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Comparative renal risk of long-term use of beta-lactams in combination with vancomycin across the continuum of care.

作者信息

Dolly Lauren M, Rivera Christina G, Jensen Kelsey L, Mara Kristin C, Schreier Diana J, Virk Abinash, Arensman Hannan Kellie N

机构信息

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.

出版信息

Ther Adv Infect Dis. 2023 Aug 11;10:20499361231189589. doi: 10.1177/20499361231189589. eCollection 2023 Jan-Dec.

Abstract

BACKGROUND

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).

METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eef/10422906/2ff329558249/10.1177_20499361231189589-fig1.jpg

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