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Optimal use of recombinant factor VIIa in the control of bleeding episodes in hemophilic patients

Authors John Puetz

Published 28 June 2010 Volume 2010:4 Pages 127—137

DOI https://doi.org/10.2147/DDDT.S6628

Review by Single-blind

Peer reviewer comments 3

John Puetz

Saint Louis University, Department of Pediatrics, St Louis, Missouri, USA

Abstract: One of the last remaining clinical hurdles in the treatment of people with hemophilia is the development of inhibitors. Alloantibodies or autoantibodies directed at coagulation factors render the infusion of coagulation factor concentrates ineffective, and alternative means must be used to achieve hemostasis. Recombinant factor VIIa (rFVIIa) was developed to control bleeding episodes in hemophilic patients with inhibitors. Clinical efficacy in achieving hemostasis in inhibitor patients was demonstrated by a compassionate-use protocol, as well as in randomized controlled trials. To date, over 1.5 million doses of rFVIIa have been given to inhibitor patients, with an excellent efficacy and safety record. Because of its short half-life, alternative means of dosing and infusing rFVIIa have been explored and are reviewed here.
Keywords: hemophilia, inhibitor, recombinant, factor VIIa, inhibitors

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