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Clinical indicators predict refractory Mycoplasma pneumoniae pneumonia in children

Clinical indicators predict refractory Mycoplasma pneumoniae pneumonia in children
Photo by asif mohomed / Unsplash
Key Takeaway
Note that specific clinical indicators predict refractory Mycoplasma pneumoniae pneumonia in children.

This retrospective case–control analysis included 522 children with Mycoplasma pneumoniae pneumonia (MPP) to assess predictors of refractory Mycoplasma pneumoniae pneumonia (RMPP). The study compared children with RMPP against those with MPP without RMPP, evaluating clinical indicators such as fever duration, platelet levels, pleural effusion, atelectasis, extrapulmonary complications, and MP antibody titers. Demographic indicators like age and gender showed no statistically significant differences between the two groups.

Analysis revealed several independent risk factors for RMPP. A prolonged duration of fever was associated with an odds ratio (OR) of 1.407 (P < 0.05). Lower platelet counts (PLT) were linked to an OR of 0.997 (P < 0.05). The presence of pleural effusion yielded an OR of 2.084 (P < 0.05), while atelectasis resulted in an OR of 3.116 (P < 0.05). Extrapulmonary complications carried the highest risk, with an OR of 4.251 (P < 0.05). Conversely, an MP antibody titer ≥1:320 acted as a protective factor, associated with an OR of 0.420 (P < 0.05).

The prediction model constructed from these variables achieved an area under the curve (AUC) of 0.870 (95%CI: 0.837, 0.904). Sensitivity was 82.2% and specificity was 80.5%. No safety data, adverse events, or discontinuations were reported in this observational analysis. Limitations inherent to the retrospective design and lack of reported follow-up duration should be considered when interpreting these findings for clinical practice.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedApr 2026
View Original Abstract ↓
ObjectiveThis 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.MethodsThis 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.ResultsDiffering 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.ConclusionWe 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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