
Signs Point To Possible Future Medicare Coverage Of Obesity Meds
Roughly 40% of adult Americans are considered obese. Obesity increases the risk of developing conditions such as diabetes, heart disease, osteoarthritis and some cancers. Rates of obesity have been steadily rising since 1980. Medications known as glucagon-like peptide-1 agonists, or GLP-1s, have become popular as weight loss therapeutics. Taken in accordance with the instructions on the label and an appropriate diet and exercise regimen, GLP-1s are effective at lowering a person's weight.
But Medicare doesn't allow coverage of weight loss medications that are strictly being used for obesity. It can only pay for them if they're prescribed for a related condition, such as diabetes or heart disease. Lawmakers have resubmitted different versions of a bill to permit such coverage numerous times since 2013. Senator Bill Cassidy (R-LA) reintroduced the Treat and Reduce Obesity Act this summer to 'combat the obesity crisis in the United States by providing regular screenings. The bill would also prevent diseases associated with obesity through expanded coverage of new healthcare specialists and chronic weight management medications for Medicare recipients.' However, it's this last item which would lift the 20-year prohibition on coverage that's been a limiting factor that has prevented previous versions of the legislation from passage.
The cost of reimbursing these medications has often been cited as a stumbling block. The nonpartisan Congressional Budget Office, for instance, published projections late last year that estimated it would cost Medicare a cumulative $35 billion from 2026-2034 to cover anti-obesity medications. While CBO included savings from improved health, these were not nearly sufficient to offset the costs of the medications.
Part of the problem is that patients who are treated with GLP-1s discontinue such treatments at a relatively high rate. One study, for example, found that approximately 53% of patients with overweight or obesity taking semaglutide-based followed for up to a year didn't persist on treatment past two months. The cost estimates used by the Centers for Medicare and Medicaid Services assume that a relatively high percentage of patients will stop taking them shortly after beginning their regimen.
And so, there are still questions about whether this latest reintroduction of TROA will be successful. Moreover, even if the proposed legislation were to pass, enactment wouldn't happen until at least two years after passage.
Another route is possible, via a regulatory pathway initiated by the executive branch. At the end of its tenure, the Biden administration proposed a regulatory change that would permit coverage of obesity drugs with some restrictions. Upon taking office, the Trump administration nixed the proposal. Nevertheless, it now intends to pursue a demonstration project under authority granted by the Affordable Care Act to experiment with models that seek to improve quality of care and lower costs.
Under a Center for Medicare and Medicaid Innovation initiative, state Medicaid programs and Medicare outpatient drug (Part D) plans could soon voluntarily choose to cover obesity drugs for weight management, the Washington Post reported, citing documents from the Centers for Medicare and Medicaid. A Medicaid experiment would commence in Apr. 2026; Medicare in Jan. 2027.
Timing for the Medicare portion of the planned model coincides with implementation of a maximum fair price for Wegovy in 2027. Together with Ozempic, another semaglutide-based product, Wegovy was selected for Medicare price negotiation earlier this year under an Inflation Reduction Act provision. Presumably, this would provide the federal government with an even lower net price than is currently attainable.
Nonetheless, challenges lie ahead. The plan has not been finalized. Nor have any details been divulged. Without information on how prescription drug plans or Medicare Advantage insurers would be incentivized to sign up, it's unclear who would be interested in adding coverage.
Aside from government-initiated changes, it's possible that certain commercial insurers and perhaps even some Medicaid payers will decide to revisit their coverage decisions if net costs decrease sufficiently, combined with more data showing the benefits of weight loss drugs when taken consistently and in conjunction with an appropriate nutrition regimen and physical activity. There's encouraging data in this regard which was posted in late June by the pharmacy benefits manager Prime Therapeutics. Recent initiators on high potency Wegovy and Zepbound—who started treatment in 2024—appear to be staying on their medications longer. The year-over-year persistence analysis found one-year persistence nearly doubling from 33.2% in 2021 to 62.7% in 2024. This in turn could confer improved, sustained benefits, in which case there would likely be less weight rebound upon discontinuation. But more research is needed to confirm the observed trend.
Another thing that could galvanize payers towards targeted coverage is if they adopt an evidence-based approach that differentiates sub-populations by risk. All or nothing reimbursement makes little sense for insurers in both the commercial and public sectors. At current prices, most cost-effectiveness analyses fail to show cost savings except for when applied to high-risk groups, such as people with established cardiovascular disease, chronic kidney disease or severe obesity. A differentiated approach to access could also help mitigate costs for Medicare which in turn could serve as an impetus to pass legislation.
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'We may get to a place where they're even reimbursed by insurance,' she said. 'I do think increasingly we are going to see providers begin to adopt these technology tools as a way to meet their patients' needs.' But for now, her message is clear: The chatbots are not there yet. 'Ideally, chatbot design should encourage sustained, meaningful interaction with the primary purpose of delivering evidence-based therapy,' said Dartmouth's Heinz. Until then, don't rely on them too heavily, the experts cautioned — and remember, they are not a substitute for professional help.


Medscape
5 minutes ago
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GLP-1s Don't Increase Suicide Risk
It's not uncommon for me, when discussing a GLP-1 medication with patients, to have them inquire about the drug's purported risk in increasing suicidal ideation. What has never occurred? Patients asking about the possible benefits of GLP-1 medications to mood and to their decreasing the risk of suicidal ideation. On the face of existing data, that's odd considering there is far more substantial evidence that GLP-1 users see improvements in mood: with no increase —and possibly decreased — risk of suicide. It's not odd, though, when considering things through the lens of how risk is overestimated by the public along with the lens of weight bias where, at least with obesity medications, negative findings — however small, tenuous, or early — tend to be readily internalized and amplified, while positive findings are often minimized and ignored. Where and how did the concern about suicide arise? On July 11, 2023, the European Medicines Agency (EMA) released a statement that, consequent to the Icelandic medicines agency's highlighting three case reports involving suicide among GLP-1 users, they would be investigating further. The EMA's statement rightly and explicitly noted, ' The presence of a signal does not necessarily mean that a medicine caused the adverse event in question .' But much of the media didn't seem to care how premature or unsubstantiated the putative risk, and this story definitely had legs gaining scary coverage in most major media outlets. By way of example, the BBC, in its story headlined Weight-loss jabs investigated for suicide risk , rather than responsibly covering the prematurity of concluding anything at all, chose this quote from the EMA's statement to highlight, ' A signal is information on a new or known adverse event that is potentially caused by a medicine and that warrants further investigation .' No doubt this sort of reporting is in part why, to this day, patients still recount suicidality as a concern when discussing these medications. But what has happened on this file since the July 2023 initiated investigation of those three purported cases? While nonexhaustive, here's a brief rundown: In April 2024, the EMA's own investigation exonerated GLP-1 medications as a source of increased suicide risk in April 2024. The US FDA also conducted its own investigation and similarly found no ties between GLP-1s and suicide risk. In June 2024. a paper was published demonstrating no increase risk in suicidality among 36,083 adults prescribed GLP-1 medications. In August 2024, a paper was published investigating GLP-1 medications and their impact on 22 neurological and psychiatric outcomes over 12 months. It found no impact among 23,386 GLP-1 users. In September 2024, a paper was published demonstrating no increased risk in suicidality among a cohort of 124,517 adults prescribed GLP-1 medications over a 1-year period. In October 2024, a paper was published demonstrating a 33% reduction in suicide ideation or attempts among 6912 adolescents with obesity for those who initiated treatment with GLP-1s over 3 years of follow-up. In February 2025. a paper was published of a nationwide (France) case-time-control of individuals who had attempted or died by suicide which found no linkage with GLP-1 use. In May 2025. a paper was published demonstrating in a meta-analysis of doubly blind randomized controlled trials that, among the 107,000 patients studied, GLP-1 use was not associated with increased risk of psychiatric adverse events or worsening depressive symptoms relative to placebo. Instead, GLP-1 use was associated with improvements in both physical and mental health-related quality of life. Finally, in June 2025, a paper was published describing a multinational self-controlled case series analysis of suicide or self-harm attempts in Hong Kong, Taiwan, and the United Kingdom that yes, again, demonstrated no increased risk among GLP-1 users and that, compared with the nontreatment period, lower suicide attempt or self-harm risk following GLP-1 treatment was observed, especially after longer periods of treatment. Negative publication bias appears to extend beyond academia into society at large. However, it manifests somewhat differently. The studies receiving the most attention are often those reporting literally negative (ie, adverse) outcomes. In contrast, more rigorous studies that challenge these negative findings, even if publicized, rarely achieve comparable societal penetration or awareness.