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Antimicrobial Agents and Chemotherapy, 08 1995, 1711-1716, Vol 39, No. 8
JM Hyatt, DE Nix, CW Stratton and JJ Schentag
The time-kill curve methodology was used to determine the pharmacodynamics
of piperacillin, ciprofloxacin, piperacillin- tazobactam and the
combinations piperacillin-ciprofloxacin and
ciprofloxacin-piperacillin-tazobactam. Kill curve studies were performed
for piperacillin, ciprofloxacin, and piperacillin-tazobactam at
concentrations of 0.25 to 50 times the MICs for 13 strains of bacteria:
four Pseudomonas aeruginosa, three Enterobacter cloacae, three Klebsiella
pneumoniae, and three Staphylococcus aureus isolates (tazobactam
concentrations of 0.5, 4, and 12 micrograms/ml). By using a sigmoid Emax
model and nonlinear least squares regression, the 50% lethal concentrations
and the maximum lethal rates of each agent were determined for each
bacterial strain. For piperacillin-ciprofloxacin and
ciprofloxacin-piperacillin-tazobactam, kill curve studies were performed
with concentrations obtained by the fractional maximal effect method (R. C.
Li, J. J. Schentag, and D. E. Nix, Antimicrob. Agents Chemother.
37:523-531, 1993) and from individual 50% lethal concentrations and maximum
lethal rates. Ciprofloxacin-piperacillin- tazobactam was evaluated only
against the four P. aeruginosa strains. Interactions between piperacillin
and ciprofloxacin were generally additive. At physiologically relevant
concentrations of piperacillin and ciprofloxacin, ciprofloxacin had the
highest rates of killing against K. pneumoniae. Piperacillin-tazobactam (12
micrograms/ml) had the highest rate of killing against E. cloacae.
Piperacillin- ciprofloxacin with relatively higher ciprofloxacin
concentrations had the greatest killing rates against S. aureus. This
combination had significantly higher killing rates than piperacillin (P
< 0.002). For all the bacterial strains tested, killing rates by
ciprofloxacin were significantly higher than those by
piperacillin-tazobactam (4 and 12 micrograms/ml had significantly higher
killing rates than piperacillin alone (P < 0.02 and P < 0.004,
respectively).(ABSTRACT TRUNCATED AT 250 WORDS)
Copyright © 1995 by the American Society for Microbiology. All rights reserved.
In vitro pharmacodynamics of piperacillin, piperacillin-tazobactam, and ciprofloxacin alone and in combination against Staphylococcus aureus, Klebsiella pneumoniae, Enterobacter cloacae, and Pseudomonas aeruginosa
Clinical Pharmacokinetics Laboratory, Millard Fillmore Hospital, Buffalo, New York 14209-1194, USA.
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