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多沙唑嗪与阿替洛尔治疗轻至中度高血压患者的多中心双盲比较。

Multicenter, double-blind comparison of doxazosin and atenolol in patients with mild to moderate hypertension.

作者信息

Ott P, Storm T L, Krusell L R, Jensen H, Badskjaer J, Faergeman O

出版信息

Am J Cardiol. 1987 May 29;59(14):73G-77G. doi: 10.1016/0002-9149(87)90161-5.

Abstract

In a double-blind multicenter study, the new alpha 1-adrenoceptor inhibitor doxazosin was compared with atenolol for efficacy, safety and effect on serum lipids. One hundred and twenty-six patients with mild to moderate hypertension were randomly assigned to receive either doxazosin (n = 63) or atenolol (n = 63). The mean final dosages, administered once daily, to obtain 24-hour blood pressure (BP) control were doxazosin 12 mg (range 1 to 16) and atenolol 91.8 mg (range 50 to 100). Of 12 doxazosin and 7 atenolol patient withdrawals from the study, 7 doxazosin and 4 atenolol patients withdrew for treatment-related reasons. No statistically significant differences between treatment groups were found after 20 weeks in changes from baseline in standing and sitting BPs measured 24 hours after administration. Sitting BP (systolic/diastolic) was reduced by 10.5/9.8 mm Hg after doxazosin treatment and by 10.9/10.7 mm Hg after atenolol therapy. Standing BP was reduced by 8.8/7.7 mm Hg after doxazosin administration and 9.7/9.3 mm Hg after treatment with atenolol. Supine BP was measured in a small cohort of the study population, and doxazosin had a smaller effect than atenolol. After 20 weeks of treatment, both drugs reduced heart rate with atenolol producing a statistically significantly greater decrease than doxazosin (standing, doxazosin 5 beats/min, atenolol 16.2 beats/min, p less than 0.001; sitting, doxazosin 5 beats/min, atenolol 13.1 beats/min, p less than 0.001). Side effects were reported by 37 patients receiving doxazosin therapy and 34 patients receiving atenolol therapy.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在一项双盲多中心研究中,对新型α1肾上腺素能受体抑制剂多沙唑嗪与阿替洛尔的疗效、安全性及对血脂的影响进行了比较。126例轻至中度高血压患者被随机分为两组,分别接受多沙唑嗪(n = 63)或阿替洛尔(n = 63)治疗。为实现24小时血压(BP)控制,每日给药一次的平均最终剂量为:多沙唑嗪12 mg(范围1至16 mg),阿替洛尔91.8 mg(范围50至100 mg)。在退出研究的12例服用多沙唑嗪和7例服用阿替洛尔的患者中,7例服用多沙唑嗪和4例服用阿替洛尔的患者因与治疗相关的原因退出。给药后24小时测量的站立位和坐位血压自基线的变化,在20周后治疗组之间未发现统计学上的显著差异。多沙唑嗪治疗后坐位血压(收缩压/舒张压)降低10.5/9.8 mmHg,阿替洛尔治疗后降低10.9/10.7 mmHg。多沙唑嗪给药后站立位血压降低8.8/7.7 mmHg,阿替洛尔治疗后降低9.7/9.3 mmHg。在一小部分研究人群中测量了仰卧位血压,多沙唑嗪的效果小于阿替洛尔。治疗20周后,两种药物均降低了心率,阿替洛尔降低的幅度在统计学上显著大于多沙唑嗪(站立位,多沙唑嗪降低5次/分钟,阿替洛尔降低16.2次/分钟,p<0.001;坐位,多沙唑嗪降低5次/分钟,阿替洛尔降低13.1次/分钟,p<0.001)。37例接受多沙唑嗪治疗的患者和34例接受阿替洛尔治疗的患者报告了副作用。(摘要截短于250字)

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