Bremner A D, Baur M, Oddou-Stock P, Bodin F
Health Centre, Glasgow, Scotland, UK.
Clin Exp Hypertens. 1997 Nov;19(8):1263-85. doi: 10.3109/10641969709083217.
A total of 501 elderly patients with essential hypertension were randomized to receive valsartan or lisinopril in this one year multi-center, double-blind, parallel group trial. Patients received valsartan 40 mg (n = 334) or lisinopril 2.5 mg (n = 167) daily for 2 weeks with subsequent titration (alone or in combination with hydroclorothiazide), depending on response to treatment. The primary efficacy variable was the percentage of patients with a response, defined as sitting diastolic blood pressure < 90 mmHg or drop of > or = 10 mmHg from baseline. A high percentage of patients responded to treatment in both valsartan and lisinopril groups: 80% for both groups at 12 weeks and 81% and 87%, respectively, at 52 weeks with no statistically significant difference between treatments (12 weeks, p = 0.925; 52 weeks, p = 0.148). More patients on lisinopril experienced drug-related cough (7.5% on valsartan, 17.4% on lisinopril). In 5.4% of lisinopril treated patients, cough led to discontinuation of therapy compared to 0.6% on valsartan. Valsartan 80 mg daily provides comparable short and long-term antihypertensive efficacy to lisinopril in elderly patients with a lower incidence of drug-related cough.
在这项为期一年的多中心、双盲、平行组试验中,共有501例老年原发性高血压患者被随机分配接受缬沙坦或赖诺普利治疗。患者每日服用缬沙坦40毫克(n = 334)或赖诺普利2.5毫克(n = 167),持续2周,随后根据治疗反应进行滴定(单独或与氢氯噻嗪联合使用)。主要疗效变量是有反应的患者百分比,定义为坐位舒张压<90毫米汞柱或较基线下降≥10毫米汞柱。缬沙坦组和赖诺普利组中都有很高比例的患者对治疗有反应:12周时两组均为80%,52周时分别为81%和87%,治疗之间无统计学显著差异(12周,p = 0.925;52周,p = 0.148)。更多服用赖诺普利的患者出现与药物相关的咳嗽(缬沙坦组为7.5%,赖诺普利组为17.4%)。在接受赖诺普利治疗的患者中,5.4%的患者因咳嗽导致停药,而缬沙坦组为0.6%。每日服用80毫克缬沙坦在老年患者中提供了与赖诺普利相当的短期和长期降压疗效,且药物相关咳嗽的发生率较低。