Comparison of the ability of double-robust estimators to correct bias in propensity score matching analysis. A Monte Carlo simulation study

Tri Long Nguyen, Gary S. Collins, Jessica Spence, Philip J. Devereaux, Jean Pierre Daurès, Paul Landais, Yannick Le Manach*

*Corresponding author for this work
10 Citations (Scopus)

Abstract

Objective: As covariates are not always adequately balanced after propensity score matching and double- adjustment can be used to remove residual confounding, we compared the performance of several double-robust estimators in different scenarios. Methods: We conducted a series of Monte Carlo simulations on virtual observational studies. After estimating the propensity scores by logistic regression, we performed 1:1 optimal, nearest-neighbor, and caliper matching. We used 4 estimators on each matched sample: (1) a crude estimator without double-adjustment, (2) double-adjustment for the propensity scores, (3) double-adjustment for the unweighted unbalanced covariates, and (4) double-adjustment for the unbalanced covariates, weighted by their strength of association with the outcome. Results: The crude estimator led to highest bias in all tested scenarios. Double-adjustment for the propensity scores effectively removed confounding only when the propensity score models were correctly specified. Double-adjustment for the unbalanced covariates was more robust to misspecification. Double-adjustment for the weighted unbalanced covariates outperformed the other approaches in every scenario and using any matching algorithm, as measured by the mean squared error. Conclusion: Double-adjustment can be used to remove residual confounding after propensity score matching. The unbalanced covariates with the strongest confounding effects should be adjusted.

Original languageEnglish
JournalPharmacoepidemiology and Drug Safety
Volume26
Issue number12
Pages (from-to)1513-1519
Number of pages7
ISSN1053-8569
DOIs
Publication statusPublished - 2017
Externally publishedYes

Keywords

  • adjustment
  • causal inference
  • confounding
  • pharmacoepidemiology
  • propensity score

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