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Sedation-Induced Burst Suppression Predicts Positive Outcome Following Traumatic Brain Injury

While electroencephalogram (EEG) burst-suppression is often induced therapeutically using sedatives in the intensive care unit (ICU), there is hitherto no evidence with respect to its association to outcome in moderate-to-severe neurological patients. We examined the relationship between sedation-in...

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Autores principales: Frohlich, Joel, Johnson, Micah A., McArthur, David L., Lutkenhoff, Evan S., Dell'Italia, John, Real, Courtney, Shrestha, Vikesh, Spivak, Norman M., Ruiz Tejeda, Jesús E., Vespa, Paul M., Monti, Martin M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8727767/
https://www.ncbi.nlm.nih.gov/pubmed/35002918
http://dx.doi.org/10.3389/fneur.2021.750667
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author Frohlich, Joel
Johnson, Micah A.
McArthur, David L.
Lutkenhoff, Evan S.
Dell'Italia, John
Real, Courtney
Shrestha, Vikesh
Spivak, Norman M.
Ruiz Tejeda, Jesús E.
Vespa, Paul M.
Monti, Martin M.
author_facet Frohlich, Joel
Johnson, Micah A.
McArthur, David L.
Lutkenhoff, Evan S.
Dell'Italia, John
Real, Courtney
Shrestha, Vikesh
Spivak, Norman M.
Ruiz Tejeda, Jesús E.
Vespa, Paul M.
Monti, Martin M.
author_sort Frohlich, Joel
collection PubMed
description While electroencephalogram (EEG) burst-suppression is often induced therapeutically using sedatives in the intensive care unit (ICU), there is hitherto no evidence with respect to its association to outcome in moderate-to-severe neurological patients. We examined the relationship between sedation-induced burst-suppression (SIBS) and outcome at hospital discharge and at 6-month follow up in patients surviving moderate-to-severe traumatic brain injury (TBI). For each of 32 patients recovering from coma after moderate-to-severe TBI, we measured the EEG burst suppression ratio (BSR) during periods of low responsiveness as assessed with the Glasgow Coma Scale (GCS). The maximum BSR was then used to predict the Glasgow Outcome Scale extended (GOSe) at discharge and at 6 months post-injury. A multi-model inference approach was used to assess the combination of predictors that best fit the outcome data. We found that BSR was positively associated with outcomes at 6 months (P = 0.022) but did not predict outcomes at discharge. A mediation analysis found no evidence that BSR mediates the effects of barbiturates or propofol on outcomes. Our results provide initial observational evidence that burst suppression may be neuroprotective in acute patients with TBI etiologies. SIBS may thus be useful in the ICU as a prognostic biomarker.
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spelling pubmed-87277672022-01-06 Sedation-Induced Burst Suppression Predicts Positive Outcome Following Traumatic Brain Injury Frohlich, Joel Johnson, Micah A. McArthur, David L. Lutkenhoff, Evan S. Dell'Italia, John Real, Courtney Shrestha, Vikesh Spivak, Norman M. Ruiz Tejeda, Jesús E. Vespa, Paul M. Monti, Martin M. Front Neurol Neurology While electroencephalogram (EEG) burst-suppression is often induced therapeutically using sedatives in the intensive care unit (ICU), there is hitherto no evidence with respect to its association to outcome in moderate-to-severe neurological patients. We examined the relationship between sedation-induced burst-suppression (SIBS) and outcome at hospital discharge and at 6-month follow up in patients surviving moderate-to-severe traumatic brain injury (TBI). For each of 32 patients recovering from coma after moderate-to-severe TBI, we measured the EEG burst suppression ratio (BSR) during periods of low responsiveness as assessed with the Glasgow Coma Scale (GCS). The maximum BSR was then used to predict the Glasgow Outcome Scale extended (GOSe) at discharge and at 6 months post-injury. A multi-model inference approach was used to assess the combination of predictors that best fit the outcome data. We found that BSR was positively associated with outcomes at 6 months (P = 0.022) but did not predict outcomes at discharge. A mediation analysis found no evidence that BSR mediates the effects of barbiturates or propofol on outcomes. Our results provide initial observational evidence that burst suppression may be neuroprotective in acute patients with TBI etiologies. SIBS may thus be useful in the ICU as a prognostic biomarker. Frontiers Media S.A. 2021-12-22 /pmc/articles/PMC8727767/ /pubmed/35002918 http://dx.doi.org/10.3389/fneur.2021.750667 Text en Copyright © 2021 Frohlich, Johnson, McArthur, Lutkenhoff, Dell'Italia, Real, Shrestha, Spivak, Ruiz Tejeda, Vespa and Monti. https://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) and the copyright owner(s) 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 Neurology
Frohlich, Joel
Johnson, Micah A.
McArthur, David L.
Lutkenhoff, Evan S.
Dell'Italia, John
Real, Courtney
Shrestha, Vikesh
Spivak, Norman M.
Ruiz Tejeda, Jesús E.
Vespa, Paul M.
Monti, Martin M.
Sedation-Induced Burst Suppression Predicts Positive Outcome Following Traumatic Brain Injury
title Sedation-Induced Burst Suppression Predicts Positive Outcome Following Traumatic Brain Injury
title_full Sedation-Induced Burst Suppression Predicts Positive Outcome Following Traumatic Brain Injury
title_fullStr Sedation-Induced Burst Suppression Predicts Positive Outcome Following Traumatic Brain Injury
title_full_unstemmed Sedation-Induced Burst Suppression Predicts Positive Outcome Following Traumatic Brain Injury
title_short Sedation-Induced Burst Suppression Predicts Positive Outcome Following Traumatic Brain Injury
title_sort sedation-induced burst suppression predicts positive outcome following traumatic brain injury
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8727767/
https://www.ncbi.nlm.nih.gov/pubmed/35002918
http://dx.doi.org/10.3389/fneur.2021.750667
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