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Low Dose of Direct Oral Anticoagulants after Left Atrial Appendage Occlusion

The optimal antithrombotic strategy following left atrial appendage occlusion (LAAO) is not yet clearly established. Low-dose non-vitamin K antagonist oral anticoagulants (NOAC) might represent a valid alternative, but data regarding their usage is scarce. The aim of this study was to examine the ef...

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Autores principales: Cepas-Guillen, Pedro Luis, Flores-Umanzor, Eduardo, Regueiro, Ander, Brugaletta, Salvatore, Ibañez, Cristina, Sanchis, Laura, Sitges, Marta, Rodés-Cabau, Josep, Sabaté, Manel, Freixa, Xavier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8623304/
https://www.ncbi.nlm.nih.gov/pubmed/34821695
http://dx.doi.org/10.3390/jcdd8110142
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author Cepas-Guillen, Pedro Luis
Flores-Umanzor, Eduardo
Regueiro, Ander
Brugaletta, Salvatore
Ibañez, Cristina
Sanchis, Laura
Sitges, Marta
Rodés-Cabau, Josep
Sabaté, Manel
Freixa, Xavier
author_facet Cepas-Guillen, Pedro Luis
Flores-Umanzor, Eduardo
Regueiro, Ander
Brugaletta, Salvatore
Ibañez, Cristina
Sanchis, Laura
Sitges, Marta
Rodés-Cabau, Josep
Sabaté, Manel
Freixa, Xavier
author_sort Cepas-Guillen, Pedro Luis
collection PubMed
description The optimal antithrombotic strategy following left atrial appendage occlusion (LAAO) is not yet clearly established. Low-dose non-vitamin K antagonist oral anticoagulants (NOAC) might represent a valid alternative, but data regarding their usage is scarce. The aim of this study was to examine the efficacy and safety of low-dose NOAC compared to single (SAPT) or dual antiplatelet therapies (DAPT) after LAAO. We included consecutive patients with non-valvular atrial fibrillation who underwent LAAO and received low-dose apixaban, SAPT, or DAPT at discharge. The primary objective of this study included an efficacy endpoint (thromboembolic events and device related thrombosis (DRT)) and a safety endpoint (incidence of major bleeding) within the first three months after LAAO. A total of 139 patients were included. This group involved SAPT in 26 (18%), DAPT in 73 (53%), and apixaban in 40 (29%) patients. Follow-up at three-months showed no significant differences in the primary efficacy endpoint (2 (8%) SAPT, 3 (4%) DAPT and 0 (0%) apixaban; p value = 0.25). In contrast, the primary safety endpoint occurred more frequently in DAPT patients (7 (10%) DAPT, 0 (0%), SAPT and 0 with apixaban; p value = 0.03). Combining both efficacy and safety outcomes, low dose apixaban had a lower rate of events (2 (8%) with SAPT, 9 (12%) with DAPT and 0 (0%) with apixaban; p = 0.046). Low-dose apixaban after LAAO may be a valid alternative to DAPT and SAPT as depicted by the reduction in the occurrence of major bleedings and combined DRT/major bleedings respectively. Randomized data will be necessary to validate this strategy.
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spelling pubmed-86233042021-11-27 Low Dose of Direct Oral Anticoagulants after Left Atrial Appendage Occlusion Cepas-Guillen, Pedro Luis Flores-Umanzor, Eduardo Regueiro, Ander Brugaletta, Salvatore Ibañez, Cristina Sanchis, Laura Sitges, Marta Rodés-Cabau, Josep Sabaté, Manel Freixa, Xavier J Cardiovasc Dev Dis Article The optimal antithrombotic strategy following left atrial appendage occlusion (LAAO) is not yet clearly established. Low-dose non-vitamin K antagonist oral anticoagulants (NOAC) might represent a valid alternative, but data regarding their usage is scarce. The aim of this study was to examine the efficacy and safety of low-dose NOAC compared to single (SAPT) or dual antiplatelet therapies (DAPT) after LAAO. We included consecutive patients with non-valvular atrial fibrillation who underwent LAAO and received low-dose apixaban, SAPT, or DAPT at discharge. The primary objective of this study included an efficacy endpoint (thromboembolic events and device related thrombosis (DRT)) and a safety endpoint (incidence of major bleeding) within the first three months after LAAO. A total of 139 patients were included. This group involved SAPT in 26 (18%), DAPT in 73 (53%), and apixaban in 40 (29%) patients. Follow-up at three-months showed no significant differences in the primary efficacy endpoint (2 (8%) SAPT, 3 (4%) DAPT and 0 (0%) apixaban; p value = 0.25). In contrast, the primary safety endpoint occurred more frequently in DAPT patients (7 (10%) DAPT, 0 (0%), SAPT and 0 with apixaban; p value = 0.03). Combining both efficacy and safety outcomes, low dose apixaban had a lower rate of events (2 (8%) with SAPT, 9 (12%) with DAPT and 0 (0%) with apixaban; p = 0.046). Low-dose apixaban after LAAO may be a valid alternative to DAPT and SAPT as depicted by the reduction in the occurrence of major bleedings and combined DRT/major bleedings respectively. Randomized data will be necessary to validate this strategy. MDPI 2021-10-28 /pmc/articles/PMC8623304/ /pubmed/34821695 http://dx.doi.org/10.3390/jcdd8110142 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cepas-Guillen, Pedro Luis
Flores-Umanzor, Eduardo
Regueiro, Ander
Brugaletta, Salvatore
Ibañez, Cristina
Sanchis, Laura
Sitges, Marta
Rodés-Cabau, Josep
Sabaté, Manel
Freixa, Xavier
Low Dose of Direct Oral Anticoagulants after Left Atrial Appendage Occlusion
title Low Dose of Direct Oral Anticoagulants after Left Atrial Appendage Occlusion
title_full Low Dose of Direct Oral Anticoagulants after Left Atrial Appendage Occlusion
title_fullStr Low Dose of Direct Oral Anticoagulants after Left Atrial Appendage Occlusion
title_full_unstemmed Low Dose of Direct Oral Anticoagulants after Left Atrial Appendage Occlusion
title_short Low Dose of Direct Oral Anticoagulants after Left Atrial Appendage Occlusion
title_sort low dose of direct oral anticoagulants after left atrial appendage occlusion
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8623304/
https://www.ncbi.nlm.nih.gov/pubmed/34821695
http://dx.doi.org/10.3390/jcdd8110142
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