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◆ Frontiers in Pediatrics2026-08-28· Medicine

Prediction of risk factors for respiratory failure in children with mycoplasma pneumoniae pneumonia based on clinical pulmonary infection scores

Jiao Lian, Xiyao Si, Xiaolong Li, Tao Xue, Zhenying Liu

原始摘要(英文原文)· Original abstract
Background Mycoplasma pneumoniae pneumonia (MPP) remains a leading cause of community-acquired pneumonia in children, with respiratory failure occurring in 15%–20% of hospitalized cases. Despite advances in understanding MPP pathogenesis, validated tools for early prediction of respiratory failure are lacking. This study aimed to develop and validate a nomogram based on Clinical Pulmonary Infection Score (CPIS) for individualized risk stratification in pediatric MPP. Methods We conducted a retrospective cohort study of 305 children with confirmed MPP admitted to our hospital between July 2020 and December 2024. Patients were categorized into respiratory failure ( n = 62) and non-respiratory failure ( n = 243) groups. Demographics, clinical features, laboratory parameters, chest imaging findings, and CPIS were collected. Independent risk factors were identified through multivariate logistic regression, and a nomogram was constructed and validated using ROC curve analysis, calibration plots, and decision curve analysis. Results Respiratory failure was associated with significantly higher rates of tachypnea (91.9% vs. 16.5%), interstitial changes (87.1% vs. 25.5%), and pleural effusion (74.2% vs. 24.7%) (all P < 0.001). The respiratory failure group exhibited elevated NLR (5.2 vs. 3.7), CRP, D-dimer, and CPIS (7.4 vs. 5.3), with lower SpO 2 (89.6% vs. 94.3%) (all P < 0.001). Multivariate logistic analysis identified interstitial changes (OR = 2.522, P = 0.001), NLR (OR = 2.716, P < 0.001), and CPIS (OR = 1.932, P < 0.001) as independent risk factors, while older age (OR = 0.467, P < 0.001) and higher SpO 2 (OR = 0.772, P < 0.001) were protective. The nomogram demonstrated exceptional discriminative ability (AUC = 0.918, 95% CI: 0.880–0.956), good calibration (Hosmer-Lemeshow P = 0.71), and positive net benefit across threshold probabilities of 5%–40%. Conclusions This CPIS-based nomogram provides a highly accurate, clinically practical tool for predicting respiratory failure in pediatric MPP. By integrating radiographic, inflammatory, and physiological parameters, it enables early identification of high-risk patients for enhanced monitoring and preemptive respiratory support, potentially improving outcomes in severe MPP.
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