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[GRADE指南:18. 如何使用ROBINS-I和其他评估非随机研究偏倚风险的工具来对证据体的确定性进行评级]

[GRADE guidelines: 18. How ROBINS-I and other tools to assess risk of bias in nonrandomized studies should be used to rate the certainty of a body of evidence].

作者信息

Morche Johannes, Freitag Simone, Hoffmann Frauke, Rissling Olesja, Langer Gero, Nußbaumer-Streit Barbara, Toews Ingrid, Gartlehner Gerald, Meerpohl Jörg J

机构信息

Abteilung Fachberatung Medizin. Gemeinsamer Bundesausschuss, Berlin, Deutschland.

Abteilung Fachberatung Medizin. Gemeinsamer Bundesausschuss, Berlin, Deutschland.

出版信息

Z Evid Fortbild Qual Gesundhwes. 2020 Apr;150-152:124-133. doi: 10.1016/j.zefq.2019.11.003. Epub 2020 Jan 22.

Abstract

OBJECTIVE

To provide guidance on how systematic review authors, guideline developers, and health technology assessment practitioners should approach the use of the risk of bias in nonrandomized studies of interventions (ROBINS-I) tool as a part of GRADE's certainty rating process.

STUDY DESIGN AND SETTING

The study design and setting comprised iterative discussions, testing in systematic reviews, and presentation at GRADE working group meetings with feedback from the GRADE working group.

RESULTS

We describe where to start the initial assessment of a body of evidence with the use of ROBINS-I and where one would anticipate the final rating would end up. The GRADE accounted for issues that mitigate concerns about confounding and selection bias by introducing the upgrading domains: large effects, dose-effect relations, and when plausible residual confounders or other biases increase certainty. They will need to be considered in an assessment of a body of evidence when using ROBINS-I.

CONCLUSION

The use of ROBINS-I in GRADE assessments may allow for a better comparison of evidence from randomized controlled trials (RCTs) and nonrandomized studies (NRSs) because they are placed on a common metric for risk of bias. Challenges remain, including appropriate presentation of evidence from RCTs and NRSs for decision-making and how to optimally integrate RCTs and NRSs in an evidence assessment.

摘要

目的

为系统评价作者、指南制定者和卫生技术评估从业者提供指导,说明他们应如何将干预性非随机研究的偏倚风险(ROBINS-I)工具作为GRADE证据确定性评级过程的一部分来使用。

研究设计与环境

研究设计与环境包括反复讨论、在系统评价中进行测试,以及在GRADE工作组会议上进行展示并获得该工作组的反馈。

结果

我们描述了使用ROBINS-I对一组证据进行初步评估的起始点以及预计最终评级的终点。GRADE通过引入升级领域来考虑减轻对混杂和选择偏倚担忧的问题:效应大、剂量-效应关系,以及当似是而非的残余混杂因素或其他偏倚增加确定性时。在使用ROBINS-I评估一组证据时需要考虑这些因素。

结论

在GRADE评估中使用ROBINS-I可能会使随机对照试验(RCT)和非随机研究(NRS)的证据比较更加理想,因为它们基于共同的偏倚风险衡量标准。挑战依然存在,包括如何恰当地呈现RCT和NRS的证据以供决策,以及如何在证据评估中最佳地整合RCT和NRS。

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