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Comparative Study
. 2009 Dec;88(6):1864-9.
doi: 10.1016/j.athoracsur.2009.08.004.

Valve-in-valve implantation using a novel supravalvular transcatheter aortic valve: proof of concept

Affiliations
Comparative Study

Valve-in-valve implantation using a novel supravalvular transcatheter aortic valve: proof of concept

Ali N Azadani et al. Ann Thorac Surg. 2009 Dec.

Abstract

Background: Transcatheter valve implantation within degenerated bioprostheses is a potentially promising treatment for high-risk surgical patients. Clinical experience is limited; however, we have shown in vitro that currently available transcatheter aortic valve sizes did not provide acceptable hemodynamics in small bioprostheses. The objective of this study was to develop a new transcatheter valve that would provide good hemodynamics within degenerated bioprostheses.

Methods: Supravalvular transcatheter valves were created using a Dacron covered stainless steel stent at the base and trileaflet pericardial leaflets in an open stent above the bioprosthesis. The transcatheter valves were implanted within 19-, 21-, and 23-mm Carpentier-Edwards Perimount bioprostheses with simulated degeneration using BioGlue to achieve a mean pressure gradient of 50 mm Hg. Hemodynamics of valve-in-valve implantation were studied in a pulse duplicator.

Results: Supravalvular transcatheter valves successfully relieved bioprosthetic stenosis. Acceptable hemodynamics were achieved with a significant reduction in mean pressure gradient of 54.0 +/- 3.5 to 9.2 +/- 6.3 mm Hg in 23-mm bioprostheses (p < 0.001), from 49.3 +/- 3.1 to 14.4 +/- 4.7 mmHg (p < 0.001) in 21 mm, and from 53.9 +/- 3.8 to 28.3 +/- 9.8 mm Hg (p = 0.013) in 19-mm bioprostheses. Effective orifice area after valve-in-valve implantation increased significantly and was comparable to rereplacement with the same size bioprosthesis.

Conclusions: Valve-in-valve implantation was performed using a novel supravalvular transcatheter valve, which successfully relieved bioprosthetic stenosis. The hemodynamics were comparable with standard surgical valve replacement. Further studies are required to assess device safety and efficacy in patients.

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Comment in

  • Invited commentary.
    Walther T, Walther C. Walther T, et al. Ann Thorac Surg. 2009 Dec;88(6):1870. doi: 10.1016/j.athoracsur.2009.09.008. Ann Thorac Surg. 2009. PMID: 19932251 No abstract available.

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