Medicaid & CHIP Payment & Access Commission Issues Public Comment on OMB Notice
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On behalf of the Medicaid and
(MACPAC), I am offering these comments on the request for information (RFI) noted above. As you may know, MACPAC is a nonpartisan legislative branch agency that provides policy and data analysis and makes recommendations to
We are encouraged by the Administration's interest in making equity a governmentwide effort and urge ongoing sustained attention to combating institutional racism in health care and addressing racial and ethnic disparities in health care and health outcomes. The Medicaid program should be a key target for such work given that 60 percent of Medicaid's 81 million beneficiaries identify as Black, Hispanic, or other non-white race or ethnicity. Moreover, the research literature is replete with examples of disparities in access, quality, and care within the program (MACPAC 2021d).
The work of the
Focus on data needs
Given the
Our analysis of more recent T-MSIS data (2018) continues to show high levels of missing or unknown data on race and ethnicity, in some cases worse performance than in 2016. Specifically, 11 states are missing race data for 10-30 percent of their enrollees and 5 states are missing more than 30 percent. In addition, 14 states have 10-30 percent unknown race data, and 7 states have more than 30 percent unknown race data. States with high levels of unknown data and those with high levels of missing data rarely overlap. In short, just 19 states had more than 90 percent of beneficiary records reporting an identifiable race and ethnicity.
Missing data may indicate several issues. Beneficiaries may not disclose their race and ethnicity when applying for or renewing coverage due to concerns about how the data might be used, and states may not report these data to CMS.
Moreover, data contained in T-MSIS may be inaccurate, given that in many cases, these data conflict with benchmarks such as the
Insufficient and inaccurate data make it difficult to assess disparities, develop appropriate interventions, and monitor progress. CMS should place a higher priority of these fields in its data validation activities and support states in gathering these data. For example, the agency could provide technical assistance to states on approaches to capture data on race and ethnicity at enrollment, including proven methods that not only improve data collection but build trust with enrollees regarding the use of such data. The latter could improve completeness by addressing hesitancy regarding self reporting of race and ethnicity.
Moreover, CMS could do more to highlight the importance of these data by disaggregating key measures by race and ethnicity in its own data reports.
Focus on policies and practices that promote equity
While better data are crucial to the work of federal and state agencies in documenting specific disparities in health care, in the Commission's view, the work to develop and implement more equitable policies does not have to wait until data improvement efforts are complete or disparities can be measured with scientific precision. There are multiple areas of opportunity that could be addressed through subregulatory guidance, waiver opportunities, and technical assistance such as:
* developing more robust approaches to monitoring access, both generally as well as for specific services for which Medicaid plays a predominant role (e.g., behavioral health services, housing supports, and long-term services and supports);
* critically examining network adequacy and payment levels in relation to access;
* providing sustained attention to measure and address disparities in Adult and Child Core Set quality measures;
* making investments in outreach and enrollment efforts to reach those who are eligible but not enrolled;
* designing payment and delivery system policies that value improvements in equity as an outcome measure;
* focusing on efforts to reach and support beneficiaries whose primary language is not English; and
* considering how to improve cultural competency in program operations and policies, including state Medicaid programs themselves, their advisory committees, managed care organizations with Medicaid contracts, and providers serving the Medicaid population.
Such efforts should also consider other disparities including those affecting people with disabilities and those residing in rural areas.
Finally, as you are well aware, communities of color have been disproportionately affected by the COVID-19 pandemic. They have experienced higher rates of infections, hospitalizations, deaths, and lower vaccination rates. As the pandemic attenuates, plans to unwind emergency authorities and return to normal operations should be designed to ensure that people of color are not disproportionately affected by activities such as the resumption of regular eligibility redeterminations or the ending of waiver flexibilities. In addition, state policies regarding use of telehealth have the potential to improve access for this population assuming appropriate attention to the availability of technology and sufficient connectivity. The way in which these activities are managed will be an important test of how CMS will prioritize equity considerations.
Thank you for your attention to MACPAC's input. If you have additional questions, please feel free to reach out to
Sincerely,
Chair
Cc:
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References
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The notice can be viewed at: https://www.regulations.gov/document/OMB-2021-0005-0001
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