Hacettepe University Faculty of Medicine, Department of Internal Medicine, Ankara, Turkey.
Hacettepe University Faculty of Medicine, Department of Infectious Diseases and Clinical Microbiology, Ankara, Turkey.
Int J Antimicrob Agents. 2018 Aug;52(2):180-184. doi: 10.1016/j.ijantimicag.2018.03.024. Epub 2018 Apr 9.
The combination of piperacillin/tazobactam (TZP) and vancomycin (VAN) provides a wide spectrum of activity against many pathogens acquired in healthcare settings. However, there have been reports of increased potential for nephrotoxicity with this combination. The aim of this study was to evaluate the nephrotoxic effect of TZP+VAN and to compare it with that of TZP and VAN monotherapies as well as VAN + meropenem (MEM), another broad-spectrum combination. A total of 402 patients receiving any of the antimicrobial regimens for >48 h were evaluated retrospectively over a 2-year period (2012-2013). Patients admitted to the intensive care unit, those with a baseline serum creatinine >2.0 mg/dL, patients on haemodialysis or peritoneal dialysis, pregnant women and those in septic shock were excluded. The presence and severity of acute kidney injury (AKI) was assessed according to the AKIN criteria. The incidence of AKI was significantly higher in the TZP+VAN group (41.3%) compared with the TZP (16.0%), VAN (15.7%) and VAN+MEM (10.1%) groups (P < 0.001). In the multivariate analysis, the risk of AKI increased 3.5-fold in patients treated with TZP+VAN and 1.7-fold in those who were receiving a potentially nephrotoxic drug when the antibiotic regimen was started compared with patients treated with VAN alone. Combined use of TZP+VAN carries a much higher risk of AKI than either antibiotic monotherapy regimen. Therefore, this broad-spectrum combination should be used cautiously in patients with a high likelihood of developing kidney injury.
哌拉西林/他唑巴坦(TZP)和万古霉素(VAN)的联合使用提供了针对许多在医疗机构获得的病原体的广泛活性谱。然而,已有报道称这种联合使用会增加肾毒性的潜在风险。本研究旨在评估 TZP+VAN 的肾毒性作用,并将其与 TZP 和 VAN 单药治疗以及另一种广谱联合药物 VAN+美罗培南(MEM)进行比较。
在 2 年期间(2012-2013 年),我们回顾性评估了接受任何一种抗菌方案治疗>48 小时的 402 例患者。排除了入住重症监护病房的患者、基线血清肌酐>2.0mg/dL 的患者、接受血液透析或腹膜透析的患者、孕妇和感染性休克患者。根据 AKIN 标准评估急性肾损伤(AKI)的存在和严重程度。TZP+VAN 组(41.3%)的 AKI 发生率明显高于 TZP(16.0%)、VAN(15.7%)和 VAN+MEM(10.1%)组(P<0.001)。在多变量分析中,与单独使用 VAN 的患者相比,开始使用抗生素方案时接受 TZP+VAN 治疗的患者 AKI 风险增加 3.5 倍,接受潜在肾毒性药物治疗的患者 AKI 风险增加 1.7 倍。
与任何一种抗生素单药治疗方案相比,TZP+VAN 的联合使用都会导致 AKI 的风险大大增加。因此,在有发生肾损伤高风险的患者中,应谨慎使用这种广谱联合药物。