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轻度高血压患者每日一次服用双醋洛尔的安全性和有效性:一项安慰剂对照研究。

The safety and efficacy of once-daily dilevalol in patients with mild hypertension: a placebo-controlled study.

作者信息

Soberman J, Greenberg S, Frishman W

机构信息

Department of Medicine, Albert Einstein College of Medicine, Bronx, New York.

出版信息

J Clin Hypertens. 1987 Sep;3(3):271-7.

PMID:3312501
Abstract

Dilevalol is a stereoisomer of labetalol, with a unique combination of beta-adrenergic blocking effects and selective beta 2-agonist activity. The safety and efficacy of dilevalol in patients with systemic hypertension were evaluated in a placebo-controlled, double-blind, randomized study. After a 4-week placebo run-in period, patients with mild hypertension (supine diastolic blood pressure of 95-105 mmHg) were randomized to receive either placebo (n = 14) or increasing doses of dilevalol (n = 15), 100-800 mg, once daily, to achieve normalization of pressure and/or a reduction of supine diastolic pressure of greater than or equal to 10 mmHg. This was followed by a 4-week maintenance phase. Compared with placebo, dilevalol, 200-800 mg/day, lowered supine and standing systolic and diastolic blood pressures significantly, while causing a modest reduction in heart rate. The drug was well tolerated without evidence of orthostasis. Dilevalol, in doses of 200-800 mg/day, is a safe and effective drug for the treatment of patients with mild hypertension.

摘要

地来洛尔是拉贝洛尔的立体异构体,具有β肾上腺素能阻断作用和选择性β2激动剂活性的独特组合。在一项安慰剂对照、双盲、随机研究中评估了地来洛尔对系统性高血压患者的安全性和有效性。在为期4周的安慰剂导入期后,轻度高血压患者(仰卧位舒张压为95 - 105 mmHg)被随机分配接受安慰剂(n = 14)或递增剂量的地来洛尔(n = 15),100 - 800 mg,每日一次,以实现血压正常化和/或仰卧位舒张压降低大于或等于10 mmHg。随后是为期4周的维持阶段。与安慰剂相比,200 - 800 mg/天的地来洛尔显著降低了仰卧位和站立位的收缩压和舒张压,同时使心率略有降低。该药物耐受性良好,无体位性低血压的证据。200 - 800 mg/天剂量的地来洛尔是治疗轻度高血压患者的一种安全有效的药物。

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