ArticleMayo Clinic proceedings. Digital health2025
External Validation of Persistent Severe Acute Kidney Injury Prediction With Machine Learning Model.
Article in Mayo Clinic proceedings. Digital health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Beyond binary AKI classification: development and external validation of a distributional model predicting serum creatinine and urine output trajectories in ICU patients.Critical care (London, England) · 2026Article
- Artificial Intelligence in Critical Care Nephrology: Current Applications, Emerging Techniques, and Challenges to Clinical Integration.Kidney360 · 2026Review
- Transforming nephrology through artificial intelligence: a state-of-the-art roadmap for clinical integration.Clinical kidney journal · 2026Review
- Validation of a cancer population derived AKI machine learning algorithm in a general critical care scenario.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025Article
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Authors and funding
5 authors.
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Abstract
Objective: To externally validate the persistent electronic alert (PersEA) machine learning model for predicting persistent severe acute kidney injury (psAKI), addressing the scarcity of validated prediction models. Patients and Methods: We included adult patients (18 years or older) admitted to intensive care unit with at least stage 2 acute kidney injury (AKI) at a tertiary medical center, using retrospective data collected between January 1st, 2017 and December 31st, 2022. The data were accessed and analyzed during the period from March 1st, 2023, through July 28th, 2023. The psAKI was defined as AKI stage 3 lasting for ≥72 hours or AKI leading to death in 48 hours or kidney replacement therapy in 1 day. The performance of the PersEA model, a boosted tree algorithm fed by hourly patient data via electronic health records to provide real-time psAKI predictions, was evaluated using specific metrics that penalize late alarms. We measured the area under the receiver operating characteristic and the area under the precision-recall curves. Results: After screening, 4479 patients from the Mayo Clinic cohort were included in the current external validation study, with 234 (5.22%) having psAKI. Results from the Amsterdam UMCdb (531 patients, 59 [11.11%] positive) and MIMIC-III (495 patients, 57 [11.52%] positive) cohorts were obtained in a prior development study. The model demonstrated an area under the receiver operating characteristic curve of 0.98 (95% CI, 0.97-0.98) and an area under the precision-recall curve of 0.67 (95% CI, 0.60-0.73), and when applying the threshold that reached 0.80 sensitivity on the internal cohort, PersEA achieved 0.88 sensitivity, 0.94 specificity, and 0.47 precision, all based on Mayo Clinic data. Conclusion: The PersEA model performed excellently on an external cohort, showing that it is scalable on high-quality data with little to no tuning once a noisy training set is chosen.
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