Association between piperacillin/tazobactam use and acute kidney injury in critically ill patients: a retrospective multicentre cohort study

哌拉西林/他唑巴坦 医学 头孢吡肟 哌拉西林 急性肾损伤 他唑巴坦 内科学 万古霉素 回顾性队列研究 重症监护医学 抗生素 亚胺培南 微生物学 抗生素耐药性 金黄色葡萄球菌 细菌 铜绿假单胞菌 生物 遗传学
作者
Bruno Martins Tomazini,Bruno Adler Maccagnan Pinheiro Besen,Leandro Utino Taniguchi,Fernando G. Zampieri,Alexandre Biasi Cavalcanti
出处
期刊:Journal of Antimicrobial Chemotherapy [Oxford University Press]
卷期号:79 (3): 552-558 被引量:1
标识
DOI:10.1093/jac/dkae001
摘要

Abstract Background Piperacillin/tazobactam is one of the most common antibiotics prescribed in the ICU and the combination of piperacillin/tazobactam with vancomycin has been associated with acute kidney injury (AKI) in critically ill patients. However, data on the risk of AKI with piperacillin/tazobactam, despite vancomycin co-exposure, are lacking. Objectives To investigate the association of piperacillin/tazobactam with AKI and renal replacement therapy (RRT) among adult ICU patients. Methods We analysed data from patients included in two open access databases (MIMIC-IV and eICU). Critically ill patients who received piperacillin/tazobactam or cefepime (a cephalosporin with similar broad-spectrum activity to piperacillin/tazobactam) during their first ICU stay were eligible for the study. Marginal structural Cox models, accounting for time-fixed covariates and time-dependent covariates were performed. The primary outcomes were AKI and need of RRT. Results A total of 20 107 patients were included, with 11 213 in the piperacillin/tazobactam group and 8894 in the cefepime group. Exposure to piperacillin/tazobactam was associated with AKI (HR 1.77; 95% CI 1.51–2.07; P < 0.001) and with need of RRT (HR 1.31; 95% CI 1.08–1.57; P = 0.005). Tests for interaction were not statistically significant for occurrence of AKI and RRT in the subgroup of patients exposed to vancomycin or not (P = 0.26 and P = 0.6, respectively). Conclusions In critically ill patients, exposure to piperacillin/tazobactam was associated with increased risk of AKI and with increased risk of RRT, regardless of combination therapy with vancomycin.
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