Surveillance of susceptibility patterns in 1297 Europeans and US anaerobic and capnophilic isolates to co-amoxiclav and five other antimicrobials agents

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Abstract

In vitro susceptibility data were collected for co-amoxiclav and other antimicrobial agents against 1297 recent anaerobe isolates collected in Europe and the USA. The co-amoxiclav (amoxicillin/clavulanic acid) MIC50/90s (amoxicillin/clavulanic acid concentration in a ratio of 2:1, expressed in terms of amoxicillin concentration in mg/L) were 0.5/4 for Bacteroides fragilis, ≤0.125/1 for Prevotella species, ≤0.125/0.25 for Fusobacterium, nucleatum, 0.5/1 for Eikenella corrodens, 0.25/8 for Peptostreptococcus anaerobius, ≤0.125/0.5 for Micromonas (Peptostreptococcus) micros, ≤25/0.5 for Fingoldia (Peptostreptococcus) magna, and ≤0.125/0.125 for Porphyromonas species. The co-amoxiclav susceptibility rate for B. fragilis was 94.6%, for P. anaerobius 84.3% and for all other species tested 100%. These data indicate that co-amoxiclav remains an effective drug for the antimicrobial treatment and prophylaxis of many anaerobic infections. Among the comparator drugs, metronidazole was very active against all bacterial species (>96% susceptible) except E. corrodens (MIC50/90 of >32/>64 mg/L), which is a capnophilic organism. Imipenem was also highly active against all species (>98% susceptible). Levofloxacin and clindamycin were the least potent agents tested, particularly against Bacteroides, Prevotella and Peptostreptococcus (levofloxacin susceptibility rates: Bacteroides 72.7%, Prevotella 71.5%, F. magna 72.4%; clindamycin susceptibility rates: Bacteroides 79.5%, Prevotella 92.1%, F. magna 84.7%. © The British Society for Antimicrobial Chemotherapy 2004; all rights reserved.

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Koeth, L. M., Good, C. E., Appelbaum, P. C., Goldstein, E. J. C., Rodloff, A. C., Claros, M., & Dubreuil, L. J. (2004). Surveillance of susceptibility patterns in 1297 Europeans and US anaerobic and capnophilic isolates to co-amoxiclav and five other antimicrobials agents. Journal of Antimicrobial Chemotherapy, 53(6), 1039–1044. https://doi.org/10.1093/jac/dkh248

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