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急性心肌梗死中静脉注射组织型纤溶酶原激活剂与早期静脉注射肝素的随机对照试验。

A randomized controlled trial of intravenous tissue plasminogen activator and early intravenous heparin in acute myocardial infarction.

作者信息

Topol E J, George B S, Kereiakes D J, Stump D C, Candela R J, Abbottsmith C W, Aronson L, Pickel A, Boswick J M, Lee K L

机构信息

Department of Internal Medicine, University of Michigan, Ann Arbor.

出版信息

Circulation. 1989 Feb;79(2):281-6. doi: 10.1161/01.cir.79.2.281.

DOI:10.1161/01.cir.79.2.281
PMID:2492454
Abstract

To evaluate the coronary thrombolytic efficacy of tissue plasminogen activator (t-PA) and early intravenous heparin, 134 patients with acute myocardial infarction were randomly assigned to combination therapy or t-PA only. At a median of 2.78 hours from symptom onset, 64 patients received both t-PA (1.5 mg/kg/4 hr) and a bolus of 10,000 units heparin, whereas 70 patients received t-PA alone at the same dose. All patients underwent coronary angiography 90 minutes after initiation of therapy to determine infarct vessel patency status, after which time the control group patients were eligible to receive heparin. Baseline demographic and angiographic characteristics were similar for the groups. Infarct vessel patency was 50 of 63 (79%) for combination t-PA and heparin and 54 of 68 (79%) for t-PA alone. Bleeding complications, as reflected by need for transfusion, were similar in the two groups: 13% in the patients treated with t-PA and heparin compared with 18% in patients treated with t-PA only (p = 0.53). The only intracranial hemorrhage in the trial occurred in a patient initially treated without heparin. Fibrinogen at 50 minutes after therapy was 32% decreased from baseline for the t-PA and heparin-treated patients compared with a 39% decrease in the control group. Predischarge left ventricular ejection fraction was similar for the two groups: 49.0 +/- 10.1% versus 50.2 +/- 11.9% for combined versus t-PA only therapy, respectively. We conclude that early intravenous heparin does not facilitate the fibrinolytic effect of t-PA at the doses tested.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为评估组织型纤溶酶原激活剂(t-PA)和早期静脉注射肝素的冠状动脉溶栓疗效,134例急性心肌梗死患者被随机分为联合治疗组或仅用t-PA组。在症状发作后的中位时间2.78小时,64例患者接受了t-PA(1.5mg/kg/4小时)和10000单位肝素的静脉推注,而70例患者接受相同剂量的单独t-PA治疗。所有患者在治疗开始后90分钟接受冠状动脉造影以确定梗死血管通畅情况,此后对照组患者有资格接受肝素治疗。两组的基线人口统计学和血管造影特征相似。联合使用t-PA和肝素治疗的63例患者中有50例(79%)梗死血管通畅,单独使用t-PA治疗的68例患者中有54例(79%)梗死血管通畅。两组因输血需求反映出的出血并发症相似:t-PA和肝素治疗的患者为13%,仅接受t-PA治疗的患者为18%(p=0.53)。该试验中唯一的颅内出血发生在最初未接受肝素治疗的一名患者身上。治疗后50分钟,t-PA和肝素治疗患者的纤维蛋白原较基线下降32%,而对照组下降39%。两组出院前左心室射血分数相似:联合治疗组为49.0±10.1%,仅用t-PA治疗组为50.2±11.9%。我们得出结论,在所测试的剂量下,早期静脉注射肝素并不能促进t-PA的纤溶作用。(摘要截短为250字)

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