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Antithrombotic treatment in patients with atrial fibrillation and acute coronary syndromes: results of the European Heart Rhythm Association survey

Lane, D. A.; Dagres, N.; Dan, G. A.; García Seara, Javier; Iliodromitis, K.; Lenarczyk, R.; Lip, G. Y. H.; Mansourati, J.; Marin, F.; Scherr, D.; Potpara, T. S.
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URI: http://hdl.handle.net/20.500.11940/15667
PMID: 30874724
DOI: 10.1093/europace/euz033
ISSN: 1099-5129
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Europace. 2019 Jul 1;21(7):1116-1125. (376.7Kb)
Acceso a la versión del editor (120.0Kb)
Fecha de publicación
2019
Título de revista
EUROPACE
Tipo de contenido
Artigo
DeCS
anticoagulantes | humanos | fibrinolíticos | fibrilación atrial | inhibidores de la agregación plaquetaria | síndrome coronario agudo
MeSH
Fibrinolytic Agents | Platelet Aggregation Inhibitors | Anticoagulants | Humans | Atrial Fibrillation | Acute Coronary Syndrome
Resumen
The management of an acute coronary syndrome (ACS) in a patient with existing atrial fibrillation (AF) often presents a management dilemma both in the acute phase and post-ACS, since the majority of AF patients will already be receiving oral anticoagulation (OAC) for stroke prevention and will require further antithrombotic treatment to reduce the risk of in-stent thrombosis or recurrent cardiac events. Current practice recommendations are based largely on consensus option as there is limited evidence from randomized controlled trials. Prior to the launch of the new European Heart Rhythm Association (EHRA) consensus document, a survey was undertaken to examine current clinical management of these patients across centres in Europe. Forty-seven centres submitted valid responses, with the majority (70.2%) being university hospitals. This EHRA survey demonstrated overall the management of ACS in AF patients is consistent with the available guidance. Most centres would use triple therapy for a short duration (4 weeks) and predominantly utilize a strategy of OAC (vitamin K antagonist, VKA or non-vitamin K antagonist oral anticoagulant, NOAC) plus aspirin and clopidogrel, followed by dual therapy [(N)OAC plus clopidogrel] until 12 months post-percutaneous coronary intervention, followed by (N)OAC monotherapy indefinitely. Where NOAC was used in combination with antiplatelet(s), the lower dose of the respective NOAC was preferred, in accordance with current recommendations.

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