The in-vitro activity of
gemifloxacin, a new
fluoroquinolone, against a wide range (c. 700) of recent clinical isolates, was compared with that of three other
fluoroquinolones and other relevant agents.
Gemifloxacin inhibited 90% of the Enterobacteriaceae strains at 0.5 mg/L or less, exceptions being Serratia spp. (MIC(90) 1 mg/L) and strains possessing a putative mechanism of resistance to
fluoroquinolones. Ninety per cent of Pseudomonas aeruginosa were inhibited by 4 mg/L.
Gemifloxacin had good activity against respiratory pathogens, with 90% of Streptococcus pneumoniae, Haemophilus influenzae and Moraxella catarrhalis being inhibited by 0.06 mg/L or less. Staphylococcus aureus (MSSA) were highly susceptible (MIC(90) 0.06 mg/L) but MRSA less susceptible (MIC(90) 8 mg/L) to
gemifloxacin. Enterococcus spp. were markedly more susceptible to the study agent than to
ciprofloxacin.
Gemifloxacin showed good activity against Bacteroides fragilis (MIC(90) 0.5 mg/L) and anaerobic cocci. A tentative in-vitro breakpoint of 0.5 mg/L was studied using a 1 microg disc content for all genera except Pseudomonas where a 5 microg disc content was employed. The false sensitivity reporting rate was 0.5% and false resistance rate was 6.0%, which was considered acceptable. In conclusion,
gemifloxacin is a highly active
fluoroquinolone that should prove clinically useful in the treatment of a wide range of
infections. Susceptibility testing criteria have been developed that should prove robust in a clinical laboratory.