The assessment of antimalarial drug efficacy in vivo

<p>Currently recommended methods of assessing the efficacy of uncomplicated falciparum malaria treatment work less well in high-transmission than in low-transmission settings. There is also uncertainty how to assess intermittent preventive therapies and seasonal malaria chemoprevention (SMC),...

Full description

Bibliographic Details
Main Author: White, NJ
Format: Journal article
Language:English
Published: Cell Press 2022
_version_ 1797111482549272576
author White, NJ
author_facet White, NJ
author_sort White, NJ
collection OXFORD
description <p>Currently recommended methods of assessing the efficacy of uncomplicated falciparum malaria treatment work less well in high-transmission than in low-transmission settings. There is also uncertainty how to assess intermittent preventive therapies and seasonal malaria chemoprevention (SMC), and&nbsp;<em>Plasmodium vivax</em>&nbsp;radical cure. A pharmacometric antimalarial resistance monitoring (PARM) approach is proposed specifically for evaluating slowly eliminated antimalarial drugs in areas of high transmission. In PARM antimalarial drug concentrations at recurrent parasitaemia are measured to identify outliers (i.e., recurrent parasitaemias in the presence of normally suppressive drug concentrations) and to evaluate changes over time. PARM requires characterization of pharmacometric profiles but should be simpler and more sensitive than current molecular genotyping-based methodologies. PARM does not require parasite genotyping and can be applied to the assessment of both prevention and treatment.</p>
first_indexed 2024-03-07T08:09:32Z
format Journal article
id oxford-uuid:64d3acab-b7af-4cd6-bd00-bb936f79a55e
institution University of Oxford
language English
last_indexed 2024-03-07T08:09:32Z
publishDate 2022
publisher Cell Press
record_format dspace
spelling oxford-uuid:64d3acab-b7af-4cd6-bd00-bb936f79a55e2023-11-20T13:30:37ZThe assessment of antimalarial drug efficacy in vivoJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:64d3acab-b7af-4cd6-bd00-bb936f79a55eEnglishSymplectic ElementsCell Press2022White, NJ<p>Currently recommended methods of assessing the efficacy of uncomplicated falciparum malaria treatment work less well in high-transmission than in low-transmission settings. There is also uncertainty how to assess intermittent preventive therapies and seasonal malaria chemoprevention (SMC), and&nbsp;<em>Plasmodium vivax</em>&nbsp;radical cure. A pharmacometric antimalarial resistance monitoring (PARM) approach is proposed specifically for evaluating slowly eliminated antimalarial drugs in areas of high transmission. In PARM antimalarial drug concentrations at recurrent parasitaemia are measured to identify outliers (i.e., recurrent parasitaemias in the presence of normally suppressive drug concentrations) and to evaluate changes over time. PARM requires characterization of pharmacometric profiles but should be simpler and more sensitive than current molecular genotyping-based methodologies. PARM does not require parasite genotyping and can be applied to the assessment of both prevention and treatment.</p>
spellingShingle White, NJ
The assessment of antimalarial drug efficacy in vivo
title The assessment of antimalarial drug efficacy in vivo
title_full The assessment of antimalarial drug efficacy in vivo
title_fullStr The assessment of antimalarial drug efficacy in vivo
title_full_unstemmed The assessment of antimalarial drug efficacy in vivo
title_short The assessment of antimalarial drug efficacy in vivo
title_sort assessment of antimalarial drug efficacy in vivo
work_keys_str_mv AT whitenj theassessmentofantimalarialdrugefficacyinvivo
AT whitenj assessmentofantimalarialdrugefficacyinvivo