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醋丁洛尔治疗高血压——与安慰剂对照的双盲试验

Acebutolol in hypertension--double-blind trial against placebo.

作者信息

Martin M A, Phillips C A, Smith A J

出版信息

Br J Clin Pharmacol. 1978 Oct;6(4):351-6. doi: 10.1111/j.1365-2125.1978.tb00863.x.

Abstract
  1. Eleven hypertensive patients were studied in a double-blind comparison of acebutolol, a beta-adrenoceptor blocker, and placebo. 2. Optimum dosage defined in an open assessment varied from 200--600 mg twice daily. 3. Blood pressure and pulse rate fell significantly while patients were lying, standing and after exercise. 4. Blood pressure remained as well controlled on each patient's optimum daily dose when taken once daily, and assessed 24 h post dose. 5. There was no correlation between blood pressure reduction and changes in heart rate. On once daily therapy while blood pressure remained unchanged at 24 h post dose there was a signficant reduction in beta-adrenoceptor blockade as measured by percentage reduction in exercise tachycardia. 6. There was no significant change in urinary catecholamine excretion or echocardiographically estimated cardiac output. 7. A correlation was found between the change in plasma renin activity (log transformed) and blood pressure reduction.
摘要
  1. 对11名高血压患者进行了一项双盲研究,比较β-肾上腺素受体阻滞剂醋丁洛尔和安慰剂。2. 在开放评估中确定的最佳剂量为每日两次,每次200 - 600毫克。3. 患者卧位、站立位及运动后血压和脉搏率均显著下降。4. 当每日一次服用每位患者的最佳日剂量并在给药后24小时进行评估时,血压仍得到良好控制。5. 血压降低与心率变化之间无相关性。在每日一次治疗中,给药后24小时血压保持不变,但运动性心动过速的百分比降低表明β-肾上腺素受体阻滞作用显著降低。6. 尿儿茶酚胺排泄或超声心动图估计的心输出量无显著变化。7. 发现血浆肾素活性变化(对数转换)与血压降低之间存在相关性。

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