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[运动诱发的无症状性心肌缺血患者服用缓释5-单硝酸异山梨酯3天后缺乏耐受性:与安慰剂对照]

[Lack of tolerance after administration of delayed-action isosorbide-5-mononitrate for 3 days in patients with exercise-induced silent ischemia: control with placebo].

作者信息

Scardi S, Pandullo C, Humar F, Spanghero M, Mazzone C

机构信息

Centro Cardiovascolare, Ospedale Maggiore, Trieste.

出版信息

G Ital Cardiol. 1992 May;22(5):549-57.

PMID:1426792
Abstract

In order to assess the development of tolerance we analyzed in a placebo-controlled study the effect of monotherapy with isosorbide-5-mononitrate (IS-5-MN) 60 mg in a controlled release formulation (Durules) once-a-day. The IS-5-MN was evaluated after the first dose and after once-a-day therapy for three days in 11 ambulatory patients (10 males, 1 female, aged 54 +/- 9 years) with stable exercise-induced silent myocardial ischaemia and significant coronary stenoses. The drug was given at 8 o'clock in the morning, and a bicycle ergometer exercise test was performed after 4 hours. The ST segment depression was evaluated by a computer-assisted system. Standing blood pressure decreased during all three periods of active treatment with IS-5-MN, (in comparison with placebo p < 0.001 and p < 0.01, p < 0.01 respectively). Heart rate did not change significantly. Compared with placebo baseline values, ischaemic threshold increased during the first day of treatment (188 sec, p < 0.0001 at 4 hours), and to a lesser extent both in second (103 sec, p < 0.003) and third day (116 sec, p < 0.003). The total exercise time increased during all three days of active therapy but significantly so only during the first day. The exercise stress test performed in the 5th day during placebo demonstrated a high reproducibility of ischaemic-threshold (235 vs 241 sec, p: ns), implying that the improvement during the active treatment with IS-5-MN was not due to a "training effect". Headache in 2 patients was the only significant side-effect.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为评估耐受性的发展,我们在一项安慰剂对照研究中,分析了采用控释制剂(杜利)每日一次服用60毫克5-单硝酸异山梨酯(IS-5-MN)进行单一疗法的效果。在11例患有稳定运动诱发型无症状心肌缺血且冠状动脉有明显狭窄的门诊患者(10名男性,1名女性,年龄54±9岁)中,于首剂用药后以及每日一次治疗三天后对IS-5-MN进行了评估。药物于上午8点服用,4小时后进行自行车测力计运动试验。采用计算机辅助系统评估ST段压低情况。在IS-5-MN所有三个积极治疗阶段,站立血压均下降(与安慰剂相比,p分别<0.001、p<0.01、p<0.01)。心率无显著变化。与安慰剂基线值相比,治疗第一天缺血阈值增加(4小时时为188秒,p<0.0001),第二天(103秒,p<0.003)和第三天(116秒,p<0.003)增加幅度较小。积极治疗的所有三天中总运动时间均增加,但仅第一天增加显著。在安慰剂治疗第5天进行的运动应激试验显示缺血阈值具有高度可重复性(235秒对241秒,p:无显著性差异),这意味着IS-5-MN积极治疗期间的改善并非由于“训练效应”。2例患者出现头痛,这是唯一显著的副作用。(摘要截取自250字)

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