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溶栓剂:具有临床意义的药物相互作用。

Thrombolytics: drug interactions of clinical significance.

作者信息

Harder S, Klinkhardt U

机构信息

Institute of Clinical Pharmacology of the J.W. Goethe University, Frankfurt am Main, Germany.

出版信息

Drug Saf. 2000 Nov;23(5):391-9. doi: 10.2165/00002018-200023050-00004.

Abstract

Thrombolytic agents activate plasminogen and induce a systemic fibrinolytic and anticoagulant state. Interaction of fibrinolysis with coagulation and platelet aggregation might be important for synergistic interactions with other antiplatelet or anticoagulant drugs. Thrombolytic agents are most often used in patients with coexisting cardiovascular medication, including various antihypertensives, beta-blocking agents, nitrates and aspirin (acetylsalicylic acid). In acute coronary syndromes, anticoagulants and antiplatelet compounds such as clopidogrel or glycoprotein IIb/IIIa receptor antagonists might be given. Inducers or inhibitors of the cytochrome P450 system are not reported to affect the pharmacokinetics of any thrombolytic agent. Since the elimination of the recombinant plasminogen activators saruplase and alteplase is dependent on liver blood flow, drugs affecting hepatic blood flow could theoretically affect the hepatic clearance of these agents. In fact, a reduction in thrombolytic activity has only been demonstrated for alteplase with nitroglycerin (glyceryl trinitrate). Pharmacodynamic interactions occur more often. The additive and beneficial effect of aspirin as concomitant therapy to thrombolysis has been demonstrated without excessive bleeding rates. No data are available on the interaction between ticlopidine or clopidogrel and thrombolytic agents in humans. Anticoagulation by heparin concomitantly with thrombolysis improves the patency rate of the occluded coronary vessel, but bleeding complications are seen more frequently. Although there has been no controlled study on the interaction between oral anticoagulants and thrombolytic agents, patients with myocardial infarction who were taking an oral anticoagulant before admission seem to be at higher risk for intracranial haemorrhage during thrombolytic therapy. Currently, no recommendations can be given for possible dose adjustment of thrombolytic therapy in patients receiving antiplatelet comedication. For comedication with heparin, it has been advised to monitor activated partial thromboplastin time frequently and to avoid values >2.5-fold normal. Patients receiving thrombolytic treatment should be monitored frequently for bleeding and the physician should be aware of any comedication exerting antiplatelet (e.g. aspirin, clopidogrel and ticlopidine) or anticoagulant (e.g. warfarin) effects.

摘要

溶栓药物可激活纤溶酶原并诱导全身性纤维蛋白溶解和抗凝状态。纤维蛋白溶解与凝血及血小板聚集之间的相互作用,对于与其他抗血小板或抗凝药物的协同相互作用可能很重要。溶栓药物最常用于同时服用心血管药物的患者,这些药物包括各种抗高血压药、β受体阻滞剂、硝酸盐类药物和阿司匹林(乙酰水杨酸)。在急性冠状动脉综合征中,可能会给予抗凝剂和抗血小板化合物,如氯吡格雷或糖蛋白IIb/IIIa受体拮抗剂。未报道细胞色素P450系统的诱导剂或抑制剂会影响任何溶栓药物的药代动力学。由于重组纤溶酶原激活剂沙芦普酶和阿替普酶的消除依赖于肝血流量,理论上影响肝血流量的药物可能会影响这些药物的肝脏清除率。事实上,仅在阿替普酶与硝酸甘油(三硝酸甘油酯)合用时,才证明其溶栓活性降低。药效学相互作用更为常见。已证明阿司匹林作为溶栓治疗的辅助疗法具有相加且有益的效果,且不会出现过高的出血率。尚无关于噻氯匹定或氯吡格雷与溶栓药物在人体中相互作用的数据。肝素与溶栓治疗同时进行抗凝可提高闭塞冠状动脉血管的通畅率,但出血并发症更为常见。尽管尚未有关于口服抗凝剂与溶栓药物相互作用的对照研究,但入院前服用口服抗凝剂的心肌梗死患者在溶栓治疗期间发生颅内出血的风险似乎更高。目前,对于接受抗血小板联合用药的患者,无法给出关于溶栓治疗可能的剂量调整建议。对于联合使用肝素的情况,建议频繁监测活化部分凝血活酶时间,并避免该值超过正常水平的2.5倍。接受溶栓治疗的患者应频繁监测出血情况,医生应了解任何具有抗血小板(如阿司匹林、氯吡格雷和噻氯匹定)或抗凝(如华法林)作用的联合用药情况。

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