计算计划进行的个体参与者数据荟萃分析的功率,以检查二元结果的预后因素效应。

IF 5 2区 生物学 Q1 MATHEMATICAL & COMPUTATIONAL BIOLOGY
Rebecca Whittle, Joie Ensor, Miriam Hattle, Paula Dhiman, Gary S. Collins, Richard D. Riley
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引用次数: 0

摘要

为个体参与者数据荟萃分析(IPDMA)项目收集数据可能会耗费大量的时间和资源,而且可能仍然没有足够的力量来回答感兴趣的问题。因此,研究人员应在收集 IPD 之前考虑其计划的 IPDMA 功率。在此,我们提出了一种方法来估算计划中的 IPDMA 项目的功率,该项目旨在综合多项队列研究,以调查潜在预后因素对二元结局的(未调整或调整后的)影响。我们考虑了二元因素和连续因素,并提供了一种分三步的方法,在假定每个相关因素的真实预后效应的前提下,在收集 IPD 之前对功率进行估计。第一步使用每项研究的常规可用(已公布)汇总数据来近似费雪信息矩阵,从而估算出每项研究中未调整预后因素效应的预期方差。然后,在第 2 步中使用这些方差来估计 IPDMA 预测预后效应汇总的预期方差。最后,步骤 3 根据双侧 Wald 检验和假定的真实效应,使用该方差估算相应的 IPDMA 功率。该方法提供了扩展功能,可根据与相关预后因素相关的其他协变量的存在(通过使用方差膨胀因子)调整功率计算,并考虑预后效应的研究间异质性。本文提供了一个示例进行说明,并提供了 Stata 代码,以便研究人员实施该方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Calculating the power of a planned individual participant data meta-analysis to examine prognostic factor effects for a binary outcome

Calculating the power of a planned individual participant data meta-analysis to examine prognostic factor effects for a binary outcome

Collecting data for an individual participant data meta-analysis (IPDMA) project can be time consuming and resource intensive and could still have insufficient power to answer the question of interest. Therefore, researchers should consider the power of their planned IPDMA before collecting IPD. Here we propose a method to estimate the power of a planned IPDMA project aiming to synthesise multiple cohort studies to investigate the (unadjusted or adjusted) effects of potential prognostic factors for a binary outcome. We consider both binary and continuous factors and provide a three-step approach to estimating the power in advance of collecting IPD, under an assumption of the true prognostic effect of each factor of interest. The first step uses routinely available (published) aggregate data for each study to approximate Fisher's information matrix and thereby estimate the anticipated variance of the unadjusted prognostic factor effect in each study. These variances are then used in step 2 to estimate the anticipated variance of the summary prognostic effect from the IPDMA. Finally, step 3 uses this variance to estimate the corresponding IPDMA power, based on a two-sided Wald test and the assumed true effect. Extensions are provided to adjust the power calculation for the presence of additional covariates correlated with the prognostic factor of interest (by using a variance inflation factor) and to allow for between-study heterogeneity in prognostic effects. An example is provided for illustration, and Stata code is supplied to enable researchers to implement the method.

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来源期刊
Research Synthesis Methods
Research Synthesis Methods MATHEMATICAL & COMPUTATIONAL BIOLOGYMULTID-MULTIDISCIPLINARY SCIENCES
CiteScore
16.90
自引率
3.10%
发文量
75
期刊介绍: Research Synthesis Methods is a reputable, peer-reviewed journal that focuses on the development and dissemination of methods for conducting systematic research synthesis. Our aim is to advance the knowledge and application of research synthesis methods across various disciplines. Our journal provides a platform for the exchange of ideas and knowledge related to designing, conducting, analyzing, interpreting, reporting, and applying research synthesis. While research synthesis is commonly practiced in the health and social sciences, our journal also welcomes contributions from other fields to enrich the methodologies employed in research synthesis across scientific disciplines. By bridging different disciplines, we aim to foster collaboration and cross-fertilization of ideas, ultimately enhancing the quality and effectiveness of research synthesis methods. Whether you are a researcher, practitioner, or stakeholder involved in research synthesis, our journal strives to offer valuable insights and practical guidance for your work.
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