Predicting Nephrotoxic Acute Kidney Injury in Hospitalized Adults: A Machine Learning Algorithm.

Griffin BR, Mudireddy A, Horne BD, Chonchol M, Goldstein SL, Goto M, Matheny ME, Street WN, Vaughan-Sarrazin M, Jalal DI, Misurac J. Predicting Nephrotoxic Acute Kidney Injury in Hospitalized Adults: A Machine Learning Algorithm. Kidney medicine. 2024 Dec 1; 6(12):100918.

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Abstract:

RATIONALE AND OBJECTIVE: Acute kidney injury (AKI) is a common complication among hospitalized adults, but AKI prediction and prevention among adults has proved challenging. We used machine learning to update the nephrotoxic injury negated by just-in time action (NINJA), a pediatric program that predicts nephrotoxic AKI, to improve accuracy among adults. STUDY DESIGN: A retrospective cohort study. SETTING AND POPULATION: Adults admitted for  >  48 hours to the University of Iowa Hospital from 2017 to 2022. EXPOSURE: A NINJA high-nephrotoxin exposure ( = 3 nephrotoxins on 1 day or intravenous aminoglycoside or vancomycin for  = 3 days). OUTCOMES: AKI within 48 hours of high-nephrotoxin exposure. ANALYTICAL APPROACH: We collected 85 variables, including demographics, laboratory tests, vital signs, and medications. AKI was defined as a serum creatinine increase of  = 0.3 mg/dL. A gated recurrent unit (GRU)-based recurrent neural network (RNN) was trained on 85% of the data, and then tested on the remaining 15%. Model performance was evaluated with precision, recall, negative predictive value, and area under the curve. We used an artificial neural network to determine risk factor importance. RESULTS: There were 14,480 patients, 18,180 admissions, and 37,300 high-nephrotoxin exposure events meeting inclusion criteria. In the testing cohort, 29% of exposures developed AKI within 48 hours. The RNN-GRU model predicted AKI with a precision of 0.60, reducing the number of false alerts from 2.5 to 0.7 per AKI case. Lowest hemoglobin, lowest blood pressure, and highest white blood cell count were the most important variables in the artificial neural network model. Acyclovir, piperacillin-tazobactam, calcineurin inhibitors, and angiotensin-converting enzyme inhibitor/angiotensin receptor blockers were the most important medications. LIMITATIONS: Clinical variables and medications were not exhaustive, drug levels or dosing were not incorporated, and Iowa''s racial makeup may limit generalizability. CONCLUSIONS: Our RNN-GRU model substantially reduced the number of false alerts for nephrotoxic AKI, which may facilitate NINJA translation to adult hospitals by providing more targeted intervention.