Comparison of Three Different Commercial Methods for Fosfomycin Susceptibility Testing in .

The lack of internationally approved breakpoint and a handy susceptibility testing reduces fosfomycin usefulness against . Previous works defined low or moderate agreement between commercial methods and the reference method (agar dilution [AD]). In particular, data lack about testing against . We compared disk diffusion (DD), E-test (ET), and automated broth microdilution (BMD) to AD by testing 150 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