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Direct Current Cardioversion in Atrial Fibrillation Patients on Edoxaban Therapy Versus Vitamin K Antagonists: a Real-world Propensity Score-Matched Study.

Authors :
Rago A
Papa AA
Attena E
Parisi V
Golino P
Nigro G
Russo V
Source :
Cardiovascular drugs and therapy [Cardiovasc Drugs Ther] 2021 Oct; Vol. 35 (5), pp. 1003-1007. Date of Electronic Publication: 2020 Sep 18.
Publication Year :
2021

Abstract

Purpose: The purpose of the present study was to compare the long-term effectiveness and safety of newly initiated anticoagulation with edoxaban (EDO) versus uninterrupted vitamin K antagonist (VKA) therapy in patients with atrial fibrillation (AF) scheduled for transesophageal echocardiogram (TEE)-guided direct electrical current cardioversion (DCC).<br />Methods: A propensity score-matched cohort observational study was performed comparing the safety and effectiveness of edoxaban versus well-controlled VKA therapy among a cohort of consecutive non-valvular AF patients scheduled for DCC. The primary safety outcome was major bleeding. The primary efficacy outcome was the composite of stroke, transient ischemic attack (TIA), and systemic embolism (SE).<br />Findings: A total of 130 AF patients receiving edoxaban 60-mg (EDO) treatment were compared with the same number of VKA recipients. The cumulative incidence of major bleedings was 1.54% in the EDO group and 3.08% in the VKA group (P = 0.4). The cumulative incidence of thromboembolic events was 1.54% in the EDO group and 2.31% in the VKA group (P = 0.9). A non-significant trend in improved adherence was observed between the EDO and VKA groups with a total anticoagulant therapy discontinuation rate of 4.62% (6/130) vs 6.15% (8/130), respectively (P = 0.06).<br />Implications: Our study provides the evidence of a safe and effective use of edoxaban in this clinical setting, justified by no significant difference in major bleedings and thromboembolic events between edoxaban and well-controlled VKA treatments.<br /> (© 2020. The Author(s).)

Details

Language :
English
ISSN :
1573-7241
Volume :
35
Issue :
5
Database :
MEDLINE
Journal :
Cardiovascular drugs and therapy
Publication Type :
Academic Journal
Accession number :
32946035
Full Text :
https://doi.org/10.1007/s10557-020-07078-7