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Abstract
Fluid overload, while common in the ICU and associated with serious sequelae, is hard to predict and may be influenced by ICU medication use. Machine learning (ML) approaches may offer advantages over traditional regression techniques to predict it. We compared the ability of traditional regression techniques and different ML-based modeling approaches to identify clinically meaningful fluid overload predictors. This was a retrospective, observational cohort study of adult patients admitted to an ICU ≥ 72 h between 10/1/2015 and 10/31/2020 with available fluid balance data. Models to predict fluid overload (a positive fluid balance ≥ 10% of the admission body weight) in the 48–72 h after ICU admission were created. Potential patient and medication fluid overload predictor variables (n = 28) were collected at either baseline or 24 h after ICU admission. The optimal traditional logistic regression model was created using backward selection. Supervised, classification-based ML models were trained and optimized, including a meta-modeling approach. Area under the receiver operating characteristic (AUROC), positive predictive value (PPV), and negative predictive value (NPV) were compared between the traditional and ML fluid prediction models. A total of 49 of the 391 (12.5%) patients developed fluid overload. Among the ML models, the XGBoost model had the highest performance (AUROC 0.78, PPV 0.27, NPV 0.94) for fluid overload prediction. The XGBoost model performed similarly to the final traditional logistic regression model (AUROC 0.70; PPV 0.20, NPV 0.94). Feature importance analysis revealed severity of illness scores and medication-related data were the most important predictors of fluid overload. In the context of our study, ML and traditional models appear to perform similarly to predict fluid overload in the ICU. Baseline severity of illness and ICU medication regimen complexity are important predictors of fluid overload.
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1 University of Georgia College of Pharmacy, Department of Clinical and Administrative Pharmacy, Augusta, USA (GRID:grid.213876.9) (ISNI:0000 0004 1936 738X)
2 University of Georgia Franklin College of Arts and Sciences, Department of Statistics, Athens, USA (GRID:grid.213876.9) (ISNI:0000 0004 1936 738X)
3 Emory University, Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, Atlanta, USA (GRID:grid.189967.8) (ISNI:0000 0001 0941 6502)
4 University of North Carolina Medical Center, Department of Pharmacy, Chapel Hill, USA (GRID:grid.410711.2) (ISNI:0000 0001 1034 1720)
5 Emory University School of Medicine, Department of Biomedical Informatics, Atlanta, USA (GRID:grid.189967.8) (ISNI:0000 0001 0941 6502); Georgia Institute of Technology, Department of Biomedical Engineering, Atlanta, USA (GRID:grid.213917.f) (ISNI:0000 0001 2097 4943)
6 LaJolla Pharmaceuticals, Waltham, USA (GRID:grid.213876.9)
7 Oregon Health and Science University, Department of Pharmacy, Portland, USA (GRID:grid.5288.7) (ISNI:0000 0000 9758 5690)
8 Northeastern University School of Pharmacy, Boston, USA (GRID:grid.261112.7) (ISNI:0000 0001 2173 3359); Brigham and Women’s Hospital, Division of Pulmonary and Critical Care Medicine, Boston, USA (GRID:grid.62560.37) (ISNI:0000 0004 0378 8294)