Vancomycin With Concomitant Piperacillin/Tazobactam vs. Cefepime or Meropenem Associated Acute Kidney Injury in General Ward Patients: A Multicenter Propensity Score-Matched Study

Author:

Komerdelj Ivan A.1,Buckley Mitchell S.2ORCID,D’Alessio Paul A.3,Ziadat Delia S.2,Kobic Emir2,Rangan Pooja24,Agarwal Sumit K.4,Tinta Nicole C.2,Yerondopoulos Melanie J.2,Kane-Gill Sandra L.5

Affiliation:

1. Department of Pharmacy, Banner MD Anderson Cancer Center, Gilbert, AZ, USA

2. Department of Pharmacy, Banner University Medical Center Phoenix, Phoenix, AZ, USA

3. Department of Pharmacy, Banner Baywood Medical Center, Mesa, AZ, USA

4. Department of Medicine, University of Arizona-College of Medicine Phoenix, Phoenix, AZ, USA

5. Department of Pharmacy and Therapeutics, School of Pharmacy, University of Pittsburgh, Pittsburgh, PA, USA

Abstract

Background: Concurrent administration of vancomycin and piperacillin/tazobactam (VAN+PTZ) may increase the risk of acute kidney injury (AKI) in hospitalized patients. Comprehensive characterization of VAN+PTZ associated AKI and recovery patterns remains lacking in previous reports. Objective: To compare the incidence of AKI associated with VAN+PTZ compared to either cefepime (CEF) or meropenem (MER) with VAN in adult general ward patients. Methods: A multicenter, retrospective, propensity score cohort study was conducted in non-critically ill adult patients. Included patients were concurrently administered VAN+PTZ or VAN+CEF/MER. Patients developing AKI ≤48 hours following combination therapy were excluded. The primary endpoint was to compare the incidence of AKI between study groups. Multivariable Cox regression modeling in predicting AKI was also conducted. Results: A total of 3199 patients met inclusion criteria and were evaluated. The incidence of AKI in VAN+PTZ and VAN+CEF/MER groups were 16.4% and 8.7%, respectively ( P < .001). The onset to AKI was 1.8 days earlier with VAN+PTZ compared to VAN+CEF/MER ( P < .001). Multivariable prediction model showed concomitant VAN+PTZ was identified as an independent risk factor of developing AKI (HR 2.34, 1.82-3.01, P < .001). The VAN+PTZ group experienced significantly higher rates of severe AKI (stage II or III) compared to the VAN+CEF/MER group ( P = .002). No differences in the AKI recovery patterns were found between study groups. Conclusions: Concomitant VAN+PTZ in adult general ward patients was independently associated with an increased risk of AKI overall. More severe AKI was also associated with VAN+PTZ.

Publisher

SAGE Publications

Subject

Pharmacology (medical)

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