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[两种不同剂量酮色林对老年高血压患者的血流动力学和体液影响]

[Hemodynamic and humoral effects of 2 different doses of ketanserin in aged patients with hypertension].

作者信息

Rizzoni D, Castellano M, Beschi M, Agabiti-Rosei E

机构信息

Cattedra di Terapia Medica Sistematica, Università degli Studi di Brescia.

出版信息

Ann Ital Med Int. 1990 Oct-Dec;5(4 Pt 2):489-96.

PMID:2102136
Abstract

The purpose of this double blind, cross-over, randomized study was to assess the antihypertensive efficacy and tolerability of ketanserin given at two different doses (i.e. 20 or 40 mg b.i.d.) in a group of patients with essential hypertension aged over 60 years. In addition, we evaluated the effect of ketanserin on some indexes of the sympathetic nervous system activity and the renin-angiotensin-aldosterone system, as well as the pharmacokinetic characteristics of the drug after acute administration per os and during chronic treatment. Twelve hypertensive patients, 6 males and 6 females gave their informed consent to the study. Each patient underwent a non invasive blood pressure monitoring after a wash out period with placebo, after 5 weeks of treatment with ketanserin (20 or 40 mg b.i.d.), after a second wash out period with placebo, and after a second period of treatment (5 weeks) with ketanserin (40 or 20 mg b.i.d.). In addition, we evaluated ketanserin plasma levels during acute and chronic administration. During treatment with ketanserin 20 mg b.i.d. systolic and diastolic blood pressure showed a small, statistically not significant reduction. The higher dose (40 mg b.i.d.) reduced systolic and diastolic blood pressure. Three hours after administration of 40 mg of the drug, ketanserin plasma levels were higher than after administration of 20 mg; this difference disappeared after 24 hours. A statistically significant relationship between mean blood pressure reduction during chronic treatment and ketanserin plasma levels was detected. No adverse effects were detected. In conclusion, ketanserin seems to be well tolerated and useful in antihypertensive therapy in elderly patients, particularly at the dose of 40 mg b.i.d.

摘要

这项双盲、交叉、随机研究的目的是评估酮色林在两组不同剂量(即每日两次,每次20或40毫克)下,对60岁以上原发性高血压患者的降压疗效和耐受性。此外,我们评估了酮色林对交感神经系统活动和肾素 - 血管紧张素 - 醛固酮系统某些指标的影响,以及口服急性给药和慢性治疗期间该药物的药代动力学特征。12名高血压患者,6名男性和6名女性,已对该研究给予知情同意。每位患者在服用安慰剂洗脱期后、服用酮色林(每日两次,每次20或40毫克)5周后、第二次服用安慰剂洗脱期后以及第二次服用酮色林(每日两次,每次40或20毫克)治疗期(5周)后,均接受无创血压监测。此外,我们评估了急性和慢性给药期间酮色林的血浆水平。在每日两次服用20毫克酮色林治疗期间,收缩压和舒张压有小幅下降,但在统计学上无显著意义。较高剂量(每日两次,每次40毫克)可降低收缩压和舒张压。服用40毫克药物三小时后,酮色林血浆水平高于服用20毫克后;24小时后这种差异消失。检测到慢性治疗期间平均血压降低与酮色林血浆水平之间存在统计学上的显著关系。未检测到不良反应。总之,酮色林似乎耐受性良好,对老年患者的降压治疗有用,尤其是在每日两次,每次40毫克的剂量下。

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