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Recombinant Activated Factor VII as a Second Line Treatment for Postpartum Hemorrhage
BACKGROUND: Severe or massive postpartum hemorrhage (PPH) has remained a leading cause of maternal mortality for decades across the world and it results in critical obstetric complications. Recombinant activated factor VII (rFVIIa) has emerged as a gold standard adjunctive hemostatic agent for the t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Society of Critical Care Medicine
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6786683/ https://www.ncbi.nlm.nih.gov/pubmed/31723654 http://dx.doi.org/10.4266/kjccm.2016.00787 |
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author | Park, Soon Chang Yeom, Seok Ran Han, Sang Kyoon Jo, Young Mo Kim, Hyung Bin |
author_facet | Park, Soon Chang Yeom, Seok Ran Han, Sang Kyoon Jo, Young Mo Kim, Hyung Bin |
author_sort | Park, Soon Chang |
collection | PubMed |
description | BACKGROUND: Severe or massive postpartum hemorrhage (PPH) has remained a leading cause of maternal mortality for decades across the world and it results in critical obstetric complications. Recombinant activated factor VII (rFVIIa) has emerged as a gold standard adjunctive hemostatic agent for the treatment of life-threatening PPH refractory to conventional therapies although it remains off-licensed for use in PPH. We studied the effects of rFVIIa on coagulopathy, transfusion volume, prognosis, severity change in Korean PPH patients. METHODS: A retrospective review of medical records between December 2008 and March 2011 indicating use of rFVIIa in severe PPH was performed. We compared age, rFVIIa treatment, transfusion volume, and Sequential Organ Failure Assessment (SOFA) score at the time of arrival in the emergency department and after 24 hours for patients whose SOFA score was 8 points or higher. RESULTS: Fifteen women with SOFA score of 8 and above participated in this study and eight received rFVIIa administration whereas seven did not. Patients’ mean age was 31.7 ± 7.5 years. There was no statistically significant difference in initial and post-24 hours SOFA scores between patients administered rFVIIa or not. The change in SOFA score between initial presentation and after 24 hours was significantly reduced after rFVIIa administration (P = 0.016). CONCLUSIONS: This analysis aimed to support that the administration of rFVIIa can reduce the severity of life-threatening PPH in patients. A rapid decision regarding the administration of rFVIIa is needed for a more favorable outcome in severe PPH patients for whom there is no effective standard treatment. |
format | Online Article Text |
id | pubmed-6786683 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Korean Society of Critical Care Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-67866832019-11-13 Recombinant Activated Factor VII as a Second Line Treatment for Postpartum Hemorrhage Park, Soon Chang Yeom, Seok Ran Han, Sang Kyoon Jo, Young Mo Kim, Hyung Bin Korean J Crit Care Med Original Article BACKGROUND: Severe or massive postpartum hemorrhage (PPH) has remained a leading cause of maternal mortality for decades across the world and it results in critical obstetric complications. Recombinant activated factor VII (rFVIIa) has emerged as a gold standard adjunctive hemostatic agent for the treatment of life-threatening PPH refractory to conventional therapies although it remains off-licensed for use in PPH. We studied the effects of rFVIIa on coagulopathy, transfusion volume, prognosis, severity change in Korean PPH patients. METHODS: A retrospective review of medical records between December 2008 and March 2011 indicating use of rFVIIa in severe PPH was performed. We compared age, rFVIIa treatment, transfusion volume, and Sequential Organ Failure Assessment (SOFA) score at the time of arrival in the emergency department and after 24 hours for patients whose SOFA score was 8 points or higher. RESULTS: Fifteen women with SOFA score of 8 and above participated in this study and eight received rFVIIa administration whereas seven did not. Patients’ mean age was 31.7 ± 7.5 years. There was no statistically significant difference in initial and post-24 hours SOFA scores between patients administered rFVIIa or not. The change in SOFA score between initial presentation and after 24 hours was significantly reduced after rFVIIa administration (P = 0.016). CONCLUSIONS: This analysis aimed to support that the administration of rFVIIa can reduce the severity of life-threatening PPH in patients. A rapid decision regarding the administration of rFVIIa is needed for a more favorable outcome in severe PPH patients for whom there is no effective standard treatment. Korean Society of Critical Care Medicine 2017-11 2017-11-30 /pmc/articles/PMC6786683/ /pubmed/31723654 http://dx.doi.org/10.4266/kjccm.2016.00787 Text en Copyright © 2017 The Korean Society of Critical Care Medicine This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Park, Soon Chang Yeom, Seok Ran Han, Sang Kyoon Jo, Young Mo Kim, Hyung Bin Recombinant Activated Factor VII as a Second Line Treatment for Postpartum Hemorrhage |
title | Recombinant Activated Factor VII as a Second Line Treatment for Postpartum Hemorrhage |
title_full | Recombinant Activated Factor VII as a Second Line Treatment for Postpartum Hemorrhage |
title_fullStr | Recombinant Activated Factor VII as a Second Line Treatment for Postpartum Hemorrhage |
title_full_unstemmed | Recombinant Activated Factor VII as a Second Line Treatment for Postpartum Hemorrhage |
title_short | Recombinant Activated Factor VII as a Second Line Treatment for Postpartum Hemorrhage |
title_sort | recombinant activated factor vii as a second line treatment for postpartum hemorrhage |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6786683/ https://www.ncbi.nlm.nih.gov/pubmed/31723654 http://dx.doi.org/10.4266/kjccm.2016.00787 |
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