Why the study?
Does transcatheter aortic valve replacement provide comparable 7-year outcomes and valve durability compared to surgical aortic valve replacement in low-risk patients with severe aortic stenosis?
RCT (n=1,000)
Randomized
Does transcatheter aortic valve replacement provide comparable 7-year outcomes and valve durability compared to surgical aortic valve replacement in low-risk patients with severe aortic stenosis?
Answers are grounded in this paper and cite their sources.
Captured external expert commentary on this paper, strongest first. Original sources are linked where available.
“These data showing longer-term TAVR durability in a low-risk surgical population will be valuable in counseling patients. With this evidence in hand, I expect that most of my older patients will now choose TAVR over surgery. However, I will caution my younger patients about the higher rates of paravalvular leak with TAVR and the need for even longer-term data to see if these leaks reflect worse durability.”
“What is very clear is that... TAVR won the first year, no question about it, but surgery wins after that. There is catch-up occurring with surgery so that by 7 years, they are roughly equal in all components.”
“The more we advance on the follow-up, the more durability becomes an issue. If the life expectancy of the patient is less than 7 years, durability is not an issue. But now we have patients who have a life expectancy of 10 or 15 years and durability is very important to demonstrate.”
The 7-year follow-up of the PARTNER 3 trial demonstrates that balloon-expandable TAVR has comparable intermediate-term durability to SAVR without structural deterioration penalties, though its early clinical advantage attenuates over time and distinct device-specific complications necessitate lifetime strategy planning.
Few advances in cardiovascular medicine have transformed clinical practice as rapidly as transcatheter aortic valve replacement (TAVR).Initially developed for patients considered inoperable or at prohibitive surgical risk, TAVR has progressively expanded into high-, intermediate-, and ultimately low-risk populations (1,2).The question has been whether long-term outcomes and durability can truly match those achieved with surgical aortic valve replacement (SAVR) rather than whether TAVR works.This concern is not unfounded.Surgical valves are implanted under direct visualization with leaflets maintained in their native configuration, whereas transcatheter valves require leaflet crimping before deployment.For more than a decade, this difference has fueled concerns about accelerated structural deterioration, higher reintervention rates, or reduced durability relative to surgical bioprosthesis (3).Earlier-generation valves such as the SAPIEN XT did show higher structural valve deterioration than surgery at 5 years, although the third-generation SAPIEN 3 did not (4).The 7-year report of PARTNER 3, published by Leon and colleagues, is the most robust long-term randomized comparison of balloon-expandable TAVR and SAVR in low-risk patients to date and will likely guide practice until the planned 10-year follow-up (5).The primary composite endpoints were similar, valve durability remained comparable, and patient-reported health status was favorable in both arms.At first glance, these findings appear to establish equivalence, but closer examination suggests a more nuanced conclusion.The most important contribution of PARTNER 3 is not that TAVR and surgery are identical, but that the anticipated durability penalty of TAVR has not emerged through 7 years while mortality has remained comparable.These conclusions remain conditional on long-term event trajectories, differential follow-up completeness, and the potential consequences of device-specific complications.Together, these considerations reestablish the importance of lifetime planning for patients with severe aortic stenosis (6).
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Weze et al. (2026) conducted an RCT in Severe aortic stenosis (n=1,000). Transfemoral transcatheter aortic valve replacement (TAVR) vs. Surgical aortic valve replacement (SAVR) was evaluated on Composite of death, stroke, or rehospitalization related to the procedure, valve, or heart failure (HR 0.87, 95% CI 0.70-1.08).
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