TY - JOUR
T1 - Impact of Pharmacists to Improve Patient Care in the Critically Ill
T2 - A Large Multicenter Analysis Using Meaningful Metrics With the Medication Regimen Complexity-ICU (MRC-ICU) Score
AU - Sikora, Andrea
AU - Ayyala, Deepak
AU - Rech, Megan A.
AU - Blackwell, Sarah B.
AU - Campbell, Joshua
AU - Caylor, Meghan M.
AU - Condeni, Melanie Smith
AU - Depriest, Ashley
AU - Dzierba, Amy L.
AU - Flannery, Alexander H.
AU - Hamilton, Leslie A.
AU - Heavner, Mojdeh S.
AU - Horng, Michelle
AU - Lam, Joseph
AU - Liang, Edith
AU - Montero, Jennifer
AU - Murphy, David
AU - Plewa-Rusiecki, Angela M.
AU - Sacco, Alicia J.
AU - Sacha, Gretchen L.
AU - Shah, Poorvi
AU - Smith, Michael P.
AU - Smith, Zachary
AU - Radosevich, John J.
AU - Vilella, Antonia L.
AU - Chase, Aaron
AU - Jun, Ah Hyun
AU - Hollis, Allison
AU - Yan Yeung, Amy Siu
AU - Martinelli, Ashley
AU - Jois, Bhavna
AU - Bissell, Brittany
AU - Cheng, Carly
AU - Forehand, Christy Cecil
AU - Masic, Dalila
AU - Khan, Sadaf
AU - Louie, Derex
AU - Ali, Dina
AU - Liang, Edith
AU - Metts, Elise
AU - Murray, Brian
AU - Huang, Ellen
AU - Howington, Gavin
AU - Ndongai, George
AU - Mease, James
AU - Davis, Jason
AU - Ho Chui, Jason Sai
AU - Huang, Karen
AU - Williams, Karen
AU - Soriano, Vincent
AU - Smith, Susan E.
AU - Stevković-Rašeta, Nataša
AU - Spezzano, Katherine
AU - Kaier, Kelsie
AU - Pandya, Komal
AU - Bastin, Melissa Thompson
AU - Ramos, Victoria
AU - Ruggero, Michael A.
AU - Armahizer, Michael
AU - Won, Sarah
AU - Wilson, Sharon
AU - Adriaens, Thomas
AU - Yoo, Tina
N1 - Funding Information:
Dr. Newsome has received research funding through the National Center for Advancing Translational Sciences of the National Institutes of Health under Award Numbers UL1TR002378 and KL2TR002381. Dr. Rech’s institution received funding from Spero Pharmaceuticals; she received funding from Harm Reduction Therapeutics. Dr. DePriest received funding from Baxter. Dr. Flannery’s institution received funding from the National Institute of Diabetes and Digestive and Kidney Diseases, the American Society of Nephrology, and La Jolla Pharmaceutical Company. The remaining authors have disclosed that they do not have any potential conflicts of interest.
Publisher Copyright:
© 2022 Lippincott Williams and Wilkins. All rights reserved.
PY - 2022/9/1
Y1 - 2022/9/1
N2 - OBJECTIVES: Despite the established role of the critical care pharmacist on the ICU multiprofessional team, critical care pharmacist workloads are likely not optimized in the ICU. Medication regimen complexity (as measured by the Medication Regimen Complexity-ICU [MRC-ICU] scoring tool) has been proposed as a potential metric to optimize critical care pharmacist workload but has lacked robust external validation. The purpose of this study was to test the hypothesis that MRC-ICU is related to both patient outcomes and pharmacist interventions in a diverse ICU population. DESIGN: This was a multicenter, observational cohort study. SETTING: Twenty-eight ICUs in the United States. PATIENTS: Adult ICU patients. INTERVENTIONS: Critical care pharmacist interventions (quantity and type) on the medication regimens of critically ill patients over a 4-week period were prospectively captured. MRC-ICU and patient outcomes (i.e., mortality and length of stay [LOS]) were recorded retrospectively. MEASUREMENTS AND MAIN RESULTS: A total of 3,908 patients at 28 centers were included. Following analysis of variance, MRC-ICU was significantly associated with mortality (odds ratio, 1.09; 95% CI, 1.08-1.11; p < 0.01), ICU LOS (β coefficient, 0.41; 95% CI, 00.37-0.45; p < 0.01), total pharmacist interventions (β coefficient, 0.07; 95% CI, 0.04-0.09; p < 0.01), and a composite intensity score of pharmacist interventions (β coefficient, 0.19; 95% CI, 0.11-0.28; p < 0.01). In multivariable regression analysis, increased patient: Pharmacist ratio (indicating more patients per clinician) was significantly associated with increased ICU LOS (β coefficient, 0.02; 0.00-0.04; p = 0.02) and reduced quantity (β coefficient,-0.03; 95% CI,-0.04 to-0.02; p < 0.01) and intensity of interventions (β coefficient,-0.05; 95% CI,-0.09 to-0.01). CONCLUSIONS: Increased medication regimen complexity, defined by the MRC-ICU, is associated with increased mortality, LOS, intervention quantity, and intervention intensity. Further, these results suggest that increased pharmacist workload is associated with decreased care provided and worsened patient outcomes, which warrants further exploration into staffing models and patient outcomes.
AB - OBJECTIVES: Despite the established role of the critical care pharmacist on the ICU multiprofessional team, critical care pharmacist workloads are likely not optimized in the ICU. Medication regimen complexity (as measured by the Medication Regimen Complexity-ICU [MRC-ICU] scoring tool) has been proposed as a potential metric to optimize critical care pharmacist workload but has lacked robust external validation. The purpose of this study was to test the hypothesis that MRC-ICU is related to both patient outcomes and pharmacist interventions in a diverse ICU population. DESIGN: This was a multicenter, observational cohort study. SETTING: Twenty-eight ICUs in the United States. PATIENTS: Adult ICU patients. INTERVENTIONS: Critical care pharmacist interventions (quantity and type) on the medication regimens of critically ill patients over a 4-week period were prospectively captured. MRC-ICU and patient outcomes (i.e., mortality and length of stay [LOS]) were recorded retrospectively. MEASUREMENTS AND MAIN RESULTS: A total of 3,908 patients at 28 centers were included. Following analysis of variance, MRC-ICU was significantly associated with mortality (odds ratio, 1.09; 95% CI, 1.08-1.11; p < 0.01), ICU LOS (β coefficient, 0.41; 95% CI, 00.37-0.45; p < 0.01), total pharmacist interventions (β coefficient, 0.07; 95% CI, 0.04-0.09; p < 0.01), and a composite intensity score of pharmacist interventions (β coefficient, 0.19; 95% CI, 0.11-0.28; p < 0.01). In multivariable regression analysis, increased patient: Pharmacist ratio (indicating more patients per clinician) was significantly associated with increased ICU LOS (β coefficient, 0.02; 0.00-0.04; p = 0.02) and reduced quantity (β coefficient,-0.03; 95% CI,-0.04 to-0.02; p < 0.01) and intensity of interventions (β coefficient,-0.05; 95% CI,-0.09 to-0.01). CONCLUSIONS: Increased medication regimen complexity, defined by the MRC-ICU, is associated with increased mortality, LOS, intervention quantity, and intervention intensity. Further, these results suggest that increased pharmacist workload is associated with decreased care provided and worsened patient outcomes, which warrants further exploration into staffing models and patient outcomes.
KW - burnout
KW - metrics
KW - patient safety
KW - pharmacy
KW - quality
KW - workload
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U2 - 10.1097/CCM.0000000000005585
DO - 10.1097/CCM.0000000000005585
M3 - Article
C2 - 35678204
AN - SCOPUS:85136910417
SN - 0090-3493
VL - 50
SP - 1318
EP - 1328
JO - Critical Care Medicine
JF - Critical Care Medicine
IS - 9
ER -