<p>Sleep stage classification is crucial in sleep medicine, but manual scoring is time-consuming, and automated solutions often struggle with complex sleep patterns. This study introduces a novel approach combining multi-scale temporal fusion with sequential XGBoost (eXtreme Gradient Boosting) processing. The approach analyzes polysomnographic data at multiple time scales (30, 15, and 5&#xa0;s) while incorporating temporal context through sequential processing. Developed from direct clinical experience in sleep scoring, where experts evaluate both brief events and broader stage transitions, the method prioritizes practical applicability in sleep medicine settings. The method was validated on a clinical dataset (224 polysomnographic recordings) and the Sleep-EDF expanded database, achieving accuracy rates of 81.5% (Cohen's kappa [κ] = 0.742) on clinical data and up to 91.5% (κ = 0.826) on Sleep-EDF data. The sequential processing notably enhanced non-rapid eye movement stage 1 (N1) detection, with F1-score improvements ranging from 27 to 61% across datasets. For datasets of approximately 170 recordings, model training and validation requires up to 12&#xa0;min on standard hardware. The results suggest this combined approach shows promise as a practical tool for automated sleep staging, though further research is needed to improve its performance and validate its utility across diverse clinical settings.</p>

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Automated sleep staging using sequential XGBoost and multi-scale temporal fusion

  • Jiří Kuchyňka,
  • Oldřich Vyšata

摘要

Sleep stage classification is crucial in sleep medicine, but manual scoring is time-consuming, and automated solutions often struggle with complex sleep patterns. This study introduces a novel approach combining multi-scale temporal fusion with sequential XGBoost (eXtreme Gradient Boosting) processing. The approach analyzes polysomnographic data at multiple time scales (30, 15, and 5 s) while incorporating temporal context through sequential processing. Developed from direct clinical experience in sleep scoring, where experts evaluate both brief events and broader stage transitions, the method prioritizes practical applicability in sleep medicine settings. The method was validated on a clinical dataset (224 polysomnographic recordings) and the Sleep-EDF expanded database, achieving accuracy rates of 81.5% (Cohen's kappa [κ] = 0.742) on clinical data and up to 91.5% (κ = 0.826) on Sleep-EDF data. The sequential processing notably enhanced non-rapid eye movement stage 1 (N1) detection, with F1-score improvements ranging from 27 to 61% across datasets. For datasets of approximately 170 recordings, model training and validation requires up to 12 min on standard hardware. The results suggest this combined approach shows promise as a practical tool for automated sleep staging, though further research is needed to improve its performance and validate its utility across diverse clinical settings.