Intracardiac echocardiography-guided implantation of the Watchman FLX left atrial appendage closure device.


Journal

Journal of cardiovascular electrophysiology
ISSN: 1540-8167
Titre abrégé: J Cardiovasc Electrophysiol
Pays: United States
ID NLM: 9010756

Informations de publication

Date de publication:
03 2021
Historique:
received: 20 10 2020
revised: 23 12 2020
accepted: 29 12 2020
pubmed: 4 2 2021
medline: 10 8 2021
entrez: 3 2 2021
Statut: ppublish

Résumé

The next-generation Watchman FLX left atrial appendage closure (LAAC) device has: (1) an atraumatic closed distal end, (2) reduced height, (3) a recessed screw hub to decrease device-related thrombus (DRT), (4) two rows of J-shape anchors so redeployment is possible after full recapture, and (5) ability to treat a greater size range of LAA ostia. To report, for the first time, the feasibility and safety of intracardiac echocardiography (ICE)-guided Watchman FLX implantation. A single-center prospective registry of atrial fibrillation patients planned for LAAC with the FLX device underwent ICE-guided implantation with conscious sedation. Transesophageal echocardiography (TEE) imaging was done preprocedure (to assess LAA size and exclude thrombus) and at clinical follow-up at 6-12 weeks. Clinical outcomes were LAA closure success, complications, leak, or DRT on follow-up TEE and major safety events. The study included 30 patients: age 75 ± 8 years, 53% men, CHA The Watchman FLX device can be safely implanted with intraprocedural ICE imaging instead of TEE.

Sections du résumé

BACKGROUND
The next-generation Watchman FLX left atrial appendage closure (LAAC) device has: (1) an atraumatic closed distal end, (2) reduced height, (3) a recessed screw hub to decrease device-related thrombus (DRT), (4) two rows of J-shape anchors so redeployment is possible after full recapture, and (5) ability to treat a greater size range of LAA ostia.
OBJECTIVE
To report, for the first time, the feasibility and safety of intracardiac echocardiography (ICE)-guided Watchman FLX implantation.
METHODS
A single-center prospective registry of atrial fibrillation patients planned for LAAC with the FLX device underwent ICE-guided implantation with conscious sedation. Transesophageal echocardiography (TEE) imaging was done preprocedure (to assess LAA size and exclude thrombus) and at clinical follow-up at 6-12 weeks. Clinical outcomes were LAA closure success, complications, leak, or DRT on follow-up TEE and major safety events.
RESULTS
The study included 30 patients: age 75 ± 8 years, 53% men, CHA
CONCLUSION
The Watchman FLX device can be safely implanted with intraprocedural ICE imaging instead of TEE.

Identifiants

pubmed: 33533089
doi: 10.1111/jce.14927
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

717-725

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2021 Wiley Periodicals LLC.

Références

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Auteurs

Mohit K Turagam (MK)

Department of Cardiovascular Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.

Petr Neuzil (P)

Department of Cardiovascular Medicine, Homolka Hospital, Prague, Czech Republic.

Jan Petru (J)

Department of Cardiovascular Medicine, Homolka Hospital, Prague, Czech Republic.

Pavel Hala (P)

Department of Cardiovascular Medicine, Homolka Hospital, Prague, Czech Republic.

Tomas Mraz (T)

Department of Cardiovascular Medicine, Homolka Hospital, Prague, Czech Republic.

Jiri Baroch (J)

Department of Cardiovascular Medicine, Homolka Hospital, Prague, Czech Republic.

Veronika Lekesova (V)

Department of Cardiovascular Medicine, Homolka Hospital, Prague, Czech Republic.

Milena Prokopova (M)

Department of Cardiovascular Medicine, Homolka Hospital, Prague, Czech Republic.

Srinivas R Dukkipati (SR)

Department of Cardiovascular Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.

Vivek Y Reddy (VY)

Department of Cardiovascular Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Department of Cardiovascular Medicine, Homolka Hospital, Prague, Czech Republic.

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