Characteristics of the Western Province, Zambia, trial site for evaluation of attractive targeted sugar baits for malaria vector control.


Journal

Malaria journal
ISSN: 1475-2875
Titre abrégé: Malar J
Pays: England
ID NLM: 101139802

Informations de publication

Date de publication:
18 May 2024
Historique:
received: 01 03 2024
accepted: 14 05 2024
medline: 19 5 2024
pubmed: 19 5 2024
entrez: 18 5 2024
Statut: epublish

Résumé

The attractive targeted sugar bait (ATSB) is a novel malaria vector control tool designed to attract and kill mosquitoes using a sugar-based bait, laced with oral toxicant. Western Province, Zambia, was one of three countries selected for a series of phase III cluster randomized controlled trials of the Westham ATSB Sarabi version 1.2. The trial sites in Kenya, Mali, and Zambia were selected to represent a range of different ecologies and malaria transmission settings across sub-Saharan Africa. This case study describes the key characteristics of the ATSB Zambia trial site to allow for interpretation of the results relative to the Kenya and Mali sites. This study site characterization incorporates data from the trial baseline epidemiological and mosquito sugar feeding surveys conducted in 2021, as well as relevant literature on the study area. CHARACTERIZATION OF THE TRIAL SITE: The trial site in Zambia was comprised of 70 trial-designed clusters in Kaoma, Nkeyema, and Luampa districts. Population settlements in the trial site were dispersed across a large geographic area with sparsely populated villages. The overall population density in the 70 study clusters was 65.7 people per square kilometre with a total site population of 122,023 people living in a geographic area that covered 1858 square kilometres. However, the study clusters were distributed over a total area of approximately 11,728 square kilometres. The region was tropical with intense and seasonal malaria transmission. An abundance of trees and other plants in the trial site were potential sources of sugar meals for malaria vectors. Fourteen Anopheles species were endemic in the site and Anopheles funestus was the dominant vector, likely accounting for around 95% of all Plasmodium falciparum malaria infections. Despite high coverage of indoor residual spraying and insecticide-treated nets, the baseline malaria prevalence during the peak malaria transmission season was 50% among people ages six months and older. Malaria transmission remains high in Western Province, Zambia, despite coverage with vector control tools. New strategies are needed to address the drivers of malaria transmission in this region and other malaria-endemic areas in sub-Saharan Africa.

Sections du résumé

BACKGROUND BACKGROUND
The attractive targeted sugar bait (ATSB) is a novel malaria vector control tool designed to attract and kill mosquitoes using a sugar-based bait, laced with oral toxicant. Western Province, Zambia, was one of three countries selected for a series of phase III cluster randomized controlled trials of the Westham ATSB Sarabi version 1.2. The trial sites in Kenya, Mali, and Zambia were selected to represent a range of different ecologies and malaria transmission settings across sub-Saharan Africa. This case study describes the key characteristics of the ATSB Zambia trial site to allow for interpretation of the results relative to the Kenya and Mali sites.
METHODS METHODS
This study site characterization incorporates data from the trial baseline epidemiological and mosquito sugar feeding surveys conducted in 2021, as well as relevant literature on the study area.
RESULTS RESULTS
CHARACTERIZATION OF THE TRIAL SITE: The trial site in Zambia was comprised of 70 trial-designed clusters in Kaoma, Nkeyema, and Luampa districts. Population settlements in the trial site were dispersed across a large geographic area with sparsely populated villages. The overall population density in the 70 study clusters was 65.7 people per square kilometre with a total site population of 122,023 people living in a geographic area that covered 1858 square kilometres. However, the study clusters were distributed over a total area of approximately 11,728 square kilometres. The region was tropical with intense and seasonal malaria transmission. An abundance of trees and other plants in the trial site were potential sources of sugar meals for malaria vectors. Fourteen Anopheles species were endemic in the site and Anopheles funestus was the dominant vector, likely accounting for around 95% of all Plasmodium falciparum malaria infections. Despite high coverage of indoor residual spraying and insecticide-treated nets, the baseline malaria prevalence during the peak malaria transmission season was 50% among people ages six months and older.
CONCLUSION CONCLUSIONS
Malaria transmission remains high in Western Province, Zambia, despite coverage with vector control tools. New strategies are needed to address the drivers of malaria transmission in this region and other malaria-endemic areas in sub-Saharan Africa.

Identifiants

pubmed: 38762448
doi: 10.1186/s12936-024-04985-0
pii: 10.1186/s12936-024-04985-0
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

153

Subventions

Organisme : Bill & Melinda Gates Foundation
ID : INV-007509
Pays : United States

Informations de copyright

© 2024. The Author(s).

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Auteurs

Annie Arnzen (A)

PATH, Seattle, WA, USA. aarnzen@path.org.

Joseph Wagman (J)

PATH, Washington, DC, USA.

Chama Chishya (C)

PATH, Kaoma, Zambia.

Erica Orange (E)

PATH, Seattle, WA, USA.

Thomas P Eisele (TP)

Centre for Applied Malaria Research and Evaluation, Tulane School of Public Health and Tropical Medicine, New Orleans, LA, USA.

Joshua Yukich (J)

Centre for Applied Malaria Research and Evaluation, Tulane School of Public Health and Tropical Medicine, New Orleans, LA, USA.

Ruth A Ashton (RA)

Centre for Applied Malaria Research and Evaluation, Tulane School of Public Health and Tropical Medicine, New Orleans, LA, USA.

Javan Chanda (J)

PATH, Lusaka, Zambia.

Jimmy Sakala (J)

PATH, Lusaka, Zambia.
Jhpeigo, Lusaka, Zambia.

Benjamin Chanda (B)

PATH, Kaoma, Zambia.

Rayford Muyabe (R)

PATH, Kaoma, Zambia.

Tresford Kaniki (T)

PATH, Kaoma, Zambia.

Mwansa Mwenya (M)

PATH, Kaoma, Zambia.

Gift Mwaanga (G)

Macha Research Trust, Choma, Zambia.

Will T Eaton (WT)

Centre for Applied Malaria Research and Evaluation, Tulane School of Public Health and Tropical Medicine, New Orleans, LA, USA.

Brooke Mancuso (B)

Centre for Applied Malaria Research and Evaluation, Tulane School of Public Health and Tropical Medicine, New Orleans, LA, USA.

Alice Mungo (A)

Macha Research Trust, Choma, Zambia.

Monicah M Mburu (MM)

Macha Research Trust, Choma, Zambia.

Nchimunya Bubala (N)

Macha Research Trust, Choma, Zambia.

Ackim Hagwamuna (A)

Macha Research Trust, Choma, Zambia.

Edgar Simulundu (E)

Macha Research Trust, Choma, Zambia.

Kochelani Saili (K)

PATH, Kaoma, Zambia.

John M Miller (JM)

PATH, Lusaka, Zambia.

Kafula Silumbe (K)

PATH, Lusaka, Zambia.

Busiku Hamainza (B)

National Malaria Elimination Centre, Lusaka, Zambia.

Willy Ngulube (W)

National Malaria Elimination Centre, Lusaka, Zambia.

Hawela Moonga (H)

National Malaria Elimination Centre, Lusaka, Zambia.

Jacob Chirwa (J)

National Malaria Elimination Centre, Lusaka, Zambia.

Thomas R Burkot (TR)

Australian Institute of Tropical Health and Medicine, James Cook University, Cairns, QLD, Australia.

Laurence Slutsker (L)

Independent Consultant, Atlanta, GA, USA.

Megan Littrell (M)

PATH, Washington, DC, USA.

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