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物理治疗和职业治疗与不治疗相比在轻至中度帕金森病中的临床疗效和成本效益:一项大型实用随机对照试验(PD REHAB)

Clinical effectiveness and cost-effectiveness of physiotherapy and occupational therapy versus no therapy in mild to moderate Parkinson's disease: a large pragmatic randomised controlled trial (PD REHAB).

作者信息

Clarke Carl E, Patel Smitaa, Ives Natalie, Rick Caroline E, Woolley Rebecca, Wheatley Keith, Walker Marion F, Zhu Shihua, Kandiyali Rebecca, Yao Guiqing, Sackley Catherine M

机构信息

Institute for Applied Health Research, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.

Department of Neurology, Sandwell and West Birmingham Hospitals NHS Trust, City Hospital, Birmingham, UK.

出版信息

Health Technol Assess. 2016 Aug;20(63):1-96. doi: 10.3310/hta20630.

Abstract

BACKGROUND

Cochrane reviews of physiotherapy (PT) and occupational therapy (OT) for Parkinson's disease found insufficient evidence of effectiveness, but previous trials were methodologically flawed with small sample size and short-term follow-up.

OBJECTIVES

To evaluate the clinical effectiveness and cost-effectiveness of individualised PT and OT in Parkinson's disease.

DESIGN

Large pragmatic randomised controlled trial.

SETTING

Thirty-eight neurology and geriatric medicine outpatient clinics in the UK.

PARTICIPANTS

Seven hundred and sixty-two patients with mild to moderate Parkinson's disease reporting limitations in activities of daily living (ADL).

INTERVENTION

Patients were randomised online to either both PT and OT NHS services (n = 381) or no therapy (n = 381). Therapy incorporated a patient-centred approach with individual assessment and goal setting.

MAIN OUTCOME MEASURES

The primary outcome was instrumental ADL measured by the patient-completed Nottingham Extended Activities of Daily Living (NEADL) scale at 3 months after randomisation. Secondary outcomes were health-related quality of life [Parkinson's Disease Questionnaire-39 (PDQ-39); European Quality of Life-5 Dimensions (EQ-5D)], adverse events, resource use and carer quality of life (Short Form questionnaire-12 items). Outcomes were assessed before randomisation and at 3, 9 and 15 months after randomisation.

RESULTS

Data from 92% of the participants in each group were available at the primary time point of 3 months, but there was no difference in NEADL total score [difference 0.5 points, 95% confidence interval (CI) -0.7 to 1.7; p = 0.4] or PDQ-39 summary index (0.007 points, 95% CI -1.5 to 1.5; p = 1.0) between groups. The EQ-5D quotient was of borderline significance in favour of therapy (-0.03, 95% CI -0.07 to -0.002; p = 0.04). Contact time with therapists was for a median of four visits of 58 minutes each over 8 weeks (mean dose 232 minutes). Repeated measures analysis including all time points showed no difference in NEADL total score, but PDQ-39 summary index (curves diverging at 1.6 points per annum, 95% CI 0.47 to 2.62; p = 0.005) and EQ-5D quotient (0.02, 95% CI 0.00007 to 0.03; p = 0.04) showed significant but small differences in favour of the therapy arm. Cost-effective analysis showed that therapy was associated with a slight but not significant gain in quality-adjusted life-years (0.027, 95% CI -0.010 to 0.065) at a small incremental cost (£164, 95% CI -£141 to £468), resulting in an incremental cost-effectiveness ratio of under £4000 (£3493, 95% -£169,371 to £176,358). There was no difference in adverse events or serious adverse events.

CONCLUSIONS

NHS PT and OT did not produce immediate or long-term clinically meaningful improvements in ADL or quality of life in patients with mild to moderate Parkinson's disease. This evidence does not support the use of low-dose, patient-centred, goal-directed PT and OT in patients in the early stages of Parkinson's disease. Future research should include the development and testing of more structured and intensive PT and OT programmes in patients with all stages of Parkinson's disease.

TRIAL REGISTRATION

Current Controlled Trials ISRCTN17452402.

FUNDING

This project was funded by the NIHR Health Technology Assessment programme and will be published in full in Health Technology Assessment; Vol. 20, No. 63. See the NIHR Journals Library website for further project information. The Birmingham Clinical Trials Unit, University of Birmingham, received support from the UK Department of Health up to March 2012. Catherine Sackley was supported by a NIHR senior investigator award, Collaboration for Leadership in Applied Health Research and Care East of England and West Midlands Strategic Health Authority Clinical Academic Training award.

摘要

背景

Cochrane关于帕金森病物理治疗(PT)和职业治疗(OT)的综述发现,有效性证据不足,但以往试验在方法上存在缺陷,样本量小且随访期短。

目的

评估帕金森病个体化PT和OT的临床有效性和成本效益。

设计

大型实用随机对照试验。

地点

英国38家神经内科和老年医学门诊。

参与者

762例轻度至中度帕金森病患者,报告日常生活活动(ADL)受限。

干预措施

患者通过网络随机分组,分别接受PT和OT两项NHS服务(n = 381)或不接受治疗(n = 381)。治疗采用以患者为中心的方法,包括个体评估和目标设定。

主要结局指标

主要结局为随机分组后3个月,由患者完成的诺丁汉扩展日常生活活动(NEADL)量表所测量的工具性ADL。次要结局包括健康相关生活质量[帕金森病问卷-39(PDQ-39);欧洲五维健康量表(EQ-5D)]、不良事件、资源利用以及照顾者生活质量(简易12项问卷)。结局指标在随机分组前以及随机分组后3、9和15个月进行评估。

结果

每组92%参与者的数据在3个月的主要时间点可得,两组间NEADL总分[差值0.5分,95%置信区间(CI)-0.7至1.7;p = 0.4]或PDQ-39总结指数(0.007分,95% CI -1.5至1.5;p = 1.0)无差异。EQ-5D指数在有利于治疗组方面具有临界显著性(-0.03,95% CI -0.07至-0.002;p = 0.04)。与治疗师的接触时间中位数为8周内4次,每次58分钟(平均剂量232分钟)。包括所有时间点的重复测量分析显示,NEADL总分无差异,但PDQ-39总结指数(曲线每年相差1.6分,95% CI 0.47至2.62;p = 0.005)和EQ-5D指数(0.02,95% CI 0.00007至0.03;p = 0.04)显示有利于治疗组的显著但微小差异。成本效益分析表明,治疗与质量调整生命年的轻微但不显著增加相关(0.027,95% CI -0.010至0.065),增量成本较小(164英镑,95% CI -1

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