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Population-Wide Malaria Testing and Treatment with Rapid Diagnostic Tests and Artemether-Lumefantrine in Southern Zambia: A community Randomized Step-Wedge Control Trial Design

Reducing the human reservoir of malaria parasites is critical for elimination. We conducted a community randomized controlled trial in Southern Province, Zambia to assess the impact of three rounds of a mass test and treatment (MTAT) intervention on malaria prevalence and health facility outpatient...

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Autores principales: Larsen, David A., Bennett, Adam, Silumbe, Kafula, Hamainza, Busiku, Yukich, Joshua O., Keating, Joseph, Littrell, Megan, Miller, John M., Steketee, Richard W., Eisele, Thomas P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society of Tropical Medicine and Hygiene 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426577/
https://www.ncbi.nlm.nih.gov/pubmed/25802434
http://dx.doi.org/10.4269/ajtmh.14-0347
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author Larsen, David A.
Bennett, Adam
Silumbe, Kafula
Hamainza, Busiku
Yukich, Joshua O.
Keating, Joseph
Littrell, Megan
Miller, John M.
Steketee, Richard W.
Eisele, Thomas P.
author_facet Larsen, David A.
Bennett, Adam
Silumbe, Kafula
Hamainza, Busiku
Yukich, Joshua O.
Keating, Joseph
Littrell, Megan
Miller, John M.
Steketee, Richard W.
Eisele, Thomas P.
author_sort Larsen, David A.
collection PubMed
description Reducing the human reservoir of malaria parasites is critical for elimination. We conducted a community randomized controlled trial in Southern Province, Zambia to assess the impact of three rounds of a mass test and treatment (MTAT) intervention on malaria prevalence and health facility outpatient case incidence using random effects logistic regression and negative binomial regression, respectively. Following the intervention, children in the intervention group had lower odds of a malaria infection than individuals in the control group (adjusted odds ratio = 0.47, 95% confidence interval [CI] = 0.24–0.90). Malaria outpatient case incidence decreased 17% in the intervention group relative to the control group (incidence rate ratio = 0.83, 95% CI = 0.68–1.01). Although a single year of MTAT reduced malaria prevalence and incidence, the impact of the intervention was insufficient to reduce transmission to a level approaching elimination where a strategy of aggressive case investigations could be used. Mass drug administration, more sensitive diagnostics, and gametocidal drugs may potentially improve interventions targeting the human reservoir of malaria parasites.
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spelling pubmed-44265772015-05-12 Population-Wide Malaria Testing and Treatment with Rapid Diagnostic Tests and Artemether-Lumefantrine in Southern Zambia: A community Randomized Step-Wedge Control Trial Design Larsen, David A. Bennett, Adam Silumbe, Kafula Hamainza, Busiku Yukich, Joshua O. Keating, Joseph Littrell, Megan Miller, John M. Steketee, Richard W. Eisele, Thomas P. Am J Trop Med Hyg Articles Reducing the human reservoir of malaria parasites is critical for elimination. We conducted a community randomized controlled trial in Southern Province, Zambia to assess the impact of three rounds of a mass test and treatment (MTAT) intervention on malaria prevalence and health facility outpatient case incidence using random effects logistic regression and negative binomial regression, respectively. Following the intervention, children in the intervention group had lower odds of a malaria infection than individuals in the control group (adjusted odds ratio = 0.47, 95% confidence interval [CI] = 0.24–0.90). Malaria outpatient case incidence decreased 17% in the intervention group relative to the control group (incidence rate ratio = 0.83, 95% CI = 0.68–1.01). Although a single year of MTAT reduced malaria prevalence and incidence, the impact of the intervention was insufficient to reduce transmission to a level approaching elimination where a strategy of aggressive case investigations could be used. Mass drug administration, more sensitive diagnostics, and gametocidal drugs may potentially improve interventions targeting the human reservoir of malaria parasites. The American Society of Tropical Medicine and Hygiene 2015-05-06 /pmc/articles/PMC4426577/ /pubmed/25802434 http://dx.doi.org/10.4269/ajtmh.14-0347 Text en ©The American Society of Tropical Medicine and Hygiene This is an Open Access article distributed under the terms of the American Society of Tropical Medicine and Hygiene's Re-use License which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Larsen, David A.
Bennett, Adam
Silumbe, Kafula
Hamainza, Busiku
Yukich, Joshua O.
Keating, Joseph
Littrell, Megan
Miller, John M.
Steketee, Richard W.
Eisele, Thomas P.
Population-Wide Malaria Testing and Treatment with Rapid Diagnostic Tests and Artemether-Lumefantrine in Southern Zambia: A community Randomized Step-Wedge Control Trial Design
title Population-Wide Malaria Testing and Treatment with Rapid Diagnostic Tests and Artemether-Lumefantrine in Southern Zambia: A community Randomized Step-Wedge Control Trial Design
title_full Population-Wide Malaria Testing and Treatment with Rapid Diagnostic Tests and Artemether-Lumefantrine in Southern Zambia: A community Randomized Step-Wedge Control Trial Design
title_fullStr Population-Wide Malaria Testing and Treatment with Rapid Diagnostic Tests and Artemether-Lumefantrine in Southern Zambia: A community Randomized Step-Wedge Control Trial Design
title_full_unstemmed Population-Wide Malaria Testing and Treatment with Rapid Diagnostic Tests and Artemether-Lumefantrine in Southern Zambia: A community Randomized Step-Wedge Control Trial Design
title_short Population-Wide Malaria Testing and Treatment with Rapid Diagnostic Tests and Artemether-Lumefantrine in Southern Zambia: A community Randomized Step-Wedge Control Trial Design
title_sort population-wide malaria testing and treatment with rapid diagnostic tests and artemether-lumefantrine in southern zambia: a community randomized step-wedge control trial design
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426577/
https://www.ncbi.nlm.nih.gov/pubmed/25802434
http://dx.doi.org/10.4269/ajtmh.14-0347
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