Treatment Coverage Estimation for Mass Drug Administration for Malaria with Dihydroartemisinin-Piperaquine in Southern Province, Zambia
Mass drug administration (MDA) is currently being considered as an intervention in low-transmission areas to complement existing malaria control and elimination efforts. The effectiveness of any MDA strategy is dependent on achieving high epidemiologic coverage and participant adherence rates. A com...
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Published in | The American journal of tropical medicine and hygiene Vol. 103; no. 2_Suppl; pp. 19 - 27 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
The American Society of Tropical Medicine and Hygiene
01.08.2020
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Subjects | |
Online Access | Get full text |
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Summary: | Mass drug administration (MDA) is currently being considered as an intervention in low-transmission areas to complement existing malaria control and elimination efforts. The effectiveness of any MDA strategy is dependent on achieving high epidemiologic coverage and participant adherence rates. A community-randomized controlled trial was conducted from November 2014 to March 2016 to evaluate the impact of four rounds of MDA or focal MDA (fMDA)-where treatment was given to all eligible household members if anyone in the household had a positive malaria rapid diagnostic test-on malaria outcomes in Southern Province, Zambia (population approximately 300,000). This study examined epidemiologic coverage and program reach using capture-recapture and satellite enumeration methods to estimate the degree to which the trial reached targeted individuals. Overall, it was found that the percentage of households visited by campaign teams ranged from 62.9% (95% CI: 60.0-65.8) to a high of 77.4% (95% CI: 73.8-81.0) across four rounds of treatment. When the maximum number of visited households across all campaign rounds was used as the numerator, program reach for at least one visit would have been 86.4% (95% CI: 80.8-92.0) in MDA and 83.5% (95% CI: 78.0-89.1) in fMDA trial arms. As per the protocol, the trial provided dihydroartemisinin-piperaquine treatment to an average of 58.8% and 13.3% of the estimated population based on capture-recapture in MDA and fMDA, respectively, across the four rounds. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-News-1 ObjectType-Feature-3 content type line 23 Financial support: The trial was an investigator-initiated study supported by a grant from the Bill & Melinda Gates Foundation. Authors’ addresses: Timothy P. Finn, Joshua O. Yukich, Travis R. Porter, Joseph Keating, and Thomas P. Eisele, Department of Tropical Medicine, Center for Applied Malaria Research and Evaluation, Tulane University School of Public Health and Tropical Medicine, New Orleans, LA, E-mails: tfinn2@tulane.edu, jyukich@tulane.edu, tporter1@tulane.edu, jkeating@tulane.edu, and teisele@tulane.edu. Adam Bennett, Malaria Elimination Initiative, Global Health Group, University of California San Francisco, San Francisco, CA, E-mail: adam.bennett@ucsf.edu. Christopher Lungu, Kafula Silumbe, and John M. Miller, PATH Malaria Control and Elimination Partnership in Africa (MACEPA), Lusaka, Zambia, E-mails: clungu@path.org, ksilumbe@path.org, and jmiller@path.org. Busiku Hamainza and Elizabeth Chizema Kawesha, National Malaria Elimination Centre, Zambia Ministry of Health, Chainama Hospital, Lusaka, Zambia, E-mails: bossbusk@gmail.com and e.chizema5@gmail.com. Ruben O. Conner and Richard W. Steketee, PATH Malaria Control and Elimination Partnership in Africa, Seattle, WA, E-mails: rconner@path.org and rsteketee@path.org. Disclaimer: The funding source had no role in the conduct, analysis, or interpretation of results of the study. All authors had full access to all the data in the study. |
ISSN: | 0002-9637 1476-1645 |
DOI: | 10.4269/ajtmh.19-0665 |