Synergistic efficacy of ceftazidime/avibactam and aztreonam against carbapenemase-producing Pseudomonas aeruginosa: insights from the hollow-fiber infection model.

Infectious diseases (London, England) Pub Date : 2025-01-01 Epub Date: 2024-08-30 DOI:10.1080/23744235.2024.2396882
María M Montero, Sandra Domene-Ochoa, Núria Prim, Eliana Ferola, Carla López-Causapé, Daniel Echeverria, Mario F Ampuero Morisaki, Victoria Vega-Toribio, Luisa Sorlí, Sonia Luque, Eduardo Padilla, Antonio Oliver, Juan P Horcajada
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Abstract

Background: Combination therapy is an attractive therapeutic option for extensively drug-resistant (XDR) Pseudomonas aeruginosa infections. Existing data support the combination of aztreonam and ceftazidime/avibactam (CZA) against class serine-β-lactamase (SBL)- and metallo-β-lactamase (MBL) - producing Enterobacterales. However, data about that combination against SBL- and MBL-producing P. aeruginosa are scarce. The objective of the study was to assess the in vitro activity of CZA and aztreonam alone and in combination against SBL- and MBL-producing XDR P. aeruginosa isolates.

Methods: The combination was analyzed by means of the hollow-fiber infection model in three selected carbapenemase-producing P. aeruginosa isolates that were representative of the three most common XDRP. aeruginosa high-risk clones (ST175, ST111, ST235) responsible for global nosocomial infection outbreaks.

Results: The three isolates were nonsusceptible to CZA and nonsusceptible to aztreonam. In the dynamic hollow-fiber infection model, the combination of CZA plus aztreonam exerts a bactericidal effect on the isolates, regardless of their resistance mechanism and demonstrates synergistic interactions against three isolates, achieving a bacterial reduction of 5.07 log10 CFU/ml, 5.2 log10 CFU/ml and 4 log10 CFU/ml, respectively.

Conclusion: The combination of CZA and aztreonam significantly enhanced the in vitro efficacy against XDR P. aeruginosa isolates compared to each monotherapy. This improvement suggests that the combination could serve as a feasible treatment alternative for infections caused by carbapenemase-producing XDR P. aeruginosa, especially in scenarios where no other treatment options are available.

头孢他啶/阿维菌素和阿兹曲南对产碳青霉烯酶铜绿假单胞菌的协同疗效:中空纤维感染模型的启示。
背景:对于广泛耐药(XDR)铜绿假单胞菌感染而言,联合疗法是一种极具吸引力的治疗选择。现有数据支持氨曲南和头孢唑肟/阿维巴坦(CZA)联合治疗产生丝氨酸-β-内酰胺酶(SBL)和金属-β-内酰胺酶(MBL)的肠杆菌。然而,有关该组合针对产 SBL 和 MBL 的铜绿假单胞菌的数据却很少。本研究的目的是评估 CZA 和阿曲南单药及联合用药对产 SBL 和 MBL 的 XDR 铜绿假单胞菌分离物的体外活性:方法:通过空心纤维感染模型,对三种精选的产碳青霉烯酶铜绿假单胞菌分离株进行了联合用药分析,这三种分离株代表了导致全球医院内感染爆发的三种最常见的 XDRP.铜绿假单胞菌高危克隆(ST175、ST111、ST235):结果:这三种分离株对 CZA 和阿曲南均无敏感性。在动态中空纤维感染模型中,无论分离菌株的耐药机制如何,CZA 和阿曲南均能发挥杀菌作用,并对三种分离菌株产生协同作用,分别减少了 5.07 log10 CFU/ml、5.2 log10 CFU/ml 和 4 log10 CFU/ml:结论:与单一疗法相比,CZA和阿曲南经体外联合治疗可显著提高对XDR铜绿假单胞菌分离株的疗效。这一改善表明,联合用药可作为产碳青霉烯酶 XDR 铜绿假单胞菌感染的一种可行的替代治疗方法,尤其是在没有其他治疗选择的情况下。
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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