个体参与者数据荟萃分析的批判性评价工具的开发与验证:一项改良的电子德尔菲研究方案

Development and validation of critical appraisal tool for individual participant data meta-analysis: protocol for a modified e-Delphi study.

作者信息

Otalike Edith Ginika, Clarke Mike, Veroniki Areti Angeliki, Tricco Andrea C, Moher David, Shea Beverley, Doherty-Kirby Amanda, Kandala Ngianga-Bakwin, Gagnier Joel

机构信息

Epidemiology and Biostatistics, University of Western Ontario, London, Ontario, Canada

Northern Ireland Methodology Hub, Queen's University Belfast, Belfast, UK.

出版信息

BMJ Open. 2025 Jun 25;15(6):e097297. doi: 10.1136/bmjopen-2024-097297.

Abstract

INTRODUCTION

Individual participant data meta-analysis (IPD-MA) is regarded as the gold standard for evidence synthesis. However, diverse recommendations and guidance on its conduct exist, and there is no consensus-based tool for the critical appraisal of a completed IPD-MA. We aim to close this gap by systematically identifying quality items and developing and validating a critical appraisal checklist for IPD-MA.

METHODS AND ANALYSIS

This study will comprise three phases, as follows:Phase 1: a systematic methodology review to identify potential checklist domains and items; this will be conducted according to the Cochrane methods for systematic reviews and reported following the Preferred Reporting Items for Systematic Reviews and Meta-analysis 2020 guidance. We will include studies that address methodological guides and essential statistical requirements for IPD-MA. We will use the proposed items to prepare a preliminary checklist for the e-Delphi study.Phase 2: at least two rounds of an e-Delphi survey will be conducted among panels with expertise in IPD-MA research, consensus development, healthcare providers, journal editors, healthcare policymakers, patients and public partners from diverse geographic locations with experience in IPD-MA. Participants will use Qualtrics software to rate items on a 5-point Likert scale. The Wilcoxon matched signed rank test will estimate response stability across rounds. Consensus on including an item will be achieved if ≥75% of the panel rates the item as 'strongly agree' or 'agree' and items will be excluded if ≥75% rates it as 'strongly disagree' or 'disagree'. A convenience sample of 10 reviewers with experience in conducting an IPD-MA will pilot-test the checklist to provide practical feedback that will be used to refine the checklist.Phase 3: critical appraisal checklist validation: to improve confidence in the tool's uptake, a subset of the e-Delphi participants and graduate students of epidemiology and biostatistics will conduct content validity and reliability testing, respectively, per the Consensus-based Standards for the Selection of Health Measurement Instruments.

ETHICS AND DISSEMINATION

Ethics approval has been obtained from the Western University Health Science Research Ethics Board in Canada. The validated checklist will be published in a peer-reviewed open-access journal and shared across the networks of this study's steering committee, Cochrane IPD-MA group and the institutions' social media platforms.

摘要

引言

个体参与者数据荟萃分析(IPD-MA)被视为证据综合的金标准。然而,关于其实施存在各种建议和指南,且对于已完成的IPD-MA,尚无基于共识的批判性评价工具。我们旨在通过系统识别质量项目并开发和验证IPD-MA的批判性评价清单来填补这一空白。

方法与分析

本研究将包括以下三个阶段:

第1阶段:进行系统的方法学综述,以识别潜在的清单领域和项目;这将根据Cochrane系统评价方法进行,并按照《系统评价和荟萃分析的首选报告项目2020》指南进行报告。我们将纳入涉及IPD-MA方法指南和基本统计要求的研究。我们将使用提议的项目为电子德尔菲研究准备初步清单。

第2阶段:将在IPD-MA研究、共识发展、医疗保健提供者、期刊编辑、医疗保健政策制定者、患者以及来自不同地理位置且有IPD-MA经验的公众合作伙伴等方面的专家小组中进行至少两轮电子德尔菲调查。参与者将使用Qualtrics软件以5点李克特量表对项目进行评分。威尔科克森符号秩检验将估计各轮的反应稳定性。如果≥75%的专家小组将项目评为“强烈同意”或“同意”,则该项目将达成纳入共识;如果≥75%的专家小组将其评为“强烈不同意”或“不同意”,则该项目将被排除。10名有IPD-MA实施经验的评审人员组成的便利样本将对清单进行预测试,以提供用于完善清单的实际反馈。

第3阶段:批判性评价清单验证:为提高对该工具应用的信心,电子德尔菲参与者的一个子集以及流行病学和生物统计学研究生将分别根据《基于共识的健康测量工具选择标准》进行内容效度和信度测试。

伦理与传播

已获得加拿大西部大学健康科学研究伦理委员会的伦理批准。经验证的清单将发表在同行评审的开放获取期刊上,并在本研究指导委员会、Cochrane IPD-MA小组以及各机构的社交媒体平台网络中共享。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b401/12198787/0bf691053d4c/bmjopen-15-6-g001.jpg

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