In vitro activity of cefiderocol and other newly approved antimicrobials against multi-drug resistant Gram-negative pathogens recovered in intensive care units in Spain and Portugal.

D Gijón, J García-Castillo, M C Fernández-López, G Bou, M Siller, J Calvo-Montes, C Pitart, J Vila, N Torno, C Gimeno, H Cruz, H Ramos, X Mulet, A Oliver, P Ruiz-Garbajosa, R Canton
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Abstract

Objective: The antimicrobial resistance is a significant public health threat, particularly for healthcare-associated infections caused by carbapenem-resistant Gram-negative pathogens which are increasingly reported worldwide. The aim of this study was to provide data on the in vitro antimicrobial activity of cefiderocol and that of commercially available comparator antibiotics against a defined collection of recent clinical multi-drug resistant (MDR) microorganisms, including carbapenem resistant Gram-negative bacteria collected from different regions in Spain and Portugal.

Methods: A total of 477 clinical isolates of Enterobacterales, Pseudomonas aeruginosa, Acinetobacter baumannii and Stenotrophomonas maltophilia were prospectively (n=265) and retrospectively (n=212) included (2016-2019). Susceptibility testing was performed using standard broad microdilution and results were interpreted using CLSI-2021 and EUCAST-2021 criteria.

Results: Overall, cefiderocol showed a good activity against Enterobacterales isolates, being 99.5% susceptible by CLSI and 94.5% by EUCAST criteria. It also demonstrated excellent activity against P. aeruginosa and S. maltophilia isolates, all being susceptible to this compound considering CLSI breakpoints. Regarding A. baumannii (n=64), only one isolate was resistant to cefiderocol.

Conclusions: Our results are in agreement with other studies performed outside Spain and Portugal highlighting its excellent activity against MDR gram-negative bacteria. Cefiderocol is a therapeutic alternative to those available for the treatment of infections caused by these MDR bacteria.

[头孢iderocol和其他新批准的抗菌药物对在西班牙和葡萄牙重症监护室康复的耐多药革兰氏阴性病原体的体外活性]。
目的:抗微生物耐药性是一个重大的公共健康威胁,特别是对于由碳青霉烯耐药性革兰氏阴性病原体引起的医疗保健相关感染,这种病原体在世界范围内越来越多地报道。本研究的目的是提供关于头孢地罗醇和市售对照抗生素对近期临床耐多药(MDR)微生物的体外抗菌活性的数据,包括从西班牙和葡萄牙不同地区收集的碳青霉烯耐药革兰氏阴性菌。方法:前瞻性(n=265)和回顾性(n=212)纳入477株肠杆菌、铜绿假单胞菌、鲍曼不动杆菌和嗜麦芽窄食单胞菌的临床分离株(2016-2019)。使用标准宽微量稀释法进行敏感性测试,并使用CLSI-2021和EUCAST-2021标准解释结果。结果:总体而言,头孢iderocol对肠杆菌分离株表现出良好的活性,CLSI敏感率为99.5%,EUCAST标准敏感率为94.5%。它还显示出对铜绿假单胞菌和嗜麦芽假单胞菌分离株的优异活性,考虑到CLSI断点,所有分离株都对该化合物敏感。关于鲍曼不动杆菌(n=64),只有一个分离株对头孢地罗醇具有耐药性。结论:我们的结果与西班牙和葡萄牙以外的其他研究一致,这些研究强调了其对耐多药革兰氏阴性菌的优异活性。头孢iderocol是治疗由这些耐多药细菌引起的感染的替代品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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