Aortic Disease and Treatment Approaches / Cardiac Valve Diseases and Treatments / Congenital Heart Disease Studies · Journal article
Journal of Cardiothoracic Surgery · August 6, 2026
A consensus or society position rather than new primary data.
This narrative review summarizes the 2025 ESC/EACTS guideline shift toward earlier and broader TAVR use in aortic valve disease, informed by registry data showing reintervention rates of 0.3–1.7% at 8 years and superior short-term survival with redo-TAVR versus explantation. The evidence highlights structural valve deterioration, leaflet thrombosis, and endocarditis as dominant failure modes, requiring long-term surveillance and refined patient selection in younger cohorts.
Narrative review integrating guideline statements and observational registries. Patients with aortic stenosis and aortic regurgitation; registry data from EXPLANT-TAVR, EXPLANTORREDO-TAVR, and FRANCE 2/FRANCE TAVI (2020–2025).. Intervention: TAVR; redo-TAVR; explantation.. Compared with: Redo-TAVR versus explantation for short-term mortality comparison..
Reintervention rates 0.3–1.7% at 8 years across EXPLANT-TAVR, EXPLANTORREDO-TAVR and FRANCE 2/FRANCE TAVI registries Redo-TAVR 30-day mortality 1.5–6.2% versus explantation 11.9–13.6%, favouring redo approach for short-term survival Structural valve deterioration, leaflet thrombosis, and endocarditis identified as predominant TAVR failure causes
Redo-TAVR 30-day mortality 1.5–6.2% versus explantation 11.9–13.6%, favouring redo approach for short-term survival
Clinicians should use this to inform shared decision-making with Heart Teams, balancing the expanded indications for earlier TAVR intervention (as per 2025 ESC/EACTS guidelines) against the long-term reintervention risk and durability concerns in younger patients. Structured surveillance for structural valve deterioration and thrombosis, and readiness for redo procedures, are warranted.
A narrative review synthesizing guideline updates and registry evidence on TAVR durability and reintervention; informs clinical decision-making but lacks original comparative effectiveness data.
As stated by the source record.
Quoted from the source exactly as published.
Clinicians should use this to inform shared decision-making with Heart Teams, balancing the expanded indications for earlier TAVR intervention (as per 2025 ESC/EACTS guidelines) against the long-term reintervention risk and durability concerns in younger patients. Structured surveillance for structural valve deterioration and thrombosis, and readiness for redo procedures, are warranted.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
Abstract Background The 2025 European Society of Cardiology (ESC) and European Association for Cardio-Thoracic Surgery (EACTS) guidelines for valvular heart disease represent a pivotal update, emphasizing earlier intervention for aortic stenosis (AS) and broader indications for transcatheter aortic valve replacement (TAVR). These changes are driven by randomized trial data demonstrating TAVR’s safety in lower-risk patients. However, as TAVR expands to younger cohorts, long-term durability remains a concern. Main body This narrative review examines key guideline updates for aortic valve disease, focusing on aortic stenosis (AS) and aortic regurgitation (AR), and integrates insights from recent registries (2020–2025) on TAVR explantation and redo-TAVR outcomes. Data from the EXPLANT-TAVR, EXPLANTORREDO-TAVR and FRANCE 2/FRANCE TAVI registries reveal reintervention rates of 0.3–1.7% at 8 years, with redo-TAVR offering superior short-term survival (30-day mortality 1.5–6.2%) compared to explantation (11.9–13.6%). Structural valve deterioration (SVD), leaflet thrombosis, and endocarditis predominate failure causes, underscoring the need for lifetime management strategies. Conclusion Implications include refined patient selection, enhanced imaging surveillance, and Heart Team-driven decisions to balance procedural benefits against reintervention risks.
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