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Journal of Clinical Microbiology, 12 1995, 3191-3193, Vol 33, No. 12
EF Marley, C Mohla and JM Campos
We determined the E-Test and National Committee for Clinical Laboratory
Standards standardized agar dilution MICs of ceftazidime, ciprofloxacin,
piperacillin, and tobramycin for Pseudomonas aeruginosa during tests of 100
rough and mucoid P. aeruginosa isolates from cystic fibrosis patients. The
levels of agreement (+/- 1 log2 dilution) between quantitative E-Test and
agar dilution MIC results were 80, 97, 73, and 89% for ceftazidime,
ciprofloxacin, piperacillin, and tobramycin, respectively. Comparison of
the results after converting the MIC data to qualitative categories
(susceptible, intermediate, and resistant) yielded levels of agreement of
84, 96, 88, and 93% for the same agents, respectively. Of the 39
qualitative discrepancies, 36 were minor and 3 were very major. We conclude
that use of the E-Test is easier and more practical than use of the agar
dilution method for most laboratories and that the E-Test furnishes results
which are at least as accurate as those obtained by the agar dilution
method. However, the higher cost of the E-Test method would likely
discourage most laboratories from selecting it over disk diffusion for
routine antimicrobial susceptibility testing of P. aeruginosa isolates from
cystic fibrosis patients.
Copyright © 1995 by the American Society for Microbiology. All rights reserved.
Evaluation of E-Test for determination of antimicrobial MICs for Pseudomonas aeruginosa isolates from cystic fibrosis patients
Department of Pathology, George Washington University Medical Center, Washington, DC 20037, USA.
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