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Multichannel EEG abnormalities during the first 6 hours in infants with mild hypoxic–ischaemic encephalopathy

BACKGROUND: Infants with mild HIE are at risk of significant disability at follow-up. In the pre-therapeutic hypothermia (TH) era, electroencephalography (EEG) within 6 hours of birth was most predictive of outcome. This study aims to identify and describe features of early EEG and heart rate variab...

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Autores principales: Garvey, Aisling A., Pavel, Andreea M., O’Toole, John M., Walsh, Brian H., Korotchikova, Irina, Livingstone, Vicki, Dempsey, Eugene M., Murray, Deirdre M., Boylan, Geraldine B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8370873/
https://www.ncbi.nlm.nih.gov/pubmed/33879847
http://dx.doi.org/10.1038/s41390-021-01412-x
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author Garvey, Aisling A.
Pavel, Andreea M.
O’Toole, John M.
Walsh, Brian H.
Korotchikova, Irina
Livingstone, Vicki
Dempsey, Eugene M.
Murray, Deirdre M.
Boylan, Geraldine B.
author_facet Garvey, Aisling A.
Pavel, Andreea M.
O’Toole, John M.
Walsh, Brian H.
Korotchikova, Irina
Livingstone, Vicki
Dempsey, Eugene M.
Murray, Deirdre M.
Boylan, Geraldine B.
author_sort Garvey, Aisling A.
collection PubMed
description BACKGROUND: Infants with mild HIE are at risk of significant disability at follow-up. In the pre-therapeutic hypothermia (TH) era, electroencephalography (EEG) within 6 hours of birth was most predictive of outcome. This study aims to identify and describe features of early EEG and heart rate variability (HRV) (<6 hours of age) in infants with mild HIE compared to healthy term infants. METHODS: Infants >36 weeks with mild HIE, not undergoing TH, with EEG before 6 hours of age were identified from 4 prospective cohort studies conducted in the Cork University Maternity Services, Ireland (2003–2019). Control infants were taken from a contemporaneous study examining brain activity in healthy term infants. EEGs were qualitatively analysed by two neonatal neurophysiologists and quantitatively assessed using multiple features of amplitude, spectral shape and inter-hemispheric connectivity. Quantitative features of HRV were assessed in both the groups. RESULTS: Fifty-eight infants with mild HIE and sixteen healthy term infants were included. Seventy-two percent of infants with mild HIE had at least one abnormal EEG feature on qualitative analysis and quantitative EEG analysis revealed significant differences in spectral features between the two groups. HRV analysis did not differentiate between the groups. CONCLUSIONS: Qualitative and quantitative analysis of the EEG before 6 hours of age identified abnormal EEG features in mild HIE, which could aid in the objective identification of cases for future TH trials in mild HIE. IMPACT: Infants with mild HIE currently do not meet selection criteria for TH yet may be at risk of significant disability at follow-up. In the pre-TH era, EEG within 6 hours of birth was most predictive of outcome; however, TH has delayed this predictive value. 72% of infants with mild HIE had at least one abnormal EEG feature in the first 6 hours on qualitative assessment. Quantitative EEG analysis revealed significant differences in spectral features between infants with mild HIE and healthy term infants. Quantitative EEG features may aid in the objective identification of cases for future TH trials in mild HIE.
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spelling pubmed-83708732021-08-30 Multichannel EEG abnormalities during the first 6 hours in infants with mild hypoxic–ischaemic encephalopathy Garvey, Aisling A. Pavel, Andreea M. O’Toole, John M. Walsh, Brian H. Korotchikova, Irina Livingstone, Vicki Dempsey, Eugene M. Murray, Deirdre M. Boylan, Geraldine B. Pediatr Res Clinical Research Article BACKGROUND: Infants with mild HIE are at risk of significant disability at follow-up. In the pre-therapeutic hypothermia (TH) era, electroencephalography (EEG) within 6 hours of birth was most predictive of outcome. This study aims to identify and describe features of early EEG and heart rate variability (HRV) (<6 hours of age) in infants with mild HIE compared to healthy term infants. METHODS: Infants >36 weeks with mild HIE, not undergoing TH, with EEG before 6 hours of age were identified from 4 prospective cohort studies conducted in the Cork University Maternity Services, Ireland (2003–2019). Control infants were taken from a contemporaneous study examining brain activity in healthy term infants. EEGs were qualitatively analysed by two neonatal neurophysiologists and quantitatively assessed using multiple features of amplitude, spectral shape and inter-hemispheric connectivity. Quantitative features of HRV were assessed in both the groups. RESULTS: Fifty-eight infants with mild HIE and sixteen healthy term infants were included. Seventy-two percent of infants with mild HIE had at least one abnormal EEG feature on qualitative analysis and quantitative EEG analysis revealed significant differences in spectral features between the two groups. HRV analysis did not differentiate between the groups. CONCLUSIONS: Qualitative and quantitative analysis of the EEG before 6 hours of age identified abnormal EEG features in mild HIE, which could aid in the objective identification of cases for future TH trials in mild HIE. IMPACT: Infants with mild HIE currently do not meet selection criteria for TH yet may be at risk of significant disability at follow-up. In the pre-TH era, EEG within 6 hours of birth was most predictive of outcome; however, TH has delayed this predictive value. 72% of infants with mild HIE had at least one abnormal EEG feature in the first 6 hours on qualitative assessment. Quantitative EEG analysis revealed significant differences in spectral features between infants with mild HIE and healthy term infants. Quantitative EEG features may aid in the objective identification of cases for future TH trials in mild HIE. Nature Publishing Group US 2021-04-20 2021 /pmc/articles/PMC8370873/ /pubmed/33879847 http://dx.doi.org/10.1038/s41390-021-01412-x Text en © The Author(s) 2021 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Clinical Research Article
Garvey, Aisling A.
Pavel, Andreea M.
O’Toole, John M.
Walsh, Brian H.
Korotchikova, Irina
Livingstone, Vicki
Dempsey, Eugene M.
Murray, Deirdre M.
Boylan, Geraldine B.
Multichannel EEG abnormalities during the first 6 hours in infants with mild hypoxic–ischaemic encephalopathy
title Multichannel EEG abnormalities during the first 6 hours in infants with mild hypoxic–ischaemic encephalopathy
title_full Multichannel EEG abnormalities during the first 6 hours in infants with mild hypoxic–ischaemic encephalopathy
title_fullStr Multichannel EEG abnormalities during the first 6 hours in infants with mild hypoxic–ischaemic encephalopathy
title_full_unstemmed Multichannel EEG abnormalities during the first 6 hours in infants with mild hypoxic–ischaemic encephalopathy
title_short Multichannel EEG abnormalities during the first 6 hours in infants with mild hypoxic–ischaemic encephalopathy
title_sort multichannel eeg abnormalities during the first 6 hours in infants with mild hypoxic–ischaemic encephalopathy
topic Clinical Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8370873/
https://www.ncbi.nlm.nih.gov/pubmed/33879847
http://dx.doi.org/10.1038/s41390-021-01412-x
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