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Clinical experiences and current evidence for therapeutic recombinant factor VIIa treatment in nontrauma settings

The hemostatic properties of recombinant activated factor VII (rFVIIa) are established in patients with inherited or acquired hemophilia with inhibitors and in patients with congenital factor VII deficiencies. Emerging clinical evidence suggests that there may be a wider role for rFVIIa in the manag...

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Detalles Bibliográficos
Autores principales: Grounds, R Michael, Bolan, Charles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3226121/
https://www.ncbi.nlm.nih.gov/pubmed/16221317
http://dx.doi.org/10.1186/cc3783
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author Grounds, R Michael
Bolan, Charles
author_facet Grounds, R Michael
Bolan, Charles
author_sort Grounds, R Michael
collection PubMed
description The hemostatic properties of recombinant activated factor VII (rFVIIa) are established in patients with inherited or acquired hemophilia with inhibitors and in patients with congenital factor VII deficiencies. Emerging clinical evidence suggests that there may be a wider role for rFVIIa in the management of hemorrhage associated with traumatic injury/accident and severe bleeding associated with critical surgery. This article considers recent data from studies in which rFVIIa was used in an attempt to control bleeding in clinical situations as diverse as coagulopathy associated with chronic liver disease, massive perioperative bleeding and bleeding during prostatectomy, organ transplantation and orthopedic surgery, uncontrollable obstetric hemorrhage, and intracerebral hemorrhage. In nontrauma settings involving acute and potentially life threatening bleeding, there may be a place for rFVIIa as adjunctive therapy in the control of hemostasis.
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spelling pubmed-32261212011-11-30 Clinical experiences and current evidence for therapeutic recombinant factor VIIa treatment in nontrauma settings Grounds, R Michael Bolan, Charles Crit Care Review The hemostatic properties of recombinant activated factor VII (rFVIIa) are established in patients with inherited or acquired hemophilia with inhibitors and in patients with congenital factor VII deficiencies. Emerging clinical evidence suggests that there may be a wider role for rFVIIa in the management of hemorrhage associated with traumatic injury/accident and severe bleeding associated with critical surgery. This article considers recent data from studies in which rFVIIa was used in an attempt to control bleeding in clinical situations as diverse as coagulopathy associated with chronic liver disease, massive perioperative bleeding and bleeding during prostatectomy, organ transplantation and orthopedic surgery, uncontrollable obstetric hemorrhage, and intracerebral hemorrhage. In nontrauma settings involving acute and potentially life threatening bleeding, there may be a place for rFVIIa as adjunctive therapy in the control of hemostasis. BioMed Central 2005 2005-10-07 /pmc/articles/PMC3226121/ /pubmed/16221317 http://dx.doi.org/10.1186/cc3783 Text en
spellingShingle Review
Grounds, R Michael
Bolan, Charles
Clinical experiences and current evidence for therapeutic recombinant factor VIIa treatment in nontrauma settings
title Clinical experiences and current evidence for therapeutic recombinant factor VIIa treatment in nontrauma settings
title_full Clinical experiences and current evidence for therapeutic recombinant factor VIIa treatment in nontrauma settings
title_fullStr Clinical experiences and current evidence for therapeutic recombinant factor VIIa treatment in nontrauma settings
title_full_unstemmed Clinical experiences and current evidence for therapeutic recombinant factor VIIa treatment in nontrauma settings
title_short Clinical experiences and current evidence for therapeutic recombinant factor VIIa treatment in nontrauma settings
title_sort clinical experiences and current evidence for therapeutic recombinant factor viia treatment in nontrauma settings
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3226121/
https://www.ncbi.nlm.nih.gov/pubmed/16221317
http://dx.doi.org/10.1186/cc3783
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