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Brain tissue oxygen monitoring in traumatic brain injury: part I—To what extent does PbtO(2) reflect global cerebral physiology?
BACKGROUND: The primary aim was to explore the association of global cerebral physiological variables including intracranial pressure (ICP), cerebrovascular reactivity (PRx), cerebral perfusion pressure (CPP), and deviation from the PRx-based optimal CPP value (∆CPPopt; actual CPP-CPPopt) in relatio...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10472704/ https://www.ncbi.nlm.nih.gov/pubmed/37653526 http://dx.doi.org/10.1186/s13054-023-04627-y |
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author | Svedung Wettervik, Teodor Beqiri, Erta Bögli, Stefan Yu Placek, Michal Guilfoyle, Mathew R. Helmy, Adel Lavinio, Andrea O’Leary, Ronan Hutchinson, Peter J. Smielewski, Peter |
author_facet | Svedung Wettervik, Teodor Beqiri, Erta Bögli, Stefan Yu Placek, Michal Guilfoyle, Mathew R. Helmy, Adel Lavinio, Andrea O’Leary, Ronan Hutchinson, Peter J. Smielewski, Peter |
author_sort | Svedung Wettervik, Teodor |
collection | PubMed |
description | BACKGROUND: The primary aim was to explore the association of global cerebral physiological variables including intracranial pressure (ICP), cerebrovascular reactivity (PRx), cerebral perfusion pressure (CPP), and deviation from the PRx-based optimal CPP value (∆CPPopt; actual CPP-CPPopt) in relation to brain tissue oxygenation (pbtO(2)) in traumatic brain injury (TBI). METHODS: A total of 425 TBI patients with ICP- and pbtO(2) monitoring for at least 12 h, who had been treated at the neurocritical care unit, Addenbrooke’s Hospital, Cambridge, UK, between 2002 and 2022 were included. Generalized additive models (GAMs) and linear mixed effect models were used to explore the association of ICP, PRx, CPP, and CPPopt in relation to pbtO(2). PbtO(2) < 20 mmHg, ICP > 20 mmHg, PRx > 0.30, CPP < 60 mmHg, and ∆CPPopt < − 5 mmHg were considered as cerebral insults. RESULTS: PbtO(2) < 20 mmHg occurred in median during 17% of the monitoring time and in less than 5% in combination with ICP > 20 mmHg, PRx > 0.30, CPP < 60 mmHg, or ∆CPPopt < − 5 mmHg. In GAM analyses, pbtO(2) remained around 25 mmHg over a large range of ICP ([0;50] mmHg) and PRx [− 1;1], but deteriorated below 20 mmHg for extremely low CPP below 30 mmHg and ∆CPPopt below − 30 mmHg. In linear mixed effect models, ICP, CPP, PRx, and ∆CPPopt were significantly associated with pbtO(2), but the fixed effects could only explain a very small extent of the pbtO(2) variation. CONCLUSIONS: PbtO(2) below 20 mmHg was relatively frequent and often occurred in the absence of disturbances in ICP, PRx, CPP, and ∆CPPopt. There were significant, but weak associations between the global cerebral physiological variables and pbtO(2), suggesting that hypoxic pbtO(2) is often a complex and independent pathophysiological event. Thus, other variables may be more crucial to explain pbtO(2) and, likewise, pbtO(2) may not be a suitable outcome measure to determine whether global cerebral blood flow optimization such as CPPopt therapy is successful. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-023-04627-y. |
format | Online Article Text |
id | pubmed-10472704 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-104727042023-09-02 Brain tissue oxygen monitoring in traumatic brain injury: part I—To what extent does PbtO(2) reflect global cerebral physiology? Svedung Wettervik, Teodor Beqiri, Erta Bögli, Stefan Yu Placek, Michal Guilfoyle, Mathew R. Helmy, Adel Lavinio, Andrea O’Leary, Ronan Hutchinson, Peter J. Smielewski, Peter Crit Care Research BACKGROUND: The primary aim was to explore the association of global cerebral physiological variables including intracranial pressure (ICP), cerebrovascular reactivity (PRx), cerebral perfusion pressure (CPP), and deviation from the PRx-based optimal CPP value (∆CPPopt; actual CPP-CPPopt) in relation to brain tissue oxygenation (pbtO(2)) in traumatic brain injury (TBI). METHODS: A total of 425 TBI patients with ICP- and pbtO(2) monitoring for at least 12 h, who had been treated at the neurocritical care unit, Addenbrooke’s Hospital, Cambridge, UK, between 2002 and 2022 were included. Generalized additive models (GAMs) and linear mixed effect models were used to explore the association of ICP, PRx, CPP, and CPPopt in relation to pbtO(2). PbtO(2) < 20 mmHg, ICP > 20 mmHg, PRx > 0.30, CPP < 60 mmHg, and ∆CPPopt < − 5 mmHg were considered as cerebral insults. RESULTS: PbtO(2) < 20 mmHg occurred in median during 17% of the monitoring time and in less than 5% in combination with ICP > 20 mmHg, PRx > 0.30, CPP < 60 mmHg, or ∆CPPopt < − 5 mmHg. In GAM analyses, pbtO(2) remained around 25 mmHg over a large range of ICP ([0;50] mmHg) and PRx [− 1;1], but deteriorated below 20 mmHg for extremely low CPP below 30 mmHg and ∆CPPopt below − 30 mmHg. In linear mixed effect models, ICP, CPP, PRx, and ∆CPPopt were significantly associated with pbtO(2), but the fixed effects could only explain a very small extent of the pbtO(2) variation. CONCLUSIONS: PbtO(2) below 20 mmHg was relatively frequent and often occurred in the absence of disturbances in ICP, PRx, CPP, and ∆CPPopt. There were significant, but weak associations between the global cerebral physiological variables and pbtO(2), suggesting that hypoxic pbtO(2) is often a complex and independent pathophysiological event. Thus, other variables may be more crucial to explain pbtO(2) and, likewise, pbtO(2) may not be a suitable outcome measure to determine whether global cerebral blood flow optimization such as CPPopt therapy is successful. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-023-04627-y. BioMed Central 2023-08-31 /pmc/articles/PMC10472704/ /pubmed/37653526 http://dx.doi.org/10.1186/s13054-023-04627-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Svedung Wettervik, Teodor Beqiri, Erta Bögli, Stefan Yu Placek, Michal Guilfoyle, Mathew R. Helmy, Adel Lavinio, Andrea O’Leary, Ronan Hutchinson, Peter J. Smielewski, Peter Brain tissue oxygen monitoring in traumatic brain injury: part I—To what extent does PbtO(2) reflect global cerebral physiology? |
title | Brain tissue oxygen monitoring in traumatic brain injury: part I—To what extent does PbtO(2) reflect global cerebral physiology? |
title_full | Brain tissue oxygen monitoring in traumatic brain injury: part I—To what extent does PbtO(2) reflect global cerebral physiology? |
title_fullStr | Brain tissue oxygen monitoring in traumatic brain injury: part I—To what extent does PbtO(2) reflect global cerebral physiology? |
title_full_unstemmed | Brain tissue oxygen monitoring in traumatic brain injury: part I—To what extent does PbtO(2) reflect global cerebral physiology? |
title_short | Brain tissue oxygen monitoring in traumatic brain injury: part I—To what extent does PbtO(2) reflect global cerebral physiology? |
title_sort | brain tissue oxygen monitoring in traumatic brain injury: part i—to what extent does pbto(2) reflect global cerebral physiology? |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10472704/ https://www.ncbi.nlm.nih.gov/pubmed/37653526 http://dx.doi.org/10.1186/s13054-023-04627-y |
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