In vitro activity of lomefloxacin against multiply resistant Pseudomonas aeruginosa, Enterobacter cloacae, and Staphylococcus epidermidis

Diagn Microbiol Infect Dis. 1989 May-Jun;12(3 Suppl):13S-16S. doi: 10.1016/0732-8893(89)90059-x.

Abstract

Lomefloxacin is a promising new difluorinated quinolone with good antimicrobial activity and favorable pharmacokinetic properties. The in vitro activity of lomefloxacin was compared to other quinolones, expanded spectrum beta-lactams, and gentamicin. The lomefloxacin MIC90 against multiply resistant strains of P. aeruginosa was 4 mcg/ml, comparable to norfloxacin and ofloxacin. Lomefloxacin was also active against methicillin-resistant S. epidermidis and JK corynebacteria. The role of lomefloxacin in the treatment of infections caused by multiresistant organisms remains to be determined in clinical trials.

Publication types

  • Comparative Study

MeSH terms

  • Anti-Infective Agents / pharmacology*
  • Ciprofloxacin / pharmacology
  • Drug Resistance, Microbial
  • Enterobacter / drug effects*
  • Enterobacteriaceae
  • Fluoroquinolones*
  • Humans
  • Microbial Sensitivity Tests
  • Norfloxacin / pharmacology
  • Pseudomonas aeruginosa / drug effects*
  • Quinolones*
  • Staphylococcal Infections / drug therapy
  • Staphylococcus epidermidis / drug effects*
  • Staphylococcus epidermidis / isolation & purification

Substances

  • Anti-Infective Agents
  • Fluoroquinolones
  • Quinolones
  • Ciprofloxacin
  • lomefloxacin
  • Norfloxacin