Incorporating uncertainty in the baseline risk: An R Shiny tool and an empirical study

M. Hassan Murad, Lifeng Lin
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Abstract

The common practice in meta-analysis and clinical practice guidelines is to derive the absolute treatment effect (also called risk difference, RD) from a combination of a pooled relative risk (RR) that resulted from a meta-analysis, and a user-provided baseline risk (BR). However, this method does not address the uncertainty in BR. We developed a web-based R Shiny tool to perform simple microsimulation and incorporate uncertainty in BR into the precision of RD. We empirically evaluated this approach by estimating the impact of incorporating this uncertainty when BR is derived from the control group rates in 3,128 meta-analyses curated from the Cochrane Library (26,964 individual studies). When BR was derived from the largest study in each meta-analysis, the median width of the CI of BR was 11.6% (interquartile range (IQR), 6.30%–18.5%). Incorporating this uncertainty in BR led to expansion of the RD CI by a median of 8 per 1,000 persons (IQR 2–24). This expansion increased in a linear fashion with BR imprecision and was more prominent in meta-analyses with low BR. This study provides a web-based tool to perform simple microsimulation and incorporate uncertainty in BR into the CI of RD.

Abstract Image

将不确定性纳入基线风险:一个R Shiny工具和实证研究
在荟萃分析和临床实践指南中,常见的做法是从荟萃分析得出的汇总相对风险(RR)和用户提供的基线风险(BR)的组合中得出绝对治疗效果(也称为风险差异,RD)。然而,这种方法并没有解决BR中的不确定性。我们开发了一个基于网络的R Shiny工具来执行简单的微观模拟,并将BR中的不确定性纳入RD的精度。我们通过评估纳入这种不确定性的影响来评估这种方法,当BR来自Cochrane图书馆(26,964项单独研究)的3128项meta分析的对照组比率时。当从每个荟萃分析中最大的研究中得出BR时,BR的CI的中位数宽度为11.6%(四分位间距(IQR), 6.30%-18.5%)。将这种不确定性纳入BR,导致RD CI的中位数增加了8 / 1000人(IQR 2-24)。随着BR不精确,这种扩展呈线性增长,在低BR的meta分析中更为突出。本研究提供了一个基于网络的工具来执行简单的微观模拟,并将BR中的不确定性纳入RD的CI中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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