Clinical factors related to successful or unsuccessful cardioversion in the EdoxabaN versus warfarin in subjectS UndeRgoing cardiovErsion of Atrial Fibrillation (ENSURE‐AF) randomized trial

Background EdoxabaN versus warfarin in subjectS UndeRgoing cardiovErsion of Atrial Fibrillation evaluated use of nonvitamin K antagonist oral anticoagulant edoxaban vs enoxaparin‐warfarin in patients with nonvalvular atrial fibrillation undergoing electrical cardioversion. Hypothesis To assess clini...

Full description

Saved in:
Bibliographic Details
Published inJournal of Arrhythmia Vol. 36; no. 3; pp. 430 - 438
Main Authors Lip, Gregory Y. H., Merino, Jose L., Banach, Maciej, Al‐Saady, Naab, Jin, James, Melino, Michael, Winters, Shannon M., Kozieł, Monika, Goette, Andreas
Format Journal Article
LanguageEnglish
Published Japan Wiley 01.06.2020
John Wiley & Sons, Inc
John Wiley and Sons Inc
Subjects
Online AccessGet full text
ISSN1880-4276
1883-2148
DOI10.1002/joa3.12341

Cover

More Information
Summary:Background EdoxabaN versus warfarin in subjectS UndeRgoing cardiovErsion of Atrial Fibrillation evaluated use of nonvitamin K antagonist oral anticoagulant edoxaban vs enoxaparin‐warfarin in patients with nonvalvular atrial fibrillation undergoing electrical cardioversion. Hypothesis To assess clinical factors related to successful or unsuccessful cardioversion. To evaluate whether differences in adverse events based on anticoagulation strategy may exist. Methods In this multicenter prospective randomized open‐label blinded end‐point evaluation trial, 2199 patients were randomized to edoxaban 60 mg once daily (30 mg for creatinine clearance 15‐50 mL/min, weight ≤ 60 kg, and/or concomitant use of P‐glycoprotein inhibitor) or enoxaparin‐warfarin. Successful cardioversion was confirmed by 12‐lead electrocardiography‐documented sinus rhythm. Results Cardioversion was successful in 1578 patients; in 355 patients, cardioversion was unsuccessful. Male, high body weight, high body mass index (BMI), coronary artery disease, concomitant aspirin, or prior statins use were more common in patients with unsuccessful cardioversion; international normalized ratio control did not differ by cardioversion success. On multivariate analysis, gender (P < .05), body weight (P = .0196) and BMI (P = .0377) emerged as independent predictors of successful cardioversion. There were no significant differences in primary efficacy (a composite of stroke, systemic embolic event, myocardial infarction, and cardiovascular death during overall study period) regardless of cardioversion success. There were no significant differences in bleeding rates, regardless of cardioversion outcome; notwithstanding low numbers, edoxaban and enoxaparin‐warfarin did not differ. Conclusions Male gender, higher mean weight and higher mean BMI were associated with unsuccessful cardioversion. Efficacy and safety outcomes were low and did not differ by cardioversion success.
Bibliography:FUNDING INFORMATION
The ENSURE‐AF study was sponsored and funded by Daiichi Sankyo. GYHL: Consultant for Bayer/Janssen, BMS/Pfizer, Medtronic, Boehringer Ingelheim, Novartis, Verseon, and Daiichi‐Sankyo. Speaker for Bayer, BMS/Pfizer, Medtronic, Boehringer Ingelheim, and Daiichi‐Sankyo. No fees are directly received personally. JM: Personal fees from Abbott, Bayer, Biotronic, Boston Scientific, Bristol‐Myers Squibb, Cardiome, Daiichi Sankyo, LivaNova, Medtronic, Pfizer, and Sanofi outside the submitted work. MB: Consultant for Abbott Vascular, Akcea, Amgen, Esperion, Eli Lilly, Merck Sharp & Dohme, Resverlogix, and Sanofi‐Aventis; a speaker for Abbott/Mylan, Abbott Vascular, Actavis, Akcea, Amgen, Biofarm, KRKA, Merck Sharp & Dohme, Sanofi‐Aventis, and Valeant; and reports grants from Sanofi‐Aventis and Valeant. NA‐S: Employee of Covance, which received funding from Daiichi Sankyo for the management of the study. JJ: Employee of Daiichi Sankyo. SMW and MM: Employees of Daiichi Sankyo at the time of writing. AG: Personal fees from AstraZeneca, Bayer, Berlin‐Chemie, Boehringer Ingelheim, Bristol‐Myers Squibb, Daiichi Sankyo, Omeicos, Medtronic, Pfizer, and Sanofi‐Aventis outside the submitted work.
ObjectType-Article-2
SourceType-Scholarly Journals-1
content type line 14
ObjectType-Feature-3
ObjectType-Evidence Based Healthcare-1
ObjectType-Article-1
ObjectType-Feature-2
content type line 23
ISSN:1880-4276
1883-2148
DOI:10.1002/joa3.12341