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Clinical Use of Cerebral Microdialysis in Patients with Aneurysmal Subarachnoid Hemorrhage—State of the Art

OBJECTIVE: To review the published literature on the clinical application of cerebral microdialysis (CMD) in aneurysmal subarachnoid hemorrhage (SAH) patients and to summarize the evidence relating cerebral metabolism to pathophysiology, secondary brain injury, and outcome. METHODS: Study selection:...

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Autores principales: Helbok, Raimund, Kofler, Mario, Schiefecker, Alois Josef, Gaasch, Maxime, Rass, Verena, Pfausler, Bettina, Beer, Ronny, Schmutzhard, Erich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5676489/
https://www.ncbi.nlm.nih.gov/pubmed/29163332
http://dx.doi.org/10.3389/fneur.2017.00565
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author Helbok, Raimund
Kofler, Mario
Schiefecker, Alois Josef
Gaasch, Maxime
Rass, Verena
Pfausler, Bettina
Beer, Ronny
Schmutzhard, Erich
author_facet Helbok, Raimund
Kofler, Mario
Schiefecker, Alois Josef
Gaasch, Maxime
Rass, Verena
Pfausler, Bettina
Beer, Ronny
Schmutzhard, Erich
author_sort Helbok, Raimund
collection PubMed
description OBJECTIVE: To review the published literature on the clinical application of cerebral microdialysis (CMD) in aneurysmal subarachnoid hemorrhage (SAH) patients and to summarize the evidence relating cerebral metabolism to pathophysiology, secondary brain injury, and outcome. METHODS: Study selection: Two reviewers identified all manuscripts reporting on the clinical use of CMD in aneurysmal SAH patients from MEDLINE. All identified studies were grouped according to their focus on brain metabolic changes during the early and subacute phase after SAH, their association with mechanisms of secondary brain injury and outcome. RESULTS: The review demonstrated: (1) limited literature is available in the very early phase before the aneurysm is secured. (2) Brain metabolic changes related to early and delayed secondary injury mechanisms may be used in addition to other neuromonitoring parameters in the critical care management of SAH patients. (3) CMD markers of ischemia may detect delayed cerebral ischemia early (up to 16 h before onset), underlining the importance of trend analysis. (4) Various CMD-derived parameters may be associated with patient outcome at 3–12 months, including CMD-lactate-to-pyruvate-ratio, CMD-glucose, and CMD-glutamate. CONCLUSION: The clinical use of CMD is an emerging area in the literature of aneurysmal SAH patients. Larger prospective multi-center studies on interventions based on CMD findings are needed.
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spelling pubmed-56764892017-11-21 Clinical Use of Cerebral Microdialysis in Patients with Aneurysmal Subarachnoid Hemorrhage—State of the Art Helbok, Raimund Kofler, Mario Schiefecker, Alois Josef Gaasch, Maxime Rass, Verena Pfausler, Bettina Beer, Ronny Schmutzhard, Erich Front Neurol Neuroscience OBJECTIVE: To review the published literature on the clinical application of cerebral microdialysis (CMD) in aneurysmal subarachnoid hemorrhage (SAH) patients and to summarize the evidence relating cerebral metabolism to pathophysiology, secondary brain injury, and outcome. METHODS: Study selection: Two reviewers identified all manuscripts reporting on the clinical use of CMD in aneurysmal SAH patients from MEDLINE. All identified studies were grouped according to their focus on brain metabolic changes during the early and subacute phase after SAH, their association with mechanisms of secondary brain injury and outcome. RESULTS: The review demonstrated: (1) limited literature is available in the very early phase before the aneurysm is secured. (2) Brain metabolic changes related to early and delayed secondary injury mechanisms may be used in addition to other neuromonitoring parameters in the critical care management of SAH patients. (3) CMD markers of ischemia may detect delayed cerebral ischemia early (up to 16 h before onset), underlining the importance of trend analysis. (4) Various CMD-derived parameters may be associated with patient outcome at 3–12 months, including CMD-lactate-to-pyruvate-ratio, CMD-glucose, and CMD-glutamate. CONCLUSION: The clinical use of CMD is an emerging area in the literature of aneurysmal SAH patients. Larger prospective multi-center studies on interventions based on CMD findings are needed. Frontiers Media S.A. 2017-11-03 /pmc/articles/PMC5676489/ /pubmed/29163332 http://dx.doi.org/10.3389/fneur.2017.00565 Text en Copyright © 2017 Helbok, Kofler, Schiefecker, Gaasch, Rass, Pfausler, Beer and Schmutzhard. 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
Helbok, Raimund
Kofler, Mario
Schiefecker, Alois Josef
Gaasch, Maxime
Rass, Verena
Pfausler, Bettina
Beer, Ronny
Schmutzhard, Erich
Clinical Use of Cerebral Microdialysis in Patients with Aneurysmal Subarachnoid Hemorrhage—State of the Art
title Clinical Use of Cerebral Microdialysis in Patients with Aneurysmal Subarachnoid Hemorrhage—State of the Art
title_full Clinical Use of Cerebral Microdialysis in Patients with Aneurysmal Subarachnoid Hemorrhage—State of the Art
title_fullStr Clinical Use of Cerebral Microdialysis in Patients with Aneurysmal Subarachnoid Hemorrhage—State of the Art
title_full_unstemmed Clinical Use of Cerebral Microdialysis in Patients with Aneurysmal Subarachnoid Hemorrhage—State of the Art
title_short Clinical Use of Cerebral Microdialysis in Patients with Aneurysmal Subarachnoid Hemorrhage—State of the Art
title_sort clinical use of cerebral microdialysis in patients with aneurysmal subarachnoid hemorrhage—state of the art
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5676489/
https://www.ncbi.nlm.nih.gov/pubmed/29163332
http://dx.doi.org/10.3389/fneur.2017.00565
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