Patanwala Asad E, Nix David E, Hills Thomas E, Erstad Brian L
Faculty of Medicine and Health, School of Pharmacy, The University of Sydney, Sydney, New South Wales, Australia.
Department of Pharmacy, Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
Clin Infect Dis. 2025 Apr 30;80(4):770-776. doi: 10.1093/cid/ciae600.
Cefepime and piperacillin-tazobactam are commonly used broad-spectrum antibiotics used to treat patients with potential gram-negative bacterial sepsis. Piperacillin-tazobactam has been shown to be associated with acute kidney injury (AKI). However, it has not been compared with cefepime in patients with septic shock. We compared the effects of cefepime and piperacillin-tazobactam on the incidence of severe AKI in patients with septic shock.
This was a retrospective, multicenter, inverse probability-of-treatment weighted cohort study conducted in 220 geographically diverse community and teaching hospitals across the United States. Adult patients were included if they had septic shock on hospital admission and received cefepime or piperacillin-tazobactam. The proportions of patients in whom stage 3 AKI occurred during hospitalization were compared between groups.
Of the 8427 patients included in the final cohort, 4569 received cefepime and 3858 received piperacillin-tazobactam. Patients had a mean (SD) age of 66.2 (15.2) years, and 45.3% were female; the mean (SD) estimated glomerular filtration rate was 48 (24) mL/min/1.73 m2 on the day of admission. In the weighted cohort, stage 3 AKI occurred in 9.9% receiving cefepime and 9.8% receiving piperacillin-tazobactam (odds ratio, 0.98 [95% confidence interval, .84-1.15]; P = .82). In terms of secondary outcomes, there was no significant difference between cefepime and piperacillin-tazobactam with regard to renal replacement therapy, in-hospital death, major adverse kidney events, stage 1 AKI, stage 2 AKI, maximum recorded serum creatinine, or hospital length of stay.
Among hospitalized patients with septic shock, there was no difference between cefepime and piperacillin-tazobactam in the occurrence of severe AKI.
头孢吡肟和哌拉西林-他唑巴坦是常用的广谱抗生素,用于治疗有潜在革兰氏阴性菌败血症的患者。已表明哌拉西林-他唑巴坦与急性肾损伤(AKI)有关。然而,在感染性休克患者中,它尚未与头孢吡肟进行比较。我们比较了头孢吡肟和哌拉西林-他唑巴坦对感染性休克患者严重AKI发生率的影响。
这是一项回顾性、多中心、治疗概率反向加权队列研究,在美国220家地理位置不同的社区医院和教学医院进行。纳入入院时患有感染性休克并接受头孢吡肟或哌拉西林-他唑巴坦治疗的成年患者。比较两组住院期间发生3期AKI的患者比例。
在最终队列纳入的8427例患者中,4569例接受头孢吡肟治疗,3858例接受哌拉西林-他唑巴坦治疗。患者的平均(标准差)年龄为66.2(15.2)岁,45.3%为女性;入院当天平均(标准差)估计肾小球滤过率为48(24)mL/min/1.73 m²。在加权队列中,接受头孢吡肟治疗的患者中有9.9%发生3期AKI,接受哌拉西林-他唑巴坦治疗的患者中有9.8%发生3期AKI(优势比,0.98 [95%置信区间,0.84 - 1.15];P = 0.82)。在次要结局方面,头孢吡肟和哌拉西林-他唑巴坦在肾脏替代治疗、住院死亡、主要不良肾脏事件、1期AKI、2期AKI、最高记录血清肌酐或住院时间方面无显著差异。
在住院的感染性休克患者中,头孢吡肟和哌拉西林-他唑巴坦在严重AKI的发生方面没有差异。