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头孢地尔在美欧医院 2020 年至 2021 年收集的包括对β-内酰胺类药物不敏感的分子特征分离株的肠杆菌科和 属的活性评估。

activity assessment of cefiderocol against Enterobacterales, and spp., including β-lactam nonsusceptible molecularly characterized isolates, collected from 2020 to 2021 in the United States and European hospitals.

机构信息

JMI Laboratories/Element Iowa City, North Liberty, Iowa, USA.

出版信息

Microbiol Spectr. 2024 Nov 5;12(11):e0147424. doi: 10.1128/spectrum.01474-24. Epub 2024 Oct 10.

Abstract

This study reports the activity of cefiderocol against Enterobacterales, , and spp. isolates collected from the United States and Europe, including Israel and Turkey, from 2020 to 2021. Among Enterobacterales, 2.8% were carbapenem nonsusceptible (CNSE); cefiderocol inhibited 96.6%/85.1% [Clinical Laboratory Standards Institute (CLSI)/European Committee on Antimicrobial Susceptibility Testing (EUCAST) breakpoints] of these isolates. Imipenem-relebactam, meropenem-vaborbactam, and ceftazidime-avibactam displayed susceptibilities lower than cefiderocol against CNSE isolates (67.4-84.6% susceptible, CLSI). Cefiderocol was the only agent active against CNSE isolates carrying metallo-β-lactamase (MBL) carbapenemase or multiple carbapenemase genes (84.6%-92.3% susceptible, CLSI). Approximately 18% of carbapenem-susceptible , , and carried extended-spectrum-β-lactamases and/or plasmid-borne AmpC-encoding genes; cefiderocol inhibited 99.8%-100.0% (CLSI) of these genotypic groups. Multi-drug resistance (MDR) phenotypes were observed in 16.9% and 52.5% of and isolates, respectively. Carbapenemase genes were rare (4.9%) among cephalosporin and/or carbapenem nonsusceptible , compared to 87.6% carriage in , respectively. Against the MDR and carbapenemase-carrying and subsets, cefiderocol was active against 98.6%/98.7% and 97.1%/97.4% (CLSI), respectively. Only 69 isolates (0.3%) across all species groups were identified as cefiderocol nonsusceptible per CLSI criteria (>4 mg/L). Cefiderocol was the most active agent against Enterobacterales, and spp., with uniform activity against all phenotypic- and genotypic-resistant subsets. Coupled with the low incidence of nonsusceptibility observed across species groups, these results demonstrate cefiderocol as an important option for treating infections caused by pathogens with diverse mechanisms of resistance in US and European hospitals.IMPORTANCEThe worldwide spread of multi-drug-resistant and carbapenem-resistant Enterobacterales and spp. poses a serious challenge in healthcare settings as infections caused by these organisms are commonly refractory to many frontline therapeutic agents. Multiple global health organizations highlighted these pathogens as critical priorities for new antibiotic development, thus necessitating continued surveillance of the activities of currently available antimicrobial agents and circulating mechanisms of resistance. To meet this need, this study phenotypically and genotypically characterized priority Gram-negative pathogens collected from patients in US and European hospitals to examine the activity of cefiderocol and other currently available treatment options, including carbapenems and β-lactam-β-lactamase inhibitor combinations. The results presented here provide a detailed perspective to healthcare practitioners of cefiderocol's broad applicability, manifested in high activity and low nonsusceptibility rates, across phenotypic and genotypic organism groups relative to other agents and further support its use against the most intransigent infections.

摘要

本研究报告了头孢地尔在来自美国和欧洲(包括以色列和土耳其)的 2020 年至 2021 年期间收集的肠杆菌科、 和 种属分离株中的活性。在肠杆菌科中,2.8%为碳青霉烯类药物不敏感(CNSE);头孢地尔抑制了 96.6%/85.1%(临床实验室标准协会(CLSI)/欧洲抗菌药物敏感性测试委员会(EUCAST)的断点)的这些分离株。亚胺培南-雷巴他定、美罗培南-沃巴他定和头孢他啶-阿维巴坦对 CNSE 分离株的敏感性低于头孢地尔(67.4-84.6%敏感,CLSI)。头孢地尔是唯一对携带金属β-内酰胺酶(MBL)碳青霉烯酶或多种碳青霉烯酶基因的 CNSE 分离株具有活性的药物(84.6%-92.3%敏感,CLSI)。大约 18%的耐碳青霉烯类的 、 和 携带超广谱β-内酰胺酶和/或质粒携带的 AmpC 编码基因;头孢地尔抑制了这些基因群的 99.8%-100.0%(CLSI)。16.9%和 52.5%的 和 分离株分别表现出多药耐药(MDR)表型。与 分别为 87.6%的携带率相比,头孢菌素类和/或碳青霉烯类不敏感的 中罕见携带碳青霉烯酶基因(4.9%)。针对 MDR 和携带碳青霉烯酶的 和 亚群,头孢地尔对 98.6%/98.7%和 97.1%/97.4%(CLSI)具有活性。根据 CLSI 标准(>4mg/L),所有种属组中只有 69 株(0.3%)被鉴定为头孢地尔不敏感。头孢地尔是肠杆菌科、 和 种属的最有效药物,对所有表型和基因型耐药亚群均具有一致的活性。结合所有种属组观察到的不敏感性发生率低,这些结果表明头孢地尔是治疗美国和欧洲医院中具有多种耐药机制的病原体引起的感染的重要选择。

重要性

多药耐药和碳青霉烯类耐药肠杆菌科和 种属的全球传播给医疗机构带来了严重挑战,因为这些生物体引起的感染通常对许多一线治疗药物具有抗性。多个全球卫生组织将这些病原体列为新抗生素开发的关键优先事项,因此需要继续监测目前可用的抗菌药物的活性和循环耐药机制。为了满足这一需求,本研究从美国和欧洲医院的患者中表型和基因型鉴定了优先革兰氏阴性病原体,以检查头孢地尔和其他目前可用的治疗选择(包括碳青霉烯类药物和β-内酰胺类/β-内酰胺酶抑制剂联合用药)的活性。这里呈现的结果为医疗保健从业者提供了一个详细的视角,即头孢地尔在表型和基因型生物体组中具有广泛的适用性,表现在与其他药物相比,其具有高活性和低不敏感性率,进一步支持其用于治疗最顽固的感染。

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