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在群组随机试验中,基线协变量不均衡对处理效应估计偏差的影响:以种族为例。

Impact of baseline covariate imbalance on bias in treatment effect estimation in cluster randomized trials: Race as an example.

机构信息

Department of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC, United States of America.

Department of Medicine, Duke University School of Medicine, Durham, NC, United States of America; Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC, United States of America.

出版信息

Contemp Clin Trials. 2020 Jan;88:105775. doi: 10.1016/j.cct.2019.04.016. Epub 2019 Jun 20.

DOI:10.1016/j.cct.2019.04.016
PMID:31228563
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8337048/
Abstract

Individual-level baseline covariate imbalance could happen more frequently in cluster randomized trials, and may influence the observed treatment effect. Using computer and real-data simulations, this paper quantifies the extent and impact of covariate imbalance on the estimated treatment effect for both continuous and binary outcomes, and relates it to the degree of imbalance for different numbers of clusters, cluster sizes, and covariate intraclass correlation coefficients. We focused on the impact of race as a covariate, given the emphasis of regulatory and funding bodies on understanding the influence of demographic characteristics on treatment effectiveness. We found that bias in the treatment effect is proportional to both the degree of baseline covariate imbalance and the covariate effect size. Larger numbers of clusters result in lower covariate imbalance, and increasing cluster size is less effective in reducing imbalance compared to increasing the number of clusters. Models adjusted for important baseline confounders are superior to unadjusted models for minimizing bias in both model-based simulations and an innovative simulation based on real clinical trial data. Higher outcome intraclass correlation coefficients did not affect bias but resulted in greater variance in treatment estimates.

摘要

个体水平的基线协变量不均衡在整群随机试验中可能更为常见,并可能影响观察到的治疗效果。本文通过计算机模拟和真实数据模拟,量化了协变量不均衡对连续和二分类结局的估计治疗效果的影响程度,并将其与不同数量的群组、群组大小和协变量组内相关系数的不均衡程度联系起来。我们重点关注种族作为协变量的影响,因为监管机构和资助机构强调了解人口统计学特征对治疗效果的影响。我们发现,治疗效果的偏差与基线协变量不均衡的程度和协变量效应大小成正比。更多的群组会导致较低的协变量不均衡,而增加群组大小相对于增加群组数量来说,在减少不均衡方面效果较差。对于重要的基线混杂因素进行调整的模型在基于模型的模拟和基于真实临床试验数据的创新模拟中都优于未调整的模型,可最大限度地减少偏差。较高的结局组内相关系数不会影响偏差,但会导致治疗估计值的方差更大。