Li Ranyi, Li Yanli, Xu Chenqi, Shen Ziyan, Xu Xialian, Ding Xiaoqiang, Li Xiaoyu, Lv Qianzhou, Pan Kunming
Department of Pharmacy, ZhongShan Hospital, Fudan University, Shanghai, China.
Department of Nephrology, ZhongShan Hospital, Fudan University, Shanghai, China.
J Pharm Technol. 2025 Jul 26:87551225251350894. doi: 10.1177/87551225251350894.
: To explore whether vancomycin (VAN) plus piperacillin-tazobactam (PTZ) was associated with an increased risk of acute kidney injury (AKI) compared with VAN plus other beta-lactams (BLs) or monotherapy in critically ill patients, where the evidence remains controversial. PubMed, Cochrane, Web of Science, and Embase were searched from inception to June 2024. Studies comparing the risk of AKI with one group receiving VAN+PTZ, and other groups receiving VAN plus other BLs, or monotherapy in critically ill. This analysis included 20 articles with 28 243 participants. The majority of included studies were retrospective (95%, 19/20) and had moderate risks of bias (80.0%, 16/20). The results indicated VAN+PTZ was associated with a significantly higher risk of AKI compared with VAN plus other BLs (OR = 1.66, 95% CI = 1.42-1.94, < 0.001). Subgroup analyses showed that compared with adults, children were associated with a higher risk of AKI when receiving VAN+PTZ (OR = 3.16 vs 1.59). Also, VAN+PTZ was associated with a significantly higher risk of severe stage 2 to 3 AKI than VAN plus other BLs (OR = 1.63, 95% CI = 1.28-2.06, < 0.001). No significant difference was identified in mortality, dialysis, time to AKI, and length of stay between patients receiving VAN plus PTZ and other combinations. : In critically ill, VAN plus PTZ was associated with an increased risk of AKI and severe stage 2 to 3 AKI compared with VAN plus other BLs, especially in children. However, more high-quality multicenter, prospective cohort studies, and randomized controlled studies are needed.
为探讨在重症患者中,与万古霉素(VAN)联合其他β-内酰胺类药物(BLs)或单药治疗相比,万古霉素(VAN)联合哌拉西林-他唑巴坦(PTZ)是否会增加急性肾损伤(AKI)的风险,目前相关证据仍存在争议。检索了PubMed、Cochrane、Web of Science和Embase数据库,检索时间从建库至2024年6月。纳入比较一组接受VAN+PTZ与其他组接受VAN联合其他BLs或单药治疗的重症患者AKI风险的研究。该分析纳入了20篇文章,共28243名参与者。纳入的研究大多为回顾性研究(95%,19/20),且存在中度偏倚风险(80.0%,16/20)。结果表明,与VAN联合其他BLs相比,VAN+PTZ与AKI风险显著升高相关(OR = 1.66,95%CI = 1.42 - 1.94,P < 0.001)。亚组分析显示,与成人相比,儿童接受VAN+PTZ时AKI风险更高(OR = 3.16 vs 1.59)。此外,与VAN联合其他BLs相比,VAN+PTZ与2至3期严重AKI风险显著升高相关(OR = 1.63,95%CI = 1.28 - 2.06,P < 0.001)。接受VAN联合PTZ与其他联合治疗的患者在死亡率、透析、发生AKI的时间和住院时间方面未发现显著差异。在重症患者中,与VAN联合其他BLs相比,VAN联合PTZ与AKI及2至3期严重AKI风险增加相关,尤其是在儿童中。然而,需要更多高质量的多中心前瞻性队列研究和随机对照研究。