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A non-randomized controlled trial to assess the protective effect of SMC in the context of high parasite resistance in Uganda

BACKGROUND: Until recently, due to widespread prevalence of molecular markers associated with sulfadoxine-pyrimethamine (SP) and amodiaquine (AQ) resistance in east and southern Africa, seasonal malaria chemoprevention (SMC) has not been used at scale in this region. This study assessed the protecti...

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Autores principales: Nuwa, Anthony, Baker, Kevin, Bonnington, Craig, Odongo, Musa, Kyagulanyi, Tonny, Bwanika, John Baptist, Richardson, Sol, Nabakooza, Jane, Achan, Jane, Kajubi, Richard, Odong, David Salandini, Nakirunda, Maureen, Magumba, Godfrey, Beinomugisha, Geofrey, Marasciulo-Rice, Madeleine, Abio, Hilda, Rassi, Christian, Rutazaana, Damian, Rubahika, Denis, Tibenderana, James, Opigo, Jimmy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945593/
https://www.ncbi.nlm.nih.gov/pubmed/36814301
http://dx.doi.org/10.1186/s12936-023-04488-4
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author Nuwa, Anthony
Baker, Kevin
Bonnington, Craig
Odongo, Musa
Kyagulanyi, Tonny
Bwanika, John Baptist
Richardson, Sol
Nabakooza, Jane
Achan, Jane
Kajubi, Richard
Odong, David Salandini
Nakirunda, Maureen
Magumba, Godfrey
Beinomugisha, Geofrey
Marasciulo-Rice, Madeleine
Abio, Hilda
Rassi, Christian
Rutazaana, Damian
Rubahika, Denis
Tibenderana, James
Opigo, Jimmy
author_facet Nuwa, Anthony
Baker, Kevin
Bonnington, Craig
Odongo, Musa
Kyagulanyi, Tonny
Bwanika, John Baptist
Richardson, Sol
Nabakooza, Jane
Achan, Jane
Kajubi, Richard
Odong, David Salandini
Nakirunda, Maureen
Magumba, Godfrey
Beinomugisha, Geofrey
Marasciulo-Rice, Madeleine
Abio, Hilda
Rassi, Christian
Rutazaana, Damian
Rubahika, Denis
Tibenderana, James
Opigo, Jimmy
author_sort Nuwa, Anthony
collection PubMed
description BACKGROUND: Until recently, due to widespread prevalence of molecular markers associated with sulfadoxine-pyrimethamine (SP) and amodiaquine (AQ) resistance in east and southern Africa, seasonal malaria chemoprevention (SMC) has not been used at scale in this region. This study assessed the protective effectiveness of monthly administration of SP + AQ (SPAQ) to children aged 3–59 months in Karamoja sub-region, Uganda, where parasite resistance is assumed to be high and malaria transmission is seasonal. METHODS: A two-arm quasi-experimental, open-label prospective non-randomized control trial (nRCT) was conducted in three districts. In two intervention districts, 85,000 children aged 3–59 months were targeted to receive monthly courses of SMC using SPAQ during the peak transmission season (May to September) 2021. A third district served as a control, where SMC was not implemented. Communities with comparable malaria attack rates were selected from the three districts, and households with at least one SMC-eligible child were purposively selected. A total cohort of 600 children (200 children per district) were selected and followed using passive surveillance for breakthrough confirmed malaria episodes during the five-month peak transmission season. Malaria incidence rate per person-months and number of malaria episodes among children in the two arms were compared. Kaplan–Meier failure estimates were used to compare the probability of a positive malaria test. Other factors that may influence malaria transmission and infection among children in the two arms were also assessed using multivariable cox proportional hazards regression model. RESULTS: The malaria incidence rate was 3.0 and 38.8 per 100 person-months in the intervention and control groups, respectively. In the intervention areas 90.0% (361/400) of children did not experience any malaria episodes during the study period, compared to 15% (29/200) in the control area. The incidence rate ratio was 0.078 (95% CI 0.063–0.096), which corresponds to a protective effectiveness of 92% (95% CI 90.0–94.0) among children in the intervention area. CONCLUSION: SMC using SPAQ provided high protective effect against malaria during the peak transmission season in children aged 3–59 months in the Karamoja sub-region of Uganda.
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spelling pubmed-99455932023-02-23 A non-randomized controlled trial to assess the protective effect of SMC in the context of high parasite resistance in Uganda Nuwa, Anthony Baker, Kevin Bonnington, Craig Odongo, Musa Kyagulanyi, Tonny Bwanika, John Baptist Richardson, Sol Nabakooza, Jane Achan, Jane Kajubi, Richard Odong, David Salandini Nakirunda, Maureen Magumba, Godfrey Beinomugisha, Geofrey Marasciulo-Rice, Madeleine Abio, Hilda Rassi, Christian Rutazaana, Damian Rubahika, Denis Tibenderana, James Opigo, Jimmy Malar J Case Study BACKGROUND: Until recently, due to widespread prevalence of molecular markers associated with sulfadoxine-pyrimethamine (SP) and amodiaquine (AQ) resistance in east and southern Africa, seasonal malaria chemoprevention (SMC) has not been used at scale in this region. This study assessed the protective effectiveness of monthly administration of SP + AQ (SPAQ) to children aged 3–59 months in Karamoja sub-region, Uganda, where parasite resistance is assumed to be high and malaria transmission is seasonal. METHODS: A two-arm quasi-experimental, open-label prospective non-randomized control trial (nRCT) was conducted in three districts. In two intervention districts, 85,000 children aged 3–59 months were targeted to receive monthly courses of SMC using SPAQ during the peak transmission season (May to September) 2021. A third district served as a control, where SMC was not implemented. Communities with comparable malaria attack rates were selected from the three districts, and households with at least one SMC-eligible child were purposively selected. A total cohort of 600 children (200 children per district) were selected and followed using passive surveillance for breakthrough confirmed malaria episodes during the five-month peak transmission season. Malaria incidence rate per person-months and number of malaria episodes among children in the two arms were compared. Kaplan–Meier failure estimates were used to compare the probability of a positive malaria test. Other factors that may influence malaria transmission and infection among children in the two arms were also assessed using multivariable cox proportional hazards regression model. RESULTS: The malaria incidence rate was 3.0 and 38.8 per 100 person-months in the intervention and control groups, respectively. In the intervention areas 90.0% (361/400) of children did not experience any malaria episodes during the study period, compared to 15% (29/200) in the control area. The incidence rate ratio was 0.078 (95% CI 0.063–0.096), which corresponds to a protective effectiveness of 92% (95% CI 90.0–94.0) among children in the intervention area. CONCLUSION: SMC using SPAQ provided high protective effect against malaria during the peak transmission season in children aged 3–59 months in the Karamoja sub-region of Uganda. BioMed Central 2023-02-22 /pmc/articles/PMC9945593/ /pubmed/36814301 http://dx.doi.org/10.1186/s12936-023-04488-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Study
Nuwa, Anthony
Baker, Kevin
Bonnington, Craig
Odongo, Musa
Kyagulanyi, Tonny
Bwanika, John Baptist
Richardson, Sol
Nabakooza, Jane
Achan, Jane
Kajubi, Richard
Odong, David Salandini
Nakirunda, Maureen
Magumba, Godfrey
Beinomugisha, Geofrey
Marasciulo-Rice, Madeleine
Abio, Hilda
Rassi, Christian
Rutazaana, Damian
Rubahika, Denis
Tibenderana, James
Opigo, Jimmy
A non-randomized controlled trial to assess the protective effect of SMC in the context of high parasite resistance in Uganda
title A non-randomized controlled trial to assess the protective effect of SMC in the context of high parasite resistance in Uganda
title_full A non-randomized controlled trial to assess the protective effect of SMC in the context of high parasite resistance in Uganda
title_fullStr A non-randomized controlled trial to assess the protective effect of SMC in the context of high parasite resistance in Uganda
title_full_unstemmed A non-randomized controlled trial to assess the protective effect of SMC in the context of high parasite resistance in Uganda
title_short A non-randomized controlled trial to assess the protective effect of SMC in the context of high parasite resistance in Uganda
title_sort non-randomized controlled trial to assess the protective effect of smc in the context of high parasite resistance in uganda
topic Case Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945593/
https://www.ncbi.nlm.nih.gov/pubmed/36814301
http://dx.doi.org/10.1186/s12936-023-04488-4
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