Procedural and clinical outcomes of type 0 versus type 1 bicuspid aortic valve stenosis undergoing trans-catheter valve replacement with new generation devices: Insight from the BEAT international collaborative registry.


Journal

International journal of cardiology
ISSN: 1874-1754
Titre abrégé: Int J Cardiol
Pays: Netherlands
ID NLM: 8200291

Informations de publication

Date de publication:
15 02 2021
Historique:
received: 29 05 2020
revised: 01 10 2020
accepted: 15 10 2020
pubmed: 6 11 2020
medline: 28 5 2021
entrez: 5 11 2020
Statut: ppublish

Résumé

Although bicuspid aortic valve (BAV) is not considered a "sweet spot" to trans-catheter aortic valve replacement (TAVR), a certain number of BAV underwent TAVR. Whether BAV phenotype affects outcomes following TAVR remains debated. We aimed at evaluating the impact of BAV phenotype on procedural and clinical outcomes after TAVR using new generation trans-catheter heart valves (THVs). patients included in the BEAT registry were classified according to the BAV phenotype revealed at multi-slice computed tomography (MSCT) in type 0 (no raphe) vs. type 1 (1 raphe). Primary end-point was Valve Academic Research Consortium-2 (VARC-2) device success. Secondary end-points included procedural complications, rate of permanent pacemaker implantation, clinical outcomes at 30-day and 1-year. Type 0 BAV was present in 25(7.1%) cases, type 1 in 218(61.8%). Baseline characteristics were well balanced between groups. Moderate-severe aortic valve calcifications at MSCT were less frequently present in type 0 vs. type 1 (52%vs.71.1%,p = 0.05). No differences were reported for THV type, size, pre and post-dilation between groups. VARC-2 success tended to be lower in type 0 vs. type 1 BAV (72%vs86.7%;p = 0.07). Higher rate of mean transprosthetic gradient ≥20 mmHg was observed in type 0 vs. type 1 group (24%vs6%,p = 0.007). No differences were reported in the rate of post-TAVR moderate-severe aortic regurgitation and clinical outcomes between groups. Our study confirms TAVR feasibility in both BAV types, however a trend toward a lower VARC-2 device success and a higher rate of mean transprosthetic gradient ≥20 mmHg was observed in type 0 vs. type 1 BAV.

Sections du résumé

BACKGROUND
Although bicuspid aortic valve (BAV) is not considered a "sweet spot" to trans-catheter aortic valve replacement (TAVR), a certain number of BAV underwent TAVR. Whether BAV phenotype affects outcomes following TAVR remains debated. We aimed at evaluating the impact of BAV phenotype on procedural and clinical outcomes after TAVR using new generation trans-catheter heart valves (THVs).
METHODS
patients included in the BEAT registry were classified according to the BAV phenotype revealed at multi-slice computed tomography (MSCT) in type 0 (no raphe) vs. type 1 (1 raphe). Primary end-point was Valve Academic Research Consortium-2 (VARC-2) device success. Secondary end-points included procedural complications, rate of permanent pacemaker implantation, clinical outcomes at 30-day and 1-year.
RESULTS
Type 0 BAV was present in 25(7.1%) cases, type 1 in 218(61.8%). Baseline characteristics were well balanced between groups. Moderate-severe aortic valve calcifications at MSCT were less frequently present in type 0 vs. type 1 (52%vs.71.1%,p = 0.05). No differences were reported for THV type, size, pre and post-dilation between groups. VARC-2 success tended to be lower in type 0 vs. type 1 BAV (72%vs86.7%;p = 0.07). Higher rate of mean transprosthetic gradient ≥20 mmHg was observed in type 0 vs. type 1 group (24%vs6%,p = 0.007). No differences were reported in the rate of post-TAVR moderate-severe aortic regurgitation and clinical outcomes between groups.
CONCLUSIONS
Our study confirms TAVR feasibility in both BAV types, however a trend toward a lower VARC-2 device success and a higher rate of mean transprosthetic gradient ≥20 mmHg was observed in type 0 vs. type 1 BAV.

Identifiants

pubmed: 33148461
pii: S0167-5273(20)34003-1
doi: 10.1016/j.ijcard.2020.10.050
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

109-114

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest None.

Auteurs

Alfonso Ielasi (A)

Clinical and Interventional Cardiology Unit, Istituto Clinico Sant'Ambrogio, Milan, Italy, Italy. Electronic address: alielasi@hotmail.com.

Elisabetta Moscarella (E)

Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Naples, Italy.

Antonio Mangieri (A)

GVM Care and Research, Maria Cecilia Hospital, Cotignola, Ravenna, Italy.

Francesco Giannini (F)

GVM Care and Research, Maria Cecilia Hospital, Cotignola, Ravenna, Italy.

Didier Tchetchè (D)

Groupe CardioVasculaire Interventionnel, Clinique Pasteur, Toulouse, France.

Won-Keun Kim (WK)

Kerckhoff Heart Center, Department of Cardiology, Bad Nauheim, Germany.

Jean-Malte Sinning (JM)

Cardiology Department, University Hospital Bonn, Bonn, Germany.

Uri Landes (U)

Cardiology Department, Rabin Medical Center, Petah Tikva, Israel.

Ran Kornowski (R)

Cardiology Department, Rabin Medical Center, Petah Tikva, Israel.

Ole De Backer (O)

The Heart Center-Rigshospitalet, Copenhagen, Denmark.

Georg Nickenig (G)

Cardiology Department, University Hospital Bonn, Bonn, Germany.

Chiara De Biase (C)

Groupe CardioVasculaire Interventionnel, Clinique Pasteur, Toulouse, France.

Lars Søndergaard (L)

The Heart Center-Rigshospitalet, Copenhagen, Denmark.

Federico De Marco (F)

Department of Cardiology, IRCCS Policlinico San Donato, Milan, Italy.

Francesco Bedogni (F)

Department of Cardiology, IRCCS Policlinico San Donato, Milan, Italy.

Marco Ancona (M)

San Raffaele Scientific Institute, Milan, Italy.

Matteo Montorfano (M)

San Raffaele Scientific Institute, Milan, Italy.

Damiano Regazzoli (D)

Clinical and Interventional Cardiology Unit, Cardio Center, Humanitas Research Hospital, Rozzano, Milan, Italy.

Giulio Stefanini (G)

Clinical and Interventional Cardiology Unit, Cardio Center, Humanitas Research Hospital, Rozzano, Milan, Italy.

Stefan Toggweiler (S)

Heart Center Lucerne, Luzerner Kantonsspital, Lucerne, Switzerland.

Corrado Tamburino (C)

Cardiology Division, CAST Policlinico Hospital, University of Catania, Catania, Italy.

Sebastiano Immè (S)

Centro Cuore Morgagni, Catania, Italy.

Giuseppe Tarantini (G)

Interventional Cardiology Unit, University of Padova, Italy.

Horst Sievert (H)

Cardiovascular Center Frankfurt, Frankfurt, Germany and Anglia Ruskin University, Chelmsford, United Kingdom.

Ulrich Schäfer (U)

UKE, Hamburg, Hamburg, Germany.

Jörg Kempfert (J)

Deutsches Herzzentrum Berlin, Charité Universitätsmedizin, Berlin, Germany.

Jochen Wöehrle (J)

Ulm University, Ulm, Germany.

Azeem Latib (A)

Department of Cardiology, Montefiore Medical Center, NY, New York, United States of America; Division of Cardiology, Department of Medicine, University of Cape Town, Cape Town, South Africa.

Paolo Calabrò (P)

Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Naples, Italy.

Massimo Medda (M)

Clinical and Interventional Cardiology Unit, Istituto Clinico Sant'Ambrogio, Milan, Italy, Italy.

Maurizio Tespili (M)

Clinical and Interventional Cardiology Unit, Istituto Clinico Sant'Ambrogio, Milan, Italy, Italy.

Antonio Colombo (A)

GVM Care and Research, Maria Cecilia Hospital, Cotignola, Ravenna, Italy; EMO GVM Centro Cuore Columbus, Milan, Italy.

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