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Vol. 286, Issue 1, 29-35, July 1998
Clinique de Réanimation des Maladies Infectieuses,
Hôpital Bichat-Claude Bernard, Paris, France (J-P.B.),
Institut
National de la Santé et de la Recherche Médicale U13,
Hôpital Bichat-Claude Bernard, Paris, France (E. A-D., M. M-J.,
B.V., J-J. P.),
Laboratoire de Biologie, Centre Hospitalier
Emile-Roux, Eaubonne, France (E.V.) and
Département
d'Anesthésie-Réanimation Chirurgicale, Centre Hospitalier
de Bicêtre, Le Kremlin Bicêtre, France (P.M.)
We looked for associations between pharmacokinetic (Pk) and
pharmacodynamic (Pd) parameters of ciprofloxacin (CPFX) and
sparfloxacin (SPFX) and the in vivo efficacy of these
antimicrobials in an immunocompetent mouse model of severe
Streptococcus pneumoniae pneumonia. Bacterial killing
curves recorded in the lungs during the 24 h after single
subcutaneous injections of the fluoroquinolones (FQs) in doses ranging
from 6.25 to 200 mg/kg were compared with mean Pk/Pd parameters in the
serum of the same mice. The impact of the dosing interval on the
antimicrobial dose response was evaluated based on the survival of mice
treated for 3 days with CPFX (25-200 mg/kg) or SPFX (6.25-50 mg/kg)
administered at various intervals from 3 to 24 h. Bacterial
killing curves showed that the maximal bacterial decrease achieved in
the lungs was correlated, similarly for both FQs, with the area under
the curve (AUC) above the minimal inhibitory concentration (MIC)
(overall correlation: r = 0.968, P < 10
). CPX attained higher maximal
bactericidal effect values, a steeper killing slope and
a shorter time to maximal bactericidal effect in comparison with SPX
for the highest doses tested. The lower MIC of SPFX compared with CPFX
(0.25 vs. 0.75 µg/ml) and its higher AUC/dose ratio
(resulting from a lower serum peak but a longer half-life) translated
into a greater area under the bactericidal curve. In the dose
fractionation experiments, the Pk/Pd parameter most closely correlated
with the survival rate for both FQs was the daily AUC/MIC ratio
(r = 0.976, P < 10
. When the AUC/MIC ratio was greater than
160, the probability of a clinical cure was 100%, independently of the
dosage schedule.
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