2003
DOI: 10.1016/s0924-8579(03)00087-6
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Activity of linezolid against anaerobic bacteria

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Cited by 48 publications
(21 citation statements)
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“…A previous study has also reported 100% susceptibility in 265 clinical anaerobic isolates [20]. Susceptibility cut off for linezolid has not been described by CLSI, previous surveys have used a cut off of 4 ug/mL as susceptible and 8 ug/mL as resistant [20].…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…A previous study has also reported 100% susceptibility in 265 clinical anaerobic isolates [20]. Susceptibility cut off for linezolid has not been described by CLSI, previous surveys have used a cut off of 4 ug/mL as susceptible and 8 ug/mL as resistant [20].…”
Section: Discussionmentioning
confidence: 99%
“…Susceptibility cut off for linezolid has not been described by CLSI, previous surveys have used a cut off of 4 ug/mL as susceptible and 8 ug/mL as resistant [20]. Linezolid has been reported to be very potent drug against all strains of Fusobacteria, Prevotella and Porphyromonas and is also reported to provide microbiological clearance as well as clinical improvement in anaerobic sepsis due to multidrug resistant B. fragilis infection [20,21].…”
Section: Discussionmentioning
confidence: 99%
“…Thus, a fluoroquinolone might not be a suitable substitute for carbapenems. Behra-Miellet et al reported that linezolid is likely to be active against most anaerobes (5). It may be a potential candidate for antimicrobial therapy if resistance to carbapenems develops.…”
Section: Discussionmentioning
confidence: 99%
“…and Staphylococcus spp., including vancomycinresistant enterococci, meticillin-resistant Staphylococcus aureus (MRSA) and meticillin-resistant CoNS [6][7][8][9]. Linezolid is also active against anaerobes, atypical microbes such as Chlamydia and Mycoplasma spp., some rapidly growing mycobacteria, and selected Gram-negative bacilli [10][11][12]. Linezolid, or N-([S]-[3-[3-fluoro-4-morpholinophenyl]-2-oxo-5-oxazolidinyl] methyl) acetamide, is a totally synthetic antimicrobial agent structurally unrelated to other agents, with unique mechanism of action [6,7].…”
Section: Introductionmentioning
confidence: 99%