Estimating the causal effect of zidovudine on CD4 count with a marginal structural model for repeated measures

被引:240
|
作者
Hernán, MA
Brumback, BA
Robins, JM
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[2] Univ Washington, Dept Biostat, Seattle, WA 98195 USA
[3] Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
关键词
repeated measures; time-varying exposure; confounding; causality; HIV disease;
D O I
10.1002/sim.1144
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Even in the absence of unmeasured confounding factors or model misspecification, standard methods for estimating the causal effect of a time-varying treatment on the mean of a repeated measures outcome (for example, GEE regression) may be biased when there are time-dependent variables that are simultaneously confounders of the effect of interest and are predicted by previous treatment. In contrast, the recently developed marginal structural models (MSMs) can provide consistent estimates of causal effects when unmeasured confounding and model misspecification are absent. We describe an MSM for repeated measures that parameterizes the marginal means of counterfactual outcomes corresponding to prespecified treatment regimes. The parameters of MSMs are estimated using a new class of estimators - inverse-probability of treatment weighted estimators. We used an MSM to estimate the effect of zidovudine therapy on mean CD4 count among HIV-infected men in the Multicenter AIDS Cohort Study. We estimated a potential expected increase of 5.4 (95 per cent confidence interval -1.8, 12.7) CD4 lymphocytes/mul per additional study visit while on zidovudine therapy. We also explain the theory and implementation of MSMs for repeated measures data and draw upon a simple example to illustrate the basic ideas. Copyright (C) 2002 John Wiley Sons, Ltd.
引用
收藏
页码:1689 / 1709
页数:21
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