Abstract
The antiphospholipid syndrome (APS) is considered the most common acquired hypercoagulable disorder associated with thrombosis. It is an antibody-mediated prothrombotic state characterized by venous and/or arterial thrombosis or obstetrical morbidity in conjunction with laboratory identification of antiphospholipid antibodies (aPL). These antibodies, recently referred to as the “antiphospholipid triangle,” include anticardiolipin antibodies (aCL), anti-β2-glycoprotein I antibodies (aβ2GPI), and the lupus anticoagulant (LA) [1]. Antiphospholipid antibodies identified in otherwise healthy individuals after a venous or arterial thrombotic or obstetrical event is referred to as primary APS. Secondary APS is the term used when APS coexists with an underlying systemic autoimmune disease such as systemic lupus erythematosus (SLE). Antibodies also occur in asymptomatic individuals with no history of thrombosis. They can also be detected in persons on medications particularly important to the cardiac patient including procainamide, hydralazine, quinidine, and the angiotensin-converting enzyme (ACE) inhibitors [2].
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Bartholomew, J.R. (2013). Perioperative Management of Anticoagulation in the Patient with the Antiphospholipid Syndrome in Cardiac Surgery and Cardiac Interventions. In: Mandell, B. (eds) Perioperative Management of Patients with Rheumatic Disease. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-2203-7_9
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