Publication | Open Access
In Vitro Activities of Tigecycline against the <i>Bacteroides fragilis</i> Group
65
Citations
10
References
2004
Year
B. Fragilis GroupAntimicrobial ChemotherapyBacterial PathogensVitro ActivitiesDrug ResistanceInfection ControlAntimicrobial ResistanceHealth SciencesAntimicrobial Drug DiscoveryOther Bacteroides SpeciesAntibacterial AgentAntimicrobial PharmacokineticsAntimicrobial CompoundPharmacologyClinical MicrobiologyBacteroides Fragilis GroupAntimicrobial SusceptibilityAntibioticsMicrobiologyMedicine
The in vitro activities of tigecycline were tested against 831 isolates of the Bacteroides fragilis group representing all of the species within the group. On a weight-to-weight basis (8 microg/ml), tigecycline was more active than clindamycin, minocycline, trovafloxacin, and cefoxitin and less active than imipenem or piperacillin-tazobactam against all isolates of the B. fragilis group. Tigecycline geometric mean MICs were statistically higher against B. distasonis than other Bacteroides species (P value of 0.0001).
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