Collecting Data to Ensure Equity in Payment Policy

This discussion proceedings addresses the critical role of data collection in promoting equitable health care payment models.

This publication is part of a collaborative initiative with the Center for Medicare & Medicaid Innovation (CMMI) aimed at transforming the U.S. health system toward higher quality and efficiency.

The proceedings emphasizes the importance of collecting comprehensive demographic and social determinants of health data, including race, ethnicity, language, disability status, sexual orientation, and gender identity.

Accurate and standardized data collection is essential for identifying health disparities, informing payment policy reforms, and advancing health equity.

Key challenges highlighted include inconsistent data collection methods, lack of standardized data collection standards, and limited resources for implementation.

The publication outlines actionable steps to address these challenges, such as enhancing data collection standards, providing technical assistance, engaging communities, and building a robust data infrastructure.

By implementing these strategies, policy makers and health care providers can develop payment models that promote equitable access to care and improve health outcomes for all populations.