Because patients with cystic fibrosis (CF) have pulmonary exacerbations sec
ondary to multi-antibiotic-resistant Gram-negative bacilli, antibiotics, li
ke meropenem, are often utilized. We studied the pharmacokinetics of merope
nem (2 g i.v. administered every 8 h in clinically stable CF patients to de
termine if the recommended maximum doses could sustain adequate concentrati
ons during the dosing interval. These pharmacokinetic data were similar to
those obtained in non-CF populations. Using this regimen, concentrations of
meropenem exceed the susceptibility breakpoint (4 mug/ml) for 50% of the d
osing interval, and therefore provide optimization of the pharmacodynamic p
rofile of the compound. Copyright (C) 2001 S. Karger AG, Basel.