Fogari R, Poletti L, Tettamanti F, Cesana B, Savonitto S
Dipartimento di Medicina Interna e Terapia Medica, Università di Pavia, Italy.
G Ital Cardiol. 1990 Apr;20(4):309-15.
The aim of this study was to compare the effect of dilevalol and captopril on blood pressure and heart rate in hypertensive subjects, both at rest and during bicycle exercise. Thirty mild hypertensive patients (24 men, 6 women), aged 34-55, were studied in a randomized, double-blind, parallel group trial. After a 3-week placebo run-in, patients were randomized to receive either dilevalol (200 mg once daily) or captopril (50 mg twice daily) for 4 weeks. Dilevalol-treated patients whose diastolic blood pressure had not decreased by more than 8 mmHg from baseline (or to less than 95 mmHg) were given 400 mg once daily for a further 2 weeks. Treatment was stopped for all other patients. Blood pressure and heart rate were measured at rest and during bicycle exercise tests 4 ("peak") and 24 hours ("trough") after dosing in the dilevalol group and 4 ("peak") and 12 hours ("trough") after dosing in the captopril group. At the end of the placebo run-in, mean resting blood pressure was 156/102 mmHg in the dilevalol group and 157/103 in the captopril group. Six patients had blood pressure normalization with captopril and 9 with dilevalol 200 mg; a further 2 patients achieved normalized blood pressure levels with dilevalol 400 mg.(ABSTRACT TRUNCATED AT 250 WORDS)
本研究旨在比较双醋洛尔和卡托普利对高血压患者静息及自行车运动时血压和心率的影响。30例轻度高血压患者(24例男性,6例女性),年龄34 - 55岁,参与了一项随机、双盲、平行组试验。经过3周的安慰剂导入期后,患者被随机分为两组,分别接受双醋洛尔(每日一次,200毫克)或卡托普利(每日两次,50毫克)治疗4周。双醋洛尔治疗组中舒张压较基线下降未超过8 mmHg(或未降至95 mmHg以下)的患者,再给予每日一次400毫克的剂量,持续2周。其他所有患者停止治疗。在双醋洛尔组给药后4小时(“峰值”)和24小时(“谷值”)以及卡托普利组给药后4小时(“峰值”)和12小时(“谷值”),测量静息及自行车运动试验时的血压和心率。在安慰剂导入期结束时,双醋洛尔组的平均静息血压为156/102 mmHg,卡托普利组为157/103 mmHg。卡托普利治疗使6例患者血压正常化,双醋洛尔200毫克治疗使9例患者血压正常化;另有2例患者使用双醋洛尔400毫克后血压达到正常水平。(摘要截选至250字)