Friday's health stories

Medical school graduates are returning to ERs


New doctors' interest in emergency medicine is rebounding after the field became the embodiment of professional burnout during the pandemic.
Why it matters: New data out Friday from The National Resident Matching Program shows medical school graduates are continuing to choose higher-paying specialties like orthopedic surgery, ophthalmology, thoracic surgery and radiology.
Safety risks hang over CAR-T therapies for myeloma
Food and Drug Administration advisers Friday will weigh the risk of premature patient deaths from adverse events when they consider expanding the use of two CAR-T therapies for multiple myeloma.
Why it matters: CAR-T treatments have shown promise in the way they can reprogram a patient's immune cells to attack cancer cells but are pricey and have been flagged before for safety concerns.

New curbs on medical device sterilizer ease fears of shortages
New federal restrictions on a cancer-causing chemical that's essential for sterilizing medical devices may have balanced out long-running concerns about protecting public health without choking the medical supply chain.
- But the tradeoffs won't entirely go away until scientists can create a reliable alternative to ethylene oxide, the odorless gas that's been the subject of numerous civil claims and lawsuits.

Hypothetical Disease X drives real spending
Disease X may still be a hypothetical threat. But the risk from a new pathogen many times deadlier than COVID-19 is driving more spending decisions on rapid tests, antimicrobial drugs and other countermeasures.
Why it matters: The fiscal 2025 budget the Biden administration rolled out this week and the intelligence community's annual threat assessment point out biodefense vulnerabilities that were laid bare by the COVID-19 experience.

EPA finalizes curbs on medical device sterilizer
The Environmental Protection Agency on Thursday finalized a rule aimed at sharply reducing emissions of ethylene oxide, a cancer-causing chemical that's essential for sterilizing medical devices.
Why it matters: The FDA has expressed concern about the possibility of resulting device shortages. There are no ready alternatives that can be used at the scale of ethylene oxide, or EtO, at this point, according to the agency.
Zoom in: The new requirements will reduce the amount of EtO coming from commercial sterilizers by an estimated 90% over time. That's an additional 10% over what EPA estimated in its proposed standards.
- The final rule extends compliance timelines for sterilizing plants compared to the proposed standards.
- Its standards aim to protect people living near sterilizing facilities while "minimizing any potential impacts to the medical device supply chain," the EPA said in a release.
- The agency received more than 40,000 comments on its proposed standards and worked closely with the Health and Human Services Department to develop the final regulations, EPA officials said.
State of play: The FDA in April began a pilot program to reduce medical sterilizers' dependence on EtO, and put out guidance last month encouraging companies to use an alternative sterilizing chemical.
- FDA estimates that EtO is used on 20 billion devices in the United States.
Flash back: A 2016 report concluded with "high" confidence that ethylene oxide is "carcinogenic to humans." The odorless gas is the subject of many civil claims and lawsuits.
What they're saying: "For years, I have called for environmental justice, urging protections for workers and fenceline communities from the dangers of EtO pollution," HHS Secretary Xavier Becerra said in a news release.
- "We will continue to work together with EPA to achieve our shared goals of lowering EtO exposure while also mitigating potential risks of medical device shortages."
- "The EPA's final ethylene oxide standards for commercial sterilizers are grounded in science and will save lives," said Senate Environment and Public Works Committee Chair Tom Carper (D-Del.). "I'm grateful for the Biden administration's years of work to develop these strong standards."
Go deeper: Inside an interagency fight over a chemical tied to cancer risks

How Medicare can start covering a popular weight-loss drug for more people
Federal regulators' recent approval of anti-obesity drug Wegovy to reduce cardiovascular risks in overweight people opens the door for Medicare to cover the pricey treatment for more people — though takeup is likely to be slow initially.
Why it matters: More than 40% of Medicare enrollees have at least one heart condition, meaning the new Wegovy approval could greatly expand older adults' access to a drug that so far has been limited for this group.

Maternal death rates may be sharply overstated: study
Rising maternal death rates in the U.S. may have been sharply overstated due to flawed record-keeping, according to new research that found mortality held steady and was in line with other developed nations over two decades.
Why it matters: Maternal health statistics have become a critical public health focus with millions of women living in areas with little to no access to maternity care and with more restricted access to abortion.

Kristi Noem faces lawsuit over video praising Texas dentist
South Dakota Gov. Kristi Noem (R) is being accused in a lawsuit of breaching D.C. consumer protection laws over online video posts this week that praised a Texas dentist.
Why it matters: The lawsuit consumer advocacy group Travelers United filed against Noem on Wednesday comes weeks after presumptive 2024 Republican nominee former President Trump hinted that she's among the frontrunners on his vice presidential shortlist.







