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Antimicrobial Agents and Chemotherapy, July 1998, p. 1837-1841, Vol. 42, No. 7
Division of Infectious Diseases and the St.
John's Cardiovascular Research Center, Harbor-UCLA Medical Center,
Torrance, California 90509,1 and
the
UCLA School of Medicine, Los Angeles, California
900242
Received 17 February 1998/Returned for modification 30 March
1998/Accepted 6 May 1998
Therapeutic options for severe infections caused by strains of
oxacillin-resistant Staphylococcus aureus (ORSA) and
coagulase-negative staphylococci (ORSE) are very limited. With the
increasing resistance of such strains to aminoglycosides, rifampin, and
currently available quinolone agents, as well as the recent
documentation of increasing resistance of ORSA to vancomycin
(VANCO), new treatment alternatives are imperative. The in vivo
efficacy of trovafloxacin (TROVA), a new quinolone agent with excellent
antistaphylococcal activity in vitro, against experimental
endocarditis (IE) due to
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Efficacy of Trovafloxacin, a New Quinolone Antibiotic, in
Experimental Staphylococcal Endocarditis Due to
Oxacillin-Resistant Strains
-lactamase-producing ORSA and ORSE strains
(ORSA and ORSE IE) was evaluated. TROVA (25 mg/kg of body weight
intravenously [i.v.] twice daily [b.i.d.]) was compared to VANCO
(20 mg/kg i.v. b.i.d.) and two regimens of ampicillin-sulbactam
(AMP-SUL; 200 mg/kg intramuscularly [i.m.] three times a day
[t.i.d.] and 20 mg/kg i.m. b.i.d.), with all agents given for 3 or 6 days. AMP-SUL was included as a comparative treatment regimen because
of its proven efficacy against experimental ORSA and ORSE IE. For both
ORSA and ORSE IE, TROVA, AMP-SUL, and VANCO each reduced
staphylococcal densities in vegetations compared to
untreated controls (P < 0.01). For ORSA IE, TROVA was
the most rapidly bactericidal agent
although not to a statistically
significant degree
correlating with its superior bactericidal effect
in vitro compared to those of VANCO and AMP-SUL.
*
Corresponding author. Mailing address: Division of
Infectious Diseases, Harbor-UCLA Medical Center, 1000 West Carson St., Bldg. RB2/Room 225, Torrance, CA 90509. Phone: (310) 222-6422. Fax:
(310) 782-2016. E-mail: Bayer{at}HUMC.EDU.
Present address: Division of Infectious Diseases, Pettis VA Medical
Center, Loma Linda, CA 92357.
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