Evidence map›Paper›PMID 39161202›Full record

ArticleJournal of the Chinese Medical Association : JCMA2024

Comparable efficacy and safety for bicuspid aortic valve stenosis patients undergoing transcatheter aortic valve replacement with balloon-expandable or self-expanding valves using Wei's sizing method.

Yung-Tsai Lee, Wei-Hsian Yin, Tien-Ping Tsao, Kuo-Chen Lee, Huan-Chiu Lin, Chun-Ting Liu, Ming-Chon Hsiung, Jeng Wei

Abstract readComparative Study
In one paragraph

Article in Journal of the Chinese Medical Association : JCMA, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Yung-Tsai LeeHeart Center, Cheng Hsin General Hospital, Taipei, Taiwan, ROC.
Wei-Hsian YinHeart Center, Cheng Hsin General Hospital, Taipei, Taiwan, ROC.
Tien-Ping TsaoHeart Center, Cheng Hsin General Hospital, Taipei, Taiwan, ROC.
Kuo-Chen LeeHeart Center, Cheng Hsin General Hospital, Taipei, Taiwan, ROC.
Huan-Chiu LinHeart Center, Cheng Hsin General Hospital, Taipei, Taiwan, ROC.
Chun-Ting LiuHeart Center, Cheng Hsin General Hospital, Taipei, Taiwan, ROC.
Ming-Chon HsiungHeart Center, Cheng Hsin General Hospital, Taipei, Taiwan, ROC.
Jeng WeiHeart Center, Cheng Hsin General Hospital, Taipei, Taiwan, ROC.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe present study aimed to investigate whether proper sizing can improve the procedural and clinical outcomes of transcatheter aortic valve replacement (TAVR) with new-generation self-expanding valves (SEVs) and balloon-expandable valves (BEVs) for treating bicuspid aortic stenosis (BAS).

methodsWe retrospectively evaluated consecutive patients who underwent TAVR with Sapien 3 valves (Edwards Lifesciences, Irvine, CA) or Evolut R/PRO valves (Medtronic, Minneapolis, MN) for severe BAS from 2017 to 2022. The primary endpoints were device success rate and major adverse cardiac and cerebral events (MACCEs), including mortality, nonfatal myocardial infarction or disabling stroke, transcatheter heart valve failure, or clinically relevant valve thrombosis during follow-up. Our team used a complementary approach of supraannular sizing in addition to the conventional annular sizing method (Wei's method) to guide the TAVR procedures.

resultsWe recruited a total of 75 consecutive patients, of whom 43 (57%) were treated with BEVs from October 2017 to June 2021, and 32 (43%) were treated with SEVs from July 2021 to December 2022. Device success was similar between the BEV and SEV groups (93% vs 94%; p > 0.99), and no cases of annular rupture occurred in either group. Similar rates of moderate-to-severe paravalvular leak were observed in the BEV and SEV groups (5% vs 6%, p > 0.99). At a median follow-up of 464 days, the MACCE rates were comparable between the two groups. In multivariate analysis, the presence of previous percutaneous coronary interventions (hazard ratio: 5.43; p = 0.039) and New York Heart Association functional class III/IV heart failure at 30 days of follow-up after TAVR (hazard ratio: 9.90; p = 0.037) were independently associated with long-term MACCEs.

conclusionOur results demonstrated comparable efficacy and safety for BAS patients undergoing TAVR using either BEVs or SEVs when using Wei's sizing method.

Indexed as

Aortic Valve StenosisBicuspid Aortic Valve DiseaseTranscatheter Aortic Valve ReplacementAgedAged, 80 and overAortic ValveFemaleHeart Valve ProsthesisHumansMaleRetrospective Studies

Identifiers

PMID39161202
PMCPMC12718791

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.