Postpartum acquired haemophilia: clinical recognition and management

Haemophilia. 2001 May;7(3):327-30. doi: 10.1046/j.1365-2516.2001.00506.x.

Abstract

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

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Autoantibodies / blood
  • Blood Coagulation Factors / administration & dosage
  • Blood Loss, Surgical
  • Dilatation and Curettage
  • Factor VIII / immunology
  • Female
  • Hemophilia A / diagnosis
  • Hemophilia A / etiology*
  • Hemophilia A / immunology
  • Humans
  • Hysterectomy
  • Postpartum Hemorrhage / etiology*
  • Postpartum Hemorrhage / immunology
  • Pregnancy
  • Pregnancy Complications, Hematologic / etiology
  • Pregnancy Complications, Hematologic / surgery

Substances

  • Autoantibodies
  • Blood Coagulation Factors
  • Factor VIII
  • anti-inhibitor coagulant complex