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Cost effectiveness of recombinant factor VIIa for treatment of intracerebral hemorrhage
BACKGROUND: Phase I/II placebo-controlled clinical trials of recombinant Factor VIIa (rFVIIa) suggested that administration of rFVIIa within 4 hours after onset of intracerebral hemorrhage (ICH) is safe, limits ICH growth, and improves outcomes. We sought to determine the cost-effectiveness of rFVII...
| Autores principales: | , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2008
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2397434/ https://www.ncbi.nlm.nih.gov/pubmed/18489750 http://dx.doi.org/10.1186/1471-2377-8-17 |