Evidence map›Paper›PMID 40101226›Full record

ArticleJournal of medical Internet research2025

Machine Learning to Assist in Managing Acute Kidney Injury in General Wards: Multicenter Retrospective Study.

Nam-Jun Cho, Inyong Jeong, Se-Jin Ahn, Hyo-Wook Gil, Yeongmin Kim, Jin-Hyun Park, Sanghee Kang, Hwamin Lee

Abstract readMulticenter Study
In one paragraph

Article in Journal of medical Internet research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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.

Nam-Jun Cho *Department of Internal Medicine, Soonchunhyang University Cheonan Hospital, Cheonan, Republic of Korea.ORCID 0000-0002-9053-0499
Inyong Jeong *Department of Biomedical Informatics, Korea University College of Medicine, Seoul, Republic of Korea.ORCID 0009-0009-1504-0463
Se-Jin AhnDepartment of Biomedical Informatics, Korea University College of Medicine, Seoul, Republic of Korea.ORCID 0009-0003-5379-3673
Hyo-Wook GilDepartment of Internal Medicine, Soonchunhyang University Cheonan Hospital, Cheonan, Republic of Korea.ORCID 0000-0003-2550-2739
Yeongmin KimDepartment of Biomedical Informatics, Korea University College of Medicine, Seoul, Republic of Korea.ORCID 0009-0001-3234-0101
Jin-Hyun ParkDepartment of Biomedical Informatics, Korea University College of Medicine, Seoul, Republic of Korea.ORCID 0009-0007-8062-7696
Sanghee KangDepartment of Surgery, Korea University Guro Hospital, Seoul, Republic of Korea.ORCID 0000-0002-6097-8831
Hwamin LeeDepartment of Biomedical Informatics, Korea University College of Medicine, Seoul, Republic of Korea.ORCID 0000-0002-6482-3511

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMost artificial intelligence-based research on acute kidney injury (AKI) prediction has focused on intensive care unit settings, limiting their generalizability to general wards. The lack of standardized AKI definitions and reliance on intensive care units further hinder the clinical applicability of these models.

objectiveThis study aims to develop and validate a machine learning-based framework to assist in managing AKI and acute kidney disease (AKD) in general ward patients, using a refined operational definition of AKI to improve predictive performance and clinical relevance.

methodsThis retrospective multicenter cohort study analyzed electronic health record data from 3 hospitals in South Korea. AKI and AKD were defined using a refined version of the Kidney Disease: Improving Global Outcomes criteria, which included adjustments to baseline serum creatinine estimation and a stricter minimum increase threshold to reduce misclassification due to transient fluctuations. The primary outcome was the development of machine learning models for early prediction of AKI (within 3 days before onset) and AKD (nonrecovery within 7 days after AKI).

resultsThe final analysis included 135,068 patients. A total of 7658 (8%) patients in the internal cohort and 2898 (7.3%) patients in the external cohort developed AKI. Among the 5429 patients in the internal cohort and 1998 patients in the external cohort for whom AKD progression could be assessed, 896 (16.5%) patients and 287 (14.4%) patients, respectively, progressed to AKD. Using the refined criteria, 2898 cases of AKI were identified, whereas applying the standard Kidney Disease: Improving Global Outcomes criteria resulted in the identification of 5407 cases. Among the 2509 patients who were not classified as having AKI under the refined criteria, 2242 had a baseline serum creatinine level below 0.6 mg/dL, while the remaining 267 experienced a decrease in serum creatinine before the onset of AKI. The final selected early prediction model for AKI achieved an area under the receiver operating characteristic curve of 0.9053 in the internal cohort and 0.8860 in the external cohort. The early prediction model for AKD achieved an area under the receiver operating characteristic curve of 0.8202 in the internal cohort and 0.7833 in the external cohort.

conclusionsThe proposed machine learning framework successfully predicted AKI and AKD in general ward patients with high accuracy. The refined AKI definition significantly reduced the classification of patients with transient serum creatinine fluctuations as AKI cases compared to the previous criteria. These findings suggest that integrating this machine learning framework into hospital workflows could enable earlier interventions, optimize resource allocation, and improve patient outcomes.

Indexed as

Acute Kidney InjuryMachine LearningAgedCreatinineFemaleHumansMaleMiddle AgedRepublic of KoreaRetrospective StudiesCreatinineacute kidney injurycreatininekidneymachine learningpatient roomsrecovery of function

Identifiers

PMID40101226
PMCPMC11962325

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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.