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Experiences with recombinant activated factor VII in the treatment of severe refractory thrombocytopenia

Grazyna Wróbel1, Grzegorz Dobaczewski, Dariusz Patkowski

  • 1Department of Bone Marrow Transplantation, Paediatric Haematology and Oncology, Medical University of Wroclaw, Wroclaw, Poland. gw@pedhemat.am.wroc.pl

Pediatric Blood & Cancer
|August 26, 2006
PubMed

Approximately 5% of chronic immune thrombocytopenic purpura (ITP) manifests itself as symptomatic, severe thrombocytopenia requiring splenectomy. The surgical procedure increases the risk of serious hemorrhage, especially in patients refractory to platelet transfusions. Recombinant factor VIIa (rFVIIa) has been found to enhance thrombin generation on activated platelets and may be a promising agent in preventing life-threatening bleedings. The administration of rFVIIa in two patients with severe refractory ITP, who underwent splenectomy, is presented. Combined therapy with agents of different mechanisms of action could be useful in cases with the highest probability of bleeding.

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