“…Given the low diagnostic yield, routine evaluation for venous hypercoagulability was not performed unless suggested by a clinical history of hypercoagulable states, e.g., a family history of venous thrombosis, thrombosis at an early age (Ͻ 45 years) with pulmonary embolus, recurrent venous thrombosis, and coumadin-induced thrombosis [6]. Similarly, the presence of a primary antiphospholipid syndrome was not routinely assessed, unless additional clinical features were present, e.g., a history of recurrent thromboses or fetal loss, thrombocytopenia, or livedo reticularis [7].…”