Centre for Statistics in Medicine, Nuffield Department of Orthopaedics, Rheumatology, and Musculoskeletal Sciences, University of Oxford, Oxford, England.
School of Medicine and Public Health, University of Newcastle, Callaghan, Australia.
JAMA. 2021 Sep 21;326(11):1045-1056. doi: 10.1001/jama.2021.14075.
Mediation analyses of randomized trials and observational studies can generate evidence about the mechanisms by which interventions and exposures may influence health outcomes. Publications of mediation analyses are increasing, but the quality of their reporting is suboptimal.
To develop international, consensus-based guidance for the reporting of mediation analyses of randomized trials and observational studies (A Guideline for Reporting Mediation Analyses; AGReMA).
DESIGN, SETTING, AND PARTICIPANTS: The AGReMA statement was developed using the Enhancing Quality and Transparency of Health Research (EQUATOR) methodological framework for developing reporting guidelines. The guideline development process included (1) an overview of systematic reviews to assess the need for a reporting guideline; (2) review of systematic reviews of relevant evidence on reporting mediation analyses; (3) conducting a Delphi survey with panel members that included methodologists, statisticians, clinical trialists, epidemiologists, psychologists, applied clinical researchers, clinicians, implementation scientists, evidence synthesis experts, representatives from the EQUATOR Network, and journal editors (n = 19; June-November 2019); (4) having a consensus meeting (n = 15; April 28-29, 2020); and (5) conducting a 4-week external review and pilot test that included methodologists and potential users of AGReMA (n = 21; November 2020).
A previously reported overview of 54 systematic reviews of mediation studies demonstrated the need for a reporting guideline. Thirty-three potential reporting items were identified from 3 systematic reviews of mediation studies. Over 3 rounds, the Delphi panelists ranked the importance of these items, provided 60 qualitative comments for item refinement and prioritization, and suggested new items for consideration. All items were reviewed during a 2-day consensus meeting and participants agreed on a 25-item AGReMA statement for studies in which mediation analyses are the primary focus and a 9-item short-form AGReMA statement for studies in which mediation analyses are a secondary focus. These checklists were externally reviewed and pilot tested by 21 expert methodologists and potential users, which led to minor adjustments and consolidation of the checklists.
The AGReMA statement provides recommendations for reporting primary and secondary mediation analyses of randomized trials and observational studies. Improved reporting of studies that use mediation analyses could facilitate peer review and help produce publications that are complete, accurate, transparent, and reproducible.
随机试验和观察性研究的中介分析可以为干预措施和暴露因素影响健康结果的机制提供证据。中介分析的出版物越来越多,但报告的质量并不理想。
制定国际共识指南,用于报告随机试验和观察性研究的中介分析(中介分析报告指南;AGReMA)。
设计、设置和参与者:AGReMA 陈述是使用增强健康研究质量和透明度(EQUATOR)方法框架制定报告指南的。指南制定过程包括:(1)对系统评价进行概述,以评估报告指南的需求;(2)对中介分析报告的相关证据进行系统评价;(3)与包括方法学家、统计学家、临床试验人员、流行病学家、心理学家、应用临床研究人员、临床医生、实施科学家、证据综合专家、EQUATOR 网络代表和期刊编辑在内的小组委员会成员进行德尔菲调查(n=19;2019 年 6 月至 11 月);(4)召开共识会议(n=15;2020 年 4 月 28 日至 29 日);(5)进行为期 4 周的外部审查和试点测试,包括方法学家和 AGReMA 的潜在用户(n=21;2020 年 11 月)。
先前对 54 项中介研究系统评价的概述表明,需要制定一份报告指南。从 3 项中介研究系统评价中确定了 33 个潜在的报告项目。在 3 轮中,德尔菲小组成员对这些项目的重要性进行了排名,提供了 60 条关于项目细化和优先级的定性意见,并提出了新的项目供考虑。所有项目都在为期两天的共识会议上进行了审查,与会者同意了一份主要关注中介分析的 25 项 AGReMA 陈述和一份次要关注中介分析的 9 项短式 AGReMA 陈述。这两份清单由 21 名专家方法学家和潜在用户进行了外部审查和试点测试,这导致了清单的细微调整和合并。
AGReMA 陈述为报告随机试验和观察性研究的主要和次要中介分析提供了建议。改进使用中介分析的研究报告可以促进同行评审,并有助于发表完整、准确、透明和可重复的研究报告。