In vitro activity of trovafloxacin (CP 99,219), a new fluoroquinolone against hospital isolates

Citation
Tkw. Ling et al., In vitro activity of trovafloxacin (CP 99,219), a new fluoroquinolone against hospital isolates, CHEMOTHERA, 45(1), 1999, pp. 22-27
Citations number
10
Categorie Soggetti
Pharmacology,"Pharmacology & Toxicology
Journal title
CHEMOTHERAPY
ISSN journal
00093157 → ACNP
Volume
45
Issue
1
Year of publication
1999
Pages
22 - 27
Database
ISI
SICI code
0009-3157(199901/02)45:1<22:IVAOT(>2.0.ZU;2-K
Abstract
The susceptibility of 492 Enterobacteriaceae, 227 other gram-negative bacte ria, 448 grampositive bacteria and 108 anaerobic organisms was determined b y the agar dilution method against trovafloxacin and other antibiotics. Tro vafloxacin was highly active against most of the Enterobacteriaceae includi ng Enterobacter spp. and Citrobacter spp. [minimum inhibitory concentration (MIC)90 <1 mg/l], Acinetobacter spp. and Pseudomonas aeruginosa (MIC90 = 0 .25 and 2 mg/l, respectively). The antimicrobial activity was extended to t he gram-positive bacteria including streptococci, Streptococcus pneumoniae, coagulase-negative staphylococci and methicillin-sensitive Staphylococcus aureus with MIC90 <1 mg/l. Enterococci and methicillin-resistant S. aureus were inhibited (MIC90 = 2 mg/l; sparfloxacin and ciprofloxacin were 16 and 64 mg/l, respectively). Almost all anaerobic organisms were inhibited by tr ovafloxacin (MIC90 = 1 mg/l).