@article{Chirehwa2021,
abstract = {Ethionamide is recommended as part of regimens to treat multidrug-resistant and rifampicin-resistant tuberculosis. This study was conducted to (i) describe the distribution of ethionamide MICs, (ii) describe the pharmacokinetics of ethionamide, and (iii) determine the probability of attaining target area under the concentration-time curve from 0 to 24 h (AUC0-24)/MIC values associated with suppression of resistant subpopulation and microbial kill. Participants received 15 to 20mg of drug/kg of body weight of ethionamide daily (in 500- or 750-mg doses) as part of a multidrug regimen. Pretreatment MICs of ethionamide for Mycobacterium tuberculosis sputum isolates were determined using Sensititre MYCOTB MIC plates. Plasma concentrations of ethionamide (measured predose and at 2, 4, 6, 8, and 10h postdose) were available for 84 patients. A one-compartment disposition model, including a liver compartment capturing hepatic extraction, best described ethionamide pharmacokinetics. Clearance and volume were allometrically scaled using fat-free mass. Isoniazid coadministration reduced ethionamide clearance by 31{\%}, resulting in a 44{\%} increase in AUC0-24. The median (range) MIC (n=111) was 2.5mg/liter (,0.3 to.40mg/liter). Simulations showed increased daily doses of ethionamide (1,250mg, 1,500mg, and 1,750mg for patients weighing {\#}45kg, 46 to 70kg, and.70kg, respectively) resulted in the probability of attaining an area under the concentration-time curve from 0 to 24 h for the free, unbound fraction of a drug (fAUC0-24)/MIC ratioof {\$}42 in more than 90{\%} of patients only at the lowest MIC of 0.3mg/liter. The WHO-recommended doses of ethionamide do not achieve target concentrations even for the lowest MIC measured in the cohort.},
author = {Chirehwa, M.T. and Court, R. and de Kock, M. and Wiesner, L. and de Vries, N. and Harding, J. and Gumbo, T. and Maartens, G. and Warren, R. and Denti, P. and Denti, P. and McIlleron, H.},
doi = {10.1128/AAC.00278-21},
journal = {Antimicrobial Agents and Chemotherapy},
number = {10},
title = {{Effect of isoniazid intake on ethionamide pharmacokinetics and target attainment in multidrug-resistant tuberculosis patients}},
volume = {65},
year = {2021}
}

{"_id":"gT7MD8jEwyPngHdBk","bibbaseid":"chirehwa-court-dekock-wiesner-devries-harding-gumbo-maartens-etal-effectofisoniazidintakeonethionamidepharmacokineticsandtargetattainmentinmultidrugresistanttuberculosispatients-2021","author_short":["Chirehwa, M.","Court, R.","de Kock, M.","Wiesner, L.","de Vries, N.","Harding, J.","Gumbo, T.","Maartens, G.","Warren, R.","Denti, P.","Denti, P.","McIlleron, H."],"bibdata":{"bibtype":"article","type":"article","abstract":"Ethionamide is recommended as part of regimens to treat multidrug-resistant and rifampicin-resistant tuberculosis. This study was conducted to (i) describe the distribution of ethionamide MICs, (ii) describe the pharmacokinetics of ethionamide, and (iii) determine the probability of attaining target area under the concentration-time curve from 0 to 24 h (AUC0-24)/MIC values associated with suppression of resistant subpopulation and microbial kill. Participants received 15 to 20mg of drug/kg of body weight of ethionamide daily (in 500- or 750-mg doses) as part of a multidrug regimen. Pretreatment MICs of ethionamide for Mycobacterium tuberculosis sputum isolates were determined using Sensititre MYCOTB MIC plates. Plasma concentrations of ethionamide (measured predose and at 2, 4, 6, 8, and 10h postdose) were available for 84 patients. A one-compartment disposition model, including a liver compartment capturing hepatic extraction, best described ethionamide pharmacokinetics. Clearance and volume were allometrically scaled using fat-free mass. Isoniazid coadministration reduced ethionamide clearance by 31%, resulting in a 44% increase in AUC0-24. The median (range) MIC (n=111) was 2.5mg/liter (,0.3 to.40mg/liter). Simulations showed increased daily doses of ethionamide (1,250mg, 1,500mg, and 1,750mg for patients weighing #45kg, 46 to 70kg, and.70kg, respectively) resulted in the probability of attaining an area under the concentration-time curve from 0 to 24 h for the free, unbound fraction of a drug (fAUC0-24)/MIC ratioof $}42 in more than 90{%} of patients only at the lowest MIC of 0.3mg/liter. The WHO-recommended doses of ethionamide do not achieve target concentrations even for the lowest MIC measured in the cohort.","author":[{"propositions":[],"lastnames":["Chirehwa"],"firstnames":["M.T."],"suffixes":[]},{"propositions":[],"lastnames":["Court"],"firstnames":["R."],"suffixes":[]},{"propositions":["de"],"lastnames":["Kock"],"firstnames":["M."],"suffixes":[]},{"propositions":[],"lastnames":["Wiesner"],"firstnames":["L."],"suffixes":[]},{"propositions":["de"],"lastnames":["Vries"],"firstnames":["N."],"suffixes":[]},{"propositions":[],"lastnames":["Harding"],"firstnames":["J."],"suffixes":[]},{"propositions":[],"lastnames":["Gumbo"],"firstnames":["T."],"suffixes":[]},{"propositions":[],"lastnames":["Maartens"],"firstnames":["G."],"suffixes":[]},{"propositions":[],"lastnames":["Warren"],"firstnames":["R."],"suffixes":[]},{"propositions":[],"lastnames":["Denti"],"firstnames":["P."],"suffixes":[]},{"propositions":[],"lastnames":["Denti"],"firstnames":["P."],"suffixes":[]},{"propositions":[],"lastnames":["McIlleron"],"firstnames":["H."],"suffixes":[]}],"doi":"10.1128/AAC.00278-21","journal":"Antimicrobial Agents and Chemotherapy","number":"10","title":"Effect of isoniazid intake on ethionamide pharmacokinetics and target attainment in multidrug-resistant tuberculosis patients","volume":"65","year":"2021","bibtex":"@article{Chirehwa2021,\nabstract = {Ethionamide is recommended as part of regimens to treat multidrug-resistant and rifampicin-resistant tuberculosis. This study was conducted to (i) describe the distribution of ethionamide MICs, (ii) describe the pharmacokinetics of ethionamide, and (iii) determine the probability of attaining target area under the concentration-time curve from 0 to 24 h (AUC0-24)/MIC values associated with suppression of resistant subpopulation and microbial kill. Participants received 15 to 20mg of drug/kg of body weight of ethionamide daily (in 500- or 750-mg doses) as part of a multidrug regimen. Pretreatment MICs of ethionamide for Mycobacterium tuberculosis sputum isolates were determined using Sensititre MYCOTB MIC plates. Plasma concentrations of ethionamide (measured predose and at 2, 4, 6, 8, and 10h postdose) were available for 84 patients. A one-compartment disposition model, including a liver compartment capturing hepatic extraction, best described ethionamide pharmacokinetics. Clearance and volume were allometrically scaled using fat-free mass. Isoniazid coadministration reduced ethionamide clearance by 31{\\%}, resulting in a 44{\\%} increase in AUC0-24. The median (range) MIC (n=111) was 2.5mg/liter (,0.3 to.40mg/liter). Simulations showed increased daily doses of ethionamide (1,250mg, 1,500mg, and 1,750mg for patients weighing {\\#}45kg, 46 to 70kg, and.70kg, respectively) resulted in the probability of attaining an area under the concentration-time curve from 0 to 24 h for the free, unbound fraction of a drug (fAUC0-24)/MIC ratioof {\\$}42 in more than 90{\\%} of patients only at the lowest MIC of 0.3mg/liter. The WHO-recommended doses of ethionamide do not achieve target concentrations even for the lowest MIC measured in the cohort.},\nauthor = {Chirehwa, M.T. and Court, R. and de Kock, M. and Wiesner, L. and de Vries, N. and Harding, J. and Gumbo, T. and Maartens, G. and Warren, R. and Denti, P. and Denti, P. and McIlleron, H.},\ndoi = {10.1128/AAC.00278-21},\njournal = {Antimicrobial Agents and Chemotherapy},\nnumber = {10},\ntitle = {{Effect of isoniazid intake on ethionamide pharmacokinetics and target attainment in multidrug-resistant tuberculosis patients}},\nvolume = {65},\nyear = {2021}\n}\n","author_short":["Chirehwa, M.","Court, R.","de Kock, M.","Wiesner, L.","de Vries, N.","Harding, J.","Gumbo, T.","Maartens, G.","Warren, R.","Denti, P.","Denti, P.","McIlleron, H."],"key":"Chirehwa2021","id":"Chirehwa2021","bibbaseid":"chirehwa-court-dekock-wiesner-devries-harding-gumbo-maartens-etal-effectofisoniazidintakeonethionamidepharmacokineticsandtargetattainmentinmultidrugresistanttuberculosispatients-2021","role":"author","urls":{},"metadata":{"authorlinks":{}}},"bibtype":"article","biburl":"https://drive.google.com/uc?export=download&id=1-9gwO2GBrWfUK-fFo05cgfzXdRK_w9xL","dataSources":["wrEvssexmuYudwQw9","9bX4N36CTXtCXNFMd","6GMFi5DCojy3jHY44"],"keywords":[],"search_terms":["effect","isoniazid","intake","ethionamide","pharmacokinetics","target","attainment","multidrug","resistant","tuberculosis","patients","chirehwa","court","de kock","wiesner","de vries","harding","gumbo","maartens","warren","denti","denti","mcilleron"],"title":"Effect of isoniazid intake on ethionamide pharmacokinetics and target attainment in multidrug-resistant tuberculosis patients","year":2021}