Transcarotid Approach for Transcatheter Aortic Valve Replacement With the Sapien 3 Prosthesis: A Multicenter French Registry.


Journal

JACC. Cardiovascular interventions
ISSN: 1876-7605
Titre abrégé: JACC Cardiovasc Interv
Pays: United States
ID NLM: 101467004

Informations de publication

Date de publication:
11 03 2019
Historique:
received: 22 10 2018
revised: 09 11 2018
accepted: 13 11 2018
pubmed: 18 2 2019
medline: 6 5 2020
entrez: 18 2 2019
Statut: ppublish

Résumé

This study sought to describe the procedural and clinical outcomes of patients undergoing transcarotid (TC) transcatheter aortic valve replacement (TAVR) with the Edwards Sapien 3 device. The TC approach for TAVR holds the potential to become the optimal alternative to the transfemoral gold standard. Limited data exist regarding safety and efficacy of TC-TAVR using the Edwards Sapien 3 device. The French Transcarotid TAVR prospective multicenter registry included patients between 2014 and 2018. Consecutive patients treated in 1 of the 13 participating centers ineligible for transfemoral TAVR were screened for TC-TAVR. Clinical and echocardiographic data were prospectively collected. Perioperative and 30-day outcomes were reported according to the updated Valve Academic Research Consortium (VARC-2). A total of 314 patients were included with a median (interquartile range) age of 83 (78 to 88) years, 63% were males, Society of Thoracic Surgeons mortality risk score 5.8% (4% to 8.3%). Most patients presented with peripheral artery disease (64%). TC-TAVR was performed under general anesthesia in 91% of cases, mostly using the left carotid artery (73.6%) with a procedural success of 97%. Three annulus ruptures were reported, all resulting in patient death. At 30 days, rates of major bleeding, new permanent pacemaker, and stroke or transient ischemic attack were 4.1%, 16%, and 1.6%, respectively. The 30-day mortality was 3.2%. TC-TAVR using the Edwards Sapien 3 device was safe and effective in this prospective multicenter registry. The TC approach might be considered, in selected patients, as the first-line alternative approach for TAVR whenever the transfemoral access is prohibited. Sapien 3 device was safe and effective in our multicenter cohort.

Sections du résumé

OBJECTIVES
This study sought to describe the procedural and clinical outcomes of patients undergoing transcarotid (TC) transcatheter aortic valve replacement (TAVR) with the Edwards Sapien 3 device.
BACKGROUND
The TC approach for TAVR holds the potential to become the optimal alternative to the transfemoral gold standard. Limited data exist regarding safety and efficacy of TC-TAVR using the Edwards Sapien 3 device.
METHODS
The French Transcarotid TAVR prospective multicenter registry included patients between 2014 and 2018. Consecutive patients treated in 1 of the 13 participating centers ineligible for transfemoral TAVR were screened for TC-TAVR. Clinical and echocardiographic data were prospectively collected. Perioperative and 30-day outcomes were reported according to the updated Valve Academic Research Consortium (VARC-2).
RESULTS
A total of 314 patients were included with a median (interquartile range) age of 83 (78 to 88) years, 63% were males, Society of Thoracic Surgeons mortality risk score 5.8% (4% to 8.3%). Most patients presented with peripheral artery disease (64%). TC-TAVR was performed under general anesthesia in 91% of cases, mostly using the left carotid artery (73.6%) with a procedural success of 97%. Three annulus ruptures were reported, all resulting in patient death. At 30 days, rates of major bleeding, new permanent pacemaker, and stroke or transient ischemic attack were 4.1%, 16%, and 1.6%, respectively. The 30-day mortality was 3.2%.
CONCLUSIONS
TC-TAVR using the Edwards Sapien 3 device was safe and effective in this prospective multicenter registry. The TC approach might be considered, in selected patients, as the first-line alternative approach for TAVR whenever the transfemoral access is prohibited. Sapien 3 device was safe and effective in our multicenter cohort.

Identifiants

pubmed: 30772290
pii: S1936-8798(18)32303-3
doi: 10.1016/j.jcin.2018.11.014
pii:
doi:

Types de publication

Journal Article Multicenter Study Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

413-419

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019. Published by Elsevier Inc.

Auteurs

Pavel Overtchouk (P)

Lille University Hospital, Lille, France.

Thierry Folliguet (T)

Henri Mondor Hospital, Créteil, France.

Frédéric Pinaud (F)

Angers University Hospital, Angers, France.

Oliver Fouquet (O)

Angers University Hospital, Angers, France.

Mathieu Pernot (M)

Bordeaux University Hospital, Pessac, France.

Guillaume Bonnet (G)

Bordeaux University Hospital, Pessac, France.

Maxime Hubert (M)

Brabois University Hospital, Vandoeuvre les Nancy, France.

Joël Lapeze (J)

Infirmerie Protestante, Lyon, France.

Jean Philippe Claudel (JP)

Infirmerie Protestante, Lyon, France.

Said Ghostine (S)

Marie Lannelongue Hospital, Plessis-Robinson, France.

Alexandre Azmoun (A)

Marie Lannelongue Hospital, Plessis-Robinson, France.

Christophe Caussin (C)

Institut Mutualiste Montsouris, Paris, France.

Konstantinos Zannis (K)

Institut Mutualiste Montsouris, Paris, France.

Majid Harmouche (M)

Rennes University Hospital, Rennes, France.

Jean-Philippe Verhoye (JP)

Rennes University Hospital, Rennes, France.

Antoine Lafont (A)

Hôpital Européen Georges Pompidou, Paris, France.

Chekrallah Chamandi (C)

Hôpital Européen Georges Pompidou, Paris, France.

Vito Giovanni Ruggieri (VG)

Robert Debré University Hospital, Reims, France.

Alessandro Di Cesare (A)

Robert Debré University Hospital, Reims, France.

Florence Leclercq (F)

Montpellier University Hospital, Montpellier, France.

Thomas Gandet (T)

Montpellier University Hospital, Montpellier, France.

Thomas Modine (T)

Lille University Hospital, Lille, France. Electronic address: thomas.modine@chru-lille.fr.

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