Dolly Lauren M, Rivera Christina G, Jensen Kelsey L, Mara Kristin C, Schreier Diana J, Virk Abinash, Arensman Hannan Kellie N
Department of Pharmacy, U.S. Department of Veterans Affairs, 2501 W 22nd Street, Sioux Falls, SD 57105, US.
Department of Pharmacy, Mayo Clinic, Rochester, MN, USA.
Ther Adv Infect Dis. 2023 Aug 11;10:20499361231189589. doi: 10.1177/20499361231189589. eCollection 2023 Jan-Dec.
Data are controversial regarding nephrotoxicity risk with vancomycin plus piperacillin-tazobactam (VPT) compared to vancomycin alone or in combination with other beta-lactams (BLs) in acute care use. Furthermore, data are lacking on the incidence of acute kidney injury (AKI) with long-term use of VPT including outpatient parenteral antimicrobial therapy (OPAT).
This retrospective study included 826 adult patients on an intravenous vancomycin plus BL for ⩾2 weeks, including cefepime, piperacillin/tazobactam, ertapenem, or meropenem, from August 2017 to January 2022. The primary outcome was incidence of AKI. Univariate and multivariable Cox proportional hazard regression analyses were conducted to adjust for confounding variables. A secondary analysis based on the propensity score (PS)-matched cohort was performed.
AKI occurred in 14.4% of patients in the VPT group ( = 15/104) compared to 5.5% in the other BL group ( = 40/722) ( < 0.001). Average time to AKI from start of combination therapy was 9.4 (1.7-12.0) days in the VPT group and 10.9 (5-22.7) days in the other BL group ( = 0.20). The median duration of vancomycin and BL in the overall cohort was approximately 1 month. Beyond BL selection, patient characteristics were not associated with AKI other than the receipt of concomitant acyclovir [hazard ratio (HR) 2.48 (95% confidence interval (CI): 1.33-4.65), = 0.004]. In the PS-matched cohort, AKI occurred in 14.4% of patients in the VPT group ( = 15/104) and 5.3% in the other BL group ( = 11/208) ( = 0.006). Receipt of VPT [HR: 2.55 (1.36-4.78), = 0.004] and acyclovir [HR: 2.38 (1.19-4.74), = 0.014) remained significantly associated with AKI in the multivariable model.
Clinicians should exercise caution when using VPT for >2 weeks, including in the OPAT setting, even when no renal dysfunction is observed during the initial week of combination therapy.