Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/28038
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dc.contributor.authorLivermore, D.-
dc.contributor.authorCarter, M.-
dc.contributor.authorBagel, S.-
dc.contributor.authorWiedemann, B.-
dc.contributor.authorBaquero, F.-
dc.contributor.authorLoza, E.-
dc.contributor.authorEndtz, H.-
dc.contributor.authorvan den Braak, N.-
dc.contributor.authorFernandes, C.-
dc.contributor.authorFernandes, L.-
dc.contributor.authorFrimodt-Moller, N.-
dc.contributor.authorRasmussen, L.-
dc.contributor.authorGiamarellou, H.-
dc.contributor.authorGiamarellos-Bourboulis, E.-
dc.contributor.authorJarlier, V.-
dc.contributor.authorNguyen, J.-
dc.contributor.authorNord, C.-
dc.contributor.authorStruelens, M.-
dc.contributor.authorNonhoff, C.-
dc.contributor.authorTurnidge, J.-
dc.contributor.authoret al.-
dc.date.issued2001-
dc.identifier.citationAntimicrobial Agents and Chemotherapy, 2001; 45(6):1860-1867-
dc.identifier.issn0066-4804-
dc.identifier.issn1098-6596-
dc.identifier.urihttp://hdl.handle.net/2440/28038-
dc.description.abstractErtapenem (MK-0826, L-749,345) is a 1-β-methyl carbapenem with a long serum half-life. Its in vitro activity was determined by broth microdilution against 3,478 bacteria from 12 centers in Europe and Australia, with imipenem, cefepime, ceftriaxone, and piperacillin-tazobactam used as comparators. Ertapenem was the most active agent tested against members of the familyEnterobacteriaceae, with MICs at which 90% of isolates are inhibited (MIC₉₀s) of ≤1 μg/ml for all species. Ertapenem also was more active than imipenem against fastidious gram-negative bacteria and Moraxella spp.; on the other hand, ertapenem was slightly less active than imipenem against streptococci, methicillin-susceptible staphylococci, and anaerobes, but its MIC₉₀s for these groups remained ≤0.5 μg/ml.Acinetobacter spp. and Pseudomonas aeruginosawere also much less susceptible to ertapenem than imipenem, and mostEnterococcus faecalis strains were resistant. Ertapenem resistance, based on a provisional NCCLS MIC breakpoint of ≥16 μg/ml, was seen in only 3 of 1,611 strains of the familyEnterobacteriaceae tested, all of them Enterobacter aerogenes. Resistance was also seen in 2 of 135 anaerobes, comprising 1 Bacteroides fragilis strain and 1Clostridium difficile strain. Ertapenem breakpoints for streptococci have not been established, but an unofficial susceptibility breakpoint of ≤2 μg/ml was adopted for clinical trials to generate corresponding clinical response data for isolates for which MICs were as high as 2 μg/ml. Of 234 Streptococcus pneumoniae strains tested, 2 required ertapenem MICs of 2 μg/ml and one required an MIC of 4 μg/ml, among 67 non-Streptococcus pyogenes, non-Streptococcus pneumoniae streptococci, single isolates required ertapenem MICs of 2 and 16 μg/ml. These streptococci also had diminished susceptibilities to other β-lactams, including imipenem as well as ertapenem. The Etest and disk diffusion gave susceptibility test results in good agreement with those of the broth microdilution method for ertapenem.-
dc.description.statementofresponsibilityDavid M. Livermore, Michael W. Carter, Simone Bagel, Bernd Wiedemann, Fernando Baquero, Elena Loza, Hubert P. Endtz, Nicole Van Den Braak, Clarence J. Fernandes, Lorna Fernandes, Niels Frimodt-Moller, Laura S. Rasmussen, Helen Giamarellou, Evangelos Giamarellos-Bourboulis, Vincent Jarlier, Jacqueline Nguyen, Carl-Erik Nord, Marc J. Struelens, Caire Nonhoff, John Turnidge, Jan Bell, Reinhard Zbinden, Stefan Pfister, Lori Mixson, and Daniel L. Shungu-
dc.language.isoen-
dc.publisherAmer Soc Microbiology-
dc.rightsCopyright © 2000, American Society for Microbiology. All Rights Reserved.-
dc.source.urihttp://dx.doi.org/10.1128/aac.45.6.1860-1867.2001-
dc.subjectBacteria-
dc.subjectCarbapenems-
dc.subjectAnti-Bacterial Agents-
dc.subjectMicrobial Sensitivity Tests-
dc.subjectQuality Control-
dc.subjectAustralia-
dc.subjectEurope-
dc.titleIn vitro activities of ertapenem (MK-0826) against recent clinical bacteria collected in Europe and Australia-
dc.typeJournal article-
dc.identifier.doi10.1128/AAC.45.6.1860-1867.2001-
pubs.publication-statusPublished-
dc.identifier.orcidTurnidge, J. [0000-0003-4240-5578]-
Appears in Collections:Aurora harvest 6
Molecular and Biomedical Science publications

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