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Journal of Clinical Microbiology, October 1999, p. 3296-3299, Vol. 37, No. 10
Departments of Pathology (Clinical
Microbiology), Hershey Medical Center, Hershey, Pennsylvania
17033,1 and Case Western Reserve
University, Cleveland, Ohio 441062
Received 29 April 1999/Returned for modification 15 June
1999/Accepted 25 June 1999
This study evaluated the susceptibility of pneumococci to
cefditoren by agar dilution and microdilution methods (both in air) and
by E-test (AB Biodisk, Solna, Sweden) and disk diffusion methods (both
in CO2). By the three MIC tests, the MICs at which 50 and 90% of isolates were inhibited (MIC50s and
MIC90s) were, respectively, as follows (in micrograms per
milliliter): for the 65 penicillin-susceptible strains tested, 0.016 and 0.03 (by agar dilution), 0.016 and 0.03 (by microdilution), and
0.016 and 0.03 (by E test); for the 68 penicillin-intermediate strains
tested, 0.125 and 0.5 (by agar dilution), 0.125 and 0.5 (by
microdilution), and 0.25 and 0.5 (by E test); and for the 67 penicillin-resistant strains tested, 1.0 and 1.0 (by agar dilution),
0.5 and 1.0 (by microdilution), and 1.0 and 1.0 (by E test). With
tentative cefditoren breakpoints (in micrograms per milliliter) of
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Comparison of Agar Dilution, Microdilution, E-Test,
and Disk Diffusion Methods for Testing Activity of Cefditoren against
Streptococcus pneumoniae
2.0 (susceptible), 4.0 (intermediate), and
8.0 (resistant), all
strains were susceptible to cefditoren by agar, microdilution, and
E-test results; with breakpoints of
1.0, 2.0, and
4.0 µg/ml, 97%
of strains were cefditoren susceptible by agar dilution results, 98%
were susceptible by microdilution results, and 99% were susceptible by
E-test results. When microdilution and E-test results were compared to
those from the reference agar dilution method, 191 (95.5%) and 183 (91.5%) of strains gave essential agreement (±1 log2
dilution); 8 (2.7%) minor discrepancies were found for both methods
with a breakpoint of
1.0 µg/ml, and no discrepancies were found
with a breakpoint of
2.0 µg/ml. Disk test results (breakpoint,
1.0 µg/ml) produced 2 major and 30 minor errors, with corresponding
zone diameters (in millimeters) of
20 (susceptible), 17 to 19 (intermediate), and
16 (resistant); a
2.0-µg/ml breakpoint
yielded zone diameters of
16 mm (susceptible). All three methods for
testing the MIC of cefditoren showed excellent correlation.
*
Corresponding author. Mailing address: Department of
Pathology, Hershey Medical Center, 500 University Dr., Hershey, PA
17033. Phone: (717) 531-5113. Fax: (717) 531-7953. E-mail:
pappelbaum{at}psghs.edu.
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