Development and validation of a medication regimen complexity scoring tool for critically ill patients
- Morgan E. Gwynn,
- Margaret O. Poisson,
- Jennifer L. Waller,
- Andrea Sikora Newsome(corresponding author)
- University of Georgia,
- Augusta University,
- Children's Hospital of Georgia,
Sustainable Development Goals
- SDG 3 Good Health and Well
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.
Publication Information
Output type
Original language
English (US)Article number
zxy054Pages from-to (Number of pages)
Pages S34-S40Journal (Volume, Issue Number)
American Journal of Health-System Pharmacy (Volume 76)Publication milestones
- Published - 03/15/2019
Publication status
ISSN
1079-2082Publication IDs
- Scopus: 85068608699
- PubMed: 31067298
- ORCID: /0000-0003-4066-4541/work/68515652
