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Vancomycin With Concomitant Piperacillin/Tazobactam vs. Cefepime or Meropenem Associated Acute Kidney Injury in
Ivan A Komerdelj1, Mitchell S Buckley2, Paul A D'Alessio3
1Department of Pharmacy, Banner MD Anderson Cancer Center, Gilbert, AZ, 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.
Insights
Concurrent vancomycin and piperacillin/tazobactam (VAN+PTZ) significantly increases acute kidney injury (AKI) risk in hospitalized patients. This combination therapy led to earlier and more severe AKI compared to vancomycin with cefepime or meropenem.
Area of Science:
- Nephrology
- Infectious Diseases
- Pharmacology
Background:
- Concurrent vancomycin and piperacillin/tazobactam (VAN+PTZ) use is common in hospitalized patients.
- Previous reports lack comprehensive data on VAN+PTZ associated acute kidney injury (AKI) and recovery patterns.
- Understanding the nephrotoxic potential of antibiotic combinations is crucial for patient safety.
Purpose of the Study:
- To compare the incidence of AKI in adult general ward patients receiving VAN+PTZ versus vancomycin with cefepime (CEF) or meropenem (MER).
- To identify VAN+PTZ as an independent risk factor for AKI.
- To evaluate the severity and recovery patterns of AKI in different antibiotic combination groups.
Main Methods:
- A multicenter, retrospective, propensity score cohort study design.
- Inclusion of non-critically ill adult patients receiving either VAN+PTZ or VAN+CEF/MER.
- Exclusion of patients with AKI within 48 hours of combination therapy initiation.
- Primary endpoint: AKI incidence comparison; Secondary analysis: Multivariable Cox regression for AKI prediction.
Main Results:
- A total of 3199 patients were analyzed.
- AKI incidence was significantly higher in the VAN+PTZ group (16.4%) compared to the VAN+CEF/MER group (8.7%) (P < .001).
- VAN+PTZ was an independent risk factor for AKI (HR 2.34, P < .001) and associated with earlier onset and more severe AKI (stage II/III).
Conclusions:
- Concomitant VAN+PTZ is independently associated with an increased risk of AKI in adult general ward patients.
- The VAN+PTZ combination leads to a higher incidence of overall and severe AKI.
- No significant differences in AKI recovery patterns were observed between the studied antibiotic combinations.
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