Myburgh D P, Smith R, Diamond T H, Faitelson H L, Sommers D K
S Afr Med J. 1983 Feb 19;63(8):263-5.
The anti-arrhythmic efficacy of sotalol, a beta-blocking agent which possesses class III anti-arrhythmic properties, was compared with that of nadolol. Nadolol, like sotalol, is non-cardioselective, is water-soluble, has no first-pass effect, is excreted unchanged in the urine, has a comparatively long half-life requiring only once-daily dosage, and has no intrinsic sympathomimetic activity and no membrane-stabilizing action. Twenty-two patients with stable chronic ventricular arrhythmias after myocardial infarction were studied; to qualify for entry they had to exhibit a minimum frequency of 30 ventricular ectopic beats per hour over a 24-hour Holter monitoring period. The study was of single-blind, cross-over format with placebo periods before active drug administration and during the cross-over periods. Nadolol 80 and 160 mg and sotalol 160 and 320 mg were administered for 7-day periods. Routine laboratory tests were performed and serum drug concentrations measured at regular intervals. Both drugs at all dosages suppressed ventricular ectopic beats significantly (P less than 0,001). No statistically significant prolongation of the QTc interval could be demonstrated with either drug. Side-effects were negligible.
索他洛尔是一种具有Ⅲ类抗心律失常特性的β受体阻滞剂,将其抗心律失常疗效与纳多洛尔进行了比较。纳多洛尔与索他洛尔一样,无心脏选择性,水溶性,无首过效应,以原形经尿液排泄,半衰期相对较长,只需每日给药一次,无内在拟交感活性,无膜稳定作用。对22例心肌梗死后稳定的慢性室性心律失常患者进行了研究;符合入选条件者在24小时动态心电图监测期间每小时室性早搏频率至少为30次。该研究采用单盲、交叉设计,在给予活性药物前及交叉期间设置安慰剂期。纳多洛尔80毫克和160毫克以及索他洛尔160毫克和320毫克给药7天。进行常规实验室检查并定期测量血清药物浓度。两种药物在所有剂量下均能显著抑制室性早搏(P<0.001)。两种药物均未显示出QTc间期有统计学意义的延长。副作用可忽略不计。