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Mitral valve-in-valve hemodynamic performance: An in vitro study.
Morgane Evin1, Carine Guivier-Curien2, Regis Rieu2
1Aix-Marseille Université, CNRS, ISM UMR 7287, 13288 Marseille cedex 09, France; Protomedlabs, Marseille, France.
The Journal of Thoracic and Cardiovascular Surgery
|January 16, 2016
Summary
The valve-in-valve procedure in mitral bioprostheses can lead to stenosis if the surgical valve
Area of Science:
- Cardiovascular Research
- Biomedical Engineering
- Prosthetic Valve Technology
Background:
- The valve-in-valve (VinV) procedure is an option for high-risk patients with failed mitral surgical bioprostheses.
- Assessing the hemodynamic performance of different VinV configurations is crucial for patient selection and procedural success.
Purpose of the Study:
- To evaluate the hemodynamic function of various valve-in-valve (VinV) configurations in failed mitral surgical bioprostheses.
- To identify factors influencing hemodynamic outcomes in the VinV procedure for mitral valve replacement.
Main Methods:
- An in vitro study utilizing a double activation duplicator to test 11 surgical bioprostheses and 15 VinV configurations.
- Hemodynamic conditions were simulated under 8 different scenarios.
- Internal orifice diameter (IOD) of surgical bioprostheses was measured using a Smartscope.
Main Results:
- The VinV procedure resulted in significantly worse antegrade hemodynamic parameters, including reduced effective orifice area and increased regurgitant fraction, compared to surgical bioprostheses alone.
- Moderate to severe mitral stenosis occurred in 52 of 120 tested VinV configurations.
- Internal orifice diameter (IOD) was the primary determinant of effective orifice area and regurgitant fraction; IOD < 22 mm increased stenosis risk, especially with >20% oversizing, while IOD > 23 mm with <8% oversizing increased paravalvular regurgitation risk.
Conclusions:
- The valve-in-valve procedure in mitral surgical bioprostheses generally yields satisfactory hemodynamic results.
- Significant mitral stenosis risk increases with a surgical bioprosthesis IOD < 22 mm, particularly with >20% oversizing.
- Significant paravalvular regurgitation is infrequent, associated with larger IODs and <8% oversizing.
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