Comparison and Evaluation of Carbenicillin Disks in Diffusion Susceptibility Testing

Author:

Matsen John M.123,Lund Marlys E.123,Brooker Doris C.123

Affiliation:

1. Department of Laboratory Medicine and Pathology, University of Minnesota School of Medicine, Minneapolis, Minnesota 55455

2. Department of Pediatrics, University of Minnesota School of Medicine, Minneapolis, Minnesota 55455

3. Department of Microbiology, University of Minnesota School of Medicine, Minneapolis, Minnesota 55455

Abstract

A broad variety of bacterial strains, including 79 Pseudomonas aeruginosa , were studied in an in vitro evaluation of carbenicillin disk susceptibility testing. Regression analysis with both 50-μg and 100-μg carbenicillin disks was carried out. Organisms having minimal inhibitory concentration values of 100 to 200 μg/ml demonstrated zones of less than 11 mm with the 50-μg disk, resulting in very little opportunity for appropriate discrimination of results. The line of regression for the 50-μg disk intersected the ordinate at a point just above the minimal inhibitory concentration value considered to be the limit of intermediate susceptibility for Pseudomonas . These considerations, together with evidence of greater disk content variation in the 50-μg than in the 100-μg disks assayed, considerable manufacturer-to-manufacturer variability with the 50-μg disk, and the more appropriate performance of the 100-μg disk, lead us to conclude that the 100-μg disk better serves the clinical test requirements for this agent than does the 50-μg disk, which is currently the only disk available for laboratory testing.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference24 articles.

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3. Carbenicillin therapy or gram-negative bacilli infections;Bodey G. P.;Amer. J. Med. Sci.,1969

4. Titrage de la sensibilitk des germes aerobies aux antibiotiques par la methode de la cupule en gelose;Chabbert Y.;Ann. Inst. Pasteur (Paris),1949

5. Collins C. H. 1967. Microbiological methods p. 149-150. 2nd ed. Butterworth and Co. London.

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