Dolly Lauren M, Rivera Christina G, Jensen Kelsey L, Mara Kristin C, Schreier Diana J, Virk Abinash, Arensman Hannan Kellie N
Department of Pharmacy, U.S. Department of Veterans Affairs, 2501 W 22nd Street, Sioux Falls, SD 57105, US.
Department of Pharmacy, Mayo Clinic, Rochester, MN, USA.
Ther Adv Infect Dis. 2023 Aug 11;10:20499361231189589. doi: 10.1177/20499361231189589. eCollection 2023 Jan-Dec.
Data are controversial regarding nephrotoxicity risk with vancomycin plus piperacillin-tazobactam (VPT) compared to vancomycin alone or in combination with other beta-lactams (BLs) in acute care use. Furthermore, data are lacking on the incidence of acute kidney injury (AKI) with long-term use of VPT including outpatient parenteral antimicrobial therapy (OPAT).
This retrospective study included 826 adult patients on an intravenous vancomycin plus BL for ⩾2 weeks, including cefepime, piperacillin/tazobactam, ertapenem, or meropenem, from August 2017 to January 2022. The primary outcome was incidence of AKI. Univariate and multivariable Cox proportional hazard regression analyses were conducted to adjust for confounding variables. A secondary analysis based on the propensity score (PS)-matched cohort was performed.
AKI occurred in 14.4% of patients in the VPT group ( = 15/104) compared to 5.5% in the other BL group ( = 40/722) ( < 0.001). Average time to AKI from start of combination therapy was 9.4 (1.7-12.0) days in the VPT group and 10.9 (5-22.7) days in the other BL group ( = 0.20). The median duration of vancomycin and BL in the overall cohort was approximately 1 month. Beyond BL selection, patient characteristics were not associated with AKI other than the receipt of concomitant acyclovir [hazard ratio (HR) 2.48 (95% confidence interval (CI): 1.33-4.65), = 0.004]. In the PS-matched cohort, AKI occurred in 14.4% of patients in the VPT group ( = 15/104) and 5.3% in the other BL group ( = 11/208) ( = 0.006). Receipt of VPT [HR: 2.55 (1.36-4.78), = 0.004] and acyclovir [HR: 2.38 (1.19-4.74), = 0.014) remained significantly associated with AKI in the multivariable model.
Clinicians should exercise caution when using VPT for >2 weeks, including in the OPAT setting, even when no renal dysfunction is observed during the initial week of combination therapy.
在急性护理中,与单独使用万古霉素或与其他β-内酰胺类药物(BLs)联合使用相比,万古霉素联合哌拉西林-他唑巴坦(VPT)的肾毒性风险数据存在争议。此外,关于长期使用VPT(包括门诊胃肠外抗菌治疗(OPAT))导致急性肾损伤(AKI)的发生率的数据尚缺乏。
这项回顾性研究纳入了2017年8月至2022年1月期间826例接受静脉注射万古霉素加BL治疗≥2周的成年患者,包括头孢吡肟、哌拉西林/他唑巴坦、厄他培南或美罗培南。主要结局是AKI的发生率。进行单变量和多变量Cox比例风险回归分析以调整混杂变量。基于倾向评分(PS)匹配队列进行了二次分析。
VPT组14.4%的患者发生了AKI(n = 15/104),而其他BL组为5.5%(n = 40/722)(P < 0.001)。VPT组从联合治疗开始到发生AKI的平均时间为9.4(1.7 - 12.0)天,其他BL组为10.9(5 - 22.7)天(P = 0.20)。整个队列中万古霉素和BL的中位使用时间约为1个月。除了BL的选择外,除了同时接受阿昔洛韦治疗外,患者特征与AKI无关[风险比(HR)2.48(95%置信区间(CI):1.33 - 4.65),P = 0.004]。在PS匹配队列中,VPT组14.4%的患者发生了AKI(n = 15/104),其他BL组为5.3%(n = 11/208)(P = 0.006)。在多变量模型中,接受VPT治疗[HR:2.55(1.36 - 4.78),P = 0.004]和阿昔洛韦治疗[HR:2.38(1.19 - 4.74),P = 0.014]仍然与AKI显著相关。
临床医生在使用VPT超过2周时应谨慎,包括在OPAT环境中,即使在联合治疗的第一周未观察到肾功能障碍。