Efficacy of therapeutic plasma exchange in a patient with coagulation inhibitors (acquired haemophilia A) - A case report

Transfus Apher Sci. 2020 Aug;59(4):102809. doi: 10.1016/j.transci.2020.102809. Epub 2020 May 24.

Abstract

Acquired haemophilia A (AHA) is a rare disorder with mostly idiopathic aetiology that leads to factor VIII (FVIII) deficiency due to coagulation inhibitors formation. Treatment protocol includes immunosuppression and Factor VIII bypassing agents including activated Prothrombin Complex Concentrates (PCC). Nevertheless, the role of plasma exchange is not clear in the treatment of AHA. We report a case of 73 year old male who presented with haematuria, prolonged activated partial thromboplastin time (APTT) and a very high titres of Factor VIII inhibitors of 98 Bethesda units (BU) and was diagnosed with acquired haemophilia A. He failed to respond to multiple immunosuppressive therapies including rituximab. Therefore, therapeutic plasma exchange (TPE) therapy was planned due to persistence of haematuria despite immunosuppressive therapies. After five cycles of plasma exchange, APTT became normal, haematuria subsided and Factor VIII inhibitors became negative. Patient was discharged without any bleeding and in a stable condition. In this index case, plasma exchange played a very crucial role, resulting in recovery of the patient. These results advocate that therapeutic plasma exchange is an effective therapy for acquired haemophilia A.

Keywords: Acquired haemophilia A – AHA; Activated partial thromboplastin time – APTT; Bethesda units – BU; Prothrombin Complex Concentrates PCC; Therapeutic Plasma Exchange – TPE.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Anticoagulants / pharmacology
  • Anticoagulants / therapeutic use*
  • Hemophilia A / drug therapy*
  • Humans
  • Male
  • Plasma Exchange / methods*

Substances

  • Anticoagulants