The efficacy of amiodarone has been proved in longterm maintenance of sinus
rhythm (SR) in patients with paroxysmal atrial fibrillation (AF), The pres
ent study evaluates the efficacy and safety of a single oral dose of amioda
rone in patients with recent-onset AF (<48 hours). Seventy-two patients wer
e randomized to receive 30 mg/kg of either amiodarone or placebo. Conversio
n to SR was verified by 24-hour Holter monitoring. Ten patients were exclud
ed because of SR in the beginning of monitoring or technical failure during
Holter monitoring. The remaining study groups were comparable (n = 31 for
each), except that in the placebo group beta blockers were more common. The
patients receiving amiodarone converted to SR more effectively than those
receiving placebo (p <0.0001). At 8 hours, approximately 50% of patients in
the amiodarone group and 20% in the placebo group (Holter successful) had
converted to SR, whereas after 24 hours the corresponding figures were 87%
and 35%, respectively. The median time for conversion (8.7 hours for amioda
rone and 7.9 hours for placebo) did not differ in the groups. Amiodarone wa
s hemodynamically well tolerated, and the number of adverse events in the s
tudy groups was similar. Amiodorone as a single oral dose of 30 mg/kg appea
rs to be effective and safe in patients with recent-onset AF. (C) 2000 by E
xcerpta Medico, Inc.