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贝那普利与美托洛尔控释片单用及联用对慢性稳定性心绞痛患者心肌缺血的影响

Effects of benazepril and metoprolol OROS alone and in combination on myocardial ischemia in patients with chronic stable angina.

作者信息

Klein W W, Khurmi N S, Eber B, Dusleag J

机构信息

Department of Cardiology, University Hospital, Graz, Austria.

出版信息

J Am Coll Cardiol. 1990 Oct;16(4):948-56. doi: 10.1016/s0735-1097(10)80347-x.

Abstract

The efficacy of benazepril, metoprolol OROS and their combination was evaluated in 29 patients (42 to 74 years of age) with chronic stable angina and documented coronary artery disease in a placebo-controlled, double-blind, crossover trial using serial quantitated exercise testing and ambulatory electrocardiographic (ECG) monitoring. The mean (+/- SEM) exercise time was 8.5 +/- 0.7 min with placebo, 8.3 +/- 0.6 min (95% confidence interval [CI]-1.06 to 0.54) with benazepril, 9.4 +/- 0.5 min (95% CI -0.32 to 2.14) with metoprolol OROS and 9.6 +/- 0.5 min (95% CI -0.25 to 2.47) with the combination of benazepril and metoprolol OROS. The mean exercise time to the development of 1 mm ST segment depression was prolonged from 6.0 +/- 0.6 min with placebo to 6.3 +/- 0.6 min (95% CI -0.93 to 1.45) with benazepril, 7.9 +/- 0.5 min (95% CI 0.83 to 3.0) with metoprolol OROS and 8.1 +/- 0.6 min (95% CI 0.88 to 3.29) with the combination of benazepril and metoprolol OROS. Benazepril did not alter the rest or maximal heart rate, whereas metoprolol OROS alone and in combination significantly lowered the heart rate at rest and during maximal exercise. Systolic blood pressure at rest was nonsignificantly reduced, whereas diastolic blood pressure was lowered significantly by all treatments in comparison with placebo. At maximal exercise, only metoprolol OROS, whether given alone or in combination with benazepril, was able to blunt significantly systolic blood pressure and rate-pressure product.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在一项安慰剂对照、双盲、交叉试验中,采用连续定量运动试验和动态心电图(ECG)监测,对29例(42至74岁)慢性稳定型心绞痛且有冠状动脉疾病记录的患者,评估了贝那普利、美托洛尔控释片及其联合用药的疗效。安慰剂组平均(±标准误)运动时间为8.5±0.7分钟,贝那普利组为8.3±0.6分钟(95%置信区间[CI] -1.06至0.54),美托洛尔控释片组为9.4±0.5分钟(95% CI -0.32至2.14),贝那普利与美托洛尔控释片联合用药组为9.6±0.5分钟(95% CI -0.25至2.47)。出现1毫米ST段压低的平均运动时间从安慰剂组的6.0±0.6分钟延长至贝那普利组的6.3±0.6分钟(95% CI -0.93至1.45),美托洛尔控释片组为7.9±0.5分钟(95% CI 0.83至3.0),贝那普利与美托洛尔控释片联合用药组为8.1±0.6分钟(95% CI 0.88至3.29)。贝那普利未改变静息或最大心率,而美托洛尔控释片单独使用及联合使用均显著降低静息和最大运动时的心率。静息收缩压无显著降低,而与安慰剂相比,所有治疗均显著降低舒张压。在最大运动时,只有美托洛尔控释片,无论单独使用还是与贝那普利联合使用,都能显著降低收缩压和心率-血压乘积。(摘要截断于250字)

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