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Intermittent preventive treatment for malaria among children in a refugee camp in Northern Uganda: lessons learned

Northern Uganda hosts a large population of refugees from South Sudan, and malaria is one of the major health problems in the area. In 2015, intermittent preventive treatment for malaria (IPTc) was implemented in two refugee camps among children aged 6 months to 14 years. Three distributions of dihy...

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Autores principales: Coldiron, Matthew E., Lasry, Estrella, Bouhenia, Malika, Das, Debashish, Okui, Peter, Nyehangane, Dan, Mwanga, Juliet, Langendorf, Celine, Elder, Greg, Salumu, Léon, Grais, Rebecca F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5442684/
https://www.ncbi.nlm.nih.gov/pubmed/28535793
http://dx.doi.org/10.1186/s12936-017-1869-x
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author Coldiron, Matthew E.
Lasry, Estrella
Bouhenia, Malika
Das, Debashish
Okui, Peter
Nyehangane, Dan
Mwanga, Juliet
Langendorf, Celine
Elder, Greg
Salumu, Léon
Grais, Rebecca F.
author_facet Coldiron, Matthew E.
Lasry, Estrella
Bouhenia, Malika
Das, Debashish
Okui, Peter
Nyehangane, Dan
Mwanga, Juliet
Langendorf, Celine
Elder, Greg
Salumu, Léon
Grais, Rebecca F.
author_sort Coldiron, Matthew E.
collection PubMed
description Northern Uganda hosts a large population of refugees from South Sudan, and malaria is one of the major health problems in the area. In 2015, intermittent preventive treatment for malaria (IPTc) was implemented in two refugee camps among children aged 6 months to 14 years. Three distributions of dihydroartemisinin–piperaquine (DP) were conducted at 8-week intervals. The first dose was directly administered at IPTc distribution sites and the second and third doses were given to caregivers to administer at home. A multi-faceted evaluation was implemented, including coverage surveys, malaria prevalence surveys, reinforced surveillance, and pharmacovigilance. Programme coverage exceeded 90% during all three distributions with a total of 40,611 participants. Compared to same period during the previous year (only available data), the incidence of malaria in the target populations was reduced (IRR 0.73, 95% CI 0.69–0.77 among children under 5 years old; IRR 0.70, 95% CI 0.67–0.72 among children aged 5–14 years). Among those not targeted for intervention, the incidence between the 2 years increased (IRR 1.49, 95% CI 1.42–1.56). Cross-sectional surveys showed a prevalence of parasitaemia (microscopy or PCR) of 12.9–16.4% (95% CI 12.6–19.3) during the intervention, with the highest prevalence among children aged 5–14 years, but with a large increase 8 weeks after the final distribution. A total of 57 adverse events were reported during the intervention period, including one severe adverse event (death from varicella). Adverse events were of mild to moderate severity, and were mainly dermatologic and gastrointestinal. This is the first documentation of an IPTc programme in a refugee camp. The positive impact of DP on the incidence of malaria, together with its favourable safety profile, should lead to further use of IPTc in similar settings. Expanding coverage groups and decreasing intervals between distributions might provide more benefit, but would need to be balanced with the operational implications of a broader, more frequent distribution schedule.
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spelling pubmed-54426842017-05-25 Intermittent preventive treatment for malaria among children in a refugee camp in Northern Uganda: lessons learned Coldiron, Matthew E. Lasry, Estrella Bouhenia, Malika Das, Debashish Okui, Peter Nyehangane, Dan Mwanga, Juliet Langendorf, Celine Elder, Greg Salumu, Léon Grais, Rebecca F. Malar J Case Study Northern Uganda hosts a large population of refugees from South Sudan, and malaria is one of the major health problems in the area. In 2015, intermittent preventive treatment for malaria (IPTc) was implemented in two refugee camps among children aged 6 months to 14 years. Three distributions of dihydroartemisinin–piperaquine (DP) were conducted at 8-week intervals. The first dose was directly administered at IPTc distribution sites and the second and third doses were given to caregivers to administer at home. A multi-faceted evaluation was implemented, including coverage surveys, malaria prevalence surveys, reinforced surveillance, and pharmacovigilance. Programme coverage exceeded 90% during all three distributions with a total of 40,611 participants. Compared to same period during the previous year (only available data), the incidence of malaria in the target populations was reduced (IRR 0.73, 95% CI 0.69–0.77 among children under 5 years old; IRR 0.70, 95% CI 0.67–0.72 among children aged 5–14 years). Among those not targeted for intervention, the incidence between the 2 years increased (IRR 1.49, 95% CI 1.42–1.56). Cross-sectional surveys showed a prevalence of parasitaemia (microscopy or PCR) of 12.9–16.4% (95% CI 12.6–19.3) during the intervention, with the highest prevalence among children aged 5–14 years, but with a large increase 8 weeks after the final distribution. A total of 57 adverse events were reported during the intervention period, including one severe adverse event (death from varicella). Adverse events were of mild to moderate severity, and were mainly dermatologic and gastrointestinal. This is the first documentation of an IPTc programme in a refugee camp. The positive impact of DP on the incidence of malaria, together with its favourable safety profile, should lead to further use of IPTc in similar settings. Expanding coverage groups and decreasing intervals between distributions might provide more benefit, but would need to be balanced with the operational implications of a broader, more frequent distribution schedule. BioMed Central 2017-05-23 /pmc/articles/PMC5442684/ /pubmed/28535793 http://dx.doi.org/10.1186/s12936-017-1869-x Text en © The Author(s) 2017 Open AccessThis article is 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, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Study
Coldiron, Matthew E.
Lasry, Estrella
Bouhenia, Malika
Das, Debashish
Okui, Peter
Nyehangane, Dan
Mwanga, Juliet
Langendorf, Celine
Elder, Greg
Salumu, Léon
Grais, Rebecca F.
Intermittent preventive treatment for malaria among children in a refugee camp in Northern Uganda: lessons learned
title Intermittent preventive treatment for malaria among children in a refugee camp in Northern Uganda: lessons learned
title_full Intermittent preventive treatment for malaria among children in a refugee camp in Northern Uganda: lessons learned
title_fullStr Intermittent preventive treatment for malaria among children in a refugee camp in Northern Uganda: lessons learned
title_full_unstemmed Intermittent preventive treatment for malaria among children in a refugee camp in Northern Uganda: lessons learned
title_short Intermittent preventive treatment for malaria among children in a refugee camp in Northern Uganda: lessons learned
title_sort intermittent preventive treatment for malaria among children in a refugee camp in northern uganda: lessons learned
topic Case Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5442684/
https://www.ncbi.nlm.nih.gov/pubmed/28535793
http://dx.doi.org/10.1186/s12936-017-1869-x
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