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全踝关节置换术与关节融合术(TARVA):一项多中心随机对照试验方案

Total ankle replacement versus arthrodesis (TARVA): protocol for a multicentre randomised controlled trial.

作者信息

Goldberg Andrew J, Zaidi Razi, Thomson Claire, Doré Caroline J, Skene Simon S, Cro Suzie, Round Jeff, Molloy Andrew, Davies Mark, Karski Michael, Kim Louise, Cooke Paul

机构信息

UCL Institute of Orthopaedics and Musculoskeletal Science (IOMS), Royal National Orthopaedic Hospital (RNOH), London, UK.

Surgical Intervention Trials Unit, University of Oxford, Botnar Research Centre, Oxford, UK.

出版信息

BMJ Open. 2016 Sep 6;6(9):e012716. doi: 10.1136/bmjopen-2016-012716.

Abstract

INTRODUCTION

Total ankle replacement (TAR) or ankle arthrodesis (fusion) is the main surgical treatments for end-stage ankle osteoarthritis (OA). The popularity of ankle replacement is increasing while ankle fusion rates remain static. Both treatments have efficacy but to date all studies comparing the 2 have been observational without randomisation, and there are no published guidelines as to the most appropriate management. The TAR versus arthrodesis (TARVA) trial aims to compare the clinical and cost-effectiveness of TAR against ankle arthrodesis in the treatment of end-stage ankle OA in patients aged 50-85 years.

METHODS AND ANALYSIS

TARVA is a multicentre randomised controlled trial that will randomise 328 patients aged 50-85 years with end-stage ankle arthritis. The 2 arms of the study will be TAR or ankle arthrodesis with 164 patients in each group. Up to 16 UK centres will participate. Patients will have clinical assessments and complete questionnaires before their operation and at 6, 12, 26 and 52 weeks after surgery. The primary clinical outcome of the study is a validated patient-reported outcome measure, the Manchester Oxford foot questionnaire, captured preoperatively and 12 months after surgery. Secondary outcomes include quality-of-life scores, complications, revision, reoperation and a health economic analysis.

ETHICS AND DISSEMINATION

The protocol has been approved by the National Research Ethics Service Committee (London, Bloomsbury 14/LO/0807). This manuscript is based on V.5.0 of the protocol. The trial findings will be disseminated through peer-reviewed publications and conference presentations.

TRIAL REGISTRATION NUMBER

NCT02128555.

摘要

引言

全踝关节置换术(TAR)或踝关节融合术是终末期踝骨关节炎(OA)的主要外科治疗方法。踝关节置换术的普及程度在不断提高,而踝关节融合术的比例保持不变。两种治疗方法均有效,但迄今为止,所有比较这两种方法的研究都是观察性的,没有进行随机分组,并且对于最合适的治疗方法尚无已发表的指南。全踝关节置换术与融合术(TARVA)试验旨在比较全踝关节置换术与踝关节融合术在治疗50 - 85岁终末期踝骨关节炎患者中的临床疗效和成本效益。

方法与分析

TARVA是一项多中心随机对照试验,将对328例年龄在50 - 85岁的终末期踝关节炎患者进行随机分组。研究的两组将分别接受全踝关节置换术或踝关节融合术,每组164例患者。多达16个英国中心将参与。患者将在手术前以及术后6周、12周、26周和52周进行临床评估并完成问卷调查。该研究的主要临床结局是一种经过验证的患者报告结局指标,即曼彻斯特牛津足部问卷,在术前和术后12个月进行收集。次要结局包括生活质量评分、并发症、翻修、再次手术以及卫生经济学分析。

伦理与传播

该方案已获得国家研究伦理服务委员会(伦敦,布卢姆斯伯里14/LO/0807)的批准。本手稿基于方案的V.5.0版本。试验结果将通过同行评审出版物和会议报告进行传播。

试验注册号

NCT02128555。

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