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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页码:81 / 88
页数:8
相关论文
共 39 条
[1]   In vitro, in vivo and clinical studies comparing the efficacy of ceftazidime-avibactam monotherapy with ceftazidime-avibactam-containing combination regimens against carbapenem-resistant Enterobacterales and multidrug-resistant Pseudomonas aeruginosa isolates or infections: a scoping review [J].
Aslan, Abdullah Tarik ;
Ezure, Yukiko ;
Horcajada, Juan Pablo ;
Harris, Patrick N. A. ;
Paterson, David L. .
FRONTIERS IN MEDICINE, 2023, 10
[2]   Epidemiological Expansion, Structural Studies, and Clinical Challenges of New β-Lactamases from Gram-Negative Bacteria [J].
Bush, Karen ;
Fisher, Jed F. .
ANNUAL REVIEW OF MICROBIOLOGY, VOL 65, 2011, 65 :455-478
[3]  
Committee E., 2022, EUCAST CLIN BREAKPOI
[4]   Selecting the dosage of ceftazidime-avibactam in the perfect storm of nosocomial pneumonia [J].
Das, Shampa ;
Zhou, Diansong ;
Nichols, Wright W. ;
Townsend, Andy ;
Newell, Paul ;
Li, Jianguo .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 2020, 76 (03) :349-361
[5]   Pseudomonas aeruginosa epidemic high-risk clones and their association with horizontally-acquired β-lactamases: 2020 update [J].
del Barrio-Tofino, Ester ;
Lopez-Causape, Carla ;
Oliver, Antonio .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2020, 56 (06)
[6]  
del Barrio-Tofino E, 2017, ANTIMICROB AGENTS CH, V61, DOI [10.1128/AAC.01589-17, 10.1128/aac.01589-17]
[7]  
Drusano GL, 2018, ANTIMICROB AGENTS CH, V62, DOI [10.1128/AAC.01682-18, 10.1128/aac.01682-18]
[8]  
Drusano GL, 2016, ANTIMICROB AGENTS CH, V60, P1194, DOI 10.1128/AAC.02231-15
[9]   Pseudomonas aeruginosa: arsenal of resistance mechanisms, decades of changing resistance profiles, and future antimicrobial therapies [J].
El Zowalaty, Mohamed E. ;
Al Thani, Asmaa A. ;
Webster, Thomas J. ;
El Zowalaty, Ahmed E. ;
Schweizer, Herbert P. ;
Nasrallah, Gheyath K. ;
Marei, Hany E. ;
Ashour, Hossam M. .
FUTURE MICROBIOLOGY, 2015, 10 (10) :1683-1706
[10]   Pseudomonas aeruginosa: new insights into pathogenesis and host defenses [J].
Gellatly, Shaan L. ;
Hancock, Robert E. W. .
PATHOGENS AND DISEASE, 2013, 67 (03) :159-173