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Brain Tissue Oxygenation and Cerebral Metabolic Patterns in Focal and Diffuse Traumatic Brain Injury

Introduction: Neurointensive care of traumatic brain injury (TBI) patients is currently based on intracranial pressure (ICP) and cerebral perfusion pressure (CPP) targeted protocols. There are reasons to believe that knowledge of brain tissue oxygenation (BtipO(2)) would add information with the pot...

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Autores principales: Purins, Karlis, Lewén, Anders, Hillered, Lars, Howells, Tim, Enblad, Per
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4013462/
https://www.ncbi.nlm.nih.gov/pubmed/24817863
http://dx.doi.org/10.3389/fneur.2014.00064
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author Purins, Karlis
Lewén, Anders
Hillered, Lars
Howells, Tim
Enblad, Per
author_facet Purins, Karlis
Lewén, Anders
Hillered, Lars
Howells, Tim
Enblad, Per
author_sort Purins, Karlis
collection PubMed
description Introduction: Neurointensive care of traumatic brain injury (TBI) patients is currently based on intracranial pressure (ICP) and cerebral perfusion pressure (CPP) targeted protocols. There are reasons to believe that knowledge of brain tissue oxygenation (BtipO(2)) would add information with the potential of improving patient outcome. The aim of this study was to examine B(ti)pO(2) and cerebral metabolism using the Neurovent-PTO probe and cerebral microdialysis (MD) in TBI patients. Methods: Twenty-three severe TBI patients with monitoring of physiological parameters, ICP, CPP, B(ti)pO(2), and MD for biomarkers of energy metabolism (glucose, lactate, and pyruvate) and cellular distress (glutamate, glycerol) were included. Patients were grouped according to injury type (focal/diffuse) and placement of the Neurovent-PTO probe and MD catheter (injured/non-injured hemisphere). Results: We observed different patterns in B(ti)pO(2) and MD biomarkers in diffuse and focal injury where placement of the probe also influenced the results (ipsilateral/contralateral). In all groups, despite fairly normal levels of ICP and CPP, increased MD levels of glutamate, glycerol, or the L/P ratio were observed at B(ti)pO(2) <5 mmHg, indicating increased vulnerability of the brain at this level. Conclusion: Monitoring of B(ti)pO(2) adds important information in addition to traditional ICP and CPP surveillance. Because of the different metabolic responses to very low B(ti)pO(2) in the individual patient groups we submit that brain tissue oximetry is a complementary tool rather than an alternative to MD monitoring.
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spelling pubmed-40134622014-05-09 Brain Tissue Oxygenation and Cerebral Metabolic Patterns in Focal and Diffuse Traumatic Brain Injury Purins, Karlis Lewén, Anders Hillered, Lars Howells, Tim Enblad, Per Front Neurol Neuroscience Introduction: Neurointensive care of traumatic brain injury (TBI) patients is currently based on intracranial pressure (ICP) and cerebral perfusion pressure (CPP) targeted protocols. There are reasons to believe that knowledge of brain tissue oxygenation (BtipO(2)) would add information with the potential of improving patient outcome. The aim of this study was to examine B(ti)pO(2) and cerebral metabolism using the Neurovent-PTO probe and cerebral microdialysis (MD) in TBI patients. Methods: Twenty-three severe TBI patients with monitoring of physiological parameters, ICP, CPP, B(ti)pO(2), and MD for biomarkers of energy metabolism (glucose, lactate, and pyruvate) and cellular distress (glutamate, glycerol) were included. Patients were grouped according to injury type (focal/diffuse) and placement of the Neurovent-PTO probe and MD catheter (injured/non-injured hemisphere). Results: We observed different patterns in B(ti)pO(2) and MD biomarkers in diffuse and focal injury where placement of the probe also influenced the results (ipsilateral/contralateral). In all groups, despite fairly normal levels of ICP and CPP, increased MD levels of glutamate, glycerol, or the L/P ratio were observed at B(ti)pO(2) <5 mmHg, indicating increased vulnerability of the brain at this level. Conclusion: Monitoring of B(ti)pO(2) adds important information in addition to traditional ICP and CPP surveillance. Because of the different metabolic responses to very low B(ti)pO(2) in the individual patient groups we submit that brain tissue oximetry is a complementary tool rather than an alternative to MD monitoring. Frontiers Media S.A. 2014-05-01 /pmc/articles/PMC4013462/ /pubmed/24817863 http://dx.doi.org/10.3389/fneur.2014.00064 Text en Copyright © 2014 Purins, Lewén, Hillered, Howells and Enblad. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Purins, Karlis
Lewén, Anders
Hillered, Lars
Howells, Tim
Enblad, Per
Brain Tissue Oxygenation and Cerebral Metabolic Patterns in Focal and Diffuse Traumatic Brain Injury
title Brain Tissue Oxygenation and Cerebral Metabolic Patterns in Focal and Diffuse Traumatic Brain Injury
title_full Brain Tissue Oxygenation and Cerebral Metabolic Patterns in Focal and Diffuse Traumatic Brain Injury
title_fullStr Brain Tissue Oxygenation and Cerebral Metabolic Patterns in Focal and Diffuse Traumatic Brain Injury
title_full_unstemmed Brain Tissue Oxygenation and Cerebral Metabolic Patterns in Focal and Diffuse Traumatic Brain Injury
title_short Brain Tissue Oxygenation and Cerebral Metabolic Patterns in Focal and Diffuse Traumatic Brain Injury
title_sort brain tissue oxygenation and cerebral metabolic patterns in focal and diffuse traumatic brain injury
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4013462/
https://www.ncbi.nlm.nih.gov/pubmed/24817863
http://dx.doi.org/10.3389/fneur.2014.00064
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