Testing causal effects in observational survival data using propensity score matching design

被引:13
|
作者
Lu, Bo [1 ]
Cai, Dingjiao [2 ]
Tong, Xingwei [3 ]
机构
[1] Ohio State Univ, Div Biostat, Coll Publ Hlth, Columbus, OH 43210 USA
[2] Henan Univ Econ & Law, Sch Math & Informat Sci, Zhengzhou, Henan, Peoples R China
[3] Beijing Normal Univ, Dept Stat, Beijing 100875, Peoples R China
基金
美国国家科学基金会;
关键词
observational studies; paired test; proportional hazards assumption; unmeasured confounding; MARGINAL STRUCTURAL MODELS; INFERENCE; DIFFERENCE;
D O I
10.1002/sim.7599
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Time-to-event data are very common in observational studies. Unlike randomized experiments, observational studies suffer from both observed and unobserved confounding biases. To adjust for observed confounding in survival analysis, the commonly used methods are the Cox proportional hazards (PH) model, the weighted logrank test, and the inverse probability of treatment weighted Cox PH model. These methods do not rely on fully parametric models, but their practical performances are highly influenced by the validity of the PH assumption. Also, there are few methods addressing the hidden bias in causal survival analysis. We propose a strategy to test for survival function differences based on the matching design and explore sensitivity of the P-values to assumptions about unmeasured confounding. Specifically, we apply the paired Prentice-Wilcoxon (PPW) test or the modified PPW test to the propensity score matched data. Simulation studies show that the PPW-type test has higher power in situations when the PH assumption fails. For potential hidden bias, we develop a sensitivity analysis based on the matched pairs to assess the robustness of our finding, following Rosenbaum's idea for nonsurvival data. For a real data illustration, we apply our method to an observational cohort of chronic liver disease patients from a Mayo Clinic study. The PPW test based on observed data initially shows evidence of a significant treatment effect. But this finding is not robust, as the sensitivity analysis reveals that the P-value becomes nonsignificant if there exists an unmeasured confounder with a small impact.
引用
收藏
页码:1846 / 1858
页数:13
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