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To evaluate the efficacy and safety of vernakalant hydrochloride — a new, relatively atrial-selective antiarrhythmic agent — in patients with recent-onset atrial fibrillation (AF), researchers conducted a post hoc analysis of a subset of adult patients with AF duration of 3 to 48 hours from two large phase III trials.
Overall, 59.4% of 229 patients who received vernakalant (3 mg/kg intravenous infusion over 10 minutes) converted to normal sinus rhythm within 90 minutes, compared to 4.9% of 61 placebo recipients. The median time to cardioversion with vernakalant was 12 minutes. Hypotension occurred in 9.1% of vernakalant-treated patients in the first 24 hours and bradycardia in 8.7%; the drug was discontinued in 1.7% of patients. No patient d…