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Community-based intermittent mass testing and treatment for malaria in an area of high transmission intensity, western Kenya: study design and methodology for a cluster randomized controlled trial

Most human Plasmodium infections in western Kenya are asymptomatic and are believed to contribute importantly to malaria transmission. Elimination of asymptomatic infections requires active treatment approaches, such as mass testing and treatment (MTaT) or mass drug administration (MDA), as infected...

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Autores principales: Samuels, Aaron M., Awino, Nobert, Odongo, Wycliffe, Abong’o, Benard, Gimnig, John, Otieno, Kephas, Shi, Ya Ping, Were, Vincent, Allen, Denise Roth, Were, Florence, Sang, Tony, Obor, David, Williamson, John, Hamel, Mary J., Patrick Kachur, S., Slutsker, Laurence, Lindblade, Kim A., Kariuki, Simon, Desai, Meghna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5463392/
https://www.ncbi.nlm.nih.gov/pubmed/28592250
http://dx.doi.org/10.1186/s12936-017-1883-z
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author Samuels, Aaron M.
Awino, Nobert
Odongo, Wycliffe
Abong’o, Benard
Gimnig, John
Otieno, Kephas
Shi, Ya Ping
Were, Vincent
Allen, Denise Roth
Were, Florence
Sang, Tony
Obor, David
Williamson, John
Hamel, Mary J.
Patrick Kachur, S.
Slutsker, Laurence
Lindblade, Kim A.
Kariuki, Simon
Desai, Meghna
author_facet Samuels, Aaron M.
Awino, Nobert
Odongo, Wycliffe
Abong’o, Benard
Gimnig, John
Otieno, Kephas
Shi, Ya Ping
Were, Vincent
Allen, Denise Roth
Were, Florence
Sang, Tony
Obor, David
Williamson, John
Hamel, Mary J.
Patrick Kachur, S.
Slutsker, Laurence
Lindblade, Kim A.
Kariuki, Simon
Desai, Meghna
author_sort Samuels, Aaron M.
collection PubMed
description Most human Plasmodium infections in western Kenya are asymptomatic and are believed to contribute importantly to malaria transmission. Elimination of asymptomatic infections requires active treatment approaches, such as mass testing and treatment (MTaT) or mass drug administration (MDA), as infected persons do not seek care for their infection. Evaluations of community-based approaches that are designed to reduce malaria transmission require careful attention to study design to ensure that important effects can be measured accurately. This manuscript describes the study design and methodology of a cluster-randomized controlled trial to evaluate a MTaT approach for malaria transmission reduction in an area of high malaria transmission. Ten health facilities in western Kenya were purposively selected for inclusion. The communities within 3 km of each health facility were divided into three clusters of approximately equal population size. Two clusters around each health facility were randomly assigned to the control arm, and one to the intervention arm. Three times per year for 2 years, after the long and short rains, and again before the long rains, teams of community health volunteers visited every household within the intervention arm, tested all consenting individuals with malaria rapid diagnostic tests, and treated all positive individuals with an effective anti-malarial. The effect of mass testing and treatment on malaria transmission was measured through population-based longitudinal cohorts, outpatient visits for clinical malaria, periodic population-based cross-sectional surveys, and entomological indices.
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spelling pubmed-54633922017-06-08 Community-based intermittent mass testing and treatment for malaria in an area of high transmission intensity, western Kenya: study design and methodology for a cluster randomized controlled trial Samuels, Aaron M. Awino, Nobert Odongo, Wycliffe Abong’o, Benard Gimnig, John Otieno, Kephas Shi, Ya Ping Were, Vincent Allen, Denise Roth Were, Florence Sang, Tony Obor, David Williamson, John Hamel, Mary J. Patrick Kachur, S. Slutsker, Laurence Lindblade, Kim A. Kariuki, Simon Desai, Meghna Malar J Case Study Most human Plasmodium infections in western Kenya are asymptomatic and are believed to contribute importantly to malaria transmission. Elimination of asymptomatic infections requires active treatment approaches, such as mass testing and treatment (MTaT) or mass drug administration (MDA), as infected persons do not seek care for their infection. Evaluations of community-based approaches that are designed to reduce malaria transmission require careful attention to study design to ensure that important effects can be measured accurately. This manuscript describes the study design and methodology of a cluster-randomized controlled trial to evaluate a MTaT approach for malaria transmission reduction in an area of high malaria transmission. Ten health facilities in western Kenya were purposively selected for inclusion. The communities within 3 km of each health facility were divided into three clusters of approximately equal population size. Two clusters around each health facility were randomly assigned to the control arm, and one to the intervention arm. Three times per year for 2 years, after the long and short rains, and again before the long rains, teams of community health volunteers visited every household within the intervention arm, tested all consenting individuals with malaria rapid diagnostic tests, and treated all positive individuals with an effective anti-malarial. The effect of mass testing and treatment on malaria transmission was measured through population-based longitudinal cohorts, outpatient visits for clinical malaria, periodic population-based cross-sectional surveys, and entomological indices. BioMed Central 2017-06-07 /pmc/articles/PMC5463392/ /pubmed/28592250 http://dx.doi.org/10.1186/s12936-017-1883-z Text en © The Author(s) 2017 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 Case Study
Samuels, Aaron M.
Awino, Nobert
Odongo, Wycliffe
Abong’o, Benard
Gimnig, John
Otieno, Kephas
Shi, Ya Ping
Were, Vincent
Allen, Denise Roth
Were, Florence
Sang, Tony
Obor, David
Williamson, John
Hamel, Mary J.
Patrick Kachur, S.
Slutsker, Laurence
Lindblade, Kim A.
Kariuki, Simon
Desai, Meghna
Community-based intermittent mass testing and treatment for malaria in an area of high transmission intensity, western Kenya: study design and methodology for a cluster randomized controlled trial
title Community-based intermittent mass testing and treatment for malaria in an area of high transmission intensity, western Kenya: study design and methodology for a cluster randomized controlled trial
title_full Community-based intermittent mass testing and treatment for malaria in an area of high transmission intensity, western Kenya: study design and methodology for a cluster randomized controlled trial
title_fullStr Community-based intermittent mass testing and treatment for malaria in an area of high transmission intensity, western Kenya: study design and methodology for a cluster randomized controlled trial
title_full_unstemmed Community-based intermittent mass testing and treatment for malaria in an area of high transmission intensity, western Kenya: study design and methodology for a cluster randomized controlled trial
title_short Community-based intermittent mass testing and treatment for malaria in an area of high transmission intensity, western Kenya: study design and methodology for a cluster randomized controlled trial
title_sort community-based intermittent mass testing and treatment for malaria in an area of high transmission intensity, western kenya: study design and methodology for a cluster randomized controlled trial
topic Case Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5463392/
https://www.ncbi.nlm.nih.gov/pubmed/28592250
http://dx.doi.org/10.1186/s12936-017-1883-z
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