Wu Dong, Wang Xiaowu, Li Guangli, Chai Xiuli, Guo Shaobo, Zhou Lulu, Wang Xiaojuan
Department of Pharmacy, Fuyang People's Hospital, Fuyang, China.
Department of Clinical Laboratory, Fuyang Second People's Hospital, Fuyang, China.
Expert Opin Drug Saf. 2025 Apr;24(4):499-506. doi: 10.1080/14740338.2024.2393263. Epub 2024 Aug 19.
Vancomycin (VAN) is empirically used with other broad-spectrum antibiotics, such as piperacillin-tazobactam (PTZ) or carbapenem (CBP). However, conflicting literature on the rates of acute kidney injury (AKI) of VAN with PTZ has been reported.
A multicenter, retrospective cohort study of the risk of AKI was conducted in patients receiving VAN and concomitant PTZ or CBP from January 2019 and June 2023.
In total, 514 eligible patients were included. AKI occurred in a total of 91 patients (17.70%). The prevalence of AKI was significantly higher in the VAN+PTZ group than in the VAN+CBP group (23.37% vs 15.27%, = 0.028). The survival curves depicting the time to AKI showed the increased incidence and more rapid onset of AKI among patients in the VAN+PTZ group compared to those of the VAN+CBP group (HR 2.186, 95%CI 1.351-3.538, = 0.0015). VAN+PTZ was associated with a consistently higher AKI rate over VAN+CBP (HR 1.762, 95%CI 1.111-2.795, = 0.0161) throughout the 14-day combination therapy. VAN with concomitant PTZ, duration of combination therapy ≤ 4 days and VAN trough concentration > 20 mg/L were independent risk factors associated with AKI.
The prevalence of AKI was found to be higher in patients receiving VAN+PTZ therapy compared to those receiving VAN+CBP therapy based on creatinine-defined AKI.
万古霉素(VAN)通常与其他广谱抗生素联合经验性使用,如哌拉西林 - 他唑巴坦(PTZ)或碳青霉烯类(CBP)。然而,关于VAN与PTZ联用导致急性肾损伤(AKI)发生率的文献报道存在矛盾。
对2019年1月至2023年6月期间接受VAN并同时使用PTZ或CBP的患者进行了一项多中心回顾性队列研究,以评估AKI风险。
共纳入514例符合条件的患者。总计91例患者(17.70%)发生了AKI。VAN + PTZ组的AKI患病率显著高于VAN + CBP组(23.37%对15.27%,P = 0.028)。描绘发生AKI时间的生存曲线显示,与VAN + CBP组相比,VAN + PTZ组患者中AKI的发生率更高且发病更快(风险比2.186,95%置信区间1.351 - 3.538,P = 0.0015)。在整个14天的联合治疗期间,VAN + PTZ组的AKI发生率始终高于VAN + CBP组(风险比1.762,95%置信区间1.111 - 2.795,P = 0.0161)。VAN与PTZ联用、联合治疗持续时间≤4天以及VAN谷浓度>20 mg/L是与AKI相关的独立危险因素。
基于肌酐定义的AKI,接受VAN + PTZ治疗的患者中AKI患病率高于接受VAN + CBP治疗的患者。