This retrospective cohort study included 307 pediatric patients diagnosed with Mycoplasma pneumoniae pneumonia. The setting was not reported. Researchers utilized machine learning algorithms, including XGBoost, logistic regression, random forest, and support vector machine, to predict the development of plastic bronchitis. Patients with MPP without plastic bronchitis served as the comparator group for analysis. The study aimed to assess specific predictive performance using historical data.
Performance metrics were reported for both training and test sets. On the training set, the area under the curve was 0.948 (95% CI: 0.919–0.973), with sensitivity at 0.904 and specificity at 0.858. On the test set, the AUC was 0.905 (95% CI: 0.843–0.957). Sensitivity and specificity on the test set were 0.812 and 0.852, respectively. Secondary outcomes included calibration, net clinical benefit, and feature importance. These metrics indicate strong discriminative ability across the study cohorts.
Safety data, including adverse events and tolerability, were not reported. Key limitations were not reported. The practice relevance suggests these tools could help clinicians identify children at high risk of developing plastic bronchitis earlier. This may allow for timely bronchoscopy intervention and nutritional support as well as anti-inflammatory therapy. However, the observational nature limits causal inference. External validation is needed before clinical adoption occurs.
View Original Abstract ↓
BackgroundMycoplasma pneumoniae pneumonia (MPP) can cause plastic bronchitis (PB), a rare, life-threatening condition. However, current diagnostic methods often fail to identify early-stage PB in children.The aim of our study was to develop machine learning algorithms to identify early-stage PB in pediatric patients with MPP.MethodsThis retrospective cohort study involved 307 pediatric patients with MPP who underwent bronchoscopy intervention from April 2023, to June 2025.Patients were randomly split into training and test sets (7:3). After feature selection using LASSO and Boruta algorithms, four algorithms, namely, extreme gradient boosting (XGBoost), logistic regression, random forest, and support vector machine, were employed to construct machine learning (ML) models through 5-fold cross-validation. Model performance was evaluated using the area under the curve (AUC), calibration curves, and decision curve analysis (DCA). The best-performing ML was selected using AUC, and feature importance in the model was ranked using SHapley Additive exPlanations (SHAP). Finally, a web-based risk predictor was constructed to facilitate user operability.ResultsMPP children with PB demonstrated more significant abnormalities in inflammation- and nutrition-related indices compared to those without PB. The XGBoost algorithm exhibited the best predictive performance, surpassing other models (logistic regression, random forest, and support vector machine) with an AUC of 0.948 (95% CI: 0.919–0.973), a sensitivity of 0.904, and a specificity of 0.858 on the training set, and an AUC of 0.905 (95% CI: 0.843–0.957), a sensitivity of 0.812, and a specificity of 0.852 on the test set. This algorithm also presented good calibration and net clinical benefit. SHAP analysis identified the retinol-binding protein 4 level, M. pneumoniae cycle-threshold value, D-dimer level, fever duration before admission, C-reactive protein-to-albumin ratio, and presence of pleural effusion as key predictors. To facilitate the clinical adoption, a freely accessible online calculator has been developed (https://plasticbronchitis.shinyapps.io/plastic_bronchitis_risk_calculator/).ConclusionThe developed interpretable ML models deployed in the network application can help clinicians identify children at high risk of developing PB earlier and tailor timely bronchoscopy intervention and nutritional support as well as anti-inflammatory therapy.