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Screening Strategies for a Sustainable Endpoint for Gambiense Sleeping Sickness

BACKGROUND: Gambiense human African trypanosomiasis ([gHAT] sleeping sickness) is a vector-borne disease that is typically fatal without treatment. Intensified, mainly medical-based, interventions in endemic areas have reduced the occurrence of gHAT to historically low levels. However, persistent re...

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Autores principales: Castaño, M Soledad, Aliee, Maryam, Mwamba Miaka, Erick, Keeling, Matt J, Chitnis, Nakul, Rock, Kat S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7289553/
https://www.ncbi.nlm.nih.gov/pubmed/31876949
http://dx.doi.org/10.1093/infdis/jiz588
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author Castaño, M Soledad
Aliee, Maryam
Mwamba Miaka, Erick
Keeling, Matt J
Chitnis, Nakul
Rock, Kat S
author_facet Castaño, M Soledad
Aliee, Maryam
Mwamba Miaka, Erick
Keeling, Matt J
Chitnis, Nakul
Rock, Kat S
author_sort Castaño, M Soledad
collection PubMed
description BACKGROUND: Gambiense human African trypanosomiasis ([gHAT] sleeping sickness) is a vector-borne disease that is typically fatal without treatment. Intensified, mainly medical-based, interventions in endemic areas have reduced the occurrence of gHAT to historically low levels. However, persistent regions, primarily in the Democratic Republic of Congo (DRC), remain a challenge to achieving the World Health Organization’s goal of global elimination of transmission (EOT). METHODS: We used stochastic models of gHAT transmission fitted to DRC case data and explored patterns of regional reporting and extinction. The time to EOT at a health zone scale (~100 000 people) and how an absence of reported cases informs about EOT was quantified. RESULTS: Regional epidemiology and level of active screening (AS) both influenced the predicted time to EOT. Different AS cessation criteria had similar expected infection dynamics, and recrudescence of infection was unlikely. However, whether EOT has been achieved when AS ends is critically dependent on the stopping criteria. Two or three consecutive years of no detected cases provided greater confidence of EOT compared with a single year (~66%–75% and ~82%–84% probability of EOT, respectively, compared with 31%–51%). CONCLUSIONS: Multiple years of AS without case detections is a valuable measure to assess the likelihood that the EOT target has been met locally.
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spelling pubmed-72895532020-06-16 Screening Strategies for a Sustainable Endpoint for Gambiense Sleeping Sickness Castaño, M Soledad Aliee, Maryam Mwamba Miaka, Erick Keeling, Matt J Chitnis, Nakul Rock, Kat S J Infect Dis Supplement Articles BACKGROUND: Gambiense human African trypanosomiasis ([gHAT] sleeping sickness) is a vector-borne disease that is typically fatal without treatment. Intensified, mainly medical-based, interventions in endemic areas have reduced the occurrence of gHAT to historically low levels. However, persistent regions, primarily in the Democratic Republic of Congo (DRC), remain a challenge to achieving the World Health Organization’s goal of global elimination of transmission (EOT). METHODS: We used stochastic models of gHAT transmission fitted to DRC case data and explored patterns of regional reporting and extinction. The time to EOT at a health zone scale (~100 000 people) and how an absence of reported cases informs about EOT was quantified. RESULTS: Regional epidemiology and level of active screening (AS) both influenced the predicted time to EOT. Different AS cessation criteria had similar expected infection dynamics, and recrudescence of infection was unlikely. However, whether EOT has been achieved when AS ends is critically dependent on the stopping criteria. Two or three consecutive years of no detected cases provided greater confidence of EOT compared with a single year (~66%–75% and ~82%–84% probability of EOT, respectively, compared with 31%–51%). CONCLUSIONS: Multiple years of AS without case detections is a valuable measure to assess the likelihood that the EOT target has been met locally. Oxford University Press 2020-06-15 2019-12-26 /pmc/articles/PMC7289553/ /pubmed/31876949 http://dx.doi.org/10.1093/infdis/jiz588 Text en © The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America. http://creativecommons.org/licenses/by/4.0/ 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Supplement Articles
Castaño, M Soledad
Aliee, Maryam
Mwamba Miaka, Erick
Keeling, Matt J
Chitnis, Nakul
Rock, Kat S
Screening Strategies for a Sustainable Endpoint for Gambiense Sleeping Sickness
title Screening Strategies for a Sustainable Endpoint for Gambiense Sleeping Sickness
title_full Screening Strategies for a Sustainable Endpoint for Gambiense Sleeping Sickness
title_fullStr Screening Strategies for a Sustainable Endpoint for Gambiense Sleeping Sickness
title_full_unstemmed Screening Strategies for a Sustainable Endpoint for Gambiense Sleeping Sickness
title_short Screening Strategies for a Sustainable Endpoint for Gambiense Sleeping Sickness
title_sort screening strategies for a sustainable endpoint for gambiense sleeping sickness
topic Supplement Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7289553/
https://www.ncbi.nlm.nih.gov/pubmed/31876949
http://dx.doi.org/10.1093/infdis/jiz588
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