Background: Critically ill patients are managed with complex medication regimens that require medication management to optimize safety and efficacy. When performed by a critical care pharmacist (CCP), discrete medication management activities are termed medication interventions. The ability to define CCP workflow and intervention timeliness depends on the ability to predict the medication management needs of individual intensive care unit (ICU) patients. The purpose of this study was to develop prediction models for the number and intensity of medication interventions in critically ill patients. Methods: This was a retrospective, observational cohort study of adult patients admitted to an ICU between June 1, 2020 and June 7, 2023. Models to predict number of pharmacist interventions using both patient and medication related predictor variables collected at either baseline or in the first 24 hours of ICU stay were created. Both regression and supervised machine learning models (Random Forest, Support Vector Machine, XGBoost) were developed. Root mean square derivation (RMSE), mean absolute error (MAE), and symmetric mean absolute percentage error (sMAPE) were calculated. Results: In a cohort of 13,373 patients, the average number of interventions was 4.7 (standard deviation (SD) 7.1) and intervention intensity was 24.0 (40.3). Among the ML models, the Random Forest model had the lowest RMSE (9.26) while Support Vector Machine had the lowest MAE (4.71). All machine learning models performed similarly to the stepwise logistic regression model, and these performed better than a base model combining severity of illness with medication regimen complexity scores. Conclusions: Intervention quantity can be predicted using patient-specific factors. While inter-institutional variation in intervention documentation precludes external validation, our results provide a framework workload modeling at any institution.
Competing Interest StatementThe authors have declared no competing interest.
Funding StatementFunding through Agency of Healthcare Research and Quality for Dr. Sikora was provided through R21HS028485 and for Drs. Sikora and Shen through R01HS029009.
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
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The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
This was a retrospective, observational study that was reviewed by the University of Georgia (UGA) Institutional Review Board (IRB) and determined to be exempt from IRB oversight (Project00001541).
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Data AvailabilityAll data produced in the present study are available upon reasonable request to the authors
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