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Título
Combined explainable deep learning model to predict pediatric sleep apnea from ECG and SpO2
Autor
Año del Documento
2026-03
Editorial
Elsevier
Documento Fuente
Measurement, Marzo 2026, vol. 264, n. 10, p. 120259
Resumen
Combining deep learning (DL) with eXplainable Artificial Intelligence (XAI) techniques has led to clinically applicable models that simplify the diagnosis of pediatric obstructive sleep apnea (OSA) using a restricted number of cardiorespiratory signals. However, no prior study has applied these techniques to concurrently analyze electrocardiogram (ECG) and oxygen saturation (SpO2) data. Here, we present an explainable DL approach integrating convolutional neural networks with overnight SpO2 and ECG signals to identify pediatric OSA. SHapley Additive exPlanations (SHAP) XAI technique was used to extract relevant patterns linked to pediatric OSA and explain the model decisions. Patients (n = 3,320) from the semi-public Childhood Adenotonsillectomy Trial (CHAT) and Pediatric Adenotonsillectomy Trial for Snoring (PATS), and the private University of Chicago (UofC) databases were analyzed. Performance obtained Cohen’s 4-class kappa of 0.549, 0.457, and 0.378 in CHAT, PATS, and UofC, respectively. Shapley values increased with OSA severity and highlighted the complementarity of SpO2 and ECG, with SpO2 being more relevant in moderate and severe cases and ECG in mild or no OSA cases. SHAP visualizations identified SpO2 desaturations linked to clusters of apneic events and those occurring independently. It also highlighted bradycardia-tachycardia and ECG cardiovascular risk patterns, including variations in P and T waves, PQ and QT intervals, and the QRS complex. Shapley values identified correlations between respiratory and cardiac patterns, showing that desaturations in OSA are linked to cardiac changes. Therefore, our interpretable DL approach may improve pediatric OSA diagnosis by integrating breathing information and accompanying cardiac changes, supporting its effective adoption in clinical settings
Materias Unesco
3325 Tecnología de las Telecomunicaciones
1203.04 Inteligencia Artificial
3314 Tecnología Médica
ISSN
0263-2241
Revisión por pares
SI
Patrocinador
This research is part of the project PID2023-148895OB-I00, funded by MICIU/AEI/10.13039/501100011033 and FSE+, and part of the project CPP2022-009735, funded by MICIU/AEI/10.13039/501100011033 and the European Union NextGenerationEU/PRTR. This research was also supported by the project “0043_NET4SLEEP_2_E”, cofunded by the European Union through the Interreg VI-A Spain-Portugal Program (POCTEP) 2021-2027; and by “CIBER-Consorcio Centro de Investigación Biomédica en Red” (CB19/01/00012) through “Instituto de Salud Carlos III (ISCIII)”, co-funded with European Regional Development Fund. The Childhood Adenotonsillectomy Trial (CHAT) was supported by the National Institutes of Health (HL083075, HL083129, UL1-RR-024134, UL1 RR024989). The National Sleep Research Resource was supported by the National Heart, Lung, and Blood Institute (R24 HL114473, 75N92019R002). The Pediatric Adenotonsillectomy Trial for Snoring (PATS) study was supported by the U.S. National Institutes of Health, National Heart, Lung, and Blood Institute (1U01HL125307, 1U01HL125295). The National Sleep Research Resource was supported by the U.S. National Institutes of Health, National Heart, Lung, and Blood Institute (R24 HL114473, 75N92019R002). C. García-Vicente was supported by ‘Ayudas para contratos predoctorales para la Formación de Doctores’ grant (PRE2021-100792) from the “Ministerio de Ciencia, Innovación y Universidades”. David Gozal was supported in part by NIH grants HL166617 and HL169266.
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Propietario de los Derechos
© 2025 The Authors
Idioma
spa
Tipo de versión
info:eu-repo/semantics/publishedVersion
Derechos
openAccess
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