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Antiphospholipid syndrome (APS) is an autoimmune disorder characterized by thrombotic events, obstetric complications, or both, in combination with persistently positive autoantibodies. For patients with thrombotic APS, long-term anticoagulation is recommended, usually with vitamin K antagonists (VKAs). But treatment decisions are still challenging, given the disease’s clinical heterogeneity and the lack of definitive trial data. Here, investigators describe anticoagulation practices and recurrence rates from a retrospective, U.K.-based study involving 500 patients with APS diagnosed after a first thrombotic event.
At initial presentation, roughly 70% of patients had venous thrombosis (mostly women), and 30% had arterial th…