Division of Hematology and Hematological Malignancies, Departments of Medicine and Community Health Sciences, University of Calgary, Calgary, Canada; and Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Canada.
Blood. 2018 Nov 22;132(21):2219-2229. doi: 10.1182/blood-2018-05-848697.
Antiphospholipid syndrome (APS), heparin-induced thrombocytopenia, and paroxysmal nocturnal hemoglobinuria are 3 acquired thrombophilias that carry a high risk of venous and arterial thromboembolism. Management of these conditions has largely included anticoagulation with a vitamin K antagonist after an initial period of a parenteral anticoagulant, for as long as the thrombotic risk is still present. The available evidence for the use of direct oral anticoagulants (DOACs) is limited and primarily consists of case series and cohort studies, which are summarized in this chapter. Randomized trials evaluating DOACs in patients with APS are reviewed. Further research is needed prior to widely adopting DOACs for use in these high-risk acquired thrombophilias; however, there may be selected low-risk subgroups where DOAC use is possible after careful consideration and patient discussion.
抗磷脂综合征 (APS)、肝素诱导的血小板减少症和阵发性夜间血红蛋白尿症是 3 种获得性血栓形成倾向,它们具有发生静脉和动脉血栓栓塞的高风险。这些疾病的治疗在很大程度上包括初始使用静脉或皮下给予抗凝药物,当血栓形成的风险仍然存在时,需要长期使用维生素 K 拮抗剂抗凝。目前关于直接口服抗凝剂(DOAC)的应用证据有限,主要是病例系列和队列研究,本章对此进行了总结。本章还回顾了随机临床试验评估 DOAC 在 APS 患者中的应用。在广泛采用 DOAC 治疗这些高危获得性血栓形成倾向之前,还需要进一步研究;然而,在仔细考虑和与患者讨论后,某些低危亚组可能可以使用 DOAC。