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Updated: Jul 8, 2025

Standardized Technique of Aortic Valve Re-implantation for Valve-sparing Aortic Root Replacement
Published on: December 11, 2017
Five-Year Follow-Up from the CoreValve Expanded Use Transcatheter Aortic Valve-in-Surgical Aortic Valve Study.
Tanvir K Bajwa1, Roger J Laham2, Kamal Khabbaz2
1XXX, Aurora Cardiovascular Services, Aurora Sinai/Aurora St. Luke's Medical Centers, Milwaukee, Wisconsin.
Transcatheter aortic valve replacement (TAVR) in failed surgical valves (TAV-in-SAV) is a safe option for extreme-risk patients. Five-year outcomes show stable clinical and hemodynamic results, with low rates of severe paravalvular regurgitation.
Area of Science:
- Cardiology
- Interventional Cardiology
- Cardiac Surgery
Background:
- Transcatheter aortic valve replacement (TAVR) offers an alternative for extreme-risk patients needing reoperation for a failed surgical aortic bioprosthesis.
- Long-term data for TAV-in-SAV procedures are limited, necessitating further investigation into their durability and safety.
Purpose of the Study:
- To evaluate the 5-year outcomes of TAV-in-SAV using the CoreValve Expanded Use Study.
- To analyze outcomes based on the mode of surgical aortic valve failure (stenosis, regurgitation, or combined).
Main Methods:
- The CoreValve Expanded Use Study enrolled 226 extreme-risk patients undergoing TAV-in-SAV.
- Outcomes were assessed at 5 years, stratified by surgical aortic valve failure mode.
- Echocardiographic data were reported by study sites.
Main Results:
- The 5-year all-cause mortality or major stroke rate was 47.2%.
- Mortality was higher in patients with severe prosthesis-patient mismatch (51.7% vs 38.3%).
- The overall aortic valve reintervention rate was 5.9%, with stable hemodynamic function and minimal severe paravalvular regurgitation at 5 years.
Conclusions:
- TAV-in-SAV with a supra-annular, self-expanding TAVR device is a safe and durable option for extreme-risk patients with appropriately sized failed surgical valves.
- Clinical and hemodynamic outcomes remain stable through 5 years post-procedure.
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