Contents

Search


coagulation factor VIII alloantibody

Alloantibody to factor VIII occurs in 20-25% of patients with severe hemophilia A transfused with factor VIII. Laboratory: - prolonged aPTT, NOT corrected with addition of normal plasma - coagulation factor VIII inhibitor in plasma Management: 1) immunosuppressive therapy 2) acute bleeding a) porcine factor VIII (generally less reactive with anti-human factor VIII) b) prothrombin complex concentrate c) recombinant factor VIIa concentrate d) plasmapheresis

Interactions

drug adverse effects of antithrombotic agent(s)

Related

coagulation factor VIII autoantibody (acquired hemophilia) coagulation factor VIII inhibitor in plasma coagulation factor VIII; antihemophilic factor; AHF; procoagulant component; contains: factor VIIIa heavy chain, 200 kD & 92 isoforms; factor VIII B chain; factor VIIIa light chain (F8, F8C)

General

alloantibody coagulation factor VIII antibody

References

Medical Knowledge Self Assessment Program (MKSAP) 11, American College of Physicians, Philadelphia 1998