中风康复试验中缺乏干预和剂量的依据:系统回顾。

IF 1.8 Q3 PERIPHERAL VASCULAR DISEASE Stroke Research and Treatment Pub Date : 2018-10-30 eCollection Date: 2018-01-01 DOI:10.1155/2018/8087372
Karen Borschmann, Kathryn S Hayward, Audrey Raffelt, Leonid Churilov, Sharon Kramer, Julie Bernhardt
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引用次数: 0

摘要

背景:大多数复杂中风康复试验效果不佳的原因可能是干预设计不当。本综述的主要目的是探讨卒中康复随机对照试验(RCTs)中干预措施和剂量的依据:我们在 Cochrane Stroke Group 资料库中搜索了符合以下标准的 RCT:(1) 以训练为基础的干预;(2) >50%的参与者为中风幸存者;(3) 同行评审全文;(4) 英语。我们提取了 16 个质量项目的数据,包括干预剂量(3 个)、试验设计(10 个)和偏倚风险(3 个),以及 18 个与试验方法相关的项目。进行逻辑回归分析以确定:(1) 试验质量项目的报告是否随时间推移而变化;(2) 质量项目的报告是否与阳性试验的可能性相关,并根据样本大小和结果数量进行调整。发表日期为 1979 年至 2013 年,样本量中位数为 32(IQR 20,58),49 项试验(25%)报告了主要结果。总质量得分的中位数为4(IQR为3,6),并且每年都有显著提高(OR为1.12,95% CI为1.07, 1.16,p结论:为了开发突破性的治疗方法,我们需要建立研究干预和干预剂量测试的理论基础。这将通过一项集体研究议程来实现,该议程旨在了解推动康复的机制原理,并为临床试验确定更明确的目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Rationale for Intervention and Dose Is Lacking in Stroke Recovery Trials: A Systematic Review.

Background: The ineffectiveness of most complex stroke recovery trials may be explained by inadequate intervention design. The primary aim of this review was to explore the rationales given for interventions and dose in stroke rehabilitation randomised controlled trials (RCTs).

Methods: We searched the Cochrane Stroke Group library for RCTs that met the following criteria: (1) training based intervention; (2) >50% participants who were stroke survivors; (3) full peer-reviewed text; (4) English language. We extracted data on 16 quality items covering intervention dose (n= 3), trial design (n= 10), and risk of bias (n= 3) and 18 items related to trial method. Logistic regression analyses were performed to determine whether (1) reporting of trial quality items changed over time; (2) reporting of quality items was associated with the likelihood of a positive trial, adjusted for sample size and number of outcomes.

Results: 27 Cochrane reviews were included, containing 9,044 participants from 194 trials. Publication dates were 1979 to 2013, sample size was median 32 (IQR 20,58), and primary outcome was reported in 49 trials (25%). The median total quality score was 4 (IQR 3,6) and improved significantly each year (OR 1.12, 95% CI 1.07, 1.16, p<0.001). Total quality score was not associated with likelihood of a positive trial, but trials containing a biological rationale for the intervention were more likely to find a difference in patient outcome (OR 2.18, 95% CI 1.14, 4.19, p=0.02).

Conclusion: To develop breakthrough treatments we need to build the rationale for research interventions and testing of intervention dosage. This will be achieved through a collective research agenda to understand the mechanistic principles that drive recovery and identification of clearer targets for clinical trials.

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来源期刊
Stroke Research and Treatment
Stroke Research and Treatment PERIPHERAL VASCULAR DISEASE-
CiteScore
3.20
自引率
0.00%
发文量
14
审稿时长
12 weeks
期刊最新文献
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