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.

The aim of this prospective study is to investigate the effectiveness of a new method for arthroscopic all-inside meniscus repair (Clearfix meniscal screw system-Innovasive Devices Inc.).This system consists of delivery cannulae,screw implants and a screw driver.After tear debridement a screw is located on the driver and passed through the cannula to the insertion site, holding the two sides of the tear together under linear compression.In this study, 46 patients (48 repairs)are included, mean age 32,7 years,with a follow-up ranging from 6 to 48 months (average 18,8 months).Only longitudinal lesions in the red/red zone or red/white areas were repaired. Ligament stabilizing procedures were done in 39 patients (84,8%) who had ACL deficient knees,.Thirty-four (71%) injuries were considered chronic (injury to repair time more than 4 weeks) and 14 (29%) injuries were considered acute (injury to repair time less than 4 weeks).The evaluation of the results was based on the clinical examination,the “OAK ” knee evaluation scheme and the MRI.Criteria for clinical success included absence of joimt line tenderness, swelling and a negative Mc Murray test.Thirteen out of 48 repairs (27%) were considered as failures according to the above mentioned criteria.The average time for the procedure was 8 minutes.Postoperatively there were no complications directly associated with the device.Magnetic resonance imaging, however,showed a persisting grade III and IV lesion in 72,8% of the patients (n=35) according to Reicher classification.

Though the system offers two main advantages,that is the absence of serious complications and the reduced operative time, the failure rate in this study is quite high. This clinical study is in agreement with the recent experimental studies referring to the limited pull-out strength of this device.

Removal of well-fixed, cementless, acetabular components during revision arthroplasty remains a challenging problem. Further damage to host bone may limit options for reconstruction and compromise the long-term result of the revision operation. We report the results of 31 hips with well-fixed, cementless sockets which were removed using a new cup extraction system. In all hips the socket was removed without difficulty and with minimal further bone loss.

Purposes of the study and background: This study tests the hypothesis that it is possible to visualise the cervical spine musculature using ultrasound. The use of diagnostic ultrasound is well established for assessing other anatomical regions; whereas the cervical spine has received little attention. Other available imaging procedures can be resource intensive with recognized risks and do not give an indication of structural detail. Ultrasound has the potential to resolve these inadequacies and would therefore be appealing.

Summary of the methods and the results: 10 healthy volunteers (age range: 21–36 years, 6 females, 4 males) were evaluated using a 8-16MHz linear array transducer (Diasus Dynamic Imaging, UK) and a 16MHz CL15-7 linear array scanhead transducer (Phillips ATL HDI 5000 SonoCT, Netherlands). Subjects were seated with their neck in a neutral position. The transducer was orientated transversely, and initially placed on the thyroid cartilage. Successive images were taken as the transducer was moved laterally across the anterior triangle, over the sternocleidomastoid, into the posterior triangle, ending in the posterior midline. Landmarks, with characteristic ultrasonic appearances, were identified to aid orientation e.g. carotid artery. Both machines produced images that clearly displayed the musculature of the cervical spine. Composite images were obtained of the anterior and posterior aspects of the neck (Figure 1) to provide information regarding the spatial orientation and relationship between the muscles.

Conclusion: This study concludes that modern ultrasound equipment provides cervical spine soft tissue images of a quality suitable for diagnostic applications. It also has the advantages of being a risk free, economic and portable procedure.

Purposes of the study and background: Diagnostic interventional procedures are often performed on patients who suffer from cervical facet joint pain and discogenic pain emanating from the cervical region. These procedures require radiographic imaging to confirm placement of instruments e.g. needles. However, these techniques are unable to provide real-time images hence prolonging the intervention. It would be of benefit to have an imaging tool that is capable of visualising needle insertion in real-time whilst preventing side effects. The purpose of this study was to determine the ultrasonic appearance of cervical facet joints in vivo and describe a standardized transducer position to visualise intervertebral discs and facet joints.

Summary of the methods and the results: 10 healthy volunteers (age range: 21–36 years, 6 females, 4 males) were evaluated using an 8-16MHz linear array transducer (Diasus Dynamic Imaging). Subjects were scanned in a prone, lateral position. The transducer was placed in the posterior triangle orientated longitudinally, initially along the posterior border of sternocleidomastoid and then moved in a cranial-caudal direction. By adjusting the angle (in the antero-posterior direction) of the transducer about a fixed position; facet joints and discs were located. The characteristic V shaped appearance of the facet joint emanates from the hyperechoic signal of the closely spaced transverse processes of adjacent vertebra (Figure1). Disc regions appeared as areas of high signal penetration into the spine with low amplitude signals returning from the disc.

Conclusion: The detail of facet joint and disc anatomy captured using ultrasound reveal it to be a viable imaging tool for interventional procedures. Noteworthy advantages of ultrasound include: its ability to provide real-time images economically, the option of portability and no known side effects.

There is a recognised incidence of anterior knee pain following Anterior Cruciate Ligament (ACL) reconstruction using a patella tendon autograft.

This study examined two group of patients both pre ACL ligament reconstruction and post ACL reconstruction using patella tendon grafts to define if anterior knee pain is a result of patella tendon harvest or a primary consequence of an ACL injury.

The two groups of patients were best matched for age, sex and physical activity.

The pre-operative group of twenty-five patients had a confirmed ACL rupture and exhibited symptoms of instability requiring an ACL reconstruction.

The operative group of twenty-five patients were a minimum of a year post operation.

The graft was harvested by an open procedure and the graft bone blocks were secured with interference screws.

The patients’ anterior knee pain score was assessed using the Shelbourne scoring system that evaluates knee function in relation to anterior knee pain using five parameters. The maximum score is 100.

The scores were compared using the unpaired student test.

There was no significant age difference between the two groups, preoperative group age 32. 2 years (range 22 to 46) and postoperative age 34. 8years (range 19 to 48).

The mean anterior knee pain score for the preoperative group was 71. 6 (49 to 100), the postoperative group was 77. 7 (45 to 100), this was not significantly different.

We found no significant difference in knee function due to anterior knee pain between the two groups. Studies have shown significant anterior knee pain following hamstring reconstruction (Spicer).

This study shows anterior knee pain in the ACL deficient knee is present prior to surgery.

We conclude that patella tendon autografts produce no significant incidence of anterior knee pain post surgery.

The purpose of this retrospective study was to analyze the indications for spinal instrumentation, report the clinical features, operative details and outcome in 16 patients with active pyogenic spinal infection.

Between January 1991 to October 1999, 81 patients with spontaneous pyogenic spinal infection were treated at the authors’ institution. Surgery (other than biopsy) was indicated in 24 patients for neurological deterioration, deformity or instability. Sixteen of these patients were treated with instrumentation in the presence of active spinal infection. Six patients underwent combined anterior and posterior procedures. 10 had a posterior procedure only. Outcomes assessed were control of infection, neurology, fusion, back pain and complications.

At a mean follow up period of 26. 9 months, all surviving patients were free of clinical infection. None of the patients had neurological deterioration. All patients who had neurological deficit preoperatively improved by at least one Frankel grade. A solid fusion was achieved in 15 patients. 12/15 patients remained asymptomatic or had very little pain. The remaining 3 patients had mild to moderate back pain. The mean correction of the kyphotic deformity was 18. 92 degrees. Postoperative complications included bronchopneumonia, nonfatal pulmonary embolism and seizures in 3 patients. One patient developed progressive kyphosis despite instrumentation but eventually fused in kyphus.

Given early recognition of pyogenic spinal infection, most cases can be managed non-operatively. Our results support that instrumented fusion with or without decompression may be used safely when indicated without the risk of recurrence of infection. Instrumentation facilitates nursing care and allows early mobilisation. For biomechanical reasons, a combined procedure is probably indicated for lesions above the conus. For lesions below the conus, we were able to achieve successful results with posterior approach only.

We have performed a study comparing the radiological results of Total hip replacements performed by a single, experienced specialist hip surgeon with those reported from the Trent Regional Arthroplasty Study (TRAS) [presented at BOA congress 2000]. Results from TRAS have revealed that inadequate cementation grades and a cement mantle width of < 2mm were the most significant associations predicting early aseptic loosening. Interestingly, their respective incidences were as large as 20% and 50% in a random sample of THRs from the TRAS register.

Data is lacking as to whether poorer radiographic cementation grades have a trend towards individual surgeons or whether they are more evenly distributed amongst the surgical population including those adhering to modem techniques.

Therefore, we have undertaken an independent review of A-P and lateral radiographs of 33 consecutive Charnley THRs performed by a specialist hip surgeon using carefully controlled modem cementing techniques and compared the results with the same random cohort of THRs from the TRAS.

Our results show that the specialist surgeon achieved a significantly higher proportion (82%) of complete cement mantles (> 2mm in all zones) than those achieved by TRAS (50%) [Chi²=7. 79, p=0. 0052]. This suggests that improved cement mantles can be achieved by the adoption of carefully controlled modem cementing techniques. However, use of the Barrack system of grading was unable to detect differences in cementation quality between specialist (88%) and TRAS group (81%) [Chi²=0. 235; p=0. 631 suggesting less sensitivity in this technique for assessing cementation quality. These results are important for the following reasons. Achievement of adequate mantle (> 2mm) can be improved upon by adoption of carefully controlled modem cementing technique. However, regardless of the method of assessment of cementation quality, approximately 18% will appear ‘inadequate’ despite modern techniques suggesting that factors outside the surgeon’s control are involved in determining cementation grade. This has important medico-legal implication in the current climate in which surgeons are being criticised, in negligence cases arising out of the 3M Capital Hip experience, for achieving ‘inadequate’ cementation.

Aims: To determine which radiological features were most significant in aseptic loosening (AL) of Charnley total hip replacement (THR) and to compare the prevalence of these features between a specialist hip surgeon and those from the general setting. Method: An analysis was performed of the initial post-operative radiographs of three groups of Charnley femoral stems: I: Failed stems within 5 years due to AL, as registered in the Trent Regional Arthroplasty Study (TRAS). II: 44 consecutive Charnley THRs performed by a single, ‘specialist’ hip surgeon. III Controls: A randomly selected cohort group from the TRAS (proven to be clinically and radiologically intact at 5 years). Results: The most significant radiographic features of failure were: (i) mantle width < 2mm in any zone giving an odds ratio of 21.0 for failure (CI 3.3 to∞; p< 0.05); (ii) “inadequate” cementation grade (Barrack grades C and D) giving an odds ratio of 9.5 for failure (CI 3.2 to 28; p< 0.05). The specialist hip surgeon achieved a significantly higher proportion (79.5%) of complete cement mantles (> 2mm) than the controls (50%) (Chi^2 = 9.455, df = 1, p=0.002). There were also a higher proportion of adequate cementation grades (88.6% vs 82%) although this difference was not significant (Chi^2= 0.947, df = 1, p=0.330). Conclusion: We have demonstrated features identified on radiographs of Charnley femoral stems predictive of failure. In our study a specialist hip surgeon achieved fewer flaws than those detected across a regional ‘average’. This suggests surgical technique can influence radiological results and thus outcome. This needs to be emphasized, particularly during training, in the hope of improving overall results in the future. However, even a specialist’s cementation appeared inadequate in 11.4% of cases, suggesting that factors outside the surgeon’s control, influence cement grading. This is important from a medico-legal standpoint because surgeons are being criticised for not achieving adequate cementation in negligence cases.

The corticosteriods in the treatment of Duchenne’s or Becker’s muscular dystrophies causes muscular weakness and osteoporosis characteristic of these patients and result in different fractures which are of difficult resolution because prolonged immobilization increases morbidity. How can this problem be solved in highly risk patients? The diverse models of external fixators have given us the possibility of treating them without immobilization and in consequence obtain a quicker return to previous functional status including gait .

4 patients with Duchenne’s and Becker’s muscular dystrophies were treated. 1 patient recovered its ambulatory ability and the rest maintain their gait. 1 of them still has an external fixator but he is able to walk. Patients presented a diaphyseal fracture of the femur, a proximal fracture of the tibia, an introchanteric fracture of the hip and a supracondylar fracture of the femur.

We consider that external fixators open an endless range of options, not very much used until recently, that help our patients to extend their functional status and gait. Patients accept them easily because they give them independence and avoid the depression that stems from the loss of capabilities.

Objective: To assess the validity of the Tokuhashi and Tomita scoring systems in the prediction of prognosis following spinal surgery for skeletal metastases.

Design: A retrospective cohort study of patients treated in a specialist spinal unit

Subjects: All patients undergoing definitive surgery for metastastes of the spine were considered eligible. Time to death or current length of survival was available in 147* of these which was confirmed by the Cancer Registry. Medical and nursing case notes were reviewed and prognostic scores using the methods of Tokuhashi et al, and Tomita et al. were calculated for each patient.

*

death data for further patients currently awaited from Cancer Registry.

Outcome measures: Mean survival period with 95% confidence intervals for patients grouped according to prognostic score.

Results: Thirty-two patients were still alive and 113 had confirmed death dates. Forty-three patients had Tokuhashi scores of 9 or greater with a mean survival of 20.1 months (95% confidence interval 5.8 months) compared to 9.5 months (2.9 months) for scores 6–8 and 3.5 months (1.8 months) for scores below this. Tomita scoring showed a similar trend with those with better prognostic profiles but without the same degree of statistical significance. The overall 30-day mortality was 8.2% with no significant difference between any other groups.

Conclusion: In patients presenting with metastatic disease involving the spine, published prognostic profiles offer some guidance to likely survival of the patient and so the appropriateness of surgical treatment.

Aim: We conducted a prospective, randomised study of 50 patients, 40 (80%) male and 10 (20%) female, with anterior cruciate ligament (ACL) rupture to compare the results of ligament reconstruction by middle third patellar tendon graft (M) or synthetic Leeds-Keio (LK) ligament.

Method: The patients were randomised into two groups. 26 (52%) underwent PTG repair and 24 (48%) LK repair. Subjective knee function was classified using the Lysholm score, Tegner activity score and IKDC grading. Laxity was tested by clinical examination including anterior draw, pivot shift and arthrometric measurements using the Stryker Laxometer (Stryker Corporation, Kalamazoo, Michigan, USA).

Results: We present the early (two to five-year follow-up) results of this on-going trial. There was no statistical difference between the two groups in activity levels, both pre-injury and current. However, both pivot shift and anterior laxity were significantly greater in the LK group at two years and greater.

Discussion: While the LK group did develop significantly greater laxity, it is demonstrated that the functional outcome is not affected. We conclude therefore that if the results of surgery were to be based on a functional outcome rather than objective measurements of laxity, it would seem logical that the LK is an acceptable alternative to autogenous PTG.

However whilst function appears to be as good the less successful objective criteria do suggest reservations for the long term results of the Leeds-keio graft.

Objective: To measure intradiscal pressures in scoliotic spines to further understand the role of mechanical forces in the development of scoliosis.

Design: Pressure readings were obtained in consented patients with ethical approval. A needle mounted pressure transducer was introduced into the disc during routine anterior scoliosis surgery.

Subjects: Ten human scoliotic discs from three patients.

Outcome measures: Intradiscal pressure profiles.

Results: Nuclear hydrostatic pressures varied from 0.2 to 0.6 MPa. The mean nuclear pressures for the three spines were 0.27+0.12, 0.35+0.06 and 0.47+0.12 MPa.

High stress, non- hydrostatic regions were consistently recorded in the concave annulus.

Conclusions: Nuclear pressures in these scoliotic patients were significantly higher than the 0.12 and 0.15 MPa recorded previously in non-scoliotic recumbent individuals^1;2 suggesting that spinal loading is abnormal in scoliosis.

Introduction: The progress of post tubeculous kyphosis in children during ‘growth spurt’ is unpredictable and has not been clearly documented in literature.

Methods: The progression of deformity in 63 children treated conservatively and belonging to a controlled clinical trial was studied over 15 years.

Results: The average Kyphosis increased from 35.2 degrees to 41.3 degrees in the ‘Active Stage’ (Phase I), there was an increase in all patients. In the ‘Healed stage’ (Phase II), a variable progress continued which was more prominent during the ‘growth spurt’. In Type I, there was a worsening which occured either continuously (Type 1a; n=19.30%), or suddently after a gap of few years (Type 1b;n=6.9%). In Type II, an improvement occured either after an initial increase or a plateau (Type IIa; n=18.29%), or continuously after disease cure (Type IIb; n=9.15%). In Type III, the deformity was static (n=11.17%). The average increase in Type Ia was 24.2 degrees, Type IIb was 20;5 degrees, Type Ib was 58.4 degrees; the decrease in Type IIa was 4.9 degrees, Type IIb was 20.5 degrees and the decrease in Type III was 1.7 degrees. Overall, the growth spurt sresulted in an increase in deformity in 25 (39%) children, a decrease in 27 (44%) and no change in 11 (17%).

Conclusion:

Post-tuberculous kyphosis in children is a ‘Dynamic deformity’ which changes till skeletal maturity.

Many factors have been demonstrated to influence the range of knee movement that an individual can achieve.

The purpose of this study was to objectively demonstrate how range of knee movement is affected when the influence of pain is abolished.

Sixty-eight patients with degenerative joint disease presenting for primary total knee arthroplasty were recruited. Using a digital camera, images were taken before and after the induction of anaesthesia with the lower limb in four positions- extension, forced extension, flexion and forced flexion. Camera set up was standard and the range of knee motion was measured from the digital images.

Average arc of motion before anaesthesia was 96° (range, 41°–157°). After induction of anaesthesia, the arc of motion increased to 115° (range, 410–161°). Knee extension improved by an average of 5° (range, 0–15°) and flexion improved by an average of 16° (range, 0–65°).

In conclusion, these results demonstrate that pain has a significant inhibitory effect on the measured range of knee movement before surgical intervention.

Dislocation of the polyethylene-rotating platform is a recognised complication of LCS knee arthroplasty.

We report ten cases of rotating platform dislocation out of 2151 primary total knee arthroplasties (0.5%) performed to date in our unit.

Of the ten cases (3 male: 7 female), six patients had a preoperative valgus deformity, two had a varus deformity and the remaining two patients were in neutral alignment, although the wear was predominantly within the lateral compartment. Two patients also had a previous patellectomy on the side of the platform spinout.

Of the ten cases, six patients were symptomatic as a result of their platform dislocation. The remaining four patients were asymptomatic and mobilising without any difficulty. In these patients, the dislocated platform was diagnosed on x-ray at outpatient review. Time to detection of the platform dislocation ranged from six days to two years.

Three patients required revision of their original insert to a larger, deeper dish insert. Three were managed by open reduction of the original insert. Of the remaining patients, one was managed successfully by closed reduction, one required an arthrodesis and one had the tibial insert cemented to the tibial tray. All patients at latest review have a functional and stable knee joint.

In conclusion, we feel that surgical error was to blame for the majority of our ten cases. Furthermore, we emphasise the importance of producing equal and balanced flexion and extension gaps at the time of knee arthroplasty in order to prevent mobile bearing dislocation. A novel technique for reducing a dislocated rotating platform is also described.

The aim of this trial was to assess the clinical examination findings commonly used for the ACL deficient knee.

For reliability testing and criterion validation 102 patients with ACL injuries were assessed by a single observer, 35 by a second observer and 47 again by the initial observer. For construct and criterion validation 30 patients were assessed pre-operatively and a mean of 1.7 years after ACL reconstruction. The Lysholm 11, Tegner and Cincinnati outcome measures were assessed along with instrumented knee laxity (Stryker test), the one hop test (OHT) and graded tests (including anterior draw, Lachman test, quality of end point, and pivot shift test).

The outcome measures were found to be reliable except the Cincinnati system. All examination findings were of unsatisfactory reliability, with the exception of the OHT and the Stryker test. Construct validation revealed a significant improvement in all outcome measure scores and examination findings following ACL reconstruction. Criterion validation revealed that of the examination findings only the OHT had a satisfactory correlation with the symptom of giving way and the Lysholm/Tegner measures. Comparison of the difference between the desired and actual Tegner activity levels with the examination findings revealed an improvement in all levels of correlation.

With the exception of the OHT, the clinical examination findings used for the ACL deficient knee are unreliable and correlate poorly with the functional outcome of the patient. They may, however, have some benefit in assessment of deficiency of the anatomical structures and the findings should be presented individually, rather than forming part of the functional assessment of the patient.

The aim of this randomised prospective study was to establish whether the use of knee splints following total knee replacement is necessary.

The study included 81 patients undergoing total knee replacement who were randomised into a ‘splint’ and a ‘no splint’ group postoperatively. Patients in the ‘splint’ group had their knee splinted in extension in the early post-operative period but the splint was removed for the patients to do exercise. Splintage was completely removed when the patient could straight leg raise. Patients in the ‘no splint’ group had a wool and crepe bandage applied around their knee and allowed to fully mobilise from the first postoperative day. The following parameters were recorded: The range of movement preoperatively, 5 days post-operatively and 6 weeks postoperatively; the length of time to straight leg raise; the blood drained from the wound. and the amount of postoperative analgesia required.

Using the unpaired 2 tailed t-test it was found that patients in the four ‘no splint’ group achieved significantly greater flexion at 5 days and 6 weeks post-operatively but drained significantly more blood from the wound. Transfusion requirements were similar in the two groups. There was no other significant difference in the parameters measured between the two groups.

In conclusion we found no evidence to advocate the use of knee splints following total knee arthroplasty.