Rademaker M, Corrie J, Lindsay B A, Flapan A D, Padfield P L
Department of Medicine, Western General Hospital, Edinburgh, Scotland, UK.
J Hum Hypertens. 1989 Jun;3(3):173-7.
Thirty patients with moderate to severe, uncontrolled hypertension were treated with a captopril/frusemide combination. The initial dose of captopril (6.25 mg or 12.5 mg) produced an acute fall in BP from 162 +/- 6/102 +/- 3 to 132 +/- 6/85 +/- 3 mmHg but at a dose of 12.5 mg three times daily outpatient BPs were not controlled. Frusemide (40 mg/day) was added and increased as necessary at two week intervals until BP was satisfactorily controlled or a total daily dose of 160 mg was reached. During long-term follow-up over a mean period of two years good BPs were achieved with an average daily dose of frusemide of 95 mg and captopril 52 mg (148 +/- 3/90 +/- 2 mmHg). There was no overall change in renal function or plasma potassium although small rises in blood urea were seen in some patients. In a group of 28 patients controlled on this regimen a change to a twice daily schedule without alteration of the dose of captopril or frusemide did not affect clinic BPs. In addition, BP remained controlled throughout the day as measured at home with an electronic sphygmomanometer. No case of glucose interolence was observed despite high doses of frusemide (HbA1 = 7.1 +/- 0.12%) and in 12 patients, where prospective measurements of HbA1 were measured, there was a fall from 7.6 +/- 0.21% to 6.9 +/- 0.16% suggesting an effect of captopril on insulin sensitivity. We conclude that low dose captopril with a variable frusemide dosage represents a simple and effective treatment for moderate to severe hypertension.
30例中重度、血压控制不佳的高血压患者接受卡托普利/速尿联合治疗。卡托普利初始剂量(6.25毫克或12.5毫克)使血压从162±6/102±3急性降至132±6/85±3毫米汞柱,但每日3次服用12.5毫克剂量时,门诊血压未得到控制。加入速尿(40毫克/天),并根据需要每两周增加剂量,直至血压得到满意控制或达到每日160毫克的总剂量。在平均为期两年的长期随访中,平均每日速尿剂量95毫克、卡托普利52毫克时,血压控制良好(148±3/90±2毫米汞柱)。尽管部分患者血尿素略有升高,但肾功能或血钾无总体变化。在一组按此方案血压得到控制的28例患者中,改为每日2次服药方案,卡托普利或速尿剂量不变,未影响门诊血压。此外,用电子血压计在家测量显示,全天血压均得到控制。尽管速尿剂量较大(糖化血红蛋白A1=7.1±0.12%),但未观察到糖耐量异常病例;在12例对糖化血红蛋白A1进行前瞻性测量的患者中,糖化血红蛋白A1从7.6±0.21%降至6.9±0.16%,提示卡托普利对胰岛素敏感性有影响。我们得出结论,低剂量卡托普利联合可变剂量速尿是治疗中重度高血压的一种简单有效的方法。