Wylde Vikki, Artz Neil, Marques Elsa, Lenguerrand Erik, Dixon Samantha, Beswick Andrew D, Burston Amanda, Murray James, Parwez Tarique, Blom Ashley W, Gooberman-Hill Rachael
Musculoskeletal Research Unit, School of Clinical Sciences, University of Bristol, Learning and Research Building (Level 1), Southmead Hospital, Bristol, BS10 5NB, UK.
School of Health Professions, University of Plymouth, Peninsula Allied Health Centre, Derriford Road, Plymouth, Devon, PL6 8BH, UK.
Trials. 2016 Jun 13;17(1):289. doi: 10.1186/s13063-016-1418-x.
Primary total knee replacement is a common operation that is performed to provide pain relief and restore functional ability. Inpatient physiotherapy is routinely provided after surgery to enhance recovery prior to hospital discharge. However, international variation exists in the provision of outpatient physiotherapy after hospital discharge. While evidence indicates that outpatient physiotherapy can improve short-term function, the longer term benefits are unknown. The aim of this randomised controlled trial is to evaluate the long-term clinical effectiveness and cost-effectiveness of a 6-week group-based outpatient physiotherapy intervention following knee replacement.
METHODS/DESIGN: Two hundred and fifty-six patients waiting for knee replacement because of osteoarthritis will be recruited from two orthopaedic centres. Participants randomised to the usual-care group (n = 128) will be given a booklet about exercise and referred for physiotherapy if deemed appropriate by the clinical care team. The intervention group (n = 128) will receive the same usual care and additionally be invited to attend a group-based outpatient physiotherapy class starting 6 weeks after surgery. The 1-hour class will be run on a weekly basis over 6 weeks and will involve task-orientated and individualised exercises. The primary outcome will be the Lower Extremity Functional Scale at 12 months post-operative. Secondary outcomes include: quality of life, knee pain and function, depression, anxiety and satisfaction. Data collection will be by questionnaire prior to surgery and 3, 6 and 12 months after surgery and will include a resource-use questionnaire to enable a trial-based economic evaluation. Trial participation and satisfaction with the classes will be evaluated through structured telephone interviews. The primary statistical and economic analyses will be conducted on an intention-to-treat basis with and without imputation of missing data. The primary economic result will estimate the incremental cost per quality-adjusted life year gained from this intervention from a National Health Services (NHS) and personal social services perspective.
This research aims to benefit patients and the NHS by providing evidence on the long-term effectiveness and cost-effectiveness of outpatient physiotherapy after knee replacement. If the intervention is found to be effective and cost-effective, implementation into clinical practice could lead to improvement in patients' outcomes and improved health care resource efficiency.
ISRCTN32087234 , registered on 11 February 2015.
初次全膝关节置换术是一种常见手术,旨在缓解疼痛并恢复功能。术后常规提供住院物理治疗以促进出院前的恢复。然而,出院后门诊物理治疗的提供在国际上存在差异。虽然有证据表明门诊物理治疗可改善短期功能,但长期益处尚不清楚。这项随机对照试验的目的是评估膝关节置换术后为期6周的基于小组的门诊物理治疗干预的长期临床疗效和成本效益。
方法/设计:将从两个骨科中心招募256名因骨关节炎等待膝关节置换的患者。随机分配到常规护理组(n = 128)的参与者将获得一本关于运动的手册,并在临床护理团队认为适当时转介接受物理治疗。干预组(n = 128)将接受相同的常规护理,并额外被邀请参加术后6周开始的基于小组的门诊物理治疗课程。为期1小时的课程将在6周内每周进行一次,将包括以任务为导向的个性化运动。主要结局将是术后12个月时的下肢功能量表。次要结局包括:生活质量、膝关节疼痛和功能、抑郁、焦虑和满意度。数据收集将通过手术前以及手术后3、6和12个月的问卷调查进行,并且将包括一份资源使用问卷以进行基于试验的经济评估。将通过结构化电话访谈评估试验参与情况和对课程的满意度。主要统计和经济分析将在意向性分析基础上进行,包括有和没有缺失数据插补的情况。主要经济结果将从国民健康服务(NHS)和个人社会服务的角度估计该干预措施每获得一个质量调整生命年的增量成本。
本研究旨在通过提供膝关节置换术后门诊物理治疗的长期有效性和成本效益的证据,使患者和NHS受益。如果发现该干预措施有效且具有成本效益,将其应用于临床实践可能会改善患者的结局并提高医疗保健资源效率。
ISRCTN32087234,于2015年2月11日注册。