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[肝素诱导的血小板减少症。新的治疗选择]

[Heparin-induced thrombocytopenia. New therapeutical options].

作者信息

Seculini Patiño Carina E, Tabares Aldo H

机构信息

Servicio de Clínica Médica, Hospital Privado Centro Médico de Córdoba, Córdoba, Argentina. E-mail:

Servicio de Medicina Vascular y Trombosis, Hospital Privado Centro Médico de Córdoba, Córdoba, Argentina.

出版信息

Medicina (B Aires). 2016;76(4):230-4.

Abstract

Heparin-induced thrombocytopenia (HIT) is an immune-mediated adverse reaction due to antibodies to a multimolecular complex of heparin and platelet factor 4 (PF4) characterized by moderate thrombocytopenia and paradoxical arterial or venous thrombosis. It is a relatively infrequent complication related to the administration of any type of heparin. In patients undergoing percutaneous coronary revascularization or coronary artery by-pass graft the prevalence of HIT is higher than in other clinical settings. Recognizing clinical and laboratory features of HIT allow immediate discontinuation of heparin and the use of alternative anticoagulants to avoid serious thrombotic complications. In this review, we summarize different therapeutic options for the treatment of HIT with special emphasis on direct oral anticoagulants (DOACS) such as dabigatran, rivaroxaban and apixaban. DOACS might represent a therapeutic alternative for HIT treatment.

摘要

肝素诱导的血小板减少症(HIT)是一种免疫介导的不良反应,由针对肝素与血小板因子4(PF4)多分子复合物的抗体引起,其特征为中度血小板减少以及矛盾性动脉或静脉血栓形成。它是与任何类型肝素使用相关的相对罕见的并发症。在接受经皮冠状动脉血运重建或冠状动脉旁路移植术的患者中,HIT的发生率高于其他临床情况。认识到HIT的临床和实验室特征可立即停用肝素并使用替代抗凝剂,以避免严重的血栓并发症。在本综述中,我们总结了治疗HIT的不同治疗选择,特别强调了直接口服抗凝剂(DOACs),如达比加群、利伐沙班和阿哌沙班。DOACs可能是治疗HIT的一种替代疗法。

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