TY - JOUR
T1 - Universal Difference-in-Differences for Causal Inference in Epidemiology
AU - Tchetgen Tchetgen, Eric J.
AU - Park, Chan
AU - Richardson, David B.
N1 - E.J.T.T. was supported by NIH grants R01AI127271, R01CA222147, R01AG065276, and R01GM139926. D.B.R. was supported by grant R01OH011409 from the National Institute for Occupational Safety and Health of the Centers for Disease Control and Prevention, and R01CA242852 from the U.S. National Cancer Institute.
PY - 2024/1/1
Y1 - 2024/1/1
N2 - Difference-in-differences is undoubtedly one of the most widely used methods for evaluating the causal effect of an intervention in observational (i.e., nonrandomized) settings. The approach is typically used when pre- and postexposure outcome measurements are available, and one can reasonably assume that the association of the unobserved confounder with the outcome has the same absolute magnitude in the two exposure arms and is constant over time; a so-called parallel trends assumption. The parallel trends assumption may not be credible in many practical settings, for example, if the outcome is binary, a count, or polytomous, as well as when an uncontrolled confounder exhibits nonadditive effects on the distribution of the outcome, even if such effects are constant over time. We introduce an alternative approach that replaces the parallel trends assumption with an odds ratio equi-confounding assumption under which an association between treatment and the potential outcome under no treatment is identified with a well-specified generalized linear model relating the pre-exposure outcome and the exposure. Because the proposed method identifies any causal effect that is conceivably identified in the absence of confounding bias, including nonlinear effects such as quantile treatment effects, the approach is aptly called universal difference-in-differences. We describe and illustrate both fully parametric and more robust semiparametric universal difference-in-differences estimators in a real-world application concerning the causal effects of a Zika virus outbreak on birth rate in Brazil. A supplementary digital video is available at: http://links.lww.com/EDE/C90.
AB - Difference-in-differences is undoubtedly one of the most widely used methods for evaluating the causal effect of an intervention in observational (i.e., nonrandomized) settings. The approach is typically used when pre- and postexposure outcome measurements are available, and one can reasonably assume that the association of the unobserved confounder with the outcome has the same absolute magnitude in the two exposure arms and is constant over time; a so-called parallel trends assumption. The parallel trends assumption may not be credible in many practical settings, for example, if the outcome is binary, a count, or polytomous, as well as when an uncontrolled confounder exhibits nonadditive effects on the distribution of the outcome, even if such effects are constant over time. We introduce an alternative approach that replaces the parallel trends assumption with an odds ratio equi-confounding assumption under which an association between treatment and the potential outcome under no treatment is identified with a well-specified generalized linear model relating the pre-exposure outcome and the exposure. Because the proposed method identifies any causal effect that is conceivably identified in the absence of confounding bias, including nonlinear effects such as quantile treatment effects, the approach is aptly called universal difference-in-differences. We describe and illustrate both fully parametric and more robust semiparametric universal difference-in-differences estimators in a real-world application concerning the causal effects of a Zika virus outbreak on birth rate in Brazil. A supplementary digital video is available at: http://links.lww.com/EDE/C90.
KW - Difference-in-differences
KW - Equi-confounding
KW - Extended propensity score
KW - Generalized linear models
KW - Odds ratios
KW - Selection bias
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U2 - 10.1097/EDE.0000000000001676
DO - 10.1097/EDE.0000000000001676
M3 - Article
C2 - 38032801
AN - SCOPUS:85178501968
SN - 1044-3983
VL - 35
SP - 16
EP - 22
JO - Epidemiology
JF - Epidemiology
IS - 1
ER -