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Interpretive criteria for the agar diffusion susceptibility test with enoxacin
The Journal of Antimicrobial Chemotherapy
|September 1, 1984
Summary
This study evaluated enoxacin disc diffusion tests for antimicrobial susceptibility. Results show that disc concentration and method influence accuracy, with specific zone interpretations recommended for clinical use.
Area of Science:
- Microbiology
- Antimicrobial Susceptibility Testing
Background:
- Accurate antimicrobial susceptibility testing (AST) is crucial for guiding effective treatment of infectious diseases.
- Enoxacin is a fluoroquinolone antibiotic used to treat various bacterial infections.
- Standardization of AST methods ensures reliable interpretation of results.
Purpose of the Study:
- To determine the correlation between Minimum Inhibitory Concentration (MIC) and inhibition zone diameters for enoxacin discs.
- To evaluate the performance of different enoxacin disc concentrations (5 and 10 µg) and AST methods (ICS and Kirby-Bauer).
- To establish reliable zone interpretation criteria for enoxacin susceptibility testing.
Main Methods:
- Regression analysis was performed on 300 clinical isolates from 15 species.
- Enoxacin discs (5 and 10 µg) were tested using both the International Clinical Standards (ICS) and Kirby-Bauer methods on Iso-Sensitest and Mueller-Hinton agars.
- MIC breakpoints and zone cut-off points were calculated and compared.
Main Results:
- Correlation between MIC and zone diameter decreased with higher enoxacin disc content and with the Kirby-Bauer method.
- No major errors in zone interpretation were found using preliminary breakpoints.
- Minor errors occurred in 3.7% (ICS, 5 µg discs) and 11.0% (Kirby-Bauer, 10 µg discs).
Conclusions:
- Recommended zone interpretations for enoxacin susceptibility testing were proposed for both ICS and Kirby-Bauer methods.
- The study provides guidance for accurate interpretation of enoxacin susceptibility results in clinical microbiology laboratories.
- Optimized disc concentrations and methods can improve the reliability of AST for enoxacin.