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Design and rationale of the Edoxaban Treatment in routiNe clinical prActice for patients with Atrial Fibrillation in Europe (ETNA-AF-Europe) study

Authors :
De Caterina, R.
Kelly, P.
Monteiro, P.
Deharo, J. C.
de Asmundis, C.
López-de-Sá, E.
Weiss, T. W.
Waltenberger, J.
Steffel, J.
de Groot, J. R.
Levy, P.
Bakhai, A.
Zierhut, W.
Laeis, P.
Reimitz, P. -E.
Kirchhof, P.
on behalf of the ETNA-AF-Europe investigators
Clinical sciences
Heartrhythmmanagement
Institute of Clinical Physiology
National Council of Research
NS Research
Novartis Institutes for BioMedical Research (NIBR)
Division of Medicine
University College of London [London] (UCL)
Neurovascular Clinical Science Unit, Catherine McAuley Centre
Mater Misericordiae University Hospital
Département de Cardiologie [Hôpital de la Timone - APHM]
Assistance Publique - Hôpitaux de Marseille (APHM)- Hôpital de la Timone [CHU - APHM] (TIMONE)
Laboratoire d'Economie de Dauphine (LEDa)
Université Paris Dauphine-PSL
Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)
Laboratoire d'Economie et de Gestion des Organisations de Santé (Legos)
Department of Medicine, Royal Free (DEPARTMENT OF MEDICINE, ROYAL FREE)
Royal Free and University College London School of Medicine
Daiichi Sankyo Inc.
Daiichi Sankyo Co.
ACS - Heart failure & arrhythmias
Cardiology
University of Zurich
De Caterina, Raffaele
Source :
Journal of Cardiovascular Medicine, Journal of Cardiovascular Medicine, 2019, 20 (2), ⟨10.2459/JCM.0000000000000737⟩, Journal of Cardiovascular Medicine, 20(2), 97-104. Lippincott Williams and Wilkins
Publication Year :
2019
Publisher :
Ovid Technologies (Wolters Kluwer Health), 2019.

Abstract

AIM: Edoxaban, a nonvitamin K antagonist oral anticoagulant, is an oral factor Xa inhibitor approved for the prevention of stroke and systemic embolism in adult patients with atrial fibrillation and for the treatment and secondary prevention in adult patients with venous thromboembolism (VTE). This study details the design of the Edoxaban Treatment in routiNe clinical prActice for patients with Atrial Fibrillation in Europe (ETNA-AF-Europe) study - a postauthorization observational study, which is part of the postapproval plan for edoxaban agreed with the European Medicines Agency. METHODS: The ETNA-AF-Europe study (Clinicaltrials.gov: NCT02944019) is a multicenter, prospective, observational study that enrolled 13 980 patients with atrial fibrillation treated with edoxaban from 852 sites across 10 European countries (Austria, Belgium, Germany, Ireland, Italy, the Netherlands, Portugal, Spain, Switzerland, and the United Kingdom). Patients treated with edoxaban were prospectively enrolled and will be followed up for 4 years with yearly follow-up visits. ASSESSMENTS: The primary objective of the ETNA-AF-Europe study is to assess the real-world safety of edoxaban by evaluating bleeding events, including intracranial hemorrhage; drug-related adverse events, such as hepatic events; and cardiovascular and all-cause mortality. In addition, efficacy will be assessed by recording major adverse cardiovascular events including stroke, systemic embolic events, transient ischemic attacks, and also VTE episodes, acute coronary syndromes, and hospitalizations related to cardiovascular condition. Event rates will be compared with event rates reported in the PREvention oF thromboembolic events-European Registry in Atrial Fibrillation in atrial fibrillation (PREFER in AF) and PREFER in AF Prolongation registries, and in the Effective Anticoagulation with Factor Xa Next Generation in Atrial Fibrillation - Thrombolysis in Myocardial Infarction 48 study datasets.

Details

ISSN :
15582027
Volume :
20
Database :
OpenAIRE
Journal :
Journal of Cardiovascular Medicine
Accession number :
edsair.doi.dedup.....881c83ffb201e2554a06282aef504e3f
Full Text :
https://doi.org/10.2459/jcm.0000000000000737