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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
- 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.
- Subjects :
- Research design
Time Factors
medicine.drug_mechanism_of_action
Pyridines
Administration, Oral
Major bleeding
030204 cardiovascular system & hematology
chemistry.chemical_compound
0302 clinical medicine
Edoxaban
Stroke prevention
Atrial Fibrillation
Epidemiology
Routine clinical practice
Prospective Studies
Registries
030212 general & internal medicine
Prospective cohort study
Stroke
[QFIN]Quantitative Finance [q-fin]
Atrial fibrillation
General Medicine
3. Good health
Europe
JEL: I - Health, Education, and Welfare/I.I1 - Health/I.I1.I11 - Analysis of Health Care Markets
Treatment Outcome
ETNA-AF-Europe study
Research Design
10209 Clinic for Cardiology
epidemiology
Cardiology and Cardiovascular Medicine
Registry
medicine.medical_specialty
Factor Xa Inhibitor
610 Medicine & health
Hemorrhage
2705 Cardiology and Cardiovascular Medicine
03 medical and health sciences
Nonvitamin K antagonist oral anticoagulants
Internal medicine
medicine
Humans
cardiovascular diseases
Safety outcomes
business.industry
PREFER in AF
medicine.disease
JEL: I - Health, Education, and Welfare/I.I1 - Health/I.I1.I12 - Health Behavior
Thiazoles
Real-world
chemistry
business
Factor Xa Inhibitors
Subjects
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