Evidence map›Paper›PMID 41330939›Full record

ArticleScientific reports2025

Development and validation of a machine learning model for critical progression risk in pediatric severe community-acquired pneumonia.

Xiaoqian Ma, Wu Zhao, Qi Sun, Hang Hang, Meng Li, Di Wu, Binbin Liu, Hengtian Zhu

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Xiaoqian MaDepartment of Pediatrics, The First Affiliated Hospital of Bengbu Medical University, Bengbu, Anhui, China.
Wu ZhaoDepartment of Pediatrics, The First Affiliated Hospital of Bengbu Medical University, Bengbu, Anhui, China. jellifish@163.com.
Qi SunDepartment of Pediatrics, The First Affiliated Hospital of Bengbu Medical University, Bengbu, Anhui, China.
Hang HangDepartment of Pediatrics, The First Affiliated Hospital of Bengbu Medical University, Bengbu, Anhui, China.
Meng LiDepartment of Pediatrics, The First Affiliated Hospital of Bengbu Medical University, Bengbu, Anhui, China.
Di WuDepartment of Pediatrics, The First Affiliated Hospital of Bengbu Medical University, Bengbu, Anhui, China.
Binbin LiuDepartment of Pediatrics, The First Affiliated Hospital of Bengbu Medical University, Bengbu, Anhui, China.
Hengtian ZhuDepartment of Pediatrics, The First Affiliated Hospital of Bengbu Medical University, Bengbu, Anhui, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to utilize various machine learning algorithms to develop a predictive model for the progression of severe community-acquired pneumonia (SCAP) in children to critical severe community-acquired pneumonia (cSCAP). Retrospective analysis of clinical data of SCAP patients admitted to the Department of Pediatric Intensive Care Medicine at the First Affiliated Hospital of Bengbu Medical University from January 2021 to April 2023. Logistic regression (LR) and Least Absolute Shrinkage and Selection Operator (LASSO) were jointly employed to screen model variables. The selected variables were then incorporated into seven algorithms, namely LR, Decision Tree (DT), Random Forest (RF), Extreme Gradient Boosting (XGBoost), Naive Bayes (NB), k-Nearest Neighbor (KNN), and Support Vector Machine (SVM), to establish a predictive model for the progression of SCAP in children to a critically severe stage. The effectiveness of the model was evaluated based on the area under the receiver operating characteristic curve (AUC), accuracy, sensitivity, specificity, positive predictive value, negative predictive value, and F1 score. Finally, the Shapley Additive Explanation (SHAP) algorithm was used to interpret the established machine learning model. A total of 211 patients were included. Red Cell Distribution Width-Coefficient of Variation (RDW-CV), procalcitonin (PCT), blood urea nitrogen (BUN), and lactate dehydrogenase (LDH) were selected as predictors. The XGBoost model outperformed six other algorithms, with an AUC of 0.98 (95% CI,0.93-1.00 ), accuracy 0.89 (95% CI, 0.78-0.94), sensitivity 0.98 (95% CI, 0.95-1.00), and specificity 0.75 (95% CI, 0.45-0.87). SHAP analysis identified PCT, LDH, RDW-CV, and BUN as the most important contributors, supporting their clinical relevance for early risk stratification. This study developed an accurate predictive model for the cSCAP in children using machine learning techniques, providing clinical support for decision-making by clinicians.

Indexed as

Community-Acquired InfectionsMachine LearningPneumoniaAlgorithmsBayes TheoremChildChild, PreschoolCommunity-Acquired PneumoniaDisease ProgressionFemaleHumansInfantMaleRetrospective StudiesROC CurveSeverity of Illness IndexChildrenCritical severe community-acquired pneumoniaMachine learningPediatric intensive care unit

Identifiers

PMID41330939
PMCPMC12673147

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.