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. 2014 Sep 3:7:603.
doi: 10.1186/1756-0500-7-603.

Impact of minimal inhibitory concentration breakpoints on local cumulative bacterial susceptibility data and antibiotic consumption

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Impact of minimal inhibitory concentration breakpoints on local cumulative bacterial susceptibility data and antibiotic consumption

Sofia Stokkou et al. BMC Res Notes. .

Abstract

Background: The phenotypic antimicrobial susceptibility testing (AST) of bacteria depends on minimal inhibitory concentration breakpoints issued by national and international breakpoint committees. The current study was performed in order to test the influence of different AST standards on local cumulative AST data and on antibiotic consumption.

Methods: Automated AST was performed with clinical isolates of Pseudomonas aeruginosa, Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, Staphylococcus aureus, coagulase-negative staphylococci, Enterococcus faecalis, and E. faecium. From each species 100 prospectively collected non-duplicate clinical isolates were tested and MIC data were interpreted according to the interpretation standards issued by DIN and EUCAST, respectively. In addition cumulative AST data from clinical isolates and antibiotic consumption were monitored before and after implementation of new EUCAST MIC breakpoints.

Results: The susceptibility rate of P. aeruginosa against piperacillin and gentamicin, and of C. freundii against piperacillin/tazobactam increased significantly, whereas the susceptibility rates of E. cloacae, S. marcescens, and M. morganii against ciprofloxacin decreased significantly after switching from DIN to EUCAST MIC breakpoints. These changes in the cumulative antibiotic resistance pattern were reflected by enhanced consumption of piperacillin/tazobactam after implementation of EUCAST MIC breakpoints.

Conclusions: These data show that changes of AST breakpoints have a significant influence on local cumulative AST data and on antibiotic consumption.

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Figures

Figure 1
Figure 1
Antibiotic consumption of selected antibiotics before and after implementation of EUCAST MIC breakpoints. The prescribed defined daily doses per 1000 patient days was calculated for the study periods of 12 month before (open bars) and 12 month after (closed bars) implementation of EUCAST MIC breakpoints. Indicated are the means and standard deviations of the 4 quarters before and the 4 quarters after implementation of EUCAST MIC breakpoints. The asterisk indicates a statistically significant (p < 0.05) change of antibiotic consumption.

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