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磺达肝癸钠(安卓)治疗期间发生的迟发性2型肝素诱导的血小板减少症。

Delayed-onset heparin-induced thrombocytopenia type-2 during fondiparinux (Arixtra) therapy.

作者信息

Modi Chirag, Satani Dhaval, Cervellione Kelly L, Cervantes Jose, Gintautas Jonas

机构信息

Jamaica Hospital Medical Center, Jamaica, NY, USA.

出版信息

Proc West Pharmacol Soc. 2009;52:5-7.

Abstract

Heparin is the most commonly used anticoagulant drug for prevention and treatment of thromboembolic diseases. Heparin-induced thrombocytopenia (HIT) is a well-known and potentially fatal side-effect of heparin therapy. HIT type 1 (HIT-1) is transient and relatively common; it usually develops within 1-7 days of initial heparin exposure. Type 2 HIT (HIT-2) is more severe and is associated with thrombocytopenia and thrombosis. HIT-2 usually develops 5 or more days after initial heparin exposure. It is an immune-mediated disorder that is presumably caused by development of platelet activating antibody against platelet factor 4 (PF4)/heparin complex. Fondaparinux (Arixtra) is a fast-acting selective inhibitor of factor Xa believed to be non-reactive to HIT sera and therefore may be used as prophylaxis for thrombosis in patients with a history of HIT-1 or HIT-2. Development of HIT-2 in patients currently taking fondaparinux prophylaxis is rare. Here we present a fatal case of delayed-onset HIT-2 (1 year after heparin exposure) manifesting while on fondaparinux prophylaxis.

摘要

肝素是预防和治疗血栓栓塞性疾病最常用的抗凝药物。肝素诱导的血小板减少症(HIT)是肝素治疗一种众所周知且可能致命的副作用。1型HIT(HIT-1)是短暂的且相对常见;通常在初次接触肝素后的1 - 7天内发生。2型HIT(HIT-2)更严重,与血小板减少症和血栓形成有关。HIT-2通常在初次接触肝素5天或更久之后发生。它是一种免疫介导的疾病,推测是由针对血小板因子4(PF4)/肝素复合物的血小板活化抗体的产生所引起。磺达肝癸钠(安卓)是一种起效迅速的Xa因子选择性抑制剂,据信对HIT血清无反应,因此可用于有HIT-1或HIT-2病史患者的血栓形成预防。目前正在接受磺达肝癸钠预防治疗的患者中发生HIT-2的情况罕见。在此,我们报告一例延迟发生的HIT-2(肝素接触后1年)致死病例,该病例在接受磺达肝癸钠预防治疗时出现。

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