Hjortdahl P, von Krogh H, Daae L, Holme I, Hjermann I
Acta Med Scand. 1987;221(5):427-34. doi: 10.1111/j.0954-6820.1987.tb01276.x.
The new alpha1-adrenoceptor antagonist, doxazosin (DOX), was compared with hydrochlorothiazide (HCTZ), both drugs administered once daily, in a randomized double-blind study including 115 patients. The mean final daily doses used were DOX, 10.8 mg; HCTZ, 89.1 mg. There were no statistically significant differences between treatment groups for blood pressure (BP) changes except that HCTZ produced a significantly greater fall (p = 0.04) in supine systolic BP than DOX. The statistically significant mean differences in changes in lipid parameters (total cholesterol and total triglycerides) were in favour of DOX. The number of patients reporting side-effects were DOX, 27/57; HCTZ, 29/53, with two DOX- and five HCTZ-treated patients withdrawn due to side-effects. In the HCTZ-treated group, laboratory serum tests indicated 11 patients with abnormally low potassium and seven with abnormally high uric acid concentrations. The overall results suggest a benefit-to-risk ratio in favour of DOX.
在一项纳入115例患者的随机双盲研究中,将新型α1肾上腺素能受体拮抗剂多沙唑嗪(DOX)与氢氯噻嗪(HCTZ)进行比较,两种药物均每日给药一次。最终使用的平均每日剂量分别为:DOX 10.8毫克;HCTZ 89.1毫克。除了HCTZ导致仰卧位收缩压下降幅度显著大于DOX(p = 0.04)外,各治疗组间血压(BP)变化无统计学显著差异。脂质参数(总胆固醇和总甘油三酯)变化的统计学显著平均差异有利于DOX。报告有副作用的患者人数分别为:DOX组27/57;HCTZ组29/53,有2例接受DOX治疗和5例接受HCTZ治疗的患者因副作用退出研究。在HCTZ治疗组中,实验室血清检查显示11例患者血钾异常低,7例患者尿酸浓度异常高。总体结果表明,DOX的效益风险比更佳。