Nephrotoxicity of Vancomycin in Combination With Beta-Lactam Agents: Ceftolozane-Tazobactam vs Piperacillin-Tazobactam.

Autor: Alosaimy, Sara, Lagnf, Abdalhamid M, Hobbs, Athena L V, Mubarez, Musa, Kufel, Wesley D, Morrisette, Taylor, Polisetty, Radhika S, Li, David, Veve, Michael P, Simon, Sam P, Truong, James, Finch, Natalie, Venugopalan, Veena, Rico, Matthew, Amaya, Lee, Yost, Christine, Cubillos, Ashley, Chandler, Elisabeth, Patch, Megan, Smith, Ian Murphy Kelsey
Předmět:
Zdroj: Clinical Infectious Diseases; 2/1/2023, Vol. 76 Issue 3, pe1444-e1455, 12p
Abstrakt: Background Vancomycin (VAN)-associated acute kidney injury (AKI) is increased when VAN is combined with certain beta-lactams (BLs) such as piperacillin-tazobactam (TZP) but has not been evaluated with ceftolozane-tazobactam (C/T). Our aim was to investigate the AKI incidence of VAN in combination with C/T (VAN/C/T) compared with VAN in combination to TZP (VAN-TZP). Methods We conducted a multicenter, observational, comparative study across the United States. The primary analysis was a composite outcome of AKI and risk, injury, failure, loss, end stage renal disease; Acute Kidney Injury Network; or VAN-induced nephrotoxicity according to the consensus guidelines. Multivariable logistic regression analysis was conducted to adjust for confounding variables and stratified Kaplan–Meir analysis to assess the time to nephrotoxicity between the 2 groups. Results We included VAN/C/T (n = 90) and VAN-TZP (n = 284) at an enrollment ratio of 3:1. The primary outcome occurred in 12.2% vs 25.0% in the VAN-C/T and VAN-TZP groups, respectively (P =.011). After adjusting for confounding variables, VAN-TZP was associated with increased odds of AKI compared with VAN-C/T; with an adjusted odds ratio of 3.308 (95% confidence interval, 1.560–6.993). Results of the stratified Kaplan–Meir analysis with log-rank time-to-nephrotoxicity analysis indicate that time to AKI was significantly shorter among patients who received VAN-TZP (P =.004). Cox proportional hazards analysis demonstrated that TZP was consistent with the primary analysis (P =.001). Conclusions Collectively, our results suggest that the AKI is not likely to be related to tazobactam but rather to piperacillin, which is a component in VAN-TZP but not in VAN-C/T. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index