Key result
Sotalol drives marked arrhythmia reduction in ~59% of patients vs placebo.
Why the study?
Sotalol has unique class III antiarrhythmic actions in experimental models, but its clinical efficacy for suppressing ventricular arrhythmias required testing.
Does sotalol reduce the frequency of ventricular arrhythmias in patients with chronic premature ventricular complexes?
RCT (n=56)
Double-blind
randomized
Yes
Does sotalol reduce the frequency of ventricular arrhythmias in patients with chronic premature ventricular complexes?
Sotalol at doses of 320 and 640 mg/day is highly effective and well-tolerated for suppressing frequent, complex ventricular arrhythmias.
Sotalol supports arrhythmia suppression in chronic PVCs; confirms RCT efficacy versus placebo.
Sotalol is a unique beta-adrenergic blocking agent with additional actions characteristic of Vaughn-Williams class III antiarrhythmic agents in experimental models. To test the efficacy of sotalol to suppress ventricular arrhythmias, a 6 week parallel, placebo-controlled out-patient study of two doses (320 and 640 mg/day, in two divided doses) was performed in four hospitals in 56 patients with chronic premature ventricular complexes at a frequency of 30/h or more (mean +/- SE, 528 +/- 60/h) on 48 hour ambulatory electrocardiographic recording. During a placebo week, no change occurred in arrhythmia frequency (532 +/- 76/h). Subsequent sotalol therapy significantly reduced median arrhythmia frequency in patients receiving both low (n = 19) and high (n = 18) doses compared with that in patients receiving placebo (by 77 and 83%, respectively, versus 6%; p less than 0.001). Twenty-two (59%) of 37 sotalol-treated patients, 11 in each group, reached the prospectively defined criterion of efficacy (greater than or equal to 75% arrhythmia reduction) versus 2 (11%) of 19 placebo control patients (p less than 0.001). Sotalol reduced the median frequency of couplets by 94% (p less than 0.0001) and that of runs by 89% (p less than 0.0007). The electrocardiographic effects of sotalol included reductions in heart rate (by 17 to 27%) and increases in the QTc (by 6 to 9%) and PR (by 6%) intervals. Ejection fraction was unchanged. The most common adverse side effect was fatigue, but drug discontinuation was required in only three patients taking 640 mg/day. No proarrhythmic events or biochemical abnormalities were observed. In summary, sotalol displays significant antiarrhythmic activity of moderately high degree with good tolerance in doses of both 320 and 640 mg/day. Its antiarrhythmic actions are distinguished from those reported for other beta-blockers by its effects on the QTc interval and its moderately high degree of antiarrhythmic activity.
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Anderson et al. (1986) conducted an RCT in chronic premature ventricular complexes (n=56). Sotalol vs. Placebo was evaluated on prospectively defined criterion of efficacy (≥75% arrhythmia reduction) (p=<0.001). Sotalol therapy significantly increased the proportion of patients achieving ≥75% arrhythmia reduction compared to placebo (59% vs 11%; p<0.001).
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