Antiphospholipid syndrome: State of the art with emphasis on laboratory evaluation

Authors
Citation
M. Greaves, Antiphospholipid syndrome: State of the art with emphasis on laboratory evaluation, HAEMOSTASIS, 30, 2000, pp. 16-25
Citations number
41
Categorie Soggetti
Cardiovascular & Hematology Research
Journal title
HAEMOSTASIS
ISSN journal
03010147 → ACNP
Volume
30
Year of publication
2000
Supplement
2
Pages
16 - 25
Database
ISI
SICI code
0301-0147(2000)30:<16:ASSOTA>2.0.ZU;2-H
Abstract
Antiphospholipid antibodies (aPLs) are associated with arterial and venous thrombosis, recurrent pregnancy loss and thrombocytopenia. Although aPLs ha ve not yet been con elusively shown to be causal in thrombosis and miscarri age, they are useful laboratory markers for the antiphospholipid syndrome ( APS). The syndrome can complicate another autoimmune disease, most commonly systemic lupus erythematosus, but more often occurs alone - primary APS. I dentification of the syndrome is clinically important because of the risk o f recurrent thrombosis and the need for antithrombotic therapy in many case s. Diagnosis and treatment of APS represent significant challenges, however , owing to the protean clinical manifestations and associations, limitation s of currently available laboratory tests for aPLs, and the lack of clear e vidence-based guidance on optimal management. Copyright (C) 2001 S. Karger AG Basel.