Clinical outcomes in patients with atrial fibrillation treated with DOACs in a specialized anticoagulation center

Direct oral anticoagulants (DOAC) are progressively replacing vitamin K antagonists in the prevention of thromboembolism in patients with atrial fibrillation. However, their real-world clinical outcomes appear to be contradictory, with some studies reporting fewer and others reporting higher complic...

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Detalles Bibliográficos
Autores: Moret, Carla|||0000-0002-0704-7456, Acosta-Isaac, René|||0000-0002-7000-3886, Mojal, Sergi|||0000-0003-0523-3869, Corrochano, Mariana|||0000-0003-1070-3845, Jiménez, Blanca, Plaza, Melania|||0000-0002-1471-3672, Souto, Juan Carlos|||0000-0003-2092-5142
Tipo de recurso: artículo
Fecha de publicación:2023
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:302838
Acceso en línea:https://ddd.uab.cat/record/302838
https://dx.doi.org/urn:doi:10.1371/journal.pone.0279297
Access Level:acceso abierto
Palabra clave:Administration, Oral
Aged, 80 and over
Anticoagulants
Atrial Fibrillation
Humans
Prospective Studies
Pyridines
Stroke
Descripción
Sumario:Direct oral anticoagulants (DOAC) are progressively replacing vitamin K antagonists in the prevention of thromboembolism in patients with atrial fibrillation. However, their real-world clinical outcomes appear to be contradictory, with some studies reporting fewer and others reporting higher complications than the pivotal randomized controlled trials. We present the results of a clinical model for the management of DOACs in real clinical practice and provide a review of the literature. The MACACOD project is an ongoing, observational, prospective, single-center study with unselected patients that focuses on rigorous DOAC selection, an educational visit, laboratory measurements, and strict follow-up. A total of 1,259 patients were included. The composite incidence of major complications was 4.93% py in the whole cohort vs 4.49% py in the edoxaban cohort. The rate of all-cause mortality was 6.11% py for all DOACs vs 5.12% py for edoxaban. There weren't differences across sex or between Edoxaban reduced or standard doses. However, there were differences across ages, with a higher incidence of major bleeding complications in patients.