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Updated: Jun 5, 2026

Standardized Technique of Aortic Valve Re-implantation for Valve-sparing Aortic Root Replacement
Published on: December 11, 2017
Percutaneous treatment of a dysfunctional aortic bioprosthesis with the CoreValve(®) prosthesis
José M Hernández-García1, Antonio J Muñoz-García, Juan H Alonso-Briales
1Servicio de Cardiología, Hospital Universitario Virgen de la Victoria, Málaga, España.
Insights
Percutaneous aortic valve replacement using the CoreValve prosthesis is a viable option for patients with severe aortic stenosis and high surgical risk. Initial outcomes show successful implantation and asymptomatic patients after medium-term follow-up.
Area of Science:
- Cardiology
- Interventional Cardiology
- Cardiac Surgery
Background:
- Severe symptomatic aortic stenosis poses a significant risk for traditional surgery.
- Percutaneous aortic valve replacement is an emerging alternative for high-risk patients.
Purpose of the Study:
- To report the initial experience with CoreValve percutaneous aortic valve implantation.
- To evaluate in-hospital and medium-term outcomes for aortic bioprosthesis dysfunction.
Main Methods:
- Four patients with aortic bioprosthesis dysfunction underwent percutaneous CoreValve implantation.
- Procedures were performed under local anesthesia with angiographic guidance.
Main Results:
- Successful prosthesis implantation in all four patients.
- One patient required a second prosthesis due to initial high positioning.
- No major complications were observed during the study period.
Conclusions:
- Percutaneous CoreValve implantation is a safe and effective treatment for aortic bioprosthesis dysfunction.
- All patients remained asymptomatic at a mean follow-up of 7 months.
Abstract:
Recently, percutaneous aortic valve replacement has emerged as a therapeutic option for patients with severe symptomatic aortic stenosis and a high surgical risk. We report our initial experience in four patients with percutaneous implantation of a CoreValve aortic prosthesis to treat aortic bioprosthesis dysfunction involving aortic stenosis or regurgitation. In-hospital and medium-term outcomes were analyzed. The procedure was performed under local anesthesia and guided by angiography. The prosthesis was implanted successfully in all patients, although a second prosthesis was required in one case because the first was positioned too high. There were no major complications. After a mean follow-up of 7 months (SD, 4.7), all patients remained asymptomatic.
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