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在连续护理过程中长期联合使用β-内酰胺类药物和万古霉素的肾脏比较风险。

Comparative renal risk of long-term use of beta-lactams in combination with vancomycin across the continuum of care.

作者信息

Dolly Lauren M, Rivera Christina G, Jensen Kelsey L, Mara Kristin C, Schreier Diana J, Virk Abinash, Arensman Hannan Kellie N

机构信息

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.

出版信息

Ther Adv Infect Dis. 2023 Aug 11;10:20499361231189589. doi: 10.1177/20499361231189589. eCollection 2023 Jan-Dec.

Abstract

BACKGROUND

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).

METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

背景

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。

方法

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。

结果

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。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eef/10422906/2ff329558249/10.1177_20499361231189589-fig1.jpg

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