Evaluating Model Specification When Using the Parametric G-Formula in the Presence of Censoring

被引:1
作者
Chiu, Yu-Han [1 ,2 ,3 ,6 ]
Wen, Lan [2 ,3 ,4 ]
McGrath, Sean [5 ]
Logan, Roger [2 ,3 ]
Dahabreh, Issa J. [2 ,3 ,5 ]
Hernan, Miguel A. [2 ,3 ,5 ]
机构
[1] Penn State Univ, Coll Med, Dept Publ Hlth Sci, Hershey, PA 17033 USA
[2] Harvard Univ, CAUSALab, Boston, MA USA
[3] Harvard Univ, Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA USA
[4] Univ Waterloo, Fac Math, Dept Stat & Actuarial Sci, Waterloo, ON, Canada
[5] Harvard Univ, Harvard TH Chan Sch Publ Hlth, Dept Biostat, Boston, MA USA
[6] Penn State Coll Med, Dept Publ Hlth Sci, Hershey, PA USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
censoring; inverse probability weighting; model misspecification; noniterative conditional expectation parametric g-formula; HIV-POSITIVE INDIVIDUALS; CORONARY-HEART-DISEASE; ANTIRETROVIRAL THERAPY; CAUSAL INFERENCE; RISK; INTERVENTIONS; MORTALITY; EXPOSURE; CONSUMPTION; INITIATION;
D O I
10.1093/aje/kwad143
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
The noniterative conditional expectation (NICE) parametric g-formula can be used to estimate the causal effect of sustained treatment strategies. In addition to identifiability conditions, the validity of the NICE parametric g-formula generally requires the correct specification of models for time-varying outcomes, treatments, and confounders at each follow-up time point. An informal approach for evaluating model specification is to compare the observed distributions of the outcome, treatments, and confounders with their parametric g-formula estimates under the "natural course." In the presence of loss to follow-up, however, the observed and natural-course risks can differ even if the identifiability conditions of the parametric g-formula hold and there is no model misspecification. Here, we describe 2 approaches for evaluating model specification when using the parametric g-formula in the presence of censoring: 1) comparing factual risks estimated by the g-formula with nonparametric Kaplan-Meier estimates and 2) comparing natural-course risks estimated by inverse probability weighting with those estimated by the g-formula. We also describe how to correctly compute natural-course estimates of time-varying covariate means when using a computationally efficient g-formula algorithm. We evaluate the proposed methods via simulation and implement them to estimate the effects of dietary interventions in 2 cohort studies.
引用
收藏
页码:1887 / 1895
页数:9
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