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

被引:0
|
作者
Montero, Maria M. [1 ,2 ,3 ,4 ]
Domene-Ochoa, Sandra [1 ,2 ]
Prim, Nuria [5 ]
Ferola, Eliana [1 ,2 ]
Lopez-Causape, Carla [6 ,7 ]
Echeverria, Daniel [8 ]
Morisaki, Mario F. Ampuero [9 ]
Vega-Toribio, Victoria [5 ]
Sorli, Luisa [1 ,2 ,3 ,4 ]
Luque, Sonia [4 ,8 ]
Padilla, Eduardo [5 ]
Oliver, Antonio [4 ,6 ,7 ]
Horcajada, Juan P. [1 ,2 ,3 ,4 ]
机构
[1] Hosp del Mar, Infect Dis Serv, Passeig Maritim 25-29, Barcelona 08003, Spain
[2] Hosp del Mar Res Inst IMIM, Infect Pathol & Antimicrobials Res Grp IPAR, Barcelona, Spain
[3] Univ Pompeu Fabra Barcelona, Dept Med & Life Sci MELIS, Barcelona, Spain
[4] Inst Hlth Carlos III, CIBER Infect Dis CIBERINFEC CB21 13 00002 & CB21 1, Madrid, Spain
[5] Lab Referencia Catalunya, MicrobiologyServ, Barcelona, Spain
[6] Hosp Son Espases, Serv Microbiol, IdISBa, Palma De Mallorca, Spain
[7] Hosp Son Espases, Unidad Invest, IdISBa, Palma De Mallorca, Spain
[8] Hosp del Mar, PharmacyServ, Barcelona, Spain
[9] Hosp Univ Ramon & Cajal, Microbiol Serv, Madrid, Spain
关键词
Pseudomonas aeruginosa; ceftazidime/avibactam; aztreonam; PK/PD; hollow-fiber; BETA-LACTAM; COMBINATION; PHARMACODYNAMICS; AMINOGLYCOSIDE; METAANALYSIS; RESISTANCE; AVIBACTAM; THERAPY;
D O I
10.1080/23744235.2024.2396882
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
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-beta-lactamase (SBL)- and metallo-beta-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.
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页数:8
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