Pedersen O L
Eur J Clin Pharmacol. 1978 Mar 17;13(1):21-4. doi: 10.1007/BF00606677.
Verapamil was evaluated as an antihypertensive agent in a pilot study. Intravenous administration of 0.1 mg/kg, followed by constant infusion of 0.0035 mg/kg min, reduced both systolic and diastolic blood pressure significantly; the maximal average decrease of 23/16 mm Hg occurred after 5 min. The resting pulse rate rose during infusion and prolongation of the atrio-ventricular conduction time was a constant finding. After the initial drop in blood pressure, a rise toward control levels was observed, despite an increase in the infusion rate. Five patients received oral treatment with verapamil 320-640 mg daily for 7 weeks. In four of the five patients a blood pressure reduction was obtained (mean: 14/12 mm Hg), but normotension was not achieved in any of them. In contrast to the acute studies, the atrio-ventricular conduction time showed no change and a decrease in resting pulse rate was noted. Two patients experienced sensations of heat and reddening of face during treatment. It is concluded that verapamil has a rather modest antihypertensive effect and it is not suitable for the treatment of arterial hypertension.
在一项初步研究中对维拉帕米作为抗高血压药物进行了评估。静脉注射0.1mg/kg,随后以0.0035mg/kg·min的速度持续输注,可显著降低收缩压和舒张压;5分钟后平均最大降幅为23/16mmHg。静息心率在输注期间升高,房室传导时间延长是一个持续的发现。在血压最初下降后,尽管输注速率增加,但仍观察到血压回升至对照水平。5名患者接受了维拉帕米口服治疗,每日320 - 640mg,持续7周。5名患者中有4名血压下降(平均:14/12mmHg),但无一例达到正常血压。与急性研究不同,房室传导时间无变化,且静息心率下降。两名患者在治疗期间出现发热感和面部发红。结论是维拉帕米的抗高血压作用相当有限,不适合用于治疗动脉高血压。