Enhancing the Quality of Race and Ethnicity Data Can Advance Health Equity
New research by the Urban Institute, American Benefits Council, and Deloitte's Health Equity Institute, funded by Elevance Health, highlights the importance of high-quality race and ethnicity data in addressing health disparities. The report identifies challenges related to inconsistent data, which hinders the tracking of health inequities. Key recommendations include enhancing community engagement, ensuring data privacy, and modernizing data collection practices to promote health equity. The COVID-19 pandemic has intensified the urgency for comprehensive data to tailor care for marginalized communities.
- Funding of new research to improve health equity data collection.
- Collaboration with key health stakeholders to enhance data quality.
- Inconsistent and incomplete data makes tracking health disparities difficult.
- Concerns about data privacy may hinder data sharing.
- New research highlights the role of high-quality data on race and ethnicity as a critical tool in reducing health disparities, but data availability problems can limit this potential.
- Solutions include clarifying the value of such data, building consumer trust, strengthening community engagement, reducing actual and perceived legal concerns, and modernizing data collection practices.
The report, “Collection of Race and Ethnicity Data for Use by Health Plans to Advance Health Equity,” finds that improved collection of race and ethnicity data for use by health insurers, and others, can help identify and address inequities in health care.
Perspectives from various health care stakeholders -- including commercial health insurance plans, health care providers, employers, community-based organizations, foundations, and research organizations -- offer several potential actions to improve the availability of high-quality race and ethnicity data:
- Developing a collective understanding of the value of improving the quality and availability of race and ethnicity data.
- Including community engagement and trusted community partners in efforts to improve data collection.
- Providing transparency about the reasons for collecting data, as well as creating and sharing guardrails to ensure data security and patient privacy while preventing harm to historically marginalized people and communities.
- Addressing concerns about the legality and permissibility of data collection and sharing among employers and others, through clarifying language from the federal government.
- Contributing to and enhancing current efforts by federal leadership to develop more inclusive standards for self-reported and voluntary identification of individuals’ race and ethnicity.
- Investing in updated data collection standards, interoperable data systems, and robust training on data collection for frontline health workers.
“Health plans play a critical role in reducing health disparities, yet we sometimes lack complete data to support a whole health approach, which is why we funded this work,” said
“Employers are the source of health coverage for most Americans and are committed to ensuring high-quality care for their workforces and the communities in which they live. This include addressing disparities in care,” said
“The COVID-19 pandemic has exacerbated health inequities in communities of color and increased the urgency for both more complete self-reported race and ethnicity data, and better data collection processes,” said
A related survey separately conducted by Deloitte’s
“We can’t improve what we don’t measure,” said
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eric.lail@elevancehealth.com
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