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Outcomes of Redo Transcatheter Aortic Valve Implantation for Structural Valve Degeneration of Transcatheter Aortic Valve

Background: The outcome of redo transcatheter aortic valve (TAV) implantation (TAVI) is unknown for TAV structural valve degeneration (SVD). This paper reports the initial results of redo TAVI for TAV-SVD in Japanese patients. Methods and Results: Of 630 consecutive patients, 6 (1.0%) underwent redo...

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Autores principales: Tsuda, Masaki, Mizote, Isamu, Ichibori, Yasuhiro, Mukai, Takashi, Maeda, Koichi, Onishi, Toshinari, Kuratani, Toru, Sawa, Yoshiki, Sakata, Yasushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Circulation Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7890286/
https://www.ncbi.nlm.nih.gov/pubmed/33693129
http://dx.doi.org/10.1253/circrep.CR-18-0025
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author Tsuda, Masaki
Mizote, Isamu
Ichibori, Yasuhiro
Mukai, Takashi
Maeda, Koichi
Onishi, Toshinari
Kuratani, Toru
Sawa, Yoshiki
Sakata, Yasushi
author_facet Tsuda, Masaki
Mizote, Isamu
Ichibori, Yasuhiro
Mukai, Takashi
Maeda, Koichi
Onishi, Toshinari
Kuratani, Toru
Sawa, Yoshiki
Sakata, Yasushi
author_sort Tsuda, Masaki
collection PubMed
description Background: The outcome of redo transcatheter aortic valve (TAV) implantation (TAVI) is unknown for TAV structural valve degeneration (SVD). This paper reports the initial results of redo TAVI for TAV-SVD in Japanese patients. Methods and Results: Of 630 consecutive patients, 6 (1.0%) underwent redo TAVI for TAV-SVD (689–1,932 days after the first TAVI). The first TAV were 23-mm balloon-expandable valves (BEV, n=5) and a 26-mm self-expandable valve (SEV, n=1). All patients underwent multidetector computed tomography (MDCT) before redo TAVI, which showed first-TAV under-expansion (range, 19.1–21.0 mm) compared with the label size. Two BEV and 4 SEV were successfully implanted as second TAV, without moderate/severe regurgitation or 30-day mortality. One of 2 patients with a BEV-inside-BEV implantation had a high transvalvular mean pressure gradient post-procedurally (34 mmHg) and required surgical valve replacement 248 days after the redo TAVI. This, however, was unnoted in patients with SEV implantation during redo TAVI. Planned coronary artery bypass grafting was concomitantly performed in 1 patient with a small sino-tubular junction and SEV-inside-SEV implantation because of the risk of coronary malperfusion caused by the first TAV leaflets. Five of the 6 patients survived during the follow-up period (range, 285–1,503 days). Conclusions: Redo TAVI for TAV-SVD appears safe and feasible, while specific strategies based on MDCT and device selection seem important for better outcomes.
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spelling pubmed-78902862021-03-09 Outcomes of Redo Transcatheter Aortic Valve Implantation for Structural Valve Degeneration of Transcatheter Aortic Valve Tsuda, Masaki Mizote, Isamu Ichibori, Yasuhiro Mukai, Takashi Maeda, Koichi Onishi, Toshinari Kuratani, Toru Sawa, Yoshiki Sakata, Yasushi Circ Rep Original article Background: The outcome of redo transcatheter aortic valve (TAV) implantation (TAVI) is unknown for TAV structural valve degeneration (SVD). This paper reports the initial results of redo TAVI for TAV-SVD in Japanese patients. Methods and Results: Of 630 consecutive patients, 6 (1.0%) underwent redo TAVI for TAV-SVD (689–1,932 days after the first TAVI). The first TAV were 23-mm balloon-expandable valves (BEV, n=5) and a 26-mm self-expandable valve (SEV, n=1). All patients underwent multidetector computed tomography (MDCT) before redo TAVI, which showed first-TAV under-expansion (range, 19.1–21.0 mm) compared with the label size. Two BEV and 4 SEV were successfully implanted as second TAV, without moderate/severe regurgitation or 30-day mortality. One of 2 patients with a BEV-inside-BEV implantation had a high transvalvular mean pressure gradient post-procedurally (34 mmHg) and required surgical valve replacement 248 days after the redo TAVI. This, however, was unnoted in patients with SEV implantation during redo TAVI. Planned coronary artery bypass grafting was concomitantly performed in 1 patient with a small sino-tubular junction and SEV-inside-SEV implantation because of the risk of coronary malperfusion caused by the first TAV leaflets. Five of the 6 patients survived during the follow-up period (range, 285–1,503 days). Conclusions: Redo TAVI for TAV-SVD appears safe and feasible, while specific strategies based on MDCT and device selection seem important for better outcomes. The Japanese Circulation Society 2019-01-16 /pmc/articles/PMC7890286/ /pubmed/33693129 http://dx.doi.org/10.1253/circrep.CR-18-0025 Text en Copyright © 2019, THE JAPANESE CIRCULATION SOCIETY This article is licensed under a Creative Commons [Attribution-NonCommercial-NoDerivatives 4.0 International] license.https://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Original article
Tsuda, Masaki
Mizote, Isamu
Ichibori, Yasuhiro
Mukai, Takashi
Maeda, Koichi
Onishi, Toshinari
Kuratani, Toru
Sawa, Yoshiki
Sakata, Yasushi
Outcomes of Redo Transcatheter Aortic Valve Implantation for Structural Valve Degeneration of Transcatheter Aortic Valve
title Outcomes of Redo Transcatheter Aortic Valve Implantation for Structural Valve Degeneration of Transcatheter Aortic Valve
title_full Outcomes of Redo Transcatheter Aortic Valve Implantation for Structural Valve Degeneration of Transcatheter Aortic Valve
title_fullStr Outcomes of Redo Transcatheter Aortic Valve Implantation for Structural Valve Degeneration of Transcatheter Aortic Valve
title_full_unstemmed Outcomes of Redo Transcatheter Aortic Valve Implantation for Structural Valve Degeneration of Transcatheter Aortic Valve
title_short Outcomes of Redo Transcatheter Aortic Valve Implantation for Structural Valve Degeneration of Transcatheter Aortic Valve
title_sort outcomes of redo transcatheter aortic valve implantation for structural valve degeneration of transcatheter aortic valve
topic Original article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7890286/
https://www.ncbi.nlm.nih.gov/pubmed/33693129
http://dx.doi.org/10.1253/circrep.CR-18-0025
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