Simplicity is a virtue.

From Washington, DC,

• Beckers Health IT reports,
  • “The Department of Health and Human Services finalized a rule Oct. 26 eliminating 14 federal health IT certification criteria and scaling back AI transparency requirements, with the agency projecting more than $1.5 billion in regulatory cost savings.
  • “The final rule, known as Health Data, Technology, and Interoperability: ONC Deregulatory Actions to Unleash Prosperity, or HTI-5, reduces compliance requirements for developers participating in the Office of the National Coordinator for Health Information Technology’s certification program.
  • “HHS initially proposed eliminating 34 of the program’s 60 certification criteria in December 2025. The final rule takes a narrower approach, removing 14 criteria and revising seven while leaving 39 unchanged.
  • “Among the changes is the elimination of AI model-card requirements within the decision support interventions certification criterion. Those requirements, established under the HTI-1 rule, were intended to give healthcare organizations information about predictive algorithms and other decision-support tools incorporated into certified health IT.
  • “The rule also removes or revises requirements involving care coordination, patient engagement and certain health data exchange capabilities, and formally removes a clinical decision support criterion that expired Jan. 1, 2025.”
• More is information about the final rule can be found at healthit.gov/hti5, on LinkedIn, or by following @ONC_HealthIT on X.

• Healthcare Dive adds,
  • “The healthcare industry is slowly but surely moving away from the old, fragmented and manual way of handling prior authorization toward a modernized electronic system.
  • “CMS-regulated payers, such as Medicare Advantage, Medicaid and marketplace insurers, are now confronting a Jan. 1 deadline to implement the three prior authorization application programming interfaces — sets of rules that enable computer programs to communicate directly with one another —  under a federal interoperability rule that was finalized in 2024.

• Beckers Hospital Review considers five big questions as the 340B drug rebate pilot nears launch on January 1, 2027.

• Beckers Payer Issues relates,
  • “Ghost networks have long been a point of frustration, with health plan members sometimes left scrambling to check if a provider is in network — or available at all.
  • “Several health insurers — including Elevance Health and Blue Shield of California, in recent months — have faced lawsuits concerning the accuracy of their provider directories. Some of these complaints said that seemingly bigger networks draw more customers, even if that appearance is ultimately misleading.
  • “But more recent developments have pointed to ongoing issues. One study published in October found more than half of secret-shopper calls made to psychiatrists and psychologists across six Blue Cross Blue Shield plans’ directories indicated errors. Separately, this fall, UnitedHealthcare mistakenly told members that eight clinicians had died before correcting the issue. 
  • “While the No Surprises Act, state laws and CMS rules have targeted ghost networks and network adequacy before, there has been a renewed focus on getting directories right.
  • “On Oct. 13, DataSpring, powered by CAQH, rolled out a new standard to measure provider directory data quality for individual clinicians. DataSpring convened major insurers, the American Medical Association and the National Committee for Quality Assurance to develop a framework rooted in the CMS quality foundation for provider directories.”

• Per a Department of Health and Human Services news release,
  • “U.S. Department of Health and Human Services (HHS) Secretary Robert F. Kennedy, Jr. brought his “Take Back Your Health Tour” to Texas and Florida last week to advance President Trump’s Make America Healthy Again agenda. Across four days, Secretary Kennedy announced new actions on kidney disease and dementia, promoted stronger nutrition education for future doctors, and worked to expand access to women’s healthcare.
  • “From Tuesday through Friday, Secretary Kennedy met with healthcare providers, patient advocates, medical educators, and pharmaceutical manufacturers in Fort Worth, Texas, and Orange Park, Fort Lauderdale, and Miami, Florida.  At each stop, he advanced concrete actions to prevent chronic disease, improve patient care, and give Americans more information and choices to protect their health.
  • “President Trump has directed us to confront chronic disease and put patients first,” said HHS Secretary Robert F. Kennedy, Jr. “Across Texas and Florida, we put that mission into action — detecting kidney disease earlier, strengthening nutrition education for future doctors, advancing prevention and care for families facing dementia, and expanding access to women’s health treatments. HHS is moving prevention to the center of American health care and giving patients more control over their health.”

• Bloomberg Law notes,
  • “One of the Department of Labor’s key policy advisers is departing the Employee Benefits Security Administration, following completion of the agency’s recent rulemaking on pharmacy benefit managers and healthcare price transparency.
  • “EBSA Senior Policy Advisor Caitlin Soto announced on LinkedIn that Friday would be her last day, calling her time at the DOL “the honor of my career.”
  • “Leading the Department’s PBM Fee Disclosure rulemaking, after nearly a decade of PBM transparency work, was the highlight,” she wrote in her post. “I’m also proud of our work on behalf of this administration to advance fertility benefits, transparency in coverage, and mental health parity. The list goes on.”
  • “The department is expected to release a rule in the coming days requiring PBMs — which negotiate drug prices for health plans — to disclose detailed compensation information to employers and other health plan sponsors. DOL also recently finalized a rule aimed at strengthening price transparency for medical services.”

From the U.S. Office of Personnel Management front,

• Federal News Network reports,
  • “More details are emerging on the Trump administration’s revisions to paid administrative leave. Agencies’ ability to pay employees not to work during workforce reduction efforts has been formalized. Paid leave will also be allowed during reduction-in-force notice periods, the Office of Personnel Management said. OPM’s latest guidance comes after it finalized regulations to conform with the rules for the deferred resignation program. OPM is expected to soon update other online resources to reflect the new regulations. — Drew Friedman (Revised administrative leave regulations – Office of Personnel Management)”
• and
  • “The White House is following a court’s order when it comes to reduction-in-force policies. The Office of Management and Budget and the Office of Personnel Management have formally rescinded two memos calling for reductions in force during shutdowns. The Trump administration agreed to terminate the two memos as part of its settlement in September to end a lawsuit by a coalition of federal employee unions including the American Federation of Government Employees, National Federation of Federal Employees and National Treasury Employees Union. Along with the removing the two memos, the Trump administration agreed to rescind every RIF notice issued during the 2026 shutdown and reinstate employees with back pay from the State Department, General Services Administration and Small Business Administration. Additionally, agencies must remove from their shutdown contingency plans any language authorizing RIFs, or RIF work, during a lapse in appropriations, unless a statute expressly permits it. — Jason Miller (OMB rescinds memo allowing RIFs during shutdowns – Office of Management and Budget)

From the U.S. Food and Drug Administration front,

• Bloomberg Law reports,
  • “A recently launched FDA initiative targeting rare diseases is a top focus to carry out, the agency’s acting chief said ahead of a public meeting Wednesday to solicit feedback on the framework. 
  • “We’ve got to make sure that that process is in place. We’re working really hard to do it,” Kyle Diamantas, acting commissioner for the Food and Drug Administration, said Monday at the National Organization for Rare Disorders’ breakthrough summit. “It’s a top priority of mine.”
  • “Earlier this month, the agency introduced the Rare Disease Framework Initiative, which seeks to give patients more input and drug companies more transparency in the regulatory process for rare treatments. The initiative aims to develop a fit-for-purpose plan that considers the nuances of each disease and patient needs.”

• Michigan Engineer relates,
  • “Conventional methods of pulling clots out through the blood vessels can damage fragile vessel walls.
  • “The newly FDA-cleared technology gently pulls on the clot with suction, stretches and thins it with an agitator, and vacuums it out of the body. 
  • “The device was designed by a team of neurosurgeons and engineers at the University of Michigan and is being commercialized by U-M startup Endovascular Engineering.”

• Per a Pfizer news release,
  • “Pfizer Inc. (NYSE: PFE) today announced that the U.S. Food and Drug Administration (FDA) has expanded approval of TALZENNA^® (talazoparib) in combination with XTANDI^® (enzalutamide) to the treatment of men with metastatic androgen pathway modulation-naïve or -sensitive (mAPMN/S) prostate cancer (PC) with homologous recombination repair (HRR) gene mutations, including both BRCA and non-BRCA mutations. mAPMN/S is also known as metastatic hormone-sensitive prostate cancer (mHSPC).
  • “This approval makes TALZENNA, an oral poly ADP-ribose polymerase (PARP inhibitor), plus XTANDI, an androgen receptor pathway inhibitor (ARPI), available in an earlier line, providing an opportunity to delay disease progression at a critical stage when more patients may experience greater benefit.”

From the judicial front,

• Bloomberg Law reports,
  • “Eli Lilly & Co. is forming a new battlefront over a weight loss treatment that has yet to secure FDA approval, intensifying a legal drive to protect its blockbuster obesity franchise.
  • “The pharmaceutical giant has filed at least 11 federal lawsuits against a range of online vendors and wellness clinics making copycat versions of its experimental drug retatrutide, accusing them of illegally selling or facilitating access to a product not approved by any regulator in the world.
  • “The crackdown escalates the company’s broader legal campaign against businesses making copies of its powerful therapies, establishing a new wave of aggressive challenges over a drug predicted to outperform currently marketed weight loss treatments. Retatrutide is still in clinical trials for obesity, type 2 diabetes, and other related conditions.” * * *
  • “Lilly’s endeavor to protect retatrutide is also focusing on the FDA, as it plans to submit an application to the regulator in the first quarter of next year. 
  • “The drugmaker is simultaneously in a legal battle with the regulator after the agency determined a few years ago that retatrutide is a drug and not a biologic — a crucial designation that shapes its market exclusivity and when Medicare can negotiate its price.
  • “A biologic designation would grant retatrutide 12 years of protection from competitors, while small molecule drugs get five. Significant for Lilly, a biologic classification would prohibit compounded versions. 
  • “The FDA earlier this month doubled down on retatrutide’s drug label after a federal court sent the determination back to the agency for review, concluding the product doesn’t meet an amino acid length threshold that would count it as a biologic.
  • “An appeals court is now weighing whether it has jurisdiction to review the battle.”

From the public health and medical / Rx research front,

• Beckers Clinical Leadership reports,
  • “Nearly 1 in 10 adults hospitalized with respiratory syncytial virus infection died in the hospital or within 30 days of discharge, according to preliminary CDC data.
  • “Researchers analyzed RSV hospitalization data from the CDC’s Respiratory Virus Hospitalization Surveillance Network, which tracks hospitalizations with lab-confirmed influenza, COVID-19 or RSV in 14 states and more than 300 hospitals. The analysis included 18,301 RSV hospitalizations among adults across eight seasons from 2014 to 2024.” 

• MedPage Today lets us know,
  • “Obesity in young adulthood was associated with significantly increased likelihood of early-onset cancers in an observational study, a risk that persisted into middle age.
  • “Men had a higher cancer risk than women, and abdominal fat further increased cancer risk beyond BMI alone.
  • “Cancer rates were highest for thyroid, endometrial, and ovarian cancers.”

• STAT News relates,
  • “Women’s hearts are different from men’s. Research from clinical trials that have required female participants only since 1993 have repeatedly drummed home that message, from varying chromosomes in heart muscle cells to different heart attack symptoms and causes. Yet wide gaps remain in heart health care for girls and women across specialties. 
  • “Recognizing that clinical fragmentation and the resulting harm to women’s health, four medical societies — the American Heart Association, American Academy of Pediatrics, Society for Maternal-Fetal Medicine, and the American College of Obstetricians and Gynecologists — have issued a framework intended to unite clinicians and patients over a lifetime of care, all aimed at dethroning cardiovascular disease as the leading cause of death in women. In that spirit, three articles offering guidance across the course of a woman’s life were published Monday in Circulation.
  • “Their message: Because female-specific biology affects girls’ and women’s hearts throughout their lives, it requires connected, holistic care starting in adolescence to reflect transitions not found in the male models that have dominated health care: periods, pregnancy, perimenopause, and menopause.” 

• Radiology Business points out,
  • “The performance of digital breast tomosynthesis—commonly referred to as 3D mammography—improves steadily with patient age, underlying the effectiveness of screening in an elderly population. 
  • “That’s according to new large-scale research from Massachusetts General Hospital, published Friday in RSNA’s Radiology Imaging Cancer. 
  • Current mammography guidelines remain largely age-based, with the influential U.S. Preventive Services Task Force’s last update in 2024 advocating for screening starting at 40. However, USPSTF claimed current evidence was insufficient to weigh the benefit of screening for women 75 and older. 
  • “Researchers with the Harvard University-affiliated institution recently sought to address this knowledge gap, analyzing data from over 300,000 mammograms. They found screening to be increasingly effective, particularly among the elderly, based on common quality benchmarks. 
  • “Cancer detection and sensitivity increased, false-positive rates declined, and specificity improved, resulting in particularly strong performance among female individuals aged 70 years and older,” lead author Leslie R. Lamb, MD, MSc, with Boston-based Mass General’s Department of Radiology, and colleagues wrote Oct. 23. “These findings provide a contemporary benchmark for screening DBT performance across age groups and contribute to the ongoing reassessment of age-based screening guidelines,” they added later. 

• Healio notes,
  • “Most U.S. women know physical activity reduces breast cancer risk, but only one-quarter meet recommended levels.
  • “A majority know alcohol raises cancer risk, but two-thirds consume alcohol to some extent.”

• Health Day adds,
  • Marijuana legalization may be landing more people in the hospital with heart problems, a new study suggests.
  • For the study, researchers analyzed more than 50 million hospital discharge records spanning 2012 to 2018. They compared Western states, where recreational marijuana sales began in 2014, with other U.S. regions.
  • The study — led by Dr. Samuel Slavin, of the Boston University Chobanian & Avedisian School of Medicine — found that hospital admissions for several serious heart conditions rose faster after legalization.
  • For each year of sales, admission rates were nearly 4% higher for heart failure, 3% higher for heart attacks and just over 2% higher for atrial fibrillation — an abnormal heart rhythm.
  • Rates for stroke, deep vein blood clots and tachycardia — a fast heartbeat — were also higher, but not statistically significant.
  • While the study cannot prove cause and effect, researchers said their findings “point to potential adverse effects of recreation legalization on population health.”

• The Washington Post tells us about “the most important things to do to stay healthy while traveling.
  • “An infectious-diseases doctor shares essential tips to prepare for any health issues while traveling in another country.”

• Beckers Behavioral Health informs us,
  • “Nearly 1 in 3 young adults in the U.S. reported using generative AI to seek substance-related information, with higher rates of use among Black and male respondents, according to a study published Oct. 19 in JMIR Formative Research.
  • “Researchers at Rutgers, the State University of New Jersey in New Brunswick, surveyed 995 U.S. adults ages 18-29 in April 2026 through the online research platform Prolific. The cross-sectional study examined the prevalence and frequency of, and reasons for, substance-related AI use, along with demographic differences and perceptions of the technology.”
• and
  • “Researchers have identified evidence supporting a potential subtype of clinical depression, known as “circadian depression,” defined by disrupted sleep-wake patterns and associated with more severe symptoms and poorer responses to commonly prescribed antidepressants, according to a study published Oct. 20 in The British Journal of Psychiatry.
  • “The study, led by researchers from the University of Sydney’s Brain and Mind Centre, analyzed data from 11,380 adults with depression in the Australian Genetics of Depression Study. Researchers classified participants as having a circadian subtype if they met at least three of six criteria related to sleep and circadian disruption: social jetlag, seasonality, delayed sleep midpoint, evening chronotype, morning tiredness and hypersomnia. They compared clinical characteristics, self-reported antidepressant responses and genetic risk profiles between groups.”

• Physicians’ Weekly informs us,
  • “Compared with patients with normal weight or overweight, the odds of death after emergency general surgery increase 92% for patients with underweight and 59% for patients with frailty, according to findings presented at the American College of Surgeons (ACS) Clinical Congress 2026 in Washington, DC.
  • “Our study shows that patients who are both underweight and frail have the worst outcomes,” said lead study author Ellen Cohn, MD, MPH, of the University of Chicago, in a news release. “We also saw that frailty reduces the positive impact of the obesity paradox — the finding that patients who are overweight, but not at the extremes of obesity, tend to have better outcomes. That protective effect is lost if a patient is frail.”   

• Per Fierce Pharma,
  • “Fresh off the excitement of Rasonque’s big splash in pancreatic cancer, the oncology community has another impressive clinical win to celebrate. Amgen’s T-cell engager Imdelltra has posted a massive survival benefit in small cell lung cancer, delivering what Chief Medical Officer Paul Burton, M.D., Ph.D., called a “watershed moment” for the field.
  • “When added on top of AstraZeneca’s Imfinzi, Imdelltra reduced the risk of death by 58% as a first-line maintenance therapy for patients with extensive-stage SCLC who had not progressed following initial treatment with Imfinzi and chemotherapy.
  • “The result came from the phase 3 DeLLphi-305 study, which showed that, compared with Imfinzi alone, Imdelltra plus Imfinzi improved median overall survival by 8.4 months to 21.1 months. These data are being presented during a presidential symposium at the European Society for Medical Oncology Congress 2026 and simultaneously published in The New England Journal of Medicine.”
• and
  • “As a cornerstone of Merck & Co.’s post-Keytruda oncology strategy, sac-TMT has cleared a clinical milestone. In its first global phase 3 win, the TROP2 antibody-drug conjugate delivered results that are “pretty consistent” with earlier China data, according to Marjorie Green, M.D., Merck’s head of oncology clinical development.
  • “Sac-TMT, partnered with China’s Kelun-Biotech, reduced the risk of death by 32%—and the risk of disease progression or death by 41%—compared with chemotherapy in patients with previously treated endometrial cancer. The patients had received prior treatment with platinum-base chemo and PD-(L)1 inhibitor therapy.
  • “Derived from the TroFuse-005 trial and presented at the European Society for Medical Oncology 2026 Congress, the data gave sac-TMT its first positive global phase 3 report out of 18 trials that Merck has launched in one of the industry’s broadest clinical development programs for a single drug.” 
• and
  • “Novartis lifted the veil on its phase 3 wins in relapsing multiple sclerosis (RMS), announced in early September. 
  • “Not only did the company’s BTK inhibitor Rhapsido reduce relapses and disease progression compared to Aubagio, an older RMS treatment from Sanofi, but it did so without inciting any liver issues, a side effect that has proven to be an ongoing barrier to success of the drug class in this indication. 
  • “Novartis said it plans to seek regulatory approval globally in RMS. Its applications will be backed by data from the Remodel-1 and Remodel-2 trials presented at MSToronto last week and simultaneously published in The Lancet.”

• BioPharma Dive adds,
  • “An antibody-drug conjugate from BioNTech and DualityBio met its main goal in a Phase 3 study in breast cancer, but may only have a “limited” impact in people with the condition, the companies said Monday.
  • “The treatment, known as trastuzumab pamirtecan, successfully delayed tumor progression in a trial of people whose breast tumors express low, but still detectable levels of the HER2 protein. The improvement on that measure was “modest,” though, and treatment was also associated with higher rates of interstitial lung disease — a potentially deadly kind of lung inflammation — than the companies had seen in earlier testing.” 

• The Wall Street Journal reports,
  • “Roche Holding ROP said it expects a pill it is developing to become the new standard treatment for an advanced form of lung cancer, and the company’s first shot at an emerging field within the oncology market.
  • “The Swiss drugmaker is working on several drugs that target a driver of cancers that long eluded the industry. A breakthrough in pancreatic cancer from U.S. biotech Revolution Medicines put the field on investors’ radar, and Roche aims to venture into it with lung-cancer medicine divarasib.
  • “In study results presented Sunday at the annual congress of the European Society for Medical Oncology in Madrid, Roche said its drug lowered the risk of death by 44% compared with available treatments from Amgen and Bristol-Myers Squibb. The late-stage clinical trial compared the effects of the drugs on patients with a specific type of lung cancer who had been previously treated.
  • “Fewer participants who took divarasib dropped out of the trial due to side effects than those who received the existing drugs, Roche said.
  • “The data are practice-changing,” Roche’s Deputy Chief Medical Officer, Stefan Frings, said in an interview.”

From the U.S. healthcare business and artificial intelligence front,

• Fierce Healthcare reports,
  • “Earlier this year, UnitedHealthcare unveiled Avery, a generative AI companion aimed at supporting care coordination for its members.
  • “At the time, the tool was available to about 6.5 million of its members in employer plans and 160,000 people enrolled in Medicare Advantage. Now, the insurer is expanding access to 21 million of its members, growing the tool’s reach at a faster clip than was initially expected.
  • “To date, the company has found that Avery has resolved 90% of its member interactions, and in the remaining 10% of cases, can complete a handoff to a human advocate to offer member support. 
  • “As we’re seeing some of the statistics and some of the feedback that we’re getting from users around the success we’ve had within the early phases of Avery, it’s just making sense to open up that application into more and more of the population,” Craig Kurtzweil, chief data and analytics officer at UnitedHealthcare, told Fierce Healthcare.”
• and
  • “Building stronger bridges between payers and providers will prove critical in addressing the biggest challenges facing healthcare: affordability and access.
  • “It’s with that backdrop that Aetna is releasing its latest provider survey, a quarterly poll that seeks to better understand providers’ perspective on their insurer counterparts and where there’s room to continue developing trust between the two. In the third quarter survey, provided first to Fierce Healthcare, Aetna found a trust score of 6 out of 10, on par with the 6.1 score seen in Q2.
  • “The tally makes for a significant increase from the first quarter, where the trust score was 5.4.
  • Steve Nelson, president of Aetna, told Fierce that “trust is at an all-time low,” so the insurer has been putting an emphasis on addressing some of the biggest pain points that erode that trust, including administrative burdens like prior authorization and increasing transparency.
  • “It’s not just a hope and a prayer here,” he said. “We’re actually making progress.” 
• and
  • “Doximity inked a partnership with Wolters Kluwer Health to embed UpToDate’s evidence-based clinical content directly within Doximity Ask, the company’s AI clinical decision support tool.
  • “In the coming weeks, at health systems that use both products, clinicians will see an answer based on UpToDate’s 13,000 clinical topics and best practice guides alongside Doximity Ask’s response, without leaving the Ask workflow.
  • “Doximity is a digital platform for U.S. medical professionals that offers workflow tools such as a telehealth solution, a clinician-to-patient dialer tool and digital faxing capabilities.
  • “The company aims to become a leading AI platform for doctors with plans to scale its clinical AI suite, including its ambient note-taking tool Scribe and clinical AI assistant and medical search engine Ask. A year ago, Doximity acquired clinical AI company Pathway and then integrated Pathway’s datasets and its AI into its free Doximity GPT product to offer DoxGPT (now Ask).”
    
• Beckers ASC Review relates,
  • “On Oct. 26, Cincinnati-based Bon Secours Mercy Health agreed to acquire Brentwood, Tenn.-based Surgery Partners through its affiliate HealthSpan Partners in a take-private deal valued at about $5.7 billion including debt. 
  • “The transaction would add more than 200 ASCs, surgical hospitals and physician practices across 30 states, along with about 5,000 affiliated physicians, to a 47-hospital system — making the latest in a growing group of health systems that have shifted ambulatory care from a nice-to-have to a strategic imperative.
  • “It most recently follows St. Louis-based Ascension’s $3.9 billion acquisition of Nashville, Tenn.-based Amsurg, which closed earlier this year, and comes as Dallas-based Tenet Healthcare keeps adding to United Surgical Partners International, its surgical arm and the nation’s largest ASC portfolio.”

• Beckers Hospital Review lets us know where “Kaiser’s Risant Health stands after Integris” agreement and “Anthropic IPO filing flags healthcare, drug discovery as growth bets.“