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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/23283
Title: Pharmacokinetic and pharmacodynamic assessment of co-amoxiclav in the treatment of melioidosis
Authors: Wirongrong Chierakul
Jinda Wangboonskul
Thida Singtoroj
Wirichada Pongtavornpinyo
Jennifer M. Short
Bina Maharjan
Vanaporn Wuthiekanun
David A B Dance
Prapit Teparrukkul
Niklas Lindegardh
Sharon J. Peacock
Nicholas P. Day
Wipada Chaowagul
Nicholas J. White
Mahidol University
Khon Kaen University
Nuffield Department of Clinical Medicine
Health Protection Agency
Sappasitthiprasong Hospital
Keywords: Immunology and Microbiology;Pharmacology, Toxicology and Pharmaceutics
Issue Date: 1-Dec-2006
Citation: Journal of Antimicrobial Chemotherapy. Vol.58, No.6 (2006), 1215-1220
Abstract: Objectives: We conducted a prospective pharmacokinetic study of oral co-amoxiclav in patients with melioidosis to determine the optimal dosage and dosing interval in this potentially fatal infection. Patients and methods: Serial plasma concentrations were measured after administration of two 1 g tablets of Augmentin® (1750 mg of amoxicillin and 250 mg of clavulanate) to 14 adult patients with melioidosis. Monte Carlo simulation was used to predict the concentration of each drug following multiple doses of co-amoxiclav at different dosages and dose intervals. The proportion of the dose-interval above MIC (T > MIC) was calculated from 10 000 simulated subject plasma concentration profiles together with chequerboard MIC data from 46 clinical isolates and four reference strains of Burkholderia pseudomallei. Results: The median (range) observed maximum plasma concentrations of amoxicillin and clavulanate were 11.5 (3.3-40.2) mg/L and 5.1 (0.8-12.1) mg/L, respectively. The median (range) elimination half-lives were 94 (73-215) and 89 (57-140) min, respectively. Simulation indicated that co-amoxiclav 1750/250 mg given at 4, 6, 8 or 12 hourly dosing intervals would be associated with a T > MIC of ≤50% in 0.7%, 2.8%, 8.6% and 33.2% of patients, respectively. Corresponding proportions for T > MIC of ≥90% were 95.8%, 78.6%, 50.2% and 10.8%, respectively. Conclusions: The dosing interval for co-amoxiclav (750/250 mg) in melioidosis should not be greater than 6 h. © 2006 Oxford University Press.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33845357081&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/23283
ISSN: 14602091
03057453
Appears in Collections:Scopus 2006-2010

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