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Population pharmacokinetic models describing drug-drug interactions and variability in HIV infected South Africans on protease inhibitor-based antiretroviral regimens with and without tuberculosis

Includes abstract.

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Bibliographic Details
Main Author: Chao, Zhang
Other Authors: McIlleron, Helen
Format: Thesis
Language:English
Published: Department of Medicine 2014
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access_status_str Open Access
author Chao, Zhang
author2 McIlleron, Helen
author_browse Chao, Zhang
McIlleron, Helen
author_facet McIlleron, Helen
Chao, Zhang
author_sort Chao, Zhang
collection Thesis
description Includes abstract.
format Thesis
id oai:open.uct.ac.za:11427/3372
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:32:38.580Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2014
publishDateRange 2014
publishDateSort 2014
publisher Department of Medicine
publisherStr Department of Medicine
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/3372 Population pharmacokinetic models describing drug-drug interactions and variability in HIV infected South Africans on protease inhibitor-based antiretroviral regimens with and without tuberculosis Chao, Zhang McIlleron, Helen Medicine Includes abstract. Includes bibliographical references. Lopinavir/ritonavir is an important component of the first-line and second-line antiretroviral treatment for young children and adults respectively in the current World Health Organization guidelines. Rifampicin, a key component of antituberculosis treatment, profoundly reduces lopinavir concentrations. Therefore, investigation of the optimal dosage regimens of lopinavir/ritonavir when co-administered with rifampicin-based antituberculosis treatment is needed urgently. Moreover, treatment adherence is associated with virological and clinical responses to antiretroviral treatment, and reduced adherence leads to the development of drug resistance. The projects in this thesis were designed to characterize the population pharmacokinetic parameters of lopinavir and ritonavir in HIV infected South Africans, to account for the drug-drug interactions between lopinavir, ritonavir and rifampicin, to investigate optimal dose regimens of lopinavir/ritonavir when administered with rifampicin, and to investigate new approach to evaluate adherence. 2014-07-29T09:02:58Z 2014-07-29T09:02:58Z 2012 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/3372 eng application/pdf Department of Medicine Faculty of Health Sciences University of Cape Town
spellingShingle Medicine
Chao, Zhang
Population pharmacokinetic models describing drug-drug interactions and variability in HIV infected South Africans on protease inhibitor-based antiretroviral regimens with and without tuberculosis
thesis_degree_str Doctoral
title Population pharmacokinetic models describing drug-drug interactions and variability in HIV infected South Africans on protease inhibitor-based antiretroviral regimens with and without tuberculosis
title_full Population pharmacokinetic models describing drug-drug interactions and variability in HIV infected South Africans on protease inhibitor-based antiretroviral regimens with and without tuberculosis
title_fullStr Population pharmacokinetic models describing drug-drug interactions and variability in HIV infected South Africans on protease inhibitor-based antiretroviral regimens with and without tuberculosis
title_full_unstemmed Population pharmacokinetic models describing drug-drug interactions and variability in HIV infected South Africans on protease inhibitor-based antiretroviral regimens with and without tuberculosis
title_short Population pharmacokinetic models describing drug-drug interactions and variability in HIV infected South Africans on protease inhibitor-based antiretroviral regimens with and without tuberculosis
title_sort population pharmacokinetic models describing drug drug interactions and variability in hiv infected south africans on protease inhibitor based antiretroviral regimens with and without tuberculosis
topic Medicine
url http://hdl.handle.net/11427/3372
work_keys_str_mv AT chaozhang populationpharmacokineticmodelsdescribingdrugdruginteractionsandvariabilityinhivinfectedsouthafricansonproteaseinhibitorbasedantiretroviralregimenswithandwithouttuberculosis