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

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

fondiparinux (Arixtra)治疗期间迟发性肝素诱导的2型血小板减少症。
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)是众所周知的肝素治疗的潜在致命副作用。HIT 1型(HIT-1)是短暂的,相对常见;通常在初次接触肝素后1-7天内发病。2型HIT (HIT-2)更为严重,与血小板减少和血栓形成有关。HIT-2通常在初次接触肝素后5天或更长时间发生。它是一种免疫介导的疾病,可能是由血小板活化抗体对血小板因子4 (PF4)/肝素复合物的发展引起的。Fondaparinux (Arixtra)是一种速效选择性Xa因子抑制剂,据信对HIT血清无反应,因此可用于有HIT-1或HIT-2病史的患者的血栓预防。目前使用氟达哌啶钠预防的患者很少出现HIT-2。在这里,我们提出了一个致命的病例延迟发作的HIT-2(1年后肝素暴露),而表现为fondaparinux预防。
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