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Mycoplasma pneumoniae infection prediction model for hospitalized community-acquired pneumonia children
Jiande Chen1, Yong Yin1,2,3, Liebin Zhao3
1Department of Respiratory Medicine, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Insights
A new nomogram accurately predicts Mycoplasma pneumoniae (Mp) infection in hospitalized children with community-acquired pneumonia (CAP). This tool aids physicians in risk stratification and clinical decisions for pediatric CAP cases.
Area of Science:
- Pediatrics
- Infectious Diseases
- Medical Diagnostics
Background:
- Community-acquired pneumonia (CAP) is a common pediatric illness.
- Mycoplasma pneumoniae (Mp) is a frequent cause of CAP in children.
- Accurate prediction of Mp infection aids in appropriate treatment and management.
Purpose of the Study:
- To develop and validate a nomogram for predicting Mp infection in hospitalized children with CAP.
- To compare the predictive performance of the nomogram with a simpler model based on age and fever duration.
Main Methods:
- Retrospective analysis of 5904 hospitalized children with CAP.
- Development of a nomogram using five predictors: age, fever duration, ESR, leukocyte count, and neutrophil proportion.
- Validation of the nomogram using concordance index (C-index), Brier scores, and decision curve analysis (DCA).
Main Results:
- The nomogram demonstrated good predictive accuracy with C-indices of 0.74 and 0.75 in training and validation sets.
- Calibration plots showed moderate agreement between predicted and actual outcomes.
- Decision curve analysis indicated good clinical utility, allowing risk stratification into low, medium, and high groups.
Conclusions:
- A validated nomogram incorporating five clinical and laboratory variables effectively predicts Mp infection in pediatric CAP.
- The nomogram serves as a valuable tool for clinical decision-making and risk assessment in pediatric infectious diseases.
- The developed nomogram outperformed a simpler model based on age and fever duration.
Objectives:
We sought to develop a nomogram to predict Mycoplasma pneumoniae (Mp) infection among hospitalized children with community-acquired pneumonia (CAP) and compare it with another model developed from age and duration of fever.
Methods:
Data on 5904 CAP children who were enrolled at Shanghai Children's Medical Center were retrospectively collected and divided into a training set (n = 4133) and a validation set (n = 1771). The model's performance was determined by concordance index (C-index), calibration curves, Brier scores, and decision curve analyses (DCAs). Akaike information criterion (AIC) and Bayesian information criterion (BIC) were used for model comparisons.
Results:
Incorporating five factors (age, duration of fever, erythrocyte sedimentation rate, leukocyte count, and neutrophil proportion), the nomogram achieved good C-index values of 0.74 (95% confidence interval [CI]: 0.72-0.76) and 0.75 (95% CI: 0.73-0.78) and good Brier scores of 0.14 (95% CI: 0.13-0.15) and 0.17 (95% CI: 0.15-0.18) in predicting Mp infection in the training and validation cohorts, respectively, and had moderate fitted calibration plots. The DCAs showed good clinical usefulness of the nomogram. Patients were effectively divided into low, medium, and high risk groups by two cut-off score points of the nomogram, 210 and 300. With the lower AIC (3673.5) and BIC (3774.7) value, the model of five predictors is the better model.
Conclusions:
By using five predictor variables, a simple nomogram of good predictive accuracy for Mp infection and moderate agreements between the actual outcome and the predicted probability was constructed. It could serve as a tool to aid physicians in clinical decision-making processes.
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