Ali Saied, Tobin Aideen, Lapthorne Susan, Collison Meadhbh, Murphy Doireann, Chan Grace, Doyle Maeve
Department of Clinical Microbiology, University Hospital Waterford, Waterford, Ireland.
Royal College of Surgeons in Ireland, Dublin, Ireland.
J Med Microbiol. 2025 Feb;74(2). doi: 10.1099/jmm.0.001955.
Carbapenems are usually employed as first-line antimicrobials against bacteria harbouring extended-spectrum beta-lactamases (ESBLs). These enzymes confer resistance often to multiple classes of antimicrobials. This indiscriminate use of carbapenems and the inevitable development of carbapenem resistance have prompted the need for carbapenem-sparing strategies. The non-carbapenem antimicrobial susceptibility patterns of 60 ESBL-producing (ESBL-PE) isolates responsible for bloodstream infections, in 2022-2023 inclusive, processed at our institution were reviewed. The non-carbapenem antimicrobial susceptibility patterns of 60 ESBL-PE isolates from bloodstream infections during the study period were determined. was the most common species isolated (87%, =52), with the majority of cases (73.3%, =44) originating from a presumed urinary source. Temocillin (TMC), mecillinam (MEC), cefiderocol (FDC), amikacin and fosfomycin (FOS) displayed excellent activity against all ESBL-PE isolates tested, with susceptibility rates of≥85%. Ciprofloxacin and amoxicillin-clavulanic acid were the least efficacious agents, with susceptibility rates≤20%. TMC, MEC, FDC and FOS offer promising alternatives to carbapenems, demonstrating efficacy against ESBL-PE. The use of these agents not only broadens the therapeutic arsenal against ESBL-PE but also mitigates the potential for escalating carbapenem resistance, especially in regions where the incidence of carbapenem resistance is increasing.
碳青霉烯类药物通常被用作针对携带超广谱β-内酰胺酶(ESBLs)细菌的一线抗菌药物。这些酶常常使细菌对多种抗菌药物产生耐药性。碳青霉烯类药物的这种滥用以及不可避免出现的碳青霉烯类耐药性,促使人们需要采取碳青霉烯类药物节省策略。我们回顾了2022年至2023年(含)期间在我们机构处理的60株导致血流感染的产ESBLs(ESBL-PE)分离株的非碳青霉烯类抗菌药物敏感性模式。确定了研究期间60株来自血流感染的ESBL-PE分离株的非碳青霉烯类抗菌药物敏感性模式。 是最常分离出的菌种(87%,=52),大多数病例(73.3%,=44)源自推测的泌尿道感染源。替莫西林(TMC)、美西林(MEC)、头孢地尔(FDC)、阿米卡星和磷霉素(FOS)对所有测试的ESBL-PE分离株均表现出优异的活性,敏感率≥85%。环丙沙星和阿莫西林-克拉维酸是疗效最差的药物,敏感率≤20%。TMC、MEC、FDC和FOS为碳青霉烯类药物提供了有前景的替代方案,对ESBL-PE显示出疗效。使用这些药物不仅拓宽了针对ESBL-PE的治疗手段,还减轻了碳青霉烯类耐药性上升的可能性,尤其是在碳青霉烯类耐药性发生率正在上升的地区。