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Sub-vastus approach versus the medial parapatellar approach in primary total knee: a randomised controlled trial [ISRCTN44544446]

机译:初次全膝总管下入路与内侧para骨旁入路:一项随机对照试验[ISRCTN44544446]

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Background Thirty thousand knee replacements are performed annually in the UK. There is uncertainty as to the best surgical approach to the knee joint for knee arthroplasty. We planned a randomised controlled trial to compare a standard medial parapatellar arthrotomy with sub-vastus arthrotomy for patients undergoing primary total knee arthroplasty in terms of short and long term knee function. Methods Patients undergoing primary total knee arthroplasty at the local NHS Trust are to be recruited into the study. Patients are to be randomised into either the subvastus or medial parapatellar approache to knee arthroplasty. The primary outcome measures will be the American Knee Society and WOMAC Scores. The secondary outcome measures will be patient based measures of EuroQol and SF-36. All outcomes will be measured pre-operatively, 1, 6, 12 and 52 weeks post-operatively. We will also review pain intensity using a pain and analgesia diary. Ease of surgical exposure and complications will also be analysed. Discussion Evidence is lacking concerning the best surgical approach to the knee joint for patients undergoing primary total knee replacement. This pragmatic randomised trial tests the hypothesis that the sub-vastus approach is significantly superior to the standard medial parapatellar approach in terms of short and long term knee function.
机译:背景技术英国每年进行三万次膝关节置换手术。膝关节置换术的最佳膝关节手术方法尚不确定。我们计划进行一项随机对照试验,以比较标准的内侧para副关节切开术和输精管下切开术在短期和长期膝关节功能方面对初次全膝关节置换术的患者的疗效。方法应在当地NHS Trust进行初次全膝关节置换术的患者入选本研究。患者将被随机分为膝关节置换术的vas下或内侧para旁入路。主要结果指标将是美国膝关节学会和WOMAC评分。次要结果指标是基于患者的EuroQol和SF-36指标。所有结果将在术前,术后1、6、12和52周进行测量。我们还将使用疼痛和止痛日记来回顾疼痛强度。还将分析手术暴露的难易程度和并发症。讨论缺乏关于进行一次全膝置换的患者最佳的膝关节手术方法的证据。这项实用的随机试验检验了以下假设:就短期和长期膝关节功能而言,输精管下入路明显优于标准内侧para上入路。

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