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Efficacy of Trovafloxacin against Experimental Staphylococcus aureus Endocarditis
Author(s) -
Glenn W. Kaatz,
Susan M. Seo,
Jeffrey R. Aeschlimann,
Heather H. Houlihan,
Renée-Claude Mercier,
Michael J. Rybak
Publication year - 1998
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.42.2.254
Subject(s) - trovafloxacin , vancomycin , nafcillin , microbiology and biotechnology , staphylococcus aureus , antimicrobial , endocarditis , medicine , bacteremia , antibacterial agent , antibiotics , pharmacology , biology , surgery , penicillin , bacteria , genetics
Trovafloxacin is a new fluoronaphthyridone chemically and functionally related to members of the fluoroquinolone class of antimicrobial agents. The in vivo efficacy of the drug was compared with that of vancomycin by using the rabbit model of left-sided endocarditis. Rabbits infected with either a nafcillin-susceptible or -resistant test strain were treated with trovafloxacin (13.3 mg/kg of body weight every 12 h) or vancomycin (25 mg/kg of body weight every 8 h) for 4 days. In comparison with untreated controls, both antimicrobial agents effectively cleared bacteremia and significantly reduced bacterial counts in vegetations and tissues of animals infected with either test strain. No resistance to trovafloxacin emerged in test strains during therapy. We conclude that in this model trovafloxacin is as efficacious as vancomycin is and may serve as a viable alternative to vancomycin for use in humans with similar infections.

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