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急性心肌梗死患者静脉推注阿替普酶后的冠状动脉再通率。

Coronary recanalization rate after intravenous bolus of alteplase in acute myocardial infarction.

作者信息

Tranchesi B, Chamone D F, Cobbaert C, Van de Werf F, Vanhove P, Verstraete M

机构信息

Instituto do Coraaâo (INCOR), University of São Paulo, Brazil.

出版信息

Am J Cardiol. 1991 Jul 15;68(2):161-5. doi: 10.1016/0002-9149(91)90737-6.

DOI:10.1016/0002-9149(91)90737-6
PMID:1829574
Abstract

The demonstration in animals that recombinant tissue-type plasminogen activator produces prolonged thrombolysis after its clearance from the circulation has prompted a few pilot studies of bolus administration in patients. Alteplase (bolus dose of 70 mg) resulted in the highest recanalization rate in our previous pilot study comparing bolus doses of 50, 60 and 70 mg of alteplase in patients with acute myocardial infarction. The aim of the present trial was to assess the efficacy and safety of the same bolus dose in a larger number of patients. A further objective was to study the angiographic reocclusion rate at 12 to 24 hours in patients who had a recanalized infarct-related coronary artery at 90 minutes and were randomized at that time to a bolus dose or an infusion for 3 hours of 30 mg of alteplase. Sixty patients with acute myocardial infarction and angiographically documented total occlusion of the infarct-related coronary artery before thrombolysis were treated within 5 hours of onset of symptoms with an intravenous 70-mg bolus dose of alteplase (or 80 mg if body weight was greater than or equal to 90 kg). Each patient received 5,000 IU of heparin intraarterially and 100 mg of aspirin by mouth before administration of alteplase. Coronary angiography was repeated 60 and 90 minutes after alteplase administration. The recanalization rate of the infarct-related coronary artery was 55% (95% confidence interval, 43 to 66%) at 60 minutes and 48% (95% confidence interval, 37 to 60%) at 90 minutes. Pretreatment levels of lipoprotein (a) were not significantly related to recanalization.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

动物实验表明,重组组织型纤溶酶原激活剂从循环中清除后仍能产生延长的溶栓作用,这促使了一些关于在患者中推注给药的初步研究。在我们之前的一项初步研究中,比较了急性心肌梗死患者使用50毫克、60毫克和70毫克阿替普酶推注剂量,结果显示阿替普酶(推注剂量70毫克)导致再通率最高。本试验的目的是评估在更多患者中使用相同推注剂量的疗效和安全性。另一个目标是研究在90分钟时梗死相关冠状动脉再通且当时随机接受30毫克阿替普酶推注剂量或3小时输注的患者在12至24小时的血管造影再闭塞率。60例急性心肌梗死且溶栓前血管造影记录梗死相关冠状动脉完全闭塞的患者在症状发作5小时内接受静脉推注70毫克阿替普酶(如果体重≥90千克则为80毫克)治疗。每位患者在给予阿替普酶前动脉内接受5000国际单位肝素和口服100毫克阿司匹林。阿替普酶给药后60分钟和90分钟重复进行冠状动脉造影。梗死相关冠状动脉的再通率在60分钟时为55%(95%置信区间,43%至66%),在90分钟时为48%(95%置信区间,37%至60%)。脂蛋白(a)的治疗前水平与再通无显著相关性。(摘要截选至250字)

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