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

Stat Med. 2018 May 20;37(11):1846-1858. doi: 10.1002/sim.7599. Epub 2018 Feb 5.

Abstract

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.

Keywords: observational studies; paired test; proportional hazards assumption; unmeasured confounding.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Bias
  • Biostatistics
  • Causality
  • Cohort Studies
  • Computer Simulation
  • Confounding Factors, Epidemiologic
  • Humans
  • Kaplan-Meier Estimate
  • Liver Cirrhosis, Biliary / drug therapy
  • Liver Cirrhosis, Biliary / mortality
  • Logistic Models
  • Observational Studies as Topic / statistics & numerical data*
  • Penicillamine / therapeutic use
  • Propensity Score
  • Proportional Hazards Models
  • Survival Analysis*

Substances

  • Penicillamine