Os I, Bratland B, Dahløf B, Gisholt K, Syvertsen J O, Tretli S
Department of Medicine, Ullevål Hospital, University of Oslo, Norway.
J Hypertens. 1991 Dec;9(12):1097-104.
In a randomized, parallel, double-blind study, lisinopril (n = 412; average dose 18.8 mg) reduced systolic and diastolic blood pressure (change = 20.2/13.8 mmHg; P less than 0.01/P less than 0.01) more than nifedipine (n = 416; average dose 37.4 mg; change = 13.3/11.2 mmHg) after 10-week treatment in patients, aged 40-70 years, with mild-to-moderate essential hypertension. Lisinopril was better tolerated than nifedipine. The withdrawals from treatment were fewer in the lisinopril-treated group (11 versus 46; P less than 0.01). The frequency of adverse experiences reported after a general question of discomfort was significantly lower for lisinopril than for nifedipine (P less than 0.01). When questioned on specific symptoms, frequency of coughing was higher with lisinopril (P less than 0.01), while flushing, edema, palpitations, dizziness, tiredness and rash were reported more frequently (P less than 0.01, for all) in the nifedipine-treated group. Quality of life was assessed by both patients and spouses. No significant changes in wellbeing were observed for either drug, except for the highest dose level of nifedipine which caused a deterioration.
在一项随机、平行、双盲研究中,对于年龄在40至70岁、患有轻度至中度原发性高血压的患者,经过10周治疗后,赖诺普利(n = 412;平均剂量18.8毫克)降低收缩压和舒张压的幅度(变化值 = 20.2/13.8毫米汞柱;P < 0.01/P < 0.01)大于硝苯地平(n = 416;平均剂量37.4毫克;变化值 = 13.3/11.2毫米汞柱)。赖诺普利的耐受性优于硝苯地平。赖诺普利治疗组的治疗退出人数较少(11人对46人;P < 0.01)。在询问一般不适问题后报告的不良事件发生率,赖诺普利显著低于硝苯地平(P < 0.01)。在询问具体症状时,赖诺普利组咳嗽的发生率较高(P < 0.01),而硝苯地平治疗组潮红、水肿、心悸、头晕、疲劳和皮疹的报告更为频繁(所有P值均 < 0.01)。生活质量由患者及其配偶进行评估。除了最高剂量水平的硝苯地平导致生活质量恶化外,两种药物均未观察到幸福感有显著变化。