CMAJ. 1987 Nov 1;137(9):803-8.
Therapy with 10 to 40 mg once daily of enalapril, a new angiotensin converting enzyme inhibitor, was compared with therapy with 50 to 100 mg once daily of atenolol in a double-blind randomized multicentre trial in 180 patients with a diastolic blood pressure (determined with the patient seated) of 95 to 115 mm Hg between March 1984 and April 1986. A total of 86 patients (61 men and 25 women with a mean age of 49.4 years and a mean blood pressure [and standard deviation] at entry into the trial of 155.5 [15.7]/101.0 [6.3] mm Hg) received enalapril, and 94 patients (63 men and 31 women with a mean age of 50.9 years and a mean blood pressure at entry of 156.6 [16.6]/101.2 [5.7] mm Hg) received atenolol. After a placebo run-in period the patients received increasing dosages of medication every 2 weeks until the target diastolic blood pressure of 90 mm Hg or less was achieved on two consecutive visits, the maximum dosage was reached, or the patient withdrew because of adverse effects. At 14 weeks the mean blood pressure was 141.6 (18.0)/90.1 (9.5) mm Hg in the enalapril group (61 patients) and 140.0 (17.1)/88.4 (8.7) mm Hg in the atenolol group (54 patients). The target diastolic blood pressure was achieved on completion of therapy (between weeks 10 and 14) in 67 (77%) of the patients receiving enalapril and 75 (79%) of the patients receiving atenolol. Compliance was similar in the two groups. Seven patients withdrew because of adverse effects, three in the enalapril group and four in the atenolol group. The results suggest that once-daily monotherapy with enalapril, 10 to 40 mg, is effective in the treatment of mild to moderate hypertension and is as effective as and tolerated as well as once-daily therapy with atenolol, 50 to 100 mg.
1984年3月至1986年4月,在一项双盲随机多中心试验中,对180例舒张压(患者坐位时测定)为95至115毫米汞柱的患者进行了比较,一组接受每日一次10至40毫克的新型血管紧张素转换酶抑制剂依那普利治疗,另一组接受每日一次50至100毫克的阿替洛尔治疗。共有86例患者(61名男性和25名女性,平均年龄49.4岁,试验开始时平均血压[及标准差]为155.5[15.7]/101.0[6.3]毫米汞柱)接受依那普利治疗,94例患者(63名男性和31名女性,平均年龄50.9岁,试验开始时平均血压为156.6[16.6]/101.2[5.7]毫米汞柱)接受阿替洛尔治疗。在经过安慰剂导入期后,患者每2周增加一次药物剂量,直至连续两次就诊时达到目标舒张压90毫米汞柱或更低、达到最大剂量或患者因不良反应退出。在第14周时,依那普利组(61例患者)的平均血压为141.6(18.0)/90.1(9.5)毫米汞柱,阿替洛尔组(54例患者)的平均血压为140.0(17.1)/88.4(8.7)毫米汞柱。接受依那普利治疗的患者中有67例(77%)在治疗结束时(第10至14周之间)达到目标舒张压,接受阿替洛尔治疗的患者中有75例(79%)达到目标舒张压。两组的依从性相似。7例患者因不良反应退出,依那普利组3例,阿替洛尔组4例。结果表明,每日一次服用10至40毫克依那普利进行单一疗法治疗轻至中度高血压有效,其疗效与每日一次服用50至100毫克阿替洛尔相当,耐受性也相似。