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Real-World GLP Costs, Rocket Off Hold, and TAVR Deterioration
August 25, 2025
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“Medicine is the only field in America where people pay massive tuition and lose 15 years of earning potential just for the privilege of practicing. By the time they’re called ‘young’ or ‘early career,’ many are in their 40s. “

Jason Locasale, PhD

Thanks to everyone who attended our webinar on new solutions for arterial plaque analysis last week! If you weren’t able to attend, don’t worry – you can watch the entire event on demand.

Obesity Care

GLP-1s Work, But Not for Free

Real-world semaglutide (Wegovy) patients might be experiencing a healthcare cost paradox, after a recent analysis in JAMA showed that GLP-1s successfully reduce weight and improve cardiovascular risk factors, but lead to increased patient healthcare expenditures in the short term.

  • Semaglutide is a GLP-1 receptor agonist approved for weight management and CV risk reduction, with established cardiovascular benefits in clinical trials like STEP 1.
  • The drug has shown dramatic trial results, but real-world cost-effectiveness data has been limited until now.

The real-world analysis examined 23.5k adults prescribed semaglutide between January 2018 and January 2025 across two large U.S. health systems and found over a 13-24 month follow-up that…

  • Patients achieved meaningful clinical benefits including 3.8% average weight reduction, 1.5 mmHg diastolic BP decrease, and 12.8 mg/dL total cholesterol reduction.
  • However, total monthly healthcare expenditures (excluding drug costs) increased by $80 per patient, with inpatient costs driving approximately half the increase.
  • The cost increase was consistent across diabetic ($67/month) and non-diabetic ($81/month) populations.

Even with proven clinical efficacy, the findings reveal a disconnect between immediate clinical benefits and short-term healthcare economics, raising questions about how long GLP-1s take to become cost-effective.

  • The increase suggests more hospital visits for cardiometabolic conditions may be driving higher expenditures after medication initiation.
  • Real-world weight loss (5% in non-diabetics) was also less dramatic than trial results (nearly 15% in STEP 1), likely due to shorter treatment duration (6-7 months on average).

Given the complexity of real-world GLP-1 use, multiple factors may be influencing the cost-effectiveness equation beyond the medication’s direct clinical effects.

  • Drug shortages, coverage changes, and co-pays may contribute to discontinuation patterns that affect long-term cost outcomes.
  • Additional healthcare utilization may also come from insurance-mandated follow-up visits, dose adjustments, and increased monitoring.
  • The analysis also couldn’t measure how early discontinuation impacts expenditures.

The Takeaway

For a while people have said, “GLP1s are expensive, but they will pay for themselves by reducing downstream healthcare costs.” They probably meant fewer heart attacks and delayed/avoiding chronic diseases (diabetes, HF, etc) and those things might still be true in the long run, but this study does not support that theory within months 13-24.

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The Wire

  • Spironolactone’s Lacking Hemodialysis Benefits: Fresh results from the ALCHEMIST trial suggest spironolactone might not provide any CV benefits to high-risk hemodialysis patients. After the study’s median 32.6-month follow-up, major cardiovascular events occurred in 24% of both patients who took either spironolactone or placebo (HR: 1.00). Hyperkalaemia rates were also similar between groups (42% vs. 41%) leading to the conclusion that spironolactone provides no cardiovascular benefit in hemodialysis patients, thus not supporting its off-label use.
  • Powerful Medical + Roche: Powerful Medical partnered with Roche to integrate PMcardio AI-powered ECG interpretation into Roche’s Cobas pulse point-of-care system. This collaboration combines real-time ECG analysis with high-sensitivity cardiac troponin T testing to streamline chest pain diagnostics in emergency departments. The duo believes this new solution will ultimately accelerate heart attack diagnosis, particularly STEMI detection, enabling faster clinical decisions within the critical 90-minute window. PMcardio is approved for use in Europe, and awaiting FDA clearance.
  • FDA Updates Breakthrough List: The FDA last week updated the list of medical devices in its Breakthrough Devices Program. During the first six months of 2025, the FDA granted breakthrough designation to 136 devices, compared to 165 for all of 2024. For the life of the program, the FDA has given breakthrough designation to 1.2k devices, with cardiovascular products dominating at 243 submissions. Twenty-one breakthrough devices have received marketing authorization so far in 2025.
  • Rocket Back on the Launchpad: Rocket Pharmaceuticals announced that the FDA lifted the clinical hold on RP-A501’s pivotal Phase 2 trial for Danon disease after just three months. The gene therapy trial will resume with a reduced dose of 3.8 x 10¹³ GC/kg and modified immunomodulation protocols based on successful Phase 1 pediatric data. Six patients have already been treated in the 12-patient study, which evaluates efficacy through LAMP2 protein expression improvements and left ventricular mass reduction.
  • Heart and Kidney Gene Link: Temple University researchers have potentially discovered why chronic kidney disease patients often die from heart problems. In a mouse model study, the researchers found that when kidney function declines, harmful toxins accumulate and activate cellular sensors. When combined with high-fat diets, this triggers dangerous blood vessel inflammation through a gene called NR1H3. The team also identified a protective protein, YBX2, that fights oxidative stress. These findings could lead to new treatments preventing cardiovascular complications in kidney disease patients.
  • FDA Clears Artrya’s Coronary Plaque Software: A new competitor is entering the red-hot U.S. arterial plaque analysis segment. Australian software developer Artrya got FDA clearance for its Salix Coronary Plaque AI-powered solution, which calculates plaque burden and composition from coronary CT angiography exams. The solution integrates with Artrya’s Salix Coronary Anatomy platform, and is eligible for reimbursement through Plaque CCTA’s Category I CPT code, which will pay $950 per assessment starting January 2026.
  • Valve Anatomy Matters in TAVR Choice: A study of nearly 1.5k patients with bicuspid aortic valve stenosis found that both self-expanding and balloon-expandable TAVR valves produce similar three-year survival and stroke rates. However, each valve type had different complications: self-expanding valves were more likely to require pacemakers or additional valve implants, while balloon-expandable valves had higher risks of annulus rupture and pressure gradients. Despite these differences in short-term complications, both valve types offered comparable long-term cardiovascular outcomes, suggesting anatomy should guide valve selection rather than survival expectations.
  • Early TAVR Deterioration Rates: Another TAVR study of over 4k heart valve replacement patients found that about 6% develop early signs of valve problems within one year. These “hemodynamic valve deterioration” issues occur when the replacement valve doesn’t work as efficiently as expected, often due to poor blood flow patterns. Interestingly, patients who received larger valves had better protection against these problems. While this deterioration didn’t increase death rates, it did predict who might need another valve procedure within five years.
  • Finerenone Goes Fine with Diuretics: Adding to our understanding of finerenone’s (Bayer’s Kerendia) HF benefits, a recent study confirmed it works safely and effectively regardless of what diuretics patients are already taking. In fact, the study of 5.4k HF patients revealed an exciting bonus: finerenone actually reduced the need for higher doses of diuretics and allowed some patients to use lower doses overall. This “diuretic-sparing effect” means patients might avoid some side effects from stronger water pills, while still getting better heart outcomes.
  • When the Lights Go Out: A 77-year-old woman died during heart surgery at the UK’s Scunthorpe General Hospital after a 10-minute power outage disrupted her procedure. The patient was receiving a stent when the electrical failure prevented doctors from using the X-ray imaging needed to complete the surgery. Staff had to wait for an engineer to restore power, creating a critical delay. The coroner concluded she likely would have survived without the power loss, noting that the power reset button was located elsewhere in the hospital.
  • Radiation? No Problem for Bypass: New research suggests patients who previously received chest radiation therapy can safely undergo heart bypass surgery using internal thoracic artery grafts. Researchers compared 294 radiation patients with matched controls and found that despite radiation patients being older, more often female, and having more lung disease, they faced no increased risk of death or other surgical complications. The results suggest that prior chest radiation shouldn’t prevent patients from receiving this preferred type of heart bypass surgery.

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The Resource Wire

  • New Horizons in Structural Heart: TAVR and TMVR rates are rising rapidly, placing more pressure on interventional planning. Tune into this Circle CVI and Radcliffe Cardiology breakout detailing how to leverage modern CT workflows to produce efficient and accurate pre-procedural plans.
  • Vista AI Reduces Patient Backlog: Cardiac MRI is infamous for its complexity and backlogs, but it doesn’t need to be that way. See how Vista Cardiac delivered a 50% reduction in scan time variability, enabling shorter scheduling blocks and eliminating a one-month backlog.
  • Rethink Your Workflow with GE HealthCare: Just 15 minutes could change the way you think about cardiovascular IT. Register now for GE HealthCare’s August 28th webinar on how technology can help care teams replace paperwork with automated reporting, integrate tools that speak the same language and standardize reporting, inventory, and billing all in one platform.
  • How to Improve Cardiology Workflows and Get More Patient Time: Complex processes and reporting requirements can mean cardiologists spend more time with clinical systems than they do with their patients. See how Merge Hemo and Merge Cardio work together to help you streamline and scale your clinical and data management workflows, so you can have more time in front of your patients.
  • Accurate and Efficient Remote Cardiac Patient Monitoring: The expansion of remote cardiac patient monitoring is creating more care opportunities, but also new operational challenges for cardiology teams. Check out this Cardiac Wire Show, where ARTELLA Solutions’ Jacinta Fitzsimons shares how the right combination of technology and service can help physicians get the most out of their cardiac RPM programs – today and into the future.
  • Siemens Healthineers’ Cardiac Ultrasound Efficiency S&T Theater at ASE 2025: Looking to reduce your exam times and ergonomic movement during cardiac ultrasound? Sign up to have lunch with Siemens Healthineers’ experts while learning how the AI-powered tools on the ACUSON Origin ultrasound system deliver consistent, reliable measurements with minimal need for manual edits.

The Industry Wire

  1. Doctors push against RFK Jr. on back-to-school COVID vaccines.
  2. Omega-3 may help to protect women from Alzheimer’s disease.
  3. Judge signs off on Blues plans’ $2.8B antitrust settlement with providers.
  4. UnitedHealth, Elevance to exit Colorado ACA marketplace.
  5. Ransomware attack on DaVita exposes data from 2.7M.
  6. Legionnaires’ outbreak in NYC kills 6, infects 111.
  7. White House data sharing is ambitious, but lacks details.
  8. UnitedHealth forms an enhanced governance board.
  9. Trump could fast-track healthcare mergers.
  10. Plague emerges in California.