Offers practical recommendations to improve telemedicine interventions to be more equitable for diverse populations, particularly those with low incomes.

Includes patient- and staff-reported measures to help complex care programs better understand the impacts of interventions.

Presents a framework and tools to help health care organizations and communities design a community-based palliative care program to meet patient needs in rural settings.

Disparities in transitional care training for caregivers of older adults based on race or financial status demonstrate need for changes in discharge processes and strategies to address bias.

Toolkit details how hospitals and health systems can use patient race, ethnicity, and language data to advance health equity and eliminate disparities.

Many physicians report low confidence in caring for patients with disability and negative perceptions about quality of life with a disability, which may reflect biased views that potentially contribute to persistent health disparities.

Health care organizations can use population-level data sources about the experiences of people with disabilities to improve care.

The value of community health workers in advancing health equity.

When identifying patients with complex health needs for interventions, algorithms that rely on cost data as a proxy for health status may lead to under-identification of Black patients.

Tailoring palliative care interventions for people who are members of ethnic and racial minority groups may support increased access to palliative care and end of life services.

Permanent supportive housing programs with a “Housing First” approach can improve health outcomes and reduce acute care use for people experiencing homelessness with disabling conditions.

Strategies for health centers and supportive housing providers to advance health equity by partnering to provide person-centered care.