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The duration of pre-existing pain in the in the fracture group varied from 3 days to 6 months (average 55 days). None of these patients received oncological input during this time period. Of these 15 patients, 12 subsequently required surgery.
Patient survival times in the operated group averaged 3 months (2 days to 9 months) – with the exception of one patient who survived for 36 months. This compared equally with survival times for the unoperated group.
Only 2/43 patients received preoperative oncology input. In the postoperative group (27 patients), 16 (59%) received radiotherapy. Of the remaining 11 patients, 9 (33%) did not receive radiotherapy due to significant postoperative complications and died within 8 weeks.
This is a retrospective study performed to analyse the functional outcome, complications and survival following intramedullary nailings for pathological fractures of long bones in a District General Hospital.
There were fifteen intramedullary nailings (Femur-11, Tibia- 2 , Humerus- 2) done in twelve patients during June 1999 and December 2002. There were twelve nailings in pathological fractures and three cases of prophylactic nailings. Nine patients had metastasis with known primary cancers from Ca Breast (3), Ca Bronchus (3), Ca Prostate (1), Ca Oesophagus (1) and Renal Cell Carcinoma (1). Two patients had metastasis without known primary site. There was one patient who had multiple myeloma with pathological fracture of femur.
We assessed the outcome of the treatment based on pain relief, post-fixation mobility and complications associated with the procedure.
Pain relief was achieved in about 92% cases. 67% cases with fracture of lower limbs were able to walk within a week postoperatively following nailing. One patient had deep infection leading to implant failure that needed nail removal to eradicate the infection. One patient had nonfatal pulmonary embolism. There was an incidence of thromboembolism of brachial artery that was treated by embolectomy without any sequelae.
The patients survival rate was 33% at six months and 0% at 2 years.
Reamings sent from nailing were helpful in confirming the diagnosis in 75% cases.
Despite poor life expectancy our results show good functional improvement following intramedullary nailing of pathological fractures of long bones. It is a safe way to restore limb function and improve quality of life.
130 consecutive patients with metastatic tumours of the extremity bones treated with resection with or without major endoprosthetic reconstruction were studied retrospectively to determine the indication for surgery, complications, clinical outcome and oncological results of treatment.
The mean age at diagnosis was 61 (22 – 84). The tumours originated from a variety of organs. Lower extremity was involved in 104 and upper extremity in 26. Metastatic disease was solitary in 55 patients and multiple in 75 at the time of surgery. The median follow-up possible from the time of operation to review was 18 months (0–103)
The indication for surgery was radical treatment of solitary metastases with curative intent in 33, pathological fracture in 46, impending fracture in 27, failure of prior fixation devices in 17, painful swelling or extremity in 37. Surgical treatment included excision of expendable bones without reconstruction in 20 patients and resection with endoprosthetic reconstruction in 110 patients. 7 patients received adjuvant chemotherapy and the majority received adjuvant radiotherapy.
At the time of review, 58 patients had died at a mean time of 23 months (0–90) from surgery (53 from progressive metastatic disease and 5 from other causes). 72 were alive at mean follow-up of 22 months (1–103) from surgery. 36 patients (28%) were alive at 2 years post-surgery and 8 (6%) at 5 years. One patient died intra-operatively. Post-operative complications occurred in 32 patients (25%). 18 patients required further surgical procedures for dislocation, infection haematoma, stiff joint, plastic surgical procedures. All the patients had control of pain and 90% achieved desired mobility.
There was no difference in the survival of patients who presented with solitary and multiple metastases, renal and non-renal metastases, and upper or lower limb metastases.
We conclude that selected patients with bone metastases can benefit from resection and major bone reconstruction with acceptable morbidity. We have not identified predictable prognostic factors in these selected patients.
Between April 1999 and December 2001 forty-one patients (forty-five femora) with metastatic lesions in the proximal femur involving intertrochanteric and subtrochanteric regions were stabilised with Proximal Femoral Nail (PFN). Thirty-eight patients (forty-two femora) were followed up for a mean period of 20 months (range 3 weeks to 35 months). There was an overall increase in mobility in 60% of the patients and the rest remained the same. Mean Preoperative Visual analog scale rating for thigh pain was 8.1 versus 3.4 for postoperative score (p< 0.01). There were no complications with respect to PFN. There were three post operative complications – chest infection, superficial wound dehiscence and pulmonary embolism. All these complications resolved without any further deterioration. Since these lesions do not usually heal well a cephalomedullary device is ideal to withstand long-term cyclic loading. Minimal operative trauma, mechanical stability, early mobilisation, pain relief and short hospital stay are the advantages of PFN in stabilising impending fractures of the proximal femur.
The weights of evidence (WE) are logs of the likelihood ratios and can be added and a probability then calculated. e.g. a 36 yr old with a 10cm, deep, painless lump that is increasing in size scores −0.39 + 0.4 + 0.4 – 0.11 + 0.58 = 0.88. This equates to a risk of the lump being malignant of 70%.
Metastatic bone disease resulting in acetabular destruction can provide the orthopaedic surgeon with the difficult challenge of achieving a stable reconstruction of the hip to provide pain relief and restoration of mobility.
We review of twenty patients with metastatic disease requiring major acetabular reconstruction presenting to our orthopaedic oncology unit over a five year period was undertaken. This yielded 15 female and 5 male patients with mean age 59 years. The primary lesion was breast (8 cases), renal (3) prostate (2), myeloma (2) and others (5) with a solitary acetabular metastasis in 75% of cases. Eight patients had received radiotherapy to the region pre-operatively.
In all cases, diseased bone was macroscopically cleared from the pelvis and reconstruction performed by means of a Harrington procedure with threaded pins passed antegrade from the iliac crest 915 cases) or mesh and screws (5 cases), all reinforced with cement around which a total hip arthroplasty was performed.
Mean follow-up was 16 months. Complications were broken pin (1 case), dislocation of femoral prosthesis (1) and deep venous thrombosis (1). Three patients died of their disease at a mean of 12 months from surgery. The remaining 17 patients continue to function at a satisfactory level with no patients having required revision surgery for loosening or deep infection.
We believe that surgical reconstruction of the acetabulum is worthwhile and can provide these deserving patients with improvement in quality of life.
In contrast to bony metastases, soft tissue metastases from carcinoma are rare. We reviewed all referrals to our Sarcoma Unit over an eight-year period, and found an incidence of soft tissue metastases from carcinoma of 1.4%. The most common mode of presentation was a painless soft tissue lump in a patient with an occult primary. Lung and kidney were the most frequent primary sources. Overall, prognosis was poor, with a mean survival of 9.4 months. Renal tumours however had a much better prognosis that other types of tumours. Treatment should be individualised according to the underlying disease and the prognosis. Although much rarer than primary soft tissue sarcomas, soft tissue metastases from carcinoma should remain a differential diagnosis in any patient presenting with a suspicious soft tissue lump.
Demographic, diagnostic, clinical, radiological and treatment data was collected on all patients.
All but one patient (Case 6) underwent radiotherapy or chemotherapy or both. Case 6 presented with a soft tissue lump over the shoulder, which on biopsy was found to be metastatic adenocarcinoma of large bowel origin. CT scan of the head confirmed multiple brain metastases. He declined any treatment and died within 2 months of presentation. In total, nine of the ten patients have died of their disease. The mean duration from diagnosis of soft tissue metastasis to death was 9.4 months (range 2–31 months). The duration of survival was significantly better for metastatic carcinoma of the kidney (23 months) compared to the other carcinomas (7 months).
Soft tissue metastases from carcinoma are rare, which again contrasts to bony metastases from carcinoma. Tolia and Whitmore (
Damron and Heiner (
All patients in our series underwent pre-operative MR scans, the appearances of which were not diagnostic of metastases, though highly suggestive of malignancy. Subsequently patients underwent either Tru-cut or open biopsy which gave the definitive diagnosis. As part of the pre-operative work-up, all patients had a CT of the chest and abdominal ultrasound scanning.
Rao et al (
Proximal femoral replacement gives reliable relief of pain and return to function in proximal femoral metastases. However, there can be technical problems with reattachment of muscles and tendons to the prosthesis, inadequate reattachment can lead to loss of function and joint stability.
We were keen to establish how effective our current method of abductor reattachment was. All the post operative x-rays of patients who had undergone Stanmore Mets Proximal Femoral Replacement, over the last 2 years at the Royal Shrewsbury and Robert Jones and Agnes Hunt Orthopaedic Hospitals, were reviewed. Particular note was made of the position of the trochanteric osteotomy, whether it remained attached or not to the prosthesis.
The Stanmore Mets Proximal Femoral Replacement has a plate which secures the trochanteric osteotomy to the prosthesis. Two screws go through the plate, osteotomy and into the prosthesis..
There were six patients, 4 male and 2 female with a mean age of 67 years. The primary carcinomas included 2 breast, 2 prostate and 1 lung and 1 renal. In five of the six patients the trochanters became detached. In 3 of the 5 patients the trochanter became detached in the first post operative week and by 2 months all 5 trochanters were detached.
We have since changed our method of attachment of the trochanteric osteotomy to the prosthesis to a hooked trochanteric plate. The plate is attached to the prosthesis by wires. Short term follow up of five patients have shown that all the trochanters have remained all attached.
Between 1972 and 2002 74 patients were treated under the combined care of the orthopaedic oncology service and lymphoma clinic with primary bone lymphoma. We reviewed the seventeen cases affecting the upper limb (23%). Of the seventeen patients nine remain alive. Assessment of the patient’s clinical presentation, histopathological definition, treatment and function outcome was made. The nine survivors were assessed clinically and with the Oxford shoulder score and the Toronto extremity salvage score.
Average time from first presentation to diagnosis was 7 months. All seventeen were diagnosed as a B –cell non-Hodgkin’s lymphoma, fifteen cases were high grade and two cases were low grade. The scapula was involved in six, humerus eight and clavicle three cases. Seven patients sustained pathological fractures three of which were at presentation; of these two were treated surgically. Eight patients have subsequently died of their disease. Functional outcome in surviving patients after medical treatment was very good with average TESS score of 79% (52%–99%) and OSS of 27 (12–52).
The presentation of lymphoma of the shoulder girdle may mimic benign shoulder conditions and lead to a delay in radiological and histopathological diagnosis. Pathological fracture is a common presentation and complication of treatment, however these fractures have a high chance of healing with medical treatment alone. Although shoulder stiffness remains a problem following medical treatment, overall upper limb function is good. There is little evidence that these patients require surgery in the short to medium term.
All cases were biopsied. 37% of these were excisional biopsies, 29% were incisional biopsies and 17% were needle biopsies. 21 patients (88%) received definitive surgery. Of these 5 had forequarter amputations (24%), 11 cases were excised marginally (52%), and 5 cases curetted (24%). Surgical choice was highly dependent on grade (X2=4.9256, p=0.005). In all cases the intent was curative.
2 patients had metastasis disease at diagnosis, and 5 developed metastases after definitive surgery. 4 patients had local recurrence (all had undergone wide local excision). All patients with grade 1 tumours remained disease free. Cumulative survival at 5 years was 57% and at 10 years 42%. Patient age did not affect survival. 5 year survival in grade 1, 2 and 3 tumours was 100%, 83% and 20% respectively. 4 of 5 patients undergoing amputation developed metastases and survival was significantly worse in the amputation group. Local recurrence in the wide local excision group did not diminish prospects for survival.
Curettage was chosen for most grade 1 and some grade 2 tumours. Although maintenance of function is far better, our study provides no evidence that curettage results in increased local recurrence rates. Indeed, local recurrence in the wide local excision group did not depress survival figures. Because of early death in the amputation group, we would recommend avoidance of amputation in favour of wide local excision in almost all cases if possible. Age alone should not be a factor in determining surgical treatment.
Retrospective analysis of 25 consecutive metal on metal proximal femoral replacements performed at our unit between 1965 and 1979.
The concentration of Cr, Co, Ti, Al, V, Mo & Ni in whole blood and urine was also measured by High-Resolution Inductively Coupled Mass Spectrometry and compared with controls and patients with other implants.
Retrieved prostheses (in situ for in excess of 25 years) were analysed for roughness and wear using a Mitutoya form tracer and an electron microscope.
In the retrieved prostheses the contact zones were found to be smoother (Ra 0.05?m), have fewer and smaller carbides together with evidence of ‘self-healing’ when compared to the original surface (Ra 0.32?m).
Blood & urine levels of Co & Cr were significantly elevated. Co levels were exceptionally elevated in loose prostheses but levels quickly fell following revision.
After resection of a malignant tumour, the options for reconstruction include the use of massive allografts. The potential benefits of allografts include the ability to shape the graft to match the defect at the time of surgery and high rates of union in metaphyseal bone. The options for fixation of allografts include intramedullary nails and plating.
The AO-LISS DF (less invasive stabilisation system for the distal femur) is a new plate designed for fractures of the femur. The screws lock into the plate and the system is thought to provide excellent purchase in metaphyseal bone. A jig allows percutaneous screw insertion.
We describe a case in which a 28 year old woman with a high grade sarcoma of the distal femur underwent reconstruction using an intercalated allograft and two LISS-DF plates. This technique allowed the knee joint to be preserved. Although the surgical approach to the femur was medial, the LISS-DF jig allowed a plate to be placed on the lateral side of the femur in a “less invasive” fashion. Although the plate is designed for application to the lateral side of the femur, in this case adequate fit on the medial side was obtained with a plate from the contralateral limb. This reconstruction provided excellent early stability at the junctions between host and allograft bone.
Growing prostheses have been utilised in the United Kingdom since the late 1970s. Various mechanisms have been tried, but to date all have required some form of surgical intervention. This has led to multiple hospital admissions and a large amount of resources, both in theatre time and rehabilitation. Over the last ten years the Department of Bio-Medical Engineering at University College, London, together with the Royal National Orthopaedic Hospital, Stanmore, have developed a prosthesis which does not require surgical intervention to elongate. The total cost of the development has been something in the order of £350,000.00. The design features are the power worm screw mechanism where one turn equals 1 mm of elongation, but attached to this mechanism is an epicyclic gearbox, which has been reduced in size so that it can fit in to the body of the prosthesis. The speed reduction achieved by the gear box is 13061 to 1. The mechanism is capable of withstanding an axial load of 1,350 newtons. When an external magnetic field is applied an external coil speed of 3,000 revs per minute leads to a lengthening of 0.23 mm per minute. To date the prosthesis has been inserted in three patients ages 11, 12 and 13. All were suffering from osteosarcoma of the distal femur and had previously received neo-adjuvant chemotherapy. Early elongation had been achieved in all patients without any major discomfort and without the need for either analgesia or inpatient admission. There had been no loss of range of movement in the early post-lengthening period.
This new prosthesis represents a significant advance in the management of skeletal sarcomas in children.
Retrospective analysis of all uncemented massive endoprostheses inserted at our unit in the management of primary bone tumours with a minimum follow up of 5 years.
The rate of infection was 12.5%, aseptic loosening 6%, amputation due to local recurrence 10% and the mortality 21%.
All the deaths occurred within 3 years of the implant being inserted and were all due to systemic progression of the disease. The amputations for local recurrence occurred throughout the follow up period, the latest being at 71 months. Revisions for infections and aseptic loosening all occurred early (within 3 years). All cases of aseptic loosening occurred in distal femoral replacements (10%) and were related to divergent canals. Proximal tibial replacements had the highest rate of infection (23%). Rates of infection were not higher in the minimally invasive grower (12.5 %) when compared to the group as a whole.
A 36 year old gentleman presented to the Metabolic Bone Disease Clinic with a progressive history of thoracic and lower limb pain. He had originally been seen by the podiatrists with worsening foot pain for which no cause had been found. Initial investigation revealed a hypophosphataemic osteomalacia and a bone scan demonstrated multiple abnormalities suggesting old fractures.
Investigations were performed to establish the cause of the osteomalacia and we discuss the differential diagnosis and the progression towards a diagnosis based on the results of these tests. The most useful investigation in this case was an octreotide scan which indicated the presence of an endocrine tumour in the medial femoral condyle of the right knee.
Plain x-rays revealed no clear bony abnormality in the area of increased uptake on the octreotide scan. The lesion was therefore localised with an MRI scan.
This subsequently demonstrated the exact location of the lesion and in image guided biopsy was performed in theatre. This confirmed the presence of a benign Phosphaturic Mesenchymal tumour. This rare tumour is usually found in soft tissues and this case is atypical given that the lesion was wholly within the femoral condyle.
Despite the benign appearance of the tumour cells there were some areas of locally invasive growth and excision rather than curettage of the tumour was recommended. It was possible to preserve both the bulk of the femoral condyle and the articular surface although the knee was protected with a hinged brace for six weeks following surgery.
Follow up biochemistry results demonstrate that the serum phosphate and alkaline phosphatase are returning to normal. Symptomatically the patient is much improved.
In view of the size of the lesions these were both fully investigated with pre-operative radiology and an image guided biopsy. The first case was found to be a large degenerate myxoid cyst involving the majority of the tibial plateau. The second case appeared similar radiologically yet was a large metastasis from a bladder cancer. The only history offered by the after this had been established was that she had had a benign polyp removed some years previously.
The aim of the study is to review the results of prophylactic reconstruction of subtrochanteric metastatic bone disease of femur using a Long Gamma Nail. Metastasis in the subtrochanteric region of femur can be challenging to treat not only due to peculiarities in biomechanics and anatomy, but also due to weak and deficient bone stock due to metastasis. Between 1996 and 2002, 28 subtrochanteric metastatic lesions of femur in 25 patients (3 bilateral) were treated with Long Gamma Nail. The outcome measures used in this study were pain relief, postoperative mobilization, and medical and implant related complications rate. There were 16 female and 9 male patients with an average age of 64 years. All patients reported marked pain relief. All but one regained pre-operative mobilization status. There were no intra-operative deaths including 3 bilateral nailings. Significant surgical and implant related complications were seen in 3(12%) patients. Postoperative medical complications were seen in 3 (12%) patients. There were no implant failures and reoperations. At the time of study 14 patients died with an average survival of 9 months and 11 patients were alive with an average survival of 16.5 months.
Long Gamma Nail is valuable reconstruction device for the prophylactic treatment of subtrochanteric metastatic bone disease of femur. It is strong, versatile and biomechanically superior to extramedullary devises and compares favourably with other intramedullary devices. In our experience Long Gamma Nail allows immediate unrestricted mobilization with marked pain relief.
A 52 year old male presented with a pathological subtrochanteric femoral fracture secondary to multiple myeloma. While stabilising the fracture with a Long Proximal Femoral Nail (PFN) distal femur fracture occurred, while introducing the distal locking screw, which was fixed with two cables. Partial weight bearing was allowed for the first six weeks.
Three months after surgery the distal static locking screw broke. Eighteen months post surgery patient developed sudden spontaneous right hip pain and was treated with further chemotherapy and radiotherapy. Radiographs showed the fracture had not healed but there was no evidence of implant failure. Two years later patient presented with sudden increase in right hip pain with inability to walk. Radiographs showed that the nail had broken at the proximal hip screw hole.
At revision surgery, with difficulty the broken distal locking screws were removed and the broken nail was removed by pushing it from below through the knee. The non union was stabilised with another long PFN. At four months post revision surgery there were radiological signs of bone healing and patient had no symptoms.
This is the first reported incidence of failure of long PFN in a pathological femoral fracture stabilisation.
Squamous cell carcinoma arising within bone is a rare lesion and is only seen essentially in the jaw and skull bones. Review of the medical literature showed that malignant change has been described in epidermoid cyst particularly in neurosurgical and orthodontic literature. However, no cases have been described in long bones as yet. Diagnosis of these tumours based on radiology and histology can be difficult and primary tumour elsewhere must be excluded. Here , a case of well differentiated squamous cell carcinoma arising from apparently a pre-existing intra-osseous epidermoid cyst in the distal tibia of a 45-year-old woman is reported. Initially treated with curettage and impact bone graft, then subsequently when the histopathology confirmed the above diagnosis, below knee amputation was performed. The differential diagnosis from other bone tumours with epithelial differentiation such as adamantinoma is discussed. This represents a rare primary neoplasm of bone of unknown histogenesis and also warns us to always try to get a histological diagnosis of what could look like clinically and radiologically a benign cyst.
Liposarcoma is the most common soft tissue sarcoma accounting for 20% of all mesenchymal malignancies.We report a rare histological variant arising from the dorsum of the foot. A 55 year old lady presented with a slow growing, well defined swelling on the dorsum of the foot. Histological examination following complete excision showed a tumor with zones of dense collagenous tissue containing pleomorphic spindle cells and scattered atypical adipocytes. A diagnosis of spindle cell sarcoma was made and referred to the local Sarcoma unit. Repeat excision and histology confirmed margins free of tumor. Four years after primary excision, patient is well with no evidence of recurrence or metastasis.
Spindle cell liposarcoma is a rare variant of well differentiated liposarcoma characterized by prominent spindle cell component. Previously reported cases originated in the subcutaneous tissues of shoulder girdle and upper limb. Main differential diagnoses include benign lesions such as spindle cell lipoma, and diffuse neurofibroma as well as dermatofibrosarcoma pro-tuberans and other malignancies such as sclerosing liposarcoma, myxofibrosarcoma, malignant peripheral nerve sheath tumor and fibromyxoid sarcoma. Spindle cell Liposarcomas tend to recur locally and may dedifferentiate with a potential for metastasis. Wide excision and long term follow up looking for recurrence and metastasis is necesssary in these rare variants of liposarcoma especially those arising at atypical sites as in our case.
A fifty year old lady with history of rheumatoid arthritis (RA) for 24 years and COPD for 10 years was admitted for investigation of persistent chest infection and for the control of RA flare-up. She was on Sulphasalazine, NSAIDs and had completed a course of gold injections and on admission started on methotrexate, folic acid, Calcium, bisphosphonates and alendronate. Urinanalysis was positive for Bence Jones’ Proteins (BJP). Four days after admission patient developed spontaneous pain in the right thigh with inability to move the right leg. Radiographs showed a supracondylar femoral fracture through a lytic lesion, which was stabilised with a Distal femoral nail. At surgery bone quality of right femur was found to be very poor. Radiographs of the left femur showed a lytic lesion in the subtrochanteric region, which was stabilised prophylactically with a Proximal Femoral Nail. Histopathological examination of the marrow reamings from right femur showed no neoplastic changes and from left femur showed occasional plasma cells. 24 hour urinanalysis showed BJP of 0.22g/hour and protein electrophoresis showed monoclonal antibodies. Bone marrow biopsy was performed which showed only reactive cells. A week later 24 hour urine BJP was down to 0.13g/hour. At three weeks, symptoms of RA were under control and the protein electrophoresis showed no monoclonal banding. Chest infection resolved with appropriate antibiotics. Computerised Tomography of chest showed bronchiectasis with no evidence of neoplasm.
A 78 year old lady attended casualty with complaints of low back pain and calf pain following a fall. Radiographs of lumbar spine did not reveal any bony injury. Clinically deep vein thrombosis (DVT) of the calf could not be excluded. Hence, venogram was performed that confirmed the diagnosis of below knee DVT. Patient was then discharged. Patient attended casualty 2 months later with complaints of sudden increase in back pain and difficulty in mictuirition. Radiographs of lumbar spine revealed a collapse of L1 vertebra. Routine blood tests were all normal except for raised International Normalised Ratio (INR), 3.5. Patient developed parapaeresis within three days. Coagulation status was controlled but no obvious primary source could be identified. After discussion with Neurosurgeons, urgent Computerised Tomography (CT) guided biopsy was arranged which was performed one week after presentation. Histopathological examination of the specimens revealed only fibrous tissue and blood. At 3 weeks after presentation patient started recovering rapidly though there was some amount of residual power loss in the lower limbs. Patient did not regain bladder control. A repeat CT guided biopsy at 6 weeks, again revealed only fibrous tissue.
This case is presented to discuss the rarer etiologies that can present as a metastatic spinal cord compression.
We reviewed 36 patients (39 shoulders) who had undergone arthroscopic Mumford procedure via a two superior portal technique for isolated acromioclavicular joint pain, using the Simple Shoulder Score (SSS) and a subjective outcome questionnaire, which included views about the cosmesis of the scars. The mean age of the 32 men and four women was 36 years (19 to 57) and 14 shoulders were on the dominant side. The mean follow-up was 22.7 months (14 to 47). Twenty-five patients reported a history of trauma, including six rugby injuries and five repetitive injuries sustained while bodybuilding.
The mean SSS was 11.5 out of 12. Subjectively 25 shoulders were rated excellent, eight good, two moderate and four poor. In 31 shoulders (79.5%) pain resolved completely. Twenty-five patients considered small scars either very important or extremely important and 33 were either extremely happy or very happy with their scars.
Arthroscopic excision of the distal clavicle via superior portals preserves the capsule-ligamentous structures stabilising the acromioclavicular joint. The procedure gives an excellent subjective outcome. Those patients with a poorer subjective outcome were older, with an increased possibility of occult shoulder pathology.
The results of arthroscopic repair of tears of the sub-scapularis tendon in nine men and six women, ranging in age from 53 to 73 years, were followed up at a mean of 14 months (6 to 24). Three were complete tears, six 50%-tears and six 30%-tears. In seven patients there were associated tears of the supraspinatus and infraspinatus tendons, which were repaired arthroscopically during the same procedure.
In each case the subscapularis tear was identified. In most patients a biceps tenotomy was necessary. The subscapularis footprint was prepared and the tendon was repaired using one or two anchors, each with two sutures, depending on the size of the tear. The mean pre-operative and postoperative Constant scores were 48 and 88 respectively.
In most patients, power returned to almost normal and pain was almost completely relieved. Arthroscopic subscapularis repair is a relatively new procedure and seems to give good results.
The outcome of the shoulder Delta prosthesis in 22 men and nine women was prospectively studied. The mean age was 74 years (62 to 86). Indications for surgery were cuff deficient arthritis (18), fracture malunion (three), ‘pseudo-paralysis’ (six) and failed total prostheses (four). The mean preoperative Constant score of 39 increased to 69 (10 to 39) at 33 months postoperatively, with the major increases in the scores for active forward elevation and pain relief. The subjective satisfaction was 79%. Although this was a small series with a short follow-up, early results seem satisfactory.
This study retrospectively reviewed the pathology after the first traumatic incident of shoulder subluxation or dislocation in 12 male and four female patients with a mean age of 14.9 years (12 to 16). All had undergone surgery and were seen over a five-year period. Patients seen after a second traumatic dislocation were excluded.
All patients had been treated conservatively for between 4 and 18 months. When conservative treatment failed, all patients underwent examination and shoulder arthroscopy. All 16 had Hill-Sachs lesions of varying degrees. Bankart repairs were done in 14 patients with Bankart lesions. Two patients had more than 25% bone loss of the glenoid, and Latarjet procedures were undertaken. One SLAP-III and three SLAP-II repairs were done. The follow-up period varied from three months to five years.
All patients were either examined or interviewed by telephone. Failures were defined as recurrence of symptoms or redislocations. All patients resumed their sporting activities at similar or higher levels. Two patients with multidirectional shoulder laxity had further possible subluxations but were treated conservatively. One sustained a massive bony Bankart lesion a year after a Bankart repair and a Latarjet procedure was subsequently performed.
Patients in this age group should be considered at high risk for recurrence. If intensive short-term rehabilitation fails, they should be managed surgically immediately.
This paper retrospectively reviews the type and outcome of shoulder surgery in 61 professional rugby players (mean age 24.7 years). All competed at provincial level or higher, with 20 competing internationally. Forty-three of the patients played the position of forward, while 33 played back. Most shoulders (41) were on the dominant side. Ten players had multiple procedures and over a seven-year period 76 procedures were performed. The procedures included 16 Latarjets, four arthroscopic stabilisations, four SLAP repairs, four arthroscopic shoulder decompressions, three biceps tenodeses, three HAGL repairs, two revision Latarjets, one posterior Bankart, one pectoralis major repair, one Weaver-Dunn and four combination procedures.
All but two players returned to their previous level of competition. The mean time to return to full contact participation was 3.6 months (1 to 12). The time to return was one month for an arthroscopic Mumford and six months for a stabilisation procedure.
Over a six-year period, one surgeon operated on 46 men with instability associated with antero-inferior glenoid loss. Thirty-three of them played rugby at a competitive level. The mean number of preoperative dislocations was five (2 to 22). Modifications included a change in orientation of the coracoid bone block and the addition of capsular closure.
A Walch-Duplay score for instability was calculated at follow-up. The mean follow-up was 38 months with a minimum of 6 months. Only one patient had recurrent instability. Thirty-one returned to sport at the same level. Walch-Duplay scores were excellent in 70%, good in 25%, mild in 3.75% and poor in 1.25%. Complications included two fibrous unions (excellent outcome), three broken screws (excellent outcome) and two fixation failures owing to patient non-compliance.
There was no decrease in the range of internal rotation. Eight patients had mild restriction in forward flexion (mean 5°) and 20 patients had mildly reduced external rotation at 90° abduction (mean 5°). All but one patient with recurrent dislocation rated the outcome excellent and would have the operation again. The Latarjet procedure confers outstanding stability and gives excellent subjective and objective outcomes.
Over one year a bio-absorbable corkscrew was used in 19 rotator cuff repairs in 17 patients (10 men and seven women) with a mean age of 52 years (25 to 68). Seven were partial thickness tears. The 12 full thickness tears involved only the supraspinatus in all but four patients. Open surgery was performed on these four patients, who had an isolated subscapularis tear, an isolated teres minor tear, a combined supraspinatus and infraspinatus tear and a combined supraspinatus, infraspinatus and subscapularis tear. The remaining patients underwent arthroscopic repair. All patients had an acromioplasty and 13 had the acromioclavicular joint excised. Two patients had a concomitant SLAP repair. One corkscrew was used in 10 cases, two in six and three in two.
The mean follow-up was 8 months (3 to 24). The mean Constant score at follow-up was 80. There were five complications (26%) in which the corkscrew or a fragment of it came loose in the subacromial space. Two patients required further surgery to remove the corkscrew.
The corkscrew was found to be a useful device for rotator cuff repairs, but the complication rate was high.
Of 81 elbow replacements performed over a seven-year period, 11 were total elbow revision (TER) procedures, which were done on two men and nine women with a mean age of 61 years (40 to 70). Seven of the patients had rheumatoid arthritis, three had post-traumatic osteoarthritis and one had haemophilia. The reason for revision was aseptic loosening in eight patients and aseptic loosening with fracture in the other three. The prostheses revised were the Souter in eight patients, the Kudo in one, the GSB I in one and the Dee in one. In revision TER, one long stem Souter prosthesis was used, two Pretoria, one GSB 3 and seven Morrey. The mean time from primary to revision TER was 10 years (2 to 31).
At a mean follow-up of 30 months (6 to 48), all except one patient were pain-free and the arc of flexion had increased by 30°. Complications included one dislocation, one radial nerve palsy, which recovered after six months, and one aseptic loosening. There were no cases of sepsis.
Revision TER is a technically demanding procedure with a high risk of complications. In this series patient satisfaction was high. Our policy is to use a hinged prosthesis, preferably the Morrey, in revision TER.
This is a retrospective review and analysis of cases of tennis elbow or lateral epicondylitis treated from 1996 to 2002. Of 191 patients treated, only 150 were contactable. These were sent self-administered Disabilities of the Arm, Shoulder, and Hand (DASH) questionnaires, which 55% patients returned completed. The rest of the patients were interviewed telephonically. Treated conservatively with avoidance of painful activities,non-steroidal anti-inflammatory medication, steroid injection, bracing, and physiotherapy, 83% of patients responded favourably and did not require surgical treatment. DASH scores ranged from 38 to 105 (mean disability < 12%) and compared favourably with those reported in the literature.
Conservative treatment of lateral epicondylitis is usually successful and minimal residual disability can be anticipated. The few patients who fail to respond to conservative treatment can be salvaged predictably with low residual disability.
This study looks at the outcomes of 112 full thickness rotator cuff tears treated by arthroscopic decompression, without repair of the rotator cuff, from 1994. The decision not to repair the tear was taken only if four criteria were met. First, if there was no clinical weakness on manual testing of the individual rotator cuff muscles, secondly, if there was full abduction, thirdly, if there was no riding up of the humeral head on the anteroposterior radiograph and fourthly, if there was well-developed ‘cable’ on arthroscopic visualisation of the rotator cuff.
The mean age of the patients, 38% of whom were men, was 62 years (47 to 83). In 44% the right shoulder was operated on. There were 32% type-II acromions and 68% type-III. There were 58% C2 tears and 42% C3 tears. All had arthroscopic acromioplasty and acromioclavicular joint excision. Later, three required an open acromioclavicular joint excision with one open cuff repair. At a mean follow-up time of 71 months (11 to 110), the clinical and surgical notes and radiographs were reviewed and a modified Simple Shoulder Test (SST) used to evaluate outcomes by telephone. The mean postoperative SST was 11.5 out of 12 (3 to 12). Complete relief was reported in 84% of cases. These subjective results suggest that, with careful selection, not all full thickness tears of the rotator cuff need repair.
From two orthopaedic theatres at Pretoria Academic Hospital 28 samples were randomly selected, including Hibiscrub soap dispensers and both fully-sealed and partially-used bottles of iodine/alcohol, Hibitane/alcohol and Hibitane/water. Samples were taken from the solutions and the bottlenecks and basic microbiological cultures were done. Only the Hibitane/water bottles yielded positive cultures, with Bacillus species cultured from three out of four.
We concluded from this small random study that with the exception of Hibitane/water mixtures it should be safe to use the same bottle of solution in different cases.
This was a prospective study to evaluate the changes in bacterial colonisation of the skin during hospital admission for elective surgery. It involved 48 patients who were admitted the day before surgery to Pretoria Academic and Pretoria East Hospitals. Within two hours of admission, cotton-tipped pus swabs were used to obtain samples from 56 skin sites in 48 patients. Postoperative specimens were obtained the day after surgery. The pre-operative cultures revealed a 73% Coagulase Negative Staphylococcus (CNS). Postoperative cultures revealed a 63% CNS. Preoperative methicillin resistance of the CNS was 6% and postoperative resistance to 49% (p < 0.01). The resistance of the organism to Cefazolin increased from 11% to 37%.
This study clearly indicates that multiple drug-resistant organisms colonise the skin of patients in the perioperative hospital stay. The postoperative rise in methicillin resistance of the CNS was alarming. Questions arising from this study include optimal admission time, length of postoperative stay, choice of perioperative antibiotic, use of occlusive dressings to prevent colonisation of wound site and routine screening for Methicillin-resistant CNS skin contaminants.
Over 40 months, 264 arthroscopic rotator cuff repairs were assessed prospectively. Preoperatively all patients were assessed using a modified Constant score and Visual Analogue Pain Scale (VAPS). The mean age at surgery was 59 years (19 to 83). In 151 cases (62%) the shoulders were on the dominant side. All patients underwent postoperative ultrasonography to assess cuff integrity at three weeks. Twenty-two patients were lost to follow-up. Of the rest, 210 were clinically reviewed and Constant scores produced. The remaining 32 were assessed using the VAPS and a subjective satisfaction questionnaire.
The Constant score improved by a mean of 29.6, with 166 patients (69%) reporting complete resolution of pain. The subjective outcome was rated excellent by 162 patients, good by 55, moderate by 20 and poor by five. There were 13 retears, 11 of which were identified on the three-week ultrasound. When four of these were revised, two required subscapularis repair. Importantly, five patients with retears had excellent subjective outcome. Complications were five superficial infections, 13 cases of transient neuritis following interscalene nerve blocks, four cases of bursitis, which required debridement and suture removal, and two anchor pull-outs. The overall reoperation rate was 4%.
Arthroscopic rotator cuff repair offers excellent objective and subjective outcomes, particularly pain relief. Ultrasonography at three weeks is a good indicator of whether or not a repair has taken.
In this prospective study of partial articular supraspinatus tendon avulsion (PASTA) lesions treated arthroscopically by an ‘all inside’ method, 12 patients (nine men and three women) with a mean age of 31 years (22 to 36) were followed up for a mean of 16 months (8 to 32). The deep partial rotator cuff tears were usually viewed from the glenohumeral joint side. Viewing the subacromial space usually revealed an entirely normal cuff with no sign of subacromial impingement. With the arthro-scope in the glenohumeral joint, the footprint area of the supraspinatus tendon was prepared and one or two anchors, each preloaded with two sutures, were passed through the rotator cuff into the footprint area of the greater tuberosity. The sutures attached to these anchors were passed through the tendon and tied in the subacromial space.
The Constant score improved from a preoperative mean of 72 to a postoperative mean of 91. The greatest increase was in power and overhead motion, especially abduction and external rotation.
PASTA lesions are difficult to diagnose, even with MRI. The ‘all inside’ method of arthroscopic repair obviates the need to detach intact fibres.
This study was undertaken to determine the most effective way of treating intracapsular femoral neck fractures in HIV-positive patients. Ten patients with a mean age of 36 years were treated. Excision Girdlestone was performed In three patients in whom previous internal fixation had failed: all had poor nutritional status and low CD4 counts (mean 162). Three patients with undis-placed fractures were treated with percutaneous AO screws and a dynamic hip screw. In the remaining four patients, total hip arthroplasty (THA) was performed. At a mean follow-up of 14 months, all patients were fully ambulant with no signs of infection.
The decision to proceed with THA in HIV-positive patients should be made only after weighing the ratio of risks and benefits. The ultimate outcome depends on a number of factors, including displacement of fractures, previous surgery, co-existent medical problems, nutritional status and the stage of the disease.
Over 13 months we prospectively monitored C-Reactive Protein (CRP) to assess surgical site infection (SSI) in 148 patients undergoing hip arthroplasty, including 34 hemiprostheses for femoral neck fracture, 35 hemiprostheses for osteosynthesis failure, 17 primary total hip arthroplasties (THAs) and 62 revisions of hemi-arthroplasty or THA. Ten patients who had probably had interaction with CRP were included.
In four out of seven patients with SSI, CRP values peaked three days after the operation, compared to eight out of 131 without SSI (p =0.0001). This gives a 60% sensitivity for detecting SSI by the CRP curve, with a specificity of 94%. The positive predictive value was 33%, and the negative predictive value 98%.
Previous studies have established the normal CRP curve after major joint replacement surgery. This study shows that a peak in CRP after day three may indicate SSI, or point to other deep infections such as pneumonia.
Over a four-year period, nine patients with tuberculosis of the wrist were treated. The mean time to diagnosis was 5 months (1 to 20). Restricted wrist motion and an increased sedimentation rate were universal. Swelling, pain on motion and severe restriction of metacarpopha-langeal joint flexion, especially in patients with extensor involvement were common. In three patients, the disease involved the carpal bones, while in five it was limited to the tenosynovium. One patient had a cold abscess not involving tendon, sheath or bone. Granulomatous inflammation on the paraffin section was seen in most patients. Only four had a positive tissue culture of Mycobacterium tuberculosis.
These patients were treated either medially or surgically. In the group treated medically, an incisional biopsy was done and antituberculous chemotherapy administered for a minimum of six months. In the group treated surgically, surgical synovectomy and debridement were done and antituberculous drugs administered. All patients had a brief period of splintage followed by intensive physiotherapy.
At a mean follow-up of 12 months (6 to 24) all patients showed improvement in symptoms, with an increased range of motion. At final follow-up 50% of the patients had some residual loss of wrist motion. Those with extensor involvement seldom regained functional metacarpophalangeal joint flexion. The results showed no recurrence of infection in this study. The treatment resulted in good recovery of function, with low morbidity.
This is a retrospective study of 14 cases from clinical records and the Bone Tumour Registry over the last 20 years. The mean follow-up time was 27 months (3 to 60). Two of the cases were referred elsewhere for final treatment and the relevant clinical records were obtained by correspondence with the treating doctor. Most tumours occurred about the knee, with two in the distal femur and five involving the proximal tibial metaphysis. Three were in the forearm and one in the humerus.
Once diagnosis had been made on clinical and radiological grounds, the tumours were curetted. Cryosurgery was used in four cases and phenol in two. Structural integrity was restored by autogenous bone grafting in most cases. Two of these were vascularised free grafts. Two patients had arthrodeses (one ischiofemoral and one wrist) and two were referred for custom-made joint replacements. There was only one local recurrence. Of the adverse outcomes, three required late amputations, one for varus malunion and recurrence, and two for nonunion and chronic sepsis.
Giant cell tumour of bone has a low rate of recurrence. The treatment challenge is to avoid sepsis and graft collapse. Large bone grafts often fail to incorporate fully, which can lead to angular deformities. A combination of bone cement, reinforced with Ender rods with bone cement to the subchondral surface, promises to be a more satisfactory method in and around the knee.
To try to find a solution to the high complication rate associated with harvesting bone graft from the iliac crest, a retrospective and prospective study was undertaken to document bone grafting from the proximal tibia in 37 adult patients undergoing a variety of foot procedures. The hospital charts of 17 patients were evaluated retrospectively for complications (mean follow-up of 27 months), while 20 patients were assessed prospectively by means of a questionnaire (mean follow-up of 7 months). There was an overall complication rate of 10.8%, 5.8% in the retrospective group and 15% in the prospective group. All complications were minor and resolved.
Although our overall complication rate is slightly higher than in similar studies, ours is the only prospective study that actively followed the healing of patients’ donor sites. We recommend the proximal tibia as an alternative harvest site. Contrary to popular belief, the proximal tibia provides a large volume of cancellous graft material.
Between January 1998 and December 2002, 418 hip revisions were performed. Of these, 45 hips were diagnosed as infected and two-stage revisions were done six weeks apart. These were excluded from the study, leaving 373 revisions for mechanical failure. In 310 cases both components were exchanged, in 59 the acetabular prostheses only and in three the stem only. One permanent resection arthroplasty was done for bone loss. Where necessary bone graft was used liberally. In 83 patients (22%) specimens taken at surgery cultured positive.
A first generation cephalosporin was given as systemic prophylaxis. Routine usage of Gentamycin was reinforced by Vancomycin or fucidic acid in the cement and bone grafts. Double lumen irrigation was inserted in only 5% of cases on the basis of operative findings. Gram stains done intraoperatively in suspected cases were non-contributory. Seventy-six percent of cultures were gram positive, with a preponderance of coagulase negative staphylococcus. Twelve percent were gram negative and 12% were mixed cultures of gram positive and gram negative organisms. One methicillin-resistant Staphylococcus aureus and one fungus were identified. As most of these patients were referred from elsewhere, we did not know whether or not Gentamycin had been used in the cement during previous surgery.
Implant failure due to low-grade infection was under-diagnosed in this series. Because of the relatively low number of failures caused by infection in this group, we recommend, with some improvements, the revision protocol presented. The expense of more detailed preoperative evaluation should be weighed against the success of the protocol.
From May 2002 to April 2003, a prospective, non-randomised, blinded study was undertaken in 30 patients with fractures of the femur and tibia, all treated with unreamed intramedullary (AO) nail fixation. There were 17 (57%) femoral shaft fractures and 13 (43%) tibial shaft fractures. Most of the patients (23) had been injured in road findings accidents, 17 of them pedestrian. No patient had any known co-morbidities.
Fourteen patients (47%) were HIV positive, nine with femoral fractures and five with tibial fractures. Three patients with compound femoral fractures were HIV positive, two HIV negative. The mean age of HIV-positive patients with femoral shaft fractures, two men and seven women, was 33 years (18 to 48). The mean age of the eight HIV-negative men with femoral shaft fractures was 28 years. Five tibial fractures were compound, three in HIV-positive patients and two in HIV-negative patients. The mean age of HIV-positive patients with tibial fractures, three men and two women, was 31 years (18 to 56). The mean age of the HIV-negative patients, seven men and one woman, was 28 years. All the fractures were Gustillo-Anderson grade- II.
At 12 weeks, 29 fractures had united. In one HIV-positive patient with a compound tibial fracture there were no radiological signs of union at 12 weeks, but after bone grafting the fracture united uneventfully. An HIV-positive patient, who had sustained a gunshot femur injury, developed deep wound infection four months after fixation. In all other patients, the wounds healed uneventfully. In asymptomatic HIV-positive patients, wound healing and fracture union rates are comparable with those of HIV-negative patients.
The aim of this retrospective study was to compare the rate of recovery and eventual level of function following total hip arthroplasty (THA) and hip resurfacing. Participants were 47 patients who had undergone THA and 43 who had undergone hip resurfacing. In all cases medical records were reviewed and function assessed, using the Harris hip score, visual assessment of gait and a functional score.
The rate of recovery, as measured by functional activities and range of motion, was notably better in patients who underwent hip resurfacing than in patients who underwent THA. No significant discrepancy was found in the presence of deformity and the levels of postoperative pain following either procedure.
We conclude that the hip resurfacing procedure may have important advantages over conventional THA, including more rapid mobilisation, higher levels of final function, increased range of motion, less physical limitation and shorter hospital stays. An important advantage is that the hip resurfacing procedure allows patients to resume work and sport earlier.
This study evaluated the early results of a new and minimally invasive posterior gluteus maximus splitting approach for total hip arthroplasty (THA) and metal-on-metal (MOM) resurfacing. The approach was used to do 30 THAs through an incision of mean length 7.5 cm and 20 MOM resurfacing procedures through an incision of mean length 8.8 cm. Intraoperative fluoroscopy was not used.
The results were compared retrospectively with a matched control group in which the conventional posterior approach had been used. The mean length of the incision in the control group was 20.5 cm. The groups were not significantly different in respect of body mass index (BMI), preoperative Oxford hip scores, estimated blood loss, or length of hospital stay. BMI was less than 33 in both groups. There was no infection, nerve palsy component malposition or dislocation. Postoperative scores were not significantly different. Patients who underwent minimally invasive hip surgery expressed great satisfaction with the cosmetic appearance of the surgical incision.
THA and MOM resurfacing can be done safely through this approach, with excellent early results and no complications.
In this study, 40 patients who underwent total hip arthroplasty (THA) and had a history of previous steroid injections were compared retrospectively with 40 carefully matched patients who underwent THA in the same period but had never received steroid injections. The development of sepsis under standard care was one of the outcome measures. This occurred in 20% of steroid patients within the first 36 months after THA, compared to 0% in the control group. Further, in a detailed analysis of Harris and Oxford scores, patients treated with steroid had a higher incidence of night pain, more severe pain, and greater loss of function in activities of daily living at one year. There were two revisions for deep infection in the steroid and control groups.
Based on the incidence of pain and infectious complications in the first postoperative year, and pending completion of the study, we provisionally suggest that steroid injection of hips may be ill advised in patients who are likely candidates for future THA.
This is an overview of South African iliac crest bone histomorphometric findings. The examination Bone in health: a study of 346 healthy black and white South African subjects revealed thicker trabeculae and greater osteoid and erosion values in blacks. If this finding reflects greater bone turnover, then bone in blacks would be renewed more frequently and be less prone to fatigue failure. The finding of higher bone marrow cellularity in blacks is in keeping with greater bone turnover. Greater bone turnover and sturdier micro architecture may contribute to the lower fragility fracture rates in blacks.
Bone disease in black teenagers is discussed. Rickets, due to dietary calcium deficiency, is associated with grotesque limb deformities and severe osteomalacia (OM). Dietary calcium deficiency was found to aggravate Rickets in endemic fluorosis. Genu valgum and varum deformities were also found to be attributable to dietary calcium deficiency. Some patients developed nutritional secondary hypoparathyroidism before going on to OM. The most severe OM was seen in boys aged 16 to 19 years. Teenagers with slipped upper femoral epiphysis were found to be osteopoenic. This may explain why the slip in blacks is more severe and more frequently bilateral than in whites.
In black adults, African haemosiderosis (from traditional beer brewed in iron pots) was found to be associated with increased erosion depth and disconnection of the trabecular network. Bone formation was not impaired. Alcohol bone disease, on the other hand, showed predominantly osteoblast impairment. Patients with femoral neck fractures (FNF) had both haemosiderosis and alcohol bone disease. FNFs were found in younger black patients than white and were predominantly in males. The osteoporosis was also more severe and OM was not seen.
This was an international single blind phase-III study of patients undergoing orthopaedic surgery to assess the efficacy and safety of HBOC-201. Patients who were expected to require two or more units of red blood cells (RBC) were randomised to HBOC-201 or RBC. Efficacy was defined as the proportion of patients in the HBOC-201 group who did not receive RBC. The HBOC-201 group comprised 350 patients and the RBC group 338. At randomisation, mean haemoglobin levels were similar (~9 g/dl) in the two groups (p =0.760). In the HBOC-201 group, transfusion was avoided in 337 patients (96.3%) on day one, 246 patients (70.3%) through day seven, and 208 patients (59.4%) through day 42. Fewer units of allogeneic red cell units were administered in the HBOC-201 group than in the RBC group, namely 1.4 units v 3.1 units (p < 0.001).
Adverse events in the HBOC-201 group were transient and mild in intensity and did not result in discontinuation of HBOC-201. There was no significant difference in mortality between the groups (p.=0.450). The efficacy of HBOC-201 was demonstrated by the avoidance of allogeneic RBC in about 60% of patients receiving this oxygen-carrying solution over a six-week period. HBOC-201 was well tolerated and appears to be a feasible alternative to RBC.
We operated on five men and seven women, aged 17 to 48 years, for avascular necrosis of the femoral head. Eleven had subchondral collapse and one Calvé-Legg Perthes’ disease. The hip was dislocated through an anterolateral approach. The cartilage over the necrotic area was elevated as a flap with the base towards fovea capitis femoris. The necrotic/cystic area was debrided and channels were drilled into well-perfused bone. Autologous bone from the iliac crest was transplanted, slightly overcorrecting the defect. The cartilage flap was sutured back and the hip relocated.
Postoperatively patients were limited to 15 kg of weight-bearing for 12 weeks and then gradually resumed full weight-bearing over six weeks. Follow-up ranged from three months to three years. No patients have been operated on again and no major complication has occurred. Preoperatively the mean joint space was 4.3 mm (3 to 5 mm); at the last follow-up, it was 3.9 mm (2.3 to 5 mm). The roundness of the femoral head was judged better postoperatively than preoperatively. No patient has so far been scheduled for arthroplasty, but two patients have had relapses of more severe pain.
The Trap Door procedure may postpone the need for arthroplasty in patients with avascular necrosis of the femoral head. Our initial results have been encouraging, but further follow-up is required.
This study reviews the short-term results of 36 hip resurfacings performed to treat avascular necrosis (AVN) of the femoral head over a four-year period. The mean age of the 32 patients, 30 men and two women, was 41 years (25 to 50). Treatment options were discussed with patients, who usually preferred resurfacing to osteotomy, vascular fibular grafting, or total hip arthroplasty. No hips were revised, but in one patient both hips will probably be revised because of symptoms arising from anterior impingement between the femoral neck and acetabular cup rim. The other patients had no or minimal symptoms. One manual labourer and one truck driver (the patient with symptoms of impingement) have been unable to resume their previous work. Another manual labourer returned to permanent light duty. All the others resumed levels of work and sports activity comparable to their previous activities.
Resurfacing of the hip is generally advocated for young, active patients. It is therefore an option for treatment of AVN, which typically occurs in the fourth and fifth decades, most commonly in physically and economically active males.
This paper looks at technical details and other issues in 30 primary total hip arthroplasty procedures performed through a direct lateral exposure in which the skin incision was limited according to the preoperatively templated acetabular component external diameter (D), using a formula D/2 + 1cm. All patients were positioned in the lateral decubitis position and stabilised with a vacuum beanbag.
Unpaired t-tests were used to determine difference in outcome between these patients and those operated on conventionally. No differences were noted between the two groups with regard to preoperative diagnosis, Oxford Hip Score, Harris Hip Score, demographic details, and body mass index. No statistically significant differences were noted with regard to operation time, blood loss, postoperative narcotic requirements, time to mobilise, length of hospital stay, postoperative complications and six-week postoperative Harris Hip and Oxford Hip functional outcome scores.
The mini-incision technique does not appear to carry short-term advantages for the patients. We did not encounter technical problems, but the mini-exposure does create technical challenges that could potentially have an adverse effect on the ultimate outcome. We do not advocate its use.
In a prospective study we assessed the accuracy of 3D-CT in defining the acetabular deficiency in developmental dysplasia of the hip (DDH), comparing pre-operative 3D-CT with plain radiographs, intraoperative stability testing and intraoperative acetabular morphology.
Twenty children (25 hips) with DDH who had open reduction and/or pelvic osteotomy from 1999 to 2001 were studied. On 3C-CT the morphology of the deficiency was described as normal, anterolateral deficient (overlapping shadows), lateral (increased acetabular index only) and global (double acetabulum). At open reduction, the position in which the hip was most stable with axial loading was assessed (Zadeh and Caterall, 2001). The surgeon’s assessment of the acetabular morphology intraoperatively was the standard against which the other modalities were tested. One hip was normal, five had a global and 19 an anterolateral deficiency.
3D-CT correlated well with the acetabular morphology (84%). Plain radiography correlated poorly, especially with the global type (60%). Mid-superior appearance on 3D-CT and lateral appearance on plain radiograph equated with an anterolateral deficiency morphologically. In the global type the hip was unstable in all positions, while the anterolateral type, while in the anterolateral type the hip was always stable in flexion and abduction and in only 31% of hips stable also in abduction and internal rotation.
The mean age at surgery was 3 years (1 to 7). The one hip with a normal acetabulum required open reduction only, the five global types an acetabuloplasty (Tonnis), and the 19 hips with anterolateral deficiency a redirectional (Salter) osteotomy.
3D-CT is helpful in appropriate osteotomy for a specific type of acetabular deficiency in DDH.
The first 100 consecutive patients with cups inserted a minimum of 10 years ago were recalled and assessed clinically and radiologically. Fixation of the cups was excellent, with no loosening or migration. One liner was replaced because of wear and granuloma formation. The granuloma was curetted and allograft impacted. The patient recovered rapidly and the bone graft showed evidence of incorporation with remodelling after a year. One liner was revised following dislocation and instability. There were no further episodes of dislocation. Five liners had wear of more than 0.2 mm per year. Surprisingly, this occurred not in the patients who were very active but in the patients with smaller cups, where the liner thickness was less than 8 mm.
There was excellent fixation at 10 years. Wear remains a concern, however, and we now recommend that a 22-mm head be used in cups smaller than 52 mm. This ensures polyethylene thickness of at least 9 mm, which will improve wear properties.
From 1999 to 2002, eight children, ranging in age from 2 to 12 years, were treated for acute septic arthritis of the hip by arthroscopic debridement. The hip was initially aspirated under image control and distended with clear saline and a routine medium, or a small joint arthro-scope was introduced into the joint. The hip was irrigated and a suction drain inserted. All patients who presented early did well; those presenting later had a poor result. The functional recovery rate was faster than with the classical arthrotomy. Arthroscopic drainage may be a valuable tool in the treatment of acute septic arthritis.
We retrospectively reviewed 45 children treated between 1987 and 2002. Their mean age was 9 years (3 to 13). Fifteen patients had subacute osteitis. Only patients with Bledhill and Roberts type II, III and IV were included. Biopsy provided histological proof of subacute osteitis in nine patients, and six were successfully treated non-surgically with flucloxacillin. Six patients had Ewing’s sarcoma, 24 had osteosarcoma, 23 Enneking stage-IIB (extracompartmental) and one Enneking stage-IIA (intracompartmental).
The preoperative clinical signs, radiographs and MRI studies were reviewed. On plain radiographs, cortical destruction and periosteal reaction were assessed. On MRI the extent and nature of bone marrow involvement and the size of the soft tissue mass/oedema was analysed and correlated clinically. On plain radiographs, cortical destruction was present in all patients with Ewing’s sarcoma and stage-IIB osteosarcoma and in 50% of patients with subacute osteitis. An ill-defined zone of transition was found in all patients with Ewing’s sarcoma and osteosarcoma and in 50% of those with subacute osteitis. These findings therefore did not help to differentiate between the two groups.
The periosteal reaction was well-defined in subacute osteitis and lucencies between laminations were thin. In the malignant group the periosteal reaction was always ill-defined, with or without a Codman’s triangle, sunray spicules and hair-on-end. Lucencies between laminations were broad and broken. This was useful in differentiating between the two groups.
On MRI, patients with subacute osteitis had no soft tissue mass, with an infiltrative type of bone marrow involvement. In the malignant group, the soft tissue mass was large and the bone marrow involvement well demarcated.
We concluded that where there was a well-defined periosteal reaction on plain radiographs, and no soft tissue mass with infiltrative bone marrow involvement on MRI, patients could initially be treated as subacute osteitis without biopsy.
This is an ongoing retrospective study of 35 children treated from 1986 to 2001 for chronic osteomyelitis following acute haematogenous osteomyelitis. The purpose was to validate the use of a modified Cierny classification to predict behaviour, to assess the timing of sequestrectomy in relation to involucrum formation, and to evaluate the results of dealing with the resultant defect by conventional methods of bone grafting.
The mean age of the patients was 7 years (1 to 12). All except 18, who were treated within five days of acute onset, were delayed presentations or transfers. In 14 children the tibia was involved, in 13 the femur, in five the humerus and in three the fibula. Monthly radiographs were taken and the size and location of the sequestrum and involucrum was documented.
Our classification represents the size and location of the sequestrum. We divided the patients into cortical (one), medullary (three), corticomedullary (12) and structural (19) types. Fractures occurred in all the structural types, as well as in five of the 12 corticomedullary types. A sequestrum was apparent at a mean of 2.4 months (1 to 3). The mean length of the sequestrum at diagnosis was 8.5 cm and at surgery 5.8 cm, suggesting partial resorption. Involucrum formed in 69% of patients at a mean of 1.9 months (1 to 3) after sequestrum. In 31% of patients no involucrum formed from 4 to 12 months after surgery. This suggests that involucrum formation depends on viable periosteum and not on the sequestrum, and in the absence of involucrum early rather than late sequestrectomy is warranted.
The resultant incomplete bone defects in the corticomedullary type ranged from 1 cm to 15 cm, but had an intact cortical bed on one or more sides. These and complete defects of less than 6 cm in the structural type united after autogenous cancellous bone grafting, with or without an exoskeleton. Four structural defects greater than 6 cm united after fibular strut grafting (humerus) or bone grafting from fibula to tibia via a posterolateral approach (tibia).
Patients were followed up both clinically and radiologically for a mean of 2.9 years. Twenty patients (57%) had an excellent result and 15 (43%) a good result.
At Sheffield Children’s Hospital 40 children with leg length discrepancies (caused variously by sepsis, trauma, hemihypertrophy, congenital longitudinal deficiencies) were assessed using three clinical methods: measuring blocks in the standing erect position, supine measurement from the anterior superior iliac spine to the medial malleolus, and prone measurement with the knees flexed, which allowed separate measurement of femoral and tibial discrepancies. All were then subjected to comparative CT scanogram.
The mean age of the 24 boys and 16 girls was 10 years (5 to 16). Children with abnormal pelvic architecture or a fixed pelvic obliquity were excluded from the study. The mean clinical length discrepancy was 29 mm (0 to 80 mm). The mean CT scanogram measurement was 26.4 mm (0 to 75 mm). The mean difference between clinical measurements taken prone and CT scanogram measurements was only 3.6 mm (0 to 14). There was little difference in the accuracy of measuring femoral and tibial discrepancies clinically or by CT scanogram. The prone method of measurements is a useful adjunct to Staheli’s rotational profile in the prone position.
This was a retrospective study of all patients with soccer injuries admitted to our orthopaedic unit over 42 months. Patients treated as outpatients were assessed for purposes of comparison.
Thirty-two patients were admitted with severe injuries, including 18 fractures of the tibial and femoral shaft. Two tibial shaft fractures were compound. There were four tibial plateau fractures and five epiphyseal injuries. One patient had a fracture dislocation of the hip. One patient with a popliteal artery injury, who presented 48 hours after a soccer injury, underwent an above-knee amputation. In the same period, 122 patients were treated as outpatients.
The types of injuries in this group were similar to soccer injuries reported in other countries. Very serious injuries are sustained in community soccer players in South Africa and urgent measures need to be taken to prevent such injuries.
Seven children, aged four to nine years, underwent fibular transfer between 1990 and 2002. Five had chronic osteomyelitis and two had septic compound fractures. Bone defects measured 5 cm to 20 cm. Reconstruction was performed in two stages. Debridement, sequestrectomy, and Gentamycin bead insertion were performed first. Two children required skin grafting and one a gastrocnemius flap.
Fibular transfer was performed as a second stage at four to six weeks, when infection was cleared. Through an anterolateral approach the fibula was divided proximally below the physis and transferred from the lateral to the anterior compartment deep to the tibialis anterior muscle belly. The fibula was fixed with screws to the lateral tibial metaphysis in two children, and placed into the medullary canal and fixed with wires in four. Distal procedures were performed in five children.
Patients were immobilised in a cast for three to six months until bone healing occurred, after which the bone was supported with a calliper. Follow-up ranged from 11 months to 13 years. All transfers united to the proximal tibia by 12 weeks. Fibular hypertrophy occurred in all children. There was shortening of 3 cm to 10 cm. Equinus deformity occurred in two children and varus of the ankle in three. All are ambulant with boots and crutches.
Fibular transfer is a useful salvage procedure and an alternative to ablation in severe tibial infections with defects. It has a free blood supply and hypertrophies with weight-bearing.
We retrospectively reviewed the clinical notes and radiographs of children with proven non-accident injury (NAI) who had sustained long bone fractures between 1997 and 2002, and compared them to the clinical and radiological appearances of 32 osteogenisis imperfecta (OI) patients, seen over the last 20 years, who sustained fractures before the age of one year.
In the five-year period, 501 children had NAI. Sexual abuse was involved in 35%, soft tissue injuries in 31%, head injuries in 26% and long bone fractures in 3.6% (18 children). The mean age of these 18 children was 11 months. Six had more than one fracture, and there were 29 fractures (15 femora, five humeri, three elbows, two forearms, two clavicles and two tibiae). Fifty-seven percent of fractures were diaphyseal and 43% were metaphyseal. There were only three metaphyseal buckle or corner lesions (distal femur). In none of these children were there radiological features of osseous fragility, i.e., osteopoenia, anterolateral bowing of the femur and tibia and gracile bones (thin bones with thin cortices).
Of the 32 OA patients, 23 were Sillence type I. There was a positive family history in 84% and 95% had blue sclera and Wormian bones. One patient was unclassifiable. All OI patients had fractures in the first year of life, 38% of them occurring perinatally. All had femoral fractures, with or without other fractures, and 90% were diaphyseal. Two or more features of osseous fragility were present in all type-III and 20 type-I patients. Three type-I patients and the unclassifiable patient had osteopoenia only, without bowing or gracile bones. Howeve, three of the four had a positive family history and all had blue sclera and Wormian bones.
In all patients, the differential diagnosis between NAI and OI could be made radiologically. The family history, blue sclera and Wormian bones were adjuncts.
Nine children with knee and foot deformities were treated by Ilizarov external fixation from 1989 to 2000 at the Sheffield Children’s Hospital. Sixteen cases of arthrogryposis were identified. Progressive correction was combined with soft tissue release, soft tissue distraction or bony correction. Clinical outcomes were assessed and comparisons made between the different treatment modalities. Three fixed flexion deformities of the knee treated with progressive correction and soft tissue distraction were corrected initially, but recurred some time after the removal of fixators. Out of five clubfoot deformities treated with an Ilizarov frame with progressive soft tissue distraction alone, three recurred despite long-term splinting. Eight clubfoot deformities were treated with a bony procedure combined with gradual correction in the circular frame, and all corrections were maintained at follow-up.
The mean treatment time in the fixator was 17 weeks (12 to 50), and the mean follow-up time was 36 months. Complications included four cases of pin-tract sepsis, one case of osteitis requiring a sequestrectomy, one of transient neuropraxia and one fracture following removal of the fixator.
The treatment of joint deformities in arthrogryposis remains challenging and complications occur. Combining the Ilizarov device with a bony procedure seems to give better results, with fewer recurrence of deformities than pure progressive soft tissue correction.
Talectomy was performed on 31 rigid clubfeet in 13 boys and 10 girls. Sixteen patients had myelomeningocele and seven arthrogryposis. The procedure was undertaken as a salvage operation on 22 feet. Seven patients had an additional cuboidectomy. The mean age of the patients was 3.7 years (2 to 9).
The patients were followed up for a mean of 4.5 years. Assessment included foot position, appearance and mobility, orthotic or shoe-wear fitting and walking capacity. Calcaneal position at the ankle was assessed radiologically. The results in 18 feet were good and in seven were satisfactory. There were six failures. Primary talectomy produced better results in children above the age of two years than ssecondary procedure in the older children. One of the patients developed a severe vascular complication, followed by sepsis, and required amputation of the foot. The other failures were due to recurrence of equines deformity.
Talectomy performed for severe rigid clubfoot achieved satisfactory correction in most of our patients. Excision of the talus as a salvage procedure carries a risk of incomplete correction and vascular complication.
Over 11 months to January 2001, we stabilised 15 pathological humeral fractures (14 patients) with a new nail that is secured in the medullary canal by hydraulic inflation. Filled with Ringer’s solution through a unidirectional valve, the nail expands by up to 50% of its original diameter. The expanded nail’s cross-section is characterised by four external longitudinal bars that are forced against the cancellous and cortical bone and prevent rotation. The entire length of the nail provides frictional contact. The fact that no locking screws are needed reduces radiological exposure for both theatre staff and patients and shortens operation times.
Ten patients had fractures in highly osteoporotic humeri, four had metastases and one a pseudarthrosis after plate fixation. There were no remarkable intra-operative or postoperative complications. Postoperative radiographic evaluation demonstrated correct axial alignment in all cases. No revisions were required and there were no intraoperative radial nerve injuries. The operative time was around 30 minutes. All fractures were stable enough to permit mobilisation of the arm and all united.
Thirty-four acute traumatic dislocations in children aged 5 to 13 years, treated between 1994 and 2002, were reviewed retrospectively. All injuries were caused by a fall. Two injuries were compound. Two children had ulnar nerve injuries, one a radial nerve injury, and one median nerve and brachial artery injury. Posterolateral dislocations were seen in 22 children, posteromedial in eight, posterior in one, anteromedial in two and anterolateral in one. Pure dislocations occurred in eight children and 26 had associated elbow injuries, including 11 medial epicondyle, five lateral mass, one olecranon, one radial head and eight combined injuries. In the combined group, six children had associated fractures and two had divergent dislocation of the proximal radio-ulnar joint. Twenty required open reduction. The injury was initially missed in eight.
The child with vascular and median nerve injury had not recovered by four months. Among the others, at follow-up of 4 to 48 months 22 results were excellent to good, 10 fair and one poor. Complications included pseudarthrosis of the medial epicondyle in one child and loss of flexion and rotation of 10° to 30° in 15. Radial and ulnar nerve injuries recovered. A high index of suspicion, good clinical examination and compared radiographs are recommended to avoid missed injuries.
One hundred and thirty-eight patients from South Africa were part of an international study aimed to determine whether the rate of healing of compound tibial fractures treated with intramedullary nails improved with recombinant human bone morphogenetic protein-2 (rhBMP-2). There were 118 men and 20 women, with a mean age of 33.3 years. According to the Gustilo-Anderson classification, there were 32 type-I, 50 type-II, 38 type-IIA and 18 type-IIIB fractures.
Patients were randomised to one of three groups: the standard care (SC) group, in which 47 patients were treated with intramedullary nail fixation and soft-tissue management, the group treated with SC and 0.75 mg/ml of rhBMP-2, which comprised 50 patients, and the group treated with SC and 1.50 mg/ml of rhBMP-2, which comprised 40 patients.
At 20 and 26 weeks, there was a significant difference (p < 0.027) in the rate of fracture healing in the three groups. At one year follow-up union was achieved in 30 patients (63.8%) in the SC group and in 27 patients (54%) and 30 patients (73.2%) in the two rhBMP-2 groups respectively. All patients with type-IIIB fractures developed nonunion in the SC group, but 56% in the 0.75-mg/ml rhBMP-2 group and 50% in the 1.5-mg/ml rhBMP-2 group achieved union.
Secondary intervention and medical costs were reduced in patients treated with rhBMP-2.
With the aim of identifying appropriate treatment and diagnosis, this paper discusses 12 of 107 elbow dislocations and 56 elbow fracture dislocations seen over four years.
One patient presented with arterial injury, two with olecranon fractures and dislocation, and three with radial head, olecranon and coronoid fractures. One patient had an intra-articular fracture, two had collateral ligamentous injuries and two had radial head fractures and dislocations.
Depending on treatment, the results can be very poor or excellent. An awareness of the pitfalls in dislocations and fracture dislocations of the elbow is necessary to prevent poor outcomes.
In a retrospective study, we reviewed 45 peri-trochanteric fractures treated between April 1995 and November 2002. The mean age of the 24 men and 21 women was 71 years (57 to 91). There were 34 inter-subtrochanteric, four reverse obliquity intertrochanteric fractures and nine subtrochanteric fractures. On the AO classification, there were 11 type-31A2-2, 21 type-31A2-3 and four type-31A3-1 intertrochanteric fractures. The fracture extended into the femoral neck in one case and into the diaphysis in three. Cardiopulmonary diseases were present in more than 60% of patients.
In most cases, fractures were reduced by closed reduction or reduction through a short incision. In 42 cases, a Smith and Nephew femoral reconstruction nail was used. Three fractures were stabilised with AO undreamed femoral nail with spiral blade. Distal locking screws were inserted in all cases. Progressive passive hip and knee movement was introduced from day one postoperatively. Partial weight-bearing was permitted from the onset. All but two fractures healed within 3 to 6 months. Union was delayed in two subtrochanteric fractures. Functional hip and knee movement was present in all patients. There was no sepsis. Proximal screws backed out in four cases, but this was of no functional significance. In one case the superior proximal screw was too long and required removal. In one case screws backed out of the femoral neck and further surgery was required. No breakage of screws or nail was observed. Inter-subtrochanteric and subtrochanteric fractures in the elderly may be successfully managed with intramedullary femoral reconstruction nails.
In a prospective, consecutive study we reviewed the results of 32 supracondylar femoral fractures treated by Smith & Nephew intramedullary supracondylar nailing between January 1996 and October 2002. The mean age of 23 women and nine men was 67 (58 to 89). All fractures were closed. Two patients had associated upper limb fractures. In four cases, fractures occurred around total knee prostheses. Four patients had previously undergone ipsilateral total hip replacement or had had a sliding hip screw. On the AO classification the majority of fractures were type-33A1 and A2; seven fractures were classified as C1 and C2. The patients were placed in the supine position on a radiolucent operating table with the knee in 30° of flexion.
Postoperatively a hinged knee brace was applied and worn until union. Supported, progressive knee movement was introduced from day one. Partial weight-bearing was permitted as soon as pain subsided and continued until there were radiological signs of union. Within three to six months all but two fractures united. These united after prolonged bracing. There was no sepsis or fixation failure. A functional range of knee movement was observed in all patients.
Retrograde intramedullary nailing is a safe and successful method of management of supracondylar femoral fractures in the elderly and offers a minimally invasive alternative.
All patients who had received an Austin Moore hemi-arthroplasty between 6 February 1998 and 14 July 2002 were included in the study. Of the 101 patients, 34 were lost to follow-up, 34 had passed away and one did not give consent for the study. The Physical Performance of Activities of Daily Living (PODL) was evaluated, using a modified version of the functional status index by Jette. The level of social functioning was determined by a questionnaire developed by House . Muscular function was evaluated by a timed ‘carpet run’ of 20 m and measuring the time it took to rise twice from an armless chair. The data were compared to an age-matched control group of 44 volunteers.
The 45% complication rate in the study group included four dislocations (12%), two femoral fractures (6%) and three deep infections (9%). The social functioning questionnaire showed an average or above average score in most of the patients, 22 of whom (69%) were satisfied with the results. On the PODL score 19 patients (60%) were above average in dependency. Ten (31%) reported no functional pain and four (10%) reported severe pain. Muscular function tests showed a statistically significant difference between the operated group and the control group, with the mean ‘carpet run’ three times longer.
Even though the study showed good results as far as dependency and social functioning was concerned, there was a high complication rate and a low objective functional outcome. We concluded it was an effective procedure for patients who did not have high functional expectations, and that physiological status should play a greater role than chronological age in therapeutic decision-making.
Since October 2001 we have used the FIXION® proximal femoral (PF) intramedullary nailing system to stabilise 93 proximal femoral fractures, 81 of which were pertrochanteric and 12 subtrochanteric.
Postoperative radiographs showed correct axial alignment in all cases. All patients recovered satisfactorily and mobilised early and without pain. Good callus formation was noted about 10 weeks after the procedure. We compared the use of the FIXION® PF with the use of Gamma nails and noted considerably shorter operation and radiological examination times.
This prospective study included 236 open tibial fractures treated by unreamed AO nailing at three to four days after injury. Ten patients were lost to follow-up and 24 were excluded. We reviewed 202 consecutive open tibial fractures treated between January 1994 and December 2000. The mean age was 31 years (18 to 66) and 152 patients were men. There were 74 Gustilo grade-I, 66 grade-II, 32 grade-IIIA and 30 grade-IIIB fractures. The soft tissue injuries were managed by delayed primary closure, split skin graft or local flap. Most fractures were stabilised by unreamed nailing and statically locked.
Below-knee casts were applied routinely for six weeks. Full weight-bearing was permitted and maintained 6 to 12 weeks after the operation. In 16 patients (8%), union was delayed, but union occurred within 12 to 30 weeks in 194 patients (96%). Nonunion was observed in eight fractures (4%). Functional union occurred in all patients. Ten (5%) had mild knee pain. Acceptable shortening was noted in seven cases (3.5%) and varus/valgus angulations in 12 (6%). In two patients the nail was too long and required exchange. Eight locking screws bent or broke. There was no sepsis but three wounds were superficially infected. Compartment syndrome developed in one patient. Twelve additional operations (exchange nailing, bone grafting, fibular osteotomy and dynamisation) were performed for delayed unions and nonunions. Seven additional operations were undertaken for surgical errors where the nail was too long, there was early excessive rotation, or there were missed locking screws.
The delay in final treatment of open tibial fractures allows safe selection of patients for secure and cost-effective unreamed intramedullary nailing, with minor complications.
This study reviews the use of intramedullary fibular allograft in treating nonunion of the humeral neck in 11 patients. Nine women and two men with a mean age of 76 years (63 to 89) were followed up for a mean of 61 months (14 to 72). The nonunion was exposed through a deltopectoral approach and fibular allograft was inserted across the fracture site. As the fibula is a very dense cortical bone, a T-plate could then be applied to the humerus with the screws directed into the intra-medullary fibular peg. Supplementary corticocancellous bone from the iliac crest was used. Bony union was achieved in every case. The preoperative mean Constant score was 26 and the postoperative mean Constant score was 75. The most notable improvement was in patients’ ability to elevate the arm actively. Decreases in pain levels were observed but were less dramatic than the increases in function.
Twenty-four patients with 26 symptomatic recurrences of deformity after previous hallux valgus procedures were included in this study. Exclusion criteria were hallux metatarsophalangeal joint fusion, Keller/Mayo procedures, insulin-dependent diabetes, previous ankle or subtalar fusions, peripheral vascular disease or peripheral neuropathy. An AAOS Foot and Ankle Outcomes Data Collection questionnaire, a Visual Analogue Pain Scale (VAPS), and the AOFAS Hallux Metatarsopha-langeal Interphalangeal Scale (HMIS) were administered preoperatively, at six months and then annually. Weight-bearing radiographs were taken preoperatively, at 6 weeks, 3 months, 6 months and 12 months. The mean follow-up was 21.6 months (6 to 36).
At final follow-up, the mean HMIS scores increased from 47.5 to 87.8 and the mean VAPS improved from 6.2 to 1.3. The mean hallux valgus angle improved from 37° to 14° and the mean intermetatarsal angle improved from 18° to 7°. In 77%, patients were very satisfied, in 4% satisfied, and in 19% somewhat satisfied.There were no cases of hallux varus. Complications included three nonunions, all of which occurred in smokers, and two superficial wound infections.
In appropriately selected patients, the Lapidus procedure is a reliable and effective alternative for failed hallux valgus surgery.
Between 1997 and 2002, seven talipes equino varus deformities in six patients were treated using gradual distraction and correction with the Ilizarov external fixator. Three patients had poliomyelitis, four patients had neglected clubfeet and two patients had relapsed club-feet. The mean age of patients was 13.3 years (5 to 21) and the mean duration of fixator application was 3.25 months. When the plantigrade position was achieved the fixator was removed and a below-knee walking cast was applied. Four months after fixator removal, additional bony correction surgery (triple arthrodesis) was done in three patients. At the time of fixator removal, a plantigrade foot was achieved in all patients.
The mean follow-up time from surgery was 26 months. Pin-tract sepsis in two patients was treated effectively with oral antibiotics. Other complications included meta-tarsophalangeal subluxation from flexor tendon contractures in one foot. There have been no recurrences of deformities.
Compared to preoperative status, gait was subjectively improved in all patients. Correction of the deformity in the patients who had a triple arthrodesis of the foot was achieved with less bone loss than in patients who had undergone a primary triple arthrodesis. These results suggest that treatment with Ilizarov frames is effective in the management of neglected and relapsed clubfoot deformities.
We treated 31 feet in 17 children with myelomeningocele by extra-articular subtalar arthrodesis. Two patients were lost to follow-up. In the rest, we assessed the correction of valgus deformity and the growth of the tarsal bones. At operation the mean age of the eight girls and nine boys was 6.3 years (3 to 9). At a mean follow-up period of 5.5 years (3 to 9) patients were evaluated clinically and radiologically. We assessed calcaneal growth by calculating the ratio of calcaneal and naviculo-metatarsal longitudinal length on the preoperative and follow-up lateral radiographs.
Results of valgus correction were good in 19 feet. In eight they were unsatisfactory owing to progressive valgus of the ankle. Orthotic fitting was difficult and pressure sores over the medial malleolus often developed. Four of the patients underwent further correction by distal tibial osteotomy. The growth ratio was increased in 15 feet, remained the same in seven and decreased in five. Extra-articular subtalar arthrodesis produced satisfactory partial correction of a complex valgus deformity and stability of the hindfoot, and did not have a detrimental effect on the growth of the calcaneus.
Between June 1996 and April 2002, 56 patients underwent closed reduction and percutaneous fixation of calcaneal fractures. Of the 39 men and 17 woman, five were lost to follow-up. The patients’ mean age was 38 years (17 to 64). Four had bilateral procedures.
Using the AOFAS Ankle and Hindfoot Scale (AHS) and Visual Analogue Pain Scale (VAPS), we assessed patients preoperatively and at 6 and 12-monthly intervals. Clinical examination was undertaken preoperatively and postoperatively at 2-week, 6-week, 3-month, 6-month and 12-monthly intervals. Except at two weeks, radiographs included weight-bearing axial and lateral views at all intervals. Follow-up was for a mean period of 42 months (12 to 72). The mean time to union was 10.2 weeks (8 to 14).
The AHS improved from 34 preoperatively to 85 at the most recent follow-up. The VAPS improved from 9.1 preoperatively to 2.2 at three years. The satisfaction rate was 86%. Functional results depended on the quality of the reduction of the posterior facet and the severity of the initial injury. Complications included a 5% sural nerve injury and a 3% peroneal tendinopathy. No wound complications were encountered.
In selected cases, closed reduction and internal fixation of calcaneal fractures may produce results similar to those of conventional open reduction and internal fixation, with fewer complications. This technique is best performed within 24 to 72 hours of injury.
The purpose of this prospective study was to evaluate the functional outcome of patients who underwent the Lapidus procedure as a treatment for moderate to severe metatarsus primus varus and hallux valgus deformities. Inclusion criteria were failure of non-surgical management for moderate or severe deformity, inter-metatarsal angles of more than 14° and hallux valgus angles of more than 30°. Exclusion criteria were any previous hallux valgus procedures, insulin-dependent diabetics, previous ankle or subtalar fusions, peripheral vascular disease or peripheral neuropathy. Bilateral procedures had to be at least six months apart to be included. The AOFAS Hallux Metatarsophalangeal Interphalangeal Scale (HMIS), Visual Analogue Pain Scale (VAPS), Musculoskeletal Function Assessment Scale, clinical examination and weight-bearing radiographs were used for assessment.
All patients were followed up for at least six months. Patients lost to follow-up in less than a year were excluded from the analysis. For a mean of 3.7 years (1 to 6.2), 126 feet in 110 patients were followed up, 105 of them (91 patients) for at least one year. At most recent follow-up, HMIS scores increased from 52 preoperatively to 87 (p < 0.0001). VAPS improved from 5.3 to 1.3 (p < 0.0001). The hallux valgus angle improved from 37° to 16° and the intermetatarsal angle improved from 18° to 8.2°. At 3.7 years, 88.5% of patients were very satisfied, 5% somewhat dissatisfied and 1.5% dissatisfied.
With proper technique and attention to detail, the Lapidus procedure is an excellent alternative for moderate to severe metatarsus primus varus and hallux valgus deformities.
From October 1999 to April 2003, 123 patients (127 ankles) underwent an Agility total ankle replacement. Prospective data were collected preoperatively, at 6 and 12 months after surgery, and thereafter annually, and included the AOFAS Ankle and Hindfoot Scale (AHS), Musculoskeletal Functional Assessment Injury and Arthritis Survey (MFA), Visual Analogue Pain Scale, patient satisfaction and standardised radiographs.
Fifty-six percent of the operations were performed for post-traumatic degenerative joint disease, 41% for primary degenerative joint disease, 1% for rheumatoid arthritis and 2% for avascular necrosis. At least one previous surgical procedure had been performed on 62% of ankles. In 6% there were intra/perioperative complications, including seven wound problems (one major, six minor), five lateral fractures, one medial malleolus fracture, one bone stock deficiency, one tibial nerve injury, one ankle in varus and one flap necrosis. Late complications included eight syndesmosis nonunions that needed bone grafting, one infection that led to a fusion, one unrelated talar fracture that led to a fusion, and one component subsidence that was revised. There were two patients with progressive varus and two with progressive valgus deformities. One patient underwent a below-knee amputation for chronic infection. Most of the perioperative complications occurred in the first 40 patients. The preoperative AHS of 43 (4 to 70) increased six months postoperatively to 75.45 and to 85 at two years. Patient satisfaction preoperatively was 0.92 out of 5 and 4.2 at two years. Baseline MFA values indicative of severe dysfunction (9.26) showed marked improvement in all parameters at two-year follow-up (21.83).
The Agility ankle replacement procedure is technically demanding and there are pitfalls and complications. The early results are promising, but follow-up has not been long enough to permit an objective opinion.
This paper compares over an 18-month period anterior and posterior procedures in 40 patients treated surgically for dislocations and fracture dislocations of the cervical spine. Patients were followed up for a minimum of 12 months. Fifteen patients were neurologically intact, 13 were severely neurologically compromised and 12 presented with radicular symptoms. There were unifacet dislocations in 33 patients and bifacet dislocations in seven. In 23 patients there were associated fractures of the posterior elements. There was a high incidence (35%) of non-spinal injuries.
Posterior fusion (interspinous wiring) was done in 20 patients, anterior surgery (plating) in 18 and combined approaches used in two. Owing to posterior column fractures, four patients undergoing posterior surgery required two-level fusion.
Two of 13 patients with quadriplegia had useful return of function. There were no postoperative neurological complications. Reduction was successful in two of six patients who presented late (after more than 30 days) and the remaining four patients underwent an in situ fusion. In the anterior and posterior approaches operation time, blood loss, hospital stay and time to fusion were comparable. Anterior surgery without instrumentation was inadequate, but patients treated by anterior surgery had less neck and graft site pain, a lower rate of instrument failure and did not require multisegment fusion.
The anterior approach with instrumentation was safe and useful, obviating the need for two-level fusions and reducing the need for orthotic support, especially in the quadriplegic patients.
The results of fluoroscopically-guided closed needle (3.5-mm diameter) biopsies performed under general anaesthesia on 70 consecutive patients with lumbar spine pathology were reviewed. There were 36 men and 34 women with a mean age of 38 years. Sixty-four patients were Frankel-E, four were Frankel-D and two were Frankel-C.
The mean duration of the procedure (three tissue cores) was 17 minutes. Consultants performed 42% of the procedures and registrars the rest under supervision. All specimens were subjected to histological, cytological and microbiological evaluation. The results show a histological diagnostic yield of 88.57%. Of the 47 infective lesions, 34 were due to tuberculosis, three were pyogenic and 10 were reported as chronic non-specific inflammations.
In the 14 patients with neoplastic lesions, nine were metastatic and five were primary bone tumours. Histological diagnosis was inconclusive in six patients. Traction artefacts were noted in two patients with sclerotic lesions and one patient revealed normal bone. In tuberculosis, the culture was positive in only 29% of patients. The combined Lowenstein-Jensen and mycobacterial growth indicator tube media improved detection time and recovery rate of mycobacteria from smear negative specimens by 10%. The overall diagnostic yield for tuberculosis was 72.34%.
The diagnostic accuracy and safety of fluoroscopically-guided closed needle biopsy is comparable to that of CT scan and it is more cost effective. It should be an integral part of the management algorithm for spinal pathology.
This paper reviews 32 patients (seven boys and 25 girls, mean age 14.5 years) with adolescent idiopathic scoliosis treated by anterior spinal release, fusion and instrumentation from 1989 to 2001. In 22 patients the thoracic curve was involved, in six the thoracolumbar and in four the lumbar curve. The mean preoperative kyphosis (thoracic curves) was 22.3° and the mean Cobb Angle was 56°. Routine exposure through the convexity was performed (sixth rib for thoracic curve and 10th rib for other curves).
After discectomy (four to nine levels), morselised rib was used as bone graft and instrumentation was applied with correction of deformity and saggital profile. Costo-plasty was performed in 10 patients. The mean operation time was three hours; mean blood loss was 180 ml. Intraoperative problems were partial pull-out of screws from the first proximal vertebra in three patients. In one asthmatic patient, who was on steroids, instrumentation was abandoned because of pull-out of several screws.
The mean hospital stay was 10 days. Two patients developed superficial wound sepsis and one sustained a burn to the right shoulder (cause unknown). Rod breakage occurred in two patients. Angulation at the level below the lowest instrumented vertebra occurred in five patients and was attributed to inappropriate fusion levels. Pseudarthrosis developed in two patients. At final follow-up, the mean Cobb angle was 26° and the mean thoracic kyphosis 30°.
The advantages of anterior surgery for idiopathic scoliosis include fewer fusion levels, correction by shortening the spinal column and less blood loss. Difficulty may be encountered in selection of fusion levels and instrumentation of the proximal vertebrae. In cases of very rigid curves, posterior spinal release may improve results.
From April 2001 to January 2003, 60 patients were selected for a circumferential fusion with an ALIF Brantigan cage and posterior titanium instrumentation. The aim of this study was to analyse the complications and the effects of circumferential fusion on functional outcome and lumbar lordosis. Circumferential fusion restored lordosis, provided a higher fusion rate, and showed a tendency towards better functional outcome and reduced back and leg pain.
The aim of this study was to assess whether the pro-lapsed disc fragment type was predictive of recurrent disc herniation or sciatica after discectomy. The records of 39 patients treated by lumbar discectomy only were reviewed. Within two months of surgery, the type of disc fragment prolapse and state of the annulus were assessed on CT scans or MRI. Patients who presented later with recurrent sciatica or disc prolapse were reviewed with MRI. All other patients were contacted and asked whether they had had recurrent sciatica or had undergone repeat surgery elsewhere. The follow-up period was three years.
The results suggest that patients in whom discs required annulotomy at surgery had poorer results than those with extrusion through an annular fissure. The degree of annular competence can be used to assess the risk of recurrence of herniation or sciatica.
Thirteen consecutive patients with scoliosis, treated with anterior spinal fusion with a single rigid rod, were followed up clinically and radiographically for 19 months.
The mean major curve, 52° preoperatively, improved to 10° at follow-up.
The results of anterior single-rod spinal fusion in patients with idiopathic scoliosis are excellent. No development of kyphosis or incidence of hardware failure was seen.
This paper retrospectively reviews 40 quadriplegics treated from 1997 to 2000. Hospital records, spinal unit records and telephonic interviews were used to obtain data on age, sex, mechanism of injury, levels involved, delay in admission, associated injuries, treatment, morbidity, mortality, rehabilitation time and placement on discharge. The mean age of the 36 men (89%) and four women (11%) was 36 years (18 to 66). The mechanism of injury in 34 of the patients (85%) was motor vehicle accidents. Five patients (13%) had sustained gunshot wounds and one patient had hit a wall (2%). The mean delay to admission was 5 days (0 to 42). Injuries were at C5/6 in 40% of the patients. Twenty-five patients (62.5%) were treated conservatively and 15 (37.5%) surgically. The 37.5% mortality rate was related to admission delay, associated injuries and patient age. Placement after discharge was problematic in 36% of the patients.
Between 1964 and 2002, 26 pairs of conjoint twins were recorded at the Red Cross Hospital. The available radiographs and notes were reviewed, with specific attention to the incidence of spinal anomalies that result in scoliosis. Structural scoliosis was noted to occur only in the ischiopagus and pygopagus subsets, namely those joined by the pelvic outlet and the rump respectively. The abnormalities were largely those of failure of formation, with early onset of severe deformity. The hemi-vertebrae were often remote to the area of conjunction, mostly in the thoracic area. All six ischiopagi had vertebral abnormalities, with two of the four pygopagi demonstrating abnormalities. There were associated lower limb neurological abnormalities in the ischiopagi.
The association of conjoint twinning and vertebral anomaly is currently thought to be due to non-specific teratogenic insult with hypoxia. The fact that the ischiopagus and pygopagus are involved is important: these groups constitute up to 45% of survivors and are reported to have a longer life expectancy. Because they will later develop severe deformities, they need early active management.
A subgroup of nine patients, five women and four men, who received lumbar disc prostheses in a segment adjacent to previous posterolateral instrumented fusions (one or two levels) is reviewed. Two patients underwent double-level disc replacement. The mean age was 46.1 years (33 to 62). All patients had marked flattening of the lumbar spine before the operation. One patient developed subsidence within two weeks of the procedure but went on to a satisfactory result. One patient with a double-level disc replacement needed another operation because of a missed far out lateral disc. On day five after the procedure, the top-level disc was removed, the level properly decompressed and the disc reinserted, with good results.
The mean postoperative hospital stay was 3.9 days (3 to 8). Within a mean time of 32 days (21 to 42), all patients returned to their previous occupations. Follow-up ranged from 3 to 19 months. At the latest follow-up, four of the patients were satisfied and five were very satisfied.
Disc replacement seems an ideal salvage procedure for junctional failure after previous fusions. The short-term clinical results are good.
This pilot study was undertaken to assess the prevalence of low back pain among nurses. Fifty-two women (mean age 44.28 years) working at a provincial hospital completed a questionnaire about low back pain and other health conditions. The duration of pain, number of episodes a year, duration of each episode and treatment were assessed.
Twenty-nine professional, three staff and 17 enrolled nurses responded. Their mean length of service was 18.32 years. Their mean weight was 78.55 kg, with a body mass index (BMI) of 32.2. They commuted a mean distance of 29.02 km (1 to 80), taking 37.12 mins (10 to 90). On average they had 2.18 dependents and 24 had help with household chores. Seventeen respondents participated in sports such as tennis, soccer and swimming.
Forty-six reported episodes of pain lasting five or more days. Symptoms had been present for 6.62 years. Twenty-three had fewer than eight episodes a year. Thirty-eight patients (82.6%) required treatment, including rest, medication and physiotherapy. Seven were admitted to hospital and one had surgery. Sick leave accounted for 751 lost work days. Forty-one nurses (78.8%) wanted to participate in a back care programme.
The results of an accelerated rehabilitation programme were collected retrospectively from 293 case notes between January 1995 and December 1998. Different grafts were used: bone patellar-tendon bone (BPTB) grafts, hamstrings grafts and allografts. The criteria used to evaluate the knees of these patients were based on patient satisfaction, clinical examination and Cybex evaluation. All 293 patients were followed up for six months or longer. Four to six months after the reconstruction procedure, 94.2% returned to sport activities.
Anterior knee pain seemed not to be a problem when using autogenous BPTB grafts. The rehabilitation programme should decrease the postoperative morbidity.
Between February 2000 and August 2002, 60 Oxford unicompartment knee replacements were done on 51 patients, nine of whom had bilateral surgery. The mean age of patients, 82% of whom were women, was 66 years (45 to 83). Primary osteoarthritis was the pathology in 97% and post-traumatic arthritis in 3%.
A full radiological assessment was done to determine positioning of the prostheses as well as the interfaces. The mean range of movement increased from 113° pre-operatively to 120° at the most recent follow-up. Complications included one case of deep venous thrombosis, one patient with bilateral tibial component loosening and three patients with loose cement particles in the joint. Most patients have no pain, but some have mild or occasional pain. One patient with bilateral unicompartmental replacements now has lateral knee pain.
Unicompartment knee replacements are an alternative to total knee replacements, but there is a significant learning curve, particularly with regard to cementing techniques. Attention needs to be paid to removing all loose cement from the joint. Patient selection is critical. The complication rate remains low, however, and the results seem satisfactory.
To determine the prevalence of osteoarthritis in the knee in the long term after anterior cruciate ligament (ACL) reconstruction, the files of patients who underwent the procedure from June 1984 to December 1990 were examined. Forty-three patients were contacted, of whom 33 (subgroup A) were willing to be examined clinically and radiologically. The other 10 agreed to a telephonic interview.
The Lysholm Knee Score (LKS) and the Petersson radiographic grading system for evaluation of osteoarthritis were used as the main measurements of outcome. The mean age at injury was 24.35 years. The mean interval between injury and surgery was 83.83 months. the mean LKS was 84.35. In subgroup A, 18.18% knees were Petersson grade 0, 30.3% grade I, 12,12% grade II, 30.3% grade III and 9.09% grade IV.
The results show that even in the long term a relatively positive outcome may be expected after ACL reconstruction
This study was to evaluate the stability of a delta keel tibial tray using a block prosthesis and to determine whether a long intramedullary stem is a necessary adjunct to augment construct stability. An experimental technique was used employing strain gauges and deflection transducers to assess the stiffness and principle strains conferred to human cadaveric tibiae under various axial loading conditions.
As a control measure, tests were conducted in the absence of any bone loss, and repeated in a simulated bone defect treated with a metal block. The latter was analysed with and without augmentation of the tibial tray with an intramedullary stem. With axial loading of 2000N, the tray and block configuration resulted in 21% less proximal bone strain than the tray alone. The combined tray, block and stem resulted in 35% less proximal bone strain than the tray alone. Using the tray and block produced 1.06 times more deflection of the tibial tray and using the tray, block and stem 1.03 times more deflection of the tibial tray than the tray alone in the absence of a bony defect.
There was no statistical difference in overall construct stability (p < 0.05) despite the large strain-offsetting effect recorded using the tibial tray in conjunction with the block and stem
These results suggest that isolated bone defects that can be dealt with using a single block and modern standard tibial tray may not require additional supplementation with a long intramedullary stem.
Sixty-one lumbar disc replacements in 50 consecutive patients were performed between June 2001 and October 2002. The mean age of the patients was 42.42 years (24 to 61). All presented with mechanical back and/or leg pain. The primary diagnosis was degenerative disc disease. Three patients underwent fusions of another level during the same operation. Seven patients presented with adjacent level disc disease after previous instrumented posterolateral fusion.
The mean postoperative hospital stay was 3.6 days (2 to 8). One patient with a double-level disc replacement and misplacement of the proximal prosthesis underwent revision surgery three days later. Six patients had subsidence on one of the endplates, all within six weeks postoperatively. All but one patient went back to their previous occupation at a mean time of 26 days (7 to 91).
Patients completed questionnaires at 3, 6, 12 and 24 months postoperatively. In the latest follow-up questionnaire, 47 patients said they were satisfied or very satisfied. Forty-five patients would undergo the same operation again or recommend it to friends, two patients were uncertain and two indicated they would not undergo the procedure again. One patient from another country was lost to follow-up, but a telephonic enquiry six months after surgery suggested that he was doing well.
Although our follow-up period is short, the clinical results compare favourably to those in the literature. The rate of immediate subsidence, which seems to be linked to the anchoring teeth, is of concern.
Twenty-seven patients with neurological deficit due to burst fractures were treated with fresh frozen allografts following anterior spinal decompression. Their mean age was 28 years. In 19 patients the injury was due to motor vehicle accidents and in five to falls. The mean preoperative kyphosis was 19° (4° to 33°). Three patients with laminae fractures, which resulted in entrapment of the dura, underwent posterior decompression and transpedicular fixation before anterior decompression. Corpectomy was performed in all patients. An appropriate length of femoral allograft was positioned by interference fit and the spine was stabilised with an anterior rod screw construct in 21 patients.
The follow-up ranged from 29 to 72 months. Bridwell grade-I fusion was seen in 23 patients at two years. Subsequent follow-up revealed no fracture, resorption or collapse. The mean neurological recovery was 1.4 Frankel grades. Nine patients (37%) made a complete recovery but in four (16%) there was no improvement. The mean postoperative kyphosis was 9° and at two years the mean loss of correction was 3°. One patient presented with a psoas abscess at two-year follow-up. At surgery the graft was partially resorbed but was stable. At six-year follow-up the patient was asymptomatic with a grade-II fusion.
The use of allografts saves considerable time in surgery and avoids potential donor site morbidity. They are versatile and are easily available.
Four low-cost hip prostheses, explanted because of clinical failure within three years, were subjected to a retrieval analysis study to determine the cause of the early failure. The study aimed to determine whether the low-cost prosthesis was substandard and had consequently contributed to the need for early revision. The retrieval analysis included a photographic record, a fractographic examination, an analysis of the material composition of the components, and a mechanical property analysis. These investigations were done in accordance with the ASTM F561 standards.
Results demonstrated substandard qualities in respect of all parameters analysed. We conclude that the inferior quality of these low-cost hip prostheses contributed appreciably to their early failure and revision.
We have previously reported on early lytic lesions occurring when collared titanium prostheses are used. Previous finite element analysis studies (FEAs) showed that lytic lesions of the calcar were due to concentration of polyethylene wear particles under the collar by a ‘pumping action’. Further follow-up of these calcar lytic lesions showed that their rate of increase in size progressively slowed down. Further FEAs were performed to determine why this was so.
An FEA mesh construct was developed, incorporating the new parameters of no contact between the collar and the calcar bone. A mechanical model to determine displacement parameters was also developed. These FEA studies demonstrated that the pumping action of the collar became less efficient as the size of the lytic lesions increased. This led to less concentration of polyethylene particles under the collar and fewer granulomatous reactions. The change in the proximal prosthesis-cement-bone construct may lead to cement mantle deterioration and earlier failure. We still recommend caution when a collared prosthesis is used, and the material and geometry of the prosthesis remain important.
We managed three elderly patients who had central fracture dislocations with early total hip arthroplasty (THA), using anteprotrusio supports. Bone grafting was used to re-establish acetabular bone stock.
Intraoperatively and postoperatively, these patients had no more complications than did patients undergoing THA for hip fractures. However, the surgical times were longer than for routine THA and blood replacement was slightly higher. Patients were mobilised early and aggressively. All became independent walkers and regained good range of movement. Radiologically the acetabular/pelvic fractures united and good bone-implant interfaces were established. There was no excessive heterotrophic bone formation.
We regard THA in the management of acetabular fractures in the elderly as a reasonable approach, enabling patients to mobilise early and keeping morbidity to an acceptable level.
This paper investigates the association between risk factors recorded prospectively before primary total hip arthroplasty (THA) and the risk for later revision surgery. The National Health Screening Service in Norway invited 56 818 people born between 1925 and 1942 to participate in an investigation of risk factors for cardiovascular disease and 92% participated. Matching these screening data with data from the Norwegian Arthroplasty Register about primary THA and revision THA, we identified 504 men and 834 women who had undergone primary THA at a mean age of 62 years. Of these, 75 and 94 were revised during follow-up. The mean age at screening was 49 years and the mean age at censoring was 68 years. The mean age of those who underwent revision THA was 57 years. Men had a 1.9 times higher risk of undergoing hip revision during follow-up (95% CI). For each year’s increase in age at primary THA, the risk of revision THA during follow-up decreased by 14% for men and 17% for women. Men who at screening had the highest level of physical leisure activities had 5.5 times the risk of later revision than those with the lowest level of physical activity (95% CI).
Men have a higher risk for revision THA. The older the patient, the lower the risk for revision. Men with intense physical activity in middle age are at increased risk of undergoing revision THA before they reach 70.
In June 1999 we instituted a prospective, randomised, double blind study to determine whether in the use of the Profix® total knee replacement system the addition of screws improved the fixation of the tibial base plate. There were 145 arthroplasties in 137 patients, 77% of them female. Their mean age was 66 years. In 86% of the patients there was osteoarthritis and in 14% an inflammatory arthritis. On a random basis, supplementary screws were inserted through the base plate into the tibia in 49% of arthroplasties and the remaining 51% were not fixed. In both groups the postoperative femoral angle measured 95% and at 12-month evaluation the tibial angle measured 89°, giving a total valgus angle of 6°. To date no tibial base plates have come loose. It is felt that the large central titanium peg plays a major role in assisting fixation of the base plate to the tibia and that supplementary screws are unnecessary. There is a small cost saving when screws are not used. We postulate that one may in the future minimise polyethylene debris tracking and osteolysis.
From September 1995 to March 2003, 15 patellofemoral joint replacements were done on 13 patients. The mean age of the one man and 12 women was 62 years. Osteoarthritis was the reason for surgery in 13 of the 15 knees. In the other two it was post-traumatic arthritis. Three different products were used: Avon (eight), Link Lubinus (five) and LCS patellofemoral prostheses (two). One patient has subsequently been revised to a total knee replacement. Recommendations are made regarding selection of patients and implants.
In a retrospective review, 38 consecutive Workers’ Compensation (WC) patients undergoing primary total knee arthroplasty (TKA) were matched to a cohort of non-WC patients for demographics and preoperative diagnosis. Outcome measures included the Knee Society Score (KSS), the Oxford Knee Score, the McGrory Modified Knee Score (MMKS), patient satisfaction and number of postoperative clinic visits. Unpaired t-tests were used to determine differences in outcomes. Pre-operative KSS, pain and flexion range as measured by KSS, and Oxford scores displayed no statistical differences. The differences in the two groups at six weeks was significant in respect of KSS (p =0.0005) pain as measured by KSS (p =0.015), and flexion range (p =0.012). At six months similar results were noted in pain as measured by KSS (p =0.018), Oxford scores (p =0.005) and flexion range (p =0.035), but KSS function was not significant (p =0.073). One-year Oxford scores (p =0.013) and flexion range (p =0.013) were statistically significant, as were MMKS (p =0.001), patient expectations (p =0.030), perceived quality of life (p =0.009), and number of postoperative clinic visits (p =0.003).
The short-term outcomes of primary TKA in patients receiving workers’ compensation benefits are inferior to those obtained by non-workers’ compensation patients. Workers’ compensation patients are seen more often for postoperative follow-up, which we would attribute to the persistence of subjective complaints following primary TKA.
Over five years, 85 low-cost primary total arthroplasties (Eortopal Bulteamex) were done at a referral hospital. These were followed up for a mean of 48 months (minimum of 18 months). There were 11 revisions (13%), with four (4.7%) necessary for aseptic loosening, two (2.3%) for recurrent dislocations, four (4.7%) for sepsis and one (1.3%) for a periprosthetic fracture.
When these results were compared with the Trent Regional Arthroplasty Register, the revision rate was noted to be four times higher than in the Trent study, with aseptic revisions being twice as high and infection rates three times higher. Dislocation rates were half those in the Trent study. We concluded that our lower dislocation rate probably reflected the quality of our surgery. Our higher sepsis rate was probably related to the hospital environment, and the high aseptic loosening rate due to the quality of the ‘low-cost’ prosthesis.
We conclude that to be cost-efficient, ‘low-cost’ pros-theses must be of good quality and that the hospital environment must be optimal. This study highlights the need for an Arthroplasty Register in South Africa.
Complex acetabular defects after failed total hip arthroplasty (THA) remain a major challenge in revision surgery. We managed 29 patients, of whom 27 had type-III and two type-IV defects (AAOS classification).The mean age of the 16 men and 13 women was 68 years (22 to 96).
Use of a modular uncemented acetabular revision system allowed us accurately to position the construct, and then optimise the orientation of the polyethylene liner in respect of stability in the reduced hip. The modularity of the system allowed good access to do an impaction bone graft to restore the defects in the bone stock.
Our follow-up ranged from 2 to 25 months. The orientation of the acetabular construct was measured radiologically and was at 50°. Our complications included four dislocations, two transient nerve palsies, one deep infection, four deep venous thromboses and one death from a pulmonary embolism. We conclude that the use of a modular acetabular reconstruction system is promising in these extremely difficult cases.
The purpose of this study was to compare old and new techniques in hemiprosthesis for primary femoral neck fractures. We implemented a new technique for inserting the Charnley stem via the Hardinge approach. This included a distal centraliser, broaches and specific entry into the femoral canal via the piriformis fossa. We then compared stem alignment and cement mantle quality in old and new techniques. The sample comprised 42 patients (34 women) who had been operated on with the old technique and 49 patients (39 women) exposed to the modern technique.
Postoperative anteroposterior and true lateral radiographs were taken and evaluated for cementing quality, mantle thickness in the 14 Gruen zones and alignment of the femoral stem in both planes. On the Barrack classification there were nine grade-A with the new technique, compared to none with the old. There was one Grade-B with the old technique. With the new technique, cement mantle thickness and uniformity was better in Gruen zones 1 to 3, 5 to 10, and 12. Alignment as measured in the lateral plane by the mean antero-posterior angle was 5.2° with the old technique and 2.2° with the new (p =0.0001). In the frontal plane there was no difference.
It is hoped the advantages associated with this modern technique for inserting the Charnley stem will confer longer survival.
The purpose of this study was to document difficulties encountered by orthopaedic surgeons with the removal of titanium implants.
A postal questionnaire was sent to all members of the New Zealand Orthopaedic Association seeking to document difficulties with the removal of titanium implants: screws, plates or intramedullary nails. The questionnaire included length of device implantation, estimated increase in theatre operating time over the expected time for the procedure, and complications encountered during the device removal.
Twenty six surgeons responded to the study. Six reported no difficulties in removing implants, 18 reported significant difficulties, and 2 had not had to remove titanium implants. Of the 18 surgeons reporting difficulties, 10 had problems with intramedullary nails, 4 with plates, 6 with screws and 1 with another device. The estimated increase in operating time varied between 20 and 140 minutes. Major complications reported included breaking intramedullary nails, screw heads shearing off, and damage to the underlying bone.
This survey demonstrates significant problems in removing titanium implants. Surgeons need to be aware that when using these devices difficulties with their removal can be encountered and patients should be warned that further injury may be sustained during device removal.
Hallux rigidus was first described by Davies-Colley and Cotterill in 1887 and varied management techniques have been described by authors since. This paper carries out an audit looking at the management of hallux rigidus in 108 patients.
A retrospective study was carried out on 108 patients coded as hallux rigidus/hallux valgus over a ten year period from 1992 to 2002 (33 male and 75 female) with a follow-up range from 3 to 144 months. Thirty three toes (27 patients) were fused, 20 toes had Tel Aviv procedures (17 patients) and 61 patients were managed conservatively.
Of the 33 toes fused, 18 required a second procedure in the form of wire removal, two developed transient transfer metatarsalgia, one developed IP joint pain and one had asymptomatic fibrous non-union. Of the 20 Tel Aviv procedures, one toe developed hallux valgus requiring re-operation and two toes had unrelated complications, one requiring re-operation.
A single method of MTP fusion when the audit was performed revealed an interesting outcome. Hallux rigidus must be managed as an ongoing continuum, not a static state.
We have correlated the ‘bedding-in’ response (the high femoral head penetration seen in the first two years after operation) with changes in offset and leg length from opposite normal hip.
Fifteen patients with serial x-rays taken in the first 5 years after operation had measurement of PE wear, femoral offset and leg length change from the opposite normal hip.
There was a weak correlation between increasing the leg length and increasing the offset during operation and increased femoral head penetration (‘bedding-in’) seen during the first two years after the operation. There was no correlation between offset and PE wear after two years in the PCA prosthesis.
Increased tissue tension in the first two years caused an increase in femoral head penetration. This effect is not continued beyond two years.
The aim of this study was to improve data collection, audit and research data by integrating a comprehensive patient data collection database into the day to day running of an orthopaedic department.
The day to day processes of the house surgeon and registrar junior staff were analysed and tasks identified that would allow accurate recording and recall of orthopaedic-specific patient data by automating and performing tasks that would improve junior staff efficiency. A database was then designed and implemented with a “front end” that performed such tasks as generating operating lists, tracking ward locations of patients, producing discharge summaries and auditing complications. This database was then introduced on the hospital intranet and the “back end” constructed to gather accurate patient and injury data to allow improved data collection and research.
Information and data collected was a significant improvement on previous methods available to the department. Junior doctor compliance for data entry was high but the system needed monitoring and “cleaning” on a weekly basis to maintain its accuracy. This method of data collection was more accurate than anything available in the hospital and has been surprisingly useful in producing data to support concerns within the department regarding managerial changes in hospital systems.
Use of a database collection system that gathers information by performing day to day tasks for junior staff has been an effective and reasonably accurate method of obtaining useful patient data. It requires regular monitoring to be most effective but has been easily integrated and accepted within the hospital system.
We have assessed the comparative function of young patients with hip or knee replacement using a high level function score.
A high level function score was developed for assessing running, walking, stair climbing and recreational activity. This was used on a series of patients after a total of 153 joint replacements including 99 THR and 54 TKR.
The groups were comparable with respect to age (average 57 years), gender and follow-up. Comparison between the groups showed that there was no significant difference in walking, stair-climbing and recreational activity. Patients with THR scored better on running ability and overall total score. Other differences noted included lower scores in bilateral joint replaced patients and posterior cruciate sacrificed knees.
Young patients undergoing hip or knee replacement have similar functional outcomes using a high activity function score. There were trends towards superior running ability and overall scores in the THR group.
We have developed and tested the accuracy of a completely automated method for polyethylene (PE) wear measurement of digitised antero-posterior and lateral radiographs.
New computer algorithms have been developed to measure PE wear on digitised hip radiographs. The only user input required is the file name of the x-ray. Validation was performed by simulation of PE wear in an acrylic phantom. Radiographs were analysed with the new software and results were compared to know penetration of the femoral head.
Accuracy using 10 antero posterior and lateral phantom radiographs was within ±0.08mm (95% CI) of the real femoral head penetration. There was no inter or intra-observer error (identical results with all measurements). Perhaps most importantly, this system gave accurate results in 94% of 600 clinical radiographs of variable quality. Only 74% of this same group of radiographs were considered of sufficient quality to allow reliable manual measurement.
This new method of PE wear measurements eliminated inter and intra-observer error, allowing comparison of wear results between different institutions. Accuracy is improved, but still limited by resolution of the scanned image.
Urinary tract infection is a source of organisms responsible for deep infection of hip and knee joint prostheses. In an attempt to reduce the occurrence of post operative urinary sepsis, some orthopaedic surgeons insert indwelling urethral catheters (IDC) immediately prior to surgery with the aim of avoiding urine retention. The purpose of this study was to determine if preoperative indwelling urethral catheterisation reduces the incidence of urine retention following total hip and total knee arthroplasty.
124 patients who underwent total hip and total knee arthroplasty in New Plymouth between April 2001 and July 2002, were randomly allocated to either have an indwelling urethral catheter inserted preoperatively (IDC group), or no catheter (control group). Prior to surgery all patients completed a questionnaire enquiring about a history of urinary obstructive symptoms, or previous urinary tract infection. The two groups were compared with regard to demographic data, questionnaire findings and the amount of post operative opiate usage. The primary outcome measure for the study was post operative urine retention. Urinary tract infection post operatively was considered as a secondary outcome measure.
No difference was noted between the two groups with regard to age sex arthroplasty type, history of urinary obstruction, or previous urinary tract infection. Post operative urinary retention occurred in a significantly less number of patients in the IDC group compared with the control group. No difference in post operative urinary tract infection was noted between the groups with the sample size used in this study.
Our study suggests that the prophylactic use of indwelling urethral catheters prior to total hip and total knee arthroplasty is effective in reducing the occurrence of post operative urine retention.
Forty six periprosthetic femoral fractures adjacent to a hip prosthesis have been retrospectively reviewed. Follow up included chart and radiograph review, Oxford Hip Score and SF-12 Global Function Score. Fractures were treated with internal fixation or revision arthroplasty without the use of allograft.
All the fractures united and functional outcome was good. The mean Oxford Hip Score was 26 and the SF-12 was 33. Complications were related to the severity of the fracture according to the Vancouver classification.
These results and a review of the literature support the ongoing management of periprosthetic femoral fractures without allograft.
Our aim was to assess the clinical and radiological medium-term outcome of a series of 153 consecutive total hip arthroplasties performed by two surgeons in Christchurch using the ABG hydroxyapatite-coated femoral stem and Duraloc 100-series uncemented acetabulum.
An independent clinical review using interviews and patient notes and radiological review of immediate postoperative and most recent x-rays was carried out.
At six to eleven years with approximately 95% follow-up, there were no stem failures, but two revisions following a fracture from significant trauma. Two cups were revised for loosening and one cup bone grafted for osteolysis. A dislocation occurred in 4.7% of cases requiring two liner exchanges and one cup revision. A low incidence of thigh pain and excellent radiographic results of the stem with high rates of bony ingrowth and no incidence of significant loosening was a feature of this series.
We report excellent results at medium-term follow up for an unceme4nted HA- coated femoral stem.
Although a number of agents have been shown to reduce the risk of thromboembolic disease, their use in total hip replacement (THR) remains controversial. Uncertainty exists regarding the safety of chemical prophylaxis as well as the choice of the most effective agent. Previous studies suggested that pneumatic compression with foot-pumps provide the best balance of safety and effectiveness, however too few patients were investigated in randomised clinical trials to draw evidence-based conclusions.
The purpose of this randomized clinical trial was to compare the safety and efficacy of pneumatic compression with foot-pumps versus low-molecular-weight heparin (LMWH) for prophylaxis against DVT.
Inclusion criteria were hip osteoarthritis and age less than 80 years. Exclusion criteria were history of thromboembolic disease, heart disease, and bleeding diatheses. 216 consecutive patients were considered for inclusion in the trial and were randomized either for management with LMWH (Fraxiparin, Sanofi-Synthelabo, France) or with the A-V Impulse foot-pump (Orthofix Vascular Novamedix, UK). Patients were monitored for DVT using serial duplex sonography and phlebography.
DVT was detected in 3 of 100 patients managed with the foot-pump compared with 6 of 100 patients who received chemical prophylaxis (p< .05). Sixteen patients did not tolerate continuous use of the foot-pump and were excluded from the study. The average postoperative drainage was 259ml in the foot-pump group and 328ml in the LMWH group (p< .05). Patients with foot-pump had less swelling of the thigh (10mm compared with 15mm) (p< .05). The patients of the foot-pump group had less postoperative oozing and bruising than did those who had received LMWH. One patient developed heparin-induced thrombocytopenia.
This study confirms the safety and efficacy of mechanical prophylaxis of DVT in THR. Some patients cannot tolerate the foot-pump.
To assess the efficacy of stabilising a femur following debridement of established osteomyelitis with a silver coated titanium plate.
A 19 year old male, with an established staphylococcus aureus osteomyelitis of the proximal femur, was treated with debridement and stabilisation of the proximal femur with a silver coated titanium plate, and intravenous then oral antibiotics.
The plate was removed six months postoperatively. Specimens were obtained for microbiology, histology and the implant sent for electron microscopic examination. Serum silver levels were obtained pre and post implantation and following plate removal.
The debrided defect of the femur healed. Specimens obtained at the time of removal showed no evidence of infection, either on culture or electron microscopic examination. Serum silver levels remained well below occupational safety guidelines.
This is an encouraging preliminary report of the potential for stabilisation of established osteomyelitis or infected non-union with a silver coated titanium implant.
We reviewed the diagnostic and clinical experience with acute osteomyelitis of the pelvis at Tauranga and Waikato Hospitals.
A retrospective review from a prospectively maintained data base was undertaken looking at all cases of pelvic osteomyelitis between 1988 and February 2003 at the two hospitals. Analysis of the diagnostic pathways, time to diagnosis, blood parameters, organism isolation, and type of imaging was carried out. Subsequent treatment including duration of intravenous antibiotic use was correlated with patient outcome.
There were 15 cases of acute pelvic osteomyelitis treated with an average patient age of 11.9 years. The most common causative organism isolated was Staphylococcus Aureus (S. Aureus) with no cases of MRSA. Inflammatory markers (ESR and CRP ) were elevated in the majority of patients but 75% had a normal white cell count. Blood cultures were positive in 90% of cases.3 patients required surgical drainage ( 1 case of turberculosis, 2 cases of staphylococcus aureus) The average duration of intravenous antibiotic therapy was 10 days with subsequent oral therapy for an average of 4 weeks. The minimum patient follow up was for 3 months, and there was no reoccurrence of infection in any patient. At final review all patients had returned to normal activities
Staphylococcus aureus is the most common causative agent in this population. ESR and CRP are the most useful markers and blood cultures are essential. Most cases can be managed non surgically and a shorter course of intravenous antibiotic therapy in this group was not associated with any adverse outcomes or reoccurrences of infections
We report a case of septic arthritis of the hip caused by toxigenic Corynebacterium diphtheria in a healthy, immunized child.
A four-year-old boy was admitted to our hospital with a four-day history of right thigh pain, inability to bear weight on the right leg and sore throat of one-day duration.
He was born in New Zealand and had been immunized against diphtheria. On admission he was febrile (37.3°C) with a congested throat. The right hip was flexed and externally rotated. His inflammatory markers were elevated. Aspiration of the hip yielded 8ml of yellow turbid fluid. Gram stain showed gram-positive bacilli. An arthrotomy was performed and the hip drained
Cultures of the aspirate grew Corynebacterium diphtheriae, the toxigenicity confirmed by the national reference laboratory.
The patient was treated with intravenous and oral antibiotics for 6 weeks and he made a full recovery.
Our patient had a history of immunization to diphtheria and this induces a protective level of antibodies against the toxin but does not prevent the bacteria from invading the blood stream and causing infection.
This is to our knowledge the first reported case of septic arthritis caused by toxigenic strain of Corynebacterium diphtheria.
Several surgical techniques have been described of resistant lateral epicondylitis or tennis elbow with variable results. This retrospective study presents the long-term outcome of a single surgeons experience with a modified surgical technique for the treatment of resistant lateral epicondylitis.
Between 1986 and 2001, the senior author performed 171 surgical procedures in 158 patients for resistant lateral epicondylitis. 147 elbows in 136 patients (88%) were independently evaluated at a mean time to follow up of 9.8 years. Patients were assessed using a functional questionnaire and physical assessment. In addition to physical assessment, provocative testing of the extensor origin and grip strength was performed. Patients subjectively rated the result of surgery and these results were compared to objective elbow performance scores.
Subjectively, 97% of patients assessed the result from surgery as good to excellent. Objectively, 97% results were good to excellent using elbow performance scores. Synovial fistulate developed in two patients by day ten postoperatively. One patient required further surgery for a synovial fistula which healed with no sequelae. There were no other complications following surgery. The postoperative range of motion improved in all patients but remained reduced in four patients. There was a significantly worse outcome for patients with Worker’s compensation claim and for cigarette smokers. There was no difference between grip strengths between the operated arm and the non-operated arm. The majority of patients returned to work by six weeks and were pain free by twelve weeks. Less than 5% of patients experienced lateral epicondylitis pain in their elbow post-operatively. A small group of patients altered their occupation or recreational activities due to tennis elbow symptoms.
The surgical technique described produces excellent results in greater than 87% of patients in the treatment of resistant lateral epicondylitis. This procedure produces a low complication rate and is associated with a high rate of patient satisfaction. Patient selection is critical in the surgical treatment of resistant lateral epicondylitis.
The purpose of this study was to highlight uncommon and confusing clinical problem of unilateral prolapsed intervertebral disc (PIVD) producing contralateral symptoms based on case reports and literature review.
Four cases of patients with disc prolapse contralateral to the symptomatic limb are presented. Two patients had cervical disc herniations, and one patient had a lumbar disc prolapse. All three patients had resolution of their contralateral radicular pain following discectomy.
Few reports have been published of patients with unilateral sciatica following contralateral lumbar disc herniation. The authors described the unique features of their patients’ anatomy and related this to their respective pathology. Coexistence of lumbar spondylosis and lateral recess stenosis, as well as the unique features of the attachments of the dural sac and nerve root sleeves to the surrounding osseous structures serve to provide an explanation for contralateral symptoms.
The cervical spine is quite different from the lumbar spine. Here the spinal cord rather than the more flexible cauda equina fills most of the spinal canal. A number of reports can be found describing Brown-Sequard syndrome as a consequence of cervical disc herniation. The two cases presented are in our opinion also the consequence of direct pressure on the spinal cord. We suggest that pressure on the ascending spinothalamic tracts leads to contralateral pain without other neurological symptoms.
Surgeons working in orthopaedic operating theatres are exposed to significant noise pollution due to the use of powered instruments. This may carry a risk of noise-induced hearing loss (NIHL). This study was designed to quantify the noise exposure experienced by orthopaedic surgeons and establish whether this breaches occupational health guidelines for workplace noise exposure.
A sound dosimeter was worn by the operating surgeon during 3 total hip replacements and 2 total knee replacements. A timed record of the procedures was kept concurrently. Noise levels experienced during each part of the procedure were measured and total noise exposures calculated. Quantified noise exposures were compared with occupational health guidelines.
Noise exposure in total hip replacement averaged 4.5% (1.52–6.45%) of the allowed daily dose (average duration 77.28 min). Total knee replacement exposure was 5.74% (4.09–7.39%) of allowed exposure (average duration 69.76min). Maximum sound levels approached, but did not exceed recommended limits of 110 dBA (108.3dBA in total hip replacement and 107.6dBA in total knee replacement). Transient peak sound levels exceeded occupational health maximum limits of 140dB on multiple occasions during surgery.
Overall total noise dose during orthopaedic surgery was acceptable, however orthopaedic surgeons experience brief periods of noise exposure in excess of legislated guidelines. This constitutes a noise hazard and carries a significant, but unquantified risk for NIHL.
We report intermediate term results of a technique of acetabular augmentation using block femoral head autograft and the uncemented expansion cup for adult hip dysplasia.
A retrospective review of one surgeon (BFH) series of consecutive total hip replacements for hip dysplasia using femoral head acetabular augmentation was carried out. The technique involves sectioning the femoral head longitudinally reversing and fixing it to the deficient acetabulum with 6.5mm AO screws. This is then reamed to accept the uncemented expansion cup. Patients were identified from audit databases. Patients completed clinical questionnaires, examination and radiographic evaluation.
Fifteen hips were identified in twelve patients (three bilateral). The average at age at surgery was 54 (44–58) years. There were eight females (eleven hips). Three patients (three hips) were unable to be contacted. Average follow up was 8.4 (4.8–11.4) years. Preoperative centre edge angle was 14 (−10–30) degrees. One patient developed a deep infection requiring early staged revision. One patient was not satisfied with her results at follow up. Mean Harris Hip Score was 83 (63–100), mean WOMAC Score was 76 (50–95). Range of motion was well maintained in all patients. Four patients had other co-morbidities affecting their results. Radiological review shows all grafts to have united with no screw breakage and no cup loosening.
At eight year follow up there is high satisfaction, good clinical and radiological results. These results demonstrate good intermediate term results using this technique in total hip replacement with acetabular dysplasia.
A retrospective audit to evaluate the effectiveness of Tranexamic Acid (TXA) in reducing blood transfusion requirements in primary total knee and hip joint replacements operated on by a single surgeon (SMD).
A survey is being sent to all Fellows of the New Zealand Orthopaedic Association who are currently in clinical practice to evaluate the strategies currently in use for reducing blood transfusion requirements in joint replacement surgery.
All primary total knee and hip joint replacements are included in this trial since February 2003. Two doses of TXA (Cyclokapron) are given at a dose of 10mg/kg intravenously. The first dose is given 10 minutes before the skin incision and the second dose 10 minutes before wound closure in the case of hip replacements and just before tourniquet release in total knee replacements. Haemostasis is secured by diathermy in the case of total knee joint replacements after tourniquet release. One deep suction drain is used.
The use of Tranexamic acid was continued until September when the numbers were collated and compared to a six-month period prior to the use of TXA. Blood loss (both measured and calculated ) and the need for transfusion were the major outcome measures. Complications related to the use of TXA were recorded.
The response rate was 89%. Various strategies to reduce blood loss were used. The mean calculated blood loss in the control group and TXA group were 1196 and 948 ml respectively. The mean measured blood loss in the control group and TXA were 595 ml and 468 ml respectively. This small number of cases – (control 8 and TXA 13) did not reach statistical significance but there was a trend in favour of reduced blood loss with the use of TXA. There was one wound haematoma in the TXA group.
A wide variety of blood conservation strategies are used by New Zealand Orthopaedic Surgeons. The use of TXA in knee joint replacements is a promising strategy.
The aim of this study was to determine the outcome of carpal tunnel decompression in elderly patients and whether this can be predicted by the severity of pre-operative nerve conduction studies.
A retrospective study was undertaken of all patients over 70 years who had carpal tunnel release (CTR) at Dunedin Hospital between April 1999 and April 2002 with a minimum one year follow up. A grading system for pre-operative nerve conduction studies (NCS) was formulated which scored patients from 1 to 6 according to severity. Patients were followed up by postal questionnaire (Boston Carpal Tunnel Score) with telephone follow up of non-responders.
There were 105 CTR procedures performed in 96 patients. Median pre-operative NCS Score was 4 with 47% scoring 5 or 6. 4 Patients had died. Post-operative symptom severity scores were low and the majority of patients were very satisfied with the results of surgery.
Despite nerve conduction studies consistent with severe median nerve compression, patients had low postoperative symptom severity scores and overall were very satisfied. Carpal tunnel release in patients over 70 years of age is justified and associated with good outcome.
To assess the radiological outcome of instrumented posterolateral lumbar fusion in a prospective randomised study comparing the use of allograft (fresh frozen human femoral head) to autologous bone (from the posterior iliac crest), using a validated method.
One hundred and twenty four radiographs of patients who had undergone instrumented posterolateral spinal fusion were assessed for fusion or non-fusion by three independent observers using the same criteria, and a second time by one of the observers. The Kappa scores for the inter-observer and intra-observer agreement were calculated. Thirty-three of these patients had fusion status verified by the gold randomised to one of two groups, to receive either allograft bone or autologous bone. The same surgeon using the same surgical technique performed or supervised all cases. The radiological results of the two groups were assessed as well as the quality of fusion.
Both the inter-observer and intra-observer kappa scores (k) were 100%. The sensitivity of the method was 87.9% and the specificity was 100%. Thirty-seven patients received allograft and 32 patients received autograft. There was no significant difference in the fusion rate, or the quality and quantity of the graft between the groups.
There is no difference in the fusion rates comparing the use of autograft and allograft for posterolateral instrumented lumbar fusion.
This is to report an audit of outcomes improvement in Lumbar Fusion patients in a private practice setting using routine application of a robust functional outcomes instrument – the Modified Rowland Questionnaire (MRQ). The MRQ is a validated responsive disease specific functional questionnaire. It ranges from 23 points (maximum disability) to zero (no disability). Potential changes in score are 46 points (−23 to 23). A 4 point improvement is clinically significant.
Two hundred and sixteen patients undergoing lumbar fusion procedures, over a five year period completed an MRQ prior to surgery and at the routine one-year follow up. Changes to the score were documented and analysed in relation to diagnosis, Accident Compensation corporation (ACC) coverage, and revision procedures.
Data completion was 88%. Median disability improvement was 10 points on the MRM questionnaire. Benefit occurred in 80.0% of patients. Improvements were more marked in degenerative spondylolisthesis and isthmic spondylolisthesis than fusions for discogenic back pain although this was not statistically significant. There was a trend to lesser functional improvements in those on ACC and those who had undergone previous surgery.
This study reports an attempt to audit outcomes in a spinal sub specialist private practice using an instrument that can be applied preoperatively and at one year follow up without undue additional work load for the patients or staff. The data completion was acceptable. Functional improvements were significant in all diagnostic groups. Outcomes in revision and ACC patients were not significantly inferior, as they have been described in similar overseas studies.
L5-S1 interbody fusion is a successful technique for treating patients with isolated degenerative disc disease. Traditionally through an open technique, the anterior laparoscopic approach for this was first described in 1991.
The purpose of this study was to review the long-term outcome results of L5-S1 interbody spinal fusion, using an anterior endoscopic technique, performed on patients with isolated degenerative L5-S1 disc disease. The first 41 spinal fusions performed by the senior authors were analysed. Patients received clinical, functional and radiological review by an independent assessor.
Clinical outcomes were excellent with > 90% of patients having significant improvement in back assessment scores (Fraser and Greenough, Japanese Orthopaedic Association). There were no intraoperative complications, no vascular complications, and no reports of retrograde ejaculation.
The anterior endoscopic approach for L5-S1 inter-body fusion results in good clinical outcomes, with a very low rate of morbidity. Surgical recovery time is quicker compared to open techniques, however, two skilled surgeons and an increase in theatre resources is required.
Spinal epidural sepsis is more widely recognised with MRI. Treatment includes antibiotics, multisystem support and drainage of pus. Neurological loss will often be stabilised but dramatic recovery is infrequent, explaining the importance of early intervention. This series highlights a very sinister spectrum of spinal infective disease despite ideal traditional treatment for spinal skeletal infection.
This is a retrospective case series review of five patients.
All patients presented with regional spinal pain, fever and regional musculoskeletal infective foci (e.g. discitis). Mild neurological abnormality existed in three patients. Rapid multisystem collapse occurred with the need for ventilatory support, despite institution of appropriate antibiotic treatment for all patients. All had grown Staphylococcus Aureus from blood cultures. Subsequent extensive quadriparesis/plegia developed, and repeat imaging demonstrated wide spread epidural pus in the cervical spine. Surgical treatment was considered but not performed when the prognosis was so poor neurologically and medically, and when the widespread epidural pus was so inaccessible. All patients died rapidly upon withdrawal of supportive treatment.
This paper describes a sinister spectrum of spinal infection with catastrophic complications despite “appropriate” treatment for previously diagnosed spinal foci infection. Positive blood cultures and fever alert to these dangers, and multisystem collapse heralded the development of cervical epidural infection. Possible interventions include early MRI scanning of the whole spine, more aggressive (than traditionally accepted) surgical treatment of infective foci in the spine in these circumstances, and minimally invasive cervical canal decompression procedures with multiple laminotomies.
To investigate the effect of pressurizing vertebral bodies during vertebroplasty using different materials in the development of fat embolism (FE) and any associated cardiovascular changes.
Polymethylmethacrylate (PMMA) is the material of choice for vertebroplasty (VP). However, PMMA has several disadvantages such as exothermic curing, uncertain long-term biomechanical effects and biocompatibility. As a result alternative materials are being developed to overcome these problems.
In order to determine the role of PMMA in the generation of cardiovascular changes following vertebroplasty we compared injection of cement with wax in an animal model.
In twenty sheep, four vertebral bodies were augmented either with PMMA or bone wax. Heart rate, arterial, central venous and pulmonary artery pressure, cardiac output and blood gas values were recorded. At postmortem the lungs were subjected to histological evaluation.
The consecutive augmentation of four vertebral bodies with PMMA induced cumulative fat embolism causing significant deterioration of baseline mean arterial blood pressure (MABP) and blood gas values. Injection of bone wax resulted in similar cardiovascular changes and amount of intravascular fat in the lungs.
Conclusion: In this animal model cardiovascular complications during multiple VP happen regardless of the augmentation material used. The deteriorating baseline MABP during VP is associated with the pressurization and displacement of bone marrow/fat into the circulation rather than caused by polymethylmethacrylate.
To assess the outcome and safety of transarticular C1-C2 screw fixation
The clinical and radiological outcomes of 15 patients treated with posterior atlantoaxial transarticular screw fixation and posterior wiring was assessed at a minimum follow up of six months. Indications for fusion were rheumatoid arthritis in eight (instability in six and secondary degenerative changes in two), non union odontoid fracture four, symptomatic osodontoideum one, C1-C2 arthrosis one and irreducible odontoid fracture one. Fusion was assessed with plain x-rays including flexion – extension films.
Twenty nine screws were placed under fluroscopic guidance. Bilateral screws were placed in 14 patients and a single screw in one patient. This patient had a single screw placed due to the erosion of the controlateral C2 pars by an anomolous vertebral artery. All patients had radiological union. Two screws (7%) were malpositioned, neither was associated with clinical sequelae. No neurological or vascular injuries were noted.
Transarticular C1-C2 fusion yielded a 100% fusion rate. The risk of neurological or vascular injury can be minimised by thorough assessment of pre operative CT scans to assess position of the vertebral artery and use of intra operative lateral and AP fluroscopy.
Recent years have seen a decided swing from the longstanding inpatient model of rehabilitation to an outpatient model for all branches of medicine in Australia. This swing has been largely cost-driven and is unlikely to change.
This paper reports on the development of a Paediatric Spinal Outreach Team (ORT) in New South Wales (NSW). The ORT was formed in 1993 and consists of a nurse, physiotherapist, occupational therapist and a social worker. It functions in close collaboration with the two children’s hospitals in Sydney. Approximately 10–11 new cases of paraplegia/quadriplegia occur in children/adolescents (up to 18 years of age) in NSW each year (population approx. 6 million). Their therapeutic needs change with growth, development and maturation. Families in regional NSW have special requirements and web-site information services (distance education) will play an important role for them in the future. Integration with an organisation which provides ancillary services is essential for a comprehensive, state-wide programme.
It is suggested that a comparable service would play an equally important role in other countries. Case studies to demonstrate savings to be made with this type of service need to be done to secure recurrent government funding.
The purpose of this study was to assess the technique of ultrasonographic evaluation of anterior shoulder translation from an anterior approach.
Anterior translation in the right shoulders of 23 volunteers was evaluated using ultrasound with a 10 MHz, 6 cm wide linear transducer. A translatory force of 90 Newtons (N) was used to translate the humeral head in the adduction and internal rotation position (Position 1), while 60 N was used in the more clinically relevant position of 90° abduction and external rotation position (Position 2).
The overall intraobserver coefficients of variation ranged from 0–13% (mean 3.8 ± 2.5%) for examiner 1 and 0.5–20.9% (mean 5.1 ± 3.9%) for examiner 2. The overall interobserver variation ranged from 0–29.8% (mean 9.3 ± 7.3%). The anterior translation in Position 1 ranged from –2.6 to 12.9 mm (mean 2.1 ± 3.1 mm) for examiner I and from −4.1 to 4.7 mm (mean 1.1 ± 2.2 mm) for examiner II. The anterior translation in Position 2 ranged from −3.3 to 3.7 mm (mean 0.3 ± 1.9 mm) for examiner I and from −8.3 mm to 4.5 mm (mean −0.7 ± 2.6 mm) for examiner II. The intraclass correlation coefficients (r) for the measured anterior translation between the 2 examiners for the 2 positions were 0.029 and −0.058 respectively.
The interobserver coefficient of variation remains excessive and there was poor agreement in the measured anterior translation. The finding of negative values in the measured anterior translation despite translatory force raises further concerns about the prospective clinical use of this technique at the present moment.
Unicompartmental knee arthroplasty has been a popular treatment option for osteoarthritis, since popularised by Marmor in the early 1970’s. The Miller-Galante prosthesis has been in widespread use in Taranaki since 1992. The initial results were encouraging, however, recently a number of failures have caused us to review our results.
The indications for the procedure were osteonecrosis or osteoarthritis limited to one tibiofemoral compartment of the knee. 145 patients were available for assessment from January 1992 – December 2001. Patients were retrospectively reviewed with a clinical assessment, questionnaire and radiographic examination. The Knee Society Scoring System was used. There were 175 knees available for review.
There was 100% follow-up. The average age of patient was 69 years. The average follow-up time was 6 years. The10 year survival was 94%. The major cause for failure was polyethylene wear (4.5). There was no statistical difference between age, tibial insert size and different surgeons.
The unicompartmental Miller-Galante knee prosthesis has very good results at 10 years. However, a high percentage of polyethylene wear is a concern and requires further investigation into the possible causes for this.
Traumatic shoulder dislocations at young age result in a significant re-dislocation rate and lead to chronic instability. Conservative treatment fails in 25–96% of cases especially in young active patients. The accepted standard treatment is the classical open Bankart repair which almost always results in loss of motion. The development of new techniques and devices has lead to an increase in arthroscopic techniques for shoulder stabilisations.
Between September 1996 and October 2000 262 arthroscopic shoulder stabilisations were performed by the senior author: 159 cases FASTak® titanium anchors, 26 Panalok® anchors and 57 cases Suretac® anchors were used. Minimum follow up was 12 months with a mean follow up of 24.9 months (12–50). Rowe score and a visual analogue scale was used to measure patient satisfaction.
The Rowe score increased to 83,1 +/− 20,9. The visual analogue score demonstrated overall patient satisfaction. Complications included redislocations(4.7%) sub-luxations (6.3%) and ongoing instability (6.3%). Return to sports occurred in 89.1% of patients with 68.4% being able to return to their previous sports activity level.
This study demonstrates that arthroscopic shoulder stabilisation is comparable to the gold standard open Bankart repair. It is associated with a high patient satisfaction, lower morbidity, faster return to the previous activity level, better range of motion and less postoperative pain. The disadvantage of the technique is a long learning curve and the potentially longer operating times.
Posttraumatic shoulder instability is a common problem in the field of sports medicine. Especially overhead athletes need intact stabilisers to meet the functional requirements. Open procedures often result in limitations of movement postoperatively. Arthroscopic techniques offer potential advantages such as better range of motion and shorter rehabilitation times.
Between September 1996 and October 2000 159 arthroscopic shoulder stabilisations were performed with FASTak® anchors. The mean follow up was 24.9 months (12–50). Rowe score and a visual analogue scale were used to measure patient satisfaction. 72 patients (m=57, f=15)with a mean age of 27.6 years (17–65) were included and clinically examined.
The Rowe score increased to 83.1 after primary stabilisation and 68.1 after revision procedures. The visual analogue score demonstrated overall patient satisfaction. 89.1% (n=64) of the patients could return to sports with 68,4% (n=49) being able to return to their previous sports activity level. Overhead athletes returned to sports in 89.4% of cases and 63.3% to their pre-injury level. In the non-overhead athletes 86% returned to sports with 60% to their pre-injury level.
This study demonstrates that arthroscopic shoulder stabilisation with FASTak® anchors may be offered to the athlete regardless of the sports activity. It allows return to sports in a high percentage and does offer the potential advantages of a faster return to the previous activity level, better range of motion and less postoperative pain. Disadvantages of the technique is a long learning curve and should therefore only be performed by dedicated and experienced shoulder surgeons.
The aim of this study was to assess the benefit and durability of isolated lateral release for advanced osteoarthritis of the lateral facet of the patellofemoral joint.
A retrospective study of 23 knees in 20 patients who had isolated lateral patellofemoral joint arthrosis treated with arthroscopic debridement and limited open lateral release was carried out. Patients completed a specific patellofemoral questionnaire (35 points) including questions for pain and functional improvement and pain and functional Fisual Analogue Scores (VAS). Eighteen knees in 15 patients were clinically and radiologically examined.
Patients averaged 50 years of age and 2 years from surgical treatment. Visual analogue scores for pain improved 28% and function 40% with little radiological change. Similar improvements were seen in the patello femoral specific questionnaire. The results appeared to be durable over the 2 year follow up period.
Lateral release for treatment of isolated arthrosis of the lateral compartment of the patellofemoral joint is an effective, reliable, durable procedure in carefully selected patients.
Calcification of a thoracic intervertebral disc (IVD) with prolapse and root syndromes/spinal cord compression in humans are well-documented entities. The mineral phases have been identified. Similar pathology occurs very rarely in children. It is also seen in dogs, especially the short-legged, chondrodystrophoid (CD) breeds, which are prone to disc degeneration, and in older sheep. The latter exhibit some morphological CD features.
This study is based on radiological/histological/electron microscopic/x-ray diffraction studies of human operative specimens and post-mortem adult animal tissues
The transitional zone (TZ), the interface between the nucleus pulposus and the annulus fibrosus, is the area of the IVD most sensitive in children and adults to the events which lead to dystrophic calcification. The TZ is the “growth plate” of the IVD and the site of maximal proteoglycan and protein synthesis. Giant hydroxyapatite crystallites are the dominant mineral phase in the human (children and adults) and canine pathology. Nucleation occurs in degraded matrix.
The new observation of the type and distribution of calcification in the elderly ovine IVD suggests this animal is a suitable model for further research into the enigmatic phenomenon of so-called dystrophic IVD calcification.
Single-stage bilateral total knee arthroplasty is an uncommon and often controversial procedure. Recent reports have refined the data relative to bilateral total knee arthroplasty and complications which include myocardial infarction, deep vein thrombosis, pulmonary embolus and death. Less significant complications, including post-operative ileus and pseudo-obstruction are also more common following bilateral replacement.
A retrospective study of the cases of total knee arthroplasty performed by the senior authors in the last ten years, examines details of surgery and anaesthesia, pre and post-operative management to identify the occurrence of complications. Patients also completed an Oxford Knee Score and a questionnaire relating to their experience of having a bilateral procedure.
While the outcomes and cost benefits of single stage bilateral replacement are established, the risk of complications remains. This study establishes the low complication rate associated with this procedure in the senior authors’ hands, and documents the high patient satisfaction from it.
The study demonstrates that, in selected patients, simultaneous bilateral knee replacement surgery can be performed with good outcomes without a definite increase in perioperative risk.
A new method of polyethylene wear measurement for analysis of serial radiographs of the same patients over a 10 year period is described.
Eighteen patients with a PCA THJR had serial radiographs performed with a minimum of 8.5 year follow up. A total of 560 A-P and lateral radiographs were analysed.
The graphs of PE wear v time fell into two groups: Group 1 – (7 patients) had accelerated PE wear with eventual development of osteolysis. Group 2 – (11 patients) had PE wear of less than 0.16mm/year and their latest radiograph showed no evidence of osteolysis.
With improved accuracy and elimination of user error, measurement of PE wear may now have the ability to make predictions about the longterm survival of a THJR. Clinical decisions may be able to be made based on individual patient measurements.
To determine whether increased sagittal laxity has an effect on functional outcome following posterior cruciate retaining total knee replacement using two differing tibial insert designs.
Ninety-seven patients were reviewed clinically, radiologically and underwent KT1000 testing of their TKR at a minimum follow up of 5 years (mean 6.5 yrs). The femoral component design was the same in all patients (Duracon/PCA). Fifty two patients had a relatively flat tibial insert design (group 1), while 45 patients had an AP lipped insert (group 2) following a change in design in 1995.
The 2 groups were comparable for age, sex, Charnley category, BMI, tibial slope and follow up. There was no significant difference in laxity measurements, IKS or WOMAC scores between the groups. There was no significant correlation between laxity and outcome score or flexion range.
Increased sagittal laxity in a knee replacement does not have a strong influence on functional outcome. The differing tibial insert designs had no significant effect on either laxity or function.
To review local experience using the Avon patellofemoral arthroplasty
All patients were retrospectively reviewed with respect to function, radiology and satisfaction
Fourteen patients were followed up. There were no revisions and very good functional outcome. Patient satisfaction was high.
The Avon patellofemoral arthroplasty is an effective implant in selected patients.
High tibial osteotomies are commonly performed for varus/valgus malalignment of the knee. In the past we have been well aware that a high tibial osteotomy corrects the coronal plane but we did not consider changes of the tibial slope. Altering the slope has an impact on the in situ forces of the cruciate ligaments and influences the stability of the knee. The purpose of this study was to investigate the amount of alteration of the tibial slope by a closed wedge osteotomy.
From January 2001 to September 2001 we reviewed retrospectively all Xrays of patients that underwent a high tibial osteotomy or were admitted for removal of hardware. 80 patients were included. 67 patients could be followed up.
The slope on the preoperative xrays was 6,1 degrees (0–12). A closed wedge osteotomy decreased the slope by a mean of 4,88 degrees. A high tibial osteotomy of six degrees in the coronal plane decreased the slope by 4.29 degrees, a HTO of eight degrees decreased the slope by 7 degrees, a HTO of ten degrees by altered the slope by 4.75 and of twelve degrees by decreased the slope by 6.5 degrees.
A closed wedge osteotomy decreases the tibial slope. It is the preferred technique when a combined procedure (HTO and ACL reconstruction) is planned. There is no correlation between the degree of correction of the coronal plane by a closed wedge high tibial osteotomy and changes of the tibial slope.
Aspetic loosening is a major problem of total hip arthroplasty, especially in young and/or active patients. This study was performed to assess the clinical performance of non-cemented, metal-on-metal implant and complications including loosening and osteolysis at medium-term follow-up.
Between 1994 and 1998, 38 patients (45 hips) had a THA with a Metasul articulation. Thirty-two patients (39 hips) were available for follow up an average of 5.3 years following the operation. Patients were independently assessed by clinical examination, with use of the Harris Hip Score, patient self-assessment forms and radiographs.
The average age was 53.5 years (range 29 to 68) with a diagnosis of primary OA accounting for 34 hips and other diagnoses for 5 hips. The average Harris Hip Score for those patients without a revision was 94.7 points (range 71 to 100). One patient had a revision of a loose femoral component at 16 months, at last review he had a Harris Hip Score of 99.7 points. No patient had a loose or revised acetabular component. Two patients had an early dislocation without sequelae. Thirty-six hips were rated as very good or excellent. There was no radiological evidence of progressive radiosclerotic lines and no other evidence of loosening.
This group of young and/or active patients with Metasul articulations has clinical results equivalent to metal-on-polyethylene articulations. There is no evidence to suggest that the rate of loosening is higher as was documented by previous metal-on-metal designs. At medium term follow up there is no evidence that the metal-on-metal articulation gave rise to any new problems or complications.
The aim of this retrospective study was to assess the long-term results (minimum ten years) following treatment of medial compartment osteoarthrosis of the knee with high tibial osteotomy using a simple, reproducible technique with minimal internal fixation and early mobilisation.
Between 1980 and 1993, seventy-five lateral, closing wedge osteotomies were performed in sixty-five patients by a single surgeon (ALP). A lateral approach was utilised, with stabilisation achieved using two staples and no use of external splints. Twenty-three patients had died prior to this review (twenty-six knees) and the remaining forty-two patients were invited to attend for independent review. The patients were assessed using the Knee Society Knee Score, Tegner and Lysholm activity score, a patient self-assessment questionnaire and radiological review.
The average age of the patients at surgery was sixty-two years (range twenty-six to seventy-seven years), reviewed between ten and twenty-three years (average seventeen years) following the procedure. Results will be presented with end-points of conversion to arthroplasty and patient dissatisfaction and complications discussed. There were no major complications observed during conversion to total knee joint replacement.
The current role of high tibial osteotomy for the treatment of medial compartment osteoarthrosis will be discussed.
The aim of this study was to evaluate the efficacy of the anteromedial opening wedge osteotomy for PCL deficient varus knees with medial compartment degenerative changes
Twelve patients had undergone an anteromedial opening wedge high tibial osteotomy for the PCL deficient varus knee using a Puddu plate. All patients were followed for a minimum of one year. Patients were evaluated prospectively pre-operatively and at follow up by visual analogue pain and patellofemoral pain scores, IKDC II, WOMAC, SF-36 and a radiographic evaluation.
All patients improved from Grade III to Grade I PCL instability. Patients reported a significant improvement in visual analogue pain and patellofemoral pain scores, IKDC II, WOMAC and SF-36.
This technique shows encouraging early results for a complex problem.
Osteochondral autologous transplantation (OATS) is a new technique for the treatment of osteochondral defects.
In a prospective study between April 1996 und May 2001 we used the OATS technique to treat 201 patients (125 male, 76 female) with a mean osteochondral defect of 3,3 cm2. The defect was in the medial femoral condyle in 96 cases, the lateral femoral condyle in 16, the patella in 22, the trochlea in seven, the tibial plateau in one, the talus in 48, the tibial plafond in two and capitellum in four. There were 17 other locations. The procedure was performed either open or arthroscopically. A mean of 2,2 cylinders was transplanted.
The Lysholm score in the lower limbs increased from a preoperative mean of 58,3 (20 to77) to a mean of 90,2 (70 to 100). Treatment by OATS alone increased the score from 65,2 to 91,6. With additional ACL/PCL reconstruction, the score increased from 49,9 to 82,6. The combination of OATS, HTO, ACL/PCL reconstruction increased the Lysholm score from 55,5 to 85,5. Ten per cent of patients complained of pain at the donor site in the lateral femoral condyle. There were no complications related to OATS performed in the upper limbs, and control MRI three months postoperatively showed incorporation of all cylinders.
The results are encouraging, and give rise, to the hope that this cost-effective and safe treatment for limited osteochondral defects may delay or even prevent the onset of osteoarthritis.
Two hundred and thirty six posterior stabilized total knee arthroplasties were performed consecutively. Twenty seven patellar clunk syndromes were identified in 25 patients. Insall-Salvati ratio, position of joint line, postoperative patellar height and anterior-posterior position of tibial tray were measured. We found that post-operative low-lying patella (p< 0.001) and anterior placement of tibial tray (p=0.011) was associated with patellar clunk syndrome. Thirteen patients had bilateral total knee replacements of the same prosthesis (5 bilateral AMK and 8 bilateral IB) but unilateral patellar clunk syndrome. The non-clunk sides were used as control for comparison with the clunk sides. The congruency and tilting of the patellar button in the skyline view were documented. We observed that the congruency of the patella button was less satisfactory in the clunk side (p=0.019).
Our aim was to determine from the general community an understanding of the implications of informed consent, expectations in regard to self-autonomy, appreciation of risk in surgery, the implications of surgical complications, the degree of acceptability of risk for a given complication and views on surgeon liability.
One thousand questionnaires were distributed to members of the general public attending the Palmerston North Hospital as outpatients or visitors (inpatients were excluded).
Less than 20% of respondents appreciated the concepts of battery, negligence, self-autonomy and confidentiality. 59% wanted to know about potential complications in order to assist them in making a decision on whether or not to proceed with surgery. Given options and a discussion of the risks, 64% wished to take responsibility for which surgical procedure they would undergo. 9% were unaware that surgical procedures had risks of serious complications. 10% would not undertake surgery if the risk of a serious complication was one in a million, while 30% would undertake surgery regardless of the risk involved. 21% felt the surgeon would be liable in the event of an unmentioned rare complication.
The grasp of the perceived objective of informed consent is poor amongst the general population. The tolerance for medical negligence is low and expectations in regard to self-autonomy seem unrealistically high. We feel it is necessary to revisit ‘informed consent’ and for the public (and the legal profession) to make ‘informed consent’ a practical goal-orientated patient/doctor friendly process rather than the existing ‘legal obstacle’ that it is.
The ability to assess the blood flow to a bone (IBF) is important for orthopaedic surgeons when deciding the fate of an injured or diseased bone. Currently there is no easy and effective method for quickly assessing the blood flow status of a bone. There is accumulating evidence that suggests that IBF may be correlated to intraosseous pressure (IOP).
Therefore, we aimed to investigate whether the two variables are correlated so that the orthopaedic surgeon could confidently use IOP as an indicator of IBF.
Using 8 mature female ewes (B.W. ~56 kg) we measured cardiovascular (eg. arterial blood pressure – ABP), and intraosseous (ie. IOP and IBF) responses to nor-adrenaline (0–1.5 μg/kg/min. i.v.) and nitroglycerine (0–80 μg/kg. i.v.) IBF was measured using semi-quantitative technique of laser Doppler flowmetry (LDF).
Our results revealed that changes in ABP were directly correlated to changes in IOP (p < 0.001). Due to technical difficulties that were encountered when using LDF, the collected IBF data were limited. However, there was compelling evidence that there is a positive and direct correlation between IBF and IOP.
This opens an exciting possibility of using IOP for quickly and accurately assessing IBF as well as providing insight into the pathological mechanisms responsible for bone and joint disorders.
Regeneration of bone is an important goal in orthopaedic surgery, such as in augmentation of fracture healing, spinal fusion and filling of osseous defects. The repair of a critical skull defect is a well-established model for investigating the efficacy of cell signalling factors and biomaterials in inducing new bone formation. We aimed to investigate a 5-mm critical skull defect in the mouse, as an in vivo tool for analysis of potential bone active factors that have been bioprospected from dairy milk protein.
Adult Swiss CD1 mice were divided into 2 groups. Each group contained animals treated with vehicle (n=11), milk protein (4mg, n=10) and TGF-b1 (2μg, n=6). Under anaesthetic a high-speed burr was used to create a 5-mm craniotomy in the left parietal bone and a precut collagen sponge with 20ml of the test factor inserted. Fluorochrome labels were administered to facilitate quantitative histological analysis of the defect. The animals were sacrificed on days 14 and 28 and the calvariae excised and fixed. The defects were assessed for percent closure using radiography, transillumination and histology.
The formal analysis of this study is underway at present. Preliminary work in our laboratory with this milk protein has shown it to be a novel bone active factor. In vivo, local injection above the calvariae in adult mice resulted in significant increase in bone area and dynamic histomorphometric indices of bone formation. In vitro, the protein is anabolic, an effect that is consequent upon its potent proliferative and anti-apoptotic actions in osteoblasts, and its ability to inhibit osteoclastogenesis.
TGF-b1 has been shown in the literature to augment the healing of critical skull defects and is included in this study as a positive control.
We believe the critical skull defect in the mouse may be a useful means to assess the role of potential bone active factors in wound healing.
The purified milk protein used in this study may have a physiological role in bone growth and a potential therapeutic application in bone regeneration. We await formal analysis of the specimens to further elucidate this statement. Further experiments will be required to determine whether it provides results that are reproducible and/or comparable to other models of fracture repair.
We compared initial fixation strength of two commonly used tibial side hamstring ACL reconstruction fixation implants – the RCI interference screw and the Intrafix device.
Using a sheep model 36 hamstring grafts were prepared and implanted into the distal femoral metaphyseal bone using either a RCI screw or an Intrafix device. They were then pulled out until failure using an Instron Materials Testing Machine. Maximum strength of graft fixation and mode of failure were recorded.
The average strength of the graft was 48kg using the RCI screw and 90 kg using the Intrafix device. This difference was statistically significant. The maximum pull-out strength was 91kg for the RCI screw and 130 kg for the Intrafix device. The most common mode of failure in the RCI screw fixation was graft shredding on the screw and whole graft pullout whereas in the Intrafix device it was intratendinous failure.
The Intrafix device demonstrated a clear strength advantage over the RCI screw with regard to initial fixation strength. The Intrafix device may reduce tibial side graft creep which is a problem with hamstring ACL reconstruction.
The aim of this surgery was to determine current practice amongst orthopaedic surgeons in New Zealand with regard to Anterior Cruciate Ligament Reconstruction.
All current members of the NZOA were sent a questionnaire on the numbers and proportions of grafts performed, methods of fixation, operative technique and return to sport.
One hundred and ten of 140 questionnaires were returned completed. Ninety two orthopaedic surgeons were performing ACL reconstructions. Eight per cent performed patellar tendon grafts in preference to hamstring grafts, whereas 16% preferred hamstring over patellar tendon grafts. Almost 2000 patellar tendon grafts at an average of just over 20 per surgeon are performed each year compared to just over 500 hamstring grafts at an average of just over 15 per surgeon. Metal interference screws were the most common fixation device in patellar tendon and hamstring grafts.
Patellar tendon grafts are the most common grafts used for ACL reconstruction with 80 % of those surveyed preferring to use patellar tendon over hamstring grafts. Metal interference screws were the most common fixation device. There is reasonable consensus regarding return to activity and sport.
The aim of this study was to assess the injury pattern of patient’s 60 years plus who have required acute orthopaedic admission and the influence this population group will have on orthopaedic services in the future.
A retrospective analysis of orthopaedic patients obtained from our database covering a three-year period (2001–2003) was conducted. We identified those that had been treated with surgical and non-surgical procedures. The demographic injury pattern and length of stay was in-turn assessed in relation to anticipated changes in the population from projected data obtained from Statistics New Zealand.
A review of 1209 orthopaedic patients (60% males) indicated that the majority (92%) required acute orthopaedic admission. Within this group, the most common injury type was a fracture, experienced particularly in the lower limb. Length of hospital stay ranged from 0–188 days. Racial distribution incorporated a number cultures including New Zealand European, New Zealand Maori, Pacific Island, Asian, Middle Eastern, and Indian.
Orthopaedics like many other services should already have begun planning for this population group. Relevant specifications may include increased follow up visits, imbalance between males and females, and the percentage of urban-based patients. With regards to orthopaedic staffing and their skill base services need to look at the possible inclusion of an aged care specialist as part of the orthopaedic hospital team and enhancement of communication between orthopaedics and staff from the geriatric ward. Training packages for orthopaedic staff, in relation to healthcare of the elderly should also be made available.
Bone autograft contains living cells that participate in the healing process. Fragmentation and heat production during cutting will kill cells. We have investigated how excessive graft fragmentation and heating can be avoided.
Two prototype cutters were fabricated. Each had a single cutting edge at the front end of a 12 mm diameter collection barrel. The principal difference between the cutters was the rake angle (at the cutting edge): 23° on cutter #1 and 45° on cutter #2.
Thrust load, feed-rate, and torque were measured using an instrumented drill press. A total of 58 tests on specimens of fresh bovine cancellous bone (distal femur, ex-abattoir) and medium density polyurethane foam (Sawbones, WA. USA) (density 252 kg/m3) were conducted: twenty-four at 100 rpm and thirty-four at 200 rpm.
Small flake-like fragmented bone chips were encountered at low thrust loads. As thrust load was increased the chips became thicker. The average cutting energy for bone was 43.7 Nm (s.d. 48.2 Nm) for cutter 1 and 37 Nm (s.d. 27 Nm) for cutter 2. The average cutting energy for the foam was 13.9 Nm (s.d. 6.0 Nm) for cutter 1 and 8.1 Nm (s.d. 3.0 Nm) for cutter 2. Polyurethane results showed a similar trend.
A higher rake angle on a bone graft tool is associated with a lower cutting energy. In turn, a lower cutting energy will generate a lower temperature in the graft, a result that is beneficial for cell survival. Graft tool design can also influence bone chip size. These experimental results are being used for the development of cell-friendly tooling.
Current research efforts aim at enhancing osseointegration of cementless implants to improve early bone fixation.
The aim of the present study was to investigate whether bone morphogenic protein (BMP) 2 had a positive effect on the osseointegration of hydroxyapatite coated implants.
Hydroxyapatite (HA) implants were coated with BMP-2 and hyaluronic acid (HY) as the carrier or with HY alone. Uncoated HA-implants served as controls. The osseointegration of the implants was evaluated either by light microscopy and pullout tests after 1, 2 and 4 weeks of unloaded implantation in the cancellous bone of 18 sheep.
The BMP-2 coating significantly increased bone growth into the perforations of HA-implants. The proportion of bone-ingrowth at 4 weeks was 32% for the BMP-implants compared to 12% for HA implants. However, BMP-2 did not enhance the percentage of bone implant contact and interface shear strength values.
Conclusion: This study indicates that BMP-2 may help to increase bone growth across gaps of cementless implants in the early stages of bone healing improving fixation and decreasing the risk of loosening.
Our aim was to assess the impact of the increasing number of patients on orthopaedic waiting lists on general practitioners in New Zealand.
A 10-point questionnaire was developed in association with the General Practice Department at the Wellington School of Medicine, and mailed to 250 randomly chosen general practitioners around New Zealand. One hundred and fifty general practitioners returned the survey.
Sixty three per cent of general practitioners reported having between eleven and thirty patients on an orthopaedic waiting list in their practice. 85% of general practitioners reported spending up to an extra 6 hours per month looking after problems caused by having to provide extra care for the patients. In 90% of cases general practitioners reported that their patients required considerably greater community support in the form of extra physiotherapy, meals-on-wheels and occupational therapy. In 138 cases, general practitioners reported greater levels of stress in the families of patients on waiting lists. The majority of general practitioners reported an increased need for analgesia and night sedation during the period on a waiting list. They also reported substantial increases in paperwork necessary to access social supports.
This study documents the burden on general practitioners produced by the increasing waiting lists, and the re-alignment of waiting lists. This burden is reducing the general practitioner’s ability to deal with routine general practice problems, and likely adversely affects the health of other New Zealanders. There is a need for a study of patients on waiting lists to further assess their needs.
Periprosthetic bone density (BD) changes can be tracked using computed-tomography (CT) assisted osteodensitometry. Patient-specific computer-generated models allow for good visualisation of density changes in bone. We describe techniques for generating smooth and realistic finite element (FE) models that contain both BD and geometry from quantitative CT data using cubic Hermite elements.
FE models were created for three patients who had a total hip replacement. CT-scans were performed at 10 days, one year, and 3 years after the operation and calibrated using a synthetic hydroxyapatite phantom. FE models of the proximal femur were automatically generated from the CT data. Each model had on average 300 tri-cubic Hermite elements. Models were least squares fitted to the entire dataset. BD data was also sampled and fitted using the same cubic interpolation functions. Density was displayed using a colour spectrum.
Realistic patient-specific FE models were obtained. Density and changes in BD were easy to identify. The error in the geometric fitting (RMS distance between data points and the model surface) was generally less then 0.5 mm. The average error for the density fitting (RMS difference between each density data point and the interpolation function value at the same point) was 61.64 mg/ml or 3.08%.
CT osteodensitometry’s potential use as a clinical tool for monitoring changes to BD can be significantly enhanced when used in conjunction with realistic patient-specific finite element (FE) models. Realistic models can be generated with an economic use of scan data, thus keeping radiation dosage down.
Paget’s disease of bone is a common disorder characterised by focal areas of increased bone resorption coupled to increased and disorganised bone formation. Pagetic osteoclasts have been studied extensively, however, due to the integral cross-talk between osteoclasts and osteoblasts, we propose that pagetic osteoblasts may also play a key role in the pathogenesis of Paget’s disease. Any phenotypic changes in the diseased osteoblasts are likely to result from alterations in the expression levels of specific genes. To determine any differences in expression between pagetic and non-pagetic osteoblasts and their precursors the gene expression profiles of RANK, RANKL, OPG, VEGF, IL-1beta, IL-6, MIP-1, TNF and M-CSF were investigated in primary cultures of human osteoblasts and in the osteoblast precursor population of bone marrow stromal cells. We present preliminary data of this study.
Trabecular bone explants were finely chopped, washed free of marrow and cellular debris then either snap frozen in liquid nitrogen or placed in flasks to culture outgrowth osteoblast-like cells. Mononuclear stromal cells from bone marrow were isolated and grown in culture flasks. RNA and conditioned media were collected from cultured osteoblasts and stromal cells at confluency. The innovative method of Real-Time PCR, the most accurate technique available at present to quantitatively measure gene expression, was used for the comparison of gene expression levels in our samples. 18S ribosomal RNA was used as an endogenous control to normalise the expression in the various samples.
RANK, MIP-1 and TNF were only detected in stromal cells whereas RANKL, OPG, VEGF, IL-1beta, IL-6 and M-CSF were detected in both osteoblasts and stromal cells. OPG displayed higher expression in osteoblasts while IL-1beta showed higher expression in stromal cells.
To date we have not seen any significant differences in gene expression between pagetic and non-pagetic subjects when comparing a small number of samples. A larger cohort is currently being investigated. We are also comparing levels of secreted proteins in the conditioned media from pagetic and non-pagetic cell cultures. This may lead to further candidate genes involved in the pathology of the pagetic lesion.
Surgical waiting lists have led to development of clinical priority access criteria (CPAC) for prioritisation of patients selected for surgery. Although introduced widely into clinical practice in New Zealand CPAC tools have not been validated. Reliability studies were therefore undertaken by the CPAC Evaluation Consortium.
Methodology Thirty eight orthopaedic surgeons practising in public hospitals were randomly selected to participate in a prioritisation exercise using computer administered clinical vignettes. Fifty vignettes were developed from the clinical histories of patients selected for total knee arthroplasty (15), carpal tunnel decompression (15) and miscellaneous orthopaedic procedures (20). These were prioritised using each of 3 priority tools producing scores between 0 and 100: visual analogue scale reflecting global clinical opinion (VAS), a generic point scoring system based on points assigned to 5 clinical domains (GOPC), and diagnosis-specific 5 point Likert scale of priority combined with a predetermined table of a range of scores for each diagnosis (ISS).
The extent of inter-surgeon variability was striking but significantly less for ISS than GOPC or VAS. This was entirely explained by the complication of a predetermined table. The other two tools were similar except that the inter centile gap was larger for the clinical opinion based tool (VAS).
As access to elective surgery is determined by a fixed financial threshold a reliable scoring system will ensure equity of access. This seems to be best achieved by using the Integrated Scoring System.
The aim of this study was to document the medium-term results of the use of fluted, tapered, titanium femoral stem in revision total hip arthroplasty.
Seventy patients undergoing total hip revision using a tapered, grid-blasted titanium modular femoral stem were reviewed at a mean follow-up time of 47 months. Femoral defects were classified according to the Pak and Paprosky system, and femoral bone quality was assessed with the Bohm and Bischel system. Clinical function was measured by the Oxford Hip Score. Radiograpic analysis was performed in all cases.
Stems were classified as a failure or re-revision in 4.3% of the cases. Three required reoperation for recurrent dislocation, in each case the femoral component alone had been revised during the most recent revision. The postoperative mean Oxford Hip Score was 20.9. Subsidence of the component was noted in 84% of hips but did not cause a significant problem. Final leg length discrepancy was 5.4mm.
The results of this titanium, tapered, grid-blasted modular stem compares favourably with other revision stems including the Oxford Hip Score compared to the results for revisions recorded in the National Joint Register (Oxford Score 24.3). Although technically demanding this stem offers a very satisfactory solution for revision of total hips in almost all circumstances.
Impaction bone grafting in conjunction with a cemented polished double-taper stem as a technique for revision of the femoral component was introduced in 1987 at our institution.
As at January 2000, 540 cases in 487 patients had been performed by multiple surgeons. All procedures have been studied prospectively, and there are no patients lost to follow-up. We present the survivorship and outcome data for these patients.
Survivorship at 15 years is 90.6 percent (95 percent confidence interval:88–93 percent). Four hundred and six hips in 365 patients remain under active follow up, with 122 patients (134 hips) deceased.
Averaged clinical scores taken preoperatively, 2 years postoperatively and at latest follow up showed marked and sustained improvement: Charnley Pain 2.7, 5.5, 5.3; Charnley Function 2.1, 4.1, 3.6; Charnley Range of Motion 4.0, 5.4, 5.3; Harris Pain 19, 38, 36; Harris Function 18, 32, 28; and Oxford Hip Score 41, 22, 25. There have been 45 failures (8.3 percent) at an average 7.6 year follow up (range 2.6–15.3 years). Technical error contributed to 13 of the 24 non-infective complications, but with improved technique plus the addition of long stemmed impaction grafting, there have been no technical errors since 1996.
Our results show that revision of the femoral component with impaction bone grafting is a reliable and durable technique with an acceptably low complication rate with excellent survivorship at 15 years.
In severe hip dysplasia the fixation of the cup becomes a technical hazard, and the augmentation of the acetabulum with an autologous bone graft is helpful when the bone stock is deficient.
Twenty-four patients (25 hips) were operated on between 1993 and 1994; the mean age at operation was 49 years (range, 28 to 71 years). The mean Sharp acetabular angle was 55degrees (range, 45 to 63degrees). The dislocation of the femoral head was graded Crowe 1 in 4 hips, grade II in 5 hips, Grade III in 10 hips, and grade IV in 6 hips. Autologus bone was harvested from the femoral head and from the proximal metaphysis of the femur. The fixation of the graft to the anterior wall and to the roof of the acetabulum was achieved using impaction using the reinforcement ring with hook of Ganz. A separate cohort of 25 patients (25 hips) operated on between 1998 and 1999 was investigated using radiostereometry (RSA).
The clinical outcome of the hips was prospectively reviewed using the Harris hip score at an average of 8.3 years (range 8 to 9 years) postoperatively. Twenty-four hips were pain-free, and had a range of motion of 210 degrees or more except 3. A positive Trendelenburg sign disappeared in 88% of the hips. One cup (4%) showed radiological loosening with migration and required revision surgery. No signs of migration or progressive radiolucent lines were present in the remaining hips. The graft appeared united without resorption in 24 hips. The results of micromotion analysis using RSA confirm the stable fixation of the reinforcement ring in dysplasia.
Satisfactory middle term results of total hip replacement for severe dysplasia can be achieved using appropriate surgery and specific components. The use of reinforcement ring is important to obtain adequate primary stability, and to protect the graft during healing.
In 2002, one hundred and thirty nine patients had their names removed from the orthopaedic surgical waiting list at Taranaki Base Hospital for financial reasons. They fell below the “financially sustainable threshold” for access to publicly funded services. We wished to determine the status of these patients and the effects of this management decision.
All patients were invited to attend clinic for assessment. They completed the SF-36 Health Survey and were interviewed regarding effects of not having surgery. In addition, hips were assessed using Harris Hip Scores and knees were assessed using Knee Society Scores.
These standardised methods of assessment allowed comparisons to be made with overseas data. Our group of patients are experiencing significant impairment as a result of not being able to have surgery. A number of resulting medical and social problems were identified in the course of assessment. Patients also expressed a high level of discontent with the process.
Removing patients who have been assessed and placed on an orthopaedic surgical waiting list is an inefficient means of utilising health resources. It has also been met with a high level of patient dissatisfaction.
This study explores the outcomes of a pilot project involving five Orthopaedic services in developing approaches to improve the consistency and equity of clinical decision-making for access to treatment.
The pilot was conducted in two phases; the first involved development of retrospective and prospective data collection and analysis tools including use of:
The Orthopaedic Integrated CPAC tool: Euroquol and Oxford Hip and Knee quality of life measures, A surgical decision construct tool to identify patterns in clinical judgement A clinician survey Phase two involved a locally managed feedback and improvement process.
Large variations in internal equity were found within most services. Additionally a significant, systemic equity issue is apparent between patients prioritised for major joints versus other conditions. The pilot has made useful progress in developing improvement tools and processes targeting electives service management, improvements in prioritisation and clinical decision making, and funding and planning decisions. The pilot has also raised issues for further CPAC development and national service policy.
This is a retrospective study on the Taranaki experience with the Harris-Galante uncemented total hip joint replacement.
Ninety-six Harris-Galante total hip joint replacements were performed in ninety patients between September 1986 and September 1989. Twenty-nine patients died during the study and thirteen patients left the Taranaki area and were lost to follow-up. This left forty-eight patients (fifty hips) for evaluation with an average follow-up of fourteen years (range, thirteen to sixteen years). Results were analysed by questionnaire, clinical examination and x-rays.
Four hips were revised giving a Kaplan-Meier survivorship analysis of 89% at 14 years. Two femoral component was revised due to aseptic loosening at six and eleven years and two acetabular components were revised at 10 and 11 years due to liner dissociation.
The average Harris Hip score improved from 47 points preoperatively to 90 points at six years follow-up then declined to 83 at 14 years follow-up.
Osteolytic lesions were identified adjacent to 17% of acetabular components at follow-up and all were confined to zone two. Eighty-nine percent of femoral radiographs showed evidence of stress shielding however there were no grade four changes.
Osteolytic lesions were identified adjacent to 17% of femoral components at follow-up and were predominantly seen distally in zones three, four and five.
This study demonstrates satisfactory results for the Harris-Galante 1 total hip joint replacement at fourteen years follow-up. Cases should be kept under annual review to assess for progressive osteolysis, liner dissociation and the need for revision surgery.
Femoral fractures are a common injury in the paediatric population. The purpose of this study was to audit the cost and early outcomes of femur fractures treated at the Starship Childrens Hospital
Forty-eight femur fractures treated between January 1998 and December 2002 were reviewed. 25 fractures were treated by application of an early hip spica, 12 by IM nails and 11 by other methods.
Children treated by early hip spica averaged 3.8 years in age. They went to theatre an average of 29.1 hours after admission and had an average length of stay of 3.8 days. In the 30 days after discharge, five patients were readmitted for loss of fracture position.
Children treated with IM elastic nails averaged 9.5 years and went to theatre on average 35.1 hours after admission. Their length of stay averaged 8.3 days. Complications in hospital included return to theatre to shorten a wire (1 patient), remanipulation and application of a hip spica (2 patients) and difficulty mobilizing (1 patient). In the first 30 days after discharge, two patients required readmission for further surgery due to prominence of the wire.
Children treated with external fixator (7), femoral rod (1) or crossed k-wires (3) averaged 8.7 years in age. They went to theatre on average 58 hours after injury and had an average length of stay of 24 days. Two patients were readmitted with superficial pin-site infections.
Most femur fractures are being operated on the next day, however surgery is delayed in some patients. The readmission rate in the first 30 days is significant and is not reduced by operative fixation. Cost containment should focus on ways to reduce the early readmission rate.
Open long bone fractures have been considered orthopaedic emergencies requiring immediate irrigation, debridement and stabilization. Concomitant traumatic brain injuries may preclude the immediate operative treatment of open fractures. The purpose of this study was to review patients with open tibial diaphyseal fractures whose operative tibial fracture management was delayed because of a concomitant traumatic brain injury to determine if there is an increased rate of infection or non-union.
After obtaining IRB approval, the trauma registry was scanned for patients who sustained both traumatic brain injury with an Abbreviated Injury Scale (AIS) equal to two or greater and an open tibial diaphyseal fracture. From January 1, 1996 to June 1, 2001, 28 patients with 31 open tibial shaft fractures were identified (Grade I=1, II=6, IIIA=17, IIIB= 7). There were 24 males and 4 females with an average age of 35 years (range 13–69 years of age). The mechanism of injury was motor vehicle collision or pedestrian versus motor vehicle accident for all patients. The mean time to operative irrigation, debridement, and stabilization was 11 hours (range 2–152 hours). Thirteen patients underwent operative orthopaedic treatment within 8 hours (mean 4.4 ± 1.3 hours), and 15 patients underwent delayed debridement (mean 35 ± 35 hours). Twenty fractures were stabilized with intramedullary nailing, 9 fractures were stabilized with external fixation, one fracture was stabilized with a compression plate, and one fracture treated in a cast. A review of clinic records and telephone follow-up interviews was used to determine the rates of infection or non-union. Infection was defined as a positive deep surgical culture for bacteria upon repeat irrigation and debridement. Non-union was defined as any clinically and radiographically unhealed fracture requiring further operative procedures.
The average length of follow up was 2.9 years (range 1 month to 6.5 years). Of the 31 open tibial diaphyseal fractures, four fractures (12.9%) were complicated by infection and four fractures (12.9%) went on to non-union. There was no statistical difference in the rates of infection or non-union in patients who underwent irrigation and debridement within eight hours and those that underwent irrigation and debridement after eight hours from the time of initial presentation (odds ratio=1.02, p=0.15). Furthermore there was no correlation between the ultimate presence of infection/non-union and grade of open tibial shaft fracture, initial method of fixation, timing of wound closure (immediate, delayed primary closure, or split-thickness skin graft or flap), severity of overall injury, and epidemiological characteristics.
In this subset of 28 patients with 31 open tibial shaft fractures and concomitant traumatic brain injuries, there was no difference in the incidence of infection or non-union in patients who underwent operative treatment within eight hours of admission to hospital and those who underwent operative treatment after eight hours. The results of this study should be considered in the prioritization of care for the multiply injured trauma patient.
The purpose of this study was to evaluate the clinical outcome of a hydroxyapatite (HA)-coated tapered stem and to assess bone remodelling of the proximal femur using quantitative computed tomography osteodensitometry.
Fifty consecutive hips were managed with total hip replacement using the Cerafit Multicone H-A.C. stem with HA coating and the Cerafit Triradius-M press-fit cup (Ceraver Osteal, Paris, France). The mean follow-up was 3 years (range, 2.9 to 4 years). Current criteria were used for clinical and radiological assessment.
Forty-nine hips (98%) were clinically rated good or excellent. The mean preoperative Harris Hip Score was rated 57, and it has improved to 96 at the time of follow-up. The radiographs showed stable fixation by bone ingrowth in all hips. Fifteen patients (15 hips) were eligible for osteodensitometry. The mean decrease of the overall bone density (BD) in the metaphyseal portion of the femur 3 years after insertion of the stem was rated 14.21%, and the mean decrease of the cortical BD was rated 15.52%. The mean decrease of the overall BD in the diaphyseal portion of the femoral component was rated 10.00%, and the mean decrease of cortical BD was rated 7.76%. Little changes were observed underneath the tip of the stem.
The clinical and radiological outcomes of the tapered stem with HA coating at a mean follow-up of 3 years compares favourably with other reports. Results of osteodensitometry show less proximal femur BD loss in comparison to similar investigations performed using uncemented stems.
The period of time acute orthopaedic patients await surgery at Middlemore Hospital is of concern to a number of the Health Professionals involved in their care. This study has arisen out of that concern in an attempt to quantify the extent of these delays.
Every patient operated on at Middlemore Hospital between 01 June and 31 December 2002 who had a fracture that fell within the categories studied was analysed. The six categories analysed were: compound fractures, tibial shaft fractures, femoral shaft fractures, ankle fractures, neck of femur fractures and distal radial fractures. Data regarding the age and time to surgery for each patient was analysed and compared with established guidelines. For the patients with neck of femur fractures additional data regarding their medical fitness for theatre was also analysed.
The study showed there was significant delay in acute patients receiving operative treatment at Middlemore Hospital. Furthermore the study highlighted the large volume of acute patients presenting to Middlemore Hospital.
Further investigation should be undertaken to consider how a department such as Middlemore can provide operative treatment within an acceptable timeframe to nearly 6000 orthopaedic patients a year, while still providing timely surgery for elective patients.
There has been a growing concern amongst the Orthopaedic Department at Auckland Hospital regarding the time Orthopaedic acute patients are waiting for surgery. To address this concern this study was undertaken to examine the extent of the problem and to establish recommended practice guidelines for waiting times.
A literature search was undertaken to identify universally accepted delays for surgery for the six categories of fracture studied – compound fractures, femoral shaft fractures, tibial shaft fractures, ankle fractures, neck of femur fractures and distal radial fractures. Current practise guidelines were then compared with the literature to ensure they are an acceptable standard of care. Every patient operated on at Auckland Hospital in 2002 that had a fracture that fell within the six categories was included in the study. Data regarding the age and time to surgery for each patient was analysed.
The study demonstrated major discrepancies between recommended practise guidelines and the present acute service. The general trend is that the more acute the fracture, the less likely it is to be operated on within the guidelines.
Further investigation should be undertaken to look at reasons behind the delays and ways to improve access. This will assist in identifying responsibility for ensuring that an acceptable standard of care is maintained.
This is a report of a retrospective clinical review of atypical Achilles tendon rupture. The main purpose to describe pathoanatomy and outcome of these ruptures.
Typically an Achilles tendon rupture is noted 4 to 6 cms above the insertion into the calcaneus and is usually related to a sporting event. However, atypical ruptures are different from the typical ruptures: site of rupture; type of rupture and presentation. In the authors experience, atypical ruptures are not common but probably underreported. The author discusses clinical findings, pathogenesis, operative findings and treatment.
Since 1998, 5 cases of atypical Achilles ruptures were seen at Hawkes Bay Hospital. There were 2 coronal Z ruptures and 3 sagittal ruptures All were treated surgically.
At minimal 18 months follow-up all Z ruptures did very well.
This study highlights atypical Achilles tendon ruptures. Their exact incident is not known but these 5 cases were seen among 104 Achilles tendon ruptures operated on by the author.
We reviewed Complete Proximal Hamstring Ruptures to assess the functional disability and to describe the early and late surgical repair
In the last two years five patients have been seen and treated with this relatively uncommon injury. A retrospective review of the patients diagnosed with complete proximal hamstring rupture, the method of injury, investigations to confirm injury, and the surgical technique was undertaken. Patient assessment using a questionnaire and VAS to compare pre and post operative functional abilities was also performed.
All patients reported a significant improvement in functional ability and a decrease in pain
Surgical repair of complete proximal hamstring rupture is a worthwhile procedure and can be performed both early and late.
The purpose of this study is to review the current treatment of Colles fractures by long term follow up and to compare these results with a similar paper published in 1965 by G.B. Smail. And secondly, to evaluate the degree of bone density in these patients and to see what, if any, treatment is being received in those with evidence of osteopenia.
The records and radiographs of 82 patients treated at Hutt Hospital between January 1997 and January 1998 were reviewed. Of these, thirty-two attended for re-examination. Subjective measures of pain, appearance and functional limitations were recorded, as were complications and whether the wrist had reached a stable state.
Anterior-posterior and lateral radiographs of both wrists were taken, from which measurements of residual dorsal tilt and shortening of radius were made.
Of the thirty two patients that presented for re-examination twenty went on to have bone density measurements.
When comparing results from two similar studies, spaced thirty seven years apart, subjective findings show that from a functional and appearance perspective there appears to be little difference between the two cohorts. With respect to pain, patients treated in 1997 complained of a lot less residual pain compared to those treated in 1960.
Objectively, the range of movement in the wrist joint was once again found to be similar in the two cohorts, as was the range of movement in shoulder, elbow appeared to be similar. Finger movement was difficult to compare.
Radiologically the degree of ventral dorsal tilt does not correlate with range of movement at the wrist.
Bone density scan results suggest that the majority of patients with evidence of osteoporosis are not been treated appropriately.
Overall conclusion is that the outcome for treatment of Colles’s fractures has not changed significantly in the past thirty seven years.
The aim of this study was to determine the outcome of patients treated with Achilles tendon rupture randomized to surgical or non-surgical treatment where both groups received the same early motion and weight bearing rehabilitation protocol.
Fifty patients between the ages of 18 and 50 years with a clinical diagnosis of Achilles tendon rupture were randomized to surgical or conservative treatment. All injuries had occurred within ten days. Both groups received the same rehabilitation program with initial cast immobilization then splintage in a removable orthosis with ankle motion commencing at two weeks. Patients completed the MFAI, a validated outcome questionnaire and clinical assessment including range of motion and calf squeeze response at 2, 6 and 12 weeks, 6 months and one year.
There was no difference between the surgical and non-surgical groups for difference in dorsiflexion and plantar flexion between the injured and non-injured sides. There was no difference in the MFAI quality of life scores for either treatment group. There was the same number of re-ruptures in both groups. There were no infections in the operated patients.
Early motion rehabilitation after Achilles tendon rupture results in similar functional results and patient satisfaction in both surgically and non-surgically treated patients.
We assessed the functional outcome of fractures of the os calcis a minimum of twenty- four months following injury.
Eighty-three patients with 85 fractures were assessed a minimum of two years following fracture of the os calcis, using a validated functional outcome measure designed specifically for fractures of the os calcis, and an EQ5D. Radiographic analysis of all fractures was performed to attempt to correlate outcome scores with the fracture pattern.
Sixty per cent of the questionnaires were returned completed. Forty percent of the fractures were treated surgically, the remainder with a period of weight relief, followed by physiotherapy and graded weight-bearing. The majority of patients reported a mild hind foot pain (8/10 on a VAS), and all reported some difficulties with walking on uneven terrain. There was no appreciable difference in the outcomes comparing patients treated by open reduction and internal fixation and those treated non-operatively.
This study demonstrates a surprisingly high patient satisfaction rate following fractures of the os calcis whether they are treated operatively or non-operatively. Patients seemed to have compensated for any altered function very well. We were not able to identify specific fracture patterns that were associated with poorer outcomes.
The aim of the study was to evaluate the results of the LISS system for distal femur fractures.
Eighteen consecutive patients with fractures of the distal femur treated with the LISS system were followed until fracture union. This group included intra-articular, extra-articular and periprosthetic fractures occurring from both high and low energy trauma.
Fractures united in 17 out of 18 cases and only 1 patient required bone grafting. The patient with the fracture that didn’t unite had an early above knee amputation for major pressure areas and peripheral vascular disease. There were no infections but 2 cases of plate failure proximally.
The LISS system is a good treatment option for fractures of the distal femur in both the osteoporotic patient and the patient with high energy trauma.
This case presentation highlights the problem of thermal necrosis of the tibia following reaming, in a tibia with a narrow canal.
A 2 year follow up of a 19 yr old aspiring dancer, who had a closed low velocity fracture to her midshaft left tibia. This was treated with intramedullary nailing of the tibia. Difficulty encountered while reaming of the canal at the time of operation because of the narrowness of the canal. She subsequently had a refracture of the shaft of the tibia, above the united fracture after the removal of the intramedullary nail. This happened in the narrow isthmic part of the tibia proximal to the fracture and was confirmed to have avascularity with isotope bone scan. This subsequently showed no appreciable sign of healing.
Patient had renailing of the tibia with bone grafting and the fracture. Latest review shows the fracture to be consolidating.
Surgeons have to be aware of the dangers of narrow canal in tibia before intramedullary nailing and appropriate reamers to be used if the canal is too narrow.
Treatment of displaced intracapsular fracture of the hip by hemiarthroplasty in old patients is generally satisfactory.
Middlemore Hospital’s agreed criteria for hemiarthroplasty were reviewed and tested.
Two hundred and thirty three patients who had hemiarthroplasty for displaced intracapsular fracture neck of femur between June 199- June 2001. All the patients’ data collected from the hospital computer system and then a search started for these patients to review their current status regarding pain and mobility.
Ninety nine patients (42%) were still alive, of them 13 demented, 13 moved or lost and 7 in a wheel chair.
Sixty six patients reviewed for pain and mobility using Sikorski and Barrington scoring criteria for pain and mobility.
Thirteen patients had painful hemiarthroplasty. Clinical notes of the most active group of these patients (7 patients) reviewed individually to identify the causes.
Two patients had revision to total hip joint replacement within 3 months because of technical errors and two patients placed on the waiting list for revision. The rest had deterioration in their general health that made total hip arthroplasty a risky operation for them.
The revision rate was 1.7 %. We concluded that hemiarthroplasty was an acceptable option for these patients. The selection criteria were correct in 98.2% of the cases. Patients who live in their own home will need a careful assessment before deciding on a hemiarthroplasty for them.
We assessed the functional and health outcomes of patients treated for a hip fracture ,6–12 months following the injury.
One hundred and ninety six patients over 60 years of age ,admitted with a subcapital or intertrochanteric fracture were sent two questionnaires, an EQ-5D, and a Hip specific outcome questionnaire based on the WOMAC .Patients with pre-existing dementia were excluded.108 (55%) returned completed questionnaires.
There were 36 males and 72 females with an average age of 81. The average time since fracture was 8.44 months. There were 46 intertrochanteric and 62 sub-capital fractures.WOMAC scores averaged 35 for intertrochanteric fractures and 25 for subcapital fractures. Males scored higher than females (31 v’s 24)Age had no influence on WOMAC scores.EQ 5D results were compared with the general population, and showed significant problems with mobility, pain, performance of usual activities, and self care.
This study shows that despite seemingly successful treatment of the fracture, patients suffer very significant reductions in function and quality of life. Greater effort needs to be made to address these issues rather than concentrating on the development of new fixation devices, if we are to improve the results of treatment of these increasingly common fractures.
This study was designed to prospectively evaluate the efficacy of indomethacin as prophylaxis for heterotopic ossification (HO) after operatively treated acetabular fractures.
An IRB approved, prospective double blind placebo controlled clinical trial was performed at two level I trauma centres to evaluate the efficacy of indomethacin as prophylaxis for heterotopic ossification after the operative treatment of acetabular fractures. Between January 1, 1999 and May 31, 2003, two hundred and thirty-two patients with acetabular fractures were treated operatively through a posterior approach. Patients with the following conditions were excluded from study participation: age < 18, spinal cord injury, ankylosing spondylitis, burns, gastrointestinal bleed, Glasgow coma scale < 12, cerebrovascular accident, pregnancy and use of other non-steroidal anti-inflammatory drugs. One hundred and fifty-seven eligible patients were identified and one hundred and twenty-five patients were enrolled in the clinical trial. One hundred and seven patients have sufficient follow up to be included in data analysis. All patients underwent operative stabilization of their ace-tabular fractures by either a combined anterior and posterior approach or an isolated posterior Kocher-Lan-genbock approach. After fixation and prior to wound closure, any necrotic gluteus minimus muscle was debrided to viable muscle. Sixty-one patients were randomized to the placebo group and forty-six patients to the indomethacin treatment group. Indomethacin 75 mg SR and the placebo were administered to the patients by the investigational drug pharmacy in a blinded fashion. The medication was taken once daily for six weeks. Patient compliance was measured by obtaining indomethacin serum levels at the first postoperative visit (2 weeks). The extent of HO was evaluated on plain radiographs (AP and Judet) at three months postoperatively. The radiographs were scored for the presence of HO using the Brooker classification as modified by Moed. The data were analyzed two ways: 1) by excluding patients with protocol deviations and 2) by using an intent-to-treat model, where all enrolled subjects with 3 month Brooker scores were included in the analysis, regardless of whether they withdrew or were dropped from the study for clinical reasons. The sample size was estimated to produce a statistical power of 80% to detect a difference of 15% between the two treatment groups with alpha = .05.
There were no significant differences with regards to age, sex, body mass index (BMI), ISS (injury severity score) and complications between the two treatment groups. The overall incidence of HO (Brooker I-IV) was 52.8% and the overall incidence of significant HO (Brooker III/IV) was 19.6%. There were four patients with Brooker IV HO. There was no significant difference between the treatment groups in the incidence of HO according to Brooker class (p=0.23). Significant HO (Brooker grades III-IV) occurred in 8 cases (17%) in the indomethacin group and 13 cases (21%) in the placebo group. There was no significant difference in the presence of moderate to severe HO (Brooker III/IV) between the two treatment groups (Fisher’s exact test p=0.81). Eighty-two of one hundred and seven patients enrolled completed the protocol. Twenty-five patients did not complete the treatment protocol for the following reasons: stopped medication due to side effects, did not receive medication at discharge, lost medication, or medication stopped by another physician who did not understand the purpose of the study. Nine patients (8.4%) did not receive the full medication course, sixteen patients (15%) were dropped or withdrew from the study for adverse events or gastrointestinal symptoms. Twelve patients dropped or withdrew from the indomethacin group and three from the placebo group. Forty percent of patients in the indomethacin group had non-detectable serum levels at two weeks. Complications identified in the indomethacin treatment group included deep venous thrombosis (5), wound infection (2), nonunion (1), gastrointestinal bleed (1) and perforated ulcer (1). Complications identified in the placebo group included deep venous thrombosis (6) and wound infection (2).
In this prospective randomized study, a placebo provided as effective prophylaxis against the development of heterotopic ossification as indomethacin. More patients withdrew from the indomethacin group for gastrointestinal side effects or adverse events than in the placebo group. Patient compliance with indomethacin was poor with 40% of patients having no detectable indomethacin serum level. Serious gastrointestinal complications (gastrointestinal bleed and perforated ulcer) occurred in two patients treated with indomethacin.
Elbow contracture is a recognized sequel of elbow trauma. We aim at reviewing the clinical outcome of surgical capsulectomy and elbow debridement.
The operative notes as well as pre and post-operative clinical records were reviewed for 15 patients who sustained an elbow trauma which resulted in elbow contracture and were managed with open capsulectomy and debridement. In addition two patients had anterior transfer of the ulnar nerve, twohad removal of loose bodies, two had excision of heterotopic bone, one patient had reconstruction of the medial collateral ligament and one patient had repair of the lateral collateral ligament .
These patients were followed up for a mean of 21 months (6 to 37).
Elbow flexion contracture improved from a mean of 37° (10° to 55°), to a mean of 10° (0° to 25°). Elbow flex-ion improved from a mean of 125° (95° to 140°) to a mean of 129° (90° to 140°). There were no major complications. Two patients underwent repeat debridement due to recurrence of contracture. One patient developed serious collection that settled gradually.
We conclude that open capsulectomy and debridement is a satisfactory way of management of post-traumatic elbow contracture in the short and intermediate term.
Minimally invasive hip replacement surgery has become the catch cry of the past 18 months. The technique of two incision surgery has been touted as allowing safe insertion of hip replacement components and early discharge of patients in comparison to standard procedures. The early results and technique developed by the author are discussed with specific reference to early complications and early radiographic and clinical results.
After extensive cadaveric dissection and anatomical study, a comparison was made of the existing exposures used in two incision surgery including pitfalls and benefits.
Following initial study, a two incision approach has been used on forty patients initially chosen as being suitable for the procedure based upon age, weight, and suitability for cementless hip replacement. Data relating to surgical time, hospital stay, post op complications and radiographic and clinical results have been prospectively analysed.
Early clinical results have been very favourable, including no increase in complication, and earlier discharge and recovery from surgery. The results are being validated by a randomised prospective international study, but the ability to discharge patients within 24 hours of surgery does not appear to be a viable option and possibly not a safe option considering the concerns relating to recovery from anaesthesia and post operative postural hypotension. A radiographic assessment has revealed accurate placement of implants compared to an historic group using conventional exposure.
Clinical scores have been better at six weeks and three months compared to mini incision and standard incision patients.
Further research and experience is required for this technique to be fully applicable and available to the general orthopaedic population. Technically the procedure is more challenging and does require adequate instruction and does have a significant learning curve. However, the early clinical results do support earlier discharge and more rapid recovery compared to standard hip replacement surgery.
We report early major complications encountered following TEN fixation of femoral fractures in children.
A case series of four children aged 8– 16 years who had primary TEN fixation of isolated femoral diaphyseal fractures.
Three of the four patients had major complications. These were: significant knee stiffness requiring manipulation, haemarthrosis requiring washout and nail removal, loss of position and refracture. Two required revision to locked intramedullary nails without early complication.
In the skeletally immature child TEN fixation of femoral fractures has a significant major complication rate. This needs to be recognised when comparing TEN fixation with other treatment options.
The Harris-Galante II acetabular prosthesis was used in Taranaki from 1992 until 1999. An increasing number of failures were noted due to liner dissociation. This lead us to retrospectively review the 237 patients with the Harris-Galante II acetabular prosthesis inserted for primary arthroplasty to assess true failure rates and mechanism of failure.
All of the cases were followed up with clinic interview, home interview, phone interview or review of notes. Harris hip scores were performed and radiographs were taken.
Forty-eight failures were found of which 66% were due to liner dissociation. The Kaplan-Meier 10 year estimate of implant survival was 72.9% ± 7.8%.
Several methods of revision were performed. Forty per cent of cases managed with polyethylene liner exchange alone required further revision for liner dissociation.
The poor survival of the Harris-Galante II cup appeared primarily due to failure of the capture mechanism of the cup. Dislocation and small shell size were both found to be significant independent factors which contributed to the incidence of failure.
Minimally invasive surgery (MIS) for THR may accelerate rehabilitation. The objectives of this study were to determine the effect of 3 surgical approaches (standard, mini (< 10cm), 2 incision Stryker approach (MIS), on length of stay, rehabilitation rates, clinical outcome, quality of life, patient safety, complications and implant position.
This study was conducted in accordance with Good Clinical Practice. Each surgeon completed 6–8 documented cases using the MIS technique before commencing enrolment to eliminate any learning curve effect. Prior to enrolment patients were assessed for eligibility and provided signed informed consent. Patient demographics, medical histories and surgical details were collected. Post-operative rehabilitation was independently documented by a physiotherapist. Clinical evaluations (HHS) were collected pre-operatively, 10 days, 6 weeks, 3 months and 1 year. Patient outcomes (SF 12/WOMAC) were collected pre-operatively and 1 year. Radiological evaluations were completed at 6 weeks. CTs/x-rays were subject to an independent review.
A sample size of 48 patients was determined based on the primary objective – length of stay. Enrolment commenced at the end of 2002 and these results are based on the first cohort of patients; based on current recruitment rates, the authors anticipate that the majority of patients will be enrolled by presentation time.
Preliminary results show mean incision lengths (cm) of 3.5/5.8 for the 2 incision MIS compared to 8.8 and 13.5 for the mini and standard respectively. Mean duration of surgery (mins) was 79 (MIS), 62 (mini) and 42 (standard). The median time (hours:minutes) from end of surgery until the first episode of knee flexion > 45°, straight leg raise, active abduction, standing, out of/in to bed, stair climbing and walking > 20 metres was shortest for MIS compared to mini and standard surgical approaches. The maximum distance walked was greatest for the MIS group. The mean length of stay (days) was shortest for the MIS group. 2.5 compared to 4.7 (mini) and 3.7 (standard).
Mean blood loss (cc) was greatest for the MIS group, 667 compared to 525 (mini) and 467 (standard). There were no intra/post-operative complications or blood transfusions.
Results suggest accelerated rehabilitation, decreased hospital stay and increased surgery duration for the MIS group. There are no safety concerns, however the procedure is felt to be quite technically demanding requiring an appropriate level of training/experience. The authors believe this is the only controlled study of this nature currently being conducted internationally.
Rising health costs have seen increased emphasis on cost containment. Outpatient follow-up after total joint arthroplasty is one such accumulating cost. Enthusiastic recent media interest in failing implants and unacceptable waiting lists adds further interest to the area.
We wished to determine the current post-operative follow-up practices and views of New Zealand Orthopaedic Surgeons. A postal survey was sent to all New Zealand Orthopaedic Surgeons.
The response rate was 83% (131/158). There was wide variation in routine practice and beliefs. For cemented THJRs, 13% of surgeons routinely saw their patients for less than one year, 38% followed their patients for less than five years and 53% continued to see patients indefinitely. Follow-up for uncemented/hybrid prostheses was higher: 8% for < one year, 29% for < 5 years and 59% indefinitely. A system of periodically re-calling patients for x-rays without necessarily seeing them is used by 20% of surgeons.
The most frequent reasons given for follow-up were the detection of osteolysis, wear, loosening and patient symptoms.
Similar figures for total and uni-compartmental knee replacements were reported.
Almost a third of surgeons reported that they were unable to follow-up their patients as they would like to because of resource limitations within the public health sector. 44% believed that future changes in medico-legal expectations will necessitate longer follow-up of patients.
This survey demonstrates wide variation in practice. Higher follow-up rates for un-cemented/hybrid prostheses may reflect uncertainty about the long-term results. There is concern amongst surgeons that their ability to follow-up patients within the public health-care sector is constrained by cost. Periodic questionnaire and x-ray assessment was suggested by many as a possible alternative for long-term follow-up of selected patients. Few surgeons are however presently using such a system. We propose a standard of care.
The use of modular components for hip and knee arthroplasty, available since the late 1970’s, has become increasingly popular. Modularity increases the inventory of components required for arthroplasty with the increased possibility of implantation of mismatched components.
All members of the New Zealand Orthopaedic Association were sent a confidential questionnaire asking whether they had selected mismatched components for arthroplasty within the last five years and if so, how often. Information was requested on which components were involved, how and when the mismatch was discovered and what action was taken once mismatch identified. Surgeons were asked to comment on factors contributing to the mismatch occurring and their standard practise to avoid this possibility occurring.
One hundred and forty eight questionnaires were sent out and 120 replies received giving a response rate of 81%. Twenty-eight surgeons (23%) had implanted mismatched components within the last five years, occurring during total hip arthroplasty in 20 cases, knee arthroplasty in six and others in four. The mismatch was discovered prior to wound closure in 39%, during the admission in 51% and after discharge in a further 10%. The mismatch led to a further surgical procedure in 13 patients (46%). The elements contributing to the mismatch will be discussed.
Modular arthroplasty is popular and enables the surgeon to modify the components to the individual patient. This is valued by surgeons accordingly and is unlikely to diminish in frequency. The mismatch rate may be higher than recognised as some mismatches may not have been noted if there was no clinical problem. Strategies to avoid this complication occurring will be discussed.
A comparison of the clinical status and outcome of a group of patients treated with tw-stage revision using either excision arthroplasty or an articulating spacer (the Kiwi Prostalac) as the first stage is presented.
Clinical scores were obtained before revision, after the first stage, and after the second stage revision, along with the outcome of the success of the revision procedure in terms of eradication of the infection, from the two study groups. Seven patients received excision arthroplasty and eight were treated with the Kiwi Prostalac spacer, at the treating surgeon’s discretion.
A comparison of the clinical status of the two groups will be presented at the varying stages of treatment, along with hospitalisation duration, and morbidity and ultimate outcome.
Our results demonstrate that two-stage revision with an antibiotic cement-coated THJR prosthesis (The Kiwi Prostalac) is an effective and safe method of managing deep peri-prosthetic infection around a THJR with significant advantages to the patient.
The brief intervention aimed to facilitate problem-solving, encourage self-management and early return to normal function. Physiotherapists undertook a one-day training programme in communication skills and cognitive-behavioural approaches. In the ‘Usual’ physiotherapy intervention treatment was provided at the discretion of the individual physiotherapist.
The main outcome measures were the Neck Pain Questionnaire, a specific measure of functional disability due to neck pain, the SF-36 a generic health-related quality of life measure, the Tampa Scale for Kinesophobia, a measure of fear- and-avoidance of movement and the use of healthcare services. Data was collected at baseline, at 3 months and at 12 months.
The intended early contact (within first week) of workers absent with musculoskeletal disorders only occurred at one experimental site; the control sites had no procedure for early contact. Absence rates improved over the four years at the intervention sites compared with the control sites: a decrease of 2.0 v an increase of 0.9 days/1000 working hours. The median return-to-work time for early intervention compared with controls was 4 days v 5 days (P=NS). Considering return-to-work time irrespective of whether the intervention was delivered early or late, the median durations were also 4 days v 5 days (P< 0.05). When looking at work retention over 12 months, the median duration of subsequent absence for early intervention was 5 days compared with 11 days for controls (P=NS). For the larger number of workers receiving a late intervention, the median duration of subsequent absence was median 4 days v 11 days for controls (P< 0.05).
As part of a 10 year follow-up study investigating the relationship between MRI-diagnosed disc disease and low back pain (LBP), a comparison of MRI image acquisition protocols was conducted. The aim was to establish whether the modern protocol produced improved diagnoses of lumbar disc disease. This is of significance when attempting to determine links between lumbar disc disease and LBP. The proposed hypothesis was that little difference in the pathology reported of MRI lumbar spines between the surface coil acquired images (Coil-MRI) and phased-array acquired images (Phased-MRI) would be found.
Four male patients aged 33, 44, 45 and 52 years, who had undergone different spinal stabilisation procedures consisting of flexible stabilisation (DNESYS), posterior instrumented fusion, and anterior interbody fusion with facet fixation were investigated. Images were acquired and analysed in the same way except that a larger number of images (500 per screening) was utilised in each case. Four operated levels and 2 adjacent levels were analysed. All motion patterns were easily distinguishable from those of the normal subjects. The PLIF and DYNESYS stabilisations demonstrated no motion at the instrumented levels. The anterior inter-body fusion-transfacet fixation patient was shown to have developed a pseudarthrosis.
Pain drawings are quick and easy for patients to complete. Our study demonstrates pain drawings can reliably be used to predict outcome following intradiscal electrothermal therapy.
Phase I Results Were Previously Reported At SBPR
i. Measurement of depression and of other mood states in pain patients has been criticised in recent years on the grounds that most questionnaires were not developed in pain populations and suffer from criterion contamination by somatic items. In addition, there is no accepted measurement for positive emotions which are more than the absence of depression. The aim of this study was to develop a reliable and brief tool to assess mood in pain patients.
ii. Nonsomatic items concerning depression, anxiety and positive outlook were extracted using exploratory factor analysis from commonly used instruments (the Beck Depression Inventory and the Hospital Anxiety and Depression Scale) completed by over 900 chronic pain patients. Confirmatory factor analysis was used to test the internal structure of the final item set. Items were then reworded and presented as a new questionnaire(the Depression, Anxiety and Positive Outlook Scale: DAPOS) to two new samples: patients attending pain management and patients attending osteopathy. The new questionnaire was compared with several well-known questionnaires (SF36, BDI, PCS). The structure was calibrated and tested using confirmatory factor analysis on both samples. Finally, a sub-set of patients carried out a sorting task to test for face validity. iii. The DAPOS performed well, indicating that it is a reliable measure of the three mood states with good initial evidence of validity in these samples
self complete proforma video recording.
ii) A check-list of treatment modalities was constructed from this proforma. Twelve sessions were recorded on video (one new and one review patient for each therapist). The recordings were rated by 3 blinded, independent observers using the checklist. These were compared with the self-report audit forms relating to the same physiotherapy session.
* Left sided retroperitoneal muscle splitting approach * Anterior hybrid interbody grafting * Pedicle screw fixation without grafting
There was radiographic evidence of fusion in 81.3% of patients. There was an improvement in mean pain VAS, and mean scores of all physical components of the SF36. Patient satisfaction was high (71%).
Subgroup analysis demonstrates that the fusion rates in non-smokers versus smokers, and primary fusions versus previous surgery, were the same. The fusion rate following multiple level fusions was lower at 72.2%.
This study sought to determine the post-operative management of spinal patients in the UK, and to determine if uniformity exists between surgeons and if there is any published evidence for this practice.
A reply-paid questionnaire was sent to members of the British Association of Spinal Surgeons and the Society for Back Pain Research. The questionnaire documented the surgeon’s experience, where they work, their operative population, the types of spinal surgery performed, and whether they have a routine for post-operative management or any written instructions for patients concerning post operative management. It also asked about the nature and duration of professionally supervised rehabilitation. Of the 89 questionnaires distributed, 63 (71%) were returned, of which 51 could be used in the analysis. The 12 not used were either completed incorrectly, had missing data or the surgeon had since retired. The replies demonstrated wide variation: only 35% of surgeons provide their patients with written post-operative instructions; there was limited referral to physiotherapy, with only 45% referring to a physiotherapist (for an average of 1.8 sessions); only a modest fraction of surgeons advocated the use of a post-operative corset (18%), others restricting sitting or encouraging bed rest; and a range of recommendations regarding return to work. There was also only a limited correlation between restrictions on sitting and recommendations about return to sedentary work or driving (Spearman r=0.08 and 0.36, respectively).
In summary, although individual surgeons may be certain of their practice, the overall variation indicates ongoing uncertainty across the profession. This was further substantiated by our literature search, which revealed limited evidence for current practices, and a paucity of research into postoperative management.
The objective of this study was to explore and identify perceptions, attitudes and beliefs held by practitioners from these three professional groups about their approaches to the care of LBP patients.
Preliminary categories of themes that emerged were: Evidence; Perceived Knowledge; Personality Characteristics; Professional Identity; The Patient; and Motivation. Of particular interest, practitioners seem to have mixed opinions with regard to basing their practice on evidence from external research.
Listening to people’s life stories and examining the narrative they use to explain their back problems can enable the multi disciplinary team to better understand individuals and their problems and assist in their own professional development as well as improving services for patients.
Patient satisfaction has been identified as a key dimension in the assessment of outcome in LBP. However what outcome is important to the patient is often not considered, or is poorly assessed. Goal Attainment Scaling (GAS) is a method for systematically targeting individualised goals, and quantifying their achievement. This will provide a valid outcome measure of genuine importance to the patient.
The average age of patients with a good outcome was 20.9 years. The average age of patients with a poor outcome was 30.9 years.
There was no correlation between the correction of either the Sharp angle or the centre-edge angle and outcome. Sphericity of the head was unrelated to outcome. Obesity was associated with a poorer outcome in older patients.
There has been a rapid uptake in the use of Resurfacing Hip Replacement (RHR) in the United Kingdom, and its use is likely to accelerate both in Europe and the USA. The current level of use of RHR is not accurately known.
It was decided to audit the use of RHR amongst Consultant Orthopaedic Surgeons in the United Kingdom, and to identify the number of operations performed in the last twelve month period, and the specific training undertaken before offering this procedure.
A questionnaire was sent to 1600 Consultant Orthopaedic Surgeons with 894 responding.
19% had performed RHR in the previous year.
Excluding surgeons that do not perform Total Hip Replacement, 23.5% of surgeons had performed RHR.
29.5% of all orthopaedic surgeons had observed RHR surgery and 23% had been on an RHR course. 65% of all consultants who had attended a course were offering RHR surgery.
7.8% of those performing RHR had neither been on a course nor observed surgery.
There was no relationship between years in practice and RHR surgery.
There was a weak association with British Hip Society membership and with a previous fellowship in Hip Surgery.
Of those performing RHR, 72% perform less than 20 cases per year. The majority of surgeons perform 6-10 RHRs per year.
Although interest in RHR is increasing, it is currently performed by the minority of consultants. Given the steep learning curve, the lack of knowledge of long-term survival, and concerns regarding metal on metal bearing surfaces, RHR should be used by surgeons with a specialist interest in hip arthroplasty. We believe RHR should be used in accordance with the guidance given by the National Institute for Clinical Excellence.
Hip resurfacing has in recent years become increasingly popular as an arthroplasty technique, particularly amongst younger patients with more active lifestyles. The procedure has been heralded as a more conservative option, aimed at those wishing to continue strenuous work and recreational activities. In the populalapress and the internet, many claims are made regarding aspects of this procedure, but little evidence has appeared in the scientific literature, either with the results of resurfacing or comparing resurfacing to conventional total hip arthroplasty.
We compare the outcomes of a consecutive series of 44 hybrid hip resurfacings against a similar series of 50 conventional hybrid hip arthroplasties (THR’s), all performed in patients aged 60 or under by a single consultant Surgeon. Data on operation time, blood loss, and length of stay, as well as complications, were all prospectively recorded. A modified Harris Hip score was also documented preoperatively, as well as at 6, 26 and 52 weeks postoperatively. In the resurfacing group, there were 28 Male and 16 female, mean age 47.6 years. In the THR group, there were 22 male and 28 female patients, of mean age 51.9 years. The results for the two groups were analysed, and p value of < 0.05 was taken as statistically significant.
The results showed no difference in operation time or blood loss. There was a small reduction in average length of stay from 7.1 to 6.4 days, which was not clinically significant, while the Modified Harris Hip Scores at 6 and 52 weeks were the same for both groups. We conclude that whilst it has been previously shown that there is an overall preservation of bone stock following resurfacing arthroplasty, there is no evidence to back additional claimed benefits.
We report a series of 668 patients (699 hips) with an average follow up of 10.5 years (range, 10–11 years) following THR using a cemented custom-made titanium femoral stem and a cemented high-density polyethyl-ene acetabular component. The fate of every implant is known.
The mean age at operation was 68 years (24 – 94 years). The indication for THR was as follows: primary OA (629), RA (18), AVN (10), intracapsular femoral neck fracture (5), Perthes disease (3), developmental hip dysplasia (2) and SUFE (1). The mean pre-operative Harris Hip Score was 19 (range 10 – 42).
One hundred and seventy-four patients (26%) were deceased at the time of their 10-year review. Four hundred and ninety-four patients were subsequently reviewed of which 88 patients (13%) were assessed by telephone review as they were too frail to attend.
The average 10-year Harris Hip Score was 92 (range 43 – 100). The average 10-year Oxford Hip Score was 19 (range 12 – 46). 99.2% reviewed at 10 years stated that they were satisfied with their THR.
Revision surgery occurred in 21 cases (3%). Seventeen femoral components were revised for infection, one for recurrent dislocation and one was iatrogenically loosened during socket revision. There were no cases of revision for aseptic loosening of the stem. Dislocation occurred in 18 cases, of which 4 became recurrent (0.6%). Six patients had a postoperative sciatic nerve palsy (0.9%) with 4 making a full recovery. There was one case of femoral nerve palsy. Eleven patients developed a DVT (1.6%). Six patients had a PE (0.9%) all of which were non-fatal. There were 16 deep and 3 superficial wound infections. Thirty-eight patients had symptomatic trochanteric bursitis post-surgery.
In conclusion, the 10-years results of the custom femoral stem are encouraging with an overall high level of patient satisfaction.
We describe the survival at 10 years of 134 consecutive JRI Furlong H.A.-coated uncemented total hip replacements.
The follow-up was a minimum of 10 years (10.5 to 12.0 years).
Patients were assessed by clinical and radiological means. We used Merle d’Aubigné and Postel clinical score.
Radiological assessments identified radio lucent lines, spot welding, pedestal formation and migration in order to assess fixation and stability of the femoral stem according to Engh’s criteria.
DeLee and Charnley zones were used to assess loosening of the ace tabular cup. Subsidence, migration and cup-angle were also measured.
The criteria for failure was revision or impending revision due to either pain, septic or aseptic loosening.
The mean results of the Merle d’Aubigné and Postel score were 7.4 pre-op. and 15.9 post-op.
None of the acetabular cups in this series were revised.
No femoral stem was revised for loosening.
Six patients were lost to follow-up. Of the 128 femoral stems reviewed, only 1 was revised for periprosthetic fracture following a fall.
There is an increasing interest amongst surgeons and demand from patients for hip resurfacing. One concern regarding resurfacing is the incidence of femoral neck fracture post operatively. McMinn and Treacy report an incidence of 0.4% in their series, our finding was of an incidence of over four times as high (1.9%). We looked at our database of hip resurfacings and tried to identify the risk factors for fracture.
We identified 11 fractures and compared these with 22 controls selected by choosing the cases performed by the surgeon immediately before and after the fracture case. We analysed their medical notes and x-rays. Statistical analysis was performed using a package in ™Excel. The implants were either Birmingham Hip (Midland Medical Technologies) or Cormet (Corin) resurfacings.
No statistically significant correlation was found for sex, age or body mass index. We found that fracture was twice as likely in the presence of possible or probable osteopenia. We did not find that fracture was more likely to occur in patients with a previous diagnosis of Perthes, DDH, SUFE and avascular necrosis (AVN).
We found patients with a superior overhang of the femoral component on the neck did not risk fracture, however we could not demonstrate that notching in itself increased the risk of fracture.
There was no correlation with neck-shaft and stem-shaft angle or neck lengthening and offset and subsequent neck fracture.
In 13 bilateral cases there was fracture in 3 (incidence 23%). Apart from one fracture that occurred at 18 weeks post-operatively all the others occurred before eight weeks. Five fractures occurred in patients who subsequently on histological analysis were found to have avascular necrosis.
We conclude that bilateral surgery is probably unwise. That a superior overhang seems to protect against fracture as long as this is not at the expense of creating an inferior notch. Finally, we find AVN in a number of retrieved heads, what is the true incidence of AVN and does the approach adopted cause the avascular process and if so why do we see so few fractures?
The practice of selecting patients with a low ASA(American Society of Anesthesiologists) grade to have joint replacement performed at remote centres such as DTCs (Diagnosis and Treatment Centres) and by teams of visiting surgeons is becoming more commonplace. This leaves NHS Hospitals with a patient population skewed towards the higher ASA grades. This study was undertaken to identify the extra burden that this may place on a District General Hospital.
All patients undergoing total hip or knee arthroplasty at Blackpool Victoria Hospital in the year 2002 were identified. Of 191 patients, 132 were classified as ASA grade I or II. 59 patients (31%) were classified as ASA grade III or IV. The immediate postoperative complication rate for the patients with ASA grade III and IV was found to be 25%. All complications were treated appropriately and all patients had a satisfactory outcome at 6 weeks. The reported immediate postoperative complication rate for hip and knee replacement ranges from 3–6%. It is clear from these figures that removal of fitter patients from waiting lists will effectively increase the complication rate following arthroplasty in NHS Hospitals. We feel that the Government has not identified the extra care involved in treating these higher risk patients.
With the demand for total hip arthroplasty continuing it is essential that the longest follow-up cases remain under continuous review.
Fifty one of the primary Charnley low-frictional torques arthroplasties have passed 30 years follow-up: mean 31 years (30–36): 42 are women and 9 men. Their mean age at surgery was 47 years (24–64). At the latest follow-up two have had a late deep infection, three a dislocation, nine a radiologically loose cup, two a loose stem and one had had a fracture of the shaft of the femur, and one a fractured stem, with only the fractured stem coming to revision.
Clinical results remain satisfactory. Wear and loosening of the cup remains the long term problem. Further improvement and even longer follow-up and successful results of the Charnley LFA will come from materials which offer the greatest resistance to wear.
Salvage procedures for complications following revision arthroplasty are becoming an increasingly necessary intervention. Total femoral replacement (TFR), initially developed for limb salvage in the management of bone malignancy is the most extreme example of this.
Over the last 25 years, 14 patients have undergone TFR at the author’s institution following complications of revision arthroplasty surgery.
We have retrospectively reviewed the medical records and radiographs on this patient group (in terms of operative indication, morbidity and mortality). The clinical outcome has been evaluated using the International Symposium of Limb salvage (ISOLS) criteria.
14 patients, 9 male 5 female were treated with TFR between 1978 and 2003. The average age was 64 years (range 44–79 years). The duration of symptoms from primary intervention to total femoral replacement was on average 8 years (range 1–15 years) and during this period the number of revision procedures undertaken ranged from 1– 4.
In 86 % of cases the operative indication for TFR was for the management of deep sepsis. Other indications include non-union and periprosthetic fracture with massive bone loss.
The post operative course was varied with 4 patients experiencing no significant complications, 2 needing further surgery as a consequence of infection, 5 needed surgery for dislocation with 2 of these patients being left with a permanently dislocated hip.
As all patients had undergone some form of limb salvage procedure prior to TFR their level of function was assessed pre-operatively by the ISOLS criteria. This showed a range 0 – 33% (poor function). Clinical outcome following TFR measured by the same ISOLS criteria showed a range 36 – 80% (poor to good function).
Total femoral replacement has a definite role in the management of complex problems arising following hip and knee revision arthroplasty surgery. Pain can be controlled to an acceptable level and independence can be maintained.
From February 1992 to December 1997, 379 total hip arthroplasties in 342 patients were performed. 13 patients were lost to follow up, with 33 unrelated deaths. All arthroplasties were performed via the posterior approach in the lateral position. All patients were enrolled in an arthroplasty register at the time of surgery by the operating surgeon. Patients underwent clinical and radiological follow up. Kaplan-Meier survivorship analysis was used to determine the failure rate of the prosthesis, with revision surgery or decision to revise as the end-point.
The overall survivorship from all causes of failure at 5–10 years was 99.4%.
There were two stem revisions. One stem was revised for aseptic loosening at 4 years and one revised for recurrent dislocation. The stem aseptic loosening rate was 0.26%.
The cup aseptic loosening rate was 0%. The dislocation rate was 0.53% (2 from 379).
The superficial infection rate was 0.53% (2 from 379). There were no deep infections in this series.
At 12 months 71.2% had no pain (270 from 379), and 53.8% (204 from 379) had normal function. 94.5% said the procedure was worthwhile or very good. At 12 months radiological follow-up revealed progressive radioluceny in 7.65% (29 from 379) acetabuli, and progressive radiolucency in 2.90% (11 from 379) femora (one progressing to revision for aseptic loosening). No acetabular cups required revision.
In patients aged 65 years or younger at the time of surgery the survivorship was 100% for both components. Attention to meticulous and consistent operative technique in acetabular and femoral preparation, in particular a complete cement mantle with good zone 7 cement and osseointegrated cement bone interfaces, enables these results to be achieved.
In 2004 the Charnely Hip replacement remains the Gold Standard hip replacement.
The median time between the first and second stage was 147 (range 50–619) days.
Fractures of the Biomet antibiotic loaded acrylic spacer occurred in 11% revisions when associated with an increase in time between stages and there was a 7% dislocation rate.
Patients did not receive a revision prosthesis in 19% cases and had early recurrent sepsis following their two stage procedure in 6%. Three patients had a single episode of dislocation of their revision hip prosthesis within a month postoperatively. Two patients had a proximal DVT and one patient had a pulmonary embolus. The mortality within eight weeks was 7%, rising to 10% within a year. This may be related to patient sepsis and comorbidities or the energy expenditure required to mobilise following a first stage procedure that we have analysed.
The Biomet antibiotic loaded cement system articulates and maintains soft tissue length in the majority of patients for the duration required between stages.
Previous studies have confirmed a very strong correlation between penetration depth and the incidence of cup loosening due to impingement of the neck of the stem on the rim of the cup. The Charnley stem has been consistently manufactured in stainless steel – originally in EN58J then 316L. Introduction of the high nitrogen content stainless steel (ORTRON) allowed the reduction of the diameter of the neck from 12.5mm to 10mm. A prospective study was set up to establish the value of the reduced diameter neck in the context of the long-term survivorship of the cup revisions for wear and aseptic loosening. The benefit of the reduced diameter neck was clear from theoretical considerations – our objective was to establish the level of that benefit.
We compared the results where the 12.5mm diameter neck had been used with patients where the reduced 10mm diameter neck was used. We have analysed the correlation between the depth of cup penetration (mm) and the incidence of radiograph cup loosening as well as revision for aseptic cup loosening. The two groups comprised 1047 and 387 hips with a mean follow-up of 16.6 years (1–36) and 12.7 years (1–20) respectively.
When there was no measurable cup penetration, not only were there no revisions for aseptic cup loosening, but none of the cups were radiologically loose. At 1mm the decrease is 5% (from 9.4% to 4.4%), at 5mm the decrease is nearly 35% (from 56.7% to 22.2%). The effect on the reduction of the revision rate was nearly 3% at 1mm to nearly 8% at 5mm. The overall “gain” in the UHMWPE thickness is about 1mm which does suggest 10 years extra at a mean of 0.1mm penetration per year.
Acetabular component loosening and pelvic osteolysis continue to be a significant clinical challenge in revision hip arthroplasty. We present results of 339 cases of acetabular reconstruction with impacted allograft.
All patients who under went acetabular reconstruction with impaction allograft between July 1995 and July 1999 were included. Clinical and radiographic data was collected prospectively.
There were 339 patients identified. Average age was 71 years. The majority were first time revisions (201) but the group includes 2nd, 3rd and 4th revisions with 34 two-stage revisions and 44 primary arthroplasties.
There were multiple surgeons with 2/3 being consultants and 1/3 fellows. Pre and post-operative clinical assessment included Oxford and Harris hip scores, and a modified Charnley score for pain, function and range of movement.
Pre-operative radiographs were classified with the Paprosky classification. Follow up radiographs were assessed for graft thickness, component migration, graft reabsorption and lucent lines.
There were 10 grade I, 205 grade II, and 103 grade III defects with 3 pelvic discontinuities. Reconstruction methods included impaction only, rim and/or medial mesh, KP plate fixation and reinforcement cages.
Follow up average was 6.1 years (4.3 – 8.4) and no patient was lost. Infection was identified in 13 patients (5 recurrent 89% eradication and 8 new 2.6%). There were 6 nerve injuries, 2 remain unresolved and 13 patients dislocated (3.8%). There have been 46 deaths in the group with 3 being peri-operative.
There have been 18 re-operations for aseptic loosening. 7 KP plates fractured, 1 cage migrated and 10 rim meshes failed.
Factors associated with aseptic loosening include use of a large rim mesh particularly with an allograft thickness of > 2cm.
We conclude that impaction allografting is a reliable method for acetabular reconstruction. Careful consideration should be given when allograft thickness will be > 2cm and a large rim mesh is required.
The mean diameter of the proximal femur increased from 12.99mm in males less than 60 years to 13.47mm in those of over 60. This increase was not statistically significant (p-value 0.064, 95% CI). In females there was a statistically significant increase in the mean diameter from 11.38mm in the under 60 age group to 12.90mm in those over 60 ( p-value 0.000, 95% CI).
220 consecutive hip resurfacing procedures were reviewed at a minimum of two years follow up to assess the incidence of heterotopic ossification and its effect on function and clinical outcome. We also reviewed the pre-operative diagnosis, gender and previous surgery. The overall percentage of heterotopic ossification was 58.63%. The incidence of Brooker 1 was 37.27%, Brooker 2 was 13.18% and Brooker 3 was 8.18%.
Male osteoarthritics had the highest incidence of heterotopic bone formation. Three males underwent excision of heterotopic bone, two for pain and stiffness and one for decreased range of movement.
Both antero-posterior and lateral radiographs were reviewed for evidence of heterotopic bone formation. 12.7% had no evidence of heterotopic bone formation on one view but clearly had on the second view.
Overall we found no evidence that heterotopic bone formation affected the clinical or functional outcome of the hip resurfacing at a mean of 3 years follow up.
Average estimated peri-operative blood loss for the standard incision group was 3.45 units and for the minimal incision group was 3.05 units (statistically significant, p-value 0.039, 95%CI). One patient after minimal incision had a superficial wound infection, which responded to oral antibiotics. There was one dislocation (standard incision).
The aim of this study was to determine whether there is evidence to support the [often quoted] concept of a threshold effect of implant wear rate on osteolysis risk after total hip arthroplasty (THA). The study design was a case control study of 115 subjects with osteolysis after Charnley THA for idiopathic osteoarthritis (mean age at primary surgery 61.1 years; M:F =49:66; osteolysis-free survival 10.9 years) compared with 115 individually case-matched subjects following Charnley THA for idiopathic osteoarthritis with no current radiographic evidence of osteolysis (mean age 61.3 years; M:F = 49:66; osteolysis-free survival 11.0 years).
Calculated median (interquartile range) annual linear wear rate (measured using the EBRA method) was 0.12mm (0.08 to 0.18) and 0.07mm (0.05 to 0.10) in the osteolysis and control groups, respectively (Wilcoxon, P< 0.001). Subjects were divided into wear quintiles based on wear rate (n=46 subjects per quintile). The proportions of osteolysis subjects in each successive wear quintile groups were 0.22, 0.39, 0.48, 0.61, and 0.80 (χ2 P< 0.001). The proportion of subjects with osteolysis thus increased in a uniform manner with no evidence of a disproportionate increase between groups. The odds-ratio for osteolysis for each incremental increase in annual linear wear above the median wear rate in the control subjects was 2.4 (logistic regression analysis, 95% CI 1.7 to 3.3, P< 0.001).
In summary, the proportion of subjects with osteolysis increases steadily by wear quintile. Our data suggest a continuous gradient of risk for osteolysis associated with increasing annual wear rate in the Charnley prosthesis. We found no evidence to support the concept of a defined threshold above which the risk of osteolysis is disproportionately increased. The implication of this finding is that the goal of advances in bearing surface technologies should be aimed at the elimination of wear, rather than simply it’s reduction to below an arbitrarily-defined level
Information on the complication rates of revision THA is well documented. However, there is little data on functional outcome of revision THA. We aimed to determine the functional outcome of revision THA (n=72 subjects) versus individually matched THA controls. All subjects underwent THA for idiopathic osteoarthritis, and the same investigator made all clinical assessments. The mean ages (±SD) at primary THA were 61.3±7.2 years (THA revisions) and 61.1±7.4 years (THA controls). The male: female ratio was 36:36 in both groups. The groups were also individually matched for primary THA year (median 1984), presence of bilateral THA (43 subjects per group), and total follow up time (mean 14±4 years). Revision-free survival in the THA revision group was 9.8±3.9 years, and post revision follow up was 4.5±3.0 years.
Sixteen subjects had revision of 1 implant component and 56 had both revised. Allograft was required in 25 and 17 of the cup and stem revisions, respectively. The median (Interquartile range) Oxford and Harris Hip Scores in the revision and control groups were 28 (21 to 39) and 72 (60 to 86) versus 21 (16 to 32) and 89 (79 to 97), respectively (Wilcoxon, P< 0.001 both comparisons). The largest difference in Harris Hip Score was found in the function domain; revision THA median score 24 (17 to 36) versus 38 (28 to 44) in the controls (P< 0.001). Male subjects had slightly better outcomes versus females in both groups (P< 0.05). Revision of both versus 1 component, bilateral THA, age at revision, and use of allograft did not affect outcome (P> 0.05 all comparisons).
The clinical outcome of revision hip arthroplasty for aseptic loosening is worse than that of primary arthroplasty, principally in terms of function. However, use of allograft, number of components revised, and age at revision are not strongly associated with clinical outcome of revision surgery.
Minimally invasive approaches to the hip may be divided into two categories: single mini-incisions derived from standard approaches and two-incision approaches designed specifically for minimally invasive total hip replacement. The authors have a number of specific concerns about the latter based on its apparent transgression of basic surgical principles and favour a mini-lateral approach to the hip which they describe and review.
The two-incision approach requires two short (2–5cm) incisions from two different directions. Unlike other minimally invasive techniques, these incisions run close to the major neurovascular structures, which have been damaged. Visibility is limited as demonstrated by the need for navigation systems and illuminated retractors by some groups. Accurate resection of the femoral neck is obscured by the presence of the femoral head. Precise siting of the socket may be compromised by poor visibility. Most series accomodate only the use of uncemented components. Claims for more rapid mobilisation appear to depend more on anaesthetic rather than surgical technique.
We have developed the mini-lateral approach to the hip, in parallel with others, over the last five years. It is a scaled-down version (< 10cm) of the Hardinge approach which has been used successfully for 25 years. It relies on a precise appreciation of the regional anatomy requires no additional equipment and avoids the problems posed by the two-incision approach. A short video presentation will be given.
We present a consecutive retrospective series of 99 patients having 103 cemented C-stem THA for OA over a three-year period. Patients were assessed for duration of surgery, blood loss and length of postoperative stay. At follow-up (mean 18/12) they were assessed using the Oxford Hip Score, radiographic analysis and their incisions were measured. No hips have been revised and none are considered to be at risk. No nerve or vascular injuries have been reported.
We describe our early experience with the implantation of the first consecutive 231 primary Birmingham Hip resurfacings. At a mean follow up of 33 months, survivorship was 99.14 %, with revision in one patient for a loose acetabular component and one unrelated death.
Mean Harris Hip score improved from a mean of 62.54 ( Range : 8–92) to 97.74. (Range: 61 – 100) Mean flexion improved from a mean of 91.52°, ( Range : 25° –140°) to a mean 110.41°. ( Range : 80° – 145°)
1 patient presented at 6 weeks post resurfacing with pain and no history of trauma. An undisplaced fracture of the superior femoral neck was seen, which healed with a period of non-weight bearing.
96.94% of patients rated their prosthesis as good / excellent, the remainder rated it good/fair.
We have implanted 371 CLS acetabular components in our centre since 1989. Despite design changes in the component we report 4 cases of failure by fracture through the metal backing of the cup. Our aim is to highlight this uncommon mechanism of failure and advise that in cases of unexplained hip pain in those with CLS acetabular components X rays in at least 2 planes are performed.
There is a difference in age between the two groups with the bilateral group being younger (p< 0.01).
Although group A had a higher death rate, it was not statistically significant. The deep infection and revision rate was similar for both groups. The average length of stay for group A was 13 days compared to 8 days for group B.There was a significant difference in the likelihood of blood transfusion with a transfusion rate of 78% in group A and 22% in group B (p< 0.001).
Only 23% of GP’s thought that their training in orthopaedics and trauma was adequate .85% felt that they would benefit from further training. 80% of these felt that clinical teaching would be the best way to achieve this.
There is a legal and ethical obligation to gain informed consent before treatment commences. A number of bodies have issued guidelines for obtaining consent and these include the Department of Health, the GMC, The Royal College Surgeons of England, and the B.O.A. For a patient to give their informed consent to surgery they must receive sufficient information about their illness, proposed treatment and its prognosis. There are no specific guidelines regarding joint replacement. With this in mind a retrospective case note study was undertaken involving 100 patients who had undergone a hip replacement. Noting the documented discussion at all stages of patient contact.Fifty percent of patients had been seen and listed in the Outpatients by a Consultant, 25% were discussed with the Consultant responsible and the remainder were listed without Consultant input. In only 33 % of cases were any specific risks recorded. This had fallen to 4% on their visit to pre operative assessment clinic. All the consent forms were completed at the time of admission for surgery. Forty percent of these on the day of surgery. The majority were completed by SHOs (58%), while only 4% were completed by consultants. None of the forms noted the lead surgeon. All the consent forms noted some frequently occurring risks. However there was a large variance in the details recorded. The study highlights that the majority of complications are only documented on the consent form, with little note of the dialogue leading up to it. It is also apparent that there is no agreement as to what represents a significant or frequent complication.
This review raises a number of important issues. There needs to be a national standardisation of the process of consent. We propose the introduction of a specific consent form for hip replacements that provide improved documentation of the standardised risks involved. This should also include guidelines regarding prosthesis choice, surgical approach and the extent of trainee involvement. In addition we would also suggest there is a need to improve sequential documented discussion up to the point of surgery and introduce specific training for juniors carrying out consent.
Giant synovial cyst is commonly seen in association with rheumatoid arthritis. The Baker’s cyst around the knee is the commonest example but it has also been described at the elbow and hip. The possibility of a synovial cyst around the hip is unfamiliar to most clinicians including those who regularly deal with inguinal swellings and those specialising in musculoskeletal conditions. This is often overlooked as a cause of symptoms in inguinal area and lower limb.
We present a report on two patients in whom abnormal pulsatile masses in the groin caused diagnostic difficulty. Patients were initially admitted under vascular surgeons with a clinical diagnosis of aneurysm. Ultrasound examination was useful in excluding aneurysm. Detailed clinical examination revealed painful restricted hip movements and an X–ray showed evidence of arthritis in hip joint. CT Scan confirmed it to be a synovial cyst. Computed Arthrotomogram or Arthrography showed communication of the cyst with hip joint.
Synovial cysts and iliopsoas bursa enlargement may be more common than previously reported. They may present as a pulsatile mass due to close proximity to femoral vessels and should be considered as a differential diagnosis in patients with unusual inguinal swelling.
On reviewing the patients’ histories further: One patient had reported a broken tooth reported at the time of surgery and been given reassurancethat it was safe to proceed. One patient had an overt dental abscess ongoing for 15 years and one patient had an occult dental abscess revealed on radiology. Two other patients had extensive dental caries with blackened stumps as teeth. Follow-up after antibiotic treatment and revision arthroplasty is limited in these cases but results appear satisfactory at up to five years.
Ten had bilateral surgery.92 (66%) were female and 48 (34%) were male.The mean age at operation was 58 (range 34–90).The mean length of follow up was 50 months (range 36–76).
Standardised anteroposterior radiographs of the pelvis were compared at one year with the three to six year reviews.Radiological demarcation of the acetabular component was assessed using the Hodgkinson grading system by the senior author.
92% of sockets showed no increase in demarcation during the review period whilst 3% had developed evidence of radiological loosening with grades 2 to 4.
Fiat Cinquecento 500mls Morris 1000 1 litre Austin 1100 1.1 litres Allegro1400 1.4 litres The Mark E Cortina 1.6 litres Wolsey 1.8 litres Rover 2.0 litres Jaguar 3.0 litres Bentley 4.5 litres
Total hip arthroplasty (THA) patients often require peri-operative blood transfusion. Variables that predict transfusion requirement may allow us to target cross-matching of individual patients.
153 patients underwent primary unilateral THA for osteoarthritis or rheumatoid arthritis during 2002 in our institution. 75 casenotes from these subjects were reviewed. Age, sex, diagnosis, weight, height, pre-operative haemoglobin (Hb) and haematocrit (Hct), anticoagulation type and timing were recorded, along with post-operative Hb and timing and quantity of any blood transfusion. Potential predictors of transfusion were examined using logistic regression analysis. ROC analysis was used to compare the relative predictive value of significant variables.
Mean (±SD) age at surgery was 67±11 years (53% females). Mean pre-operative Hb was 13.8±1.4g/dl, mean post-operative Hb was 10.2±1.0g/dl. 27 patients (36%) needed a transfusion; the most frequently given volume was 2 units and the mean number of units given was 0.85. The most common reason for transfusion was an asymptomatic low Hb (< 8.0g/dl). Pre-operative Hb and Hct were predictive of post-operative transfusion (logistic regression analysis P< 0.01). Age, gender, diagnosis and anticoagulation were not predictive. Using ROC analysis the optimal ‘cut-off’ value of pre-op Hb as a predictor was 12.7 g/dl, giving a sensitivity of 41% and a specificity of 88% for blood transfusion requirement. The optimal ‘cut-off’ for Hct was 0.41, sensitivity 74% and specificity 61%. There was no significant difference in the overall predictive value between these variables (comparison of area under ROC curves, P> 0.05).
In summary, subjects with a pre-operative Hb< 12.7 or Hct < 0.41 are more likely to require a blood transfusion after unilateral primary THA than those with an Hb or Hct above these values. In treatment centres where cross-matched blood is not available at short notice on demand, pre-operative cross-match of patients with blood counts below these values may be appropriate.
There is no doubt that the closed body-exhaust system plays an important role in reducing infection rate in total hip arthroplasty. This demands a secure body-exhaust air hose. The current method in securing the air hose by tying the hose ribbons around the waist often fails to hold the hose in place. Soon after the operation begins; the hose that is secured to the body starts to migrate its way up to reach the surgeon’s neck. This will inevitably undermine the effectiveness of the body exhaust system, interfere with the sterility of the surgeon’s gown, and cause discomfort to the arthroplasty surgeon.
A new and simple method is described to stop the body exhaust pipe from slipping and migrating up the surgeon’s body. The surgeon’s own buttocks are used to anchor the hose tapes instead of fastening the air hose ribbons around the surgeon’s waist.
The new method of using the surgeons buttocks as anchors to secure the body-exhaust hose in place can improve the effectiveness of the body exhaust system and raise its potential to the maximum without causing any discomfort to the surgeon or jeopardise the sterility of the surgeons clothing.
The placement of the guide wire in the dynamic hip screw operation can be a challenging task to the trauma surgeon. Complications can arise related to incorrect guide wire entry point, making wrong tracks, or even accepting an unsatisfactory lag screw placement. Insisting to optimise the guide wire position can lead to increase in operation and radiation exposure times.
A new non-invasive technique is described to assist precision placement of the guide wire in the dynamic hip screw fixation of the neck of femur fractures using no more than a size A4 plain folded paper and a non-permanent marker pen.
The new non-invasive “no high tech” method can help the trauma surgeons to shorten the operation time and reduce the radiation exposure time needed to place the guide wire in the dynamic hip screw fixation of the neck of femur fractures.
In this study, we reviewed the records of 881 patients with fracture neck of femur over 5 years. Of these, 372 patients underwent hemiarthroplasty (231 cemented and 141 uncemented). The aim was to analyse the factors, which may contribute towards the mortality in cemented versus uncemented group.
The mean age in the cemented and uncemented group was 82 and 81 years respectively. 136 (58.8%) patients were operated within 24 hours of admission in the cemented group as compared to 63 (44.6%). The mean operative time was 81minutes for cemented hemiarthroplasty and 61 minutes for uncemented hemiarthroplasty. 77% of the cemented hemiarthroplasty was performed by Registrar grade as compared to 69% in the uncemented group. Of the 231 patients in the cemented group, 52% received general and 48% received spinal anaesthesia. Of the 141 patients in the uncemented group, 30% received general and 70% received spinal anaesthesia.
There was an 8% 30-day mortality compared to 11% 30-day mortality in uncemented group (p< 0.05). The mean age of patients in the mortality group was age 86 yrs in cement and 84 yrs in uncemented group. Most operations were done within 24–48 hours. There was significant co morbidity in patients who died. The average operative time of patients who died in both groups was same.
There was an increased mortality rate in the uncemented group as compared to the cemented group (p< 0.05). Based on our study, we conclude that cement is not a risk factor. Duration and timing of surgery is not associated with increased mortality. There was no difference in 30-day mortality rates between patients receiving general or spinal anaesthesia. Significant co morbid factor is associated with increased mortality.
The advantages are preservation of bone stock, non violation of the proximal femur, reduction of stress shielding in the proximal femur and it is quite physiological.
The one important thing is to avoid notching the neck to prevent disastrous fractures. The implant is less forgiving and the learning curve is steep. The ultimate usefulness can only be gauged once longer follow-ups are available.
Autologous drains are used frequently in total knee replacement surgery but not in total hip replacement surgery (THR). Previous studies have shown that these drains are not cost effective in THR surgery. We studied the effectiveness of autologous drains in THR surgery compared with normal suction drains.
All the patients had an uncemented hip. The Bellovac®A.B.T (Astra) autologous drainage system was used. Patients using the drains were studied prospectively and the volume of drainage, volume of autotransfusion, amount of homologous blood transfused and the hospital stay were all recorded. A group of patients who had normal suction drains were studied retrospectively to determine the transfusion rate and hospital stay using these drains.
In the group using standard suction drains there were 43 patients with a mean age of 72. The mean drainage was 641 ml (Range 500 – 1070). 10 patients out of 43 had a transfusion (Transfusion rate 23%). A total of 21 units of blood were used. The mean hospital stay was 14 nights. In the group using autologous drains there were 38 patients with a mean age of 67. The mean drainage was 703 ml (Range 200 – 1700), and of this the mean volume of blood that was given back to the patient was 445 ml (Range 50 – 1050). 2 out of 38 patients have required a blood transfusion, a transfusion rate of 5 % . This reduction in transfusion rate is significant (p< 0.005). The mean hospital stay was 9 nights. The difference in the hospital stay was not statistically significant.
Using the autologous drainage system in uncemented total hip replacement surgery reduces the need for a homologous blood transfusion. It is simple and easy to use and avoids the complications of a blood transfusion. It was also found to be cost effective.
Injuries to the lower urinary tract are well recognized following fractures to the pelvic ring. The overall incidence of pelvic fractures is similar in men and women. However associated urological injuries occur less frequently in women. There are very few reported cases of combined bladder and urethral injury or combined intra- and extraperitoneal bladder rupture in women. Only two cases have been reported describing communication of the hip joint and an extra peritoneal bladder rupture.
To our knowledge we are the first to describe a pelvic ring injury complicated by combined intra and extra-peritoneal bladder rupture, urethral injury and direct intraperitoneal communication of the ruptured bladder with a central dislocation of the hip joint. The mechanism of bladder laceration was gross displacement of the quadrilateral plate and pubic rami following acetabular fracture. This bone was found at laparotomy to be lying within the bladder cavity.
Revision hip surgery is increasing each year. We describe a case of revision hip surgery of a fully ingrown modular stem in which the supplied manufactures replacement modular head did not fit the original taper. This resulted from a change in the manufacturing process and taper dimensions between the primary index hip replacement and the revision operation. The manufacturing company was not aware of this change in their manufacturing process. This caused problems during surgery.
A thirty-nine year old male patient had a Mittel-meier uncemented hip prosthesis performed for avascular necrosis of the femoral head in 1988. Twelve years following the index primary hip replacement the cup was loose and migrating so revision of the acetabular component was planned.
A selection of Mittelmeier heads was obtained from the company. The ceramic head was removed and the acetabular component revised for a cemented cup. It was then discovered, during the operation, that the supplied heads did not fit the taper on the stem. The manufacturers had changed the dimensions of the taper since the original prosthesis had been implanted in 1988. Several companies had marketed this prosthesis since 1988 and the current supplier was unaware of a change in the taper. With the cup already cemented in place there were limited options. By chance the Exeter heads fitted the taper on the femoral component and were used. The patient recovered uneventfully.
The Mittlemier is not the only prosthesis to change its taper during its lifetime. If as in this case the manufacturers are unaware of a change in the manufacturing process the surgeon has no way of confirming the information provided prior to the surgery. This case highlights the potential problems when trying to partially revise a modular component.
In shallow or deficient sockets, we describe a simple technique by 180° rotation of the Cormet 2000 metal-on-metal resurfacing pegged acetabular prosthesis. This works by utilising ischio-pubic splines for superolateral socket engagement. We have used this technique in three patients with successful outcome avoiding the need of structural graft augmentation. In one patient, this technique was supplemented with cadaveric allograft.
The Austin Moore Prosthesis (AMP) is a recognised treatment option in the management of displaced intracapsular femoral neck fractures in elderly patients. Peri-prosthetic femoral fractures are a potential complication of both cementless and cemented hemiarthroplasty and can occur intra-operatively or at any stage following implant insertion.
Over a two-year period, 244 patients underwent hemiarthroplasty for a displaced intracapsular femoral neck fracture. Seventy patients had an AMP inserted whilst 174 patients were treated using a cemented Thompson stem. All of the AMP’s were inserted by, or under the supervision of an orthopaedic consultant.
Five patients (7%) from the AMP group sustained a periprosthetic femoral fracture. Four required revision surgery. The remaining case was managed non-operatively.
When compared to the cemented Thompson hemiarthroplasties performed over the same time period, despite the operating time being significantly less, the number of periprosthetic femoral fractures was significantly greater with the AMP. Furthermore, the early mortality rate was significantly higher for the AMP group who, were also significantly older and more likely to require postoperative blood transfusion. There was no significant difference in gender or ASA grade between the two groups.
These findings suggest that for displaced intracapsular femoral neck fractures in elderly patients, when hemiarthroplasty is the treatment of choice, a cemented prosthesis is preferable.
Telephone interview is an important tool for patient follow-up after THR and a useful adjunct to life-long review.
Revision hip surgery is becoming increasingly common, 300 procedures being performed in 2001 at our institution. In order to achieve a good outcome bone stock needs to be of good quantity frequently necessitating the use of impaction bone grafting using allograft bone.
Donor bone may frequently take three months before it becomes available for use due to the stringent screening procedure. Donor patients must have a clean bill of health, swabs taken at the time of surgery must obviously demonstrate no growth and blood samples taken at donation and an interval of three months, free from viral infectious diseases. It is thus easy to see the lag from the time of donation to availability and why, with increasing demand, need for allograft bone is rapidly exceeding supply.
We need to look for an alternative supply of human bone allograft.
We have compared the harvest of bone at the time of primary total knee replacement with that of the femoral head by both mass and volume. Sixty consecutive patients undergoing primary hip or knee arthroplasty were included in the study, and the masses and volume of the femoral heads compared with that of the total bone cuts in knee arthroplasty. The type of knee replacement used was documented as was whether the femoral head had had a bone block removed. It was found that the mass of femoral heads was 81g, that of knee cuts 95g this is a statistically significant difference; the volume of femoral heads 66ml and that of knee cuts 75ml.
The volumes of bone available from knee arthroplasty cuts are at least comparable femoral heads obtained using hip replacement and could, perhaps, provide a realistic source of bone allograft.
Between 1999 and 2002, we revised 72 hips in 69 patients using this technique (mean age 65years, 28 to 88). Fifty-six cases had aseptic loosening, 8 had infection (2 stages), 7 had peri-prosthetic fractures and 1 had a broken stem. The mean time to revision was 8.5years (1 to 21). Patients were assessed clinically and with the Oxford Hip Score (OHS) pre- and post-operatively. Fifty-seven patients also had acetabular revision. Four patients required femoral osteotomy to remove the old prosthesis. We used a mean of 1.8 (1 to 4) femoral heads per operation.
Complications included 6 peri-operative femoral fractures diagnosed at operation and fixed successfully, 6 infections, 10 dislocations (2 were recurrent), one deep vein thrombosis, 2 pulmonary embolism and one gastrointestinal haemorrhage. The average blood transfusion was 1.8 units (0 to 9).
The OHS improved from 45 (26 to 58) pre-operatively to 24.3 post-operatively (12 to 43). No hip has been re-revised for aseptic loosening at a mean follow-up of 32.7 months (16 to 51).
Two cases of assymptomatic hip dislocation discovered incidentally are presented.
Both these patients were mobilising independently and did not suffer from any neurological abnormality. Both these patients had asked to be discharged after an initial 2-year follow-up. They had not experienced any problem with the hip replacement. These dislocated prosthesis were discovered incidentally. Revision arthroplasty was carried out successfully in both these patients
These cases emphasise the need for long-term clinical and radiological follow-up in hip arthroplasty patients as hip dislocations can be assymptomatic and not detected by clinical examination. Radiological review alongside evaluation using scoring systems is recommended.
Beighton and Kozlowski, in 1980, first defined this disorder, in Afrikaners, the syndrome , evident at birth, is constantly manifested by dwarfism, ligamentous hyperlaxity, congenital scoliosis, and multiple dislocations(hip dislocation, radial head dislocation, scoliosis, spatulate thumbs, and generalized ligamentous hyperlaxity, children are of normal intelligence potential.
We report A Tunisian family, in which the proband , and her parents family have the presumptive diagnosis of Beighton dysplasia(spondyloepimetaphyseal dysplasia), the proband manifested the full clinical criteria of the disorder, whereas the mother, and other family members are partially manifesting the disorder, but dysplastic hips is the common feature in most of the family members examined(from both paternal and maternal side), up to four family subjects are variably affected, ranging between congenital hip dislocation in two subjects and post adulthood dysplastic arthrosis.
The striking clinical findings evolved from the study is the accompaniment of diverse skeletal abnormalities rather than the hip dysplasia, the mother is with adolescent type kyphosis, and two other family subjects are with short stature and scoliosis, fractures were encountered in three family subjects, this was secondary to osteoporosis, which in fact a general clinical feature in all the family subjects.
The mode of inheritance of the disorder is compatible with autosomal recessive trait.
The purpose of this study is to indicate the importance of the precise recognition of the underlying etiologies in children presented with congenital dysplastic hips, as a matter of fact this is our main strategy in the department.
The 10 year survival in the bilateral hip arthroplasty group for the Charnley femoral component (Median follow up 138 months) and Harvard femoral component (Median follow up 120 months) using aseptic loosening as an end point was 95.2% (92.4%-98%) and 77.2% (69.2%-85.2%) respectively.
The posterior capsule is variously incised and excised during total hip replacement (THR). There is no consensus on the direction of the capsulotomy and the need to repair the posterior capsule. The objective of this study was to determine the orientation of the collagen fibres and nerves in the posterior hip capsule in patients undergoing THR.
Specimens from five patients with osteoarthrosis of the hip (with no fixed deformity) were obtained and fixed in 10% neutral buffered formalin. Sutures were placed to mark the head and trochanteric end before excising. A standard posterior approach was used. The samples were examined and reported by a pathologist. Samples were processed overnight in a VIP5 automatic tissue processor and embedded in paraffin wax, preserving the location of the suture sites on embedding. Sections were cut at 5 Ïm and routinely stained with haematoxylin and eosin. The van Gieson stain was used for collagen fibres. Nerve fibres were highlighted using immunohistochemistry for S100 protein and blood vessels using an antibody to CD34.
The collagen bundles seen were predominantly parallel to the axis of the specimen. Dispersed within the collagen bundles were small vascular leashes that were parallel with the collagen fibres. The S100 staining revealed that these were neurovascular leashes, with small nerves running alongside the vessels and the collagen. Nerves that separate from the vessels were likely to serve proprioceptive and nociceptive functions.
The direction of the capsulotomy during THR by posterior approach has been traditionally perpendicular to the direction of the capsular fibres. However, if possible, capsulotomy along the orientation of the collagen fibres may be advantageous. As this study demonstrates, it will result in less damage to the capsular collagen fibres, blood vessels and nerves resulting in better capsular repair and healing, and better conservation of pro-prioceptive and nociceptive functions.
The management of leg-length inequality following total hip replacement remains controversial. Many leg length discrepancies are well tolerated and need no treatment. Some patients require only a heel raise, but some patients remain dissatisfied after their hip replacement surgery.
A recent report has suggested that leg-lengthening following total hip replacement does not correlate with patient satisfaction nor joint-specific or generic health scores[
All 4 patients underwent revision surgery which equalised leg length and resulted in immediate and complete resolution of their symptoms. We discuss the clinical findings, x-ray appearances and surgical technique employed to correct this problem. We have never had to revise a hip because of a shortened leg on the operated side.
We present the early results of a bone conserving implant, the Thrust Plate Prosthesis (TPP) used for the revision of failed resurfacings of the hip in nine patients.
Four revisions were for fractured neck of femurs. The original implant in this fracture group was a McMinn resurfacing. The original acetabular component was retained. Five revisions were due to aseptic loosening. Four of the original implants in this group were Beuchal Pappas (BP) resurfacings and one was a Cormet2000 resurfacing.
In the fracture group the average age was 46yrs (34–70). The time from primary to revision surgery was 5.8 months (3–11). The Harris hip scores improved in all patients to their pre fracture level of 90 (83–99).
In the aseptic loosening group the average age was 62yrs (53–67). The time from primary to revision surgery was 121 months for the BP resurfacings and 19 months for the Cormet. The Harris hip scores also improved in this group to an average of 73.8 (50–100).
Hip resurfacing presents an attractive option for the younger patient. It is a bone conserving procedure with the added benefit of increased stability by using a large diameter head. Fracture of the femoral neck is a specific early complication. The usual treatment of this complication has been revision to a more traditional design, loosing the benefits of bone conservation.
The TPP is a bone preserving implant that has metaphyseal fixation of the proximal femur. It has satisfactory long term results (
Further tests were carried out in which an abductor load was included in the model. Testing was done at 600N and repeated thrice for each femur. The principal strains were calculated and compared with the principal strains without the abductor load.
Modern cementation techniques in hip arthroplasty are enhanced by the use of a cement restrictor. Failure of cemented hip replacements is commonly caused by aseptic loosening. Cement plugs which occlude the medullary canal are widely used to increase cementation pressures. Many plug types with variable performance exist. Ideally, plug performance should be sufficient regardless of other factors. All plug designs are circular in cross section, yet the vast majority of human femora are of oval section, the average ellipticity for human femora being 1.3. This study aims to determine (I) the effect of cement viscosity, canal shape and canal size on plug performance and (II) which designs of cement restrictor are able to withstand cementation pressures, regardless of values of other potentially influential factors.
Research is the quest for information. It is not an excuse for attending meetings in exotic places, nor is it an escape from clinical work that has become uninteresting. The early orthopaedic joumals contained reports of patients who have been treated by individual surgeons in specific, often novel, ways. There was little scientific structure, but nevertheless these papers were valuable as they disseminated knowledge to other Surgeons and also stimulated enquiry.
Orthopaedic research has developed dramatically over the last two or three decades. Patient related research has been advanced as a result of the availability of new techniques for example electron microscopy, DNA sequencing and the Genome, together with the discovery of the fine details of the cytokine control of cellular processes. This has gone hand in hand with the development of surgical sophistication allowing more adventurous interventions.
Joint replacement and internal fixation have led to close associations between orthopaedic surgeons and scientists from other disciplines, notably engineers and material scientists. This multi-disciplinary involvement is typical of orthopaedic surgeons and results in each discipline benefiting from the specialist knowledge of the others. The natural tendeney for orthopaedic surgeons to be interested in mechanical items is clear from a study of the distribution of interesting cars in the hospital car park!
The efficacy of different treatment methods should be challenged and this has resulted in the need for careful audit and epidemiological review. In some instances this has resulted in the conclusion that often used treatments are not effective. The assiduous application of the Cochrane principles is often very revealing, not least in that it indicates the lack of properly conducted orthopaedic trials.
Academic orthopaedics is in danger. In many countries the speciality is under pressure, normally as a result of economic measures that restrict the avallability of salarles and grants. In spite of these restrictions, it is surprising that there is a steady supply of excellent papers. How much better it could be with more funding.
The purpose of publícation is to share information. It should be the aim of every research worker to make a contribution to the understanding of the subject and to share his findings with his colleagues. Curiously many researchers feeI that their commitment to their project is complete as soon as they finish the trial and have the results. The preparafion of their work for dissemination through publication is often a very weak link and in some instances is absent. This is a dangerous tendency as their information may not be broadcast, wasting the scientific endeavour and endangering the status of the fundíng organisation, whose charitable status often depends on sharing the fruitg of research.
The incentive to publish is very variable. In some institutions the very existenee of a research department depends on a ‘paper score’ which is normally calculated from the product of the number of papers and the impact factor of the j ournal in which they are published. The calculation used to determine the impact factor of ajournal does not favour orthopaedic journals, as most orthopaedic papers are not quoted prolifically within the first year of publication. In contrast orthopaedic papers tend to have a much longer and more valuable lifetime and to some this is the more important and relevant feature. Unfortunately, the long-term value of the papers is not part of the calculation of impact factor. In order to achieve a high impact factor the publication must be in a rapidly changing field and contain at least a tiny element of special originality, which leads to it being quoted by most of the workers in that field. In the publishing world there is an ongoing discussion conceming an index that is more relevant than the impact factor.
For some, the competition for publication is so intense that there is ‘salami slicing’. Salami slicing is a process of publishing very small morsels of information in short papers instead of producing the complete study. It is done intentionally to increase the number of papers published and is frowned upon by scientific editors. Even worse there are cases of plagiarism and fraud, sadly occurring more commonly in surgical publication, than in other disciplines.
It may be time to ask fundamental questions about the need for research, articularly the need for every doctor in training to improve or embellish his or her Curriculum Vitae by decorating it with published works. There ís a tendeney for the more wealthy and better respected grant awarding bodies to fund successful rescarch teams, rather than to risk their limited resources on a spectacular project from an unknown team.
Funding is avallable from commercial sources. The role of this type of rescarch may require special assessment. There are issues of intellectual property rights and instances of commercial organisations delaymg or preventing publication if the findings of the study are not favourable. Many cynical readers give no weight to papers that are sponsored by commercial sources.
It is essential that rescarch in orthopaedics continues and that every possible step is taken in order to facilitate high quality research. There may be strength in numbers and it could be that the newly revitalised European Orthopaedic Research Society could help in supporting the endeavours of rescarch workers, particularly when it comes to European funding.
Total joint arthroplasty is the most significant advance in the treatment of end-stage arthritic disease of major joints. Despite the clinical success of this surgical procedure, however, some total joint prostheses fail, and although a failed prosthesis can be replaced, the results of revision arthroplasty are not as good as the first time. Studying the failed prosthesis and the associated bone and soft tissues provides insight into the causes of failure.
Most prosthetic failures are the result of structural limitations of the implant components. Although material failure may be sudden, a much more common cause is gradual aseptic loosening of the prostheses. Aseptic loosening is caused by both mechanical (gradual loss of material by wear) and biological (osteoclastic resorption of adjacent bone) factors. Wear particles induce a foreign body reaction characterized by a pseudomembrane composed of granulomatous tissues including macrophages, fibroblasts, giant cells, and osteoclasts in addition to debris particles. The extent of this response is driven by the number, size, composition, surface area, and types of particles present. Although there are differences in the relative local toxicity of each of these particles, the end result is the same. These mechanical and biological factors are unavoidable, and the success of a total joint prosthesis depends on the rate with which they occur. Polyethylene wear particles (1–200 ?) are the primary cause of loosening. They are strongly birefringent under polarized light microscopy. Smaller particles are phagocytized by histiocytes, whereas larger particles are surrounded by foreign body giant cells. Fragmentation of PMMA may also cause particulate debris. The presence of these particles (30–100 ?) may be deduced by empty spaces into the soft tissues, often bordered by foreign body giant cells, since PMMA is dissolved by xylene during routine histological techniques. Metal oxides form on the surface of chrome-cobalt or titanium alloys due to an electrolytic process, and stresses on the surface of the metal shear the oxides into the surrounding tissues, causing a black pigmentation of the tissues. Histologically, the black deposits of oxidized metals are seen extracellularly as well as in the cytoplasm of histiocytes. In addition to oxidation, metal undergoes corrosion and, as a result, metal ions enter the soft tissues and the bloodstream. A ceramic-on-ceramic coupling generates a significantly lower amount of debris as compared to the conventional metal-on polyethylene solution. When present, ceramic debris cause a mild histiocytic reaction without giant cells and virtually no osteoclastic bone resorption. There are various secretory proteins at the interfacial membrane that can affect bone turnover, including the cytokines IL-1, IL-6, Il-10, and TNF-a. Other factors involved with bone resorption include the enzymes responsible for catabolism of the organic component of bone, such as MMPs. Prostaglandins, in particular PGE2, are also known to be important intercellular messengers in the osteolytic cascade. More recently, several mediators known to be involved in stimulation or inhibition of osteoclast differentiation and maturation, such as RANKL and osteoprotegerin, have been suggested as key factors in the development and progression of osteolysis.
Infection around a prosthesis also causes loosening in approximately 1–5% of cases. Total joint prostheses become infected by two mechanisms, wound contamination at the time of surgery by Staph. aureus or Staph.epidermidis, and late hematogenous spread of organisms (Staphylo- and Streptococci, E. Coli, Pseudomonas, and anaerobes). The following factors facilitate bacterial growth. First, reaming and sawing, as well as PMMA polymerization, cause necrosis of necrotize bone adjacent to the implant, and such nonvascularized area permits bacteria to grow, safe from circulating host defenses. Second, a highly hydrated matrix of extracellular polymeric substances (biofilm) is formed that defends bacteria from antibiotics and phagocytosis. Third, some metals, such as nickel or cobalt, may depress macrophage function. The distinguishing histologic features of an infected prosthesis is an acute inflammatory reaction: a finding of > 5 PMN or of > 50 lymphocytes/hp field are presumptive for infection. Because some low-grade infections fail to stimulate an acute inflammatory reaction, they go undiagnosed until postoperative period when microbacterial culture results are available. To date, no single routinely used clinical or laboratory test has been shown to achieve ideal sensitivity and specificity for the diagnosis of prosthetic joint infection, and in most cases the diagnosis depends on a combination of clinical features, radiographic findings, and laboratory results. Intra-operative tissue cultures may be falsely negative because of prior antimicrobial exposure, a low number of organisms, inappropriate culture media, or atypical organisms. Conversely, cultures may be falsely positive because of contamination in the operating room, during transport, or in the laboratory. If the implant is removed, the entire prosthesis can be cultured. Moreover, because prosthetic joint infection is a biofilm-mediated infection, techniques that sample bacteria in biofilm, such as sonication or enzymatic treatment, may improve the diagnosis of prosthetic joint infection. More recently, molecular techniques are being used to detect nucleic acid in samples from infected patients even when conventional techniques are negative because of unusual microbial growth requirements or failure to grow after antimicrobial exposure or due to unfavourable environmental conditions. A disadvantage of such approach is its extreme sensitivity, leading to the possibility of false positive results.
The clinical presentation of prosthetic joint infection may be indistinguishable from that of aseptic implant failure. In many cases, culture of granulomatous tissue around failed prostheses, preoperatively diagnosed as aseptically loosened, reveals the presence of bacteria that may per se significantly contribute to the recruitment, maturation and activation of osteoclasts and that superimpose to the foreign body reaction to wear debris. The presence of a smouldering infection in case of “aseptic” failure observed in revision arthroplasties. A systematic investigation on all retrieved implants is mandatory to define the precise role of each potential factor contributing to the pathogenesis of failure, in order to further improve the quality of care of patients having total joint arthroplasty.
The aims of Total Knee Arthroplasty (TKA) are to relieve pain and to recreate joint function and stability. Knee joint stability is intimately associated with the concept of joint motion. A stable knee joint is one that maintains an appropriate minimum contact force between the articulating surfaces throughout the functional range of motion of the joint. Thus a TKA is stable when moving through its range of motion it can carry the required functional loads without pain, maintaining contact on non-peripheral located regions and produce joint contact force of normal intensity on the polyethylene insert. Any factors causing an abnormal joint contact force and/or abnormal eccentric position of joint contact force might lead to polyethylene and component loosening. The TKA stability and function are strictly related to the interplay among the implant component alignment, articular surface geometry (flat or congruent polyethylene insert), cruciate-retaining or cruciate-substituting prosthesis design, soft tissue balancing and muscle action. Tibial component loosening continues to be a common mode of failure following TKA. Tibial component fixation is critically dependent on an equilibrium between the mechanical loads and bone resistance to them. Even if it is difficult to find a strict correlation between locomotor lower limb function and knee kinematics, TKR kinematics and position of the point of contact between femur and tibial insert are fundamental biomechanical parameters to understand the reason of extensor mechanism deficit often found in TKA patients and the risk of polyethylene wear. In the present study we will present TKA kinematics and position of the point of contact between femur and tibial insert in fixed and mobile insert focusing in TKA design features. Different knee joint kinematic patterns has been found between fixed and mobile TKA design particularly when congruent artificial joint surface is coupled with mechanical constraint such as the spine-cam mechanism.
Total hip replacement procedures provide a very effective treatment modality for a wide range of diseases and injures to joints.
The annual number of primary and surgeries has been increasing. In Region Emilia Romagna, 4000000 inhabitants, 4587 total hip replacements (THA) were performed in 1997 and the number raised up to 5410 in 2002 ( + 18%). Emiarthoplasties were respectively 1914 and 2215 (+ 16%). Parallely number of revision raised from 550 to 938 (+71%).
In 2003 incidence of primary THAs in Emilia-Romagna is 107/100.000 inhabitants, higher than mean national value (76/100000).
Data of both primary and revision surgeries are collected by RIPO (Register for Orthopaedic Prosthetic Implantology) that started its activity in Rizzoli Institute on January 1990 and in Regione Emilia-Romagna on January 2000. The recording of data is done for each joint replacement operation and it consists on the identification of the patient, information about diagnosis or reason for re-operation, surgical approach, antibiotic and antithromboembolic prophylaxis, perioperative complications. Acetabular, femoral and head components are separately registered, on the basis of stickers with catalogue numbers provided by manufacturers with the implants. Fixation of the components is recorded as well.
Among the purposes of the Register there are the identification of early prosthesis failures, the information of surgeons on the outcome of their patients, the creation of a benchmarking tool for consultants and the speedy identification of relevant patients if a particular prosthesis or a particular batch gives cause for concern.
As for Scandinavian registers, revision is used as an end-point in the analyses. On this basis it is possible to calculate survival curves either aggregated or stratified.
By Cox multivariate analysis it has been ascertained that risk factors in total hip arthroplasties are represented by sex (females have lower risk than males), by age (younger than 40 are more at risk than 40–70s, and older than 70 are less at risk than 40–70s) and by pathology (fracture, coxites and Paget diseases have higher risk than coxarthrosis).
Basing on these data, survival analysis was normalized and the influence of articular coupling and fixation of the components on prosthesis outcome have been evaluated.
It resulted that failures are more likely to occur when metal on metal, or metal on polyethylene or ceramic on polyethylene devices rather than ceramic on ceramic implants are implanted.
Similarly cemented and hybrid THAs fail at higher rate than uncemented ones. All data are referred to a 11 years follow-up.
At present time Kaplan Meier analysis indicates a survival rate of total hip arthroplasties performed at Istituto Rizzoli of nearly 90% at ten years follow-up (9717 primary implants, 435 failures).
Main reasons for revisions are aseptic loosening of the cup (33%),aseptic loosening of both components (18%), aseptic loosening of the stem (17%), deep infection (7.9%),dislocation (7.6%),prosthesis fracture (3%) etc. Aseptic loosening represent, therefore, the most frequent cause for revision.
Results obtained at Istituto Rizzoli fit in the benchmarking set by the British NICE (National Institute for Clinical Excellence) that states that the revision rate should be of 10% or less at 10 years.
To improve these results attention should be pointed on new models: hip prosthesis technology is continually changing, with new designs and techniques being introduced. There is a need to strike a balance between using prostheses with published long-term performance data, and the need to develop and improve hip prosthesis. A solution to this problem could be to entrust reference clinical centers the evaluation of the effectiveness of any new prosthesis for at least three years, before opening free distribution in standard orthopaedic units,as suggested by NICE. Only models that reach the ‘entry benchmark’ in adequately sized, well conducted observational studies, can be implanted with a good safety. At present time it is unlikely that clinical evaluation data on long term effectiveness is required by Notified Body for ‘CE’ marking, unless new materials are involved in the manufacture. This happens despite the fact that even small changes to existing prostheses can have a significant impact on implant performance and revision rate.
Other factors than the already discussed can influence the surgery outcome, and among these the volume of operations performed in the hospital, the ability of the surgeon and its confidence with the technique, the compliance of the patient. Only an overall view of the situation will allow to reach the goal of reduction of need for revision of total hip arthroplasties.
Although dynamic hip screw (DHS) is considered the treatment of choice for pertrochanteric fractures, we theorized that external fixation would produce clinical outcomes equal to, if not better than, outcomes obtained with conventional treatment. As external fixation is minimally-invasive, we expected a lower rate of morbidity and a reduced need for blood transfusions. We compared fixation with DHS vs. Orthofix pertrochanteric fixator (OPF) in elderly pertrochanteric fracture patients. Forty consecutive pertrochanteric fracture patients were randomized to receive either 135A1 4-hole DHS (Group A) or OPF with 4 HA-coated pins (Group B). Inclusion criteria were: female, age B3 65 years, AO type A1 or A2 and BMD less than −2.5 T score. There were no differences in patient age, fracture type, BMD, ASA, hospital stay or quality of reduction. Operative time was 64 B1 6 minutes in Group A and 34 B1 5 minutes in Group B (p < 0.005). Average number of post-operative blood transfusions was 2.0 B1 0.1 in Group A, and none in Group B (p < 0.0001). Pain was measured 5 days post-operatively and was lower in Group B (p < 0.005). Fracture varization at 6 months was 6 B1 8A1 in Group A and 2 B1 1A1 in Group B (p = 0.002). In Group B, no pin-tract infections occurred. Pin fixation improved over time, as shown by pin extraction torque (2770 B1 1710 N/mm) greater than insertion torque (1967 B1 1254 N/mm), (p= 0.001). Harris hip score at 2 years was 62 B1 20 in Group A and 63 B1 17 in Group B. This study shows that OPF with HA-coated pins is an effective treatment for this patient population. Operative time is brief, blood loss is minimal, fixation is adequate and the reduction is maintained over time.
The release of metallic elements from the surfaces of orthopaedic prostheses, either by leaching or breakdown of the device into the body, is a potential health problem to patients. During the endurance of this bio-material metal alloys undergo to corrosion with the possibility that metal ions interact with biofluids and tissues inducing adverse biological effects (local or systemic damage such as cytotoxicity, delayed hypersensitivity, effects on angiogenesis and mutagenicity). Indeed, as the metal ions are released over a period of time, they will continue to stimulate the inflammatory response and to influence those cells within the chronic response.
The safe evaluation of biocompatibility of metallic-based orthopaedic prostheses is a prerequisite for their use in medicine. In this context, the use of in vitro model systems is of growing importance, not only as components of the initial phases of the safe evaluation process, but also as alternative (non-animal) methods for regulatory purpose through the cycle of research, development, validation and acceptance by regulatory authorities.
The aim of this work is to review the activity of IMETOX (In vitro Metal Toxicology) project of ECVAM in relation to biomaterials for hard tissue substitute. The research is aiming at integrating aspects of metal toxicity in different toxicological areas (e.g. systemic toxicity, reproductive toxicity, immunotoxicity, carcinogenicity).
Examples of tier testing as basis for new in vitro strategies for the evaluation of immunotoxicity, basal cyto-toxicity, and carcinogenic potential of metals of interest as components of medical devices (e.g. Ag, Co, Cr, Pt, Ti, V) investigated by cell cultures (mouse fibroblasts Balb/3T3, human keratinocytes HaCaT) are presented.
Key factors influencing cellular metal toxicity (low dose exposure, speciation, interaction among elements) and the new emerging problems of the cytotoxic potential of metal-nanoparticles are discussed.
Recent improvements in HA-coating technique make it possible to apply HA by different methods. The most promising is the precipitation technique. A thin Ca-P of 10 – 30 microns thickness can be applied using precipitation in fluid. The process takes place at room temperature in stead of at temperatures of many thousends of degrees centigrade. Still providing an HA-coating of similar type as the plasma-spray technique, there are several advantages associated with its use. To start with, the coating is of a micro-crystalline type in stead of macro-crystalline. This provides enhanced bioactivity because the exposed surface area of a micro-crystralline surface is much greater. At second it is possible to coat irregular surfaces, including porous materials that can not be coated using conventional techniques because the pores would be closed down. At third it is possible to include biological factors in the coating such as growth factors, bone-morphogenetic proteins or antibiotics at the time of manufacturing because the process takes place at room temperature. The high temperatures used with plasma-sprayed HA-coatings would preclude this. Experiments confirm these improvements. They show much enhanced bone apposition. Also the combination with antibiotics, growth factors or BMP’s is attractive because it may lead to a reduction in the need for bone graft materials or infection especially in revision surgery. This will greatly influence the possibilities of bone repair especially in revision surgery. Several experimental and clinical studies are currently ongoing and it is expected that these new enhanced coatings will expand the use of HA-coatings on more implant surface structures.
The world-wide experience with metallic implants provides the evidence for biocompatibility of modern cobalt- and titanium-based alloys. However, a corrosion process leading to release of ions has to be taken into account, and controversial data are available about the ‘endogenous’ metal exposure resulting from implants.
Adverse tissue reactions, cytotoxicity and toxic/ sensitizing effects of corrosion products on the immune system, as well as an involvement of metal ions in the pathogenesis of prosthesis loosening, are the main undesired effects. Moreover, metal ions could be responsible of long-term toxic effects, such as genotoxicity and carcinogenicity.
The aim of our study was to analyze the levels of serum metal ions in a large series of patients who underwent total hip and knee replacement (THR and TKR, respectively); both stable and loosened implants were considered. Furthermore, a group of subjects with fracture fixation devices was evaluated.
A consecutive series of 471 individuals (193 M; 278 F) was enrolled in the study, including 151 with hip prosthesis loosening (Group A: 52 M; 99 F; median age 67; median follow up 90 months) and 100 patients with stable hip prosthesis (Group B: 44 M; 56 F; median age 59; median follow up 34 months). Group A and B comprised implants with different coupling, i.e. ceramic-on-ceramic (alumina), metal-on-metal and metal-on-polyethylene, and different stem alloy (TiAlV-THR and CoCrMo-THR). 20 patients with knee prosthesis loosening (Group C: 3 M; 17 F; median age 67; median follow up 25 months), and 12 subjects with failed fracture fixation devices (Group D: 6 M; 6 F; median age 35; median follow up 12 months) were enrolled, too. Osteoarthritis was the most frequent disease that led to joint replacement (59%), followed by hip dysplasia (19%), and trauma (13%). Ion reference ranges were obtained from 188 subjects (88 M; 100 F; median age 52), including 56 healthy subjects and 132 candidates to primary THR or TKR. Serum samples were analyzed for chromium (Cr), cobalt (Co), molybdenum (Mo), nickel (Ni), aluminum (Al), titanium (Ti) and vanadium (V) content, in relation with the presence in the implant alloy, using a graphite furnace atomic absorption spectrometer (GFAAS), equipped with double background correction Deuterium/ Zeeman, autosampler and pyrolytic carbon-coated graphite tubes (Unica Solaar 939 QZ, Cambridge, UK). The highest value found for subjects with no implant was considered the upper reference limit for each element.
Group A (loosened THR) and B (well-fixed THR) patients, compared with controls, showed different behaviour depending on the prosthesis coupling and stem composition.
Metal-on-PE coupling and CoCrMo/Ni stem: a significant increase of Cr and Co serum values was observed, in both groups, even if the increase in loosened implants was higher than in the stable ones. Mo and Ni concentration did not show a significant variation. Ceramic-on-ceramic coupling: a high Cr release, and a high Al, Ti release was shown in loosened implants with CoCrMo stem, and TiAlV stem, respectively, whereas normal values were measured in patients with stable prostheses. Metal-on-metal coupling and CoCrMo stem: a significantly higher Co and Cr release, both in group A and B patients. The conspicuous corrosion rate in metal-on-metal implants, even if stable, was confirmed in the same population in the short- and medium-term.
A serum Co, Cr increase was demonstrated in Group C patients, too, who had a failed knee prosthesis, and a Cr, Ni increase was observed in Group D patients with stainless steel fracture fixation devices.
Metal corrosion leading to ion release needs further consideration, because it may enhance the inflammatory reaction, depress the immune system, and facilitate peri-prosthetic bacterial growth. Especially metal-on-metal coupling introduces additional biologic risks associated with increased degradation products of prosthetic materials. Otherwise, histiocytic/giant-cell reaction and peri-prosthetic osteolysis induced by polyethylene particles represent the main problem in knee and hip joint implants with metal/PE coupling, and the systemic effects due to the ion release become negligible. On the contrary, ceramic-on-ceramic coupling represents a good alternative, as demonstrated by the absence of metal release in stable implants, even if, in case of loosening, a serum ion increase is observed, probably due to the fretting at the head/neck connection.
Also, metal corrosion of fixation devices is a concern; consequently, it could be appropriate to remove the implants, as early as their function is accomplished.
In conclusion, ion profile should be carefully monitored and the epidemiological survey implemented, in order to establish the tolerance values in patients with implants, especially in young patients, where a long-term ‘endogenous’ exposure has to be faced. In particular, concerning systemic toxic effects, the ‘gene expression profiling’, through the use of microarray technology, could contribute to an improved understanding of the biological responses to metal ions released from orthopedic implants. In such a way a real risk-to-benefit ratio for the patient could be established.
Finally, ion monitoring, as demonstrated by the different serum ion levels in stable and loosened implants, could allow to detect early signs of failure, when radiographic and clinical data are unclear, and to avoid the need of revision using a proper treatment.
The aim is: to point out, in respect of Italian case law trends, the concept and the boundaries of surgeon malpractice liability in evaluating and implanting new prosthesic materials.
The surgeon is liable for damages caused by fraudulent intention or fault during his clinical and operating activity. In a civil perspective, it could be the result of either a breach of a contract or a tort, depending on the existing relationship between the surgeon and the patient; but in both case there might be a serious inexperience or a light imprudence or negligence to admit a fair compensation for damages. While in a criminal perspective, the personal injuries might be the result of a serious fault also in the area of imprudence and negligence to admit the application of criminal sanctions. Of course, personal liability of surgeon stands by vicarious liability of health unit.
Civil sanctions are more effective than criminal sanctions, not only because they have a wider area of application, but also because they are more incisive in quantitative terms, considering the new guidelines on pecuniary and biological damages that make out, at the same time, a compensatory and punitive function.
The surgeon, to be sure not to be affected by civil and criminal actions, might inform the patient about the operating features and the consequences of non operating, follow standardized protocols, use products and materials tested and certified by the most influential scientific literature, be care of post-operating effects and adopt all remedies and treatments that can eliminate or reduce post-operating risks, use the best and up-to-date techniques available. In any case he is not liable for unforeseeable events, even if they are in a causative relationship with surgical activity.
Metals represent the main components of orthopaedic implants. Being in contact with biological fluids, the metallic alloys used for the fabrication of artificial joints undergo corrosion or degradation, therefore they release ions and molecules. Although these do not have antigenic properties, they bind to protein carriers and may act as haptens eliciting a delayed-type hypersensitivity reaction (DTH). Biomaterial-related hypersensitivity is considered as an immunotoxic effect, although little is known about its clinical incidence and its impact on implant failure. The main question about the sensitivity against metals used in the joint prosthesis concern the cause-effect relation with the implant failure. In metal-exposed workers, the diagnosis of DTH is made in vivo by patch testing. For the occupational exposure standard patch-testing protocols are available, but some concerns exist about their applicability to study the hypersensitivity to metal implants. In this case-control study, a panel of representative haptens was used to assess the incidence of positive patch testing in patients undergoing ‘total hip replacement’ (THR) and ‘total knee replacement’ (TKR). The main goal of this study was to evaluate the validity of this relatively simple and safe procedure in the diagnosis of the hypersensitivity reactions to the implant components.
A consecutive series of 286 individuals was enrolled in the study. Five groups of patients were evaluated: Group A included 75 patients (20 M; 55 F; median age 59) candidates to primary THR or TKR; Group B included 98 patients with loosening of THR (27 M; 71 F; median age 67; median follow up: 102 months); Group C included 53 patients with stable THR (13 M; 40 F; median age 68; median follow up: 60 months); Group D included 40 patients with failed TKR (14 M; 26 F; median age 68; median follow up: 24 months); Group E included 20 patients with stable TKR (4 M; 16 F; median age 70; median follow up: 16 months). Osteoarthritis was the most frequent disease that led to joint replacement (59%), followed by hip dysplasia (19%), and trauma (13%). Patients with rheumatoid arthritis were excluded from the study, as well as patients who assumed cortico-steroids or other immunosuppressive drugs.
Fifty-eight patients (21%) had an additional implant at another site. Hypersensitivity to metals was tested by using the most relevant components of Cobalt-Chromium based alloys (CoCrMo), Ti-based alloys (TiAlV), and bone cements. A drop of each hapten was smeared on the Haye’s chamber test, which was applied to the dorsum of the patient. After 48–72 hours, skin reactions were evaluated and graded as 0 (no reaction), 1 (erythema), 2 (edema), 3 (vesicles), or 4 (bulla).
All patients with a medical history of metal DTH showed positive skin reaction. The incidence of positive patch testing to at least one hapten, as well as the frequency of DTH to metal, resulted significantly higher in patients with TKR, while the incidence of positive skin testing to bone cements was similar in all groups. Group B patients with CoCrMo-THR showed a low frequency of nickel-DTH in comparison to Group A (9% and 22%, respectively). In patients with TiAlV-THR the immune status seemed to be unaffected, and these individuals showed a high incidence of vanadium-DTH (Group A: 8%; Group B: 21%; Group C: 19%; p= 0.04). A high incidence of vanadium hypersensitivity was found also in patients with TKR (Group D: 33%; Group E: 20%). The median duration of the implant resulted significantly lower in patients who had a positive patch testing to metals (71 vs 106 months; p= 0.008).
Our results demonstrated the reliability of the panel used for skin testing, which was able to identify a systemic hypersensitivity status. A remarkable finding concerned the prevalence of DTH related to the metal composition of the implant. A significant low frequency of metal DTH, namely nickel, was found in patients with CoCrMo-failed implant. Because nickel is the most common metal sensitizer and its amount in both CoCrMo and TiAlV alloys is very low, we may consider the incidence of nickel DTH as informative for the immune status of the examined group. In the TiAlV group the immune status seems to be unaffected; on the contrary, theese patients showed a high prevalence of vanadium skin reaction. These results confirm the conclusion of previous studies, where the immunocompromised status of patients who had a CoCrMo had been shown and related to the high serum level of chromium and cobalt. Although the cause-effect relation between DTH and implant failure cannot be established, the hypersensitivity should be considered when deciding what type of prosthesis to use. Either if the sensitization precedes or follows the loosening, it participates in the network of events that are responsible for prosthetic loosening, because contributes to mantain the inflammatory process.
Bone marrow is the tissue where hemopoiesis occurs in close contact with the stromal microenvironment which support hemopoietic stem cell growth and differentiation. The bone marrow stroma is composed of a variety of different cell types providing structural and functional support for hemopoiesis: endothelial cells, adipocytes, smooth muscle cells, reticular cells, osteoblasts and stromal fibroblasts. Among these cell types, stromal fibroblasts have a peculiar biologic relevance. They are in fact able to support hemopoiesis, to differentiate towards osteogenic, chondrogenic and adipogenic lineage and to form a bone structure complete of hemopoietic marrow in in vivo assays. Their in vitro clonogenic counterpart is represented by Colony Forming Units-fibroblasts (CFU-f), which in turn give rise to Bone Marrow Stromal Cells (BMSC). In vivo bone formation by BMSC has been strikingly demonstrated and therefore these cells are considered a progenitor compartment for osteoblasts, responsible for the maintenance of bone turnover throughout life.
BMSC can be easily isolated from bone marrow aspirates. Nevertheless, given the low frequency of BMSC in a marrow sample, a step of extensive in vitro expansion is required to obtain a consistent number of cells available for both reconstruction and repair of mesodermally derived tissues. Moreover, their use for gene and cell therapy of skeletal diseases requires the long-lasting engraftment of BMSC endowed with a residual proliferation potential sufficient to sustain the low, but continuous, bone turnover in adulthood. The maintenance of BMSC stemness and the possibility to reprogram their commitment is therefore a field of primary interest given their potential use in regenerative medicine. Cell therapy of bone lesions by ex vivo expanded BMSC is passing from the phase of experimental animal model to the phase of clinical trials. Bone is repaired via local delivery of cells within a scaffold. Extremely appealing is the possibility of using mesenchymal progenitors in the therapy of genetic bone diseases via systemic infusion. Under some conditions where the local microenvironment is either altered (i.e. injury) or under important remodelling processes (i.e. fetal growth), engraftment of stem and progenitor cells seems to be enhanced. A better understanding of the mechanisms controlling BMSC differentiation and engraftment is required for their exploitation in therapy of human diseases. Furthermore, a better understanding of the interactions occurring between BMSC and biomaterials used to deliver cells in vivo will hopefully extend the field of therapeutic applications of mesenchymal progenitors. In this talk we will go through our experimental evidences on: a) influence of signaling molecule; b) transplantation route and engraftment; c) biomaterials.
Growth factors are essential for a number of cellular functions. Our results show that FGF-2 supplemented BMSC primary cultures display better differentiation potential, a higher degree of osteogenicity and undergo an early increase in telomere size followed by a gradual decrease, whereas in control cultures telomere length decreases with increasing population doublings. In conjunction with clonogenic culture conditions, FGF-2 supplementation extends the life-span of BMSC to over 70 doublings and preserves their differentiation potential up to 50 doublings. All together, these data suggest that FGF-2 supplementation in vitro selects for the survival of a particular subset of cells enriched in pluripotent mesenchymal precursors and may be useful to obtain a large number of cells for mesenchymal tissue repair.
BMSC intravenous infusion has been proposed as a means to support the hematopoiesis in Bone Marrow Transplants or as a vehicle for gene therapy. However, it seems that this route of injection leads to engraftment of a small proportion of BMSC. We have transplanted human BMSC transduced with the human erythropoietin gene, either intravenously or subcutaneously in NOD/SCID mice. Efficiency of engraftment was evaluated monitoring the hematocrit levels. Systemic infusion never increased hematocrit levels, whereas subcutaneous transplantation of the same number of cells induced an important increase of the hematocrit for at least two months. To determine whether the transient effect was due to cell loss or to reduction in expression, we recovered the cells implanted into a tridimensional scaffold, after the normalization of the hematocrit, expanded them in vitro, and re-implanted them in a new group of mice. Again the hematocrit levels rose one week after the transplantation. These results demonstrate that ex-vivo expanded human BMSC are not transplantable by systemic infusion, whereas the local implantation into a 3D scaffold allows their long term engraftment.
Biomaterials for bone regeneration should have a suitable structure to allow cell adhesion and an ideal level of vascularisation, a key factor to achieve new bone formation. Furthermore, they have to be informative, driving the cells towards osteogenesis and allowing the deposition of bone extracellular matrix. Our results indicate that BMSC need a mineralized scaffold to initiate bone formation which will occur with an extent proportional to the availability of biomaterial surface.
Tissue engineering regards the generation, regeneration, augmentation or limitation of the structure and function of living tissues by the application of scientific and engineering principles. Skeletal defects resulting from tumor resection, congenital abnormalities or trauma often require surgical intervention to restore the function. Current option for bone replacement include autografts,allografts,metals,ceramic and polymers.However, all these materials have drawbacks, and their selection usually require some compromises.
Skeletal tissues are under extensive investigation in tissue engineering research and beside the biological issues, the scaffolds design plays an important role. A number of biodegradable and bioabsorbable materials as well as scaffold designs, have been experimentally and, in some cases clinically studied. An appropriate scaffold should posses highly porous with interconnected pore network for cell growth and flow transport of nutrient and metabolic waste; biocompatible and bioresorbable with a controlled degradation and resorption rate to match cell/ tissue growth, suitable surface chemistry for cell attachment, proliferation and differentiation, and mechanical properties to match those of the implanted tissue. Synthetic biodegradable polymers and inorganic materials are promising as extracellular matrix analogue to facilitated tissue development and growth; these include: polyglycolic acid, poly-l-lactic acid, copolymers, poly-caprolactones, hydroxyapatite, tricalcium phosphates. All these scaffolds are well performing from biological and chemical-physical but they have some limitations from mechanical point of view. To overcome this problem a composite structure made by Polycaprolactone and Hydroxyapatite is studied by mechanical and biological analysis. To obtain a porous structure, the casting and salt leaching technique is implemented. The composite shows mechanical properties in the range of the spongy bone and interesting biological properties with regards to osteoblasts.
Injectable gels made of collagen are analysed to carry cells, a preliminary results of collagen gel loaded with MSC cells have been performed and rheological and proliferation study are showing the feasibility to obtain a bioactive materials/cells to be inject in the defined body site defects avoiding massive surgery.
The placement of orthopaedic, as well as dental, oral and craniofacial implants, are common practices in medicine and denstistry today. Challenges to the successful outcome of such implants include loosening of the device and inadequate filling of bone defects. The engineering of bone tissue is a recent strategy to provide new solutions to such problems. Since skeletal tissue regeneration requires three components, i.e. cells, growth and differentiation factors, and extracellular matrix, the approach of bone engineering is to mimic the biological process by delivering to the injured site: 1. cells capable of differentiating into osteoblasts, 2. inductive factors, and 3. a scaffold, biodegradable or not, to support cells. Prior to experimental and clinical application of the innovative surfaces or scaffolds, the three components have to be tested in the Labs using reliable in vitro methods.
1. Cells. The source of cells is a key point: osteoblast is the differentiated cell able to form bone in vivo and in vitro, and should be used, but primary human osteoblasts (hOB) are seldom available to the Labs, whereas osteoblast-like cell lines and bone cells from animals are an easy source, but may give different responses. An additional aspect which cannot be disregarded is the source of the bone cells, since the age and gender of the donor, as well as the site of retrieval and the method of isolation, have been shown to affect the yield of cells, the proliferation rate and their ability to form bone in vitro.
Stromal cells from bone marrow (MSC), and other sites, have been shown to be a promising source of cells with high replicative and bone-forming potential. The same drawbacks outlined for osteoblasts apply to MSC.
In our lab human osteoblasts are mainly obtained from trabecular bone fragments and stromal cells from bone marrow of patients undergoing surgical revision of hip implants. HOB are usually isolated by seeding minced bone chips in culture plates to get outgrowth of single cells from fragments, as the isolation technique (mechanical vs enzymatic) appeared to have no effect on the differentiation process. Confluence of the cell layer is reached in approximately four weeks (14–40 dd) and the bone phenotype is assessed by alkaline phosphatase (ALP) cytochemistry and morphology, as well as mineralization after addition of ascorbic acid and b-glycerophosphate. MSC are isolated by gradient centrifugation and adherence to culture plastic; their replicative potential is evaluated by the colony forming assay, and ALP staining provides the test for differentiation toward bone-forming cells.
Preliminary evaluation of our cell isolates from orthopaedic patients showed that there is no direct correlation between the age of donor and the yield of hOB in terms of proliferation rate and ALP activity. As far as MSC are concerned, the addition of dexamethasone during cell expansion stimulated only a small increase in the number of colonies and ALP positive staining.
2. Inductive factors include growth factors, cytokines, peptide sequences and angiogenetic factors. The experience of our Lab will be given in a different presentation.
3. Specifically tailored biomaterials are crucial tools in tissue engineering: our experience is concerning in vitro testing of artificial materials developed by material scientists to replace bone.
Such materials have to provide biocompatibility, i.e. no inflammatory reaction or immunorejection, controlled biodegradation if necessary, and biomechanical features to comply with the anatomical requirements.
From a methodological point of view, the ‘engineered’ biomaterials can be classifieded as bi-dimensional (2D) materials or three-dimensional (3D) scaffolds.
2D surfaces are often well known materials already in clinical use, but innovations concern the ‘biomimetic approach’ applied to their surface. This means to recreate the ‘nanotopography’ of natural tissues, by modifying the roughness, or by mimicking the extracellular matrix (ECM) on the surface: both strategies aim to recruit bone cells and to promote bone formation.
In the framework of a national research project both 2D and 3D materials were assayed in our Lab.
Two types of titanium with different surfaces were tested with human osteoblasts, and compared to a commercial titanium with smooth surface. At 4 hours from seeding onto surfaces, hOB on smooth Ti were elongated, with evident spreading. On the rougher surfaces small focal contact patches were evident, and hOB showed a more rounded morphology whereas stitching to the irregular surface. By prolonging the culture time, all the surfaces were covered by cells, and differences were less evident. Therefore early osteoblast adhesion seems to be different on micro-rough and smooth titanium, but then hOB exhibited a similar proliferation rate. Our results show that surface roughness is not always increasing cell adhesion, and primary cells do require specific micro or nano-topography to spread and proliferate, unlike continuous cell lines which are easily growing on any substrate.
A second approach to control cell adhesion and spreading onto surfaces is the deposition of RGD sequence (Arg-Gly-Asp), the cell-binding domain shared by a number of bone related proteins, including collagen, fibronectin, bone sialoprotein, thrombospondin, vitronectin, etc. The process for immobilization of peptides on the surfaces is crucial, and the amount and pattern of immobilized peptide has to be controlled, as adhesion sites should have a specific spatial arrangement to be recognized by cell adhesion molecules. Inadequate distribution of such binding motifs has also been shown to promote apoptosis of cells, instead of enhanced adhesion.
In our lab polymers with irradiation treatment and RGD-addition were tested using human osteoblasts. In comparison with smooth surface, irradiated surfaces were found to promote cell adhesion and RGD immobilization was further increasing the number of cells highly spread, with well defined cytoskeleton, and evident stress fibers along the cell body. Therefore, RGD immobilization onto surfaces, if adequately tailored, is a powerful tool to recruit cells and to stimulate their function. Further improvements will make use of sequences which specifically bind osteoblasts to the functionalized surface.
3D scaffolds are conceived as bone substitutes for large bone defects: therefore they have to be able to host bone cells, to promote bone formation and to be replaced gradually by regenerated bone. They are mostly approved polymers which are modulated in terms of cristallinity, porosity, interconnections, etc. to get a controlled degradation rate, and often added with bone-like components (hydroxyapatite or b-tricalciumphosphate) to improve osteoconduction. Moreover, the scaffold can be loaded with cells or growth factors (BMPs), to fasten tissue regeneration, or with drugs for treatment of infection, cancer therapy, and so on. Naturally derived polymers, including the recent ‘bioscaffolds’, besides difficulty in preparation, suffer from poor control of enzymatic degradation and weak mechanical performance: therefore many research groups rely on synthetic polymers.
Poly-e-caprolactone (PCL) matrices, with micro- or macro-porosity, and with or without hydroxyapatite (HA) particles, have been extensively assayed in our Lab for their ability to support osteoblast growth and activity. In our hands the presence of HA particles within and onto the PCL scaffold was found to increase osteoblast adhesion and function. We have been able to detect surface colonization by continuous and primary bone cells, and also mineral formation after 3–4 weeks with proper additives, but the presence of viable cells in the ‘core’ of the scaffold is still a matter of debate. The employment of a spinner flask for cell seeding into matrices has been found to improve ‘conditioning’ of the scaffold, but not definitely cell entrance in depth. Confocal microscopy is to some extent faded by the autofluorescence of the polymer matrix, and light microscopy suffer from poor resolution. Results from our experience with hOB and MSC seeded on different 3D PCL scaffolds are presented.
Hydrophilic and hydrophobic polyurethane-based scaffolds (PU) were assayed in our lab, too. Despite high hydrophilicity and addition of the polymeric matrix with HA and b-tricalciumphosphate (TCP), hOB were not able to adhere and grow to confluence onto such porous polymers.
In summary, in vitro models with osteoblasts are a powerful tool to analyse biological compatibility of innovative surfaces or scaffolds, even if they are unable to model physiological function in vivo. Actually, that these models can work in the body has to be demonstrated in experimental in vivo testing, prior to clinical trial. However, the design and improvement of materials rely on the understanding of how cells basically respond to surfaces.
In conclusion, the challenge in bone engineering is to link clinical needs to material technology. In vitro and in vivo studies have demonstrated that the ability of materials to support bone formation can be enhanced by modifying the physical, chemical and biological characteristics of the surface, and surface micropatterning is a powerful tool for constructing elaborate intelligent bio-materials. But the biological response of bone cells and bone tissue, and therefore the orthopaedic research, is a critical step in material research and bone engineering.
Autologous chondrocyte transplantation is a widely used technique for the treatment of cartilage lesions. This therapeutic strategy has been recently improved by the use of biocompatible scaffolds which allow a better fixation of the cells inside the defect together with the maintenance of their original phenotype. We have recently reported that human chondrocytes can efficiently grow on a hyaluronan acid derivative biomaterial (Hyaff-11, Fidia Advanced Biopolymers, Abano Terme, Italy) and are able to express and produce collagen type II and proteoglycans, molecules expressed by differentiated cells (Grigolo et al. Biomaterials 2002). However, from the histological evaluations of the grafted tissues there is not always evidence of hyaline cartilage neo-formation even in presence of good clinical symptoms. Only few studies deals with cellular, and biochemical processes that occur during the remodeling of the graft tissue after transplantation in humans. Biopsy samples harvested from the graft have been examined using a panel of specific antibodies. It was found that cell transplantation is followed not only by a process of cartilage repair but in some cases also by a regeneration achieved through the turnover of the initial fibrocartilagineous tissue via enzymatic degradation and synthesis of newly formed collagen type II. Therefore, we examined the expression of genes encoding extracellular matrix proteins and regulatory factors essential for cell differentiation in human cartilage biopsies of patients who underwent autologous chondrocyte transplantation.
Human cartilage biopsies of patients treated by autologous chondrocyte transplantation and from a multi-organ donor were used. A Real-Time RT-PCR analysis was performed in isolated chondrocytes to evaluate the expression of collagen type I, II, X, aggrecan, cathepsin B, early growth response protein-1 (Egr-1) and Sry-type high-mobility-group box transcription factor-9 (Sox-9) mRNAs. Immunohistochemical analysis for ECM proteins and regulatory proteins was carried out on paraffin embedded sections.
Real-time RT-PCR analysis showed that collagen type I mRNA was expressed in all the samples evaluated while collagen type II was present even if at lower levels compared to control. Collagen type X messenger was undetectable. Aggrecan mRNA was present in all the samples at lower levels compared to donor. Cathepsin B messenger was higher in the samples compared to control. Egr-1 and Sox-9 mRNAs were expressed at lower levels compared to donor. The immunohistochemical analysis showed a slight positivity for collagen type I in all the sections. Collagen type II was found in all the samples evaluated with a positivity confined inside the cells, while the control displayed a positivity which was diffuse in the ECM. Cathepsin B was slightly positive in all the samples while the control was negative. Egr-1 protein was particularly evident in the areas negative for collagen type II. Sox-9 was positive in all the samples, with evident localization in the superficial layer.
Our results provide evidence that the remodelling of the graft tissue after autologous chondrocyte transplantation is regulated by a sophisticated gene expression machinery control addressed to new cartilage formation.
Angiogenesis is the formation of new blood vessels occurring in an adult through migration and proliferation of endothelial cells, and tubular structures formation. Angiogenesis is modulated by growth factors, cytokines, adhesion molecules, integrins, and enzymes. Angiogenesis plays a role in many physiological processes (i.e. remodeling of ischemic muscle, woumd healing, fracture repair) as well as in pathological process such as rheumathoid arthritis and metastases. In bone, vasculature is essential for cartilage resorption and angiogenesis temporally precedes osteogenesis: the origin of bone is the artery carrying calcium and phosphate ions. Osteogenesis takes place near newly formed vessels, that mediate delivery of osteoprogenitor cells, secrete mitogens for osteoblasts, and transport nutrients and oxygen. Inadequate bone vascularity is associated with decreased bone formation and bone mass. In animals, inhibition of angiogenesis during fracture repair results in the formation of fibrous tissue. A poor blood supply is therefore considered as a risk factor for an impaired bone healing. Angiogenesis is vital in tissue engineering, especially when matrices are colonized by cells with an aerobic metabolism. The scaffold must not only support the growth of the cells making up the organ which should be replaced in vivo (i.e. osteoblasts); it must also support the growth of endothelial cells and develop an effectively functioning vasculature to supply the cells with oxygen. Osteogenesis of tissue engineered materials could be limited by a lack of vascularization, and the bioengineered graft may be potentially resorbed in the same way as a conventional bone graft. In rats, angiogenesis in coralline materials implanted in ectopic muscular sites, was higher when the biomaterial was combined with a vascular pedicle or was coated with bone marrow stromal cells. A combination of both enhanced vascularization and osteogenesis to a greater extent. Endothelial cells release growth factors and cytokines promoting bone deposition: PDGF-AB, TGF-beta 1 and 2, FGF-2, EGF, BMP. However, under inflammatory stimula, endothelial cells release bone resorbing cytokines: IL-6, M-CSF, GM-CSF. Bone marrow stromal cells release angiogenetic proteins such as VEGF, FGF-2, PDGF, TGF, and, after induction with BMP, PlGF. A conversation between bone marrow stromal cells and endothelial cells may therefore be hypothesized. Cultures of bone marrow stromal cells with endothelial cell conditioned medium showed significantly higher phosphatase alkaline activity and osteocalcin production. It was also be hypothesized that stromal cells may acquire immunophenotypic characteristics consistent with endothelial cells. Therefore scaffold requirements are also the ability to favour angiogenesis; endothelial cells growing on the artificial scaffold should mantain a normal phenotype and should not exhibit a pro-inflammatory and bone.resorbing phenotype. Endothelial cell cultures are useful supplementary in vitro tests for the evaluation of scaffolds for bone tissue engineering. Endothelial cell cultures are derived both from animals (usually ox, calf or pig vessels) and from human tissues, mainly the human umbilical vein and the vessels of microcirculation (derma or subcutaneous fat). Endothelial cells in non-human species show different reactions: they have usually a faster replication rate and grow better on the artificial substrata. Endothelial cells from different organs are intrinsically different and exhibit different responses to stimula. if the use of endothelial cells from bone microcirculation should be desirable, they require transfection with viral vectors to be immortalized. To study the response of endothelial cells cultured in vitro on artificial scaffolds, their adhesion, growth, viability and production of metabolites should be evaluated. Adhesion and growth on the materials may be evaluated indirectly by the uptake of Alamar Blue, which measures the amount of oxido-reduction reactions in the cell. A direct evaluation may be obtained by fluorescence microscopy using specific staining for the different cell structures. By studying the expression of adhesins and integrins, the interference of the scaffold with the cell/cell and cell/substrate adhesion should be verified. The release of substances in conditioned medium, as well as the evaluation of specific mRNAs in cells, should be assayed. Among the metabolites released by endothelial cells, the substances promoting bone deposition or favouring resorption, should be investigated. In particular, the release of growth factors may be explored, as they favour cell proliferation and the incorporation of the engineered scaffold within tissues. For the enhancement of bone formation, growth factors may be delivered in different ways: through incorporation on the scaffold, through transfection of bone marrow stromal cells, through platelet gel. Angiogenic growth factors are stored in platelet alpha granules and released during activation. A significant increase in the proliferation of bovine bone endothelial cells was demonstrated after 72 hour incubation with platelet gel in comparison with serum free conditions; the proliferation was similar to the growth induced by the fetal calf serum supplementation (platelet gel: 82.2B18.1x103 cells; serum free: 19.5B11.1x103 cells; fetal calf serum: 72.4B12.4x103 cells). However, the platelet gel inhibited the formation of tubular structures on Matrigel
In conclusion, the development of newly formed vessels on the bone cell engineered scaffold improves the incorporation in the host tissues and the success of the device. The use of exogenous growth factors or of platelet gel favours angiogenesis, besides osteoblast differentiation. The in vitro evaluation of the scaffold should be supplemented by tests on the adhesion, growth and functionality of endothelial cells.
When investigating orthopaedic biomaterials and tissue engineered devices, biological investigations by means of in vitro and in vivo tests are mandatory to obtain a overall picture of biocompatibility and therapeutic efficacy. However, various aspects requiring careful consideration should be kept in mind and can explain the complex situations encountered by researchers when the skeletal tissue is involved. This presentation aimed to summarize some useful information in improving in vivo methodology to test present and future therapies for orthopaedic surgery. Some in vivo biological tests to study innovative reconstructive surgical techniques are summarized on the basis of the experience of the Experimental Surgery Department –IOR.
After in vitro and in vivo biocompatibility tests, for the study of bone defect healing and of biomaterial osteo-inductive properties the subcutaneous and intramuscular implants are usually performed in laboratory animals while osteoconduction and bone healing evaluation require the development of “nonunions” (sites that never achieve functional bone continuity) and “critical size defects” (the smallest defect that will heal with less than 10% bony growth) models. Biomaterial osteointegration properties are investigated by means of metaphyseal, diaphyseal and intramedullary implantation. The use of pathological animals is also recommended to take into account the clinical situation where biomaterials are often implanted in aged and osteoporotic patients. As far as articular cartilage pathology is concerned, chondral and osteochondral “critical size defects” may be performed and the development of osteoarthritic animals could be also useful.
At different experimental times post-explantation evaluations by means of radiology, histology, histomorphometry and biomechanics provide a complete characterization of biomaterials and biotechnologies showing their potential therapeutic efficacy for skeletal reconstruction.
In vivo studies provide important pre-clinical information on new biomaterials and biotechnologies for the skeletal reconstruction Among the factors that are increasingly improving the reliability of in vivo testing are the continuous improvement in knowledge on bone biology and comparative science between humans and animals, the awareness that animal suffering should be reduced as much as possible, and, finally, the amount and the accuracy of in vivo post-explantation findings.
Despite biomechanical well established implants and improved operation techniques we still have a too high rate of complications in orthopaedic and trauma surgery like non-union, implant loosening or implant associated infections. The development of bioactive implants could improve the clinical outcome.
Growth factors are important regulators of bone metabolism. During fracture healing many growth factors or cytokines were locally released at the facture site. In several studies, different growth factors demonstrated osteoinductive and fracture stimulating properties.
In vitro and in vivo studies showed a stimulating effect of Insulin-like growth factor-I (IGF-I), Transforming growth factor-A71 (TGF-A71) and Bone morphogenetic protein-2 (BMP-2) on osteo- and chondrogenetic cells. The exact effectiveness and the interaction of these growth factors during fracture healing is not known so far. Further, the local application of these factors for therapeutically use in fracture treatment is still a problem.
A biodegradable poly(D,L-lactide)-coating of implants allows the local and controlled release of incorporated growth factors directly at the fracture site. The coated implant serves on the one hand for fracture stabilization and on the other hand as a drug delivery system. The coating has a high mechanical stability. The incorporated growths factors remain biologically active in the coating and were released in a sustained and controlled manner.
To investigate the effect of locally released growth factors IGF-I, TGF-A71 and BMP-2 and the carrier PDLLA on fracture healing, standardised closed fracture models were developed with a close relationship to clinical situation. Further, possible local and systemic side effects were analysed.
The results demonstrated a significantly higher stimulating effect of IGF-I on fracture healing compared to TGF-A71. The combined application of both growth factors showed a synergistic effect on the mechanical stability and callus remodeling compared to single treatment.
The local release of BMP-2 also enhanced fracture healing significantly – comparable to combination of IGF-I and TGF-A71. However, a higher rate of mineralisation was measurable outside the fracture region using BMP-2 in a rat fracture model.
Using a large animal model on pigs with a 1 mm osteotomy gap, the effectiveness of locally released growths factors could be confirmed. Further, the PDLLA-coating without any incorporated growth factors demonstrated a significantly effect on healing processes in both models. These investigations showed, that the local release of growth factors from PDLLA coated implants significantly stimulate fracture healing without any local or systemic side effects.
Comparing systemic with local stimulation techniques, we found an improvement of fracture healing by systemic administration of growth hormone and local application of IGF-I and TGF-A71. However, the combined use of both simulation techniques did not lead to a further increase of healing processes.
Investigations on the effectiveness and the interaction of growth factors during fracture healing demonstrated an dramatic effect in the early phases of healing processes. The growth factors stimulate the differentiation of osteoblasts with a higher production of collagen I in vitro and increase osteogenesis and vascularisation of the fracture callus in vivo.
Further applications of the coating technology are the use of PDLLA and growth factor coated cages for the stimulation of intervertebral fusion and the use of PDLLA and Gentamicin coated implants in order to prevent implant associated infections.
The first patients with open tibia fractures were treated with PDLLA and Gentamicin coated IM nails.
The purpose of this study is to demonstrate the validity of the autologous chondrocytes transplantation (A.C.T.) technique implemented over the last 6 years in the treatment of osteochondral lesions of the talus.
Our case study included 22 patients (12 males and 10 females), with an average age of 27 years affected by osteochondral lesions of the talus surface. All lesions were > 1.5 cm2, monofocal, and post-traumatic in origin. The first 9 patients received ACT (Genzyme technique) and the remaining 13 patients received ACT with an arthroscopic technique. In 6 of the patients, the cartilage harvested from the detached osteochondral fragment was used for culturing, avoiding the first step arthroscopy in the knee. Before surgery, all patients were assessed clinically, radiographically, and using MRIs. For clinical evaluation patients were assessed using the American Foot & Ankle Society 100 point score. Before surgery the mean score was 48.4 points. 11 patients underwent second-look arthroscopy at one year during which a biopsy was harvested for histologic analysis of the reconstructed cartilage. Of these, 9 patients (Genzyme technique) also had hardware removed.
The mean follow-up of the 22 patients was 36 months. At follow-up, all patients but one were satisfied with their results. With regards to the clinical results evaluated using the American Foot and Ankle Society score, an average of 90.5 was obtained at 24 months, while at 36 months the average score (19 patients) was 94.0 (range 54–100). During follow-up arthroscopy, 4 patients had mild fibrosis and 1 patient required regularization of flap overgrowth causing pain.
The clinical and histological results have confirmed the validity of the surgical technique utilized with no subjective nor objective complications. An improvement of the symptoms and of articular function has also been observed: laboratory data confirmed the histological appearance of the newly formed hyaline cartilage in all cases evaluated. Immunohistochemistry showed a positive staining for collagen type II located in the extracellular matrix and in the chondrocytes in the healthy and transplanted cartilage biopsies. All the specimens studied were also positive for proteoglycans expression as was the Alcian blue reaction, which highlighted the presence of these fundamental components of a cartilaginous matrix.
The reconstruction of large bone segments is a major goal in orthopaedic surgery. Autologous cancellous bone is recognized as the most biologically active graft material, but autologous bone harvest is associated with significant morbidity and founds its limit in the available quantity. Biomaterials or allografts do not encounter these limitations, but have no osteogenic and limited osteinductive potential. In order to enhance tissue regeneration and healing we have tried to obtain a graft with osteconductive, inductive and osteogenic properties. The day before operation 350 cc of autologous blood is donated from the patient and centrifuged to obtain a platelet-rich plasma. Bone marrow is aspirated from the posterior iliac crests with the patient under spinal anaesthesia and is processed to increase its stem cell content. The structural scaffold used is morcellized cancellous bone provided from our Bone Bank. At operation bone is mixed with bone marrow buffy coat and Platelet Rich Plasma in a sterile glass becker with addition of CaCl2 till clot formation to produce a gel-like component that is handled easily. We have utilized this technique from November 2000 till January 2004 for 68 patients: 41 of these patients required healing of large bone defects: 22 males and 19 females. Fresh bone marrow alone was used for a percutaneous injection in 11 cases; open surgery with autologous growth factors, bone marrow buffy coat and allograft was used in 30 patients. The radiological and clinical results showed early healing of the defects treated with this technique and no complications related to the procedure at an average follow up of 23 months (3–40).
The use of autologous grafts for vertebral arthrodesis is associated with a number of complications that should be properly considered: pain at the harvesting site, increased blood loss, prolonged surgical time, and additional scar. Moreover, in many cases, the amount of autologous bone is insufficient. Novel materials, either natural or synthetic, are therefore needed to be used as bone substitutes in vertebral surgery. For this purpose, a number of synthetic materials have been developed, their characteristics varying considerably in terms of ostoinduction, osteoconduction, biomecanics, and cost.
In particular, clinical and experimental studies have highlighted the potential of demineralized bone matrix (DBM), alone or in combination with autologous grafts, and of collagenic mineralized matrix (Healos).
Aim of this study was the evaluation of the clinical value of these materials in vertebral surgery. We have analyzed a series of 60 patients who underwent vertebral arthrodesis by the addition of either DBM (30 cases) or Healos (30 cases).
Bone substitutes were used both in posterior-lateral arthrodeses (on one side, the other being treated with autologous graft as a control) and in intersomatic arthrodeses in association with titanium or carbon fiber scaffolds.
Patients were followed-up for a minimum 1-year interval, and evaluated with regard to clinical (Oswestry score, SF-36) and radiographic (static and dynamic X-rays, spiral CT, MRI) parameters. The area of arthrodesis was independently analyzed by three independent observers.
Clinical results showed the reliability of both materials as a tool for a stable arthrodesis, since they were found to be able to achieve results comparable to those obtained with autologous grafts in the control arm of the study.
Autologous chondrocyte transplantation has become a possible solution for the treatment of chondral knee lesions. In the last years matrix autologous chondrocyte transplantation procedures were developed by various scientists. We selected a biodegradable, hyaluronian-based biocompatible scaffold for cell proliferation. This nonwoven three-dimensional structure consists of a network of 20 – B5-thick fibers with interstices of variable sizes which constitute an optimal physical support to allow cell-cell contacts, cluster formation, and extracellular matrix deposition in order to create a bioengenerized cartilage Hyalograft C. The easy handling of Hyalograft C in open surgery has suggested us to investigate its possible use by an arthroscopic procedure.
Arthroscopic technique has been used from December 2000 in 88 cases. At December 2003 45 patients achieved at least 1 year follow up and 22 patients – 2 years follow up.
All the patients were clinically evaluated was analyzed according to the International Repair Cartilage Society score at 12 and 24 months. Returning back to sport was also recorded. We were able to obtain CT scans or MRI images for all patients at 6, 12 and 24 months of follow up.
No complications related to the implant and no serious adverse events were observed during the treatment and follow up period. The IKDC objective score improved after 12 months in all patients, showing a normal or nearly normal knee in 96,7% of patients. The mean IKDC subjective score obtained was 41,3 at baseline, 76.9 at the 12 months follow-up control, and 75,9 after 24 months. The worsening of IKDC score was noted in 1 of 22 patients analyzed at 12 and 24 months follow up.
A second look arthroscopy was performed in 11 patients at 12 months follow up and a complete healing of the defect and the excellent quality of regenerated cartilage was noted at macroscopic examination. The histological evaluation in 6 cases has demonstrated the hyaline type of new cartilage, although not completely mature.
This matrix autologous chondrocyte transplantation procedure avoids the use of periosteal flap, simplify the surgical procedure and permit to perform the arthroscopic implant. Thus, complications as hypertrophy or ossification of periosteal flap are avoided and the surgical morbidity and the recovery time for the patient are extremely reduced. The preliminary clinical and histological results are encouraging but the decree absolute on the efficiency of this method will be assessed at longer follow up.
Composite tissue defects in absence of general contra-indications are now routinely dealt by composite free tissue transfers which now stand as routine procedures. When dealing with amputations of the thumb several reconstructive procedures are now available and should be tailored on individual basis.
Microvascular surgical techniques are especially gratifying when the appropriate indications are followed: young age, absence of systemic diseases no alcohol or smoke abuse.
A custom – made thumb can be reconstructed assembling in a single composite tissue graft different tissues harvested from various parts of the body.
An outcome study as been performed on 72 patients where the wrap-around technique, the second and great toe transfer have been carried out.
Overall assessment included, as a preliminary analysis, the of vassessement behaviour of each single transferred tissue: the nail complex, the pulp and the bone. Donor – site problems at the foot were assessed by gait analysis. Vascular complications were recorded in 5% of the patients, and 89% of the patients had excellent outcomes.
A stiff prosthetic stem in the proximal femur alters the load-bearing model af the bone and leads to changes of the lamellar organization, known as “stress shielding”.
To avoid this problem in the 70th a stem with a higher elastic modulus was developed and implanted in patiens (isoelastic stem of Mathys and Morscher).
A group of 17 isoelastic stems of this type which have remained in the femur from 6 to 8 years, were removed and are the object of the study. Analysis of the polyacetile surface was carried out with a low enlargement microscope. The stems were then radiographed and cut with a low speed saw to investigate structural changes between the polyacetile cover and the steinless steel core.
Two type of material lesions were observed:
- loss of polyacetile material from the surface (wear) - structural yielding lesions.
Distribution and frequency of each type of lesion was registerd in relation to four zones of the stem: a) cone with the metallic head; b) proximal stem (metaphyseal); c) body of the stem (diaphyseal); a)apex of the stem.
Wear of the polyacetile stem is evidence that no fixation of the stem was achieved, therefore a fraction of the load energy was dissipated at the prosthesis-endosteal surface.
However the presence of structural yielding lesions demonstrate that another fraction of the load energy was carried out by the stem. The topography of these lesions allowed to understand the biomechanical behavior of the “isoelastic” stem inside the femur with vertical longitudinal (piston) and rotational in the horizontal plane movements.
Failure of polyacetile and decoupling of polyacetile cover and stainless steel core were the other main findings.
The theory of an isoelastic stem is appealing by a biomechanical point of view, however two practical problems caused failure in this series: 1) lack of fixation at the implant-bone interface; 2) failure of materials.
Biomaterials improve the quality of life for an ever increasing number of people each year. The range of applications is vast and includes such things as joint and limb replacements, artificial arteries and skin, contact lenses and dentures.
Ceramic biomaterials can be divided roughly into three main types governed by their in vivo behaviour and tissue response. In broad terms, there are the bioresorbable ceramics (b-tricalciumphosphate), bioreactive (hydroxyapatite, fluorapatite and bioglass) and bioinert (alumina, zirconia and pyrolytic carbon). The resorbable ones are incorporated into the surrounding tissue, or may even dissolve completely over a period of time. The bioreactive ones, like hydroxyapatite (used for coatings on metallic pins), encourage bonding to surrounding tissue with, for example, new bone growth being stimulated. The bionert ceramics are mostly used for structural components. Alumina and Zirconia are known for their general chemical inertness and hardness. These properties are exploited for implant purposes, where they are used as an articulating surface in hip and knee joints. Their ability to be polished to a high surface finish make them an ideal candidate for this wear application, where they operate against materials such as ultra high molecular weight polyethylene (UHMWPE).
Alumina is a highly inert material and resistant to most corrosive environments, including the highly dynamic environment that is the human body. Under physiological conditions, it is classed as nearly inert, with evidence of any response from surrounding tissues and remaining essentially unchanged after many tyears of service. However, the body does recognise it as a foreign material and does attempt to isolate it by forming a layer of non adherent fibrous tissue around the implant where possible. Porous alumina may also be used to replace large sections of bone that have been removed for reasons such as cancer.
Alumina has been used in dental applications. Specifically, it has been used for tooth replacements. The term high alumina ceramics is referred to materials that have the minimal content of 97% of alumina. If the percentage of minimal alumina is of 99% it is called high purity alumina ceramics. In its α phase (better famous like corundum), characterized from its particular structure and stability, the high purity alumina is used in orthopaedics, in the articulations of the hip and knee prostheses.
From more than 30 years, the alumina has been successfully used. Today, more than 3,5 million of ball-heads e and 350 thousand of inserts of alumina BIOLOXA8 have been implanted confirming, in clinical use, the characteristics of low wear and biocompatibility that has allowed to reduce the problems of osteolisis induced by the polyethylene. The increase of the mechanical characteristics, the new shapes and the conical fixation have raised the reliability of the ball-heads and inserts of alumina.
The BIOLOXA8forte (in commerce from 1994) is an high purity alumina (ca 99,7 %) with a small percentage of magnesium oxide (MgO). Approximately 50 years ago, magnesium oxide was introduced in the phase of sintering of the alumina, because it was discovered that a small amount of this additive prevented the increase of grains of alumina during the sintering process. It was therefore possible to have a more homogenous and dense microstructure, both characteristic directly correlated with the mechanical resistance. The suffix ‘forte’ derives from the increased mechanical characteristic caught up with the continuous optimization of the fabrication technology.
Many laboratory tests and clinical cases have shown that the wear rate of alumina-alumina bearing coupling is extremely low (0.001 mm/year). If compared with metal-polyethylene (0,2 mm/year), it evidences the drastic reduction of particles of debris and therefore of the osteolysis problem.
One of the main factors that the reduction of the wear rate involves is the characteristic molecular structure of alumina. Its superficial layer is composed of oxygen atoms that create a residual electric power which interacts with polarized molecules of the lubricant, binding it to the surface by strong Van der Waals ties. It is therefore guaranteed the presence of a fluid film that reduces the coefficient of clutch between the two surfaces involved during the articulation.
The colour of alumina components is subjected to variations. Originally it is ivory, but it can easy stretch to the brown after sterilization with gamma beams that interact with the free valences introduced by the MgO. This change of colour does not induce changes of the mechanical characteristics.
Currently the systems are completely modular and allow a wide choice of couplings. Ceramic acetabulum has been abandoned and replaced by ceramic inserts. In 1984 and subsequently in 1995, the introduction of ISO standards for the production of ceramics ball-heads and inserts and the concept of conical fixation has allowed to catch up higher reliability. The third generation of alumina has reduced the complications rates to values around 0.01% (for the 28 mm ball-heads and inserts), maintaining the excellent tribology and wear characteristics.
Today, the alumina BIOLOXA8forte components are prepared in clean-room, sintered with high quality control processes, marked by laser and accurately inspected and tested. The dimension of grains of the microstructure, currently reduced to inferior values of 2 B5m, has allowed to raise the value of the mechanical resistance of about 45% (580 Mpa) of the value requested by ISO standard (400 Mpa). The tolerances between ceramics (ball-heads and inserts) and metallic parts (taper and metal shell) are fundamental for lengthening the implant reliability. It is important to control and certificate the stems and cups which the ceramic parts are applied on. Correct assembling and the respect of the compatibilities between parts (angle, material, producer) guarantee the longevity of the implants.
Actually, in the orthopaedic field, the alumina application is mainly used in standard applications of the hip prostheses. Ball-heads of 22 milimeters of diameter, lengths of neck type XL, and the knee prostheses are not possible because of the mechanical characteristics of alumina not allowing to catch up the elevate stress values requested for these special applications.
Between 1975 and 1977, the first studies issued that the strenght of alumina could be reinforced by the introduction of ceramic oxides. It was discovered that the strenght and toughness of alumina could endure a remarkable increment through the realization of composites with oxide of zirconium (zirconia). In the zirconia, during the phase of cooling from temperatures over 1170A1C, the grains endure a change of phase (from tetragonal to monoclinic), with an increase of 3% of volume. At ambient temperature the phase monoclina is stable. This transformation is martensitic, with energy absorption, and involves a heat-proof change of the simmetry of the structure. In the case of dispersed grains of zirconia in the alumina matrix, the transformation absorbs the energy of the crack and the tenacity of the ceramics increases. The Yttria (Y2O3) use, as stabilizing of the zirconia, has allowed to exceed the problem of the defects of the structure. It was introduced a percentage of zirconia stabilized with yttria (Y-TZP) in the alumina matrix and other mixed oxides to counterbalance the reduction of the hardness caused by particles of zirconia and to create lengthened particles during the sintering.
All this studies have been used to create the new ceramics BIOLOXA8delta. Tests of biocompatibility in agreement with norms EN 30993 have been carried out allowing the implants of these new composite ceramics. The BIOLOXA8delta has a bending strenght around 1000 MPa, that is more than the double of the alumina standard (400 MPa). In the minimum fracture load test, ball-heads of 28 mm AF millimeter (neck L) have caught up values around 100 KN, very beyond the 46 KN requested by the FDA.
Multiple cycles of sterilization in autoclaves have demonstrated that the BIOLOXA8delta does not endure alterations of the mechanical and tribological characteristics.
On the basis of these results, BIOLOXA8delta will allow the realization of medical ceramics devices, already in study phase, like knee prosthesis, 22 mm ball-heads, thinner wallthickness of inserts, whose realization was not possible with the ceramic materials up to now available.
Shape, surface composition and topography are key factors to achieve post surgery and long-term mechanical stability of endosseous dental titanium implants and to enhance implant osteointegration [
Recent research has studied the morphology of implant surfaces [
Our in vitro research shows that sand-blasted surfaces positively influence osteoblast metabolic activity by modifying phenotype, surface adhesion levels and proliferation rate [
A few days after surgery, osteogenic activity was markedly enhanced in the sand-blasted implants which presented more new tissue closely adhering to the implant surface. Three months later there were no major differences in the three samples examined and all showed perfect osteointegration.
Our results suggest that the shorter osteointegration rate obtained with sand-blasted implant surfaces is not only the result of the increased surface area in contact with newly formed bone tissue, but is also correlated to the enhanced osteoblast osteogenesis induced by the concave surfaces geometric design.
The SEM analyses indicated that the PEs surface which was directly in contact with bone shows an anomalous degradation. The surface looks as it has been corroded or “bitten” and its morphology is significantly different from that of surfaces abraded either in vivo or in vitro.
Bone reconstruction in pediatric oncology always has to face two major problems: the frequent unavailability of small prosthetic tools and the difficulty in finding bone allografts of adequate size.
Aim of this work is to present the research lines in this field, currently active in our institution to improve the planning and the results of reconstructive tumor surgery in children. Starting from patient’s CT data sets, subject-specific 3D models of bone segments can be created and compared with the similar models obtained by the CT analysis of massive allografts stored in the Rizzoli Bone Bank.
In the same time the computer modelling technologies allow the development of three-dimensional environment, where the surgeon can navigate and exploit both artificial (prostheses, metallic plates and screws) or biological tools (bone allografts or autografts).
The presented method has been utilized with success in 10 children (mean age 8, range 4–13) that underwent a skeletal reconstruction of the limbs in the last year (proximal humerus 1, diaphyseal humerus 1, total humerus 1, distal radius 1, proximal femur 3, diaphyseal femur 1, proximal tibia 1, diaphyseal tibia
Compressive tests showed no statistical differences between PMMA cylinders containing Methotrexate and controls before and after aging in saline.
In vitro cell interactions were evaluated with human osteoblasts (HOB, 2nd passage) isolated from the trabecular bone of the femoral head of patients undergoing total hip replacement and cultured following the usual procedure. HOB cells (1x105 cells/sample) were kept in contact with the scaffolds for 7 and 14 days. At each time endpoint HOB metabolic activity, intracellular and released ALP were evaluated.
HOB cells grown on scaffold samples showed an increase of metabolic activity from 7 to 14 days. The amount of intracellular ALP increased too, whereas the amount of ALP in the medium was quite low. HOB cells, after 14 days, appeared closely adherent to the scaffolds, with an elongated and flattened shape.
Bone marrow would represent a useful source of cells for skeletal tissue engineering. Marrow mesenchymal stem cells (MSC) can generate cartilage, bone and fat. The differentiation of this multipotent population into fibroblast, chondrocytes or osteoblasts can be inducted in vitro by the addiction of growth factor like bFGF, TGFA7, BMP-2.
In order to evaluate the possibility of inducing cell differentiation by cell-matrix interaction, we studied the in vitro behaviour of human MSC cultured on various scaffolds.
Bone marrow was obtained during surgery for pelvic fractures or hip arthroplasty. MSC were isolated by cell sorting (CD45/glycophorin A micromagnetic beads), expanded and characterised by FACSCalibur flow cytometry system (CD3, CD34, CD14, CD45, CD90 and CD105). Then cells were grown for 30 days on different scaffolds: type I and type II collagen, type I collagen + hydroxyapatite. Histochemical (alcian blue, safranin O, ALP and von Kossa stains), immunohistochemical (type I e II collagen, chondroitin sulphate, osteonectin), histomorphometric (area %) and spectrophotometric (cell proliferation, PG synthesis, ALP activity) analyses were performed after 15 and 30 days of culture.
Among the scaffolds tested in the present study, we observed a great variability in terms of MSC adhesion and proliferation. MSC grown on type II collagen differentiated into cells expressing chondrocytes markers (S100, collagen II, chondroitin-S). MSC grown on type I collagen + hydroxyapatite differentiated into osteoblast-like cells.
These data evidenced that MSC-matrix interaction can influence phenotype expression, cell adhesion and growth rate.
X-ray exams were performed immediately after the surgery. Clinical, ultrasound and x-ray exams were performed after 20 days and then every month.
Autogenous cancellous bone is the most effective material in stimulating osteogenic response and the standard graft augmentation for patients with nonunions or bone defects. However it may not be available in sufficient quantity and bone harvesting may give rise to morbidity. Allograft does not have the osteogenic potential of autogenous bone and may be complicated by immunological reaction and transmission of infections.
The search of bone substitutes has led to study several growth factors capable of inducing bone formation. Bone morphogenetic proteins (BMPs) have been shown to have a central role in endochondral and intramembranous bone formation and are thought to promote normal bone healing process. Recent studies demonstrated that platelet-rich plasma (PRP) provides several growth factors and stimulates osteogenesis.
The aim of the study was the evaluation of rhBMP-7 (rhOP-1) and PRP effects on the different cells detected at the site of nonunion, such as osteoblast-like cells, fibroblast-like cells and mesenchymal cells.
During the surgical treatment of seven nonunion cases, cancellous bone and nonunion tissue were harvested. Osteoblast-like cells and fibroblast-like cells were isolated and characterized. Mesenchymal cells were obtained from bone marrow samples of the same patients. Each cell type was incubated with rhBMP-7 and PRP at different concentrations. Proliferation rate and alkaline phosphatase (ALP) activity were assessed at 3, 7, 15, and 30 days. cytochemical and immunocytochemical analysis were performed at 15 and 30 days.
Proliferation rate was higher in osteoblast-like cells and mesenchymal cells than in fibroblast-like cells. Growth factors induced mesenchymal cells to express osteoblast phenotype markers.
The results show that fibroblast-like cells at the site of nonunion are responsive to growth factors stimulation, though their low osteoblastic differentiation rate, even at highest concentration of growth factors. These data suggest that the use of growth factors in nonunion treatment should be combined with autologous cancellous bone and/or bone marrow graft, sources of target cells, in order to enhance osteogenic response.
Cage implants are designed in order to separate contiguous vertebrae allowing an adequate stress transfer and favoring bone growth. In this paper the biomechanical and histological properties of novel composite cages and commercial titanium implants have been in vitro and in vivo investigated.
Several chemical modifications of Hyaluronic acid (HA), a biodegradable linear polysaccharide, have been devised to provide mechanically and chemically robust materials in medical applications.
This study was specially designed to assess whether such a kind of materials are capable to substitute natural NP by suitable viscoelastic properties.
Small amplitude oscillatory shear tests were performed to study linear viscoelastic properties by using a strain controlled rheometer (Bohlin VOR). In particular, the elastic modulus (G’) and the viscous modulus G’’ were evaluated.
The same rheological behaviour was observed for all HA derivatives. In particular, G’ and G’’ were respectively equal to 400 and 91Pa for HYADD3A8 solutions at 1Hz and at 20mg/ml (0,15M), and 210 and 51Pa for HYAFF120p50A8 at 50 mg/ml(0M).
The groups were thus divided:
Group 1: lyophilized bone chips. Group 2: lyophilized bone chips + platelet gel Group 3 lyophilized bone chips + platelet gel + packed autologous medullary cells (buffy coat).
At six weeks X-rays, MRI and needle biopsies were carried out. The tissue underwent morphological and microstructural tests.
The purposes of our study were: 1) to apply a French translation of the EVGS to standard video recordings of a group of independent walking spastic diplegic CP patients 2) to evaluate the intraobserver and interobserver reliability and 3) to compare the results of gait analysis with experienced and inexperienced observers.
Classification of the Complications was in three grades :
- I : Benign complication without any unexpected surgery or anaesthesia - II : Serious complication with unexpected surgery or anaesthesia - III : Severe complication
The complications were recorded in four periods: surgery, elongation, consolidation and late complications
Articular complications do not show any significant difference between the different methods. The main complications are seen in neurological and post infectious diseases. The mean percentage of lengthening in these complications is not different of the mean percentage of the series.
Preoperative positioning and the incision
Psoas tenotomy, capsular exposure and the capsulotomy
Facilitation of the Gigli saw osteotomy
Sizing and procurement of the graft
Displacement and fixation of the osteotomy
Application of the hip spica
Some questions are worthy of debate:-
Can the osteotomy be safely combined with open reduction of the high dislocation?
Should the osteotomy be fixed before reducing the femoral head?
Are there alternatives to autogenous bone graft and K-wire fixation?
Is minimally invasive surgery an option?
Are the contraindications and alternatives to the Salter osteotomy fully appreciated?
Between June 1987 and July 2003, 62 cases were so far treated. There were 13 adults (19 – 35 years) and 49 children and adolescents (2.5 years – 18 years). All patients had a clinical and radiological evidence for osteoid osteoma (hyperfixation on scintigraphy, visible nidus on CT scan). The nidus was mostly localized in the lower limb (53 cases) especially femoral neck (23), femoral shaft (13), tibial shaft (14).
Statistical analysis by ordinal regression analysis showed there was no correlation between slip severity and duration of symptoms. In addition, there was no correlation between slip severity and age or weight.
Half the patients had received surgical treatment before reaching the hospital, either at civilian hospitals, forward military surgical units or both. None of this surgery was strictly “life or limb-saving”. Amputations performed prior to admission were in the proximal tibia and followed the long posterior flap pattern appropriate to an adult amputation for vascular disease regardless of the level of injury. Several had primary closure of war wounds. After admission, four patients required plastic surgical procedures, two had ophthalmic surgery, one had a laparotomy and one had a facial reconstruction procedure in addition to surgery for extremity trauma. One child with fragment wounds was undergoing treatment for acute lymphoblastic leukaemia.
An arthroscopic evaluation of the joint associated with an arthroscopic capsular release (release of the coracohumeral ligament) was performed in 4 cases. In addition, the latissimus dorsi was transfered. Pre and Post operative passive external rotation were measured in degrees in R1 position.
Pre and post operative medial rotation were evaluated according to the Mallet classification. A comparative evaluation of the glenohumeral deformities were performed between pre-operative MRI and arthroscopic results.
Arthroscopic release is a safe but demanding technique which allows an increase in the external passive rotation in OBPP. It should be noted that this technique requires a significant practice.
The aim of this study was to evaluate whether duration of surgery correlates with the survival and final outcome of the patient with metastatic bone disease.
Between 1999 and 2002, 23 consecutive patients with impending or complete pathological fractures of the femur due to metastatic bone disease caused by variety of malignancies or an unknown primary were reviewed. These fractures were treated with intramedullary fixation in the form of long intramedullary hip screw, long Gamma nail or AO nail. These patients were followed up clinically and radiologically until death from the primary disease.
The results obtained demonstrate a mean survival time between 9 days to 12 months. Pain relief was achieved in 90% patients. Ambulatory status was improved in 47% patients. The postoperative course was complicated by four technical and five systemic complications. Intramedullary nailing is a safe and effective method in the treatment of metastatic bone disease. It provides good functional result with pain relief and improved mobility. The operating time does not predictably correlate with the survival and final outcome of the patient.
The histological findings from the heads of femur or bone biopsy taken from 90 patients with suspected pathological fractures of the femoral neck were studied to determine the rates of significant abnormal pathological findings.The mean age at the time of fracture was 80.41 years (44–99). 29 patients were males and 71 females. The patients were divided into four groups. Group I: 34 patients with fracture without history of fall or trauma. Group II: 21 patients with suspicious radiology of pelvis. Group III: 27 patients with past history of malignancy without known bone metastases. Group IV: 8 patients with past history of malignancy and known bone metastases
None of the patients in groups I and II had significant abnormalities other than osteoporosis. 4 patients (15%) in group III had metastases and 6 patients (75%) in group IV had metastases on histological examination.
We conclude that the absence of history of fall or trauma or subtle radiographic findings in patients with fracture of the neck of the femur is usually not associated with sinister pathology and the cause of fracture in these patients is often osteoporosis. Patients with previous history of malignancy without known bone metastases have a 15% risk of finding of metastatic disease even in the absence of radiological abnormalities. Patients with fractured neck of femur with past history of malignancy and who are known to have bone metastases must be considered as having pathological fractures through metastatic disease until unless proven otherwise
6 patients had primary bone tumour and were referred to the tumour specialist. Of the remaining patients with suspected MBD all required fixation and in all cases intramedullary reamings were sent for histology. 18 patients had a known primary tumour of which 8 (44%) had no evidence of malignancy on histology. 22 patients had an unknown primary tumour of which 19 (86%) had no evidence of malignancy on histology.
The average tumour volume was higher in the patients with lytic lesion and associated fracture than those with no fracture, 27.3 and 20.7cm³. 17(85%) of the lytic lesions, with volume larger than 10 cm³ had pathological fracture.
Post operatively all patients were allowed to fully weight bear. 70 % of patients regained their initial level of mobility or increased their level of dependence by a factor of one. Mean hospital stay was 20.8 days (mode 7 days). Patients that died post operatively had a mean survival of 299 days (range 2–1034). Those patients that were still alive at the last follow up had a mean survival of 475 days (range 7–1384). There were no cases of fixation or implant failure. There was one case of deep infection that was treated by implant removal.
The generally unfavourable prognosis and perceived risks have led surgeons to palliate, stabilise in situ or amputate for distal femoral metastases despite recognised morbidity and life style restrictions. We conclude that DF EPR should be considered as a limb salvage option in patients with distal femoral mets.
Presenting features included a discrete lump or diffuse swelling in 115 patients (95.8%). Pain was not a feature in 69 patients. 3 patients (2.5%) presented with pain alone and 2 patients (1.7%) with varicosities. 116 patients (96.7%) were referred to our unit as a possible soft tissue sarcoma. 4 patients were referred as suspected benign lesions requiring specialist assessment owing to size and location. 46 patients (38.3%) ignored their swelling, resulting in a delay to presentation to their local units. In only 13 patients was pain a feature. These were not considered to be true delayed referrals. 24 patients (20%) experienced a delayed referral to our unit. An alternative diagnosis was suggested in 7 patients by preliminary imaging investigations. A ‘Whoops procedure’ was performed in 14 patients. 3 patients were initially misdiagnosed as muscular injuries, with consequent conservative management resulting in delay.
Much controversy surrounds synovial sarcomas, including prognostic indicators and optimal treatment. This paper reviews these subjects on the 65 cases of synovial sarcoma on the hospital’s database.
At 40 months 3 cases were excluded. 2 on review of the diagnosis and 1 had definitive treatment elsewhere. At 80 months 5 additional patients were lost to follow up.
The Kaplan-Meier 5 year survival rate for all patients in this review was 52.1%. Excluding patients who presented with metastases, this figure rose to 60.1%. All deaths were due to metastatic disease. Univariate analysis showed age of patient and size of tumour to be significant prognostic indicators for survival. Size of tumour only, was a significant predictor of metastatic spread using univariate analysis. Multivariate analysis showed only tumour size to be a significant indicator of survival and metastatic spread.
The local recurrence rate at 5 years was 22.3%. No convincing clinical features were shown to influence the local recurrence rate.
Adjuvant therapy was not shown to influence outcome significantly.
At 80 months follow up the 5 year survival rate increased to 54.9% (SE = 6.9%) and without metastases 61.7% (SE = 7.2%). The significance of established prognostic indicators did not change at final follow up.
The amputation rate was 21%. 3 patients had limb preserving surgery using an endoprosthetic replacement.
Tumour size and metastases appear to be the only consistent prognostic indicators of survival. Endoprosthetic replacement surgery should be considered a surgical option for synovial sarcomas involving bone. Doubling the follow up did not statistically affect survivorship data.
Responses were gained from 56 European databases. National databases were less able to identify this detailed anatomical site than regional ones. 30 databases from 12 countries responded with complete data representing 1.619 billion total population person-years. Four malignant tumours at the medial end of clavicle were identified from a total of 233.2 million children-years at risk.
Free, vascularised fibular grafting is well described in limb salvage surgery. The mechanical properties of the fibula make it ideal for replacement of bony defects after tumour resection and it can be sacrificed with minimal morbidity. We review the outcome of a consecutive series of 24 patients.
Between 1993 and 2002 we performed free vascularised fibular grafts in 24 patients as part of a limb salvage procedure following tumour excision. Pre-operatively patients were staged using the Musculoskeletal Tumour Society (MSTS) system. Post-operatively patients were followed up with radiographs and clinical examination. From the radiographs graft hypertrophy and time to bony union was documented. Functional outcome was assessed using the MSTS scoring system. Complications were recorded.
There were 15 women and 9 men with a mean age of 26 years (6–52). Mean follow up was 51 months (12–106). There were 19 malignant tumours, all stage 2b, and 5 giant cell tumours. The mean length of graft was 12.5 cm. (4.5–25). 16 grafts were used in the upper limb and 8 in the lower limb. Arthrodesis was performed in 8 cases and intercalary reconstruction in 16 cases. Fixation of grafts was achieved with a plate and screws in 21, a blade plate in 2 and an IM nail in 1. In 6 cases the resected tumour bone was reinserted as autograft after extracorporeal irradiation. In all but one patient the tumour margins were clear. Primary bony union was achieved in 22 patients (92%) at a mean of 35 weeks (12–78). Graft hypertrophy was seen in 7/29 cases (24%). Complications included 2 wound breakdowns, 3 stress fractures, 1 muscle contracture, 1 malunion and 1 painful plate. Overall 8 patients (33%) required second operation. 2 patients died of recurrent disease and one has metastases. The mean MSTS functional score was 87% (80–93).
Free vascularised fibula grafts offer a reliable method of reconstruction after excision of bone tumours. The complication rate appears high and some patients require a revision procedure. However, the problems are relatively easy to correct, bony union is achieved in the majority and functional outcome is good.
Clear cell sarcoma of soft tissues is a rare, poorly understood tumour with little written about it in peer reviewed literature. The aim of this paper is to present a consecutive series of patients treated at our institution.
All patients were staged using the system of the musculo-skeletal tumour society (MSTS). The aim of surgery was to achieve a wide excision. Adjuvant chemotherapy or radiotherapy was used in some patients depending on the margins, age and general health of the patient. Follow-up comprised clinical examination, magnetic resonance imaging (MRI) of the tumour bed and chest x-rays. Patients were seen 3 monthly for the first 2 years and then 6 monthly.
Between 1997 and 2003 14 patients were included. There were 5 males and 9 females with a mean age of 49 years (21–82). Mean follow-up was 42 months (1–84). Seven tumours occurred in the upper limb and 7 in the lower limb. Four patients were lymph node positive at presentation. The mean maximum diameter of the tumour was 5.6 cm (2–8). Ten patients were referred prior to excision but 4 patients had already undergone inadvertent excision biopsy elsewhere. Four patients developed local recurrence and 3 patients developed metastases. Seven patients remain disease free, 2 have no active disease, 1 is alive with disease and 4 have died of the disease.
The 2 year survival in this series is 71%. Poor prognostic factors include positive lymph nodes at diagnosis, maximum diameter of the tumour greater than 5cm and incomplete initial excision. It is important that these patients are treated early and that wide excision is achieved. We recommend early referral to a recognised musculo-skeletal tumour centre.
The purpose of this study was to review the outcomes of patients treated with injectable calcium phosphate cement (Norian SRS, Norian Corporation, Cupertino, California) for contained bone defects after resection of benign or low-grade malignant bone tumours.
The clinical records and radiographs of 17 patients who had been treated with calcium phosphate cement were reviewed, looking for incorporation into bone, reabsorption of the material and complications.
The 17 patients had a mean age of 29.8 years (range 7 to 64). The diagnosis was giant cell tumour in 9 cases, fibrous dyplasia in 2, low grade chondrosarcoma in 2, and one each of enchondroma, chondromyxoid fibroma, osteofibrous dysplasia, and chondroblastoma. The tibia was involved in 9 cases, the femur in 6 and the radius in 2. The mean follow up was 11 months (range 3 to 25).
The material is radioopaque and well visualised on plain radiographs. In most cases, incorporation of the material into the bone structure appeared good, but there was little absorption of the material during the followup available. The exceptions were 2 cases in which the material was absorbed following local recurrence of giant cell tumour.
One fracture associated with a giant cell tumour healed well in the presence of the material. In three patients, there were clinical and radiological features at follow up suggestive of periostitis related to the material. In one case a florid effusion of the knee may have been due to the material.
Injectable calcium phosphate cement may have a role in the management of contained defects requiring mechanical support following resection of benign or low-grade malignant tumours of bone. However, problems with periostitis, possibly synovitis and absorption in the presence of local recurrence should be considered.
This preliminary report demonstrates the effective use of Apapore in the management of benign cystic bone lesions.
The use and development of bone graft substitutes over the past ten years has increased dramatically to improve their osseo-integration to a level similar to autografting techniques without the drawbacks of comorbidity from the graft site.
Apapore is a synthetic bone graft substitute which consists of a scaffold of synthetic phase-pure hydroxy apatite with micro- and macroporosity and inter-connectivity to favour bone repair.
Nineteen patients (12M:7F) with a mean age of 18.6years (8–33 years) having had procedures for the management of benign cystic lesions of bone with grafting using Apapore were followed up retrospectively for a mean period of 8 months (1–16months). In each case the diagnosis of a benign cystic lesion was made histologically prior to surgery. The subsequent definitive procedure was performed by a consultant on the Bone Tumour Unit at the Royal National Orthopaedic Hospital (Stanmore) in each case involving curettage and impaction of Apapore into the cavity in a standard fashion as a general anaesthetic procedure in the operating theatre.
There have been no complications to date. All patients have made uneventful recoveries. Short-term radiological follow-up demonstrates excellent incorporation of the bone graft substitute and osseo-integration.
The Government has set a target of two weeks for referral of suspicious tumours to specialist centres, but what symptoms should raise suspicion of chondrosarcoma and what factors affect survival and local recurrence? A retrospective study of 320 cases of chondrosarcoma from the Scottish Bone Tumour Registry was performed. Presenting symptoms and were related to tumour grade and duration of disease free status and survival. Pain, swelling and loss of function were the most common presenting features. Rapid progression of pain was significantly associated with high-grade tumours. Longer duration of symptoms from onset to presentation was associated with low-grade tumours. High-grade tumour and metastasis at diagnosis were associated with poor prognosis. Thus, patients with a longer history of symptoms actually appear to have longer disease free survival after presentation. Expert opinion should be sought for patients presenting with pain, swelling and loss of function. Practitioners should make prompt referral of patients presenting with pain that is rapidly increasing in severity.
When managing malignant bone tumours in the distal femur with limb salvage, resection and reconstruction with a distal femoral replacement (DFR) conventionally entails prosthetic replacement of the knee joint. In younger patients it is desirable to try to preserve the knee joint. We now use a new Joint-Sparing distal femoral prosthesis in those cases where it is possible to resect the tumour and preserve the femoral condyles. Purpose of study: To look at our early results with knee joint preserving DFR’s. Methods: Between June 2001 and March 2004 the prosthesis was implanted in 8 patients (5 males and 3 females) aged between 8 and 24 years at the time of surgery. The diagnosis was osteosarcoma in 6 cases and chondrosarcoma in 2 cases. All patients were followed regularly and knee range of movement was recorded as well as any complications that occurred. Patients were functionally evaluated using the MSTS Scoring System. Results: Six of the patients had a mean follow-up of 20 months (range 8–33) and in this group 4 had good knee flexion with a mean flexion of 122° (110–130), 1 patient had fair flexion of 60° and 1 patient had poor flexion of 20°. The mean fixed flexion deformity in the 3 patients who had such a deformity was 10° (5–15). There were no intraoperative complications but the patient with poor flexion required an arthrolysis and because of the poor result is under consideration for conversion to a conventional DFR. Two patients had follow-up periods of 3 months or less and are still in their early rehabilitation period. One patient in this group developed sepsis that resolved after an open washout. Conclusions: Our early results with this prosthesis, in the patients with adequate follow-up, have been good in the majority but the two cases of fair and poor knee flexion are disappointing. This particular problem may relate to design and technical factors, which will be discussed in detail.
The cumulative 14-year recurrence rate was 40% and the mean time to recurrence was 20.2 months.
Our study sets out to show whether vascular endothelial growth factor (VEGF) expression in stage 2B osteosarcomas around the knee influences disease-free and overall survival.
Fifty-two such patients treated in out unit were identified and followed-up for for a minimum of 92 months. All were treated according to the current MRC protocol and had resection of their tumour. Tissue from their resected tumours was stained for VEGF using immunohistochemical methods and the percentage of tumour cells staining for VEGF was assessed. The relationship between VEGF expression and survival was assessed using the log-rank test and Kaplan-Meier survival curves.
At follow-up 32 (62%) patients were dead, all from metastatic disease. Twenty-six (50%) tumours showed expression of VEGF. Statistical analysis showed that patients with tumours with VEGF expression in more than 25% of the cells had significantly shorter overall survival (p=0.019) and disease free intervals (p=0.009).
VEGF is peptide which acts as a stimulator of new blood vessel growth in normal tissues, as well as in some solid tumours and their metastases. A tumour which is able to induce a blood supply has an increased ability to grow, seed metastases and threaten life. Our study is the first to look at VEGF expression in the tumour cells surviving after chemotherapy. It is this population of cells which is important as it is these cells which may go on to develop into metastatic or locally recurrent tumours. The over-expression of VEGF by osteosarcoma cells is thought to be associated with a worse prognosis due to a number of mechanisms. This study shows that VEGF expression is an important prognostic factor in osteosarcomas. Suppression of tumour angiogenesis by inhibition of the action of VEGF has shown promise in animal models as a potential new treatment for osteosarcoma, and warrants further study.
When managing malignant long bone tumours in skeletally immature patients it is desirable, after resection, to reconstruct with a prosthesis that can be lengthened at appropriate intervals to keep pace with growth of the contralateral side. In an attempt to avoid multiple surgical procedures to achieve such lengthening we have recently developed a prosthesis that can be lengthened non-invasively.
We performed a retrospective analysis of massive endoprostheses inserted at our unit in the management of Giant Cell Tumours of the distal femur with a minimum follow up of 5 years.
We reviewed our experience with diaphyseal endoprostheses to determine the survival of this type of reconstruction and factors affecting that survival.
Bone lesions of the tibia are encountered commonly in radiology practice.
The range of pathologies is large and it can be difficult to reach a diagnosis based upon conventional radiographic features alone. Cross-sectional imaging (CT and MRI) can help narrow down the differential and in many cases provide a definitive diagnosis.
We present a pictorial review of the imaging features a comprehensive range of pathologies involving the tibia on conventional radiography, CT and MRI and discuss features to aid accurate diagnosis.
The purpose of this paper is to present the rare occurrence of clear cell chondrosarcoma in a patient suffering from Niemann-Pick disease (NPD).
NPD is a rare autosomal recessive inborn error of metabolism. It is a lysosomal storage disorder affecting children and adolescents often causing death in early childhood although in milder form patient may survive up to adulthood. Although chondrosarcoma is a relatively common malignant bone lesion, these lesions rarely affect patients suffering from Niemann-Pick disease. This article presents the case of a 50-year-old man with a chondrosarcoma in the olecranon of the left ulna who also suffered from milder form of Niemann-Pick disease. Radiography and MRI showed cortical disruption and an expansile lesion. Histologically, the tumour was classified as grade 2 clear cell chondrosarcoma with classical differentiation according to the American Joint Committee of Cancer pathologic staging system. Amputation of an above elbow type was performed to obtain clear surgical margins. A case report and discussion of this rare association of a patient suffering from milder form of NPD who developed a clear cell chondrosarcoma is presented here. NPD and clear cell chondrosarcoma are rare diseases and together their occurrence was not found reported in the literature. NPD patients rarely live to the age of 50 years. This raises a possibility that if Niemann-Pick patients survived long enough they might develop chondrosarcoma. Alternatively this could just be coincidental. More research is needed to clarify this possibility.
Relevant literature is reviewed.
A case report of an 11 year old boy who underwent tibial osteotomy to prevent angulation of his right tibia.
As a 7 year old, LH sufered a minor injury to his right tibia. A lump appeared at the same site. Soon the lump grew to be similar to “a second knee cap”. However, it only caused him pain when he traumatised it. He and his parents were disturbed by the lump, and the fact that it was creating an anterior-posterior bowing of his tibia. They sought medical advice. His original hospital carried out X rays that demonstrated the deformity and a cloud like lump at the tibial tuberosity.
A bone scan confirmed a solitary osseous lesion. In July 2002 he was referred to the RNOH, where the decision was taken to resect the tibial tuberosity and undertake a corrective osteotomy. Post surgery in August 2002, LH was mobilised in a full cast for 9 weeks and graduated slowly from non to full weight bearing. Histology revealed a probable endchondroma, or unusual growth plate reaction.
A year after the procedure LH is a symptom free, happy and active boy. Radiographs confirm normal angulation of his Tibia.
In conclusion an osteotomy can be a very successful treatment for a childhood lesion that leads to progressive deformity.
Breast carcinoma is the most common cause for bony metastases. Skeletal complications in women with meta-static breast carcinoma often occur multiple times in a single patient and significantly contribute to the patient morbidity. We describe a 62 year old lady with a known metastatic breast carcinoma who presented with simultaneous quadruple extremity diaphyseal long bone fractures after a trivial fall. To the author’s best knowledge, similar report has never been previously described in the literature.
The wish and general condition of the patient, and concurrent occurrence of four long bone fractures dictated the non-operative mode of treatment in this case.Where the life expectancy is assumed to be less than six weeks, the multidisciplinary team should give careful consideration on selection of best treatment choice between simultaneous or sequential surgical fixation of multiple long bone fractures and conservative palliative treatment. With treatment suited for an end-of-life circumstance, the educational lesson for dissemination to the readers is that in a patient where there is an extremely high likelihood of imminent perioperative mortality after sustaining quadruple extremity diaphyseal proximal long bone fractures simultaneously, conservative palliative treatment should be primarily considered over an aggressive operative fixation.
We report a rare case of an intracortical chondroma in the region of the medial femoral condyle of the femur extending into the femoral sulcus and the patellofemoral joint.A sixteen year old Asian boy presented with repeated episodes of right sided anterior knee pain and giving way over a three year period. The patient had been treated previously for multiple bony swellings at another hospital and a diagnosis of multiple enchondromatosis had been made. Examination revealed that the patellofemoral compression test was positive with fullness over the medial eminence of the femur in the region of the trochlear groove.Pre-operative X-rays and MRI scan showed the presence of an intracortical lesion over the medial femoral condyle extending into the femoral sulcus. The lesion demonstrated intermediate signal intensity on T1 and high intensity on T2 weighted images with variable low signal intensity foci due to the presence of a calcified matrix. The patient underwent arthroscopic examination. An intra-articular lesion (2cmx 3cm.) was identified and excised through a mini-arthrotomy. The lesion was entirely intra-articular arising from the medial femoral condyle proximal to the femoral sulcus, extending partially into the supra-patellar pouch. Histopathological examination confirmed the presence of a low grade cartilaginous neoplasm best diagnosed as an atypical chondroma. At a two year follow up appointment the patient was found to be asymptomatic with no evidence of radiological recurrence.
Although there have been several reports of periosteal chondromas developing around the knee the majority deal with soft tissue chondromas in para-articular locations or intra-cortical tumours in extra-articular regions. Our tumour is unique due to its intra-articular and intracortical location. A detailed review of the literature of this rare tumour is presented with a pictorial presentation of the case including arthroscopic radiological and histopathological findings.
The soft tissue sarcomas (STS) are a diverse collection of malignant tumours of the connective tissues arising from the primitive mesoderm and ectoderm. While the primary treatment of most is surgery, chemotherapy can be offered to patients presenting with locally advanced or metastatic disease although sarcomas are resistant to the majority of anticancer drugs. The reasons for this are not fully understood but it is thought that p53 abnormalities and mdm2 overexpression may be involved. Samples from twenty eight adult patients with soft tissue sarcomas have been analysed for p53 mutations in exons 4 to 9 both by denaturing high performance liquid chromatography (dHPLC) and by direct automated sequencing. By sequencing we found mutations in 7/28 patients, giving a mutation rate of 25%. 4/6 were point mutations in exons 5, 7 and 8 and the remaining three were deletions in exons 4, 7 and 8. Six of these samples gave abnormalities in dHPLC analysis with a concordance rate of 97.5% between the sequencing and dHPLC data. Thirty nine and forty samples have been assessed by immunohistochemistry for p53 and mdm2 expression respectively. Do7 antibody which recognises the N terminus of p53 and F4-14 which recognises the carboxy-terminus of mdm2 were used. Immunohistochemistry was scored semiquantitatively by two independent observers and the results scored accordingly: low (< 20%), intermediate (20–80%) and high (> 80%). The initial results showed that 23/40 (58%) of patients were high staining for mdm2 in contrast to only 15/39 (38%) of patients for p53. All patients with deletions in p53 had intermediate staining for mdm2. 2/3 of these had intermediate staining for p53 and 1/3 had high staining for p53. One patient with a point mutation had high staining for both p53 and mdm2 but the other two have yet to be analysed by immunohistochemistry. These results confirm the overexpression of mdm2 in STS. Future experiments are planned using fluorescent in situ hydridisation (FISH) to determine whether MDM2 amplification is one of the mechanisms involved in mdm2 overexpression.
We report our clinical experience with three patients in whom squamous cell carcinomas developed secondarily to chronic bone infections. The diagnosis was delayed in each case.
There are several well recognised warning signs which should alert the physician to the possibility of malignant change having occurred in the region of chronic bony infection.
Close attention to these signs will prevent undue delay in diagnosis and avoid the associated complications.
As chronic osteomyelitis becomes less common in first world countries we need to remain aware of the possible complications which can be encountered.
The diagnosis in each of our cases was delayed by the fact that the possibility of malignant change was not considered by several experienced orthopaedic surgeons.
When there is change in signs and symptoms or altered flora within the discharge one must be alerted to the possibility of malignant change. This should prevent delays in diagnosis. Radiological progression should probably be regarded as malignant change until proven otherwise.
With early diagnosis and treatment the prognosis for a patient with squamous cell carcinoma is good. Key words: Osteoclastoma, Osteomyelitis, Sinus tract, Squamous cell carcinoma.
Soft tissue tumours on the sole of the foot are rare and difficult to diagnose, we report a series of five patients who presented with a late diagnosis of a soft tissue tumour on the soles of their feet.
We reviewed the notes of five patients who presented with lesions on the soles of their feet. There were 3 males and two females with an age range from 35yrs to 78 yrs. Our results showed that there was at least a one year delay in their diagnosis from their initial symptoms. They all sought medical treatment late, and were all originally diagnosed with benign lesions at their first presentation. All but one, were found to have malignant lesions on biopsy which required surgical excision. As a consequence of the delay in their presentation and diagnosis, there was also a delay in their treatment.
Our conclusions are that tumours on the soles of the feet are difficult to diagnose and almost invariably present late.
* Posterior portal: anterior branch of the axillary nerve and posterior circumflex artery 3.4 cm (range: 1.4 – 5); cutaneous branch of the axillary nerve 6.3 cm (range: 3.8 – 8.3), suprascapular nerve 2.8 cm (range: 2.1–3.3). * Anterosuperior portal: main branch of the musculocutaneous nerve 6.5 cm (range: 3.8 – 11). * Lateral subacromial portal: axillary nerve and posterior circumflex artery 3.7 cm (range: 2– 5.5). * Anteroinferior subaxillary portal 4 cm (range: 3.1 –6). * Supraspinatus portal: suprascapular nerve 3.2 cm (range: 2.4 – 4).