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Malaria risk in young male travellers but local transmission persists: a case–control study in low transmission Namibia
BACKGROUND: A key component of malaria elimination campaigns is the identification and targeting of high risk populations. To characterize high risk populations in north central Namibia, a prospective health facility-based case–control study was conducted from December 2012–July 2014. Cases (n = 107...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5303241/ https://www.ncbi.nlm.nih.gov/pubmed/28187770 http://dx.doi.org/10.1186/s12936-017-1719-x |
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author | Smith, Jennifer L. Auala, Joyce Haindongo, Erastus Uusiku, Petrina Gosling, Roly Kleinschmidt, Immo Mumbengegwi, Davis Sturrock, Hugh J. W. |
author_facet | Smith, Jennifer L. Auala, Joyce Haindongo, Erastus Uusiku, Petrina Gosling, Roly Kleinschmidt, Immo Mumbengegwi, Davis Sturrock, Hugh J. W. |
author_sort | Smith, Jennifer L. |
collection | PubMed |
description | BACKGROUND: A key component of malaria elimination campaigns is the identification and targeting of high risk populations. To characterize high risk populations in north central Namibia, a prospective health facility-based case–control study was conducted from December 2012–July 2014. Cases (n = 107) were all patients presenting to any of the 46 health clinics located in the study districts with a confirmed Plasmodium infection by multi-species rapid diagnostic test (RDT). Population controls (n = 679) for each district were RDT negative individuals residing within a household that was randomly selected from a census listing using a two-stage sampling procedure. Demographic, travel, socio-economic, behavioural, climate and vegetation data were also collected. Spatial patterns of malaria risk were analysed. Multivariate logistic regression was used to identify risk factors for malaria. RESULTS: Malaria risk was observed to cluster along the border with Angola, and travel patterns among cases were comparatively restricted to northern Namibia and Angola. Travel to Angola was associated with excessive risk of malaria in males (OR 43.58 95% CI 2.12–896), but there was no corresponding risk associated with travel by females. This is the first study to reveal that gender can modify the effect of travel on risk of malaria. Amongst non-travellers, male gender was also associated with a higher risk of malaria compared with females (OR 1.95 95% CI 1.25–3.04). Other strong risk factors were sleeping away from the household the previous night, lower socioeconomic status, living in an area with moderate vegetation around their house, experiencing moderate rainfall in the month prior to diagnosis and living <15 km from the Angolan border. CONCLUSIONS: These findings highlight the critical need to target malaria interventions to young male travellers, who have a disproportionate risk of malaria in northern Namibia, to coordinate cross-border regional malaria prevention initiatives and to scale up coverage of prevention measures such as indoor residual spraying and long-lasting insecticide nets in high risk areas if malaria elimination is to be realized. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12936-017-1719-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5303241 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53032412017-02-15 Malaria risk in young male travellers but local transmission persists: a case–control study in low transmission Namibia Smith, Jennifer L. Auala, Joyce Haindongo, Erastus Uusiku, Petrina Gosling, Roly Kleinschmidt, Immo Mumbengegwi, Davis Sturrock, Hugh J. W. Malar J Research BACKGROUND: A key component of malaria elimination campaigns is the identification and targeting of high risk populations. To characterize high risk populations in north central Namibia, a prospective health facility-based case–control study was conducted from December 2012–July 2014. Cases (n = 107) were all patients presenting to any of the 46 health clinics located in the study districts with a confirmed Plasmodium infection by multi-species rapid diagnostic test (RDT). Population controls (n = 679) for each district were RDT negative individuals residing within a household that was randomly selected from a census listing using a two-stage sampling procedure. Demographic, travel, socio-economic, behavioural, climate and vegetation data were also collected. Spatial patterns of malaria risk were analysed. Multivariate logistic regression was used to identify risk factors for malaria. RESULTS: Malaria risk was observed to cluster along the border with Angola, and travel patterns among cases were comparatively restricted to northern Namibia and Angola. Travel to Angola was associated with excessive risk of malaria in males (OR 43.58 95% CI 2.12–896), but there was no corresponding risk associated with travel by females. This is the first study to reveal that gender can modify the effect of travel on risk of malaria. Amongst non-travellers, male gender was also associated with a higher risk of malaria compared with females (OR 1.95 95% CI 1.25–3.04). Other strong risk factors were sleeping away from the household the previous night, lower socioeconomic status, living in an area with moderate vegetation around their house, experiencing moderate rainfall in the month prior to diagnosis and living <15 km from the Angolan border. CONCLUSIONS: These findings highlight the critical need to target malaria interventions to young male travellers, who have a disproportionate risk of malaria in northern Namibia, to coordinate cross-border regional malaria prevention initiatives and to scale up coverage of prevention measures such as indoor residual spraying and long-lasting insecticide nets in high risk areas if malaria elimination is to be realized. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12936-017-1719-x) contains supplementary material, which is available to authorized users. BioMed Central 2017-02-10 /pmc/articles/PMC5303241/ /pubmed/28187770 http://dx.doi.org/10.1186/s12936-017-1719-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 | Research Smith, Jennifer L. Auala, Joyce Haindongo, Erastus Uusiku, Petrina Gosling, Roly Kleinschmidt, Immo Mumbengegwi, Davis Sturrock, Hugh J. W. Malaria risk in young male travellers but local transmission persists: a case–control study in low transmission Namibia |
title | Malaria risk in young male travellers but local transmission persists: a case–control study in low transmission Namibia |
title_full | Malaria risk in young male travellers but local transmission persists: a case–control study in low transmission Namibia |
title_fullStr | Malaria risk in young male travellers but local transmission persists: a case–control study in low transmission Namibia |
title_full_unstemmed | Malaria risk in young male travellers but local transmission persists: a case–control study in low transmission Namibia |
title_short | Malaria risk in young male travellers but local transmission persists: a case–control study in low transmission Namibia |
title_sort | malaria risk in young male travellers but local transmission persists: a case–control study in low transmission namibia |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5303241/ https://www.ncbi.nlm.nih.gov/pubmed/28187770 http://dx.doi.org/10.1186/s12936-017-1719-x |
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