ArticleScientific reports2025
Development and validation of a machine learning model for critical progression risk in pediatric severe community-acquired pneumonia.
Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Predictive value of bronchoalveolar lavage fluid leukotriene C4 for airway hyperresponsiveness in children withTranslational pediatrics · 2026Article
- Prediction of severe pediatric community-acquired pneumonia using multimodal fusion of chest radiographs and clinical data.BMC pediatrics · 2026Article
- A leakage-controlled and SHAP driven machine learning framework for paediatric respiratory disease classification using Indian hospital EHR data.BMC medical informatics and decision making · 2026Article
- Machine learning-based identification of inflammatory biomarkers for predicting pulmonary consolidation in children with Chlamydia pneumoniae infection.Frontiers in pediatrics · 2026Article
- A multicenter, clinically interpretable prediction model for malignancy risk in C-TIRADS 3-4 thyroid nodules.Frontiers in oncology · 2026Article
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Authors and funding
8 authors.
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Abstract
This study aimed to utilize various machine learning algorithms to develop a predictive model for the progression of severe community-acquired pneumonia (SCAP) in children to critical severe community-acquired pneumonia (cSCAP). Retrospective analysis of clinical data of SCAP patients admitted to the Department of Pediatric Intensive Care Medicine at the First Affiliated Hospital of Bengbu Medical University from January 2021 to April 2023. Logistic regression (LR) and Least Absolute Shrinkage and Selection Operator (LASSO) were jointly employed to screen model variables. The selected variables were then incorporated into seven algorithms, namely LR, Decision Tree (DT), Random Forest (RF), Extreme Gradient Boosting (XGBoost), Naive Bayes (NB), k-Nearest Neighbor (KNN), and Support Vector Machine (SVM), to establish a predictive model for the progression of SCAP in children to a critically severe stage. The effectiveness of the model was evaluated based on the area under the receiver operating characteristic curve (AUC), accuracy, sensitivity, specificity, positive predictive value, negative predictive value, and F1 score. Finally, the Shapley Additive Explanation (SHAP) algorithm was used to interpret the established machine learning model. A total of 211 patients were included. Red Cell Distribution Width-Coefficient of Variation (RDW-CV), procalcitonin (PCT), blood urea nitrogen (BUN), and lactate dehydrogenase (LDH) were selected as predictors. The XGBoost model outperformed six other algorithms, with an AUC of 0.98 (95% CI,0.93-1.00 ), accuracy 0.89 (95% CI, 0.78-0.94), sensitivity 0.98 (95% CI, 0.95-1.00), and specificity 0.75 (95% CI, 0.45-0.87). SHAP analysis identified PCT, LDH, RDW-CV, and BUN as the most important contributors, supporting their clinical relevance for early risk stratification. This study developed an accurate predictive model for the cSCAP in children using machine learning techniques, providing clinical support for decision-making by clinicians.
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