Resistance characteristics of blood culture isolates ofEnterobacter cloacaewith special reference to beta-lactamases and relation to preceding antimicrobial therapy
Autor: | Hans Jørn Kolmos, Merete Weischer, Helga Schumacher |
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Rok vydání: | 1994 |
Předmět: |
Microbiology (medical)
Imipenem medicine.drug_class Cephalosporin Antibiotics Drug resistance beta-Lactamases Pathology and Forensic Medicine Microbiology Amp resistance Enterobacter cloacae medicine Humans Immunology and Allergy Cefoxitin biology Enterobacteriaceae Infections Drug Resistance Microbial General Medicine biochemical phenomena metabolism and nutrition Antimicrobial biology.organism_classification Enzyme Induction Ampicillin Resistance medicine.drug |
Zdroj: | APMIS. 102:356-366 |
ISSN: | 1600-0463 0903-4641 |
DOI: | 10.1111/j.1699-0463.1994.tb04884.x |
Popis: | Resistance characteristics of 53 blood culture isolates of E. cloacae were examined and correlated with antimicrobial treatment preceding bacteraemia. Resistance patterns of 22 antimicrobial agents, presence of resistant mutants, and inducibility of beta-lactamase were investigated; furthermore, population analysis and investigation of beta-lactamase production of selected isolates were performed. Thirty-two isolates (60%) were resistant to cephalothin and/or cefoxitin and/or ampicillin, and 14 isolates (26%) had further resistance characteristics, 7 of the 14 being resistant to non-beta-lactam antibiotics. All ampicillin-susceptible and 76% of cefotaxime-susceptible isolates had resistant mutants in the zone of inhibition when high inoculum was used. All isolates investigated had inducible chromosomal beta-lactamases, and, in addition, two isolates had an enzyme corresponding with TEM-1. Correlation of resistance patterns and antimicrobial treatment preceding bacteraemia showed that treatment with a third-generation cephalosporin was associated with beta-lactam multiresistance. In conclusion, susceptibility testing of beta-lactam antibiotics of Enterobacter must be interpreted with caution and monotherapy with an extended-spectrum cephalosporin should be avoided unless presence of resistant mutants and inducibility of beta-lactamase can be excluded. |
Databáze: | OpenAIRE |
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