An automated bedside measure for monitoring neonatal cortical activity: a supervised deep learning-based electroencephalogram classifier with external cohort validation

被引:23
作者
Moghadam S.M. [1 ,2 ]
Airaksinen M. [1 ,2 ]
Nevalainen P. [1 ]
Marchi V. [3 ]
Hellström-Westas L. [4 ]
Stevenson N.J. [5 ]
Vanhatalo S. [1 ,2 ]
机构
[1] BABA Center, Pediatric Research Center, Department of Clinical Neurophysiology, Children's Hospital, HUS imaging, HUS Diagnostic Center, University of Helsinki and Helsinki University Hospital, Helsinki
[2] Department of Physiology, University of Helsinki, Helsinki
[3] Department of Developmental Neuroscience, Stella Maris Scientific Institute, IRCCS Fondazione Stella Maris Foundation, Pisa
[4] Department of Women's and Children's Health, Uppsala University
[5] Brain Modelling Group, QIMR Berghofer Medical Research Institute, Brisbane, QLD
基金
欧盟地平线“2020”; 芬兰科学院;
关键词
Brain - Classification (of information) - Long short-term memory - Patient monitoring - Sleep research - Unsupervised learning - Wakes;
D O I
10.1016/S2589-7500(22)00196-0
中图分类号
学科分类号
摘要
Background: Electroencephalogram (EEG) monitoring is recommended as routine in newborn neurocritical care to facilitate early therapeutic decisions and outcome predictions. EEG's larger-scale implementation is, however, hindered by the shortage of expertise needed for the interpretation of spontaneous cortical activity, the EEG background. We developed an automated algorithm that transforms EEG recordings to quantified interpretations of EEG background and provides simple intuitive visualisations in patient monitors. Methods: In this method-development and proof-of-concept study, we collected visually classified EEGs from infants recovering from birth asphyxia or stroke. We used unsupervised learning methods to explore latent EEG characteristics, which guided the supervised training of a deep learning-based classifier. We assessed the classifier performance using cross-validation and an external validation dataset. We constructed a novel measure of cortical function, brain state of the newborn (BSN), from the novel EEG background classifier and a previously published sleep-state classifier. We estimated clinical utility of the BSN by identification of two key items in newborn brain monitoring, the onset of continuous cortical activity and sleep-wake cycling, compared with the visual interpretation of the raw EEG signal and the amplitude-integrated (aEEG) trend. Findings: We collected 2561 h of EEG from 39 infants (gestational age 35·0–42·1 weeks; postnatal age 0–7 days). The external validation dataset included 105 h of EEG from 31 full-term infants. The overall accuracy of the EEG background classifier was 92% in the whole cohort (95% CI 91–96; range 85–100 for individual infants). BSN trend values were closely related to the onset of continuous EEG activity or sleep-wake cycling, and BSN levels showed robust difference between aEEG categories. The temporal evolution of the BSN trends showed early diverging trajectories in infants with severely abnormal outcomes. Interpretation: The BSN trend can be implemented in bedside patient monitors as an EEG interpretation that is intuitive, transparent, and clinically explainable. A quantitative trend measure of brain function might harmonise practices across medical centres, enable wider use of brain monitoring in neurocritical care, and might facilitate clinical intervention trials. Funding: European Training Networks Funding Scheme, the Academy of Finland, Finnish Pediatric Foundation (Lastentautiensäätiö), Aivosäätiö, Sigrid Juselius Foundation, HUS Children's Hospital, HUS Diagnostic Center, National Health and Medical Research Council of Australia. © 2022 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY-NC-ND 4.0 license
引用
收藏
页码:e884 / e892
页数:8
相关论文
共 31 条
[1]  
Abend N.S., Mani R., Tschuda T.N., Et al., EEG monitoring during therapeutic hypothermia in neonates, children, and adults, Am J Electroneurodiagn Technol, 51, pp. 141-164, (2011)
[2]  
Boylan G., Burgoyne L., Moore C., O'Flaherty B., Rennie J., An international survey of EEG use in the neonatal intensive care unit, Acta Paediatr, 99, pp. 1150-1155, (2010)
[3]  
de Vries L.S., Hellstrom-Westas L., Role of cerebral function monitoring in the newborn, Arch Dis Child Fetal Neonatal Ed, 90, pp. F201-E207, (2005)
[4]  
Tsoi K., Yam K.K.M., Cheung H.M., Et al., Improving consistency and accuracy of neonatal amplitude-integrated electroencephalography, Am J Perinatol, (2021)
[5]  
Dilena R., Raviglione F., Cantalupo G., Et al., Consensus protocol for EEG and amplitude-integrated EEG assessment and monitoring in neonates, Clin Neurophysiol, 132, pp. 886-903, (2021)
[6]  
Chalak L., Hellstrom-Westas L., Bonifacio S., Et al., Bedside and laboratory neuromonitoring in neonatal encephalopathy, Semin Fetal Neonatal Med, 26, (2021)
[7]  
Deshpande P., McNamara P.J., Hahn C., Shah P.S., Guerguerian A.M., A practical approach toward interpretation of amplitude integrated electroencephalography in preterm infants, Eur J Pediatr, 181, pp. 2187-2200, (2022)
[8]  
Walsh B.H., Murray D.M., Boylan G.B., The use of conventional EEG for the assessment of hypoxic ischaemic encephalopathy in the newborn: a review, Clin Neurophysiol, 122, pp. 1284-1294, (2011)
[9]  
Watanabe K., Hayakawa F., Okumura A., Neonatal EEG: a powerful tool in the assessment of brain damage in preterm infants, Brain Dev, 21, pp. 361-372, (1999)
[10]  
Menache C.C., Bourgeois B.F., Volpe J.J., Prognostic value of neonatal discontinuous EEG, Pediatr Neurol, 27, pp. 93-101, (2002)