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EEG monitoring during anesthesia in children aged 0 to 18 months: amplitude-integrated EEG and age effects
BACKGROUND: The amplitude-integrated EEG (aEEG) is a widely used monitoring tool in neonatology / pediatric intensive care. It takes into account the amplitudes, but not the frequency composition, of the EEG. Advantages of the aEEG are clear criteria for interpretation and time compression. During t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8962600/ https://www.ncbi.nlm.nih.gov/pubmed/35346111 http://dx.doi.org/10.1186/s12887-022-03180-x |
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author | Schultz, Barbara Schultz, Michael Boehne, Martin Dennhardt, Nils |
author_facet | Schultz, Barbara Schultz, Michael Boehne, Martin Dennhardt, Nils |
author_sort | Schultz, Barbara |
collection | PubMed |
description | BACKGROUND: The amplitude-integrated EEG (aEEG) is a widely used monitoring tool in neonatology / pediatric intensive care. It takes into account the amplitudes, but not the frequency composition, of the EEG. Advantages of the aEEG are clear criteria for interpretation and time compression. During the first year of life, the electroencephalogram (EEG) during sedation / anesthesia changes from a low-differentiated to a differentiated EEG; higher-frequency waves develop increasingly. There are few studies on the use of aEEG during pediatric anesthesia. A systematic evaluation of the aEEG in defined EEG stages during anesthesia / sedation is not yet available. Parameters of pediatric EEGs (power, median frequency, spectral edge frequency) recorded during anesthesia and of the corresponding aEEGs (upper and lower value of the aEEG trace) should be examined for age-related changes. Furthermore, it should be examined whether the aEEG can distinguish EEG stages of sedation / anesthesia in differentiated EEGs. METHODS: In a secondary analysis of a prospective observational study EEGs and aEEGs (1-channel recordings, electrode positions on forehead) of 50 children (age: 0–18 months) were evaluated. EEG stages: A (awake), Slow EEG, E(2), F(0), and F(1) in low-differentiated EEGs and A (awake), B(0–2), C(0–2), D(0–2), E(0–2), F(0–1) in differentiated EEGs. RESULTS: Median and spectral edge frequency increased significantly with age (p < 0.001 each). In low-differentiated EEGs, the power of the Slow EEG increased significantly with age (p < 0.001). In differentiated EEGs, the power increased significantly with age in each of the EEG stages B(1) to E(1) (p = 0.04, or less), and the upper and lower values of the aEEG trace increased with age (p < 0.001). A discriminant analysis using the upper and lower values of the aEEG showed that EEG epochs from the stages B(1) to E(1) were assigned to the original EEG stage in only 19.3% of the cases. When age was added as the third variable, the rate of correct reclassifications was 28.5%. CONCLUSIONS: The aEEG was not suitable for distinguishing EEG stages above the burst suppression range. For this purpose, the frequency composition of the EEG should be taken into account. |
format | Online Article Text |
id | pubmed-8962600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-89626002022-03-30 EEG monitoring during anesthesia in children aged 0 to 18 months: amplitude-integrated EEG and age effects Schultz, Barbara Schultz, Michael Boehne, Martin Dennhardt, Nils BMC Pediatr Research BACKGROUND: The amplitude-integrated EEG (aEEG) is a widely used monitoring tool in neonatology / pediatric intensive care. It takes into account the amplitudes, but not the frequency composition, of the EEG. Advantages of the aEEG are clear criteria for interpretation and time compression. During the first year of life, the electroencephalogram (EEG) during sedation / anesthesia changes from a low-differentiated to a differentiated EEG; higher-frequency waves develop increasingly. There are few studies on the use of aEEG during pediatric anesthesia. A systematic evaluation of the aEEG in defined EEG stages during anesthesia / sedation is not yet available. Parameters of pediatric EEGs (power, median frequency, spectral edge frequency) recorded during anesthesia and of the corresponding aEEGs (upper and lower value of the aEEG trace) should be examined for age-related changes. Furthermore, it should be examined whether the aEEG can distinguish EEG stages of sedation / anesthesia in differentiated EEGs. METHODS: In a secondary analysis of a prospective observational study EEGs and aEEGs (1-channel recordings, electrode positions on forehead) of 50 children (age: 0–18 months) were evaluated. EEG stages: A (awake), Slow EEG, E(2), F(0), and F(1) in low-differentiated EEGs and A (awake), B(0–2), C(0–2), D(0–2), E(0–2), F(0–1) in differentiated EEGs. RESULTS: Median and spectral edge frequency increased significantly with age (p < 0.001 each). In low-differentiated EEGs, the power of the Slow EEG increased significantly with age (p < 0.001). In differentiated EEGs, the power increased significantly with age in each of the EEG stages B(1) to E(1) (p = 0.04, or less), and the upper and lower values of the aEEG trace increased with age (p < 0.001). A discriminant analysis using the upper and lower values of the aEEG showed that EEG epochs from the stages B(1) to E(1) were assigned to the original EEG stage in only 19.3% of the cases. When age was added as the third variable, the rate of correct reclassifications was 28.5%. CONCLUSIONS: The aEEG was not suitable for distinguishing EEG stages above the burst suppression range. For this purpose, the frequency composition of the EEG should be taken into account. BioMed Central 2022-03-26 /pmc/articles/PMC8962600/ /pubmed/35346111 http://dx.doi.org/10.1186/s12887-022-03180-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Schultz, Barbara Schultz, Michael Boehne, Martin Dennhardt, Nils EEG monitoring during anesthesia in children aged 0 to 18 months: amplitude-integrated EEG and age effects |
title | EEG monitoring during anesthesia in children aged 0 to 18 months: amplitude-integrated EEG and age effects |
title_full | EEG monitoring during anesthesia in children aged 0 to 18 months: amplitude-integrated EEG and age effects |
title_fullStr | EEG monitoring during anesthesia in children aged 0 to 18 months: amplitude-integrated EEG and age effects |
title_full_unstemmed | EEG monitoring during anesthesia in children aged 0 to 18 months: amplitude-integrated EEG and age effects |
title_short | EEG monitoring during anesthesia in children aged 0 to 18 months: amplitude-integrated EEG and age effects |
title_sort | eeg monitoring during anesthesia in children aged 0 to 18 months: amplitude-integrated eeg and age effects |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8962600/ https://www.ncbi.nlm.nih.gov/pubmed/35346111 http://dx.doi.org/10.1186/s12887-022-03180-x |
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