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These breakpoints were used on the basis of recommendations as previously described [ 16].
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CLSI breakpoints were used for imipenem and meropenem [ 9] since European Committee on Antimicrobial Susceptibility Testing (EUCAST) breakpoints were not available when the study was initiated.
The European Committee on Antimicrobial Susceptibility Testing (EUCAST) breakpoints were used to define reduced susceptibility.
Post-2008 MIC breakpoints were used for penicillin resistance.
NCCLS breakpoints were used for interpretation of MIC's [ 29].
NCCLS (2002) breakpoints were used to interpret the data.
FDA breakpoints were used for doripenem since CLSI breakpoints for doripenem were not available when the study was initiated.
However, because no breakpoints have been established for levofloxacin and gatifloxacin, moxifloxacin breakpoints were used for interpretation of these results.
The European Committee on Antimicrobial Susceptibility Testing (EUCAST) zone diameter interpretive standards and MIC breakpoints were used for CIP and FA [ 55].
These breakpoints were used based on the recommendations from the National Committee for Clinical Laboratory Standards (NCCLS) and a large clinical trial [ 10, 11].
The simplified explanation is that breakpoints are used to specify when a site layout will change when the browser window reaches certain dimensions.
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