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Rheumatology

Antiphospholipid syndrome

Thrombosis or pregnancy morbidity with persistent antiphospholipid antibodies. Who to test, how anticoagulants wreck the lupus anticoagulant assay, why warfarin beats DOACs in high-risk APS, the obstetric regimen, catastrophic APS, and the non-criteria features (livedo, valve disease, thrombocytopenia) examiners use.

Tier 2Condition

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At a glance

  • Antiphospholipid syndrome (APS) is an acquired autoimmune thrombophilia: venous, arterial or microvascular thrombosis, or pregnancy morbidity, with persistent antiphospholipid antibodies (aPL).
  • Primary APS occurs alone. About a third of people with SLE carry aPL; around 10 to 15% of those with SLE develop APS. See SLE.
  • Three tests: lupus anticoagulant (LA), anticardiolipin (aCL) and anti-beta2-glycoprotein I (anti-β2GPI). Positives must persist 12 weeks or more apart.

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Last updated
14 November 2026
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