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Preclinical trauma studies of recombinant factor VIIa
Preclinical studies in animals and ex vivo human blood have provided a solid rationale for conducting prospective randomized trials in trauma patients. Small animal models have been utilized to study the efficacy of recombinant activated factor VII (rFVIIa; NovoSeven(®)) in treating thrombocytopenic...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3226120/ https://www.ncbi.nlm.nih.gov/pubmed/16221316 http://dx.doi.org/10.1186/cc3782 |
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author | Schreiber, Martin A Holcomb, John B Rojkjaer, Rasmus |
author_facet | Schreiber, Martin A Holcomb, John B Rojkjaer, Rasmus |
author_sort | Schreiber, Martin A |
collection | PubMed |
description | Preclinical studies in animals and ex vivo human blood have provided a solid rationale for conducting prospective randomized trials in trauma patients. Small animal models have been utilized to study the efficacy of recombinant activated factor VII (rFVIIa; NovoSeven(®)) in treating thrombocytopenic rabbits and for the reversal of anticoagulation. Safety models in the rabbit also exist to test for systemic activation of clotting and pathologic thrombosis. Animal models simulating traumatic injuries in humans have primarily been performed in pigs because of species similarities in terms of coagulation characteristics and the larger internal organs. The pig studies, utilizing human rFVIIa, have shown increased strength of clot formation, decreased bleeding, and improved survival. However, these findings are not uniform and are dependant on the model chosen. All of the animal models described have provided good safety data and suggest that the use of rFVIIa is not associated with systemic activation of coagulation or microthrombosis of end organs. |
format | Online Article Text |
id | pubmed-3226120 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32261202011-11-30 Preclinical trauma studies of recombinant factor VIIa Schreiber, Martin A Holcomb, John B Rojkjaer, Rasmus Crit Care Review Preclinical studies in animals and ex vivo human blood have provided a solid rationale for conducting prospective randomized trials in trauma patients. Small animal models have been utilized to study the efficacy of recombinant activated factor VII (rFVIIa; NovoSeven(®)) in treating thrombocytopenic rabbits and for the reversal of anticoagulation. Safety models in the rabbit also exist to test for systemic activation of clotting and pathologic thrombosis. Animal models simulating traumatic injuries in humans have primarily been performed in pigs because of species similarities in terms of coagulation characteristics and the larger internal organs. The pig studies, utilizing human rFVIIa, have shown increased strength of clot formation, decreased bleeding, and improved survival. However, these findings are not uniform and are dependant on the model chosen. All of the animal models described have provided good safety data and suggest that the use of rFVIIa is not associated with systemic activation of coagulation or microthrombosis of end organs. BioMed Central 2005 2005-10-07 /pmc/articles/PMC3226120/ /pubmed/16221316 http://dx.doi.org/10.1186/cc3782 Text en Copyright ©2005 BioMed Central Ltd |
spellingShingle | Review Schreiber, Martin A Holcomb, John B Rojkjaer, Rasmus Preclinical trauma studies of recombinant factor VIIa |
title | Preclinical trauma studies of recombinant factor VIIa |
title_full | Preclinical trauma studies of recombinant factor VIIa |
title_fullStr | Preclinical trauma studies of recombinant factor VIIa |
title_full_unstemmed | Preclinical trauma studies of recombinant factor VIIa |
title_short | Preclinical trauma studies of recombinant factor VIIa |
title_sort | preclinical trauma studies of recombinant factor viia |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3226120/ https://www.ncbi.nlm.nih.gov/pubmed/16221316 http://dx.doi.org/10.1186/cc3782 |
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