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.
The diagnosis and subsequent treatment of patients with “Anterior Knee Pain” remains a challenge and an enigma at times. The 4 main parameters, which need to be assessed, are:
Bony anatomy of the PFJ Cartilage structure within the PFJ Tracking of the patella with active knee extension Structure of the soft tissues in the extensor mechanism While plain radiographs, CT scans and static MRI sans and arthroscopic assessments highlight some of the parameters none of them are comprehensive. The type of MRI scanning used in this study assesses all 4 parameters. The equipment required for resisted quadriceps contraction is inexpensive and readily available.
Radiological diagnosis and grading of subluxation if present. Clinical scoring of 26 patients who returned the questionnaires. Oxford, Lysholm and Tegner scores were used and correlated with the radiological scores. Development of a Treatment Algorithm based o the scan results.
Insertion of the femoral component was associated with generating a larger microembolic load than the other phases of the operation.
Between June 1986 and 1993, 208 Protek CLS total hip replacements were inserted in 174 patients. These have been reviewed clinically and radiologically by independent observers at 3 yearly intervals. One hundred and sixty six hips in 137 patients were available for review 9 to 15.5 years from insertion (mean just over 10.5 years). There has been no significant clinical or radiological change when compared to reviews three and six years ago with regard to the Harris Hip Score and the pain and function components of this. There has also been no change in subsidence, heterotopic ossification or lucencies. There has been no significant difference in results between males or females, nor between other factors such as pre-operative diagnosis, the use of metal or ceramic heads, age at time of operation or length of follow up. The failure rate remains low, less than 4%, i.e. survival rate greater than 96%. The reasons for failure in general do not relate to the fixation of either the acetabular or femoral components. The results of this long-term follow up of a large group of relatively young patients at time of insertion of arthroplasty remain very satisfactory.
Traditionally, immobilisation following achilles tendon rupture has been for 10 to 12 weeks. We have previously published a series of 71 consecutive repairs with no re-ruptures, using a lateral surgical approach. The latter part of this cohort were immobilised for six weeks instead of 12, with early weight bearing. The lack of any re-ruptures encouraged us to pursue the accelerated rehabilitation. This study documents a further 34 cases followed prospectively for 6–24 months (mean 15.9 months). All were repaired with a single Kessler-type suture using loop PDS, through a lateral approach. Patients were partial weight-bearing immediately in an Aircast boot with three cork heel wedges. At two-weekly intervals the wedges were reduced, and the boot abandoned after six weeks. There have been no re-ruptures. Thirty of the 34 patients returned to pre-injury activity levels. All patients were satisfied or very satisfied with the immobilisation device and the accelerated rehabilitation regime. Cost savings were also made through use of a single removable orthosis rather than sequential casts. We advocate this regimen of careful operative achilles tendon repair and accelerated weight bearing rehabilitation with a removable orthosis.
The purpose of the study was to review and present a series of early failures of the Miller Galante unicom-partmental knee replacement (UKR). Following several early failures all Miller Galante UKR’s inserted by the author (60 patients, 72 knees) were recalled for clinical and radiological review including assessment using the American Knee Society Score and the Oxford Knee Score. All knees with effusions were aspirated and specimens sent for histological analysis. There were 22 females and 38 males with a mean age of 67 years. The mean follow up was 3.4 years. Six failures were noted with follow up from 10 months to 4 years. These 6 cases will be discussed in more detail including operative findings at revision and possible reasons for failure. Early failure of this arthroplasty is unacceptable and caution should be exercised if contemplating using this implant unless more definite causative factors are identified.
Traditionally, immobilisation following Achilles tendon rupture has been for 10 to 12 weeks. We have previously published a series of 71 consecutive repairs with no re-ruptures, using a lateral surgical approach. The latter part of this cohort were immobilised for six weeks instead of 12, with early weight bearing. The lack of any re-ruptures encouraged us to persue the accelerated rehabilitation. This study documents a further 34 cases followed prospectively for 6–24 months (mean 15.9 months). All were repaired with a single Kessler-type suture using loop PDS, through a lateral approach. Patients were partial weight-bearing immediately in an Aircast boot with three cork heel wedges. At two-weekly intervals the wedges were reduced, and the boot abandoned after six weeks. There have been no re-ruptures. Thirty of the 34 patients returned to pre-injury activity levels. All patients were satisfied or very satisfied with the immobilisation device and the accelerated rehabilitation regime. Costs savings were also made through use of a single removable orthosis rather than sequential casts. We advocate this regimen of careful operative achilles tendon repair and accelerated weight bearing rehabilitation with a removable orthosis.
Isolated patello-femoral arthritis occurs in up to 10% of patients suffering osteoarthritis of the knee. Previous reports of several different patello-femoral designs have given indifferent results. The Lubinus prosthesis has a reported 50% failure rate at eight years in a study of 76 cases. The main reasons for failure were mal-alignment, wear, impingement and disease progression. The Avon patello-femoral arthroplasty was designed to solve some of these problems. The first cases were implanted in September 1996 and entered into a prospective review. The outcome was assessed using pain scores, Bartlett’s patella score and the Oxford knee score. To date 207 knees have been treated and 95 knees have reviewed at two to five years. The median pain score improved from 15/40 points to 35 at five years. The movement increased from 114° to 120° at five years. The Bartlett patella score improved from 10/30 points to 26 at five years. The Oxford knee score improved from 19/48 points to 40 points at five years. Two patients developed mal-alignment (1%) one of which required distal soft tissue realignment. There have been no cases of deep infection, fracture, wear or loosening. Fifteen knees (7%) developed evidence of disease progression, twelve of which (6%) have required revision to a total knee replacement. The functional results are similar to those of a total knee replacement. Results to date suggest that this improved design has all but eliminated the previous problems of mal-alignment and early wear. The functional results are as good as or better than those of a total knee replacement. There is a low complication rate and an excellent range of movement. Disease progression remains a potential problem. This type of prosthesis offers a reasonable alternative to total knee replacement in this small group of patients with isolated, early patello-femoral disease.
The aim of this study was to examine causes of the failed knee arthroplasty. Since 1980 the Bristol Knee Replacement Registry has prospectively recorded data on 3024 patients. Complete original and 5 year follow up data was available on 999 knees. The surgery was judged a failure if there was no improvement in the American Knee Society score at 5 years or if there had been a revision within that time. The prosthesis used was Kinematic in 471 knees, the Medial Unicompartmental Sled in 258 knees, the Kinemax Plus in 134 knees and a variety of other designs. At 5 years, 79 (7. 9%) either showed no improvement in the American Knee Society score or had been revised. The failure rate was 7% for the Kinematic, 7% for the medial Sled and 5% for the Kinemax Plus. 20% of the less frequently used designs failed. Five (0. 5%) knee replacements failed because of infection. 22 knees (2. 2%) had significant comorbidity that precluded a satisfactory functional outcome. For 7 knees (0. 7%), the patient exhibited patterns of abnormal illness behaviour that were thought to explain the poor outcome. A further 27 knees (2. 7%) failed because of technical errors either at the time of surgery (13 cases, 1. 3%), or in selecting a prosthesis which failed prematurely (14 cases 1. 4%). No cause for failure could be identified in 12 cases (1. 2%). The high failure rate amongst infrequently used prosthesis emphasises the need to use established designs. No cause for failure could be identified in 12 cases and 5 were due to infection; such cases are hard to avoid. This study shows the importance of assessing both the overall physical and psychological state of the patient if disappointing results are to be avoided. The most frequent cause of an unsatisfactory outcome was a technical one, which should be avoidable.
Isolated patellofemoral arthritis occurs in up to 10% of patients suffering osteoarthritis of the knee. Previous reports of several different patellofemoral designs have given indifferent results. The Lubinus prosthesis has been shown to have a 50% failure rate at eight years in a study of 76 cases. The main reasons for failure were mal-alignment, wear, impingement and disease progression. As a result of these studies, a new prosthesis was designed to solve some of these problems. The Avon patellofemoral arthroplasty was first implanted in September 1996. The cases have been entered into a prospective review with evaluations at eight months, two years and five years. The outcome was assessed using pain scores, Bartlett’s patella score and the Oxford knee score. To date, 186 knees have been treated; over 100 knees have been reviewed at two years and 20 knees at five years. The main pain score improved from a pre-operative level of 13.5 points out of 40 to 33.5 points at two years and 36 at five years. The mean pre-operative movement was 109° and this increased to 120° at five years. The Bartlett patella score improved from a pre-operative level of 10.5 points out of 30 pre-operatively to 23 points at two years and 25 at five years. The Oxford knee score was 20 points out of 48 pre-operatively and this improved to 35 points at two years and 40 points at five years. One patient developed subluxation, which required distal soft tissue realignment. No other patient has developed problems with alignment or wear. Ten knees have developed evidence of disease progression usually in the medial compartment of which six have required revision to a total knee replacement. The results to date suggest that this improved design has all but eliminated the previous problems of malalignment and early wear. The functional results are as good or better than those of a total knee replacement. There is a low complication rate and an excellent range of movement. Disease progression remains a potential problem. This type of prosthesis offers a reasonable alternative to total knee replacement in this small group of patients with isolated, early patellofemoral disease.
The Bristol Knee Replacement Registry was established in the 1970’s and contains prospectively recorded data on 3024 patients. The present study examines the group of 812 patients for whom complete pre-operative and five year post-operative data is available in order to relate their eventual health status to the pre-operative demographic data and to disease severity. The group comprised 593 women and 219 men who had undergone either Kinematic, Total or Sled unicompartmental knee replacement. Pre-operatively, the average American Knee Society Score (AKSS) was 89 with the elderly, rheumatoid patients and women having significantly lower scores. Five years later the average AKSS had risen to 161 with patients of all ages, (including the over 80’s) gaining considerably. However, the rheumatoid patients remained more disabled as did women who had a final AKSS of 157 as opposed to 171 for the men (p<
0.01). In addition, a statistically significant finding was that those with the lowest pre-operative scores also had the lowest 5 year scores - they never catch up. 173 patients underwent bilateral knee replacement at separate times. Their pre-operative AKSS was significantly higher at the time of the second knee replacement (90) than the first (82) p<
0.01. We conclude that since patients present earlier for their second TKR and those with most disability fail to catch up the procedure should be performed earlier in the natural history of the disease, especially in women.
The aim of this study was to report our experience of patellofemoral arthroplasty in isolated osteoarthrosis. Material and Methods: The Lubinus Patellofemoral Arthroplasty was performed between 1989 and 1995 in 76 knees. The Avon Patella Femoral Arthroplasty was used from 1996 to 2001 in 187 knees. The average age of the patients was 65.5 years (range 36–87) with a male to female ratio of 1: 5. All the patients have been prospectively reviewed with standard radiographs, the Bristol Knee Score, and more recently Bartlett and Oxford scores.
The Avon Arthroplasty with improved design features for better tracking and congruity was introduced in 1996 and 187 have now been inserted in 147 patients. One hundred and nine knees have been followed for 8 months and 82 have completed the 2 year follow-up. Two patients have undergone revision to a TKR 97.5% (survivorship 2 out of 82). Three patients have had a unicompartmental arthroplasty added for disease progression. There have been no cases of patella maltracking or subliaxation. Four year survivorship for moderate pain and revision is 96% (79 out of 82). Functional scores compared favourably with parallel series of total knee replacements. Conclusion: The medium-term results of the Lubinus Patello Femoral Arthroplasty are unsatisfactory. We suggest the use of this prosthesis should be discontinued. The Avon Arthroplasty has improved results in the short-term.
The purpose of this study was to determine the rate of polyethylene wear in a fixed bearing knee replacement in order to establish a norm against which mobile bearing implants can be judged.
Linear wear was measured using an electronic micrometer and volumetric wear by creating a mould of the defect using dental wax, and subsequently weighing the wax. Results: All components developed dishing which varied in orientation but matched the alignment of the femoral component. A near congruous articulation was thus produced correctly aligned for that particular arthroplasty. The mean linear penetrative wear for the group was 0.33mm (0.09mm per year) and the volumetric wear 124mm³ (26mm³ per year). The rate of wear seemed greatest during the second year.
The latest government targets state that by the end of 2005 the maximum waiting time for an outpatient appointment will be 3 months. These recommendations will not only increase the size of the outpatient clinics, but also the resources required thereafter. The purpose of this study was to analyse the outcome of new knee referrals to one consultant’s knee outpatient service in order to quantify the resources required to investigate and treat these patients. All new patients attending one consultant’s knee out-patient service in the time period January 1st 1997 to December 31st 1997 were prospectively entered into a database recording patient details, source of referral and provisional diagnosis. Eighteen months after the time period a cohort of 200 patients was randomly selected and the notes were analysed retrospectively. The number of outpatient appointment episodes (OPAs), MRI scans, physiotherapy referrals and surgical episodes generated were recorded for each patient. Analysis of the initial database records show that a total of 662 new knee referrals were seen in 1997. 52% (341) were made up of the five most common diagnoses, these being osteoarthritis, anterior knee pain, major anterior cruciate ligament injury, medial ligament injury and medial meniscus injury. Retrospective analysis of the 200 patient notes revealed that these patients required a total of 511 OPAs, 38 MRI scans, 178 courses of physiotherapy and 93 surgical episodes (53 elective and 40 daycase/emergency). These figures can be extrapolated to account for the total number of patients seen: The resource implications of a new knee referral are substantial. Extra resources must accompany each new patient, otherwise, although government targets will be reached the time taken to complete each patient’s treatment will become longer. It is imperative that before an agreement is made to see new patients the resources required to manage them are in place.
