Supporting elimination of lymphatic filariasis in Samoa by predicting locations of residual infection using machine learning and geostatistics
dc.contributor.author | Mayfield, Helen | |
dc.contributor.author | Sturrock, Hugh | |
dc.contributor.author | Arnold, Benjamin F. | |
dc.contributor.author | Andrade-Pacheco, Ricardo | |
dc.contributor.author | Kearns, Therese | |
dc.contributor.author | Graves, Patricia | |
dc.contributor.author | Naseri, Take | |
dc.contributor.author | Thomsen, Robert | |
dc.contributor.author | Gass, Katherine | |
dc.contributor.author | Lau, Colleen | |
dc.date.accessioned | 2022-10-11T00:51:59Z | |
dc.date.available | 2022-10-11T00:51:59Z | |
dc.date.issued | 2020 | |
dc.date.updated | 2021-11-28T07:22:22Z | |
dc.description.abstract | The global elimination of lymphatic filariasis (LF) is a major focus of the World Health Organization. One key challenge is locating residual infections that can perpetuate the transmission cycle. We show how a targeted sampling strategy using predictions from a geospatial model, combining random forests and geostatistics, can improve the sampling efficiency for identifying locations with high infection prevalence. Predictions were made based on the household locations of infected persons identified from previous surveys, and environmental variables relevant to mosquito density. Results show that targeting sampling using model predictions would have allowed 52% of infections to be identified by sampling just 17.7% of households. The odds ratio for identifying an infected individual in a household at a predicted high risk compared to a predicted low risk location was 10.2 (95% CI 4.2–22.8). This study provides evidence that a ‘one size fits all’ approach is unlikely to yield optimal results when making programmatic decisions based on model predictions. Instead, model assumptions and definitions should be tailored to each situation based on the objective of the surveillance program. When predictions are used in the context of the program objectives, they can result in a dramatic improvement in the efficiency of locating infected individuals. | en_AU |
dc.description.sponsorship | Tis work received fnancial support from the Coalition for Operational Research on Neglected Tropical Diseases, which is funded at Te Task Force for Global Health primarily by the Bill & Melinda Gates Foundation, by the United States Agency for International Development through its Neglected Tropical Diseases Program, and with UK aid from the British people. Colleen Lau was supported by an Australian National Health and Medical Research Council (NHMRC) Fellowship (1109035). | en_AU |
dc.format.mimetype | application/pdf | en_AU |
dc.identifier.issn | 2045-2322 | en_AU |
dc.identifier.uri | http://hdl.handle.net/1885/274427 | |
dc.language.iso | en_AU | en_AU |
dc.provenance | Tis 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. Te 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/. | en_AU |
dc.publisher | Nature Publishing Group | en_AU |
dc.relation | http://purl.org/au-research/grants/nhmrc/1109035 | en_AU |
dc.rights | © The Author(s) 2020 | en_AU |
dc.rights.license | Creative Commons Attribution 4.0 International License | en_AU |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | en_AU |
dc.source | Scientific Reports | en_AU |
dc.title | Supporting elimination of lymphatic filariasis in Samoa by predicting locations of residual infection using machine learning and geostatistics | en_AU |
dc.type | Journal article | en_AU |
dcterms.accessRights | Open Access | en_AU |
local.bibliographicCitation.issue | 1 | en_AU |
local.bibliographicCitation.lastpage | 11 | en_AU |
local.bibliographicCitation.startpage | 1 | en_AU |
local.contributor.affiliation | Mayfield, Helen, College of Health and Medicine, ANU | en_AU |
local.contributor.affiliation | Sturrock, Hugh, University of California | en_AU |
local.contributor.affiliation | Arnold, Benjamin F., University of California | en_AU |
local.contributor.affiliation | Andrade-Pacheco, Ricardo, University of California | en_AU |
local.contributor.affiliation | Kearns, Therese, Charles Darwin University | en_AU |
local.contributor.affiliation | Graves, Patricia, James Cook University | en_AU |
local.contributor.affiliation | Naseri, Take , Ministry of Health, Samoa | en_AU |
local.contributor.affiliation | Thomsen , Robert , Ministry of Health, Samoa | en_AU |
local.contributor.affiliation | Gass , Katherine , Neglected Tropical Disease Support Centre | en_AU |
local.contributor.affiliation | Lau, Colleen, College of Health and Medicine, ANU | en_AU |
local.contributor.authoremail | u5651486@anu.edu.au | en_AU |
local.contributor.authoruid | Mayfield, Helen, u1028048 | en_AU |
local.contributor.authoruid | Lau, Colleen, u5651486 | en_AU |
local.description.notes | Imported from ARIES | en_AU |
local.identifier.absfor | 000000 - Internal ANU use only | en_AU |
local.identifier.ariespublication | a383154xPUB15969 | en_AU |
local.identifier.citationvolume | 10 | en_AU |
local.identifier.doi | 10.1038/s41598-020-77519-8 | en_AU |
local.identifier.scopusID | 2-s2.0-85096622255 | |
local.identifier.uidSubmittedBy | a383154 | en_AU |
local.publisher.url | https://www.nature.com/ | en_AU |
local.type.status | Published Version | en_AU |
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