Skoularigis J, Strugo V, Zambakides C, Eintracht S, Reddy K, Tshele E, Smith D, Sareli P
Division of Cardiology, Baragwanath Hospital, Johannesburg, South Africa.
Int J Clin Pharmacol Ther. 1996 Jun;34(6):263-8.
A double-blind, randomized, parallel-group study was performed to compare the efficacy and tolerability of captopril-thiazide and enalapril-thiazide combinations. After a 3-week placebo run-in period, 47 Black patients with mild to moderate essential hypertension (mean 24-hour diastolic blood pressure (BP) > 90 mmHg and < 115 mmHg) were randomized to receive 1 of 2 combination tablets: captopril 50 mg plus hydrochlorothiazide 25 mg (CAP, n = 24) or enalapril 20 mg plus hydrochlorothiazide 12.5 mg (COR, n = 23) once daily. After 12 weeks of active treatment the mean 24-hour ambulatory BP was reduced from 152 +/- 11/99 +/- 6 to 133 +/- 13/86 +/- 7 mmHg (p < 0.005) in the CAP group and 157 +/- 15/100 +/- 6 to 141 +/- 18/90 +/- 12 in the COR group (p < 0.005). Target BP (24-hour diastolic BP < 90 mmHg) was achieved in 75% (18/24) of patients on CAP and 48% (11/23) on COR (p = n.s.). 24-hour BP load fell significantly with both CAP (from 69% to 34%, p < 0.001) and COR (from 67% to 37%, p < 0.001). Left ventricular mass index decreased by 7% with CAP and 11% with COR. Cardiac index and fractional shortening remained essentially unchanged in both groups. Both treatments were well tolerated and overall incidence of side effects was very low. It is concluded that both CAP and COR are effective, safe first-line antihypertensive choices in Black patients with mild to moderate hypertension with the former showing a trend towards greater efficacy than the latter.
进行了一项双盲、随机、平行组研究,以比较卡托普利-噻嗪组合与依那普利-噻嗪组合的疗效和耐受性。在为期3周的安慰剂导入期后,47例轻度至中度原发性高血压黑人患者(平均24小时舒张压(BP)>90 mmHg且<115 mmHg)被随机分配接受2种复方片剂中的1种:卡托普利50 mg加氢氯噻嗪25 mg(CAP组,n = 24)或依那普利20 mg加氢氯噻嗪12.5 mg(COR组,n = 23),每日1次。积极治疗12周后,CAP组的平均24小时动态血压从152±11/99±6 mmHg降至133±13/86±7 mmHg(p<0.005),COR组从157±15/100±6 mmHg降至141±18/90±12 mmHg(p<0.005)。CAP组75%(18/24)的患者和COR组48%(11/23)的患者达到目标血压(24小时舒张压<90 mmHg)(p=无统计学意义)。CAP组和COR组的24小时血压负荷均显著下降(分别从69%降至34%,p<0.001;从67%降至37%,p<0.001)。CAP组左心室质量指数下降7%,COR组下降11%。两组的心脏指数和缩短分数基本保持不变。两种治疗耐受性良好,副作用总发生率很低。结论是,CAP和COR都是治疗轻度至中度高血压黑人患者有效的、安全的一线降压选择,前者的疗效有高于后者的趋势。