Antiphospholipid Syndrome: A Review

M. Hossain, Md. Akhter Hossain, Y. Rahman, M. Hasan
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Abstract

Antiphospholipid syndrome (APS) is an autoimmune disease characterized by venous thromboembolism, arterial thrombosis, and obstetric morbidities in the setting of persistently positive levels of antiphospholipid antibodies. It may be primary or secondary. The latest classification criteria (Sydney 2006) recognize just three tests to define this syndrome- lupus anticoagulant, anticardiolipin antibodies and anti-?2-glycoprotein-1 antibodies. Treatment of thrombotic events involves lifelong anticoagulation with vitamin K antagonist warfarin. Antiphospholipid antibody syndrome (APS) with only pregnancy morbidity is treated with thromboprophylaxis with heparin during pregnancy and postpartum for 6 weeks. In this review we discuss the pathogenesis, diagnosis, treatment and prognosis of the APS.
抗磷脂综合征:综述
抗磷脂综合征(APS)是一种自身免疫性疾病,在抗磷脂抗体持续阳性的情况下,以静脉血栓栓塞、动脉血栓形成和产科发病率为特征。它可以是主要的,也可以是次要的。最新的分类标准(悉尼2006)只承认三种测试来定义这种综合征——狼疮抗凝血剂、抗心磷脂抗体和抗?2-glycoprotein-1抗体。治疗血栓事件涉及终身抗凝与维生素K拮抗剂华法林。抗磷脂抗体综合征(APS)只有妊娠发病率在妊娠期间和产后6周用肝素治疗血栓预防。现就该病的发病机制、诊断、治疗及预后作一综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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