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Prognostic value of neonatal EEG following therapeutic hypothermia in survivors of hypoxic-ischemic encephalopathy

OBJECTIVE: Early prediction of neurological deficits following neonatal hypoxic-ischemic encephalopathy (HIE) may help to target support. Neonatal animal models suggest that recovery following hypoxia-ischemia depends upon cortical bursting. To test whether this holds in human neonates, we correlate...

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Autores principales: Koskela, Tuomas, Kendall, Giles S., Memon, Sara, Sokolska, Magdalena, Mabuza, Thalitha, Huertas-Ceballos, Angela, Mitra, Subhabrata, Robertson, Nicola J., Meek, Judith, Whitehead, Kimberley
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8407358/
https://www.ncbi.nlm.nih.gov/pubmed/34284244
http://dx.doi.org/10.1016/j.clinph.2021.05.031
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author Koskela, Tuomas
Kendall, Giles S.
Memon, Sara
Sokolska, Magdalena
Mabuza, Thalitha
Huertas-Ceballos, Angela
Mitra, Subhabrata
Robertson, Nicola J.
Meek, Judith
Whitehead, Kimberley
author_facet Koskela, Tuomas
Kendall, Giles S.
Memon, Sara
Sokolska, Magdalena
Mabuza, Thalitha
Huertas-Ceballos, Angela
Mitra, Subhabrata
Robertson, Nicola J.
Meek, Judith
Whitehead, Kimberley
author_sort Koskela, Tuomas
collection PubMed
description OBJECTIVE: Early prediction of neurological deficits following neonatal hypoxic-ischemic encephalopathy (HIE) may help to target support. Neonatal animal models suggest that recovery following hypoxia-ischemia depends upon cortical bursting. To test whether this holds in human neonates, we correlated the magnitude of cortical bursting during recovery (≥postnatal day 3) with neurodevelopmental outcomes. METHODS: We identified 41 surviving infants who received therapeutic hypothermia for HIE (classification at hospital discharge: 19 mild, 18 moderate, 4 severe) and had 9-channel electroencephalography (EEG) recordings as part of their routine care. We correlated burst power with Bayley-III cognitive, motor and language scores at median 24 months. To examine whether EEG offered additional prognostic information, we controlled for structural MRI findings. RESULTS: Higher power of central and occipital cortical bursts predicted worse cognitive and language outcomes, and higher power of central cortical bursts predicted worse motor outcome, all independently of structural MRI findings. CONCLUSIONS: Clinical EEG after postnatal day 3 may provide additional prognostic information by indexing persistent active mechanisms that either support recovery or exacerbate brain damage, especially in infants with less severe encephalopathy. SIGNIFICANCE: These findings could allow for the effect of clinical interventions in the neonatal period to be studied instantaneously in the future.
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spelling pubmed-84073582021-09-03 Prognostic value of neonatal EEG following therapeutic hypothermia in survivors of hypoxic-ischemic encephalopathy Koskela, Tuomas Kendall, Giles S. Memon, Sara Sokolska, Magdalena Mabuza, Thalitha Huertas-Ceballos, Angela Mitra, Subhabrata Robertson, Nicola J. Meek, Judith Whitehead, Kimberley Clin Neurophysiol Article OBJECTIVE: Early prediction of neurological deficits following neonatal hypoxic-ischemic encephalopathy (HIE) may help to target support. Neonatal animal models suggest that recovery following hypoxia-ischemia depends upon cortical bursting. To test whether this holds in human neonates, we correlated the magnitude of cortical bursting during recovery (≥postnatal day 3) with neurodevelopmental outcomes. METHODS: We identified 41 surviving infants who received therapeutic hypothermia for HIE (classification at hospital discharge: 19 mild, 18 moderate, 4 severe) and had 9-channel electroencephalography (EEG) recordings as part of their routine care. We correlated burst power with Bayley-III cognitive, motor and language scores at median 24 months. To examine whether EEG offered additional prognostic information, we controlled for structural MRI findings. RESULTS: Higher power of central and occipital cortical bursts predicted worse cognitive and language outcomes, and higher power of central cortical bursts predicted worse motor outcome, all independently of structural MRI findings. CONCLUSIONS: Clinical EEG after postnatal day 3 may provide additional prognostic information by indexing persistent active mechanisms that either support recovery or exacerbate brain damage, especially in infants with less severe encephalopathy. SIGNIFICANCE: These findings could allow for the effect of clinical interventions in the neonatal period to be studied instantaneously in the future. Elsevier 2021-09 /pmc/articles/PMC8407358/ /pubmed/34284244 http://dx.doi.org/10.1016/j.clinph.2021.05.031 Text en © 2021 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Koskela, Tuomas
Kendall, Giles S.
Memon, Sara
Sokolska, Magdalena
Mabuza, Thalitha
Huertas-Ceballos, Angela
Mitra, Subhabrata
Robertson, Nicola J.
Meek, Judith
Whitehead, Kimberley
Prognostic value of neonatal EEG following therapeutic hypothermia in survivors of hypoxic-ischemic encephalopathy
title Prognostic value of neonatal EEG following therapeutic hypothermia in survivors of hypoxic-ischemic encephalopathy
title_full Prognostic value of neonatal EEG following therapeutic hypothermia in survivors of hypoxic-ischemic encephalopathy
title_fullStr Prognostic value of neonatal EEG following therapeutic hypothermia in survivors of hypoxic-ischemic encephalopathy
title_full_unstemmed Prognostic value of neonatal EEG following therapeutic hypothermia in survivors of hypoxic-ischemic encephalopathy
title_short Prognostic value of neonatal EEG following therapeutic hypothermia in survivors of hypoxic-ischemic encephalopathy
title_sort prognostic value of neonatal eeg following therapeutic hypothermia in survivors of hypoxic-ischemic encephalopathy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8407358/
https://www.ncbi.nlm.nih.gov/pubmed/34284244
http://dx.doi.org/10.1016/j.clinph.2021.05.031
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