IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Department of Medical and Surgical Sciences, Alma Mater Studiorum, University of Bologna, Bologna, Italy.
Eur J Clin Microbiol Infect Dis. 2024 Sep;43(9):1861-1864. doi: 10.1007/s10096-024-04879-8. Epub 2024 Jul 17.
We evaluated the activity of piperacillin in relation to INCREASING TAZOBACTAM CONCENTRATION against ESBL-producing Enterobacterales collected from patients with bacteraemia. Increasing tazobactam concentration (4, 12 or 24 mg/L) exerted a reduction of piperacillin MICs under the clinical breakpoint in a concentration-dependent manner (0%, 60% and 90% of clinical isolates). Also, activity of piperacillin/tazobactam based at higher achievable serum concentrations (123/14 mg/L) is needed to reduce the bacterial growth in 92% of ESBL-producers. CHANGES IN THE PIPERACILLIN MIC IN RELATION TO INCREASING TAZOBACTAM SUGGEST THAT REALTIME TDM COULD BE USED FOR DRIVEN ANTIMICROBIAL THERAPY WITH PIPERACILLIN/TAZOBACTAM IN BSI DUE TO ESBL STRAINS.
我们评估了哌拉西林与增加他唑巴坦浓度对抗血培养分离的产 ESBL 肠杆菌科的活性。增加他唑巴坦浓度(4、12 或 24mg/L)以浓度依赖方式降低了临床折点下哌拉西林 MIC(临床分离株的 0%、60%和 90%)。此外,为了减少 92%产 ESBL 细菌的生长,需要更高的可达到血清浓度(123/14mg/L)的哌拉西林/他唑巴坦基础上的活性。哌拉西林 MIC 的变化与增加他唑巴坦浓度有关,提示由于 ESBL 株,实时 TDM 可用于驱动 BSIs 中哌拉西林/他唑巴坦的经验性抗菌治疗。