Structural Nested Cumulative Failure Time Models to Estimate the Effects of Interventions

被引:25
作者
Picciotto, Sally [1 ]
Hernan, Miguel A. [2 ,3 ]
Page, John H. [3 ]
Young, Jessica G. [2 ]
Robins, James M. [2 ,3 ]
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
关键词
Causal inference; Coronary heart disease; Epidemiology; G-estimation; Inverse probability weighting; CORONARY-HEART-DISEASE; RISK-FACTORS; SURVIVAL; QUESTIONNAIRE; VALIDATION; OUTCOMES; TRIALS;
D O I
10.1080/01621459.2012.682532
中图分类号
O21 [概率论与数理统计]; C8 [统计学];
学科分类号
020208 ; 070103 ; 0714 ;
摘要
In the presence of time-varying confounders affected by prior treatment, standard statistical methods for failure time analysis may be biased. Methods that correctly adjust for this type of covariate include the parametric g-formula, inverse probability weighted estimation of marginal structural Cox proportional hazards models, and g-estimation of structural nested accelerated failure time models. In this article, we propose a novel method to estimate the causal effect of a time-dependent treatment on failure in the presence of informative right-censoring and time-dependent confounders that may be affected by past treatment: g-estimation of structural nested cumulative failure time models (SNCFTMs). An SNCFTM considers the conditional effect of a final treatment at time m on the outcome at each later time k by modeling the ratio of two counterfactual cumulative risks at time k under treatment regimes that differ only at time m. Inverse probability weights are used to adjust for informative censoring. We also present a procedure that, under certain "no-interaction" conditions, uses the g-estimates of the model parameters to calculate unconditional cumulative risks under nondynamic (static) treatment regimes. The procedure is illustrated with an example using data from a longitudinal cohort study, in which the "treatments" are healthy behaviors and the outcome is coronary heart disease.
引用
收藏
页码:886 / 900
页数:15
相关论文
共 31 条
[1]  
[Anonymous], 1999, STAT MODELS EPIDEMIO
[2]  
Bickel P., 1993, EFFICIENT AND ADAPTI
[3]   VALIDATION OF QUESTIONNAIRE INFORMATION ON RISK-FACTORS AND DISEASE OUTCOMES IN A PROSPECTIVE COHORT STUDY OF WOMEN [J].
COLDITZ, GA ;
MARTIN, P ;
STAMPFER, MJ ;
WILLETT, WC ;
SAMPSON, L ;
ROSNER, B ;
HENNEKENS, CH ;
SPEIZER, FE .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1986, 123 (05) :894-900
[4]   The Nurses' Health Study: 20-year contribution to the understanding of health among women [J].
Colditz, GA ;
Manson, JE ;
Hankinson, SE .
JOURNAL OF WOMENS HEALTH, 1997, 6 (01) :49-62
[5]  
Gooley TA, 1999, STAT MED, V18, P695, DOI 10.1002/(SICI)1097-0258(19990330)18:6<695::AID-SIM60>3.3.CO
[6]  
2-F
[7]   Structural accelerated failure time models for survival analysis in studies with time-varying treatments [J].
Hernán, MA ;
Cole, SR ;
Margolick, J ;
Cohen, M ;
Robins, JM .
PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2005, 14 (07) :477-491
[8]   A structural approach to selection bias [J].
Hernán, MA ;
Hernández-Díaz, S ;
Robins, JM .
EPIDEMIOLOGY, 2004, 15 (05) :615-625
[9]   Marginal structural models to estimate the joint causal effect of nonrandomized treatments [J].
Hernán, MA ;
Brumback, B ;
Robins, JM .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 2001, 96 (454) :440-448
[10]   Compound Treatments and Transportability of Causal Inference [J].
Hernan, Miguel A. ;
VanderWeele, Tyler J. .
EPIDEMIOLOGY, 2011, 22 (03) :368-377