ArticleBMC medical imaging2025
Development and validation of a radiomics-based model for early prediction of delayed radiological recovery from Mycoplasma pneumoniae pneumonia: a multicenter study.
Article in BMC medical imaging, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed.
- Based on a radiomics-clinical nomogram to predict the therapeutic effect of pulmonary cryptococcosis pneumonia.Scientific reports · 2026Article
- Early risk stratification of adverse progression in pediatricFrontiers in medicine · 2026Article
- Early identification of refractoryFrontiers in medicine · 2026Article
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6 authors.
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Abstract
objectiveTo develop and validate a radiomics-based model for the early prediction of delayed radiological recovery from Mycoplasma pneumoniae pneumonia (MPP).
methodsThe study cohort included MPP patients admitted to three medical centers from July 2023 to October 2023. Patients were divided into two groups based on clinical and imaging outcomes at two weeks post-treatment: recovery and delayed recovery. Image segmentation, feature extraction, and selection were performed using the uAI Research Portal V1.1. A logistic regression model was constructed. A total of 1904 radiomics features were automatically extracted from the raw images using the Pyradiomics V3.0 tool built into the uAI Research Portal V1.1. Feature selection was performed with Z-score normalization, Spearman correlation analysis, and least absolute shrinkage and selection operator methods. Clinical-imaging, radiomics, and integrated (clinical + imaging + radiomics features) models were constructed. Model performance was assessed by calculating the area under the receiver operating characteristic curve (AUC), sensitivity, and specificity. Decision curve analysis was used to evaluate the net benefit.
resultsA total of 576 eligible patients were included in the study. Multivariate logistic regression analysis revealed that D-dimer levels (odds ratio [OR]: 4.06, 95% confidence interval [CI]: 2.52-6.55; p < 0.001), the systemic immune-inflammation index (SII) (OR: 6.61, 95% CI: 2.08-21.00; p = 0.001), and the consolidation pattern (OR: 2.82, 95% CI = 1.52-5.24; p = 0.001) were significantly associated with delayed recovery. With the training set, the integrated model outperformed the radiomics model in terms of predictive efficacy (AUC: 0.982 vs. 0.872, p = 0.01). However, there was no statistically significant difference between the integrated and clinical-imaging models (AUC: 0.982 vs. 0.894, p = 0.07). There was no significant difference in performance between the radiomics and clinical-imaging models with both the training and external validation sets (AUC: 0.894 vs. 0.872, p = 0.75; AUC: 0.807 vs. 0.837, p = 0.638). With the external validation set, the integrated model achieved an AUC of 0.865 (95% CI: 0.770-0.960), sensitivity of 0.933, and specificity of 0.720.
conclusionThe MPP delayed recovery prediction model, based on 16 radiomics features, D-dimer, SII, and a consolidation pattern, showed excellent predictive performance. It can be used by clinicians as an effective tool for early identification and intervention.
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