Postpartum acquired haemophilia: clinical recognition and management

Postpartum acquired haemophilia is a rare but serious complication of an ot herwise normal pregnancy. Patients usually present with postpartum haemorrh age (PPH) or uncontrolled bleeding following surgical interventions, which fail to respond to conservative treatment. A high index of clinical suspici on along with early laboratory diagnosis and prompt institution of appropri ate therapy is essential for the management of acute bleeding episodes. Our patient, a 32-year-old female, presented with severe PPH and shock. She ha d undergone dilation and curettage three times, with subsequent total abdom inal hysterectomy and internal iliac artery ligation, before she was diagno sed with acquired haemophilia (factor VIII autoantibodies) and an inhibitor level of 8 Bethesda units (BU). The patient underwent an abdominal laproto my for removal of the abdominal packing used in the previous operation, and blood and blood clots, and was given FEIBA (R) therapy. The patient respon ded to these measure and the factor VIII inhibitor level decreased to 2 BU at the time of discharge 10 weeks later.