医学
头孢吡肟
哌拉西林/他唑巴坦
美罗培南
万古霉素
哌拉西林
急性肾损伤
相伴的
内科学
他唑巴坦
重症监护室
麻醉
抗生素
亚胺培南
微生物学
细菌
铜绿假单胞菌
抗生素耐药性
生物
遗传学
金黄色葡萄球菌
作者
Mitchell S. Buckley,Ivan Komerdelj,Paul A. D’Alessio,Pooja Rangan,Sumit Agarwal,Nicole C. Tinta,Brandon Martinez,Delia S. Ziadat,Melanie Yerondopoulos,Emir Kobic,Sandra L. Kane‐Gill
标识
DOI:10.1016/j.jcrc.2021.10.018
摘要
The risk of acute kidney injury (AKI) associated with concomitant vancomycin and piperacillin/tazobactam in the intensive care unit (ICU) remains controversial. The aim of this study was to compare the AKI incidence associated with concomitant vancomycin and piperacillin/tazobactam compared to either cefepime or meropenem with vancomycin in the ICU.A multicenter, retrospective, propensity score-matched cohort study was conducted in adult ICU patients administered vancomycin in combination with either piperacillin/tazobactam, cefepime, or meropenem were included. Patients developing AKI ≤48 h following combination therapy initiation were excluded. The primary endpoint was to compare the incidence of AKI associated with concomitant antimicrobial therapy. Multivariable Cox regression modeling in predicting AKI was also conducted.A total of 1044 patients were matched. The AKI incidence in vancomycin- piperacillin/tazobactam and vancomycin-cefepime/meropenem groups were 21.9% and 16.8%, respectively (p = 0.068). Multivariable prediction models showed concomitant vancomycin-piperacillin/tazobactam was an independent risk factor of AKI using serum creatinine only (HR 1.52, 1.10-2.10, p = 0.011) and serum creatinine with urine output-based KDIGO criteria (HR 1.77, 1.18-2.67, p = 0.006). No significant differences between groups were observed for AKI recovery patterns or mortality.Concomitant vancomycin and piperacillin/tazobactam administration in adult ICU patients was independently associated with an increased risk of AKI.
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