Safety and Efficacy of Single Versus Dual Antiplatelet Therapy After Left Atrial Appendage Occlusion.


Journal

The American journal of cardiology
ISSN: 1879-1913
Titre abrégé: Am J Cardiol
Pays: United States
ID NLM: 0207277

Informations de publication

Date de publication:
01 11 2020
Historique:
received: 20 06 2020
revised: 29 07 2020
accepted: 03 08 2020
pubmed: 8 9 2020
medline: 1 12 2020
entrez: 7 9 2020
Statut: ppublish

Résumé

The optimal antiplatelet strategy after left atrial appendage (LAA) occlusion able to protect from device-related thrombosis, paying the lowest price in terms of bleeding increase, is unclear. In a real-world, observational study we performed a head-to-head comparison of single versus dual antiplatelet therapy (SAPT vs DAPT) in patients who underwent LAA occlusion. We included 610 consecutive patients, stratified according to the type of post-procedural antiplatelet therapy (280 on SAPT and 330 on DAPT). Primary outcome measure was the incidence of the net composite end point including Bleeding Academic Research Consortium classification 3-5 bleeding, major adverse cardiovascular events or device-related thrombosis at 1-year follow-up. The use of SAPT compared with DAPT was associated with similar incidence of the primary net composite end point (9.3% vs 12.7% p = 0.22), with an adjusted hazard ratio (HR) of 0.69, 95% confidence interval 0.41 to 1.15; p = 0.15) at multivariate analysis. However, SAPT significantly reduced Bleeding Academic Research Consortium classification 3-5 bleeding (2.9% vs 6.7%, p = 0.038; adjusted HR 0.37, 0.16 to 0.88; p = 0.024). The occurrence of ischemic events (major adverse cardiovascular events or device-related thrombosis) was not significantly different between the 2treatment strategies (7.8% vs 7.4%; adjusted HR 1.34, 0.70 to 2.55; p = 0.38). In patients who underwent LAA occlusion, post-procedural use of SAPT instead of DAPT was associated with reduction of bleeding complications, with no significant increase in the risk of thrombotic events. These hypothesis-generating findings should be confirmed in a specific, randomized study.

Identifiants

pubmed: 32892987
pii: S0002-9149(20)30857-2
doi: 10.1016/j.amjcard.2020.08.013
pii:
doi:

Substances chimiques

Platelet Aggregation Inhibitors 0
Clopidogrel A74586SNO7
Aspirin R16CO5Y76E

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

83-90

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Giuseppe Patti (G)

University of Eastern Piedmont and Maggiore della Carità Hospital, Novara, Italy. Electronic address: giuseppe.patti@uniupo.it.

Alessandro Sticchi (A)

Campus Bio-Medico University, Rome, Italy.

Giuseppe Verolino (G)

Campus Bio-Medico University, Rome, Italy.

Vincenzo Pasceri (V)

San Filippo Neri Hospital, Rome, Italy.

Vincenzo Vizzi (V)

Luigi Sacco Hospital, Milan, Italy.

Elvis Brscic (E)

Maria Pia Hospital, Turin, Italy.

Gavino Casu (G)

San Francesco Hospital, Nuoro, Italy.

Paolo Golino (P)

University of Campania "Luigi Vanvitelli", Naples, Italy.

Vincenzo Russo (V)

University of Campania "Luigi Vanvitelli", Naples, Italy.

Antonio Rapacciuolo (A)

Federico II University of Naples, Naples, Italy.

Giacomo Boccuzzi (G)

S.G. Bosco Hospital, Turin, , Italy.

Antonio Mangieri (A)

GVM Care & Research Maria Cecilia Hospital, Cotignola, Italy.

Paolo Antonio Pagnotta (PA)

Humanitas Research Hospital, Rozzano-Milan, Italy.

Antonio Colombo (A)

EMO-GVM Centro Cuore Columbus, Milan, Italy.

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Classifications MeSH