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Impact of Four Rounds of Mass Drug Administration with Dihydroartemisinin-Piperaquine Implemented in Southern Province, Zambia.
Eisele, Thomas P; Bennett, Adam; Silumbe, Kafula; Finn, Timothy P; Porter, Travis R; Chalwe, Victor; Hamainza, Busiku; Moonga, Hawela; Kooma, Emmanuel; Chizema Kawesha, Elizabeth; Kamuliwo, Mulakwa; Yukich, Joshua O; Keating, Joseph; Schneider, Kammerle; Conner, Ruben O; Earle, Duncan; Slutsker, Laurence; Steketee, Richard W; Miller, John M.
Affiliation
  • Eisele TP; 1Department of Tropical Medicine, Center for Applied Malaria Research and Evaluation, Tulane University School of Public Health and Tropical Medicine, New Orleans, Louisiana.
  • Bennett A; 2Malaria Elimination Initiative, Global Health Group, University of California San Francisco, San Francisco, California.
  • Silumbe K; 3PATH Malaria Control and Elimination Partnership in Africa (MACEPA), Lusaka, Zambia.
  • Finn TP; 1Department of Tropical Medicine, Center for Applied Malaria Research and Evaluation, Tulane University School of Public Health and Tropical Medicine, New Orleans, Louisiana.
  • Porter TR; 1Department of Tropical Medicine, Center for Applied Malaria Research and Evaluation, Tulane University School of Public Health and Tropical Medicine, New Orleans, Louisiana.
  • Chalwe V; 4Institute for Medical Research and Training, University Teaching Hospital, Lusaka, Zambia.
  • Hamainza B; 5National Malaria Elimination Centre, Zambia Ministry of Health, Lusaka, Zambia.
  • Moonga H; 5National Malaria Elimination Centre, Zambia Ministry of Health, Lusaka, Zambia.
  • Kooma E; 5National Malaria Elimination Centre, Zambia Ministry of Health, Lusaka, Zambia.
  • Chizema Kawesha E; 5National Malaria Elimination Centre, Zambia Ministry of Health, Lusaka, Zambia.
  • Kamuliwo M; 6Zambia Ministry of Health, Southern Provincial Health Office, Choma, Zambia.
  • Yukich JO; 1Department of Tropical Medicine, Center for Applied Malaria Research and Evaluation, Tulane University School of Public Health and Tropical Medicine, New Orleans, Louisiana.
  • Keating J; 1Department of Tropical Medicine, Center for Applied Malaria Research and Evaluation, Tulane University School of Public Health and Tropical Medicine, New Orleans, Louisiana.
  • Schneider K; 7PATH MACEPA, Seattle, Washington.
  • Conner RO; 7PATH MACEPA, Seattle, Washington.
  • Earle D; 3PATH Malaria Control and Elimination Partnership in Africa (MACEPA), Lusaka, Zambia.
  • Slutsker L; 7PATH MACEPA, Seattle, Washington.
  • Steketee RW; 7PATH MACEPA, Seattle, Washington.
  • Miller JM; 3PATH Malaria Control and Elimination Partnership in Africa (MACEPA), Lusaka, Zambia.
Am J Trop Med Hyg ; 103(2_Suppl): 7-18, 2020 08.
Article in En | MEDLINE | ID: mdl-32618247
ABSTRACT
Over the past decade, Zambia has made substantial progress against malaria and has recently set the ambitious goal of eliminating by 2021. In the context of very high vector control and improved access to malaria diagnosis and treatment in Southern Province, we implemented a community-randomized controlled trial to assess the impact of four rounds of community-wide mass drug administration (MDA) and household-level MDA (focal MDA) with dihydroartemisinin-piperaquine (DHAP) implemented between December 2014 and February 2016. The mass treatment campaigns achieved relatively good household coverage (63-79%), were widely accepted by the community (ranging from 87% to 94%), and achieved very high adherence to the DHAP regimen (81-96%). Significant declines in all malaria study end points were observed, irrespective of the exposure group, with the overall parasite prevalence during the peak transmission season declining by 87.2% from 31.3% at baseline to 4.0% in 2016 at the end of the trial. Children in areas of lower transmission (< 10% prevalence at baseline) that received four MDA rounds had a 72% (95% CI = 12-91%) reduction in malaria parasite prevalence as compared with those with the standard of care without any mass treatment. Mass drug administration consistently had the largest short-term effect size across study end points in areas of lower transmission following the first two MDA rounds. In the context of achieving very high vector control coverage and improved access to diagnosis and treatment for malaria, our results suggest that MDA should be considered for implementation in African settings for rapidly reducing malaria outcomes in lower transmission settings.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Quinolines / Malaria, Falciparum / Artemisinins / Mass Drug Administration / Antimalarials Type of study: Clinical_trials / Evaluation_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Country/Region as subject: Africa Language: En Journal: Am J Trop Med Hyg Year: 2020 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Quinolines / Malaria, Falciparum / Artemisinins / Mass Drug Administration / Antimalarials Type of study: Clinical_trials / Evaluation_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Country/Region as subject: Africa Language: En Journal: Am J Trop Med Hyg Year: 2020 Type: Article