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Development of resistance in Pseudomonas aeruginosa obtained from patients with cystic fibrosis at different times
Authors:F. B. Spencker  L. Staber  T. Lietz  R. Schille   A. C. Rodloff
Affiliation:Institute for Medical Microbiology and Epidemiology of Infectious Diseases, and;Department of Pediatrics, University of Leipzig, Leipzig, Germany
Abstract:Objective  Determination of the extent of changes in quantitative resistance in Pseudomonas aeruginosa isolates from patients with cystic fibrosis over a period of approximately 2 years.
Methods  Three hundred and ninety nine isolates of P. aeruginosa collected from 34 pediatric patients in the period between April 1994 and April 1996 were investigated. During the 2 years the children were treated with a combination of a betalactam and an aminoglycoside, approximately every 3 months. In between they received ciprofloxacin orally, when required. The minimal inhibitory concentrations (MICs) of 38 clones of P. aeruginosa defined by different patterns in macrorestriction analysis (pulse field gel electrophoresis, PFGE) were established for 12 antibiotics: gentamicin, amikacin, tobramycin, ciprofloxacin, levofloxacin, moxifloxacin, trovafloxacin, imipenem, meropenem, ceftazidime, cefepime, and piperacillin by means of broth microdilution tests according to DIN 58940.
Results  Twenty-four of the 38 clones developed increased MIC values during the time of observation especially for aminoglycosides and quinolones. Comparatively less affected were ceftazidime, imipenem and meropenem. An association between the number of the intravenous treatment courses and the increase of the MIC values could not be verified.
Conclusions  A trend towards an increase of the MICs against antipseudomonal agents was observed over a limited period of time. It is necessary to prevent this development possibly by employing suitable combinations of antibiotics and the introduction of new substances.
Keywords:Pseudomonas aeruginosa    antibiotic resistance    minimal inhibitory concentrations (MICs)    cystic fibrosis
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