Resuscitation from hemorrhagic shock after traumatic brain injury with polymerized hemoglobin

Abstract 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...

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Main Authors: Cynthia R. Muller, Vasiliki Courelli, Alfredo Lucas, Alexander T. Williams, Joyce B. Li, Fernando Dos Santos, Clayton T. Cuddington, Savannah R. Moses, Andre F. Palmer, Erik B. Kistler, Pedro Cabrales
Format: Article
Language:English
Published: Nature Publishing Group 2021-01-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-81717-3
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spelling doaj-498e933377124b19800d64b418baa6772021-01-31T16:26:52ZengNature Publishing GroupScientific Reports2045-23222021-01-0111111110.1038/s41598-021-81717-3Resuscitation from hemorrhagic shock after traumatic brain injury with polymerized hemoglobinCynthia R. Muller0Vasiliki Courelli1Alfredo Lucas2Alexander T. Williams3Joyce B. Li4Fernando Dos Santos5Clayton T. Cuddington6Savannah R. Moses7Andre F. Palmer8Erik B. Kistler9Pedro Cabrales10Department of Bioengineering, University of California San DiegoDepartment of Bioengineering, University of California San DiegoDepartment of Bioengineering, University of California San DiegoDepartment of Bioengineering, University of California San DiegoDepartment of Bioengineering, University of California San DiegoDepartment of Anesthesiology and Critical Care, University of California San DiegoWilliam G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State UniversityWilliam G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State UniversityWilliam G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State UniversityDepartment of Anesthesiology and Critical Care, University of California San DiegoDepartment of Bioengineering, University of California San DiegoAbstract 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.https://doi.org/10.1038/s41598-021-81717-3
collection DOAJ
language English
format Article
sources DOAJ
author Cynthia R. Muller
Vasiliki Courelli
Alfredo Lucas
Alexander T. Williams
Joyce B. Li
Fernando Dos Santos
Clayton T. Cuddington
Savannah R. Moses
Andre F. Palmer
Erik B. Kistler
Pedro Cabrales
spellingShingle Cynthia R. Muller
Vasiliki Courelli
Alfredo Lucas
Alexander T. Williams
Joyce B. Li
Fernando Dos Santos
Clayton T. Cuddington
Savannah R. Moses
Andre F. Palmer
Erik B. Kistler
Pedro Cabrales
Resuscitation from hemorrhagic shock after traumatic brain injury with polymerized hemoglobin
Scientific Reports
author_facet Cynthia R. Muller
Vasiliki Courelli
Alfredo Lucas
Alexander T. Williams
Joyce B. Li
Fernando Dos Santos
Clayton T. Cuddington
Savannah R. Moses
Andre F. Palmer
Erik B. Kistler
Pedro Cabrales
author_sort Cynthia R. Muller
title 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_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_sort resuscitation from hemorrhagic shock after traumatic brain injury with polymerized hemoglobin
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-01-01
description Abstract 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.
url https://doi.org/10.1038/s41598-021-81717-3
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