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Suboptimal Antituberculosis Drug Concentrations and Outcomes in Small and HIV‐Coinfected Children in India: Recommendations for Dose Modifications

This work aimed to evaluate the once‐daily antituberculosis treatment as recommended by the new Indian pediatric guidelines. Isoniazid, rifampin, and pyrazinamide concentration–time profiles and treatment outcome were obtained from 161 Indian children with drug‐sensitive tuberculosis undergoing thri...

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Autores principales: Guiastrennec, Benjamin, Ramachandran, Geetha, Karlsson, Mats O., Kumar, A.K. Hemanth, Bhavani, Perumal Kannabiran, Gangadevi, N. Poorana, Swaminathan, Soumya, Gupta, Amita, Dooley, Kelly E., Savic, Radojka M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6004234/
https://www.ncbi.nlm.nih.gov/pubmed/29247506
http://dx.doi.org/10.1002/cpt.987
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author Guiastrennec, Benjamin
Ramachandran, Geetha
Karlsson, Mats O.
Kumar, A.K. Hemanth
Bhavani, Perumal Kannabiran
Gangadevi, N. Poorana
Swaminathan, Soumya
Gupta, Amita
Dooley, Kelly E.
Savic, Radojka M.
author_facet Guiastrennec, Benjamin
Ramachandran, Geetha
Karlsson, Mats O.
Kumar, A.K. Hemanth
Bhavani, Perumal Kannabiran
Gangadevi, N. Poorana
Swaminathan, Soumya
Gupta, Amita
Dooley, Kelly E.
Savic, Radojka M.
author_sort Guiastrennec, Benjamin
collection PubMed
description This work aimed to evaluate the once‐daily antituberculosis treatment as recommended by the new Indian pediatric guidelines. Isoniazid, rifampin, and pyrazinamide concentration–time profiles and treatment outcome were obtained from 161 Indian children with drug‐sensitive tuberculosis undergoing thrice‐weekly dosing as per previous Indian pediatric guidelines. The exposure–response relationships were established using a population pharmacokinetic‐pharmacodynamic approach. Rifampin exposure was identified as the unique predictor of treatment outcome. Consequently, children with low body weight (4–7 kg) and/or HIV infection, who displayed the lowest rifampin exposure, were associated with the highest probability of unfavorable treatment (therapy failure, death) outcome (P(unfavorable)). Model‐based simulation of optimized (P(unfavorable) ≤ 5%) rifampin once‐daily doses were suggested per treatment weight band and HIV coinfection status (33% and 190% dose increase, respectively, from the new Indian guidelines). The established dose‐exposure–response relationship could be pivotal in the development of future pediatric tuberculosis treatment guidelines.
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spelling pubmed-60042342018-10-10 Suboptimal Antituberculosis Drug Concentrations and Outcomes in Small and HIV‐Coinfected Children in India: Recommendations for Dose Modifications Guiastrennec, Benjamin Ramachandran, Geetha Karlsson, Mats O. Kumar, A.K. Hemanth Bhavani, Perumal Kannabiran Gangadevi, N. Poorana Swaminathan, Soumya Gupta, Amita Dooley, Kelly E. Savic, Radojka M. Clin Pharmacol Ther Research This work aimed to evaluate the once‐daily antituberculosis treatment as recommended by the new Indian pediatric guidelines. Isoniazid, rifampin, and pyrazinamide concentration–time profiles and treatment outcome were obtained from 161 Indian children with drug‐sensitive tuberculosis undergoing thrice‐weekly dosing as per previous Indian pediatric guidelines. The exposure–response relationships were established using a population pharmacokinetic‐pharmacodynamic approach. Rifampin exposure was identified as the unique predictor of treatment outcome. Consequently, children with low body weight (4–7 kg) and/or HIV infection, who displayed the lowest rifampin exposure, were associated with the highest probability of unfavorable treatment (therapy failure, death) outcome (P(unfavorable)). Model‐based simulation of optimized (P(unfavorable) ≤ 5%) rifampin once‐daily doses were suggested per treatment weight band and HIV coinfection status (33% and 190% dose increase, respectively, from the new Indian guidelines). The established dose‐exposure–response relationship could be pivotal in the development of future pediatric tuberculosis treatment guidelines. John Wiley and Sons Inc. 2018-02-02 2018-10 /pmc/articles/PMC6004234/ /pubmed/29247506 http://dx.doi.org/10.1002/cpt.987 Text en © 2017 The Authors Clinical Pharmacology & Therapeutics published by Wiley Periodicals, Inc. on behalf of American Society for Clinical Pharmacology and Therapeutics This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research
Guiastrennec, Benjamin
Ramachandran, Geetha
Karlsson, Mats O.
Kumar, A.K. Hemanth
Bhavani, Perumal Kannabiran
Gangadevi, N. Poorana
Swaminathan, Soumya
Gupta, Amita
Dooley, Kelly E.
Savic, Radojka M.
Suboptimal Antituberculosis Drug Concentrations and Outcomes in Small and HIV‐Coinfected Children in India: Recommendations for Dose Modifications
title Suboptimal Antituberculosis Drug Concentrations and Outcomes in Small and HIV‐Coinfected Children in India: Recommendations for Dose Modifications
title_full Suboptimal Antituberculosis Drug Concentrations and Outcomes in Small and HIV‐Coinfected Children in India: Recommendations for Dose Modifications
title_fullStr Suboptimal Antituberculosis Drug Concentrations and Outcomes in Small and HIV‐Coinfected Children in India: Recommendations for Dose Modifications
title_full_unstemmed Suboptimal Antituberculosis Drug Concentrations and Outcomes in Small and HIV‐Coinfected Children in India: Recommendations for Dose Modifications
title_short Suboptimal Antituberculosis Drug Concentrations and Outcomes in Small and HIV‐Coinfected Children in India: Recommendations for Dose Modifications
title_sort suboptimal antituberculosis drug concentrations and outcomes in small and hiv‐coinfected children in india: recommendations for dose modifications
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6004234/
https://www.ncbi.nlm.nih.gov/pubmed/29247506
http://dx.doi.org/10.1002/cpt.987
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