This study evaluates the effectiveness and safety of intravenous diltiazem and veraparnil for the acute treatment of atrial fibrillation (AF). A double - blind, parallel, randomized and comparative study protocol was used. The study involved 24 patients with AF, a ventricular rate > 120 beats/min and systolic blood pressure >90 mmHg. Patients were randomized to receive either intravenous diltiazem (n= ı2 ) 0.35 mg/kg (maximum 25 mg) or intravenous veraparnil (n= 1 2) O.ı5 mg/kg (maximum ı O mg). Therapeutic response was defined as a 20 % decrease in ventricular rate from basel ine, a heart rate bel o w ı 00/min. and conversion to sinus rhythm. Eleven of 12 patients (% 92) in diltiazem group and 12 of 12 (100 %) in veraparnil group responded (p>0.05). The mean time to achieve response was 2.7±1 minutes for diltiazem and 3.9±5 minutes for veraparnil (p>0.05). The mean reduction in heart rate from baseline was % 35 with veraparnil and % 24 with diltiazem. Veraparnil reduced systolic blood pressure from baseline by 24 % and diastolic blood pressure by 20 %, diltiazem by ll % and ı3 %, respectively. Symptomatic hypotension was observed in 4 patients in veraparnil group and none in diltiazem group (p<0.05). It is concluded that intravenous diltiazem and veraparnil are equally effective in reducing the heart rate and diltiazem seems to be a safer drug to be used for the acute treatment of AF, for symptomatic hypotension is seen more frequently with veraparniL
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