J Cardiovasc Pharmacol. 1985;7 Suppl 1:S77-81. doi: 10.1097/00005344-198507001-00015.
A total of 270 patients with mild to moderate essential hypertension were evaluated in a multicenter double-blind randomized study that compared the effect of captopril plus a thiazide diuretic with that of propranolol plus a diuretic. All patients were previously uncontrolled with diuretics alone. Following a 4-week placebo control period, during which diuretic was not withdrawn, the patients were treated either with 37.5-75 mg/day of captopril (n = 133) or with 60-120 mg/day of propranolol (n = 137) for 12 weeks, the diuretic being continued in both groups. Blood pressure in both groups was significantly reduced after 2 weeks of treatment. Reduction in systolic but not diastolic blood pressure after 10 and 12 weeks of treatment was significantly greater in the captopril group than in the propranolol group (p less than 0.05). Treatment was considered to be effective in 77% of the captopril patients and in 61% of the propranolol group. The difference was significant (p less than 0.05). Side effects occurred in 6 of the 133 patients (4.5%) treated with captopril and in 16 of the 137 patients (11.7%) treated with propranolol. The difference between the two groups was significant (p less than 0.05). There were few significant changes in laboratory data in either group. The serious side effects previously reported with higher doses of captopril were not observed. The results indicate that low-dose captopril plus a diuretic is more efficacious than propranolol plus a diuretic in mild to moderate essential hypertension previously uncontrolled with a diuretic alone.
在一项多中心双盲随机研究中,对270例轻至中度原发性高血压患者进行了评估,该研究比较了卡托普利加噻嗪类利尿剂与普萘洛尔加利尿剂的效果。所有患者此前单独使用利尿剂时血压均未得到控制。在为期4周的安慰剂对照期内(在此期间利尿剂未停用),患者被随机分为两组,一组接受37.5 - 75毫克/天的卡托普利治疗(n = 133),另一组接受60 - 120毫克/天的普萘洛尔治疗(n = 137),为期12周,两组均继续使用利尿剂。治疗2周后,两组血压均显著降低。治疗10周和12周后,卡托普利组收缩压的降低幅度显著大于普萘洛尔组,而舒张压降低幅度两组无显著差异(p < 0.05)。卡托普利组77%的患者治疗有效,普萘洛尔组为61%。差异具有统计学意义(p < 0.05)。接受卡托普利治疗的133例患者中有6例(4.5%)出现副作用,接受普萘洛尔治疗的137例患者中有16例(11.7%)出现副作用。两组之间的差异具有统计学意义(p < 0.05)。两组实验室数据均无明显显著变化。未观察到之前报道的高剂量卡托普利出现的严重副作用。结果表明,在轻至中度原发性高血压患者中,此前单独使用利尿剂血压未得到控制时,低剂量卡托普利加利尿剂比普萘洛尔加利尿剂更有效。