肝素诱导血小板减少症
阿加曲班
磺达肝素
肝素
比伐卢定
医学
血小板因子4
抗凝剂
低分子肝素
血小板
血小板活化
血栓形成
直接凝血酶抑制剂的发现与发展
药理学
抗体
免疫学
内科学
凝血酶
静脉血栓栓塞
心肌梗塞
经皮冠状动脉介入治疗
出处
期刊:PubMed
日期:2023-06-01
卷期号:24 (6): 424-431
摘要
Heparin-induced thrombocytopenia (HIT) is a potentially fatal, immune-mediated adverse drug reaction to heparin (both unfractionated and low molecular weight heparin) which is caused by the formation of IgG antibodies against an epitope composed by platelet-derived PF4 and heparin. Binding of IgG to PF4/heparin neoantigen induces platelet activation which may cause venous or arterial thrombosis, associated with thrombocytopenia. HIT diagnosis is based on both pre-test clinical probability evaluation and the detection of platelet activating antibodies. Laboratory diagnosis is based on immunologic and functional assays. When HIT is diagnosed any type of heparin should be stopped immediately and non-heparin alternative anticoagulant must be started in order to halt the pro-thrombotic process. Argatroban and danaparoid are currently the only drugs approved for HIT treatment. Bivalirudin and fondaparinux are also used for the treatment of this rare but severe condition.
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