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慢性疼痛中富集入组、随机撤药试验设计的系统评价:设计与报告的新框架

Systematic review of enriched enrolment, randomised withdrawal trial designs in chronic pain: a new framework for design and reporting.

作者信息

Moore R Andrew, Wiffen Philip J, Eccleston Christopher, Derry Sheena, Baron Ralf, Bell Rae F, Furlan Andrea D, Gilron Ian, Haroutounian Simon, Katz Nathaniel P, Lipman Arthur G, Morley Stephen, Peloso Paul M, Quessy Steve N, Seers Kate, Strassels Scott A, Straube Sebastian

机构信息

Pain Research and Nuffield Division of Anaesthetics, University of Oxford, Oxford, United Kingdom Centre for Pain Research, University of Bath, Bath, United Kingdom Division of Neurological Pain Research and Therapy, Department of Neurology, University Hospital, Kiel, Germany Centre for Pain Management and Palliative Care & Regional Centre for Excellence in Palliative Care, Haukeland University Hospital, Bergen, Norway Institute for Work & Health, Toronto, ON, Canada Queen's University, Kingston General Hospital, Departments of Anesthesiology & Perioperative Medicine and Biomedical & Molecular Sciences, Kingston, ON, Canada Division of Clinical and Translational Research, Department of Anesthesiology, Washington University School of Medicine, St Louis, MO, USA Analgesic Solutions, Natick, MA, USA Department of Pharmacotherapy, University of Utah, Salt Lake City, UT, USA Leeds Institute of Health Sciences, University of Leeds, Leeds, United Kingdom Department R449, AbbVie, North Chicago, IL, USA qd Consulting, LLC, Durham, NC, USA RCN Research Institute, Warwick Medical School, University of Warwick, Coventry, United Kingdom 8002 Davis Dr, Clayton, MO, USA Division of Preventive Medicine, University of Alberta, Edmonton, AB, Canada.

出版信息

Pain. 2015 Aug;156(8):1382-1395. doi: 10.1097/j.pain.0000000000000088.

Abstract

Enriched enrolment, randomised withdrawal (EERW) pain trials select, before randomisation, patients who respond by demonstrating a predetermined degree of pain relief and acceptance of adverse events. There is uncertainty over the value of this design. We report a systematic review of EERW trials in chronic noncancer pain together with a critical appraisal of methods and potential biases in the methods used and recommendations for the design and reporting of future EERW trials. Electronic and other searches found 25 EERW trials published between 1995 and June 2014, involving 5669 patients in a randomised withdrawal phase comparing drug with placebo; 13 (median, 107 patients) had a randomised withdrawal phase of 6 weeks or less, and 12 (median, 334) lasted 12 to 26 weeks. Risks of bias included short duration, inadequate outcome definition, incomplete outcome data reporting, small size, and inadequate dose tapering on randomisation to placebo. Active treatment was usually better than placebo (22/25 trials). This review reduces the uncertainty around the value of EERW trials in pain. If properly designed, conducted, and reported, they are feasible and useful for making decisions about pain therapies. Shorter, small studies can be explanatory; longer, larger studies can inform practice. Current evidence is inadequate for valid comparisons in outcome between EERW and classical trials, although no gross differences were found. This systematic review provides a framework for assessing potential biases and the value of the EERW trials, and for the design of future studies by making recommendations for the conduct and reporting of EERW trials.

摘要

富集入组、随机撤药(EERW)疼痛试验在随机分组前,选择那些通过表现出预定程度的疼痛缓解和对不良事件的接受程度来做出反应的患者。这种设计的价值存在不确定性。我们报告了对慢性非癌性疼痛EERW试验的系统评价,同时对所使用方法中的方法和潜在偏倚进行了批判性评估,并对未来EERW试验的设计和报告提出了建议。电子检索和其他检索发现了1995年至2014年6月期间发表的25项EERW试验,在随机撤药阶段有5669名患者参与,将药物与安慰剂进行比较;13项试验(中位数为107名患者)的随机撤药阶段为6周或更短,12项试验(中位数为334名患者)持续12至26周。偏倚风险包括持续时间短、结局定义不充分、结局数据报告不完整、样本量小以及随机分组至安慰剂时剂量递减不充分。积极治疗通常优于安慰剂(22/25项试验)。本评价减少了围绕EERW试验在疼痛方面价值的不确定性。如果设计、实施和报告得当,它们对于做出疼痛治疗决策是可行且有用的。较短、较小的研究可以提供解释;较长、较大的研究可以为实践提供信息。尽管未发现明显差异,但目前的证据不足以对EERW试验和经典试验的结局进行有效比较。本系统评价提供了一个框架,用于评估潜在偏倚和EERW试验的价值,并通过对EERW试验的实施和报告提出建议来指导未来研究的设计。

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