Nine patients underwent arthrodesis of the knee using a customised coupled nail (the Mayday arthrodesis nail), five after infected arthroplasty, one following failed arthrodesis, one for intractable anterior knee pain, one for Charcot instability and one after trauma. Comparison was made with 17 arthrodeses, eight undertaken using external fixation, four with dual compression plates, and five with long Küntscher nails. Union was achieved in all patients (100%) at a mean time of ten months using the customised implant. There were no complications despite early weight-bearing. No further procedures were required. This contrasted with a rate of union of 53% and a complication rate of 76% with alternative techniques. Of this second group, 76% required a further operative procedure.

We compared the Mayday arthrodesis nail with other techniques of arthrodesis of the knee. The differences in the need for further surgery and occurrence of complications were statistically significant (p < 0.001), and differences in the rate of nonunion and inpatient stay of less than three weeks were also significant (p < 0.05) using Fisher’s exact test.

We conclude that a customised coupled intramedullary nail can give excellent stability allowing early weight-bearing, and results in a high rate of union with minimal postoperative complications.

A randomised, prospective trial comparing the percutaneous compression plate (PCCP) and the classic hip screw was performed for intertrochanteric fractures of the femur in 108 patients. The PCCP offers the ability to stabilise fractures with a minimal exposure and periosteal stripping thus preserving soft tissue cover.

Over a 19-month period all patients with extra-capsular fractures apart from subtrochanteric and pathologic fractures were included. They were classified as per Evans classification.

The patient’s pre-operative haemoglobin, premorbid mobility, medical and mental status were noted. The duration of the procedure, screening time, blood loss and any technical difficulty encountered along with the post-operative haemoglobin, drainage and transfusion requirements, as well as the length of stay in the orthopaedic unit and total length of stay in the hospital were recorded. Results were analysed using the Chi-square test and Student’s test.

The operating time was significantly longer in the PCCP group (mean 59vs49mins,P< 0.05). There was no significant difference between the two groups with regard to the other parameters measured.

There was no difference in the failure rate (2 cut-outs in the CHS group and one screw back-out in the PCCP.) With the device being of fixed single angled design it proved to be unsuitable for 3 patients.

The PCCP would appear to be as good as the more conventional device though it does not confer the perceived advantages of decreased duration of stay or significant reduction in transfusion requirement which are associated with other percutaneous procedures. The device is a single fixed angle one and is therefore not universally applicable to all patients.

Introduction: Traditionally adolescent anterior knee pain is considered to be a self limiting condition with no long term sequelae. However recently two publications have suggested the condition may be longer lasting. We wish to suggest that adolescent anterior knee pain may lead to patello femoral arthritis.

Method: We have carried out a comparative study assessing the incidence of previous adolescent anterior knee in patients who underwent patello femoral replacement for isolated patello femoral arthritis and have compared them with a matched group of patients who had medial unicompartmental replacement for isolated medial compartment arthritis without patello femoral disease.

All patients were sent a postal questionnaire enquiring about adolescent anterior knee pain, knee injury and patella instability.

Results: Ninety-three PFR patients and 86 UKR patients replied. The incidence of adolescent AKF and patella instability was higher in the PFR.group.

Conclusion: Adolescent anterior knee pain may not always be a benign self limiting condition since this as well as patella injury and instability was associated with subsequent isolated patello femoral arthritis.

The aim of this study was to investigate the hypothesis that unicompartmental knee replacement (UKR) of a single arthritic tibio femoral compartment can slow the progression of arthritis to the other compartment.

Method: Since 1974, a prospective database has been established in Bristol to register and follow up the results of unicompartmental knee replacement. Forty two prostheses that had survived for more than 10 years were examined using the Ahlbach radiological scoring system and compared to a control group of patients from the Bristol “OA 500” series, in which patients being treated conservatively for gonarthritis were regularly reviewed by clinical scoring and radiological analysis. The groups were sex matched.

All AP and lateral standing knee radiographs at entry and 8 years were scored using the Ahlbach scoring system. The Ahlbach system has been shown to have good inter and intra observer correlation, and to relate closely to pathological findings at operation. An intra and inter observer error study of our results confirmed good correlation.

Results: The groups were well matched but the OA 500 group showed a lower average age, though not a significant difference (62 years compared to 67 years). The lateral compartment of all knees in both groups were Ahlbach grade 0 or 1 group before operation or entry to the OA 500 register.

In the UKR group, four out of 42 knees showed progression of a single Ahlbach grade (9.5%). 2 revisions for arthritic progression were added to this group making a total of six out of 42 (14.3%). In the control group 12 of the 42 knees progressed by one or two Ahlbach grades and a further case underwent surgery making a total of 13 (31%). This difference was significant (p< 0.01).

Conclusion: Recent studies have shown that with a better understanding of design, improved selection of patients and better surgical technique, a UKR can have at least as good, if not better, results than a TKR at 5 year follow up, and has benefits of preservation of anatomy, earlier rehabilitation, preservation of bone stock and easier revision. Our radiological findings in this study will need to be correlated with further randomised prospective clinical studies, but suggest that progression of Osteoarthritis is reduced by UKR, and that this should be an additional stated benefit of this surgical technique.

The aim of this study was to demonstrate the effectiveness of a customised coupled arthrodesis nail.

Knee arthrodesis is now infrequently performed and is usually reserved as a salvage for infected Joint arthroplasty or occasionally for intractable pain. Many methods have been used. Recently locked intramedullary coupled nails have gained in popularity. To deal with all size combinations a large inventory is required. We wish to report our series using a customised implant and to compare the outcome with other methods of knee arthrodesis.

Nine patients underwent arthrodesis using this implant, six following infected arthroplasty, two for intractable anterior knee pain and following trauma. Comparison was made with 17 arthrodeses performed since 1993 using external fixation (8), plates (4), and long K-nails (5). Union was achieved in nine patients (100%) at a mean time of 10 months using the customised implant. There were no complications despite early weight-bearing. No further procedures were required. This contrasted with a union rate of 65% with a 76% complication rate using alternative techniques. Seventy six percent of this second group required a further operative procedure.

We conclude that a customised coupled intramedullary nail can give excellent stability allowing early weight-bearing, and results in a high union rate with minimal post-operative complications. The differences in need for further surgery and occurrence of complications were statistically significant (p< 0.001), and differences in in-patient stay and non-union rate were also significant (p< 0.05) using Fisher’s exact test.

The aim of this study was to analyse the kneeling ability of patients before and at one and two years after total (TKR), unicompartmental (UKR) and selective patellofemoral (PFR) knee arthroplasty, for osteoarthritis. Method: Data was prospectively collected on 253 knees, which underwent either TKR, UKR or PFR. A kneeling score was obtained by analysis of the relevant section of the Oxford Knee Score questionnaire. Scores were obtained pre-operatively and at 1 and 2 years post-operatively (minimum score 0, maximum 4). Absolute values and change following arthroplasty were recorded. Correlations with pain and other knee functions were also made.

Results: Kneeling ability prior to surgery was poor in all three groups (mean score 0.7 out of 4) and improved significantly after surgery (mean score at one year 1.13 and at two years 1.46 out of 4) (P< 0.001). Kneeling ability at 1 year differed significantly with operation type (p = 0.02). Kneeling ability improved most in the first year post-operatively but continued to improve between one and two years although the final function was still not good. Kneeling ability was best in UKR and worst in PFR, with the difference between these prostheses being statistically significant (P< 0.001).

Conclusion: Kneeling ability in osteoarthritic knees is poor but improves with arthroplasty. However, the majority of patients will still have difficulty kneeling.

In Total Knee Arthroplasty (TKA) and Total Hip Arthroplasty (THA) the total blood loss is composed of ‘visible’ blood loss from the surgical field and wound drainage, and blood loss into the tissues which is ‘hidden’. Blood management should be aimed at addressing the total blood loss.

56 TKAs and 46 THAs were prospectively studied. TKAs were performed with tourniquet. After tourniquet release, all drained blood was salvaged and significant volumes reinfused. No reinfusion was used for THAs.

The true total blood loss was calculated in the following way:

Patient Blood Volume (PBV) is: [1]

PBV = k1 x height3 + k2 x weight + k3

Therefore patient total Red Blood Cell volume (RBCv) is:

RBCv = PBV x Hct. (where Hct is Haematocrit)

Total RBCv loss = PBV x (Hct preop – Hct postop) + ml RBC transfused

The result is reconverted to Whole Blood volume.

Hidden Loss = Total Loss – Visible Loss.

In TKA, the mean total true blood loss was 1474ml. The mean hidden loss was 735ml. Therefore hidden loss is 50% of the total loss and the total true loss following TKA is twice the visible volume. In THA, the mean total true blood loss was 1629ml. The mean hidden loss was 343ml.

Thus hidden loss in THA is much smaller. (21%) Total loss is 1.3 times the visible loss. In the TKA group, comparing patients with large losses receiving reinfusion and those with small losses not receiving reinfusion, the proportion of total true loss which was hidden was the same, at 50%.

Patients with Body Mass Index (BMI) > 30 were compared with those with a BMI < 30 and no correlation was found between BMI and Hidden Loss.

Joint Replacement Surgery involves a ‘hidden’ blood loss which is not revealed and cannot be measured or reinfused in practice, but which should be taken into account when planning blood loss management. In TKA it is substantial. In THA it is much smaller and probably not of as much clinical concern. Hidden loss is no greater in the Obese patient.

Aim: To assess the functional results of revision TKR with the PFC/TC3 system, and to correlate this with the reasons for revision and restoration of joint height.

Method: One hundred and fifty three patients underwent revision TKR using the PFC/TC3 system. Data was prospectively collected (using the Bristol Knee Score) pre-operatively and at a mean of 4.2 years post-revision. Forty three revisions were for infection and 81 revisions were for aseptic loosening. Measurements of the joint height were made pre and post-operatively using Figgie’s method and were divided into three groups: lower by more than 5mm, restored and elevated more than 5mm. Use of distal augments and polyethylene thickness were recorded.

Results: The mean pre-op function score was 12 and post-operatively was 19 for the infection group and 20 for the aseptic loosening group. Revision after initial UKR gave a mean score of 21, while revision after TKR gave a mean score of 18 (max 27). Knees in which the joint line was elevated by more than 5 mm had a mean score of 17 while those where the joint line was restored had a mean score of 1 9. Recent increasing use of distal augments improved the joint line and results.

Conclusion: Revision using the PFC/TC3 system produced acceptable medium term functional results and good survival. Better restoration of joint line and functional results were achieved by distal femoral rather than proximal tibial augmentation.

Objective: To report the survivorship rate and clinical outcome of a large series of lateral unicompartmental replacements.

Method: 88 lateral St Georg Sled LTKRS were performed between 1978 and 1999. Clinical and radiological data was prospectively recorded at regular follow up and only 5 knees were lost during the 22 year period.

Results: 15 knees were revised after an average of 8 years. (eight for progressive arthritis, six for loosening and four for femoral fracture) 29 patients (30 knees) died during the course of the study. At final follow up (average 9 years) 50 of the 63 remaining knees were rated as good or excellent, nine as fair and nine poor. The mean range of flexion was 110°.

At 10 years the cumulative survival rate was 83% and at 15 years 78% (10 knees at risk). The “worst case scenario” where knees with pain or lost to follow up are added to revisions shows a 10 year survivorship of 74%.

Conclusion: Although the results are not as good as medial UKR. These clinical outcomes suggest that the conservative surgical procedure of lateral UKR with the fixed bearing St George Sled prosthesis can give acceptable results in the uncommon situation of severely symptomatic isolated lateral tibio femoral arthritis.

Purpose: To compare the ten-year survivorship results of an established total and medial compartment knee replacement performed in a single centre over an eighteen year period.

Method: Since 1978 knee replacements have been prospectively recorded in Bristol on a database. Regular clinical and radiological review has been undertaken every two or three years up to twenty years. 408 medial St Georg Unicompartmental replacements and 531 Kinematic total knee replacements have been subject to survivorship analysis using three failure end points. One - revision or removal of the implant. Two – revision or removal and moderate or severe pain. Three – the worst case including all patients lost to follow-up.

Results: The follow-up rate was 97% in both groups. 212 patients (562 knees) died and 31 patients (35 knees) were lost to follow-up. At ten years 25 medial Sled and 20 Kinematic knee arthroplasties had been revised. There was no significant difference (p > 0.05) in the number of good and excellent results. The mean range of movement at the last follow-up was 109 degrees for the medial Sled and 100 degrees for the Kinematic (p< 0.01). 94% of the medial Sled patients obtained a range of movement equal to or greater than 90 degrees whereas only 84% of Kinematic patients obtained this range (p < 0.05).

The ten-year survivorship figures were similar for both groups. Revision as the end point was 87.5% for the medial Sled and 89.6% for the Kinematic knees. When moderate and severe pain was considered in addition to revision ten-year survivorship was 79.4% in both groups. The worst case survivorship was also 74% in both groups.

Conclusion: The ten-year survivorship results of a fixed bearing, non-congruous, Unicompartmental arthroplasty are as good as those of a total knee replacement when performed in a single centre by two consultant surgeons and a variety of trainees. The advantages of a more rapid recovery and better quality result are offset by an easier though slightly higher revision rate.

We describe 88 knees (79 patients) with lateral unicompartmental osteoarthritis which had been treated by the St Georg Sled prosthesis.

At a mean follow-up of nine years (2 to 21) 15 knees had revision surgery, nine for progression of arthritis, six for loosening, four for breakage of a component and four for more than one reason. Six patients complained of moderate or severe pain at the final follow-up. Only five knees were lost to follow-up in the 21-year period.

We performed survivorship analysis on the group using revision for any cause as the endpoint. At ten years the cumulative survival rate was 83%, and at 15 years, when ten knees were still at risk, it was 74%.

Based on our clinical results and survival rate the St Georg Sled may be considered to be a suitable unicompartmental replacement for isolated lateral compartment osteoarthritis.

Purpose: This study analyses the kneeling ability of patients following Unicompartmental knee replacement (UKR), Patellofemoral replacement (PFR) and Total knee replacement (TKR).

Method: Data was prospectively collected on 272 knees (254 patients) that had undergone various forms of arthroplasty procedures for osteoarthritis of the knee. All patients completed the Oxford Knee Questionnaire preoperatively and 1 year postoperatively, thus graded their kneeling ability into one of 5 categories. Absolute values and change following arthroplasty were recorded. In addition the reported kneeling ability of 75 patients was checked by clinical examination.

Results: Preoperatively only 2% of all patients could kneel with PFR group being more able than the others (UKR 0%, TKR 0% and PFR 6%). In all groups the kneeling ability was better one year following replacement than preoperatively (23% of UKR, 18% of TKR and 9% of PFR) being able to kneel with little or no difficulty.

Conclusions: No form of arthroplasty used resulted in good kneeling ability, though this function was always improved particularly by UKR. Good range of movement and younger age appeared to correlate with better kneeling ability but many patients thought they had been told not to kneel and reported less ability than they demonstrated on examination. Instruction to avoid kneeling seems unnecessary.

Traditional dogma states that anterior knee pain in adolescence does not lead to patello-femoral arthritis. However analysis of 642 new knee referrals seen in one year showed that over 25% had anterior knee pain and that patients were of all ages. This lead to us questioning whether anterior knee pain or adolescent chondromalacia patellae is in fact a benign self limiting condition.

Method: A postal questionnaire was sent to 150 patients who had undergone isolated patello femoral replacement (PFR) enquiring about patella problems earlier in life. The same questionnaire was sent to a matched group of patients who had undergone unicompartmental replacement; because of the selection policy of the unit, these would not have had changes of patellofemoral arthritis.

Results: 118 patients who had undergone PFR retumed the form. 107 were female; the average age at surgery was 66 years. 26 (22%) reported adolescent anterior knee pain at an average age of 18. 112 forms were returned form the UKR group in which females predominated and who had an average age at surgery of 67 years. Only 7 (6%) reported adolescent anterior knee pain, at an average age of 19. 16 (14%) of the PFR group reported adolescent patella instability as opposed to 1 on the UKR group.

Discussion: The finding that significantly more patients with isolated patello-femoral arthritis had suffered from adolescent anterior knee pain suggests a possible causal relationship. Further long-term studies are needed to determine whether adolescent anterior knee pain is benign, as traditionally believed, or whether certain subsets are precursors of patello-femoral arthritis.

Aim: MRI examination of tibial tunnel enlargement after hamstring ACL surgery.

Methods and Results: 101 primary hamstring ACL reconstructions were carried out employing a transtibial over-the-top route with fixation provided by the Soffix buttonhole polyester double loop device (1186 N mean UTL to failure with young human cadaveric STG tendons). 24 were reviewed and bony tunnel enlargement was evaluated. 18 prospective reconstructions at 4 months and 6 randomly selected cases at a mean of 14 months were subjected to MRI scanning performed perpendicular to the tibial tunnel axis and the cross sectional area (CSA) was calculated with a computer programme.

In 7 cases there was no enlargement, in 5 cases there was cylindrical enlargement, in 12 cases there was conical enlargement but no cavitation was noted. A maximum mean CSA of 33% ± 38.84 sd was noted at the upper tibial tunnel exit whilst the CSA increase at the distal tibial tunnel entrance was 13% ± 16.77 sd.

In addition the MRI scan showed no evidence of excessive granulation tissue ingrowth or synovial fluid between the graft and the tunnel wall. It would appear that micro-motion which is a major factor in tunnel enlargement is eliminated by the combination of a tight fitting graft, the strength and stiffness of the fixation device and highly accurate, low stress placement of the tibial tunnel. Post operative KT 2000 arthrometric testing of the mean side to side difference (SSD) was 1.71 mm ± 1.82 sd confirming that the graft remained stiff in vivo.

Conclusion: We concluded that our technique avoids excessive tunnel enlargement and leads to greater post-operative graft stiffness than that reported in other series, where hamstring reconstruction has been employed.

We have studied the long-term outcome of 408 primary medial St George Sled unicompartmental arthroplasties of the knee and 531 primary Kinematic total knee arthroplasties using survivorship analysis. The operations were performed by a number of surgeons under the supervision of two consultants at one orthopaedic centre. Prospective clinical assessment was carried out before and at 2, 5, 8, 10, 12 and 15 years after operation. Failure was defined as follows: revision or removal of the implant; the presence of moderate or severe pain; or ‘worst-case’ with all patients lost to follow-up.

Cumulative survival rates at ten years were calculated using life tables. The follow-up rate was 97%. At ten years, 25 medial sled arthroplasties and 20 Kinematic knee arthroplasties had been revised. With revision or removal as the survivorship endpoint at ten years there was a success rate of 87.5% for the medial sled and 89.6% for the Kinematic knee arthroplasty. When moderate or severe pain was included these rates became 79.4% for both arthroplasties. There was no statistically significant (p > 0.05) difference between the rates of survival for the two arthroplasties using either of the endpoint criteria.

Good or excellent results were recorded for 77.9% of the medial sled knees and 75.1% for the Kinematic knees. The former had 93.8% of cases with a final range of movement in excess of 90° compared with 83.7% for the Kinematic knees (p < 0.01). We conclude that at a single orthopaedic centre in the UK, the St Georg Sled medial compartment arthroplasty for appropriate specific indications offers predictable survivorship at ten years which is comparable with that of the Kinematic total knee arthroplasty.

We performed a randomised, prospective trial in 111 patients with intertrochanteric fractures of the hip comparing the use of the Gotfried percutaneous compression plate (PCCP) with that of the classic hip screw (CHS). Blood loss and transfusion requirement were less in the PCCP group but the operating time was significantly longer. The complication rate after operation was similar in both groups, and at a minimum follow-up of six months there was no difference in the rates of fracture healing or implant failure. The PCCP gives results which are similar to those obtained with a conventional device. Its suggested advantages seem to be theoretical rather than practical and, being a fixed-angle implant, it is not universally applicable.

We present a prospective review of the outcome of 76 Lubinus patellofemoral arthroplasties carried out in 59 patients between 1989 and 1995. At a mean follow-up of 7.5 years, 62 knees in the 48 patients were reviewed; 11 patients (14 knees) had died. None was lost to follow-up.

The clinical outcome using the Bristol Knee Scoring system was satisfactory in 45% of the cases. Maltracking of the patella, resulting in lateral tilt, subluxation and polyethylene wear, was the most common complication (32%). Revision surgery was carried out in 21 knees (28%) giving a cumulative survival rate of 65% (confidence interval (CI) 49 to 77) at eight years. The survival rate for revision and moderate pain was 48% (CI 36 to 59) at six years. Progression of arthritis was seen in seven cases (9%). In five of these (6.5%), the symptoms were severe enough to need revision surgery. Due to the high proportion of unsatisfactory results, we have discontinued the use of this prosthesis.