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Fluoroquinolone susceptibility, resistance, and pharmacodynamics versus clinical isolates of Streptococcus pneumoniae from Indiana
The in vitro activity and pharmacodynamics (AUC 0–24/MIC) of levofloxacin, gatifloxacin, moxifloxacin, and gemifloxacin were evaluated against 307 clinical isolates of Streptococcus pneumoniae from Indianapolis, Indiana. Organisms were collected between January 1999 and April 2000, and MICs were det...
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Published in: | Diagnostic microbiology and infectious disease 2001-08, Vol.40 (4), p.193-198 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The in vitro activity and pharmacodynamics (AUC
0–24/MIC) of levofloxacin, gatifloxacin, moxifloxacin, and gemifloxacin were evaluated against 307 clinical isolates of
Streptococcus pneumoniae from Indianapolis, Indiana. Organisms were collected between January 1999 and April 2000, and MICs were determined by broth microdilution. Serum concentration-time profiles were simulated for the following oral regimens administered once daily: levofloxacin 500 mg and 750 mg; gatifloxacin 400 mg; moxifloxacin 400 mg; gemifloxacin 320 mg. Free 24 h area under the serum concentration-time curves (AUC
0–24) were calculated, and the average AUC
0–24/MIC was calculated for each regimen. Differences in AUC
0–24/MIC among agents were determined by analysis of variance (Scheffe post-hoc test,
p < 0.05). Overall, gemifloxacin was the most potent agent tested. Five (1.7%), 4 (1.3%), and 2 (0.7%) isolates were resistant to levofloxacin, gatifloxacin, and moxifloxacin, respectively. None of the isolates was resistant to gemifloxacin. Gemifloxacin AUC
0–24/MIC was significantly greater than all other regimens (
p < 0.0001), with the exception of moxifloxacin. However, the percent of isolates for which an AUC
0–24/MIC ≥ 30–50 can be achieved is similar for gemifloxacin, moxifloxacin, gatifloxacin, and levofloxacin 750 mg. Large comparative studies are needed to determine if the differences in AUC
0–24/MIC among fluoroquinolones are clinically significant. |
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ISSN: | 0732-8893 1879-0070 |
DOI: | 10.1016/S0732-8893(01)00277-2 |