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Antiphospholipid syndrome (APS) is an autoimmune disease leading to thrombosis and pregnancy complications associated with persistent antiphospholipid antibodies. The management of APS involves decisions regarding anticoagulant therapy, with primary prevention for those without prior thrombosis being debated, as evidence for its effectiveness is limited. Current guidelines suggest that antithrombotic therapy may not be routinely necessary for individuals with aPL without a history of thrombosis, although so

Author

KHTH BTH

Language

EN