Key result
Indirectly estimated race/ethnicity (BISG) failed to detect the differential impact of full drug coverage on clinical events seen with self-reported race (interaction P=0.83 vs P=0.05).
Why the study?
Does indirectly estimated race/ethnicity accurately describe disparities in clinical outcomes and health behaviors compared to self-reported race/ethnicity in post-MI patients?
Observational (n=2,387)
Does indirectly estimated race/ethnicity accurately describe disparities in clinical outcomes and health behaviors compared to self-reported race/ethnicity in post-MI patients?
Effect estimate: HR 0.87
p-value: p=0.83
Indirectly estimated race/ethnicity using BISG may not accurately capture disparities in clinical outcomes and health behaviors compared to self-reported race/ethnicity.
Indirect estimates may miss race-based outcome differences post-MI; leaves open whether self-reported data are required for disparity research.
BACKGROUND: Methods of estimating race/ethnicity using administrative data are increasingly used to examine and target disparities; however, there has been no validation of these methods using clinically relevant outcomes. OBJECTIVE: To evaluate the validity of the indirect method of race/ethnicity identification based on place of residence and surname for assessing clinically relevant outcomes. DATA SOURCES: A total of 2387 participants in the Post-MI Free Rx Event and Economic Evaluation (MI FREEE) trial who had both self-reported and Bayesian Improved Surname Geocoding method (BISG)-estimated race/ethnicity information available. STUDY DESIGN: We used tests of interaction to compare differences in the effect of providing full drug coverage for post-MI medications on adherence and rates of major vascular events or revascularization for white and nonwhite patients based upon self-reported and indirect racial/ethnic assignment. RESULTS: The impact of full coverage on clinical events differed substantially when based upon self-identified race (HR=0.97 for whites, HR=0.65 for nonwhites; interaction P-value=0.05); however, it did not differ among race/ethnicity groups classified using indirect methods (HR=0.87 for white and nonwhites; interaction P-value=0.83). The impact on adherence was the same for self-reported and BISG-estimated race/ethnicity for 2 of the 3 medication classes studied. CONCLUSIONS: Quantitatively and qualitatively different results were obtained when indirectly estimated race/ethnicity was used, suggesting that these techniques may not accurately describe aspects of race/ethnicity related to actual health behaviors.
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Bykov et al. (2015) conducted an observational in Post-MI (n=2,387). Indirect method of race/ethnicity identification (BISG) vs. Self-reported race/ethnicity was evaluated on Differences in the effect of full drug coverage on rates of major vascular events or revascularization (HR 0.87, p=0.83). Indirectly estimated race/ethnicity (BISG) failed to detect the differential impact of full drug coverage on clinical events seen with self-reported race (interaction P=0.83 vs P=0.05).
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