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Are current standards of reporting quality for clinical trials sufficient in addressing important sources of bias?

机译:当前报告临床试验质量的标准是否足以解决重要的偏倚来源?

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摘要

Determining the quality of a randomized clinical trial (RCT) is necessary for decision-makers to determine the believability and applicability of the trial findings. Issues that are likely to affect the utility of RCT evidence include issues of bias, random error and applicability. In this article we focus primarily on issues of bias and examine the evidence for whether reporting methodological items, including allocation concealment, sequence generation, and blinding of participants can be relied upon as evidence of bias. We present the findings of a systematic review of meta-epidemiological studies and a simulation study demonstrating that commonly examined sources of bias likely play little role in treatment exaggeration. We discuss other issues that may additionally influence trial outcomes including sample size, publication bias, and expertise of trialists. We conclude by discussing strategies to moderate the effect of known biases in assessing overall estimates of treatment effects. (C) 2015 Elsevier Inc. All rights reserved.
机译:对于决策者来说,确定随机临床试验(RCT)的质量对于确定试验结果的可信度和适用性是必要的。可能影响RCT证据实用性的问题包括偏见,随机误差和适用性问题。在本文中,我们主要关注偏见问题,并研究是否可以依靠报告方法论项目(包括分配隐藏,序列生成和参与者盲目)作为偏见的证据。我们介绍了对元流行病学研究的系统评价和一项模拟研究的结果,这些结果表明,通常检查出的偏见来源在夸大治疗中可能起的作用很小。我们讨论了可能另外影响试验结果的其他问题,包括样本量,出版物偏倚和试验人员的专业知识。我们通过讨论在评估治疗效果的总体评估中缓和已知偏见的效果的策略来得出结论。 (C)2015 Elsevier Inc.保留所有权利。

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