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

Author:

Tomazini Bruno Martins123ORCID,Besen Bruno Adler Maccagnan Pinheiro234,Taniguchi Leandro Utino234ORCID,Zampieri Fernando Godinho35,Cavalcanti Alexandre Biasi13

Affiliation:

1. Research Institute, Hospital do Coração (Hcor) , Sao Paulo , Brazil

2. Intensive Care Unit, Hospital Sírio-Libanês , Sao Paulo , Brazil

3. Scientific Committee, Brazilian Research in Intensive Care Network (BRICNet) , Sao Paulo , Brazil

4. Medical ICU, Internal Medicine Department, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo , Sao Paulo , Brazil

5. Department of Critical Care Medicine, Faculty of Medicine and Dentistry, University of Alberta , Edmonton , Canada

Abstract

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.

Publisher

Oxford University Press (OUP)

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