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Novel approaches to risk stratification to support malaria elimination: an example from Cambodia

BACKGROUND: Accurate malaria stratification is essential for effective targeting of interventions but represents a particular challenge in pre-elimination settings. In these settings transmission is typically sufficiently low and spatially heterogeneous to warrant a need for estimates of malaria ris...

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Autores principales: Cox, Jonathan, Sovannaroth, Siv, Dy Soley, Lek, Ngor, Pengby, Mellor, Steven, Roca-Feltrer, Arantxa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4177243/
https://www.ncbi.nlm.nih.gov/pubmed/25233886
http://dx.doi.org/10.1186/1475-2875-13-371
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author Cox, Jonathan
Sovannaroth, Siv
Dy Soley, Lek
Ngor, Pengby
Mellor, Steven
Roca-Feltrer, Arantxa
author_facet Cox, Jonathan
Sovannaroth, Siv
Dy Soley, Lek
Ngor, Pengby
Mellor, Steven
Roca-Feltrer, Arantxa
author_sort Cox, Jonathan
collection PubMed
description BACKGROUND: Accurate malaria stratification is essential for effective targeting of interventions but represents a particular challenge in pre-elimination settings. In these settings transmission is typically sufficiently low and spatially heterogeneous to warrant a need for estimates of malaria risk at sub-district or village level but is also likely to be sufficiently high to render the type of decision support systems appropriate to the final stages of malaria elimination impractical. In such a scenario it is arguably more feasible to strengthen existing passive malaria surveillance systems so that routinely generated case data can provide an effective basis for stratifying malaria risk. This paper explores the utility of routine malaria surveillance data for the stratification of malaria risk in Cambodia, where the target is malaria elimination by 2025. METHODS: A malaria information system (MIS) was developed to generate timely, routine data on temporal and spatial variations in malaria cases reported through public health facilities and village malaria workers (VMWs). The MIS was implemented across all malaria endemic districts in the country during 2010–11. In 2012 MIS data were extracted and assessed on the basis of coverage and completeness. Village-level incidence estimates for 2011 were generated using predefined data inclusion criteria. RESULTS: In 2011, the MIS covered 681 health facilities and 1,489 VMW villages; the overall completeness of monthly reporting was 82& and 97& for health facilities and VMWs respectively. Using these data it was possible to estimate malaria incidence for 89& of villages covered by the MIS. The resulting stratification highlights the highly heterogeneous nature of malaria transmission in Cambodia and underlines the importance of village-level data for effective targeting of interventions, including VMWs. Challenges associated with implementing the MIS and the implications of these for developing viable and sustainable MIS in Cambodia and elsewhere are discussed. CONCLUSIONS: This study demonstrates the operational feasibility of introducing a system to routinely generate village level malaria case data in Cambodia. Although resulting incidence estimates are subject to various limitations and biases the data provide an objective, repeatable basis for a dynamic system of stratification which is appropriate for guiding the transition between malaria pre-elimination and elimination phases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1475-2875-13-371) contains supplementary material, which is available to authorized users.
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spelling pubmed-41772432014-09-29 Novel approaches to risk stratification to support malaria elimination: an example from Cambodia Cox, Jonathan Sovannaroth, Siv Dy Soley, Lek Ngor, Pengby Mellor, Steven Roca-Feltrer, Arantxa Malar J Research BACKGROUND: Accurate malaria stratification is essential for effective targeting of interventions but represents a particular challenge in pre-elimination settings. In these settings transmission is typically sufficiently low and spatially heterogeneous to warrant a need for estimates of malaria risk at sub-district or village level but is also likely to be sufficiently high to render the type of decision support systems appropriate to the final stages of malaria elimination impractical. In such a scenario it is arguably more feasible to strengthen existing passive malaria surveillance systems so that routinely generated case data can provide an effective basis for stratifying malaria risk. This paper explores the utility of routine malaria surveillance data for the stratification of malaria risk in Cambodia, where the target is malaria elimination by 2025. METHODS: A malaria information system (MIS) was developed to generate timely, routine data on temporal and spatial variations in malaria cases reported through public health facilities and village malaria workers (VMWs). The MIS was implemented across all malaria endemic districts in the country during 2010–11. In 2012 MIS data were extracted and assessed on the basis of coverage and completeness. Village-level incidence estimates for 2011 were generated using predefined data inclusion criteria. RESULTS: In 2011, the MIS covered 681 health facilities and 1,489 VMW villages; the overall completeness of monthly reporting was 82& and 97& for health facilities and VMWs respectively. Using these data it was possible to estimate malaria incidence for 89& of villages covered by the MIS. The resulting stratification highlights the highly heterogeneous nature of malaria transmission in Cambodia and underlines the importance of village-level data for effective targeting of interventions, including VMWs. Challenges associated with implementing the MIS and the implications of these for developing viable and sustainable MIS in Cambodia and elsewhere are discussed. CONCLUSIONS: This study demonstrates the operational feasibility of introducing a system to routinely generate village level malaria case data in Cambodia. Although resulting incidence estimates are subject to various limitations and biases the data provide an objective, repeatable basis for a dynamic system of stratification which is appropriate for guiding the transition between malaria pre-elimination and elimination phases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1475-2875-13-371) contains supplementary material, which is available to authorized users. BioMed Central 2014-09-19 /pmc/articles/PMC4177243/ /pubmed/25233886 http://dx.doi.org/10.1186/1475-2875-13-371 Text en © Cox et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Cox, Jonathan
Sovannaroth, Siv
Dy Soley, Lek
Ngor, Pengby
Mellor, Steven
Roca-Feltrer, Arantxa
Novel approaches to risk stratification to support malaria elimination: an example from Cambodia
title Novel approaches to risk stratification to support malaria elimination: an example from Cambodia
title_full Novel approaches to risk stratification to support malaria elimination: an example from Cambodia
title_fullStr Novel approaches to risk stratification to support malaria elimination: an example from Cambodia
title_full_unstemmed Novel approaches to risk stratification to support malaria elimination: an example from Cambodia
title_short Novel approaches to risk stratification to support malaria elimination: an example from Cambodia
title_sort novel approaches to risk stratification to support malaria elimination: an example from cambodia
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4177243/
https://www.ncbi.nlm.nih.gov/pubmed/25233886
http://dx.doi.org/10.1186/1475-2875-13-371
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