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Pharmacokinetic/pharmacodynamic-based treatment of disseminated Mycobacterium avium

Journal

FUTURE MICROBIOLOGY
Volume 6, Issue 4, Pages 433-439

Publisher

FUTURE MEDICINE LTD
DOI: 10.2217/FMB.11.25

Keywords

disseminated Mycobacterium avium; ethambutol; moxifloxacin; optimized dosing; pharmacokinetics-pharmacodynamics

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Disseminated Mycobacterium avium complex (MAC) is treated with a macrolide and ethambutol. However, the kill rates are extremely slow so that therapy takes many months to years to achieve and even then more than 40% of patients are not completely cured. Recent studies have demonstrated that assays that detect extracellular MAC have a limited predictive value. Antibiotics kill at a much slower and more disappointing rate against bacilli within macrophages. Use of pharmacodynamic/pharmacokinetic models has resulted in design of new doses and dosing schedules for disseminated MAC, as well as new susceptibility breakpoints for ethambutol and moxifloxacin.

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