Tariq A R, Maheendran K, Kamsiah J, Christina P
Department of Pharmacology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Jalan Raja Muda, Kuala Lumpur.
Med J Malaysia. 1992 Sep;47(3):182-9.
Twenty eight patients who satisfied the entry criteria and had completed an initial 2 weeks treatment with placebo were titrated fortnightly with doses of Nicardipine ranging from 30 mg to 90 mg daily in two or three divided doses. Nicardipine treatment significantly reduced blood pressures both in the supine and standing positions (p < 0.0004) when compared with placebo treatment. Heart rates however did not change significantly. Forty six percent (13/28) of patients on 20 mg twice daily, 25% (7/28) on 10 mg three times daily, 18% (5/28) of patients on 20 mg three times daily and 11% (3/28) on 30 mg three times daily achieved supine diastolic blood pressures < 90 mm Hg. Nicardipine treatment at 16 weeks and at 24 weeks did not significantly alter the lipid profile when compared to the end of placebo treatment period. No other biochemical abnormalities were reported during the study period. Except for 2 cases of mild pedal oedema and 2 cases of transient headaches, no serious side-effects were encountered.
28名符合入选标准且已完成2周安慰剂初始治疗的患者,开始接受尼卡地平治疗,剂量为每日30毫克至90毫克,分两到三次服用,每两周调整一次剂量。与安慰剂治疗相比,尼卡地平治疗显著降低了仰卧位和站立位的血压(p < 0.0004)。然而,心率没有显著变化。每日两次服用20毫克的患者中有46%(13/28)、每日三次服用10毫克的患者中有25%(7/28)、每日三次服用20毫克的患者中有18%(5/28)以及每日三次服用30毫克的患者中有11%(3/28)的仰卧位舒张压降至<90毫米汞柱。与安慰剂治疗期结束时相比,16周和24周的尼卡地平治疗未显著改变血脂水平。在研究期间未报告其他生化异常情况。除2例轻度足部水肿和2例短暂头痛外,未出现严重副作用。