EHR Data and Inclusion of Multiracial Asian American, Native Hawaiian, and Pacific Islander People-Opportunities for Advancing Data-Centered Equity in Health Research (JAMA Network Open)
Summary: This article highlights the underrepresentation of Asian American, Native Hawaiian, and Pacific Islander (AANHPI) individuals in health research due to insufficient data disaggregation and limited inclusion in electronic health record (EHR) systems.
Authors emphasize the need for more comprehensive data collection and analysis methods to accurately represent the diverse health experiences within the AANHPI communities. They argue that the current lack of disaggregated data hinders efforts to address health disparities and effectively allocate resources for these populations. By incorporating EHR data that includes ethnicity and race identifiers, researchers can gain insights into the unique health needs and challenges faced by multiracial AANHPI individuals.
The article discusses the potential benefits of leveraging EHR data to inform policies and interventions aimed at reducing health inequities. With improved data collection practices, health care providers and policymakers can develop targeted strategies to address the specific health concerns of AANHPI communities and promote better health outcomes.
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