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贝那普利对慢性稳定型心绞痛患者心肌缺血的影响。

Effect of benazepril on myocardial ischaemia in patients with chronic stable angina pectoris.

作者信息

Tzivoni D, Gottlieb S, Khurmi N S, Medina A, Gavish A, Stern S

机构信息

Heiden Department of Cardiology, Bikur Cholim Hospital, Jerusalem, Israel.

出版信息

Eur Heart J. 1992 Aug;13(8):1129-34. doi: 10.1093/oxfordjournals.eurheartj.a060325.

Abstract

The anti-ischaemic properties of benazepril, a non-sulfhydryl inhibitor of angiotensin-converting enzyme, were assessed in 20 patients with chronic stable angina pectoris, by repeated exercise tests and repeated 72-h ambulatory electrocardiographic monitoring. The study was a double-blind, placebo-controlled cross-over; 11 patients received benazepril 10 mg b.i.d. and nine received 20 mg b.i.d. All patients had a positive treadmill stress test and at least three ischaemic episodes during 24 h of ambulatory electrocardiographic monitoring. Benazepril at a dose of 10 mg b.i.d. did not improve the exercise duration, the time taken to reach 1 mm ST depression. Similar findings were observed during treatment with 20 mg b.i.d. Benazepril at a dose of 10 mg b.i.d. was ineffective in improving ischaemic parameters during daily activities. However, among the nine patients who received 20 mg b.i.d. the number of ischaemic episodes was reduced from 142 to 103, and the total duration of ischaemic was reduced from 1099 to 531 min. The number of weekly anginal attacks was reduced from 58 to 33, and the weekly sublingual nitroglycerin tablets consumption was reduced from 31 to 14. When the two doses (10 mg and 20 mg) were combined (N = 20), the number of ischaemic episodes was reduced from 314 to 260 (P = 0.074), and the duration of ischaemic was reduced from 3453 to 2514 min (P = 0.072).

摘要

贝那普利是一种非巯基血管紧张素转换酶抑制剂,通过重复运动试验和重复72小时动态心电图监测,对20例慢性稳定型心绞痛患者的抗缺血特性进行了评估。该研究为双盲、安慰剂对照交叉试验;11例患者接受每日两次10毫克贝那普利治疗,9例患者接受每日两次20毫克贝那普利治疗。所有患者平板运动试验均为阳性,且在24小时动态心电图监测期间至少有三次缺血发作。每日两次10毫克剂量的贝那普利未改善运动持续时间,即达到ST段压低1毫米所需的时间。每日两次20毫克剂量治疗期间观察到类似结果。每日两次10毫克剂量的贝那普利在改善日常活动期间的缺血参数方面无效。然而,在接受每日两次20毫克剂量的9例患者中,缺血发作次数从142次减少至103次,缺血总时长从1099分钟减少至531分钟。每周心绞痛发作次数从58次减少至33次,每周舌下含服硝酸甘油片的用量从31片减少至14片。当将两种剂量(10毫克和20毫克)联合使用时(N = 20),缺血发作次数从314次减少至260次(P = 0.074),缺血时长从3453分钟减少至2514分钟(P = 0.072)。

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