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View my account settingsA longer stay in the hospital after primary total hip replacement is consistent with an increased morbidity and slower recovery for patients. In addition, it is among the more costly aspects of a total joint replacement. A process, which reduces the length of stay following this procedure and synchronically maintains the high standards of safe care would certainly improve the clinical practice and provide financial benefits.
Our objective was to evaluate the efficiency of a holistic perioperative, accelerated recovery programme following this procedure and in particular to assess its impact in the shot term patient’s recovery, morbidity, complications, readmission rate and cost savings for the NHS.
Eighty-nine patients participated in our rapid recovery programme, which is a comprehensive approach to patient care, combining individual pre-operative patient education, pain management, infection control, continuous nursing and medical staff motivation as well as intensive physiotherapy in the ward and the community. Forty-eight male and 41 female patients with an average age of 69 (range-50 to 87) underwent a total hip replacement in an NHS District General Hospital. The average BMI was 28 (range-18 to 39) and the average ASA 2.3 (range-1 to 4). The procedure was performed by 3 different surgeons using the same operative standards. A standardised post-operative protocol was followed and the patients were discharged when they were medically fit and had achieved the ward physiotherapy requirements. They were then daily followed up by a community orthopaedic rehabilitation team in patient’s own environment as long as it was required.
The average length of stay was reduced from 7.8 days to 5. There was no increase in complications–or readmissions rate while there were significant cost savings. The waiting list for this surgery was reduced and the patient’s satisfaction was high.
The rapid recovery programme for primary total hip replacement surgeries has been proved to be an efficient method of reducing the length of stay in hospital and consequently the financial costs while it ensures the safe and effective peri-operative management of patients.
The ‘gold standard’ for treatment of chronic ankle instability is Brostrom-Gould procedure, which is an ‘open’ surgery.
Most authors recommend this type of operation even after an arthroscopic inspection of the joint.
The arthroscopic methods, including thermal shrinkage, propose in the past didn’t received a widely spread support.
We present a method of arthroscopic lateral ligament ‘repair’ with an anchor placed in the fibula.
We used this technique on 31 consecutive patients (28 were available for follow-up).
21 patients were victims of work or traffic accidents and 3 had sport-related lesions.
The patients were evaluated after a 24,5 month follow-up.
The average post-op AOFAS score was 85,3 and average satisfaction was 3,77 (1 to 5)
We had two ‘relapses’ (another sprain without instability on the stress XR). On 3 patients we had some wound healing problems and we had 3 lesions of the superficial peroneal nerve, one of these is persistent. One patient developed a deep vein thrombosis post operatively.
With this method, we achieved good results with relatively few complications, even more considering that most of the patients were work-compensation cases. It’s a simple procedure, less ‘aggressive’ then the traditional one’s, producing an anatomical and functional repair of the lateral ligament.
We report 114 of 117 (97% follow up) consecutive metal-on-metal hip resurfacings in 105 patients with a minimum of 5 years follow up implanted between October 1999 and May 2002. Revision of either the femoral or acetabular component during the study period is defined as failure. No other revisions have been performed or are impending. We had 4 failures giving us survivorship at 5 years of 97% (95% confidence interval (CI) 94 – 100). The mean follow up was 72 months and the mean age at implantation was 54.5 years old (Range 35 – 75). All patients were followed up clinically and radiographically.
The mean Harris hip score at follow up was 96.4. The mean Oxford Hip Score fell from 41.6 preoperatively (Range 16 – 57) to 15.3 postoperatively (Range 12 – 49) p< 0.0001. The UCLA Activity Scale rose from 3.93 preoperatively (Range 1 – 10) to 7.54 postoperatively (Range 4 – 10) p< 0.001.
Radiographic analysis revealed an average stem shaft angle of 130.6 degrees (Range 112 – 148) with average cup alignment of 36 degrees (Range 22 – 47). Neck thinning was present in 12 hips (10%) and we define a technique for measuring thinning. Heterotropic ossification was present in 17 hips and lucent lines around the femoral component in 10 hips.
This study confirms that metal-on-metal resurfacing produces an excellent clinical and functional outcome in the younger patient who requires surgical intervention for hip disease. The results compare favourably with those from the originating centre and confirm that resurfacing is well suited for younger higher demand patients. It is the first study with a minimum 5 year follow up from outside the originating centre.
Venous thromboembolism (VTE) is a potentially fatal complication after total hip replacement (THR) and may be associated with a considerable economic burden. In many centres, thromboprophylaxis using a subcutaneous (sc) anticoagulant in patients undergoing THR is restricted to 14 days or less. Rivaroxaban is a once-daily, oral, direct Factor Xa inhibitor in advanced clinical development for thromboprophylaxis after major orthopaedic surgery; it does not require monitoring or dose adjustment. In a phase III study, RECORD2, oral rivaroxaban 10 mg, given once daily for 35±4 days, significantly reduced the incidence of the primary endpoint (deep vein thrombosis, pulmonary embolism and all-cause mortality), compared with 40 mg sc enoxaparin, given for 14 days (2.0% vs 9.3%, respectively; relative risk reduction 79%; p< 0.001). The incidence of bleeding was low and similar in both groups, despite extended thromboprophylaxis with rivaroxaban. This analysis demonstrates the economic impact of extended thromboprophylaxis with oral rivaroxaban. The effect of rivaroxaban on healthcare costs was based on the primary efficacy results, and the associated reduced administration and monitoring costs, and includes non-drug costs only. The cost of symptomatic VTE was taken from published sources in the US and the UK 2007 NICE Guidelines. It was assumed that nurses spent 3 mins/day administering enoxaparin and training patients to self-inject for outpatient use. Hospital duration was 5 days. In the UK, full blood counts should be taken every 3 days when receiving enoxaparin. The total US health-care resource cost was $192/patient for enoxaparin and $39 for rivaroxaban (excluding drug costs). This saving of $153 was driven by reduced hospital costs associated with fewer VTEs when using rivaroxaban. In the UK, the total healthcare cost/patient was £44 with enoxaparin and £2 with rivaroxaban – savings driven equally by reduced hospitalization and monitoring costs with rivaroxaban prophylaxis. The different cost savings in the US and UK are due to higher US hospital costs. The costs of post-thrombotic syndrome (PTS) were excluded in this analysis. PTS has an estimated 5-year rate of 21% after asymptomatic VTE and 30% after symptomatic VTE, at a total cost/patient of more than $11,000 in the US and £4000 in the UK. Given the reduction in all VTE events with rivaroxaban, there are potential further healthcare cost savings due to reduced PTS. The RECORD2 study showed that extended prophylaxis (35 days) with rivaroxaban was significantly more effective than short-term enoxaparin (14 days) for the prevention of VTE, and was not associated with an increased risk of bleeding. This analysis illustrates an additional benefit of once-daily, oral rivaroxaban in the reduction in healthcare costs related to administration and monitoring.
extent of fracture in percentage along the intertrochanteric line angle of the fracture line.
Both these parameters were measured on a plain anteroposterior radiograph. To measure the length of fracture we have drawn a straight line along the medial border of femoral shaft extending proximally in to the pelvis. Then we measured the distance between the most superior point of the fracture line on the lateral cortex and the midpoint of lesser trochanter on the first line. Then we measured the length of the fracture starting from the most superior point on the lateral cortex. We estimated the percentage of this fracture length in relation to line.
To estimate the angle, again we have drawn a straight line along the medial border of femoral shaft extending proximally in to the pelvis. We have drawn another line in the direction of fracture staring from most superior point of fracture on the lateral cortex joining the first line. We measured the angle between these two lines (Fig 2). We used our Hospital PACS system to measure the angles and the length of the fracture.
Clostridium difficile associated diarrhoea (CDAD) has emerged as a healthcare associated infection of great clinical and economic significance especially in the frail and vulnerable group of fracture neck of femur patients. A major risk factor for the development of CDAD in patients who undergo operation for fracture neck of femur is the perioperative antibiotic exposure, with cephalosporins being particularly implicated. The type ‘027’ strains of C. Difficile are multi-resistant and cause severe morbidity and mortality. A retrospective audit was performed to study the effect of C. Difficile infection in operated fracture neck of femur patients.
There were 19 (55.5%) trauma admissions with fractures and 15 (45.5%) elective admissions. There were 12 (35.2%) patients with previous gastric problems. There were 20 (59%) patients who were on gastric irritant medications, out of which only 5 (25%) were on gastro protective medications. All 34(100%) patients were on low molecular weight heparin for thromboprophylaxis. There were 2 patients on steroids and 2 patients on warfarin.
Coffee ground vomitus occurred preoperatively in 4 (13.4%) and postoperatively in 26 (86.6%). It happened with in the first six hours after surgery in 25 (96.5%) patients. Only in one patient it happened after 3 weeks.
All patients were kept nil by mouth, started on fluid resuscitation and intravenous ranitidine followed by oral omeprazole. Patients who were haemodynamically unstable were investigated by endoscopy. 17 (50%) patients had oral gastroduodenoscopy. 2 patients had blood transfusion because of significant drop in haemoglobin and one died before the transfusion was started.
There were 5 (14.7%) deaths in our study group. The cause of 2 deaths was directly related to gastrointestinal bleeding and the other three were confirmed to have had concurrent chest infection.
We present a retrospective analysis of 50 cases of cuff tear arthropathy, treated over past seven year period by use of reverse geometry shoulder prosthesis. 98% follow-up was achieved with average follow up of 3 years. Mean (SD) age was 81.3 (9.2) years and female to male ratio was 5:1. Six patients had bilateral reverse geometry shoulder replacements. Patients were assessed with preoperative Oxford and American Shoulder and Elbow Scores Society score (pre-op ASES) and post-operative American Shoulder and Elbow Society Score (post-op ASES), Oxford, Constant and SF36 scores. Mean pre-op ASES was 22.29 (95%CI: 9.1 – 37.9) and post-op ASES score was 65.2 (95%CI: 48.5 – 81.9), (P< 0.001, Paired t-test). Mean post operative Oxford score was 27.25 (95% CI: 18.4 – 27.6). Mean post operative Constant score was 63.2 (95% CI: 52.6 – 79.6). X-ray review was performed to assess scapular notching and Sirveaux score was used to grade extent of notching. 11 patients had Sirveaux grade 0, 5 had grade 1, 6 had grade 2, 12 had grade 3 and 8 had grade 4 notching. Intra-operative complications included 2 glenoid fractures. Post-operative complications included 2 acromion fractures and 2 episodes of subsidence with dislocation. None of the patients developed post operative haematoma. There was one episode of infection in one patient that required further surgery. Iteration of approach with increasing experience over the years will be discussed. Ours is the biggest series of reverse geometry prosthesis used for irreparable rotator cuff tear arthropathy published so far in the literature and our results have shown superior results in terms of improvement in function and complications. We conclude reverse geometry shoulder replacement provides reasonable improvement in pain and function in elderly population with massive cuff tear arthropathy of shoulder.
Manoli and Schaeffer in 1987, showed that fixation by antiglide plate demonstrated superior static biomechanical properties compared to lateral plating.
However there are some shortcomings in their study and hence we decided to perform our biomechanical study. The shortcomings of the Manoli study are. They did not use an interfragmentary lag screw for lateral plate fixation. It was a cadaveric study where the bone does not accurately represent the live bone. The quality of the bone ranging from normal to osteoporotic bone varies from cadaver to cadaver and hence there is no uniformity between the samples.
These bones were custom made for the experiment. We used two sets of bones, one representative of normal bone (Set A n=10) and the other of osteoporotic bone quality (Set B n=10). Each of the sets A & B will have two types of fixations for artificially created Weber B Fractures.
Lateral plate with interfragmentary lag screw. Antiglide plate with interfragmentary lag screw.
The strength of the fixation was measured by restressing the bone until the fixation failed using an Instron machine which simultaneously applied torque and compressive forces to the fibular construct. The resulting data was analysed on a computer and statistical analysis was performed.
Single Photon Emission Computed Tomography – Computed Tomography (SPECT-CT) combines metabolic information with an exact anatomical localization. We hypothesised that diagnostic infiltration with a local anaesthetic of a painful hindfoot or midfoot joint showing 99mTc-DPD-uptake in SPECT-CT, leads to a positive OA pain response.
Periprosthetic humeral fractures are rare but their numbers tend to increase because of the development of shoulder prostheses. We analysed our cases to see if some therapeutic guidelines can be provided.
Histomorphological examinations including synovial cell coating, appearance of tendon and tissue interface, inflammation and scarring of the site of surgery were done. The results were analyzed statistically (Kruskal-Wallis-test; Jonckheere Terpstra-test).
Secondly, we proposed that fixation with alternate cortical screws from both sides of the cortices (2C) may confer a stronger mechanical stability than fixation with all screws from one side (1C).
The concept of tension band wiring is based on the fact that the distractive force applied to one surface of the bone will result in compression on the opposite articular surface.
Clinical outcomes of TBW are not equivocal. It is associated with significant morbidity such as non union, failure of fixation, especially in osteoporotic bone and infection which sometimes leads to amputation. Often a second procedure for removal of prominent metal work is required.
In our biomechanical study we investigated this concept as we believe that the forces generated by TBW construct do not generate significant compressive forces required for healing of fracture.
The advantage of using 4th generation composite bone model is that it provides uniformity which is not achievable in cadaveric studies. Two different bone models representative of Olecranon and patella were used. Transverse fractures were created in the bones and fixed with TBW technique as described in A.O. manual.
Two 0.062-inch Kirschner wires and figure of eight configuration of 18G Stainless steel wire with single knot technique was used. Micro motion transducers (DVRT: MicroStrain, Williston, Vermont) with an accuracy of ± 1μm were placed across the fracture site both anteriorly and posteriorly. Continuous information regarding fracture distraction and compression, as determined by the transducers was recorded from both sites simultaneously during the experiment.
The tension band wire construct was loaded up to a maximum force of 4000 Newtons for patella and 500 for the olecranon. The fractures were subjected to cyclic loading at 1Hz using a servo hydraulic materials-testing system (model 8500; Instron, Canton, Massachusetts). The results were analysed on a computer and statistical analysis performed.
The ability of hMSCs to differentiate into several mesenchymal cell lineages including the osteoblast lineage plays a key role in skeletogenesis and bone regeneration. Although the importance of physical factors in the development and maintenance of bone tissue has been recognized for many years and we previously demonstrated that mechanical strain constitutes an inherent stimulus for osteogenic differentiation of undifferentiated hMSCs, there is strong evidence to suggest that obesity is an independent factor in the risk of implant failure due to aseptic loosening or fracture after TJR. While mechanical complications and overload have been widely suggested, we hypothesized that the osteogenic mechanoresponse of hMSCs may be profoundly altered in obese patients.
hMSCs were isolated from bone marrow of 10 donors (BMI ranging from 18.7 to 37.6 kg/m2). The individual response of unidfferentiated hMSCs to cyclic tensile strain (CTS) was determined in a two-armed study design (strained versus unstrained (CTR)) using a 4-point bending device, where strain was restricted to a maximum of 3,000 μstrain. Phenotypic effects were characterized by analyzing cell numbers, cell viability and ALP activity; mRNA levels of marker genes related to early osteogenic differentiation (RUNX2, ALPL, SPARC, SPP1), protein synthesis (COL1A1), and cell cycle (MKI67) were determined by real-time RT-PCR. Possible contributions to anthropomorphometric variables and individual triglycerides, cholesterin, glucose, leptin, adiponectin, resistin, and estradiol levels were evaluated by linear regression analysis.
We found a significant up-regulation of the osteogenic marker genes due to CTS, including RUNX2 (1.9 fold), ALPL (2.4 fold), SPP1 (2.8 fold), and SPARC (4.1 fold), which was accompanied by an increase in cell-based ALP activity from 6.1 ± 1.2 μM/min/106 in CTR to 8.5 ± 1.7 μM/min/106 in CTS (plus 39.6 ± 9.8% SEM, P< 0.05). Cell density was significantly lower following CTS (minus 20.0 ± 4.7%, P< 0.05), which was also found for cell viability (XTT minus 17.8 ± 5.6%, P< 0.05). As a consequence, the phenotypic CTS response (ALP activity w/o normalization) ranged widely between donors (−30.8% to +60.1%) and was highly significant inverse correlated to donor’s BMI (r= −0.91, P< 0.0001). Additionally, leptin and estradiol levels determined within bone marrow plasma were significantly correlated with the phenotypic mechanoresponse (r=−0.71, P=0.028, and r=0.67; P=0.039; respectively).
The findings demonstrate that the osteogenic mechanosensitivity of hMSCs is highly affected by physiological factors related to donor’s BMI. Such an upstream imprinting process within bone marrow may be an important area of further research, since obesity-linked problems constitute increasing concerns in orthopaedic surgery within the western world.
Mesenchymal stem cells (MSCs) from bone marrow are multipotent cells capable of forming cartilage, bone, and other connective tissues. The objective of this study was to determine whether the use of allogenic mesenchymal stem cells could functionally heal defect in the distal femoral physis in rabbits without the use of immunosuppressive therapy. An iatrogenic defect was created in the lateral femoral condyle of thirty-two New Zealand white rabbits, 7 weeks old, that weighed 2.25 ? 0.24 kg. Each defect, 3.5 mm in width and 12 mm in length, in the right distal femoral physis was treated with allogenic mesenchymal stem cells in new composite hyaluronate/ collagen type I/fibrin scaffold. The healing response was evaluated radiographically, by MRI (at three weeks and four months after implantation), and also histologically, by Pearls’ reaction and with immunofluorescency (at four months after implantation). The results were compared with the data for the control defects (without stem cell implantation) in left distal femoral physes. In average, right femurs with damaged distal physis and transplanted MSCs grew more in length (0.55? 0.21 cm) as compared with left femurs with physeal defect without stem cell transplantation (0.46? 0.23 cm). Valgus deformity of right femurs with physeal defect and transplanted MSCs was mild (0.2? 0.1°). On the contrary, left femurs with physeal defect without transplantated MSCs showed significant valgus deformity (2.7? 1.6°). For defects treated with allogenic mesenchymal stem cell implants, no adverse immune response and implant rejection were detected in this model. Histologically, no lymphocytic infiltration occurred. At four months after transplantation, hyalinne cartilage had formed throughout the defects treated with allogenic MSCs. Labeled mesenchymal stem cells/diferentiated chondrocytes were detected in the physeal defects based on magnetic resonance imaging and immunofluorescency. The results of this study demonstrated that allogenic mesenchymal stem cells in a new composite hyaluronate/collagen type I/fibrin scaffold repaired iatrogenic defects in the distal femoral physes in rabbits without the use of immunosuppressive therapy. The use of allogenic mesenchymal stem cells for the repair of physeal defects may be an alternative to autologous MSCs transplantation. An allogenic approach would enable mesenchymal stem cells to be isolated from any donor, providing a readily available source of cells for cartilage tissue repair.
In finite element (FE) analysis of long bones it is now common practice to calculate the material properties based on CT data. Although a unique material property is calculated for each element, assigning each element an individual material property results in excessively large models. To avoid this, it is usual to group the elements based on their material properties and to assign each group a single material property (Zannoni 1998). No study has analysed the effect the number of material properties used in a long bone FE model has on the accuracy of the results.
The aim of this study was to evaluate the variation in the calculated mechanical environment as a function of the number of material properties used in an FE model.
An FE mesh of a cadaveric human tibia containing 47,696 ten-node tetrahedron elements and 75,583 nodes was created using CT scans. Material properties were calculated for each element of the mesh based on previous work (Rho 1995, 1996). Eleven FE models were created by varying the number of groups (1, 2, 4, 8, 16, 32, 64, 128, 256, 512, 1024) the elements were divided into. A single material property was assigned to each group. All models were subject to an axial point load of 300N applied on the medial condyle of the tibial plateau while the distal end was fixed. The variation in maximum and minimum principal strains and deflections, at 17 well distributed surface nodes and at 65 randomly distributed nodes within the bone were plotted against the number of element groups. The total strain energy was also plotted against the number of groups. The errors for strain, deflection, and total strain energy were calculated for each model assuming that the model using 1024 element groups was accurate.
The parameter to converge with the least number of element groups was the total strain energy. At 512 element groups the error was less than 0.001% (0.7% for the two material model). The next to converge were the displacements. Using 512 materials the maximum error in displacement at the surface nodes was 0.001% (4.7% for the 2 material model), while for the internal nodes the maximum error was 0.53% (36.7% for the 2 material model). The least convergence occurred for principal strains. The maximum errors when 512 materials were used were 1.06% (57.7% for the 2 material model) and 3.02% (104.5% for the 2 material model) for the surface and the internal nodes respectively.
This study demonstrates the relationship between the accuracy of calculated mechanical environment and the number of material properties assigned to the model. While this study will allow the analyst to make an informed decision on the number of material properties for modelling the human tibia it also helps examine the validity of previous studies which, usually due to limited resources, used fewer material properties.
The immunosuppressive drug rapamycin (RAPA) prevents rejection in organ transplantation by inhibiting interleukin-2-stimulated T-cell division. RAPA has also been suggested to possess strong anti-angiogenic activities linked to a decrease in production of vascular endothelial growth factor (VEGF). Because VEGF is a key growth factor in fracture healing, the present study was conducted to analyze the effect of RAPA on bone repair.
For the herein introduced study 35 SKH-1Hr mice were treated by a daily intraperitoneal (i.p.) injection of RAPA (1.5mg/kg/d) from the day of fracture until sacrifice. Two or five weeks after fracture, animals were killed and bone healing was analyzed using radiological (n=16 at 2 weeks; n=16 at 5 weeks), biomechanical (n=2x8), and histomorphometric (n=2x8)
X-ray analyses demonstrated that RAPA treatment inhibits callus formation after 2 weeks of fracture healing. The radiologically observed lack of callus formation after RAPA treatment was confirmed by histomorphometric analyses, which revealed a significantly diminished callus size and a reduced amount of bone formation when compared to vehicle-treated controls. Biomechanical testing further demonstrated that RAPA significantly reduces torsional stiffness of the callus (11.5±5.9% of the contralateral unfractured femur vs. 28.3±13.9% in controls; p< 0.05). Of interest, this was associated with a decrease of callus VEGF and PCNA expression. After 5 weeks of fracture healing, however, the negative impact of RAPA on fracture healing was found blunted and the radiological, histomorphometric and biomechanical differences observed after 2 weeks could not longer be detected.
We demonstrate that RAPA treatment leads to a severe alteration of early fracture healing. The negative action of RAPA on fracture repair at 2 weeks is most probably due to an inhibition of VEGF expression within the callus as suggested by the results of the Western blot analysis, demonstrating during the early phase of fracture healing a significantly reduced expression of VEGF and PCNA after RAPA treatment. This indicates a substantial alteration of cell proliferation and angiogenic vascularization during initial fracture healing. Since T-cells contribute to delayed fracture healing, RAPA may promote bone healing at later stages due to a reduction of interleukin-2-stimulated Tcell division.
A variety of scaffolds, including collagen-based membranes, fleeces and gels are seeded with osteoblasts and applied for the regeneration of bone defects. However, different materials yield different outcomes, despite the fact that they are generated from the same matrix protein, i.e. type I collagen. Recently we showed that in fibroblasts MMP-3 is induced upon attachment to matrix proteins in the presence of TGFbeta.
The reconstruction of bone defects with biomaterials represents a potential alternative to the transplantation of autologous and allogenic bone. Ceramic materials can be combined with growth factors (i.e. BMPs) to render them osteoinductive. Coating of biomaterials with growth factors has mostly been attempted by adsorption onto the material’s surface. The superficial deposition usually results in an immediate passive release of the proteins, thus restricting their temporal availability during bone healing. It was hypothesized that a co-precipitation of proteins onto calcium phosphate ceramics may provide the possibility to achieve a prolonged release of proteins from the material without impairing the biologic activity of growth factors.
Tritium labelled bovine serum albumin ([3H]BSA) and recombinant human BMP2 (rhBMP2) were coated onto biphasic calcium phosphate (BCP) ceramics using a coprecipitation technique of proteins together with calcium phosphate (Liu Y et al. 2001). The co-precipitation was compared to conventional adsorption of proteins to ceramic materials. The passive and cell-mediated release of [3H]BSA was investigated during 19 days. To analyze the cell-mediated protein release, murine bone marrow cells were seeded onto ceramics and differentiated to osteoclasts or to monocytes/macrophages. To assess whether rhBMP2 co-precipitated to BCP ceramics retained its biologic activity the growth factor’s ability to induce the differentiation of primary murine osteoblasts was studied.
After 19 days 71.7±5.3% of the adsorbed [3H]BSA was passively released (63.0±6.0% within 4 days). The passive liberation of [3H]BSA was effectively reduced using the coprecipitation technique (12.5±2.0% within 19 days, 10.1±2.3% within 4 days, p< 0.001). Further analysis demonstrated a sustained, osteoclast-mediated release of coprecipitated [3H]BSA from calcium phosphate ceramics which was blocked by the addition of calcitonin. Passive release of adsorbed and co-precipitated BMP2 led to a temporally restricted stimulation of murine osteoblasts. Cell-mediated liberation of co-precipitated BMP2 induced a sustained stimulation of the differentiation of osteoblasts.
The successful application of exogenously added growth factors depends critically on the mode of delivery. It has been shown that a sustained availability of BMP2 is beneficial for bone healing. Application of the co-precipitation technique resulted in a long-term release of proteins from BCP ceramics mediated by active resorbing osteoclasts without impairing the biologic activity of rhBMP2. Co-precipitating growth factors onto BCP ceramics provides a potential to shift the initial extensive liberation to a sustained release of bioactive proteins. This method of protein delivery may represent a possibility to achieve a more physiological availability of growth factors during bone regeneration.
Meniscal samples were processed for histology, immunohistochemistry and in situ hybridization, for assessment of cell density, cells actively dividing as well as apoptotic cells, distribution of COMP and estimate the proteoglycan content.
The main mode of failure of the acetabular component in total hip arthroplasty is aseptic loosening. Successive generations of cementation techniques have evolved to alleviate this problem.
This paper evaluates one such method, Negative Pressure Intrusion cementation. Two groups of machined bovine cancellous bone samples were created; experimental (n = 26) and control (n = 26). The experimental group was cemented using the negative pressure technique and control group was cemented in the absence of negative pressure. The relative cement intrusion depths were then assessed for each group using MicroCT. These samples were then further machined and tested to failure in torsion to estimate their mechanical properties.
Results show mean cement intrusion depth for the negative pressure group to be 8676μm and 6042 μm for the control group (p = 0.078). Mechanical testing also revealed a greater mean torque in the negative pressure group (1.6223Nm vs 1.2063Nm) (p = 0.095).
This work quantifies the effect of negative intra-osseous pressure on cement intrusion depth in cancellous bone and for the first time relates this to increased mechanical strength.
Physeal cartilage is known to have poor self-repair capacity after injury. Evaluation of the ability of cultured mesenchymal stem cells to repair damaged physis is the actual research topics. In 10 immature New Zealand white rabbits autogenous mesenchymal stem cells were transplanted into iatrogenic physeal defect in lateral portion of distal growth plate of the right femur. The same defect without stem cells transplantation in the left femoral distal physis served as a control. In our study, we used our own technique of implantation of MSCs with a newly modified gel scaffold (New Composite Hyaluronate/Collagen Type I/Fibrin Scaffold). The rabbits were euthanized 4 months after transplantation. Bone length discrepancy and valgus deformity were measured from femoral radiographs. Healing of the defect was investigated histologically. The ability of mesenchymal stem cells to survive and promote cartilage healing in the physeal defect was assessed by immunofluorescence. Average difference in femur length measured from surgery to euthanasia (4 months) was 0.61? 0.19 cm after preventive transplantation of MSCs in right femur, but only 0.11 ? 0.07 cm in left femur. Average angular (valgus) deformity of right femur with MSCs preventively transplanted to iatrogenically damaged distal femoral physis was 1.2? 0.72°. Valgus deformity in left femur was 5.4? 2.5°. Prophylactic transplantation of autogenous mesenchymal stem cells to iatrogenically damaged distal growth plate of rabbit femur prevented bone bridge formation and resulted in healing of the physeal defect with hyaline cartilage. Immunofluorescence examination showed that the chondrocytes newly formed in growth zone are the result of implanted MSCs differentiation. Femur growth in traumatized physis was maintained even after transplantation of autogenous MSCs. As compared with the opposite femur (with physeal defect but without transplanted MSCs), the bone showed no significant shortening or valgus deformity (p=0.018).
The torsion testing in Ibandronate had 51% greater toughness than placebo and 69% greater than the non-OVX group. Ibandronate increased trabecular number significantly over the placebo and was not significantly different from the non-OVX group. Trabecular separation was less in Ibandronate compared to the placebo group. Volume in the trabecular neck increased by 35% for the Ibandronate over the placebo.
For patients where curative surgery was an option, primary wide local excision (15 patients) or primary amputation (2 patients) was performed. The remaining 2 patients presented with unresectable disease due to the location and localised spread; an embolisation was performed for palliation in both cases. Revision surgery was needed in 9 patients for either a positive resection margin confirmed by histology, or a recurrence; these included 3 secondary amputations. A histologically proven recurrence occurred in 6 patients after an average of 15.8 (4 to 41) months. Local adjuvant radiotherapy was administered to 7 patients and a combination of radio–and chemotherapy was used in 2 patients for metastases. Mortality was 53% (9 patients) by the end of 36 months follow-up period.
Results: EndoTAG-1® treatment of AIA mice with developing or in established disease showed a strong attenuation of the course of the disease as well as a potent anti-inflammatory effect. Histological analysis of knee sections demonstrated a dramatic reduction of the pannus and infiltration of inflammatory cells. Enrichment of EndoTAG at the synovial vasculature of AIA mice was observed when compared with healthy mice. Treatment of AIA mice with EndoTAG-1® concomitant to disease induction showed a complete remission of the course of the disease as shown by a significant decrease of clinical scores compared to both control and Taxol® treated groups. A complete inhibition (98%) of neo-vascularisation was observed in the synovial vasculature of mice with AIA that were treated with EndoTAG-1® whereas Taxol® alone showed only 50% inhibitory effect. Rolling and adhesion of platelets were reduced to 53% (paclitaxel 5%) and 98% (paclitaxel 57%), respectively.
Conventional: UHMWPE gamma sterilized in inert, SXL: sequentially irradiated and annealed UHMWPE irradiated to a cumulative dose of 100kGy (33 kGy irradiation + 8 hour annealing in air, repeated 3 times) and gas plasma sterilized, and E-Poly: UHMWPE irradiated to 100kGy, stabilized with α-tocopherol, and gamma sterilized in inert.
Four specimens from each group were subjected to a reciprocating mechanical stress of 10 MPa at a frequency of 0.5 Hz in an environmental chamber maintained at 80°C. Control samples were placed in the chamber but not subjected to cyclic mechanical stress. When a visible crack was observed on a sample’s surface or when a sample fractured, it and its corresponding control sample were analyzed by FTIR to quantify oxidation.
Fibula autograft reconstruction, both vascularised (v) and non-vascularised (nv), has been established as a standard method in limb salvage surgery of bone and soft tissue tumours of the extremities. This study retrospectively analyses the results of fibula autograft procedures in general and in relation to vascular reconstruction or simple bone grafting.
Since the implementation of the Vienna Tumour Registry in 1969, 26 vascularised and 27 non-vascularised fibula transfers have been performed at our institution in 53 patients, 26 males and 27 females with an average age of 21 years (range 4 to 62 years). Indications included osteosarcoma in 18, Ewing’s Sarcoma in 15, adamantinoma in 5, leiomyosarcoma in 3 and others in 12. Thirty patients were operated for reconstruction of the tibia (8v/22 nv), 7 for the femur (6v/1nv), 7 for defects of the forearm (4v/3nv), 5 for metarsal defects (all v), 3 for the humerus (1v/2nv) and one patient was treated for a pelvic defect (nv).
Average follow-up was 63 months (range 2 to 259 months). 43 patients showed successful primary bony union of the autograft. In 12 cases pseudarthrosis indicated further surgical revision, 9 of these patients were primarily reconstructed by use of a nv autograft. 4 patients, 2 with v and 2 with nv reconstruction, suffered a fracture of the transplant and were operated for secondary osteosynthesis. 10 patients with v bone graft developed wound healing disturbances which led to surgery, 2 patients with nv grafts suffered such complications. In 2 patients recurrent infection of a nv and a v fibula transfer led to the implantation of a modular tumour prostheses or amputation, retrospectively. Function of all patients with primary bone healing was rated satisfactory.
The use of fibula autograft in limb-salvage surgery under oncological conditions allows biological reconstruction with good functional outcome, especially when primary bone healing is achieved. Vascularised bone grafting seems to have a better outcome in terms of primary bone healing than simple fibula bone grafting, and thus represents a feasible choice in the reconstruction of bone defects from tumour resection.
The study was designed to assess the reproducibility and reliability of Mirels scoring system and the conventional scoring system for impending pathological fractures. The results of both classification systems influence the choice of therapeutic procedures offered to these patients.
Blinded plain antero-posterior radiographs from forty-seven patients with bone metastases were scored by eight independent observers (four orthopaedic surgeons and four radiologists with varying clinical experience). Each observer scored the radiographs as per the Mirels and the conventional systems. After twelve weeks, the radiographs were scored again by the same observers. Inter– and intra-observer agreement was assessed based on the weighted kappa coefficient values for both systems.
For intra-observer reproducibility, kappa values for the conventional system had a mean of 0.495 (SD 0.12) showing a moderate agreement, while Mirels scoring system had a mean of 0.386 (SD 0.143) showing a fair agreement. For inter-observer reliability, kappa values for the conventional scoring system were 0.322 for the first test and 0.47 for the second test giving fair and moderate agreements respectively. For Mirels’ scoring system, kappa coefficient for inter-observer reliability was 0.183 for the first test and 0.218 for the second giving poor and fair agreements respectively.
The conventional scoring system showed a better inter and intra-observer agreement compared to Mirels’ scoring system. Consultants had a better intra-observer agreement compared to their registrars. We also found that radiologists, in our study, had better intra-observer agreement compared to orthopaedic surgeons. Radiographs should be scored cautiously by experienced doctors in a multi-disciplinary setting to achieve the best decision of whether to proceed with a prophylactic surgery or not.
Purpose of this paper was to review the Rizzoli experience in prosthetic reconstruction of the knee after resection of bone tumors with special attention to major complications and functional outcome.
Since abrupt data could be misleading due to the oncologic population and related deaths (although 2/3 of the patients were cured or long survivors), to censore the implant unrelated events a statistical analysis of the implant survival was performed and Kaplan-Meyer curves of implant survival were studied.
In 543 HMRS prostheses major complications were infection 8%, stem breakage 2%, aseptic loosening 4%, while revision for polyethylene wear components rated 7.4%.
Techniques of revisions were analyzed, as well as the outcome of revised cases, which showed that about 2/3 of the patients treated for major complications do well, although the risk for further complications is significantly incresed in revised implants.
Discussion: The reduction of major complication rate with the newer designs of the modular prosthesis was statistically significant and this seems to confirm that newer materials and a modified stem design positively affected the implant survival. Also the wear of polyethylene component was dramatically decreased in the newer prosthetic design. Functional results were satisfactory in most of the patients that did not experience major complications, with a trend to improvement in the newer design. Revision surgery is technically demanding and sometimes newer ‘hybrid’ techniques are suggested, implying the use of bone allografts.
Appropriate timing of revisions is crucial. An early treatment of complications can improve the final outcome.
The 38 procedures were identified from September 1995 to June 2007 and included 17 distal femoral replacements, 12 proximal femoral replacements, 4 proximal humeral replacements, 2 distal humeral replacements, 2 hemi-pelvic replacements and 1 total femoral replacement. EPR survivorship was calculated using a Kaplan-Meier survival curve. The quality of patients’ mobility and performance of activities of daily living was used to assess functional outcome.
87.4% of patients who underwent a lower limb EPR achieved a satisfactory or very satisfactory functional outcome. 100% of patients achieved a satisfactory or very satisfactory functional outcome in the upper limb EPR group.
3 implants failed, 2 as a result of infection and required staged revisions, 1 eventually requiring amputation, and 1 failed as a result of aseptic loosening. 2 patients dislocated their proximal femoral replacements, both were treated successfully by closed reduction. Despite the salvage surgery subsequent amputation was only required in one patient.
Ewing’s sarcoma family tumors (ESFT) express the EWS-FLI1 fusion gene generated by the chromosomal translocation t(11;22)(q24;q12). Expression of the EWS-FLI-1 fusion protein in a permissive cellular environment is believed to play a key role in ESFT pathogenesis. However, EWS-FLI1 induces growth arrest or apoptosis in differentiated primary cells and the identity of permissive primary human cells that can support its expression and function has until now remained elusive. Here we show that expression of EWS-FLI1 in primary human mesenchymal stem cells (hMSC) is not only stably maintained without inhibiting proliferation, but that it induces a gene expression profile bearing striking similarity to that of ESFT, including genes that are among the highest ESFT discriminators.
Expression of EWS-FLI-1 in MSCs may recapitulate the initial steps of Ewing’s sarcoma development, allowing identification of genes that play an important role early in its pathogenesis. These observations are consistent with our recent findings using mouse mesenchymal progenitor cells and provide compelling evidence that hMSCs are candidate cells of origin of ESFT.
We prospectively assessed a consecutive series of patients undergoing MTPJ arthroplasty with the MOJE prosthesis. All patients entered into the study were assessed preoperatively with the AOFAS 100-point Hallux Meta-tarsophalangeal-Interphalangeal Joint Scale and the range of motion was recorded. Patients were assessed on table postoperatively for range of motion (ROM) and then at 3, 12 and 24 months with AOFAS scores and ROM.
Forty-two toes (40 patients) were recruited into the study. There were 24 women and 16 men. The mean patient age on the day of surgery was 59 (range 37 to 73). 18 operations were carried out on the left hallux and 24 on the right. All operations were carried out for a diagnosis of hallux rigidus (although one patient also had hallux valgus, with an intermetatarsal angle of 24° and a hallux valgus angle of 40°).
The mean pre-op AOFAS score increased from 36.0 to 82.2 at 3 months (p< 0.001) and was 87.0 at 12 months and 84.2 at 24 months. There was no significant change in scores from 3 months onwards. Only 2 patients had a follow-up of 36 months; both of them had AOFAS scores of 95.
The mean arc of motion reduced from 70.8° on-table to 33.3° by 24 months (p< 0.001). The difference in arc of motion from 3 months to 12 months was a decrease from 45.6 to 40.0 which was borderline significant.
In 4 radiographs there was evidence of progressive loosening (figure 4). This was at 24 months in all 4 cases. For 3 of the patients the AOFAS score was 85. For the 4th patient the AOFAS score was 65
One patient had a spontaneous fusion of the toe. There were also three episodes of wound breakdown, one patient had intra-operative division of the EHL tendon that was repaired. We also noted post-operatively that: three feet developed Morton’s neuromata; one patient developed tarsometatarsal joint osteoarthritis of the great toe, one sesamoid osteoarthritis and one plantar fasciitis.
At the most recent follow-up appointment 33 out of 40 patients (82.5%) were satisfied with the results of their operation, 2 were dissatisfied (5%) and results regarding satisfaction were not available for 5 patients.
The results obtained in this paper demonstrate good, prospective, short-term results with the press-fit zirconium ceramic Moje implant. We believe that in the correct patient group good short term results can be achieved in the treatment of 1st MTPJ osteoarthritis as an alternative to fusion, particularly in those patients who are unwilling to have permanent stiffness in this joint for cosmetic or functional reasons
Fractures were Classified based on the Weber’s system. Pre-operative medial clear space measurement was done by 2 independent observer using PACS measurement tool. Intraoperative details for the method of fixation and the medial soft tissue were analysed.
Most common method of fixation is Neutralisation plate for the lateral side. In Weber B type 1/3 rd of the cases had both plate on the lateral side and syndesmotic screw fixation. 2/3rd of them had only plate fixation.
In Webers C type, only syndesmotic screw in n=3, Plate and screw n=4, only plate in n=9 cases
Radiological measurement of medial clear space average = 9.08mm, range= 5 –22 mm Less than 50% of the patients only had medial clinical signs. 26.6% had soft tissue (periosteal injury) and only 6.6% had deltoid ligament injury Out come assessment criterias: The failure of fixation or any on going medial symptoms in group A. – one case of failure of fixation. Final clinical assessment with ankle score (Olerud and Molander score.) at 6 months average (between 3–18 months). No significant difference in the score, on follow up.
Medial clear space does not correlate with any degree of medial soft tissue injury. Exploration is indicated if widening persist after lateral side fixation. Routine exploration of the medial side has no long term impact on the clinical outcome.
if subjects with medial tibial stress syndrome demonstrate increased navicular drop and medial longitudinal-arch deformation during quiet standing and gait compared to healthy subjects, the relationship between medial longitudinal-arch deformation during quiet standing and gait.
Distal tibial bone loss involving the ankle is a devastating injury with few options for reconstruction. The purpose of our study was to look at the long term results of ilizarov technique used to achieve lengthening of tibia and fusion at the ankle.
17 cases (16 post traumatic and one post tumor resection) admitted to one institution between 1994 and 2003. 13 cases were done in bifocal and four in trifocal mode.
The duration of follow up was 12 to 84 months The average age was 33 years (Range 7–71). The mean length of the defect was 4.5 cm (Range 1–12).
Union of the fusion site occurred in 88% (15/17) of the patients with mean duration to docking and union being 8 months. The mean time in fixator was 13 months (Range 5 to 29).
Average number of surgeries per patient was 3.2. Five patients required free vascularised grafts before the index procedure and 4 patients required realignment at the docking site. Functional results – Fourteen (77.5%) of the patients could walk without support or bracing and twelve patients (71%) returned to same or modified occupation.
Complications – Two non-union.
Deformity – Fusion site equinus deformity occurred with non union after re-fracture in one case. There were 2 cases of residual fore-foot equinus.
Residual low grade infection with discharging sinus was present in two patients. One patient needed change of wires for Pin tract infection.
Our study showed 76% good and excellent scores on functional scoring but also demonstrates the high morbidity associated with this procedure. In spite of the steep learning curve and high complication rates the procedure can be undertaken in specialised centers for highly motivated patients to achieve good functional results.
Between January 1996 and December 2006, 130 patients were operated on for acquired varus equinus foot deformity. The most frequent aetiologies were stroke or brain damage due to head trauma. The primary indications for surgery included pain, caused by pressure of the foot or toes on the floor or in shoes, ankle instability due to varus deformity, or difficulty wearing orthopaedic shoes or braces. Split anterior tibial transfer was generally done after lengthening of Achillis tendon and tenotomy of long and short toe flexors during the same session. The author did compare preoperative and postoperative autonomy, and shoe or orthosis requirements. The results of this study include significant improvement in patient autonomy demonstrated by an improved ability to ambulate independently and a decreased need to wear orthopedic shoes and orthoses, as well as an increased ability to wear normal shoes, or the ability to ambulate bare foot. Adequate knee flexion during swing phase of the stride was the best indicator for better result. This procedure is safe and yields good results with minimal complications. The indications are very common, inasmuch as the number of young hemiplegic patients surviving after a stroke or head injury is increasing. This procedure can result in definite improvement for these disabled patients and can increase their autonomy.
From Jul 1999 to Jan.2006 77 patients were treated according to the above technique.
5 revisions were performed; 2 for stiffness (1 tibial component, 1 insert), 2 for stress fractures (tibial component only) and 1 insert fracture. 3 of these cases required further surgery following their first revision (1 fusion for deep infection, 1 insert exchange for edge loading and one arthoscopic debridement plus calcaneal osteotomy for painful varus deformity).
There were no primary revisions for aseptic loosening or deep infection. 3 radiographs demonstrated non-progressive lucent lines behind the tibial component.
Further surgery was required in 8 other ankles (6 calcaneal osteotomies and 2 arthroscopic debridements). Complete correction of pre-operative deformity was ultimately achieved in all but 4 ankles.
The mean postoperative American Orthopaedic Foot and Ankle Society Score was 77.
Protocol 1: 6 weeks NWB, 3 weeks partial weight bearing (PWB), 3 weeks FWB in plaster. Protocol 2: 2 weeks NWB, 4 weeks PWB, 6 weeks FWB in plaster.
The advantages of this technique over single K wire are:
Less post operative complications like pain and pin tract infection. Achieving normal biomechanics of the foot by fixing the PIP joint at 15–20 degrees of flexion. Using two K wires gives more rotational stability of the toes and reduces the complications of over riding, under riding and hyperextension of the toes. 15–20 degrees flexion at PIP joint will give good digital purchase and push off in stance phase. As the K wire engages the cortex of proximal phalanx, there is almost negligible chance of loosening of K wires which is a common problem in large single K wire which usually is driven in to the medullary cavity of proximal phalanx.
Objective parameters of AOFAS scale like adduction/ abduction, flexion, rotational deformities are significantly less with two wire fusions compared with single wire procedures (Coughlin et al). Radiological analysis of the foot showed that 97% had bony union compared 81% with single pin, and only 3% had fibrous union compared to 19% with single wire. Both the procedures didn’t have any non-unions. Only one patient had superficial wound infection, and surprisingly none had pin tract infection.
The long term results of Total Ankle Arthroplasty still remain largely unsatisfactory and Ankle Arthrodesis remains the gold standard treatment for severe degenerative ankle joint disease resulting from trauma and other causes. We describe the method and results of ankle fusion performed with a single anterior midline incision using the standard AO T-Plate.
18 patients underwent fusion of the tibio-talar joint with this technique over the past 5 years with a follow up range of 10 months to 5 years (mean-19 months). Though the commonest indication was post-traumatic degenerative joint disease (this included 6 patients who had previous internal fixation), other causes included primary osteoarthritis, rheumatoid arthritis, neuro-pathic joint (Charcot’s) and failed arthrodesis with other
There was radiological union in all 18 patients. Excellent clinical results were finally achieved in 16 (89%). Complications included persistent pain(1), delayed union(2), infection(2, including one deep) and 2 under-went removal of plate with good final result.
This technique is a modification of that described previously by Rowan and Davey. In our practice the plate is contoured to the surface of talus and the distal screws are directed more vertically towards the sustenaculum talus. We found it helpful to obtain more compression of adjacent surfaces.
With the use of an anterior T-plate not only a better stability in biomechanical terms is achieved, less dissection and better soft tissue cover of the metalwork help in overall patient satisfaction. Though we have performed ankle arthrodesis with different
Hallux varus is a rare cause of pain in the foot mostly occurring after failed hallux valgus surgery. We reviewed 12 patients with unilateral hallux varus treated with soft tissue techniques (4x), arthrodesis of the first metatarso-phalangeal joint (3x) or with a distal chevron osteotomy (5x) with medial transposition of the first metatarsal head and reconstruction of the soft tissues on the lateral side of the metatarsophalangeal joint. 10 patients had previous hallux valgus surgery, in 2 cases the deformities were of unknown origin. 1 male and 11 female patients were followed up on average 26.4 months postoperatively. AOFAS hallux score improved from 46 (range 10–75) to 86 (range 72–95) points. The metatarsophalangeal angle measured with the center-head to center-base method was reduced from −16.1° (range −35° to −8°) to 5.1° (range −15° to 21°). The intermetatarsal angle increased from 5.8° (0–11°) t o 10.5° (0–19°). All patients were subjectively satisfied with the procedure. Our results indicate that joint preserving operation techniques are viable methods in the correction of mild and moderate symptomatic hallux varus deformities. Mild remaining varus deformities are well tolerated.
In case of severe varus deformity or major signs of osteoarthritis in the first metatarsophalangeal joint MTP arthrodesis provides good results.
Twenty-five Regnauld’s procedures were performed in 20 patients with painful hallux valgus. This procedure involves the removal of proximal one-third of the proximal phalanx which is fashioned into a ‘hat-shaped graft’ and replaced as an osteochondral autogenous graft. The average age at operation was 56 years (range 39–76). After a mean follow-up of 3 years, 4 months (range 2.5–5.7 years), all the patients were assessed clinically and radiologically. The mean hallux valgus angle preoperatively was 29.3° (range 20–50°). At follow-up, a mean correction of 16.9° was obtained. In our study, 92% of patients were satisfied with the operation, but 8 patients (40%) showed progression of osteoarthritis of the first metatarsophalangeal joint. At 10 year follow up all these patient are satisfied with procedure and doing well. In view of the high incidence of degenerative changes in the first metatarsophalangeal joint, this procedure should be reserved for those patients over the age of 65 years or those with early osteoarthritic changes in the first metatarsophalangeal joint.
Between October 2006 and September 2007, eight consecutive patients with syndesmotic diastasis of the ankle had Tight Rope suture –endobutton fixation. We present our early results following this fixation. There were 3 males and 5 females with a mean age of 42 years (range 21 – 67). All were followed up for a mean of 7 months. Five patients had right side involvement. Majority were twisting injuries. These patients were compared with a cohort group (10 patients) who had diastasis screw fixation for similar fractures during the same period.
We recommend the use of this new suture endobutton fixation for ankle diastasis with promising early functional results. Further prospective studies are needed to evaluate this new type of fixation device.
Hallux rigidus is a common condition involving the first Metatarsophalyngeal (MTP) joint. Total joint arthroplasty is an acceptable modality of treatment. A number of different prosthesis have been used. Our study aims to evaluate the outcome of uncemented ceramic on ceramic (MOJE) prosthesis, in the treatment of painful hallux rigidus.
Between March 2000 and June 2005, 38 patients (53 feet) with painful hallux rigidus were treated with uncemented ceramic on ceramic (MOJE) prosthesis. There were 30 female and 8 male patients. The hallux meta-tarsophalangeal-interphalangeal scoring scale, by the American Orthopaedic Foot and Ankle Society, was used to assess these patients, pre-operatively and at follow up. A total score of 100 is possible in a patient with no pain, full range of MTP joint movement and good alignment.
The average follow up was for 34 months (range 12–68 months). Three revisions were carried out in three patients, 2 for deep infection, and 2 for persisting pain. Five patients showed radiological signs of osteolysis but had no symptoms. There was one late subluxation after 32 months. One patient developed a superficial infection, which was treated successfully.
The average AOFAS score pre-operatively was 45, compared to 91 post-operatively (p< 0.05). 23 patients (36 feet) classed the outcome as excellent to good. Ten of the patients subjectively described the out come of the procedure as excellent.
The preop range of movement (combined dorsiflex-ion and plantarflexion) was improved from a mean of 22 degrees to 68 degrees postoperatively.
The ceramic/ceramic (MOJE) total arthroplasty gave excellent results in 77% of patients. The early outcome is encouraging. We ewcommend continued use of this prosthesis for painful hallux rigidus.
This study assesses the pre and post-operative pedal pressures during stance phase of dynamic gait cycle to identify objective biomechanical factors which influence the final outcome.
Pedobarography was performed before and 8 months after surgery, on an average. Sole was divided into eight segments i.e. heel, midfoot, lateral forefoot, central forefoot, medial forefoot, II–V toes, hallux and total sole area. Variables compared were contact area, peak pressure, mean pressure and contact time. Manchester-Oxford foot questionnaire (MOXFQ) was used to assess the clinical disability. The inter-metatarsal and metatarso-phalengeal angles were measured radiographically. Both clinical and radiological assessments were performed pre and post-operatively.
The inter-metatarsal angle reduced from 15 to 7 (p 0.001) and the metatarso-phalengeal angle reduced from 32 to 9 (p 0.001).
There was significant reduction in heel contact area (p 0.002), the medial forefoot (p 0.030) and II – V toes (p 0.048) contact time.
We prospectively enrolled and evaluated 30 patients with unilateral or bilateral hallux valgus. At the time of our preliminary follow-up, 8 patients (14 feet) with unilateral or bilateral hallux valgus who had either a Scarf or a combined Scarf-Akin procedure from June 2006 to December 2006 were evaluated. Three surgeons practicing within one practice performed the procedures. Exclusion criteria for this study included concomitant forefoot pathology, such as hammertoes, clawtoes, and transfer metatarsalgia, which required concomitant surgery. We also excluded patients with excessive first ray instability which would have required 1st metatarsal-cuneiform fusion. The average age of the patients at surgery was 37.8 years (range, 14–76 years).
Average follow-up time was 6.5 months. Four of the eight patients (8/14 feet) required an Akin osteotomy in addition to the Scarf procedure. Patients showed an average improvement of AOFAS score from 65.7 to 86.3. The ACFAS 1st ray score improved from 63.2 to 86.8. The intermetatarsal and hallux valgus angles improved from mean pre-operative values of 14.3° and 25.9° to 9.5° and 10.2°, respectively. Similarly, the 1st metatarsal declination angle also improved from a mean of 38.7° pre-operatively to 20.9° post–operatively. There was no significant change in first metatarsal dorsiflexion before and after surgery (64.5 to 68.7). Pre op and post op plantarflexion was also assessed. The mean hallux plantarflexion remained virtually identical at 11.3 degrees of motion. Pedobarographic analysis showed medialization of peak plantar pressure following surgery. Peak plantar pressure increased under the hallux (Increasing from 91.5 kPa to 144.6 kPa) and first metatarsal while decreasing under the 2nd, 3rd, 4th, and 5th metatarsals following surgery. Average time to return to work and to activities of daily living were 2.6 weeks and 3 weeks respectively.
We conclude that the Scarf osteotomy and Akin closing wedge osteotomy of the proximal phalanx of the great toe appear to be safe and effective for the treatment of hallux valgus and restoration of normal forefoot pressure. Our data suggest the Scarf osteotomy normalizes the function of the hallux during the propulsive phase of the gait cycle. This was reflected in the increased peak pressure under the first metatarsal head and the reduction of peak pressure under the second metatarsal head. We have found pedobarography to be useful as a pre-operative tool and to assess outcomes in forefoot surgery.
Many studies have evaluated bilateral versus unilateral surgery in large joints, however, limited research is available to compare outcomes of bilateral-staged foot surgeries versus synchronous-bilateral foot surgery. 186 consecutive cases of first metatarsophalangeal joint surgery were prospectively included in this study; 252 procedures were performed: 120 were unilateral or staged-bilateral, and 66 were synchronous-bilateral operations. Patients were evaluated at 6–and 12-weeks for specific early complications, and surveyed about there return to work, activities of daily living, shoe gear requirements, satisfaction, and reasons for choosing staged or synchronous surgery. Additionally, a cost analysis was performed on all surgical scenarios. Student-t test showed no statistical significance between groups in all clinical settings to a 95% confidence level. Complication rates were similar and few in all situations. Patients were very satisfied when choosing bilateral-synchronous surgery and would elect to repeat it the same way 97% of the time. The economic costs to the health system average 25% greater when patients undergoing first metatarsophalangeal joint surgery have the procedure performed one foot at a time. Combined with the time lost from work, this reveals a significant economic cost to both society and patient.
The remainders (10 patients) had a delayed reloading on the lower limb.
In this study the clinical and radiological results of the fracture group were compared to those of a control group of 15 patients.
Postoperative complication rate (deep venous thrombosis, infection, dislocation) were not different between the groups.
There was a significant increase of duration of the stay of the patient in the rehabilitation center (p=0.007) in the fracture group and the patient spend more time with the physiotherapist (p=0.001)as they left the center.
The fracture rate was lower when the patients were operated by a senior surgeon (p=0.021).
One of the best procedures to prevent haemarthrosis in haemophilia has been radioactive synovectomy (synoviorthesis). Since the first report of radioactive synovectomy in haemophilia of Ahlberg in 1971, (7) many centers adopted this procedure as the one of choice to, through fibrosing the synovial membrane, prevent further haemarthrosis.
Since 1976 we have performed 119 such radioactive synoviorthesis in 110 patients with age from 3 to 40 years with a mean of 10 years of age, 71 of these patients were under 12 years of age. The knees were injected in 71 cases, elbow in 29 cases, ankles in 16 and shoulders in 3 cases. The clinical results of this procedure gives an 80% of excellent results with no further bleeding. In case of failure a new injection can be given in the same joint at a 6 month interval, or an injection for the same purpose in other joint. One of the criticisms against this method is the possible chromosomal damage induced by the radioactive material.
In our center, 4 studies have been made in order to see whether these changes, in case of appearance, are everlasting and all have demonstrated that chromosomal changes are reversible. The radioactive material used in the 2 first studies was 189 Au. In 1978, 354 metaphases were studied with 61 ruptures, 17.23%, (non premalign) and 6 structural changes -considered premalign-, 1.69%. Any number below 2% is considered non dangerous. A further study was done in 1982, in the same group of patients with a result of 21 ruptures, 3.34% and
Rivaroxaban is a novel, oral, once-daily, direct Factor Xa inhibitor in advanced development for the prevention and treatment of venous thromboembolism (VTE). This study analysed the potential economic benefit attributable to the use of oral rivaroxaban relative to subcutaneous enoxaparin for extended VTE prophylaxis (35±4 days) after total hip replacement (THR). In RECORD1, rivaroxaban reduced the incidence of the composite primary efficacy endpoint (total VTE, including all-cause mortality) by 70%, compared with enoxaparin (p< 0.001). Symptomatic VTE occurred in 0.3% and 0.5% (p=0.22) of patients receiving rivaroxaban and enoxaparin, respectively. Major bleeding was low and similar in both groups: 0.3% and 0.1% (p=0.18), respectively.
Potential savings associated with oral rivaroxaban were based on any reduction in the incidence of symptomatic VTE events, and reduced administration and monitoring costs. Analyses for both the US and the UK included only non-drug costs incurred by the healthcare sector. It was assumed that nurses spent 3 minutes/day administering enoxaparin and training patients to self-inject; assumed duration of hospital stay was 5 days. UK costs (based on the 2007 NICE Guidelines) also included full blood counts (FBCs) every 3 days, for up to 14 days, in patients receiving enoxaparin.
Two analyses were performed: one assumed no difference in the occurrence of symptomatic VTE between treatments; the other assumed that the observed difference was real, but did not reach statistical significance.
In the first analysis, assuming no difference in symptomatic VTE incidence, the total resource cost in the US was $46/patient for enoxaparin and $42.5/patient for rivaroxaban: a saving of $3.5/patient. For the UK, the total resource cost was £33/patient for enoxaparin and £7.5/per patient for rivaroxaban: a saving of £25.5/ patient. Savings were driven by reduced monitoring (FBCs) and administration costs.
In the second analysis, assuming the observed difference in symptomatic VTE incidence was real, the US total resource cost was $57/patient for enoxaparin and $42.5/patient for rivaroxaban: a saving of $14.5/patient. For the UK, the total resource cost was £30/patients for enoxaparin and £7.5/patient for rivaroxaban: a saving of £22.5/patient. Savings were again driven by reduced monitoring and administration costs, and also reduced VTE incidence.
Over 400,000 US patients undergo THR, and ~60,000 patients in England and Wales undergo THR annually. Thus, the potential cumulative cost savings with rivaroxaban are considerable.
Recent changes in health care policy relating to pre hospital triage and closure of acute services in district general hospitals have placed unanticipated strains on financially challenged larger trusts in London. The financial implications for the presumed ‘designated’ regional trauma centre have previously not been scrutinised. Our study investigates how these changes and the resultant ‘out of area’ trauma has impacted on workload at our London teaching hospital and looks at the financial implications for the Trauma and Orthopaedics department.
A retrospective analysis of all attendances to the A& E department over a four month period (July – October) in 2006 was compared to a similar period in 2005. All admitted, major orthopaedic trauma cases bought in by ambulance or HEMS services were included. Review of case notes and phone interviews were used to ascertain how many of the incidents had occurred outside our region of referral.
An 83% increase in major trauma admissions was observed (32 cases in 2005, 53 cases in 2006; P value = 0.03). Of these cases, 27/32 and 46/53 could be assessed. Two patients in 2005 (7%) and twelve patients in 2006 (26%) were out of area (P value = 0.07). As these patients were bought in as ‘local’ cases, and not as regional referrals for treatment, the Trust was not reimbursed appropriately. Fiscal analysis of the out of area trauma cases was carried out to ascertain the shortfall incurred by the department.
This study surveys our patients to determine their experiences at airport security, establishes the detectability of common orthopaedic implants in an airport security scanner
A volunteer with metal implants strapped on and patients with implants in-situ walked through a gate scanner at a UK airport. Also, standard operating procedures at UK airports were ascertained.
There were 111 total knee replacements (TKR), 20 unicompartmental knee replacements (UKR), 2 bilateral UKR replacements, 17 bilateral TKR.
Unlike previous studies from the U.K., virtually all patients with a TKR activated the gate scanner. Conversely, those with unicompartmental replacements did not.
Patients are concerned about this possibility but are not informed at time of surgery and do not know what the procedures are if their implant is detected.
The patient with the bilateral UKR did not set off the scanners where as the patient with the TKR did.
A variety of surprisingly large trauma implants escaped detection.
Mechanical prophylaxis with foot-pumps provides an interesting alternative to chemical agents in the prevention of thomboembolic disease following major orthopaedic surgery procedures. Recent studies have suggested that simultaneous use of graduated compression stockings (GCS) may hinder the pneumatic compression effect of foot pumps. The hypothesis of this prospective study was that the use of foot-pumps without GCS does not affect the efficacy of DVT prophylaxis, and improves patient compliance. 846 consecutive patients admitted at a single institution undergoing total hip (THR) or knee replacement (TKR) were included in the study. The A-V Impulse System® foot-pump units (Orthofix Vascular Novamedix, Andover, UK) was used in all patients. Forty-six patients discontinued the use of foot-pumps, leaving 400 patients who received foot-pumps in combination with GCS and 400 patients with foot pumps alone. Eleven patients of the stocking group (2.7%) and 9 patients of the no-stockings group (2.3%) developed postoperative symptomatic DVT (p=0.07). DVT was more frequent in TKR (10 of 364; 2.7%) than in THR (10 of 436; 2.3%). Non-fatal pulmonary embolism occurred in 4 patients out of 20 with symptomatic DVT, 2 each of the stockings and no stockings groups. The foot pump discontinuation rate of patients treated with stockings was 7%, versus 4% of patients treated without stockings (p< 0.05). In conclusion, management of patients with foot-pumps without GCS does not reduce efficacy of DVT prophylaxis after THR and TKR, and improves patient compliance.
Thirty-eight patients were treated with scaphoid excision and 4-corner fusion using dorsal circular plate. Thirty-nine patients were treated with total wrist fusion using one single, dorsal, precontoured and tapered plate for osteosynthesis and third carpometacarpal joint (CMCJ-3) was included. All patients were immobilised in a cast for 4 weeks after surgery.
Postoperative complications, pain (visual analogue scale), clinical and functional outcome based on Green and O’Brien score, grip strength, X-ray evaluation, time to return to work and activity level were evaluated and compared.
The average time to return to work was 17 weeks (4-corner) and 16,2 weeks (total fusion). All patients return to work. Twelve percent of four-corner fusion and 72% of total wrist fusion return to the same work level with restrictions (until 33% of activity). Twenty-two percent of 4-corner fusion and 28% of total wrist fusion were unable to return to their previous activity level, performing lower intensity work activities. Overall satisfaction was high in both groups with 85% (4corner) and 93% (total fusion).
Total wrist fusion had less surgical failures, better level of satisfaction, lesser lost of force than 4-corner fusion, with less potential for further deterioration with time. However, 4-corner fusion allows return to work with a similar activity level and preserve a functional range of motion in patients with high levels of activity.
Recent NICE guidelines have recommended that heparin should be routinely administered to patients under-going THR to prevent thromboembolism, although it is unclear from the existing evidence if heparin is the most effective. However, research has suggested that aspirin, which is a low cost prophylactic agent, is effective in preventing DVT and PE after orthopaedic surgery. The aim of this study was to determine the 90-day mortality rate after THR using aspirin as a prophylactic agent.
Primary THR One patient (0.04%) died within 30 days of surgery and a further 3 (0.13%) died between day 30 and day 90, giving a total mortality at 90 days of 0.17% (4/2,286). One patient (0.04%) died from PE and the other 3 patients (0.13%) died from non-vascular causes. Revision hip replacement One patient (0.27%) died within 30 days of surgery and a further 1 patient (0.27%) died between day 30 and day 90, giving a total mortality at 90 days of 0.54% (2/367). Both patients died from non-vascular causes.
80 porcine deep flexor tendons were harvested from adult porcine forelimbs and randomized into four groups of twenty tendons. Three groups were repaired using either a two, four or six strand repair, and the remaining group was repaired with the new device. Half of each group was repaired using a core technique alone; the remainders were supplemented with a Silfverskiöld Peripheral Cross Stitch.
The repairs were pre-loaded to 1N in a Zwick Linear Tensiometer, with subsequent distraction to failure at 10mm/min. When preloaded the tendon dimensions were measured at the repair site as well as above and below in order to assess repair site bulk. During loading the Force to Produce 3mm Gap (FPG) was recorded as was the Ultimate Strength (US) following failure.
The FPG of the new device was superior to the Cruciate when used alone and was equivalent to the Savage when augmented with a peripheral repair. The US of the new device was superior to the Cruciate both with and without a peripheral repair.
We plan to continue development of the device to optimize its hold on the tendon. We also plan to perform cyclical testing in physiological conditions
In addition, it seems that the radiological findings do not walk along with the clinical features and the wrist functionality in a major percentage. Our results indicate the importance of anatomical reduction and especially the restoration of radial length in order to obtain good functional future outcome.
The aim of this study was to investigation how the rotational axis of the wrist moves as the hand goes from full ulna to full radial deviation.
End-to-side neurorraphy (4 groups) Group A bFGF (20ng) Group B NGF (25ng) Group C (normal saline) Group X [bFGF (20ng) + NGF (25ng)] Negative control group (G) Animal keeping was conform to standard conditions set by the NIH (appropriate cages for housing; standard rat chow and water ad libitum; 12h – light/darkness exposure).
All experimental procedures were performed under the supervision of a veterinarian and were prospectively approved by the Animal Experimental Ethics Committee.
We observed similar effect in individual domains of pain, mobility and range of motion. Survival of the implant at nine years with revision due to any reason was 93.5%. We observed a significant difference in survival of procedures done by pioneer surgeons and by non pioneering surgeons (p < 0.01) (log rank test). There were 119 complications of which there were 30 fractures, 21 occurring within the first six months of operation.
110 patients completed the study, with 2 comparative groups for epidemiologic and radiological criteria (n = 63 for pins and 57 for external fixator).
Correlation between Crowe, Hartofilakidis and Eftekhar classifications with distance between ideal and postoperative center rotation and medial bone bulk were calculated using Pearson correlation. Correlation was also analyzed using information about distance between ideal acetabular roof point and medial pelvic rim.
The incidence of cancer needs to be interpreted with caution and can only be ascertained by a prospective study.
Metal-on-metal articulations are increasingly used in THR. Hypersensitivity reactions to the metal ions can occur. The symptoms and signs are similar to a patient presenting with an infected prosthesis. Correct diagnosis before revision surgery is crucial to implant selection and operation planning. We present a practical approach to this diagnostic problem.
The history, clinical findings, hip scores, radiology, serum metal ions, ESR, C-RP, hip arthroscopy and aspirate results, synovial fluid metal ion levels, labelled white cell/colloid scan, 99m-technetium scan, revision hip findings and histology of a typical patient who had an allergic response to a metal-on-metal hip articulation are presented, and how the findings differ from a patient with an infected implant. Clinical examination, hip scores and serum metal ion levels were repeated one year after revision of the metal-on-metal hip articulation to a ceramic-on-ceramic.
In hypersensitivity, the periarticular tissues undergo lymphocyte-dominated infiltration, the histology differs from that found in infection. The white cell labelled/colloid scan also uses this difference for diagnosis. Hip aspiration is the single best investigation for infection.
We report the difficulties encountered during surgery, and the long term results of patients who had Crowe 3 or 4 DDH and a technically difficult primary hip arthroplasty using the modular S-ROM stem.
4 patients had a technical complication during surgery. The average pre-op Harris Hip Score was 37, at 5 years it was 83, and at 10 years 81. The SF12 measure of physical and mental wellbeing was 43.90 physical/54.48 mental at 5 years, and 41.64 physical/54.03 mental at 10 years. The WOMAC average score (the lower the score the better the outcome) was 27 at 5 years and 23 at 10 years.
None of the S-ROM stems had been revised, 2 hips had undergone acetabular revision and one hip had a liner exchange. None of the S-ROM stems were loose at latest follow-up. Four hips had osteolysis in Gruen zone 1, one hip had osteolysis in zone 7, and one hip had osteolysis in zone 1 and 7. There was no evidence of osteolysis around or distal to the sleeve.
S-ROM stem/sleeve modularity allows femoral component anteversion independent of the position of best fit in the proximal femur, and helps overcome the technical difficulty in these patients.
For RSA, the wear rate for the 28mm femoral head group was 0.05±0.02 while the 36mm femoral head group was 0.03±0.02, p=0.13.
For the Martell analysis, the average steady-state wear rate was −0.002 ± 0.01 mm per year and −0.026 ± 0.13 mm per year for 28mm and 32mm head sizes, respectively, p=0.62. There was no correlation between wear and time in situ or femoral head size for any of the clinical studies.
In comparing the Martell and Devane programs, the total average wear rates were significantly different, 0.07±0.05 and 0.03±0.06mm/year respectively, p=0.01. However, when the absolute values of the Martell results were used, there was no difference, p=0.22.
In 2006 the standard prosthesis for hip hemiarthroplasty in our unit was changed from the traditional Thompson prosthesis used for over 20 years to the monobloc Exeter Trauma Stem (ETS). The principle anticipated advantages were ease of stem implantation, improvement of orientation positioning and a consistency with modern proven femoral THR stem design.
All patients selected for hemiarthroplasty replacement for a displaced subcapital fracture of the hip were eligible for inclusion. Failed previous surgical cases were excluded.
The last 100 Thompson’s prostheses used before and the first 100 Exeter Trauma Stems undertaken after the changeover date were studied. Outcomes measured included surgical complications including infection, dislocation, fracture, necessity to ream etc. and technical adequacy of implant positioning based upon post-operative radiographs. Surgeon grade was recorded. There were no changes in surgical personnel.
206 consecutive patients were included in the study (age range 76–96); 67 men and 139 women. Data were collected prospectively as part of a comprehensive hip fracture audit.
Initial results show that the rate of surgical complications is similar in both prosthesis groups. Radiographs demonstrate the presence of a learning curve in the use of the new prosthesis. On six occasions after December 2006 the Thompson prosthesis was used – this was due to unavailability of ETS prosthesis or where a very large femoral head (56mm) was required.
The introduction of the ETS for hip hemiarthroplasty was successful. Initial conversion problems involved maintaining sufficient stock of the most commonly used size of prosthesis. Advantages were a low dislocation rate despite the greater potential for erroneous implant version and a reduction in the amount of femoral preparation required including reaming. Limitations of this study are the lack functional outcome and long term survivorship analysis.
Analyses of six different cementing techniques (cemtech) were performed using high viscosity (HVC) (Smart Set GHV, DePuy, Blackpool, England) and low viscosity cement (LVC) (Endurance, DePuy, Blackpool, England):
Manual application HVC ¼filling of the component with LVC and manual appl. ¼filling HVC and manual appl. ½filling LVC ½filling HVC Complete filling with LVC
A force of 150N was used to press five shells in each cemtech group on foam specimens. During seating cement pressures and polymerization heat 5 mm under the foam surface were measured.
Specimens were cut into quarters, surfaces were digitalized and cement penetration areas and depths were quantified using a pixel-analysis-software. The effects of the cemtech were examined by Kruscal-Wallis and Mann-Whitney-U-tests (two-sided, p-value< 0.05, SPSS)
Maximum temperatures were A) 36.0± 4.1°C, B) 45.0±5.7°C, C) 36.2±4.2°C, D) 53.5±2.5°C, E) 48.3±6.5°C and F) 53.2±12.6°C. D, E and F exceeded 50°C.
A provided even cement penetration over the available fixation area without involvement of the internal area and the stem. Cemtech that used LVC cement (B, D and F) showed higher interior area cement contents than HVC (A, E and C). The cement content in the interior area was A) 39.3±26.4mm2, B) 72.1±16.9mm2, C) 37.7±10.5mm2, D) 99.0±24.6mm2, E) 67.5±15.6mm2 and F) 121.0±29.0mm2.
A showed mainly complete seating with a cement mantle thickness of 0.5±0.7 mm. All other cemtech had incomplete seating in all specimens with significantly thicker polar cement mantles (p=0.032) up to a maximum of 4.6±1.2mm for E.
Metal-metal hip resurfacing offers the advantage of conservation of femoral bone stock. In addition, the implant may offer enhanced resistance to dislocation in comparison with conventional total hip arthroplasty.
We present a series of 32 female patients with one to 4 year follow up (mean age 57 ranges 50–70 at time of surgery)
All patients required hip arthroplasty. Careful preoperative selection was carried out with particular attention paid to estimation of bone density. A standard resurfacing operation was carried out. Patients had pre and postoperative WOMAC and SF36 scoring. All patients were followed closely in the post operative period. No significant complications were noted at follow up.
In our study we have shown that given careful patient selection Birmingham hip resurfacing can be safe and reliable form of arthroplasty.
We developed a mathematical model of the pelvis to evaluate the influence of the pelvis movements on anteversion and inclination of an acetabular cup arbitrarily implanted with 10° of anteversion and 45° of abduction. Measurment were particularly focused on evaluating the influence of a −15 to 15 degrees pelvic rotation around the three space axes.
When considering the anteroposterior axis, the ranges of variation are almost 30° for abduction and 6° for anteversion. When considering vertical and mediolateral axes, the magnitude of variation is 30° for anteversion and 3° for abduction
We demonstrate a close relationship between acetabular cup anteversion and pelvic rotations in all planes. In contrast, acetabular cup abduction is mainly related to the rotation around the anteroposterior axis. The influence of the pelvic position on the evaluation of acetabular cup alignement requires very precise CT measurement protocols to make the evaluation accurate and reproductible.
Acetabular centre positioning in the pelvis has a profound effect on hip joint function. The force–and moment-generating capacities of the hip muscles are highly sensitive to the location of the hip centre. We describe a novel 3D CT-based system that provides a scaled frame of reference (FOR) defining the hip centre coordinates in relation to easily identifiable pelvic anatomic landmarks. This FOR is more specific than the anterior pelvic plane (APP) alone, giving depth, height and width to the pelvis for both men and women under-going hip surgery.
CT scans of 22 normal hips were analysed. There were 14 female and 8 male hips. The APP was used as the basis of the coordinate system with the origin set at the right anterior superior iliac spine. After aligning the pelvis with the APP, the pelvic horizontal dimension (Dx) was defined as the distance between the most lateral points on the iliac crests, and its vertical dimension (Dy) was the distance between the highest point on the iliac wing and the lowest point on ischial tuberosity. The pelvic depth (Dz) was defined as the horizontal distance between the posterior superior iliac spine and the ipsilateral ASIS. The ratios of the hip centre’s x, y, and z coordinates to their corresponding pelvic dimensions (Cx/Dx, Cy/Dy, Cz,Dz) were calculated. The results were analysed for men and women.
For a given individual the hip centre coordinates can be derived from pelvic landmarks. We have found that the mean Cx/Dx measured 0.09 ± 0.02 (0.10 for males, 0.08 for females), Cy/Dy was 0.33 ± 0.02 (0.30 for males, 0.35 for females), and Cz/Dz was 0.37 ± 0.02 (0.39 for males and 0.36 for females). There was a statistically significant gender difference in Cy/Dy (p=0.0001) and Cz/Dz (p=0.03), but not in Cx/Dx (p=0.17). Anteversion for the male hips averaged 19° ± 3°, and for the female hips it was 26° ± 5°. Inclination measured 56° ± 1° for the males and 55° ± 4° for the females. Reliability testing showed a mean intra-class correlation coefficient of 0.95. Bland-Altman plots showed a good inter-observer agreement.
This method relies on a small number of anatomical points that are easily identifiable. The fairly constant relationship between the centre coordinates and pelvic dimensions allows derivation of the hip centre position from those dimensions. Even in this small group, it is apparent that there is a difference between the sexes in all three dimensions. Without the need for detailed imaging, the pelvic points allow the surgeon to scale the patient’s pelvis and thereby know within a few millimetres the ‘normal’ position of the acetabulum for both men and women. This knowledge may be of benefit when planning or undertaking reconstructive hip surgery especially in patients with hip dysplasia or bilateral hip disease where there is no reference available for planning the surgery.
We report the results of cementless total hip arthroplasty using the Bi-metric titanium femoral stem at a minimum follow up of 10 years and a mean of 12.2 years (range 10–17).
64 hips (43 male/21 female) were implanted consecutively into 54 patients between 1988 and 1995. The mean age at operation was 54.3 years (range 42–65). All patients had a Bi-metric uncemented stem (Biomet UK). The first 13 patients received a metal backed screw in acetabular cup (TTAP-ST, Biomet UK) with the remainder receiving metal backed pressfit cups (Universal, Biomet UK).
All patients were followed up annually and assessed using the Hip Society Score (HSS; max 40 points) to record pain, function and mobility. Survivorship was calculated using the Kaplan-Meier method.
57 hips were followed up for a minimum of ten years. There were 4 deaths (6 hips) before completion of follow up and 1 patient was lost to follow up.
Using revision for any reason as the end point of the study; survivorship for the total hips at 10 years was 89.5% (95% confidence interval: 78.1–96.1%) with a mean Hip Society Score of 34.9 (range 20–40) compared to 14.5 (range 8–24) pre-operatively (p< 0.01 student t test).
Survivorship for the femoral stem in isolation was 100% at 10 years (95% CI 93.7–100%) and there continues to be no revisions to date at a mean follow up of 12.2 years.
The screw fix cup performed poorly with 3 acetabular revisions (including 1 liner change) before the 10 year follow up, a failure rate of 23.1%. There has sub-sequently been a further 4 acetabular revisions.
Ten year survivorship for the pressfit cup is 93.5% (95% CI 82.0–98.8%) with 3 revisions (including 2 liner changes) at ten years. There has subsequently been one further acetabular revision and 9 further liner changes (29.5% failure rate).
There have been no recorded infections and no instances of thigh pain.
Radiographs at ten years showed all the femoral stems were stable with no evidence of migration. Two stems had small radiolucent lines at the bone-implant interface but no signs of loosening. One stem had an area of osteolysis in Gruen zone 7 but didn’t require revision. Rates of osteolysis were extremely low given the large amounts of particulate debris in the hip from the worn acetabular liners.
In conclusion, although neither cup has proved to be particularly successful the Bi-metric stem has performed well at 10 year follow up and continues to do so. This is inspite of the fact they were implanted into a young and active group of patients.
A clinical and radiographic study was conducted on 97 total hip arthroplasties (79 patients) performed for congenital hip dislocation using three-dimensional custom cementless stem. The mean age was 48 years (17 to 72). The mean follow up was 123 months (83 to 182).
According to Crowe, there were 37 class 1, 28 class 2, 13 class 3 and 19 class 4. The average lengthening was 25 mm (5 to 58 mm), the mean femoral anteversion 38.6° (2° to 86°) and the correction in the prosthetic neck −23.6° (71° to 13°). The average Harris hip score improved from 58 to 93 points. Six hips (6.2%) required a revision. The survival rate was 97.7% ± 0.3% at 13 years.
Custom cementless stem allows anatomical reconstruction and good functional results in a young and active population with disturbed anatomy, while avoiding a femoral osteotomy.
The purpose of this study was to evaluate the clinical and radiological findings in patients with avascular necrosis of the femoral head after implantation of a porous tantalum implant combined with autologous growth factors (AGF).
The study included 40 hips in 30 patients. Of the 40 hips, 1 hip was stage I, 9 hips were stage II, 22 hips were stage III, and 8 hips were stage IV, according to the Steinberg classification system. Follow-up was 2 to 4 years. The porous tantalum (diameter of 10 mm, length ranging from 70 –110 mm) was implanted in the center of the necrotic area under fluoroscopic control.
Clinical evaluation using the Harris hip score showed an increase from 66 to 96 points preoperatively to postoperatively in hips with stage II disease, from 60 to 85 points in hips with stage III, and from 60 to 80 points in hips with stage IV (p< 0,001). Of the 40 hips, the radiological stage in 20 hips (50%) remained stable, 17 (42.5%) progressed to an advanced stage and 3 hips (7.5%) underwent total hip arthroplasty (p< 0,001). Of the 17 hips that progressed, 7 were stage II, 7 were stage III, and 3 were stage IV. No material damage or implant migration was observed.
Although failures are still observed with the use of porous tantalum, the minimal invasive technique and short operative time make tantalum a reasonable alternative in the treatment of AVN of the femoral head.
In a qualitative analysis the head-neck contour of all femora was assigned to one of the following four groups: regular waisting, mildly reduced waisting, reduced to distinctly reduced waisting or completely lacking waisting. In a quantitative analysis, angle alpha according to Nötzli et al. (2002) was measured. Furthermore, the CCD angle was measured to assess the orientation of the femoral neck in the frontal plane as well as the LCE-angle according to Wiberg and the acetabular index of the weightbearing zone to rule out any acetabular anomalies.
TAD is <
25mm. To establish whether there was a correlation between TAD and surgeon grade or fracture type. To establish positions of screws on both radio graphs. To ensure SHS are used in the correct fracture types.
The majority of cases were operated on by Registrars 67%, Staff grade 15%, Research fellows 9%, SHOs 6% and Consultant grades 3%. Registrars achieved Centre–Centre positions in 62% of cases with staff grade 47% of cases. The majority of SHS were performed for Types 2 and 4 according to Jensen & Michaelson classification. SHS implants were used in one subtrochanteric fracture and zero reverse oblique fractures. 21 cases had a TAD> 25mm and one of these has gone on to failure, requiring THR.
It is unclear which length of thread may be most advantageous for the internal fixation of an intracapsular fracture with cancellous screws. We have compared the 16mm versus the 32mm threads on cancellous screws within a randomised trial for 432 patients. All fractures were fixed with three screws and patients followed-up for a minimum of one year from injury.
The characteristics of the patients in the two groups was similar with a mean age of 76 years. 23% were male. The most common complication encountered was non-union of the fracture which for undisplaced fractures occurred in 7/107(6.5%) of short threaded screws versus 11/133(8.3%) of long threaded screws. For displaced fractures the figures were 29/104(27.9%) versus 24/89(27.0%). Other complications for the short versus long threaded group were avascular necrosis (two cases versus five cases) and fracture below the implant (two cases in each group). Elective removal of the screws for discomfort was undertaken in five and three cases respectively. None of these differences between groups was statistically significant. In summary there is no difference in fracture healing complications related to the length of the screw threads.
While squeaking ceramic bearings in total hip arthroplasty are increasingly reported in the literature, the etiology remains unclear. Cup inclination and anteversion have been correlated with the phenomenon but even amongst well positioned cups bearing noise is observed. Most studies do not distinguish between different types of noise or incidence rate and do only investigate actively complaining patients. This study analysed the incidence of ceramic bearing noise in a single type of hip implant and investigates correlations with patient, implant and surgery parameters.
In a consecutive series of 145 ceramic-on-ceramic primary hips (Stryker ABG-II, 28mm head) in 132 patients (m/f=72/60, avg. age=54yrs) and an average follow-up of 3.0 (1–7) years, noisy bearings were identified by a patient questionnaires stating the type of noise (squeaking, clicking, scratching, combinations), time of initial incidence, incidence rate (permanent, often, sometimes, rare) and type of movement. Patient demographics (age, gender, height, weight, BMI, side of surgery, leg length difference), implant parameters (cup and stem size, neck length) and surgery parameters (cup and stem position, leg length correction) were recorded and compared between the noisy and silent groups (t-test, Fisher Exact test).
Twenty-eight noisy hips (19.3%) were identified with 14 patients reporting squeaking, 16 clicking and 5 scratching including 7 with a combination of noises. Quasi permanent noises were reported for 7 hips (2 often) but in 17 cases the noise appeared only sometimes (2 rare). The average time of first incidence was 1.74 years port-op with 7 hips reporting noise directly after operation and 15 after 2 years or more. Silent and noisy hips were statistically not different regarding age, gender, follow-up time, side of operation, height, weight, BMI, cup and stem size, leg length difference or stem position. Significant differences were identified with the noise group having a steeper cup inclination (49.9° vs 46.9°, p< 0.05) and less frequent shorter (−2.7mm) necks (0 vs 22%, p< 0.01) but more frequent longer (+4mm) necks (50% vs 37%, p< 0.05). Leg length correction was performed less frequent (31 vs 55%, p< 0.01). In the noise group 5 (17%) and in the silent group only 1 (0.9%) cup revisions was performed (p< 0.01).
The incidence of noisy ceramic bearings was higher than usually reported (< 5%) as not only actively complaining subjects but all patients were interviewed. Cup position was confirmed to be a contributing factor but patient weight, height or BMI did not play a role. However, the use of long necks, the absence of short necks and less frequently performed leg length corrections significantly contributed to producing bearing noise. Biomechanical restoration, preoperative planning and soft tissue tension seem to be important factors in bearing noise etiology.
A neck of femur fracture is known to be a high risk factor for the development of pressure sores with an associated morbidity, mortality and cost. We have attempted to identify risk factors in these patients for the development of pressure sores by analysing prospectively collected data of 4654 consecutive patients (1003 males/3473 females). 3.8% developed pressure sores in the sacral, buttock or heel areas.
Patients factors that increased the risk of pressure sores were increased age (82.1 years versus 76.6 years), lower mental test score (4.65 versus 5.76), diabetes mellitus (pressure sore incidence 10.4%), higher ASA score (3.0 versus 2.7) and lower admission haemoglobin concentration (120gms versus 124gms). Those patients with an extracapsular fracture were more likely to develop pressure sores compared to patients with an intracapsular fracture (4.5% versus 3.1%). Being male was not a risk factor.
While the time interval between fall and admission was not significant, the time interval between admission and surgery was found to be an extremely significant risk factor. A fall in blood pressure during surgery (5.6%) was found to increase risk. Patients who underwent a dynamic hip screw were more likely to develop pressure sores (incidence 4.7%). Patients with an intracapsular fracture treated with internal fixation were less likely to develop pressure sores in comparison to those fractures treated with a hemiarthroplasty or a sliding hip screw (2.0% versus 4.7 versus 4.4%). No relationship was seen related to length of surgery or type of anaesthesia. Our incidence of pressure sores is lower than previously reported (30%). Whilst determining factors that increase the risk of pressure sores may not be sufficiently reliable to be used for the individual patient, taking appropriate preventative measures can reduce the incidence, particularly with reference to (optimising the patient pre-operatively and) reducing delays to surgery.
The health care system has to deal with substantial health care costs, which are expected to continue to rise due to the increasingly elderly populations. One way of saving has been a reduction of the amount of beds at hospitals. The consequence is that acute patients inappropriately are admitted to non specialized wards because of limited beds. These patients are also known as ‘outliers’. In this study consecutive patients with a hip fracture treated at the orthopaedic department (n=273) are compared with patients treated at other departments (n=147) according to incidence of complications and length of stay (LOS) before and after introduction of an evidence based clinical pathway. There was no medical difference between the populations. However the strict demands of saving costs, with limited beds, have resulted not only in economic consequences with prolonged hospitalization, but also in patient suffering and inconvenience of postoperative complications because of an increasing number of complications.
Patients treated at non specialized wards had an extra LOS of stay of 3.7 days in the acute hospital settings and furthermore 13.6 days of LOS including rehabilitation compared to patients treated at the orthopaedic department. In addition we consider the implemented evidence based clinical pathway to be successful since the number of complications was reduced. It is a major challenge to establish effective treatment and rehabilitation for patients after a hip fracture aiming to avoid complications and reduce LOS. Theses fragile patients with a hip fracture ought to be treated at the orthopaedic department, or at departments with geriatric and rehabilitation knowledge. Physiotherapists, occupational therapists and nurses specialising in orthopaedics and geriatricians should take an active part in these patients care, to improve the quality of care and patient safety in patients with a hip fracture.
Hip fractures constitute a major cause of hospital admission and length of stay in the elderly, resulting in increased disability and mortality. In this study the influence of optimized treatment of consecutively included patients with hip fracture on time to operation, bed days, reoperations and mortality within one year were investigated. The study period was April 1st 2003 and March 31st 2004. Comparisons are made between the 210 first patients and the 210 last patients who followed the new clinical pathway introduced at the University Hospital in Lund, Sweden. Early surgery, within 24 hours, was not associated with reduced mortality, but it was significantly associated with reduced length of stay (p< 0.001). Significantly more patients operated with osteosynthesis for femoral neck fracture, were reoperated compared to all other types of surgery (p< 0.001) also when reoperations with extraction of the hook-pins in healed fractures were excluded. Mortality was higher in men than in women at four (p = 0.025) and twelve months (p = 0.001) after the fracture. Mortality was significantly higher in medically fit patients with administrative delay to surgery compared to patients with no delay (p< 0.001).
The presentation is based on the results of the nursing intervention program by using telephone contact to elderly patients with hip replacement after discharge.
Due to an ageing population the numbers of patients with hip fractures are increasing. They often suffer from concomitant diseases and are therefore prone to be affected by complications such as pressure ulcers. The prevention of pressure ulcers among patients with a hip fracture is crucial. The aim of this study was to improve the quality of care and patient safety in patients with a hip fracture. A new evidence based clinical pathway was introduced to prevent hospital acquired pressure ulcers. Furthermore the purpose was to bring the staff’s attention to pressure ulcer prevention and to facilitate changes in clinical practice to improve quality of care and patient safety. A total of 478 patients with a hip fracture were consecutively included between April 1st 2003 and March 31 st 2004. The new evidence based clinical pathway was introduced on October 1st 2003. The results from the first 210 patients in the control group and the last 210 patients in the intervention group are presented in this article. In the intervention group hospital acquired pressure ulcers decreased by 50% (p< 0.007). It is possible to reduce the development
We evaluated used sizes of standard and offset stems and cups, neck length, material of bearing surfaces and on the AP X-ray postoperative in standing position the inclination and anteversion angle of the cup as well as the stem position, postoperative leg length and Trendelenburg sign.
The range of cup inclination angle was in safe zone with an average of 45,8°, neutral stem position in 92,2%.
Leg length equal in 73% and lengthening or shortening +/−in average 8,4mm and 6,5 mm.
The Trendelenburg sign was negativ in 93% at the time of removal of skin sutures.
Patients were allocated a deprivation category by retrospective application of the Scottish Index of Multiple Deprivation (SIMD) quintiles.
Femoral stress shielding in cementless THA is a potential complication commonly observed in distally loading press-fit stems. This prospective study describes long-term femoral bone remodeling in cementless THA at a mean of 17 years (range: 15 to 20) in 208 consecutive fully HA-coated stems (Corail, DePuy Int. Ltd, Leeds, UK). All THA were performed by one group of surgeons between 1986 and 1991. The concept of surgical technique included impaction of metaphyseal bone utilizing bland femoral broaches until primary stability was achieved without distal press-fit. Radiographic evaluation revealed a total of five (2.4%) stems with periprosthetic osteolysis, which were associated with eccentric polyethylene wear. They were either revised or awaiting revision surgery. The remaining 97.6% stems revealed biologic load transfer in the metaphysis alone (52%) or in both metaphysis and diaphysis (48%). Stem survival of 97.6% after 15 to 20 years without stress shielding were considered to be related to: impaction of metaphyseal bone, bland broaches, HA coating, and unique prosthetic design.
Hip fractures are one of the leading causes of morbidity in the elderly population. A large reduction in morbidity can be achieved if these individuals can have definitive treatment rapidly. However, this is not always achievable to a multi factorial host of contributing factors. Therefore, to enable us to understand some aspect of why these delays, if any occur, the following study was undertaken.
The purpose of the study is to relate the place at which the patient fell, to the time of day for admission to casualty. This will enable us to ascertain whether there is a relationship between the location of injury and the time taken to admission into hospital; if there is such a correlation, then it will enable us to identify factors which will expedite an individuals attendance to hospital.
Despite advances in total hip arthroplasty, failure of acetabular cup remains a concern. The role of bone marrow stromal cells (BMSCs) to aid osseointegration of orthopaedic implants have been recently studied. We investigated the hypothesis that autologous BMSCs sprayed on the surface of acetabular cups would improve bone formation and bone implant contact.
Total hip replacements were implanted in 11 sheep, randomly assigned to receive either acetabular implants sprayed with autologous BMSCs suspended in fibrin (study group) or fibrin only (control group). Sheep were sacrificed after six months and the acetabulum with the implant was retrieved and prepared for undecalcified histology. Implant bone contact in both groups was compared microscopically, by noting the presence or absence of new bone or fibrous tissue along the implant at 35 consecutive points (every 1000 μm). The observers undertaking the histological analysis were blinded.
Significantly increased bone implant contact was noted in the BMSC treated group 30.71% ± 2.95 compared to the control group 5.14% ± 1.67 (p = 0.014). The mean thickness of fibrous tissue in contact with the implant was greater at the periphery 887.21mm ± 158.89 and the dome 902.45mm ± 80.67 of the implant in the control group compared to the BMSC treated group (327.49mm ± 20.38 at the periphery and 739.1 mm ± 173.72 at the centre). Conversely, direct bone contact with the implant surface was significantly greater around the cups with BMSCs.
Our data demonstrate that BMSC sprayed on surface of acetabular implants improves bone implant contact. Spraying acetabular cups using stem cells could be used in humans where acetabular bone contact is compromised such as in revision procedures.
Surgery and postoperative regime were identical in the two groups.
CR-migration during cementation and stem insertion was calculated and the quality of cementation was evaluated on the post-operative X-ray according to the criteria by Barrack et Al(
Mean values are presented with 95% CI. An unpaired T-test was used to analyse the differences in CR migration and the quality of cementation quality.
Regarding quality of cementation the mean value in the Imset group were 2.8 which was significantly better in the Hardinge group=2.1 (P=0.003)
Dysplasia of the hip in children, characterised by a shallow acetabulum and a deficient coverage of the femoral head, generally causes altered biomechanics of the hip joint. A kinematic analysis on the individual and comparative spatial movement of the acetabulum with some of the pelvic osteotomy techniques is performed. The osteotomy providing greater correction in most of the parameters potentially leading to greater reduction in loading is the choice of the surgeon.
Adult saw bone hip models have been used. Points of reference have been carefully chosen and data has been obtained using the Polhemus Electromagnetic measuring system before and after the osteotomy. Five techniques (Chiari, Salter, Steel, Tonnis and Ganz) have been performed, parameters like the Centre-edge angle, Sharp’s angle, Acetabular Head index (Femoral head cover), translation and rotation in 3 planes have been analysed.
Results show an improvement in most of the parameters when the above pelvic osteotomies are performed. Centre-Edge angle improved by a mean (in degrees) of 7.4 (Chiari), 9.6(Salter), 16.9(steel), 28.4(Tonnis) and 31.0(Ganz). There has been marked increase in Femoral head cover with mean 24% with Tonnis and Ganz. Significant changes in rotational parameters in all 3 planes were achieved, particularly with Ganz and Tonnis techniques.
Traditionally acetabular dysplasia correction has been assessed in one or two dimensions by plain radiographs and true three dimensional movement of the acetabulum is difficult to assess with simple techniques. This study describes a simple and reproducible method to compare the various pelvic osteotomies and comparative effects these can produce on the kinematics of the hip joint. It is intended to extend this study to include kinetics to compare the forces and stress distribution changes caused by performing the above techniques and a larger study is recommended, based on this technique and the initial trend of results shown.
The clinical outcome was measured using Harris, Charnley, Oxford hip scores and quality of life using SF-36. Radiographs were systematically analysed for implant position, fixation, and loosening.
The clinical scores were respectively, Harris 85 (25–100), Oxford 21.5 (12–52), mean Charnley score 4.8 for pain, 5.3 for movement and 4.3 for mobility; the mean SF-36 score were 44 (12–58) for the physical and 51.4 (19–71) for the mental component. With an end point of definite or probable aseptic loosening, the probability of survival at 5 years was 100% and 97.3% (95% CI = 2.9) for acetabular and femoral components respectively. Overall survival at 5years with removal or repeat revision of either component for any reason as the end point was 91% (95% CI: 82 to 97%).
There is only a paucity of information on the outcome of resurfacing arthroplasty in patients suffering from hip osteoarthritis secondary to developmental dysplasia (DDH). When performing arthroplasty in dysplastic hips, the anatomic abnormalities offer reconstructive challenges, in particular in resurfacing. The present study was therefore conducted to address the following questions: Can hip resurfacing arthroplasty provide satisfactory clinical results in patients with DDH? Can the patients return to sports and recreational activities? Can the hip biomechanics be restored? And finally, can surface arthroplasty reestablish a normal, symmetric gait pattern? The study comprised 24 consecutive patients (32 hips) with a mean age of 44.2 years who underwent surface replacement due to hip osteoarthritis secondary to DDH. Surgery was performed by two senior surgeons using either the Durom implant or the Birmingham Hip Resurfacing prosthesis, dependent on the surgeon’s preference. At a mean follow-up of 43 months, all patients were evaluated cross-sectionally. We assessed clinical and radiographical data and investigated spatiotemporal gait parameters using an electronic mat. The Harris Hip Score improved from 54.7 +/−13.3 to 97.3 +/−5.2 (p< 0.001) and University of California at Los Angeles (UCLA) activity levels increased from 5.3 +/−2.0 to 8.6 +/−1.6 (p< 0.001), respectively. Hip flexion improved from 95.7° +/−16.5° to 106.7° +/−10.6° (p< 0.001). At a mean of 11.2 +/−4.8 weeks after surgery, all patients returned to sports activity. They participated in a mean of 6.0 +/−2.6 different disciplines, 2.8 +/−1.3 times and 4.1 +/−3.6 hours per week. The most common disciplines were cycling, swimming, exercise walking and downhill-skiing. Spatiotemporal parameters of gait demonstrated a symmetrical gait pattern without major differences to normative data. Both, the hip lever arm ratio and the femoral offset increased significantly (p< 0.001) from 0.48 +/−0.07 to 0.57 +/−0.08 and from 39.3 +/−8.2 mm to 45.6 +/−6.2 mm, respectively. Grade I heterotopic ossifications were seen in two hips, there were no Grade II or III ossifications. Two surface replacements failed, both failures could be attributed to surgical errors. The surface arthroplasty risk index was 3.2 +/−1.4 for the entire cohort and 4.5 for the revision cases. Femoral radiolucencies were detected in ten of the remaining 30 hips. The present study demonstrated that hip resurfacing achieved satisfactory clinical results in patients with hip osteoarthritis secondary to DDH. The failure rate of 6.3% did not reach our expectations, however, both failures could be attributed to surgical errors. Further follow-up is nevertheless of utmost importance to assess the significance of femoral stem radiolucencies in this young and active group of patients.
After implementing the guideline, the rate of unsupervised junior registrars performing operations declined from 20% (188/938) to 6% (21/336, p< 0.001 X2). The rate of reoperations declined from 15% (139/938) to 10% (35/336, p=0.044 X2, p=0.043 log.reg.), with a 20% (85/436) to 13% (23/174) decline for intracapsulary and an 11% (54/502) to 7% (12/162) decline for extracapsulary fractures.
Hip resurfacing preserves proximal femoral bone stock, optimises stress transfer to the proximal femur and offers inherent stability and optimal range of movement. The early results of metal–on-polyethylene resurfacing designs were poor and the resurfacing concept was largely abandoned. Modern metal-on-metal articulations enabled the introduction of a new generation of hip resurfacings with encouraging early results. In 1997 two of the authors developed a hip resurfacing system utilizing a metal-on-metal bearing. Our study reports on the clinical and radiological outcomes of the first 200 hips that were treated with the Durom hip resurfacing at an average follow up of 4.6 years (range 3.5–6).
Between May 2001 and December 2003, 200 consecutive hip resurfacings were performed on 189 patients, using the Durom hybrid metal-on-metal system. The average age of the patients was 50 years (range 22.5 – 72.3) and 119 were male. Patients were seen at 6 weeks and at 3, 6 and 12 months and annually thereafter for clinical and radiological evaluation. Clinical results were evaluated using the Harris Hip Score. A subjective assessment of patient satisfaction was obtained and patient activity was assessed using the UCLA activity score.
No patient was lost to follow up. There were no dislocations and no femoral neck fractures. One femoral component was revised due to aseptic loosening 3.9 years postoperatively. There was one late acute haematogenous infection that was successfully treated elsewhere by debridement and retention of the prosthesis. The mean Harris Hip Score improved significantly from 46.7 preoperatively to 94.4 postoperatively. The mean HHS constituents for pain, function and motion all were significantly improved from the preoperative values of 11.9, 25.7 and 4.2 to 41.8, 43.4 and 4.8 respectively following the resurfacing procedure. The mean UCLA activity score was 7.2 indicating a relatively active patient population and 179 hips were rated as excellent by the patients. No cup was considered radiographically loose. Extensive radiologic changes were observed around the femoral stem in 2.5% of the hips, with migration of the femoral component in one case and stem demarcation in 4 cases. All 5 patients maintained excellent function and had no hip pain. Pelvic osteolysis was observed in 2 cases. Neck remodelling changes were observed in 35 hips (17.5%). Kaplan-Mayer survivorship analysis demonstrated the rate of survival of the resurfacing components to be 99.5% (95% confidence interval 98.5 to 100) with revision for any reason as the endpoint.
Early results with the Durom resurfacing system appear encouraging. Although these should be regarded with caution, modern metal-on-metal hip resurfacing potentially offers the ultimate bone preservation and restoration of function in appropriately selected young patients.
Mean follow-up was 15.3 years. The mean Merle d’Aubigner hip score was 16.3±1.8 at the latest follow-up. There was no early or late instability. Radiologically, there were 31% of severe granuloma formation extending beyond zones I and VII. However, granuloma remained asymptomatic in all of the cases and did not require surgical revision of the femoral component. On the acetabular side, late complications occurred: aseptic loosening (3.3%), intra-prosthetic dislocation (3.6%), polyethylene wear that required replacement of the liner (1.8%). Survival of dual-articulation acetabular system with surgical revision for aseptic loosening as the end-point for failure was 96.4% at 15 years and 94.9% at 18 years postoperatively (p< 0.05).
The primary etiology necessitating revision is aseptic loosening.
According to the SOFCOT classification, the acetabular deficiency was grade IV 9 times, grade III 47 times, grade I or II 107 times.
All the implanted acetabular components are SERF dual-mobility implants. This system consists of a metal back which can be HA-coated and Press Fit or cemented in a Kerboull cross or in a Novae Arm. The mobile-bearing insert which allows a dual articulation between the head and the metal back is of polyethylene.
We implanted 119 HA-coated press-fit cups and cemented 44 dual-mobility cups in a support ring or in a Kerboull cross.
We reported 8 complications: 6 early dislocations and 2 acetabular revisions for secondary mobilisation of the cup.
With 4% dislocations at a mean follow-up of 56 months, the dual-mobility cup seems to provide high stability in revision hip surgery when other factors such as muscular deficiency, extended synovectomies, difficult implant placement, encourage an uncertain postoperative prosthetic stability.
These results have to be compared to those of other systems such as constrained acetabular cups or tripolar cups.
Further, we will present data on 90 days cause of death following primary THR and predictors for death, including age, gender and comorbidity (analyses are not finished yet).
The purpose of this study was to compare the clinical and radiological findings in patients with avascular necrosis of the femoral head after management with vascularized fibular graft (VFG) compared to porous tantalum implant.
The study included 60 hips in 50 patients, who were followed prospectively for 2–4 years. 28 patients (30 hips) were treated with VFG and 22 patients (30 hips) were treated with a porous tantalum implant. The two patient groups were matched for age, gender, etiology, pre-operative stage and Harris Hip Score (HHS). Of the VFG group, 14 hips were stage II and 16 were stage III, while of the tantalum group, 1 hip was stage I, 11 hips were stage II and 18 hips were stage III, according to Steinberg classification system. Mean operative time was 3 hours for VFG and 30 min for porous tantalum.
At final follow-up, there was no significant statistical difference in the radiological stage (p=0.246), and radiological progression of the disease (p=0.329) was observed between these two groups. Using HHS, the mean clinical results improved in the VFG group from 61 points preoperatively to 90 points at final follow-up, while in tantalum group HHS improved from 63 to 81 points (p=0.022). Three hips from each group underwent total hip arthroplasty.
The results of the present study suggest that although the management of AVN with VFG appears to show better results compared to the use of porous tantalum using clinical evaluation
The fractures of the hip are a main problem of health care. These fractures will be multiply by 2 in 2025 and 3 in 2050. In the population of old people, 1/3 of the women and 1/9 of the men will have a fracture of their hip. Some authors used the name of “EPIDEMIC”.
The aima of the INPECH project (Indicators of the Performance for the comparison between hospital) was to check if the comparison of performances of clinical teams, on the basis of indicators chosen by themselves, allowed to improve their performances. It was an experimentation of a volonteer processes of comparison of performance between 3 multidisciplinary teams.
The study followed some stages:
in every hospital, description of the process of care of the hip fractures with a choice of indicators of performance (difficulties of the care percepted by the professionals, possibilities of improvement, feasibility of the record of the indicators during the whole process) a first meeting of concertation with the three hospitals where a common choice of 20 indicators was done: 5 factors of adjustement corresponding to the prefracture status, 10 factors of the processes and 5 factors recorded at 3 months postoperatively a first period of inclusion (433 patients of more than 65 years-old) a second meeting of confrontation in order to analyze the results of the first inclusion period and to have exchange between the different teams about the disparities - the age, the autonomy and the mobility of the patients did not differ between the hospitals - the preoperative time was significantly different: 0.7 to 3.6 days - the time of the first get up (2 to 4 days), of the first social demand 3 to 7 days), of the hospitalization in surgery (9 to 14 days) and the rate of transfert in rehabilitation centers varied significantly between the centers. - At three months, the mortality, the levels of dependance and of autonomy were not significantly different. Each team had a reflexion about the opportunities of improvement and the actions to begin A second period of inclusion was realized in order to objectivize if the proposed improvements allowed a real change of our professional practices. (423 patients)
The analysis of this second inclusion authorized a real change in our professional practices and showed the efficacy of the indicators which were improved.
This study had permitted to show qualitative differences of care of hip fractures between the hospitals. The confrontation between the teams had authorized a positive reflexion of some of our professional practices and the improvement was underlined by the second series of inclusion.
There is an overall decrease in operative time over the 100 cases, representing a gradual learning process throughout. However, the fall from an average time of 75 minutes for the first 30 cases, to the average operative time of 30 minutes for the remaining 70 cases, is a significant learning process (40% fall in operative time). We thus, believe the learning curve to be 30 operations.
Mortality data from the Register regarding all 950 patients with one-stage BTHR surgery during the period 1992 until 2005 were compared to those 2577 who had had a twostage procedure with less than six months between the operations.
A subgroup of 481 patients in the Western Region of Sweden with complete data on individual CPP (cost per patient) was selected for the health economic analysis.
Of the 498 patients 6.6% experienced one or more symptomatic cardiovascular complications (deep vein thrombosis, pulmonary embolism (PE), myocardial infarction, and stroke, transient ischemic attack or retinal vein thrombosis). In the degenerative OA group 4.7% (95% Cl: 2.6–6.8%) had a cardiovascular event and in the secondary OA + revision group the rate was 13.4% (95% Cl: 10.2–16.6). The rate of complications directly related to the surgery (dislocation, perioperative fracture, bleeding, aseptic loosening, deep infection, peroneal palsy or superficial wound infection) was 15.4% (95% Cl: 12.3–18.6). In the degenerative OA and secondary OA/revision group the rates were: 14.2% and 19.6% respectively. Nine (1.8%) patients died, five of cardiovascular reasons (disseminated intravascular coagulation, PE followed by renal failure, PE followed by cerebral ischemia and stroke), the first three in close relation to the operation.
There were more females in our study population (61.2% v 38.8%). Statistical analysis was performed for males and females after adjusting for age, body mass index and pre -op scores.
Does cement mantle thickness affect cement penetration depth during impaction grafting? and Does cement mantle thickness affect the early mechanical stability?
In a prospective and randomised clinical study, acetabular cups were implanted free-hand (control group n=25) or with computer assistance using an image-free navigation system (study group n=25). Total hip replacement was performed in lateral position and through minimally invasive anterior approach (MicroHip). The cup position was measured postoperatively on pelvic CT using the CT-planning software.
An average inclination of 42.3° (range: 35°–56°; SD±8.0°) and an average anteversion of 24.0° (range: −5° to 54°; SD±16.0°) were found in the control group, and an average inclination of 45.0° (range: 40°–50°; SD±2.8°) and an average anteversion of 14.4° (range: 5°–25°; SS±5.0°) in the computer-assisted study group. The deviations from the desired cup position (45° inclination, 15° anteversion) were significantly lower in the computer-assisted study group (p< 0.001 each). While only 10/25 of the cups in the control group were within the Lewinnek safe zone, 18/25 of the cups in the study group were placed in this target region (p=0.003). We saw no disadvantage compared to previous studies in supine position with standard approach.
Since 1990, an uncemented titanium screw-in cup with the same outer design, but with two different types of polyethylene liners, has been used at our department. The aim of this study is to detect any differences between the two types of liners in terms of wear behaviour, focal osteolysis and revisions. We present results after a minimum 10 years of follow-up.
Since 1984, more than 1000 Bernese periacetabular osteotomies (PAO) have been performed for the treatment of developmental dysplasia of the hip (DDH) in adolescents and adults at the institution where this technique was developed. We present a concise 20-year follow-up of the first 75 PAOs whose initial and 10-year results had been published previously.
A retrospective study of the first 75 consecutive hips (63 patients) treated with PAO for DDH between April 1984 and December 1987 was performed. The mean patient age at surgery was 29.3 years ± 11.4 (13 – 56) and in 31% of all hips a previous surgical attempt to achieve sufficient coverage had been performed. Preoperatively, 58% of all hips presented with osteoarthritis and 49% with dysplasia Class 4 or higher according to Severin. Four patients (5 hips) were lost-to-follow-up and 1 patient (2 hips) died unrelated to surgery. The remaining 58 patients (68 hips) were followed for a mean of 20.4 years ± 1.1 (18.8 – 22.9) and 41 hips (60%) were preserved at last follow-up. Regarding the surviving hips with preoperatively no or slight osteoarthritis (52 hips), the survivor ship rate was 75%.
Twenty-seven hips were converted to a THA (26 hips) or hip arthrodesis (1 hip) which were defined as endpoints. The cumulative Kaplan-Meier survivorship at 20 years was 61%. The Cox regression analysis was performed to detect predictive factors for poor outcome and to calculate the corresponding hazard ratios. Six predictive factors for poor outcome were found: age over 30, a preoperative Merle d’Aubigné score less than 15, a positive preoperative anterior impingement test and limp, preoperative OA grade of more than 1, and a postoperative extrusion index of more than 20%.
Despite the fact that this series represented the learning curve of a technically demanding intervention of a very inhomogeneous patient group with various previous surgical attempts to achieve sufficient coverage and several concomitant intertrochanteric osteotomies, the 20-year results on the first 75 hips are promising.
Increased survivorship rates are expected for more recent series after identification of relative contraindications based on or analysis. PAO is an effective and successful surgical technique for correction of DDH.
With an increasing number of primary total hip arthroplasties being carried out worldwide, and a lack or inadequate follow-up leading to delays in revision surgery, more complex problems including periprosthetic fracture have to be dealt with at revision surgery.
Unawareness, that clinical results do not reflect the mechanical state of the arthroplasty, together with strain shielding in the femur, progressive endosteal cavitation and stem migration may result in deterioration of the periprosthetic bone stock and femoral fracture.
Acute onset due to the fracture, severe symptoms and poor medical status of the patient usually demands immediate surgical intervention.
We have developed a modular cemented femoral component for revisions where deficiency of the proximal femur, or the femoral fracture, demands a variable extra-femoral portion of the stem. The shaft of the stem is 200mm or longer allowing the extra-medullary position to vary up to 15cm. It has a double polished taper
Between 1985 and 2007 the stem has been used in 79 revisions where there was a periprosthetic fracture. The mean age at surgery was 70 years (37–93) and the mean follow-up was 4 years (0–14 years 10 months). In 86% the primary surgery had been performed at another hospital. In 80% the fracture had united at one year. The main post-operative problem was dislocation in 10 cases between 7 days and 9 years after revision and was most common where the abductors were absent. 2 patients died in the post-operative period. Five hips have been re-revised, 3 for dislocation, 1 for Infection and 1 stem loosening.
Overall revision for periprosthetic fracture using this implant has given good results.
Although the results of this type of surgery are encouraging, this must not be considered as an alternative to regular follow-up and early intervention in cases where progressive loosening and deteriorating bone stock are likely to lead to a more demanding surgery.
Retrieval analysis offers a direct insight into in vivo wear mechanisms. However, the 3D measurement of wear patch characteristics on spherical highly reflective bearings has been difficult. An instrument based on an optical technique has been developed over the past 3 years. It is capable of scanning metallic head and cup in a single measurement, within minutes, at a resolution of 20 nm. From the cloud of 3D points obtained during scanning (typically 35,000 To 1,000,000), a 3D image of the measured part can be obtained. The associated computer program allows for sphericity, roughness, radius and local radius to be calculated, and surface maps of the 3D model can easily be plotted.
Both head and cup of two failed MoM resurfacing devices, a wear simulator test couple and intact components were analysed using the new technique. A successful McKee Farrar head (20 years in vivo) was also scanned. Results were compared with traces obtained on a Mitutoyo RA 300 roundness machine (resolution 0.01 microns).
3D maps of the bearing surfaces of MoM devices were obtained. The maximum linear wear values on heads were 2.5 microns, 99 microns 53.5 microns and 298 microns for the simulator sample, the McKee Farrar head and the two failed resurfacing devices respectively. The corresponding maximum linear wear values on cups were 11 microns, 529 microns and 645 microns for the simulator sample and the two failed resurfacing devices respectively. These results were in good agreement with results obtained on the Mitutoyo machine. Contrary to other worn samples, the two latter cups showed that the cup had worn on the edge of the bearing surface. This resulted in an oval shaped wear patch on the head. For the McKee Farrar device and the simulator device, the wear patch was away from the edge and the outline of the wear patch was circular in shape.
This novel technique has allowed for high resolution 3D mapping of the full bearing surfaces on successful McKee Farrar device and on more recent resurfacing devices. Further studies are required. However, the results suggest that component positioning is paramount to wear performance of metal on metal devices.
The immediate postoperative X-rays showed that the rotation center of the hip was 5,2 mm [0–10] far from the ideal rotation center (26% of cases: 0 mm) and the PE cup was implanted with a lateral inclination of 42,5° [30–55]. In postoperative X-ray follow up, one case of acetabular aseptic loosening was found which didn’t need hip revision. In all other cases no modification of implants position neither of hip rotation center was noted. In 79% of cases, we had total graft incorporation; in 17% of cases, an non evolutive radiolucent area between graft and bone and in 4% of cases (loosening) a graft migration.
Ceramic-on-metal (ceramic head and metal liner, COM) hip replacements have shown reduced wear in comparison to metal-on-metal (MOM) bearings (Firkins et al., 1999). This has been attributed to a reduction in corrosive wear, differential hardness and a reduction in adhesive wear. In a clinical report on the use of a metal-on-ceramic hip replacement (Valenti et al., 2007) which consisted of a stainless steel head and alumina ceramic insert at revision 6-months post-op massive metallosis and macroscopic wear was observed.
The aim of this study was to assess the performance of ceramic and metal bearings in different configurations under adverse conditions, ceramic heads on metal liners (COM) were compared to metal heads on ceramic inserts (MOC), with head on cup rim loading under micro-separation hip joint simulation.
Components used were made of zirconia-platelet toughened alumina (Biolox Delta) and high carbon (0.2wt%) CoCrMo alloy (DePuy International Ltd, UK). Hip simulator testing applied a twin-peak loading cycle and walking motions with the prosthesis in the anatomical position. The lubricant (25% calf-serum) was changed every 0.33Mc, wear was measured gravimetrically. Testing was conducted for 2-million cycles, a standard simulator cycle was adapted so the head subluxed in the swing phase forcing the head onto the cup rim at heel strike (Williams et al., 2006).
The total overall mean wear rate for the MOC bearings (0.71±0.30mm3/Mc) was significantly higher than the wear rate for the COM bearings (0.09±0.025mm3/Mc). The contact of the head against the rim of the cup at heel strike caused deep stripe wear on the metallic heads of the MOC bearings. This region on the head is exposed to high stress conditions and susceptible to damage in edge contact, the effect of this is increased when the cup is a harder material than the head. The wear of a metal-on-metal (MOM) couple under similar conditions was almost two-fold greater than the MOC couple (1.58mm3/Mc, Williams et al., 2006) providing further evidence of the reduced wear with COM in comparison to MOM.
The explant described Valenti et al. included a stainless steel head, this is a softer material compared to CoCr, and wears at a higher level. It can be postulated that the wear under adverse conditions would be further increased.
The COM concept can provide increased design flexibility; thin metal shells can be used with larger ceramic heads. Additionally the design protects against ceramic liner chipping. COM bearings are currently undergoing clinical trials, early data suggests reduced metal ion release in patients with COM bearings compared to metal-on-metal (Williams et al., 2007).
Conclusion: The use of an antibiotic-loaded spacer in the 2-stage treatment of infected hip arthroplasties provides better infection control with good functional results and is superior to treatment in 2 stages without a spacer.
Even though the operations are largely successful, complications after joint replacement surgery occur frequently. Approximately 10% of lower limb arthroplasties need surgical revision, of which 70% are due to loosening. The purpose of this study was to assess the feasibility of 18-fluorodeoxyglucose positron emission tomography (18FFDG–PET) in detecting septic and aseptic endoprosthetic loosening of hip and knee endoprostheses.
The sensitivity/specificity for infectious loosening in hip replacement arthroplasties was 67%/83%, in the knee 14%/89%.
The aim of our study was to examine the outcome of ACL reconstruction by using four strand hamstring tendon autografts.
5 patients had laxity > 3mm when compared to the healthy knee by using the KT-1000 arhthrometric testing. 2 of the latter patients complained of a feeling of knee joint instability which occurred due to inaccurate positioning of the femoral tunnel. In 2 cases the transfix pins were displaced and removed on the 4th and 15th post-operative month.
The tunnel expansion was measured by an X-Ray or a CT scan. The tibial tunnel expansion was 0–2.5mm (mean 1.2) or 18% and the femoral tunnel expansion was 0–3 mm (mean 1.4) or 26%. 8 patients reported mild pain which did not restrict their activities. A 5 degree loss of extension was noticed in one patient who continues physiotherapy.
28 of the above patients suffered also from a meniscal injury that was managed arthroscopically.
Results and longevity of total knee arthroplasty depend on the correction of axis of the lower limb and the stability of the prosthesis. Faithful to the principle of dependent cuts, our goal was to obtain two equal correlated, rectangular extension and flexion gaps using a ligament balancing tensor called CORES® (Stryker®).
The aim of this study was to evaluate the early results of a high flexion total knee prosthesis design and patient factors affecting the final range of motion (ROM) on a consecutive series of primary total knee arthroplasty (TKA) patients. 61 knees of 42 patients of a single surgeon series were prospectively evaluated. The mean follow up was 18 (13–30) months. The results were evaluated pre–and postoperatively using the Knee Society Score, the knee flexion and the difference between the preoperative and postoperative knee flexion angles (Δ flexion). Two tailed Student t test was used to compare preoperative and postoperative variables. Knee and function scores increased significantly from 33 (range 11–54) points and 41 (range 10–70) points to 94 (range 77–100) [p< 0,0001] and 89 (range 65–100) [p< 0,0001] respectively. ROM increased significantly [p< 0,0001] from 106 (range 20–140) to 124 (range 90–160) degrees. There was a strong correlation between the preoperative and postoperative flexion [r=0,5984 p=0,0002; (95% CI: r= 0,3210 to 0,7812)]. ROC (receiver-operating characteristic) curve analysis showed that to reach ≥ 130 degrees of final flexion using a high flexion knee system, the patient has to have minimum 100 degrees of flexion preoperatively. The use of high flexion knee system by itself should not be interpreted to bring flexion ≥ 130 degrees to every TKA patient, rather a design not to compromise ROM in selected patients.
Between 1975 and 2OO1, Five Hundred unicompartmental kne arthroplasties (UKA) were performed by a surgeon (M.R.C.) In more than 6O% of the cases it was an internal UKA for knee degenerative arthritis. Axis deformity was noted in 43,2% of the cases, with a genu varum in 33,6% of the cases. Isolated necrosis of the medial femoral condyle was noted in 6 cases (1,2%) and 13 cases (2,6%) showed with sequellae of a trauma. A Single procedure was performed in 425 knees. Bilateral arthroplasty was done in in 15% of the cases. Epidemiology of the series shows that the left knee was operated in 46.6% and right one in 53.4% of the cases. The Average age was 7O.6 for male and 71.8 for the female patients. 7O.4% of the patients were Female and 29.6% were Male. Several types of implants were used: The Marmor knee in 295 cases, the Miller-Galante (75 cases), Cartier (75 cases) Oxford III (5O cases), but also the Mansat and PCA prosthesis.
The correct indication should take in account the persistance of the ACL and of a mild knee deviation in the frontal axis.
patients’ pre-operative demographics for age, weight, height, BMI, intraoperative variables such as the operating surgeon (n=2), insert and component sizes, and clinical assessment criteria including pre-operative and five-year post-operative Oxford knee (OKS) and Tegner (TS) scores.
In joint arthroplasty and in knee replacement in particular, the currently used patient assessment scores like KSS, are characterized by subjective ceiling effects. To monitor patients accurately in time, objective function assessment is required which is impossible with the classic scores. A single time point comparison study showed that an acceleration based gait test is reliable to analyze gait and to distinguish between knee pathologies. How-ever the use of an accelerometer to monitor functional changes over time is never reported before and will be investigated in this study. A representative group of 29 TKP patients (11 men, mean age 72yrs, weight 85kg, height 1.68m) operated for osteoarthritis receiving unilateral TKP (Stryker Scorpio) were monitored for 3 months. Classic scores (ROM, KSS, WOMAC, VAS, PDI) and the gait test was performed pre, 2 and 6 weeks and 3 months postoperative. Gait was analyzed using a triaxial accelerometer fixed to the sacrum while walking 6 times 20meters at preferred speed. Movement parameters like step frequency, step time, step length, speed and up/down displacement were calculated based on a peak detection algorithm. The gait test was compared with the classic scores using Pearson correlation. The paired t-test was used to investigate the changes after surgery (p< 0.05). Significant correlations were shown between all classic scores and all movement parameters (except up/down displacement and step length). The function KSS and PDI showed significant correlations with most gait parameters, while all Womac scores did not. Two weeks after surgery, the classic scores reached the preoperative scores. For instance function KSS was 57.21 preoperative and reached a score of 59.75 at 2 weeks postoperative. No significant changes were shown between preoperative and 2 weeks postoperative for the VAS, KSS and PDI. In contrast all gait parameters were significantly impaired at 2 weeks postoperative (step time of 0.63s) compared to preoperative (step time of 0.72s) and reached the preoperative functional abilities only at 6 week follow up or still later (step time of 0.64s). Between the 2nd and 6th week postoperative, significant changes were shown in all classic scores, ROM and in speed, up/down displacement. After 6 weeks postoperative KSS, PDI, ROM and the frequency improved significantly. The correlations between all movement parameters and function KSS and PDI indicates that these scores are more function based due to inclusion of objective function measures like ROM, while the Womac contains only questions about ADLs. According to the classic scales, patients show at 2 weeks similar skills as preoperative, while the gait test shows that patients are performing less at 2 weeks and reach the pre operative ability at 6 weeks. This suggest that the addition of the gait test give more information about the functional changes a patient experiences after surgery.
Outcomes following TKA often are good, but patients sometimes lack adequate range of motion and strength. Reasons for these deficits may include instability and the loss of cruciate ligament function. One approach to TKA design is to retain the PCL, and configure the TKA surfaces to approximate the function of the ACL. This can be accomplished by having a lateral surface that controls tibiofemoral motion near extension, but allows femoral rollback with flexion. We have been using such a fixed-bearing TKA design since 2001. The purpose of this study was to determine if an ‘ACL-substituting’ arthroplasty design provides clinical and functional results comparable to traditional PCL-retaining arthroplasty designs.
This series consists of 407 consecutive knees in 185 male and 222 female patients (73±9 years, 28±5 BMI) operated from November 2001 to August 2006. All patients underwent TKA by the same surgeon using PCL-retention and implantation of the same cemented ‘ACL-substituting’ TKA design. Clinical outcomes were evaluated using Knee Society Scores and radiographic review for the first 100 TKA with minimum 2 year follow-up. A subset of patients participated in IRB-approved protocols to quantitatively evaluate TKA motion and strength. Functional outcomes were assessed during gait, stair-climbing and curb step-over tasks for 10 unilateral TKA using a motion capture system, force platforms and inverse dynamics to measure the dynamic knee joint flexion moment. Kinematic outcomes were studied during kneeling for 20 TKA using fluoroscopy and shape matching techniques.
Knee Society Scores averaged 96+7 (pain) and 95+12 (function) at an average of 3.2+0.7 (range, 2 to 5) years follow-up. Passive flexion averaged 122°±10°, with 70% of the TKA achieving > 120° flexion. Radiolucent lines (2–4 mm wide) were observed in 7 TKA. Peak flexion moments (dynamic strength) for the TKA averaged 79%, 80% and 85% of the patients’ contralateral normal knees during the gait, stair-climbing and step-over tasks, respectively. In maximum kneeling, knees averaged 131°±13° flexion, 10° ±4° tibial rotation, and 2mm/10mm posterior position of the medial/lateral condyles.
This series’ early clinical follow-up was comparable to any well performing TKA. Knee flexion during passive examination and kneeling were comparable to the best reported results for PCL-retaining and PCL-substituting TKA. Peak knee flexion moments, a measure of functional strength, were comparable to the strongest knees reported in the literature. These early results suggest a fixed-bearing prosthesis with ‘ACL-substitution’ can provide patient performance comparable to the best performing designs.
Midvastus (MV) vs Medial Parapatellar (MPP) approach: Quadriceps function in the early post operative period was better preserved in the MV group. Post operative pain, blood loss and the need for LRR tended to be lower in the MV group. Subvastus (SV) vs Medial Parapatellar approach: Quadriceps function was better preserved in the SV group up to 3 months post operatively. ROM was generally greater up until the 4 week time point. Post operative pain and blood loss was lower in the SV group. Midvastus vs Subvastus approach: The SV group suffered with significantly more pain at six months post operatively. Quadriceps-sparing versus Medial Parapatellar Approach: Significantly longer operative times and more complications were noted in the QS group. Modified ‘Quadriceps sparing’ Medial Parapatellar vs Mini-Subvastus (MSV) approach: A tendency for earlier restoration of SLR and better early ROM was noted in the MSV group.
MIS tends to result in an improved early quadriceps function and decreased blood loss. However, these approaches are technically more demanding, result in longer operative times and provide no long-term benefit. There is concern that they result in a greater number of major complications and risk implant mal-alignment. Eversion of the patella seems to correlate with poor quadriceps function.
Aim of this study was to compare the postoperative range of motion of three types of total knee replacements.
They were 72 posterior cruciate ligament retaining knee prostheses (group I), 61 postero-stabilized (group II), 52 ultracongruent plates (group III). Inclusion criteria were primary arthritis with varus deformity inferior to 15 degrees (°), no previous surgery on the knee, body mass index inferior to 35, preoperative flexion superior to 110°. All prostheses were performed with the same ancillary with one unique surgeon (DH). Recovery and analgesia protocols were similar in the three groups. Mobility was measured using a goniometer.
Continuous data were tested for normal distribution using Kolmogorov-Smirnov test. Normally distributed data were analyzed with two tailed t-tests, whereas non-parametric data were analyzed with Mann-Whitney U test. Statistical significance was set at p < 0.05.
At 2 years follow-up, the group I demonstrated a mean flexion of 121.8° in preoperative period and 110.3° in postoperative period. They were respectively of 121.3 and 122.2° in the group II. Regarding group III, they were 121.6 °preoperatively and 118.4° postoperatively.
Results were significant (p< 0.05) between groups I and II, and groups I and III.
No statistic correlation was found between need of mobilisation under general anesthesia (p> 0.05), flexum (p> 0.05), knee score (p> 0.05), patient satisfaction depending on type of prostheses (p> 0.05).
Posterior cruciate ligament removal tends to offer a best postoperative flexion without significant influence on the knee score or patient satisfaction.
Flexion contracture is a common deformity encountered in patients requiring total knee replacements (TKR). Both the soft tissue envelope and articular bones are involved in the knee extension lag. A few studies in the past have assessed the relationship between bone cuts and extension deficit by using goniometers and rulers. Using navigation for TKR enables the accurate measurement of knee flexion contracture and bone cuts. The aim of this study was to try to establish a relationship between extension lag correction and the size of bone cuts made.
104 continuous TKR were completed by a single consultant using the OrthoPilot® (BBraun, Aesculap) navigation system and Columbus implants. 74 knees had preoperative flexion contracture (including neutral knees) while 30 were in hyperextension. Data was recorded prospectively using the navigation system. These included preoperative flexion and extension angles, actual bone cuts of tibia and femur (both medial and lateral), postoperative correction of flexion and extension angle, size of the prosthesis with thickness of polyethylene and soft tissue release. Of the 74 knees with fixed flexion, 57 had no release and 13 had a posterior release (4 had an intermediate release and were excluded from the study).
For knees with fixed flexion (n=70) there was a significant statistical difference between the pre and post implant extension angle (p < < 0.0001). There was no correlation between the thickness of bone cuts and postoperative extension lag either for the group with no release (p=0.495) or posterior release (p=0.516). There was also no correlation between bone cuts and preoperative angles for either type of release (p=0.348 and p=0.262). There was a significant difference between the preoperative extension deformity for the two soft tissue releases performed (p=0.00019), the mean fixed flexion angles being −4.4° and −10.4° for no release and posterior release respectively.
Flexion contracture deformity in TKR can theoretically be solved in two ways: either by extensively releasing the soft tissue or by increasing the extension gap by cutting more bone (logically the distal femur). Appropriate soft tissue management and release in TKR is crucial in balancing the prosthesis in the coronal as well as the lateral plane. This study seems to confirm the supremacy of soft tissue management and release over bone cut resection. Cutting more or less bone could in fact lead to a poorer outcome as this will change the joint line level without having any additional beneficial effect in correcting the flexion contracture. Conversely adequate soft tissue release has corrected the flexion contracture when needed. In conclusion, there was no correlation between bone cut resection and extension lag correction and with large extension deficits, a posterior soft tissue release and osteophytes resection was more important than bone cuts.
In the sagital view, the centre of the circle is offset by 21mm (S.D.3mm) at an angle of 67° (S.D. 7°) from a line connecting the midpoint between the centres of the femoral condyles and the femoral head centre.
On either end of this line, the articular surface of the trochlea can be fitted to spheres of radius 30mm (S.D. 6mm) laterally and 27mm (S.D. 5mm) medially, with an rms of 0.4mm.
This can be of use in planning and performing joint reconstruction and have implications for the design of patello-femoral replacements and the rules governing their position.
Competence of the extensor mechanism is the major determinant of functional outcome after resection of the proximal tibia and tumor prosthesis implantation. Restoration of a compromised active extension of the knee and an extension lag still remains a difficult challenge. Various techniques have been proposed in the past twenty years including direct attachment of the patellar ligament to the prosthesis, transposition of the medial gastrocnemius muscle possibly associated with other muscle flaps, transposition of the fibula and combination of these techniques. Transposition of the fibula was first reported by Kotz in 1983 but not sufficiently described, so that surgeons who want to plane and manage such a procedure can have some difficulties. We present our technique of fibula transposition and report the functional results about seven patients treated for high-grade sarcomas of the proximal tibia. Fibula transposition is carried out only if the entire fibula and its soft-tissues can be preserved. Resection of the tumor and reconstruction is carried out using the same anteromedial approach. After implantation of the prosthesis, the fibula and its muscles are mobilized anteriorly in a ‘baionnette’ shape obtained by performing a two-level osteotomy. The peroneal nerve and the anterior tibial vessels are previously identified and released to prevent tension on these structures during transposition. Care must be taken to preserve as much as possible the muscular insertions on the fibula so that probability of bone fusion increases. The biceps tendon and the lateral collateral ligament inserted in the fibular head are sutured to the patellar ligament. The knee is immobilized in a knee-ankle orthosis for 6 weeks. We have performed this technique in seven cases. A medial gastrocnemius muscle flap was associated in 3 cases to cover the prosthesis. Fusion was achieved in all cases. Full active extension was obtained in all cases with an extensor strength rated 5/5. All patients were ambulatory without external support at the last follow up.
The purpose of this study was to evaluate the femoral component rotation in a small subset of patients who had developed arthrofibrosis after mobile-bearing total knee arthroplasty (TKA). Arthrofibrosis was defined as flexion less than 90 degrees or a flexion contracture greater than 10 degrees following TKA. From a consecutive cohort of 3,058 mobile-bearing TKAs, 49 (1.6%) patients were diagnosed as having arthrofibrosis, of which 38 (86%) could be recruited for clinical assessment. Femoral rotation of a control group of 38 asymptomatic TKA patients matched for age, gender, and body mass index was also evaluated. The surgical epicondylar axis was compared with the posterior condylar axis for the femoral prosthesis. Femoral components in the arthrofibrosis group were significantly internally rotated by a mean of 4.7 degrees (SD 2.2 degrees, range 10 degrees internal to 1 degrees external). In the control group, the femoral component had a mean 0.3 degrees internal rotation (SD 2.3 degrees, range 4 degrees internal to 6 degrees external). Following mobile-bearing TKA, there is a significant correlation between internal femoral component rotation and chronic arthrofibrosis.
Antibiotic-impregnated cement is frequently used for fixation of total knee prostheses as a measure to prevent postoperative infection. In recent years, more cementless knee prostheses have been implanted especially for younger patients.
In 1997 to June 2004, 35044 primary total knee arthroplasties for primary or secondary osteoarthritis were performed in Finland and registered in nationwide arthroplasty register. The patients aged 70 years (range 21–96) on average, and 71.7% were women.
During the median follow-up of 39 months (range 0–104), 978 (2.8%) knees were revised. There were 188 (0.58%), 21 (1.09%) and 10 (1.18%) reoperations due to infection after cemented, hybrid and cementless arthroplasties, respectively (p=0.003). In hybrid arthroplasties with cemented tibial component, the septic reoperation rate did not significantly differ from cemented arthroplasties. Instead, the higher number of infections after hybrid arthroplasty was related to use of cementless tibial components (5.3% vs. 0.9%, p< 0.008). In Cox regression model adjusted for age, gender and diagnosis, the hazard ratio for septic reoperation after knee replacement with cementless tibial component was 2.4 (95% CI 1.4–4.1) compared to the cemented alternative. The fixation method did not affect the rate of septic reoperations occurring after the first postoperative year.
Cementless fixation of tibial component in primary total knee arthroplasty may associate with an increased risk of early septic reoperation. Until this finding is confirmed in other materials, cementless fixation in primary knee arthroplasty should be used cautiously in patients with increased risk for infection.
Participants were asked to estimate the number of times a trainee needs to do the following procedures to achieve competency: diagnostic scope, partial medial meniscectomy, partial lateral meniscectomy, and anterior cruciate ligament (ACL) reconstruction.
The femoral component showed a median deviation from the transepicondylar axis of 1,7° (range: 3,1° external rotation to 4,4° internal rotation) in the navigated group and of 1,0° (range: 3,4° external rotation to 4,3° internal rotation) in the conventional implantations.
The tibial component showed a much greater range of rotational deviation from the medial third of the tuberosity in median 5,3° (range: 14,9° external rotation to 26° internal rotation) in the navigated group and 4,8° (range: 6,5° external rotation to 23,8° internal rotation) in the conventional implantations.
Regional anaesthesia, and the supplementation of either general or spinal anaesthesia with nerve block is well established and becoming increasingly more popular. Femoral, sciatic and obturator nerve blockade, in alone or in combination, by means of single shot or continuous infusion has been shown to significantly improve pain control and post operative nausea and vomiting (PONV). We identify equally significant morbidity associated with this practice, with delayed post operative rehabilitation, increase in length of stay, reduction in range of movement and local adverse symptoms at the site of injection and paraesthesia at 3 months post operatively.
2 surgeons were recruited to contribute 100 consecutive total knee replacements each to this study. Each worked exclusively with a one anaesthetist. Each had a predictable and different practice. One employed either spinal or general anaesthesia which the surgeon supplemented with end of operation infiltration of soft tissues in the surgical field including the capsule and skin incision with ropivacaine 300mg, adrenaline 500μg and ketorolac 30mg with normal saline added to make a volume of 100ml. The second employed either spinal or general anaesthesia but supplemented this with a single combined femoral and sciatic nerve block performed pre-operatively. Intravenous opiate analgesia administed via patient controlled analgesia pump for 24 hours post operatively, paracetamol 1g 6 hourly and ibuprofen 300mg 8 hourly where appropriate were prescribed by both anaesthetists. We recorded the incidence of insertion of urinary catheter, deep venous thrombosis diagnosed within 3 and 12 weeks, recovery of lower limb power to grade 5/5, range of movement achieved in each postoperative day and at 12 weeks post operatively, length of stay in addition to PONV and pain scores using the visual analogue scale (VAS) and collected every 6 hours. Localised pain and tenderness at the site of injection was noted at 12 weeks, and persistent paraesthesia.
As predicted patients in the group receiving nerve block has significantly less pain and post operative nausea and vomiting (p< 0.05). There was no statistically significant difference in the use of urinary catheters (p = 0.052) or the incidence of deep venous thrombosis (p=0.58). There was however a significant difference in the recovery of lower limb power (p = 0.023), range of movement recorded at 24hr intervals (p=0.038) (at 12 weeks p=0.54) and length of stay in hospital (0.038). One patient had an almost complete femoral nerve palsy at 12 weeks and required a manipulation under anaesthesia of her knee following recovery of same.
Nerve blockade is an increasingly popular method of controlling post-operative pain. We demonstrate some adverse effects on rehabilitation following this practice in addition to the increased financial and logistical burden of a longer inpatient stay.
Navigation was performed with dependant bone cuts, tibia first. The tibial trackers were implanted distally, while the femoral trackers were implanted medially close to the joint line, to prevent impingement with the stems.
Bone morphing was performed on the surface of the ancient prosthesis. The system showed the difference between the level of the ideal joint line and the real bone cut, thus indicating the height that had to be reconstructed. The provisional tibial plateau was assembled with its stem and its metallic augments and the knee was balanced with the new tibial component and the ancient femoral component still in place. Femoral reconstruction was finally performed based on an ideal position that had memorized by the computer
Bone reconstruction was required in 2 tibias (morselized allografts) and in one femur (structural femoral head allografts).
The aim of our study was to determine the occurence of cruciate ligament aplasia arthroscopically.
In our followed series consisting of 50 PFFD patients, 26 boys and 24 girls, five boys with PFFD classified respectively as Pappas III, VII, VII, VIII and IX and 3 girls with PFFD classified respectively as Pappas III, VII and VIII were examined arthroscopically. Deficiency of cruciate ligaments was also documented in a pateint with the diagnosis of isolated aplasia of the fibula.
Changes in the shape of intercondylar area of the distal femur, and aplasia or hypoplasia of the intercondylar ridge of proximal tibia in all PFFD patients were evaluated by an X-ray.
Seriousness of the anomaly was inversely related to the degree of classification according to Pappas. None of our patients suffered from problems arising from knee instability. Based on our experience we recommend a reserved approach as far an indication for cruciate ligament reconstruction in PFFD patients is concerned.
Removal of solidly fixed implants is a challenge in revision knee arthroplasty. It is fraught with the risk of intraoperative fractures and bone stock vital for the success of subsequent revision surgery. We describe the double extraction technique for extraction of solidly fixed implants. This technique was first tested in laboratory setting and then replicated in the operation theatre with successful results.
In this retrospective study we analysed all our patients in which we used the double extraction technique for the removal of solidly fixed implants. In this procedure, the surgeon and the assistant each place an osteotome on the cement metal interface at symmetric positions, directly opposite each other on the medial and lateral sides. They deliver synchronous blows with a mallet at positions around the interface until the cement fractures. The femoral component can then be easily removed. The technique was tested in a laboratory before it was used clinically. Polyurethane mouldings, representing a suitable substrate for cementing metal components were fixed on to a steel rod of similar weight and length as the lower leg. Stainless steel discs (40mm diameter x 4mm thickness) were cemented on to the polyurethane substrate to form a model of a cemented implant. The discs were instrumented to allow recording of the mechanical processes caused by the double extraction technique and to allow comparison with the single osteotome extraction technique. The methodology successfully demonstrated that the double osteotome technique increases the contact force of the second blow. When the synchronous blows are delivered, less energy is expended in the movement of tibia and more is contributed to the removal of the component.
In this study we looked at a total of 206 patients were the solidly fixed tibial and femoral components were removed using the double extraction technique. There were 86 men and 126 women. The mean age of the patients was 66.8 years (range 37–87 years). Only patients with solidly fixed implants were included in this study. Stability of implants was assessed with preoperative radiographs and then confirmed intraoperatively. Patients with loose implants intraoperatively were excluded from this study. We present our results with use of this technique in 206 patients with follow up of 1 to 5 years.
The patients were divided into 5 groups based on their BMI, BMI< 25(normal), 25–29.9(overweight), 30–34.9(obese), 35–39.9(moderately obese), 40 or more(morbidly obese).
BMI < 25 was treated as a control group for comparison.
Statistical analysis was done using t test.
The mean length of stay for revision due to aseptic loosening in 1997 was 14.3 days. The average length of stay for revision for infected arthroplasty was 35 days. In 2006, the length of stay increased to 65 days for infected arthroplasty and 15.03 days for aseptic cases.
The mean total cost of aseptic revision per patient was 12,409.92 (range 8,822.58–13,559.65) euro in 1997 with revisions for infection costing 20,888.66 euro, a difference of 68.32%.
The industry cost of implants increased by 32–35% (€3119–€4371 and €4216–€5800) between 1999 and 2006 depending on implant selection. There was a 20– 42% increase in generic hospital costs (admission, investigation and treatment related costs) in the same period.
Patients with osteoarthritis of the knee reviewed by the General practioners, are usually referred for further management to the orthopaedic surgeon. It was our observation that patients were usually referred with supine knee X-rays. This meant weight-bearing films were repeated at the clinic.
The operations were performed by 11 surgeons, with more than 80% done by 5 surgeons. 162 (74%) femur components and 181 (83%) tibia components were cemented. Patella resurfacing was performed in 135 (62%) cases.
We evaluated the results prospectively with a clinical inspection, radiographs (AP and lateral, longleg standing, patella sunrise view), and the use of the Knee Society Score, Quality-of-Life Short Form-36 and WOMAC rating score.
149 patients were examined at a mean follow up of 5,9 years (range 4,1–8,2 years). 29 were questioned on the telephone, 29 deceased, 7 revisions had to be performed and 4 (2%) were lost to follow up.
Early complications included 12 haematoma, 10 wound healing problems, 5 early infections, 2 thrombosis and 1 non lethal pulmonary embolism. 7 revisions had to be performed: 3 late infections (2 one-stage revisions with synovectomy and exchange of polyethylene inlay, one two-stage revision with semi-constrained implant LCCK© Zimmer Inc.), 3 patella resurfacing due to anterior knee pain and 1 exchange of cemented tibia plateau due to aseptic loosening. Survivorship at 6 years including any reason of failure was 96,5%.
High tibial osteotomy is an efficient treatment for medial compartment osteoarthritis of the knee; its used for middle aged patients with high activity levels and can delay the need for total arthroplasty.
The results of total knee arthroplasty after failed high tibial osteotomy are controversies; several authors reported inferior outcomes, but others have concluded that tibial osteotomy doesn’t bias following total arthroplasty. The aim of this study was to evaluate the results of failed high tibial osteotomy subsequently converted to total knee arthroplasty and compare the results to group of patients underwere primary arthroplasty; the authors evaluate some of technical problems that a previous high tibial osteotomy can generate, like scar tissue, patellar tendon shortening and changes of proximal tibial anatomy.
At an average of five years follow up, the clinical results of total knee arthroplasty after high tibial osteotomy were similar to those of primary knee prosthesis.
Restoration of the position of the prosthetic joint line to the same level as the natural joint line, is a challenging problem in primary and revision knee arthroplasty and there is no reliable method for achieving this objective. We hypothesise that there is a constant ratio between the inter-epicondylar distance and the distance from this interepicondylar line to the joint line.
We analysed one hundred Computerised Tomography (CT) scans of the knee in the non arthritic population to study this relationship. The inter-epicondylar distance and the perpendicular distance from this inter-epicondylar line to the joint line was measured using both the clinical and surgical epicondylar axes for each knee as described in previous literature.
The results showed that using the clinical epicondylar axis the inter-epicondylar distance was 3 times the perpendicular distance from the inter-epicondylar line to the joint line (the median and mean ratio 3.0, Standard Deviation ±0.21). Using the surgical epicondylar axis the inter-epicondylar distance was 3.3 times the perpendicular distance from the inter-epicondylar line to the joint line (the median and mean ratio 3.3, SD ±0.25).
Landmarks such as inferior pole of patella or fibular head have been used to estimate the joint line position, but these methods have been shown to be unreliable. Our method will give an accurate estimate of the position of the joint line from the clinical epicondylar axis distance. This distance is easily calculated when using Computer Navigation for the surgery in both the primary and revision setting and the modern software programmes for Computer Assisted TKR should be modified accordingly. We conclude that the position of the joint line from the inter-epicondylar line is one-third of the inter-epicondylar distance which is valuable especially when there is significant bone loss at the tibio-femoral articulation.
Knee Society objective and functional score of 190 or above full knee extension and a maximum flexion of 125° or above excellent subjective patient rating.
Thirty TKA of 29 patients (9 male, 20 female) with a median age of 70 years (range, 31–87) at time of surgery fulfilled the study criteria. All TKA were implanted at a single high-volume joint replacement center in 2002. In all cases both the condylar twist angle (CTA) using the clinical epicondylar axis (CEA) and the posterior condylar angle (PCA) using the surgical epicondylar axis (SEA) were used to assess rotational alignment of the femoral component.
The dynamic modulus of the normal or mildly degenerated cartilage correlated negatively with the Mankin score: r (Spearman) = −0.823, n = 348. Stiffness at the repaired site was similar to normal cartilage at adjacent sites in the knee.
Performing Bilateral Knee replacements simultaneously is a controversial issue with proponents on both sides of the argument. The advantages of simultaneous arthroplasties include the administration of a single anaesthetic, reduced hospital stay and consequent reduced costs. Reuben et al (J. Arthroplasty, 1998) reported a 36% reduction in hospital costs. Patients also have a quicker return to function and Leonard et al (J Arthroplasty 2003) reported a high patient satisfaction rate of 95%.
The primary disadvantages noted in previous studies include an increase in peri operative complications–both cardiac and pulmonary. An increase in mortality figures is perhaps the most serious complication recorded in some studies. Ritter etal (Clin. Orthop. 1997) reported a 30 day mortality rate of 0.99% in bilateral simultaneous TKA as compared to 0.3% in patients who underwent a staged procedure.
Our study comprised a total of 202 patients who underwent bilateral simultaneous total knee replacements at a District General Hospital in Harlow. Harlow is one of the centres involved in the multi centric trials for the PFC Sigma Knee System and is perhaps the only centre in the UK where bilateral simultaneous procedures are carried out in significant numbers. There were 103 males and 99 females. 12 of the patients had Rheumatoid arthritis. 45% of the patients were in the 71–80 years age group, 26% in the 61–70 years age group. The average age across the entire group was 71.3 years. 35% of patients had a BMI of 25–30, 23% a BMI of 30–35, while less than 5% had a BMI of greater than 40. Most patients (44%) were ASA grade 2. The 3 most common co morbidities included hypertension(85%), coronary artery disease(25%) and diabetes mellitus (12%). 90% of the patients had the procedure performed under a General Anaesthetic and Epidural. Tourniquet time ranged from 55–159 minutes. (average 96 minutes). The patella was resurfaced in all patients. Post operatively the average drain collection was 1200 mls(range 7002600mls). Average pre op Hb was 13.8 g/dl, the post op average being 9.7 g/dl. 71% of patients required blood transfusion after surgery (average 2.8 units). Average hospital stay was 12.4 days (range 5–38 days). 6 patients required HDU admission.
These figures are comparable to those in published literature. We have found Bilateral simultaneous Total Knee replacements to be a safe procedure with quick return to function.
Today the use of pneumatic tourniquet is commonly accepted in total knee arthroplasty (TKA) to reduce perioperative blood loss. There are a few prospective randomised and nonrandomised studies that compare the effect of tourniquet release timing in cementless or cemented unilateral TKA. However, many of these studies show an inadequate reporting and methodology. This randomized prospective study was designed to investigate the efficiency of tourniquet release timing in preventing perioperative blood loss in a simultaneous bilateral TKA study design. To our knowledge, this is the first study of its kind, in which the effect of tourniquet release timing on perioperative blood loss was investigated in simultaneous bilateral cemented TKA.
In 20 patients (40 knees) one knee was operated with tourniquet release and hemostasis before wound closure, and the other knee with tourniquet release after wound closure and pressure dressing. To determine the order of tourniquet release technique for simultaneous bilateral TKA, patients were randomized in two groups: ‘Group A’ first knee with tourniquet release and hemostasis before wound closure, and ‘Group B’ second knee with tourniquet release and hemostasis before wound closure. The blood loss was recorded 48 hours postoperative for each technique.
We found no significant difference in total blood loss between both techniques (p =.930), but a significant difference in operating time (p =.035). There were no postoperative complications at a follow-up of 6 month. Other studies report an increase the blood loss in early tourniquet release and an increase the risk of early postoperative complications in deflation of tourniquet after wound closure. In this study we found no significant difference in perioperative blood loss and no increase of postoperative complications. Therefore, we recommend a tourniquet release after wound closure to reduce the duration of TKA procedure and to avoid possible risks of extended anaesthesia.
clinical outcome, ligamentous stability and alignment after application of the various medial release techniques (capsular release and deep MCL, pie crust of superficial MCL, superficial MCL release on the tibial side, release of semimembranosus tendon) and to propose a rationale for their use.
In 255 of the 359 (71%) primary TKA’s, symmetrical gaps could be achieved by releasing the capsula and the deep MCL (group 0). In 87 cases (24%), an additional piecrust of the superficial MCL was necessary (group 1). In 55 cases out of these 87 an additional release of the insertion of the semimembranosus was performed. In 17 out of the 359 (5%), the medial tightness necessitated a distal release of the superficial MCL (group 2).
The mean preoperative mechanical femorotibial angle (MFTA) was 174.0, 172.1 and 169.5 and was corrected postoperatively to 179.1, 179.2 and 177.6 for group 0, 1 and 2 respectively.
At 12 months, mediolateral stability was clinically evaluated as normal in 97% for group 0, 95% for group 1 and 83% for group 2. Three percent (3%), 5% and 17% has a mediolateral laxity ranging from 6–9 degrees for group 0,1 and 2, respectively.
This is a non controlled experimental prospective4 clinical study that obtained satisfactory results in the chemical Synovectomy with Oxitetracycline Clorhydrate (Emicine), in dfferent joints, demonstrating that it is an Effective method in the treatment of recurrent haemarthrosis in haemophilia.
Besides the experimental demonstration of its action in rabbits is exposed.
One of the most serious complications of THA is deep infection.
Charnley realised the problem. This led to the development of clean air enclosure, total body exhaust suits and the introduction of the instrument tray system. Subsequently antibiotics were used both systematically and also as an addition to the acrylic cement. Occasional deep infection requires further intervention, either by removing the implant, or performing one or two stage revision. It has been the senior author’s practice to undertake one-stage revision provided the bone stock was of sufficiently good quality to ensure reasonable quality of component fixation. The technique is based on the accepted principle of infection management: Removal of all foreign body material and infected tissues, application of local antiseptics/antibiotics, closure of cavities, ensuring stability, drainage, rest, continuation of antibiotics.
Between January 1974 and December 2001, 185 one-stage revisions were carried out by the senior author: 162 had a minimum follow-up of 5 years with a mean of 12.3 years (5.1–27.6 years). 138 cases (85.2%) were free from infection. Presence of a sinus at revision did not affect the outcome adversely – on the contrary – 90.4% were infection free as compared with 82.7% of those without a sinus.
Attention to detail was the essential part of the operation.
The clinical results were evaluated with SF12, WOMAC, and KSCRS performed preoperatively and postoperatively at 5 and 10 years. A radiographic analysis was performed using x-rays of the last available follow-up.
Knowing patient bone density is important to select the proper fixation technique and for secondary osteoporosis medical treatment. However few studies addressing hip fractures provided data regarding patient bone mineral density.
Discussion: There are notable differences in bone mass density. Femoral neck BMD proved to be the best diagnostic site using DXA, with 15.07% of hip fracture patients having a normal age-related bone mass. Higher non-osteoporotic bone densities were found in women with hip fractures: BMD values were (27.40%) at the trochanter and (17.81%) at the Ward’s triangle.
All patients underwent a total hip replacement (ABG II, Stryker) with uncemented proximally hydroxyapatite-coated femoral stem with tantalum RSA markers. Ceramicceramic bearing surfaces were used. A uniplanar type of RSA setup was applied. The RSA examinations were performed postoperatively and at 3, 6, and 12 months.
During surgery, cancellous bone biopsy was taken from the proximal femur from the site of stem implantation. The specimens were scanned with micro-CT. 3D analysis of trabecular bone geometry and BMD was performed using CTAn software. After micro-CT imaging, the trochanteric cancellous bone specimens were subjected to a destructive compression test. Maximum force and stiffness were calculated. Linear regression analysis was applied to study correlations between different parameters investigated.
Unexpectedly, the quality of intertrochanteric cancellous bone did not predict RSA migration of the femoral stems. The femoral stems reached high stability within 3 months and there were no significant differences in the axial and rotational migration of the femoral stems between the patients with normal or poor quality of the intertrochanteric cancellous bone.
We prospectively reviewed the medication of such patients who were discharged from our Trauma Unit to identify if the NICE guidance was being followed.
We prospectively reviewed their medication to identify if a bisphosphonate had been commenced by the General Practitioner and their discharge letters to their General Practitioners to see if it had been suggested to start one.
Only one (2%) of the discharge letters (written by the Orthopaedic doctor to the General Practitioner) recommended commencing a bisphosphonate.
6 of the 47 patients (13%) had been started on a bisphosphonate by the General Practitioner.
We believe the results demonstrate a lack of health promotion opportunities to prevent future fracture. Although there is clear focus and impetus for developing falls prevention services nationwide, this enthusiasm has not been translated across to bone health, despite the potential savings in terms of morbidity, mortality and healthcare costs.
Important deficiencies in local services have been identified, particularly with respect to communication between secondary and primary care.
This study lead to an education initiative to ensure the Trauma department and our local General Practitioners were aware of the NICE guidance. A second prospective audit is currently being undertaken to assess the effect on our service.
Fracture prevention has so far been studied in patients included on the basis of low bone density, and not after a fracture. In this study the inclusion criteria was a new hip fracture irrespective of bone density. An international, multicenter, randomized, double-blind, placebo-controlled, parallel-group trial (HORIZON-RFT) studied whether the bisphosphonate, zoledronic acid (ZOL) 5 mg, reduced subsequent clinical fractures in men and women ≥50 yrs after a hip fracture.
An additional telephone survey was conducted 6–8 weeks after the first conversation to assess the influence of the intervention.
Following this a FF prevention strategy was implemented. This consisted of fracture clinic infrastructure changes, a staff awareness teaching programme and the assignment of an osteoporosis nurse specialist.
A re-audit six months later identified 16 of 175 new patients as having FF. According to BOA and NICE guidelines 88% (14 of 16 patients) and 75% (6 of 8 > 75’s) respectively were appropriately managed for secondary prevention. Fisher’s Exact Test showed a significant improvement in secondary prevention management according to BOA guidelines (p< 0.05), but not NICE guidelines (p=0.2), as a consequence of these interventions.
Type IIb, so called mobiled pseudoarthrosis according to Paley classification, is characterized by congenital pseudoarthrosis of proximal femur with an isolated small and stiff femoral head. We are unable to create a moveable hip joint but appropriate length of the affected extremity can be reached by gradual lengthening. In previous classification it is known as Type Aitken C or Pappas III.
Type IIIa, with diaphysial deficiency of femur, corresponds to Type D according to Aitken or to Type I and II according to Pappas.
In Type IIIa, the knee joint is developed and functional with the ROM more than 45 degrees. In Type IIIb the knee joint is more or less stiff and functionally unuseable.
These three groups present the most severe congenital short femur deformities, but their occurrence is fortunately very seldom – less than 1 in 300 thousand live births. Among 41 cases of congenital short femur Pappas I–IV which were collected during 30 years from the Czech population of 10 million – Pappas I was seen in one case, Pappas II in five cases, Pappas III in 16 cases and Pappas IV in 19 cases. From the 16 cases of Pappas III deformity was found in three of them – stiffness of isolated femoral head was found and these three patients were added to this group.
Distraction of the distal part of femur up to acetabular level Connection between head and diaphysis First femoral lengthening Lengthening of the tibia Contralateral epiphysiodesis around the knee Plastic surgery
Lengthening between 15 and 39 cm was reached.
In Type IIIa, ilio-femoral fusion (knee-for-hip procedure) was performed in five cases. The functional results are excellent. There was no need for Syme amputation or rotationplasty. The prerequisite is at least 60 degrees arc of motion in the knee joint. Severe restricted ROM in the knee joint may lead to pseudoarthrosis.
In Type IIIb (2 cases), the residual fragment of distal femur with unfunctional knee joint was stabilized in socket formed after pelvic osteotomy in the level of original acetabulum. The removal of telescopic proximo-distal movement stabilized the supportive function of the extremity.
Maintaining correction is perhaps the most difficult aspect of management. Parental teaching and early attention to brace complications are helpful techniques to improve parental compliance.
56 patients who had undergone lower limb lengthening in accordance with Ilizarov principles in 61 bone segments were retrospectively studied and functional outcomes were evaluated by 5 different assessment systems.
There were 17 cases of congenial bone deficiencies, 11 post poliomyelitis, 11 post traumatic, 8 post infection, and 9 miscellaneous cases.
The average lengthening was 7.6 centimeters (3–14). Among the 46 patients who had reached skeletal maturity at the time of study,79% had reached their lengthening goal. 10 patients had still open physes and would require further equalization procedures.
There were 40 side effects (complications and obstacles) and 37 problems. 27 cases required additional surgery to treat the complications. Major complications were most commonly seen in congenital femoral lengthening cases.
The functional outcome as evaluated by the five different assessment systems revealed improvement in almost all aspects. The improvement in esthetic appearance of the limb and shoe -wear, walking, sporting activities, and limp were the most common reasons for satisfaction as observed in 89% of the cases.
The healing pattern went through different phases although they were not distinctively exclusive from each other and did show considerable overlap. First phase showed formation of a bulbous mass with some continuity of scar tissue across tendon gap. The transition zone between new fibre and the original tend quite distinct. However dynamic ultrasound showed the Achilles tendon moved as a single unit. Second phase showed fibres resembling normal tendon crossing the gap and reduction of bulbous mass The transition zone was still discernible. Final stage demonstrated more homogenous fibres of Achilles tendon with an indistinct transition zone.
Two older children showed a distinctly longer process of healing. One child showed an irregular mass of fluid and soft tissue structures in the gap at six weeks The other child demonstrated a relative reduction in the proportion of tendon fibres across the gap At 12 weeks there was evidence of continuation of tendon fibres, but transition zone partly visible.
There are many established database for estimating fetal femoral length ultrasonagraphically. There is little data however on radiological measurements of fetal femoral lengths. The aim of our study was to introduce radiologically measured fetal femoral lengths in order to improve our understanding of normal fetal femoral growth.
Using the standard growth curve there was a strong correlation between our radiological measurements and previously published ultrasonographic measurements (R2= 0.9492)
The femoral growth velocity curve demonstrated a rapid growth acceleration phase peaking at 12 cm/annum at 16 weeks, followed by a rapid deceleration phase reducing to a growth rate of 5 cm/annum at birth.
The growth remaining was calculated for each week. At 24 weeks the growth achieved is 10% thus giving a multiplying factor of 10. At birth the growth achieved is 20% giving a multiplying factor of 5.
Aim: To assess the risk of iatrogenic ulnar nerve injury using the mini medial incision to reduce and stabilise displaced supracondylar fractures of the humerus in children with crossed K-wires.
The five cases of primary ischemia with absent pulse and a white hand were managed by emergency reduction followed by exploratory surgery and vascular repair which restored the radial pulse, excepting one case which required anterior fasciotomy.
A number of studies show significant differences regarding their results due to the heterogeneity of methods and scientific and geographic fields originating each series.
The present study is intended to show the age of appearance and complete fusion of the different ossification nuclei of the first radio of the foot in a present Mediterranean sample of children and its relation with several morphometric and clinical parameters.
A descriptive and qualitative assessment allowed us to determine the existence or lack of each ossification nucleus of the first radio of the foot. Risser’s scale, adapted by us, was applied in the following way: 0, lack; I, rudimentary nucleus; II, well formed nucleus; III, partial fusion to diaphysis; IV, complete fusion.
Likewise, a statistical analysis was performed relating the ages of appearance and fusion of each nucleus with the forefoot morphology (digital and metatarsal formulae) and the main pathologies motivating the x-ray examination (traumatism, our control group; flatfoot; hallux valgus; clubfoot).
As a general rule, the age of appearance of each nucleus was earlier in girls. A delay in the age of appearance of the proximal metatarsal epiphysis in clubfoot patients (3.33 years) was observed in comparison with the control group (1.96 years).
In general, there was no relation between sex and the fusion (partial and total) of each nucleus of the first radio of the foot. The exception was the age of appearance of the distal metatarsal epiphysis (when this incostant nucleus was present), earlier in boys (9.49 years) than girls (11.21 years).
A delay in the age of fusion of the proximal and distal metatarsal epiphyses and the proximal phalanx epiphysis was observed in hallux valgus patients.
In patients with egyptian foot, there seems to be a delay in the age of fusion of the distal metatarsal and distal phalanx epiphyses.
Thanks to neonatal screening, idiopathic congenital dislocation of the hip (CDH) is generally diagnosed and treated at an early age. Despite this measure, late diagnosis of CDH still occurs. The goal of this article is to analyse the results of Petit-Morel’s closed reduction (CR) technique in the treatment of CDH diagnosed between 1 and 5 years old. We reviewed 72 hips in 60 patients. The treatment method was the same for all patients, beginning by bilateral longitudinal traction to achieve ‘presentation’ of the hip. It was followed by ‘penetration’ in a hip spica cast made under general anesthesia. The third step was an almost systematic surgical treatment of the remaining acetabular dysplasia. Results were evaluated using the radiological Severin score. Average follow-up was 11.9 years. The failure of CR occurs only twice. In this two cases, open reduction showed intraarticular obstacles to reduction. The only case of avascular necrosis (AVN) occured in one of this two failures of CR. At last follow-up, 95.8% of hips were rated as normal, or midly deformed. Young age at treatment significantly influenced the prognosis in our series. Neither the gender nor the height of the dislocation did appear to have any influence on the result. The patients which did not undergo a periacetabular osteotomy were significantly younger than the other one in the series. Pelvic osteotomy is an integral part of the method, as after 18 months many hips have lost their capacity to correct the remaining dysplasia. However, we only perform this osteotomy if the hip shows no sufficient correction during the semesters following the reduction od the dislocation. Considering Severin score, it is impossible to privilege closed or open reduction, as the results of both methods are close. However, in case of failure of reduction, which occurs in both methods, a second open reduction is much more difficult to achieve than and open reduction in a hip first treated by closed reduction. The results of this second surgery on the hip are poorer, with higher rates of AVN. Moreover, long-term functional and radiological deterioration of the hip is higher after open reduction than closed reduction. Lowest rates of AVN are reported after traction followed by closed reduction compared with exteporaneous reduction or open reduction, thanks to progressive reduction of the hip. Finally, mention should be made of the cost of the treatment. Petit-Morel’s protocole is expensive, both because of the duration of stay in the hospital, and by indirect costs as parent adaptation of its work during the treatment. The cost of open reduction is lower. However, considering the prooved better results of the closed method, requiring lower rates of further surgical procedure, we think that this method is the one to be promoted for treatment of CDH in children between 1 and 5 years old.
32 calcaneonavicular coalitions were surgically excised and an autogenous free fat graft was interponed to prevent a relapse. 1 calcaneonavicluar coalition also had an interposition of the extensor digitorum brevis after resection, while 1 calcaneonavicular coalition had lengthening of the short peroneal tendon in addition to excision and autogenous free fat graft. 1 calcaneonavicular coalition had to have an arthrodesis of the talocalcaneal joint.
From 2 talocalcaneal coalitions 1 had excision the other 1 talocalcaneal arthrodesis.
Both of the coalitions that had arthrodesis had short-leg plastercasts for 12 to 13 weeks.
For patients with bilateral coalition pedobarography was performed and the foot that had been treated compared to the untreated contralateral side. For these patients the AOFAS ankle and hind foot score and pain according to the VAS were evaluated.
1 patient showed a suspicious relapse in MRI after excision of a calcaneonavicular coalition. 1 talocalcaneal coaltion that had had excision continued to have pain after surgery. Both patients did not want a revision.
1 patient who was treated by an arthrodesis of the subtalar joint had a fracture of the tibial head, where autogenous bone graft had been taken. Osteosynthesis of the tibia was performed.
4 patients had pain after excision of a calcaneonavicular coalition but could be relieved by conservative treatment.
For 5 patients adequate follow up is still pending due to short interval to surgery.
Pedobarography showed tendecies of improved pressure distribution of the treated feet that were not significant.
We present a review of 195 patients attending hip ultrasound clinic from June 2005–2006 to assess for hip dysplasia. 51 dysplastic hips were identified and if appropriate were treated with a Pavlik harness. Follow up was continued until ultrasound was normal. However three cases (7%) were found to be dysplastic on further follow up. Whilst this study does not prove the existence of ‘late’ dysplasia occurring in hips that were normal at birth, it does show that hips treated to normality in the first six months of life can develop recurrent dysplasia. It suggests that weaning from Pavlik harness maybe appropriate and highlights the need for long term follow up for dysplastic hips with pelvic x-ray at 5 months.
We have been following all modern trends in the treatment of Legg-Calve-Perthes disease during several decades (from nonoperative treatment, revascularization procedures, varization femoral osteotomies to various pelvic osteotomies). Last few years we have started to use triple pelvic osteotomy in patients older than seven years, in order to shorten treatment period, establish solid containment and subsequent remodelation of femoral head, and achieve final spheric hip congruence.
In the period from 1996 to 2004 we had 28 such surgical interventions.
Patient age at surgery was between 7 and 10 years. All hips were uncontained preoperatively, and in fragmentation stage. Twelve hips were classified as Catterall group III and sixteen hips as Catterall group IV.
Triple pelvic osteotomy according to Tonnis (modified by Vladimirov) was performed in all cases.
Average follow-up period was 40 (28–96) months.
Treatment result was good in all patients, with full functional recovery.
Spheric joint congruence was achieved in 24, and aspheric congruence in other 4 cases.
Average period for union of osteotomies was 10 weeks, followed by introduction of full weight bearing, considerably earlier than in patients with similar age and disease stage, treated by combination of Salter pelvic osteotomy and femoral shortening.
In the avian injection group of 66 Knees, 57 had pain relief at 3 months.
In the synthetic injection group of 58 Knees, 48 had pain relief at 3 months
No complications were noted in either of the groups.
Using Chi square test and with 95% confidence interval, synthetic injection has no significant difference with avian injections in pain relief at 3 months [p=0.724].
VAS data should be analyzed using non paramentrics methods because vas have non-linear properties VAS and VRS are not interchangeable and they have a low percentage of intra-scale agreement. Disagreement are aleatory and non systematic The two scales have different interpretation Probably, due to great correlation with disability measured by odi, it is recommended to use vrs
Number of patients, although we find clinically and statistically significant differences
The mean EMG frequency was significantly lower for the PL (pathologic leg, 138.3 Hz; normal leg, 158.3 Hz, p< 0.001). Lower mean EMG intensity was found in the pathologic PL and GM. The mean EMG frequency of the TA was lower in the patient group, its intensity higher.
To identify the incidence and timing of superior subluxation following total shoulder replacement (TSR) and any associated change in pain, activities of daily living and ranges of movement. Forty-six TSR in rheumatoid patients with more than 5years follow-up were identified from a prospectively compiled database held by the senior author (ANS). Modified Constant scores (excluding the power component) were measured and recorded prospectively every 2years. Pre-operative and complete follow-up scores were available for 35 joints (27 patients). A Mann-Whitney U test was used to compare patients with subluxation and those without, with regard to the changes in the components of the Constant score at last follow-up compared with the pre-operative score. Superior subluxation of the humeral head was defined as when the lower third of the humeral head had migrated level or superior to the midpoint of the glenoid component as measured on the AP radiograph. An independent observer reviewed AP radiographs, taken at each 2 yearly review, at random with identity hidden and in no particular date order. Twenty-three patients developed superior subluxation since surgery, of which 87% occurred after 5years. Of the 35 joints with both clinical and radiological follow-up, 16 had evidence of subluxation. There was no statistically significant difference between the changes in the activities of daily living (Mann-Whitney U=106, p=0.1) and range of movement (U=140, p=0.7) components of the Constant score. However, patients without subluxation had a greater improvement in their pain scores (U=80, p=0.02). Approximately half of rheumatoid patients with TSR will demonstrate radiological changes of superior subluxation, in the majority after 5 years. This change is not associated with deterioration in activities of daily living or ranges of movement. However, pain relief persists irrespective of subluxation but is greater in those without subluxation.
In the presence of tendons lesser bony wear is seen at the acromion (acetabularisation, (p< 0.005), the glenoid (superomedial wear p=0.005) as well as the humeral head (femoralization, p=0.002).
The radiological classifications according to Hamada and Favard seem not to be as appropriate to reflect accurately the location and extent of the tendino-muscular degeneration as the acromial acetabularization and humeral sphericity.
The acromio-humeral distance is a good indicator for the location and the extend of the cuff tear arthropathy. A smaller acromio-humeral distance (95% CI: 4mm + 1) is only present if the postero-superior muscles are fatty degenerated (Goutallier stade III & IV) and a larger distance is calculated (95% CI: 7mm + 3) when only the antero-superior muscles are diseased.
The coracoid tip in cuff tear arthropathy-patients is almost always positioned in the inferior half of the glenoid (84%).
A bigger supero-inferior distance of the glenoid in relation to the radius of the humeral head indicates more structural destruction of rotator cuff status (tendinous and muscular) and a worse clinical outcome.
High-resolution micro-computed tomography ([mu]CT) imaging have been instrumental in providing true quantitative and qualitative three-dimensional data on baseline bone morphology
The glenoids were cut at the glenoid neck and at the base of the coracoid process.
The total, trabecular, and cortical BMDs of the 5 regions of the glenoids were determined by use of peripheral quantitative computed tomography (pQCT) (Xtrem Ct;Scanco, Zurich, Ch) Each glenoid was fixed horizontally in a custom-made jig, and axial pQCT scans (pixel size,1536/1536; slice thickness 80 microns), perpendicular to the articular surface, were obtained at the level of each area. From the resulting binarized three-dimensional reconstruction, Scanco software was used to calculate the bone volume per tissue volume; mean trabecular separation; mean trabecular number, connectivity density.
The mean total BMD in different regions of 20 glenoid specimens ranged from 0,243 to 0,489 g/cm2. The center of the glenoid was surprisingly poor in trabecular structures as we found a bony gap at 8 mm of distance from the articular surface.
In the future, component design should use areas of stronger subchondral bone. Posterior and superior bone area could be another alternative for fixation in decreasing glenoid-loosening rates. As the inferior center of the glenoid is an area devoided of trabecular bone, center-keel design component doesn’t seem to be the best choice.
Several studies showed the efficacy of arthroscopic repair for Type II SLAP lesions without other associated lesions, but the only data reported on the association of arthroscopic repair of Type II SLAP lesion and rotator cuff tears involve young and active patient. To our knowledge, no studies have focused on patients over 50.
We evaluated the results of a randomized controlled trial of arthroscopic repair in patients over 50 with rotator cuff tears and Type II SLAP lesion in whom the repair was effected repairing the two lesions, or repairing the rotator cuff tears and performing a tenotomy of the long head of the biceps.
We recruited 63 patients. In 31 patients, we repaired the rotator cuff and the Type II SLAP lesion (Group 1). In the other 32 patients, we repaired the rotator cuff and tenotomized the long head of the biceps (Group 2). 7 patients (2 in the group 1 and 5 in the group 2) were lost to final follow up.
A modified UCLA shoulder rating scale was used to evaluate pre-operative and post-operative shoulder pain, function, active forward flexion, strength and patient satisfaction.
Of 63 patients randomized to one of the two treatments, 5.2 year results were available for 56. 7 patients (2 in the group 1 and 5 in the group 2) did not return at the final follow up.
Statistically significant differences were seen with respect to the UCLA score and ROM values at final follow-up In Group 1 (SLAP repair and rotator cuff repair), the UCLA showed a statistically significant improvement from a pre-operative average rating of 10.4 (range 6 to 14) to an average of 27.9 (24–35) postoperatively (P< 0.001). In Group 2 (biceps tenotomy and rotator cuff repair), the UCLA showed a statistically significant improvement from a pre-operative average rating of 10.1 (range 5 to 14) to an average of 32.1 (range 30 to 35) post-operatively (P< 0.001) There was statistically significant difference in total post-operative UCLA scores and ROM when comparing the two groups post-operatively (P< 0.05).
Arthroscopic management has been recommended for some SLAP lesions, but no studies have focused on patients over 50 with rotator cuff tear and Type II SLAP lesion.
We compared the clinical outcome of patients over 50 affected with rotator cuff tears and Type II SLAP lesion in whom both the defects were repaired, or the rotator cuff tear was repaired and the long head of the biceps tendon was tenotomized. In our hands, the association of rotator cuff repair and biceps tenotomy provides better clinical outcome compared with repair of Type II SLAP lesion and of the rotator cuff.
The repair of the two defects, in fact, can lead to worst clinical results compared with association Rotator cuff repair alone is sufficient to determine a good post-operative outcome, allowing to avoid post-operative stiffness of the shoulder.
Postoperative stiffness (POS) of the shoulder may occur after an apparently successful reconstruction of a rotator cuff tear.
The role of the peripheral nervous system in tissue healing has only recently been recognized.
We determined the plasma levels of SP in patients with postoperative stiffness after arthroscopic repair of a rotator cuff tear, and compared them with those in patients with a good outcome after arthroscopic rotator cuff repair.
Plasma samples were obtained at 15 months from surgery from 2 groups of patients who underwent arthroscopic repair of a rotator cuff tear. In Group 1, 30 subjects (14 men and 16 women, mean age: 64.6 years, range 47 to 78) with shoulder stiffness 15 months after arthroscopic rotator cuff repair were recruited. In Group 2, 30 patients (11 men and 19 women, mean age: 57.8 years, range 45 to 77) were evaluated 15 months after successful arthroscopic rotator cuff repair. Immunoassays were performed with commercially available assay kits to detect the plasma levels of SP.
Statistical analysis were performed with Wilcoxon Sign Rank test. Significance was set at P< 0.05
The concentrations of the neuropeptide SP in sera were measurable in all patients. Patients with postoperative stiffness had statistically significant greater plasma levels of SP than patients in whom arthroscopic repair of rotator cuff tears had resulted in a good outcome (P < 0.05)
Postoperative stiffness (POS) of the shoulder may occur after an apparently successful reconstruction of a rotator cuff tear.
An increased amount of SP in the subacromial bursa has been correlated with the pain caused by rotator cuff disease.
SP stimulates DNA synthesis in fibroblasts, which are the cellular components of the adhesive capsulitis of the shoulder. Also, SP is a pain transmitter peptide, and pain may cause a secondary muscular and/or capsular contracture.
Our results show that the plasma concentrations of substance P in patients with shoulder stiffness after arthroscopic rotator cuff repair are higher compared to plasma levels of SP in patients with a good postoperative outcome.
We cannot determine the cause of POS in our patients, but the findings of this study suggest a possible neuronal role in the pathophysiology of POS after arthroscopic repair of rotator cuff tears. The knowledge of the pathophysiological role of sensory nerve peptides in tissue repair in these patients could open new therapeutic options to manage conditions of the musculo-skeletal system with impaired tissue-nervous system interaction.
Restoring of anatomic footprint may improve the healing and mechanical strength of repaired tendons. A double row of suture anchors increases the tendon-bone contact area, reconstituting a more anatomic configuration of the rotator cuff footprint.
We aimed to investigate if there were differences in clinical and imaging outcome between single row and double row suture anchor technique repairs of rotator cuff tears.
We recruited 60 patients affected by a rotator cuff tear diagnosed on clinical grounds, magnetic resonance imaging evidence of cuff tear and inadequate response to nonoperative management, an unretracted and sufficiently mobile full-thickness rotator cuff lesion to allow a double row repair found at the time of surgery.
In 30 patients, rotator cuff repair was performed with single row suture anchor technique (Group 1). In the other 30 patients, rotator cuff repair was performed with double row suture anchor technique (Group 2). 8 patients (4 in the single row anchor repair group and 4 in the double row anchor repair group) were lost at follow up.
A modified UCLA shoulder rating scale was used to evaluate preoperative and postoperative shoulder pain, function and range of motion, strength and patient satisfaction. All patients received a post-operative MR arthrography at the final follow up appointment.
At the 2 year follow-up, no statistically significant differences were seen with respect to the UCLA score and ROM values. Post-operative MR arthrography at 2 years of follow up in group 1 showed intact tendons in 14 patients, partial thickness defects in 10 patients and full thickness defects in 2 patients. In group 2, MR arthrography showed an intact rotator cuff in 18 patients, partial thickness defects in 7 patients, and full thickness defects in 1 patient.
Biomechanical studies comparing single versus double row suture anchor technique for rotator cuff repair show that a double row of suture anchors increases the tendonbone contact area and restores the anatomic rotator cuff footprint, providing a better environment for tendon healing.
Our study shows that there are no advantages in using a double row suture anchor technique to restore the anatomical footprint. The mechanical advantages evidenced in cadaveric studies do not translate into superior clinical performance when compared with the more traditionally, technically less demanding, and economically more advantageous technique of single row suture anchor repair.
establish an epidemiological database on LHB injuries in RCT; study the dynamic behaviour of LHB in RCT; search for a correlation between injected imaging findings and arthroscopic findings.
partial or full-thickness RCT demonstrated arthroscopically, arthorscopic description of LHB, imaging with injection (arthroscan or arthro-MR), data collected on the internet site of the Socité Française d’Arthroscopie (SFA).
Other reasons for arthroscopy, past surgery and MRI were excluded. The dynamic examination consisted in a search for the incapacity to glide the LHB in its gutter during passive abduction of the arm leading to intra-articular fold (hourglass test) and instability of the LHB in its groove during external rotation (medial instability) or internal rotation (lateral instability) with the arm at 90° abduction (RE2 and RI2 tests). Extension of the RCT in the frontal and sagittal plane were determined using the classification of the French Arthroscopic Society.
Epidemiological data (static test): LHB intact 21%, tenosynovitis 51%, hypertrophy 21%, delamination 12%, pre-tears 7%, subluxation 18%, dislocation 9%, tear 2%. No influence of age, gender or side operated. Conversely, the rate of lesions increased significantly with extention of the RCT in the frontal and sagittal plane.
Imaging-dynamic arthroscopy correlation: 25% of LHB lesions were not diagnosed by injected imaging. Inversely, there was a good correlation to determine the position of the LHB in its groove.
32 patients in the tenodesis group were satisfied with the result and would do surgery again compared to 25 in the tenotomy group, complaining about the visual deformity. There was no statistical difference in score result between the tenodesis or tenotomy group.
Group 1: anatomical prosthesis (Tornier): At an average follow-up of 16,5 (range 6–55) months, 13/17 patients with an average age of 78,6 years (70–95), were evaluated. Group 2: reversed prosthesis (Depuy): At an average follow-up of 12,6 (range 6–18) months, 13/17 patients with an average age of 77,1 years (70–84), were evaluated. In this group functional treatment was started immediately after surgery.
Does the pre-operative range of active anterior elevation alter the outcome of reverse shoulder prosthesis? A review of 96 cases.
Qualitative variables are presented in absolute and percentage values. Quantitative variables are presented with mean values and standard deviation.
Placement of the prosthesis in the proper retroversion can be achieved by placing the posterior fin 1,06 cm posterior to the upper insertion of the pectoralis major or by placing the posterior fin at 24,65º with respect to the upper insertion line.
Upper insertion of the pectoralis major constitutes a reliable reference to reproduce anatomy in hemiarthroplasties for proximal humeral fractures.
Intra–and postoperatively, there were neither fibrillations and sharp waves of the MUP’s as direct signs, nor incomplete (IP’s) of the motor unit of the subscapular nerve as indirect signs of denervation.
Polymethylmethacrylate cement (PMMA), as standard in fragility fractures, does not have the capacity to undergo remodeling. Therefore in young patients, a bio-compatible/–resorbable alternative would be preferable. KyphOs FS(R), a calcium magnesium hydroxyapatite cement has been developed for use during Balloon Kyphoplasty (BKP), a minimal invasive therapy.
This single-arm multicenter study evaluates the safety and effectiveness of this cement during BKP in young patients with stable VCFs.
We describe the clinical results up to 3mo of the ongoing 1-year follow-up study.
Based on the standard deviation in the Wood study, up to 100 patients had to be enrolled to detect the minimal clinical important difference (MCID) of 2–3 pts on the primary endpoint.
Mean cervical and radicular VAS-reported pain decreased from 60 [4–84] and 65 [2–96] pre-operatively to 21[0–45] and 21[0–36] at 0–6 months and to 15 [0–40] and 16 [0–40] respectively at 6–12 months. Similarly mean NDI decreased from 25 [9–45] to 10 [0–35] at 0–6 months and to 6[0–36] at 6–12mths. All patients were satisfied with the results so far.
Quantitative radiographic analysis showed satisfactory restoration of cervical mobility at the operated levels with mean flexion-extension mobility 6.4°[1–11°] at 0–3mths and 7.1°[4–12°] at 6–12mths respectively. The adjacent level mobility was found within normal ranges at 6–12mths post-operatively. At the same follow-up period, the regional lordosis was within physiological ranges for 65% of patients at the last follow-up.
Both clinical and radiological findings in this study support the effectiveness of the Discocerv® Cervidisc Evolution prosthesis at mid-term. However further follow-up at long term is necessary in order to confirm these findings.
group A: conservative treatment – 321 pts. (49%) – the magnitude of the curves was at time of detection on average 35,7 degrees according to Cobb angle and 39,8 at time of last control with FU 13,7 year. group B: hemiepiphyseodesis – 102 pts. (16%) – the time of surgery was 6,6 years, follow up was 14,2 years. The magnitude of the curves was at time of detection on average 44,1 degrees, 44,2 preoperatively, 34,4 postoperatively and 38,4 at time of last control. Final result of correction was 9,8 degrees (22%). group C: posterior instrumentated fusion – 145 pts. (22%) – the time of surgery was 8,6 years, follow up was 18,9 years. The magnitude of the curves was at time of detection on average 59,2 degrees, 65,5 preoperatively, 39,9 postoperatively. Final result of correction was 25,6° (38%). group D1: strut graft with posterior instrumentated fusion – 27 pts. – the time of surgery was 11,8 years, follow up was 19,5 years. The magnitude of the curves was at time of detection on average 54,4 degrees, 65,6 preoperatively, 38,6 postoperatively. Final result of correction was 26° (40%). group D2: anterior osteotomy with posterior instrumentated fusion – 33 pts. – the time of surgery was 9,9 years, follow up was 18,3 years. The magnitude of the curves was at time of detection on average 58,1 degrees, 65 preoperatively, 37 postoperatively. Final result of correction was 28° (43%). group D3: combined hemivertebrectomy with posterior instrumentated fusion – 22 pts. – the time of surgery was 10,2 years, follow up was 12,1 years. The magnitude of the curves was at time of detection on average 46,4 degrees, 51,3 preoperatively, 20,3 postoperatively. Final result of correction was 31,3° (61%).
The purpose of this prospective study was to assess the functional outcome in thoracolumbar vertebra fractures that were treated nonsurgically.
From 1999 to 2005, seventy-four patients with single-level nonpathologic fractures, with angle of kyphosis less than 20° and with no or minor neurological impairment and without neurological deterioration were managed non-operatively. A custom-made thoracolumbosacral orthosis was worn by all patients for six months and early ambulation was recommended. The average follow-up period was 34 months (range, 14 to 59 months). Functional, pain, and employment status were assessed using the Denis system. Radiographic evaluation of vertebral kyphosis, local kyphosis angle, anterior body compression, and sagittal index were performed at time of injury, and final follow-up. Paired t test and Wilcoxon signed rank test were used for statistical analyses.
At final follow-up, 63 patients (86.3%) were rated P1 (no pain), 8 patients (11%) were rated P2 (occasional pain), 2 patients (2.7%) were rated P3 (moderate pain), and 0 patients (0%) were rated P5 (constant severe pain). Sixty-five patients (90%) were able to work at the same level (W1) and the rest was W2 and no W3,4,5. According to radiographic evaluation although all the results showed statistically significant differences, these were too small to be important clinically. The initial local kyphosis angle averaged 14.73° (sd 5.08), and at follow-up it averaged 15.99° (sd 4.98). The initial sagital index averaged 16.1° (sd 5.69), and at follow-up it averaged 16.79° (sd 5.63).
As conclusion nonoperative treatment of selected patients with thoracolumbar vertebral fracture predictably leads to acceptable functional and radiographic results. Conservative management resulted in minimal loss of work potential in these patients and no correlation was found between fracture type and clinical outcome.
Patients with bilateral femur shaft fractures are known to have a higher rate of complications when compared with those who have unilateral fractures. Many contributing factors have been considered responsible, however due to the heterogeneity of the studied populations solid conclusions cannot be substantiated. Patients included in our study were separated according to the presence of a unilateral (group USF) (n=146) versus bilateral femur shaft fracture (group BSF) (n=19)Endpoints of the study included the incidence of systemic (SIRS, Sepsis, Acute Lung Injuries) complications. The perioperative assessment included documentation of clinical and laboratory data assessing blood loss, coagulopathy, wound infection, and pneumonia. Local (wound infection, compartment syndrome etc.) and systemic complications (ALI, MOF, Sepsis) were documented. Statistical analyses were conducted to examine the relation between the occurrence of unilateral versus bilateral femoral fractures and variables indexing patient demographic characteristics and other indicators of initial injury severity. Independent sample t-tests were used to examine treatment group differences for variables that approximated a Gaussian distribution. For non-normal indicators of injury severity Mann-Whitney tests were performed. Pearson chi-square tests were performed for binary indicators of injury severity, except when expected cell counts did not exceed 5 participants. When this occurred, the Fisher exact test was used Evidence indicated that patients who suffered a bilateral femoral fracture were significantly more likely to have hemothorax and receive a blood transfusion upon admission to the hospital in comparison to patients who suffered a unilateral femoral fracture. Bivariate analyses also indicated that patients with bilateral femoral fractures exhibited a longer clinical recovery time and were more likely to experience clinical complications in comparison to those with unilateral fractures. However, there were no significant differences between the fracture groups in terms of the number of hours spent on a ventilator or the occurrence of pneumonia, acute lung injury, acute respiratory distress, sepsis, and multiple organ failure following surgery. Patients in borderline condition spent significantly more time in the ICU in comparison to those in stable condition. The high incidence of posttraumatic complications in poly-trauma patients with bilateral femur shaft fractures is caused by the accompanying injuries rather than by the additional femur fracture itself. It also documents that a thorough preoperative assessment can help differentiate those who have a high like hood of developing systemic complications from those who do not.
The aim of this study was to find out if a specific proprioceptive exercise as perturbation training permits a further and durable recovery of proprioception after ACL reconstruction for an early return to agonism.
They have been clinically evaluated before surgery and after 2, 3, 6 and 12 months after surgery with a kinaesthetic device constituted by a tilting platform equipped by digitalized sensor connected to a computer. The protocol included three repetition of one and two legged standing balance. The statistical analyses with t-test considered significant value of p< 0.05.
Best results in the Perturbation group are maintained at the 6th month only in the one legged stance on healthy side (p=0,014) but any difference is still present at 12 months.
The aim of this study was to document the findings and the pathology of tennis elbow during arthroscopy in patients who had failed conservative treatment for lateral elbow pain with a presumptive diagnosis of lateral epicondylitis (tennis elbow).
Of the 232 patients who had degenerative changes 186(80%) had articular cartilage changes in the lateral compartment(radial head & capitellum), partial thickness loss in n=94(51%) and full thickness cartilage loss in n=92(49%).
This diagnosis of tennis elbow is often applied to patients with degenerative changes(osteoarthritis) involving the lateral compartment.
Advanced degenerative changes involving the articular cartilage of the lateral compartment can be present in patients with little or no abnormality visible on x-ray.
We conclude that arthroscopy is a definitive diagnostic tool to evaluate the various pathologies giving rise to lateral elbow pain and also helps in planning and initiating the appropriate treatment plan directed against specific and accurate conditions causing lateral elbow pain(lateral epicondylitis)
Patients were mobilized with an AirCast® ankle brace and cranes for six weeks, then the syndesmotic screw was removed and patients started full weight bearing.
Using the x-rays of the ankle before and after and the CT of both ankles before removal of the syndesmotic screw we evaluated the radiologic results: the syndesmotic interval in the axial cuts, the Espace claire de Chaput (total clear space, TCS) und the medial clear space (MCS). Ventralization of the fibula as a measurement for the position of the fibula in the incisura was defined as the difference between the vertical reference lines of tibia and fibula in the CT. The functional results were evaluated by the scores of Phillips, Olerud/Molander and Weber.
The functional scores showed good to very good results in most patients.
Study Design: A prospective, randomized clinical trial.
The operative therapy of intraarticular fractures of the calcaneus is nowadays established surgical standard. Aim is an accurate reduction with reconstruction of the Boehler’s angle, the length and the subtalar joint. 3D-fluoroscopy with the Siremobil Iso-C 3D? mobile C-arm radiography system is a valuable assistance for the accurate reconstruction of the anatomical structures. Remaining incongruities can be recognized and corrected intraoperatively. The achieved reduction can be safely fixed by the advantages of a locked implant In the period of 10/2002 until 10/2004 we operated 59 patients with intraarticular fractures of the calcaneus by means of anatomical reduction and locked plate (Calcaneus TiFix, Litos, Germany) under control of 3D-fluoroscopy. After routine CT diagnostics, fractures were classified according to Sanders: 18 fractures were type II, 33 fractures type III and 9 were classified type IV.
Results: Surgical treatment of the fractures took place according on average after an interval of 8.5 days (7 to 11). A 3D-fluoroscopy was performed after reduction and temporary fixation of the fracture. There was no technical fault of the device. Median theatre time was 72 minutes (53–112 minutes) including 3-D-fluoroscopy. In 22 cases a remaining incongruity of > 1 mm could be seen on intraoperative 3-D-fluoroscopy. In these cases a reduction was performed again. The Boehler’s angle could be raised on average by 18° (11° to 22°), shortening of the hindfoot could be improved on average by 13 picture millimetres (9 to 17mm). Bone graft was not required in any case. At 6 months follow up, all patients had returned to work, or if unemployed, where judged fit to work by their GP. Three patients changed their position. 25 Patients were completely pain free at follow-up. In all cases the achieved reduction could be fixed by the implant until full weight bearing was reached.
Conclusion: The use of 3D Fluoroscopy had a real impact in the treatment of calcaneal fractures. If this short term advantage influences the long term result has to be shown in further follow up.
Retrospective comparative analysis of twenty five patients treated with Ilizarov bone transport [IBT] and twenty one patients treated with vascularised fibular graft [VFG] from 1994 to 2003 in one institution, for post traumatic tibial bone defects of more than six centimeters. The aim of the study was to find out if there were any differences in achieving radiological end points, bone and functional score and return to work (final outcome), hospital stay and operating time (logistic factors) and complication rates. The mean defect size in the IBT group was 11.9 centimeters and in the VFG group 14.6 centimeters.
Twenty one and sixteen patients in the IBT and VFG group respectively achieved the radiological end point that is union of the defect and graft hypertrophy [p 0.5]. Nineteen patients in the IBT group and fifteen in the VFG group returned to productive work [p 0.72]. Bone and functional results were analyzed by Paley’s evaluation system and there were no significant differences in the two groups of patients [bone result p 0.97 and functional result p 0.1]. The logistic factors were significantly less of IBT group [p < 0.05]. Two patients in the IBT group and one patient in the VFG group had amputation and one patient in VFG group died. Three cases in the VFG group had flap loss. Stress fracture of the graft occurred in eight patients in the VFG group [p 0.0007].
The final outcome was same in both groups. Hospital stay, operating time and refractures were significantly less in IBT group.
Despite continuous advances in the treatment of long bone fractures, disturbances of healing processes remain a difficult challenge. Currently, autologous cancellous bone and bone marrow grafting has become the standard treatment of delayed unions and non-unions. Platelet concentrates rich in growth factors – platelet-rich plasma (PRP) – represent a novel osteoinductive therapy that could be valuable for the treatment of disturbances of bone healing processes.
This article reports the efficiency of percutaneous autologous platelet-leukocyte rich gel (PLRG) injection as a minimally invasive method as alternative to open grafting techniques. Following the outpatient procedure, each of 32 participants was followed up on a regular basis with clinical examinations, roentgenograms, dual-energy x-ray absorptiometry (DEXA) examinations and functional evaluations. In the delayed-union group the average time to union after PLRG injection was 9,3 weeks and the union was achieved in all cases. In the nonunion group, the union was observed in 13 of 20 cases and the average time to union after PLRG injection was 10,3 weeks. Interestingly, in patients with non-union, who a union was not achieved, the ave time from the fracture and/or from the last operation was longer than 11 months. Probably the fibrous tissue in the gap interposing the bone ends becomes more ossified with time and the vascular vessels diminish, so the PLRG is no longer able to induce the bone healing processes in such cases.
This is our initial experience with the use of PLRG as biologic treatment for delayed union or nonunion. Our investigation showed that percutaneous PLRG injection in delayed union is a sufficient method to obtain union, which is less invasive procedure than bone marrow injection. Also percutaneous PLRG grafting can be an effective method for the treatment of selected cases of nonunion. One critical factor is the average time of PLRG injection to the index operation – the time less than 11 months after initial surgery seems to be critical to achieve good outcomes in percutaneous PLRG injections for nonunion.
There was a strong correlation between the length of time spent in the hanging cast and a high rate of non-union. The average length of time spent in cast for the non-union group was 48 days as opposed to 30.9days in the group that went onto unite (p=0.0601)
There was a statistically significant correlation between non-union and the radiographic degree of distraction at the time of first application of hanging cast (p=0.016) and also at the six week check (p=0.001).
Other factors associated with a poor outcome were the degree of varus angulation at presentation (p=0.0078), male sex, right humerus, dominant side, older age group, high energy injury, NSAID use, significant co-morbidities and associated injuries.
In the studies using SF36, the mean Physical Component Summary (PCS) for the amputation group was 39.76 +/−7.06 and mean Mental Component Summary (MCS) was 52.05+/−3.39. The mean PCS for the reconstruction group was 38.5+/−0.78 and the mean MCS was 50.76 +/− 3.09. The mean physical SIP score for amputation was 13.033 with SEM of 3.048, and the psychological SIP score was 15.953 with SEM of 1.153. The mean Physical SIP for reconstruction was 10.686 with SEM of 1.034 and the psychological SIP was 10.754 with SEM of 0.647. The Unpaired t test was used to compare the outcomes of amputation and reconstruction, studies using SF36 and SIP scores were compared independently. Our results show that physical morbidity in both groups is not significantly influenced by the modality of surgical intervention, but there is a statistically significant difference noted in psychological morbidity, the group with reconstruction being better. These results were consistent in studies using either of the two generic scales namely, SF36 or SIP scores.
The evolving importance of extremity trauma is clear from the quantity of its reporting. The paucity of life threatening cavity trauma is highlighted. Casualty survival off the battlefield is increasing perhaps due to the impact of personal protective equipment. The combination of changing ballistics and increasing survivability leads to an apparent increase in limb threatening and complex hand trauma being encountered by military surgeons.
Despite being rarely reported in isolation, the proportion of complex hand trauma is broadening with an increase in open fractures and mutilated soft tissue injuries resultant from high and low energy transfer ballistics.
Hand trauma is also shown to occur in deployed troops during activities unrelated to war fighting. Sporting activities and inappropriate use of equipment are responsible for soft tissue and bony injury with considerable morbidity.
The literature was analysed with regard to the classification of hand trauma. Articles relating to recent conflicts were notable for their lack of classification of these injuries.
The bulk of papers retrieved concerning military hand trauma management were published prior to the conflicts of the last decade. It is within these papers that classification and treatment priorities including the nature of debridement and fracture stabilisation are discussed and highlighted as core knowledge.
Despite a culture of ensuring that today’s trauma surgeons learn from mistakes made by their predecessors, in the field of hand trauma this is not the case.
A comprehensive review of changing orthopaedic conflict related injury patterns with special regard to hand trauma and the key learning points from historical literature are highlighted. Proposals for improving management are discussed with regard to improved training opportunities and dialogue between military trauma surgeons.
To determine the functional outcome of floating knee injury a retrospective study was undertaken at 3 level 1 trauma centers.
Experimental test were performed in a patella sow-bone models and showed superior to tension bel (patella) and Plate fixation/fibula). On the other side the locked nail system allows percutaaneous osteosynthesis of the whole ulna also in shaft, distal fractures and shortening osteotomies.
All clinical cases treated with the XS/XXS nail where recorded prospectively and re-examined after 6–12 months. From may 2000 to march 2002 76 patients with olecranon fractures were evaluated. 85% of the olecranon fracture patients could be re-examined. Most patients where treated immediately or after wound healing without splint.
71.7% of all patients with olecranon fractures showed a very good result according to the Murphy score. In 2 part fractures the rate was even 94.7%. Only in the group of more part fractures in 5.9% fair results were found. No patient showed a poor result.
The technical possibilities of XS nail osteosynthesis in ulna shaft, distal fractures and shortening osteotomies are presented.
The locked plates are commonly used to obtain fixation in periarticular and comminuted fractures. Their use has also gained popularity in fixing fractures in osteoporotic skeleton. These plates provide stable fixation and promote biological healing. We have used over 150 locked plates with varying success in last 3 years to fix periarticular fractures involving mainly Knee and Ankle. These plates need to be removed if indicated which may be implant failure, infection, non-union or a palpable symptomatic implant. There are no reports in the literature regarding complications associated with removal of these locked plates. We report our clinical experience of removing locked plates in 28 adult patients. The procedure of implant removal was associated with a complication rate of 25%. The main problems encountered were difficulty in removing the locked screws and the implant itself. The locking plate could not be removed in two patients and had to be left in situ. We recommend that surgeon should be aware of these potential complications whilst removing these plates and that fluoroscopic control and all available extra equipment mainly metal cutting burrs and screw removal set should be available in theatre.
Human recombinant Osteogenic Protein 1 or rhBMP-7 is licensed for use in tibial non-union where autologous bone grafting has failed. Through its osteoconductive and osteoinductive properties, its application may be more widely applied. We audited our use of rhBMP-7 and present the largest series currently reported in the literature.
We reviewed 107 consecutive patients on whom rhBMP-7 was used over a 5-year period (2002–2007). Demographic and clinical details (e.g indication, site, use of adjuncts, previous surgery, smoking status, time to union, mean follow up etc) were entered into an electronic spreadsheet.
RhBMP-7 was used in 112 sites on 107 patients (65 male, 42 female). Ages ranged from 16yrs to 89yrs (mean 47.6). Non-union was the main indication for surgery (82 cases). RhBMP-7 was used alone in 39 cases and with autologous bone graft (56 cases). In other cases demineralised bone matrix, USS and bone allograft were used as adjuncts. Tibia (42 cases), femur (29 cases), humerus (21 cases) were the most common sites of administration. Mean number of operations prior to use of rhBMP-7 was 1.6 (range 1–20). In all cases, union was achieved in 65% (73/112) with a mean union time 5.8 months. The ‘rhBMP-7 alone’ subgroup demonstrated union in 83% (30/36), mean union time 5.15 months. 68% (56/82) of cases treated for nonunion subsequently united with rhBMP-7.
Our results suggest rhBMP-7 is useful in the management of fracture non-union and limb reconstruction surgery irrespective of site. It promotes bone healing of non-unions subjected to multiple operations previously. It may be indicated in those patients in whom autologous bone graft harvest is undesirable or not possible or as an adjunct to bone grafting. Moreover we did not detect any adverse reactions specific to the administration of rhBMP-7.
Displaced proximal humeral fractures are common fractures with high complication rate especially in osteoporotic elderly population. The purpose of our clinical prospective case series was to evaluate the Philos locking plate developed by AO/ASIF in surgical treatment of these difficult fractures.
Between October 2005 and March 2007 42 patients were included in the study group. The patients were divided in two groups based on the age at the time of presentation. Group A consisted of patients younger than 65 years old; 14 male, 9 female; mean age 43.8 (24–63 years old) and group B were patients above the age 65; 16 female, 3 male; mean age 77.3(66–90 years old). All fractures were classified according to AO/ASIF classification and radilogical and functional outcomes were assesed.
Mean follow up was 7.8 months. The mean Constant scres were 86.3(71–92) in group A and 84.7(68–92) in group B (p> 0.05). All fracture healed uneventfully and no implant failure was observed. Displacement of tuberculum majus fragment was observed in only one case. Avascular necrosis of the humeral was not observed in any case.
This prospective study proved that when technical details are followed and supplementary suture fixation of the tubercular fragments to the plate is obtained locking plate fixation of these problem fractures in every age group has a very high radiological and functional success rate. Especially in fixation of osteoporotic fractures lack of fixation failure and initiation of early range of motion is a major advantage.
Proximal humeral fractures are common fractures that may lead to severe functional disability. In open reduction and internal fixation of these fractures deltopectoral approach is pereferred by many surgeons being an internervous plane and because of familiarity. However when this aprroach is used extensive soft tissue dissection is inevitable and control of the commonly displaced tuberculum majus fragment which is displaced posterolateraly is difficult. In this prospective study we compared deltopectoral and lateral deltoid splitting approach by using the same fixation material.
Between October 2005 and March 2007 42 patients were included in the study group. In Group A a lateral deltoid split approch and in Group B deltopectoral approach was used. Group A consisted of 22 cases; mean age 60.95 (26–90 years old); 12 female and 10 male, Group B 20 cases; mean age 56.9 (24–86 years old); 13 female, 7 male. Philos locking plate fixation (Synthes) was used in every case. When deltoid split approach was used axillary nerve was explored and protected, a C-arm was used in every case. Functional results and compications were compared at the follow up visits.
When radiological results were compared the reduction of head and tubercular fragments were better in deltoid splitting approach. The Constant score was better in Group A at an earlier time period 68.9 vs 58.4 (p< 0.01). At the 6th month follow up the difference between Constant scores was not significant, 85.9 vs 85.2 (p> 0.05). Axillary nerve lesion due to lateral deltoid split exposure was not observed in any of the cases.
Lateral deltoid split exposure with identification and protection of the axillary nerve facilitates 270 degrees control of the head and tubercular fragments in AO/ASIF type B and C fractures. Additional fixation of tubercular fragments by sutures passed through cuff tendons and fixed to the plate helps to maintain the reduction. Compared to double incision minimal invasive approach a shother plate is used without any inadvertant risk to the axillary nerve. Better Constant scores are achieved at an earlier time. We recommend this technique in AO/ASIF type B and C fractures.
During the last decade intramedullary nailing of the humerus became a more popular operation. Modern nails are successfully used in treatment of fractures involving proximal, distal and middle shaft humerus, as well as pseudarthrosis and pathological fractures. Minimal invasive insertion lessens the complications from neurovascular and soft tissue damage without significant delay in healing period in comparison with compression plates. Aim of our study is to present our experience and the clinical outcomes of this method.
In group II, two cases needed implant revision with intramedullary nail in one and circular external fixator in another for non-union. Mal-union in one case and chronic osteomyelitis in another were late complications of group II. At the last follow up satisfaction rates were as; 21/25 in group I and 18/20 in group II clinically. There was no significant difference between both groups with regard to clinical evaluation (p> 0.05).
Results were analysed using ANOVA with 95% Confidence Intervals.
The Majeed functional scoring was applied. In conclusion we could say that 81% of our patients were in the excellent and good category.
The classification system commonly used the Muller and Schatzker ones those relate grade to treatment ad outcome.
We compared all cases of closed intra-articluar fractures (AO types C2 and C3) fixed by the method described above in a one year period (June 2004 – June 2005) – Group 1 (n = 26), with the immediate previous one year period (June 2003 – June 2004) of matched closed fracture pattern fixed by formal open reduction and internal fixation – Group 2 (n = 16).
Mean follow up was 26 months. All bony and soft tissue complications were recorded. A specific assessment of foot and ankle outcome was undertaken using the American Orthopaedic Foot and Ankle Score (AOFAS). Scoring was undertaken on two separate occasions at a mean of 9 and 24 months post operatively, by orthopaedic surgeons blinded to the treatment modality. The mean of the two scores was then recorded. It has been previously demonstrated that the functional outcome in pilon fractures improves for approximately 2 years after injury.
In their presented work authors summarize the results of using Philos plate in ultimate indications. These are – dislocated proximal humeral fractures with abruption of the head in anatomical neck, where head fragment is so much thin and eventually osteoporotic, that fixation of any osteosynthetic component would be technically impossible. These cases include even situations where head fragment is then splitted into two major fragments.
Presentation supported by grants MSMT CR 57/226010NPV, GA CR 106/04/1118 and FT–TA3/131
Both groups were age and sex matched. Besides patient demographics, fracture pattern according to Dennis–Webber classification, orientation of the medial malleolar fracture, position of screw in relation to fracture, post-operative fracture displacement and union (bony and clinical) were assessed. Patients were also contacted to assess whether they had returned to their pre-injury level of activities.
In group-I, 15 patients had bi-malleolar Dennis-Webber type B fractures, 9 had bi-malleolar Dennis-Webber type C and 10 had tri-malleolar fractures. 3 had uni-malleolar fracture.
In group-II, 20 patients had bi-malleolar Dennis-Webber type B fractures, 9 had bi-malleolar Dennis-Webber type C fractures and there were 5 tri-malleolar fractures. 5 had uni-malleolar fracture.
The fracture orientation in both the groups was mostly horizontal than oblique and the screw placement was at an angle to the fracture in the majority of cases in both of them.
There was no significant difference between the two groups, in terms of clinical union, post-operative fracture displacement and return of patients to their pre-injury level of activity.
Long folllow up showed that main complications were pain and bone cysts, which required arthrodesis in 8 cases. Survivorship analysis at 108 months were 83% [IC5%: 72–95]. At follow up, clinical AOFAS ankle score was significantly raised (31% preoperative to 84% at follow up). A SF36 quality of life score was available for 85 patients. Physical score was 60, mental score 66 and total score was 64.
The aim of this study is to present guidelines for treatment of acquired adult flat foot (AAFF) and review the results of a series of patients consecutively treated. 180 patients (215 feet), mean age 54? 12 years affected by AAFF were evaluated clinically, radiographically and by MRI to chose the adequate surgical strategy. Tibialis posterior dysfunctions grade 1 were treated by tenolysis and tendon repair (48 cases), grade 2 by removal of degenerated tissue and tendon augmentation (41 cases), grade 3 by flexor digitorum longus tendon transfer (23 cases); in these cases subtalar pronation without arthritis was corrected by addictional procedures consisting of either calcaneal osteotomy (66 cases), subtalar athroereisis (25 cases) or Evans procedure (21 cases) in case of severe midfoot abduction. Subtalar arthrodesis (82 cases) or triple arthrodesis (21 cases) were performed in case of subtalar arthritis isolated or associated with midtarsal arthritis respectively. Postoperatively plastercast without weight-bearing for 4 weeks followed by walking boot for 4 weeks was advised. All patients were followed up to 5 years. Before surgery the mean AOFAS score was 48+\−11, while it was 89+\−10 at follow-up (p< 0.005). Mean heel valgus deviation at rest was 15°+\−5° preoperatively and 8°+\−4° at follow-up (p< 0.005). Mean angulation of Meary’s line at talonavicular joint level was 165°+\−12° preoperatively and 175°+\6 at follow-up. Surgical strategy in AAFF should include adequate treatment of tibialis posterior disfunction and osteotomies for correction of the skeletal deformities if joints are arthritis free; arthrodesis should be considered in case of severe joint degeneration
Displaced intra-articular fractures of the calcaneus need anatomic reduction of the joint surfaces and overall shape to restore function and minimize the risk of posttraumatic subtalar arthritis. The morbidity associated with extended approaches is a major concern. In the present study we compared the medium-term results after percutaneous reduction and screw fixation (PRSF) with that of open reduction and internal fixation (ORIF) for displaced fractures with less severe fracture patterns (Sanders type II).
To measure the edge angle of the medial (α) and lateral (β) talar dome, curves were adjusted along the medial and lateral talar body and on top of the talar dome measuring the angles in-between. To measure the radius, circles were fitted into the medial and lateral talar dome (rm and rl).
Knee braces are more comfortable to wear, and they also restrict hip movement by tightening the hamstrings. With this background we investigated the effect of a knee brace, applied in full extension, on hip flexion and adduction.
With a flexed knee, the mean hip adduction angle was 23.7 degrees (CI95 = 20.6, 26.9). With the knee braced, the mean hip adduction angle was 21.6 (CI95 = 19.2, 24.1). Hence the knee brace reduced hip adduction by 9% (2.1 deg). A paired t-test found this was not significant with P = 0.3.
Hip fracture is a common serious injury in the elderly. Between 1982 and 1998 the number of hip fractures reported annually in Scotland in patients over 55 years rose from 4,000 to 5,700. The optimum method of treatment for the various fracture types remains in contention. The purpose of this study was to compare outcome measures between displaced, intracapsular fractures in patients over 70 years fixed with cannulated screws and sliding hip screw with side plate. Between 1998 and 2005 a total of 30,482 patients were reviewed by the Scottish Hip Fracture Audit (SHFA). Of these 15,823(53.3% of the total) had sustained intracapsular fractures. 13,587 of these occurred in patients aged 70 or over. Of these 2,428 had undisplaced and 11,159 displaced fractures. We performed a Chi test statistical analysis comparing outcome measures in this group of displaced intracapsular fractures with respect to aspects of early failure. 534(3.9%) of patients were treated conservatively. 509 (4.7%) fractures were fixed using cannulated screws and 499 (4.6%) using a sliding hip screw. Readmission within 120 days for any cause occurred in 62 patients(14.1%) treated with cannulated screw fixation and in 63 patients(15.7%) for those treated with a sliding hip screw(P=0.509). Of these 36 patients(8.2%) in the former and 23 patients(5.7%) in the latter group were readmitted for complications related to hip fracture(P=0.033). Mortality within this period included 69 patients(13.5%) in the CS and 98(19.6%) in the SHS group. In terms of re-operation within 120 days of the original admission, 53 patients(10.6%) receiving cannulated screws compared to 24 patients(4.8%) treated with a sliding hip screw requiring further surgery(P=0.0006). The fracture was seen to displace in 12(22.6%) patients originally treated with cannulated screws compared to 6 patients(25%) treated with sliding hip screw(P=0.156). More significantly the fixation device was seen to have migrated in 24(45.3%) of the cannulated screw as compared to 7(29.2%) patients in the sliding hip screw group(P=0.002). Periprosthetic fractures were recorded in 4(7.5%) of the former and 3(12.5%) in the latter group(P=0.708). Wound infection was higher in the SHS group(2 patients) as compared to the screw fixation group(1 patient)(P=0.565). Statistical analysis demonstrates a dramatic difference exists between these 2 fixation types in terms of re-operation within 120 days of the original admission for which published literature has previously only recorded biomechanical, in vitro comparisons. Data regarding specific implant factors such as number of screws, position, configuration, starting point, thread length and use of washers in cannulated screws, and position, tapping, supplementary screw and compression screw in sliding hip screws was not recorded and may be considered to bias our results.
The aim of the present study was to determine the different radiological alterations observed in our series and their possible relation with other variables (sex, foot pathology and forefoot morphology).
In the 46.3% of the cases there are radiological alterations in the ossification nucleus of the proximal phalanx. In such cases, the 79.2% were sclerotic.
In the flatfoot patients a higher frequency regarding the apperance of radiological alterations was shown significant (p< 0.05) for first cuneiform, proximal metatarsal, and proximal phalanx nuclei.
In the cases with evident alterations of the proximal or distal metatarsal nuclei, the 100% of the cases was related to egyptian digital formula.
The retrospective study did not provide us with additional clinical information about symptoms that could define osteocondrosis in each case.
The biomechanical alterations of the gait in the flat-foot patients, or its treatment (insole), could be related to radiological alterations of such nuclei.
Medial patello-femoral degenerative changes were found more frequently and these lesions were more pronounced: 20% had narrowing < 50% (IKDC C) and 4% had narrowing > 50% (IKDC D). Onset of medial patellofemoral osteoarthritis was correlated with medial femorotibial osteoarthritis (p< 0,001).
Patellar height was statistically different between the operated and controlateral knee (CDI = 0.92 and 0.96, p< 0.001). Patella baja (CDI< 0.8, frequency 9.9%) was correlated with medial femoro-patellar osteoarthritis (< 0.001) and postoperative cast immobilisation (p=0.047).