Early identification of acute kidney injury progression in critically ill patients with sepsis: interpretable machine learning approach
- Journal
- Clinical kidney journal (Q1)
- Published
- 27 June 2026
- Study design
- Unclassified
- Evidence level
- Level 5, Expert Opinion (CEBM 5)
- Authors
- Xiaodong You, Yanlong Chen, Jiahui Chen, Xinyi Mao, Yifei Wang, Zhongman Zhang, et al.
- PMID
- 42571594
- DOI
- 10.1093/ckj/sfag216
Why clinicians should know about it
- Picked for Health Informatics (paper of the day, 10 August 2026).
Abstract
BACKGROUND: Acute kidney injury (AKI) is a common and severe complication of sepsis and is often associated with a poor prognosis. However, there is still a lack of an effective prediction model for early identification of AKI progression in critical septic patients, defined as AKI stage 1 or 2 to stage 3 within 7 days after diagnosis of sepsis-associated AKI (SA-AKI). METHODS: We extracted the clinical data of patients with SA-AKI from the Medical Information Mart for Intensive Care (MIMIC) datasets, eICU Collaborative Research Database (eICU-CRD) and Salzburg Intensive Care database (SICdb), with the MIMIC-IV (version 3.1) database used for training and internal validation, the MIMIC-III Clinical Database CareVue subset used as temporal validation, and the eICU-CRD and SICdb used as external validation. Lasso regression and recursive feature elimination were used for feature selection. Six machine learning (ML) algorithms, including k-nearest neighbors, logistic regression, naïve Bayes, random forest (RF), support vector machine and decision tree, were utilized to establish the prediction model. Model performance was assessed using receiver operating characteristic curves, calibration curves and decision curve analysis. SHapley Additive exPlanations (SHAP) method was used for the interpretation of the models. RESULTS: The MIMIC-IV, MIMIC-III subset, eICU-CRD and SICdb included 9193, 2178, 10 332 and 1701 patients with SA-AKI. Twelve variables were selected for model construction, including weight, liver disease, mechanical ventilation, systolic blood pressure, hemoglobin, glucose, blood urea nitrogen, creatinine, chloride, anion gap and urine output. An RF model achieved the best performance in both internal, temporal and external validation (area under the curve is 0.779, 0.758 and 0.713, respectively). A user-friendly platform was built to early predict SA-AKI progression for clinician use. CONCLUSION: ML could be a useful tool for predicting AKI progression in septic patients. We developed an RF model to predict the risk of SA-AKI progression, which may provide a reference for early identification and prompt intervention of high-risk group.
Abstract as published, via PubMed.
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