Moser M, Bode C
Innere Medizin III (Kardiologie), Universitätsklinik Freiburg, Hugstetter Strasse 55, Freiburg, Germany.
Internist (Berl). 2008 Sep;49(9):1031-7. doi: 10.1007/s00108-008-2074-3.
Inhibition of blood coagulation is an essential cornerstone of the therapy of acute myocardial infarction. Risk stratification represents a valuable tool to adjust the intensity of anticoagulation and timing of invasive therapy according to patient risk. All patients presenting with myocardial infarction should be treated with aspirin and clopidogrel. Patients with ST-segment elevation myocardial infarction and high-risk patients with myocardial infarction without ST-segment elevation who undergo invasive therapy should be treated immediately with unfractionated heparin (alternatively enoxaparin) and a glycoprotein (GP) IIb/IIIa antagonist in the catheter laboratory. The direct thrombin antagonist bivalirudin may emerge as an attractive alternative in these patients. In low-risk patients who undergo delayed urgent elective interventional therapy the factor Xa antagonist fondaparinux may be advantageous because of its low bleeding rate. In these patients administration of unfractionated heparin is necessary for percutaneous coronary intervention.
抑制血液凝固是急性心肌梗死治疗的重要基石。风险分层是根据患者风险调整抗凝强度和侵入性治疗时机的重要工具。所有心肌梗死患者均应接受阿司匹林和氯吡格雷治疗。ST段抬高型心肌梗死患者以及未出现ST段抬高的高危心肌梗死患者,若接受侵入性治疗,应在导管室立即使用普通肝素(也可用依诺肝素)和糖蛋白(GP)IIb/IIIa拮抗剂进行治疗。直接凝血酶拮抗剂比伐卢定可能成为这些患者有吸引力的替代药物。对于接受延迟紧急选择性介入治疗的低风险患者,Xa因子拮抗剂磺达肝癸钠可能因其低出血率而具有优势。在这些患者中,经皮冠状动脉介入治疗时必须使用普通肝素。