[Risk factors for plastic bronchitis in children with macrolide-unresponsive Mycoplasma pneumoniae pneumonia and
Xiao-Song Shi1, Xiao-Hua He1, Jie Chen1
1Department of Pediatrics, Provincial Hospital Affiliated to Fuzhou University/Fujian Provincial Hospital, Fuzhou 350001, China.
Insights
Older age and elevated lactate dehydrogenase and fibrinogen levels are key risk factors for plastic bronchitis (PB) in children with macrolide-unresponsive Mycoplasma pneumoniae pneumonia (MUMPP). A new nomogram model effectively predicts PB development.
Area of Science:
- Pediatric Pulmonology
- Infectious Diseases
- Medical Diagnostics
Background:
- Macrolide-unresponsive Mycoplasma pneumoniae pneumonia (MUMPP) can lead to serious complications.
- Plastic bronchitis (PB) is a rare but severe condition complicating pediatric pneumonia.
- Identifying risk factors for PB in MUMPP is crucial for early intervention.
Purpose of the Study:
- To identify risk factors associated with plastic bronchitis (PB) in children diagnosed with macrolide-unresponsive Mycoplasma pneumoniae pneumonia (MUMPP).
- To develop and validate a predictive nomogram model for PB in this pediatric population.
Main Methods:
- Retrospective analysis of 178 children with MUMPP who underwent bronchoscopy.
- Comparison of clinical and laboratory data between children with PB (n=49) and without PB (n=129).
- Development and assessment of a nomogram prediction model using logistic regression, ROC analysis, and goodness-of-fit tests.
Main Results:
- Older age, elevated lactate dehydrogenase (LDH), and higher fibrinogen levels were significant risk factors for PB in children with MUMPP (P<0.05).
- The developed nomogram model demonstrated good discriminatory ability with an AUC of 0.733.
- The model showed good fit and clinical utility, indicating its potential for practical application.
Conclusions:
- A risk nomogram incorporating age, LDH, and fibrinogen levels effectively predicts PB development in children with MUMPP.
- This model offers valuable discriminatory ability, accuracy, and predictive efficacy.
- The findings support the use of this nomogram for risk stratification and early management of PB in pediatric MUMPP.
Objectives:
To investigate the risk factors for plastic bronchitis (PB) in children with macrolide-unresponsive Mycoplasma pneumoniae pneumonia (MUMPP) and to establish a nomogram prediction model.
Methods:
A retrospective analysis was conducted on 178 children with MUMPP who underwent bronchoscopy from January to December 2023. According to the presence or absence of PB, the children were divided into a PB group (49 children) and a non-PB group (129 children). The predictive factors for the development of PB in children with MUMPP were analyzed, and a nomogram prediction model was established. The model was assessed in terms of discriminatory ability, accuracy, and clinical effectiveness.
Results:
The multivariate logistic regression analysis showed that older age and higher levels of lactate dehydrogenase and fibrinogen were closely associated with the development of PB in children with MUMPP (P<0.05). A nomogram model established based on these factors had an area under the receiver operating characteristic curve of 0.733 (95%CI: 0.651-0.816, P<0.001) and showed a good discriminatory ability. The Hosmer-Lemeshow goodness-of-fit test indicated that the predictive model had a good degree of fit (P>0.05), and the decision curve analysis showed that the model had a good clinical application value.
Conclusions:
The risk nomogram model established based on age and lactate dehydrogenase and fibrinogen levels has good discriminatory ability, accuracy, and predictive efficacy for predicting the development of PB in children with MUMPP.
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