Development and validation of a medication regimen complexity scoring tool for critically ill patients
- PMID: 31067298
- DOI: 10.1093/ajhp/zxy054
Development and validation of a medication regimen complexity scoring tool for critically ill patients
Abstract
Purpose: The purpose of this study was to develop and validate a novel medication regimen complexity-intensive care unit (MRC-ICU) scoring tool in critically ill patients and to correlate MRC with illness severity and patient outcomes.
Methods: This study was a single-center, retrospective observational chart review of adults admitted to the medical ICU (MICU) between November 2016 and June 2017. The primary aim was the development and internal validation of the MRC-ICU scoring tool. Secondary aims included external validation of the MRC-ICU and exploration of relationships between medication regimen complexity and patient outcomes. Exclusion criteria included a length of stay of less than 24 hours in the MICU, active transfer, or hospice orders at 24 hours. A total of 130 patient medication regimens were used to test, modify, and validate the MRC-ICU tool.
Results: The 39-line item medication regimen complexity scoring tool was validated both internally and externally. Convergent validity was confirmed with total medications (p < 0.0001). Score discriminant validity was confirmed by lack of association with age (p = 0.1039) or sex (p = 0.7829). The MRC-ICU score was significantly associated with ICU length of stay (p = 0.0166), ICU mortality (p = 0.0193), and patient acuity (p < 0.0001).
Conclusion: The MRC-ICU scoring tool was validated and found to correlate with length of stay, inpatient mortality, and patient acuity.
Keywords: critical care; drug therapy; patient safety; pharmacists; pharmacy; scoring tool.
© American Society of Health-System Pharmacists 2019. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
Comment in
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Significant correlation versus strength of correlation.Am J Health Syst Pharm. 2020 Jan 8;77(2):73-75. doi: 10.1093/ajhp/zxz280. Am J Health Syst Pharm. 2020. PMID: 31876930 No abstract available.
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