Evidence map›Paper›PMID 42638875›Full record

ArticleFrontiers in cellular and infection microbiology2026

Development and validation of an interpretable machine learning model for predicting multidrug-resistant infections in ICU patients.

Yimeng Yang, Jianrui Lv, Junbin Tian, Shuo Yu, Guangdong Wang, Lei Ma

Abstract readValidation Study
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yimeng YangAnesthesia and Surgical Center, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Jianrui LvAnesthesia and Surgical Center, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Junbin TianAnesthesia and Surgical Center, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Shuo YuDepartment of General Surgery, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Guangdong WangDepartment of Respiratory and Critical Medicine, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Lei MaAnesthesia and Surgical Center, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Multidrug-resistant (MDR) infections in intensive care units (ICUs) are difficult to recognize early. This study developed and validated an interpretable machine-learning model for early MDR risk prediction in ICU patients. Methods: A retrospective cohort was built from the Medical Information Mart for Intensive Care IV (MIMIC-IV, n=48,501) for model development with internal validation (7:3 split) and from MIMIC-III (n=38,583) for temporal validation. Candidate predictors at ICU admission included demographics, vital signs, laboratory indices, comorbidities, therapeutic interventions, and severity scores. Missing values were imputed using missForest. Highly correlated predictors were removed using correlation screening. Feature selection used the intersection of Least Absolute Shrinkage and Selection Operator regression and Boruta. Data imbalance was handled by Random Undersampling. Eight models were constructed including Logistic Regression, K-Nearest Neighbors, Decision Tree, Random Forest (RF), Extreme Gradient Boosting, Light Gradient Boosting Machine, Support Vector Machine, and Neural Network. Hyperparameters were optimized using grid search and cross-validation. Model performance, calibration, and clinical utility were evaluated. Model interpretability used SHapley Additive exPlanations (SHAP). A web calculator was implemented using Shiny in R. Results: RF achieved the best overall performance in internal validation (AUC 0.784, 95% CI 0.769-0.798) and remained stable in temporal validation (AUC 0.778, 95% CI 0.771-0.786). The final model included 19 predictors. SHAP identified enteral nutrition, Acute Physiology Score III, stage of acute kidney injury, blood urea nitrogen, opioids use, hemoglobin, and platelet as the leading contributors. A web-based calculator was created to output individualized risk with SHAP-based explanations. Conclusions: We developed and validated an interpretable RF model for early prediction of MDR infections in ICU patients and translated it into a web-based calculator with SHAP explanations, enabling rapid bedside risk stratification to support timely antimicrobial stewardship and resource allocation.

Indexed as

Drug Resistance, Multiple, BacterialIntensive Care UnitsMachine LearningAgedBoosting Machine Learning AlgorithmsClassification AlgorithmsFemaleHumansLogistic ModelsMiddle AgedPrediction AlgorithmsPredictive Learning ModelsRandom ForestRetrospective Studiesintensive care unitsmachine learningmultidrug-resistant infectionsprediction modelrandom forest

Identifiers

PMID42638875
PMCPMC13500264

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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.