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Sleep-wake cycle on amplitude-integrated EEG and neuroimage outcomes in newborns

BACKGROUND: The aim of this study was to evaluate the results of sleep-wake cycle monitoring using amplitude-integrated EEG (aEEG) and neuroimaging in newborn infants with a possible perinatal hypoxic insult, investigate the correlation between the findings, and determine the relevance of the findin...

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Autores principales: Rhie, Seonkyeong, Chae, Kyu Young, Jo, Heui Seung, Lee, Kyu Hyung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025544/
https://www.ncbi.nlm.nih.gov/pubmed/27633892
http://dx.doi.org/10.1186/s13052-016-0294-z
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author Rhie, Seonkyeong
Chae, Kyu Young
Jo, Heui Seung
Lee, Kyu Hyung
author_facet Rhie, Seonkyeong
Chae, Kyu Young
Jo, Heui Seung
Lee, Kyu Hyung
author_sort Rhie, Seonkyeong
collection PubMed
description BACKGROUND: The aim of this study was to evaluate the results of sleep-wake cycle monitoring using amplitude-integrated EEG (aEEG) and neuroimaging in newborn infants with a possible perinatal hypoxic insult, investigate the correlation between the findings, and determine the relevance of the findings to reasonably predict neurological outcome. METHODS: aEEG was recorded among newborn infants suspected of perinatal asphyxia between November, 2014 and June, 2015 in one neonatal intensive care unit facility. Brain imaging with serial ultrasonography and MRI when available were performed, and the infants were divided into two groups according to findings and potential neurological outcome: Group I (favorable findings) and Group II (severe findings such as high grade intraventricular hemorrhage, cerebral infarction or white matter injury). Established sleep-wake cycle times after birth was compared between the two groups. RESULTS: Among 107 newborn infants, 85 subjects were classified as Group I and the remaining 22 subjects as Group II. The total number of aEEG sessions was 207 and recording time was 2,796 h with a mean of 14.43 ± 13.40 h per study. Estimated times of cyclicity were earlier in Group I (113.34 h, 95 % CI 82.31–144.37) as compared to Group II (504.39 h, 95 % CI 319.91–688.88; p < 0.001). CONCLUSIONS: Delayed cyclicity on aEEG has a strong correlation with unfavorable brain neuroimages in newborns with possible perinatal asphyxia. If sleep-wake cycles do not appear during initial period after birth, follow-up aEEG studies are recommended. TRIAL REGISTRATION: Retrospectively registered Registration number: BD 2015–148 Name of registry: amplitude integrated EEG in neonate Date of registration: September 9, 2015
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spelling pubmed-50255442016-09-20 Sleep-wake cycle on amplitude-integrated EEG and neuroimage outcomes in newborns Rhie, Seonkyeong Chae, Kyu Young Jo, Heui Seung Lee, Kyu Hyung Ital J Pediatr Research BACKGROUND: The aim of this study was to evaluate the results of sleep-wake cycle monitoring using amplitude-integrated EEG (aEEG) and neuroimaging in newborn infants with a possible perinatal hypoxic insult, investigate the correlation between the findings, and determine the relevance of the findings to reasonably predict neurological outcome. METHODS: aEEG was recorded among newborn infants suspected of perinatal asphyxia between November, 2014 and June, 2015 in one neonatal intensive care unit facility. Brain imaging with serial ultrasonography and MRI when available were performed, and the infants were divided into two groups according to findings and potential neurological outcome: Group I (favorable findings) and Group II (severe findings such as high grade intraventricular hemorrhage, cerebral infarction or white matter injury). Established sleep-wake cycle times after birth was compared between the two groups. RESULTS: Among 107 newborn infants, 85 subjects were classified as Group I and the remaining 22 subjects as Group II. The total number of aEEG sessions was 207 and recording time was 2,796 h with a mean of 14.43 ± 13.40 h per study. Estimated times of cyclicity were earlier in Group I (113.34 h, 95 % CI 82.31–144.37) as compared to Group II (504.39 h, 95 % CI 319.91–688.88; p < 0.001). CONCLUSIONS: Delayed cyclicity on aEEG has a strong correlation with unfavorable brain neuroimages in newborns with possible perinatal asphyxia. If sleep-wake cycles do not appear during initial period after birth, follow-up aEEG studies are recommended. TRIAL REGISTRATION: Retrospectively registered Registration number: BD 2015–148 Name of registry: amplitude integrated EEG in neonate Date of registration: September 9, 2015 BioMed Central 2016-09-15 /pmc/articles/PMC5025544/ /pubmed/27633892 http://dx.doi.org/10.1186/s13052-016-0294-z Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Rhie, Seonkyeong
Chae, Kyu Young
Jo, Heui Seung
Lee, Kyu Hyung
Sleep-wake cycle on amplitude-integrated EEG and neuroimage outcomes in newborns
title Sleep-wake cycle on amplitude-integrated EEG and neuroimage outcomes in newborns
title_full Sleep-wake cycle on amplitude-integrated EEG and neuroimage outcomes in newborns
title_fullStr Sleep-wake cycle on amplitude-integrated EEG and neuroimage outcomes in newborns
title_full_unstemmed Sleep-wake cycle on amplitude-integrated EEG and neuroimage outcomes in newborns
title_short Sleep-wake cycle on amplitude-integrated EEG and neuroimage outcomes in newborns
title_sort sleep-wake cycle on amplitude-integrated eeg and neuroimage outcomes in newborns
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025544/
https://www.ncbi.nlm.nih.gov/pubmed/27633892
http://dx.doi.org/10.1186/s13052-016-0294-z
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