Publication

Evaluation of medication regimen complexity as a predictor for mortality

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Last modified
  • 06/25/2025
Type of Material
Authors
    Andrea Sikora, University of GeorgiaJohn W. Devlin, Northeastern UniversityMengyun Yu, University of GeorgiaTianyi Zhang, University of GeorgiaXianyan Chen, University of GeorgiaSusan E. Smith, University of GeorgiaBrian Murray, University of North CarolinaMitchell S. Buckley, La Jolla Pharmaceutical CompanySandra Rowe, Oregon Health & Science UniversityDavid Murphy, Emory University
Language
  • English
Date
  • 2023-12-01
Publisher
  • Nature Research
Publication Version
Copyright Statement
  • © The Author(s) 2023
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 13
Issue
  • 1
Start Page
  • 10784
End Page
  • 10784
Grant/Funding Information
  • Funding through Agency of Healthcare Research and Quality for Drs. Devlin, Murphy, Sikora, Smith, and Kamaleswaran was provided through R21HS028485 and R01HS029009.
  • Data acquisition were supported by NC TraCS, funded by Grant Number UL1TR002489 from the National Center for Advancing Translations Sciences at the National Institutes of Health, and Data Analytics at the University of North Carolina Medical Center Department of Pharmacy.
Supplemental Material (URL)
Abstract
  • While medication regimen complexity, as measured by a novel medication regimen complexity-intensive care unit (MRC-ICU) score, correlates with baseline severity of illness and mortality, whether the MRC-ICU improves hospital mortality prediction is not known. After characterizing the association between MRC-ICU, severity of illness and hospital mortality we sought to evaluate the incremental benefit of adding MRC-ICU to illness severity-based hospital mortality prediction models. This was a single-center, observational cohort study of adult intensive care units (ICUs). A random sample of 991 adults admitted ≥ 24 h to the ICU from 10/2015 to 10/2020 were included. The logistic regression models for the primary outcome of mortality were assessed via area under the receiver operating characteristic (AUROC). Medication regimen complexity was evaluated daily using the MRC-ICU. This previously validated index is a weighted summation of medications prescribed in the first 24 h of ICU stay [e.g., a patient prescribed insulin (1 point) and vancomycin (3 points) has a MRC-ICU = 4 points]. Baseline demographic features (e.g., age, sex, ICU type) were collected and severity of illness (based on worst values within the first 24 h of ICU admission) was characterized using both the Acute Physiology and Chronic Health Evaluation (APACHE II) and the Sequential Organ Failure Assessment (SOFA) score. Univariate analysis of 991 patients revealed every one-point increase in the average 24-h MRC-ICU score was associated with a 5% increase in hospital mortality [Odds Ratio (OR) 1.05, 95% confidence interval 1.02–1.08, p = 0.002]. The model including MRC-ICU, APACHE II and SOFA had a AUROC for mortality of 0.81 whereas the model including only APACHE-II and SOFA had a AUROC for mortality of 0.76. Medication regimen complexity is associated with increased hospital mortality. A prediction model including medication regimen complexity only modestly improves hospital mortality prediction.
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Keywords
Research Categories
  • Health Sciences, Medicine and Surgery
  • Health Sciences, Pharmacy

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