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- W4290963904 abstract "The lack of internationally approved breakpoint and a handy susceptibility testing reduces fosfomycin usefulness against Pseudomonas aeruginosa. Previous works defined low or moderate agreement between commercial methods and the reference method (agar dilution [AD]). In particular, data lack about testing against P. aeruginosa. We compared disk diffusion (DD), E-test (ET), and automated broth microdilution (BMD) to AD by testing 150 P. aeruginosa isolates. We obtained better categorical agreement (CA) for DD and ET for minimal inhibitory concentration >128 mg/L (84.7% and 92.7%, respectively), but with high very major error (VME). BMD had the lowest VME rate (2/42), but with 64% CA and 52/108 major errors. We cannot define a method comparable to AD. Larger studies, as well as the definition of a breakpoint value are needed for fosfomycin against P. aeruginosa." @default.
- W4290963904 created "2022-08-13" @default.
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- W4290963904 date "2022-09-01" @default.
- W4290963904 modified "2023-10-16" @default.
- W4290963904 title "Comparison of Three Different Commercial Methods for Fosfomycin Susceptibility Testing in <i>Pseudomonas aeruginosa</i>" @default.
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- W4290963904 doi "https://doi.org/10.1089/mdr.2021.0410" @default.
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