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Resuscitation from hemorrhagic shock after traumatic brain injury with polymerized hemoglobin
Traumatic brain injury (TBI) is often accompanied by hemorrhage, and treatment of hemorrhagic shock (HS) after TBI is particularly challenging because the two therapeutic treatment strategies for TBI and HS often conflict. Ischemia/reperfusion injury from HS resuscitation can be exaggerated by TBI-i...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7843604/ https://www.ncbi.nlm.nih.gov/pubmed/33510204 http://dx.doi.org/10.1038/s41598-021-81717-3 |
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author | Muller, Cynthia R. Courelli, Vasiliki Lucas, Alfredo Williams, Alexander T. Li, Joyce B. Dos Santos, Fernando Cuddington, Clayton T. Moses, Savannah R. Palmer, Andre F. Kistler, Erik B. Cabrales, Pedro |
author_facet | Muller, Cynthia R. Courelli, Vasiliki Lucas, Alfredo Williams, Alexander T. Li, Joyce B. Dos Santos, Fernando Cuddington, Clayton T. Moses, Savannah R. Palmer, Andre F. Kistler, Erik B. Cabrales, Pedro |
author_sort | Muller, Cynthia R. |
collection | PubMed |
description | Traumatic brain injury (TBI) is often accompanied by hemorrhage, and treatment of hemorrhagic shock (HS) after TBI is particularly challenging because the two therapeutic treatment strategies for TBI and HS often conflict. Ischemia/reperfusion injury from HS resuscitation can be exaggerated by TBI-induced loss of autoregulation. In HS resuscitation, the goal is to restore lost blood volume, while in the treatment of TBI the priority is focused on maintenance of adequate cerebral perfusion pressure and avoidance of secondary bleeding. In this study, we investigate the responses to resuscitation from severe HS after TBI in rats, using fresh blood, polymerized human hemoglobin (PolyhHb), and lactated Ringer’s (LR). Rats were subjected to TBI by pneumatic controlled cortical impact. Shortly after TBI, HS was induced by blood withdrawal to reduce mean arterial pressure (MAP) to 35–40 mmHg for 90 min before resuscitation. Resuscitation fluids were delivered to restore MAP to ~ 65 mmHg and animals were monitored for 120 min. Increased systolic blood pressure variability (SBPV) confirmed TBI-induced loss of autoregulation. MAP after resuscitation was significantly higher in the blood and PolyhHb groups compared to the LR group. Furthermore, blood and PolyhHb restored diastolic pressure, while this remained depressed for the LR group, indicating a loss of vascular tone. Lactate increased in all groups during HS, and only returned to baseline level in the blood reperfused group. The PolyhHb group possessed lower SBPV compared to LR and blood groups. Finally, sympathetic nervous system (SNS) modulation was higher for the LR group and lower for the PolyhHb group compared to the blood group after reperfusion. In conclusion, our results suggest that PolyhHb could be an alternative to blood for resuscitation from HS after TBI when blood is not available, assuming additional testing demonstrate similar favorable results. PolyhHb restored hemodynamics and oxygen delivery, without the logistical constraints of refrigerated blood. |
format | Online Article Text |
id | pubmed-7843604 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78436042021-01-29 Resuscitation from hemorrhagic shock after traumatic brain injury with polymerized hemoglobin Muller, Cynthia R. Courelli, Vasiliki Lucas, Alfredo Williams, Alexander T. Li, Joyce B. Dos Santos, Fernando Cuddington, Clayton T. Moses, Savannah R. Palmer, Andre F. Kistler, Erik B. Cabrales, Pedro Sci Rep Article Traumatic brain injury (TBI) is often accompanied by hemorrhage, and treatment of hemorrhagic shock (HS) after TBI is particularly challenging because the two therapeutic treatment strategies for TBI and HS often conflict. Ischemia/reperfusion injury from HS resuscitation can be exaggerated by TBI-induced loss of autoregulation. In HS resuscitation, the goal is to restore lost blood volume, while in the treatment of TBI the priority is focused on maintenance of adequate cerebral perfusion pressure and avoidance of secondary bleeding. In this study, we investigate the responses to resuscitation from severe HS after TBI in rats, using fresh blood, polymerized human hemoglobin (PolyhHb), and lactated Ringer’s (LR). Rats were subjected to TBI by pneumatic controlled cortical impact. Shortly after TBI, HS was induced by blood withdrawal to reduce mean arterial pressure (MAP) to 35–40 mmHg for 90 min before resuscitation. Resuscitation fluids were delivered to restore MAP to ~ 65 mmHg and animals were monitored for 120 min. Increased systolic blood pressure variability (SBPV) confirmed TBI-induced loss of autoregulation. MAP after resuscitation was significantly higher in the blood and PolyhHb groups compared to the LR group. Furthermore, blood and PolyhHb restored diastolic pressure, while this remained depressed for the LR group, indicating a loss of vascular tone. Lactate increased in all groups during HS, and only returned to baseline level in the blood reperfused group. The PolyhHb group possessed lower SBPV compared to LR and blood groups. Finally, sympathetic nervous system (SNS) modulation was higher for the LR group and lower for the PolyhHb group compared to the blood group after reperfusion. In conclusion, our results suggest that PolyhHb could be an alternative to blood for resuscitation from HS after TBI when blood is not available, assuming additional testing demonstrate similar favorable results. PolyhHb restored hemodynamics and oxygen delivery, without the logistical constraints of refrigerated blood. Nature Publishing Group UK 2021-01-28 /pmc/articles/PMC7843604/ /pubmed/33510204 http://dx.doi.org/10.1038/s41598-021-81717-3 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Muller, Cynthia R. Courelli, Vasiliki Lucas, Alfredo Williams, Alexander T. Li, Joyce B. Dos Santos, Fernando Cuddington, Clayton T. Moses, Savannah R. Palmer, Andre F. Kistler, Erik B. Cabrales, Pedro Resuscitation from hemorrhagic shock after traumatic brain injury with polymerized hemoglobin |
title | Resuscitation from hemorrhagic shock after traumatic brain injury with polymerized hemoglobin |
title_full | Resuscitation from hemorrhagic shock after traumatic brain injury with polymerized hemoglobin |
title_fullStr | Resuscitation from hemorrhagic shock after traumatic brain injury with polymerized hemoglobin |
title_full_unstemmed | Resuscitation from hemorrhagic shock after traumatic brain injury with polymerized hemoglobin |
title_short | Resuscitation from hemorrhagic shock after traumatic brain injury with polymerized hemoglobin |
title_sort | resuscitation from hemorrhagic shock after traumatic brain injury with polymerized hemoglobin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7843604/ https://www.ncbi.nlm.nih.gov/pubmed/33510204 http://dx.doi.org/10.1038/s41598-021-81717-3 |
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