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Updated: Jun 13, 2026

An In vitro Model to Study Immune Responses of Human Peripheral Blood Mononuclear Cells to Human Respiratory Syncytial Virus Infection
Published on: December 10, 2013
Predictive Model for Critical Illness Infection in Hospitalized Children with RSV Infection: A Retrospective Study
Xingfeng Cheng1, Sha Wei1, Jinquan Xia2
1Intensive Care Unit, Wuhan Children's Hospital (Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College, Huazhong University of Science & Technology, Wuhan 430074, China.
Insights
Predicting critical respiratory syncytial virus (RSV) pneumonia in children is crucial. Elevated interleukin-6 (IL-6), creatine kinase-MB (CK-MB), serum bilirubin excretion (SBE), and neutrophil percentage help identify high-risk infants.
Area of Science:
- Pediatrics
- Infectious Diseases
- Critical Care Medicine
Background:
- Respiratory syncytial virus (RSV) is a major cause of pediatric hospitalizations.
- Predictors for severe RSV illness remain poorly understood.
- Early identification of at-risk children is essential for timely intervention.
Purpose of the Study:
- To identify risk factors for critical RSV pneumonia in children.
- To develop a predictive model for critical RSV illness.
- To improve early risk assessment and clinical decision-making.
Main Methods:
- Retrospective analysis of 12,035 children hospitalized with RSV.
- Inclusion of 30 critically ill children and 90 non-critical controls.
- Multivariable logistic regression and nomogram development using identified predictors.
Main Results:
- Four independent predictors of critical illness were identified: IL-6, CK-MB, SBE, and neutrophil percentage.
- The developed nomogram showed excellent predictive discrimination (AUC = 0.921).
- The model demonstrated strong calibration and clinical utility across various risk thresholds.
Conclusions:
- Elevated IL-6, CK-MB, neutrophil percentage, and SBE are key indicators of critical RSV infection in children.
- A nomogram incorporating these biomarkers offers a reliable tool for early risk stratification.
- This predictive model can aid clinicians in managing pediatric RSV cases.
Abstract:
Background/Objectives: Respiratory syncytial virus (RSV) is a leading cause of hospitalization in children, but predictors of critical illness remain poorly defined. This study aimed to identify risk factors for critical RSV pneumonia and develop a predictive model. Methods: A retrospective analysis of 12,035 children hospitalized with RSV infection between 2019 and 2025 identified 304 eligible patients after applying exclusion criteria. Among these, 30 children with critical illness and 90 randomly selected non-critical controls were included. Clinical characteristics, laboratory parameters, and co-infection patterns were compared. Univariate, Lasso, and multivariable logistic regression analyses were performed to identify independent predictors, which were then incorporated into a nomogram. Model performance was assessed using the ROC curve, calibration plot, and decision curve analysis. Results: Among the 304 eligible children, 30 (9.9%) developed critical illness. Co-infection with three or more pathogens was most frequent in the critical group (43.3%), whereas single RSV infection predominated in the non-critical group (38.9%). Multivariable logistic regression identified four independent predictors of critical illness: interleukin-6 (IL-6), creatine kinase-MB (CK-MB), serum bilirubin excretion (SBE), and neutrophil percentage. The nomogram combining these factors exhibited excellent discrimination (AUC = 0.921, 95% CI: 0.868-0.974). The calibration curve closely matched the ideal 45° reference line (Hosmer-Lemeshow χ2 = 3.233, p = 0.919), and decision curve analysis demonstrated clinical benefit across threshold probabilities ranging from 0.01 to 0.99. Conclusions: Elevated IL-6, CK-MB, neutrophil percentage, and SBE are independent predictors of critical RSV infection in children. The nomogram based on these accessible biomarkers provides a robust tool for early risk assessment and guiding clinical decisions.
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