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The study was designed to compare the clinical performance of an Alumina ceramic acetabular bearing to that of a polyethylene bearing in a cementless hip couple.
The study group consisted of 15 surgeons who performed 308 total hip replacements (297 patients) between January 29, 1998 and February 1, 2000. All patients received a porous coated cementless titanium stem with an Alumina ceramic 28 mm or 32 mm head. Patients were randomized to receive a porous titanium acetabular shell with either a polyethylene or Alumina cup liner. There were 164 Alumina cups and 144 polyethylene cups. The mean age was 57.3 years and consisted of 50% males and 50% females. The preoperative diagnoses were: osteoarthritis 69.8%, avascular necrosis 19.5 %, post traumatic arthritis 2.9 %, inflammatory arthritis 3.9% and other 3.9%. The mean follow up was 12 months. The longest follow up was 38 months.
The Harris Hip Score was good and excellent in 86% of the control patients and 87% of the study patients. There has been 100% follow up and survivorship.
There were two reoperations for recurrent dislocations in each group. There were no Alumina component fractures, no progressive radiolucencies and no evidence of rapid wear.
In the short term follow-up between 12 and 38 months, there do not appear to be any differences between the patients with a bearing couple consisting of Alumina on plastic with those consisting of Alumina on Alumina. There have been no catastrophic failures of the ceramic components. The Alumina/Alumina bearing couple for total hip arthroplasty appears to be an excellent alternative bearing, providing the advantage of improved long term wear and a reduced incidence of polyethylene induced osteolysis.
A method was developed to take radiographs showing the inner articulation of bipolar hip prostheses. By this method, wear was measured in 68 hips whose inner head diameter was 22 mm. Average annual wear rate was 0.17 mm. Osteolysis was observed in 25 hips (37%) and there was no difference between the annual wear rate of hips with and without osteolysis. Studying 19 retrieved prostheses, abrasion of the rim was deeper in hips with osteolysis than those without it. Wear rate of the inner articulation in bipolar hip prosthesis is much larger than that in Charnley’s prosthesis, as linear penetration into the articulation surface reduces the motion range of the inner articulation and this increases impingement and advances rim abrasion.
Friction was studied in 67 retrieved cemented cups with 32 mm internal diameter. Friction was measured under 1.0 KN of static load. High molecular hyaluronic acid was adapted as a lubricant. Thirty cups were combined with alumina heads and 37 were combined with metal heads. The years cups were in situ was 7.5 (3.2–13.2) for alumina-polyethylene implants and 8.9 (1.5–15.7) for metal-polyethylene implants (p> 0.05).
The revision rate at 15 years follow-up was higher in metal-polyethylene (PE) implants (57%) than that of alumina-PE implants (40%) (p< 0.05). The prevalence of cup loosening was less in alumina-PE implants (12/30) than in metal-PE implants (29/37) (p< 0.01). Less wear was observed in alumina-PE implants (1.15+−0,80mm) than in metal-PE implants (1.62+−0.61mm) (p< 0.01). Less wear was observed in cups without loosening (alumina-PE implants: 1.84+−0.57mm, metal-PE implants: 1.75+−0.51mm) than in those with loosening (alumina-PE implants: 0.69+−0.56mm, metal-PE implants: 1.31+−0.73mm) in both types (alumina-PE implants: p< 0.01, metal-PE implants: p< 0.05). Less wear rate was observed in cups without loosening (alumina-PE implants: 0.11+−0.05 mm/year, metal-PE implants: 0.14+−0.05mm/year) than in those with loosening (alumina-PE implants: 0.17+−0.03 mm/year, metal-PE implants: 0.22+−0.09mm/year) in both types (alumina-PE implants: p< 0.01, metal-PE implants: p< 0.05). The coefficient of friction increased in proportion to the progress of cup wear in both types (alumina-PE implants: r2 =0.217, p< 0.01, metal-PE implants: r2 =0.183, p< 0.01). Relation between the coefficient of friction and stability of implants was not detected in both types, while alumina-PE implants had lower coefficient of friction (0.137+-0.056) than metal-PE implants (0.209+−0.098) (p< 0.01). The torque of metal-PE implants without stem loosening (0.137+−0.053) was larger than that of alumina-PE implants with stem loosening (0.274+−0.088) (p< 0.01).
The results suggest that wear has greater influence on stability of implants than the friction, whereas coefficient of friction increases in worn implants.
In revision THA, the solid acetabular reconstruction in the true acetabulum is often challenging. We are using the Kerboull acetabular reinforcement devices after packing hydroxyapatite granules for acetabular bone defects. We report our 3–7 year clinical and roentgenographical results.
Twenty-one acetabuli in 20 patients were reconstructed in the true acetabuli with Kerboull-type acetabular reinforcement devices and porous hydroxyapatite granules (Sumitomo Pharmaceutical Co. Ltd.). The mean age of the patients at operation was 68 years. The mean follow-up period was 5 years and 3 months (38–88 months). Acetabular bone deficiencies were evaluated according to AAOS classification (type II: 5 hips, type III: 16 hips). Porous hydroxyapatite granules (20–60 grams) were grafted to all the acetabuli. Autologous cortico-cancellous bone grafts or hydroxyapatite blocks were used to reconstruct the segmental defects in 6 hips. All the acetabuli were reinforced with Ker-boull-type reinforcement devices and Charnley-type cemented prostheses were implanted. Clinical and roent-genographical results were evaluated using Japanese Orthopaedic Association hip score and Hodgkinson classification. Average hip score was improved from 42 points to 75 points. No re-revision was done. No infection was noted. The roentgenograms showed neither migration nor loosening of the acetabular components.
Porous hydroxyapatite granules are one of the best bone substitutes because of their mechanical and biochemical properties. Oonishi reported very good results of his acetabular reconstruction using this material. The Kerboull-type acetabular devices are very effective to the reconstruction in the true acetabulum. Excellent results of these devices were reported by Kerboull. Ace-tabular reconstrution using both of them showed very good clinical and roentgenographical results during 3 to 7 post-operative years in our series.
Clinical evaluation was carried out using HSS, Knee Society, Tegner Activity, and Patellar scores. A three-dimensional, quantitative gait analysis and simultaneous epicutaneous electromyographic recordings of 7 muscles surrounding the knee were carried out on all patients. 11 healthy volunteers (mean age 69 years, 60-75) served as control group.
The science of tribology concerning hip arthroplasty has mainly dealt with total endoprostheses, whereas measurement values of hemiendoprosthetic implants are rare. The small amount of experimental tribologic data concerning hemiendoprosthetic implants in the form of pendulum trials, animal experiments, in-vivo measurements on human hip joints and pin on disc studies will be reviewed in the following work. The reported frictional coefficients in these studies were between 0,014-0,07. In order to test the friction coefficients of different femur head hemiendoprostheses (ceramic-cobalt chrome – and titanium heads and bipolar endoprostheses) against fresh cadaveric acetabula, the HEPFlEx-hip simulator (Hemi-EndoProsthesis Flexion Extension) was developed. In the simulator, the various hemiendoprosthetic heads are placed on a special cone and tested against a human cadaver acetabulum cast in MCP 47 woodmetal. The plane of movement of the apparatus is uniaxial with a rotating movement of +/− 35 degrees. The force is produced pneumatically dynamic with amounts of up to 5 kN. Newborn calf serum served as a lubricant. Preliminary results showed that the mean friction coefficient at 3 kN loading was μ=0.032–0.07 for ceramic against cartilage and μ=0.024–0.153 for metal against cartilage.
Patients with dislocation, severe subluxation of the hip joints were treated with cementless THA combined with subtrochanteric shortening femoral osteotomy. Total hip arthroplasty (THA) requiring subtrochanteric osteot-omy has been considered to lead to several complications. The aim of this paper is to assess the clinical results and complications of this procedure.
An acetabular component was placed into position at the site of the true acetabulum. After femoral corrective shortening osteotomy for dislocation or severe sub-luxation of the hip joints, an AML cementless stem was tightly inserted into the femoral canal to achieve bony union and osteointegration with the implant.
Twenty-one patients (23 hips; 2 men, 19 women) treated with cementless THA combined with subtro-chanteric femoral shortening osteotomy were enrolled in this study. The mean age was 55 years and the mean follow-up period was 4.5 years.
The average elongation of the limb was 48 mm after subtrochanteric shortening femoral osteotomy. Solid union of the osteotomy was obtained within an average of 5.5 months after surgery. None of these patients developed sciatic nerve palsy. There were 4 cases of non-union of the osteotomy site and 3 of aseptic loosening of the femoral component related to intraoperative femoral fracture. Upward migration of the proximal part of the femur was related to poor preoperative bone quality.
In order to diminish these complications, careful patient selection, accurate femoral reaming and suitable methods of bone cutting and augmentation of the oste-otomy site are necessary.
Clinical results were determined according to the hip joint function criteria of the Japanese Orthopaedic Association (JOA).
Fifty consecutive patients (60 hips) were included in the study who underwent primary total hip arthroplasty. There were 37 men and 13 women; the average age was 46.6 years (range, 26 to 70 years). The authors used cementless Duraloc series 100 acetabular component without a screw hole, a 22 mm (inner diameter) polyethylene liner, and a cementless IPS (Immediate Postoperative Stability) femoral component in all hips. The average follow-up was 6.3 years (range, 5 to 7 years). Thigh pain was evaluated using a visual analog scale (ten points). Clinical (Harris hip score) and radiographic follow-up was performed at six weeks; at three, six and 12 months; and yearly thereafter. Linear and volumetric wear were measured by software program. Bone remodeling and osteolysis were examined.
Preoperative hip score was 42.3 points (range, 16 to 69 points). The hip score at the final follow-up was 96 points (range, 95 to 100 points). All hips had satisfactory fit of the femoral stem in both coronal and sagittal planes. There was no aseptic loosening or revision of the components. One patient (2 %) had moderate thigh pain at three months and slight pain at six months and resolved. The average linear wear was 1.60 mm (SD, 0.068) and the wear rate per year was 0.23 mm (SD, 0.013). The average volumetric wear was 607.9 mm3 (SD, 25.8). The average volumetric wear per year was 87.4 mm3 (SD, 4.9). Four hips (8 %) had osteolysis in the calcar femorale (zone 7-A) less than 1 cm in diameter.
Accepted landmarks for determining rotation include the posterior condyles, Whiteside’s line, arbitrary 3-4° of external rotation, and transepicondylar axis (TEA). All methods require anatomical identification, which may be variable.
The purpose of this study was to radiologically evaluate femoral component rotation (CT analysis) based on a method that references to the tibial axis and balanced flexion-tension.
The purpose this prospective, randomized clinical trial was to determine if unilateral or bilateral simultaneous total hip arthroplasty procedures resulted in a differing incidence of fat embolization, degree of hemodynamic compromise, levels of hypoxemia or mental status changes. Also, the incidence of fat embolization was compared between the cemented and cementless total hip arthroplasty in the patients with a unilateral- and bilateral simultaneous total hip arthroplasty.
One hundred and fifty-six consecutive patients undergoing primary total hip arthroplasty were enrolled prospectively in the study after giving informed consent. The group consisted of fifty patients undergoing bilateral simultaneous total hip arthroplasty and 106 patients undergoing unilateral total hip arthroplasty. One hundred and three hips were cemented and 103 hips were cementless. To determine the hemodynamic changes and to detect the fat and bone marrow embolization, arterial and right atrial blood samples were obtained before implantation (baseline) and at one, three, five and ten minutes after implantation of the acetabular component. Also, arterial and right atrial blood samples were obtained at one, three, five and ten minutes after implantation of the femoral component. And then blood samples were obtained at twenty-four and forty-eight hours after the operation. Arterial blood pressure, right atrial pressure, arterial oxygen tension and carbon-dioxide tension were monitored at corresponding times. The presence of lipid was determined with oil red O fat stain and the presence of cellular contents of bone marrow was determined with Wright-Giemsa stain.
The incidence of fat embolism was not statistically different (P=1.000) between the patients with a bilateral total hip arthroplasty (twenty seven patients or 54 per cent) and the patients with a unilateral total hip arthroplasty (fifty-two patients or 49 per cent). In the semiquantitative analysis of fat globules in both groups, there was no tendency to have a higher number of fat globules in the bilateral group than in the unilateral group. Also, the incidence of bone marrow embolization was not statistically different (P=0.800) between the patients with a bilateral total hip arthroplasty (eight patients or 16 per cent) and the patients with a unilateral total hip arthroplasty (fourteen patients or 13 per cent). There was no statistical difference (P=0.800) in the incidence of the presence of fat globule between the cemented total hip (thirty-four patients or 34 per cent) and the cementless total hip arthroplasty (forty-seven patients or 44 per cent). Also, there was no statistical difference (P=0.627) in the incidence of the presence of bone marrow cells between the cemented total hip arthroplasty (thirteen patients or 13 per cent) and the cement-less total hip arthroplasty (twelve patients or 11 per cent). Four patients with positive bone marrow cells had neurological manifestation. All of these four patients developed diffuse encephalopathy with confusion and agitation for about twenty-four hours.
The present study confirmed that the incidence of fat and bone marrow embolization is similar in the patients with a bilateral simultaneous-and unilateral total hip arthroplasty as well as in the patients with cemented and cementless total hip arthroplasty. The patients with bone marrow cell emboli had a significantly lower arterial oxygen tension (p=0.022) and oxygen saturation (p=0.017) than the patients without bone marrow cell emboli. On the contrary, the number of fat globules did not affect the perioperative hemodynamic changes. Encephalopathy is related to the biochemical and/or mechanical changes by bone marrow cells.
The purpose of this study was to analyse and to recommend solutions for early complications with a new total knee mobile bearing device, that promises a logical synthesis of combined A/P translation and rotation ability, but has shown early surgical technique related complications.
The purpose of this study was to analyse a potential correlation of arthrofibrosis (AF) and femoral rotational mal-alignment in total knee arthroplasty (TKA). We hypothesized an increased internal mal-rotation of the femoral component leading to unphysiological kinematic motion of the arthroplastic knee joint. These repetitive microtrauma may then induce increased synovial hyperplasia leading to arthrofibrosis. Arthrofibrosis is an ill-defined entity that results in unsatisfactory outcome following TKA. Biological and mechanical factors have been suggested as etiology, but specific causes have not been identified.
This study has been cleared by the Ethical Committee, University of Zurich, Switzerland.
Cementless fixation in TKA remains controversial because of less predictable osseointegration and difficulty interpreting fixation interfaces. Radiolucent zone analysis (RLZ) of plain radiographs is the only practical method of evaluating the fixation interface.
Correction of fixed valgus is a challenge in primary TKA. Achieving patello-femoral and femoral-tibial stability requires superficial/deep lateral side releases if non-constrained prostheses are utilized. The medial approach has disadvantages with more reported complications. The direct lateral approach, with/without tubercle osteotomy, is an approach option utilized in two reporting centers.
We have developed lameller etched titanium (L.E.T.) structure, as a new bone-prosthesis interface. L.E.T. has a laminating structure consisting of a thin board made of porous etched titanium layer. We call this structure, a space controlled interface, because its pore shape, pore size and porosity within the interface can be controlled easily.
Although bone loss and ligamentous instability are usually indications for the use of constraining prostheses in revision total knee arthroplasty (TKA), several reports have documented a high rate of failure with these prostheses. We therefore tried using the cruciate retaining augmentable type prosthesis (NexGen CRA) if a good intraoperative ligamentous balance could be obtained with revision TKA.
CRA was used on nine knees of seven patients with an average age of 71.7 years. The follow-up lasted for an average of 1.6 years. Clinical evaluation consisted of instability ratings, knee score, range of motion and %MA (mechanical axis) as an index of the alignment. These patients showed improvement varus instability from a mean of 7.0° preoperatively to a mean of 1.5° postoperatively, and in valgus instability from 5.3° to 1.3°.
The knee score was significantly improved from 41 to 81, but the %MA resulted in an unsatisfactory improvement from −8.8% to 34.0%. The femoral anatomical-mechanical angle (FAMA) was measured as a parameter of bowing deformity of the femur, and the knees were divided into two groups, the bowing group consisting of the knees with an FMA of more than 8° (n=6, average 9.0°), the normal group of knees with an FAMA of less than 7° in FAMA (n=3, average 6.7°). The postoperative %MA showed a mean value of 40.9% for the normal group, and 30.6% in the bowing group. These results demonstrated that the discrepancy between FAMA for the bowing group(=9.0°) and the valgus angle of the stem of the femoral component (6.0°) was the cause of the malalignment in the bowing group. These clinical results suggest that the cruciate retaining augmentable type prosthesis can be used successfully for selected revision cases, but that malalignment in knees with bowed femora may remain a problem.
A changed kinematic elbow axis can cause early loosening of elbow endoprostheses and can decrease the functional outcome. Therefore, these prostheses and their alignment tools are designed to reconstruct normal joint kinematics. We investigated whether it is possible to reconstruct the pre-operative kinematic axis of the elbow when an iBP™ elbow endoprosthesis (Biomet) has been placed.
The calibrated Flock of Birds® electromagnetic tracking device registered controlled passive elbow flexion of ten embalmed upper extremities. The pre-operative kinematic elbow axes were established using helical axes.
Results were expressed in the humeral coordinate system defined by the glenohumeral joint rotation centre and the lateral and medial epicondyle of the humerus. The glenohumeral joint rotation centre was determined using a regression method. The senior author implanted the iBP™ elbow endoprosthesis using standard instrumentation for humeral component alignment. The post-operative kinematic axes were then calculated. A Student’s t-test was performed to compare the pre- and post-operative axes.
No significant differences were found in the direction of the kinematic elbow axes before and after surgery, indicating no alteration in the valgus/varus angle or change in longitudinal rotation of the ulna with respect to the humerus. However, the axis was located significantly more distal (mean difference 7.0 mm, p = 0.004) after surgery. The ventral-dorsal location of the kinematic axis was not significantly different (p = 0.748) after surgery, but there was some variation in individual axes. The iBP™ Elbow System enables the reconstruction of the direction of the pre-operative kinematic elbow axis. While the exact position of the pre-operative axis could not be reproduced in vitro, the kinematic axis of the elbow is expected to be less distal in vivo as a result of the extensive destruction of the rheumatoid elbow. Individually adjustable alignment tools might enable more precise reconstruction.
We evaluated the geometry of the resected femoral surface according to the theory for total knee arthroplasty (TKA) using three-dimensional computed tomography (3D CT).
The 3D CT scans were performed in 44 knees indicated as requiring total knee arthroplasty. The 3D images of the femurs were clipped according to the following procedures. The distal femur was cut perpendicular to the mechanical axis at 10 mm proximal from the medial condyle. Rotational alignment was fixed at 3 degrees external rotation from the posterior condylar line. The anterior condyle was resected using the anterior cortex as the reference point. The posterior condyle was cut at 10 mm anterior from the medial posterior condyle.
The medial-lateral (ML) width/anterior-posterior (AP) length was 1.58 ± 0.14 (mean ± SD). AP length of the 3D images tended to be longer than the box length of the three kinds of components provided when the ML width of the images was approximately equal to that of each component. The widths of medial and lateral posterior condyles of the images were 30.1 ± 3.8 mm and 24.8 ± 3.0 mm, respectively. In all except one case, the widths of the resected medial posterior condyles were greater than those of the medial condyles of all components when those of resected lateral posterior condyles were equal to those of the lateral condyles of the components.
The shapes of the resected femoral surface did not always match those of the components. The configuration of Japanese knee joints is different from that of American knee joints. Components with appropriate geometry should be designed for Japanese patients.
In cementless fixation system, surface character becomes important factor. Alkali and heat treatments on titanium metal has been proved to show strong bonding to bone and higher ongrowth rate. In this study we examined the effect of alkali and heat treatments on titanium rod in rabbit femur intramedurally model, in consideration of cementless hip stem. The implant had a 5mm in diameter and 25 mm in length. The implants were and half of them were immersed in 5 mol/L sodium hydroxide solution and heated at 600 åé for one hour (AH implant), and the other half were untreated (CL implant). The implants were implanted into the distal femur of the rabbits, AH implant into left femur and CL implants into right. The bone-implant interfaces were evaluated at 3, 6, and 12 weeks after implantations.
Pull-out tests showed that AH implants significantly higher bonding strength to bone than CL implants at each week after operations. At 12 weeks mean pull-out load of AH implants was 411.7 N and that of CL implants 72.2 N. As postoperative time elapsed, histological examination revealed that new bone form on the surface of the both types of the implants, but significantly more bone contacted directly on the surface of AH implants. At 12 weeks AH implant was covered by the newly formed bone about 56% of the whole surface of the implants and CL implants was about 19%.
In conclusion, alkali- and heat-treated titanium offers strong bone-bonding and high affinity to bone instead of conventional mechanical interlocking mechanism. Alkali and heat treatments on titanium may be applicable to the surface treatment for cementless joint replacement implant.
We developed an endoscopically controlled device for cement removal out of the femoral canal. This system (Swiss OrthoClast) uses simple ballistic principles to effect mechanical fracturing of the bone cement. A special extraction set facilitates removal of the distal cement layer and of the intramedullary plug. The cement removal procedure, even in the depth of the femur, is controlled with an endoscopical system via monitor. Handling of this device will be demonstrated. We report our clinical results of 45 procedures with this device.
Patellofemoral complications after TKA are mostly avoided with appropriate operative technique. Although most orthopedic surgeons performed using a medial parapatellar approach at TKA, but a large amount of the patellar blood flow is blocked by this procedure. A certain surgical exposure, including the midvastus and subvastus approach, has resulted in good clinical results. It is important to maintain the integrity of the extensor mechanism. But the southern or subvastus approach has inadequate exposure in some patients. And then we have had the primary total knee Arthroplasty using midvastus approach in 98 cases, 68 patients. Mean follow up is 30 months, between from 20 months to 43 months.
We estimated parameters of total blood loss, surgical time, difficulty of exposure, number of lateral releases. The clinical parameters of range of motion, ability to perform a straight leg raise, and the number of operative or postoperative complications were evaluated. The patients who had the midvastus approach had minor blood loss, resonable surgical time, no difficulty of exposure even in patients with severe varus or valgus deformities, required lateral retinacular releases only 5% of the cases. The range of motion was all above 120 degrees flexion, no extension loss, had a higher incidence of ability to straight leg raise and fewer complications as like superficial wound infection. The midvastus surgical approach have some more advantages with less pain and earlier control of the operative leg, and may be discharged from the hospital earlier. Because preserving the integrity of the vastus medialis insertion into the medial border of the quadriceps tendon and limited disruption of the extensor mechanism improves the rapid control of quadriceps muscle and improves the more stable patellofemoral articulation, and then evidenced a marked reduction in the need for lateral retinacular releases.
We recommend the mid-vastus surgical approach for total knee arthroplasty. The Midvastus approach is an efficacious alternative to the medial parapatellar approach for primary total knee arthroplasties in selected patients who are not obese and who have not had previous arthrotomy. And if needed more additional exposure, the muscle can be safely split by further dissection.
This cohort was reassessed by chart and radiograph review in 2000. All patients who initially had cavitary osteolysis had been revised. In addition, 13 patients with cyst osteolysis progressed to cavity and ten knees had been revised. Of the 52 knees that had line osteolysis, 21 progressed to cyst or cavity and 15 knees were revised. Furthermore, 57 additional knees had developed osteolysis with 24 knees being revised.
Osteolysis in the AMK is a silent and progressive disorder. We were unable to identify any risk factors that would classify certain patients as at risk for osteolysis. Consequently, we recommend regular periodic follow up in order to recognize osteolysis early.
As for the number of patients who requires total knee arthroplasty (TKA), Asian-Pacific countries will be the most important market. However, due to the paucity of anthropometric data on the proximal tibia in this population, many prostheses designed for Caucasian knees have been introduced without specific modification.The aim of the current study was to analyze the geometry of the proximal tibia to design the optimum component for the Japanese population.
Anthropometric data on the proximal tibia of 100 knees in 80 patients undergoing TKA was obtained. Briefly, anterior-posterior (AP) and medial-lateral (ML) lengths were measured with a combination of two different methods, namely on the computed tomography (CT) images obtained preoperatively and intraoperative direct measurement on tibial resection surface. Reproducible measurement was possible only when the intraoperative measurement was combined with the corresponding CT images while the direction of measurements being aligned to the epicondylar axis of the femur.
It was shown that smaller components with an ML of around 60 mm were rarely required. Tibial component size variation should focus on an ML length of 65 to 75 mm because 76 of 100 knees (76 %) fell into this size range. When the subjects were confined to women, 70 of 77 knees (91%) were included in this size range. The intraoperative AP to ML ratio had a negative correlation with the ML length (r = −0.412, P < 0.0001) indicating that bigger knees were shallower in the AP direction. The size variation of currently popular pros-theses were not in accordance with the geometry of the tibial resection surface shown in this study.
The results of this study applied to a cross-section of the Japanese population can be used by manufacturers to create a prosthesis suitable for most of the Asian-Pacific population.
BIONs (Bionic Neurons) are microminiature stimulators that can be injected into muscles. They receive power and commands from an external magnetic field. They have been shown to be safe and effective for stimulating muscles in animals. Clinical trials are underway to assess the efficacy and safety of BIONs for therapeutic exercise of weak or paralyzed muscles. In patients with knee osteoarthritis weakness of quadriceps muscle has been shown by different authors to be highly correlated with pain and functional impairment, while quadriceps strengthening is associated with significant improvements of clinical scores. Preliminary results of the use of BIONs to strengthen the quadriceps muscles in patients affected by knee osteoarthritis are reported.
Five patients have been recruited so far, three of them have completed the protocol. Patients are implanted with BIONs near the common femoral nerve and in the vastus medialis muscle, and stimulated for 12 weeks. Therapy starts three days after implantation with two-three stimulation sessions of 10–30 minutes each day. Stimulation parameters are intended to recruit the quadriceps muscles (up to 10 X threshold for muscle twitch) at relatively low frequencies (5–13 pps) in short trains (5–10 s) with pauses between trains (5 s). Outcome measures include WOMAC, Knee Society Score, muscle measurements with MRI, gait analysis, isokinetic tests. All patients found muscle stimulation to be agreeable. No adverse events or complications have been observed. Thresholds for eliciting muscle contractions remained stable over time. In the three patients knee function improved and pain decreased over the stimulation period, while muscle thickness, as measured by MRI, increased.
Results are preliminary but encouraging. We anticipate studying 15 patients to demonstrate clearly the safety and efficacy of this technology in this application. Plans are underway for additional clinical trials in orthopaedic patients as well as in stroke patients.
A modular neck allows to choose the offset of the femoral head and the degree of anti-retroversion, lateralization and varus-valgus intraoperatively. At the G. Pini Institute we have been using modular necks in custom prostheses since 1989. Excellent results in this application did open the way to a larger use in off-the-shelf prostheses. Modular necks can be now coupled with different stems, leaving the surgeon free to use the preferred prosthetic stem design. Modular necks have been implanted in more than 50,000 in the world. Medium term results in custom prosthesis and the experience in off-the-shelf non-cemented stems are presented, together with further improvements of this technology under study.
From 1989 to December 1999, 481 custom stems have been implanted. All patients but ten received modular necks. The prostheses were made of a titanium alloy and HA coated. 61 % of patients had dysplastic oxarthrosis. 372 implants performed between 1989 and 1996 were retrospectively evaluated. Data from off-the-shelf prosthesis, at a shorter follow-up, are also reported. Laboratory data showed that the use of an elliptical Morse cone of the neck reduced wear debris production to less than 1 mg/year. In custom implants, (mean follow-up: 7 years), we did not observe any thigh pain or radiological signs of osteolysis or fretting. Mean leg-length discrepancy was 2.8 cm pre-op and 0.3 cm post-operatively. Off-the-shelf implants also showed good clinical and radiological results. New design modular necks will increase the possible range of motion and provide more solutions for positioning the center of rotation. Modular neck is a safe and reliable solution to obtain the correct position of the center of rotation intra-operatively, without side effects. Applications in off-the-shelf prostheses allow to reduce costs while maintaining the advantages of this technology.
The success of total knee replacement surgery depends critically on proper limb alignment and implant position. Even with contemporary mechanical alignment instrumentation, errors in limb alignment and implant position do occur. To improve upon the accuracy and biomechanical efficacy of conventional surgical instrumentation while limiting the need for substantial pre-operative planning, a non-image-based computer-aided navigation system was developed for total knee replacement surgery. Clinical studies have demonstrated that use of this system, OrthoPilot® (Aesculap AG, Tuttlingen, Germany), for knee replacement surgery can lead to improved limb alignment and implant position.
In this study we investigated the repeatability and sensitivity of the OrthoPilot® computer-aided navigation system for total knee replacement surgery. To assess repeatability, total knee replacement surgeries were simulated on an idealized test bench using identical input parameters and the variation in output measurements was measured. To assess sensitivity, the effect of moderate movement of position sensors on system-level accuracy was measured. The results indicate that (1) the system functions in a highly repeatable manner if it is supplied with repeatable inputs; and (2) unintentional relative movement of position sensors during surgery can substantially affect accuracy of the system outputs.
Because computer-aided navigation systems are powerful tools for orthopaedic surgery, it is important to recognize that their accuracy and precision are highly dependent on pre-operative and intra-operative registration techniques. Like all instrumentation systems, their use is associated with a learning curve, even in the hands of experienced orthopaedic surgeons. The results of this study demonstrate that the OrthoPilot® in an inherently precise instrument that is sensitive to variations in surgical technique. It is critical that the users of these systems (i.e. surgeons) be aware of system sensitivities and pay careful attention to operative techniques required by the system.
Loosening of the glenoid component after Total Shoulder Arthroplasty is an established phenomenon with long-term follow-up studies showing radiolucency in 65% of glenoid components at 10 years (Stewart and Gray, 1997). Glenoid component designs are based on anthropometric measurements of normal shoulder joints. The purpose of this study was to study the surface anatomy of both bony and cartilaginous layers of the normal glenoid fossa in more detail.
We have developed a reproducible and inexpensive technique of surface shape assessment using laser morphometric analysis and applied this to thirty normal glenoid fossae mounted in the scapular plane. Surface analysis was carried out before and after removal of the glenoid labrum and after papain digestion of the articular cartilage allowing assessment of the skeleton alone allowing comparison with other studies using bony or cartilaginous landmarks in assessment of glenoid version. Using a specially designed program, five equi-distant lines were placed across the glenoid from which analysis of the orientation of the fossa was determined.
None of the scapulae presented a single surface that could be judged anteverted or retroverted by an amount representable by a single figure. All scapulae demonstrated a twist about the vertical axis. Two main types were identified.
Type 1 – Superior retroversion (mean 16.0 degrees) becoming progressively less to the lower pole (mean 3.0 degrees)
Type 2 – Retroverted superiorly, twisting to reach the position of maximal anteversion in the lower half of the glenoid, twisting back into more retroversion towards the lower pole. None of the specimens were morphologically equivalent to currently available glenoid prostheses. The surface shape of the glenoid is so variable that we should explore the relationship between this and the kinematics of the shoulder joint. There may be implications for the design of shoulder replacements and possibly custom prostheses.
Between 1989 and 1993, 158 patients with a total of 187 damaged knees underwent TKA using AGC-S prosthesis (Biomet). Of these patients, six required revision surgeries due to metallosis. The average period from the first operation to the revision was 68.0 months (range: 41–97 months). In all six cases, the plain X-rays taken immediately before reoperation, showed sinking of the tibial component. The withdrawn implants showed severe abrasion of the polyethylene used in the posteromedial area. The percent share of the tibial component averaged 90.3% (range: 85.3–93.5%) on the anteroposterior view, and on the lateral view averaged 83.1% (range:76.9–94.0%). The tibial components used for AGC-S type TKA can be characterized by the presence of a rim. In some cases, however, the rim cannot be placed on the tibial cortex, and this obliges the surgeon to select smaller components, resulting in a smaller percent share of the tibial component. The tibial component can sink in such cases. The sinking of the tibial component probably leads to malalignment and joint instability. Furthermore the insert with a flat surface was likely to induce articular instability, thus enhancing the abrasion of the polyeth
We present the results of our initial experience with the use of the Birmingham metal-on-metal Hip Resurfacing. The Birmingham Hip Resurfacing(BHR) consists of a high carbon chrome cobalt uncemented hydroxyapatite cupand a cemented femoral component. For patients with severe dysplasia adysplasia cup with screws was used. We utilise this kind of prosthesis for the younger patients (< 65 year). Excellent clinical results are encountered; none of the early problems aswith the old Wagner resurfacing (metal-on-poly) are seen. Our early results are similar to the encouraging results of the series of D.McMinn/R.Treacy.
From September 1998 through April 2001, 185 BHR arthroplasties were performed. The mean age was 49.7 year (16–75). More male patients were operated with this method than female patients (64%–36%). The aetiology was osteoarthritis (81%), necrosis (9%), dysplasia (CDH) (6.6%).
The mean length of stay in hospital was six days (range: 2–26). Complications were: One fractured neck of femur, one ischial nerve palsy and one guide pin was left in the femur. All patients were followed on regular basis and the X-rays were studied for angle of preoperative neck of femur, postoperative angle of the femoral component, angle of cup placement and the parallelism of both components.
This study examined the inhibitory effects of anti-TNF-a antibody (anti-TNF) and a new bisphosphonate (TRK-530) on peri-implant oseteolysis in a rat model with continuous infusion of polyethylene particles. TRK-530 is a novel synthetic bisphophonate to have a direct effect on osteoclastic bone resorption as well as suppressive effects on bone resorbing cytokines from macrophages.
We developed LET (Lamellar Etched Titanium) porous structure as a new bone-prosthesis interface, which is made by piling up and fusing the etched titanium thin layers. This method can control pore size and porosity easily and obtain definite interconnective open pore structure (average porosity 65%, average pore size 500 micrometer)
We implanted two types of interface, one with LET and the other with a conventional rough surface structure, which is made with inert gas-shielded arc spraying (ISAS) technique (Ra 40 micrometer) Both materials have coated with HA using the flame spray method. Mechanical and histological studies were performed at 2, 4, 9 and 12 weeks.
Flexion after total knee arthroplasty (TKA) has recently been improved by changing implant designs, surgical techniques and early postoperative rehabilitation protocols. Especially for Asian people, deep knee flexion is essential because of their life style. Small numbers of patients can achieve full flexion after TKA, however, most current prostheses are not designed to allow deep knee flexion safely. Furthermore, the kinematics involved in knee flexion greater than 90 degrees in cases of TKA is still unknown, even though fluoroscopic studies have shown the paradoxical anterior femoral translation in posterior cruciate retaining (CR) TKA with knee flexion up to 90 degrees. The purpose of this study was to determine the femoro-tibial contact pattern in deep knee flexion.
The knee that had been operated upon was passively flexed from 90 degrees up to the maximum flexion under anesthesia soon after the surgery. Lateral roentgenograms of the knee were taken during flexion, and the three-dimensional kinematics was analyzed using image-matching techniques. Nine patients with CR type were included.
The average maximum flexion angle was 131.8 °. The contact point moved posteriorly with deep knee flexion except for one patient. Five out of nine patients showed external rotation of the femoral condyle. Two patients showed internal rotation, and the other two exhibited no rotational movement. None of the patients showed dislocation or disengagement of the components. At the maximum flexion, the edge of the posterior flange of the femoral component contacted the polyethylene insert.
This study was performed under non-weight-bearing conditions, but deep knee flexion is not usually performed in weight-bearing conditions. Most of the CR type showed posterior roll back during deep knee flexion. The design of the posterior flange of the femoral component should be changed to prevent damage to the polyethylene.
New prosthesis designs should be compared to a standard implant in randomized studies evaluated by radiostereometric analysis (RSA). The Unique customized prosthesis (UCP) is a newly developed concept for fitting uncemented prosthesis to the exact internal shape of the proximal femur [
The role of the posterior cruciate ligament (PCL) after total knee arthroplasty has been controversial. Previous studies have reported that function of the preserved PCL after TKA was questionable and that it was difficult to determine the appropriate PCL tension to reproduce rollback. However, several in vivo studies have reported that prosthesis geometry directly affects knee kinematics, making it difficult to determine which factors most influence knee kinematics. The purpose of this two-center, two surgeons study was to evaluate knee kinematics of a single design of CR TKA. A total of 23 TKAs were studied fluoroscopically during a single-limb step-up/down maneuver. The average patient age at the time of TKA, knee score (HSS/KSS) and ROM were 70.6 years, 91.1 points and 116.9 degrees respectively. All patients had a PCL-retaining prosthesis of the same design using an unconstrained “flat” tibial insert. TKAs were performed by one surgeon at each hospital (Group 1:13 knees, Group 2: 10 knees). Both groups of knees exhibited ‘screw-home’ type axial rotations from 20° of flexion to full extension. In Group 1, rollback occurred early in the flexion range and was maintained until 80° of flexion. In Group 2, the lateral condyle exhibited rollback in early flexion, but both condyles translated forward as flexion increased to 80°. Medial and lateral contact were more posterior in Group 1 over most of the range of motion (p< 0.05). Although femoral rollback has been infrequently observed in similar studies of PCL retaining arthroplasties, our two-center, two surgeon data suggest that rollback can be achieved using this unconstrained prosthesis with PCL retention. However, there were consistent and statistically significant differences in the knee kinematics exhibited by the two groups of patients.
Polyethylene wear in total knee arthroplasty (TKA) is a complex and mutifactorial process. It is generally recognized that wear is directly related to a material wear factor, contact stress, and sliding distance. Conventional methods of predicting polyethylene wear in TKA mainly focus on peak contact stress or subsurface shear stress using finite element method analysis. By incorporating kinematics and contact stress, a new predictor for polyethylene wear in TKA (“Wear Index”) has been developed. The Wear Index was defined by multiplying deformation by femoro-tibial sliding velocity. The purpose of this study was to determine the predictive value of the Wear Index for polyethylene wear in TKA using both a numeric and an in vitro model.
Four commercially available total knee prostheses were modeled for this study. Deformation and sliding velocity were calculated based on the three-dimensional geometry of the components and the gait kinematic inputs using Hertz’s formula. One specimen of each of the four types of total knee prostheses was mounted on a custom-designed knee simulator. Vertical loads and flexion-extension uni-axial motion were simulated using computer controlled servohydraulic actuators. The same gait kinematic inputs used in the theoretical study were used in the simulation test. After the simulations, the surface of the tibial insert was examined microscopically and macroscopically and compared with the theoretically generated Wear Index.
This study showed a high correlation between the numeric model and the simulation. The depth of wear on the tibial insert correlated significantly with the Wear Index. Microscopic findings also demonstrated a good correlation between the Wear Index and observed wear patterns. Sliding velocity is an important factor for understanding wear in TKA. In conclusion, this study suggests that the Wear Index is a reliable predictor of polyethylene wear in TKA, as it incorporates both contact stress and kinematics in its calculation.
It is widely accepted that a wide contact area between bone and artificial materials is necessary in the fixation of hip joint prostheses. It is also considered important that the load should be applied to the proximal femur. However, these two concepts are contradictory in that the contact point cannot be determined in a wide contact area. Therefore, in this study, we revised the available concepts to improve the method of fixation of joint prostheses using finite-element-method (FEM) analysis of the equivalent mathematical models. The first model was designed based on the intramedullary cruciate fixation stem. In this model, the total contact area was limited to the small area of legs-on-plane. Another model was designed based on the fit-and-fill-type stem, and in this model, the total contact area of the plane-on-plane was equal to the total surface area of the stem. In the plane-on-plane model, there was an unstable vibrating pattern in stress distribution, and we considered that deterministic cha
Malalignment and cement mantle quality have been implicated in loosening of the Charnley stem [
The ‘first generation’ Metal on Metal bearing devices was typically produced from cast, high carbon CoCrMo alloy and was in the as-cast condition. They exhibited course, hard primary, and block carbides supported by a softer matrix material. This bi-phasic condition has been verified through reported literature and forensic scientific studies of ‘long-term survived’ retrieved ‘first generation’ devices. The as-cast microstructure of CoCrMo alloys possesses superior wear resistance to the microstructures formed following post cast thermal treatments. It has been well reported that the improvement of mechanical properties, such as tensile or fatigue strength, can be achieved through the thermal treatment of this alloy. Thermal treatments of this alloy have been found to alter its’ microstructure with a significant modification to the carbide phase morphology. The modifications vary with a tendency for a refinement of the carbide size through dissolution of the chromium and molybdenum through solid state solution. Through the examination of the wear patterns of retrieved devices and wear testing of this material in its’ various microstructural conditions, it has been shown that modifications to the carbide morphology, to achieve improved mechanical properties, reduces its’ bio-tribological properties/performance leading to a lower wear resistance. The as-cast carbide morphology is the most mechanically stable condition and with its’ volume fraction, reduces the potential for adhesive wear of the matrix through ‘matrix to matrix’ contact of the two opposing bearing surfaces. It has been reported that abrasive wear is the typical mechanism for metal on metal bearings due to the generation of ‘third body’ particles from carbide asperity tips fracturing during the initial ‘running-in’ period [typically 500k to 1M cycles]. After this stage the carbides become almost level with the surrounding softer matrix material with ‘third body’ scratches dominating the surface topography. Evidence of surface pitting on ‘first generation’ devices [McKee Farrar and Muller] and modern high carbon wrought devices [Metasul] has been attributed to adhesive/fatigue wear following surface-to-surface contact. Therefore, in microstructural conditions, where there is a reduced carbide volume fraction, or no carbides present, wear resistance is reduced. To test this hypothesis two wear tests have been carried out on CoCrMo samples produced from the same chemistry alloy, with varying microstructures, using Calowear [abrasive] and Pin on Dist [adhesive] tests. The as-cast microstructural condition was determined to have the lowest wear coefficient [k=mm3/Nm] in both tests, however statistical significance at 90% confidence interval was only confirmed in the Calowear Test. Examination of wear scars confirmed the mechanical stability of the as-cast carbide phase. It is noted, however that there are papers which have been published offering a divergence of opinion to this hypothesis and which have been considered by this author.
A total knee design has been developed to support high flexion requirements of post-total knee replacement lifestyles. The extent of flexion, following total knee replacement, is influenced by relative femoral tibial kinematics, posterior knee soft tissue impingement, patella and patellar tendon tracking, preoperative knee flexion, and postoperative physical therapy. A new implant design incorporates features to prevent posterior tibial displacement in high flexion, improved conformity of the femoral/tibial articular surface contact to 155 degrees of flexion, greater femoral/tibial articular surface contact area in high flexion, and a shortened patellar tendon pathway. The requirement for tibial internal-external rotation during some knee flexion activity is accommodated by a rotating tibial poly-ethylene option within the implant system. Laboratory tests indicate the achievement of greater articular surface contact in high flexion conditions through extending the posterior femoral condyle curvature and accommodating the tibial polyethylene articular surface. Joint simulator testing indicates improved wear performance of the high flexion design. A prospective controlled multicenter clinical trial has been initiated to evaluate this high flexion implant design along with surgical techniques and post-surgery physical therapy developed to support patient achievement of high knee flexion following total knee arthroplasty.
We developed K.K.S. (Keio-Kyocera Series) THA sytem. The aim is to develop original THA system suitable for Japanese patients. We produced MCF (means Medullary Canal Filling) stem, based on the anatomical anlysis of Japanese typical osteoarthritic patients (53 cases) by the measurements with CT scan. By the use of this stem, excellent canal fitting and initial rigid fixation can be obtained. We used this stem together with non-cement porous socket from 1992. At first the surface of this stem was smooth (S groupe), from 1994 the surface was altered to porous surface (P groupe), and then from 1995 HA coating to porous surface (H groupe) was added. The purpose of this study is to compare the biological fixation ability among stems with same shape and different surface.
New generation alumina-on-alumina (A-A) prostheses have been introduced to try and overcome the problem of osteolysis often attributed to polyethylene wear particles liberated within conventional metal-on-ultra high molecular weight polyethylene (UHMWPE) joints. This study uses a hip simulator to compare the volumetric wear rates of five different radial clearances of A-A joints. Atomic force microscopy (AFM) provided topographic characterisation of the prosthesis surfaces throughout the wear test.
Longevity of the implants is the most respected factor in THA. Except from this fact, complications like dislocation, wear and osteolysis are reported in literature most frequently. But there is an underestimation in the orthopedic community in the importance of joint function, which is directly related to accurate restoration of joint geometry. This might be due to a lack of functional parameters for the measurement and availability of adequate implants for accurate restoration of joint geometry.
From our point of view the two problems: stable stem fixation and joint geometry have to be addressed separately: Safe stem fixation on the one hand, adequate joint geometry on the other hand. With the use of standard implants compromises have to be made on either side. To avoid this dilemma, we propose alternative systems: A modular system with interchangeable necks as a standard implant for better fit and adequate joint geometry or a custom implant. In the presentation we address the interference of stem fit and joint geometry and discuss problems and advantages of modularity and custom implants.
Our experience with metal/metal desings in France date from 1994. The goal of this study is to communicate our primary and comparative clinical results of 90 implants followed a minimum of 6 years
A method to extensively cross-link polyethylene for total hip application has been developed and tested in hip wear simulation. Extensively cross-linked polyethylene was prepared by exposing GUR 1050 polyethylene resin to 90 kg to 110 kg of e-beam radiation. For total hip application, the material was evaluated in an AMTI joint simulator in normal debris-free conditions and in a Shorewestern simulator for the adverse condition of added bone cement and aluminum oxide debris. The normal condition testing was conducted to 30 million cycles, while the adverse condition tests were conducted to 5 million cycles. Femoral head sizes from 22 mm to 46 mm were evaluated. The wear performance of extensively cross-linked material was compared to control material (GUR 1050 gamma sterilized in nitrogen). The results demonstrate a significant improvement in wear (greater than 80 percent reduction) of extensively cross-linked GUR 1050 acetabular components compared to the control acetabular components. The adverse condition wear of both materials was greater than the normal wear; however, when compared to the controls, the extensively cross-linked material had improved wear performance in both normal and adverse conditions. The wear of femoral heads larger than normal 32 mm sizes showed accelerated wear in the control material and desirable low wear in the extensively cross-linked condition. The polyethylene particles generated in the wear simulation were of similar size and shape between the extensively cross-linked and controlled polyethylene. As demonstrated in the laboratory simulation, this extensively cross-linked polyethylene has the potential to substantially reduce particular debris generation in total hip applications. A multicenter randomized controlled clinical study of extensively cross-linked and control acetabular components is ongoing.
Infected hip prosthesis, a devastating complication of primary total hip arthroplasty (THA) can lead to a serious condition. We report here the treatment outcome of our method of two-stage revision THA for infected hip arthroplasty using a temporary antibiotic-impregnated cement spacer for the period between resection and reimplantation.
Between 1996 and 2000, we performed two-stage revision THA using a temporary antibiotic-impregnated cement spacer on eight hips in eight patients with infected hip arthroplasty including hemiarthroplasty, with the infection presenting itself between four days and 19.4 years after last operation. There were four females and four males, with a mean age of 67 years (58 to 72). The mean period of follow-up was 2.5 years (0.3 to 4.3). Cementless THA was implanted as the second srage procedure. Bone defects were restored with frozen allografts. The clinical outcome was evaluated using the hip score of the Japanese Orthopaedic Association (JOA hip score).
The duration of follow-up was 33.9 months (range, 8 to 55 months). The mean JOA hip score at follow-up improved from 32.6 (19 to 74) to 77.1 (59 to 96). The mean interval period was 10.3 weeks (range, 6 to 19 weeks). Seven patients with infected hip arthroplasty successfully received implantation by two-stage cement-less revision THA.
One patient with MRSA infection had a recurrence after four months of revision of THA. However, the two-stage procedure using a vancomicin-impregnated bone cement spacer and beads implantation successfully treated this patient 14 months after the first revision of THA. No recurrence of infection was found at 42 months of follow-up.
These results suggest that two-stage revision THA using a temporary antibiotic-impregnated cement spacer is a useful technique for infected hip arthroplasty.
There was no difference in the average number of gait cycles between females and males. However, polyethylene wear per million cycles was significantly higher in males (p=0.006). Even after adjustment for greater height and weight in males, their wear rate was still significantly higher (p< 0.01). Males walked at a higher average speed (p=0.07), spent 33.9% more time walking fast or very fast, had 4% more starts/stops per day, with 13% less strides between stops. The percentage of time spent walking slow (5–9 cycles/minute) was negatively correlated to wear (p< 0.05).
It is widely accepted that a wide contact area between bone and artificial materials is necessary in the fixation of hip joint prostheses. It is also considered be applied to the proximal femur. However, these two concepts are contradictory in that the contact point cannot be determined in a wide contact area. Therefore, in this study, we revised the available concepts to improve the method of fixation of joint prostheses using finite-element-method (FEM) analysis of the equivalent mathematical models.
The first model was designed based on the intramedullary cruciate fixation stem. In this model, the total contact area was limited to the small area of legs-on-plane. Another model was designed based on the fit-and-fill-type stem, and in this model, the total contact area of the plane-on-plane was equal to the total surface area of the stem. In the plane-on-plane model, there was an unstable vibrating pattern in stress distribution, and we considered that deterministic chaos existed in the stress filled wide
Carbon nanotubes are an exciting new type of material and have extraordinary properties (
The objective of this study was to determine the validity of this hypothesis and whether MWNTs can significantly improve the tensile properties of PMMA. Methods MWNTs (20–30 nanometers in diameter, 20–100 microns long) were grown on a fused quartz substrate by the thermal decomposition of xylene in the presence of a metal catalyst. They are formed in well-aligned mats and grow perpendicular to the walls of a tubular reactor. As a first approach MWNTs were separated and dispersed through the liquid monomer component of PMMA by using an ultrasonic probe. The remaining polymer component was then mixed with this dispersion and the product was used to prepare specimens by casting in molds. Since prior work in other polymer systems (
Since MWNTs are also electrically conducting and have magnetic properties, MWNTs may also help dissipate the heat generated by polymerization or permit bone cement with an “engineered” mechanical anisotropy. Although static tensile tests are an incomplete measure of bone cement, these preliminary results are very encouraging and motivate continuing study of the more clinically relevant (impact resistance, fatigue properties, etc.) measures of the mechanical performance of MWNT augmented bone cement.
We have utilized arthroscopic arthroplasty of the hip joint (arthroscopic partial resection of the acetabular edge) for the treatment of advanced osteoarthritis of hip joint.
We have utilized arthroscopic Arthroplasty to widen the joint space and tried to improve the outcome of joint preserving operation. We have treated advanced osteoarthritis of nine hip joints of eight patients (age from 41 to 56, averaged 44.3 years old) by arthroscopic arthroplasty in the past six years. The patient was put on the surgical traction table in the supine position. Arthroscope was inserted into the hip joint from antero-medial approach under fluoroscopic control and the acetabular edge was shaved until bleeding from subchondral bone was seen. In eight joints of seven patients, additional surgical procedures were applied later.
Acetabular edge resection alone might resulted in the lateral-proximal displacement of the femoral head and to acquire good result in the long term, some additional procedure should be considered. However, in one case of this series showed good roof osteophyte formation after arthroscopic arthroplasty with improved JOA score. This might be a result of improved blood supply at the edge of acetablum. We believe that arthroscopic arthroplasty for advanced osteoarthritis in combination with other procedures may avoid total hip arthroplasty.
Polyethylene wear is the most important risk factor affecting the durability of total knee arthroplasty. We developed a new method of measuring wear of the tibial polyethylene insert in total knee arthroplasty (TKA) on standard standing radiographs.
The traditional stem in cement-less total hip replacement was designed as a straight stem. This design was chosen to compensate for lack of initial stability provided by cement. Specifically the box shape of the implant achieved rotational stability and the wedge shape promised proximal press fit. Therefore also the first robot-assisted surgeries were performed using straight stems.
Primarily those surgeons using the antero-lateral approach soon felt limitations of the use of straight stems during robot-assisted surgery. The reamer, in order to guarantee a straight positioning of the implant, used a straight approach to the proximal femur, thereby damaging the insertion site of the gluteus muscle in some cases. This then led to persisting muscular deficit with a consecutive positive Trendelenburg sign.
Surgeons began to monitor during computer–assisted planning not only the final position, but also the cutting path, which was – as requested by the surgeons – displayed on the screen. At the same time anatomic stems became available for computer-assisted planning and surgery. With the introduction of anatomic stems also oblique cutting became available, thus avoiding compromising the greater Trochanter.
Clinical results of anatomic stems in robot-assisted surgery seem to be satisfactory. Although most users allow immediate weight bearing, no loosening or visible subsidence was reported. Cadaver studies and animal experiments suggest that exactness of robot-assisted preparation with the resulting close fit of the implant – no press fit though – provide sufficient stability to allow for anatomic designed stems in cement-less procedures.
Impaction allografting is one of the techniques for reconstruction of femur during revision total hip arthroplasties. The initial stability of the stem fixed with impacted morsellized allogtafts and cement depends on multiple factors. The aim of this study was to investigate the stability of stem in reference to the size of bone chips, femoral bone defect and implant design.
Morsellized grafts of human femoral heads were prepared using a reciprocating type bone mill or a rotating type bone mill. Femoral bone defect was created at proximal medial cortex. Two types of polished stem were tested; CPT stem and VerSys CT stem (Zimmer Inc.). The cross section of the stem was relatively rectangular in CPT stem, while round in VerSys CT stem. Morsellized grafts were impacted into an over-reamed plastic bone and the stem was fixed with PMMA bone cement. Cyclic compression test and torsional test were performed using an Instron type machanical tester. Bone chips prepared by a reciprocating type bone mill contained large chips with broad size distribution, which represented high stiffness in compression test and high maximum torque in torsional test. Femoral bone defect and implant geometry did not affect the axial stability of stem, while large bone defect and round shape stem showed significantly lower maximum torque.
These results indicated that the size of bone chips, femoral bone defect and implant geometry affected the initial stability of the stem. Impaction grafting seems to be a technically demanding procedure, however several factors can be controlled to obtain secure implant stability.
This paper outlines and defines a research, which was conducted in order to gauge the efficiency of the Elective Orthopaedic Assessment Clinic in the Department of Orthopaedics, Kilcreene Orthopaedic Hospital, Kilkenny, Ireland. The study was conducted in the year 1999. During this year, 380 patients were seen in the clinic. Of these, 328 patients were on the waiting list for joint replacement and 52 were on the waiting list for other elective procedure. In the process of the study it was observed that 204 patients were found fit on their first preassesment visit. Of all the 328 patients on the waiting list, 48 of those who were awaiting joint replacement were found to have dental caries or infected gums and 28 were diagnosed with some minor infective foci elsewhere in the body. However as according to procedure the patients that did not meet the preassessment criteria due to infection, but were pronounced fit for an operation had to wait for the infection to settle before they could be rescheduled for surgery.
The study in question has proved that the clinic acts as an intermediary between the patients and the operation theatre, by determining patient’s fitness for surgery and appropriately placing them on the corresponding waiting lists. This fact is of primary importance as it aids in preventing possible and sometimes last minute cancellations, thereby attesting to the effectives and efficiency of the clinic. The clinics efficiency can also be measured by the fact that it has initiated a number of improvements, such as the introduction of a checklist card for patients on the waiting list for joint replacements. This checklist includes dental health, and also arranges for patients to be examined by their general practioners and dentists before the preassesment checkup.
Successful outcome in TKA is influenced by the accuracy of the bone cuts, the reconstruction of the anatomical axes,implant design geometry and the active and passive soft tissue structures surrounding the articulation. They determine stability,range of motion and interface stress of the replaced knee joint and of course the clinical result. Since August 2000 we use regukarly the GALILEO-CAS and GALILEO-NAV System in TKA with the TC-PLUS(TM) Solution Knee.
Further evaluation of the mid and long term results are necessary to evaluate the effectiveness of Computer Assisted Surgery in Total Knee replacement.
polyethylene wear and degradation demand of thin components
Excellent Scratch resistance AMC Ceramics is much harder than most surgical instruments. In comparison, metal components are easily scratched and damaged during surgery with the consequence of increasing wear.
The novel AMC Ceramic offers a solution to minimise the allergic and wear related problems of knee implants. New concepts on the basis of hard on hard combination are technically already realised. The use of knee endoprosthesis with ceramic on ceramic combination is an option for ”zero” wear bearings in the knee.
The first Ceramic knee implant in a human patient was used by Dr. G. Langer of the Orthopedic Clinic at the University of Jena, Germany in 1972 [
The wear behaviour of the Ceramic components for the knee system were tested in accordance to ISO/WD 14243-3 for 5*106 cycles. Six samples were tested. The lubricant was calf serum diluted with deionized water. All tests have been performed with components made of the novel AMC Ceramic. The wear test performed showed an average gravimetric wear rate below 1 mg/1*106 cycles on each of the six components. A change of geometry was not measurable after 5 million cycles. No significant change of the surface structure was detectable with a conventional surface tracer. SEM and AFM pictures show traces of ultra mild abrasive wear at the surface.
The performed investigation on the novel knee concept shows the following potential benefits for a Ceramic knee bearing:
approx. 500 times lower volumetric wear low risk of tribologically induced failure no PE particle induced osteolysis
The novel AMC Ceramic offers a solution to minimize the allergic and wear related problems of knee implants. New concepts on the basis of hard on hard combination are to be realized. The use of knee endoprosthesis with Ceramic on Ceramic combination is an option for ”zero” wear bearings in the knee. These first results motivate to start further R& D on Ceramic on Ceramic bearings for total knee implants.
This study assesses the clinical performance of the Souter-Strathclyde elbow arthroplasty with a standardised index and long-term survivorship analysis.
We undertook assessment of 68 primary Souter-Strathclyde total elbow replacements. Of 53 patients assessed with pre-operative Souter-Strathclyde charts, nine died and one was lost to follow-up, 43 had radiographic and telephone review, and 38 (88%) had clinical examination according to the Mayo Elbow Performance Index.
Survival of the 43 elbows was to a mean of 72 months (range 8 to 187). A cohort of 25 elbows available for review with > 5-year follow up had improvement in pain, motion, stability and function. Eight of ten elbows in deceased patients had satisfactory scores at the last assessment. Ulnar neuropraxia occurred in eight elbows (12%), persistent sensory deficit in two (3%) and motor deficit in one. Two triceps abscesses required local skin flap cover. Revision was undertaken in 14 elbows (20%) for instability (6) bony injury (3), loosening (3) and intraoperative problems (2).
The survivorship at 13 years was 74% with 62 (91%) of all elbows achieving a satisfactory Mayo score.
This study addresses four questions:
Does laminar flow exist in our operating theatres?
Do perioperative warming blankets affect laminar flow?
Do perioperative warming blankets cause displacement of particles into a wound perioperatively?
Do conventional theatres have adequate airflow?
It has been widely recognised that laminar flow theatres decrease colony forming units in operating theatres and thus decrease the risk of infection in arthroplasty surgery. It is also accepted that perioperative warming blankets improve patient haemodynamic stability and may reduce the risk of wound infection.
However, there has been great debate as to whether these perioperative warming blankets cause disruption of laminar flow and excess displacement of dust into a wound, and thus increase the risk of infection of total joint arthroplasty surgery. Using digital video imaging and airflow measurement techniques as used in formula 1 racing design, this independent study reveals that the Bair Hugger system has no effect on laminar flow or paticle displacement. It also shows that factors out of the surgeon’s control disrupt laminar flow and that general theatre design may be inherently flawed. This would seriously affect the risk of infection.
Total knee arthroplasty (TKA) after proximal tibial valgus osteotomy is thought to be technical demanded and its outcome is not as sufficient as primary TKA. Purpose of this study is to identify particular surgical procedures and outcome of TKA after proximal tibial valgus osteotomy in the different type of osteotomies. Fourteen TKA after proximal tibial valgus osteotomies were underwent for 13 patients with osteoarthritis. Average age at surgery was 72 years old. The mean duration from proximal tibial valgus ostetomy to TKA was 9 years and 10 months and the mean follow up period after TKA was three years and nine months. Four closed wedged osteotomies, five modified Levy’s reversed V shaped osteotomies and five domed osteotomies were underwent before TKA. The V-Y lengthening of quadriceps tendon or osteotomy of the tibial tubercle was necessary for each one knee. Both knee had patella infera due to previous osteotomies of tibial tubercle for patello- femoral osteoarthritis. 11 lateral releases including release of lateral collateral ligament and two lengthening of iliotbial tract were needed to achieve sufficient ligament balance. The stems of tibial components could be placed almost centrally especially in knees, which had reversed V shaped oseteotomies and laterally in knees, which had domed or closed wedged osteotomies. Clinical results evaluated by Japan Orthopedic Association score had improved from 53 points before TKA to 84 points after TKA. This study suggests that 1) approach is difficult in the knee, which had previous osteotomy of tibial tubercle, 2) lateral release including lateral collateral ligament and iliotibial tract is necessary to achieve sufficient ligament balance, 3) the stem of tibial component might be placed laterally in knees, which had previous domed oseteotomy or closed wedged osteotomy, 4) outcome of TKA after proximal valgus osteotomy is as good as primary TKA.
Sciatic nerve palsy is a troublesome complication of total hip arthroplasty, and may be caused by direct injury or over-traction at the time of the operation. We investigated the effects of over-traction on the blood flow of the sciatic nerve by placing the hip and knee joints in various positions. Twenty hip joints of 10 adult dogs were examined. Using a posterior surgical approach, the sciatic nerve was exposed and a site 1 cm distal to the greater trochanter was selected for blood-flow measurement. The blood-flow was measured using a Laser Doppler Flowmetry, with the hip and knee joints at various positions. Blood flow decreased as flexion angle increased and internal rotation angle of the hip joint increased, and decreased with as flexion angle of the knee joint decreased.
When we positioned the hip joint at 160 degrees of flexion and 30 degrees of internal rotation and the knee joint at 0 degrees of flexion, we found that the mean blood-flow decreased by 69% from the value measured when the hip joint was at 90 degrees of flexion and the knee joint was 90 degrees of flexion. When knee flexion was 90 degrees there was no significant difference in average blood flow between 30 degrees of internal rotation of the hip and 0 degrees internal rotation. When knee flexion was 0 degrees there was a significant difference in average blood flow between 30 degrees of internal rotation of the hip and 0 degrees of internal rotation.
Our results suggest that surgeons should pay attention to extension of the knee and the flexion and internal rotation positions of the hip to prevent sciatic nerve palsy as a complication of total hip arthroplasty
A prospective randomized study was performed to evaluate the role of cold therapy in the postoperative treatment of total hip arthroplasty (THA). Forty consecutive patients underwent primary total hip arthroplasty for osteoarthritis. All components were not cemented. The patients were randomized: 20 were fitted with a cold therapy device for four days, and 20 were not. They were evaluated in terms of blood loss, creatine phosphokinase (CPK) level, C-reactive protein (CRP) level, and pain relief. No significant difference was found in the amount of postoperative wound drainage between the two groups of patients. The use of cold compressive dressing after THA was not associated with an increase in CPK and CRP level.
The pain score in the postoperative period of THA was significantly lower in the cold therapy group than in the control group. The results of this study support the potential benefit in pain reduction by use of the cold compressive device in the postoperative recovery of patients undergoing THA.
The use of prostheses with porous surfaces in cementless total hip arthroplasty now predominates. Beads are popular for use as a porous coating, but their mechanical strength may be insufficient because of displacement of some of the beads from the coating. In this study, we propose a new porous surface, created by making direct holes in the metal surface using a YAG laser. A titanium-alloy (Ti-6Al-4V) rod was used. A Bead-type prosthesis was made by diffusion bonding pure titanium beads to the rod; it was 5 mm in diameter and 35% in porosity. A Laser type was made by directly creating holes in the same rod surface using a YAG laser; it was 5 mm in diameter and 33.7% in porosity. Both implants were evaluated in vivo using the hemitranscortical cylindrical model in two beagle dogs. Four prostheses were implanted into each femur through the lateral cortex, for a total of eight of each type, and remained in place for 12 weeks. Except for the proximal implant, push-out tests were performed to measure the shear strength of fixation of the implants to the cortical bone. For observations of the implant-bone interface, decalcified specimens of the proximal femur were stained with toluidine blue and observed with an optical microscope. The mean push-out strength of the Laser type was approximately 10.2 MPa and that of the Beads type was approximately 10.7 MPa. There was no significant difference in interface push-out strength between the groups. Bone ingrowth into both types was sufficient, however, some specimens of the Beads type demonstrated displacement of some of the beads from the rod surface. This study indicates that a porous surface created with a YAG laser might be useful not only for its shear strength, but also for the strength of the surface itself.
Biodegradable porous scaffolds play an important role in tissue engineering as the temporary templates for transplanted cells to guide the formation of the new organs. The most commonly used porous scaffolds are constructed from two classes of biomaterials. One class consists of synthetic biodegradable polymers such as poly (α-hydroxy acids), poly(glycolic acid), poly(lactic acid), and their copolymer of poly(DL-lactic-co-glycolic acid) (PLGA). The other class consists of naturally derived polymers such as collagen. These biomaterials have their respective advantages and drawbacks. Therefore, hybridization of these biomaterials has been expected to combine their advantages to provide excellent three-dimensional porous biomaterials for tissue engineering. Our group developed one such kind of hybrid biodegradable porous scaffolds by hybridizing synthetic poly (α-hydroxy acids) with collagen. Collagen microsponges were nested in the pores of poly (α-hydroxy acids) sponge to construct the poly (α-hydroxy acids)-collagen hybrid sponge.
Observation by scanning electron microscopy (SEM) showed that microsponges of collagen with interconnected pore structures were formed in the pores of poly (α-hydroxy acids) sponge. The mechanical strength of the hybrid sponge was higher than those of either poly (α-hydroxy acids) or collagen sponges both in dry and wet states. The wettability with water was improved by hybridization with collagen, which facilitated cell seeding in the hybrid sponge. Use of the poly (α-hydroxy acids) sponge as a skeleton facilitated formation of the hybrid sponge into the desired shapes with high mechanical strength, while collagen microsponges contributed good cell interaction and hydrophilicity. One of such kind of hybrids. Additionally, our group developed a hydrostatic pressure bioreactor for chondrocyte culture. And our study showed that hydrostatic pressure (0–3 MPa) had promotional effects on the production of proteoglycan and type II collagen by cultured chondrocytes. Therefore, it would be a promising pathway for reconstructing cartilage-like tissue to culture chondrocytes in this three-dimensional hybrid sponge under physiological hydrostatic pressure.
To report and validate the early migration rates of the collarless polished tapered hip replacement using manual and computer measurements
To report early clinical results of the CPT hip
There was no significant difference between inter or intra observer measurements for hip migration.
This is the first study to date that we are aware of that describes the subsidence rates of the CPT hip which includes validation by inter and intra observer readings.
To evaluate the osseointegration enhancement, a consecutive randomized series of 50 on a total of 483 cementless titanium prostheses were prospectically studied. The features of the stem were the following: tapered, straight, low-profile neck, metaphyseal and hystmic fit, proximal 1/3 hydroxyapatite coated (HA) and titanium porous coated (PC). The acetabular component was hemispherical, titanium porous coated. A zircornia or Co/Cr head (28mm) was used. Female were 53% and average age 65. The general diagnosis was ostheoarthritis, congenital hip dysplasia, fracture, aseptic loosening, osteonecrosis, previous femoral osteotomy, previous pelvic osteotomy. Clinical objective assessment was based on the HHS. A patient oriented evaluation (Womac and SF12) was obtained. Radiological assessment was based on the Engh’s method. The general and prospectical group results have been evaluated.
In all the groups the HHS, Womac and SF12 questionnaires showed a statistically significant improvement in quality of life. Consistent evidence of proximal bone ingrowth were present in 100 % (HA) and 96 % (PC), stable proximal fibrous ingrowth in 4 % (PC). Cortical hypertrophy (50 % zone 3–5), stress shielding (56 % zone 1) and pedestal ( one case) were assessed. Nor osteolysis neither subsidence were identified. No significant general complications such as infections or periprosthetic fractures were observed. The use of HA seems to improve the mechanism of osseointegration and earlier clinical outcomes, even if this difference is not significant. Patient oriented evaluation and radiographic assessments confirmed the reliability of this cementless prosthesis. Less osteolysis could be predicted in the future, according to the reported results of other authors in the HA coated stems.
Bone Loss is the main problem in failed total hip arthroplasties. Revision surgery must be conformed to the degree of the bone loss. Since 1986, 330 cases of failed THA underwent to revision surgery. Different solutions were adopted according to Paprosky femoral defects classification. In type I, a primary cementless stem was implanted (23%). In type II and IIIa, were proximal fixation is still possible to achieve, Mid PCA-Howmedica (5%) and modular S-ROM-J& J revision stems (18%) were implanted. In all the other degree of bone loss (IIIb–IV) cementless distal fixation stems, Long PCA-Howmedica (17 %), Wagner-Sulzer (18 %) and modular (MP-Link, Profemur-Wright) (19 %), were used. Patients were clinically and radiographically evaluated by HHS and according to Engh’s criteria. Best results were observed in Type I group (HHS=90). Long and mid PCA stems presented poor clinical (HHS=60) and radiographical results and required re-revision in 15% of cases. Intermediate results were observed in Wagner prostheses. Modular revision stems showed best results although earlier F-U. (HHS=80). Of these, re-revision surgery was performed in two cases, one of which because of infection and the other one due to severe thigh pain.
Cementless modular stems seem to be the most suitable technique. Distal fixation associated with proximal fill permit to manage the majority of femoral bone defects minimizing bone grafts. The modular stems, allow to conform the design of the components to the bone defects permitting to achieve primary stability (press-fit), restoring the centre of rotation and muscles tension, reducing pain and restoring hip function.
Early micromotion of joint prostheses with respect to the bone can be assessed very accurately by a method called Roentgen Stereophotogrammetric Analysis (RSA); a method that uses two simultaneous X-ray exposures of the joint and has an accuracy of 0.1 mm for translations and 0.3 degree for rotations [
In a previous study we have developed a Model-based RSA algorithm, which does not require the attachment of markers to the prosthesis [
Because the accuracy of this NOA algorithm was not as high as the accuracy of the currently used Marker-based RSA, we have studied alternative algorithms for Model-based RSA. From a simulation study in which we used models of the Interax Total Knee Prosthesis (Stryker-Howmedica) and the G2 Hip Prosthesis (Johnson & John-son), we found that the results of the NOA algorithm can be improved substantially. The newly developed Model-based RSA algorithm is based on minimisation of the mean distance between the points of the actual contour and the virtually projected contour. The simulation study shows that the new algorithm is superior to the NOA-algorithm in situations where part of the contour is occluded, as well as in situations where the contour is distorted by noise. With the new algorithm, the residual position error can be reduced to 0.1 mm. and also the residual orientation error can be reduced to 0.3 degree, making Model-based RSA a future alternative to Marker-based RSA.
Biomechanical alignment of the knee is a major determinant in the outcome of Total Knee Arthroplasty. However, the best method to assess the alignment is yet undecided. Conventional methods use hip to ankle “long” standing x-rays but these suffer from technical difficulties and hence are a potential for error. Short x-rays are considered to have doubtful accuracy.
This study aimed to assess if the “short” AP x-rays could be used to assess the lower limb axis within a range of statistically insignificant and clinically acceptable difference.
The results indicate the readings from the short x-rays were not statistically different from those obtained from the long x-rays in four sets of observations. The largest difference between any two readings was 0.68 degrees. The analysis of data showed that the measurements from the short x-rays could indeed be used to assess the long axis of the lower limb with the provison that there is no gross femoral shaft deformity.
By 1998, 10 patients had undergone 12 revision total knee arthroplasties at our institute. One patient died three weeks after surgery due to cerebral infarction, leaving 11 knees of nine patients for evaluation. Average follow-up was 4.8 years (1 to 9 years). All components were subjected to revision surgery in five knees, the tibial tray and insert in four knees, and only the insert in two knees. Patients were evaluated with clinical examinations, radiographs, and the Knee Society Clinical Rating System.
After revision surgery, the Knee Scores and ROMs were restored to almost the same level as just after the first TKA. Re-revision was performed on two patients, one 103 months and the other 82 months after revision TKA. In those two patients, huge bone loss of the proximal tibial canal was filled with cement without bone graft. The other patients, however whose tibial trays were fixed with cement on adequate grafted bone obtained good results.
The femoral components that were not treated with revision surgery despite small flaws or scratches due to wear and tear of the tibial insert did not cause marked wear of the new tibial insert.
After having completed more than 150 primary knee arthroplasties with a new navigation system both analyzing the position of the implants as well as the soft tissue balancing in each range of motion, we performed the first revision surgeries in February 2001 using this device. At present we have revised 15 arthroplasties with the support of navigation. The reasons for revision were early loosening in 11 cases and instability in 4 cases. Intra-operatively, we were able to analyze the malpositioning of the implants and the disturbed soft tissue balance.
In most cases (n = 12), a femoral internal malposition was found. There was, therefore, extreme polyethylene wear on the medial plateau of the tibia and instability of the soft tissues on the lateral side. We were also able to find an incorrect joint-line and a malrotation of the tibial component. In all these cases specific intra-operative kinematics showed us the primary reason for early loosening. The navigation system screen provides not only information about the incorrect angle of the implant position but also indirectly via the kinematics, information about the relationship of the malpositionings between the implants. In many cases (n = 10) there were combined errors in positioning of the implants.
The first 15 cases show that malpositioning of knee implants can be analyzed with the new generation of navigation systems. These devices help the surgeon, in the operation room, to make his decision how to proceed.
The malpositioned implants showed extreme polyethylene wear demonstrating that the positioning of the implants does influence the outcome very much.
A useful navigation system in revision surgery is the one which is not related to a specific design of an implant but is usable in all cases so that every implant can be measured.
One hundred twenty eight revision hip arthroplasties performed before Dec. 1995 using the Wagner self locking prosthesis were followed for five to ten years. Obviously, the shape of this revision prosthesis complements optimal primary stability; however, one must pay attention not to undersize the stem. Hence, the most significant feature contributing to this self-locking type is the accomplishment of appropriate canal filling when revision with optimum anchorage length of prosthetic component. According to the clinical and radiological data obtained from our midterm results, we confirm the excellent validity of this system for treating the advanced cases of bone resorption for revision. Obviously the classification based on the femoral bone deficiency by the AAOS and DGOT are well documented. Even though we agree with the recent concept of Bourne-Rorabeck that is worthwhile tending to revert to a simple, but practical classification based on the cancellous bone’s quality and the intactness of the cortical tube, we believe that four of Bourne-Rorabeck had better be five in order to be clearer. Furthermore, additional seven various cases series of recent for subsidence of the femoral components were included in this study.
We beieve that the only contraindication is conversion from arthrodesis when the patient has long standing history of heavy plate and screws because of undue discrepancy of the stress shielding. Lastly, it is very unusual, however, we describe the operative technique which Wagner stem is inevitably removed.
An argument against the use of canal-filling, customised femoral stems has been that such implants have a large cross-sectional area and therefore are stiffer than standard, uncemented implants, thus inducing more stress shielding and bone loss in the proximal femur. The purpose of this study was to evaluate the association between the volume of the femoral stem and the change in periprosthetic bone mineral density (BMD) measured with DEXA.
The common factor in all (mechanical) prosthetic failure mechanisms is the induction of osteolysis around the endoprosthesis with subsequent prosthetic migration and finally loosening of the prosthesis. Both initial prosthesis-bone fixation and long-term prosthesis survival depend on the quality of the peri-prosthetic bone mass. The effects of treatment of RA patients with prednison are inhibition of osteoblastic activity and inhibition of calcium resorption from the intestines. The bone mass loss during the first six months of prednison treatment is substantial and will seldom be regained. Bisphosphonates are known to decrease osteoclastic activity and may therefore stop osteolysis at the bone-prosthesis interface.
The aim of the study was to evaluate a possible association of bisphosphonates with reduced migration of total knee prostheses (Interax, Howmedica Osteonics, Rutherfort, USA) in a high-risk group. Roentgen Stereophotogrammetric Analysis (RSA-CMS, Medis, The Netherlands) was used to measure the micromotion.
Retrospectively a group of nine RA patients treated with prednison (non-bisphosphonates group) and a group of fourteen RA patients (bisphosphonates group) treated with prednison in combination with bisphosphonates (Etidronate) were included from a prospective randomized study of 82 patients (
At the two-year follow-up evaluation, functional scores and knee scores did not differ significantly among the two groups. At the two-year follow-up evaluation, the non-bisphosphonates group subsided −0.47 ± 0.8 mm, and the bisphosphonates components subsided 0.07 ± 2.9 mm. In the analysis of variance with repeated measurements, with correction for follow-up time, sedimentation rate, and prosthesis fixation type, the bisphosphonates group migrated 1.20 mm less in the total migration (95% c.i.: 1.07–1.30 mm) compared to the non-bisphosphonates group.
In this study, bisphosphonates medication in addition to corticosteroid medication was associated with reduced migration of knee prostheses compared to corticosteroid medication alone.
Osteotomy of the greater trochanter continues to be an important surgical technique, especially in revision and difficult primary hip replacement, which implied the tightness of abductors.
We advocate the frog-leg lateral radiograph to determine the reducibility of the dislocation at the level of true acetabulum in order to identify the sufficient length of abductors while sitting. This flexibility of soft tissue structure composed of abductor is compromised once hip is reduced, because of difficulty in bringing the trochanter down to its bed.
In practice, transtrochanteric approach and shortening of proximal femur were applied and greater trochanter was transferred distally for restoring of abductors power(modified osteotomy), while reducing the possibility of trochanteric dislodgement. In fact, the wire force is reduced by 25 % while the bone union compressive force is unchanged in the modified osteotomy compared with conventional osteotomy. We evaluated 17patients(23 hips) in DDH and 15 patients in tuberculous hip. Conventional osteotomy was performed in tuberculous hip and modified osteotomy in DDH.
Nonunion of osteotomized trochanter was found in the case of 5 tuberculous hips especially irreducible in the frog-leg lateral radiograph preoperatively.
Radiographs historically have not been standardized according to magnification. Depending upon the size of a patient, a film will either magnify a bone and joint (of large patients with more soft tissue) or minify (in the case of thin patients). An orthopedic surgeon must guess at the degree of over or under magnification to select an implant that is neither too large nor too small. The surgeon may be aided by the incorporation of a marker of known size. By calculating the difference between the size of the marker displayed on the film and the actual size of the marker, the orthopedic surgeon can identify the degree of magnification/minimization and compensate accordingly when selecting a prosthetic template.
This activity takes time and also is subject to mathematical error. Digital pre-op planning allows for an image to be displayed electronically, and with the use of a known sized marker, automatically calculate the magnification and recalibrate the image so that it is sized at 100% from the perspective of the user.
Digital pre-op planning incorporates a library of electronic templates of prostheses, which can be standardized to exactly match the size of diagnostic image being displayed. Traditionally, an orthopedic surgeon places an acetate template enlarged to be 110% to 120% over an X-ray film magnified to be110% to 130%. When there is a significant variation in magnification between the template and the procedure, this can contribute to surgical error. This type of error will be virtually eliminated with digital templating that has the capability to identically scale electronic templates to the X-ray image being displayed. Digital pre-op planning enables surgeons to select from a library of templates and electronically overlay them on an image as well as perform the necessary measurements critical to the templating procedure which not only speeds up this process but, as will be shown, has the potential of delivering unprecedented accuracy.
Positioning and secure fixation of the acetabular component without bone cement in dysplastic and deficient acetabulum is technically challenging because of the distorted anatomy of the acetabulum such as shallow and very thin medial and anterior wall, deficient super-olateral dome. Several treatment options have been reported to solve these problems when total hip arthroplasty is needed.
The author developed a new technique of circumferential acetabular medial wall displacement osteotomy to get secure fixation of the cementless hemispherical acetabular component at the site of the original acetabulum. This technique preserves the thin medial wall, deepens, and enlarges the acetabulum without additional structural bone graft. The procedure can also provide appropriate positioning and sufficient coverage of the acetabular cup.
From October 1989 to October 1995, we analyzed 84 hips in 80 patients who had a cementless total hip replacement with circumferential acetabular medial wall osteotomy at the Kyung Hee University Hospital. There were 28 male and 52 female patients with an average age of 49 years (range 25–71). Initial diagnoses were congenital dislocation, severe dysplasia, infection sequelae, and secondary osteoarthritis. The follow-up period ranged from 5 years to 11 years, the average being 7.2 years. All acetabular components used in this procedure were cementless porous coated hemispherical Harris-Galante (HG) I or II cup. The acetabular cup had secure fixation at the site of the original acetabulum without bone cement in all cases. Cup coverage ratio has become 97.7% in average. There was no radiolucent line around the cup or loosening. None of the acetabular cups with circumferential acetabular medial wall osteotomy had signs of medial migration. Bone union at the site of osteotomy was achieved in all cases. Bony ingrowth into the porous surface and remodeling around osteotomized acetabular medial wall was excellent. Technical pitfalls and advantages in biomechanical viewpoint of the procedure will be discussed.
The aim of this study was on the one hand to compare the fixation of a posterior stabilised prosthesis (PS) and a PCL retaining mobile bearing design (Interax, Howmedica Osteonics, Rutherfort, USA) and on the other hand to measure the mobility of the mobile bearing. All measurements were carried out by means of Roentgen Stereophotogrammetric Analysis (RSA-CMS, Medis, Netherlands).
A prospective,randomised,double-blind study (N=28) was conducted to assess the micromotion of the components. At the one-year follow-up evaluation, the micromotion of the PS-components and the mobile bearing components were not significantly different. The PS-tibial components subsided −0.063 ± 0.177 mm and the mobile bearing knee tibial components subsided 0.067 ± 0.084 mm. The PS tibial component showed a higher variability in the migration results indicating a number of PS with rather large micromotion.
For three patients, the in vivo motion of the mobile bearing with respect to the metal backing was assessed at 30, 60 and 90 degrees of passive flexion. Two of mobile bearings moved posteriorly (2.4 and 2.9 mm) at respectively 60 and 90 degrees of flexion and showed a medial-lateral translation of 0.03 and 3.5 mm. One mobile bearing moved only 0.4 mm posteriorly at 90 degrees of flexion but showed a lateral-medial translation of 3.1 mm.
The broad range of kinematic patterns of mobile bearings during flexion that is observed in fluoroscopic studies is also observed in this study. A possible positive effect of mobile bearing movement may be found in the smaller variability of the micromotion of the mobile-bearing knees compared to the PS knees. The assumption was that shear forces in tibial bones implanted with a mobile bearing prosthesis would be better dissipated from the prosthesis-bone interface resulting in less micromotion. The kinematics of an additional number of mobile bearing knees -already included in the micro-motion study- will have to be assessed in order to determine the relation between mobility and micromotion.
The advantages of high viscosity Simplex AF cement (PMMA) compared to low viscosity Simplex P are the low porosity, the high fatigue strength, the lower polymerization time, and the lower maximum polymerization temperature. A prospective, randomized, double-blind clinical study was conducted to assess the in vivo effects of viscosity of bone cement on the micromotion of a polished tapered stem and UHMWP-cup (Exeter, Stryker-Howmedica). Roentgen Stereophotogrammetric Analysis (RSA-CMS, Medis, The Netherlands) was used to measure micromotion.
Twenty patients were included in a Simplex AF group (70 ± 4.3 years), and twenty patients were included in a Simplex P group (71 ± 7.3 years). No significant differences in body mass index and clinical hip scores were observed between the two studied groups.
There was no significant difference of the subsidence of both high and low viscosity cemented Exeter stems. The subsidence was according to the literature and showed that the viscosity of the bone cement did not influence the cement-implant bond of this polished tapered stem design.
The total migration of the cups and the migration along the medial-lateral axis were significantly larger for the Simplex AF cemented cups compared to the Simplex P cemented cups (p=0.037). This can be explained by the higher cement mantle thickness in acetabular Gruen zone 2 (p=0.003) and 3 (p=0.004) of the Simplex AF cemented cups.
We conclude from this study that the viscosity of the bone cement has no effect on the subsidence of polished tapered stems and that a high cement mantle thickness around an UHMWP-cup has a negative effect on fixation.
Polyethylene wear is a significant factor limiting survivorship of total knee arthroplasty (TKR). Crosslinking of polyethylene has been shown to significantly reduce wear in hip arthroplasty but has not been reported for TKR. This study measured wear in polyethylene cross-linked to two levels in a knee wear simulator.
Six polyethylene knee inserts were tested in a knee wear simulator. Inserts were manufactured from polyethylene crosslinked to two different levels: 2.5 Mrad (Low-X) and 10.5 Mrad (High-X). Each implant was enclosed in a closed lubricant (50% alpha fraction calf serum) recirculation chamber, maintained at 37°C and changed every 500,000 cycles. Physiologic levels of load and motion were applied at 1 Hz for a total of 6,000,000 cycles. Wear was measured by the gravimetric method before wear testing and at every 500,000 cycles. Semi-quantitative wear assessment was performed by imaging the insert surfaces at 10x magnification.
The Low-X inserts demonstrated significantly higher wear rates (mean 4.66 mg/million cycles) than the High-X inserts (mean 1.55 mg/million cycles, p < 0.001). Wear scars on the Low-X inserts were irregular and visibly deeper than those on the High-X inserts. The machining marks on the surface of the insert were also better preserved in the High-X insert wear scars. These results suggest that crosslinked PE can significantly reduce wear in TKR under physiologic conditions. This can result in reduced lysis and increased survivorship. Localized damage can cause catastrophic failure in polyethylene knee inserts. Therefore, further studies are necessary to evaluate wear under these conditions.
An anatomical cementless stem sometimes does not fit the femur of Japanese osteoarthritis (OA) patients due to deformity of the proximal femoral canal.
In order to develop a new stem, we performed morphological analysis of 36 normal femora and 113 OA femora by using a computer aided design system and a three-dimensional canal fill ratio of anatomical stem was calculated.
Thirty-six normal femora and 113 OA femora were reconstructed from 3D-CT data by using a computer aided design system. We analyzed each femur, and it became clear that there are 3 types of proximal femur in Japanese OA patients. In typeI, the configuration is the same as normal (42%). In typeII, the medial cortex is more steep (29%). In typeIII, the posterior cortex inclines anterior (26%). We chose 5 femora of the same size from each of the three types, and applied the anatomical stem of the most suitable size to each femur in the computer, we then calculated a three-dimensional canal fill ratio of the anatomical stem in the proximal portion of femoral canal.
The mean canal fill ratio was 76.4% in typeI, 60.0% in typeII, and 57.2% in typeIII. The canal fill ratio in typeI was significantly higher than the other types.
It is thought that to fill the proximal femoral canal with cementless stem is important to stabilize the stem and can lead to a good result. The anatomical stem fitted for the typeI, but did not fit for typeII and III, so we must consider developing a more suitable stem for typeII and typeIII.
We want to prove that you cannot make a good fitting stem of a THP before surgery because the resulting shape of the femoral cavity is set after all the tools have been introduced in the femur. We are fully aware that fit and fill alone is not enough to obtain good fixation therefor all the investigated implants were plasma spray coated with HA.
We have investigated two groups of patients:
Pre – operative group: custommade implant based on CT scans and manufactured before surgery. The proximal part was size for size and coated with HA; the distal part is cylindrical (44 cases, followup from 2.6 years to 6.2 years). Per – operative group: custommade implants based on a mould of the femoral cavity in the proximal femur and manufactured during surgery. The prosthesis was size for size and the HA coating was applied on the proximal 1/3 of the implant. (13 cases with a minimum follow-up of two years).
The manufacturing procedures and coating specifications for both groups were exactly the same. We’ve compared the Harris hip score for both groups and we’ve performed a radiolographical analysis.
Of the preoperative group 6 protheses had to be revised. This results in a revision rate of 13 % which is not acceptable. In the peroperative group however, no revisions have been performed. Radiografically the peroperative group showed much better results than the preoperative group.
The obtained results suggest that it is not only important to have a good bone growth initiator such as HA but the implant needs to be in close contact with the bone.
In primary malignant bone tumours, the “en – block” excision with the sacrifice of soft tissues causes a functional deficit of the interested limb. There are many possibilities for reconstruction after a wide resection of the proximal humerus. The Authors report their experience using megaprostheses, focusing to soft tissue reconstruction, in order to obtain a good and fast functional recovery of the involved limb. 13 megaprostheses of the proximal humerus were employed. All patients were affected of primary malignant bone tumors with different histology. The tumor was staged according to Enneking’s system. 8 cases were classified as IIB and the remaining as IIA. All the tumors were treated with an intrarticular resection. Soft tissues reconstruction was performed, in 8 cases, using a mesh (Trevira tube), dressed all along the prosthesis, with a high resistance to traction. Radio and/or chemotherapy were employed referring to the histology.
At a medium follow – up of two years, for the surviving patients, we have obtained excellent functional results in 1 case, good in seven cases, fair in three cases and poor in two cases. The size of the resection is a main factor in order to obtain a good functional recovery of the joint motion. A wide excision (below deltoid insertion) with the sacrifice of large muscular masses and of the osteoarticular structures can represent a functional amputation causing the loss of muscles that are important to have an acceptable joint movement.
In our experience we retain that the use of modular prostheses in reconstructive orthopaedic surgery is advantageous because of its versatility and of its quick implantation, despite of other reconstructive systems. Moreover the use of a device, as that described, for an easy anchorage of the myotendinous structures, allows a quick functional recovery offering the patients considerable advantages for their social life.
Zirconia has considered a good material for manufacturing of ball heads in total hip replacement due to high mechanical properties of this ceramic material. However in the literature the problem of heads biocompatibility is still debated. The Authors reported their experience in ten years of research on the biological properties of this material. In vitro tests were performed onto materials in form of powders, analyzing the inhibitory effects on human lymphocyte mitogenesis, and in form of plates measuring adhesion and spreading of 3T3 fibroblasts. A mutagenic test was also performed. In vivo tests were performed by injection of powders in mice and evaluating the survival of animals according to ASTM F – 750. We also inserted ceramic in form of cylinders into proximal tibial metaphysis of NZW rabbits and analysed local and systemic reaction due to material diffusion. We also developed a system of production of Zirconia particles by inserting ceramics under patellar tendon of NZW rabbits.
In vitro tests showed that Zirconia powders and plates induced a similar effect of Alumina ones; no mutagenic effect were observed using our samples, demonstrating that Zirconia has no carginogenic effects. In any case the diffusion of particles didn’t show modifications into internal organs (lung, kidney, liver, spleen) of mice and rabbits. In time (one year after operation) the connective tissue present at bone ceramic interface is transformed into lamellar bone.
Our experience demonstrates that Zirconia may be considered a good material for prosthetic implants.
The Authors analysed two cases of catastrophic failures of Total Hip Prostheses due to the disruption of the PE inlay and the Ti-alloy metal back of the acetabular components. In the cases reported the PE inlay (4 mm in thickness) was coupled with a 32 mm in diameter Alumina ball heads. At time of revision the alumina ball heads showed many black marks due to the contacts with the Ti-alloy metal back. The sockets showed severe damages, concentrated in the superolateral zone. The PE inlays were disrupted. Almost a third of the metal back is missing. A large metallosis was also visible in the membrane at the interface between implant and bone. Histologic sections showed a large amount of metallic debris in a pseudovillous membrane. At higher magnification oligonuclear cells in a rich in vessels stroma were in contact with metal particles. PE debris with the characteristic birifrangent aspect to the polarised light microscope was contained into polynuclear giant cells. SEM showed that the size of 25% of particles was less than 1 μm, while the size of 53% of wear debris is in the range from 1 to 5 mm. EDAX confirmed that these particles consisted of Ti alloy. The Authors analysed the possible roles of different factors in the etiology of this cup failures and concluded that in both the cases analysed the initiator of the failure was the size selection of the prosthesis, and in particular the PE thickness, followed by the positioning of the acetabular component. The deformation of the PE inlay leads to rupture of the inlay itself, followed by the direct contact between the Alumina ball head and the titanium alloy cup, causing the disruption of the Ti-alloy metal back, with massive release of wear debris in the surrounding tissues.
Radiographs are often used to determine the varus/ valgus alignment of the prosthesis in relation to the long axis of femur. This is usually considered to be one of the important parameters in predicting early mechanical failure of the total hip replacement.
The measurements made by the University of Dundee X-Ray Analysis Software and skilled manual operators of the varus and valgus angulations of hip prosthesis in relation to the femoral shaft were compared for inter and intra-observer reliability.
The manual measurements were carried out on the same randomly selected digitised images of 78 postoperative X-rays by two independent observers and by the same analysis software twice.
The results of the study showed a very high agreement between the readings of the two methods (the largest difference was 0.6 degrees) and two observers (the largest difference being 0.08 degrees) indicating excellent intra and inter observer reliability. The lowest correlation was 0.82 and this was between software reading 1 of observer 1 and software reading 1 of observer 2. The highest correlation of 0.99 was between software reading 1 and software reading 2 for the same observer. The software analysed the x-rays with precision and accuracy and was much faster than manual measurement. A further benefit of the computerised method is an unskilled operator can be trained in 15 minutes to use the software
The Pyramid stem is a tecnical evolution of the previous Zweimuller, in order to have the best press fit. It has no more longitudinal grooves and neck, but has a distal arcuate fissura to improve the elasticity and to avoid distal stress by a uniform contact with the bone. We show the breaking test and resistence test. It has a rectangular section, a uniform thickness along all its lenght to have a good diaphyseal anchorage on four zones of the internal cortex to avoid torsional stress and to maintain endomi-dollar vascularization. This stem has the maximum contact surface not only with the dyaphysis, but also with the metaphysis and the trochanter. It has been studied with the femur morfology, to fill the bigger ones with a cylindric canal and the smallest ones with a conic canal. Transverse section has increased by the pyramids that increase contact surface bone-prosthesis, primary stability and press-fit. It is straight both in the frontal and in the sagittal plane to realise a good primary stabilization according with the concept of the three support point. We present our surgical experience to obtain a correct position of the stem, and the best use of the instrumentation. From June 1997 to May 2001 we have used this stem in 257 hips; we have obtained excellent and good results in 87% of patients. We show some cases and the only one stem removed. This stem allows a rapid postoperative rehabilitation following our protocol as explained.
Load-controlled knee simulators, representing the passive constraints and joint loads observed in the natural knee, have been developed to assess device-dependent kinematics and wear damage of total knee replacements (TKR) in a controlled mechanical environment. Using a finite element model (FEM) to represent the simulator, our objective in this study was to quantify the variations in kinematics, contact stresses, and contact areas that occur with variations in the ‘soft-tissue’ spring stiffness and coefficient of friction for a conforming knee design.
A finite element model was created of the Insall-Burstein Posterior-Stabilized II knee system. The model conditions corresponded with the International Standards Organisation (ISO) test protocol #14243-1 and consisted of the prescribed flexion angle, the axial compressive load, the anterior-posterior (AP) force, the internal-external (IE) moment, and linear springs mounted to provide AP and IE restraints. This setup has been validated as a reasonable equivalent system for this design in the Instron-Stanmore knee simulator. The linear spring constant was set at 7.24 N/mm and the coefficient of friction was 0.01; both values were then varied by an order of magnitude. The implant kinematics and the maximum contact stress and areas of contact over the loading cycle were determined.
Varying the spring constant by a factor of two changed the AP motions and IE rotations of the tibial insert by about 20%. The maximum contact stresses, occurring during peak loads and moments, varied by 40%, while the area of contact over the full cycle changed by 30%. Changing the coefficient of friction had little effect upon the dependent variables. Wear is a function of both stresses and kinematics. This study indicates that stresses in this design are more sensitive than kinematics to changes in ‘soft-tissue’ stiffness. Therefore, both must be considered to determine wear potential.
After having completed more than 150 primary knee arthroplasties with a new navigation system both analyzing the position of the implants as well as the soft tissue balancing in each range of motion, we performed the first revision surgeries in February 2001 using this device. At present we have revised 15 arthroplasties with the support of navigation. The reasons for revision were early loosening in 11 cases and instability in 4 cases. Intraoperatively, we were able to analyze the malpositioning of the implants and the disturbed soft tissue balance.
In most cases (n = 12), a femoral internal malposition was found. There was, therefore, extreme polyethylene wear on the medial plateau of the tibia and instability of the soft tissues on the lateral side. We were also able to find an incorrect joint-line and a malrotation of the tibial component. In all these cases specific intra-operative kinematics showed us the primary reason for early loosening. The navigation system screen provides not only information about the incorrect angle of the implant position but also indirectly via the kinematics, information about the relationship of the malpositionings between the implants. In many cases (n = 10) there were combined errors in positioning of the implants.
The first 15 cases show that malpositioning of knee implants can be analyzed with the new generation of navigation systems. These devices help the surgeon, in the operation room to make his decision how to proceed.
The malpositioned implants showed extreme polyethylene wear demonstrating that the positioning of the implants do influence the outcome very much.
A useful navigation system in revision surgery is the one which is not related to a specific design of an implant but is usable in all cases so that every implant can be measured.
The surgical technique comprised cutting the tibial surface perpendicular to the long axis, ligament balancing in extension followed by femoral component rotation referenced off the proximal tibial cut to produce a rectangular flexion gap. The patella was cut to the level of the lateral facet and tibial component rotation was referenced off the center of the ankle. Lateral release was performed if congruent patello-femoral contact was not attained in knee flexion. Clinical and radiographic review was performed as per Knee Society criteria. Additional radiographic evaluation included patellar displacement, tilt, residual bone thickness and coverage ratio. A patient-administered questionnaire was used to evaluate anterior knee pain and patello-femoral function 1 year after surgery.
Currently available uncemented acetabular components appear to provide very reliable fixation for at least 10 years. However, these cups have been associated with a significant incidence of polyethylene wear. Osteolysis associated with this wear is emerging as the most significant problem in total hip replacement surgery. The purpose of this presentation is to describe the rationale for reducing polyethylene wear through the use of an uncemented acetabular component made of a polyethylene/ Tantalum (Trabecular Metal) composite and to describe the initial clinical experience with this cup.
Clinical and radiographic data were prospectively collected on the first 125 consecutively performed total hip replacements in which a tantalum (Trabecular Metal), monoblock acetabular component was used. Minimum follow-up was 24 to 46 months. Sixty three percent of the patients were female. Mean age was 61. The diagnoses were: OA-74%; AVN-12%; RA-10%; other-4%. 50% of the hips had cemented femoral components. 20% of the patients were Charnley Class 1, 30% Charnley Class 2, and 50% Charnley Class 3. At most recent follow-up, all patients were pain free (Ave. pain score pre-op.- 6.7, post-op.-1.4). No patient’s function was limited by hip function (Ave. Harris hip score pre-op.-38, post-op.-92). All hips had radiographic findings consistent with bone-ingrowth. Gaps in zone 2 were seen in 10% of hips, but filled in by one year. The rate of polyethylene wear as measured by the Martel technique was less than 0.07mm/year in the first two years.
There were three complications in the group: 2 dislocations which re. The early experience with the monoblock, tantalum cup indicates that initial fixation is secure, even without screws, and that initial polyethylene wear is very low.
It is estimated that there will be over 12,000 total shoulder replacements implanted this year. In the best series, the survivorships of these devices are 90% at 7 years. However, there are radiographic indications that the long term success will be limited to wear and damage to the polyethylene glenoid components. Like tibial insert in total knee replacements, the glenoid is subjected to both rolling sliding motions of a metal counterface. Additionally, the compressive loads on the glenoid have been estimated to be as high as 2800N under ‘normal’ conditions. In contrast to tibial inserts, glenoid components are all typically less than 6 mm thick. In metal backed glenoid devices, the polyethylene thickness is often < 3 mm. The effect of these parameters and kinematics on polyethylene damage has not previously described. Although total shoulder replacements have been in use for over 25 years, there have been no reports describing the nature and extent of glenoid polyethylene wear and damage.
We report the determination of polyethylene damage type and severity of 38 retrieved glenoid components of at least 4 different designs. Wear and damage were considered significant when either 80% of the glenoid surface was damaged or if over 25% of the component was worn away. Abrasion, burnishing and pitting were the main modes of damage. There were 2 fractured components. There was significant UHMWPE wear and damage in 17 (45%) components. In nine of these, the component was completely worn through.. These findings are consistent with high stress, high wear conditions and thin polyethylene components.
These results indicate polyethylene wear and damage is expected to be a key factor in limiting the survivor-ship total shoulder replacements and that polyethylene damage and wear in total shoulder replacements may be higher than that found for either total hip or knee replacements.
Besides the numerous variations of TKR designs addressing fixation, wear, or specific indications, there are variations from competing design philosophies such as conformity and shape of the articulating surfaces and mobile versus fixed bearing designs. With the same resected ACL and retained PCL ligament combinations and similar surgical procedure, the subset of different implants for these very indications should be expected to produce only minor variations in kinematics. This study set out on a comprehensive series of detailed and intricately controlled in-vitro tests to examine this hypothesis. Six different posterior cruciate retaining medium size knees from different manufacturers were used. Four were fixed bearing condylar types of low to high constraint; and two mobile bearing ones which allowed rotational and translational freedom, one fully and one partially conforming. The implants were aligned according to the manufacturer’s recommendations and subjected to the same ISO force-control simulation. The kinematics captured from the averaged simulated cycles of walking showed AP displacement contained within an envelope of 4 mm for most of the stance phase. This increased with most to a maximum range of 5mm just before toe-off at the end of the stance phase. In rotation, the designs showed ranges during stance from about 2–13 degrees. The kinematics from the different implant designs were thus significantly different; a controversial answer regarding the hypothesis posed. This means the “performance” must be different between these implants if installed “ideally” on the same patient with the PCL retained. Studies are worthwhile to determine if these differences in performance are reflected in clinical functional conditions.
Numerous studies have reported on the effects of modular insert design on stress at the tibial/femoral articular surface. However, while the insert / tibial component surface (“backside”) wear and motion have been investigated, backside stress is not well delineated. Because stress may be related to observed backside damage, this study addressed the backside stress response to insert thickness, material, and articular geometry.
Twelve Natural Knee II tibial inserts (Sulzer Orthopedics Inc.) with three thicknesses (6, 12.5, and 18.5 mm), two materials (Durasul and 4150 UHMWPE), and two types of condylar geometry (congruent and ultra-congruent) were tested. Fuji film was placed between the baseplate and insert. A femoral component was loaded onto the insert in axial compression at four times Body Weight. The film was scanned into Adobe Photoshop to measure mean and peak luminosity, which was converted into stress. Analysis of Variance was performed with main effects and all two-way interactions to determine significance.
The mean stress ranged from 0.61 to 3.92 MPa and the peak stress ranged from 2.17 to 10.4 MPa. Insert thickness significantly influenced both mean (p=0.001) and peak (p=0.001) backside stress. Stress for the 6 mm inserts (7.17 MPa mean, 9.91 MPa peak) were approximately 2.1 times the 12.5 mm inserts (3.47 MPa mean, 4.66 MPa peak), and were approximately 2.6 times the 18.5 mm inserts (2.74 MPa mean, 3.71 MPa peak). There was not a significant effect on mean or peak stress from material or condylar geometry. None of the interactions were significant.
This study provides two important contributions. First, it establishes the backside stress magnitude during simple loading. Second, the relationship between backside stress and the insert thickness is experimentally quantified. Understanding this stress magnitude and response may be important to controlling observed in-vivo backside damage.
We have been using a Charnley type hip prosthesis with an alumina ceramic head. Three sizes of alumina head, 28, 26 and 22mm, were employed and the Ortron 90 Charnley total hip prosthesis was used at the same period. The objective of this study was to compare the survival rate and the wear rate of those four groups. There were 90, 62, 322 and 88 hips in 28, 26, 22mm alumina head and 0rtron 90 head group. Average age at operation was 49.5, 57.8, 58.0 and 60.6, respectively. A 28 mm prosthesis was indicated for relatively young patients. The mean duration of follow-up was 156, 97, 49 and 110 months, respectively. Twenty patients were chosen at random for each of four groups and the linear wear as seen on X-ray film was measured every two years with a computer and scanner.
These results suggest that mechanism for the prevention of delamination by vitamin-E-addition is caused by increased elongation at break by increasing toughness at grain boundary. The addition of vitamin E is a simple and extremely effective method to prevent destruction of UHMWPE joint component.
Bankston et. al. reported that the clinical wear rates of molded acetabular cups was 50% less than a group of machined UHMWPE cups. However, due to covariables between groups including different femoral stems, cement technique, polyethylene resins and surgeons, unequivocal attribution of the low wear rates to direct molding could not be made.
In order to more directly assess the benefits of directly molded acetabular cups vs. machined cups, we report the comparison of hip simulation wear rates of machined and directly molded cups. These simulator results will then compared to two recent clinical reports on molded and machined cups of the same hip stem and cup design. The molded cups were made from 1900 resin and gamma sterilized in an inert atmosphere. The machined cups were made from HSS reference UHMWPE (4150) and gamma sterilized in air. The molded 1900 cups had a 55% lower wear rate after 5 million cycles on the hip simulator (14 v. 31mg/million cycles). Ranawat reported the average linear head penetration rate for 235 direct-lymolded, all polyethylene, cemented cups at a mean follow-up time of 6 years was .075mm/year. This is 56% lower than the rate of .17 mm/year he reported previously for the machined, uncemented metal-backed cups of the same design. These results provide further evidence that directly molding acetabular cups can provide wear rates over 50% less than machined cups both in both clinical and hip simulator evaluations. It is interesting to note based on other reports, that there is no osteolysis at 10 years of follow-up when the wear rates are < 1mm. The clinical and simulation wear rates reported here for the directly molded cups are within this performance range.
Polyethylene wear debris in TKA arises from several sources, including the tibiofemoral articulation and the interface between the backside surface of the tibial insert and the metal tibial tray. In this study we identify a new source of abrasive damage to the polyethylene bearing surface: impingement of resected bony surfaces, osteophytes and overhanging acrylic cement on the tibial bearing surface during joint motion.
One hundred forty-eight tibial components of 24 different designs in a retrieval collection were examined. A digital image of the articular surface of each insert was recorded. The presence, location and projected area of abrasive wear to the non-articulating edges of the insert were assessed using image analysis software.
Significant abrasive wear was observed in 24% of the retrievals with cemented femoral components and 9% from non-cemented components. Of the retrievals exhibiting this abrasive wear mode, 46% experienced multiple site damage. The average damage area for each individual abrasive scar was 78±11mm^2. Within the group of worn inserts, the abrasive scars were seen with a frequency of 69% on the extreme medial edge, 19% on the extreme lateral edge, 38% on the posterior-medial edge and 23% on the posterior-lateral edge. In posterior stabilized components with an open femoral box design, scarring of the superior surface of the tibial post was also observed. This proposed mode of damage was confirmed with several retrieved femoral components containing either fixed cement protruding from the posterior condyles, from the medial and lateral edges or osteophytes embedded in the posterior capsule. The corresponding inserts exhibited significant abrasive scarring at those locations.
We have observed a previously unrecognized source of polyethylene damage resulting in gouging, abrasion and severe localized damage in cemented and uncemented total knee replacement. Clearly, acrylic cement, in bulk or particulate form, often contributes to severe damage of the tibial surface and improvements to instruments and techniques for cementing are needed to prevent this wear mechanism.
Malfunctioning of Total Knee Replacements is often related to patella-femoral problems. As the patella groove guides the patella during flexion, the difference between anatomic- and prosthetic groove geometry may be of major influence concerning patella-femoral problems. This study focusses on the orientation or direction of the femoral patella groove, relative to the mechanical axis of the femur. Literature shows a controversy in measured groove orientation: Eckhoff et al. (1996) have measured a lateral groove, and Feinstein et al. (1996) have measured a medial groove, relative to the mechanical axis. Current femoral knee components have a lateral, or neutral directed patella groove. As most TKA surgical techniques subscribe an exorotation of the femoral component during implantation, the prosthetic in vivo situation will show a lateral groove. The objectives were to clarify the described controversy and to determine whether there is a difference in anatomic- and prosthetic groove orientation, which might cause patella-femoral problems.
The patella groove orientation of 100 human femora was measured using a 3-D measurement system. A spherical measurement probe was moved through the groove, starting at the notch and finishing at the cartilage edge, to simulate patella motion. The patella groove angle was defined as the angle between the mechanical axis and the measured groove points, in the frontal plane. A medial patella groove angle of 1.8±2.6° was measured. An implanted situation of a femoral component with neutral groove showed a lateral groove angle of 1.3°. An implanted situation of a femoral component with assymmetrical groove showed a lateral groove angle of 2.6°. The authors measured a medial oriented patella groove. This anatomical groove orientation is in contradiction with current femoral knee component design and surgical practice, because that results in a lateral oriented groove. This difference in anatomic- and prosthetic groove orientation may be a cause of patella-femoral problems.
How total knee replacements (TKR) articulate is directly related to their functional and wear performance. Recently, significant interest has concerned the center of axial rotation, or pivot point. Since the tibia exhibits internal rotation with knee flexion, the pivot point describes condylar translations: a medial pivot implies posterior lateral condylar translations with flexion, a lateral pivot implies anterior medial condylar translations with flexion.The purpose of this study was to describe the location of the pivot point, as related to TKR design, in a large number of knees studied under dynamic weight-bearing conditions.
Two hundred and four well functioning TKR’s were studied using fluoroscopy as subjects performed a stair ascent. There were 131 cruciate retaining fixed bearing knees (11 designs), 33 mobile bearing knees (5 designs), and 40 posterior stabilized knees (4 designs). CAD model based shape matching was used to determine 3D knee kinematics and the pivot point location from 21,837 images. The pivot location was described as a percentage of tibial width, −50% (lateral) to +50% (medial).
Posterior stabilized knees exhibited medial pivots (mean +14%, +7% to +30%) while cruciate retaining (mean −9%, −35% to +21%) and mobile bearing knees (mean −20%, −48% to +5%) exhibited lateral pivots on average (p< 0.001).
How a TKR design provides A/P stability dictates the location of its center of axial rotation and the A/P motions of the condyles. As the relationship between constraint and in vivo motions becomes clearer, TKR designs can be enhanced to achieve more favorable functional and wear performance.
Wear of the underside of modular tibial inserts (“backside wear”) has been reported by several authors. However, the actual volume of material lost through wear of the backside surface has not been quantified. This study reports the results of computerized measurements of tibial inserts of one design known to have a high incidence of backside wear in situ.
A series of retrieved TKA components of one design (AMK, Depuy) with evidence of severe backside wear and extrusions of the polyethylene insert were examined. The three-dimensional surface profile of the backside of each insert was digitized and reconstructed with CAD software (UniGraphics). The volume of material removed was calculated from the volume between the worn backside surface and an “initial” surface defined by unworn areas.
Computer reconstructions showed that in all retrievals, the unworn surface of the remaining pegs, the rim of material extruded over the medial edge and unworn surfaces on the anterior-lateral edge all lie in a single plane. This demonstrates that the “pegs” present on the backside of these inserts correspond to residual, unworn protrusions remaining on each retrieved component and do not represent cold flow extrusions through the base plate holes. The average volume of material lost due to backside wear was 608mm^3 ± 339mm^3 (range:80–1599 mm^3). This corresponds to an average loss of 569mg and an average linear wear rate of 103mg/year, based on the time in situ for each implant.
The volume of material removed due to backside wear is significant and is of a magnitude large enough to generate osteolysis. Our results indicate that the appearance of pegs on the underside of components with screw holes on the baseplate are not due to creep, but instead are due to severe wear of the insert. The mechanisms of material removed due to pitting and burnishing actually produce debris of a size more damaging in terms of osteolysis than wear at the articulating surface making it clear that significant improvements in implant design are needed to prevent backside wear and osteolysis.
Condylar liftoff can undoubtedly occur with total knee replacements (TKR); it occurs in the surgeon’s hands and has been shown to occur in vivo. However, the reported incidence of condylar liftoff and the implications for articular surface damage require further scrutiny. A three-part argument is made that the incidence of condylar liftoff has been overstated, and there is little direct evidence that condylar liftoff is a significant factor in the wear performance of coronally flat-on-flat TKR’s. First, an analysis of fluoroscopic measurement errors based on the uncertainty in measuring varus/valgus angles (the parameter used to determine liftoff) reveals that the standard error for liftoff measurements is 1.2mm, nearly identical to the mean liftoff value in recent published reports. Second, because most TKR’s have some anterior/posterior curvature of the tibial insert, any axial rotation of the knee induces a varus/valgus angulation that can be interpreted as liftoff, even though the condyles remain in contact. Third, condylar liftouff has been used to justify the need for coronally round-on-round geometries, yet an analysis of 100 unselected retrieved tibial inserts from three coronally flat designs reveals no difference in wear type, magnitude, severity, depth, or symmetry between the medial and lateral aspects of the tibial inserts. Although condylar liftoff certainly can occur in vivo, an argument can be made that the incidence of liftoff in experimental studies has been overstated, and that there is little evidence from retrievals that contemporary coronally flat-on-flat TKR’s are uniquely susceptible to articular damage from condylar liftoff.
The limiting factor in the growth of RSA as a wide spread clinical tool is the man-hours needed to run a study. Calibration takes more than half of the processing time. The aim of this study is to develop automatic calibration method applicable to the grid and line patterns common in all RSA systems. This method uses a Harris Corner detector to find candidate positions on an image one 16th the original area (16 times quicker). Canny edge detection in regions of interest around the candidate positions on the full size image produce circular edges for marker-balls. A conic section is fitted to this edge using the Bookstein method to produce an accurate estimation of position to a local accuracy of 0.01 mm. Scanner distortion was modeled using a stabilised B-spline mesh to produce global accuracy of 0.03mm. A model based pattern recognition method can be used to label the marker-balls correctly. For sets of 4 marker balls a Homography was calculated and used to predict the positions of the other points in the grid. If supporting marker-balls are found in the predicted positions, they are counted. The four-point set, which returns the greatest number of support marker-balls, is the best estimate of a grid. Reference markers in the grid are used to localise it.
The method had a ninety- percent success rate on a set of 20 clinical X-rays. In two X-rays not enough marker-balls were visible due to a poor exposure. It finds marker-balls in a 15-MB image in 50 seconds on a 180 MHz silicon graphics O2. Labelling speed depends on the number of marker-balls and is 45 seconds per group of 50. This method is widely implementable, as it requires just the 3D positions of the markers in each plate of the calibration object for input.
Polyethylene wear remains an important cause of failure in knee replacements. Retrieval studies, simulators and simple X-ray methods produce wear data that may be inaccurate or unrealistic. We have developed an accurate RSA system for measuring wear in-vivo. Using this system we have found wear rate in a fixed bearing TKR to be about 0.1mm/yr[
Four Oxford uni-compartmental knee replacements, with excellent clinical results were studied ten years after implantation. RSA X-rays were taken in double leg stance with the knee in full extension and 15 and 30 degrees flexion. Following RSA calibration, silhouettes of the components on the stereo X-rays were extracted using a Canny edge detector and were matched to silhouettes projected using CAD models to determine the 3D component position. The average minimum thickness of the bearing was determined and was compared with the measured minimum thickness of 14 unused bearings to calculate linear penetration.
The average linear penetration after average 10 years implantation (range 8.5 to 10.25 years) was 0.16 mm (SD 0.13 mm). The average penetration rate was 0.017 mm/year (SD 0.011 mm/year). The maximum linear penetration rate was 0.027 mm/year.
The penetration rate is similar to that obtained in a retrieval study [
The low contact stress and self-aligning properties of mobile bearing total knee replacements (TKR) make them an increasingly popular implant choice worldwide. Two variations on the mobile bearing knee concept have been commonly adopted: systems that retain the posterior cruciate ligament (PCL) and provide free rotation and translation (RT) of the mobile bearing, and systems that sacrifice the PCL and provide for rotation only (RO) motion of the mobile bearing. The purpose of this study was to evaluate the in vivo kinematics of these two types of mobile bearing TKR during gait, stair, and two deep knee flexion activities.
Twelve patients (6 RT, 6 RO) with unilateral mobile bearing knee arthroplasty and excellent functional outcomes at least one year after TKR were studied. Fluoroscopic images of the knee were acquired as patients walked on a treadmill, ascended a step, performed a deep knee bend, and knelt to maximum flexion. Knee kinematics were derived from CAD model based shape matching techniques.
The RT knees exhibited greater posterior translation of the femur on the tibia during early stance in gait (RT: 5mm vs. RO: 2mm) and during knee extension during stair ascent (RT: 5mm vs. RO: 1.5mm). There were no differences between the two groups in the flexion angles achieved during deep knee bend or kneeling.
Although there were no significant clinical or functional differences in these patients, the RO knees exhibited smaller tibio-femoral translations and less intersubject variability in knee kinematics during dynamic weight-bearing activities.
The average movement of heads in 6.5M-rad irradiated polyethylene sockets was 0.22mm one year post operation and its direction was toward backside of patients’ body. The average movement of conventional polyethylene sockets was 0.24mm one year post operation and its direction was just the same as irradiated polyethylene sockets.
The growing interest in the use of metal on metal bearings in the treatment of end stage hip arthritis in the young has raised the need to monitor metal ion levels in these patients. Blood levels are good indices of the safety of these devices. Total wear/corrosion over a given time period is best estimated from 12 or 24-hour urine collections. Whole blood samples of 52 patients with metal on metal hip arthroplasties were analysed for levels of chromium, cobalt and molybdenum using high-resolution induction coupled plasma mass-spectrometry. Fifteen of these were in an older age group (mean age 75.3years) and had metal on metal hip replacements performed 19–28 years before the assessment. The rest (37) were younger (mean age 52.9 years) and had hip resurfacings performed in the last 4 years. The results show higher levels of ions than those found in the normal population.
This agrees with other studies. However we found no significant difference between the levels in the older patients with THR and the younger patients with hip resurfacing. In another study, urine collections from 78 patients who had hip resurfacings in the past and are now at different postoperative durations (2, 4, 6, 8, 10, 12, 18, 24 and 36-month periods) were analysed for metal ions using the same technique. The mean levels show an increase compared to the preoperative values but this increase is not statistically significant.
The urinary excretion of cobalt in these groups have also been compared with the expected cobalt release due to corrosion in this alloy. They were found to rise above the corrosion levels only in the 8–12 month period, possibly due to “run-in” of the bearing. It can be concluded that the ion levels can be attributed mainly to corrosion and there is minimal contribution from wear.
An extra articular correction may be necessary in osteoarthritis with an important post traumatic or congenital deformity. In the last 5 years we performed 11 TKR associated with a tibial (9 cases) or a femoral Osteotomy (2 cases), in one time surgery. The average intra osseous deformity was 14°. The technical problems are different in varus and valgus knees.
1- Which type of osteotomy ? In varus knees with a tibial deformity (6 cases) we use a hight tibial valgus osteotomy with opening wedge. Pre operative planning with long standing X rays allows precise determination of the amount of correction needed. A rigide wire, driven up to the fibular head, is placed. A provisional wedge of the desired size (degree of correction) is maintened temporarily by a staple, which will be removed later. Once the correction has been performed and maintened, the standard instrumentation to implant the prosthesis is used. In valgus knees with a tibial deformity (2 cases) a hight tibial closing wedge osteotomy, and in valgus knees with a femoral deformity (2 cases), a low femoral closing wedge osteotomy, are used. In all cases a medial approach without any release and without fibular osteotomy is performed.
2- Which kind of prosthesis?
Two degrees of constraint are possible in fonction of particular needs.
Most of the time, a non-constrained PS articular implants will be used and when more constraint will be needed (in lateral instability), CCK-type articular surfaces will be choised.
In all cases, a stem will have to be, associated with the osteotomy (tibial or femoral). Different diameters will allow a good press-fit and if necessary, an offset stem will be used.
3- Associated osteosynthesis or not? Stability provided by the press-fit stem may allow not to use an osteosynthesis in most than 50% of cases. If a doubt remains about stability, a small plate can bee added on the medial tibial side of the tibia.
4- Which immediate post-op follow-up?
Full weight bearing will be immediate. A splint will be used only for walking during six weeks. A standard rehabilitation protocole will be followed. In our 11 patients with a short follow up (1 to 5 years) complications consisted in one hematom and one phlebitis. Post-operative alpha angle was 96° and beta angle 91°. TKR with an associated osteotomy seems to be a possible alternative when osteoarthritis is associated with an important extra articular deformity.
Metal on Metal bearings have functioned satisfactorily for up to 30 years without a full understanding of what shape the components were at the start, or as they were worn over time.
Modern metrology methods can use elegant computer driven coordinate measuring machines in both manufacturing and retrieval analysis as most manufacturers and laboratories do. This method however is fl awed in its ability to look at the much higher levels of resolution required for analysing these bearings. A method has been developed which will analyse to the sub micron deviances from roundness that the subleties of manufacturing can achieve, and allows an analysis of wear of explanted implants.
Both new and explanted Ring, McKee, Stanmore, Metasul and Resurfacing implants have demonstrated initial form variances that range from 1 to over 100 microns out of round. Roundness trace analysis has allowed linear wear on explanted implants to be measured from 0.5 to 150 microns. This represents combined head and cup linear annual wear rates from 2 to 65 microns per year.
Metal heads and cups are not manufactured as round as has been believed. The average wear rates over time for different Metal on Metal systems is not the same.
Development of the metal/ metal hip resurfacing began in 1989 with the first patient implantation in February 1991. In the first three years three methods of implant fixation were employed in a pilot study of 119 resurfacings and the optimum fixation was identified as Hydroxyapatite Coated (HA) uncemented cups and cemented femoral components.
From March 1994 until February 2001 the author has performed 1503 hybrid fixed resurfacing implants, 294 of the McMinn type (HA on Smooth Metal Cup) and 1209 Birmingham Hip resurfacings (BHR; HA on Porous Metal Cup). Mean age was 52.9 years, diagnosis – Osteoarthritis 78%; Dysplasia 7%; Inflammatory 2%; Avascular necrosis 5%; other 8%. In the 294 McMinn Resurfacings 8 have failed and 7 have been revised. Reasons for failure; 5 cup loosenings, two infections and one femoral head collapse in a patient with pre-existing avascular necrosis. High wear of the metal/ metal bearings, with altered metallurgy, is now presenting as a cause for concern with these McMinn resurfacings performed in 1996 where the metal was Solution Heat Treated (SHT) and Hot Isostatically Pressed (HIP). Patients from 1996 are exhibiting asymptomatic radiographic osteolysis and at revision metallosis is seen with high wear measured on the retrieved components. Laboratory studies have shown that SHT and HIP alters the carbide microstructure and increases wear on abrasive wear testing.
In the 1209 BHR’s 7 failures have occurred requiring revision. Reasons for revision – 4 femoral neck fractures, 2 infections and 1 collapsed femoral head from avascular necrosis. Implant fixation is reliable as judged by very low migration on an R.S.A. study. Bearing wear is very low as judged from wear analysis of explants as would be expected from the historically proven “As Cast” metal microstructure. Function is good as judged by the Harris Hip Score (mean 96.3 at 3years). Cumulative survival on all Hybrid fixed implants is 97% at 7–8 years.
Hip resurfacing, using metal on metal bearings with historically proven metallurgy using hybrid fixation, offers a viable treatment alternative for the young and more active patient with hip arthritis.
After a very short résume of his presentation in sept 2000 for the ISTA Conference in Berlin, the author looks briefly at the results of T.R.A.C knees after, what is now, four years of clinical follow-up.
Given the bad results this far regarding the femoropatellar joint and the uncemented version. M.D. François Pilon moves on to present an original concept, the latest evolution in knee systems: the rotary plateformed and posterior stabilised prosthesis, which offers a large congruence of polyethylene.
Originality of the newwave prothesis:
-Developement of a non-posteriorstabilised, fixed-plateau, prosthèses (GALICA, 8 yrs on !) -Use of GoldFinger System (4 yrs on) -First implantations in Sept. 00 (only simple clinical impressions today)
Clinical, X-ray follow-up system: All NewWave users can consult the computer Letterbox :
A NewWave reimplantation replacement prosthesis is at the moment on the drawing-board.
In four years time, Dr Pilon hopes to be presenting the real five year follow-up H.S.S. results of NewWave to the I.S.T.A..
The authors strongly recommend that: 1) a surveillance program be established for careful, regular follow-up of patients with THR in place more than 7 years; 2) CT scans be considered as part of that surveillance program, and 3) cups with screws NOT be used routinely in primary THR surgery.
It is well recognized that following excision of bone tumours around the knee, which often requires excision of the joint, cemented fixed hinged endoprosthetic replacements can give excellent results in terms of function (87%). However, for patients under 20 years of age the overall survivorship of distal femoral replacements in this age group is less than 45% at 10 years. To try and address this we have used HA ingrowth collars since 1989 and introduced the Smiles rotating hinge in 1991. In the younger patients we have also used uncemented prostheses using HA.
The HA collars at 70mm thickness are now standard protocol on all extremeity endoprosthetic replacements. We will present the results of retrieval specimens. We have also undertaken a study to determine the effect that HA collars and roating hinges have on enhancement of implant fixation. A survivorship and radiographic analysis has been carried out with three groups of patients: 1. Fixed hinge no collar. 2. Rotating hinge no collar. 3. Rotating hinge with HA collar
The selection criteria were all distal femoral replacements of patients who were over 16 years of age and had a cemented intramedullary stem. The study groups were consistent for age and amount of bone resected and all patients have been followed up.
Then SMILES (Stanmore Modular International Limb Salvage System) was first introduced in 1991 for use as a customized prosthesis in the treatment of malignant and aggressive bone tumours. However, the use of this pros-thesis has been extended to minimal customization, to be used in a situation of salvage surgery for the arthrosplasty, which has already undergone previous revision surgery. Between 1991 and 1997 32 SMILES prostheses were used in thismanner in 30 patients. 28 patients were available for review, all had a minimum of 3 years follow-up. The mean number of previous revision procedures was 2 and 6, average 2.6. There were 11 male and 19 female patients. The mean age at the time of the salvage procedure was 67 years (46 to 86). The mean age of the primary procedure was 57.8 (Range 43–71). The Knee Society score increased from 26 to 68 and the function score increase from 26 and 68 and the function score increased from 27 to 75. Average flexion improved post-operatively from 78 to 88 degrees. 84% of patients stated that they were pleased with the results in terms of pain and mobility.
We conclude that this prosthesis is a satisfactory alternative to complex reconstructions or amputation in the presence of infection, severe bone or soft tissue loss and has rendered acceptable results.
Both backside and articular surface wear have been linked to osteolysis after total knee arthroplasty (TKA). Prostheses with cementless fixation, screw holes in high load regions, and thin polyethylene are susceptible to backside wear. Factors associated with articular wear are similarly well defined. Micromotion at the modular polyethylene interface has been reported for many prostheses, but the relevance of such data compared to articular motions and wear are difficult to appreciate. This study compares in vivo motions and wear occurring at the backside and articular surfaces after TKA.
Contemporary PCL-retaining prostheses from one manufacturer were implanted by one surgeon using cement fixation. The polyethylene inserts were > 6mm thick with a full peripheral rim capture and anterior wire locking mechanism. Femoral condylar motions were measured in 20 knees using fluoroscopic analysis during stair and gait activities. All patients had good to excellent clinical outcomes at one year follow-up. Articular and backside surface damage was evaluated on 32 polyethylene inserts retrieved after 27 months (1 to 71) months in-situ for infection (9), autopsy (6), patellar resurfacing (4), patellar loosening (4), tibial loosening (3), osteolysis (2), and other (4).
Femoral condylar translation over the polyethylene articular surface ranged from 5-10 mm, which is substantially larger than the reported 50-500 micron range of backside interface micromotion measured in vitro. Damage covered < 33% of the backside surface and appeared as a cast impression of the opposed metal tibial component without scratches associated with micromotion. In contrast, damage consisting predominantly of scratching, burnishing and tractive striations covered 46% of the articular surface.
Different locking mechanisms for modular polyethylene inserts result in different degrees of backside wear. No significant backside wear was observed these retrieved inserts with a wire-supplemented peripheral capture. Given the abrasive wear mechanisms and particulate debris shed during femoral condylar sliding, efforts to control motions at the articular surface appear warranted.
Knee simulators are now widely used for the determination of performance and wear durability of TKR’s. The International Standards Organisation (ISO) force-control option synchronises AP force and IE torque with flexion angle and axial force for the walking gait cycle. The force control concept subjects the same input waveforms to different TKRs, allowing them to move (and wear) as their designs dictate. It however relies on a mechanical spring based assembly to simulate the restraint effects of ligaments in AP and rotation. The contribution of this restraint mechanism depends on the stiffnesses of the four springs, and on how they are set at the neutral position. The springs can be loose with a gap, such that compression only starts (or ends) when the motion exceeds the gap. Alternatively the springs can be pre-compressed such that they never go loose.
A detailed mathematical model was developed which included the stiffnesses of the four springs, their settings (level of pre-compression or gap), and geometry of the mechanism to calculate a matrix of AP restraint force curves with AP displacement, and how these curves change with int-ext rotation superimposed. The same was done for rotational restraint with simultaneous linear displacement. Through an interactive computational interface, the families of curves for any combination of variables were repeatedly plotted and compared to published data on the contribution of particular ligaments to the laxity of the knee (eg. Fukubayashi et al. 1982) to find the optimum spring stiffnesses and gap configuration. This was done for simulation arrangements retaining ACL, PCL or both retained or resected. The results showed the behaviour of the system to be as sensitive to the gap and level of pre-compression, as to the stiffnesses of the springs. For the resected ACL retained PCL situation, the optimum we recommend is soft (7.24 N/mm) springs on the ACL side, harder (33.8 N/mm) springs on the PCL side, with a 2.5 mm gap on each side. For both ACL and PCL resected, the soft (7.24 N/mm) springs for both sides are optimum, again with a 2.5 mm gap on each.
These settings are obviously different from each other, and are different from the tests with this simulator published by different laboratories. The same settings are a pre-cursor for valid comparison of wear and kinematics.
The perception that all cemented stems have reasonable assurance of success if implanted with contemporary cement technique has recently been questioned. Surface finish, stem shape, patient weight and high neck offset have been identified as factors contributing to early loosening. Small design changes to existing cemented stems have led to substantial differences in clinical performance. This study investigates the multi-factorial nature of stem loosening after a 24% early failure rate occurred within the initial three years.
Total hip arthroplasty was performed by the same surgeon on 67 patients with an average age and weight of 65 years (21-85) and 82 kg (49-127), respectively. Initial diagnosis was osteoarthritis (84%), osteonecrosis (7%), congenital dysplasia (4%), and other (5%). Modern femoral stems (Perfecta IMC) with increased lateral neck offset were implanted using contemporary cementing techniques. The stems are grit-blasted proximally, with intramedullary collar steps on the anterior/posterior surface. These design features are meant to enhance axial load transfer and stem-cement bonding. All acetabular cups were uncemented and used polyethylene (48 patients) or cobalt-chrome (20 patients) liners. Patients were evaluated with clinical and radiographic follow-up.
Revision for stem loosening was necessary in 16(24%) patients 9 to 38 months after index surgery, including 9 hips revised within the first 18 months. Radiolucencies at the cement/bone interface, stem subsidence and distal femoral osteolysis were consistently observed. Patients with loosening were significantly heavier than those with well-fixed stems (93 kg versus 78 kg, respectively). Revised hips included 7 cobalt-chrome and 9 polyethylene articulations.
It appears that several mechanical factors contributed to these early failures. Lateral offset stems with cement fixation appear to be at risk for loosening in young, heavy patients. Design features and a thin cement mantle may have resulted in increased cement stresses and cracks during the axial and torsional loading that occur with daily activities.
Validation of input parameters and the resulting polyethylene damage is essential for knee joint wear simulators to be useful in prospective evaluations. The purpose of this study was to compare damage patterns on polyethylene inserts wear tested on a knee simulator with inserts retrieved after well-functioning total knee arthroplasty (TKA).
Five polyethylene tibial inserts from a PCL-retaining knee prosthesis (Natural Knee) were wear tested on an Instron/Stanmore simulator in 50% bovine serum. The input consisted of ISO 14243 force-controlled testing standard to simulate human gait for 5 million cycles. Nine polyethylene tibial inserts (Natural Knee) were retrieved from patients after 52+45 months (13-124) of successful function. The inserts were retrieved post-mortem (n=7) and for pain (n=2). Articular damage was assessed and the circumference of each damage region digitized. The damage size, location and linear surface deformation were measured and the deformation rate (mm/106 cycles or mm/year) was calculated.
The linear deformation rate for all inserts decreased considerably with time. Lateral damage was located significantly more posterior than the medial damage on both the simulated and retrieved inserts, corresponding to femoral external rotation. Retrieved inserts had larger lateral damage, whereas simulator inserts had larger medial damage. The AP extent of damage on the retrieved inserts was significantly greater than the extent on the simulator inserts. Three retrieved inserts had substantial delamination, whereas none of the simulator inserts had delamination.
There was good agreement in the deformation rates for the simulator and retrieved inserts. However, retrieved inserts with delamination show an increased deformation rate and this type of damage did not occur on simulator inserts. The greater AP extent of damage and larger lateral damage on the retrieved inserts suggest that in vitro wear simulation should perhaps include a more complete range of patient activity dynamics to better predict in vivo damage.
Directly molding IB, MG and AGC UHMWPE tibial inserts has provided excellent clinical performance. This performance may be related to the oxidation resistance and higher fracture toughness provided by the direct molding process. Directly molded UHMWPE components have been reported not to oxidize after either nine years post irradiation aging on the shelf or after 11 years of implantation. Retrievals show that molded IB inserts to have lower oxidation, better polyethylene quality and less surface damage than machined IB II inserts. However, the IB, MG and AGC products were directly molded from 1900 UHMWPE resin which is no longer available. The question remains if directly molding resins other than 1900 in a contemporary modular design will provide the same benefits. We report here on the first knee simulation wear of a contemporary total knee system comprised of a directly molded 1020 esin tibial insert. This result will be compared to the knee simulation result of an IBII machined from 4150 extruded ro 4 Optetrak tibial inserts made by directly molding 1020 resin were tested on a 4 station Instron/Stanmore simulator at 1.4 Hz with a 2279 N maximum load and right knee kinematics. The lubricant was bovine calf serum with EDTA and sodium azide. Axial loads were applied from 0 to 40& #778; flexion and internal/external rotation was −3/+6 degrees. Location, type and area of surface damage, were evaluated every 1 million cycles (Mc).
The wear rate of the directly molded inserts was 6X less than reported for machined IB II inserts (2 vs 12 mg/million cycles respectively). There were no signs of delamination or pitting with either design. The more conforming Optetrak provided 52% reduction in wear area over the IB II (21 vs 32 % respectively). This demonstrates that resins other than 1900 may be directly molded in a contemporary and provide the same historical advantages.
Polyethylene (PE) wear affects survivorship in the long term while dislocation remains a significant factor in the short term. Increasing head size can reduce impingement and dislocation. However, this increases wear rates and reduces the net thickness of the liner. Several reports have demonstrated significant reduction in wear in cross-linked PE. This study reports wear rates in crosslinked PE liners with increased head size. Four groups of PE liners were tested against cobalt-chrome heads in a hip wear simulator: highly crosslinked liners with head size 28mm (28XPE) and 32mm (32XPE), and minimally crosslinked liners with head size 28mm (28PE) and 32mm (32PE). Additional liners were used as load-soak controls to monitor weight gain due to fluid absorption. Gravimetric analysis was performed every 500,000 cycles for a total of 5,000,000 cycles. 28PE and 32PE liners had mean wear rates of 12.5(±1.0) and 17.45 (±2.6) mg/million cycles. Both highly crosslinked PE liners (28XPE and 32XPE) had significant less wear rates that regular polyethylene 1.49 (±0.72) and 2.55 (±0.19) mg/million cycles respectively. Increasing head size resulted in increased wear, which is consistent with previous reports. Highly crosslinked PE significantly reduced wear rates in both head sizes. Although there was a small increase in wear in the 32XPE group compared to the 28XPE group, wear was significantly less than both 32PE and 28PE groups. These encouraging results suggest that a dual benefit (reduced wear and reduced dislocation rate) might be achieved using 32XPE liners. Further studies that evaluate fatigue damage, crack propagation and impingement are necessary.
Crosslinking of UHMWPE markedly improves its wear resistance. However, Green et al. (JBMR 53, 490, 2000) have reported that the wear debris from crosslinked PE were smaller than from non-crosslinked PE, and that particles with a mean diameter of 0.24 μm diameter caused more osteolytic activity of mouse macrophages in vitro than 0.45 μm or 1.7 μm particles. In order to predict how a new PE will behave clinically, however, it is desirable to compare its particle morphology to that of the gamma-air sterilized PE that was used in the vast majority of acetabular cups over the past three decades. We compared PE wear debris that were generated in a hip simulator and recovered by digestion and filtration of the serum lubricants, from cups crosslinked at 2.7 Mrads in air (historical controls), and cups machined from extruded bars that had been pre-gamma crosslinked at 4.5 Mrads and remelted (to extinguish free radicals and stabilize against oxidation) prior to cup machining. The debris were 85% and 92% rounded particles, respectively, and the balance were fibrils. The diameters of most of the rounded particles were from 0.07 to 0.3 μm, with very similar distributions in this range for the two materials. The total number of round particles from the 4.5 Mrad remelted PE was 32% and 76% below that of the 2.7 Mrad gamma-air non-aged and aged cups, respectively, the number of fibrils was 66% and 88% lower, respectively, and the total volume of wear debris per million cycles was 71% and 90% lower with the 4.5 Mrad-remelted PE cups, respectively. Since there was little if any systematic change in particle morphology, the substantially reduced wear and high oxidation resistance of the cups fabricated from gamma crosslinked-remelted PE could markedly reduce the incidence of clinical osteolysis.
Used in conjunction with the words “endoprosthesis” and “bone-implant interface”, fluid flow is usually referred to as a potential mechanism for loosening and implant failure. Paradoxically, recent studies have shown the importance of fluid flow in augmenting molecular transport through the osteocytic syncytium. This transport is essential for maintenance of cellular nutrition as well as communication between osteocytes, osteoblasts and osteoclasts, which are interconnected biochemically by interstitial fluid in bone. In the absence of loading, larger sized molecules are not transported efficiently through bone tissue in vivo [1]. The efficacy of load-induced fluid flow, resulting from normal physiological loading of bone, has been proven for the transport of small (300-400 Da, on the order of smaller amino acids) and larger (1800 Da, on the order of small proteins) molecular weight tracers through bone [2]. Nonetheless, using a similar model to study perfusion and fluid flow in the vicinity of endoprosthetic
Recent studies have shown that the distinct porosities within bone tissue act as molecular sieves in situ [4] and that molecules on the order of cytokines and serum derived proteins can not be transported through the lacunocanalicular system without interstitial fluid flow resulting from physiological mechanical loads. These data as a whole suggest that fluid flow regimes in a physiological range are essential for osteocyte viability and function. In order to insure implant stability, health of the tissue at the interface must be insured. Hence, fluid flow in a physiological range could be considered essential for implant stability. These issues will be discussed in light of recent developments in endoprosthetic technology and the design of future generations of implants.
Quadriceps moment arm is one of the factors determining quadriceps force. Total knee arthroplasty designs with larger quadriceps moment arms should generate less quadriceps and patellofemoral forces. A study was conducted to measure knee kinematics, quadriceps and patellofemoral forces in two knee designs with differing centers of rotation. In addition, the effect of a central dome-shaped versus a medialized patella component was determined. Six human cadaver knees were tested before implantation and after sequential implantation with two posterior cruciate retaining designs: Scorpio and Control. The quadriceps moment arm of the Scorpio design was 1 cm longer than that of the Control design. Knee kinematics was measured with an eletromagnetic tracking device while the knee was put through dynamic simulated stair climbing under peak flexion moments of 40 N-m. Quadriceps tension and patellofemoral compressive and shear forces were measured for both conditions and for the central and medialized patella components. The normal unimplanted condition showed increasing rollback with flexion while both implanted conditions displayed relatively less rollback. Overall, quadriceps tension was highest in the unimplanted condition and lowest in the Scorpio condition. The Scorpio design showed a 10-20% reduction in quadriceps tension at angles greater than 40° when compared to the Control design. Patellofemoral forces were also significantly reduced in the Scorpio design when compared to Control. There were no differences noted between the central and medialized patella component. The Scorpio design, with its more posterior center of rotation, reduced quadriceps tension and patellofemoral forces. Reduced quadriceps forces may facilitate postoperative rehabilitation and activities such as stair climbing. Reduction in patellofemoral forces could reduce patellar complications such as anterior knee pain, component wear and loosening. These results are currently undergoing validation with a prospective clinical study.
Early revision after total knee arthroplasty (TKA) is fortunately uncommon. However, instability and lack of fixation are common early failure mechanisms. Cement techniques utilizing lavage and multiple drill hole interdigitation of the resected tibial surface can reduce micromotion and produce reliable tibial component fixation. This study looks at clinical failure mechanisms, cement technique and polyethylene damage in patients needing early revision of cemented TKA.
PCL-retaining TKA with cement fixation was performed on > 1000 patients at a single institution. Cement techniques varied with surgeon, with some using lavage and drill hole preparation of the resected surface and others electing to cement the surface “as cut”. Seventeen patients were revised within three years of follow-up. Revision reasons included loosening (41%), instability (18%), infection (24%), pain (12%), and malposition (6%). Prospective outcome scores, radiographic data, revision reasons, and polyethylene wear were compared.
Pre-revision pain and function scores gradually decreased back to pre-operative levels. Leg alignment averaged 7° varus (nine patients) and 12° valgus (eight patients) pre-operatively and 5° valgus at pre-revision. Tibial radiolucent lines were present medially only in nine knees and medially and laterally in four knees. The majority of patients revised for loosening had a tibial component cemented onto the “as cut” bone without additional preparation. Damage covered 32%-85% of the polyethylene articular surface. Scratching and pitting were significantly correlated (p< 0.05) with shorter in-situ time and revision for instability and loosening. Alignment and outcome scores were not correlated with damage.
In this series of cemented TKA, loosening and instability accounted for 59% of the early failure, similar to the incidence previously reported for cementless TKA. Cement technique and component positioning, not polyethylene wear, were the primary contributing factors. Attention to ligament balancing and achieving better tibial component fixation is needed to further limit the incidence of early failure after cemented TKA.
Oxidized Zirconium (OxZr), metallic zirconium alloy oxidized to form a ceramic surface, was developed as an alternative bearing material to cobalt-chrome (CoCr) alloy for improvements in roughening resistance, frictional behavior, and biocompatibility without a risk of brittle fracture. Knee simulator testing without intentional addition of abrasives demonstrated that the ultra-high molecular weight polyethylene (UHMWPE) wear rate was 85% less with OxZr than with CoCr femorals. The relative performance of articulating materials can change when tested under abrasive conditions, so test protocols were investigated with abrasives added directly to the simulator test lubricant.
Testing was conducted on a six-station, four-axis, physiological knee simulator. OxZr and CoCr medium-sized, cruciate-retaining, femoral components were tested against UHMWPE tibial inserts sterilized by ethylene oxide. Alumina powder was mixed into 50% bovine serum lubricant at a concentration of 0.2 mg/cm3. Tests were conducted with different powder sizes in the range of 0.3 to 150 μm. Measurements included tibial insert weight and femoral surface roughness.
The lubricant in CoCr tests became opaque with gray debris while the femoral condyles became scratched. In contrast, the lubricant in OxZr tests remained normal (as in tests without abrasives), and femoral condyle scratching was much less severe. Despite these obvious effects, the UHMWPE wear produced by each material did not increase appreciably over that of tests without abrasives, with OxZr maintaining a wear rate about 85% less than for CoCr. It was noted that the scratches were aligned, or became realigned, with the translation motion and had little evidence of the swirls or cross-hatching often observed on retrieved components. Previous testing indicates that UHMWPE wear increases significantly only if scratches are oblique to the sliding direction. Thus, a test technique that produces scratches with more clinically relevant orientations is needed for a performance comparison between femoral materials under abrasive conditions.
In December 2000, the Inter-Op acetabular component (Sulzer Orthopedics Inc., TX) was recalled. Contamination by an oil-based residue that was inadvertently left in the porous coating following a change in manufacturing processes was suspected to have resulted in lack of fixation. The aim of this study was to characterize the histopathology of the these failures for consistency with this hypothesis.
In Japan, osteoarthritis of the knee joint has been developing as the number of the elderly has been increasing recently. And the total knee replacement is expected to be indicated frequently. However, the total knee prosthesis does not always fit in with the shape of the Japanese osteoarthritic knee, due in part to the imported prostheses from U.S. or Europe. Therefore, the geometry of the Japanese osteoarthritic knee should be more characterized to achieve well coverage of prostheses onto the femur and tibia.
562 osteoarthritic knees rated as stage 1 or more according to Kellgren’s osteoarthritic knee classification were selected randomly and analyzed radiologically. The width of femur (FW) and the width of tibia (TW) were measured in the region 8mm from the articular surface. The distance from the anterior surface of the femur to the farthest backward of the femoral condyle was measured as FL. The anterior-posterior length of the tibia (TL) was measured by the 7 degree posterior slope of the tibial lateral image.
The AP/ML ratios of the femur and tibia were obtained by dividing FL by FW, and TL by TW. The mean value of AP/ML ratio of femur was 0.74å}0.07, and the mean value of AP/ML ratio of tibia was 0.68å}0.04. A statistically negative high correlation was found between FW and AP/ML ratio of femur, and between TW and AP/ML ratio of tibia. The larger FW and TW became, the smaller became the AP/ML ratios of femur and tibia.
Most of tatal knee prosthesises commercially available in Japan don’t follow the negative correlation between AP/ML ratio and the width of femur and tibia. We conclude that AP/ML ratio of femur and tibia should vary with the width of femur and tibia.
A customised, uncemented femoral stem was introduced clinically in 1995 after several years of development and pre-clinical testing. All the patients operated in our hospital have entered a prospective clinical study. The aim of this study is to present the short-term clinical data. Furthermore, the measurement of implant migration and the periprosthetic bone remodelling at two years is also reported.
Titanium-alloy is a metal with excellent biocompatibility, but its osteoconduction is not as efficient as hydroxyapatite materials. Calcium-ion (Ca-ion) implantation is a surface modification technique that can improve osteoconduction of titanium without an additional layer of coating. We studied the effects of Ca-ion-implantation on osseointegration of a titanium-alloy stem in a bilateral canine THA model. The stem surface was grit-blasted and Ca-ion-implanted by the ion mixing technique. Fifteen mongrel dogs had bilateral single-stage THAs, with a Ca-ion-implanted stem used in one side and a non-Ca-ion-implanted stem in the contralateral side. They were sacrificed at 1, 6, and 12 months postoperatively, and microradiographs were taken. Undecalcified cross-sections were evaluated histologically. For quantitative evaluation, the length of new bone apposition to the implant surface was obtained using computer image analysis. Most implants were well integrated, and there was no apparent qualitative difference between the two types of stems radiographically and histologically. However, Ca-ion-implanted stems had significantly greater new bone apposition than non-Ca-ion-implanted stems at 1 month, although the overall effect of Ca-ion-implantation was not significant.
The results showed enhanced osteoconduction with Ca-ion-implantation only in the early postoperative period. This could be related to the previous data of immersion tests that the dissolution rate of Ca-ion from Ca-ion-implanted titanium decreases with time. Clinically, early osteoconduction is desirable and could accelerate rehabilitation and outcome. Although further improvement of the Ca-ion-implantation technique for a sustained osteoconductive effect is necessary, Ca-ion-implantation will be beneficial for early fixation of titanium-alloy implants.
The increasing success rates of total hip replacements (THR) have led to a younger patient population with an increased probability for revision. The survival of revised components is improved by a good bone quality. This has led to an increased interest in bone preserving THR designs. A novel type of THR was developed of which the femoral component is cemented in the neck. The load carrying area of this prosthesis is reduced in comparison with conventional cemented implants. Whether an adequate stability can be achieved was biomechanically evaluated during simulated normal walking and chair rising. In addition, the failure behaviour was investigated.
Bone mineral density (BMD) was measured in 5 fresh frozen proximal human cadaver femora. The femoral heads were resected and a 20 mm diameter canal was created in the femoral necks. Bone cement was pressurised in this canal and the polished, taper-shaped prosthesis was subsequently introduced centrally. A servohydraulic testing machine was used to apply dynamic loads up to 1.8 kN to the prosthetic head. Radiostereophotogrammetric analysis was used to measure rotations and translations between prosthesis and bone. In addition, the constructions were loaded until failure in a displacement-controlled test.
During the dynamic experiments, the femoral necks did not fail, and no macroscopical damage was detected. The initial stability of the implant did not seem to be sensitive to bone quality. Maximal values were found for normal walking with a mean rotation of about 0.2 degrees and a mean translation of about 120 microns. These motions stabilised during testing. The failure loads in this study varied between 4.1 and 5.5 kN, higher failure loads were associated with higher BMD values. Most specimens showed subtrochanteric spiral fractures.
In conclusion, the stability of the prosthetic device may be adequate under dynamic, physiological loading conditions. The static failure loads were relatively low and require further optimisation of the prosthetic implant.
We developed a computer assisted total knee arthroplasty system to help the surgeon achieving more intra-operative accuracy.
A novel CT-free image-guided navigation system for acetabular cup placement has been designed, implemented and evaluated in laboratory and clinical environments. The most common postoperative complications for total hip arthroplasty (THA), subluxation and dislocation, is directly related to acetabular component orientation. Recent developments in the area of CT-based cup navigation have proven to be a valuable aid. However, a CT scan often unwarranted and has a significant impact on the total cost of treatment.
The method proposed in this paper utilizes reference coordinates from the anterior pelvic plane (APP) to compute the angular orientation of the cup. The APP is aligned to a vertical plane of a standing patient defined by the two anterior superior iliac spines and the pubic tubercles. A hybrid strategy for the acquisition of these landmarks has been introduced involving percutaneous pointer-based digitization with the possibility of non-invasive bi-planar landmark reconstruction using multiple registered fluoroscopy images. An intuitive graphical user interface, combined with a sterile virtual keyboard control, effectively support the navigation of acetabular preparation and cup placement.
A detailed validation of the system was performed in a laboratory setting. Seven full body human specimens were used to confirm the APP reference concept using custom made software to simulate worst case scenarios.
System usability was evaluated throughout an early clinical trial involving 25 patients. A postoperative study of all patients found that the accuracy was better than 4° inclination and 5° anteversion under standard clinical conditions. This implies that there is no significant difference in performance from the established CT-based navigation methods.
Treatment of severe radiocarpal arthritis remains controversial. Since 1992, the newly designed universal total wrist arthroplasty has been used as an alternative to radiocarpal fusion.
A total of 49 patients underwent total wrist arthroplasty between 1992 and 1998. A total of 43 patients with 47 wrists were available for follow-up. Thirty-two patients had rheumatoid arthritis, nine patients had osteoarthritis and two patients had Kienboch’s disease. The average age of the patient was 55 years and the average length of follow-up was 42 months.
Results at follow-up showed 89% of the wrist were without pain. Neutral alignment was present in 96% of the wrists. A functional arc of motion was present in 87% of the wrists. Ninety-four percent of the patients were satisfied. Radiographs showed excellent alignment of the implant, without evidence of distal migration of the carpal component. Complications occurrred in 12 of 47 wrists (25.5%). Six of the wrists had a dislocation. Three wrists developed metallosis, requiring revision of the prosthesis. One patient required removal of the prosthesis and wrist fusion. The revision rate in this series was 11%. The fusion rate was 2%. Eleven of 12 patients had resolution of their complication with appropriate intervention, and did not require a salvage procedure.
This study revealed that total wrist arthroplasty can result in a painless and functional wrist in the majority of patients. We feel that total wrist arthroplasty remains a viable alternative in patients with severe radiocarpal arthritis.
Total Hip Replacement (THR) in proximal, posterior iliac dislocation of the hip often represents a problematic issue. Reviewing their selected cases (70 patients between 3700 THR from 1986 to 2001), authors focalized some key points for this demanding surgery. The most important steps are acetabular positioning, implant decisioning and surgical approach (exposure and release).
Acetabular cup positioning. The natural site (Paleoacetabulum), the ideal place to restore biomechanical and dynamic properties of the joint, many times gives few chances to achieve primary stability. So one site, at least the nearest possible to the natural site must be reached. A CT or MRI study is necessary to assess preoperative planning for cup positioning. We used two different cups, the Zweymuller and the Wagner cup, with good primary stability. A Conus stem (Wagner) or an Alloclassic stem (in less displastic femoral shape) was used.
We always performed this surgery as a one step procedure. No preventing traction or release surgery was performed. An anatomic and wide (medial and lateral) exposure of the joint must be performed. We used the Smith-Petersen approach modified by Wagner. A meticulous periarticular release of soft tissue was performed. In same cases a shortening femoral osteotomy was performed to allow refractory reduction. Possible complications are discussed. Good clinical outcomes at more than ten years are shown.
Authors describe their first experience with a computerized navigation system for cup insertion in THR (Medivision). Computer navigation systems started first at the Müller Institute (Bern) in 1991 when prof. Nolte inserted his first pedicle screw in a spine specimen.
In January 1997 a CT-based cup module for hip pros-thesis was developed in laboratory by prof. Nolte. At the end of 1998 a first clinical trial on a CT-based cup navigation started in Maastrict by Prof. Geesink. A new CT-free cup navigation module appeared on the scene at the end of 2000. The first clinical successful CT-free cup navigation was performed in Ludwigshafen by Dr. Grützner in January 2001.
More then 3000 hip implants have been done with good results in Europe. A postoperative CT accuracy study of cup orientation shows mean error of about 5° (to be published by Bernsmann et al. in summer 2001). Medivision uses in orthopedic surgery are multiple. Spine surgery, Pelvic Osteotomy, C-arm Navigator, C-arm Nailing, CT-based Cup, CT-free Cup, ACL-reconstruction, Total Knee Replacement. We used Medivision first in THA to asses cup orientation and lower limb length. First results confirm system reliability. The feeling with this computer-guided surgery is good and grew up every new case. Learning curve is not so long and deep if few principles are used.
In revision hip Arthroplasty, there often exists the intact femoral cortex under the level of loosened stem. In such cases we used a mid-length full-porous Cementless stem, because femoral bone remodeling and reinforcement could be obtained. We evaluated the readiographical change in femur after the inplantation of full-porous Cementless stem.
In this work we mean explain our clinical experience about the use of a T.R.K. mobile meniscal bearing implanted during the 2000 and 2001 in our institute. The prostheses design allows the motion of the polietilenic component 5mm in the anteroposterior directions and 12.5 degrees in the internal and external rotation.
In association with the shaping of the femural contact surfaces this design allows a huge upgrade of contact surfaces compared with other protheses already in use. We have evaluated 17 patients on short term follow up, patients operated in our division, four males and 13 females. The average ages are 68 ± 8.
The indication was in all cases gonartrosis. The evaluation protocol includes:
§ Pre and post operative x rays (after 60 days);
§ Clinical evaluation of the range of motion;
§ D.E.X.A. mineralometry;
§ Stabilometric evaluation pre operative and after 6 months.
The first results have pointed out the disappearing of pain in all the patients, an optimal recovering of the articular function with no loss of extension, a good prothesic osteointegration (even in an initial phase in our cases) and the stabilometric evaluation confirms a soon proprioceptivity recovering and the motion of the operated limb.
After all this encouraging results we have decided to continue implanting this kind of protheses as we think that not only it warrants a better range of motion, but the utmost null polietilenic debris may allows a longer life to the implant as a consequence of the reduced stress rate.
Since 1989 more than 5000 Zweymuller stems have been implanted in the Orthopaedic Institute G. Pini, Milan, Italy. This uncemented stem which has been produced since 1979 nowadays is though to be one of the best prothesical solutions and this can be affirmed both on the easy operative techniques and on the bases of our clinical studies of follow up. This is also the most used uncemented coxofemural system in Europe. The advantages in the Zweymuller design are due to the rotatory stability and the slight volume of the implant, which in the international literature are referred as the key points of this success. The bone anchorage and the distribution of the weights is achieved both proximally and distally thanks to the conical stem, which in the proximal region is anchored on one side by the great wing of the trocanteris on the other side by the wedge effect.
In the distant cortical instead the borders of the stem get wedged in the bone. This very wide anchorage allows a great stability reflected also by the lack of weigh pain at diafisys level.
The same stem is used both for first implant as well as revisions (after evaluation of the bone stock, achieved in our studies by dexa) but also for intertrocanteric osteotomies.
The chance of a rapid mobilization of the patient makes this stem convenient also in geriatric orthopaedic cases. The material is a alloy of Ti, Al and Nb: this material has been studied directly for medical appliances and not only it doesn’t contain toxic or allergenic components but provide an high resistence to breaks. Osteointegration is favoured by the rough surfaces.
In our last clinical study on the follow up of patients treated with this kind of implant in the last 18 months we have seen a difference in those cases in which a pneumatic driver for nailing had been used in the operative room. Not only the operative time for the positioning has been reduced of one third but the implant resulted to be more precise.
The use of this driver allows a better fitting of the stem to the femural shaft as the cut is more precise. In fact the surgeon has a controlled magnitude and direction of the driving force and this force is anyway limited.
There is a remarkable reduction of cases of intra operative fractures. So we have collected datas on 70 randomized patients in whom this device had been used compared to the same number of patients operated without this apparel: the operative time is reduced of 15 minutes in average and as a consequence the risk of fat emboly has diminished; revisions for malpositioning and intraoperative fractures are almost worthless. Moreover the blood loss has reduced of 100 cc. This are only partial datas but seem to suggest that this device can provide a great help to the orthopaedic surgeon in the operative room as well as reducing complicances in patients: we plan that this driver together with the Zweymuller stem will represent in the future one of the most safe solution in the total hip replacement when the surgeon puts the indication for an uncemented implant.
The pre operative evaluation of the degree of osteolisys in cotyle revision in a prothesis is very important in order to plan the best surgical treatment.
In these cases above the traditional radiological and scintigrafic exams we have achieved a evaluation techniques bases on D.E.X.A. This technique allows obtaining data on the periprotheses bone stock. These are the criterion of choice of the revision protheses, keepin’ in consideration data acquired by D.E.X.A.:
GIR 1 (loosening and acetabular widing with persistence of walls). If the cotyle is uncemented and the biological age of the patient allows, we use to treat with a first implant press fit uncemented cotyle. GIR 2 (loosening and acetabular deformation with losing a wall): uncemented with or without screws or conical screw first implant cotyle. GIR 3 (loosening and acetabular deformation with losing of one ore more columns and the bottom): oval cotyles with or without bone grafts. GIR 4 (massive periacetabular loss): oval review components with peripheral supports and obturatory ring, associated or not with bone grafts. As extrema ratio we use a McMinn cotyle.
A prospective consecutive series of uncemented, hydroxyapatite coated primary hip replacements utilizing two different types of alumina ceramic inserts and alumina ceramic heads is reported. Clinical and radiological results together with complications and reoperations are detailed.
193 hips followed up to 39 months using the Secur fit cup with ABC liner (Stryker). 40 hips using the Trident AD shell with the Trident titanium wrapped liner are reported up to 18 months.
Clinical scores (Harris and Postel Merle D’Aubigne) are similar to metal polyethylene at early review. SF 12 physical scores improved post operation. 100% bony ingrowth was seen radiologically (Engh and ARA scores).
Liner rim surface chips on insertion were seen in 1.4% of the ABC liners and none occurred after the 20th hip. No chips were seen in the Trident liners. One ABC liner sustained extensive surface rim chips in a heavy fall at 24 months. This is the first report of such a liner fracture. One Secur fit ABC cup was revised for recurrent subluxation.
The importance of early revision of ceramic fractures and the re use of shells is discussed. The addition of a titanium sandwich wrap to the ceramic liner is likely to eliminate the early chips.
Hydroxyapatite (HA) is a bioactive material with a high affinity for bone. Ti-6Al-4V is lightweight and less biotoxic. Using these materials, a cementless hip prosthesis has been clinically used, consisting mainly of a Ti femoral stem coated with plasma-sprayed biocompatible HA. However, this type of stem entails several disadvantages: HA is likely to decompose at the coating; long term HA coating layer bonding to Ti is unstable and optimal HA thickness is unfeasible. In many actual cases, debonding of HA coating layer from the Ti surface was found upon removal of stems.
To resolve these concerns, we started developing a new hip prosthesis using composite materials comprised of Ti-6Al-4V and HA containing bioinactive and highly stable glass in 1985. The cementless hip prosthesis, named HAPG-Profile, unites the bioactive stem surface with the surrounding bone via adhesive glass. In basic experiments, the glass-coated HAPG-Profile has been demonstrated to possess much higher bonding stability than the plasma-sprayed HA, with bone affinity and safety not compromised. On the basis of these results, we manufactured the HAPG-Profile jointly with DePuy International, UK, and initiated a clinical trial in January 1997 in the teaching Hospital, Nagoya University School of Medicine, and Tokyo Kosei Nenkin Hospital. A total of 63 patients were followed up for more than two year and evaluated according to the Japanese Orthopedic Association Score and Harris Hip Score (HHS) clinically, functionally and radiographically. The results of the two-year follow-up study indicated success of early fixation associated with favorable outcomes.
The great diffusion of total hip replacement in young patients has generated as a consequence an increasing in the number of prothesic failing associated with more or less extended bone loss. We mean analyze the various surgical solution to this problem. In the planning of the best surgical treatment the evaluation of the degree of osteolysis is the more correct technique; in fact we have supported the classical radiological exams with the miralometry as DEXA (supplying quantitative data on the periprotesic bone stock). Data obtained in this way allow choosing more carefully the best protheses in the preoperative planning: mid or long stem, with or without bone graft, with or without materials which may promote a bone rehabilitation. Anyway the surgeon should have all the possible protheses solutions as it happens to change the operative plan during the operation. These are the criterion of choice of the revision protheses, keepin’ in consideration data acquired by D.E.X.A.:
GIR 1 (loosening and or widing of the femural shaft with reducing of the cortical without interruption of walls): If the mobilized protheses is uncemented and DEXA supplies datas about a good bone stock we try to use a first implant uncemented protheses GIR 2 (widing of the femural shaft with reducing of the cortical with interruption of one wall): In these cases we use two kind of protheses anatomical or not with an oversized stem which increases the stability of the implant. GIR 3 (widing of the femural shaft with reducing of the cortical with interruption of two or more walls): In this cases we prefer using a long stem straight protheses, unless there is an increase of the osteolitic lesion; this protheses allows a stable anchorage thanks the optimized lenghts thus opposing to the rotational strenghts and allowing the transmission of translational strenghts both in the proximal and in the distal direction. The new calcar shape assure better adapting to the bone stock. With the increase of the osteolitic region, according to Wagner’s criteria, we have to change plan in orther to find a better anchorage. In fact SL Wagner protheses regains the coesion with the rehabsorbed bone cavity thus creating a relative stability in the immediate post operatory. Lately a high osteodeformation fills in the bone lacks. For this reason the muscolar insertion shouldn’t be receded around the thick cortical. This uncemented revision stem get anchored through a distal anchorage guaranteed by the conical shape, the stem is straight. The pre operative planning is compulsory in order to evaluate the measure of the osteotomic cut. GIR 4 (massive proximal circumferential bone loss). In the past, in case of complete femoural osteolisys the gold standard was the implant of great resection tumoral-cemented Muller’s stem as well as Kotz’s uncemented stems.
Kotz’s design, on the bases of follow up studies, seem to support Wagner’s theories about the distant anchorage: There is an attempt of periprothesic corticalization even though the huge bone loss. In the last years we have performed a revision modular distally anatomic stem characterized by a metafi sarial leaning on the proximal component.
The weight bearing is progressive on the base of the radiological evolution and DEXA as well. The complete bearing will be allowed only after a sufficient bone restoration.
In our experience uncemented protheses in the stem revision can allow in mid and long term good results expecially keeping in consideration that these patients had already coxofemural problems. The range of motion is difficulty improvable so the results must be weighted on the bases of the previous clinical situation. If patients are monitored in order to operate as soon as possible in case of mobilization, the use of uncemented protheses can be a valid way for the functional recovering of these patients.
This paper describes a development project for a minimally invasive percutaneous hip arthroplasty. The prosthesis provides a percutaneous replacement of the hip, employing the transtrochanteric approach and imaging control. (Currently Xray, but eventually real time MRI.) It is envisaged that conventional anaesthesia and operating theatre facilities will eventually be redundant. An optimal access entry is obtained using a percutaneous guide wire up the femoral neck, over which a drill is passed to accommodate a working post with a blunt end to avoid penetration of the medial acetabulum. On the post, a lateral cortical protection hoop is accurately fitted and screwed with four splayed screws. A 19 mm access tunnel is milled to receive a 1mm wall thickness H.A. coated tube.to the proper depth for neck resection. The neck is resected using an expanding cutter, and the head removed piecemeal. Using a milling end cutter on a flexible drive, located on the working tube, a spherical concave bed of decorticated bone is produced in the acetabulum.
The acetabular implant bed is formed as a “flower bud”, from titanium alloy with hydroxyapatite coating on its outer surface. This device is introduced retrograde via the tube, and opened in its definitive location under direct vision. The acetabular articular surface is metal, with profiling of the rim margins to accommodate required movements, as in the normal anatomy. The device is installed in an acrylic cement bed whose function is to retain apposition and contact of the flower “Petals” against bone, and to support the acetabular bearing surface. The femoral component comprises a 16.5 mm head and 11mm neck, and 17 mm shaft machined to fit the working tube. The device has been tested to an ultimate lateral bending strength of 1 ton, and 400,000 cyclical loading to 10 hundredweight. Optimal length of femoral component is selected to reproduce precise anatomy, and final adjustments are achieved using intratubal thrust shims. The cortical protecting hoop is replaced with a matching profile H.A. coated thrust plate reinserting the same four splayed screws. The wound is closed and the patient mobilised immediately. The approach avoids interference with muscles, and will permit accurate restoration of the anatomy.
Raised expectations and increased population of retirement age impose impossible pressures. Logistics and resources cannot to keep abreast of demand for hip arthroplasty with existing technologies. Radical solutions are required to match demand .
We followed 66 total hip arthroplasties using a cement-less Omniflex femoral component with different surface morphology in 51 patients for a mean of 98 months (72 to 138). There were 57 women and nine men, and the mean age of the patient at the time of operation was 55.4 years (39 to 70). Preoperative diagnosis was osteoarthritis secondary to congenital hip dislocation and dysplasia in 64 hips, rheumatoid arthritis in two hips. This series was divided into three groups according to the extent of surface treatment in the proximal part of the femoral component. A circumferential Hydroxyapatite or titanium plasma-spray coated Omniflex stem was used in 33 hips (Group A). A patchy titanium-beads coated stem and a smooth surfaced stem of the same design were used in 25 hips (Group B) and eight hips (Group C), respectively.
Clinically, the mean Harris Hip Score was 54 points preoperatively, which improved to 89 points at the latest follow-up. Incidence of thigh pain was the lowest in Group A ( 6%) in comparison with in Group B (28%) and Group C (25%). Radiographically, the aseptic loosening rate of the femoral component was none in Group A, 16% in Group B and 75% in Group C. Incidence of femoral osteolysis was almost the same rate among the three groups; 38% in Group A, 40% in Group B, and 50% in Group C. However only in Group A, no Osteolysis was found distal to the lesser trochanter level. The femoral revision was performed in two hips of Group C. This study elucidated that the extent of surface treatment would be one of the important factors to influence the stem stability and the occurence of femoral osteolysis.
The ROBODOC& #61650;-System contains a REVISION SOFTWARE which enables to plan and execute total hip revision surgery with ROBODOC& #61650. The greatest problem in Revision THR is the complete removal of bone cement without damaging healthy bone structures. In many cases the transfemoral approach is the only way to completely remove all existing bone cement. Postoperatively weight bearing is not allowed for 6 – 8 weeks.
Using the ROBODOC& #61650;-Revision-System two titanium pins need to be implanted preoperatively as there is no femoral neck left that could be used for surface matching. The next step is to take a CT scan of the femur and the data transfer to ORTHODOC& #61650;. The program uses a special technique to enhance the CT images so that all existing bone cement in the cavity and around the old prosthesis is clearly visible and can be distinguished from bone structures. Besides, metal artifacts caused by the existing prosthesis are minimized. four points of interest are marked: Top of implant, top of bone, base of implant and base of cement. A cutting path can be planned to remove all the existing bone cement. The next step is the planning of the new prosthesis. The prosthesis can be adjusted in any direction until a satisfactory position is reached. Intraoperatively, after the pin finding procedure, the robot mills out the existing bone cement and creates a new cavity for the planned implant. The surgeon now implants the new prosthesis.
In revision cases the average age of patients with a cemented implant at time of revision was 65.5 years, with a cementless implant 53.9 years. The average time between primary THR and revision THR was 9.5 years for the cemented group and 7.5 years for the cementless group.
Intra- / postoperative complications were dislocation in 1 case, thrombosis / embolism in 1 case, fracture of the greater trochanter in one case and infection in two cases.
Fit with the proximal femoral cortices is critical to the success of cementless femoral stems in total hip arthroplasty. Conventional femoral stems are often designed from the average geometry of the normal femora. Hip disease in Japan, however are predominantly associated with Osteoarthritis secondary to congenital hip dislocation or sublux-ation of the hip. We developed a new model of proximal fitting cementless total hip stem, the so-called FMS (for Fukui Medical School) stem, based on the endosteal geometry of Japanese proximal femoral canal with developmental dysplasia of the hip. The proximal third surface of this stem model was circumferentially hydroxyapatite-coated.
One hundred-two hips in 85 patients underwent cement-less total hip arthroplasty with the new stems were studied with a minimum follow-up period of two years. There were 78 women and 8 men, and the mean age of the patient at the time of operation was 56.4 years. Preoperative diagnosis was developmental dysplasia of the hip in 94 hips, osteonecrosis in 6 hips and rheumatoid arthritis in 2 hips. The mean follow-up period was 43 months (24 to 74). Clinically, the mean Harris Hip Score was 48 points preoperatively, which improved to 92 points at the latest follow-up. Thigh pain was present in two hips (2%) at the latest follow-up although in six hips (6%) in the study group at one-year follow-up. Radiographically, according to Engh’s criteria, spot welds associated with osseointegration were observed around the inferior border of the proximal coating in all hips. We have observed no loosening or failure of the stems at the latest follow-up. Our results indicate that the new model of proximal fitting cementless fem
There are concerns that highly crosslinked polyethylenes are not appropriate for knee implants. One concern is insufficient attachment strength of the insert to the tibial baseplate. In this study, the Natural Knee II Durasul (Sulzer Orthopedics Inc.) snap feature was optimized and then tested to evaluate if the locking mechanism withstood in vivo forces.
Initial testing showed that the anterior snap did not always fully engage if the conventional polyethylene design was employed. Therefore, a slight modification was made to the anterior face of the anterior snap feature. Subsequently, full engagement was consistently achieved.
The optimal snaplock geometry was evaluated using size 3, 22mm thick Durasul inserts in a peel-out test. Thick inserts were employed for a worst-case scenario (greatest lever arm). The modification employed resulted in a doubling of the attachment strength.
Once the optimal snap was defined, peel-out and constraint testing were conducted to determine in vivo performance characteristics the insert/baseplate attachment strength. The attachment strength of the Natural-Knee II Durasul tibial insert exceeds the maximum shear forces at the knee reported by Greenwald et al., even without an applied compressive load that would be present physiologically and would increase the attachment strength. This locking mechanism is stronger than clinically successful implants
To further verify the design, a 20° shear fatigue test was conducted on 22mm Ultracongruent inserts, again, a worst-case scenario. This study evaluated the migration of the polyethylene by monitoring anterior displacement of the femur and posterior lift-off under extreme physiological loads. All knee assemblies survived 107 fatigue cycles with no adverse effects. All inserts remained firmly attached to their respective baseplates. No polyethylene cracking was detected at the tabs of the insert or in the body of the inserts. This study shows that a successful locking mechanism can be made with the Durasul material.
Although complications associated with patello-femoral (PF) joint account for up to 50% of total knee replacement (TKR) revision procedures (Lee), the PF joint has been overlooked in wear simulations. The goal of this study was to develop an in vitro model to simulate patella wear in TKR’s. This report describes the concepts of an in vitro model for normal gait and the preliminary results of experimental validation.
The primary consideration in the development of the current model was modeling of the in vivo kinetics and kinematics. Since the in vivo kinetics are not well documented, the current model adapted a PF joint force pattern of gait measured one year postoperatively in a telemetric distal femoral replacement (Taylor et al). The maximum force was increased from 571N to 1780N (2.5xBody Weight) to compensate for muscle deficiency and to better reflect a maximum load representative of the in vivo situation. In vivo kinematics were adopted from measurements of Lafortune. Only the PF flexion was included in the model as a simplification of the complex patella motions. The phase relationship between the kinematic and kinetic waveforms was adjusted to replicate the in vivo situation. A 6-station knee simulator carried out the experimental validation with a test frequency of 1.5Hz. The test was intended to run for 5 million cycles, with CMM wear measurements (Muratoglu et al.) taken every million cycles. The preliminary measurements showed wear patterns in the tested patellae similar to retrieved patellae. Currently there are no standards for wear testing the PF joint. The current in vitro wear model presents a useful tool to critically assess the PF joint during gait. Future work should incorporate testing for adverse loading conditions, such as PF mal-alignment, rising from a chair or deep knee flexion.
The increasing number of primary hip arthroplasties leads to a corresponding increase in revision hip arthroplasty. In Germany approximately 15.000 cemented total hip arthroplasties are revised annually. In these cases cement removal remains a critical point in this procedure. Ultrasonic instruments have shown to facilitate the removal of bone cement considerably. But during the use of these divices large ammounts of fumes are emitted. For occupational safety reasons, we analized the fumes emitted from the ultrasonic instrument while removing PMMA bone under standardized in vitro conditions using GC-FID-analysis and GC-masspectrometry. The analysis revealed PMMA concentrations of 5 ml/m3 (ppm9 corresponding to 10% of the MAK-value (maximum working concentration). For occupational safety matters the PMMA fumes emitted are considered safe.
Recent advancements toward increasing the longevity of total hip replacements (THR) have made it possible to consider younger patients as candidates for this procedure. These include the development of highly crosslinked ultra high molecular weight polyethylenes (UHMWPE) and the re-introduction (most recently in the US) of metal-on-metal (MOM) articulating couples.
Early MOM designs (e.g. McKee-Farrar, Müller) were made of cast cobalt chrome (CoCr) with no polyethylene liner (a.k.a. “direct”), and to this date continue to show some degree of clinical success (20 to 30 years in-vivo). Since that time, improvements in materials and manufacturing techniques as well as clinical information from retrievals have led to the development of a new design, incorporating an UHMWPE liner between the CoCr inlay and the titanium alloy (Ti6Al4V) ace-tabular shell (a.k.a. “sandwich”). A previous study has reported that couples employing the polyethylene liner show lower wear than their solid metal counterpart [
Recently, highly crosslinked polyethylenes have emerged as an alternative bearing surface with tremendous potential for clinical success. However, the term highly cross-linked polyethylene refers to a great many materials, each manufactured under drastically different processing parameters, such as type of irradiation, dose, and warm versus cold state. It has been widely shown in laboratory hip simulator testing, that the wear resistance of UHMWPE improves significantly with increasing cross-link density, but the measurement of this parameter is somewhat controversial. While both swell testing of the polyethylene (direct) and trans-vinylene content (indirect) both yield information regarding the actual degree to which the material is crosslinked, no study to date has examined the exact relationship between these two tests. In evaluating the clinical performance of highly crosslinked polyethylenes, it is crucial that they be characterized according to the specific parameters by which they were manufactured. onship. Micro-Fourier Transform Infrared Spectroscopy (FTIR) and swelling measurements were performed on samples irradiated by either electron beam or gamma sources at varying doses, in both the cold and warm state. The trans-vinylene content was obtained from the ratio of the peaks at 965 cm-1 and 2022 cm-1, while the crosslink density was computed from Flory network theory.
The information for crosslink density was plotted versus trans-vinylene content to obtain the precise relationship between these two highly sensitive tests. This information can be used to aid in the clinical evaluation of commercially available highly crosslinked polyethylenes, and to improve our understanding of the very complex relationship between wear and the physical and chemical properties of UHMWPE.
We performed an experimental study to determine the effectiveness of computer assisted robotic bone preparation with regard to primary rotational stability in comparison to hand broaching. Forty-five synthetic femora were prepared by one of two robotic systems (Robodoc n = 12 and CASPAR n = 12) or by one experienced surgeon (n = 21). Seven different types of cementless femoral components were implanted using a standard protocol and measured in a specially designed testing machine with displacement in six degrees of freedom. For each implant at lease 3 measurements were taken for the handbroached and the robotic milled group, respectively. In addition the contact areas between the stems and the bone were visualised.
S-ROM, Antega and ABG stems were lightly more stable in hand broached femora. Osteolock (prepared by both robotic systems) and Vision 2000 stems were more stable in the robot group without changing the movement pattern. G2 and Versys ET performed higher stability with a change to more proximal fixation in the robotic group. Finally four of seven stems had an increase in rotational stability with the robotically milled cavities. The findings highlight the current difficulties in creating a perfect match of robotically milled cavity and stem geometry to achieve enhanced stability. The contact areas differed in some prosthesis in the way of preparation. In some stem geometries area of fixation and the movement pattern of the stem differ with the mode of preparation.
To elaborate upon the complex variety of successful reconstructive techniques for limb salvage surgery for the management of aggressive juxta-articular and peri-acetabular bone tumors.
Limb sparing surgery, while complex, continues to gain wider acceptance among an increasing number of highly specialised musculoskeletal oncology surgeons.
The collective experience of the Musculoskeletal Sarcoma Group at The University of Calgary has utilised a variety of limb and joint salvage techniques in its armamentarium for reconstruction of such cases.
Whether malignant or benign, aggressive lesions occur at or near the joint resulting in marked subchondral bone destruction or pathologic fractures. comprehensive stepwise plan can result in a stable, pain free and functional joint with limb sparing.
The author has utilised local tumor removal and cementation with polymethylmethacrylate with and without secondary internal fixation. ome cases have been amenable to massive osteoarticular allografts, and more recently, tumor endoprostheses.
The North American experience with massive oncology prostheses is growing, resulting in increased opportunities for limb and joint salvage surgery with decreased morbidity and complications. his presentation will review the experience of the principal author’s work in limb and joint-sparing bone tumor surgery over the past 18 years.
A first introduction of a successful metal-on-metal (m-o-m) articulation was made by G.K. McKee in 1956 using a cast CoCrMo alloy for the head and cup. Long-term clinical investigations of m-o-m and polyethylene-on-metal articulation showed similar 20 years follow-up survival rates. This and very good wear results obtained with some of the first generation m-o-m articulation led to a re-introduction of the m-o-m articulation in 1988. A healthy hip joint has a very low friction coefficient and almost no wear due to the optimal lubrication, which, under normal conditions, completely separates the two articulation surfaces. On the other hand all artificial hip prostheses are unable to produce or maintain a permanent lubrication film. Therefore, the surfaces of the prostheses are always subject to wear. Compared to polyethylene liners, wearing at an average linear rate of 0,1 to 0,2mm per year, m-o-m articulations showed generally very little wear. In vitro simulations of the second generation m-o-m articulation on a Stanmore hip simulator showed a steady wear rate of 5.6±7.3μm per million cycles, with a higher wear rate during the running-in phase of about one million cycles. The analysis of over 200 second-generation m-o-m retrieved hip implants showed an average linear wear rate of approximately 5μm per year after the running-in period, with a follow up time of up to ten years. There’s a great concern about the incidence of cancer after a total m-o-m hip replacement. It is very difficult to find a causal relationship between THR and cancer occurrence, as in some studies many cancers were detected within two years after THR, which indicate rather an associative relationship. However, the summarized results do not indicate an increased cancer risk after m-o-m total hip replacements. Over 130,000 m-o-m articulations have been implanted since 1988 and the clinical results have been excellent matching or surpassing current gold standards for hip replacement.
Advantages of custom made prosthesis are the 3D-Planing and correction of the head position using the best possible form fit. Considering these properties we examined several off the shelf systems if they can fulfil the requirements to form fit and head position. By using our fit program we simulated the implantation of five different off the shelf systems in more than 200 individual reconstructed femora. The data of these bones were used for constructing a custom made implant, so the best form fit and head position could be compared with the result of the fit. All of the patients were younger than 65 years. The data of the off the shelf prostheses systems came from 3D measurement. All systems were described as anatomical.
The fit program is an optimization program which can implant a 3D prosthesis model in a reconstructed 3D femur by variation of all six special parameters simultaneously.
Compared to the demands of our custom implants, the results of the virtual implantation of the off the shelf systems, are more or less unsatisfactory. Depending on the acceptable tolerance of the limits in offset, leg lengthening and anteversion up to 50% of the patients could not be treated with a single off the shelf system, when the best form fit was reached sufficiently. Using the results of this examination we enlarged our custom-made prosthesis system with six different sizes of an anatomical like off the shelf prostheses. By perfoming the same fit simulation with our new implants we found that more than 70% of our patients could be treated with this implant sufficiently, when using the same limits.
A good correspondence was found between the computer fit, which was calculated in advance, and the postoperative situation. The combined system of custom and off the shelf prostheses in addition with our 3D planning system based on CT examination, leads to new way of choosing the best implant for a single patient. If the virtual implantation of an off the shelf system does not give a satisfying result, the custom-made CTX prosthesis will be chosen for this patient.
The mobile bearing knee system has been designed to combine high stability and kinetic function with or without the posterior cruciate ligament. In this kontext the MBK-system is mainly qualified for patients with sufficient kollateral ligaments. Regarding to the origin anatomy a special attachment of the articulating surface allows an anterior-posterior movement of 4,5 mm and a rotation of 53 degrees. The sagital scape of the femoral component guarantees concruency to the articulating surface throughout a range of motion from 5 degress extension to 105 degress flexion. According to this fact high stresses to polyethylene with the consequence of an increase of attrition could be reduced.
From May 1997 to June 2001 236 mobile bearing knees were implanted in 220 patients. In June 2000 100 patients with 1 to 2 year follow up were investigated clinically and radiologically. The Knee Society Score was used for the clinical assessment. By using a special study questionaire pre-, intra- and postoperative data were collected.
Overall results in the first cases with 1 to 2 year follow up were good to excellent. Over 90% of the whole study group represented a plain increase of score values pre- to postoperatively. Regarding to the first 100 implantations postoperative complications were seen in 3 cases (1 deep vein thrombosis, 1 fixed flexion deformity, 1 sub-luxation of the patella). Intraoperative complications were noticed by one patient because of an uncomplicated tibial fissure. One re-admission was necessary in 1 case because of a traumatic patella fracture. A reduction of pain was noticed in 89,2% after 1 year, in 100% after 2 years. In case of the radiological follow up no signs of loosening or implant failure were seen.
Till June 2001 we had 2 more complications. One TKR has been revisised because of infection. One tibial component was changed because of instability and malrotation.
The first results in 100 cemented mobile bearing knees were very encouraging. All patients with 1 to 2 year follw up represented good clinical and radiological results. Mechanical implant failures were not seen in any cases.
In Revision-THR the great variability of acetabular defects requires a revision-cup-system, which enables the surgeon to treat even extensive unexspected bone losses with a load stable reconstruction during the surgery.
For these cases a modular revision support cup (MRS-Titan) has been developed. It allows the reconstruction of the geometric rotation centre and prevents the applied autologous or homologous bone graft in the healing phase from overlaoding. Beyond that an individual adjustment of the differently large flexible straps guarantees the solid anchoring of the revision support cup to the vital bone. The individual anatomy can be preserved in every case of acetabular destruction due to the high range of modularity the system provides. Because of the intraoperatively synthesis of all parts of the MRS-cup the approach and the traumatization of the soft tissue can be minimized.
Since 1995 we implanted 95 MRS-Titan-cups out of 250 which were implanted world wide. In all cases a stable anchoring of the implant has been reached. We will report about our own follow-up and complications. In 4 MRS revisions a revitalized acetabular bone graft has been found able to host a noncemented hemispherical cup in three cases.
A stem revision system was developed by a group of orthopedic surgeons and bioengineers. Implant specific instruments have been created to make the operation as easy as possible. The stem of the MRP prosthesis is conical and forged of a Titanium Aluminium Niobium alloy. It consists of 2 modular elements, a diaphysical and a trochantical part that can be supplemented by a head. Stem lengths from 140 mm and 200 mm are aviable with different length of diaphysical and prolongation elements so that each stem length could be realized in small steps. Also the anchoring of th diaphysical prosthesis elements in the bone makes a free construction of the total prosthesis to the femur with choice of the length and a variable adjustment of the rotation position of the neck of the femur prosthesis. Eight longitudinal ridges on the stem elements guarantee a rotation stability and the curved stems allow a reconstruction of the physiological antecurvation of th thigh also in case of fractures and segmental resections.
Since 1993 the members of the clinical working team implanted 1500 MRP prosthesis. We think that the best way for an optimal anchoring is the preservation of a great deal of the solid bone structures also in the section of the primary anchoring with partial bone resorption. The proximal anchoring of the femoral isthmus up to the middle third of the femur guarantees the most reliable long-term results. Indications for revision operations are given by resorptive bone defects up to a considerable bone loss on the proximal femur, for intraoperative stem fractures, for primary subtrochantar long distance fractures with simultaneous coxarthritis and for defect zones after bone tumor treatments. The very variable new design facilitates the revision operation and shortens the operation time.
The MRP prosthesis is able to bridge mechanically stable, damaged or missing parts of the proximal femur with revision operations and it makes an immediate partial loading possible for the patient. Defected zones of the bone fill with bone structures as a basis for the local anchored musculature. The modularity of the prosthesis lightens the revision operation.
Ceramic on ceramic hip-joint replacements (THR) are known for their excellent wear resistance. Such rigid-rigid bearings generally exhibit a biphasic wear-performance, i.e. a rapid run-in phase decreasing into a steady-state phase. However, due to the ultra-low wear of ceramics, few studies have adequately characterized these wear phases. Since this behavior was not well defined for modern alumina-on-alumina hips, we studied this phenomenon using hip simulator techniques. We also compared all-ceramic THR to UHMWPE wear-rates for exact comparison. Run-in wear was measured at 200,000 cycle intervals to 1 million cycles (1 Mc) followed by 500,000 cycle intervals to 14 Mc.
Alumina heads started off with high wear but then demonstrated a curvilinear run-in phase that smoothly transited into steady-state wear. The alumina liners had linear run-in to 0.6 Mc and then abruptly transited into steady-state by 0.8 Mc. During run-in, the liner wear was 40% greater than for the mating heads. Steady-state liner wear varied from 0.002 to 0.007 mm3/Mc. It was also clear that at least 10 million cycles were required to define the steady-state wear for alumina implants due to their ultra-low wear magnitudes. Combined head and cup run-in wear averaged 0.33 mm3/Mc and was completed within 0.8 Mc while steady-state wear was < 0.01 mm3/Mc up to 20 Mc. This was a remarkable 30-fold reduction from run-in.
The run-in phase would probably be completed by the first year of follow-up. Compared to UHMWPE cups, the alumina implants demonstrated a 9,000-fold wear-reduction over 20 million cycles in the simulator. This may correspond to 20 years in the typical patient. In addition, the alumina/UHMWPE combination has been favored historically because using CoCr/ UHMWPE bearings resulted in a doubling of the wear-rates in comparative clinical studies. Clearly the all-ceramic THR offers a much superior alternative with its massive reduction in wear-debris volume.
The results of wear testing using hip simulators have suggested that highly cross-linked polyethylene (PE) is more resistant to abrasive wear than “conventional” polyethylene that has been sterilized by 2.5 – 4 Mrad of radiation. Optimum methods for testing other mechanical properties of PE are controversial, but some studies have suggested that highly cross-linked polyethylenes have reduced impact strength when compared to either “conventional” PE or PE that has never been cross-linked. T he principle mechanism of loosening of most total hip prostheses is bone loss induced by debris particles that have been generated by abrasive wear, hence the rationale for using highly cross-linked PE for total hip arthroplasty. The principle mechanism of failure of bipolar hips, however, is less clear. If abrasive wear is important in bipolars, then the use of highly cross-linked PE is reasonable, but if impingement is an important complication of bipolar arthroplasty, then the use of highly cross-linked polyethylene might We revewied the implant registry of the Cleveland Clinic and identified 62 retrieved bipolar implants. The peripheral rim of each was evaluated, and a previously published scoring system used to grade the extent of rim damage due to impingement. A subset of implants were disassembled, and the shadowgraph method was used to measure the extent and rate of polyethylene abrasive wear. Adequate clinical information and radiographs were available in relatively few cases, but when available, the results of implant evaluation were correlated with clinical and radiographic findings.
The results suggest that both abrasive wear and rim damage due to impingement are common findings in retrieved bipolar devices. Further studies with better clinical and radiographic correlation are needed to clarify the most significant factors with respect to osteolysis and implant failure, but our results suggest caution in implementing highly cross-linked polyethylene for bipolar devices.
Alumina has been the dominant ceramic used in orthopaedics since 1970. It is near diamond hardness is superior to all other biomaterials and its wettability has been a great benefit for tribological reasons. Over the past 30 years, this ceramic has gradually been optimized with superior processing, higher purity, greater density, and somewhat higher strength. Also serial numbers have been added to uniquely identify implant components and proof-testing now ensures that every implant is pre-clinically tested, compared to prior methods of sampling only 2–3% for destructive tests. The clinical downside remaining has been the small but troublesome fracture incidence of alumina implants. Historically, this has averaged 0.015% (15 per 100,000 cases) overall but varied from 0.08% up to 13% in those clinical series experiencing fractures (Heros, Sem. Arthrop-98). As well as creating patient hardships, fracture of any implant in the USA frequently leads to major lawsuits. Thus ceramic implants must be treated w While there has as yet been no FDA-approval given to market ceramic cups in the USA, there are a number of ceramic candidates being developed for both THR and TKR. These include zir-conia-alumina composites as well as new zironia/zirconia or zirconia/alumina combinations for THR. In addition, there are new combinations of toughened aluminas and also other choices such as silicone nitrides proposed for use with either metal CoCr heads or CoCr cups. Finally an alternate approach has been to provide a metal zirconium knee joint with a ceramic zirconia coating for improved bearing performance. Thus, the state of the art of alumina implants will be reviewed and put into perspective with the “new and improved” ceramics currently on the horizon. This survey will put into perspective the physical and mechanical attributes as well as the clinical performance of ceramic implants.
The nature of human anatomy necessitates a continuum of implant sizes to recreate near-normal joint mechanics and also afford adequate fixation. Nowhere is this clearer than in the very constrained space required for design of shoulder implants. The effects of muscles acting about the humeral head clearly determine the shoulder’s mechanics. Also standard cement fixation may be undesirable due to difficulties in revision surgery be it required. To emphasize this, two recent developments will be discussed in the evolution of a shoulder design: a) adaptation of the prosthesis to the bony shaft for cement fixation and b) position adaptation of the humeral-head to recreate normal gleno-humeral kinematics.
Humeral stems are generally inserted undersized to the shaft and made ‘analog’ by the use of cement. We have studied this fixation biomechanically to find how little cement was required. Our fixation appeared satisfactory with about the proximal 4-cm of cemented stem. We also looked at shortening the stem but found indeed that stem-length was beneficial. Finally we have sought adaptability in design rather than in cement. We have achieved this by a tri-flanged design for the distal stem. This allows stem compression for intimate contact. In addition, its out of round shape, afforded more rotational stability in cement sheath.
For kinematics, Wallace et al discovered that the head could be displaced a variable distance from the center of the shaft and unique to each patient. Later studies showed that a mismatch could lead to improper mechanics with glenoid impingement. The solution proved to be a variable displacement humeral-head, which would allow the surgeon to select the direction and magnitude of displacement during surgery. Thus, this evolution of prosthetic shoulder design allows a smaller number of prostheses to be adapted satisfactorily to the continuum of humeral anatomy and also provide superior joint kinematics.
The TPP is a bone conserving Total Hip Replacement (THR). Originally designed in 1977, two modifications have been made since then and in its current form has been available since 1981.
We have used the TPP with a metal-on-metal articulation for active “younger” patients. The acetabular component has been the Armor cup.
48 TPPs have been performed in 41 patients since 1995. The age of the patients was 48 (21–54) years at the time of the operation. There were 17 females and 24 male patients. All patients are kept on an annual review. At the last review, one patient (2 THR) had died at eight weeks from a pulmonary embolism; one patient was lost to follow-up; one patient had required a revision for aseptic loosening.
We believe that this THR may offer a viable alternative for the younger patient, though it is a technically demanding procedure.
Major long-term complication of total hips is osteolysis in the more active patients. Osteolysis is a result of the biological response to the wear debris particles. This has resulted in the search for improved bearings such as metal and ceramic on polyethylene, all ceramic, and all metal total hips. Wear ranking of metal-polyethylene, ceramic-polyethylene, metal-metal, and ceramic-ceramic total hips has become clear at ratios of 1,000:500:10:1. However, wear debris from polyethylene, ceramic, and metal wear tests average about 0.6, 0.3, and 0.02 microns, respectively. From this information we can now deduce the number of particles librated is millions for ceramics, billions for polyethylene, and trillions for metal.
In recent years, studies have revealed new information on the biological response to various types of wear debris. Factors such as number of particles, particle morphology (size and shape), and surface to volume ratio are becoming keys to a partial comprehension of this biological response and osteolysis. Recent studies have demonstrated that smaller particles (< 0.1 microns) may be more toxic to cells than larger particles (> 0.1 microns). Studies have shown that crosslinking of polyethylene reduces the size of the wear debris particles and that for gamma irradiated polyethylene this reduction in size is proportional to the radiation dose. It has also been shown that crosslinking results in a significant reduction in fibril particles. Therefore, large reductions in wear rate do not necessarily mean that the total joint will be more successful. Thus, two factors, which interact, are the volume rate of wear and the morphology of the wear debris particles. Some investigators have developed a biological ind
Although good clinical results for modern metal-on-metal total hip endoprostheses are reported, in some cases early loosening is encountered. Such loosening may lead to revision surgeries, which raise some concern on the functionality of that pairing. The study contains 17 early-revised uncemented metal-on-metal (Co28Cr6Mo, ASTM F799) total hip arthroplasties from one manufacturer (Plus Endoprothetik, Switzerland) with a mean of 29 months in-situ (12–58) from 16 patients (seven male, nine female); mean age at revision surgery was 57 years (41–72). The reason for revisions was aseptic loosening of implants with increasing pain (13 stems and seven metal cups were revised). The tribologic assessment of all 17 metal pairings is conducted by 3 dimensional measurements of the metal ball heads and inlays according to ISO and through scanning electron microscopy (SEM) inspection of the articulating surfaces. Additional metal ion content (Cr, Co, Mo, Ti,Al, Nb, Ni) of selected tissue samples and synovial fluid is quantified by inductively coupled plasma – atomic emission spectrometry (ICP-AES).
The mean wear rate of both, the femoral ball head and the acetabular inlay, is 7.3um/a (2.8 – 29.4) based on the time in-situ with a mean clearance of 42.8um (32 – 56um). Adhesive and abrasive wear traces as well as third body wear particles (aluminum oxide Al2O3) are identified on all bearing surfaces only to an extent, which is typical for metal pairings. Corrosive attack is visible on one pairing as a smoky area.
Tribologic results do not indicate a significant contribution of wear due to the Al2O3-particles. The amount of wear does not seem increased and is comparable to previously published data for metal-on-metal pairings and simulator studies. Analytic results indicate a relatively high Al content from all retrieved tissue areas. The investigations on the surfaces of all 17 metal-on-metal articulations indicate no material failure that might have led to the necessity of early revision.
The Armor cup is a Titanium shell designed to press-fit into the acetabulum. It has 2 additional screw holes for screw fixation. The liner is polyetylene with a metal-on-metal articulation bearing surface.
We have performed 194 Total Hip Replacements (THR) in 167 patients using the Armor cup from 1994 to 2001. 83 THRs were performed using an uncemented stem (46 Thrust Plate Prostheses, 28 Wagner Cones and 15 Zwyemullers) and 111 THRs were carried using the cemented, polished, cannulated CF30 stem. The patient age was 54 (22–77) years at the time of the operation.
All patients are under annual review. At the last review, 3 patients had died (6 THRs); 4 patients required revision – 2 for the CF30 stem where Boneloc cement had been used, 1 for a periprosthetic fracture and 1 for a dislocated Armor cup. 1 patient was lost to follow-up.
We have therefore found the Armor cup with a metal-on-metal articulation to be a satisfactory componenet in the short to medium term. 26 patients are now over 60 months following implantation.
The mean linear wear rate in HA group was 0.19mm/yr and in the non-HA group was 0.21mm/yr, which was not significant (p> 0.05). There was no case of osteolysis or aseptic loosening of any component. Both groups had comparable outcomes in terms of HSS scores, walking ability and sports participation.
A recent study of tissues from 14 modern metal-on-metal (MM) total hips reported an intense diffuse and perivascular (p.v.) lymphocytic infiltrate, suggestive of hypersensitivity (Willert et al. Osteologie 2000; 9:2–16). This study evaluated the histopathology of tissues from modern MMs using cases obtained at revision or autopsy.
The world’s clinical experience of highly cross-linked UHMWPE cups (HCLPE) lies in the cemented THR experience beginning in Japan (H, Oonishi), then South Africa (CJ. Grobbelaar) followed by England (M. Wroblewski). The South-African THR concept was to cross-link RCH1000 to a depth of only 300um with 10 Mrad radiation dose in a pressurized acetylene atmosphere. Subsequent sterilization was 3 Mrad in air. The modified Charnley stem had a 30 mm stainless-steel head. Between 1977 and 1983, over 1,000 cases had been implanted by surgeons Grobbelaar and Weber (Grobbelaar, SABJS-99). Analysis has been performed on 100 survivors with follow-up 14 – 21 years. In the Pretoria series, there were only two of 64 cases with revision for granulomas and in the Johannesburg series two of 39 survivors with wear-related problems. Wear was only measurable in nine of 39 cases analyzed radiographically and total linear wear varied from 0.7 to 1.5 mm.
We have had the first-time opportunity to perform the retrieval analysis on Dr Weber’s cases. We now have & #65298; cases of revised cups and one sample off the shelf. These were examined by SEM to examine the microwear phenomena of the HCLPE surfaces. On the peripheral of the load-bearing area, the machine tracks were folded and their edges became fibrillated, some nodules, ripples, fibrils and folds (with attached fibrils) were observed. Fibrils were small in size and quite rare. Multi-oriented scratches and delaminations were sometimes observed.
This study is the first time review for the retrieval analysis on Dr. Weber’s HCLPE cases. The SEM study showed that the load-bearing area had very little wear evident after 20 years. This confirms the clinical and radiographic observation of Dr. Weber. While the retrieval data to date includes only 2 HCLPE cups, these results are encouraging.
The first Ceramic knee implant in a human patient was used by Dr. G. Langer of the Orthopedic Clinic at the University of Jena, Germany in 1972 [
The wear behavior of the Ceramic components for the knee system were tested in accordance to ISO/WD 14243-3 for 5*106 cycles. Six samples were tested. The lubricant was calf serum diluted with deionized water. All tests have been performed with components made of the novel AMC Ceramic.
The wear test performed showed an average gravimetric wear rate below 1 mg/1*106 cycles on each of the six components. A change of geometry was not measurable after 5 million cycles. No significant change of the surface structure was detectable with a conventional surface tracer. SEM and AFM pictures show traces of ultra mild abrasive wear at the surface. The performed investigation on the novel knee concept shows the following potential benefits for a Ceramic knee bearing:
approx. 500 times lower volumetric wear low risk of tribologically induced failure no PE particle induced osteolysis
The novel AMC Ceramic offers a solution to minimize the allergic and wear related problems of knee implants. New concepts on the basis of hard on hard combination are to be realized. The use of knee endo-prosthesis with Ceramic on Ceramic combination is an option for îzeroî wear bearings in the knee. These first results motivate to start further R& D on Ceramic on Ceramic bearings for total knee implants.
Alumina all-ceramic implants were first used in 1970 by Pierre Boutin in France and around 1972/3 in the rest of Europe. Thus the European ceramic experience is approximately 30 years. In the early 1980’s, the so-called Mittelmeier THR was introduced into the USA but the clinical results were generally far from satisfactory. However, the survivors now provide a useful benchmark of about 15–18 years in the USA. Perhaps as a result, the FDA has still not permitted use of all-ceramic THR in the USA. However, there are a number of new materials recently approved for use, including the highly crosslinked polyethylenes (HCLPE) and CoCr on CoCr. In anticipation of all-alumina THR being approved in the near future, we have examined the types of wear seen long term. Implants were retrieved after 15–25 years of successful use and compare to 10 to 20 million cycle simulator studies. This report examines the ball and cup wear seen on 2 Mittelmeier retrievals in the USA with that seen on a conventional all-ceramic THR retIn retrieved implants gray coloring matter was deposited on load-bearing area. Gray stripe areas were observed on the periphery of the head The SEM analysis showed that the main bearing area had high wear. The peripheral gray stripe area had severe wear. EDAX showed that gray color was caused by transferred CoCr particles. In the simulator study the wear progress was most sever in main load-bearing area.
All-ceramic implants had minimal wear even after 24 years. The surface of retrieved implants had different types of wear. The contact zones showed normal wear and showed relatively mild. In the periphery of the contact zones, the stripe scars corresponded with the cup rim tracking and more sever wear. Such stripe wear was not observed in the simulator experiments. The gray wear areas were caused by the metal contamination from micromotion of stem against bone. Thus, ceramic bearings proved to be excellent after 15–25years by simulator studies and clinical studies.
A retrospective study was performed to evaluate the safety and effectiveness of an alumina-based total knee arthroplasty system (Low Friction Anatomical, LFA, Kyocera, Kyoto, Japan). The system, which uses modern materials and contemporary component design, has been in clinical use in Japan since 1992. The system uses an alumina femoral component that articulates against standard polyethylene tibial and patellar components.
The retrospective study evaluated the clinical performance of amodern-style ceramic femoral component and included 60 knees (49 patients) with an average follow-up of 3.8 years. Clinical outcomes were assessed by the Japanese Orthopaedic Association (JOA) Knee Rating Scale, which is comparable to the Knee Society Rating Scale used in the United States. Radiographic outcomes were assessed by the operating surgeon and another independent reviewer. The radiographs were reviewed for the presence or absence of lytic lines, implant and anatomical alignment, and other pertinent radiographic findings. Complications during the follow-up period were noted.
Total knee replacement with the LFA system improved JOA scores in 98% of the cases. Mechanical and prosthetic alignment were satisfactory for all knees. The following results were noted:
No fractures or failures associated with the alumina ceramic femoral component No problems with subsidence or abnormal bone remodeling Absence of lytic lines in 96% of cases Absence of complication in 94% of cases Overall success rate of 96% at an average follow-up of 3.8 years.
An alumina-based total knee replacement system was found to be a safe and effective means of treating the arthritic knee joint. The use of ceramics in total knee arthroplasty applications provides an opportunity for a low friction bearing interface and a completely metal-free total joint system.
Wear of ultra-high molecular weight polyethylene (UHMWPE) is a major factor that affects longevity of the total joint replacement. In total hips, cross-linking of polyethylene acetabular cup has been shown highly effective in reducing wear both clinically and experimentally. In TKR, Schmidig 2000 showed 90% reduction of wear rate in 10 Mrad irradiated tibial inserts compared to 3 Mrad irradiated tibial inserts. Thus crosslinking should provide substantial improvement also in the wear resistance of UHMWPE tibial inserts. Our objective was to compare 3 Mrad UHMWPE with 10 Mrad HCLPE in same design but comparing standard kinematics to more severe mal-rotation kinematics. The latter offsets the tibial tray with 15 degrees internal rotation such the central tibial eminencies became involved in the wear process. Our hypothesis was that HCLPE would be more resistant than the standard UHMPE even in the mal-rotation model. The control material was Duracon 3 Mrad UHMWPE. HCLPE was radiation crosslinked to 10 Mrad mater
Navigation enables to precisely reproduce pre-operative planning. Most systems however do not tell us the target values of the planning parameters. As we operate more and more young patients with full or only slightly reduced mobility, kinematic properties of artificial hip joints become more important. The range of motion of artificial hip joints is limited, finaly resulting in impingement and thereby in wear and loosening.
This limited range of motion has to be devided under the different planes of movement and at the same time dislocation stability has to be considered. We have to search for the ideal compromise.
For this purpose a three-dimensional computer model has been developed. Input are the implant geometries and the implantation angles. As result the range of motion of the different planes of movement is calculated. Thus the surgeon knows the consequences of his implant choice and his pre-operative planning.
As a result of this investigation flexion proved to be the critical plane of movement, above all in full profile cups and if anteversion of the cup and the stem are not considered. Another critical plane of movement is external rotation.
Concerning implant design extralong heads as well as antidislocation rims proved to be problematic. The same problem we face in antidislocation cups with a closing angle of more than 180° of course.
Only by considering the kinematic results of an individual THR planning full benefit can be taken out of navigation.
The system permits a three-dimensional pre-operative planning of the correct axis and rotation as well as the correct implant size. The introperative cutting is entirely executed by the surgical robot according to the preoperative planning.
A CT scan is made of the femoral head, the distal femur and the proximal tibia including all the pins and the ankle. A rod is laid on the patient’s leg to detect the motion during CT scan. The CT data is being transferred to the ORTHODOC® workstation on an optical disk. The ORTHODOC® displays three orthogonal cross-sections of the bone on a high-resolution screen. A manipulation on one of the cross-sections is shown in nearly real-time on the other two cross-sections.
The first step is to find all the four pins on the CT scan and to check their position. The next step is to create a femoral and tibial axis using four markers (i.e. proximal and distal femur and proximal an distal tibia). The bone is then aligned along the axis. Once those steps have been performed and implant can be selected from an implant library. The femoral component is the first part of the planning. Once the correct size, alignment and rotation have been found the tibial component is added and adjusted. The final step is to select the tibial liner.
Once the planning is finished a synthetic x-ray can be created which shows the postoperative result and helps to determine if the correct axis was planned. After finishing the planning a transfer tape that can be loaded into the ROBODOC® is created. The patient’s leg is positioned using a special leg holder and thigh support plate.
The patient’s knee should be flexed to an angle of approximately 70 to 80 degrees, a gap of 1 to 2 mm should be achieved. The patient is prepared and draped in the normal manner. Surgery proceeds normally and the regular approach for TKA is used. Once the exposure is finished and the four pins are clearly accessible, two Steinmann pins are inserted, one in the femur and one in the tibia. The Hoffmann II Orthopedic Fixation System is used to connect the two Steinmann pins and to distract the knee joint.
Now the robot is moved to the OR table. The femur and the tibia must be rigidly fixated to the robot base. Following this two bone motion monitors are attached to the bone, one to the femur and one to the tibia.
The registration program is started. Using ROBODOC®’s ball probe the four pins have to be located, including the use of pin extenders so that the robot can find the patient’s position on the OR table by comparing the data to the preoperative CT data of that particular patient. First the femoral pins are found, then the tibial pins. If the registration is correct the cutter can be installed, the irrigation system is connected and the robot starts cutting the surface for the planned implant.
First the femur is prepared, then the tibia. The final cut is the cruciform in the tibia for which a special cutter is required. Should bone motion occur during any part of the cutting procedure the robot will stop and the pins have to be re-registered. Once the cutting is finished, the robot is moved away from the OR-table, the pins and fixators are removed an the surgeon inserts the planned implant manually – normally using the cementless tecnique. The surgery is finished the traditional way.
Fifty patients who had received total knee replacement using the ROBODOC® System were followed up and examined using a pre-defined protocol: 23 patients were male, 27 were female. All cases showed severe signs of osteoarthrosis. In 35 cases we saw a varus deviation, in 13 cases a valgus deviation, in two cases there was no deviation from the axis. four patients were post-traumatic cases, in one case a complex osteotomy had been performed.
In 38 patients the cementless technique was used, in eight cases the tibial component was cemented and in four cases both components were cemented due to poor bone quality.
We had an obvious learning curve, OR time went down from 130 minutes for the first procedure to 90 minutes average OR time. Due to the three-dimensional pre-operative planning of the correct axis and rotation we saw a good alignment of the femoral and tibial component in all cases. Besides the optimal size of the components could be selected for the patients in this group.
The surgeon has total control of the procedure at all times and the procedure can be finished manually if necessary. Correct aligment and rotation are the known preconditions for durability in TKR. The present disadvantages of the system are soft tissue management including ligament balancing, the rigid fixation and the use of pins (markers).
By June 2001 about 280 surgeries have been performed using the system. The development of a pinless system is already on its way and clinical testings are abour to start at BGU Frankfurt.
Despite impressive overall results at one year, lower knee scores were associated with a surgeons ‘learning curve’. After this ‘learning curve’, increased surgical experience led to further improvement with 90% achieving an excellent result, 8% a good, 2% a fair and 0% a poor result.
The middle third of quadriceps tendon is an autograft of sufficient size and strength and is stronger than the patellar tendon autograft with the same dimensions. We present the results from the use of a quadriceps autograft for the reconstruction of the chronically ACL deficient knee.
Between March 1999 and March 2000 we treated 36 patients with chronic ACL deficiency using a quadriceps tendon autograft, harvested from the middle third of the tendon with and without a patellar bone block.
The tendinous side of the graft was stabilized using the Mark II and Patella Soffix fixation systems (Surgicraft, UK). In the tibia the graft was passed through a tunnel and in the femur it was passed over the top. In those cases where the graft was harvested with a bone block, his was fixed to the tibia using interference screw fixation. The mean postoperative follow up was 21 months. The results have been evaluated using the IKDC, the Lysholm and the Tegner scales. According to the International Knee Documentation Committee rating system most of the patients had normal or nearly normal ratings. Knee laxity was evaluated using the arthrometers KT-2000 and Rolilmeter. There were no significant complications related to the harvesting site and there was no significant differences between the two groups regarding stability and function. MRI evaluation and second look arthroscopies in 7 patients revealed graft survival
The quadriceps tendon-patellar autograft is a reasonable alternative ACL reconstruction in primary and probably revision ACL reconstruction with minimal donor site morbidity and restoration of knee stability.
The study was established to assess the long-term results and differences between autogenous and synthetic anterior cruciate ligament (ACL) reconstruction.
We randomised 50 patients into 2 groups: 26 (52%) underwent reconstruction with middle third patellar tendon graft (PTG) harvested using the ‘ Graftologer ‘ (Neoligaments), and 24 (48%) underwent reconstruction with the Leeds-Keio ligament (LK).
Subjective knee function was assessed using the Lysholm score, Tegner activity score, IKDC grading, and clinical assessment of anterior knee pain. Laxity was tested clinically, including anterior draw at 20° (Lachman), pivot shift, and arthrometric measurements using the Stryker laxometer.
At five years we have noted a slight reduction in Lysholm scoring in the LK group, as well as reduced Tegner activity level. Pivot shift and laxity were significantly greater in the LK group.
Compared with earlier results, which showed little subjective difference between the groups, the autogenous PTG group show more sustainable long-term results than the synthetic (LK) group. There is no significant difference in anterior knee symptoms between the groups.
To review the results of anterior cruciate ligament (ACL) reconstruction in the skeletally immature patient.
At follow up the average subjective knee score was 86.6 (range 51.7–97). On objective testing 5 knees were rated normal, 6 knees nearly normal, 1 knee abnormal and 1 knee greatly abnormal. KT-1000 testing at 30N of force showed an average side-to-side difference of 2.77mm (range1-7mm) at maximum force side to side difference was 3.62mm (range 1–13mm). No leg length discrepancy or angulation was detected. All patients had returned to a higher level of function than pre-operatively.
68 consecutive patients undergoing total knee arthroplasty for osteoarthritis of the knee were included in the clinical part of the study. After a routine exposure the AP axis was marked on each distal femur. The AFCL was identified and the anterior cortical cut was made parallel to this line. The angle between this cortical cut and the perpendicular to the AP axis was measured with a sterile goniometer.
The improvement in alignment resulted in this trial being stopped prematurely as 6 out of 7 of the initial variables had reached significance. It shows a clear improvement in component alignment with computer navigation.
The kinematic profile of single axis design TKR was closer to normal especially near extension. During mid-flexion, abnormal anterior femoral translation was noticed with the polyradial design. No significant difference was noted between CR and CS designs.
The mechanical and anatomical axes are identified, from 3 dimensional landmarks, in both AP and lateral planes. The coronal and sagittal alignment of the pros-theses is then measured against the axes.
The rotation of the femoral component is measured relative to the transepicondylar axis. Tibial rotation was measured with reference to the posterior tibial condyles and the tibial tuberosity. Coupled femorotibial rotational alignment was assessed by superimposition of the femoral and tibial axial images.
The results of 100 scans show a low inter and intra observer error rate whilst independent assessment shows a mean measurement error of 3mm in a three dimensional plane. The radiation dose is 2.7mSV.
All surgery was performed by a single surgeon, using one prosthesis design in each group.
The data were assessed for any correlation between the pre-operative MCS and post-operative PCS, Pain, Stiffness and Function scores using Spearman’s Rank Correlation.
There was a statistically significant negative correlation between pre-operative MCS and six month WOMAC Pain, Stiffness and Function scores (P=0.025, P=0.019 and P=0.011 respectively) in the primary patients. There was no significant correlation with twelve months WOMAC scores.
There was no significant correlation in terms of pre-operative MCS and six months WOMAC scores in the revision patients, but there was a statistically significant negative correlation between pre-operative MCS and the twelve months pain score (P=0.039).
The technique was the same in all cases, involving 9cm osteotomy with screw fixation. In cases with marked restricted flexion and patella baja, the tubercle was deliberately moved proximally to gain length in the extensor mechanism.
Range of movement increased on average 45° in the revisions, and by 60° in the primaries.
An active extensor lag in 4 cases (all deliberate proximalisations) post operatively which all recovered.
5 patients underwent MUA for stiffness at 12 weeks.
We reviewed the outcome of 116 primary cemented Omnifit 7000 series total knee arthroplasties implanted into 108 patients over a period of two years with a mean follow up of 68 months (range, 48–90). During the review period, 12 patients died and 8 patients were lost to follow up (24 knees). The mean Knee Society score postoperatively at review was 86 (range, 65 to 95). The mean functional score at review was 76 (range, 60 to 100). The mean range of motion at review was 100 degrees (range, 85 to 115). Radioluscent lines greater than or equal to 1mm in width were present in 9 (10%) of the femoral views, 12 (14%) of the tibial AP views, 4 (4%) of the tibial lateral views and there was no evidence of progression of the radioluscent lines.
There were three revisions; one because of an early deep joint infection, on due to instability in the AP plane and one due to aseptic loosening. The clinical and radiographic results with a minimum five year follow up show very satisfactory results. The Omnifit 7000 series provides results, which compare well with other cemented arthroplasties in the medium term.
We wish to report our observations on a prospective series of 22 patients with high energy posterolateral corner injuries undergoing surgery at our Unit.
Since 1997, all patients presenting to our Unit with posterolateral corner injuries were analysed prospectively. Twenty two patients are presented with a mean follow-up of two years. Thirteen patients underwent acute exploratory surgery within two weeks of injury. The majority of patients had four or more injured structures identified at operation. The surgery involved reattachment of the injured structures together with selective staged intra-articular reconstruction in high demand individuals. Nine patients were referred to our unit a number of years after their original accident. The majority of these chronic cases underwent popliteofibular reconstruction using semitendinosus. All patients from both groups returned to activities of daily living after surgery. Ten patients returned to sport after reconstruction. Eight out of ten of these had undergone acute reconstruction.
Posterolateral corner injuries are high-energy multiple ligament injuries. Acute repair with staged selective intra-articular reconstruction in our series led to 61% of the acute patients returning to sport. Only 22% of the patients presenting late, returned to sport after reconstruction. This suggests that patients are more likely to return to sport if their knees are reconstructed early and we would encourage an assertive approach to these high-energy injuries.
The purpose of this study was to characterise accurately, the extent and geometry, and produce representative rigid resin models of full thickness articular cartilage lesions of various types, shapes and sizes on the articular surface of pig patellae.
Ten adult pig patellae and three adult Ox patellae were obtained and cleared of adhering tissue. Full thickness lesions were induced from oval shaped to “U” shaped scarifications by careful use of a hand held bur, and the geometry noted by taking appropriate dimensions with a Vernier cailper in the horizontal and vertical planes, and plan view photographs. MRI images using fat-suppressed weighted 1.5 mm thick slices scans in the horizontal plane, were produced in DICOM format for conversion to SLE files used in the reconstruction in the computer. The patellae were then held in a stone plaster mix to produce a male mould of the articular surface. The computer images were generated and the physical dimensions taken with the Vernier calliper were recorded from the reconstructed image in the computer using graphics software. The computer data was used to produce a rigid full scale model of the articular surface in resin using laser stereolithography which is using in the rapid prototyping industry. The resin models were matched with the male plaster moulds to confirm an accurate match of the 3-dimensional shape of the computer generated in all the types of lesions we produced. It is proposed to use the rigid models to produce sterile templates that could be used by surgeons to fashion an area around a lesion using a suitable reamer/bur using a predetermined criteria of cartilage thickness (say 2 mm), and the same geometrical data would be used to produce a suitable semi rigid scaffold shaped to the lesion. Our study has shown that very accurate 3 dimensional data can be quickly processed from MRI images to produce, using current rapid prototyping techniques, templates and implants to fit lesions accurately in the patella. There is no reason why this technology could not be applied to any joint surface that can be accessed by MRI.
Methods of accurately assessing the required dimensions of an ideal meniscal allograft for each patient are limited. One popular method used is to choose the appropriate graft according to the bony tibial plateau dimensions of the patient, as determined from plain radiographs.
Linear regression analysis was used to obtain a formula, relating each meniscal dimension to the various bony plateau measurements. The resulting equations were used to calculate an expected meniscal dimension from the measured plateau dimensions, and this was compared to the size of the actual dimension measured.
The mean percentage error between meniscal dimensions calculated from specific compartmental tibial plateau dimensions, and the actual measured meniscal dimensions was 5.3% (s.d. 4.1%). When using just total bony tibial plateau width to calculate meniscal dimensions, the percentage error was 6.2% (s.d. 4.9%). This difference was not statistically significant. The maximum error between calculated and actual meniscal dimensions was 32%.
Questionnaire of surgeons views on photographic records: This showed that less than 50% of surgeons felt they could interpret their own photographs and only 25% felt other surgeons records were useful. 80% felt that single image photographs gave clearer information than 4 small images per sheet. Retrospective audit of 70 arthroscopic records. This showed that the diagnosis was demonstrated in only 60% of records when taken. Small images had been recorded in 75% of cases. Production of guidelines for improving photographic records. Re-audit of 50 subsequent records. This showed a significant improvement such that the diagnosis was clearly demonstrated in 84% of records.
This may lead to a reduction in the need for repeat arthroscopy when patients are referred for second opinions to specialist knee surgeons, thereby reducing costs and morbidity.
The knees were mounted into an Instron materials testing machine. Paddles of pressure-sensitive Fuji Prescale Film were inserted into the lateral compartment of the knee, underneath the lateral meniscus. Each knee was then loaded to 700N for 10 seconds. The Fuji Film paddles were digitally scanned and then analysed using Scion Image Analysis software to determine the intra-articular contact pressures.
Contact pressures were then determined after (i) total lateral meniscectomy, (ii) lateral meniscal allograft transplantation using a bone plug-keyhole technique to secure the horn attachments, and (iii) after insertion of the graft by suturing only.
All 23 cases were able to partially weight bear immediately postoperatively, indicating satisfactory early press fit. No cases of loosening or cases suspicious of loosening have been noted.
Of the 23 cases 19 have been followed for at least 1 year. 18/19 showed consolidation of bone defects and in 1 case there was significant bone resorption under the tibial base plate due to stress shielding.
We wanted to know if a mobile bearing Total Knee Arthroplasty was able to cope with rotation of the tibial tray about the femoral prosthesis, by studying the tibio-femoral and patello-femoral joints.
This was a kinematic study that used a mobile bearing TKA mounted on a jig that allowed rotation of the tibial tray. The TKA was moved through a 90° range of flexion and we used photography to record the effects at the tibio-femoral and patello-femoral joints. We found that with a fixed tibia, increasing the degree of external rotation increased the degree of medial femoral condyle lift off from the polyethylene insert which was complete at 25° of tibial tray external rotation. The lift off increased with the degree of flexion. The patello-femoral joint remained congruent. If the rotated tibial tray was mounted on a tibia that was allowed to freely rotate, it led to congruity at the tibio-femoral joint. Now we found that there was medial facet impingement and lateral facet lift off of the patella button in extension and flexion.
We concluded that this mobile bearing prosthesis did not cope well with rotation of the tibial tray. The relatively low congruency at the tibio-femoral articulation meant that there was a reduced “driving force” at the tibio-femoral joint resulting in less than adequate rotation of the mobile polyethylene insert. We feel that the tibial tray must be placed in neutral to the femoral prosthesis and failure to do so will result in abnormal polyethylene loading that would increase wear and may culminate in early prosthesis revision.
The femoral antero-posterior axis (AP or Whiteside’s Line) is one of the frequently used landmarks during total knee arthroplasty for determining rotation of the femoral component. Femoral morphology is assumed to be relatively constant and bone cuts made to prepare the distal femur are referenced from this landmark. Few studies have confirmed the consistency or reproducibility of this axis in normal femora even though the effect of malrotation on patella tracking and valgusvarus knee stability has been well documented.
Fifty normal (non-degenerate) cadaveric femora (27 right, 23 left) were studied. The AP axis was identified and marked on each. An end-on photograph was taken to give a two dimensional image. The transepicondylar axis (TEA) was then drawn on each image. The angle between these two axes was recorded.
Measurement of the TEA referenced from the AP axis gave a mean angle of 90.82 degrees (range 80–102; standard deviation=4.72).
This study shows that the femoral AP axis is a reasonable method of determining femoral component rotation during total knee arthroplasty. However the variance in the results would suggest that other landmarks should also be used as a means of cross-checking femoral component rotation.
The mean age of patients was 28.3 (range 18–44) years. Mean IKDC score following reconstruction was 74.8 (range 49–100), SD±18.5. There was significant improvement in pre and post reconstruction mean Lysholm 2 and Tegner’s activity scores (p< 0.01). Subjective function of the knee on a scale of 0–10 improved from pre-operative 3.1 to post-operative 7.7 (p< 0.01). Arthrometry at 25-degree flexion and 130 N force using Laxometer showed mean anterior laxity 5.3mm on the operated side and 3.1 on the healthy side (side to side difference 2.2mm).
Pain relief was obtained in 84/193 cases (43.5%). In 122 cases where the aim was to avoid surgery, this was achieved in 52 cases (42.6%). Success rate decreased with increasing severity of disease (Fisher’s Exact test; p< 0.01). Only 25/122 cases with PFJ involvement had pain relief (21%), compared to 59/71 cases without PFJ involvement (83%), (Chi squared test; χ 2(1)=71.57, p< 0.01). Younger age (< 60 years) is a poor prognostic factor (Chi squared test; χ2(1)= 5.86, p=0.02).
Fifty-seven revision total knee arthroplasties were performed in our hospital using the TC3 system between 1995 and 1997. Twelve patients died. Forty-five patients were followed up for an average of 5.6 years (range 4 – 7 years). No patients were lost to follow-up.
All patients were clinically and radiologically evaluated. A postal patient satisfaction questionnaire was completed. Two patients were revised; one for infection and one for instability. Survivorship using revision as the end point was 93.3% at 7 years.
Indications for revision were infection(4;9%), instability(38;84%), pain and stiffness(3;7%). 32(71%) patients were satisfied with their outcome, 7(16%) were non-committal and 6(13%) were disappointed at 5 years. We have analysed the 13 dissatisfied patients and highlight the lessons learnt.
Pain and stiffness are not good indications for revision. Insert thickness of more than 17.5mm is suggestive of elevation of the joint-line. Instead the femoral component should be distalised. Step wedges should be used in preference to angular wedges. Always long stem the tibial implant if augments are used. Stems should be canal filling with adequate grip on the diaphysis.
We suggest the above lessons we have learnt from our initial revision arthroplasty learning curve may correlate to the clinical outcome of this small group of dis-satisfied patients.
Their mean age was 33 years old and 11 patients were below 17 years of age. There was a predilection for females with 22 (59.5%) out of 37 patients.
There was average 3.3 years period of time with swelling/knee symptoms before diagnosis .
The MRI scan was the cornerstone for the patient’s assessment. It has proved useful in recurrent disease and posterior ”Bakers cyst” disease.
2 of the patients had been managed with arthroscopic synovectomy alone, 10 patients have undergone simultaneous arthroscopic synovectomy combined with open excision of any “Bakers cyst” disease.
10 had “open synovectomy”. 3 patients have had radiotherapy .3 patients have had TKR Complications included 3 superficial wound infections, 1 DVT, 1 PE, 1 stress fracture after radical bone curettage, common temporary/refractory stiffness (needing physio/ MUAs). Recurrence was high and managed with repeat arthroscopic synovectomy.
100 patients were studied. 3 records were excluded, as there was no follow-up recorded. The demographics on 97 were: mean age 67 (range 37–91), male 56%, mean duration of symptoms 8.8yrs and primary OA in 65%.
Overall 43% were improved at 3 months, 31% at 6 months and 29% at 12 months. When the results were analysed according to indication, patients with ‘moderate non-mechanical osteoarthritic symptoms after failed medical management and not severe enough for arthroplasty’ did best (49% at 3 months and 38% at 6 months). Patients with ‘persisting arthritic symptoms after attempted arthroscopic debridement for mechanical type knee symptoms’ had less predictable results (42% improved at 3 months and 23% at 6 months). Patients with ‘severe or deteriorating symptoms while awaiting knee replacement’ or who were ‘too medically ill for TKR’ had a low rate of improvement (18% at 3 months).
At day 7 the swelling measured at 5cm below the joint and 5cm above the joint were significantly lower in the cold group compared with the room temperature group.
Drainage from the intra-articular drain was significantly lower in the cold group.
In the National Health Service although some units perform ACL reconstruction as a day case, others continue to admit patient’s overnight due to a possible medicolegal implication of complication including postoperative pain, nausea and vomiting and urinary retention. The aim of this study is to assess the safety, efficacy of post operative pain control, cost effectiveness of the day case procedure and the role of extended acute ‘hospitalcare in the community’ by a Rapid Response Team.
We carried out a retrospective review of data of fifty-seven patients who underwent day case ACL reconstruction with pre-emptive analgesia and postoperative pain control with analgesics and non-steroidal anti-inflammatory drugs. Rapid Response Team consisting of qualified nurses who provide intensive level of nursing cares in-patients home provided the postoperative community care. Aim of this team is to reduce the pressure of acute hospital beds.
Out of fifty-seven patients, adequate pain relief was achieved in 92.8%. One patient needed admission for pain relief, one patient needed admission for excessive bleeding and five patients had nausea and vomiting. Cost analysis showed that ACL reconstruction is cost effective. We conclude that ACL reconstruction is a safe procedure provided attention is given to patient selection, preadmission screening, patient education, preemptive analgesia with appropriate pain management and post operative community care.
Antero-inferior reattachment of a femoral peel off type injury of the Anterior Cruciate Ligament (ACL) occurs fairly commonly when an injury involves a valgus strain in addition to the more common external rotation strain of the knee.
This produces a recognisable and consistent pattern of clinical signs with an increased Lachman but with a solid end stop, an increased anterior drawer with no end stop and a pivot glide or 1+ pivot shift. This pattern of signs can be explained on a biomechanical basis.
From a functional point of view the reattachment often provides enough stability to allow a patient to return to a reasonable level of sporting activity.
Problems arise however when functional instability does occur and an inability to interpret the clinical signs, an MRI that is often interpreted as normal, and an arthroscopy when, to the inexperienced, the ACL may look relatively normal, leads to an error in decision making with regard to ACL reconstruction.
This variety of ACL injury has not been previously reported.
Information acquired from retrieved polyethylene ace-tabular components is invaluable to the design engineer in achieving better in-vivo service. The failure criteria used, namely mode-1 to 4 wear, are vague and not user-friendly. Based on an in-depth evaluation of over 100 failed acetabular cups, this study investigated a more precise classification
Although all the cups were obtained from one centre, they were not clearly marked, making an accurate assessment of the in-vivo life impossible. This, however, was not the aim of the study. We used visual inspections, magnifying glasses, colour-dye penetrant and stereo-microscopes to examine the cups. The most common defects identified were mechanical damage, cracks in the material, plastic flow, scratches, fretting, flaking and wear particles embedded in base material. These cups provided valuable data for compilation of a proposed set of failure criteria to be used in future. Visible defects should be used as a classification tool in future cup-failure analysis. They are explicit and can be used with confidence.
A scoring system that objectively weighs up the indications, contra-indications and order of priority for joint replacement is useful when assessing patients who demand surgery or when providing health fund providers with objective motivation for surgery.
The appropriate American score (Harris Hip Score or American Knee Society Rating) is applied. The scoring system goes on to assess the degree of pain and functional ability in greater depth. It takes into consideration the extent of other affected joints and the ability to perform normal activities of daily living such as driving, dressing, foot care, bathing and recreational pursuits.
The functional demands of the patient’s activities at home are then assessed, taking into account how much assistance is available, and what need there is to shop or make use of public transport, and how much walking or stair-climbing this entails. To this is added an assessment of the functional demands or stresses of the patient’s occupation. By adding the American scores and the additional scores for pain and functional ability, and subtracting from that total the score for functional demands at home and at work, one arrives at a score for the degree of compromise (American Score + pain + function – functional demand = compromise score). A lower score means greater compromise.
Finally, one determines the risk of morbidity and mortality. The greater the risk, the lower the compromise score should be. The contra-indication score is reached by multiplying the compromise score by the morbidity and mortality risks and dividing by 100. Depending on how one looks at it, the contra-indication score reflects either the urgency of surgery or the degree of resistance against it.
Primary total hip replacements are routine procedures with good outcomes. To ensure uniformly good results it is important that a thorough preoperative assessment of the patient is made. The prosthesis best suited to the patient and the pathology must be carefully selected and the optimal surgical technique must take into account patient, pathology and prosthesis parameters.
We discuss patients’ problems such as morbid obesity, the different arthritides and neuromotor abnormalities. Acetabular problems, including dysplastic acetabula and acetabula protrusio, are dealt with in detail. We examine post-traumatic hip pathologies, including retained fracture implants, nonunions and ankyloses. On the femoral side, dysplastic femurs, post-traumatic malunions and post-osteotomies are dealt with.
Anterolateral acetabular bone deficiency is one of the problems associated with total hip arthroplasty in patients with developmental dysplasia of the hips. We studied the integration of the acetabular reconstruction (cemented socket) in a bulk femoral head autograft. Between 1995 and 2003, we compared 10 patients with a second group who were treated by means of uncemented acetabular components. All the patients had complained of moderate to severe pain.
The techniques for the two procedures, cemented and uncemented, were comparable. Out of the 10 cemented procedures, one failed. In the uncemented cup procedure, one also failed after surgery. The results were comparable with published figures and encourage us to continue using the cemented procedure.
Resorption of the calcar below the collar of a titanium femoral prosthesis was observed. Biopsies of these lesions showed concentrations of polyethylene. We assessed the size of the resorption and correlated this with the size of the femoral prosthesis and the time since implantation. The age and the weight of the patient were also linked to the size of the prosthesis.
We conducted a finite element analysis (FEA) of the femoral component-femur complex in both the loaded and unloaded situation. The FEA study demonstrated changing pressure under the collar that can be translated into microbending motions, with the degree of the movement dependent on the size of the prosthesis, the material of the prosthesis and the weight of the patient.
We hypothesise that the existence of a ‘polyethylene pump’ due to the bending movements of the collared prosthesis concentrates polyethylene particles under the collar. We therefore postulated that the calcar resorption is due to the polyethylene granulomatous lesions, resulting from the micromotion of the collar of the prosthesis.
Over five years, 85 low-cost primary total arthroplasties (Eortopal Bulteamex) were done at a referral hospital. These were followed up for a mean of 48 months (minimum of 18 months). There were 11 revisions (13%), with four (4.7%) necessary for aseptic loosening, two (2.3%) for recurrent dislocations, four (4.7%) for sepsis and one (1.3%) for a periprosthetic fracture.
When these results were compared with the Trent Regional Arthroplasty Register, the revision rate was noted to be four times higher than in the Trent study, with aseptic revisions being twice as high and infection rates three times higher. Dislocation rates were half those in the Trent study. We concluded that our lower dislocation rate probably reflected the quality of our surgery. Our higher sepsis rate was probably related to the hospital environment, and the high aseptic loosening rate due to the quality of the ‘low-cost’ prosthesis.
We conclude that to be cost-efficient, ‘low-cost’ prostheses must be of good quality and that the hospital environment must be optimal. This study highlights the need for an Arthroplasty Register in South Africa.
This instructional lecture reviews the drill hole positions, how to determine the entrance and exit points, and how to do the actual drilling.
The goals of this study were to determine the outcome of surgical iliotibial band release in long-distance runners with iliotibial band friction syndrome (ITBFS).
A retrospective study of 66 patients (94 ITBFS) treated between 1995 and 1999 was performed. The diagnosis was made clinically by the presence of a positive Noble test. All other pathology was excluded. All patients had failed a trial of conservative therapy consisting of rest, physiotherapy, activity modification and corticosteroid injections.
Surgery was performed on an outpatient basis and patients were monitored postoperatively for at least two years. The outcome was assessed according to patient satisfaction, the time it took to return to running, level of activity and surgical complications.
Most patients were able to start running again within six weeks of surgery. Complications included three superficial infections and two cases of prolonged pain. The procedure was unsuccessful in three patients. Ninety-six percent of patients said that they would have this procedure again.
ITBFS is common in long-distance runners in this country. This is a safe, simple and effective surgical alternative for patients who do not respond to conservative treatment.
Because of the preconception that they are doomed to early failure, the use of rotating hinges in total knee arthroplasty (TKA) remains a controversial topic. We share our experience of more than 100 patients undergoing TKA using a rotating hinge.
As we had in mind the single purpose of allaying fears of early failure, this was a fairly simple study, using revision as a concrete endpoint. We discuss indications, contra-indications and some examples.
With our study showing a 93.6% survivorship rate at a mean of 4.8 years, we conclude that the rotating hinge has a definite place in TKA.
The main objective of the study was to determine the best method of treatment for adolescents with anterior cruciate ligament (ACL) injuries. Results were collected retrospectively from clinical notes from January 1999 to December 2001, during which time 14 patients were treated. Patient satisfaction, clinical examination and Cybex evaluation were used as criteria. A review of the literature on the subject was also conducted.
The results at four to six-month follow-up showed that 85.6% of the patients returned to active sport participation at the same level, 100% had stable knees on clinical examination, and no patient had any leg-length discrepancy or rotational or angular malalignment.
The ruptured ACL in young adolescents should be reconstructed to prevent re-injury and to decrease the incidence of traumatic degeneration in the unstable knee joint.
We conducted an engineering failure analysis of retrieved acetabular cups. From one centre, 37 properly-marked components were retrieved. The details of the patients were noted. Of the 37 components, 27 were brought to the laboratory for an engineering investigation of the cause of failure. A further 10 components were also taken to the biochemistry laboratory within an hour of retrieval, with tissue removed from the patients.
The purpose of the investigation was to determine whether any proteins were deposited inside the cups and to see whether there was wear debris on either the retrieved component or in the tissue surrounding the prosthesis. We used visual inspection, colour-dye penetrant, stereo-microscopes, scanning electron microscopes, and mass-spectometric analysis to examine the cups. Debris was captured using 0.4-um filters.
We found mechanical failure in vivo is mainly caused by plastic flow. Fretting is the second most likely cause of failure. Both of these are indicative of localised overheating between the acetabular component and the ceramic femoral head. The most likely cause of the overheating is lack of lubrication. With electrophoresis it became evident that at some time in their in-vivo service these cups had reached temperatures exceeding 60°C. These temperatures were confirmed on a five-poster hip simulator.
We suggest that an in-depth study be undertaken to establish the method of in-vivo lubrication and the lubricity of the available lubricant.
The mechanical failure of ultra-high molecular weight polyethylene (UHMWPE) acetabular cups in vivo is due mainly to a combination of excessive plastic flow and fretting. Localised overheating of the bearing surface, due to insufficient lubrication, causes this. The purpose of this study was to determine the amount of creep in UHMWPE under various conditions.
Test pieces were cut from a piece of raw material and tested according to ASTM D2990. In the first test, to determine the anisotropic behaviour of the material, test pieces of raw material were cut at various orientations. The material was then tested in the virgin state and the virgin state at different temperatures. It was also gamma sterilised under different conditions, namely 24 kGy in air, 25 kGy in a nitrogen atmosphere and 25 kGy in air, and heat treated at 80°C to get an annealing effect. Further tests were conducted to determine the effect of cross-linking on creep behaviour. These tests were administered at room temperature, at 50°C and at 60°C.
The material showed extreme anisotropic behaviour. It was more sensitive to creep in the centre of the bar than on the outside (32%). Maximum creep, however, occurred at a 45°-angle. This is significant if we assume that maximum loading of an acetabular cup occurs at an angle of 70.7°. The difference in creep for the virgin material, measured at room temperature and at 60°C, was 87.3% or 0.716 mm. The variance in creep for the different methods of sterilisation was a maximum of 0.3 mm. Creep for the cross-linked material, however, was markedly less than for the virgin material. There was a decrease of 36% (0.58 mm) in creep at room temperature and almost 83% (0.84 mm) at 60°C.
The test results show that the cross-linked material is much more stable. This may explain the good in-vivo service of these products.
The aim of total knee arthroplasty (TKA) is to align both the femoral and tibial components perpendicular to the mechanical axis of the leg. Most instrument systems cut the femur and tibia independently. Accurate alignment of the femoral component is hampered by our inability to define precisely the centre of the hip in three-dimensional space. Femoral resection is therefore based on a number of assumptions, which unfortunately do not hold true all of the time.
First, it assumes that an intramedullary rod follows a predictable path in the femur; secondly, that there is a fixed relationship between the rod and the mechanical axis of the leg, and thirdly that the shape of the distal femur is constant. Fourthly, even if the resection is correct, it assumes that the femoral component sits perfectly on cut surfaces. Further, there are inherent inaccuracies in the assessment of femoral component position, in that rotation of the limb with a 10° fixed-flexion deformity greatly affects apparent component position.
The exact entry point into the femur also influences alignment in that an intramedullary rod placed through an entry point 10 mm anterior to the intercondylar notch of the femur gives a mean valgus angle of 8°. When the tibia is cut perpendicular to its long axis in the coronal plane, assuming 3° of tibial varus, the femur needs to be cut with the corresponding degree of valgus, i.e., 5°. Even this argument is based on a small number of cadavers and does not take account of variations in the anatomy of the distal femur. In particular, a valgus bow can result in valgus malposition of the component. Extramedullary alignment carries the problem of using only a surface representation of the centre of the hip in a single plane, which becomes inaccurate as the femoral jig is rotated.
Malalignment of the tibial component increases the stress on the ultra-high molecular weight polyethylene insert, predisposing it to increased wear and subsidence. Studies comparing intramedullary and extramedullary guidance systems for cutting the proximal tibia have shown that 71% to 94% of prostheses inserted with an intramedullary guide, and 82% to 88% inserted with an extramedullary guide, are within 2° of being perpendicular to the long axis of the tibia.
To set a benchmark for comparison with computer assisted and robotic techniques currently being developed, we felt that it was important to assess the accuracy of placement of both the tibial base plate and femoral component in the coronal plane using current guidance systems.
We developed a series of radiographs allowing accurate independent assessment of femoral and tibial components. A long anteroposterior view of the distal femur with the patient prone was used to assess femoral placement. Coned views of the proximal and distal femur on the same plate were used to assess tibial placement. Correct rotational alignment of the radiograph was confirmed by the profile of the components.
Using this technique, we radiologically assessed the varus/valgus alignment of the tibial components of 350 TKAs. All the tibial components were implanted using an extramedullary guide with no posterior slope. We implanted 96.3% of components within 2° of the perpendicular to the longitudinal axis of the tibia. In order to validate our radiological assessment, a subgroup of 40 knees was re-assessed on CT scan. Analysis of this subgroup showed a close correlation between the results using the two different methods (mean difference 0.88°, SD 0.75).
We also assessed the position of the femoral component in 362 TKAs. A subgroup of 32 knees, 18 with perfect alignment and 14 with imperfect alignment, underwent CT scout scan of the femur from which the mechanical axis of the femur could be measured. Radiologically, 92% of all components were implanted within 3° of the target value and 83% were within 2° of target. There was close correlation between the CT and radiological measurements in the subgroup. Deviation from the mechanical axis was 1.16° (− 2.5° to +2°) in the perfectly aligned knees, validating both surgical technique and radiological assessment.
Although the findings for the femoral components compared favourably with other studies, there was still room for improvement. We set out to achieve this through direct measurement of the mechanical axis of the femur. In a series of 80 TKAs, patients were subjected to a preoperative CT scout scan of the femur. We took care to eliminate rotational error. The angle between the slope of the distal femur and the mechanical axis of the femur was calculated. During surgery the distal cutting block (Wright Medical Medial Pivot Arthroplasty System) was applied directly to the distal femur without use of an intramedullary alignment rod and the angle corrected so as to be perpendicular to the mechanical axis. A right-angled jig resting on the anterior femoral cortex was used to assess the flexion/extension of the cut. Patients were scanned again postoperatively.
In 76 knees (95%) the femoral component was within 2° of the mechanical axis. The remaining three were within 3°. We continue to evaluate the technique with the use of a new jig, which allows incremental 1°-correction of the distal femoral cut.
In conclusion, accurate cutting of the tibia during knee arthroplasty is possible with careful use of extra-medullary instrumentation. The use of a simple pre-operative CT scan eliminates the errors inherent in intramedullary femoral systems and takes into account the femoral anatomy of each individual patient.
Robotic-assisted surgery may offer the opportunity of accurate placement of components. It is, however, likely to be both time consuming and expensive. We should not yet abandon thoughts of improving the use of our current mechanical instruments. Robots have yet to prove their superiority.
Arthroscopic surgery performed on the medial or lateral compartments of the knee most commonly involves resection or repairs of tears of the posterior horns of the menisci. In osteoarthritic, anterior cruciate ligament-deficient, ligamentously tight, or very large adult knees, arthroscopic surgery through the conventional anterolateral and antero-medial ports can be difficult. It often gives rise to the risk of iatrogenic damage to the articular surfaces and structures of the knee. Establishing an accessory medial and/or lateral port for instrumentation has proved an easy and safe technique in conducting arthroscopic surgery to the posterior (medial and/or lateral) compartments of the knee.
This technique was used on 103 patients where access to the posterior compartments of the knee proved problematic. The technique is simple but highly effective and safe and is recommended for the inexperienced arthroscopist.
In high-demand situations, modern thinking and experience in total hip arthroplasty (THA) favours the uncemented press-fit cup over its cemented counterpart. Before its regular use in 1996, a high-demand cemented stem was designed for use as a short revision stem with a press-fit cup, with or without impaction bone grafting, in active people, especially those over 55 years.
Conceptually, a collarless double-tapered highly polished design was preferred. The clip-on hollow centraliser was designed for 5-mm subsidence. The valgus stem, with cement superior to the shoulder, limited upward pistoning in the cement sleeve, creating less debris. The stiff upper and flexible distal part resulted in a decreased contribution from shear and an increased contribution from compression in load transfer from prosthesis to cement. Three sizes are available: G1, G2 and G3. A straight type is presently being developed for smaller patients with congenital dysplasia of the hip.
The stem, made by (Thornton Heavy Engineering Sheffield, United Kingdom), from Rex 734 stainless steel to ISO-2002 standards, tapers 10 mm to 12 mm (6°). All tolerances are adequate to handle Inox or Ceramic heads.
From April 1996 to December 2002, 278 stems were implanted in Dr Weber’s practice. The first 172 hip operations (168 patients) were studied. The mean age was 58.6 years. There were 137 primary hips and 25 revisions.
The mean follow-up period was 4.5 years (3 to 7). Three patients died with the prosthesis in situ. Two reoperations were done: one cup was revised for recurrent dislocation and one fracture below the step was successfully plated. Only three cases of subsidence were documented, all of them less than 3 mm. To date there have been no stem revisions.
The prosthesis, together with the stainless steel head and cross-linked cup, can be regarded as cost-effective and can be used routinely, as a high-demand prosthesis with press-fit cup, or as a short-revision prosthesis.
Young adults are supposed to be enthusiastic, ambitious, energetic and productive. However, the disabling pain and consequent risk of job loss arising from certain pathological conditions in the hip can almost ruin their lives.
This paper discusses the biomechanical properties of the ceramic-on-ceramic total hip arthroplasty (THA) and metal-on-metal resurfacing implants, highlighting the advantages and disadvantages, and compares the survival rates of THA and new generation hip resurfacing procedures.
Short to mid-term results of hip resurfacing seem promising, but more research is necessary to find a better solution to the problem of hip pain in young adults.
This study investigated the rapid progression of osteoarthritis of the hip in elderly females, taking into account their symptoms, the clinical signs and the radiological, MRI and histological findings.
Early radiographs are often non-contributory, which can lead to inappropriate further investigations and treatment, such as lumbar spine imaging and surgery. MRI and histological findings lead me to believe that patients’ dramatic deterioration may be due to segmental avascular necrosis of the femoral head, with osteo-cartilaginous detachment.
When a patient with hip symptoms and signs has normal radiographs, one should be aware of this condition.
We have introduced a radiological scoring system to assess our technical competence in hip replacement surgery. We have also used it to assess the progress of the registrars in our training programme.
This scoring method involves several parameters, including positioning of the components and the quality of interfaces. We compared our results before and after the introduction of this scoring system, and found that the quality of our surgery had improved. We conclude that an objective scoring system is valuable as a training aid, as well as in maintaining standards in our unit.
The purpose of our study was to assess the success rate of methods used for knee arthrodesis in failed total knee arthroplasty and to do a functional evaluation after arthrodesis of the knee. A physiotherapist and occupational therapist assessed 10 patients who had undergone knee arthrodesis, using either the Orthofix or Ilizarov methods.
Both methods were successful. There were no failures. The functional outcomes were satisfactory.
Previous incisions around the knee may complicate subsequent total knee arthroplasty (TKA) because they can lead to skin problems, with wound breakdown and a risk of sepsis.
Our database contains details of 925 TKAs, 851 primary and 74 revision procedures. Of the 851 primary TKA patients, 368 had previously undergone knee surgery, 72 of them more than once. Twenty of the 74 patients who underwent revision TKA had undergone one previous procedure (excluding the primary TKA), and 24 had undergone multiple procedures. We clinically reviewed 133 TKAs, classifying previous procedures into midline (24), medial (50), lateral (26) and transverse (13) procedures. In 53 cases there had been previous arthroscopic procedures. Excluding the arthroscopies, previous scars were followed in 20 cases, partially followed in 11 cases and ignored in 53 cases.
Following up patients for a minimum of six months, we saw only six cases with minor wound edge slough. These did not require further surgery. Three of the six patients were in the group of 442 with previous scars, and three in the group of 483 without previous scars. All patients had spinal anaesthesia, peri-operative oxygen, vacuum drainage and a delayed knee-bending program, which we believe contributed to the low incidence of wound problems.
We believe that previous scars should be followed if they are approximately in the line of a normal midline TKA incision, and that scars beyond the midline can be ignored without increasing the risk of skin necrosis.
This was a retrospective study of all AML uncemented femoral prostheses and Duraloc cups in a consecutive series of patients treated between 1990 and 1995. Patients were evaluated clinically using the Merle Score. Radiological parameters included osseo-integration, subsidence and wear. Failure was defined as removal of implants or revision.
The 8 to 10-year results show a 99% survival rate. One patient was revised for femoral stem loosening following trauma. One patient with rheumatoid disease required revision for acetabular cup loosening after a few days.
We conclude that the results of the uncemented AML femoral stem and Duraloc cup are excellent in the South African population.
In a study of 76 consecutive hip resurfacing arthroplasty procedures, the reasons for choosing this procedure rather than total hip arthroplasty (THA) were reviewed. Patient age, preoperative diagnosis, presence of bone deficiency and other technical factors were considered.
The mean age of patients, 79% of whom were men, was 44 years (20 to 76). The preoperative diagnosis in 59% of patients was osteoarthritis and in 37% avascular necrosis. The decision to resurface the hip rather than to perform THA was influenced primarily by the patient’s choice. In 43 cases (57%), the patient had prior knowledge of the procedure and specifically that it be considered. Other important considerations were the patient’s level of physical activity, the expectation of non-compliance with mobilisation and rehabilitation, the expectation of instability of the hip, the quality of bone and the surgeon’s experience with the surgical technique.
As experience of the procedure grew, the mean age of patients who underwent resurfacing arthroplasty increased. The early clinical results of resurfacing indicate that the range of motion is less than in hip replacement, that the resurfaced hip demands less care against dislocation or wear, and that the patient mobilises and rehabilitates more rapidly and reaches a higher level of physical ability than with THA. As mid-term and long-term results become available, the indications for and prevalence of hip resurfacing arthroplasty are likely to increase.
The ROCC® prosthesis is a stabilised posterior cruciate ligament-sacrificing rotating mobile bearing knee. It contains a press-moulded polyethylene insert (Arcom®). It has high coronal conformity during gait and lift-off, and sagittal conformity during the weight-bearing phase. It also has a central concave-convex saddle-horse stabilisation mechanism with a progressive stop. Preferential gliding kinematics optimise the wear factor. A deep anatomical trochlea permits good patellar tracking at every degree of flexion with both resurfaced and unresurfaced patellae. The tibiofemoral displacement of the prosthesis approximates normality.
In 175 primary TKAs with the ROCC® knee, at two-year follow-up the objective measurement of pain was 8.7 out of 10 (7 to 10) in 94% of patients. In 89% of patients, the range of flexion was 128° (95° to 145°). At 3 months, the Knee Society Score was 175 in 87% of patients (function score 80), at 6 months 185 in 89% of patients (function score 90) and at 12 months 200 in 94% of patients (function score 100).
In 98% the femoral component was not cemented and there were no femoral radiolucent lines. The tibial component was not cemented in 30% and two patients in this group needed revision for loosening of the tibial plateau. There were no complications such as persistent pain, flexion contracture, Sudeck’s syndrome, instability or dislocation. Mechanical tests did not show any wear or cold flow deformation of the polyethylene insert after 3 million cycles.
Various techniques for meniscal suturing have been described: inside-out, outside-in, and all-inside. In some, the knots are intra-articular, while in others they are outside the joints. Suture materials include barbed absorbable pins, meniscal staples, absorbable and non-absorbable monofilament sutures and non-absorbable multifilament sutures. The gold standard, however, is mattress sutures with non-absorbable multifilament sutures and extra-articular knots.
Because some of the newer fixation devices are quite expensive, give inferior fixation and cause complications through breakage and synovitis following absorption of the material, a simple and inexpensive outside-in technique was developed.
With this technique, it is possible to suture the meniscus from the anterior horn to the anterior third of the posterior horn. The only requirements are two no-20 hypodermic needles, 1/0 monofilament nylon and 2/0 multifilament non-absorbable suture. Mattress-type sutures can be placed either superiorly or inferiorly in the meniscus, with the knot extra-articular. For tears in the posterior two thirds of the meniscus, which is inaccessible with this technique, one of the commercially-available all-inside techniques is used.
In June 1999 a randomised double-blind study on tibial base plate fixation was started to determine whether, when using the Profix® total knee replacement, the addition of screws improved the fixation of the tibial base plate. To date 138 total knee arthroplasties (THAs) have been performed, 119 of which were available for study. Selected randomly, 56 patients had supplementary screws inserted through the base plate and 63 did not.
After a minimum of 12 months follow-up, 27 patients had some radiolucent lines at the prosthesis-bone interface on the tibial component. These lines occurred in 14 cases with supplementary screws and 13 without screws. In one patient without supplementary screws, the tibial tray had subsided into the tibia. Statistically there was no apparent difference between the two groups.
The early results of our study raise questions about the value of supplementing base plate fixation in uncemented THAs, especially considering the additional cost of the screws and their potentially detrimental consequences.
Using the EOL+ cup, 25 operations were performed between December 1999 and February 2003. Most of them were salvage procedures for recurrent dislocations following primary and revision hip surgery.
The 18 women and seven men (mean age 65 years) had experienced a total of about 50 dislocations and 20 previous revision procedures. One patient had seven recorded dislocations, three had each had three previous revisions, and three cases had each had two previous revisions.
The mean follow-up was 22 months. No redislocations have occurred. One patient was revised to another EOL+ cup.
This cup presents an alternative salvage solution in problem cases, including those due to poor musculature, which do not respond to conventional solutions.
Uncemented double-mobility acetabular cups, first used in the late 1970s as a solution to recurrent hip dislocations, have proved efficient in reducing dislocation rates while preserving an important range of motion. The low wear-rate and low mechanical stress on the bone to cup interface enhances survival.
New instrumentation has permitted design changes that improve the dislocation coverage of the cup (upper part of the cup) and reduce the risk of impingement with the femoral stem (lower part of the cup).
Indications for the use of double-mobility cups have increased. They include primary total hip arthroplasty in relatively unstable hips, in which cases we use the Avantage® press-fit or 3P cup with an AURA II anatomical uncemented or cemented stem, dysplasia (in congenital high dislocations we use the press-fit or 3P or revision cup with an AURA revision stem, and in dysplasia we use small AURA II or Vectra or CMK dysplastic stems), muscular deficiency, in which Avantage® cups can be used with AURA II or revision stems, resection prosthesis or ARMEL calcar prosthesis, etc.)
The purpose of this study was to evaluate the early results of a new and minimally invasive posterior gluteus maximus splitting approach for total hip arthroplasty (THA) and metal-on-metal hip (MOM) resurfacing.
Thirty patients underwent THA (both cemented and uncemented) and 20 underwent MOM resurfacing. This single incision approach permitted THA through an incision ranging from 5.5 cm to 9 cm, and MOM resurfacing through an incision ranging from 7.5 cm to 10 cm. Intraoperative fluoroscopy was unnecessary. Body mass index was not a selection criterion. With the exception of the severely obese, this approach is suitable for all patients.
Fewer than 5% of patients needed blood transfusions. Patients were mobilised early and discharged from hospital. At a mean follow-up of six months, postoperative pain scores were low, cosmetic results excellent and patient satisfaction scores high. . Patients returned to normal activities early. There were no complications.
Between February 2000 and August 2002, 60 Oxford unicompartment knee replacements were done on 51 patients, nine of whom had bilateral surgery. The mean age of patients, 82% of whom were women, was 66 years (45 to 83). Primary osteoarthritis was the pathology in 97% and post-traumatic arthritis in 3%.
The mean range of movement increased from 113° preoperatively to 120° at the most recent follow-up. Complications included one case of deep vein thrombosis, one patient with bilateral tibial component loosening and three patients with loose cement particles in the joint. Most patients have no pain, but some have mild or occasional pain. One patient with bilateral unicompartmental replacements now has lateral knee pain.
Unicompartment knee replacements are an alternative to total knee replacements, but there is a significant learning curve, particularly with regard to cementing techniques. Attention needs to be paid to removing all loose cement from the joint. Patient selection is critical. The complication rate remains low, however, and the results seem satisfactory.
To investigate whether there are different patterns of patellar degeneration, 123 consecutive knee arthroplasties were investigated. Knees on which previous patellar surgery or osteotomies had been done were excluded. Areas of grade-III or more degeneration of the patella and femoral condyle were recorded.
The femur was divided into three condyles and nine areas. The patella was divided into three facets and nine areas. In 74 (60%) of the knees, patellar degeneration was less than grade III. In 49 (40%) knees, patellar degeneration was grade III or more. In these 49 knees, there were 122 lesions in the nine areas of the femur and 77 lesions in the nine areas of the patella. These lesions were analysed to determine the most common areas of degeneration in the femur and patella and to establish whether there was any pattern of degeneration between the patella and femoral lesions.
The highest incidence of degeneration was found in the medial femoral condyle, central and central-medial patella, probably the areas of highest load in the knee. The areas of least degeneration were in the lateral femur and the superior patella, which are probably the lowest weight-bearing areas. Any pattern of patellar degeneration can occur with any pattern of femoral degeneration.
Lateral and central-patellar facet degeneration are well-recognised clinical and radiological entities. In this series, medial patellar facet degeneration was commonly found. Medial patellar facet degeneration is less well recognised and in the literature is referred to only as secondary to lateral release. In this series, patients with lateral releases were excluded.
The medial facet is especially loaded in the flexed knee. A fixed flexion contracture, as is common in medial compartment osteoarthritis, explains the high incidence of medial facet degeneration. Standard patellar skyline views show only the unloaded medial facet. Medial patellar facet degeneration is probably more common than is recognised and may be a cause of unexplained anterior knee pain, especially in the flexed knee.
To stabilise the dislocating patella, one can increase the medial vectors, decrease the lateral vectors, or combine these options.
Oblique strengthening of vastus medialis increases the medial vectors. This muscle is an active secondary constraint for stabilising the patella. Strengthening this muscle is the cornerstone of treatment of patellar instability, but it is often unsuccessful if the medial patello-femoral ligament is deficient. The medial patellofemoral ligament is the primary passive constraint to lateral dislocation of the patella. Reconstruction of this ligament, which tenses in extension, stabilises the patella in most cases, without the danger of secondary late-stage patellofemoral degeneration. However, in high-riding patellae, effective ligament reconstruction may cause an extensor lag. An elevation of more than 3 mm affects the contact pressures by disturbing the unique relationship between patella and trochlea. Because it can lead to late stage patellofemoral degeneration, trochleaplasty is rarely indicated.
Tibial tubercle transfer decreases the lateral vectors and is indicated in cases of severe patella alta, a markedly increased Q-angle and lateral patellar tilt. The tubercle can be transferred distally or medially or internally rotated. The procedure changes the patellofemoral relationship, increasing the load in the medial tibio-femoral compartment and giving rise to the possibility of late-stage degeneration in both the patellofemoral and the tibiofemoral joints. It should not be undertaken lightly and the amount of shift should be conservative. The lateral retinaculum, which becomes lax in extension in right in flexion, provides about 10% of patellar stability to lateral dislocation. Because most patellae dislocate in early flexion, lateral retinacular release is seldom indicated except in the rare cases where the patella dislocates in late flexion.
In severe cases of patellar instability, it might be necessary to combine reconstruction of the medial patello-femoral ligament with tibial tubercle transfer and even with lateral retinacular release.
Because of bony lesions, revision surgery in the acetabulum is not always easy. We have a revision cross that we use to strengthen the bone cement and give extra stability in the presence of defects.
So far, two surgeons have performed operations on 60 patients. Follow-up times range from six months to five years. One patient has been lost because of sepsis.
We conclude that this is an effective way to augment revisions.
Anterior knee pain after total knee arthroplasty (TKA) occurs in 5% to 30% of patients whether or not the patella has been resurfaced. We retrospectively reviewed our patients, none of whom underwent patellar resurfacing. Only 2% had anterior knee pain, none requiring revision surgery. Our follow-up was between two and five years.
We paid particular attention to removing osteophytes and conducting a thorough peripatellar synovectomy and a circumpatellar cautery denervation.
Our results compare favourably to those in the literature, whether or not the patellae were resurfaced. We conclude that patellar resurfacing in TKA is unnecessary when careful attention is paid to the peripatellar tissues.
Sagittal knee implant design, together with soft tissue and alignment, determines the kinematics of an artificial knee joint. A single-radius design was thought to improve the kinematics and biomechanics of a knee joint prosthesis and therefore also improve rehabilitation. Two total knee joint prosthesis designs, differing only in their sagittal geometry, were compared in vivo.
To determine the three-dimensional kinematics and difference between a multi-radius and single-radius implants, six patients, all one-year postoperative, were subjected to video-fluoroscopy while walking on a treadmill, stepping up and down a 20-cm step and doing deep lunges.
In a clinical evaluation, differences in range of motion, functional knee score, 40-cm chair raise and anterior pain at 6 weeks and 3, 6 and 12 months were compared in 86 patients with multi-radius and 108 patients with single-radius implants. The age of the patients in the two groups was similar and ranged from 68 to 70 years.
Fluoroscopically-determined flexion was 105° in the multi-radius group and 123° in the single-radius group (p < 0.01). External rotation and lateral condyle movement was statistically similar. The single-radius group did not exhibit paradoxical motion of the medial condyle and had less overall movement. The objective knee scores did not differ significantly (p > 0.05). Patients in the single-radius group gained flexion significantly faster (p < 0.001). After one year, there was no difference between the groups. Three months postoperatively, 72% of the single-radius group could rise from a chair without using their arms, compared to 40% of the multi-radius group (p < 0.001). Although this improved in both groups, it remained superior in the single-radius group. Anterior knee pain was present in 59% of the multi-radius group and in only 18% of the single-radius group at three months (p < 0.001). At one-year follow-up, 4% of the single-radius and 29% of the multi-radius groups respectively complained of anterior knee pain (p < 0.001).
A single-radius sagittal design knee prosthesis leads to faster rehabilitation better and kinematics than a multi-radius design. The reduced movement of the condyles on the polyethylene insert should result in less long-term wear.
Complex acetabular defects after failed total hip arthroplasty (THA) remain a major challenge in revision surgery. We managed 29 patients, of whom 27 had type-III and two type-IV defects (AAOS classification). The mean age of the 16 men and 13 women was 68 years (22 to 96).
Use of a modular uncemented acetabular revision system allowed us accurately to position the construct, and then optimise the orientation of the polyethylene liner in respect of stability in the reduced hip. The modularity of the system allowed good access to do an impaction bone graft to restore the defects in the bone stock. Our follow-up ranged from 2 to 25 months. The orientation of the acetabular construct was measured radiologically and was at 50°. Our complications included four dislocations, two transient nerve palsies, one deep infection, four deep vein thromboses and one death from pulmonary embolism. We conclude that the use of a modular acetabular reconstruction system is promising in these extremely difficult cases.
The reported revision rate of total hip arthroplasties (THAs) due to wear and osteolysis is around 10% at 10 years. However, the actual rate is probably higher: the incidence of osteolysis is reported to be 10% to 45%. Apart from design improvements, improved or new materials and/or and combinations are important in reducing particle-induced osteolysis, especially in young and active patients.
Wear reduction of up to 40% after inert gas sterilisation of polyethylene (PE) has been demonstrated, both in vitro and in vivo. An effective means of providing further increases in wear resistance is to cross-link PE extensively. Early clinical results of non-melt-annealed PE at three years showed wear reduction of up to 85% compared to inert gas radiation-sterilised PE.
In hip joint simulator investigations, bearings with a ceramic ball-head articulating against a composite cup demonstrated wear rates similar to those of ceramic-ceramic bearings. The wear particles are benign. Clinical data collected over two years suggest no disadvantages compared to the standard articulation controls.
The wear resistance of alumina-alumina articulation has been enhanced. In-vitro investigation demonstrated that even with a cup inclination of 60° the wear rate is not increased. The effect of micro-separation of the artificial joint is also minimised. Several prospective multi-centre alumina-alumina studies have shown no additional complications with this articulation. However, alumina is a brittle material with an inherent risk of fracture. The addition of 25% zirconia to alumina (ZTA) in the manufacturing process improves its fracture resistance, increasing its strength by more than 50%, while maintaining its other properties. The wear properties of ZTA are even better than that of alumina, especially in micro-separation articulation mode.
Highly cross-linked and optimised PE and composite technology are promising concepts in address wear particle-induced osteolysis.
Severe central facture dislocations of the hip in the elderly can be catastrophic. Conservative treatment yields poor results with stiff painful hips. Reasonable hip function may be achieved with multiple surgical procedures and extended periods of immobilisation, but morbidity and mortality remain high.
We managed three elderly patients who had central fracture dislocations with early total hip arthroplasty (THA), using anteprotrusio supports. Bone grafting was used to re-establish acetabular bone stock.
Intraoperatively and postoperatively, these patients had no more complications than did patients undergoing THA for hip fractures. However, the surgical times were longer than for routine THA and blood replacement was slightly higher. Patients were mobilised early and aggressively. All became independent walkers and regained good range of movement. Radiologically the acetabular/pelvic fractures united and good bone-implant interfaces were established. There was no excessive heterotrophic bone formation.
We regard THA in the management of acetabular fractures in the elderly as a reasonable approach, enabling patients to mobilise early and keeping morbidity to an acceptable level.
In cases of tumours, severe bone loss, etc., special pros-theses are sometimes required. It is also important to have a prosthesis that permits a switch from a primary knee system to a revision knee to a hinged knee.
This paper discusses and demonstrates some locally-manufactured prostheses.
In the question of shoulder arthroplasty, the indications for hemi-arthroplasty or total arthroplasty have been well described. There are advantages and disadvantages to each.
This paper reviews 30 cases of use of the Elite® shoulder prosthesis over three years. Results have been good. The procedure calls for few instruments but is effective.
There were 98 tumours treated. In females, the most common tumours were breast (8) and renal (4) and in males, prostate (13), multiple myeloma (12) and lung (10). The thoracic spine was involved in 62, the lumbar in 18, cervical in 16 and sacral in 2. The vertebral body was involved in 76.
There were 109 operations. An instrumented fusion was performed in 82. Surgical approach was anterior in 17 (9 cervical, 8 thoracic) and posterior in 80 (5 cervical, 56 thoracic and 17 lumbar). Six patients had combined approaches (2 cervical, 3 thoracic and 1 lumbar). Two patients were treated for metachronous tumours. One patient had non-contiguous metastases treated separately. One patient was treated for local recurrence. One patient had revision for implant failure (anterior thoracic). One patient was explored after deterioration due to loss of autoregulation. Thoraco-abdominal approaches (12) were associated with ileus (2) and pneumonia (3). Of four cases with deep wound infections, three had received prior local irradiation. Two patients died of pulmonary embolus. 83 patients survived beyond three months.
All patients demonstrated improvement in pain status. Thirteen of 29 non-ambulatory cases were able to mobilise postoperatively. There were 32 whose Frankel grades improved. Seventeen of these returned to normal (15 from Grade 4 and 2 from Grade 3). One patient with complete motor and sensory loss improved to useful but subnormal status, three others improved to residual motor function. 11 other patients improved one grade. Of those whose scores did not change (76), 53 remained normal, eight maintained useful but subnormal status, five were stabilised with residual motor function, three kept some sensory perception and two had complete motor and sensory loss. One patient deteriorated from residual motor function to complete motor loss. The outcome for sphincter dysfunction (8) was not clear from the notes. In no case was a specific change in function documented.
Highly selective CT-guided epidural steroid injection was then carried out at the level of spondylolithesis by an experienced interventional radiologist. The pain diagram, VAS of pain severity and ODI were all completed again by the subjects themselves or by telephone at 1 and 3 months after injection in the presence of an independent assessor (nurse) and then reviewed and discussed with the treating doctor. All subjects were also asked to complete a functional questionnaire.
Part of the clinical work up had included an isotope bone scan, which revealed a focal area of increased uptake in the L1 vertebra. On MRI, the vertebral lesion had a ‘halo’ of high intensity signal with infraction of the upper vertebral endplate. There were no clinical symptoms arising from the vertebral lesion. The differential diagnosis of the L1 lesion suggested was either a meta-static Ewing’s tumour or an aggressive haemangioma. Given the possibility of a multifocal or metastatic lesion, a vertebrectomy and reconstruction with femoral allograft was performed. A second stage posterior stabilisation from T12 to L2 was performed. Histological examination of the resected vertebra revealed a benign capillary haemangioma. On recent review one year after treatment, the patient remains in remission from his tumour and has successful graft incorporation with minimal symptoms from his spine.
34 cysts were resected from 31 patients. Two (6%) were ligamental and 32 were facetal. 31 cysts were resected by laminectomy alone and 3 patients underwent laminectomy and bone only fusion. One cyst (3%) recurred and was managed by repeat laminectomy. One patient required instrumented lumbosacral fusion for increasing anterolisthesis. Incidental dural tear was the most common surgical complication occurring in two cases (6%). One patient demonstrated significant weakness of ankle and foot dorsiflexion which recovered incompletely. Average follow-up for the surgical group was 18 months (5–72 months). 27 scored an excellent or good outcome (79%), 3 scored a fair outcome, 3 were considered poor and one patient was worse. 30 (88%) patients were satisfied having complete improvement or improved with residual back or leg symptoms. Three responded as no change and one was worse.
The median ISS score was 24 (range 16–75) and not significantly different from patients with no spinal injury. The median number of associated injuries was 5 (range 0–23) and patients with spinal injuries were more likely to have associated thoracic, abdominal and extremity injuries and less likely to have associated head injuries than patients with no spinal injury. Patients with spinal injuries were more likely to be discharged to rehabilitation or convalescent hospitals and less likely to die than patients with no spinal injury.
The patient was treated non-operatively. On discharge at 10 weeks he had normal sensation to L3 and grade 5-power on left knee extension and grade 4-power on the right. There was no motor recovery distal to this. He had a hypotonic neurological bladder with sufficient resting tone in the sphincter to prevent incontinence.
Stereotactic navigation in cranial surgery is a well-established technique, in routine clinical use since the turn of the century. The advent of computer guided stereotaxis since the early 1990’s has led to an explosion in applications for the technology in cranial surgery, with the development of new surgical techniques, minimal access and consequent claimed reduction in morbidity and mortality.
Computer guidance also allows application of stereotactic techniques in spinal surgery. Early interventions have concentrated on the insertion of pedicle screws with improvement in accuracy and certainty of optimal screw placement. The use of fluoroscopic guidance allows the insertion of percutaneous pedicle screws and truly minimal access fusion techniques for the lumbar spine. More recently the development of improved registration has allowed the application of this technology to thoracic spinal surgery and to the cervical spine. Percutaneous techniques for C1/C2 arthrodesis, image guided vertebrectomy and transoral surgery, have been reported. The technology allows the development of surgical techniques designed not only for individual pathology but adapted to the anatomy of the individual patient. Disadvantages include a significant learning curve, especially for cervical spine surgery, the cost and need for registration which may be time consuming. Advantages include claimed accuracy in decompression, hardware placement, minimal access techniques and a three-dimensional solution to what is essentially a three dimensional problem. More recently non-computer based navigation systems have become available with improved hardware placement without the problems associated with computer based systems.
The purpose of this paper is to review computer guided spinal surgery, present new techniques based on its application to the adult spine, discuss advantages and disadvantages of those techniques and present the results of studies on the new non-computer based navigation systems.
Dorsolumbar angulation: On prone films, Cobb angle was measured at upper T12 and lower L1 end plates (normal 0°; with standard deviation +3/−3). Lumbosacral angular motion: On functional films, lines were drawn on the upper end plates of L5 and S1. The resulting differences [(+)-(−)] between functional angles were compared with the normal values obtained from the literature (i.e. in excess of 26° of combined motion). The difference between standing lateral functional radiography and the prone/supine scanography was accepted. Sacral inclination: On supine films, the angle between a vertical line (a perpendicular to horizontal baseline) and the upper S1 endplate.
Dorsolumbar angulation: 26 showed (positive) kyphotic angles up to 30°−40°. Lumbosacral angular motion: In view of the spinal rigidity found in most cases, a compensatory excess mobility was expected at 5/1 level, but the opposite was confirmed. Indeed, 27 patiens showed exaggerated (negative) extension shift (of −5°−10°); amongst these 10 were with complete loss of flexion; 12 were with partial flexion (a forward shift of up to 15°), but 5 with full flexion, permitted by a lumbar kyphosis. Sacral inclination: twenty-eight patients showed a shift to a diminished angle of 25°–35° as compared to 35°–55° in 15 control spines.
The patients were grouped according to the number of selected abnormal radiological parameters present. The cases were graded: Grade I (1 abnormality) – 2 cases, Grade II -13 cases and Grade III – 19 cases. The threshold for imbalance was (1) at least one severe thoracolumbar compression (or an equivalent combination of multiple minor thoraco-lumbar compression fractures) for D/L kyphosis and (2) a single lumbar fracture with at least 50% compression.
The mean Oswestry Disability Index scores at 2 years correlated with technical accuracy in placement of the prosthesis: Group I – 24.1; Group II – 30.3; and Group III – 36.3 (p < .05). The Mean VAS scores at 2 years correlated with technical accuracy in placement of the prosthesis: Group I – 28.3; Group II – 35.4; and Group III – 48.4 (p = 0.016). The mean flexion/extension range of motion and prosthesis function also correlated with device placement: Group I – 7.12 +/− 4.06 degrees; Group II – 7.47 +/− 4.41 degrees; and Group III – 3.15 +/− 3.51 degrees (p = 0.003).
There was no apparent difference between the clinical improvement in VAS and LBOS (p=0.91 and p=0.45 respectively) for each group. Analysis of the power of the comparison showed an 86% power for comparison of VAS improvement using a clinically important difference (delta) of 1 VAS point and there was 98% power for the LBOS improvement comparison using a clinically important difference (delta) of 10 LBOS points. Complications appeared higher in the arthroplasty group with foraminal encroachment requiring revision in 3 cases and one case of polyethylene failure in the Charité group at 3 years. This case occurred with an 8mm polyethylene insert (since removed from inventory by the manufacturer)
The outcomes for the 2002–2003 publications were better (MWp=0.02) than for the de Kleuver study. Fewer patients had disc replacement at more than one level (FEp< 0.01). The number of patients undergoing secondary surgery (FEp< 0.01) and arthrodesis (FEp=0.04) was less and the incidence of prosthetic subsidence or migration was lower (FEp=0.28). This overall improvement in recent studies highlights the importance of patient selection and the use of a disc replacement of appropriate size.
Following disc replacement, there was a significant improvement in outcome measures at six-week follow-up. This improvement was maintained at two years. While disc replacement reported significantly less pain and disability in the early period following surgery compared with the fusion, the difference was not significant by six months.
Compressive myelopathy, occurring through traumatic fracture/dislocation of vertebrae, iatrogenic injury, cervical spondylotic myelopathy (CSM), or metastatic tumour, causes much socio-economic and emotional disability for patients as well as physical consequences. In such conditions, APP is recognised as an early and specifi c marker of axonal injury. The proteolysis of APP in both acute and chronic compressive myelopathy has not yet been described. Studies analysing axonal injury after brain trauma suggest a role for Caspase-3 in the cleavage of APP
The understanding of biological systems is increasingly dependent on modelling and simulations. Numerical simulation is not intended to replace in vivo experimental studies, but to enhance the understanding of biological systems. This study tests the hypothesis that pressure pulses in the SAS are high adjacent to areas of arachnoiditis and investigates the validity of a numerical model by comparison with in vivo experimental findings.
The classification system reflects gradually increasing biological stability of the construct.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more the authors have received, or are likely to receive direct material benefits.
In relation to the conduct of this study, one or more the authors have received, or are likely to receive direct material benefits.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more the authors have received, or are likely to receive direct material benefits.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors has received, or is likely to receive direct material benefits.
In relation to the conduct of this study, one or more of the authors has received, or is likely to receive direct material benefits.
In relation to the conduct of this study, one or more of the authors has received, or is likely to receive direct material benefits.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors has received, or is likely to receive direct material benefits.
In relation to the conduct of this study, one or more of the authors has received, or is likely to receive direct material benefits.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors has received, or is likely to receive direct material benefits.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more the authors have received, or are likely to receive direct material benefits.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more the authors have received, or are likely to receive direct material benefits.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more the authors have received, or are likely to receive direct material benefits.
In relation to the conduct of this study, one or more of the authors has received, or is likely to receive direct material benefits.
In relation to the conduct of this study, one or more of the authors has received, or is likely to receive direct material benefits.
In relation to the conduct of this study, one or more of the authors has received, or is likely to receive direct material benefits.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors has received, or is likely to receive direct material benefits.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors has received, or is likely to receive direct material benefits.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a commercial source.
In relation to the conduct of this study, one or more of the authors has received, or is likely to receive direct material benefits.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
Traditional osteotomies are posterior or horizontal. A technique of an oblique osteotomy from the sciatic notch to the iliac crest has been developed at Great Ormond Street since 1996, along with a system of external fixation. It is undertaken concurrently with urological reconstruction. The system of external fixation is relatively simple compared with other published work.
Also children with classical exstrophy were divided into 4 groups on the basis of continence.
The mean post-operative percent reduction in the amount of the original diastasis was determined for all age groups. Comparison of pubic approximation was made between the two types of post-operative immobilisation
The average improvement in pubic approximation was 37% for the whole series. Chidren who were older at the time of surgery (18–60 months) were found to maintain better correction over time (76%).
Children immobilised with an external fixator maintained better closure of the pelvis than those treated with plaster cast alone. (51% and 12.2% respectively). Maintenance of pubic approximation was associated with a higher level of bladder continence.
Complications included 3 cases of infection and loosening of the external fixator requiring early removal. There were no neurovascular complications.
It is a reliable operation and the technique is applicable to all age groups.
Initially the Urologist will make an infra-umbilical incision then identify and mobilise the anatomical structures intended for their subsequent reconstruction and repair. This wound is then temporarily closed.
The Orthopaedic surgeon will then approach the ilial crest through bilateral oblique incisions made inferior to the anterior superior ilial spine as described for the Salter osteotomy
The interval is developed distal to the anterior superior ilial spine after identification and protection of the lateral femoral cutaneous nerve which is taken medially. After the interval between sartorious and tensa fascia lata are identified the iliac apophysis is split and reflected off the inner and outer ilial crests. The exposure may be improved by also developing the interval between rectus femorus and gluteus medius. Each side of the pelvis is exposed sub-periosteally from the iliac crest extending into the sciatic notch.
A Gigli saw is then passed through the sciatic notch. The line of the osteotomy is from the posterior part of the sciatic notch extending anteriorly and superiorly to exit the iliac crest 2cm posterior to the anterior superior iliac spine (figure 2). The most anterior 1.5cm of iliac crest from the distal pelvic fragment is trimmed to allow closure of the iliac apophysis after rotation.
The size of the half pin utilised is determined by the age of the patient. A baby under 18 months old will have a 3.5mm pin from the AO wrist external fixator frame and an older child over 2 years, a 4.5mm half pin. One half pin is inserted on each side of the pelvis. The half pin is placed in the distal fragment from anterior and lateral to posterior and medial with the tip of the screw just exiting the cortical bone of the medial aspect of the sciatic notch (figure 3a). Consideration of pin placement must take into account rotation of the distal fragment and preventive skin pressure areas. The iliac apophysis is repaired and the skin wounds are closed.
The Urologist completes the reconstruction procedure planned via their infra-umbilical approach.
The final stage involves the medial and superior rotation of both distal pelvic fragments and subsequent closure of the symphyseal diastasis. This position is maintained with the application of an anterior A-shaped frame from the wrist, AO fixation set in the younger infant or the AO pelvic fixator in the older child (figure 3b).
Symphyseal approximation is confirmed intra operatively by palpatation. Bilateral above knee front slabs casts are applied to prevent kicking the hips or knees.
The post-operative management involves pin site care on alternate days. The front slab casts are removed at 3 weeks and the anterior A-frame is removed at 6 weeks after union is confirmed on a pelvic radiograph. Depending on the social situation the children may go home during the post-operative period.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
From our retrospective study. The five-year estimated survival rates were 55% for the group with a pathologic fracture and 77% for the group without a fracture (p = 0.02). Eleven (37%) of the 30 patients with a fracture who were managed with limb salvage and 10 (45%) of the 22 patients with a fracture who were managed with an amputation died of the disease (p = 0.50). The performance of a limb-salvage procedure in patients with pathologic fracture did not seem to significantly increase the risk of local recurrence or death.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors has received, or is likely to receive direct material benefits.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.