Long Dustin M, Hudgens Michael G
Department of Biostatistics, West Virginia University, Morgantown, West Virginia, 26506-9190, U.S.A.
Biometrics. 2013 Dec;69(4):812-9. doi: 10.1111/biom.12103. Epub 2013 Nov 18.
Estimation of treatment effects in randomized studies is often hampered by possible selection bias induced by conditioning on or adjusting for a variable measured post-randomization. One approach to obviate such selection bias is to consider inference about treatment effects within principal strata, that is, principal effects. A challenge with this approach is that without strong assumptions principal effects are not identifiable from the observable data. In settings where such assumptions are dubious, identifiable large sample bounds may be the preferred target of inference. In practice these bounds may be wide and not particularly informative. In this work we consider whether bounds on principal effects can be improved by adjusting for a categorical baseline covariate. Adjusted bounds are considered which are shown to never be wider than the unadjusted bounds. Necessary and sufficient conditions are given for which the adjusted bounds will be sharper (i.e., narrower) than the unadjusted bounds. The methods are illustrated using data from a recent, large study of interventions to prevent mother-to-child transmission of HIV through breastfeeding. Using a baseline covariate indicating low birth weight, the estimated adjusted bounds for the principal effect of interest are 63% narrower than the estimated unadjusted bounds.
在随机研究中,治疗效果的估计常常受到因对随机化后测量的变量进行条件设定或调整而可能产生的选择偏倚的阻碍。消除此类选择偏倚的一种方法是考虑在主要分层内推断治疗效果,即主要效应。这种方法面临的一个挑战是,在没有强假设的情况下,主要效应无法从可观测数据中识别出来。在这些假设存疑的情况下,可识别的大样本界限可能是推断的首选目标。在实际中,这些界限可能很宽且信息不多。在这项工作中,我们考虑是否可以通过对分类基线协变量进行调整来改进主要效应的界限。我们考虑了调整后的界限,结果表明其永远不会比未调整的界限更宽。给出了调整后的界限比未调整的界限更精确(即更窄)的充要条件。使用一项近期关于通过母乳喂养预防艾滋病毒母婴传播干预措施的大型研究数据对这些方法进行了说明。利用一个表明低出生体重的基线协变量,感兴趣的主要效应的估计调整界限比估计的未调整界限窄63%。