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是否正在以正确的理由进行随机对照试验?

Are randomized controlled trials being conducted with the right justification?

机构信息

Department of Institutional Research, Oklahoma State University Center for Health Sciences, Tulsa, Oklahoma, USA.

出版信息

J Evid Based Med. 2020 Aug;13(3):181-182. doi: 10.1111/jebm.12405. Epub 2020 Jul 2.

Abstract

OBJECTIVE

It has been estimated that much of health research may be wasted, resulting in billions of dollars in wasteful research spending worldwide each year. Given the increased use of randomized trials and their influence on medicine, one method to combat research waste is to conduct randomized clinical trials (RCTs) only when a systematic review (SR) suggests more data are needed or when no previous SRs are identified. Here, we analyzed RCTs to determine whether SRs were cited as justification for conducting a trial.

METHODS

We analyzed phase III RCTs published between 2016 and 2018 in New England Journal of Medicine, Lancet, and JAMA. We performed duplicate and independent data extraction to ensure the accuracy and validity of our data. For each trial, we extracted whether SRs were cited as justification for conducting the clinical trial.

RESULTS

We examined 637 RCTs that cited 728 SRs. Overall, 38.1% (243/637) of RCTs cited an SR as either verbatim (6.9%, 44/637) or inferred (31.2%, 199/637) for trial justification. The 79 remaining RCTs cited SRs in other ways. Approximately, 49.5% (315/637) of RCTs did not cite a SR.

CONCLUSIONS

Less than half of the analyzed clinical trials cited a SRs as the basis for undertaking the trial. We believe trialists should be required to present relevant SRs to an ethics or peer review committee demonstrating an unmet need prior to initiating a trial. Eliminating research waste is both a scientific and ethical responsibility.

摘要

目的

据估计,大量的健康研究可能被浪费了,导致全球每年在浪费性研究上花费数十亿美元。鉴于随机试验的使用增加及其对医学的影响,对抗研究浪费的一种方法是仅在系统评价(SR)表明需要更多数据或没有先前的 SR 时进行随机临床试验(RCT)。在这里,我们分析了 RCT,以确定 SR 是否被引述为进行试验的理由。

方法

我们分析了 2016 年至 2018 年在《新英格兰医学杂志》、《柳叶刀》和《美国医学会杂志》上发表的 III 期 RCT。我们进行了重复和独立的数据提取,以确保数据的准确性和有效性。对于每个试验,我们提取了是否引用了 SR 作为进行临床试验的理由。

结果

我们检查了引用了 728 个 SR 的 637 个 RCT。总体而言,38.1%(243/637)的 RCT 引用了 SR 作为试验理由的原文(6.9%,44/637)或推断(31.2%,199/637)。其余 79 个 RCT 以其他方式引用了 SR。大约 49.5%(315/637)的 RCT 没有引用 SR。

结论

分析的临床试验中不到一半引用了 SR 作为进行试验的依据。我们认为,试验人员应该被要求向伦理或同行评审委员会提交相关的 SR,以证明在开始试验之前存在未满足的需求。消除研究浪费既是科学的责任,也是道德的责任。

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