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Piperaquine Pharmacokinetics during Intermittent Preventive Treatment for Malaria in Pregnancy
Dihydroartemisinin-piperaquine (DP) is a long-acting artemisinin combination treatment that provides effective chemoprevention and has been proposed as an alternative antimalarial drug for intermittent preventive therapy in pregnancy (IPTp). Several pharmacokinetic studies have shown that dose adjus...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8092554/ https://www.ncbi.nlm.nih.gov/pubmed/33361303 http://dx.doi.org/10.1128/AAC.01150-20 |
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author | Chotsiri, Palang Gutman, Julie R. Ahmed, Rukhsana Poespoprodjo, Jeanne Rini Syafruddin, Din Khairallah, Carole Asih, Puji B. S. L’lanziva, Anne Otieno, Kephas Kariuki, Simon Ouma, Peter Were, Vincent Katana, Abraham Price, Ric N. Desai, Meghna ter Kuile, Feiko O. Tarning, Joel |
author_facet | Chotsiri, Palang Gutman, Julie R. Ahmed, Rukhsana Poespoprodjo, Jeanne Rini Syafruddin, Din Khairallah, Carole Asih, Puji B. S. L’lanziva, Anne Otieno, Kephas Kariuki, Simon Ouma, Peter Were, Vincent Katana, Abraham Price, Ric N. Desai, Meghna ter Kuile, Feiko O. Tarning, Joel |
author_sort | Chotsiri, Palang |
collection | PubMed |
description | Dihydroartemisinin-piperaquine (DP) is a long-acting artemisinin combination treatment that provides effective chemoprevention and has been proposed as an alternative antimalarial drug for intermittent preventive therapy in pregnancy (IPTp). Several pharmacokinetic studies have shown that dose adjustment may not be needed for the treatment of malaria in pregnancy with DP. However, there are limited data on the optimal dosing for IPTp. This study aimed to evaluate the population pharmacokinetics of piperaquine given as IPTp in pregnant women. Pregnant women were enrolled in clinical trials conducted in Kenya and Indonesia and treated with standard 3-day courses of DP, administered in 4- to 8-week intervals from the second trimester until delivery. Pharmacokinetic blood samples were collected for piperaquine drug measurements before each treatment round, at the time of breakthrough symptomatic malaria, and at delivery. Piperaquine population pharmacokinetic properties were investigated using nonlinear mixed-effects modeling with a prior approach. In total, data from 366 Kenyan and 101 Indonesian women were analyzed. The pharmacokinetic properties of piperaquine were adequately described using a flexible transit absorption (n = 5) followed by a three-compartment disposition model. Gestational age did not affect the pharmacokinetic parameters of piperaquine. After three rounds of monthly IPTp, 9.45% (95% confidence interval [CI], 1.8 to 26.5%) of pregnant women had trough piperaquine concentrations below the suggested target concentration (10.3 ng/ml). Translational simulations suggest that providing the full treatment course of DP at monthly intervals provides sufficient protection to prevent malaria infection. Monthly administration of DP has the potential to offer optimal prevention of malaria during pregnancy. (This study has been registered at ClinicalTrials.gov under identifier NCT01669941 and in the ISRCTN under number ISRCTN34010937.) |
format | Online Article Text |
id | pubmed-8092554 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-80925542021-05-05 Piperaquine Pharmacokinetics during Intermittent Preventive Treatment for Malaria in Pregnancy Chotsiri, Palang Gutman, Julie R. Ahmed, Rukhsana Poespoprodjo, Jeanne Rini Syafruddin, Din Khairallah, Carole Asih, Puji B. S. L’lanziva, Anne Otieno, Kephas Kariuki, Simon Ouma, Peter Were, Vincent Katana, Abraham Price, Ric N. Desai, Meghna ter Kuile, Feiko O. Tarning, Joel Antimicrob Agents Chemother Pharmacology Dihydroartemisinin-piperaquine (DP) is a long-acting artemisinin combination treatment that provides effective chemoprevention and has been proposed as an alternative antimalarial drug for intermittent preventive therapy in pregnancy (IPTp). Several pharmacokinetic studies have shown that dose adjustment may not be needed for the treatment of malaria in pregnancy with DP. However, there are limited data on the optimal dosing for IPTp. This study aimed to evaluate the population pharmacokinetics of piperaquine given as IPTp in pregnant women. Pregnant women were enrolled in clinical trials conducted in Kenya and Indonesia and treated with standard 3-day courses of DP, administered in 4- to 8-week intervals from the second trimester until delivery. Pharmacokinetic blood samples were collected for piperaquine drug measurements before each treatment round, at the time of breakthrough symptomatic malaria, and at delivery. Piperaquine population pharmacokinetic properties were investigated using nonlinear mixed-effects modeling with a prior approach. In total, data from 366 Kenyan and 101 Indonesian women were analyzed. The pharmacokinetic properties of piperaquine were adequately described using a flexible transit absorption (n = 5) followed by a three-compartment disposition model. Gestational age did not affect the pharmacokinetic parameters of piperaquine. After three rounds of monthly IPTp, 9.45% (95% confidence interval [CI], 1.8 to 26.5%) of pregnant women had trough piperaquine concentrations below the suggested target concentration (10.3 ng/ml). Translational simulations suggest that providing the full treatment course of DP at monthly intervals provides sufficient protection to prevent malaria infection. Monthly administration of DP has the potential to offer optimal prevention of malaria during pregnancy. (This study has been registered at ClinicalTrials.gov under identifier NCT01669941 and in the ISRCTN under number ISRCTN34010937.) American Society for Microbiology 2021-02-17 /pmc/articles/PMC8092554/ /pubmed/33361303 http://dx.doi.org/10.1128/AAC.01150-20 Text en Copyright © 2021 Chotsiri et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Pharmacology Chotsiri, Palang Gutman, Julie R. Ahmed, Rukhsana Poespoprodjo, Jeanne Rini Syafruddin, Din Khairallah, Carole Asih, Puji B. S. L’lanziva, Anne Otieno, Kephas Kariuki, Simon Ouma, Peter Were, Vincent Katana, Abraham Price, Ric N. Desai, Meghna ter Kuile, Feiko O. Tarning, Joel Piperaquine Pharmacokinetics during Intermittent Preventive Treatment for Malaria in Pregnancy |
title | Piperaquine Pharmacokinetics during Intermittent Preventive Treatment for Malaria in Pregnancy |
title_full | Piperaquine Pharmacokinetics during Intermittent Preventive Treatment for Malaria in Pregnancy |
title_fullStr | Piperaquine Pharmacokinetics during Intermittent Preventive Treatment for Malaria in Pregnancy |
title_full_unstemmed | Piperaquine Pharmacokinetics during Intermittent Preventive Treatment for Malaria in Pregnancy |
title_short | Piperaquine Pharmacokinetics during Intermittent Preventive Treatment for Malaria in Pregnancy |
title_sort | piperaquine pharmacokinetics during intermittent preventive treatment for malaria in pregnancy |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8092554/ https://www.ncbi.nlm.nih.gov/pubmed/33361303 http://dx.doi.org/10.1128/AAC.01150-20 |
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