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[与肝素诱导的血小板减少症相关的十个问题]

[Ten questions related to heparin-induced thrombocytopenia].

作者信息

Toschi Vincenzo

机构信息

Servizio di Immunoematologia e Medicina Trasfusionale e Centro Emostasi e Trombosi, ASST Santi Paolo e Carlo, Milano.

出版信息

G Ital Cardiol (Rome). 2023 Jun;24(6):424-431. doi: 10.1714/4041.40201.

Abstract

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.

摘要

肝素诱导的血小板减少症(HIT)是一种潜在致命的、免疫介导的针对肝素(普通肝素和低分子肝素)的药物不良反应,它由针对由血小板衍生的PF4和肝素组成的表位的IgG抗体形成所引起。IgG与PF4/肝素新抗原的结合诱导血小板活化,这可能导致静脉或动脉血栓形成,并伴有血小板减少症。HIT的诊断基于检测前的临床概率评估和血小板活化抗体的检测。实验室诊断基于免疫学和功能测定。当诊断出HIT时,应立即停用任何类型的肝素,并必须开始使用非肝素替代抗凝剂以阻止血栓形成过程。阿加曲班和达那肝素目前是仅被批准用于治疗HIT的药物。比伐卢定和磺达肝癸钠也用于治疗这种罕见但严重的病症。

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