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Readers Speak Up About Women’s Health Issues, From Reproductive Care to Drinking

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Tue, 09 Apr 2024 09:00:00 +0000

Letters to the Editor is a periodic feature. We welcome all comments and will publish a selection. We edit for length and clarity and require full names.

Many readers responded to our data-driven coverage of how ethical and religious directives issued by the U.S. Conference of Catholic Bishops affect care options at Catholic and Catholic-affiliated hospitals in the United States. And we encourage other readers to share their feedback.

A communications specialist in Seattle stated her opinion bluntly in an X post.

“More and more women are running into barriers to obtaining care as Catholic health systems have aggressively acquired secular hospitals in much of the country.”Religion is harming healthcare. https://t.co/O4L9mIzP5K

— JoAnne Dyer (@7Madronas) February 27, 2024

— JoAnne Dyer, Seattle

The Right to Separation of Church and Care

At my most recent OB-GYN appointment, I was warned that our biggest hospital, Covenant Medical Center, is affiliated with the Roman Catholic denomination, as is its string of primary care and other clinics, Grace Clinics.

Attempting to regain some sense of control over my body, I decided to create an advance health directive to make clear I do not want to be taken to any medical facility associated with that denomination, to avoid my medical care being curtailed or impacted by ethical and religious directives, known as ERDs, issued by Roman Catholic bishops (“The Powerful Constraints on Medical Care in Catholic Hospitals Across America,” Feb. 17). To do this, I wanted to know which facilities are so affiliated. It is very hard to find that out.

First, I looked at Grace Clinic and Covenant Medical Center websites. No mention of affiliation with the church, or ERDs, or how ERDs limit the types of medical treatments a patient will be offered (or even informed of the existence of).

When I called Grace Clinic, they denied affiliation with the Catholic Church. When I called Covenant Medical Center, they also denied affiliation. They are owned by Providence, which is Roman Catholic, though you have to do a deep dive into the website to figure that out.

Either the employees are lying or are kept in ignorance so the patients will be kept in ignorance. How can a patient determine whether a hospital will deny them care because of religious beliefs, if the organization conceals its affiliation with said beliefs?

These hospitals have the right to believe whatever they want. It appears they currently also have the right to lie to patients about it. How can patients be informed health care consumers if they can’t access the information they need, and are affirmatively given incorrect information from the organizations?

I have contacted Providence through its website asking if it is affiliated with the Roman Catholic Church and, if so, where I can find a list of types of patients that won’t be treated in accordance with American Medical Association standards, as well as which treatments, procedures, and medications will not be provided or provided only on a limited basis because of that affiliation.

I’ve heard nothing.

— Helen Liggett, Lubbock, Texas

An assistant professor at the Cincinnati Children’s Hospital Medical Center also weighed in on X:

Important reporting from @KFFHealthNews on the impact of Catholic hospital care including their ethics review process:https://t.co/0k2mJpPhY0

— Elizabeth Lanphier (@EthicsElizabeth) February 19, 2024

— Elizabeth Lanphier, Cincinnati

Life at All Costs Is Costly

One aspect of IVF that’s not being discussed is the discarding of embryos found to have serious medical defects (‘What the Health?’: Alabama Court Rules Embryos Are Children. What Now? Feb. 22). For example, a family may carry a devastating condition and wish to screen potential offspring, or defects may arise spontaneously. The Alabama Supreme Court’s decision suggests that these embryos, too, must be implanted.

The court’s decision also affects babies born with severe defects. How much support must be provided a baby born without parts of the brain and skull (anencephaly), which is not terribly uncommon? Or one born without kidneys? Or one with a most severe form of brittle-bone disease (osteogenesis imperfecta), where every touch can break bones? It sounds as though Alabama law now requires maximum support in every instance — in my opinion, this would be holier-than-thou sadism. How does the court define life? Merely a beating heart? I can’t imagine a nurse or doctor not leaving/quitting when forced to torture these babies. Then there’s the parents’ torment. This is godly?

— Gloria Kohut, Grand Rapids, Michigan

On X, an anesthetist and emergency medicine doctor promoted the “What the Health?” podcast episode that delved into the topic:

Check out the latest episode of KFF Health News’ “What the Health?” podcast, where the Alabama Supreme Court’s ruling on embryo rights sparks a national debate. Plus, possible abortion bans and Catholic hospital care. Listen at: https://t.co/4hrsEaWXVb#health, #healthpolicy, …

— David Moniz (@DrDavidMoniz) February 22, 2024

— David Moniz, Chilliwack, British Columbia

Distilling Statistics on Women’s Drinking

While the distilled spirits industry is opposed to excessive consumption by any segment of our society, it’s important to note that your recent article on women and alcohol failed to include federal data showing reductions in alcohol abuse among women in the United States (“More Women Are Drinking Themselves Sick. The Biden Administration Is Concerned,” March 28). For example, the most recent National Survey on Drug Use and Health data indicates binge-drinking among women 21 and older declined more than 6% in the past five years (from 2018 to 2022).

Additionally, claims in the article that the covid-19 pandemic “significantly exacerbated binge-drinking” are not supported by multiple federal data sources that indicate that the pandemic did not produce lasting increases in drinking or harmful drinking.

For instance, a 2023 study using federal data showed that, while sales did rise at the very beginning of the pandemic, this did not necessarily translate to increased binge-drinking or overall consumption in the months following. Rather, drinking decreased — both days per month drinking and drinks per day — as did binge-drinking. Moreover, the same federal NSDUH data referenced above indicates nearly 9 out of 10 U.S. adults 21 years and older (89%) say they drink the same amount or less than they did pre-pandemic.

The article also cites an outdated Global Burdens of Disease report published in 2018 to back up claims that “no amount of alcohol is safe” while ignoring the updated GBD report published in 2022. Importantly, this most recent GBD research concluded there are drinking levels “at which the health risk is equivalent to that of a non-drinker” and that “for individuals age 40+, drinking small amounts of alcohol is not harmful to health.”

Reporting on alcohol research provides important information for consumers, so it is imperative that such reporting correctly reflects the latest evidence on alcohol and health. We encourage all adults who choose to drink — women and men — to drink in moderation, to follow the advice of the Dietary Guidelines for Americans, and to talk to their health care providers who can help determine what is best for them based on individual factors and family history.

— Amanda Berger, vice president of science and health, Distilled Spirits Council of the United States, Washington, D.C.

A lawyer who specializes in fighting insurance denials recommended our March “Bill of the Month” feature in an X post:

All too often insurance providers claim medical treatment is not medically necessary. This article explains a #Cigna denial. #healthinsurance #medicalnecessity https://t.co/rpMwsSOOup

— Scott Glovsky (@ScottGlovskyLaw) March 25, 2024

— Scott Glovsky, Pasadena, California

Working Within a Broken Health Care System

Thanks to Molly Castle Work for the excellent article about the England family’s struggles with our broken health care system (“A Mom’s $97,000 Question: How Was Her Baby’s Air-Ambulance Ride Not Medically Necessary?” March 25). One avenue of resolution that was not noted in your excellent article is the California Department of Managed Health Care. I am a physician, and we had a different, but also very expensive ($90,000), health care bill. It took two years and two appeals to that department, but, ultimately, we were reimbursed by our insurance company. This is a resource that should be more widely known.

— Erica Buhrmann, Berkeley, California

An Unfair Burden on Those Most in Need

It is difficult to understand why those most vulnerable in society, who have difficulty purchasing health insurance, are required to pay more for services with the same doctors and facilities than insurance companies pay. Insurers benefit from “negotiated pricing.” Those with no insurance are required to pay the entire “inflated” bill for medical services. Most times, the difference between the amount a doctor or medical provider bills, compared with the actual payment doctors receive from insurance companies, is approximately 20% of the amount billed.

It is patently unfair to require uninsured patients to pay more than insurance companies pay. Uninsured individuals have an unfair bargaining power, compared with insurance companies. A good example is demonstrated in your article of the woman who received an uncovered emergency medical flight before her death, and her heirs were left with an outrageous bill of $81 (“Without Medicare Part B’s Shield, Patient’s Family Owes $81,000 for a Single Air-Ambulance Flight,” Feb. 27). If her family was told they were responsible for $81,000 for the air ambulance, the transport would not have occurred.

The practice of holding uninsured persons responsible for “entire” medical bills often, in essence, causes someone who does not have coverage — mostly because of affordability — to supplement the revenue of doctors and medical providers by being required to pay the full inflated amount billed for medical services.

Insurance companies defend this practice of “negotiated pricing,” when, in essence, it is used to force those who can least pay to supplement losses suffered by the doctors for discounted payments from insurers.

There needs to be regulation that prohibits medical providers from price-gouging the uninsured, forcing them to supplement doctors’ and providers’ income to make up for underpayments from insurers. Many times, uninsured individuals are already living at or near poverty levels before incurring unexpected medical obligations. Being hit with a surprise bill for an air-ambulance ride costing $81,000 is sufficient to cause the patient to file for bankruptcy. In the U.S., the No. 1 reason people file for bankruptcy protection is because of medical bills.

Our current system of administering health care and payments for such is broken and needs to be fixed. Once this disparate system of payments is rectified, health care should become far more accessible to the general public.

— Ronald B. Kaplan, Holbrook, Massachusetts

On X, a public health scholar shared our article about the side effects of the anti-vaccine movement:

A TN law now means they foster parents, social workers & other caregivers can’t provide permission for childhood vaccines — an essential part of health care for kids. We need to take antivaxxers seriously because they are seriously harming public health. https://t.co/6jX7ltNq4i

— jenn kauffman ✨ (@jennaudrey) March 12, 2024

— Jenn Kauffman, Washington, D.C.

Not Vaccinated? Get Schooling Elsewhere

I am a father and a primary care physician. I just read Amy Maxmen’s article “How the Anti-Vaccine Movement Pits Parental Rights Against Public Health” (March 12) and commend her for her balanced and fact-based presentation.

I feel that an important aspect is missing from such articles — that being the rights of the majority of parents who support vaccination to have their children in the safest possible environment in public schools. We know that no vaccine is perfect, and that our children are still at risk for measles, covid, and other diseases, despite taking advantage of the proven benefits of vaccines.

I believe that parents who exercise their rights to not have their children vaccinated should be required to homeschool, or to send their children to private schools having policies with which they agree. I am aware that only a tiny percentage of Americans would agree with me.

— John Cottle, Mendocino, California

Clinical psychologist Carl Hindy seemed inspired by our article on a costly new postpartum depression treatment:

[Instead of gender reveal parties, we can have Pharma baby showers 😢] A New $16,000 Postpartum Depression Drug Is Here. How Will Insurers Handle It? – KFF Health News https://t.co/1CVZEX7yf8

— Carl Hindy, Ph.D., HSP, Clinical Psychologist (@DrCarlHindy) March 18, 2024

— Carl Hindy, Exeter, New Hampshire

Tending to New Mothers’ Needs

It was heartbreaking to read that private health insurers have effectively delayed the availability of a revolutionary treatment for postpartum depression, a debilitating condition that makes it difficult for new parents to care for their families, work, or even get out of bed (“A New $16,000 Postpartum Depression Drug Is Here. How Will Insurers Handle It?” March 12).

As one of the 1 in 5 new mothers who struggled with this terrible illness when my own son was born, I can only hope zuranolone is made widely available very soon. As an advocate for the rights of pregnant workers, I hope that mental health care providers are aware that there is another new and revolutionary tool that is at their disposal today to support patients struggling with prenatal and postpartum mental health conditions. A new federal law, the Pregnant Workers Fairness Act, gives workers the right to receive changes at work needed for pregnancy-related mental health conditions. The Pregnant Workers Fairness Act, which applies to employers with 15 or more employees, requires they provide reasonable accommodations for pregnancy, childbirth, and related medical conditions, so long as it does not impose an undue hardship. For example, a new mother experiencing a perinatal mental health condition may be eligible to receive a modified schedule, time off to attend mental health appointments, a more private workspace, permission to work from home, or any other “reasonable accommodation” that will address their needs. Mental health care providers should support their patients by discussing their work-related challenges, helping to identify workplace modifications, and writing effective work notes to their patients’ employers.

Health care providers and their patients can access free resources from the University of California Law-San Francisco Center for WorkLife Law on workplace accommodations for perinatal mental health conditions at pregnantatwork.org. Health care providers or employees with questions can contact the Center for WorkLife Law’s free and confidential legal helpline at 415-703-8276 or hotline@worklifelaw.org.

— Juliana Franco, San Francisco

Fear of Needles Is Sometimes Unfounded

I read your article “Needle Pain Is a Big Problem for Kids. One California Doctor Has a Plan” (March 20). I can tell you from experience that the needle is not the source of the pain. After a bone marrow transplant from a donor, I had to get all those childhood vaccines and those for adults 65 and older. The needle stick can barely be felt; it’s the medication going in that is painful. The area you get the vaccine in is then sore for several days. That has been my experience.

— Patsy Rowan, Los Angeles

Radiologist Ian Weissman chimed in on X about pain-reduction strategies:

Researchers have helped develop a five step plan to help prevent what they call “needless pain” for children getting injections or their blood drawnhttps://t.co/mCi8Tx6ILn

— Ian Weissman, DO (@DrIanWeissman) March 29, 2024

— Ian Weissman, Milwaukee

Informed on the Difference Between Mis- and Disinformation

First, I am grateful for your continued investigative reporting on covid-19.

Second, I am writing to share a perspective that I trust you can share with the writer of “Four Years After Shelter-in-Place, Covid-19 Misinformation Persists” (April 1). My focus is on the term “information” and its variants.

Specifically, I find it helpful to distinguish linguistically three variants:

  • “Information” is information that one provides to others that the informer believes to be accurate.
  • “Misinformation” is information that one provides to others that the informer believed was accurate, yet was provided information that indicates the information was less than accurate at some level. As such the informer issues an erratum and corrects the “mis” of the “mis-information.”
  • “Disinformation” is information that one provides to others with demonstrable knowledge that this information is not accurate and shares with an intent to illicit thought and action for ulterior motives — motives that are often nefarious and may result in harm, such as increasing individual and/or population morbidity and mortality.

I find the conflation of “mis” and “dis” to be in and of itself harmful to those who convey “mis” and then correct as well as giving those who use “dis” for less-than-honorable purposes cover, a safe haven, and a “get-out-of-jail card.”

For example, it is well known that Fox News internally adhered to information based on scientific data and medical evidence during the covid-19 pandemic state of emergency. Concurrently, it parlayed information externally that can only be characterized as “dis.”

What I find surprising is the fact (I stand to be corrected should I be misinformed) that no one has found at least one individual who acted upon Fox News’ disinformation that resulted in morbidity and/or mortality — or wrongful death litigation.

Keep up the good work.

Ed Shanshala, CEO of Ammonoosuc Community Health Services, Littleton, New Hampshire

A communications specialist outside Chicago called out disinformation in an X post:

Disinformation is public health enemy 1. Those who start it and spread it are toxic for our society.

— Michelle Rathman 🟧 (the real one) (@MRBImpact) April 1, 2024

— Michelle Rathman, Geneva, Illinois

States Should Not Spend Opioid Settlement Cash on Unproven Tech

Aneri Pattani did an excellent job reporting on the event in Mobile, Alabama, on Jan. 24, where the Poarch Band of Creek Indians presented a check for $500,000 from the tribe’s opioid settlement funds to the Helios Alliance (“Statistical Models vs. Front-Line Workers: Who Knows Best How to Spend Opioid Settlement Cash?” March 5).

Helios, which includes for-profit and nonprofit organizations, will use funds to build a proprietary simulation model to help leaders decide how to spend settlement funds. According to Helios, the initial system will not be completed before spring 2024.

As a digital product manager for the past 20 years, I understand the potential of technology to improve health care, but settlement funds should not be financing early-stage, proprietary technologies developed by private-sector companies. Helios’ pitch is: “… spend 5% [of settlement funds] so you get the biggest impact with the other 95%,” says Rayford Etherton, who formed the alliance. But given the nationwide settlement is $50 billion over the next 18 years, 5% means that $2.5 billion would go to a potentially proprietary solution.

While the promise of a new technology simulation model is exciting, it’s also high-risk. Moreover, while respected experts like Stephen Loyd are involved with Helios, there aren’t experienced artificial intelligence engineers, digital product experts, data scientists, or security experts listed on the Helios website.

Any technology developed using opioid settlement funds should be open-source and free to all states. More transparency from Helios is needed to describe ownership, user access terms, and licensing fees.

Settlement funds should be deployed to proven, evidence-based solutions. Given the opioid crisis has been raging for 20 years, health care experts already have data-driven insights on how to fix this: increase access to medication-assisted treatment; reduce barriers to physician licensing for buprenorphine, methadone, and naltrexone; increase education in schools; enhance social services such as employment and child care; and increase funding to law enforcement to fight illegal opioids (specifically, fentanyl).

Rather than putting large settlement investments into a not-yet-built simulation model, states should use a human-centered design approach based on research from patients, providers, family members, and community groups that have been battling the opioid crisis for decades to drive initial investments across the ecosystem of opioid crisis drivers. Once Helios has a working simulation product tested and in production, states can consider small investments to pilot usage and see if the product actually produces the desired outcomes.

The ongoing mantra of “public-private partnerships” is a great idea, but the public sector shouldn’t end up paying the bill and taking on all the risk.

— Kelly O’Connor, Washington, D.C.

A professor in Weill Cornell Medicine’s Department of Population Health Sciences shared insights on X:

Fascinating article. On the one hand “Data does not save lives. Numbers on a computer do not save lives,” vs the city has an obligation to use its settlement funds “in a way that is going to do the most good…instead of simply guessing.” https://t.co/w4QJ7zOkgM

— Bruce Schackman (@BruceSchackman) March 6, 2024

— Bruce Schackman, New York City

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Title: Readers Speak Up About Women’s Health Issues, From Reproductive Care to Drinking
Sourced From: kffhealthnews.org/news/article/letters-readers-women-health-reproductive-care-drinking-april-2024/
Published Date: Tue, 09 Apr 2024 09:00:00 +0000

Kaiser Health News

US Judge Names Receiver To Take Over California Prisons’ Mental Health Program

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kffhealthnews.org – Don Thompson – 2025-03-20 12:46:00

SACRAMENTO, Calif. — A judge has initiated a federal court takeover of California’s troubled prison mental health system by naming the former head of the Federal Bureau of Prisons to serve as receiver, giving her four months to craft a plan to provide adequate care for tens of thousands of prisoners with serious mental illness.

Senior U.S. District Judge Kimberly Mueller issued her order March 19, identifying Colette Peters as the nominated receiver. Peters, who was Oregon’s first female corrections director and known as a reformer, ran the scandal-plagued federal prison system for 30 months until President Donald Trump took office in January. During her tenure, she closed a women’s prison in Dublin, east of Oakland, that had become known as the “rape club.”

Michael Bien, who represents prisoners with mental illness in the long-running prison lawsuit, said Peters is a good choice. Bien said Peters’ time in Oregon and Washington, D.C., showed that she “kind of buys into the fact that there are things we can do better in the American system.”

“We took strong objection to many things that happened under her tenure at the BOP, but I do think that this is a different job and she’s capable of doing it,” said Bien, whose firm also represents women who were housed at the shuttered federal women’s prison.

California corrections officials called Peters “highly qualified” in a statement, while Gov. Gavin Newsom’s office did not immediately comment. Mueller gave the parties until March 28 to show cause why Peters should not be appointed.

Peters is not talking to the media at this time, Bien said. The judge said Peters is to be paid $400,000 a year, prorated for the four-month period.

About 34,000 people incarcerated in California prisons have been diagnosed with serious mental illnesses, representing more than a third of California’s prison population, who face harm because of the state’s noncompliance, Mueller said.

Appointing a receiver is a rare step taken when federal judges feel they have exhausted other options. A receiver took control of Alabama’s correctional system in 1976, and they have otherwise been used to govern prisons and jails only about a dozen times, mostly to combat poor conditions caused by overcrowding. Attorneys representing inmates in Arizona have asked a judge to take over prison health care there.

Mueller’s appointment of a receiver comes nearly 20 years after a different federal judge seized control of California’s prison medical system and installed a receiver, currently J. Clark Kelso, with broad powers to hire, fire, and spend the state’s money.

California officials initially said in August that they would not oppose a receivership for the mental health program provided that the receiver was also Kelso, saying then that federal control “has successfully transformed medical care” in California prisons. But Kelso withdrew from consideration in September, as did two subsequent candidates. Kelso said he could not act “zealously and with fidelity as receiver in both cases.”

Both cases have been running for so long that they are now overseen by a second generation of judges. The original federal judges, in a legal battle that reached the U.S. Supreme Court, more than a decade ago forced California to significantly reduce prison crowding in a bid to improve medical and mental health care for incarcerated people.

State officials in court filings defended their improvements over the decades. Prisoners’ attorneys countered that treatment remains poor, as evidenced in part by the system’s record-high suicide rate, topping 31 suicides per 100,000 prisoners, nearly double that in federal prisons.

“More than a quarter of the 30 class-members who died by suicide in 2023 received inadequate care because of understaffing,” prisoners’ attorneys wrote in January, citing the prison system’s own analysis. One prisoner did not receive mental health appointments for seven months “before he hanged himself with a bedsheet.”

They argued that the November passage of a ballot measure increasing criminal penalties for some drug and theft crimes is likely to increase the prison population and worsen staffing shortages.

California officials argued in January that Mueller isn’t legally justified in appointing a receiver because “progress has been slow at times but it has not stalled.”

Mueller has countered that she had no choice but to appoint an outside professional to run the prisons’ mental health program, given officials’ intransigence even after she held top officials in contempt of court and levied fines topping $110 million in June. Those extreme actions, she said, only triggered more delays.

The 9th U.S. Circuit Court of Appeals on March 19 upheld Mueller’s contempt ruling but said she didn’t sufficiently justify calculating the fines by doubling the state’s monthly salary savings from understaffing prisons. It upheld the fines to the extent that they reflect the state’s actual salary savings but sent the case back to Mueller to justify any higher penalty.

Mueller had been set to begin additional civil contempt proceedings against state officials for their failure to meet two other court requirements: adequately staffing the prison system’s psychiatric inpatient program and improving suicide prevention measures. Those could bring additional fines topping tens of millions of dollars.

But she said her initial contempt order has not had the intended effect of compelling compliance. Mueller wrote as far back as July that additional contempt rulings would also be likely to be ineffective as state officials continued to appeal and seek delays, leading “to even more unending litigation, litigation, litigation.”

She went on to foreshadow her latest order naming a receiver in a preliminary order: “There is one step the court has taken great pains to avoid. But at this point,” Mueller wrote, “the court concludes the only way to achieve full compliance in this action is for the court to appoint its own receiver.”

This article was produced by KFF Health News, which publishes California Healthline, an editorially independent service of the California Health Care Foundation. 

The post US Judge Names Receiver To Take Over California Prisons’ Mental Health Program appeared first on kffhealthnews.org

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Amid Plummeting Diversity at Medical Schools, a Warning of DEI Crackdown’s ‘Chilling Effect’

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kffhealthnews.org – Annie Sciacca – 2025-03-20 04:00:00

The Trump administration’s crackdown on DEI programs could exacerbate an unexpectedly steep drop in diversity among medical school students, even in states like California, where public universities have been navigating bans on affirmative action for decades. Education and health experts warn that, ultimately, this could harm patient care.

Since taking office, President Donald Trump has issued a handful of executive orders aimed at terminating all diversity, equity, and inclusion, or DEI, initiatives in federally funded programs. And in his March 4 address to Congress, he described the Supreme Court’s 2023 decision banning the consideration of race in college and university admissions as “brave and very powerful.”

Last month, the Education Department’s Office for Civil Rights — which lost about 50% of its staff in mid-March — directed schools, including postsecondary institutions, to end race-based programs or risk losing federal funding. The “Dear Colleague” letter cited the Supreme Court’s decision.

Paulette Granberry Russell, president and CEO of the National Association of Diversity Officers in Higher Education, said that “every utterance of ‘diversity’ is now being viewed as a violation or considered unlawful or illegal.” Her organization filed a lawsuit challenging Trump’s anti-DEI executive orders.

While California and eight other states — Arizona, Florida, Idaho, Michigan, Nebraska, New Hampshire, Oklahoma, and Washington — had already implemented bans of varying degrees on race-based admissions policies well before the Supreme Court decision, schools bolstered diversity in their ranks with equity initiatives such as targeted scholarships, trainings, and recruitment programs.

But the court’s decision and the subsequent state-level backlash — 29 states have since introduced bills to curb diversity initiatives, according to data published by the Chronicle of Higher Education — have tamped down these efforts and led to the recent declines in diversity numbers, education experts said.

After the Supreme Court’s ruling, the numbers of Black and Hispanic medical school enrollees fell by double-digit percentages in the 2024-25 school year compared with the previous year, according to the Association of American Medical Colleges. Black enrollees declined 11.6%, while the number of new students of Hispanic origin fell 10.8%. The decline in enrollment of American Indian or Alaska Native students was even more dramatic, at 22.1%. New Native Hawaiian or other Pacific Islander enrollment declined 4.3%.

“We knew this would happen,” said Norma Poll-Hunter, AAMC’s senior director of workforce diversity. “But it was double digits — much larger than what we anticipated.”

The fear among educators is the numbers will decline even more under the new administration.

At the end of February, the Education Department launched an online portal encouraging people to “report illegal discriminatory practices at institutions of learning,” stating that students should have “learning free of divisive ideologies and indoctrination.” The agency later issued a “Frequently Asked Questions” document about its new policies, clarifying that it was acceptable to observe events like Black History Month but warning schools that they “must consider whether any school programming discourages members of all races from attending.”

“It definitely has a chilling effect,” Poll-Hunter said. “There is a lot of fear that could cause institutions to limit their efforts.”

Numerous requests for comment from medical schools about the impact of the anti-DEI actions went unreturned. University presidents are staying mum on the issue to protect their institutions, according to reporting from The New York Times.

Utibe Essien, a physician and UCLA assistant professor, said he has heard from some students who fear they won’t be considered for admission under the new policies. Essien, who co-authored a study on the effect of affirmative action bans on medical schools, also said students are worried medical schools will not be as supportive toward students of color as in the past.

“Both of these fears have the risk of limiting the options of schools folks apply to and potentially those who consider medicine as an option at all,” Essien said, adding that the “lawsuits around equity policies and just the climate of anti-diversity have brought institutions to this place where they feel uncomfortable.”

In early February, the Pacific Legal Foundation filed a lawsuit against the University of California-San Francisco’s Benioff Children’s Hospital Oakland over an internship program designed to introduce “underrepresented minority high school students to health professions.”

Attorney Andrew Quinio filed the suit, which argues that its plaintiff, a white teenager, was not accepted to the program after disclosing in an interview that she identified as white.

“From a legal standpoint, the issue that comes about from all this is: How do you choose diversity without running afoul of the Constitution?” Quinio said. “For those who want diversity as a goal, it cannot be a goal that is achieved with discrimination.”

UC Health spokesperson Heather Harper declined to comment on the suit on behalf of the hospital system.

Another lawsuit filed in February accuses the University of California of favoring Black and Latino students over Asian American and white applicants in its undergraduate admissions. Specifically, the complaint states that UC officials pushed campuses to use a “holistic” approach to admissions and “move away from objective criteria towards more subjective assessments of the overall appeal of individual candidates.”

The scrutiny of that approach to admissions could threaten diversity at the UC-Davis School of Medicine, which for years has employed a “race-neutral, holistic admissions model” that reportedly tripled enrollment of Black, Latino, and Native American students.

“How do you define diversity? Does it now include the way we consider how someone’s lived experience may be influenced by how they grew up? The type of school, the income of their family? All of those are diversity,” said Granberry Russell, of the National Association of Diversity Officers in Higher Education. “What might they view as an unlawful proxy for diversity equity and inclusion? That’s what we’re confronted with.”

California Attorney General Rob Bonta, a Democrat, recently joined other state attorneys general to issue guidance urging that schools continue their DEI programs despite the federal messaging, saying that legal precedent allows for the activities. California is also among several states suing the administration over its deep cuts to the Education Department.

If the recent decline in diversity among newly enrolled students holds or gets worse, it could have long-term consequences for patient care, academic experts said, pointing toward the vast racial disparities in health outcomes in the U.S., particularly for Black people.

A higher proportion of Black primary care doctors is associated with longer life expectancy and lower mortality rates among Black people, according to a 2023 study published by the JAMA Network.

Physicians of color are also more likely to build their careers in medically underserved communities, studies have shown, which is increasingly important as the AAMC projects a shortage of up to 40,400 primary care doctors by 2036.

“The physician shortage persists, and it’s dire in rural communities,” Poll-Hunter said. “We know that diversity efforts are really about improving access for everyone. More diversity leads to greater access to care — everyone is benefiting from it.”

This article was produced by KFF Health News, which publishes California Healthline, an editorially independent service of the California Health Care Foundation. 

The post Amid Plummeting Diversity at Medical Schools, a Warning of DEI Crackdown’s ‘Chilling Effect’ appeared first on kffhealthnews.org

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Tribal Health Leaders Say Medicaid Cuts Would Decimate Health Programs

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kffhealthnews.org – Jazmin Orozco Rodriguez – 2025-03-19 04:00:00

As Congress mulls potentially massive cuts to federal Medicaid funding, health centers that serve Native American communities, such as the Oneida Community Health Center near Green Bay, Wisconsin, are bracing for catastrophe.

That’s because more than 40% of the about 15,000 patients the center serves are enrolled in Medicaid. Cuts to the program would be detrimental to those patients and the facility, said Debra Danforth, the director of the Oneida Comprehensive Health Division and a citizen of the Oneida Nation.

“It would be a tremendous hit,” she said.

The facility provides a range of services to most of the Oneida Nation’s 17,000 people, including ambulatory care, internal medicine, family practice, and obstetrics. The tribe is one of two in Wisconsin that have an “open-door policy,” Danforth said, which means that the facility is open to members of any federally recognized tribe.

But Danforth and many other tribal health officials say Medicaid cuts would cause service reductions at health facilities that serve Native Americans.

Indian Country has a unique relationship to Medicaid, because the program helps tribes cover chronic funding shortfalls from the Indian Health Service, the federal agency responsible for providing health care to Native Americans.

Medicaid has accounted for about two-thirds of third-party revenue for tribal health providers, creating financial stability and helping facilities pay operational costs. More than a million Native Americans enrolled in Medicaid or the closely related Children’s Health Insurance Program also rely on the insurance to pay for care outside of tribal health facilities without going into significant medical debt. Tribal leaders are calling on Congress to exempt tribes from cuts and are preparing to fight to preserve their access.

“Medicaid is one of the ways in which the federal government meets its trust and treaty obligations to provide health care to us,” said Liz Malerba, director of policy and legislative affairs for the United South and Eastern Tribes Sovereignty Protection Fund, a nonprofit policy advocacy organization for 33 tribes spanning from Texas to Maine. Malerba is a citizen of the Mohegan Tribe.

“So we view any disruption or cut to Medicaid as an abrogation of that responsibility,” she said.

Tribes face an arduous task in providing care to a population that experiences severe health disparities, a high incidence of chronic illness, and, at least in western states, a life expectancy of 64 years — the lowest of any demographic group in the U.S. Yet, in recent years, some tribes have expanded access to care for their communities by adding health services and providers, enabled in part by Medicaid reimbursements.

During the last two fiscal years, five urban Indian organizations in Montana saw funding growth of nearly $3 million, said Lisa James, director of development for the Montana Consortium for Urban Indian Health, during a webinar in February organized by the Georgetown University Center for Children and Families and the National Council of Urban Indian Health.

The increased revenue was “instrumental,” James said, allowing clinics in the state to add services that previously had not been available unless referred out for, including behavioral health services. Clinics were also able to expand operating hours and staffing.

Montana’s five urban Indian clinics, in Missoula, Helena, Butte, Great Falls, and Billings, serve 30,000 people, including some who are not Native American or enrolled in a tribe. The clinics provide a wide range of services, including primary care, dental care, disease prevention, health education, and substance use prevention.

James said Medicaid cuts would require Montana’s urban Indian health organizations to cut services and limit their ability to address health disparities.

American Indian and Alaska Native people under age 65 are more likely to be uninsured than white people under 65, but 30% rely on Medicaid compared with 15% of their white counterparts, according to KFF data for 2017 to 2021. More than 40% of American Indian and Alaska Native children are enrolled in Medicaid or CHIP, which provides health insurance to kids whose families are not eligible for Medicaid. KFF is a health information nonprofit that includes KFF Health News.

A Georgetown Center for Children and Families report from January found the share of residents enrolled in Medicaid was higher in counties with a significant Native American presence. The proportion on Medicaid in small-town or rural counties that are mostly within tribal statistical areas, tribal subdivisions, reservations, and other Native-designated lands was 28.7%, compared with 22.7% in other small-town or rural counties. About 50% of children in those Native areas were enrolled in Medicaid.

The federal government has already exempted tribes from some of Trump’s executive orders. In late February, Department of Health and Human Services acting general counsel Sean Keveney clarified that tribal health programs would not be affected by an executive order that diversity, equity, and inclusion government programs be terminated, but that the Indian Health Service is expected to discontinue diversity and inclusion hiring efforts established under an Obama-era rule.

HHS Secretary Robert F. Kennedy Jr. also rescinded the layoffs of more than 900 IHS employees in February just hours after they’d received termination notices. During Kennedy’s Senate confirmation hearings, he said he would appoint a Native American as an assistant HHS secretary. The National Indian Health Board, a Washington, D.C.-based nonprofit that advocates for tribes, in December endorsed elevating the director of the Indian Health Service to assistant secretary of HHS.

Jessica Schubel, a senior health care official in Joe Biden’s White House, said exemptions won’t be enough.

“Just because Native Americans are exempt doesn’t mean that they won’t feel the impact of cuts that are made throughout the rest of the program,” she said.

State leaders are also calling for federal Medicaid spending to be spared because cuts to the program would shift costs onto their budgets. Without sustained federal funding, which can cover more than 70% of costs, state lawmakers face decisions such as whether to change eligibility requirements to slim Medicaid rolls, which could cause some Native Americans to lose their health coverage.

Tribal leaders noted that state governments do not have the same responsibility to them as the federal government, yet they face large variations in how they interact with Medicaid depending on their state programs.

President Donald Trump has made seemingly conflicting statements about Medicaid cuts, saying in an interview on Fox News in February that Medicaid and Medicare wouldn’t be touched. In a social media post the same week, Trump expressed strong support for a House budget resolution that would likely require Medicaid cuts.

The budget proposal, which the House approved in late February, requires lawmakers to cut spending to offset tax breaks. The House Committee on Energy and Commerce, which oversees spending on Medicaid and Medicare, is instructed to slash $880 billion over the next decade. The possibility of cuts to the program that, together with CHIP, provides insurance to 79 million people has drawn opposition from national and state organizations.

The federal government reimburses IHS and tribal health facilities 100% of billed costs for American Indian and Alaska Native patients, shielding state budgets from the costs.

Because Medicaid is already a stopgap fix for Native American health programs, tribal leaders said it won’t be a matter of replacing the money but operating with less.

“When you’re talking about somewhere between 30% to 60% of a facility’s budget is made up by Medicaid dollars, that’s a very difficult hole to try and backfill,” said Winn Davis, congressional relations director for the National Indian Health Board.

Congress isn’t required to consult tribes during the budget process, Davis added. Only after changes are made by the Centers for Medicare & Medicaid Services and state agencies are tribes able to engage with them on implementation.

The amount the federal government spends funding the Native American health system is a much smaller portion of its budget than Medicaid. The IHS projected billing Medicaid about $1.3 billion this fiscal year, which represents less than half of 1% of overall federal spending on Medicaid.

“We are saving more lives,” Malerba said of the additional services Medicaid covers in tribal health care. “It brings us closer to a level of 21st century care that we should all have access to but don’t always.”

This article was published with the support of the Journalism & Women Symposium (JAWS) Health Journalism Fellowship, assisted by grants from The Commonwealth Fund.

KFF Health News is a national newsroom that produces in-depth journalism about health issues and is one of the core operating programs at KFF—an independent source of health policy research, polling, and journalism. Learn more about KFF.

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