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Newly diagnosed congenital factor VII deficiency and utilization of recombinant activated factor VII (NovoSeven(®))
This case report presents a newly diagnosed congenital factor VII deficiency treated with recombinant activated factor VII (rFVIIa). Congenital factor VII deficiency is a rare autosomal-recessive bleeding disorder that occurs in fewer than 1/500,000 persons. Its presentation can vary from epistaxis...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3601647/ https://www.ncbi.nlm.nih.gov/pubmed/23516010 http://dx.doi.org/10.2147/CPAA.S39772 |
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author | Bartosh, Nicole S Tomlin, Tara Cable, Christian Halka, Kathleen |
author_facet | Bartosh, Nicole S Tomlin, Tara Cable, Christian Halka, Kathleen |
author_sort | Bartosh, Nicole S |
collection | PubMed |
description | This case report presents a newly diagnosed congenital factor VII deficiency treated with recombinant activated factor VII (rFVIIa). Congenital factor VII deficiency is a rare autosomal-recessive bleeding disorder that occurs in fewer than 1/500,000 persons. Its presentation can vary from epistaxis to hemarthroses and severe central nervous system bleeding, and correlates poorly with factor VII levels. Our patient had not had a significant hemostatic challenge prior to his presentation and therefore never had any symptomatology suggestive of this disease. He was treated with rFVIIa, and was able to undergo repair of his fractures without bleeding. CASE REPORT: A 19-year-old African-American male presented to the emergency room after an altercation that resulted in significant trauma. He sustained bilateral mandibular angle fractures and orbital floor fractures, requiring urgent surgical correction. On initial evaluation, he was noted to have a prolonged prothrombin time of 40.1 seconds, with an International Normalized Ratio of 4.0, a normal activated partial thromboplastin time of 29.9 seconds, and a platelet count of 241. After receiving vitamin K and fresh frozen plasma, he was taken to the operating room for a temporary rigid maxillomandibular fixation. A 1:1 mixing study with normal plasma corrected the prothrombin time (decreasing from 40.7 to 14.7 seconds) and a factor VII assay revealed 5% of the normal factor VII level. The patient was diagnosed with congenital factor VII deficiency. Due to his coagulopathy and the extensive surgical correction needed, rFVIIa was administered and surgery was accomplished without hemorrhagic sequelae. CONCLUSION: This case report and review describes a rare congenital disease, the history of rFVIIa use, and its mechanism. rFVIIA use in our patient provided a treatment option that allowed the necessary surgical correction, but further prospective studies on dose optimization would ensure adequate dosing with minimal risk of severe side effects. |
format | Online Article Text |
id | pubmed-3601647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-36016472013-03-19 Newly diagnosed congenital factor VII deficiency and utilization of recombinant activated factor VII (NovoSeven(®)) Bartosh, Nicole S Tomlin, Tara Cable, Christian Halka, Kathleen Clin Pharmacol Case Report This case report presents a newly diagnosed congenital factor VII deficiency treated with recombinant activated factor VII (rFVIIa). Congenital factor VII deficiency is a rare autosomal-recessive bleeding disorder that occurs in fewer than 1/500,000 persons. Its presentation can vary from epistaxis to hemarthroses and severe central nervous system bleeding, and correlates poorly with factor VII levels. Our patient had not had a significant hemostatic challenge prior to his presentation and therefore never had any symptomatology suggestive of this disease. He was treated with rFVIIa, and was able to undergo repair of his fractures without bleeding. CASE REPORT: A 19-year-old African-American male presented to the emergency room after an altercation that resulted in significant trauma. He sustained bilateral mandibular angle fractures and orbital floor fractures, requiring urgent surgical correction. On initial evaluation, he was noted to have a prolonged prothrombin time of 40.1 seconds, with an International Normalized Ratio of 4.0, a normal activated partial thromboplastin time of 29.9 seconds, and a platelet count of 241. After receiving vitamin K and fresh frozen plasma, he was taken to the operating room for a temporary rigid maxillomandibular fixation. A 1:1 mixing study with normal plasma corrected the prothrombin time (decreasing from 40.7 to 14.7 seconds) and a factor VII assay revealed 5% of the normal factor VII level. The patient was diagnosed with congenital factor VII deficiency. Due to his coagulopathy and the extensive surgical correction needed, rFVIIa was administered and surgery was accomplished without hemorrhagic sequelae. CONCLUSION: This case report and review describes a rare congenital disease, the history of rFVIIa use, and its mechanism. rFVIIA use in our patient provided a treatment option that allowed the necessary surgical correction, but further prospective studies on dose optimization would ensure adequate dosing with minimal risk of severe side effects. Dove Medical Press 2013-03-15 /pmc/articles/PMC3601647/ /pubmed/23516010 http://dx.doi.org/10.2147/CPAA.S39772 Text en © 2013 Bartosh et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Case Report Bartosh, Nicole S Tomlin, Tara Cable, Christian Halka, Kathleen Newly diagnosed congenital factor VII deficiency and utilization of recombinant activated factor VII (NovoSeven(®)) |
title | Newly diagnosed congenital factor VII deficiency and utilization of recombinant activated factor VII (NovoSeven(®)) |
title_full | Newly diagnosed congenital factor VII deficiency and utilization of recombinant activated factor VII (NovoSeven(®)) |
title_fullStr | Newly diagnosed congenital factor VII deficiency and utilization of recombinant activated factor VII (NovoSeven(®)) |
title_full_unstemmed | Newly diagnosed congenital factor VII deficiency and utilization of recombinant activated factor VII (NovoSeven(®)) |
title_short | Newly diagnosed congenital factor VII deficiency and utilization of recombinant activated factor VII (NovoSeven(®)) |
title_sort | newly diagnosed congenital factor vii deficiency and utilization of recombinant activated factor vii (novoseven(®)) |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3601647/ https://www.ncbi.nlm.nih.gov/pubmed/23516010 http://dx.doi.org/10.2147/CPAA.S39772 |
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