Research Article | | Peer-Reviewed

Superiority of Three Directly Observed Treatment Compared to One Directly Observed Treatment in the Seasonal Malaria Chemoprevention in Children Aged Under Five in Burkina Faso: A Quasi-Experimental Trial

Received: 28 May 2025     Accepted: 15 July 2025     Published: 16 July 2025
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Abstract

The implementation of seasonal malaria chemoprevention (SMC) in Burkina Faso has not achieved its objective of reducing by at least 60% the morbidity associated with malaria in children under 5 years of age. We assessed a new approach of delivery consisting for the community health workers to directly supervise the three doses of the treatment compared to the standard of delivery (only the first dose directly observed treatment). The objective of the study was to compare the superiority of three doses supervised intake of SMC (3DOT) to the supervised intake of the first dose only. Three centers for health and social promotion were randomly selected in the Gaoua health district (3DOT) and 4 in the Boromo health district (1DOT) to receive a monthly four rounds of SMC with Sulfadoxine-pyrimethamine plus Amodiaquine (SP+AQ) in a quasi-experimental cluster randomized trial, before-after with a control group design which included in total 2440 children. The primary endpoint was the reduction in prevalence between each SMC round. The Khi-2 test was used to assess the superiority of 3DOT versus 1DOT. The reduction of malaria prevalence was significantly higher in 3DOT compared to the 1DOT, 68.60% vs 53.00% (p<.0001). The coverage in the 3DOT was significantly lower than that in the 1DOT, 81.39% versus 95.72%; p<0.0001 for optimal coverage. The 3DOT delivery approach of SMC provides better reduction of malaria prevalence than the 1DOT. However, the lower coverage obtained with the 3DOT compared to the 1DOT is a concerning issue to overcome in the perspective of the scale-up of this strategy at large scale.

Published in Science Journal of Public Health (Volume 13, Issue 4)
DOI 10.11648/j.sjph.20251304.12
Page(s) 177-188
Creative Commons

This is an Open Access article, 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 or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2025. Published by Science Publishing Group

Keywords

SMC, Method of Delivery, 3DOT, Burkina Faso

References
[1] WHO. Seasonal malaria chemoprevention with sulfadoxine-pyrimethamine plus amodiaquine in children: a field guide. Published online 2013: 56.
[2] Wilson AL, IPTc Taskforce. A systematic review and meta-analysis of the efficacy and safety of intermittent preventive treatment of malaria in children (IPTc). PLoS One. 2011; 6(2): e16976.
[3] Konaté AT, Yaro JB, Ouédraogo AZ, et al. Intermittent preventive treatment of malaria provides substantial protection against malaria in children already protected by an insecticide-treated bednet in Burkina Faso: a randomised, double-blind, placebo-controlled trial. PLoS Med. 2011; 8(2): e1000408.
[4] Meremikwu MM, Donegan S, Sinclair D, Esu E, Oringanje C. Intermittent preventive treatment for malaria in children living in areas with seasonal transmission. Cochrane Database Syst Rev. 2012; (2): CD003756.
[5] Compaoré R, Yameogo MWE, Millogo T, Tougri H, Kouanda S. Evaluation of the implementation fidelity of the seasonal malaria chemoprevention intervention in Kaya health district, Burkina Faso. PLOS ONE. 2017; 12(11): e0187460.
[6] Souares A, Lalou R, Sene I, Sow D, Le Hesran JY. Factors related to compliance to anti-malarial drug combination: example of amodiaquine/sulphadoxine-pyrimethamine among children in rural Senegal. Malar J. 2009; 8: 118.
[7] Tiono AB, Kangoye DT, Rehman AM, et al. Malaria incidence in children in South-West Burkina Faso: comparison of active and passive case detection methods. PLoS One. 2014; 9(1): e86936.
[8] Ministère de la Santé et de l’Hygiène publique Burkina. Annuaire statistique 2020.
[9] Yanogo PK, Yanogo C, Tinto H. Prevalence of Malaria among Children between 3 and 59 Months Old in Two Healthcare Districts of Burkina Faso, 2020. TIJPH. 2024; 12(04).
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[11] Cairns M, Ceesay SJ, Sagara I, et al. Effectiveness of seasonal malaria chemoprevention (SMC) treatments when SMC is implemented at scale: Case-control studies in 5 countries. PLoS Med. 2021; 18(9): e1003727.
[12] Adjei MR, Kubio C, Buamah M, et al. Effectiveness of seasonal malaria chemoprevention in reducing under-five malaria morbidity and mortality in the Savannah Region, Ghana. Ghana Med J. 2022; 56(2): 64-70.
[13] Kirakoya-Samadoulougou F, De Brouwere V, Fokam AF, Ouédraogo M, Yé Y. Assessing the effect of seasonal malaria chemoprevention on malaria burden among children under 5 years in Burkina Faso. Malar J. 2022; 21(1): 143.
[14] Kweku M, Webster J, Adjuik M, Abudey S, Greenwood B, Chandramohan D. Options for the delivery of intermittent preventive treatment for malaria to children: a community randomised trial. PLoS One. 2009; 4(9): e7256.
[15] Bojang KA, Akor F, Conteh L, et al. Two strategies for the delivery of IPTc in an area of seasonal malaria transmission in the Gambia: a randomised controlled trial. PLoS Med. 2011; 8(2): e1000409.
[16] Barry A, Issiaka D, Traore T, et al. Optimal mode for delivery of seasonal malaria chemoprevention in Ouelessebougou, Mali: A cluster randomized trial. PLoS One. 2018; 13(3): e0193296.
[17] Dabiré KR, Diabaté A, Namontougou M, et al. Distribution of insensitive acetylcholinesterase (ace-1R) in Anopheles gambiae s.l. populations from Burkina Faso (West Africa). Trop Med Int Health. 2009; 14(4): 396-403.
[18] Hancock PA, Hendriks CJM, Tangena JA, et al. Mapping trends in insecticide resistance phenotypes in African malaria vectors. PLoS Biol. 2020; 18(6): e3000633.
[19] Malaria Consortium. Coverage and quality of seasonal malaria chemoprevention supported by Malaria Consortium with philanthropic funding or cofunding in 2023: Results from Burkina Faso, Chad, Mozambique, Nigeria, South Sudan, Togo and Uganda.
Cite This Article
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    Kiswendsida, Y. P., Nadine, S. E., Traore, I. T., Chantal, Y., Tinto, H. (2025). Superiority of Three Directly Observed Treatment Compared to One Directly Observed Treatment in the Seasonal Malaria Chemoprevention in Children Aged Under Five in Burkina Faso: A Quasi-Experimental Trial. Science Journal of Public Health, 13(4), 177-188. https://doi.org/10.11648/j.sjph.20251304.12

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    ACS Style

    Kiswendsida, Y. P.; Nadine, S. E.; Traore, I. T.; Chantal, Y.; Tinto, H. Superiority of Three Directly Observed Treatment Compared to One Directly Observed Treatment in the Seasonal Malaria Chemoprevention in Children Aged Under Five in Burkina Faso: A Quasi-Experimental Trial. Sci. J. Public Health 2025, 13(4), 177-188. doi: 10.11648/j.sjph.20251304.12

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    AMA Style

    Kiswendsida YP, Nadine SE, Traore IT, Chantal Y, Tinto H. Superiority of Three Directly Observed Treatment Compared to One Directly Observed Treatment in the Seasonal Malaria Chemoprevention in Children Aged Under Five in Burkina Faso: A Quasi-Experimental Trial. Sci J Public Health. 2025;13(4):177-188. doi: 10.11648/j.sjph.20251304.12

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  • @article{10.11648/j.sjph.20251304.12,
      author = {Yanogo Pauline Kiswendsida and Sanou Estelle Nadine and Isidore Tiandiogo Traore and Yanogo Chantal and Halidou Tinto},
      title = {Superiority of Three Directly Observed Treatment Compared to One Directly Observed Treatment in the Seasonal Malaria Chemoprevention in Children Aged Under Five in Burkina Faso: A Quasi-Experimental Trial
    },
      journal = {Science Journal of Public Health},
      volume = {13},
      number = {4},
      pages = {177-188},
      doi = {10.11648/j.sjph.20251304.12},
      url = {https://doi.org/10.11648/j.sjph.20251304.12},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.sjph.20251304.12},
      abstract = {The implementation of seasonal malaria chemoprevention (SMC) in Burkina Faso has not achieved its objective of reducing by at least 60% the morbidity associated with malaria in children under 5 years of age. We assessed a new approach of delivery consisting for the community health workers to directly supervise the three doses of the treatment compared to the standard of delivery (only the first dose directly observed treatment). The objective of the study was to compare the superiority of three doses supervised intake of SMC (3DOT) to the supervised intake of the first dose only. Three centers for health and social promotion were randomly selected in the Gaoua health district (3DOT) and 4 in the Boromo health district (1DOT) to receive a monthly four rounds of SMC with Sulfadoxine-pyrimethamine plus Amodiaquine (SP+AQ) in a quasi-experimental cluster randomized trial, before-after with a control group design which included in total 2440 children. The primary endpoint was the reduction in prevalence between each SMC round. The Khi-2 test was used to assess the superiority of 3DOT versus 1DOT. The reduction of malaria prevalence was significantly higher in 3DOT compared to the 1DOT, 68.60% vs 53.00% (p<.0001). The coverage in the 3DOT was significantly lower than that in the 1DOT, 81.39% versus 95.72%; p<0.0001 for optimal coverage. The 3DOT delivery approach of SMC provides better reduction of malaria prevalence than the 1DOT. However, the lower coverage obtained with the 3DOT compared to the 1DOT is a concerning issue to overcome in the perspective of the scale-up of this strategy at large scale.},
     year = {2025}
    }
    

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    T1  - Superiority of Three Directly Observed Treatment Compared to One Directly Observed Treatment in the Seasonal Malaria Chemoprevention in Children Aged Under Five in Burkina Faso: A Quasi-Experimental Trial
    
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    AU  - Sanou Estelle Nadine
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    AU  - Yanogo Chantal
    AU  - Halidou Tinto
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    AB  - The implementation of seasonal malaria chemoprevention (SMC) in Burkina Faso has not achieved its objective of reducing by at least 60% the morbidity associated with malaria in children under 5 years of age. We assessed a new approach of delivery consisting for the community health workers to directly supervise the three doses of the treatment compared to the standard of delivery (only the first dose directly observed treatment). The objective of the study was to compare the superiority of three doses supervised intake of SMC (3DOT) to the supervised intake of the first dose only. Three centers for health and social promotion were randomly selected in the Gaoua health district (3DOT) and 4 in the Boromo health district (1DOT) to receive a monthly four rounds of SMC with Sulfadoxine-pyrimethamine plus Amodiaquine (SP+AQ) in a quasi-experimental cluster randomized trial, before-after with a control group design which included in total 2440 children. The primary endpoint was the reduction in prevalence between each SMC round. The Khi-2 test was used to assess the superiority of 3DOT versus 1DOT. The reduction of malaria prevalence was significantly higher in 3DOT compared to the 1DOT, 68.60% vs 53.00% (p<.0001). The coverage in the 3DOT was significantly lower than that in the 1DOT, 81.39% versus 95.72%; p<0.0001 for optimal coverage. The 3DOT delivery approach of SMC provides better reduction of malaria prevalence than the 1DOT. However, the lower coverage obtained with the 3DOT compared to the 1DOT is a concerning issue to overcome in the perspective of the scale-up of this strategy at large scale.
    VL  - 13
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Author Information
  • Department of Public Health, Health Science Research and Training Unit, Joseph Ki-Zerbo University, Ouagadougou, Burkina Faso. Burkina Field Epidemiology and Laboratory Training Program (BFELTP), Health Science Research and Training Unit, Joseph Ki-Zerbo University, Université Joseph Ki-Zerbo, Ouagadougou, Burkina Faso

  • Burkina Field Epidemiology and Laboratory Training Program (BFELTP), Health Science Research and Training Unit, Joseph Ki-Zerbo University, Université Joseph Ki-Zerbo, Ouagadougou, Burkina Faso

  • Higher Institute of Health Sciences, University Nazi BONI, Bobo-Dioulasso, Burkina Faso

  • Burkina Field Epidemiology and Laboratory Training Program (BFELTP), Health Science Research and Training Unit, Joseph Ki-Zerbo University, Université Joseph Ki-Zerbo, Ouagadougou, Burkina Faso

  • Clinical Research Unit of Nanoro, Institut de Recherche en Sciences de la Santé, Nanoro, Burkina Faso

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