Pre-appraisal commentary on the PARTNER 3 seven-year results: The wrong button at the top


Çiçek S.

Turkish Journal of Thoracic and Cardiovascular Surgery, vol.34, no.1, pp.1-3, 2026 (SCI-Expanded, Scopus) identifier identifier identifier

  • Publication Type: Article / Review
  • Volume: 34 Issue: 1
  • Publication Date: 2026
  • Doi Number: 10.4274/tjtcs.2025.28913
  • Journal Name: Turkish Journal of Thoracic and Cardiovascular Surgery
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.1-3
  • Keywords: low-risk patients, PARTNER 3, surgical aortic valve replacement, Transcatheter aortic valve implantation, trial methodology, valve durability
  • Istanbul University Affiliated: No

Abstract

The 7-year outcomes of the Placement of Aortic Transcatheter Valves 3 (PARTNER 3) trial comparing transcatheter aortic valve implantation (TAVI) with surgical aortic valve replacement (SAVR) in low-risk patients indicate that the narrowing difference between the two strategies reflects study design convergence rather than true clinical equivalence. Although the composite endpoint of death, stroke, and rehospitalization appeared comparable, important asymmetries persisted. Notably, approximately one quarter of patients in the SAVR group underwent concomitant coronary artery bypass grafting, whereas no patients underwent percutaneous coronary intervention, and surgical valve types were not standardized. In contrast, the incidences of valve thrombosis and paravalvular leak remained substantially higher after TAVI. Emerging trends in late mortality and crossing hazard curves further suggest potential divergence in long-term survival. Thus, the perceived equivalence of TAVI and SAVR largely reflects trial design and endpoint framing rather than durable clinical parity. Among younger patients, lifetime risk profiles differ fundamentally. As clinical enthusiasm for transcatheter therapy expands, careful interpretation grounded in valve durability, proportional hazards, and transparent analysis remains essential. Ultimately, long-term treatment standards should prioritize biological integrity over procedural convenience.