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Using non-exceedance probabilities of policy-relevant malaria prevalence thresholds to identify areas of low transmission in Somalia

BACKGROUND: Countries planning malaria elimination must adapt from sustaining universal control to targeted intervention and surveillance. Decisions to make this transition require interpretable information, including malaria parasite survey data. As transmission declines, observed parasite prevalen...

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Autores principales: Giorgi, Emanuele, Osman, Ali Abdirahman, Hassan, Abdikarin Hussein, Ali, Abdi Abdillahi, Ibrahim, Faisa, Amran, Jamal G. H., Noor, Abdisalan M., Snow, Robert W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5819647/
https://www.ncbi.nlm.nih.gov/pubmed/29463264
http://dx.doi.org/10.1186/s12936-018-2238-0
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author Giorgi, Emanuele
Osman, Ali Abdirahman
Hassan, Abdikarin Hussein
Ali, Abdi Abdillahi
Ibrahim, Faisa
Amran, Jamal G. H.
Noor, Abdisalan M.
Snow, Robert W.
author_facet Giorgi, Emanuele
Osman, Ali Abdirahman
Hassan, Abdikarin Hussein
Ali, Abdi Abdillahi
Ibrahim, Faisa
Amran, Jamal G. H.
Noor, Abdisalan M.
Snow, Robert W.
author_sort Giorgi, Emanuele
collection PubMed
description BACKGROUND: Countries planning malaria elimination must adapt from sustaining universal control to targeted intervention and surveillance. Decisions to make this transition require interpretable information, including malaria parasite survey data. As transmission declines, observed parasite prevalence becomes highly heterogeneous with most communities reporting estimates close to zero. Absolute estimates of prevalence become hard to interpret as a measure of transmission intensity and suitable statistical methods are required to handle uncertainty of area-wide predictions that are programmatically relevant. METHODS: A spatio-temporal geostatistical binomial model for Plasmodium falciparum prevalence (PfPR) was developed using data from cross-sectional surveys conducted in Somalia in 2005, 2007–2011 and 2014. The fitted model was then used to generate maps of non-exceedance probabilities, i.e. the predictive probability that the region-wide population-weighted average PfPR for children between 2 and 10 years (PfPR(2–10)) lies below 1 and 5%. A comparison was carried out with the decision-making outcomes from those of standard approaches that ignore uncertainty in prevalence estimates. RESULTS: By 2010, most regions in Somalia were at least 70% likely to be below 5% PfPR(2–10) and, by 2014, 17 regions were below 5% PfPR(2–10) with a probability greater than 90%. Larger uncertainty is observed using a threshold of 1%. By 2011, only two regions were more than 90% likely of being < 1% PfPR(2–10) and, by 2014, only three regions showed such low level of uncertainty. The use of non-exceedance probabilities indicated that there was weak evidence to classify 10 out of the 18 regions as < 1% in 2014, when a greater than 90% non-exceedance probability was required. CONCLUSION: Unlike standard approaches, non-exceedance probabilities of spatially modelled PfPR(2–10) allow to quantify uncertainty of prevalence estimates in relation to policy relevant intervention thresholds, providing programmatically relevant metrics to make decisions on transitioning from sustained malaria control to strategies that encompass methods of malaria elimination. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12936-018-2238-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-58196472018-02-26 Using non-exceedance probabilities of policy-relevant malaria prevalence thresholds to identify areas of low transmission in Somalia Giorgi, Emanuele Osman, Ali Abdirahman Hassan, Abdikarin Hussein Ali, Abdi Abdillahi Ibrahim, Faisa Amran, Jamal G. H. Noor, Abdisalan M. Snow, Robert W. Malar J Research BACKGROUND: Countries planning malaria elimination must adapt from sustaining universal control to targeted intervention and surveillance. Decisions to make this transition require interpretable information, including malaria parasite survey data. As transmission declines, observed parasite prevalence becomes highly heterogeneous with most communities reporting estimates close to zero. Absolute estimates of prevalence become hard to interpret as a measure of transmission intensity and suitable statistical methods are required to handle uncertainty of area-wide predictions that are programmatically relevant. METHODS: A spatio-temporal geostatistical binomial model for Plasmodium falciparum prevalence (PfPR) was developed using data from cross-sectional surveys conducted in Somalia in 2005, 2007–2011 and 2014. The fitted model was then used to generate maps of non-exceedance probabilities, i.e. the predictive probability that the region-wide population-weighted average PfPR for children between 2 and 10 years (PfPR(2–10)) lies below 1 and 5%. A comparison was carried out with the decision-making outcomes from those of standard approaches that ignore uncertainty in prevalence estimates. RESULTS: By 2010, most regions in Somalia were at least 70% likely to be below 5% PfPR(2–10) and, by 2014, 17 regions were below 5% PfPR(2–10) with a probability greater than 90%. Larger uncertainty is observed using a threshold of 1%. By 2011, only two regions were more than 90% likely of being < 1% PfPR(2–10) and, by 2014, only three regions showed such low level of uncertainty. The use of non-exceedance probabilities indicated that there was weak evidence to classify 10 out of the 18 regions as < 1% in 2014, when a greater than 90% non-exceedance probability was required. CONCLUSION: Unlike standard approaches, non-exceedance probabilities of spatially modelled PfPR(2–10) allow to quantify uncertainty of prevalence estimates in relation to policy relevant intervention thresholds, providing programmatically relevant metrics to make decisions on transitioning from sustained malaria control to strategies that encompass methods of malaria elimination. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12936-018-2238-0) contains supplementary material, which is available to authorized users. BioMed Central 2018-02-20 /pmc/articles/PMC5819647/ /pubmed/29463264 http://dx.doi.org/10.1186/s12936-018-2238-0 Text en © The Author(s) 2018 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
Giorgi, Emanuele
Osman, Ali Abdirahman
Hassan, Abdikarin Hussein
Ali, Abdi Abdillahi
Ibrahim, Faisa
Amran, Jamal G. H.
Noor, Abdisalan M.
Snow, Robert W.
Using non-exceedance probabilities of policy-relevant malaria prevalence thresholds to identify areas of low transmission in Somalia
title Using non-exceedance probabilities of policy-relevant malaria prevalence thresholds to identify areas of low transmission in Somalia
title_full Using non-exceedance probabilities of policy-relevant malaria prevalence thresholds to identify areas of low transmission in Somalia
title_fullStr Using non-exceedance probabilities of policy-relevant malaria prevalence thresholds to identify areas of low transmission in Somalia
title_full_unstemmed Using non-exceedance probabilities of policy-relevant malaria prevalence thresholds to identify areas of low transmission in Somalia
title_short Using non-exceedance probabilities of policy-relevant malaria prevalence thresholds to identify areas of low transmission in Somalia
title_sort using non-exceedance probabilities of policy-relevant malaria prevalence thresholds to identify areas of low transmission in somalia
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5819647/
https://www.ncbi.nlm.nih.gov/pubmed/29463264
http://dx.doi.org/10.1186/s12936-018-2238-0
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