To investigate the proprioceptive function of patients with an ACL rupture before and after reconstruction and correlate these findings with ligament laxity testing and clinical outcome measures. Fifty patients with an ACL rupture and 50 normal controls were recruited to the study. The Biodex Balance SD System was used to assess knee proprioception. This equipment measures proprioceptive function using an electronic platform. The balance of the subject is computed using stabilometry and an Overall Stability Index (OSI) is produced. A lower score reflects better proprioception. Knee stability was assessed clinically and with the Rolimeter knee arthrometer in all subjects. Participants were evaluated using the Tegner, Lysholm, Cincinnati and IKDC scoring systems. In the ACL group, 34 patients underwent ACL reconstruction and returned for their follow-up review 3 months post-operatively. The proprioceptive function of the injured knee of the ACL group (mean OSI 0.70) was significantly poorer compared to that of their uninjured knee (mean OSI 0.46, p<0.001, 95%CI 0.14, 0.34) and to the Normal Control group (mean OSI 0.49, p=0.01, 95%CI 0.05, 0.38). There was a significant improvement in proprioception of the injured knee following ACL reconstruction (mean OSI 0.47, p=0.003, 95%CI 0.10, 0.42). A significant correlation was found between pre-operative proprioception measurements and all the pre-operative knee outcome scores, however this correlation was not found post-operatively. No correlation was found between ligament laxity testing and either proprioception measurements or knee outcome scores.Purpose of Study
Summary of Methods and Results
The aim of this study was to compare immediate weight-bearing mobilisation with traditional plaster casting in the rehabilitation of non-operatively treated Achilles tendon ruptures. Forty-eight patients with Achilles tendon rupture were randomised into two groups. The treatment group was fitted with an off-the-shelf carbon-fibre orthotic and the patients were mobilised with immediate full weight-bearing. The control group was immobilised in traditional serial equinus plaster casts. The heel raise within the orthotic and the equinus position of the cast was reduced over a period of eight weeks and then the orthotic or cast was removed. Each patient followed the same rehabilitation protocol. The primary outcome measure was return to the patient's normal activity level as defined by the patient. There was no statistical difference between the groups in terms of return to normal work [p=0.37] and sporting activity [p=0.63]. Nor was there any difference in terms of return to normal walking and stair climbing. There was weak evidence for improved early function in the treatment group. There was 1 re-rupture of the tendon in each group and a further failure of healing in the control group. One patient in the control group died from a fatal pulmonary embolism secondary to a DVT in the ipsilateral leg. Immediate weight-bearing mobilisation provides practical and functional advantages to patients treated non-operatively after Achilles tendon rupture. However, this study provides only weak evidence of faster rehabilitation.
There has been very little documented regarding the impact of meniscal injuries on knee proprioception. The aim of this study was to investigate the proprioceptive function of patients with meniscal tears and asses the influence that arthroscopic partial menisectomy has on knee proprioception. One hundred subjects were recruited comprising an Arthroscopy group (50 patients) and a Normal Control group (50 subjects). The Biodex Balance SD System was used to assess proprioception. This equipment measures knee proprioception on an electronic platform. The balance of the subject is computed producing an Overall Stability Index (OSI). Lower scores reflect better proprioception. Knee stability was assessed clinically and with the Rolimeter knee arthrometer. The Lysholm and IKDC scoring systems were used to evaluate all the subjects. Of the 50 subjects within the Arthroscopy group (all of whom had a normal ACL confirmed) 34 were found to have meniscal tears. Twenty-nine of the 34 patients with meniscal tears returned for their follow-up review 3 months post-operatively. The proprioceptive function of the injured knee of the Arthroscopy group with meniscal tears (mean OSI 0.86) was significantly poorer compared to that of their uninjured knee (mean OSI 0.62, p<
0.001, 95%CI 0.14, 0.34) and to the Normal Control group (mean OSI 0.49, p<
0.001, 95%CI 0.21, 0.54). There was no significant improvement in their proprioceptive function following menisectomy (mean OSI 0.75, p=0.23, 95%CI −0.07, 0.28). There was a significant improvement of both the Lysholm (p=0.004) and IKDC (p=0.021) scores postoperatively.
We performed two independent randomised controlled trials to assess the potential benefits of immediate weight-bearing mobilisation for Achilles tendon ruptures. The first trial on surgically treated patients provides strong evidence of improved functional outcome for patients mobilised fully weight-bearing after operative repair of their Achilles tendon rupture. The two cases of re-rupture in the treatment group suggest that careful patient selection may be required as patients need to follow a structured rehabilitation regime. The second trial performed upon non-operatively treated patients provides only weak evidence of a functional benefit from immediate weight-bearing mobilisation. However, the practical advantages of immediate weight-bearing did not predispose the patients to a higher complication rate. In particular there was no evidence of tendon lengthening or a higher re-rupture rate. We would therefore advocate the use of immediate weight-bearing mobilisation for the rehabilitation of all patients with rupture of the Achilles tendon.
The aim of this study was to test the efficacy of shock-wave therapy for chronic Achilles pain. Forty-nine patients with Achilles tendon pain for a minimum of 4 months were included in the study. Patients were randomised to either shockwave therapy (n=27) or placebo control (n=22). The treatment group were given 2000 shocks at up to 1500 mJ/mm2 per shock. The control (sham) treatment was applied using the same parametres but the shockwaves were dispersed before they reached the patient. Each patient was treated once a month over 3 months. The primary outcome measure was pain on walking indicated on a 100mm visual analogue score (VAS) at 3 months. The walking pain scores were very similar at baseline between the two groups. In the treatment group the mean (standard deviation) was 55.5 mm (30.6) and in the control group 55.6mm (26.5). By 3 months, the pain scores had reduced in both groups to a mean (standard deviation) of 34.5 mm (34.2) and 50.3 mm (36.3). Although lower in the treatment group this difference was not statistically significant at the 5% level (t-test, p=0.127, 95% CI : −4.7 to 36.2). Two elderly patients in the treatment group sustained spontaneous rupture of the tendon after falls during the course of the trial. The results of this trial provided no evidence for the use of shockwave therapy in the treatment of patients with chronic Achilles tendinopathy. However, a treatment effect cannot be ruled out since the 95% confidence interval included a potential clinically relevant difference. The two cases of rupture suggest extreme caution in treating the elderly.
Return to sport was 39.0 (18.0 to 60.0) in the treatment group and 26.0 (40.0 to 90.0) in the control group, p = 0.341. Return to normal walking was 12.0 (10.0 to 18.0) in the treatment group and 18.0 (18.0 to 22.0) in the control group, p <
0.001. Return to stair climbing was 13.0 (10.0 to 15.0) in the treatment group and 22.0 (18.0 to 22.0) in the control group, p <
0.001. Return to work was 9.0 (2.0 to 9.0) in the treatment group and 4.0 (1.0 to 13.0) in the control group, p = 0.984. There were 2 re-ruptures of the tendon in the treatment group. One occurred when the patient slipped on ice whilst wearing the orthotic. The other whilst running 3 months after the initial injury. One patient who had an augmented tendon repair and then plaster casting, required plastic surgery for a major wound complication. In addition, there were 8 minor wound-related complications in the control group and 6 in the treatment group.
Acute Achilles tendon pain is a common clinical entity, particularly in sportsmen and women. Fortunately, the majority of such pain is self limiting. However, there are a significant number of people for whom the pain becomes chronic and debilitating. A recent Cochrane review found that there was no randomised controlled evidence of an effective treatment for chronic Achilles pain. The aim of this study was to test the efficacy of shockwave therapy in a double-blind randomised controlled trial. The study has the approval of Local Research Ethics Committees. Forty nine patients with Achilles tendon pain for a minimum of 4 months were included in the study. Patients were randomised to either shockwave therapy (n=27) or sham dose control therapy (n=22). Ultrasound was used to focus the shocks onto the affected area of tendon. The treatment group were given 2000 shocks at upto 1500mJ per shock, titrated to the patients pain tolerance. The control (sham) treatment was applied using the same parametres but with bubble-wrap interposition between the shockwave generator and the Achilles, to disperse the shockwaves. Each patient was treated once a month over 3 months. Primary outcome measure was pain on walking indicated on a 100mm visual analogue score (VAS) at 3 months. Secondary outcome measures included clinical and patient centred questionnaire scores. . An intention-to-treat approach was used for the analysis. Where patients had missing pain scores at 3 month follow-up, the last available pain score was carried forward. The walking pain scores were very similar at baseline between the two groups. In the treatment group the mean (standard deviation) was 55.5mm (30.6) and in the control group 55.6mm (26.5). By 3 months, the pain scores had reduced in both groups to a mean (standard deviation) of 34.5 mm (34.2) and 50.3 mm (36.3). Although lower in the treatment group this difference was not statistically significant at the 5% level (t-test, p = 0.127, 95% C.I. : −4.7 to 36.2). No statistically significant differences were found with respect to any of the other clinical variables. Two elderly patients in the treatment group sustained spontaneous rupture of the tendon after falls, during the course of the trial. The results of this trial provided no evidence for the use of shockwave therapy in the treatment of patients with chronic Achilles tendinopathy. However, a treatment effect cannot be ruled out since the 95% confidence interval was wide and included a potential clinically relevant difference. The 2 cases of rupture suggest extreme caution in treating the elderly.
Anterior knee pain attributable to the patellofemoral joint and extensor mechanism dysplasia is a common presentation to Orthopaedic surgeons. Plain radiology is likely to remain the primary investigation of the knee in most centres, but most of the radiological features of extensor mechanism dysplasia are time consuming and difficult to measure reproducibly. 137 consecutive symptomatic knees aged under 30, referred to an Orthopaedic surgeon were studied in order to identify a rapid and reproducible marker for those knees worthy of further in-depth analysis. Overall, 67 knees (49%) had at least one radiological abnormality and 70 (51%) were considered ‘normal’. There were 5 Dejour Type3 dysplasias of the femoral trochlea, 9 Type2 and 12 Type1. There were 49 cases of patella alta and 5 of patella infera. Four knees had an abnormal lateral patellofemoral (patellar tilt) angle. 15 knees had more than one abnormality. The classification of trochlear dysplasia was difficult and showed poor reproducibility. This was also true for the measurement of lateral patellofemoral angles. Patellar height was more easily measured but took time. The sulcus angle emerged as an easily and rapidly measurable feature that was reproducible and was closely related to the other features of extensor mechanism dysplasia. The sulcus angle offers a rapid and reliable ‘screening’ measurement on knee radiographs. A normal sulcus angle suggests that seeking the other radiological markers of extensor mechanism malalignment is unlikely to reveal additional useful information. Other diagnoses can then be sought. The more abnormal the sulcus angle, the more severe the other features of extensor mechanism dysplasia are likely to be. Further detailed measurements can then help to define the most appropriate surgical correction.
A prospective clinical investigation to determine the optimum knee flexion angle for the ‘skyline’ patellofemoral joint radiograph. Plain radiography of the patello-femoral joint includes the axial or ‘skyline’ radiograph. The optimum knee flexion angle for making this image remains unclear. We therefore performed a prospective clinical study in which patients underwent three skyline radiographs with knee flexion angles of 30(or minimal flexion), 50 and 90 degrees. The patients were new patients, aged between 12 and 30, presenting to a knee clinic with anterior knee pain. Two observers evaluated the radiographs, making a standardised series of measurements. Blinding was organised so that the observers were unable to use any information other than the radiographic image alone. One observer evaluated all the films on two separate occasions to allow calculation of intra- and interassessor agreement. There were 67 knees from 46 patients. There was a high level of intra- and inter-observer agreement. There were a number of patients in which the radiographic appearance of the patello-femoral varied markedly between the different views; in all cases the abnormality was best demonstrated by the 30-degree view. There were however a number of minimal flexion views in which the film contained incomplete information because part of the patello-femoral joint was missing from the image. We conclude that whilst a minimal flexion skyline view is the most sensitive method for the detection of patellar tilt and subluxation, not all knees can be successfully imaged at the required position. A flexible approach is therefore needed, to obtain satisfactory images at minimal flexion.
The positioning of components in knee replacement is related to outcome and for this reason a study has been conducted to compare the exact position of the tibial and femoral components in total knee arthroplasty with the placement as judged by the surgeon at the time of operation. Operating surgeons of a range of grades completed a pro-forma immediately after operating on 25 patients having total knee replacement. Patients were entered into the study by consent providing that they had osteoarthritis and this was their first ever lower limb joint replacement. The form detailed where the surgeon considered he had placed the femoral component in the coronal plane and in terms of rotation upon the femur. They were asked to state what lines or angles of reference they had used and whether they had used intra or extra medullary jigs. Likewise for the tibia, implant position was detailed for coronal, sagittal and transverse planes. The proforma stated the grade of operating surgeon but were otherwise kept anonymous. All study patients had pre and postoperative CT scans. These involved an AP scannogram and transverse sections, according to a protocol, through the femoral neck, femoral condyles, tibial plateau and ankle. By comparing bony landmarks seen on the pre-operative CT scans with lines of reference from the components post-operatively the exact position of the implant was determined in the transverse and coronal planes. For the sagittal plane (slope) the standard lateral X-ray was used. For the femur all operations were carried out using intra-medullary jigs. For the femoral component the difference was not significant between the measured position and the surgeons estimate in any plane (p=0.937 for coronal and p=0.432 for transverse). The measured position of the component was not related to the grade of the operating surgeon nor to the axis nor technique of reference used. For the tibial component, coronal alignment was significantly different (p=0.001) with the measured position being in more varus than was estimated. The range of transverse placement was from 4° of external rotation to 35° of internal rotation of the tibial prosthesis with reference to the tibial tubercle centre. This was significantly different to that estimated by the surgeon (p<
0.001). Estimation of slope in the sagittal plane was good. None of these differences were related to operator grade. For 15 of the TKR’s the tibail component was aligned using intra-medullary techniques. This was related to the accuracy of positioning of the prosthesis with significantly better estimation compared to those in which extra-medulary jigs had been used (p=0.002 for the transverse plane and p=0.065 for the coronal plane). This study has demonstarted that surgeons are able to accurately judge the position of insertion of the femoral component in total knee replacement. Surgeons are poor at estimating the position of the tibial component in the transverse and coronal planes but better in the sagittal plane. Due to the difficulty in its assessment rotational alignment has been ignored in arthroplasty but as with alignment in the other planes it is likely to have a bearing on outcome. Improved techniques to help us judge placement of knee components are needed.