Journal
EUROPACE
Volume 13, Issue 2, Pages 161-173Publisher
OXFORD UNIV PRESS
DOI: 10.1093/europace/euq382
Keywords
Atrial fibrillation; Flecainide; Sinus rhythm maintenance; Remodelling; Safety; Cardioversion
Categories
Funding
- Meda Pharmaceuticals
- Sanofi-Aventis
- Pfizer
- Bristol-Myers Squibb
- 3M Pharmaceuticals
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Atrial fibrillation (AF) is the most common arrhythmia in clinical practise and its prevalence is increasing. Over the last 25 years, flecainide has been used extensively worldwide, and its capacity to reduce AF symptoms and provide long-term restoration of sinus rhythm (SR) has been well documented. The increased mortality seen in patients treated with flecainide in the Cardiac Arrhythmia Suppression Trial (CAST) study, published in 1991, still deters many clinicians from using flecainide, denying many new AF patients a valuable treatment option. There is now a body of evidence that clearly demonstrates that flecainide has a favourable safety profile in AF patients without significant left ventricular disease or coronary heart disease. As a result of this evidence, flecainide is now recommended as one of the first-line treatment options for restoring and maintaining SR in patients with AF under current treatment guidelines. The objective of this article is to review the literature pertaining to the pharmacological characteristics, safety and efficacy of flecainide, and to place this drug in the context of current therapeutic management strategies for AF.
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