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Published on: February 24, 2023
Development of a predictive model based on clinical indicators for refractory Mycoplasma pneumoniae pneumonia in
Feifei Yu1,2, Yan Zhou1, Zhengxiu Luo2
1Department of Pharmacy, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Children and Adolescents' Health and Diseases, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Rare Diseases in Infection and Immunity, Chongqing, China.
Insights
This study identifies key indicators to predict refractory Mycoplasma pneumoniae pneumonia (RMPP) in children, developing a nomogram for early risk assessment and guiding treatment decisions for better outcomes.
Area of Science:
- Pediatric Infectious Diseases
- Respiratory Medicine
- Clinical Epidemiology
Background:
- Mycoplasma pneumoniae pneumonia (MPP) can lead to refractory cases (RMPP) in children, necessitating early identification.
- Predictive tools for RMPP are crucial for timely intervention and management.
- Current diagnostic and prognostic indicators for RMPP require further refinement.
Purpose of the Study:
- To screen and identify clinical indicators for predicting the occurrence of RMPP in children.
- To determine combined factors for predicting RMPP.
- To provide a basis for early identification and treatment planning for RMPP.
Main Methods:
- Retrospective case-control analysis of 522 children with MPP.
- Inclusion of 28 clinical indicators, including clinical features and laboratory data.
- Application of univariate and multivariate logistic regression, stepwise regression, ROC curve analysis, and nomogram construction.
Main Results:
- Duration of fever, pleural effusion, atelectasis, and extrapulmonary complications were identified as independent risk factors for RMPP.
- Platelet count (PLT) and MP antibody titer ≥1:320 were found to be protective factors.
- The developed prediction model demonstrated high accuracy (AUC=0.870), with 82.2% sensitivity and 80.5% specificity.
Conclusions:
- A validated visual nomogram model for predicting RMPP risk in children was constructed.
- This user-friendly tool aids in the individualized prediction of RMPP risk at initial presentation.
- The model supports clinical decision-making for macrolide therapy and identifies high-risk children for closer monitoring and adjunctive therapies.
Objective:
This study aims to screen indicators for predicting the occurrence of refractory Mycoplasma pneumoniae pneumonia (RMPP) in children, determine the combined factors for predicting RMPP, and provide a basis for the early identification of children with RMPP and the determination of treatment plans.
Methods:
This study was a retrospective case-control analysis. A total of 522 children with MPP and 28 clinical indicators were included. Clinical feature, hospitalization period, laboratory data, etc., were collected. The risk factors related to RMPP were screened through univariate analysis. A multivariate logistic regression model was established, and stepwise regression was used to screen out independent risk factors. The operating characteristic curve (ROC) of the combined predictor was drawn for predictive efficacy analysis. A visual nomogram model for predicting the probability of RMPP occurrence was constructed and validated.
Results:
Differing from other results, there were no statistically significant differences in demographic indicators such as age and gender between the two groups. The multivariate logistic regression analysis showed that duration of fever (OR = 1.407), PLT (OR = 0.997), pleural effusion (OR = 2.084), atelectasis (OR = 3.116), and extrapulmonary complications (OR = 4.251) were independent risk factors for RMPP (P < 0.05). MP antibody titer ≥1:320 (OR = 0.420) is a protective factor. The AUC of the prediction model was 0.870 (95%CI: 0.837, 0.904), the sensitivity of the prediction model was 82.2%, the specificity was 80.5%, and the prediction accuracy was relatively high. The calibration curve, close to the 45° line, exhibited good calibration.
Conclusion:
We constructed and validated a visual and user-friendly model for individualized prediction of RMPP risk in children at initial presentation, to support clinical decision-making regarding macrolide therapy. This model provides a tool for identification of high-risk children, which may inform closer monitoring and prompt consideration of adjunctive therapies.
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