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Raise the Bar: State-Based Marketplaces Using Quality Tools to Enhance Health Equity

Nurse shakes hand with patient in doctors office

Registered nurse Leslie Stavig (right) shakes hands with client Robert Reed after taking a blood sample at the Alameda County Health Care for the Homeless clinic in Oakland, Calif., on June 6, 2019. California and Washington are customizing requirements to strengthen their health quality and equity programs by collecting data stratified by race and ethnicity to identify systemic disparities and address racial discrimination. Photo: Paul Chinn/San Francisco Chronicle via Getty Images

Registered nurse Leslie Stavig (right) shakes hands with client Robert Reed after taking a blood sample at the Alameda County Health Care for the Homeless clinic in Oakland, Calif., on June 6, 2019. California and Washington are customizing requirements to strengthen their health quality and equity programs by collecting data stratified by race and ethnicity to identify systemic disparities and address racial discrimination. Photo: Paul Chinn/San Francisco Chronicle via Getty Images

Authors
  • Headshot of Jalisa Clark
    Jalisa Clark

    Research Fellow, Center on Health Insurance Reforms, Health Policy Institute, McCourt School of Public Policy, Georgetown University

  • Christine Monahan
    Christine Monahan

    Assistant Research Professor, Center on Health Insurance Reforms, Health Policy Institute, McCourt School of Public Policy, Georgetown University

Authors
  • Headshot of Jalisa Clark
    Jalisa Clark

    Research Fellow, Center on Health Insurance Reforms, Health Policy Institute, McCourt School of Public Policy, Georgetown University

  • Christine Monahan
    Christine Monahan

    Assistant Research Professor, Center on Health Insurance Reforms, Health Policy Institute, McCourt School of Public Policy, Georgetown University

One of the ways the Affordable Care Act (ACA) sought to improve health care quality was by establishing a Quality Improvement Strategy (QIS) program and Quality Rating System (QRS) for health coverage sold through the ACA marketplaces. More recently, the federal government has begun using the QIS program and QRS parameters to advance health equity. Federal rules now require all marketplace insurers to adopt a strategy for reducing health disparities and to stratify certain clinical data by race and ethnicity.

While state-based marketplaces (SBMs) have authority to supplement these federal minimum QIS and QRS standards with state-specific quality rules, most have hewed closely to the federal default approach. California and Washington are notable exceptions. Each has implemented a customized QIS program and robust data collection standards to identify and reduce racial and ethnic health disparities.

Overview of Federal Implementation of Marketplace Coverage Quality Initiatives

Quality Improvement Strategy (QIS): The ACA’s QIS program mandates that carriers participating in the marketplaces for a minimum of two years design and implement: 1) a strategy for improving performance in at least one of four key categories: health outcomes, hospital readmissions, patient safety and medical errors, and the promotion of wellness and health; and 2) a strategy dedicated to reducing disparities among people of color, LGBTQ+ people, people with disabilities, people who live in rural areas, or people otherwise adversely affected by poverty and inequality in health and health care.

Quality Rating System (QRS): The ACA’s QRS is used to help marketplace consumers understand the quality and value of the plans offered. Plans are scored on a 1-to-5-star scale. To calculate these scores, CMS mandates insurers to submit clinical data, as well as data on enrollee experience, plan efficiency, affordability, and management. The clinical data categories measure insurers’ performance in 28 areas, including screenings, immunizations, medication adherence, and disease management. For example, the “cervical cancer screening” measurement requires insurers to report the percentage of eligible enrollees screened for cervical cancer. The Centers for Medicare and Medicaid Services (CMS) requires that plans stratify 10 of the 28 clinical quality measurements by race and ethnicity.1 CMS has proposed to expand stratified race and ethnicity data for five additional clinical data measurements for 2025, bringing the total to 15.

Washington's Strategic Move to Develop Its Own Quality Improvement Strategy

In 2022, Washington began tailoring its QIS requirements to improve insurers’ performance on quality metrics. Washington designates specific QRS clinical measurements for which insurers must provide the state with data and requires them to implement a quality improvement strategy incorporating these measurements. For 2024, carriers will be required to submit QRS measurements for cervical cancer screening and antidepressant medication management.

Part of Washington’s strategy is designed to target health disparities. Historically, there have been racial and ethnic disparities in cervical cancer screening rates and antidepressant medication adherence. In 2023, Washington began requiring issuers to present both measurement results stratified by race and ethnicity to identify health disparities. (CMS requires insurers to report both measurements under the federal QRS program but does not require these measurements to be stratified by race and ethnicity.) The state was able to take this important step because it has prioritized the collection of enrollee race and ethnicity data. The marketplace already has made significant strides working with insurers to collect directly reported data and has established still higher reporting standards for future years.

California’s New Quality Transformation Initiative Lays a Foundation for Data Stratification

Covered California has rolled out an innovative Quality Transformation Initiative (QTI) and is building into the program ways to reduce health disparities. Through the QTI program, California penalizes insurers who place below the 66th national percentile for four QRS-required clinical measures: controlling high blood pressure, comprehensive diabetes care, colorectal cancer screening, and childhood immunization status. Penalties will be collected into a Quality Transformation Fund and used to finance activities that positively impact population health. Separately, carriers are also penalized for failing to report enrollees’ spoken and written language and collecting less than 80 percent of enrollees’ directly reported race and ethnicity data.

California intends to use stratified race and ethnicity data to build health equity accountability into the QTI program. California will evaluate whether carriers meet the 66th percentile threshold for each OMB-designated racial and ethnic group. (Race and ethnicity groups without sizable populations will be combined in an “all other members” group.) The financial penalties imposed on carriers will be adjusted based on the size of the respective racial or ethnic population groups. Overall population measurements can mask differences in outcomes for various demographics. By not only requiring the data to be stratified but also holding carriers to the same threshold, California's health equity methodology emphasizes the importance of ensuring that no racial or ethnic group is subjected to lower health care quality standards.

The implementation of health equity accountability is targeted for the 2026–28 QTI contract period. In the interim, Covered California mandates that insurers provide details on how they will address health disparities. For example, insurers may state the measures they are implementing to collect demographic data or strategies to ensure consumers can access health care in their preferred language.

Looking Ahead

In the reoccurring discussions about social justice, advocates have emphasized that equity cannot be optional, a principle that holds true in the realm of care quality. Washington and California highlight opportunities for other state-based marketplaces to strengthen their quality programs. These efforts also suggest that CMS could raise standards across SBMs by continuing to incorporate health equity in the QIS and QRS programs. CMS should implement its plans to mandate carriers to use directly reported race and ethnicity data for enrollees and continue to increase the number of QRS clinical measures that must be stratified by race and ethnicity. To promote transparency and allow for accountability, CMS should publicly report issuers’ stratified QRS data and provide details on the QIS programs that issuers submit to address health care disparities.

Quality reporting programs that do not rely on data stratified by race and ethnicity run the risk of making inaccurate assumptions about the actual state of health care services in America. Such oversight not only conceals existing disparities but also contributes to the perpetuation of racial discrimination within the U.S. health care system.

NOTES
  1. The 10 measurements insurers are required to stratify by race and ethnicity data are: asthma medication ratio, breast cancer screening, child and adolescent well-care visits, colorectal cancer screening, controlling high blood pressure, hemoglobin A1c (HbA1c) control for patients with diabetes: HbA1c poor control (>9.0%), immunizations for adolescents, initiation and engagement of substance use disorder treatment, prenatal and postpartum care, and well-child visits in the first 30 months of life.

Publication Details

Date

Contact

Jalisa Clark, Research Fellow, Center on Health Insurance Reforms, Health Policy Institute, McCourt School of Public Policy, Georgetown University

Citation

Jalisa Clark and Christine H. Monahan, “Raise the Bar: State-Based Marketplaces Using Quality Tools to Enhance Health Equity,” To the Point (blog), Commonwealth Fund, May 22, 2024. https://doi.org/10.26099/046M-5X35