Literature DB >> 32388870

Quantifying the bias due to observed individual confounders in causal treatment effect estimates.

Layla Parast1, Beth Ann Griffin1.   

Abstract

It is often of interest to use observational data to estimate the causal effect of a target exposure or treatment on an outcome. When estimating the treatment effect, it is essential to appropriately adjust for selection bias due to observed confounders using, for example, propensity score weighting. Selection bias due to confounders occurs when individuals who are treated are substantially different from those who are untreated with respect to covariates that are also associated with the outcome. A comparison of the unadjusted, naive treatment effect estimate with the propensity score adjusted treatment effect estimate provides an estimate of the selection bias due to these observed confounders. In this article, we propose methods to identify the observed covariate that explains the largest proportion of the estimated selection bias. Identification of the most influential observed covariate or covariates is important in resource-sensitive settings where the number of covariates obtained from individuals needs to be minimized due to cost and/or patient burden and in settings where this covariate can provide actionable information to healthcare agencies, providers, and stakeholders. We propose straightforward parametric and nonparametric procedures to examine the role of observed covariates and quantify the proportion of the observed selection bias explained by each covariate. We demonstrate good finite sample performance of our proposed estimates using a simulation study and use our procedures to identify the most influential covariates that explain the observed selection bias in estimating the causal effect of alcohol use on progression of Huntington's disease, a rare neurological disease.
© 2020 John Wiley & Sons, Ltd.

Entities:  

Keywords:  confounder; kernel estimation; nonparametric; robust; selection bias; treatment effect

Year:  2020        PMID: 32388870      PMCID: PMC8162899          DOI: 10.1002/sim.8549

Source DB:  PubMed          Journal:  Stat Med        ISSN: 0277-6715            Impact factor:   2.373


  48 in total

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2.  The design versus the analysis of observational studies for causal effects: parallels with the design of randomized trials.

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3.  Substance abuse may hasten motor onset of Huntington disease: Evaluating the Enroll-HD database.

Authors:  Jordan L Schultz; John A Kamholz; David J Moser; Shawna M E Feely; Jane S Paulsen; Peg C Nopoulos
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4.  Propensity score methods for bias reduction in the comparison of a treatment to a non-randomized control group.

Authors:  R B D'Agostino
Journal:  Stat Med       Date:  1998-10-15       Impact factor: 2.373

5.  Assessing the sensitivity of regression results to unmeasured confounders in observational studies.

Authors:  D Y Lin; B M Psaty; R A Kronmal
Journal:  Biometrics       Date:  1998-09       Impact factor: 2.571

6.  Bias formulas for sensitivity analysis of unmeasured confounding for general outcomes, treatments, and confounders.

Authors:  Tyler J Vanderweele; Onyebuchi A Arah
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7.  Understanding racial disparities in treatment intensification for hypertension management.

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Journal:  J Gen Intern Med       Date:  2010-04-13       Impact factor: 5.128

Review 8.  Selection bias in observational and experimental studies.

Authors:  J H Ellenberg
Journal:  Stat Med       Date:  1994 Mar 15-Apr 15       Impact factor: 2.373

9.  Propensity score techniques and the assessment of measured covariate balance to test causal associations in psychological research.

Authors:  Valerie S Harder; Elizabeth A Stuart; James C Anthony
Journal:  Psychol Methods       Date:  2010-09

10.  Evaluating treatment effectiveness under model misspecification: A comparison of targeted maximum likelihood estimation with bias-corrected matching.

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Journal:  Stat Methods Med Res       Date:  2014-02-12       Impact factor: 3.021

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  1 in total

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Journal:  BMC Infect Dis       Date:  2022-07-07       Impact factor: 3.667

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