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阿替洛尔对“混合型”心绞痛短暂性缺血影响的单盲、安慰剂对照研究。

A single-blind, placebo-controlled study of effects of atenolol on transient ischemia in "mixed" angina.

作者信息

Chierchia S, Glazier J J, Gerosa S

出版信息

Am J Cardiol. 1987 Jul 15;60(2):36A-40A. doi: 10.1016/0002-9149(87)90498-x.

DOI:10.1016/0002-9149(87)90498-x
PMID:3303885
Abstract

The efficacy of atenolol in preventing episodes of transient ischemia during daily life was evaluated in 10 patients with "mixed" angina who underwent a 4-week, single-blind, double-crossover placebo-controlled trial. On day 6 and 7 of each treatment phase, continuous ambulatory electrocardiographic monitoring was performed for 48 hours. On day 7 an exercise test was also performed. Two-hundred and sixty-four ischemic episodes (79% "silent") were recorded during placebo treatment; 98 were recorded during atenolol treatment (63% decrease, p less than 0.01). In agreement with previous observations, most ischemic episodes observed during placebo (156 or 59%) were not preceded by an increase in heart rate. Surprisingly, the beneficial effects of atenolol were more pronounced for these episodes than for those preceded by an increase in heart rate and apparently caused by an increase in myocardial demand (decreases of 72% and 48%, respectively). Painful and painless episodes were decreased by a similar extent. In all patients, the heart rate recorded at the beginning of ST-segment depression was widely variable and significantly lower with atenolol (64 +/- 14 beats/min) than with placebo (81 +/- 13 beats/min, p less than 0.05). During both placebo and atenolol treatment, the highest incidence of ischemic events was observed between 6 A.M. and 9 P.M., in coincidence with the highest levels of the heart rate resting.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对10例“混合型”心绞痛患者进行了一项为期4周的单盲、双交叉、安慰剂对照试验,以评估阿替洛尔在预防日常生活中短暂性缺血发作方面的疗效。在每个治疗阶段的第6天和第7天,进行48小时的动态心电图监测。在第7天还进行了运动试验。安慰剂治疗期间记录到264次缺血发作(79%为“无症状性”);阿替洛尔治疗期间记录到98次(减少63%,p<0.01)。与先前的观察结果一致,安慰剂治疗期间观察到的大多数缺血发作(156次或59%)之前心率没有增加。令人惊讶的是,阿替洛尔对这些发作的有益作用比对那些之前心率增加且显然由心肌需求增加引起的发作更明显(分别减少72%和48%)。疼痛性和无痛性发作减少的程度相似。在所有患者中,ST段压低开始时记录的心率差异很大,阿替洛尔组(64±14次/分钟)显著低于安慰剂组(81±13次/分钟,p<0.05)。在安慰剂和阿替洛尔治疗期间,缺血事件的最高发生率出现在上午6点至晚上9点之间,与静息心率的最高水平一致。(摘要截断于250字)

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