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Helminth lifespan interacts with non-compliance in reducing the effectiveness of anthelmintic treatment
BACKGROUND: The success of mass drug administration programmes targeting the soil-transmitted helminths and schistosome parasites is in part dependent on compliance to treatment at sequential rounds of mass drug administration (MDA). The impact of MDA is vulnerable to systematic non-compliance, defi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5791166/ https://www.ncbi.nlm.nih.gov/pubmed/29382359 http://dx.doi.org/10.1186/s13071-018-2670-6 |
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author | Farrell, Sam H. Anderson, Roy M. |
author_facet | Farrell, Sam H. Anderson, Roy M. |
author_sort | Farrell, Sam H. |
collection | PubMed |
description | BACKGROUND: The success of mass drug administration programmes targeting the soil-transmitted helminths and schistosome parasites is in part dependent on compliance to treatment at sequential rounds of mass drug administration (MDA). The impact of MDA is vulnerable to systematic non-compliance, defined as a portion of the eligible population remaining untreated over successive treatment rounds. The impact of systematic non-compliance on helminth transmission dynamics - and thereby on the number of treatment rounds required to interrupt transmission - is dependent on the parasitic helminth being targeted by MDA. RESULTS: Here, we investigate the impact of adult parasite lifespan in the human host and other factors that determine the magnitude of the basic reproductive number R(0), on the number of additional treatment rounds required in a target population, using mathematical models of Ascaris lumbricoides and Schistosoma mansoni transmission incorporating systematic non-compliance. Our analysis indicates a strong interaction between helminth lifespan and the impact of systematic non-compliance on parasite elimination, and confirms differences in its impact between Ascaris and the schistosome parasites in a streamlined model structure. CONCLUSIONS: Our analysis suggests that achieving reductions in the level of systematic non-compliance may be of particular benefit in mass drug administration programmes treating the longer-lived helminth parasites, and highlights the need for improved data collection in understanding the impact of compliance. |
format | Online Article Text |
id | pubmed-5791166 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57911662018-02-08 Helminth lifespan interacts with non-compliance in reducing the effectiveness of anthelmintic treatment Farrell, Sam H. Anderson, Roy M. Parasit Vectors Short Report BACKGROUND: The success of mass drug administration programmes targeting the soil-transmitted helminths and schistosome parasites is in part dependent on compliance to treatment at sequential rounds of mass drug administration (MDA). The impact of MDA is vulnerable to systematic non-compliance, defined as a portion of the eligible population remaining untreated over successive treatment rounds. The impact of systematic non-compliance on helminth transmission dynamics - and thereby on the number of treatment rounds required to interrupt transmission - is dependent on the parasitic helminth being targeted by MDA. RESULTS: Here, we investigate the impact of adult parasite lifespan in the human host and other factors that determine the magnitude of the basic reproductive number R(0), on the number of additional treatment rounds required in a target population, using mathematical models of Ascaris lumbricoides and Schistosoma mansoni transmission incorporating systematic non-compliance. Our analysis indicates a strong interaction between helminth lifespan and the impact of systematic non-compliance on parasite elimination, and confirms differences in its impact between Ascaris and the schistosome parasites in a streamlined model structure. CONCLUSIONS: Our analysis suggests that achieving reductions in the level of systematic non-compliance may be of particular benefit in mass drug administration programmes treating the longer-lived helminth parasites, and highlights the need for improved data collection in understanding the impact of compliance. BioMed Central 2018-01-31 /pmc/articles/PMC5791166/ /pubmed/29382359 http://dx.doi.org/10.1186/s13071-018-2670-6 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Short Report Farrell, Sam H. Anderson, Roy M. Helminth lifespan interacts with non-compliance in reducing the effectiveness of anthelmintic treatment |
title | Helminth lifespan interacts with non-compliance in reducing the effectiveness of anthelmintic treatment |
title_full | Helminth lifespan interacts with non-compliance in reducing the effectiveness of anthelmintic treatment |
title_fullStr | Helminth lifespan interacts with non-compliance in reducing the effectiveness of anthelmintic treatment |
title_full_unstemmed | Helminth lifespan interacts with non-compliance in reducing the effectiveness of anthelmintic treatment |
title_short | Helminth lifespan interacts with non-compliance in reducing the effectiveness of anthelmintic treatment |
title_sort | helminth lifespan interacts with non-compliance in reducing the effectiveness of anthelmintic treatment |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5791166/ https://www.ncbi.nlm.nih.gov/pubmed/29382359 http://dx.doi.org/10.1186/s13071-018-2670-6 |
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