Interventions, Barriers, and Proposed Solutions Associated With the Implementation of a Protocol That Uses Clinical Decision Support and a Stress Biomarker Test to Identify ICU Patients at High-Risk for Drug Associated Acute Kidney Injury

Author:

Williams Victoria L.1ORCID,Smithburger Pamela L.12ORCID,Imhoff Allison N.3,Groetzinger Lara M.1ORCID,Culley Colleen M.2,Burke Clayton X.3,Murugan Raghavan34,Lamberty Phillip E.15,Mahmud Mujtaba2,Benedict Neal J.12,Kellum John A.34,Kane-Gill Sandra L.124

Affiliation:

1. UPMC Presbyterian, Pittsburgh, PA, USA

2. University of Pittsburgh School of Pharmacy, Pittsburgh, PA, USA

3. UPMC Magee-Womens Hospital, Pittsburgh, PA, USA

4. Department of Critical Care Medicine, Center for Critical Care Nephrology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA

5. Department of Medicine, Division of Pulmonary, Allergy, and Critical Care Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA

Abstract

Background: Damage biomarkers are helpful in early identification of patients who are at risk of developing acute kidney injury (AKI). Investigations are ongoing to identify the optimal role of stress/damage biomarkers in clinical practice regarding AKI risk prediction, surveillance, diagnosis, and prognosis. Objective: To determine the impact of utilizing a clinical decision support system (CDSS) to guide stress biomarker testing in intensive care unit (ICU) patients at risk for drug-induced acute kidney injury (D-AKI). Methods: A protocol was designed utilizing a clinical decision support system (CDSS) alert to identify patients that were ordered 3 or more potentially nephrotoxic medications, suggesting risk for progressing to AKI from nephrotoxic burden. Once alerted to these high-risk patients, the pharmacist determined if action was needed by ordering a stress biomarker test, tissue inhibitor of metalloproteinase-2-insulin-like growth factor-binding protein 7 (TIMP-2•IGFBP7). If the biomarker test result was elevated, the pharmacist provided nephrotoxin stewardship recommendations to the team. Pharmacists recorded the response to the clinical decision support alert, ordering, and interpreting the TIMP-2•IGFBP7, and information regarding clinical interventions. An alert in conjunction with TIMP-2•IGFBP7 as a strategy for AKI risk prediction and stimulant for patient care management was assessed. In addition, barriers and solutions to protocol implementation were evaluated. Results: There were 394 total activities recorded by pharmacists for 345 unique patients. Ninety-three (93/394; 23.6%) actionable alerts resulted in a TIMP-2•IGFBP7 test being ordered. Thirty-one TIMP-2•IGFBP7 results were >0.3 (31/81; 38.3%), suggesting a high-risk of progression to AKI, which prompted 191 pharmacist/team interventions. On average, there were 1.64 interventions per patient in the low-risk patients, 3.43 in high-risk patients, and 3.75 in the highest-risk patients. Conclusion and Relevance: Stress biomarkers can be used in conjunction with CDSS alerts to affect therapeutic decisions in ICU patients at high-risk for D-AKI.

Publisher

SAGE Publications

Subject

Pharmacology (medical)

Reference27 articles.

1. Moore BJ, Torio CM. Healthcare Cost and Utilization Project. Statistical Brief #231: Acute Renal Failure Hospitalizations, 2005–2014. Rockville, MD: Agency for Healthcare Research and Quality; 2017. Accessed July 29, 2022. https://www.hcup-us.ahrq.gov/reports/statbriefs/sb231-Acute-Renal-Failure-Hospitalizations.pdf.

2. Acute kidney injury—epidemiology, outcomes and economics

3. KDIGO Clinical Practice Guidelines for Acute Kidney Injury

4. Urinary biomarkers for early detection of platinum based drugs induced nephrotoxicity

5. Nephrotoxin Stewardship

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