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喷布洛尔(Hoe 893d)用于原发性高血压。血压效应、耐受性及血浆浓度

Penbutolol (Hoe 893d) in primary hypertension. Blood pressure effects, tolerance and plasma concentrations.

作者信息

Ohman K P, Asplund J, Landahl S, Liander B

出版信息

Eur J Clin Pharmacol. 1982;22(2):95-9. doi: 10.1007/BF00542451.

Abstract

Penbutolol (Hoe 893d), a long-acting non-selective beta-adrenoceptor blocking agent, was given once daily to 23 patients with primary hypertension, WHO Stages I-II. The dose (50-100mg) needed to achieve the therapeutic goal, i.e. supine diastolic BP less than 95 mm Hg, was titrated individually. On a daily dose of penbutolol 83 +/- 19 mg (mean +/- SD) blood pressure (BP, mean +/- SD) fell from 180 +/- 21/112 +/- 8 mmHg on placebo to 154 +/- 25/94 +/- 14 mmHg. 18 patients who reached the therapeutic goal (responders) continued in a double blind, cross-over study versus placebo, during which the supine BP fell on average 20/10 mmHg on the same dose of penbutolol, and 2/1 mmHg on placebo. Plasma concentrations (mean +/- SD) of free 0.10 +/- 0.07 microgram/ml) and total (2.02 +/- 1.39 microgram/ml) penbutolol did not differ between responders and nonresponders, and were not correlated with the fall in BP. Side effects were mild and mostly well tolerated. One patient developed dermatitis and another an elevation of liver enzymes.

摘要

喷布洛尔(Hoe 893d)是一种长效非选择性β肾上腺素受体阻滞剂,对23例世界卫生组织I-II期原发性高血压患者每日给药1次。实现治疗目标(即仰卧位舒张压低于95mmHg)所需的剂量(50 - 100mg)进行个体化滴定。每日服用喷布洛尔83±19mg(均值±标准差)时,血压(均值±标准差)从安慰剂组的180±21/112±8mmHg降至154±25/94±14mmHg。18例达到治疗目标的患者(反应者)继续进行与安慰剂的双盲交叉研究,在此期间,相同剂量的喷布洛尔使仰卧位血压平均下降20/10mmHg,安慰剂组下降2/1mmHg。反应者与无反应者之间游离喷布洛尔(均值±标准差为0.10±(1克/毫升)和总喷布洛尔(2.02±1.39微克/毫升)的血浆浓度无差异,且与血压下降无关。副作用轻微,大多耐受性良好。1例患者出现皮炎,另1例出现肝酶升高。

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