Why the study?
Vernakalant offers a novel approach to pharmacological cardioversion of recent-onset AF, prompting a description of the evidence, guidelines, and local hospital implementation process.
Does vernakalant improve rapid conversion to sinus rhythm in patients with recent onset atrial fibrillation compared to placebo or amiodarone?
Does vernakalant improve rapid conversion to sinus rhythm in patients with recent onset atrial fibrillation compared to placebo or amiodarone?
Vernakalant provides a rapid and effective pharmacological alternative for the cardioversion of recent onset atrial fibrillation, potentially reducing atrial remodeling and avoiding the risks of electrical cardioversion.
May support vernakalant for rapid recent-onset AF cardioversion; leaves open head-to-head RCTs versus amiodarone or electrical cardioversion.
Atrial fibrillation (AF) is the most common arrhythmia, and there is a one in four lifetime risk of developing the condition for people who are over the age of 40. Vernakalant, a new addition to intravenous antiarrhythmic drugs for cardioversion of AF, is the first atrial-specific antiarrhythmic drug for pharmacological cardioversion of recent onset AF and is more effective than placebo and amiodarone. The drug offers patients an alternative to other pharmacological agents for chemical cardioversion and avoids the risks associated with electrical cardioversion. Its main advantage is rapid conversion of AF, which potentially reduces atrial remodelling and it can be used in patients with little or no underlying cardiovascular disease and in those with moderate disease such as stable coronary and hypertensive heart disease. Post-marketing and clinical trials suggest a favourable rate of conversion to sinus rhythm. Jersey General Hospital was the first in the UK to obtain and introduce the drug in practice. This article describes the evidence and guidelines for its use and the local implementation process.
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Angela Hall (2018) studied this question.
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