Virginia Commonwealth University, Richmond, Virginia, USA.
Sentara Norfolk General Hospitalgrid.415513.7, Department of Pharmacy, Norfolk, Virginia, USA.
Antimicrob Agents Chemother. 2022 Aug 16;66(8):e0004022. doi: 10.1128/aac.00040-22. Epub 2022 Jul 13.
Acute kidney injury (AKI) is a complication associated with vancomycin. Previous studies demonstrated that the combination of vancomycin and piperacillin-tazobactam increases the risk of AKI compared to vancomycin with meropenem or cefepime. These studies did not utilize area under the curve (AUC)-based dosing, which reduces vancomycin exposure and may decrease nephrotoxicity compared with trough-based dosing. This study evaluated the incidence of AKI in patients receiving AUC-dosed vancomycin with either concomitant piperacillin-tazobactam (VPT) or meropenem or cefepime (VMC). This retrospective cohort study included patients admitted to Sentara Norfolk General Hospital between October 2019 and September 2020 who received AUC-dosed vancomycin and concomitant piperacillin-tazobactam, meropenem, or cefepime for at least 48 h. The primary outcome was the incidence of AKI during treatment or within 24 h of discontinuation. A total of 435 patients (VPT, = 331; VMC, = 104) who received a median duration of 4 days of treatment were included. The incidence of AKI was significantly higher with VPT than with VMC (13.6% versus 4.8% [ = 0.014]). Multivariable analysis showed VPT to be an independent risk factor for the development of AKI (odds ratio [OR], 3.00 [95% confidence interval {CI}, 1.15 to 7.76]). VPT was associated with more frequent AKI than VMC, even with the relatively short courses of antimicrobial therapy administered in this population. In comparison with the precedent in the literature for trough-based vancomycin dosing, our results suggest that the use of AUC-based vancomycin dosing in combination with piperacillin-tazobactam, meropenem, or cefepime may result in a lower overall incidence of AKI.
急性肾损伤(AKI)是万古霉素相关的并发症。先前的研究表明,与万古霉素与美罗培南或头孢吡肟合用相比,万古霉素与哌拉西林他唑巴坦合用会增加 AKI 的风险。这些研究并未使用基于 AUC 的剂量给药,与基于谷值的剂量给药相比,基于 AUC 的剂量给药可降低万古霉素的暴露量,并可能降低肾毒性。本研究评估了接受 AUC 剂量万古霉素与哌拉西林他唑巴坦(VPT)或美罗培南或头孢吡肟(VMC)联合治疗的患者 AKI 的发生率。这项回顾性队列研究纳入了 2019 年 10 月至 2020 年 9 月期间在 Sentara Norfolk 综合医院住院且接受 AUC 剂量万古霉素联合至少 48 小时的哌拉西林他唑巴坦、美罗培南或头孢吡肟治疗的患者。主要结局为治疗期间或停药后 24 小时内 AKI 的发生率。共纳入 435 例患者(VPT,n=331;VMC,n=104),中位治疗时间为 4 天。VPT 组 AKI 的发生率明显高于 VMC 组(13.6%比 4.8%[P=0.014])。多变量分析显示,VPT 是 AKI 发生的独立危险因素(比值比[OR],3.00[95%置信区间{CI},1.15 至 7.76])。即使在该人群中给予相对较短疗程的抗菌治疗,VPT 与 VMC 相比,AKI 的发生率也更高。与文献中关于谷值万古霉素剂量的研究结果相比,我们的结果表明,与哌拉西林他唑巴坦、美罗培南或头孢吡肟联合使用基于 AUC 的万古霉素剂量可能会降低 AKI 的总体发生率。