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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...

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Autori principali: Kissela, Brett M, Eckman, Mark H
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2008
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2397434/
https://ncbi.nlm.nih.gov/pubmed/18489750
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2377-8-17
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