Indications for propensity scores and review of their use in pharmacoepidemiology
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Abstract: Use of propensity scores to identify and control for confounding in observational studies that relate medications to outcomes has increased substantially in recent years. However, it remains unclear whether, and if so when, use of propensity scores provides estimates of drug effects that are less biased than those obtained from conventional multivariate models. In the great majority of published studies that have used both approaches, estimated effects from propensity score and regression methods have been similar. Simulation studies further suggest comparable performance of the two approaches in many settings. We discuss five reasons that favour use of propensity scores: the value of focus on indications for drug use; optimal matching strategies from alternative designs; improved control of confounding with scarce outcomes; ability to identify interactions between propensity of treatment and drug effects on outcomes; and correction for unobserved confounders via propensity score calibration. We describe alternative approaches to estimate and implement propensity scores and the limitations of the C‐statistic for evaluation. Use of propensity scores will not correct biases from unmeasured confounders, but can aid in understanding determinants of drug use and lead to improved estimates of drug effects in some settings.
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Risk stratification can control observed confounders more efficiently than regression and may outperform propensity scores when covariates are weakly correlated with exposure.
“These methods constitute a broader strategy of risk stratification, allowing for more efficient control of observed confounders than regression-based approaches [31,32], and are a better alternative to propensity score estimation when covariates are not highly correlated with the exposure [33].”
From Social Media Use and Depressive Symptoms Among United States Adolescents (2021) · cites this paper as [32]
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- Authors
- Glynn, R. J., Schneeweiss, S., & Stürmer, T.
- Affiliations
- Brigham and Women's Hospital (US)
- Corresponding author
- Glynn, Robert J.
- Venue
- Basic & Clinical Pharmacology & Toxicology
- Publisher
- Wiley
- Published
- 2006-03
- Volume
- 98
- Issue
- 3
- Pages
- 253-259
- ISSN
- 1742-7835 (ISSN-L)
- 1742-7843
- PMC
- PMC1790968
- OpenAlex
- W2073225472
- Cited by
- 541
- References
- 32
- Citations by year
- 2026: 8 · 2025: 11 · 2024: 15 · 2023: 19 · 2022: 29 · 2021: 29 · 2020: 33 · 2019: 43 · 2018: 36 · 2017: 33 · 2016: 41 · 2015: 37 · 2014: 35 · 2013: 43 · 2012: 35
- FWCI
- 2.80
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Basic & Clinical Pharmacology & Toxicology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute on Aging (AG-18833, R56AG023178, AG-23178, R56AG018833, R01AG018833, R01AG023178)
- Topics
- Physical Sciences › Mathematics › Statistics and Probability › Advanced Causal Inference Techniques
- Physical Sciences › Mathematics › Statistics and Probability › Statistical Methods in Epidemiology
- Physical Sciences › Mathematics › Statistics and Probability › Statistical Methods in Clinical Trials
- Keywords
- propensity score, pharmacoepidemiology, confounding adjustment, observational studies, propensity score matching, unmeasured confounding, concordance index, simulation study
- MeSH terms
- Clinical Trials as Topic, Data Interpretation, Statistical, Humans, Research Design, Models, Statistical, Bias, Confounding Factors, Epidemiologic, Treatment Outcome, Outcome Assessment, Health Care, Pharmacoepidemiology, Drug-Related Side Effects and Adverse Reactions
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