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Antimicrobial susceptibility testing of Acinetobacter spp. by NCCLS broth microdilution and disk diffusion methods
Jana M Swenson1, George E Killgore, Fred C Tenover
1Division of Healthare Quality Promotion, Epidemiology and Laboratory Branch, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA. jswenson@cdc.gov
Journal of Clinical Microbiology
|November 6, 2004
Summary
Broth microdilution and disk diffusion methods show comparable results for many antibiotics against Acinetobacter spp. However, broth microdilution has interpretation challenges, especially with beta-lactams, leading to high error rates.
Area of Science:
- Clinical Microbiology
- Antimicrobial Resistance
- Infectious Diseases
Background:
- Broth microdilution (BMD) and disk diffusion (DD) are standard methods for antimicrobial susceptibility testing.
- Limited comparative data exist for Acinetobacter spp. using these methods.
Purpose of the Study:
- To compare the categorical agreement of BMD and DD for Acinetobacter spp. susceptibility testing.
- To identify discrepancies and potential interpretation issues between BMD and DD.
Main Methods:
- Tested 196 Acinetobacter spp. isolates using BMD and DD with various antimicrobial agents.
- Evaluated error rates (very major, major, minor) between the two methods.
- Assessed BMD interpretation challenges, including subtle growth patterns.
- Collaborated with six external laboratories to confirm BMD interpretation issues.
Main Results:
- High agreement between BMD and DD for amikacin, ciprofloxacin, gentamicin, imipenem, levofloxacin, meropenem, tobramycin, and trimethoprim-sulfamethoxazole.
- Frequent very major errors with beta-lactams and beta-lactam-inhibitor combinations using BMD.
- Significant interpretation difficulties and high error rates for BMD with beta-lactams and tetracyclines.
- External laboratory testing confirmed BMD interpretation variability for cefepime.
Conclusions:
- BMD and DD show good agreement for several antibiotics against Acinetobacter spp.
- BMD poses interpretation challenges, particularly with beta-lactams, leading to unacceptable error rates.
- Clinical laboratories must be aware of potential discrepancies between BMD and DD results.