Abstract
Children and adolescents comprise a significant proportion of the hemophilia population, including those patients who have developed inhibitors to factor VIII or FIX. We examine the use of rFVIIa for the treatment of bleeding episodes and the prevention of bleeding in children and adolescents with hemophilia A and B with inhibitors, focusing on registry data and recent clinical trial results. Based on this review of the literature, we conclude that recombinant FVIIa is safe and effective for use in controlling bleeding in these patient populations.
| Original language | English |
|---|---|
| Pages (from-to) | 25-32 |
| Number of pages | 8 |
| Journal | Transfusion and Apheresis Science |
| Volume | 38 |
| Issue number | 1 |
| DOIs | |
| State | Published - Feb 2008 |
| Externally published | Yes |
Keywords
- Bleeding disorder
- Hemophilia
- Inhibitors
- NiaStase
- NovoSeven
- Recombinant FVIIa
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