In vitro susceptibility of pneumococci to trovafloxacin, penicillin G, and other antimicrobial agents in the Czech Republic and Slovakia
Jazyk angličtina Země Německo Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
8894582
DOI
10.1007/bf01691161
Knihovny.cz E-zdroje
- MeSH
- antiinfekční látky farmakologie MeSH
- fluorochinolony * MeSH
- lidé MeSH
- mikrobiální testy citlivosti MeSH
- naftyridiny farmakologie MeSH
- penicilin G farmakologie MeSH
- peniciliny farmakologie MeSH
- Streptococcus pneumoniae účinky léků MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antiinfekční látky MeSH
- fluorochinolony * MeSH
- naftyridiny MeSH
- penicilin G MeSH
- peniciliny MeSH
- trovafloxacin MeSH Prohlížeč
The in vitro activity of the new naphthyridone trovafloxacin (CP 99,219) was compared with those of penicillin G and six other agents (cefpodoxime, erythromycin, azithromycin, clindamycin, ciprofloxacin, and sparfloxacin) against 316 penicillin-susceptible and -resistant pneumococci isolated in the former Czechoslovakia. Trovafloxacin was very active against strains of Streptococcus pneumoniae (MIC50 and MIC90 0.25 microgram/ml). Ciprofloxacin was less active (MIC50 1.0 microgram/ml, MIC90 2.0 micrograms/ml), and MICs of sparfloxacin were between those of trovafloxacin and ciprofloxacin (MIC50 and MIC90 both 0.5 microgram/ml). MICs of cefpodoxime, erythromycin, azithromycin, and clindamycin were higher for strains intermediately resistant or resistant to penicillin than for penicillin-susceptible strains.
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