Initial and long-term antithrombotic therapy after left atrial appendage closure with the WATCHMAN.


Journal

Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
ISSN: 1532-2092
Titre abrégé: Europace
Pays: England
ID NLM: 100883649

Informations de publication

Date de publication:
01 07 2020
Historique:
received: 05 12 2019
revised: 10 02 2020
accepted: 23 03 2020
pubmed: 29 5 2020
medline: 29 6 2021
entrez: 29 5 2020
Statut: ppublish

Résumé

Evidence regarding post-procedural antithrombotic regimen other than used in randomized trials assessing percutaneous left atrial appendage (LAA) closure is limited. The present work aimed to compare different antithrombotic strategies applied in the real-world EWOLUTION study. A total of 998 patients with successful WATCHMAN implantation were available for the present analysis. The composite ischaemic endpoint of stroke, transitory ischaemic attack, systemic embolism and device thrombus, and the bleeding endpoint defined as at least major bleeding were assessed during an initial period (from implant until first medication change) and long-term period (from first change up to 2 years). The antithrombotic medication chosen in the initial phase was dual antiplatelet therapy (DAPT) in 60%, oral anticoagulation (OAC) in 27%, single antiplatelet therapy (SAPT) in 7%, and no medication in 6%. In the second long-term phase, SAPT was used in 65%, DAPT in 23%, no therapy in 8%, and OAC in 4%. No significant differences were found between the groups regarding the ischaemic endpoint both in the initial period (Kaplan-Meier estimated rate 2.9% for DAPT vs. 4.3% for OAC vs. 3.9% for SAPT or no therapy) and in the second period (4.2% for SAPT vs. 1.8% for DAPT vs. 3.5% for no therapy). With respect to bleeding events, the only difference was found in the initial phase with a higher incidence in patients under SAPT or no therapy. Tailored antithrombotic treatment using even very reduced strategies such as SAPT or no therapy showed no significant differences regarding ischaemic complications after LAA closure.

Identifiants

pubmed: 32464648
pii: 5848358
doi: 10.1093/europace/euaa074
doi:

Substances chimiques

Anticoagulants 0
Fibrinolytic Agents 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1036-1043

Informations de copyright

Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2020. For permissions, please email: journals.permissions@oup.com.

Auteurs

Jakob Ledwoch (J)

CardioVascular Center CVC, Seckbacher Landstraße 65, 60389 Frankfurt, Germany.
Klinik für Kardiologie, Pneumologie und Internistische Intensivmedizin, München Klinik Neuperlach, Munich, Germany.

Kolja Sievert (K)

CardioVascular Center CVC, Seckbacher Landstraße 65, 60389 Frankfurt, Germany.

Lucas V A Boersma (LVA)

St. Antonius Hospital Nieuwegein, and Amsterdam UMC, The Netherlands.

Martin W Bergmann (MW)

Cardiologicum Hamburg, Hamburg, Germany.

Hüseyin Ince (H)

Vivantes Klinikum Am Urban, Berlin, Germany.

Stephan Kische (S)

Vivantes Klinikum im Friedrichshain, Berlin, Germany.

Evgeny Pokushalov (E)

State Research Institute of Circulation Pathology, Novosibirsk, Russia.

Thomas Schmitz (T)

Elisabeth Krankenhaus Essen, Essen, Germany.

Boris Schmidt (B)

Cardioangiologisches Centrum Bethanien (CCB), Frankfurt Am Main, Germany.

Tommaso Gori (T)

Universitätsmedizin Mainz und DZHK Standort Rhein-Main, Mainz, Germany.

Felix Meincke (F)

Asklepios Klinik St Georg, Hamburg, Germany.

Alexey Vladimir Protopopov (AV)

Regional State Hospital, Krasnoyarsk, Russia.

Timothy R Betts (TR)

John Radcliffe Hospital, Oxford, UK.

Patrizio Mazzone (P)

Ospedale San Raffaele, Milano, Italy.

David Foley (D)

Beaumont Hospital, Dublin, Ireland.

Marek Grygier (M)

Poznan University of Medical Sciences, Poznan, Poland.

Tom De Potter (T)

Onze Lieve Vrouw Ziekenhuis, Aalst, Belgium.

Horst Sievert (H)

CardioVascular Center CVC, Seckbacher Landstraße 65, 60389 Frankfurt, Germany.

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Classifications MeSH