Health and Health Care for American Indian or Alaska Native People: Key Issues

Published: Dec 19, 2025

Introduction

Recent and forthcoming policy changes may have important implications for American Indian or Alaska Native (AIAN) people and could widen existing disparities in health and health care. This brief provides an overview of recent policies affecting health and health care for AIAN people and their potential impacts. It draws on data from KFF’s Key Data on Health and Health Care for American Indian or Alaska Native People and KFF analysis of recent laws and policy changes. AIAN people are identified as a racial and ethnic group. However, AIAN is also a political and legal classification. This status recognizes over 570 AIAN Tribes as sovereign nations, establishing a government-to-government relationship that dictates the federal government’s trust responsibility, including the provision of health care to AIAN people in federally recognized Tribes.  Key takeaways include the following:

  • The 2025 reconciliation law makes large cutbacks in federal Medicaid spending that could negatively impact AIAN people and communities. The Congressional Budget Office (CBO) estimates that the law will reduce federal Medicaid spending over the next decade by an estimated $911 billion and increase the number of uninsured people by 10 million due to changes to Medicaid and other programs, including the ACA Marketplace. Medicaid is the primary source of health coverage for Native communities, with over one in three (35%) AIAN individuals under age 65 enrolled in Medicaid or the Children’s Health Insurance Program (CHIP), including 52% of AIAN children. Medicaid and CHIP are also the largest source of third-party funding for the Indian Health Service (IHS) and Tribal health facilities, and one of the main ways the federal government upholds its trust responsibility. To replace reductions in federal funding, states will need to increase spending or make program reductions, which could lead to eligibility and benefit cutbacks that might reduce coverage for low-income people overall, including AIAN people, and reduce funding available to IHS and other Tribal providers. Further, although the law provides exemptions for most AIAN people from new work requirements and more frequent eligibility determinations, AIAN people may face challenges documenting their eligibility for such exemptions and may experience coverage losses.
  • Similarly, changes to the ACA Marketplace may erode coverage for AIAN people. Enhanced premium tax credits are set to expire at the end of 2025, which would make coverage unaffordable for many, including AIAN people. Estimates show that as many as 40% of AIAN people enrolled in the Marketplace with tax credits will lose their coverage if these credits expire.
  • Continued underfunding of the IHS, broad reductions in federal funding and equity initiatives, and shifts in vaccination policy and attitudes may also negatively impact health and health care access for AIAN people. Despite proposed increases, FY 2026 funding for the IHS falls short of levels estimated to fully meet health care needs and fulfill the federal trust responsibility. Further, while Executive Orders focused on eliminating Diversity, Equity, and Inclusion (DEI) initiatives largely exempt Tribes, broader federal budget cuts and rollbacks to equity initiatives may reduce resources available to Tribal communities, including for data, public health surveillance, and outreach. Recent declines in vaccination rates, rising misinformation about vaccines, and shifts in federal vaccine policy may increase the risk of preventable disease outbreaks in AIAN communities, including recent measles outbreaks in the U.S.

Health Care for AIAN People

Under treaties and laws, the U.S. has a unique trust responsibility to provide health care to AIAN people. The IHS is the primary federal agency through which the federal government fulfills its trust responsibility for members of federally recognized Tribes, who make up approximately 2.8 million AIAN people from 574 federally recognized Tribes nationwide. Members of federally recognized Tribes, as well as certain other eligible AIAN individuals, can receive IHS-funded services through a network of IHS- and Tribally-run hospitals and clinics, along with Urban Indian Organizations (UIOs). AIAN people receiving services through IHS providers are not charged or billed for the cost of their services. However, the IHS has long been underfunded and lacks the resources needed to fully meet the health care needs of AIAN people. Services available through the IHS are primarily limited to primary care, although the IHS does provide some ancillary and specialty services. When care is not available within IHS or Tribal facilities, the Purchased/Referred Care (PRC) Program may fund services from outside providers. Yet, the funding for PRC has historically been insufficient and does not extend to UIOs. As a result, access to care through the IHS varies widely by location, and AIAN individuals who rely solely on the IHS often face significant barriers to obtaining needed services.

AIAN people can access health coverage through Medicaid, CHIP, and the Affordable Care Act (ACA) Marketplace, with certain unique benefits and protections. Tribal members enrolled in these programs can continue receiving care from IHS, Tribal, or UIO providers at no cost and additionally have access to a broader network of services than those available solely through IHS since they can access care through any provider participating in Medicaid and are covered by the comprehensive Medicaid benefit package. Medicaid offers specific protections for Tribal members, including exemptions from out-of-pocket costs. For the ACA Marketplace, Tribal members eligible for premium tax credits can enroll in zero or limited cost-sharing Marketplace plans and have other specific protections. For example, AIAN individuals with incomes between 100% and 300% of the federal poverty level who enroll in zero cost-sharing plans pay no out-of-pocket costs for covered services. Additionally, AIAN Marketplace enrollees have access to a Special Enrollment Period, allowing them to enroll in or switch plans once per month, beyond the standard open enrollment window that is available for other eligible people.

Health coverage improves access to care for AIAN people and strengthens Tribal health systems. Given the limitations of IHS funding and service availability, health coverage through Medicaid and the Marketplace enhances access to care for AIAN people since they can access covered care through a broader network of providers and have coverage for a comprehensive set of benefits. In addition to improving individual access to care, Medicaid is also an important source of funding for IHS and Tribal facilities and is one of the primary ways the federal government upholds its federal trust responsibility to provide health care to AIAN people. Medicaid is the largest third-party payer for the IHS, accounting for $1.3 billion out of the total almost $1.8 billion in third-party collections in fiscal year 2025. Further, unlike other Medicaid costs, which are typically shared between the federal government and states, the federal government covers 100% of the cost for services provided to AIAN Medicaid enrollees through the IHS or Tribally operated facilities whether operated directly by the IHS or on its behalf by a Tribe. Importantly, in contrast to IHS funding, Medicaid funding is not subject to annual appropriations and is provided on a continuous, claims-based basis throughout the year. As a result, Medicaid revenues are a vital funding stream that help facilities cover operational costs, pay providers, and invest in infrastructure development.

Due to a combination of lower coverage rates, additional access barriers, and historical and ongoing discrimination, AIAN people continue to face significant disparities in health and health care. AIAN people have shorter life expectancies relative to their White counterparts (70.1 vs 78.4 years at birth), higher rates of chronic diseases such as diabetes and asthma, and higher rates of suicide deaths and substance use disorder. About a quarter (26%) of AIAN adults report having fair or poor health status compared to 17% of White adults. Additionally, AIAN people face greater risks during pregnancy, including higher rates of preterm births and infant mortality. Among those under age 65, AIAN people are three times more likely to be uninsured (21%) compared to White people (7%).

Since President Trump took office in January 2025, the Administration and Congress have made significant health policy changes. While in some cases AIAN people have been specifically exempted or protected from new requirements or cutbacks, many changes may have significant impacts on health and health care for AIAN people that could exacerbate the large disparities they already face in health and health care.

Medicaid and ACA Marketplace Changes

The 2025 reconciliation legislation makes large cutbacks in federal Medicaid spending that could negatively impact low-income people overall, including AIAN people and communities. CBO estimates that the law will reduce federal Medicaid spending over the next decade by an estimated $911 billion and increase the number of uninsured people by 10 million due to changes to Medicaid and other programs, including the ACA Marketplace. Medicaid is the primary source of health coverage for Native communities with one in three (35%) AIAN individuals under age 65 enrolled in Medicaid or the Children’s Health Insurance Program (CHIP), including 52% of AIAN children. As noted, Medicaid is also the largest source of external funding for IHS and Tribal health facilities, accounting for roughly two-thirds of their third-party revenue and providing a stable funding source to support operations. To replace reductions in federal funding, states will need to increase spending or make program reductions, which could lead to broad eligibility and benefit cutbacks that might reduce coverage for low-income people overall, including AIAN people and reduce funding available to IHS and other Tribal providers.

The law imposes an array of new requirements on Medicaid enrollees but largely exempts AIAN people from these changes. The law will require more frequent Medicaid eligibility determinations (every six months), adds a new work requirement, and imposes increased cost sharing for adults enrolled in the ACA Medicaid expansion. The law exempts AIAN people from these new requirements. However, it is unclear how state Medicaid programs will verify AIAN people’s Tribal citizenship. Some AIAN people may face challenges documenting their exemption status. While states are required to use available data to verify exemption status, some AIAN people who need to document their Tribal citizenship may face challenges to submitting documents, including long distances to post offices and limited internet access, as seen during the recent unwinding of Medicaid continuous enrollment.

While the 2025 reconciliation law exempts AIAN people from changes to Marketplace coverage, the pending expiration of enhanced Marketplace subsidies could lead to declines in coverage for AIAN people. Without renewal of the enhanced tax credits, premium payments for individuals enrolled in the Marketplace are expected to more than double on average. Estimates suggest that a substantial share of AIAN people currently enrolled in a Marketplace plan could lose coverage if the enhanced premium tax credits expire, particularly in states that have not expanded Medicaid to adults.

Funding for IHS

Congressional appropriations bills for Fiscal Year (FY) 2026 increase funding for the IHS compared to prior years but still fall far short of the funding levels to fulfill the federal trust responsibility to AIAN communities. In late July 2025, both the House and Senate Appropriations Committees passed their respective FY 2026 bills, each proposing increased funding for the IHS. The House bill allocates $8.41 billion, while the Senate bill allocates $8.1 billion, both above the FY 2025 enacted level of $6.96 billion. These increases are expected to support expanded primary care, behavioral health, and preventive services, as well as help offset inflationary pressures that threaten to erode service capacity. The House bill also includes $105.99 million for Urban Indian Health and $6.05 billion in advance appropriations for FY 2027. Following the most recent government shutdown, the deadline to pass FY 2026 appropriations bills has been extended through the end of January, during which time IHS continues to operate at FY 2025 funding levels. While these bills increase funding, they fall short of estimated needs. The Tribal Budget Formulation Work Group, led by Tribal leaders across all IHS regions, has recommended full funding at $73 billion for the IHS and $1.09 billion for Urban Indian Health to meet health care needs and fill service gaps. The group has identified several areas that would benefit from increased funding including workforce shortages, Infrastructure improvement, and targeted public health initiatives, such as mental health, substance use and opioid treatment programs, efforts to eliminate HIV and hepatitis C, and culturally tailored chronic disease management through the Special Diabetes Program for Indians.

Federal Cutbacks to Staff, Diversity Initiatives, Data, and Research

Although Tribes have largely been exempted from recent reductions in DEI initiatives, broader federal program and budget cutbacks that eliminate staff and programs focused on health equity may still undermine efforts to address longstanding disparities affecting AIAN communities. While Health and Human Services (HHS) Secretary Robert F. Kennedy Jr. has suspended layoffs at IHS, Tribal leaders caution that deep cuts at other federal health agencies are causing widespread disruption. These reductions are impacting many programs Tribal communities rely on, including public health surveillance, data systems, and community outreach efforts. Tribes report that staffing losses in key federal health agencies have led to gaps in data collection, weakened communication, and delayed implementation of essential programs. Maintaining strong health data infrastructure and partnerships with Tribal communities is key for tracking health inequities and targeting resources effectively. One notable loss is the Centers for Disease Control and Prevention’s (CDC) Healthy Tribes Program, which previously provided roughly $32.5 million annually to support culturally grounded approaches, such as community gardens and incorporation of traditional wellness practices, but has now been effectively dismantled. Broader restructuring across the HHS has also affected Indian country. Tribal representatives, including the National Indian Health Board, have expressed concerns that dismantling equity-focused initiatives threatens to reverse gains addressing disparities affecting AIAN people.

Changes in Vaccine Policy

Shifts in vaccine policy, misinformation about vaccine safety, and declines in childhood vaccination rates may lead to a rise in outbreaks of once eradicated diseases with disproportionate impacts for AIAN people. HHS Secretary Kennedy, known for his longstanding opposition to vaccines and for spreading vaccine misinformation, has recently spearheaded initiatives to review the federal childhood vaccination schedule, overhaul the membership of the Advisory Committee on Immunization Practices (ACIP), and limit both COVID-19 vaccines and mRNA vaccine research. Additionally, the Trump administration has released a report advocating for a new vaccine policy framework, which includes revisiting the childhood vaccine schedule and focusing on vaccine-related injuries. Since the COVID-19 pandemic, childhood vaccination coverage has declined nationwide. Gaps in immunization are higher in AIAN communities, increasing their susceptibility to disease resurgence. Among children born in 2020, only 57% of AIAN children were fully immunized by age two, compared to 71% of non-Hispanic White children. Additionally, roughly 76% of AIAN children have received their first MMR dose, falling short of the 95% coverage required to achieve herd immunity. AIAN adults were also 30% less likely to receive a flu shot than their non-Hispanic White counterparts during the 2023–2024 season. These declines have contributed to the most severe measles outbreak in the U.S. in more than three decades. Recent measles clusters in Tribal communities, especially in the Northern Plains and Southwest, have disrupted health care access and led to temporary clinic closures. In response, IHS, Tribal, and Urban health facilities have implemented mobile vaccination units, walk-in clinics, and multilingual public health campaigns tailored to meet local needs.

At the same time, misinformation about vaccine safety continues to circulate widely. KFF polling data shows that a majority of Americans have read or heard the false claim that the MMR vaccine causes autism in children. About one-third have heard that getting the measles vaccine is more dangerous than becoming infected with measles, and 34% believe the debunked claim that MMR vaccines cause autism. Among parents, about one in ten (9%) believe the MMR vaccine can cause autism, and roughly one in six (16%) say they have ever skipped or delayed at least one childhood vaccine for any of their children. Additionally, while formally supportive of the MMR vaccine’s effectiveness, Senator Kennedy has amplified anti-vaccine narratives including debunked claims linking the MMR vaccine to autism, creating confusion and reducing clarity on vaccine safety. Beyond the existing mistrust of the health care system due to historical trauma and abuse, some Tribal leaders warn that skepticism and mistrust of the health care system among AIAN people is increasing. Together, the increased skepticism among the public about the safety and effectiveness of measles vaccines and a decline in trust of health authorities in general, have contributed to lower vaccination rates and complicated outreach and communication efforts to combat preventable disease outbreaks.

A Snapshot of Sources of Coverage Among Medicare Beneficiaries

Most in Traditional Medicare Have Supplemental Coverage that Helps Cover Medicare Cost Sharing but More Than Three Million Don’t

Published: Dec 19, 2025

Health care affordability has been a longstanding concern in the U.S., including among older adults, many of whom have relatively low incomes and modest assets to help cover the cost of premiums and medical bills. Medicare offers important financial protection by providing health insurance coverage to 69 million people in the U.S., including adults age 65 or older and younger adults with long-term disabilities. However, Medicare-covered benefits are subject to cost-sharing requirements and exclude some commonly needed services, like dental and vision care.  Additionally, traditional Medicare does not include a cap on out-of-pocket costs.

To help with cost sharing for Medicare-covered services and fill the gaps in Medicare benefits, most Medicare beneficiaries supplement traditional Medicare with additional coverage, such as Medigap, for which policyholders pay an average of $2,600 annually in premiums. More than half of people with Medicare are currently enrolled in Medicare Advantage, which offers extra benefits not available in traditional Medicare and caps annual out-of-pocket costs. Medicare beneficiaries may also have employer- or union-sponsored coverage or Medicaid coverage in addition to Medicare. But some people on Medicare lack additional coverage and face the risk of incurring high out-of-pocket costs if they need expensive medical care.

This analysis documents the different sources of coverage among people with Medicare and examines variation in beneficiary characteristics by source of coverage. The analysis draws on data from the Centers for Medicare & Medicaid Services (CMS) March 2025 Medicare Advantage enrollment files and the 2023 Medicare Current Beneficiary Survey (see Methods for details).

Key Facts

  • More than half of all people with Medicare Part A and Part B (54% or 34.1 million in 2025) are enrolled in a Medicare Advantage plan, while 46% (28.7 million) are in traditional Medicare.
  • Among traditional Medicare beneficiaries, most (87%) had additional coverage that supplements Medicare benefits in 2023, but 3.5 million beneficiaries (13%) lacked additional coverage, leaving them at risk of facing high out-of-pocket costs for medical care.
  • Overall, 14.1 million beneficiaries (23% of all Medicare beneficiaries) had employer or union sponsored coverage in 2023, either as a supplement to traditional Medicare or through group Medicare Advantage plans, another 12.2 million (20%) had Medicaid in addition to traditional Medicare or Medicare Advantage, and the same number, 12.2 million (20%) had a Medicare supplemental insurance (Medigap) policy to supplement traditional Medicare.
  • The number and share of Medicare beneficiaries with Medicaid (dual eligible individuals) were substantially higher in Medicare Advantage (68%) than traditional Medicare (32% in 2023).
  • Compared to traditional Medicare beneficiaries, Medicare Advantage enrollees were more likely to be Black or Hispanic, have incomes below $20,000 per person, and self-report fair or poor health.

More than Half of All People with Medicare Are Enrolled in Medicare Advantage

In 2025, Medicare Advantage covered more than half (54%) of Medicare beneficiaries with both Medicare Parts A and B, or 34.1 million out of about 62.8 million people. Of the total number of Medicare Advantage enrollees in 2025, most (62%) are enrolled in individual plans available to all Medicare beneficiaries. One in five (21%) are in Special Needs Plans (SNPs) and 17% are enrolled in employer- or union-sponsored group plans, where employers or unions contract with an insurer and Medicare pays the insurer a fixed amount per enrollee to provide benefits covered by Medicare. (These estimates are based on March 2025 Medicare Advantage plan enrollment data and therefore differ from those discussed below and shown in Figure 1, which are based on the 2023 Medicare Current Beneficiary Survey (MCBS)).

Compared to traditional Medicare beneficiaries, Medicare Advantage enrollees were more likely to be Black or Hispanic, have incomes below $20,000 per person, and self-report fair or poor health, based on KFF analysis of the 2023 MCBS (Figure 2, Appendix Table 1).

Medicare Advantage Enrollees Were More Likely Than Those in Traditional Medicare To Be Black or Hispanic, Low-Income, and in Poorer Health

Most Medicare Beneficiaries in Traditional Medicare Have Additional Coverage that Supplements Medicare Benefits

In 2023, most (87%) people in traditional Medicare had some form of additional coverage, either through Medigap (43%), employer coverage (29%), Medicaid (14%), or another source (1%),based on estimates from the MCBS.But 3.5 million Medicare beneficiaries in traditional Medicare (13%) had no additional coverage. A more detailed discussion of these types of coverage and the characteristics of people with each coverage type is below.

The Characteristics of Traditional Medicare Beneficiaries Vary Widely by Source of Additional Coverage

Nearly a Quarter of Medicare Beneficiaries Have Employer Coverage, Either through Group Medicare Advantage Plans or in Addition to Traditional Medicare

In total, 14.1 million Medicare beneficiaries – nearly a quarter (23%) of Medicare beneficiaries overall – had some form of employer or union-sponsored health insurance coverage in 2023 in addition to Medicare Part A and Part B. Of this total, 8.2 million beneficiaries had employer coverage in addition to traditional Medicare (29% of beneficiaries in traditional Medicare), while 5.9 million beneficiaries were enrolled in Medicare Advantage employer group plans. Most people with both Medicare Part A and Part B and employer- or union-sponsored coverage are retirees with Medicare as their primary source of health insurance coverage.

Compared to traditional Medicare beneficiaries overall in 2023, beneficiaries with employer or union-sponsored coverage in addition to traditional Medicare were more likely to have higher incomes ($40,000 or greater per person), a bachelor’s degree or higher, self-report excellent or good health, and were less likely to be under age 65 (Figure 3, Appendix Table 1).

Separately, in 2023, an estimated 5.8 million Medicare beneficiaries had Part A only, a group that primarily includes people who were active workers (either themselves or their spouses) and had primary coverage from an employer plan and Medicare as a secondary payer. People with Part A only cannot enroll in a Medicare Advantage plan, so people with coverage through Medicare Advantage employer group plans are likely to be retired.

Four in 10 People in Traditional Medicare Have a Medigap Supplemental Policy

Medicare supplement insurance, also known as Medigap, covered 2 in 10 (20%) Medicare beneficiaries overall, or 43% of those in traditional Medicare (12.2 million beneficiaries) in 2023. Medigap policies, sold by private insurance companies, fully or partially cover Medicare Part A and Part B cost-sharing requirements, including deductibles, copayments, and coinsurance. Medigap limits the financial exposure of Medicare beneficiaries and provides protection against catastrophic medical expenses. However, Medigap premiums can be costly and can rise with age, among other factors, depending on the state in which they are regulated.

Compared to all traditional Medicare beneficiaries in 2023, beneficiaries with Medigap were more likely to be White, have higher annual incomes (above $20,000 per person), self-report excellent, very good, or good health, and have a bachelor’s degree or higher (Figure 3, Appendix Table 1).

In contrast, a smaller share of traditional Medicare beneficiaries under age 65 have a Medigap policy than traditional Medicare beneficiaries ages 65 and older (1% versus 9%). Federal law provides a 6-month guarantee issue protection for adults ages 65 and older when they first enroll in Medicare Part B if they want to purchase a supplemental Medigap policy, but these protections do not extend to adults under the age of 65 with disabilities, and most states do not require insurers to issue Medigap policies to beneficiaries under age 65.

One in Five People with Medicare Also Have Coverage from Medicaid, with More Covered Under Medicare Advantage than Traditional Medicare

Medicaid, the federal-state program that provides health and long-term services and supports coverage to low-income people, was a source of supplemental coverage for 12.2 million Medicare beneficiaries with low incomes and modest assets in 2023, or 20% of all Medicare beneficiaries. A larger number and share of Medicare beneficiaries with Medicaid (known as dual-eligible individuals) were enrolled in a Medicare Advantage plan (8.3 million, or 68% of all dual-eligible individuals) than in traditional Medicare (4.0 million, or 32%) (Appendix Table 1). For these beneficiaries, Medicaid typically pays the Medicare Part B premium and may also pay a portion of Medicare deductibles and other cost-sharing requirements. Most dual-eligible individuals are also eligible for full Medicaid benefits, including long-term services and supports.

Compared to traditional Medicare beneficiaries overall in 2023, dual-eligible individuals were more likely to have low incomes and relatively low education levels, self-report fair or poor health, identify as Black or Hispanic, and be under the age of 65 (Figure 3, Appendix Table 1).

3.5 Million Traditional Medicare Beneficiaries Lack Supplemental Coverage

In 2023, 3.5 million Medicare beneficiaries – 6% overall –and 13% of beneficiaries in traditional Medicare – had no supplemental health insurance coverage. Traditional Medicare beneficiaries with no additional coverage are fully exposed to Medicare’s cost-sharing requirements, which would mean paying a $1,736 deductible for a hospital stay in 2026, daily copayments for extended hospital and skilled nursing facility stays, and a $283 deductible plus 20% coinsurance for physician visits and other outpatient services. (These costs are in addition to the standard Part B premium amount of $203 per month in 2026). Beneficiaries in traditional Medicare without additional coverage also face the risk of high annual out-of-pocket costs because there is no cap on out-of-pocket spending for Part A and B services in traditional Medicare, unlike in Medicare Advantage plans.

Beneficiaries in traditional Medicare without any form of additional coverage were more likely to have modest incomes (between $20,000 and $40,000 per person) compared to all traditional Medicare beneficiaries in 2023 (Figure 3, Appendix Table 1). Medicare beneficiaries with modest incomes have limited ability to afford Medigap premiums and are unlikely to qualify for Medicaid because their income and assets are not low enough to meet eligibility guidelines.

The number and share of traditional Medicare beneficiaries without any form of supplemental coverage has steadily declined in recent years. Between 2018 and 2023, the number of traditional Medicare beneficiaries without supplemental coverage declined from 5.6 million beneficiaries (10% of the total Medicare population, or 17% of those in traditional Medicare) to 3.5 million (6% of the total Medicare population, or 13% of those in traditional Medicare). This decline likely reflects the increase in Medicare Advantage enrollment over time, which has increased from 20 million in 2018 to 34 million in 2025.

Methods

For information on Medicare Advantage enrollment in 2025, this analysis draws on data from the Centers for Medicare & Medicaid Services (CMS) Medicare Advantage Enrollment files for March 2025 (See Methods of KFF, “Medicare Advantage in 2025: Enrollment Update and Key Trends” for more details). For information on sources of supplemental coverage within traditional Medicare and Medicare Advantage, this analysis draws on data from the CMS Medicare Current Beneficiary Survey (MCBS) 2023 Survey file data (the most recent year available), a nationally representative survey of Medicare beneficiaries.

Sources of coverage are determined based on the source of coverage held for the most months of Medicare enrollment in 2023. The analysis includes 60.4 million people with both Part A and B Medicare coverage in 2023 (weighted), including beneficiaries living in the community and in facilities. It excludes beneficiaries who were enrolled in Part A only (typically active workers or their spouses with employer or union sponsored coverage) or Part B only for most of their Medicare enrollment in 2023 (weighted n=5.4 million) and beneficiaries who had Medicare as a secondary payer (weighted n=1.7 million). (Because this analysis reflects coverage held for most months, it shows fewer Medicare beneficiaries with Part A-only or Part B-only coverage than the CMS Medicare enrollment dashboard, which reports 5.8 million with Part A only in 2023). The analysis also focuses only on coverage for Part A and Part B benefits, not Part D. This analysis of the MCBS accounted for the complex sampling design of the survey.

In this brief, the number and share of beneficiaries enrolled with both Medicare and Medicaid coverage (dual-eligible individuals) do not align with other KFF estimates due to differences in data sources and methods used. In other KFF publications, the number of dual-eligible individuals is estimated using a 100% CCW sample and include dual-eligible individuals with at least one month of enrollment in Medicare Part A or Part B, rather than those with coverage for most months of the year. The analysis in this brief is based on the MCBS because this data source provides a wider array of demographic and health status indicators than the CCW.

All reported differences in the text are statistically significant; results from all statistical tests are reported with p<0.05 considered statistically significant. Because estimates reported in the text and figures are rounded to the nearest whole number, some estimates may not sum to overall totals due to rounding.

Appendix

Sources of Coverage Among Medicare Beneficiaries, 2023

State and Federal Reproductive Rights and Abortion Litigation Tracker

Last updated on

The Supreme Court’s Dobbs ruling, overturning Roe v. Wade, returned the decision to restrict or protect abortion to states. In many states, abortion providers and advocates are challenging state abortion bans contending that the bans violate the state constitution or another state law. The state litigation tracker presents up-to-date information on the ongoing litigation challenging state abortion policy.

In addition, since the Dobbs decision, new questions have arisen regarding the intersection of federal and state authority when it impacts access to abortion and contraception. Litigation has been brought in federal court to resolve some of these questions. The federal litigation tracker presents up-to-date information on the litigation in federal courts that involves access to contraception and abortion.

Status of Abortion Litigation in State Courts, as of 2/14/2023
Status of Abortion Litigation in State Courts, as of February 15, 2023

State and Federal Reproductive Rights and Abortion Litigation Tracker

Last updated on

The Supreme Court’s Dobbs ruling, overturning Roe v. Wade, returned the decision to restrict or protect abortion to states. In many states, abortion providers and advocates are challenging state abortion bans contending that the bans violate the state constitution or another state law. The state litigation tracker presents up-to-date information on the ongoing litigation challenging state abortion policy.

In addition, since the Dobbs decision, new questions have arisen regarding the intersection of federal and state authority when it impacts access to abortion and contraception. Litigation has been brought in federal court to resolve some of these questions. The federal litigation tracker presents up-to-date information on the litigation in federal courts that involves access to contraception and abortion.

Litigation Involving Reproductive Health and Rights in the Federal Courts, as of February 15, 2023

What to Know About Pharmacy Benefit Managers (PBMs) and Federal Efforts at Regulation

Published: Dec 18, 2025

The price of prescription drugs in the U.S. continues to be a concerning issue to the public, with KFF polling consistently showing the public supports various approaches to lowering prescription drug costs. Efforts to rein in drug costs have long been a priority for both federal and state policymakers. The Trump administration has recently taken steps to address drug costs through Executive Orders and multiple pricing agreements to bring ‘Most Favored Nation’ pricing to consumers in the U.S., though the impact and savings from these efforts are not yet known. The Biden administration enacted the Inflation Reduction Act of 2022, which authorized the federal government to negotiate lower drug prices with manufacturers for some drugs covered by Medicare, among other provisions, resulting in an estimated reduction in the federal deficit of $237 billion over 10 years for the drug pricing provisions alone.

One player in the system of pharmaceutical pricing in the U.S. that has come under increasing scrutiny in recent years is the pharmacy benefit manager, or PBM. These so-called ‘middlemen’ are used by health insurance companies to manage their pharmacy benefits. PBMs have been the focus of attention from policymakers for several reasons, including their business practices, market consolidation, and lack of transparency, all of which factor into concerns that PBMs themselves have played a role in increasing drug prices, even as they work to manage pharmacy benefits and costs for insurers.

In an April 2025 Executive Order, the Trump administration directed the Assistant to the President for Domestic Policy to reevaluate the role of ‘middlemen’ to “promote a more competitive, efficient, transparent, and resilient pharmaceutical value chain”. In the current session of Congress, legislation addressing various concerns related to PBMs and their business practices has been introduced and voted on but not enacted, including provisions in recent House GOP legislation responding to the expiration of the enhanced ACA premium subsidies, which passed the House in December 2025, and in budget reconciliation legislation passed by the House but not the Senate in May 2025. This brief provides an overview of the role of PBMs in managing pharmacy benefits, discusses recent federal legislation focusing on several elements of PBM business practices, and explains the potential federal budgetary impact of this legislation, which would have a relatively modest impact on the federal deficit, based on available CBO estimates. (This brief focuses on actions at the federal level and does not address state legislative efforts related to PBMs, which have occurred in all 50 states.)

The Role of PBMs

Pharmacy benefit managers (PBMs) act as intermediaries between drug manufacturers and insurance companies that offer drug benefits to employer health plans, Medicare Part D prescription drug plans, state Medicaid programs, and other payers. In this role, PBMs serve several functions: negotiating rebates and price discounts with drug manufacturers, processing and adjudicating claims, reimbursing pharmacies for drugs dispensed to patients, structuring pharmacy networks, and designing drug benefit offerings, which includes developing formularies (lists of covered drugs), determining utilization management rules, and establishing cost-sharing requirements.

Although there are many PBMs, a few companies dominate the overall U.S. market. According to the Federal Trade Commission (FTC), the top 3 PBMs – OptumRx (owned by UnitedHealth Group), Express Scripts (owned by Cigna), and CVS Caremark (owned by CVS Health, which also owns Aetna) – manage 79% of prescription drug claims on behalf of 270 million people in 2023 (Figure 1).

In 2023, the Top 3 PBMs - CVS Caremark, Express Scripts, and OptumRx - Managed 79% of Prescription Drug Claims in the U.S.

Certain PBM Business Practices Have Given Rise to Concerns About Their Impact on Drug Prices

Sources of revenue: PBMs generate revenue in different ways. PBMs are typically paid fees for the functions they serve managing pharmacy benefits. PBMs also negotiate rebates with drug manufacturers in exchange for preferred placement of rebated drugs on a health insurance plan formulary, and they may retain a portion of the drug rebates they negotiate, though this may be more common in the commercial employer market than in the Medicare Part D market. Many state Medicaid programs and Medicaid managed care plans also contract with PBMs to manage or administer pharmacy benefits, including negotiating supplemental prescription drug rebates with manufacturers.

Rebates can help lower the cost of drug benefits for health insurers, which enables them to offer lower premiums in turn and may translate to lower out-of-pocket costs for patients at the point of sale. In order for PBMs to maximize rebate revenue, however, they may favor higher-priced drugs with higher rebates over lower-priced drugs with low or no rebates in their negotiations with drug companies. This may have an inflationary effect on drug pricing by manufacturers, increase costs for payers across the system, and raise out-of-pocket costs for patients who pay based on the list price – a particular concern for those without insurance but also for those with high-deductible insurance plans or when cost sharing is calculated as a percentage of the drug’s price, such as for Part B drugs under Medicare.

Because of these impacts, some have suggested that rebates negotiated between PBMs and drug manufacturers should be passed along in full to individuals at the point of sale and make discounts available upfront at the pharmacy counter. This arrangement would produce savings for individuals who take drugs with high rebates, since they would face lower out-of-pocket costs on their medications when they fill their prescriptions. However, if rebates are no longer being used to reduce a plan’s overall drug benefit costs, point-of-sale drug discounts could result in higher premiums for all plan enrollees.

Spread pricing: Another potential source of revenue for PBMs comes from the contracting practice of spread pricing, which is when a PBM pays a lower rate for a drug to the dispensing pharmacy than the amount the PBM charges an insurer for that drug and retains the difference or “spread” as profit. The practice of spread pricing can result in higher costs for insurers, while lower reimbursement levels put financial pressure on pharmacies.

PBMs have come under bipartisan scrutiny in recent years for spread pricing arrangements in Medicaid managed care that have increased Medicaid costs for states and the federal government. As a result, a number of states have prohibited spread pricing or adopted other reforms to increase transparency and improve oversight. Concerns about Medicaid spread pricing also led the Centers for Medicare & Medicaid Services (CMS) to issue an informational bulletin in May 2019 about how managed care plans should report spread pricing, which may have reduced the practice.

Consolidation: Consolidation in the PBM market has enabled a few PBMs to gain significant market power. As mentioned above, three PBMs manage nearly 80% of all prescription claims in the U.S. Moreover, the top three PBMs are vertically integrated with major health insurers: OptumRx is owned by UnitedHealth, Express Scripts is owned by Cigna, and CVS Caremark is owned by CVS Health, which also owns Aetna. Each of these PBMs also own mail order pharmacies and specialty pharmacies.

The FTC and members of Congress on both sides of the aisle have raised concerns that this level of market concentration and vertical integration enables PBMs to steer consumers to their preferred pharmacies, mark up the cost of drugs dispensed at their affiliated pharmacies, reimburse PBM-affiliated pharmacies at a higher rate than unaffiliated pharmacies for certain drugs, and apply pressure over certain contractual terms, all of which may disadvantage unaffiliated and independent pharmacies, contributing to pharmacy closures.

Transparency: Financial contracts between PBMs and drug manufacturers, including drug pricing information and the rebate arrangements that PBMs negotiate with drug manufacturers, are generally not made public. This means that plan sponsors often do not have insight into how much PBMs are actually paying for drugs on their formularies, and PBMs often consider this information to be proprietary. In the pharmaceutical supply chain as whole, many players operating in this market do not have information about prices, which can make informed decision-making difficult and imperfect.

In recent years, federal lawmakers have focused several Congressional hearings on the topic of PBMs, including their role in prescription drug pricing, drug spending growth, and rising out-of-pocket costs for drugs, and have introduced legislation focusing on several elements of PBM business practices. The legislation highlighted below is not an exhaustive list but includes some of the more recent and prominent legislative efforts in the 119th Congress.

In May 2025, the House passed a version of the 2025 federal budget reconciliation law that included several provisions that would have addressed some PBM operations, though the PBM provisions were not included in the final version of the bill that was passed by Congress and signed into law in July 2025 (sometimes referred to as the “One Big Beautiful Bill Act”). The provisions in the May 2025 House-passed budget reconciliation bill include:

  • Delinking PBM compensation from drug prices, rebates, and discounts that they negotiate for drug plans under Medicare Part Dand instead basing compensation on a ‘bona fide service fee’, which would be a flat dollar amount.
  • Establishing transparency and reporting requirements for PBMs, including data on utilization, pricing, and revenues for formulary covered drugs; PBM-affiliated pharmacies; contracts with drug manufacturers; and other PBM business practices. This provision would require PBMs to provide this data to Part D plan sponsors as well as the HHS Secretary.
  • Prohibiting spread pricing in Medicaid and instead basing payments on a ‘pass-through model’ in which payments made by a PBM on behalf of the State Medicaid program to the pharmacy are limited to the drug ingredient cost and a professional dispensing fee. Payments to PBMs and similar entities would be required to reflect the pharmacies’ costs and an administrative fee that is fair market value. 
  • Ensuring accurate payments to pharmacies under Medicaid: All retail pharmacies and certain non-retail pharmacies would be required to complete the National Average Drug Acquisition Cost (NADAC) survey, if they are selected for participation in the survey. This provision would require survey participation across all retail pharmacies, including larger chain pharmacies who have historically not participated in the survey and who likely obtain their drugs at lower prices, which could lower pharmacy reimbursement for some drugs and result in federal and state savings.

In December 2025, the House passed GOP legislation responding to the expiration of enhanced ACA premium subsidies, the Lower Health Care Premiums for All Americans Act (H.R. 6703), which included a separate PBM provision that would increase oversight of PBMs that provide services to employer group health plans through data transparency and reporting requirements. This provision would require PBMs to report detailed prescription drug utilization and spending data to plans, including gross and net spending, out-of-pocket spending, pharmacy reimbursement, and other details related to the plan’s pharmacy benefit.

Separately, reflecting the bipartisan support for legislation related to PBMs, Representatives Buddy Carter (R) and Vincente Gonzalez (D) introduced the PBM Reform Act of 2025 in the House, while the chairman and ranking member of the Senate Finance Committee, Senators Mike Crapo (R) and Ron Wyden (D), introduced the Pharmacy Benefit Manager (PBM) Price Transparency and Accountability Act in the Senate. These bills are similar but not the same; the PBM Reform Act of 2025 includes the provision that would increase oversight of PBMs that work with employer group health plans (as in the broader House GOP bill), which is not included in the PBM Price Transparency and Accountability Act. A bipartisan group of representatives, including Representatives Jake Auchincloss (D), Diana Harshbarger (R), and James Comer (R) also recently reintroduced the Pharmacists Fight Back Act, which includes two coordinated pieces of legislation that would regulate PBMs in certain federal health benefits programs.

  • The PBM Reform Act of 2025 (H.R.4317) includes most of the PBM provisions that were included in a preliminary version of the budget reconciliation bill that passed the House in May 2025 and includes: delinking PBM compensation from the cost of medications for drug plans under Medicare Part D, prohibiting spread pricing in Medicaid, and ensuring accurate payments to pharmacies under Medicaid. In addition, the bill includes provisions to increase oversight of PBMs that work with employer group health plans and to assure pharmacy access and choice for Medicare beneficiaries, which were not included in the May 2025 House-passed bill.
    • The provision to assure pharmacy access for Medicare beneficiaries would reinforce existing regulatory requirements that Part D plan sponsors contract with any willing pharmacy that meets their standard contract terms and conditions and have those conditions be ‘reasonable and relevant.’ These conditions would be defined and enforced according to standards determined by the Secretary of Health and Human Services (HHS).
  • The PBM Price Transparency and Accountability Act (S.3345) also includes most of the PBM provisions that were included in the May 2025 House-passed bill and includes: delinking PBM compensation from the cost of medications for drug plans under Medicare Part D, prohibiting spread pricing in Medicaid, and ensuring accurate payments to pharmacies under Medicaid. Additionally, it includes the provision to assure pharmacy access and choice for Medicare beneficiaries, which was not included in the May 2025 House-passed bill.
  • The Pharmacists Fight Back Act (H.R. 6609) and (H.R. 6610) would establish certain requirements with regard to PBMs in Medicare and Medicaid and in Federal Employee Health Benefits Plans, respectively. Plan sponsors (or PBMs acting on behalf of those sponsors) would be required to reimburse pharmacies for drugs based on pricing benchmarked to the National Average Drug Acquisition Cost (NADAC) and would be required to share a portion of rebates at the point of sale, with the remainder of the rebates being used to lower plan premiums. The legislation also prohibits PBMs from steering patients to PBM-affiliated pharmacies.

Budgetary Effects of PBM Legislation

In general, cost estimates from the Congressional Budget Office (CBO) have scored PBM provisions with relatively low savings to the federal government. CBO estimated a total federal deficit reduction of $3.2 billion over 10 years (2025-2034) attributable to the PBM provisions incorporated in the May 2025 House-passed budget reconciliation bill (which were not included in the final legislation enacted in July 2025):

  • A reduction of $400 million from delinking PBM compensation from the cost of medications for drugs under Part D and establishing PBM transparency and reporting requirements
  • A reduction of $261 million from prohibiting spread pricing in Medicaid
  • A reduction of $2.5 billion from ensuring accurate payments to pharmacies under Medicaid

The provision to increase oversight of PBMs that work with employer group health plans was scored as part of the Lower Health Care Premiums for All Americans Act (H.R. 6703) that passed the House in December 2025. CBO estimated this provision would reduce the federal deficit by $1.9 billion over 10 years (2026-2035), with $1.8 billion in additional revenues and savings of $22 million. CBO assumes this provision would modestly reduce premiums charged in the group health insurance market, which could increase wages and therefore increase federal revenues.

CBO has not provided cost estimates for the PBM Reform Act of 2025, the PBM Price Transparency and Accountability Act, or the Pharmacists Fight Back Act. The provision to assure pharmacy access and choice for Medicare beneficiaries is not reflected in any of the cost estimates above. It is also possible that the effects of the Medicaid spending reductions in the budget reconciliation law will impact estimates of savings from the Medicaid PBM provisions. The law is expected to result in fewer Medicaid enrollees, which could lower Medicaid drug spending and translate to lower savings from Medicaid PBM provisions.

VOLUME 37

ACIP Vote Drives Online Engagement About Hepatitis B Vaccine, And Posts Claim a VAERS “Cover-Up” of COVID-19 Vaccine Deaths


Highlights

Nearly two weeks after a CDC vaccine advisory panel voted to end the universal recommendation that newborns be vaccinated for hepatitis B, online conversations about childhood vaccination schedules and parental choice have continued at elevated levels, with many prominent accounts celebrating the decision as a victory for medical freedom.

Meanwhile, narratives about an FDA memo claiming COVID-19 vaccines caused 10 pediatric deaths have evolved from focusing on the unverified claims to framing the announcement as evidence of a broader government “cover-up,” as some have characterized it as vindication for those previously “silenced” for raising vaccine safety concerns.


Recent Developments

Online Conversations About Childhood Vaccination Schedule Continue Following ACIP Meeting

A medical professional puts a Band-Aid on an infant's thigh.
FotoDuets / Getty Images

What’s happening?

  • The CDC’s Advisory Committee on Immunization Practices (ACIP) voted earlier this month to end its prior recommendation that all newborns receive the hepatitis B vaccine within 24 hours of birth. The committee now recommends that parents of infants born to mothers who test negative for hepatitis B should consult with their health care provider and decide when or if their child should be vaccinated.
  • The universal birth dose of the hepatitis B vaccine has been credited with a 99 percent drop in hepatitis B infections in children and teens since the 1991 recommendation, but high-profile critics of the universal birth dose, including Department of Health and Human Services (HHS) Secretary Robert F. Kennedy Jr., have argued that vaccinating all children is unnecessary when many cases are transmitted through sexual activity or needle-sharing among adults.
  • After the vote by ACIP, President Donald Trump called for a full review of the childhood vaccination schedule, suggesting limiting the number of recommended children’s vaccinations to match that of “peer, developed countries.”

How has this contributed to online conversation?

  • KFF’s monitoring of X, Reddit, and Bluesky identified more than 50,000 posts, reposts, and comments mentioning hepatitis B on X, Reddit, and Bluesky on December 5, the day of the vote, up from a daily average of approximately 3,400 posts thus far in 2025 as of December 8. Many accounts framed the decision as a victory for parental rights or medical freedom, celebrating the move to shared clinical decision-making. Some accounts which have previously shared false information about vaccines characterized the universal birth dose as previously having been “forced” on newborns, despite ACIP’s recommendations not constituting vaccine mandates.
  • The enhanced engagement about hepatitis B has persisted beyond the initial spike on December 5, with the average number of daily posts, reposts, and comments remaining elevated at approximately 17,000 through December 12. But, the volume of posts is declining, and KFF will continue to monitor how these conversations evolve.

Who do people trust for health information in light of conflicting guidance?

Following ACIP’s vote to end the universal hepatitis B birth dose recommendation, major medical organizations including the American Medical Association (AMA) and American Academy of Pediatrics (AAP) issued statements emphasizing the importance of hepatitis B vaccination for newborns. Several Democratic governors and state health departments in Democratic-led states have also reaffirmed support for the birth dose, leaving parents with conflicting recommendations from federal and state authorities, as well as from professional medical organizations. Recent polling from the Annenberg Public Policy Center found that when the CDC and AMA issue conflicting vaccine recommendations, Americans are more likely to accept the AMA’s recommendation by a 2-to-1 margin, regardless of political affiliation. KFF polling similarly shows that larger shares of the public trust their own health care providers and physicians associations like the AMA and AAP than the CDC for reliable vaccine information. In light of conflicting recommendations, these survey findings suggest that enhanced prenatal counseling may be helpful for alleviating confusion about vaccine guidelines among parents.

Why this matters

  •  ACIP’s decision to end the universal birth dose recommendation for the hepatitis B vaccine, despite its documented effectiveness and safety record, signals a shift in how the committee weighs population-level protection against individual parental choice. Online narratives celebrated the decision as a victory for medical freedom, indicating that personal decision making may outweigh public health concerns for some parents.
  • The debate over hepatitis B vaccinations indicates further partisan divides. A recent KFF Quick Take explores findings from the KFF/Washington Post Survey of Parents, showing that very few parents report skipping or delaying the hepatitis B vaccine for their children, but Republican supporters of the Make America Great Again (MAGA) and supporters of the Make America Healthy Again (MAHA) are more likely to have done so.
  • The KFF/Washington Post poll found that similar shares report skipping or delaying other recommended childhood vaccines like MMR or chickenpox. President Trump’s call to review the full pediatric vaccine schedule suggests that concerns about the timing of hepatitis B vaccination may influence broader conversations about childhood immunization schedules that health professionals should monitor.

Claims of “Cover-Up” Emerge Following FDA Memo on Vaccine Deaths

A masked young child with dark brown hair holds a teddy bear in the background while a doctor draws liquid into a syringe in the foreground.
thianchai sitthikongsak / Getty Images

What’s happening?

  • A recent internal Food and Drug Administration (FDA) memo  claims to link at least 10 pediatric deaths to COVID-19 vaccines, based on reports from the Vaccine Adverse Event Reporting System (VAERS). The memo, which does not include children’s ages, medical histories, or other evidence, has not been published in a peer-reviewed medical journal, its claims have been criticized by 12 former FDA commissioners as well as by current FDA staff. The FDA has since announced it is expanding its investigation to examine adult deaths potentially linked to COVID-19 vaccines.
  • VAERS is a passive vaccine surveillance system, and reports of side effects can be submitted by anyone including patients, healthcare providers, or individuals without medical training. The system is intended to generate hypotheses and identify possible concerns, not establish causality. Individuals and groups opposed to vaccinations have commonly misrepresented VAERS data to cast doubt on vaccine safety by presenting unverified reports as proof of harm.

What are common online narratives?

  • Online narratives about the FDA memo have continued through December. While early discussions focused on the memo’s claims about the 10 deaths, recent conversations have framed the announcement as evidence of a broader “cover-up” of vaccine harms. The vice chair of ACIP, who has more than 1.3 million followers on X, posted that the pediatric deaths were previously identified by the CDC, but were only now being disclosed. Approximately 17% of all posts KFF identified about the FDA memo in December thus far as of December 15, used language that suggested the memo was an admission that the FDA hid vaccine deaths from the public, using terms like “cover-up,” “finally admitting,” “caught red-handed,” or claims that officials “lied” about vaccine safety.  Some also expressed feelings of “vindication” for individuals who were allegedly “silenced” or “censored” for raising concerns about COVID-19 vaccines.
  • A Substack article published in early December and shared by an account on X with more than 500,000 followers claimed that the memo may result in the FDA adding a “black-box” warning to COVID vaccines or removing them from the market.

What does the evidence say?

COVID-19 vaccines have been extensively studied in children, and multiple published, peer-reviewed studies have demonstrated no increase in mortality. The vaccines have been shown to reduce the risk of hospitalization and severe illness, and about 2,100 children have died from COVID-19 itself since the pandemic began.

Why this matters

Federal health officials framing unverified VAERS reports as evidence of vaccine-caused deaths may contribute to uncertainty among parents about the safety of COVID-19 vaccines for children. The KFF/The Washington Post Survey of Parents found that large majorities of parents had positive views of long-standing childhood vaccinations, but were more uncertain about COVID-19 vaccines. Previous KFF polling has shown that about half (52%) of adults said they did not know enough to say whether mRNA vaccines were generally safe or generally unsafe. The FDA memo may provide what appears to be official validation for these concerns, making it more difficult for health communicators to explain the limitations of VAERS and the vaccines’ established safety record.


What We Are Watching

Continued Staffing Changes Signal Ongoing Shifts in Federal Health Messaging

Recent staffing changes at federal health agencies may signal continuation of criticism around current vaccination schedules and public health recommendations. The CDC’s new principal deputy director, for example, previously ended his state’s mass vaccination campaigns and delayed outbreak notifications as Louisiana’s surgeon general, while a new chief science officer at HHS co-authored a declaration calling for an end to pandemic shutdowns and later chaired a vaccine advisory committee that made recommendations criticized by major medical organizations. The FDA also appointed a new acting director of its Center for Drug Evaluation and Research who has advocated for making it more difficult for young men to receive the COVID-19 vaccine and questioned whether the childhood vaccination schedule is scientifically justified. Health communicators should anticipate statements from federal health officials that may contradict existing guidance and potentially contribute to declining trust in government health agencies as reliable sources of vaccine information. KFF will continue to monitor how communication from these officials influences public trust in vaccines and federal health agencies.

X’s Location Transparency Feature Could Help Verify the Authenticity of Accounts That Cast Doubt on Health Information

A new feature deployed on the social media platform X in late November shows the country or region where accounts are based, designed to verify authenticity and limit the influence of bot networks and foreign “troll” accounts. Initial media reporting has focused on politically-oriented accounts, revealing that numerous high-engagement accounts that presented themselves as American were actually based overseas. The feature could prove valuable for health communicators and researchers attempting to track the origin of false health claims, and understanding where these claims originate could help public health officials and platforms develop more targeted responses.

Recent ChatGPT Updates Aim to Address Mental Health Risks, OpenAI says

OpenAI, the company that operates the popular AI chatbot ChatGPT, has introduced a number of safety updates to its default model this year after reports emerged of users experiencing mental health crises during conversations with the chatbot. The New York Times uncovered nearly 50 cases of people having mental health crises while talking with ChatGPT, with nine hospitalized and three deaths. In some cases, the chatbot’s responses validated delusional thinking or discouraged users from seeking mental health help, and the company is now facing five wrongful death lawsuits alleging that the chatbot may have encouraged users to commit suicide. The company released GPT-5 in August and deployed an October update, developed in consultation with mental health professionals, that aims to better recognize users experiencing crisis and de-escalate sensitive conversations. OpenAI says that additional features, like session break reminders, parental controls, and age verification, are designed with user safety in mind, but internal communications reported by The New York Times show that the company still prioritizes user engagement metrics. Some mental health professionals have argued that OpenAI is understating the risk to its users, noting that 5 to 15 percent of the population could be vulnerable to delusional thinking. Parents and mental health professionals should be aware of the potential for AI chatbots to reinforce harmful thoughts or provide dangerous guidance, particularly during extended conversations.

About The Health Information and Trust Initiative: the Health Information and Trust Initiative is a KFF program aimed at tracking health misinformation in the U.S., analyzing its impact on the American people, and mobilizing media to address the problem. Our goal is to be of service to everyone working on health misinformation, strengthen efforts to counter misinformation, and build trust. 


View all KFF Monitors

The Monitor is a report from KFF’s Health Information and Trust initiative that focuses on recent developments in health information. It’s free and published twice a month.

Sign up to receive KFF Monitor
email updates


Support for the Health Information and Trust initiative is provided by the Robert Wood Johnson Foundation (RWJF). The views expressed do not necessarily reflect the views of RWJF and KFF maintains full editorial control over all of its policy analysis, polling, and journalism activities. The data shared in the Monitor is sourced through media monitoring research conducted by KFF.

A Look at Nursing Facility Characteristics in 2025

Published: Dec 17, 2025

The 2025 reconciliation law could have major implications for nearly 15,000 federally certified nursing facilities and the more than 1.2 million people living in them. Nursing facilities provide medical and personal care services for older adults and people with disabilities. In 2023, Medicaid paid for 44% of long-term institutional care costs; 37% of long-term institutional care costs were paid for out-of-pocket; and the remaining 18% was covered by other public and private payers. Although provisions in the reconciliation law do not directly limit or reduce nursing facility services, changes to the Medicaid program could result in reduced payments from Medicaid for nursing facility care and may result in fewer people having Medicaid coverage of nursing facility care (see Box 1 for more on the 2025 reconciliation law.)

This data note discusses the impact of the 2025 reconciliation law on nursing facilities and examines the characteristics of nursing facilities and the people living in them with data from Nursing Home Compare, a publicly available dataset that provides a snapshot of information on quality of care in each nursing facility, and CASPER (Certification and Survey Provider Enhanced Reports), a dataset that includes detailed metrics collected by surveyors during nursing facility inspections. State-level data are also available on State Health Facts, KFF’s data repository with downloadable health indicators. Key takeaways from July 2025 data include:

  • There are 14,742 nursing facilities certified by CMS and about 1.24 million residents living in these certified nursing facilities (Figure 1).
  • Nursing facility residents receive, on average, about 3.85 hours of nursing care per day from licensed practical nurses (LPN/LVN), registered nurses (RNs), and nurse aides (Figure 2).
  • On average, nursing facilities receive 9.5 deficiencies over the course of a survey cycle (Figure 3).
  • While nearly all facilities receive at least one deficiency over the course of a survey cycle, 27% of facilities receive serious deficiencies for actual harm or jeopardy posed to a resident (Figure 3).

Box 1: Major Provisions in 2025 Reconciliation Law that Could Impact Nursing Facilities

The reconciliation law, passed on July 4, 2025, includes significant health care policy changes, including some major changes could have implications for nursing facilities.

Broader federal spending cuts: The 2025 reconciliation law is expected to reduce federal Medicaid spending by $911 billion over the next decade, which could have implications for nursing facilities. Those spending cuts are likely to leave states with difficult choices about how to respond to reduced federal support including spending on long-term care which accounts for more than one-third of all Medicaid spending. States’ options for reducing spending on nursing facility care could involve reducing payment rates or restricting eligibility so that fewer people receive services.

State-directed payments (SDPs): SDPs require managed care organizations to make certain types of payments to health care providers, generally aimed at increasing provider payment rates to increase access to or quality of care. The reconciliation law reduced the maximum payment rate in SDPs from commercial rates to Medicare rates in states that have adopted the ACA expansion and to 110% of Medicare rates in non-expansion states. As a result of these changes, states may reduce payments to nursing facilities to comply with the caps in the new law.

Moratorium on eligibility rules: The reconciliation law delays implementation of two eligibility rules that would have increased Medicaid enrollment, especially among Medicare beneficiaries (dual-eligible individuals), a group that disproportionately uses nursing facility services, until 2034. CBO estimated that delaying these rules could reduce the number of dual-eligible individuals by around 1 million.

Reduced retroactive coverage period: The law reduces the period for which states must provide Medicaid coverage for qualified medical expenses from 90 days prior to the date of application for coverage to 60 days among non-expansion enrollees. Because entering a nursing facility is often a precipitating event for people to apply for Medicaid, this change may particularly affect Medicaid payments for nursing facilities.

Staffing rule: The law delays implementation of a Biden-era rule intended to help address long-standing concerns about staffing shortages and the quality of care in nursing homes until 2034. A Texas judge overturned key requirements from the rule in May 2025; and the Trump Administration rescinded the rule in December 2025.

Freezing home equity limit: The reconciliation law reduces maximum home equity limits on the homes of Medicaid nursing facility applicants to $1 million, starting in 2028. The limits will not grow over time and thus, become more binding in future years (as of 2025, 11 states had home equity limits higher than $1 million). Once this cap takes effect, people in those states who would otherwise be eligible may no longer qualify for Medicaid long-term care. 

Immigration enforcement: The law provides additional funding to Immigration and Customs Enforcement to expand detention and deportation operations of immigrants in the U.S., raising questions about workforce shortages. Immigrants made up 21% of workers in nursing facilities in 2023.

Effective prohibition on new provider taxes or increases to existing ones: States are permitted to finance the non-federal share of Medicaid spending through healthcare-related taxes or “provider taxes” and often use those tax revenues to bolster provider payment rates. All but six states have taxes on nursing facilities. The law effectively prohibits states from enacting any new provider taxes or from increasing existing ones. Historically, states have used provider tax revenues as a mechanism to sustain Medicaid spending during budget shortfalls and to bolster payment rates, and the prohibition will reduce states’ ability to do so in the future. Recent data from a 50-state survey of state Medicaid programs show that 7 states (CO, KY, MA, MN, NJ, NC, and OK) planned to increase taxes on nursing facilities in FY 2026, though the new reconciliation law may prevent these increases from taking effect.

As of July 2025, there are 14,742 nursing facilities certified by CMS (Figure 1). The number of nursing facilities certified by CMS decreased by 6% between July 2015 and July 2025. There has generally been a steady decline during that time period. In order to receive payment under the Medicare and/or Medicaid programs, nursing facilities are required to follow certain regulations and be certified by CMS. The decreased number of nursing facilities reflects the net change in the number of certified facilities after accounting for newly-certified facilities and facilities that are no longer certified, including facilities that closed.

There are about 1.24 million residents living in certified nursing facilities (Figure 1). Since 2021, the number of nursing facility residents has gradually increased from 1.10 million to 1.24 million. However, between 2015 and 2025, the number of residents living in nursing facilities decreased by 9%, with most of that coming from a steep decline between 2020 and 2021, reflecting the effects of the COVID-19 pandemic. Prior to the pandemic, the number of residents was relatively steady, although it declined from 1.37 million in 2015 to 1.32 million in 2020. COVID-19 exacerbated the decrease in nursing facility residents—in part because nursing facility residents and staff incurred so many deaths during the pandemic.

Number of Certified Nursing Facilities and Residents, 2015-2025

Residents receive an average of 3.85 hours of nursing care per day, including 0.87 hours of LPN care, 0.68 hours of RN care, and 2.3 hours of nurse aide care (Figure 2). While staffing levels have gradually slightly increased overtime since 2022, the average hours of nursing care that nursing facility residents received declined by 7%, from 4.13 hours to 3.85 hours per resident each day, between July 2015 and July 2025. The decrease was driven by a 19% decline in registered nurse (RN) hours and a 7% decline in nurse aide hours. Licensed practical nurse (LPN) hours increased by 5% in this same time period. The 2024 rule would have required nursing facilities to meet minimum standards in staff hours for RNs and nurse aides but did not include any requirements for LPNs. A Texas judge overturned key elements of the rule in April 2025, the 2025 reconciliation law delayed all provisions of the rule until October 2034 (Box 1), and the Trump Administration rescinded the rule in December 2025. Previous KFF analysis show that just 19% of nursing facilities met the standards at the time of the rule’s passing.

The total hours of nursing care per resident decreased between 2015 and 2025, but rose briefly in 2021. The relatively higher staffing hours per resident in 2021 reflected the fact that the number of residents declined more quickly than the number of total nursing staff hours did between 2020 and 2021. In 2021, the number of staffing hours was 12% lower than in 2020 (data not shown). These lower staffing levels in the last several years align with data as of March 2024 showing that the number of workers employed at long-term care facilities continues to remain below pre-pandemic levels.

Nursing Facility Hours per Resident Day by Nurse Staff Type, 2015-2025

Box 2: Direct Care Staff in Nursing Facilities

Registered Nurse (RN): Registered nurses (RNs) are responsible for the overall delivery of care to the residents and assess needs of nursing facility residents. RNs are typically required to have between two and six years of education.

Licensed Practical Nurse (LPN) and Licensed Vocational Nurse (LVN): LPNs/LVNs provide care under the direction of an RN. Together, RNs and LPNs/LVNs make sure each resident’s plan of care is being followed and their needs are being met. LPNs/LVNs typically have one year of training. 

Certified Nurse Aides/Assistants (CNAs): CNAs work under the direction of a licensed nurse to assist residents with activities of daily living such as eating, bathing, dressing, assisting with walking/exercise, and using the bathroom. All CNAs must have completed a nurse aide training and competency evaluation program within 4 months of their employment. They must also pursue continuing education each year.

Nursing facilities receive an average of 9.5 deficiencies over the course of a survey cycle and 27% of facilities receive deficiencies for actual harm or jeopardy (Figure 3, Box 3). While nearly all facilities receive at least one deficiency during a survey cycle, this analysis focuses on the share with serious deficiencies since there is wide variation in the types of deficiencies a facility may receive. Both the average number of deficiencies and the share of facilities with serious deficiencies have increased over time, which could reflect increased oversight and low staffing levels that lead to staffing-related deficiencies. Between 2015 and 2025, the average count of deficiencies per nursing facility increased from 6.8 to 9.5, an increase of 40%. The increase was generally steady overtime, except for two stable periods: 1) between 2020 and 2022 and 2) between 2024 and 2025 (though 2024 and 2025 reported the highest number deficiencies during the 10-year period). The share of facilities reporting serious deficiencies between 2015 and 2025 increased from 17% to 27%, with a slight decrease between 2024 and 2025. A 2023 report on nursing home staffing by Abt Associates found that better-staffed nursing homes are typically cited for fewer deficiencies or violations of federal regulations, suggesting there may be a relationship between the increase in deficiencies and the general decrease in staffing levels over the 10-year time period.

Box 3: Deficiencies in Nursing Facilities

Nursing facilities receive deficiencies when they fail to meet the requirements necessary to receive federal funding. Deficiencies are often given for problems which may have negative effects on the health and safety of residents. Commonly cited deficiencies include a failure to provide necessary care, failure to report abuse or neglect, and violation of infection control requirements. Each of these categories has specific regulations that state surveyors review to determine whether facilities have met the standards.

Deficiencies are characterized by their level of severity: Deficiencies for “actual harm” or “immediate jeopardy” are the most severe and are grouped together under the term, “serious deficiencies.” CMS defines “actual harm” as a “deficiency that results in a negative outcome that has negatively affected the resident’s ability to achieve the individual’s highest functional status.” “Immediate jeopardy” is defined as a deficiency that “has caused (or is likely to cause) serious injury, harm, impairment, or death to a resident receiving care in the nursing facility.” These can include citations to facilities for physically abusing residents, failure to maintain safe living quarters, or failure to provide CPR or other basic life support when necessary for residents.

Average Deficiencies per Nursing Facility and Share of Nursing Facilities Receiving a Deficiency for Actual Harm or Jeopardy, 2015-2025

Medicaid is the primary payer for 63% of nursing facility residents; Medicare for 14% of residents; and the remaining 23% of residents have another primary payer (ex. out-of-pocket) (Figure 4). The share of residents by primary payer has stayed relatively stable over time. Medicare does not generally cover long-term care but does cover up to 100 days of skilled nursing facility care following a qualifying hospital stay. KFF polling shows that four in ten adults overall incorrectly believe that Medicare is the primary source of insurance coverage for low-income people who need nursing facility care. 

Distribution of Nursing Facility Residents by Primary Payer in 2025

Nearly three-quarters (73%) of nursing facilities are for-profit, one-fifth (20%) are non-profit, and the remaining seven percent are government-owned (Figure 5). The share of facilities by ownership type has also stayed relatively stable over time but there was increasing scrutiny over the 73% of facilities that are for-profit during the prior Administration. Despite little change in the type of ownership, there have been reports of private equity firms purchasing nursing facilities and changing operations to increase profits, resulting in lower-quality care. The GAO estimates that about 5% of nursing facilities had private equity ownership in 2022.

The Biden Administration issued a final rule in November 2023 on nursing facilities (separate from the April 2024 staffing rule that was delayed by the 2025 reconciliation law and then rescinded by the Trump Administration in December 2025). The 2023 nursing facility rule requires nursing homes enrolled in Medicare or Medicaid to disclose detailed information regarding their owners, operators, and management, including:

  • Anyone who exercises any financial control over the facility;
  • Anyone who leases or subleases property to the facility, including anyone who owns 5% or more of the total value of the property; and
  • Anyone who provides administrative services, clinical consulting services, accounting or financial services, policies or procedures on operations, or cash management services for the facilities.

Facilities must also disclose whether any of the owning or managing entities are a private equity company or real estate investment trust (REIT). Facilities began self-reporting this data to CMS in early 2024 and the data is now available to the public. However, these data may be incomplete for now as fewer than 100 facilities report private equity ownership and just over 300 facilities report REIT ownership. Other research estimates those counts to be higher. 

Distribution of Nursing Facilities by Profit Status

This work was supported in part by The John A. Hartford Foundation. KFF maintains full editorial control over all of its policy analysis, polling, and journalism activities.

Recent Changes in Federal Vaccine Recommendations: What’s the Impact on Insurance Coverage?

Author: Jennifer Kates
Published: Dec 16, 2025

The Trump administration has made several recent changes to federal routine vaccination recommendations. Specifically, under the auspices of Secretary Kennedy, who has long questioned the safety and efficacy of vaccines and stated his intention to review vaccine schedules, the CDC’s Advisory Committee on Immunization Practices (ACIP) has recommended changes (including to age group, type of vaccine, and/or clinical decision-making process) to seven vaccine usage recommendations in the United States: Meningococcal; RSV for adults; RSV for children; influenza; COVID-19; Measles, Mumps, Rubella and Varicella (MMRV); and Hepatitis B. These recommendations, which have been adopted by the HHS Secretary or Acting CDC Director, have raised questions about the implications for insurance coverage, since most insurers are required to cover ACIP/CDC recommended vaccines at no-cost, either due to requirements of the Affordable Care Act or other federal statutes.

Below, we provide an overview of each of these changes and what they mean for coverage requirements. As the table indicates, of the seven recent changes, two have no implications for coverage, two removed the coverage requirement, and three expanded the requirement. When a coverage requirement is removed, an insurer could still choose to cover a vaccine at no cost. In fact, AHIP, the trade association for the health insurance industry whose members cover more than 200 million Americans, announced that health plans will continue to cover all ACIP-recommended immunizations that were recommended as of September 1, 2025 with no cost-sharing for patients through the end of 2026. When a coverage requirement is expanded, insurers (with limited exception) must cover the vaccine at no-cost. The insurance requirement extends to vaccines with “individual decision-making” (also known as “shared clinical decision-making”) recommendations as well, which are those “individually based and informed by a decision process between the health care provider and the patient or parent/guardian”.

In addition to federal requirements for coverage, states have the authority to require state-regulated health insurers (employer plans that are fully insured and individual and small-group marketplace plans) to cover vaccines beyond minimum federal requirements (and not necessarily linked to current ACIP/CDC recommendations). As of December 2025, eight states have moved to do so (and one state authorizes the state Commissioner of Insurance to do so). Still, states cannot impose coverage requirements on self-insured employer plans, which cover most (67%) people with employer coverage.

Additional changes to ACIP-recommended vaccine schedules are likely, as President Trump has issued a Presidential Memorandum calling on HHS and CDC to begin a “process to align U.S. core childhood vaccine recommendations with best practices from ‘peer, developed countries’”. Beyond their implications for insurance coverage, changes to vaccine recommendations, particularly those that narrow or limit access, are likely to have other implications, such as driving down already falling vaccine coverage rates in the United States.

Changes to Vaccine Recommendations and Insurance Coverage
VaccinePrior RecommendationNew RecommendationDate of
Change
Insurance Implications
Meningococcal MenACWY and MenB may be administered at the same visit if indicated (for certain populations).MenABCWY vaccine may be used when both MenACWY and MenB are indicated at the same visit (for certain populations).4/16/25 (ACIP)
6/25/25 (HHS)
Expands coverage requirement to include new pentavalent (5-in-1) MenABCWY vaccine for those indicated. Applies to private insurers, Medicaid, Vaccines for Children Program.
RSV for adultsRecommended for all adults, ages 75 and older and adults ages 60-74 with increased risk. Recommended for all adults, ages 75 and older and adults ages 50-74.4/16/25 (ACIP)
6/25/25 (HHS)
Expands coverage requirement to include those ages 50-59 who are at increased risk. Applies to private insurers, Medicaid, Medicare Part D.
RSV for childrenRecommended that infants aged < 8 months born during or entering their first RSV season who are not protected by maternal vaccination receive nirsevimab.Recommended that clesrovimab, a monoclonal antibody approved in 2025, be added as an option, with no preferential recommendation between nirsevimab and clesrovimab.6/25/25 (ACIP)
7/22/25 (HHS)

 

Expands coverage requirement to include new monoclonal antibody for infants. Applies to private insurers, Medicaid, Vaccines for Children Program.
InfluenzaSingle-dose and multi-dose influenza vaccines recommendedMulti-dose influenza vaccines with Thimerosal no longer recommended6/25/25 (ACIP)
7/22/25 (HHS)
Removes coverage requirement for multi-dose flu vaccine (which will no longer be available in the U.S. market). Applies to private insurers, Medicaid, Vaccines for Children Program. Medicare Part B required to cover by statute, not linked to ACIP/CDC*.
COVID-19Recommended for everyone, ages 6 months and olderVaccination based on individual-based decision-making (also known as shared clinical decision-making) with an emphasis that the risk-benefit of vaccination is most favorable for individuals who are at an increased risk for severe COVID-19 disease and lowest for individuals who are not at an increased risk.9/19/25 (ACIP)
Last week of September (CDC)
 

 

Coverage requirement remains unchanged (vaccines recommended through individual-based decision-making must be covered at no-cost). Applies to private insurers, Medicaid, Vaccines for Children Program. Medicare Part B required to cover by statute, not linked to ACIP/CDC.
Measles, Mumps, Rubella, VaricellaBoth the combined measles, mumps, and rubella (MMR) vaccine and combined measles, mumps, rubella, and varicella (MMRV) vaccine recommended for childrenRecommendation that Varicella vaccine be given as stand-alone vaccine (combined MMRV no longer recommended)9/19/25 (ACIP)
Last week of September (CDC)
Removes coverage requirement for combined MMRV. Applies to private insurers, Medicaid, and Vaccines for Children Program.
Hepatitis BBirth dose recommended for all infantsVaccination based on individual-based decision-making for parents deciding whether to give the hepatitis B vaccine, including the birth dose, to infants born to women who test negative for the virus. For those infants not receiving the birth dose, recommendation that initial dose be administered no earlier than two months of age. Additionally, when evaluating need for subsequent dose in children, recommended that parents should consult with health care providers to decide whether to test first.12/5/25 (ACIP)
12/16/25 (CDC, change in birth dose recommendation adopted; review of screening recommendation still underway)
Coverage requirement remains unchanged (vaccines recommended through individual-based decision-making must be covered at no-cost). Applies to private insurers, Medicaid, Vaccines for Children Program. Medicare Part B required to cover by statute, not linked to ACIP/CDC.

Notes: See KFF, ACIP, CDC, and Insurance Coverage of Vaccines in the United States, for coverage criteria by payer. *While Medicare Part B is required to cover influenza vaccine by statute, not linked to ACIP/CDC, this change will result in the removal of the multi-dose vaccine from the market.

Sources:

Key Data on Health and Health Care by Race and Ethnicity

Published: Dec 16, 2025

Executive Summary

Introduction

Copy link to Introduction

Racial and ethnic disparities in health and health care remain a persistent challenge in the United States. The COVID-19 pandemic’s uneven impact on people of color drew increased attention to inequities in health and health care, which have been documented for decades and reflect longstanding structural and systemic inequities rooted in historical and ongoing racism and discrimination. KFF’s 2023 Survey on Racism, Discrimination, and Health documents ongoing experiences with racism and discrimination, including in health care settings. While inequities in access to and use of health care contribute to disparities in health, inequities across broader social and economic factors that drive health also play a major role. Since taking office, the Trump administration has implemented policies that may erode progress addressing disparities in health and health care, including eliminating equity-related initiatives, reducing federal data collection and reporting, increasing and expanding immigration enforcement, and restricting immigrant access to coverage and health and social supports. Moreover, changes in the 2025 tax and spending law are anticipated to large coverage losses, which will likely exacerbate disparities.

Data are key for identifying disparities and the factors that drive them, developing interventions and directing resources to address them, as well as for assessing progress and establishing accountability. This analysis examines how people of color fare compared to White people across 64 measures of health, health care, and social and economic factors that drive health using the most recent data available from federal surveys and administrative sets as well as the 2023 KFF Survey on Racism, Discrimination, and Health, which provides unique nationally-representative measures of adults’ experiences with racism and discrimination, including in health care (see About the Data).

Where possible, we present data for six groups: White, Hispanic, Black, Asian, American Indian or Alaska Native (AIAN), and Native Hawaiian or Pacific Islander (NHPI). People of Hispanic origin may be of any race, but we classify them as Hispanic for this analysis. We limit other groups to people who identify as non-Hispanic. When the same or similar measures are available in multiple datasets, we use the data that allow us to disaggregate for the largest number of racial and ethnic groups. Unless otherwise noted, differences described in the text are statistically significant at the p<0.05 level.

We include data for smaller population groups wherever available. Instances in which an estimate has a 95% confidence interval width greater than 20 percentage points or 1.2 times the estimate may not be reliable and are noted in the figures. Although these small sample sizes may impact the reliability, validity, and reproducibility of data, they are important to include because they point to potential underlying disparities that are hidden without disaggregated data. For some data measures throughout this brief we refer to “women” but recognize that other individuals also give birth, including some transgender men, nonbinary, and gender-nonconforming persons.

Key Takeaways

Copy link to Key Takeaways

Hispanic, Black, and AIAN people fare worse than White people across the majority of examined measures of health and health care and social determinants of health (Figure 1). Black people fare better than White people for some cancer screening and incidence measures, although they have higher rates of cancer mortality. Despite worse measures of health coverage and access, and social and economic factors, Hispanic people fare better than White people for some health measures, including life expectancy, some chronic diseases, and most measures of cancer incidence and mortality. These findings may, in part, reflect variation in outcomes among subgroups of Hispanic people, with better outcomes for some groups, particularly recent immigrants to the U.S. Examples of some key findings include:

  • Among people under age 65, AIAN (19%) and Hispanic (18%) were more than twice as likely as their White counterparts (7%) to be uninsured as of 2023.
  • Among adults with any mental illness, Hispanic (44%), Black (39%), and Asian (33%) adults were less likely than White adults (58%) to receive mental health services as of 2024.Roughly, six in ten Hispanic (65%), AIAN (65%), and Black (58%) adults went without a flu vaccine in the 2023-2024 season, compared to less than half of White adults (51%).
  • AIAN and Black people have a shorter life expectancy (70.1 and 74.0 years, respectively) compared to White people (78.4 years) as of 2023.
  • Black (10.9 per 1,000) and AIAN (9.2 per 1,000) infants were at least two times as likely to die as White infants (4.5 per 1,000) as of 2023. Pregnancy-related mortality rates are also more than three times higher among Black women compared to White women.
  • Hispanic (24%), AIAN (23%), and Black (22%) households were roughly twice as likely to experience food insecurity as White households (12%).
Health and Health Care among People of Color Compared to White People

Asian people in the aggregate fare the same or better compared to White people for most examined measures. However, they fare worse for some measures, including receipt of some routine care and screening services, and some social and economic measures, including home ownership, crowded housing, and experiences with racism and discrimination. They also have higher shares of people who are noncitizens or who have limited English proficiency (LEP), which could contribute to barriers to accessing health coverage and care. Moreover, the aggregate data may mask underlying disparities among subgroups of the Asian population.

Data gaps largely prevent the ability to identify and understand health disparities for NHPI people. Data are insufficient or not disaggregated for NHPI people for a number of the examined measures. Among available data, NHPI people fare worse than White people for the majority of measures. There are no significant differences for some measures, but this largely reflects the smaller sample size for NHPI people in many datasets, which limits the power to detect statistically significant differences.

These data highlight the persistence of disparities in health and health care. While these data provide insight into the status of disparities, ongoing data gaps and limitations hamper the ability to get a complete picture, particularly for smaller population groups and among subgroups of the broader racial and ethnic categories. Going forward, new policies may widen racial and ethnic disparities, while at the same time data to identify and measure them may become more limited. Addressing disparities is important not only for the groups impacted by them but for the nation’s overall health and productivity.

Racial Diversity Within the U.S. Today

Total Population by Race and Ethnicity

Copy link to Total Population by Race and Ethnicity

About four in ten people (43%) in the United States identify as people of color (Figure 2). This group includes 20% who are Hispanic, 12% who are Black, 6% who are Asian, 1% who are AIAN, less than 1% who are NHPI, and 5% who identify as another racial category, including individuals who identify as more than one race. The remaining 57% of the population are White. The share of the population who identify as people of color has grown over time, with the largest growth occurring among those who identify as Hispanic or Asian. The racial diversity of the population is expected to continue to increase, with people of color projected to account for over half of the population by 2050. Changes to how data on race and ethnicity are collected and reported may also influence measures of the diversity of the population.

Total United States Population by Race and Ethnicity, 2023

Racial Diversity by State

Copy link to Racial Diversity by State

Certain areas of the country—particularly in the South, Southwest, and parts of the West are more racially diverse than others (Figure 3). Overall, the share of the population who are people of color ranges from 10% or fewer in Maine and West Virginia to 50% or more of the population in California, District of Columbia, Florida, Georgia, Hawaii, Maryland, Nevada, New Mexico, and Texas. Most people of color live in the South and West. More than half (59%) of the Black population resides in the South, and nearly eight in ten Hispanic people live in the West (37%) or South (39%). About three quarters (73%) of the NHPI population, almost half (49%) of the AIAN population, and 43% of the Asian population live in the Western region of the country.

People of Color as a Share of the Total Population by State, 2023

Total Population by Age, Race, and Ethnicity

Copy link to Total Population by Age, Race, and Ethnicity

People of color are younger compared to White people. Hispanic people are the youngest racial and ethnic group, with 31% ages 18 or younger and 55% below age 35 (Figure 4). Roughly half of Black (48%), AIAN (48%), and NHPI (51%) people are below age 35, compared to 42% of Asian people and 38% of White people.

Total Population by Age, Race, and Ethnicity, 2023

Health Coverage, Access to, and Use of Care

Racial Disparities in Health Coverage, Access, and Use

Copy link to Racial Disparities in Health Coverage, Access, and Use

Overall, Hispanic, Black, and AIAN people fare worse compared to White people across most examined measures of health coverage, access to, and use of care (Figure 5). Experiences for Asian people are mostly similar to or better than White people across these examined measures. NHPI people fare worse than White people across some measures, but several measures lacked sufficient data for a reliable estimate for NHPI people.

Coverage, Access, and Use of Care Among People of Color Compared to White People

Health Coverage

Copy link to Health Coverage

Despite gains in health coverage across racial and ethnic groups over time, Hispanic, Black, AIAN, and NHPI people under age 65 remain more likely to be uninsured compared to their White counterparts. After the Affordable Care Act (ACA), Medicaid and Marketplace coverage expansions took effect in 2014, all racial and ethnic groups experienced large increases in coverage. Beginning in 2017, coverage gains began reversing, and the number of uninsured people increased for three consecutive years. However, between 2019 and 2023, there were small gains in coverage across most racial and ethnic groups, with pandemic enrollment protections in Medicaid and enhanced ACA premium subsidies. Despite these gains over time, disparities in health coverage persist as of 2023. AIAN and Hispanic people under age 65 have the highest uninsured rates at 19% and 18%, respectively (Figure 6). Uninsured rates for NHPI (13%) and Black (10%) people are also higher than the rate for their White counterparts (7%). White and Asian people have the lowest uninsured rates at 7% and 6%, respectively.

Uninsured Rate Among the Under Age 65 Population by Race and Ethnicity, 2010-2023

Access to and Use of Care

Copy link to Access to and Use of Care

Among those under age 65, most adults of color are more likely than White adults to report not having a usual doctor or provider and going without care. Roughly one third (36%) of Hispanic adults, one quarter (25%) of AIAN adults, and one in five of NHPI (22%) and Asian (19%) adults report not having a personal health care provider compared to 16% of White adults (Figure 7). The shares of Black adults (15%) who report not having a personal health care provider are similar to the share of their White counterparts (16%). In addition, Hispanic (23%), NHPI (19%), AIAN (18%), and Black (16%) adults are more likely than White adults (12%) to report not seeing a doctor in the past 12 months because of cost, while Asian adults (8%) are less likely than White adults to say they went without a doctor visit due to cost. Hispanic adults (30%) are more likely than White adults (26%) to say they went without a routine checkup in the past year, while Black (19%) adults are less likely to report going without a checkup. Hispanic (45%), AIAN (41%), and Black (36%) adults are more likely than White adults (32%) to report going without a visit to a dentist or dental clinic in the past year.

Having a Health Care Provider and Use of Care Among Adults Under Age 65 by Race and Ethnicity, 2024

Children of color are more likely than White children to go without a preventive dental visit, lack a usual source of care, or have no personal doctor. About one third of Hispanic (34%), Black (34%), and Asian (34%) children lack a usual source of care when sick compared to 15% of White children (Figure 8). Hispanic (39%), AIAN (39%), Black (33%), and Asian (28%) children are more likely to not have a personal doctor or nurse than White children (21%). Similarly, higher shares of Black (25%), Asian (23%), and Hispanic (22%) children went without a preventive dental visit in the past year compared to White children (18%). Data for NHPI children should be interpreted with caution due to large confidence intervals.    

Percent of Children Without a Usual Source of Care, Personal Doctor, and Who Did Not Have a Dental Visit by Race and Ethnicity, 2023

Among adults with any mental illness, Hispanic, Black, and Asian adults are less likely than White adults to report receiving mental health services. Nearly six in ten (58%) of White adults with any mental illness report receiving mental health services in the past year (Figure 9). In contrast, about four in ten Hispanic (44%) and Black (39%) adults, and a third (33%) of Asian adults with any mental illness report receiving mental health care in the past year. Data are not available for AIAN and NHPI adults.

Adults with Any Mental Illness Who Received Mental Health Services in the Past Year by Race and Ethnicity, 2024

Experiences across racial and ethnic groups are mixed regarding receipt of recommended cancer screenings (Figure 10). Black people (22%) are less likely than White people (27%) to go without a recent mammogram among women ages 40 and older. In contrast, AIAN (37%) and Hispanic (30%) people are more likely than White people (27%) to go without a mammogram. Among those recommended for colorectal cancer screening, Hispanic, Asian, AIAN, and NHPI people are more likely than White people to not be up to date on their screening. AIAN (47%), Asian (46%), Hispanic (40%), and Black (34%) people are more likely than their White counterparts (31%) to report not having a pap smear in the past three years. Increases in cancer screenings, particularly for breast, colorectal, and prostate cancers, have been identified as one of the drivers of the decline in cancer mortality over the past few decades.

Percent of Adults Who Are Not Up-To-Date With Cancer Screenings by Race and Ethnicity, 2024

Racial and ethnic differences persist in flu and childhood vaccinations (Figure 11). About two in three Hispanic (65%) and AIAN (65%) adults, and roughly six in ten (58%) Black adults did not receive a flu vaccine in the 2023-2024 season compared to about half (51%) of White adults. However, among children, White children (48%) are more likely than Hispanic (39%) and Asian (31%) children to go without the flu vaccine. Black (48%) and AIAN (46%) children have similar rates of flu vaccination to White children. In 2021-2023, AIAN (41%), Black (36%), and Hispanic (35%) children were more likely than White children (31%) to have not received all recommended childhood immunizations. The rate for Asian children (30%) was similar to the rate for White children (31%). Data are not available to assess flu and childhood vaccinations among NHPI adults and children.

Receipt of Flu and Childhood Vaccinations by Race and Ethnicity

Health Status and Outcomes

Racial Disparities in Health Status and Outcomes

Copy link to Racial Disparities in Health Status and Outcomes

Black and AIAN people fare worse than White people across most examined measures of health status and outcomes (Figure 12). In contrast, Asian and Hispanic people fare better than White people for a majority of examined health measures. NHPI people fare worse than White people across some measures, but several measures lacked sufficient data for a reliable estimate for NHPI people.

Health Status and Outcomes Among People of Color Compared to White People

Life Expectancy

Copy link to Life Expectancy

Black and AIAN people have a shorter life expectancy at birth compared to White people.  Hispanic, Black, and AIAN people experienced larger declines in life expectancy than White people between 2019 and 2021, followed by increases in 2022 and 2023 that brought them closer to pre-pandemic levels. Life expectancy at birth represents the average number of years a group of infants would live if they were to experience the age-specific death rates prevailing during a specified period. Life expectancy declined by 2.7 years between 2019 and 2021, largely reflecting an increase in excess deaths due to COVID-19, which disproportionately impacted Black, Hispanic, and AIAN people. AIAN people experienced the largest life expectancy decline of 6.6 years, followed by Hispanic and Black people (4.2 and 4.0 years, respectively), and a smaller decline of 2.4 years for White people. Asian people had the smallest decline in life expectancy of 2.1 years between 2019 and 2021. Recent data show that overall life expectancy increased across all racial and ethnic groups between 2021 and 2023, but racial disparities persist (Figure 13). Life expectancy is lowest for AIAN people at 70.1 years, followed by Black people at 74.0 years. White and Hispanic people have higher life expectancies at 78.4 and 81.3 years, respectively, while Asian people have the highest life expectancy at 85.2 years. Life expectancies are even lower for AIAN and Black males, at 66.7 and 70.3 years, respectively. Data are not available for NHPI people.

Life Expectancy at Birth in Years by Race and Ethnicity, 2019-2023

Self-Reported Health Status

Copy link to Self-Reported Health Status

Hispanic, Black, and AIAN adults are more likely to report fair or poor health status than their White counterparts, while Asian adults are less likely to indicate fair or poor health. Nearly three in ten (28%) AIAN adults, about a quarter of Hispanic (26%) and NHPI (25%) adults, and about one in five (22%) Black adults report fair or poor health status, compared to 17% of White adults (Figure 14). About one in ten (12%) Asian adults report fair or poor health status.

Percent of Adults Reporting Fair or Poor Health Status by Race and Ethnicity, 2024

Birth Risks and Outcomes

Copy link to Birth Risks and Outcomes

As of 2023, Black people are more than three times as likely as White people to experience a pregnancy-related death (deaths within one year of pregnancy) (49.4 vs. 14.9 per 100,000 live births) (Figure 15). Rates were lower for Hispanic (12.3 per 100,000) and Asian (10.7 per 100,000) women. Data from 2023 were insufficient to identify mortality among AIAN and NHPI women. However, earlier data from 2021 show that AIAN and NHPI people (118.7 and 111.7 per 100,000, respectively) had the highest rates of pregnancy-related mortality across racial and ethnic groups. The Dobbs decision, eliminating the constitutional right to abortion could widen the already large disparities in maternal health as people of color may face disproportionate challenges accessing abortions due to state restrictions.

Pregnancy-Related Mortality per 100,000 Births by Race and Ethnicity, 2023

Black, AIAN, and NHPI women have higher shares of preterm births, low birthweight births, or births for which they received late or no prenatal care compared to White women (Figure 16). Additionally, Hispanic women (10%) are more likely to have births for which they received late or no prenatal care compared to White women (5%). Asian women (9%) are more likely to have low birthweight births, defined as babies born weighing less than 5 pounds 8 ounces or 2,500 grams, than White women (7%). Notably, NHPI women (22%) are more than four times as likely as White women (5%) to begin receiving prenatal care in the third trimester or to receive no prenatal care at all.

Percent of Births With Selected Risk Factors by Race and Ethnicity, 2023

Teen birth rates have declined over time, but the birth rates among Hispanic, Black, AIAN, and NHPI teens are over two times higher than the rate among White teens (Figure 17). In contrast, the birth rate for Asian teens is more than four times lower than the rate for White teens.

Birth Rate per 1,000 for Teens Ages 15-19 by Race and Ethnicity, 2023

Infants born to women of color are at higher risk for mortality compared to those born to White women. As of 2023, Black (10.9 per 1,000) and AIAN (9.2 per 1,000) infants are at least two times as likely to die as White infants (4.5 per 1,000) (Figure 18). NHPI (8.2 per 1,000) and Hispanic (5.0 per 1,000) infants also have higher death rates compared to White infants. Asian infants have the lowest mortality rate at 3.4 per 1,000 live births.

Infant Mortality per 1,000 Live Births by Race and Ethnicity, 2023

HIV and AIDS Diagnoses

Copy link to HIV and AIDS Diagnoses

Black, Hispanic, AIAN, and NHPI people are more likely than White people to be diagnosed with HIV or AIDS, the most advanced stage of HIV infection. In 2023, the HIV diagnosis rate for Black people (41.9 per 100,000) is roughly eight times higher than the rate for White people (5.2 per 100,000), and the rate for Hispanic people (25.2 per 100,000) is about five times higher than the rate for White people (Figure 19). AIAN and NHPI people (9.8 and 10.1 per 100,000, respectively) also have higher HIV diagnosis rates compared to White people. Among those diagnosed in 2023, similar patterns are present among those classified as having AIDS at the time of diagnosis, the most advanced stage of HIV, reflecting barriers to treatment. Black people (20 per 100,000) have a roughly nine times higher rate of AIDS diagnosis compared to White people (2.3 per 100,000). Hispanic (10.1 per 100,000), AIAN (3.7 per 100,000), and NHPI people (4.7 per 100,000) also have higher rates of AIDS diagnoses than White people.

HIV and AIDS Diagnosis Rate per 100,000 by Race and Ethnicity, 2023

Among people ages 13 and older living with an HIV diagnosis, viral suppression rates are lower among AIAN (65%), Hispanic (66%), NHPI (62%), and Black (64%) people compared to White (72%) and Asian (70%) people (Figure 20). Viral suppression refers to having less than 200 copies of HIV per milliliter of blood. Increasing the share of people with HIV who are virally suppressed is one of four key strategies or “pillars” of the Ending the HIV Epidemic in the U.S. initiative. Viral suppression promotes optimal health outcomes for people with HIV and also offers a preventive benefit when someone is virally suppressed, as they cannot sexually transmit HIV.

Viral Supression Rates Among People Ages 13 Years and Older Living with Diagnosed HIV Infection by Race and Ethnicity, 2023

Chronic Disease and Cancer

Copy link to Chronic Disease and Cancer

The prevalence of chronic disease varies across racial and ethnic groups and by type of disease. Diabetes rates for Black (17%), AIAN (16%), and Hispanic (13%) adults are all higher than the rate for White adults (12%). Black (6%), NHPI (5%), Hispanic (4%), and Asian (2%) people are less likely than White people (8%) to have had a heart attack or heart disease. AIAN (23%) and Black (18%) adults have higher rates of asthma compared to their White counterparts (16%), while rates for Hispanic (13%) and Asian (10%) adults are lower. Among children, Black (15%) and Hispanic (11%) children are more likely to have ever had asthma compared to White children (9%), while Asian children (7%) have a lower asthma rate (Figure 21). Data are not available for NHPI children.

Percent Reporting they Have Ever Been Told by a Doctor They Have Diabetes, Heart Attack or Heart Disease, or Asthma by Race and Ethnicity, 2024

Black, AIAN, and NHPI people are roughly twice as likely as White people to die from diabetes, and Black people are more likely than White people to die from heart disease (Figure 22). Hispanic people (26.2 per 100.000) also have a higher diabetes death rate compared to White people (19.8 per 100,000). In contrast, Asian people (16.6 per 100,000) are less likely than White people to die from diabetes. Asian (78.5 per 100,000), Hispanic (108.7 per 100,000), AIAN (138.3 per 100,000), and NHPI (157.8 per 100,000) people have lower heart disease death rates than their White counterparts (169.1 per 100,000).

Age-Adjusted Death Rates per 100,000 for Selected Diseases by Race and Ethnicity, 2023

People of color generally have lower rates of new cancer cases compared to White people, but Black people have higher incidence rates for some cancer types (Figure 23). Black people (445.4 per 100,000) have lower rates of cancer incidence compared to White people (458.6 per 100,000) for cancer overall, and most of the leading types of cancer examined. However, they have higher rates of new colon and rectum (39.8 and 37.0 per 100,000, respectively) and prostate (188.2 and 112.9 per 100,000, respectively) cancer. AIAN people (42.2 per 100,000) have a higher rate of colon and rectum cancer than White people (37.0 per 100,000). Other groups have lower cancer incidence rates than White people across all examined cancer types.

Age-Adjusted Rate of Cancer Incidence per 100,000 by Race and Ethnicity, 2022

Although Black people do not have higher cancer incidence rates than White people overall and across most types of cancer, they are more likely to die from cancer. Black people (161.8 per 100,000) have a higher cancer death rate than White people (148.6 per 100,000) for cancer overall and for most of the leading cancer types (Figure 24). In contrast, Hispanic, Asian, NHPI, and AIAN people have lower cancer mortality rates across most cancer types compared to White people. The higher mortality rate among Black people despite similar or lower rates of incidence compared to White people could reflect a combination of factors, including more limited access to care, later stage of diagnosis, more comorbidities, and lower receipt of guideline-concordant care, which are driven by broader social and economic inequities.

Age-Adjusted Rate of Cancer Mortality per 100,000 by Race and Ethnicity, 2023

Obesity

Copy link to Obesity

Obesity rates vary across race and ethnicity groups. As of 2024, Black (42%), AIAN (41%), and Hispanic (36%) adults all have higher obesity rates than White adults (32%), while Asian adults (13%) have a lower obesity rate. (Figure 25).

Obesity Rate Among Adults by Race and Ethnicity, 2024

Mental Health and Drug Overdose Deaths

Copy link to Mental Health and Drug Overdose Deaths

Overall rates of mental illness are lower for people of color compared to White people but could be underdiagnosed among people of color. About one in five Hispanic (21%) and Black (21%) adults, and 17% of Asian adults report having any mental illness compared to 25% of White adults (Figure 26). Among adolescents, Black (14%), Asian (14%), and NHPI (8%) adolescents were less likely to report having a major depressive episode in the past year compared to White adolescents (19%). Research suggests that a lack of culturally sensitive screening tools that detect mental illness, coupled with structural barriers, could contribute to underdiagnosis of mental illness among people of color.

Percent of Adults with Any Mental Illness and Percent of Adolescents Who Had A Major Depressive Episode by Race and Ethnicity, 2024

AIAN and White people have the highest rates of deaths by suicide as of 2023. People of color have been disproportionately affected by recent increases in deaths by suicide compared with their White counterparts. As of 2023, AIAN (23.8 per 100,000) and White (17.6 per 100,000) people have the highest rates of deaths by suicide compared to other racial and ethnic groups (Figure 27). Rates of deaths by suicide are about two times higher among AIAN adolescents (14.1 per 100,000) than White adolescents (7.1 per 100,000). In contrast, Black (9.1 per 100,000), Hispanic (8.2 per 100,000), and Asian (6.5 per 100,000) adolescents have lower rates of suicide deaths compared to their White peers.

Suicide Death Rate per 100,000 Population by Race and Ethnicity, 2023

Drug overdose death rates are highest among AIAN and Black people. As of 2023, AIAN people continue to have the highest rates of drug overdose deaths (65 per 100,000) compared with other racial and ethnic groups. Drug overdose death rates among Black people (48.9 per 100,000) exceed rates for White people (33.1 per 100,000), reflecting larger increases among Black people in recent years (Figure 28). Hispanic (22.8 per 100,000), NHPI (26.2 per 100,000), and Asian (5.1 per 100,000) people have lower rates of drug overdose deaths than White people (33.1 per 100,000). Data on drug overdose deaths among adolescents show that while White adolescents account for the largest share of drug overdose deaths, Black and Hispanic adolescents have experienced the fastest increase in these deaths in recent years.

Age-Adjusted Drug Overdose Deaths per 100,000 by Race and Ethnicity, 2023

Social and Economic Factors

Racial Disparities in Health Status and Outcomes

Copy link to Racial Disparities in Health Status and Outcomes

Social and economic factors like socioeconomic status, education, immigration status, language, neighborhood and physical environment, employment, and social support networks, as well as access to health care have an important influence on health. There has been extensive research and recognition that addressing social, economic, and environmental factors is important for addressing health disparities. Research also shows how racism and discrimination drive inequities across these factors and impact health and well-being. 

Black, Hispanic, and AIAN people fare worse compared to White people across most examined social and economic measures (Figure 29). Experiences for Asian people are more mixed relative to White people across these examined measures. NHPI people fare worse than White people for half of the measures, however, reliable or disaggregated data are missing for a number of measures.

Social Determinants of Health among People of Color Compared to White People

Work Status, Family Income, and Education

Copy link to Work Status, Family Income, and Education

While most people across racial and ethnic groups live in a family with a full-time worker, disparities persist (Figure 30). AIAN (68%), Black (74%), NHPI (79%), and Hispanic (81%) people are less likely than White people (83%) to have a full-time worker in the family. In contrast, Asian people (86%) are more likely than their White counterparts (86%) to have a full-time worker in the family.

Percent of Under Age 65 Population With a Full-Time Worker in the Family by Race and Ethnicity, 2023

Despite the majority of people living in a family with a full-time worker, over one in five AIAN (25%) and Black (21%) people have family incomes below the federal poverty level, over twice the share as White people (10%). Rates of poverty were also higher among Hispanic (16%) and NHPI (15%) people (Figure 31).

Percent of Under Age 65 Population With Family Income Below Poverty by Race and Ethnicity, 2023

Black, Hispanic, AIAN, and NHPI people have lower levels of educational attainment compared to their White counterparts. Among people ages 25 and older, over two thirds (69%) of White people have completed some post-secondary education, compared to less than half (45%) of Hispanic people, just over half of AIAN (52%) and NHPI (54%) people, and about six in ten (58%) Black people (Figure 33). Asian people (75%) are more likely than White people (69%) to have completed at least some post-secondary education.

Educational Attainment by Race and Ethnicity, 2023

Net Worth and Homeownership

Copy link to Net Worth and Homeownership

Black and Hispanic families have less wealth than White families. Wealth can be defined using net worth, a measure of the difference between a family’s assets and liabilities. The median net worth for White households is $285,000 compared to $44,900 for Black households and $61,600 for Hispanic households (Figure 33). Asian households have the highest median net worth of $536,000. Data are not available for AIAN and NHPI people.

Family Median Net Worth by Race and Ethnicity, 2022

People of color are less likely to own a home than White people (Figure 34). Nearly eight in ten (78%) White people own a home compared to 70% of Asian people, 61% of AIAN people, 56% of Hispanic people, about half of Black people (50%), and 43% of NHPI people.

Homeownership Rates by Race and Ethnicity, 2023

Food Security, Housing Quality, and Internet Access

Copy link to Food Security, Housing Quality, and Internet Access

Hispanic, AIAN, and Black people are roughly twice as likely to experience food insecurity compared to their White counterparts (Figure 35). Asian and White people have similar rates of food insecurity (11% vs 12%, respectively).

Percent of Individuals in a Household Experiencing Food Insecurity by Race and Ethnicity, 2023

People of color are more likely to live in crowded housing than their White counterparts (Figure 36). Among White people, 3% report living in a crowded housing arrangement, defined by the American Community Survey as having more than one person per room. In contrast, almost three in ten (28%) NHPI people, roughly one in five Hispanic (18%) and AIAN (16%) people, and about one in ten Asian (12%) and Black (8%) people report living in crowded housing. However, these differences may reflect cultural preferences for multigenerational living rather than a housing challenge.

Percent of Individuals Living in Crowded Housing by Race and Ethnicity, 2023

AIAN, Black, and NHPI people are less likely to have internet access than White people (Figure 37). Higher shares of AIAN (10%) and Black (5%) people say they have no internet access compared to their White counterparts (4%). In contrast, Asian (2%) and Hispanic (3%) people are less likely to report no internet access than White people (4%).

Percent of Individuals Without Internet Access by Race and Ethnicity, 2023

Transportation

Copy link to Transportation

Black, Asian, AIAN, and Hispanic people are more likely to live in a household without access to a vehicle than White people (Figure 38). About one in eight (13%) Black people and about one in ten Asian (9%) and AIAN (9%) people live in a household without a vehicle available, followed by 7% of Hispanic people. The shares of NHPI (5%) and White (4%) people who report not having access to a vehicle in the household are similar.

Percent of Individuals Living in a Household Without Vehicle Access by Race and Ethnicity, 2023

Citizenship and English Proficiency

Copy link to Citizenship and English Proficiency

Asian, Hispanic, NHPI, and Black people include higher shares of noncitizen immigrants compared to White people. Asian and Hispanic people have the highest shares of noncitizen immigrants at 24% and 20%, respectively (Figure 39). Asian people are projected to become the largest immigrant group in the United States by 2055. Noncitizen immigrants are more likely to be uninsured than citizens and face increased barriers to accessing health care.

Percent of Total Population Who is a Noncitizen by Race and Ethnicity, 2023

Asian and Hispanic people are more likely to have LEP compared to White people. Almost one in three Asian (31%) and Hispanic (28%) people report speaking English less than very well compared to 1% of White people (1%) (Figure 40). Adults with LEP are more likely to report worse health status and increased barriers in accessing health care compared to English proficient adults.

Percent of Individuals Ages Five and Older Who Have Limited English Proficiency by Race and Ethnicity, 2023

Experiences with Racism, Discrimination, and Unfair Treatment

Copy link to Experiences with Racism, Discrimination, and Unfair Treatment

Racism is an underlying driver of health disparities, and repeated and ongoing exposure to perceived experiences of racism and discrimination can increase risks for poor health outcomes. Research has shown that exposure to racism and discrimination can lead to negative mental health outcomes and certain negative impacts on physical health, including depression, anxiety, and hypertension.

AIAN, Black, Hispanic, and Asian adults are more likely to report certain experiences with discrimination in daily life compared with their White counterparts, with the greatest frequency reported among Black and AIAN adults. A 2023 KFF survey shows that at least half of AIAN (58%), Black (54%), and Hispanic (50%) adults, and about four in ten (42%) Asian adults say they experienced at least one type of discrimination in daily life in the past year (Figure 41). These experiences include receiving poorer service than others at restaurants or stores; people acting as if they are afraid of them or as if they aren’t smart; being threatened or harassed; or being criticized for speaking a language other than English. Data are not available for NHPI adults.

Percent of People Who Report Experiences of Discrimination by Race and Ethnicity, 2023

About one in five (18%) Black adults and roughly one in eight (12%) AIAN adults, followed by roughly one in ten Hispanic (11%), and Asian (10%) adults who received health care in the past three years report being treated unfairly or with disrespect by a health care provider because of their racial or ethnic background. These shares are higher than the 3% of White adults who report this (Figure 42). Overall, roughly three in ten (29%) AIAN adults and one in four (24%) Black adults say they were treated unfairly or with disrespect by a health care provider in the past three years for any reason compared with 14% of White adults.

Percent of People Who Report Experiences of Discrimination by a Health Care Provider by Race and Ethnicity, 2023

About the Data

Data Sources

Copy link to Data Sources

This chart pack is based on the KFF Survey on Racism, Discrimination, and Health and KFF analysis of a wide range of health datasets, including the 2023 American Community Survey, the 2024 Behavioral Risk Factor Surveillance System, the 2022-2024 National Health Interview Survey, the 2024 National Survey on Drug Use and Health, and the 2022 Survey of Consumer Finances as well as from several online reports and databases including the Centers for Disease Control and Prevention (CDC) Morbidity and Mortality Weekly Report (MMWR) on vaccination coverage, the National Center for Health Statistics (NCHS) National Vital Statistics Reports, the CDC Influenza Vaccination Dashboard Flu Vaccination Coverage Webpage Report, the National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention (NCHHSTP) Atlas, the United States Cancer Statistics Incidence and Mortality Web-based Report, the 2023 CDC Natality Public Use File, CDC Web-based Injury Statistics Query and Reporting System (WISQARS) database, and the CDC WONDER online database.

Methodology

Copy link to Methodology

Unless otherwise noted, race/ethnicity was categorized by non-Hispanic White (White), non-Hispanic Black (Black), Hispanic, non-Hispanic American Indian or Alaska Native (AIAN), non-Hispanic Asian (Asian), and non-Hispanic Native Hawaiian or Pacific Islander (NHPI). Some datasets combine Asian and NHPI race categories limiting the ability to disaggregate data for these groups. Non-Hispanic White people were the reference group for all significance testing. All noted differences were statistically significant differences at the p<0.05. We include data for smaller population groups wherever available. Instances in which an estimate has a 95% confidence interval width greater than 20 percentage points or 1.2 times the estimate may not be reliable and are noted in the figures.

U.S. Global Health Country-Level Funding Tracker

Published: Dec 15, 2025

This tracker provides U.S. global health funding data by program area and country. It includes Congressionally appropriated (planned) funding amounts from FY 2006 – FY 2023, as well as obligations and disbursements from FY 2006 – FY 2025 (FY 2025 data are partially reported). Data were obtained from ForeignAssistance.gov (see About This Tracker below for more details). For examples of analyses that can be done using this tracker, please expand the section below.

Tracker

About This Tracker

The U.S. is the largest donor to global health in the world, providing bilateral (direct country-to-country) support for U.S. global health programs in over 75 countries in FY 2023, with additional countries reached through U.S. regional efforts and U.S. contributions to multilateral organizations. This tracker provides historical data on bilateral U.S. government funding for global health by country, region, and income-level. It presents data on country-specific global health funding channeled through the Department of State (State) and U.S. Agency for International Development (USAID); these agencies account for approximately 85% of all U.S. funding for global health. Funding channeled through other agencies – the National Institutes of Health (NIH), Centers for Disease Control and Prevention (CDC), and Department of Defense (DoD) – is not included, as these data are not available at the country-level. Funding directed to “regional” or “worldwide” programs, which may reach additional countries, is also not included. See our companion resource, KFF U.S. Global Health Budget Tracker, to view data on U.S. funding for global health overall, including funding channeled through these other agencies. Data in this tracker present three transaction types:

  1. Appropriated: funding amounts based on Congressional appropriations for a given fiscal year which may be obligated and disbursed over a multi-year period;
  2. Obligations: binding agreements that will result in disbursements (or outlays), immediately or in the future, and
  3. Disbursements: actual paid amounts (an outlay of funds) to a recipient in a given year.

These amounts will be updated as new data become available. Queried data can be downloaded using the button within the interactive, and the full data can be downloaded here. For questions related to this resource, or for inquiries on further analyses on U.S. global health funding, please contact globalhealthbudget@kff.org.

Sources

KFF analysis of data from the U.S. Foreign Assistance Dashboard, U.S. State Department regional classifications, and World Bank income classifications.