Pharmacodynamically Guided Levofloxacin Dosing for Pediatric Community-Acquired Pneumonia
Key Points Oral levofloxacin is recommended as a preferred treatment for pediatric community-acquired penicillin-resistant Streptococcus pneumoniae pneumonia. This article describes a pharmacodynamically guided levofloxacin regimen and the probability of the pharmacodynamic target being attained in...
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Veröffentlicht in: | Journal of the Pediatric Infectious Diseases Society 2017-06, Vol.6 (2), p.118-122 |
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Zusammenfassung: | Key Points
Oral levofloxacin is recommended as a preferred treatment for pediatric community-acquired penicillin-resistant Streptococcus pneumoniae pneumonia. This article describes a pharmacodynamically guided levofloxacin regimen and the probability of the pharmacodynamic target being attained in S pneumoniae isolates collected from pediatric patients.
Abstract
Background.
Oral levofloxacin is recommended as a preferred treatment for infection with Streptococcus pneumoniae with a penicillin minimum inhibitory concentration (MIC) of ≥4 µg/mL and as an alternative for infection with S pneumoniae with a penicillin MIC of ≤2 µg/mL. To investigate the current dosing recommendations and create a pharmacodynamically guided regimen, a Monte Carlo simulation was performed.
Methods.
The simulation included a previously published 1-compartment model, and incorporated a formula that takes into account age-appropriate weights for hospitalized patients. Three different dosing regimens, including community-acquired pneumonia guideline dosing, inhalational anthrax dosing, and a pharmacodynamically guided regimen, were assessed. The probability of target attainment was described as the proportion of patients who achieve an unbound-drug area under the concentration–time curve over 24 hours divided by the MIC above 33.7 µg/mL per hour. Microbiologic data from 2 stand-alone pediatric tertiary care centers were included.
Results.
Guideline-recommended doses of levofloxacin seem to produce suboptimal exposure in patients aged 5–14 years for pneumococci with an MIC of 1 µg/mL. Anthrax dosing was suboptimal in patients aged 15 years. The pharmacodynamically guided regimen maintained a probability of target attainment of >90% for all age groups without producing peak concentrations higher than those previously described. None of the regimens attained the pharmacodynamic targets for a levofloxacin MIC of 2 µg/mL.
Conclusions.
Current dosing recommendations were found to be suboptimal for specific age groups. A pharmacodynamically guided levofloxacin dosing regimen was determined, but it will need to be studied clinically for safety and tolerability. |
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ISSN: | 2048-7193 2048-7207 |
DOI: | 10.1093/jpids/piw006 |