Continuous vs Episodic Prophylactic Treatment With Amiodarone for the Prevention of Atrial Fibrillation: A Randomized Trial

• Published in: JAMA : the journal of the American Medical Association Vol. 300; no. 15; pp. 1784 - 1792
• Main Authors: Ahmed, Sheba, Rienstra, Michiel, Crijns, Harry J. G. M, Links, Thera P, Wiesfeld, Ans C. P, Hillege, Hans L, Bosker, Hans A, Lok, Dirk J. A, Van Veldhuisen, Dirk J, Van Gelder, Isabelle C, CONVERT Investigators, for the
• Format: Journal Article
• Language: English
• Published: Chicago, IL American Medical Association 15.10.2008
• Subjects: Aged; Amiodarone - administration & dosage; Amiodarone - therapeutic use; Anti-Arrhythmia Agents - administration & dosage; Anti-Arrhythmia Agents - therapeutic use; Atrial Fibrillation - mortality; Atrial Fibrillation - prevention & control; Atrial Fibrillation - therapy; Biological and medical sciences; Cardiac arrhythmia; Cardiac dysrhythmias; Cardiology. Vascular system; Cause of Death; Clinical trials; Drug Administration Schedule; Drug therapy; Electric Countershock; Female; General aspects; Heart; Hospitalization; Humans; Kaplan-Meier Estimate; Male; Medical sciences; Middle Aged; Mortality; Prevention and actions; Prospective Studies; Public health. Hygiene; Public health. Hygiene-occupational medicine; Risk factors; Secondary Prevention; Side effects; Antianginal agent; Arrhythmia; Continuous; Coronary vasodilator agent; Atrial fibrillation; Cardiovascular disease; Amiodarone; Antiarrhythmic agent; Iodine Organic compounds; Excitability disorder; Medicine; Prevention; Randomization; Treatment; Heart disease; Clinical trial; Comparative study
• ISSN: 0098-7484; 1538-3598
• DOI: 10.1001/jama.300.15.1784

CONTEXT Amiodarone effectively suppresses atrial fibrillation but causes many adverse events. OBJECTIVE To compare major events in patients randomized to receive episodic amiodarone treatment with those who received continuous amiodarone treatment while still aiming to prevent atrial fibrillation. DESIGN, SETTING, AND PARTICIPANTS A randomized trial of 209 ambulatory patients with recurrent symptomatic persistent atrial fibrillation, conducted from December 2002 through March 2007 at 7 Dutch medical centers. INTERVENTION Patients were randomly assigned to receive either episodic or continuous amiodarone treatment after electrical cardioversion following amiodarone loading. Episodic amiodarone treatment was discontinued after a month of sinus rhythm and reinitiated if atrial fibrillation relapsed (1 month peri–electrical cardioversion). In the continuous treatment group amiodarone was maintained throughout. MAIN OUTCOME MEASURES The primary end point was a composite of amiodarone and underlying heart disease–related major events. The secondary end points were all-cause mortality and cardiovascular hospitalizations. RESULTS After a median follow-up of 2.1 years (range, 0.4-2.5 years), 51 (48%) of those receiving episodic treatment vs 64 (62%) receiving continuous treatment had sinus rhythm (P = .05). There were 85 atrial fibrillation recurrences (80%) among the episodic treatment group vs 56 (54%) in the continuous treatment group (P < .001). No significant difference existed in the incidence of the primary composite end point between each group (37 [35%] episodic vs 34 [33%] continuous; incidence rate difference, 0.2; 95% confidence interval [CI], −10.2 to 10.6). However, there were nonstatistically significant differences in the incidence of amiodarone-related major events (20 [19%] episodic vs 25 [24%] continuous; incidence rate difference, −2.0; 95% CI, −8.7 to 4.6) and underlying heart disease–related major events (17 [16%] episodic vs 9 [9%] continuous; incidence rate difference, 3.6; 95% CI, −1.6 to 8.7). All-cause mortality and cardiovascular hospitalizations were higher among those receiving episodic treatment (56 [53%] vs 35 [34%], P = .02). CONCLUSIONS In this study population, there was no difference in the composite of amiodarone and cardiac major adverse events between groups. However, patients receiving episodic treatment had a significantly increased rate of atrial fibrillation recurrence and a significantly higher rate of all-cause mortality and cardiovascular hospitalizations. TRIAL REGISTRATION clinicaltrials.gov Identifier: NCT00392431