Antiarrhythmic drugs in patients with early persistent atrial fibrillation and heart failure: results of the RACE 3 study

Author:

Al-Jazairi Meelad I H1ORCID,Nguyen Bao-Oanh1,De With Ruben R1,Smit Marcelle D2,Weijs Bob3,Hobbelt Anne H1,Alings Marco4,Tijssen Jan G P5,Geelhoed Bastiaan1,Hillege Hans L1,Tieleman Robert G2,Van Veldhuisen Dirk J1,Crijns Harry J G M3,Van Gelder Isabelle C1,Blaauw Yuri1,Rienstra Michiel1ORCID,

Affiliation:

1. Department of Cardiology, University of Groningen, Groningen, University Medical Center Groningen, The Netherlands

2. Department of Cardiology, Martini Hospital, Groningen, The Netherlands

3. Department of Cardiology, Maastricht University Medical Centre and Cardiovascular Research Institute Maastricht, The Netherlands

4. Department of Cardiology, Amphia Hospital Breda, Julius Clinical Zeist, The Netherlands

5. Department of Clinical Epidemiology and Biostatistics, Academic Medical Centre, Amsterdam, The Netherlands

Abstract

Abstract Aims Maintaining sinus rhythm in patients with persistent atrial fibrillation (AF) is challenging. We explored the efficacy of class I and III antiarrhythmic drugs (AADs) in patients with persistent AF and mild to moderate heart failure (HF). Methods and results In the RACE 3 trial, patients with early persistent symptomatic AF and short history of mild to moderate HF with preserved or reduced left ventricular ejection fraction (LVEF) were randomized to targeted or conventional therapy. Both groups received AF and HF guideline-driven treatment. Additionally, the targeted-group received mineralocorticoid receptor antagonists, statins, angiotensin-converting enzyme inhibitors and/or receptor blockers, and cardiac rehabilitation. Class I and III AADs could be instituted in case of symptomatic recurrent AF. Eventually, pulmonary vein isolation could be performed. Primary endpoint was sinus rhythm on 7-day Holter after 1-year. Included were 245 patients, age 65 ± 9 years, 193 (79%) men, AF history was 3 (2–6) months, HF history 2 (1–4) months, 72 (29.4%) had HF with reduced LVEF. After baseline electrical cardioversion (ECV), 190 (77.6%) had AF recurrences; 108 (56.8%) received class I/III AADs; 19 (17.6%) flecainide, 36 (33.3%) sotalol, 3 (2.8%) dronedarone, 50 (46.3%) amiodarone. At 1-year 73 of 108 (68.0%) patients were in sinus rhythm, 44 (40.7%) without new AF recurrences. Maintenance of sinus rhythm was significantly better with amiodarone [n = 29/50 (58%)] compared with flecainide [n = 6/19 (32%)] and sotalol/dronedarone [n = 9/39 (23%)], P = 0.0064. Adverse events occurred in 27 (25.0%) patients, were all minor and reversible. Conclusion In stable HF patients with early persistent AF, AAD treatment was effective in nearly half of patients, with no serious adverse effects reported.

Funder

Netherlands Heart Foundation

AstraZeneca

Bayer

Biotronik

Boehringer-Ingelheim

Boston Scientific

Medtronic

Sanofi-Aventis

St Jude Medical paid to the Netherlands Heart Institute

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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