Treatment of the antiphospholipid syndrome.

Q1 Medicine
Auto-Immunity Highlights Pub Date : 2013-12-22 eCollection Date: 2014-06-01 DOI:10.1007/s13317-013-0056-5
Monica Galli
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引用次数: 36

Abstract

The antiphospholipid syndrome is characterized by a combination of laboratory findings (i.e., the presence of at least one antiphospholipid antibody) and clinical manifestations (arterial and/or venous thrombosis, obstetrical complications). Long-term oral anticoagulant is recommended to prevent recurrence of both arterial and venous thrombosis, whereas (low molecular weight) heparin plus aspirin is the treatment of choice to prevent further obstetrical complications. In the rare case of catastrophic antiphospholipid syndrome, heparin plus high-dose corticosteroids plus plasma exchange is associated with the highest recovery rate. Some new, non-antithrombotic-based treatments of antiphospholipid syndrome with rituximab, autologous stem cell transplantation, or hydroxychloroquine are also reviewed.

抗磷脂综合征的治疗。
抗磷脂综合征的特点是实验室检查结果(即至少存在一种抗磷脂抗体)和临床表现(动脉和/或静脉血栓形成、产科并发症)的结合。长期口服抗凝剂被推荐用于预防动脉和静脉血栓的复发,而(低分子量)肝素加阿司匹林是预防进一步产科并发症的治疗选择。在罕见的灾难性抗磷脂综合征病例中,肝素加大剂量皮质类固醇加血浆置换与最高的恢复率相关。一些新的,非抗血栓为基础的治疗抗磷脂综合征的利妥昔单抗,自体干细胞移植,或羟氯喹也进行了综述。
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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