Antiphospholipid Syndrome

被引:76
|
作者
Branch, Ware
Holmgren, Calla
Goldberg, James D.
机构
来源
OBSTETRICS AND GYNECOLOGY | 2012年 / 120卷 / 06期
关键词
RECURRENT PREGNANCY LOSS; SYSTEMIC LUPUS-ERYTHEMATOSUS; ANTICARDIOLIPIN ANTIBODIES; FETAL-DEATH; CLASSIFICATION CRITERIA; CLINICAL CONSEQUENCES; GROWTH-RETARDATION; WOMEN; THROMBOSIS; ANTICOAGULANT;
D O I
10.1097/01.AOG.0000423816.39542.0f
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Antiphospholipid syndrome (APS) is an autoimmune disorder defined by the presence of characteristic clinical features and specified levels of circulating antiphospholipid antibodies (Box 1 and Box 2). Diagnosis requires that at least one clinical and one laboratory criterion are met. Because approximately 70% of individuals with APS are female (1), it is reasonably prevalent among women of reproductive age. Antiphospholipid antibodies are a diverse group of antibodies with specificity for binding to negatively charged phospholipids on cell surfaces. Despite the prevalence and clinical significance of APS, there is controversy about the indications for and types of antiphospholipid tests that should be performed in order to diagnose the condition. Much of the debate results from a lack of well-designed and controlled studies on the diagnosis and management of APS. The purpose of this document is to evaluate the data for diagnosis and treatment of APS.
引用
收藏
页码:1514 / 1521
页数:8
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