AI Article Synopsis

  • A 71-year-old man diagnosed with AHA experienced severe bleeding and was initially treated with rFVIIa and prednisolone, but his condition did not improve and he faced hemorrhagic shock.
  • A successful combination therapy of rFVIIa with plasma-derived FVIIa and factor X was eventually applied, leading to effective hemostasis without causing thrombosis.

Article Abstract

Acquired hemophilia A (AHA) is a rare, life-threatening hemorrhagic disease caused by autoantibodies against factor VIII (FVIII), and bypassing agents (BPA) are used to control bleeding. However, some cases need a change of BPA or BPAs given sequentially or in combination for refractory bleeding. A 71-year-old man was admitted with subcutaneous hemorrhage. Laboratory investigations showed prolongation of activated partial thromboplastin time (APTT) and low-coagulation FVIII activity and FVIII inhibitor; we, therefore, diagnosed AHA. He was treated with recombinant factor VIIa (rFVIIa) BPA and prednisolone. However, his symptoms did not improve sufficiently, thus we switched BPA to activated prothrombin complex concentrate. Unfortunately, this was not effective and he suffered hemorrhagic shock. Therefore, we selected rFVIIa, with plasma-derived FVIIa and factor X (pd-FVIIa/FX) as combination therapy, and hemostasis was achieved without thrombosis. This case suggests that the combination of rFVIIa and pd-FVIIa/FX short-term can be well tolerated for refractory hemorrhage in AHA.

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Source
http://dx.doi.org/10.1097/MBC.0000000000001243DOI Listing

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