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Systemic, Local, and Imaging Biomarkers of Brain Injury: More Needed, and Better Use of Those Already Established?

Much progress has been made over the past two decades in the treatment of severe acute brain injury, including traumatic brain injury and subarachnoid hemorrhage, resulting in a higher proportion of patients surviving with better outcomes. This has arisen from a combination of factors. These include...

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Autores principales: Carpenter, Keri L. H., Czosnyka, Marek, Jalloh, Ibrahim, Newcombe, Virginia F. J., Helmy, Adel, Shannon, Richard J., Budohoski, Karol P., Kolias, Angelos G., Kirkpatrick, Peter J., Carpenter, Thomas Adrian, Menon, David K., Hutchinson, Peter J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4332345/
https://www.ncbi.nlm.nih.gov/pubmed/25741315
http://dx.doi.org/10.3389/fneur.2015.00026
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author Carpenter, Keri L. H.
Czosnyka, Marek
Jalloh, Ibrahim
Newcombe, Virginia F. J.
Helmy, Adel
Shannon, Richard J.
Budohoski, Karol P.
Kolias, Angelos G.
Kirkpatrick, Peter J.
Carpenter, Thomas Adrian
Menon, David K.
Hutchinson, Peter J.
author_facet Carpenter, Keri L. H.
Czosnyka, Marek
Jalloh, Ibrahim
Newcombe, Virginia F. J.
Helmy, Adel
Shannon, Richard J.
Budohoski, Karol P.
Kolias, Angelos G.
Kirkpatrick, Peter J.
Carpenter, Thomas Adrian
Menon, David K.
Hutchinson, Peter J.
author_sort Carpenter, Keri L. H.
collection PubMed
description Much progress has been made over the past two decades in the treatment of severe acute brain injury, including traumatic brain injury and subarachnoid hemorrhage, resulting in a higher proportion of patients surviving with better outcomes. This has arisen from a combination of factors. These include improvements in procedures at the scene (pre-hospital) and in the hospital emergency department, advances in neuromonitoring in the intensive care unit, both continuously at the bedside and intermittently in scans, evolution and refinement of protocol-driven therapy for better management of patients, and advances in surgical procedures and rehabilitation. Nevertheless, many patients still experience varying degrees of long-term disabilities post-injury with consequent demands on carers and resources, and there is room for improvement. Biomarkers are a key aspect of neuromonitoring. A broad definition of a biomarker is any observable feature that can be used to inform on the state of the patient, e.g., a molecular species, a feature on a scan, or a monitoring characteristic, e.g., cerebrovascular pressure reactivity index. Biomarkers are usually quantitative measures, which can be utilized in diagnosis and monitoring of response to treatment. They are thus crucial to the development of therapies and may be utilized as surrogate endpoints in Phase II clinical trials. To date, there is no specific drug treatment for acute brain injury, and many seemingly promising agents emerging from pre-clinical animal models have failed in clinical trials. Large Phase III studies of clinical outcomes are costly, consuming time and resources. It is therefore important that adequate Phase II clinical studies with informative surrogate endpoints are performed employing appropriate biomarkers. In this article, we review some of the available systemic, local, and imaging biomarkers and technologies relevant in acute brain injury patients, and highlight gaps in the current state of knowledge.
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spelling pubmed-43323452015-03-04 Systemic, Local, and Imaging Biomarkers of Brain Injury: More Needed, and Better Use of Those Already Established? Carpenter, Keri L. H. Czosnyka, Marek Jalloh, Ibrahim Newcombe, Virginia F. J. Helmy, Adel Shannon, Richard J. Budohoski, Karol P. Kolias, Angelos G. Kirkpatrick, Peter J. Carpenter, Thomas Adrian Menon, David K. Hutchinson, Peter J. Front Neurol Neuroscience Much progress has been made over the past two decades in the treatment of severe acute brain injury, including traumatic brain injury and subarachnoid hemorrhage, resulting in a higher proportion of patients surviving with better outcomes. This has arisen from a combination of factors. These include improvements in procedures at the scene (pre-hospital) and in the hospital emergency department, advances in neuromonitoring in the intensive care unit, both continuously at the bedside and intermittently in scans, evolution and refinement of protocol-driven therapy for better management of patients, and advances in surgical procedures and rehabilitation. Nevertheless, many patients still experience varying degrees of long-term disabilities post-injury with consequent demands on carers and resources, and there is room for improvement. Biomarkers are a key aspect of neuromonitoring. A broad definition of a biomarker is any observable feature that can be used to inform on the state of the patient, e.g., a molecular species, a feature on a scan, or a monitoring characteristic, e.g., cerebrovascular pressure reactivity index. Biomarkers are usually quantitative measures, which can be utilized in diagnosis and monitoring of response to treatment. They are thus crucial to the development of therapies and may be utilized as surrogate endpoints in Phase II clinical trials. To date, there is no specific drug treatment for acute brain injury, and many seemingly promising agents emerging from pre-clinical animal models have failed in clinical trials. Large Phase III studies of clinical outcomes are costly, consuming time and resources. It is therefore important that adequate Phase II clinical studies with informative surrogate endpoints are performed employing appropriate biomarkers. In this article, we review some of the available systemic, local, and imaging biomarkers and technologies relevant in acute brain injury patients, and highlight gaps in the current state of knowledge. Frontiers Media S.A. 2015-02-18 /pmc/articles/PMC4332345/ /pubmed/25741315 http://dx.doi.org/10.3389/fneur.2015.00026 Text en Copyright © 2015 Carpenter, Czosnyka, Jalloh, Newcombe, Helmy, Shannon, Budohoski, Kolias, Kirkpatrick, Carpenter, Menon and Hutchinson. http://creativecommons.org/licenses/by/4.0/ 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
Carpenter, Keri L. H.
Czosnyka, Marek
Jalloh, Ibrahim
Newcombe, Virginia F. J.
Helmy, Adel
Shannon, Richard J.
Budohoski, Karol P.
Kolias, Angelos G.
Kirkpatrick, Peter J.
Carpenter, Thomas Adrian
Menon, David K.
Hutchinson, Peter J.
Systemic, Local, and Imaging Biomarkers of Brain Injury: More Needed, and Better Use of Those Already Established?
title Systemic, Local, and Imaging Biomarkers of Brain Injury: More Needed, and Better Use of Those Already Established?
title_full Systemic, Local, and Imaging Biomarkers of Brain Injury: More Needed, and Better Use of Those Already Established?
title_fullStr Systemic, Local, and Imaging Biomarkers of Brain Injury: More Needed, and Better Use of Those Already Established?
title_full_unstemmed Systemic, Local, and Imaging Biomarkers of Brain Injury: More Needed, and Better Use of Those Already Established?
title_short Systemic, Local, and Imaging Biomarkers of Brain Injury: More Needed, and Better Use of Those Already Established?
title_sort systemic, local, and imaging biomarkers of brain injury: more needed, and better use of those already established?
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4332345/
https://www.ncbi.nlm.nih.gov/pubmed/25741315
http://dx.doi.org/10.3389/fneur.2015.00026
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