Walker L J, MacKenzie G, Adgey A A
Regional Medical Cardiology Centre, Royal Victoria Hospital, Belfast, U.K.
Eur Heart J. 1988 May;9(5):471-8. doi: 10.1093/oxfordjournals.eurheartj.a062531.
In a double-blind placebo-controlled trial to study the effect of nifedipine on ventricular arrhythmias among patients with acute myocardial infarction, 434 patients with suspected myocardial infarction were randomized within 6 h from the onset of chest pain to treatment with nifedipine (p = 217) or placebo (p = 217). During the 48-h treatment period, a 10-mg capsule containing active drug or placebo was administered sublingually every 4 h for 24 h, then orally every 4 h for the next 24 h. Acute myocardial infarction was confirmed in 295 patients (146 in the nifedipine group and 149 in the placebo group). Twenty-four hour ECG tape analysis during 1-5 h from onset of chest pain showed that there was no significant difference in the number of patients with ventricular ectopics, ventricular couplets, ventricular tachycardia (3-9 beats), self terminating or sustained ventricular tachycardia between the two treatment groups. Also during the greater than 5-24 h from onset of chest pain, the numbers of patients with ventricular ectopics, multifocal, bigeminal or couplets, self-terminating ventricular tachycardia or sustained ventricular tachycardia did not differ significantly. However, there was a significant reduction in the number of patients with short runs of ventricular tachycardia (3-9 beats) in the nifedipine-treated group. There was no significant difference among patients with ventricular fibrillation between the two treatment groups.
在一项双盲安慰剂对照试验中,为研究硝苯地平对急性心肌梗死患者室性心律失常的影响,434例疑似心肌梗死患者在胸痛发作后6小时内被随机分为硝苯地平治疗组(n = 217)或安慰剂组(n = 217)。在48小时的治疗期间,含活性药物或安慰剂的10毫克胶囊每4小时舌下含服一次,共24小时,然后在接下来的24小时内每4小时口服一次。295例患者确诊为急性心肌梗死(硝苯地平组146例,安慰剂组149例)。胸痛发作后1 - 5小时的24小时心电图磁带分析显示,两组治疗组之间室性早搏、室性成对搏动、室性心动过速(3 - 9次搏动)、自限性或持续性室性心动过速患者的数量无显著差异。同样在胸痛发作后大于5 - 24小时期间,室性早搏、多灶性、二联律或成对搏动、自限性室性心动过速或持续性室性心动过速患者的数量也无显著差异。然而,硝苯地平治疗组短阵室性心动过速(3 - 9次搏动)患者的数量显著减少。两组治疗组之间心室颤动患者无显著差异。