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Use of activated recombinant factor VII for severe coagulopathy post ventricular assist device or orthotopic heart transplant
BACKGROUND: Ventricular assist devices(VAD) implantation/removal is a complex surgical procedure with perioperative bleeding complications occurring in nearly half of the cases. Recombinant activated factor VII (rFVIIa) has been used off-label to control severe hemorrhage in surgery and trauma. We r...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1939840/ https://www.ncbi.nlm.nih.gov/pubmed/17617902 http://dx.doi.org/10.1186/1749-8090-2-32 |
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author | Gandhi, Manish J Pierce, Richard A Zhang, Lini Moon, Marc R Despotis, George J Moazami, Nader |
author_facet | Gandhi, Manish J Pierce, Richard A Zhang, Lini Moon, Marc R Despotis, George J Moazami, Nader |
author_sort | Gandhi, Manish J |
collection | PubMed |
description | BACKGROUND: Ventricular assist devices(VAD) implantation/removal is a complex surgical procedure with perioperative bleeding complications occurring in nearly half of the cases. Recombinant activated factor VII (rFVIIa) has been used off-label to control severe hemorrhage in surgery and trauma. We report here our experience with rFVIIa as a rescue therapy to achieve hemostasis in patients undergoing orthotopic heart transplant (OHT) and/or VAD implantation. METHODS: A retrospective review was conducted from Jan 03 to Aug 05 for patients who received rFVIIa for the management of intractable bleeding unresponsive to standard hemostatic blood component therapy. Blood loss and the quantity of blood products, prior to, and for at least 12 hours after, administration of rFVIIa were recorded. RESULTS: Mean patient age was 53, (38–64 yrs), mean dose of rFVIIa administered was 78.3 μg/kg (24–189 μg/kg) in 1–3 doses. All patients received the drug either intraoperatively or within 6 hours of arrival in ICU. Mean transfusion requirements and blood loss were significantly reduced after rFVIIa administration (PRBC's; 16.9 ± 13.3 to 7.1 ± 6.9 units, FFP; 13.1 ± 8.2 to 4.1 ± 4.9 units, platelets; 4.0 ± 2.8 to 2.1 ± 2.2 units, p < 0.04 for all). 5 patients expired including 3 with thromboembolic cause. One patient developed a lower extremity arterial thrombus, and another deep vein thrombosis. CONCLUSION: In this review, there was a significant decrease in transfusion requirement and blood loss after rFVIIa administration. Although, 5/17 developed thromboembolic complications, these patients may have been at higher risk based on the multiple modality therapy used to manage intractable bleeding. Nevertheless, the exact role of rFVIIa with respect to development of thromboembolic complications cannot be clearly determined. Further investigation is needed to determine rFVIIa's safety and its effectiveness in improving postoperative morbidity and mortality. |
format | Text |
id | pubmed-1939840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-19398402007-08-04 Use of activated recombinant factor VII for severe coagulopathy post ventricular assist device or orthotopic heart transplant Gandhi, Manish J Pierce, Richard A Zhang, Lini Moon, Marc R Despotis, George J Moazami, Nader J Cardiothorac Surg Research Article BACKGROUND: Ventricular assist devices(VAD) implantation/removal is a complex surgical procedure with perioperative bleeding complications occurring in nearly half of the cases. Recombinant activated factor VII (rFVIIa) has been used off-label to control severe hemorrhage in surgery and trauma. We report here our experience with rFVIIa as a rescue therapy to achieve hemostasis in patients undergoing orthotopic heart transplant (OHT) and/or VAD implantation. METHODS: A retrospective review was conducted from Jan 03 to Aug 05 for patients who received rFVIIa for the management of intractable bleeding unresponsive to standard hemostatic blood component therapy. Blood loss and the quantity of blood products, prior to, and for at least 12 hours after, administration of rFVIIa were recorded. RESULTS: Mean patient age was 53, (38–64 yrs), mean dose of rFVIIa administered was 78.3 μg/kg (24–189 μg/kg) in 1–3 doses. All patients received the drug either intraoperatively or within 6 hours of arrival in ICU. Mean transfusion requirements and blood loss were significantly reduced after rFVIIa administration (PRBC's; 16.9 ± 13.3 to 7.1 ± 6.9 units, FFP; 13.1 ± 8.2 to 4.1 ± 4.9 units, platelets; 4.0 ± 2.8 to 2.1 ± 2.2 units, p < 0.04 for all). 5 patients expired including 3 with thromboembolic cause. One patient developed a lower extremity arterial thrombus, and another deep vein thrombosis. CONCLUSION: In this review, there was a significant decrease in transfusion requirement and blood loss after rFVIIa administration. Although, 5/17 developed thromboembolic complications, these patients may have been at higher risk based on the multiple modality therapy used to manage intractable bleeding. Nevertheless, the exact role of rFVIIa with respect to development of thromboembolic complications cannot be clearly determined. Further investigation is needed to determine rFVIIa's safety and its effectiveness in improving postoperative morbidity and mortality. BioMed Central 2007-07-06 /pmc/articles/PMC1939840/ /pubmed/17617902 http://dx.doi.org/10.1186/1749-8090-2-32 Text en Copyright © 2007 Gandhi et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Gandhi, Manish J Pierce, Richard A Zhang, Lini Moon, Marc R Despotis, George J Moazami, Nader Use of activated recombinant factor VII for severe coagulopathy post ventricular assist device or orthotopic heart transplant |
title | Use of activated recombinant factor VII for severe coagulopathy post ventricular assist device or orthotopic heart transplant |
title_full | Use of activated recombinant factor VII for severe coagulopathy post ventricular assist device or orthotopic heart transplant |
title_fullStr | Use of activated recombinant factor VII for severe coagulopathy post ventricular assist device or orthotopic heart transplant |
title_full_unstemmed | Use of activated recombinant factor VII for severe coagulopathy post ventricular assist device or orthotopic heart transplant |
title_short | Use of activated recombinant factor VII for severe coagulopathy post ventricular assist device or orthotopic heart transplant |
title_sort | use of activated recombinant factor vii for severe coagulopathy post ventricular assist device or orthotopic heart transplant |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1939840/ https://www.ncbi.nlm.nih.gov/pubmed/17617902 http://dx.doi.org/10.1186/1749-8090-2-32 |
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