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Thrombocytopenia in antiphospholipid syndrome: Is anticoagulation and/or antiaggregation always required?
Stephane Zuily1, Ricard Cervera2, Thomas Foret3
1CHRU-Nancy, Vascular Medicine Division, French Referral Center for Rare Systemic and Autoimmune Diseases, F-54000 Nancy, France; Université de Lorraine, INSERM, DCAC, F-54000 Nancy, France.
Abstract:
The antiphospholipid syndrome (APS) is an autoimmune and prothrombotic condition defined by the association of thrombotic events and/or obstetrical complications and the persistence of antiphospholipid antibodies (aPL) over time. Among the new criteria recently included in the 2023 ACR/EULAR classification criteria for APS, thrombocytopenia is one of the most frequent. The occurrence of thrombocytopenia in aPL/APS patients is important to consider because it could predict APS-related clinical events with a 3-fold increased risk for thrombotic events or obstetrical morbidity or all-cause deaths. A debate on the need or not of anticoagulation and/or antiaggregation in APS patients and aPL carriers with thrombocytopenia took place on the 7th edition of the International Congress on Controversies in Rheumatology and Autoimmunity (CORA), that was organized in Turin, Italy, on March 18th, 2023, and this review summarizes the main arguments that were discussed in this session.
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