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使用组织型纤溶酶原激活剂进行冠状动脉溶栓后发生颅内出血。

Intracranial hemorrhage after use of tissue plasminogen activator for coronary thrombolysis.

作者信息

Kase C S, O'Neal A M, Fisher M, Girgis G N, Ordia J I

机构信息

Boston University School of Medicine, Massachusetts.

出版信息

Ann Intern Med. 1990 Jan 1;112(1):17-21. doi: 10.7326/0003-4819-112-1-17.

Abstract

Tissue plasminogen activator (tPA), an approved coronary thrombolytic agent, can cause serious bleeding. We report the cases of six patients with intracranial hemorrhage after tPA treatment for acute myocardial infarction. None of the patients were hypertensive at admission, and only one was hypertensive during therapy. Intravenous tPA, 100 mg, was followed by continuous intravenous heparin infusion; intracranial hemorrhage occurred between 2 and 14 hours after tPA infusion ended and between 3 and 17 hours after heparin therapy was started. The partial thromboplastin time (PTT) was excessively prolonged (from 81 s to more than 150 s) in all patients at onset of intracranial hemorrhage. The intracerebral hematomas were predominantly of lobar location, and two patients had multiple simultaneous hemorrhages. Four patients died from massive intracranial hemorrhage; the mechanism for these hemorrhages was unclear. Factors possibly related to hemorrhage include a systemic fibrinolytic state or a platelet anti-aggregant effect produced by tPA and enhanced hemorrhagic tendency caused by the combined effects of tPA and heparin. Local vascular changes at the bleeding site remain as potential contributing factors for isolated intracranial hemorrhage.

摘要

组织型纤溶酶原激活剂(tPA)是一种已获批准的冠状动脉溶栓剂,可导致严重出血。我们报告了6例急性心肌梗死患者接受tPA治疗后发生颅内出血的病例。所有患者入院时均无高血压,治疗期间仅1例出现高血压。静脉注射100mg tPA后,持续静脉输注肝素;颅内出血发生在tPA输注结束后2至14小时以及肝素治疗开始后3至17小时之间。所有患者颅内出血发作时部分凝血活酶时间(PTT)均过度延长(从81秒延长至150秒以上)。脑内血肿主要位于脑叶,2例患者同时出现多处出血。4例患者死于大量颅内出血;这些出血的机制尚不清楚。可能与出血相关的因素包括全身纤溶状态或tPA产生的血小板抗聚集作用,以及tPA与肝素联合作用导致的出血倾向增强。出血部位的局部血管变化仍然是孤立性颅内出血的潜在促成因素。

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