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False susceptibility to cefotetan reported by MicroScan for DHA-type AmpC beta-lactamase-producing Klebsiella
1Department of Laboratory Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Abstract:
This study evaluated the accuracy of cefotetan susceptibility determination using the MicroScan WalkAway system for AmpC-producing Klebsiella pneumoniae. In total, 57 K. pneumoniae isolates that showed a D-shape flattening in a double-disk synergy test were studied. Cefotetan MICs were determined by the agar dilution method. The bla(DHA) gene was detected in all 57 isolates, one of which co-harboured bla(CMY-1). According to the MicroScan system, 28 isolates were susceptible, 18 were intermediately-resistant, and 11 were resistant to cefotetan. Compared with the agar dilution method, very major, minor and major error rates were 28.1% (16/57), 47.4% (27/57) and 1.8% (1/57), respectively.
Insights
The MicroScan WalkAway system showed poor accuracy in determining cefotetan susceptibility for AmpC-producing Klebsiella pneumoniae. High error rates, particularly very major and minor errors, indicate potential issues in clinical treatment decisions.
Area of Science:
- Clinical Microbiology
- Antimicrobial Resistance
- Bacterial Genetics
Background:
- AmpC-producing Klebsiella pneumoniae is a growing concern in healthcare settings.
- Accurate susceptibility testing is crucial for effective antibiotic treatment.
- Cefotetan is a beta-lactam antibiotic used to treat infections caused by Gram-negative bacteria.
Purpose of the Study:
- To evaluate the diagnostic accuracy of the MicroScan WalkAway system for cefotetan susceptibility testing.
- To assess the performance of the MicroScan system against a reference method for AmpC-producing K. pneumoniae isolates.
Main Methods:
- Fifty-seven Klebsiella pneumoniae isolates with AmpC production (indicated by D-shape flattening in double-disk synergy test) were analyzed.
- Cefotetan Minimum Inhibitory Concentrations (MICs) were determined using the gold standard agar dilution method.
- The bla(DHA) and bla(CMY-1) genes were identified via molecular methods.
Main Results:
- The MicroScan WalkAway system classified isolates as susceptible (n=28), intermediate (n=18), or resistant (n=11).
- Comparison with agar dilution revealed high error rates: very major errors (28.1%), minor errors (47.4%), and major errors (1.8%).
- All isolates harbored the bla(DHA) gene, with one also carrying bla(CMY-1).
Conclusions:
- The MicroScan WalkAway system demonstrates significant limitations in accurately determining cefotetan susceptibility for AmpC-producing K. pneumoniae.
- The high rates of very major and minor errors suggest a potential for misinterpretation of susceptibility results.
- Clinical laboratories should exercise caution when relying solely on the MicroScan system for cefotetan susceptibility testing in these specific isolates.
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