COMPARATIVE IN-VITRO ACTIVITIES OF TROVAFLOXACIN (CP-99,219) AGAINST 445 GRAM-POSITIVE ISOLATES FROM PATIENTS WITH ENDOCARDITIS AND THOSE WITH OTHER BLOOD-STREAM INFECTIONS
Hp. Endtz et al., COMPARATIVE IN-VITRO ACTIVITIES OF TROVAFLOXACIN (CP-99,219) AGAINST 445 GRAM-POSITIVE ISOLATES FROM PATIENTS WITH ENDOCARDITIS AND THOSE WITH OTHER BLOOD-STREAM INFECTIONS, Antimicrobial agents and chemotherapy, 41(5), 1997, pp. 1146-1149
The in vitro activity of trovafloxacin (CP-99,219), a new fluoroquinol
one, was compared with the in vitro activities of other commonly used
quinolones and other antimicrobial agents against 445 gram-positive mi
croorganisms isolated between 1986 and 1995 from patients with endocar
ditis and those with other blood- stream infections. The MICs at which
90% of the isolates are inhibited (MIC90) of trovafloxacin far methic
illin-susceptible staphylococci, viridans group streptococci, and ente
rococci were 0.06, 0.25, and 0.5 mg/liter, respectively. The MIC90 of
trovafloxacin for vancomycin-resistant enterococci as well as for meth
icillin-resistant Staphylococcus aureus and methicillin-susceptible an
d ciprofloxacin-resistant S. aurcus, isolated from sources other than
blood, was 1 mg/liter. For the quinolones the rank order of activity w
as trovafloxacin > sparfloxacin > ciprofloxacin = ofloxacin > pefloxac
in. Depending on the species tested, trovafloxacin was 4- to 64-fold m
ore active than ciprofloxacin. Further experimental and in vivo studie
s are warranted to evaluate the efficacy of trovafloxacin in the treat
ment of bacterial endocarditis and other infections caused by gramposi
tive organisms.