Non-invasive neonatal jaundice detection using machine learning with support vector machine synthetic minority over-sampling technique ensemble voting
Neonatal jaundice is a common condition in newborns that can result in serious consequences such as permanent brain injury. Traditional diagnostic methods often require invasive blood tests that may cause nuisance and health risks for infants. To address this problem, we propose a non-invasive diagnostic method utilizing image processing and machine learning. The study lies in the integration of the support vector machine synthetic minority over-sampling technique (SVMSMOTE) to address the critical but underexplored challenge of class imbalance in neonatal jaundice datasets, combined with a soft-voting ensemble of adaptive boosting (AdaBoost) and extra trees (ET). This study used the Normal and Jaundiced Newborns dataset, containing facial images of newborns aged 2 to 8 days with varied skin tones. The color features were extracted from RGB and YCrCb channels. The primary challenge addressed is data imbalance, which can bias models toward the majority class and reduce sensitivity for jaundiced cases. SVMSMOTE addresses this by generating high-quality synthetic samples near the decision boundary, improving minority-class representation without introducing noise. We evaluated eight machine learning classifiers: support vector machine, multilayer perceptron, logistic regression, AdaBoost, Extra Trees, passive aggressive, and gradient boosting, as well as ensemble methods combining soft voting and hard voting. Our best-performing model achieved 99.35% accuracy, 98.81% precision, 99.55% recall, an F1-score of 99.17%, an AUC of 99.55%, and a Matthews correlation coefficient of 98.36%. This high recall is particularly clinically significant, reducing false negatives, a critical requirement for neonatal screening to prevent missed diagnoses. These findings demonstrate the promising potential of artificial intelligence-based non-invasive approaches for early neonatal jaundice, but further external clinical validation is required before real-world deployment.
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