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Optimizing one-dose and two-dose cholera vaccine allocation in outbreak settings: A modeling study
BACKGROUND: A global stockpile of oral cholera vaccine (OCV) was established in 2013 for use in outbreak response and are licensed as two-dose regimens. Vaccine availability, however, remains limited. Previous studies have found that a single dose of OCV may provide substantial protection against ch...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060364/ https://www.ncbi.nlm.nih.gov/pubmed/35442958 http://dx.doi.org/10.1371/journal.pntd.0010358 |
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author | Leung, Tiffany Eaton, Julia Matrajt, Laura |
author_facet | Leung, Tiffany Eaton, Julia Matrajt, Laura |
author_sort | Leung, Tiffany |
collection | PubMed |
description | BACKGROUND: A global stockpile of oral cholera vaccine (OCV) was established in 2013 for use in outbreak response and are licensed as two-dose regimens. Vaccine availability, however, remains limited. Previous studies have found that a single dose of OCV may provide substantial protection against cholera. METHODS: Using a mathematical model with two age groups paired with optimization algorithms, we determine the optimal vaccination strategy with one and two doses of vaccine to minimize cumulative overall infections, symptomatic infections, and deaths. We explore counterfactual vaccination scenarios in three distinct settings: Maela, the largest refugee camp in Thailand, with high in- and out-migration; N’Djamena, Chad, a densely populated region; and Haiti, where departments are connected by rivers and roads. RESULTS: Over the short term under limited vaccine supply, the optimal strategies for all objectives prioritize one dose to the older age group (over five years old), irrespective of setting and level of vaccination coverage. As more vaccine becomes available, it is optimal to administer a second dose for long-term protection. With enough vaccine to cover the whole population with one dose, the optimal strategies can avert up to 30% to 90% of deaths and 36% to 92% of symptomatic infections across the three settings over one year. The one-dose optimal strategies can avert 1.2 to 1.8 times as many cases and deaths compared to the standard two-dose strategy. CONCLUSIONS: In an outbreak setting, speedy vaccination campaigns with a single dose of OCV is likely to avert more cases and deaths than a two-dose pro-rata campaign under a limited vaccine supply. |
format | Online Article Text |
id | pubmed-9060364 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-90603642022-05-03 Optimizing one-dose and two-dose cholera vaccine allocation in outbreak settings: A modeling study Leung, Tiffany Eaton, Julia Matrajt, Laura PLoS Negl Trop Dis Research Article BACKGROUND: A global stockpile of oral cholera vaccine (OCV) was established in 2013 for use in outbreak response and are licensed as two-dose regimens. Vaccine availability, however, remains limited. Previous studies have found that a single dose of OCV may provide substantial protection against cholera. METHODS: Using a mathematical model with two age groups paired with optimization algorithms, we determine the optimal vaccination strategy with one and two doses of vaccine to minimize cumulative overall infections, symptomatic infections, and deaths. We explore counterfactual vaccination scenarios in three distinct settings: Maela, the largest refugee camp in Thailand, with high in- and out-migration; N’Djamena, Chad, a densely populated region; and Haiti, where departments are connected by rivers and roads. RESULTS: Over the short term under limited vaccine supply, the optimal strategies for all objectives prioritize one dose to the older age group (over five years old), irrespective of setting and level of vaccination coverage. As more vaccine becomes available, it is optimal to administer a second dose for long-term protection. With enough vaccine to cover the whole population with one dose, the optimal strategies can avert up to 30% to 90% of deaths and 36% to 92% of symptomatic infections across the three settings over one year. The one-dose optimal strategies can avert 1.2 to 1.8 times as many cases and deaths compared to the standard two-dose strategy. CONCLUSIONS: In an outbreak setting, speedy vaccination campaigns with a single dose of OCV is likely to avert more cases and deaths than a two-dose pro-rata campaign under a limited vaccine supply. Public Library of Science 2022-04-20 /pmc/articles/PMC9060364/ /pubmed/35442958 http://dx.doi.org/10.1371/journal.pntd.0010358 Text en © 2022 Leung et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Leung, Tiffany Eaton, Julia Matrajt, Laura Optimizing one-dose and two-dose cholera vaccine allocation in outbreak settings: A modeling study |
title | Optimizing one-dose and two-dose cholera vaccine allocation in outbreak settings: A modeling study |
title_full | Optimizing one-dose and two-dose cholera vaccine allocation in outbreak settings: A modeling study |
title_fullStr | Optimizing one-dose and two-dose cholera vaccine allocation in outbreak settings: A modeling study |
title_full_unstemmed | Optimizing one-dose and two-dose cholera vaccine allocation in outbreak settings: A modeling study |
title_short | Optimizing one-dose and two-dose cholera vaccine allocation in outbreak settings: A modeling study |
title_sort | optimizing one-dose and two-dose cholera vaccine allocation in outbreak settings: a modeling study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060364/ https://www.ncbi.nlm.nih.gov/pubmed/35442958 http://dx.doi.org/10.1371/journal.pntd.0010358 |
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