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Assessing the benefits of early pandemic influenza vaccine availability: a case study for Ontario, Canada
New vaccine production technologies can significantly shorten the timelines for availability of a strain-specific vaccine in the event of an influenza pandemic. We sought to evaluate the potential benefits of early vaccination in reducing the clinical attack rate (CAR), taking into account the timin...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915538/ https://www.ncbi.nlm.nih.gov/pubmed/29691450 http://dx.doi.org/10.1038/s41598-018-24764-7 |
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author | Champredon, David Laskowski, Marek Charland, Nathalie Moghadas, Seyed M. |
author_facet | Champredon, David Laskowski, Marek Charland, Nathalie Moghadas, Seyed M. |
author_sort | Champredon, David |
collection | PubMed |
description | New vaccine production technologies can significantly shorten the timelines for availability of a strain-specific vaccine in the event of an influenza pandemic. We sought to evaluate the potential benefits of early vaccination in reducing the clinical attack rate (CAR), taking into account the timing and speed of vaccination roll-out. Various scenarios corresponding to the transmissibility of a pandemic strain and vaccine prioritization strategies were simulated using an agent-based model of disease spread in Ontario, the largest Canadian province. We found that the relative reduction of the CAR reached 60% (90%CI: 44–100%) in a best-case scenario, in which the pandemic strain was moderately transmissible, vaccination started 4 weeks before the first imported case, the vaccine administration rate was 4 times higher than its average for seasonal influenza, and the vaccine efficacy was up to 90%. But the relative reductions in the CAR decreased significantly when the vaccination campaign was delayed or the administration rate reduced. In urban settings with similar characteristics to our population study, early availability and high rates of vaccine administration has the potential to substantially reduce the number of influenza cases. Low rates of vaccine administration or uptake can potentially offset the benefits of early vaccination. |
format | Online Article Text |
id | pubmed-5915538 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59155382018-04-30 Assessing the benefits of early pandemic influenza vaccine availability: a case study for Ontario, Canada Champredon, David Laskowski, Marek Charland, Nathalie Moghadas, Seyed M. Sci Rep Article New vaccine production technologies can significantly shorten the timelines for availability of a strain-specific vaccine in the event of an influenza pandemic. We sought to evaluate the potential benefits of early vaccination in reducing the clinical attack rate (CAR), taking into account the timing and speed of vaccination roll-out. Various scenarios corresponding to the transmissibility of a pandemic strain and vaccine prioritization strategies were simulated using an agent-based model of disease spread in Ontario, the largest Canadian province. We found that the relative reduction of the CAR reached 60% (90%CI: 44–100%) in a best-case scenario, in which the pandemic strain was moderately transmissible, vaccination started 4 weeks before the first imported case, the vaccine administration rate was 4 times higher than its average for seasonal influenza, and the vaccine efficacy was up to 90%. But the relative reductions in the CAR decreased significantly when the vaccination campaign was delayed or the administration rate reduced. In urban settings with similar characteristics to our population study, early availability and high rates of vaccine administration has the potential to substantially reduce the number of influenza cases. Low rates of vaccine administration or uptake can potentially offset the benefits of early vaccination. Nature Publishing Group UK 2018-04-24 /pmc/articles/PMC5915538/ /pubmed/29691450 http://dx.doi.org/10.1038/s41598-018-24764-7 Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Champredon, David Laskowski, Marek Charland, Nathalie Moghadas, Seyed M. Assessing the benefits of early pandemic influenza vaccine availability: a case study for Ontario, Canada |
title | Assessing the benefits of early pandemic influenza vaccine availability: a case study for Ontario, Canada |
title_full | Assessing the benefits of early pandemic influenza vaccine availability: a case study for Ontario, Canada |
title_fullStr | Assessing the benefits of early pandemic influenza vaccine availability: a case study for Ontario, Canada |
title_full_unstemmed | Assessing the benefits of early pandemic influenza vaccine availability: a case study for Ontario, Canada |
title_short | Assessing the benefits of early pandemic influenza vaccine availability: a case study for Ontario, Canada |
title_sort | assessing the benefits of early pandemic influenza vaccine availability: a case study for ontario, canada |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915538/ https://www.ncbi.nlm.nih.gov/pubmed/29691450 http://dx.doi.org/10.1038/s41598-018-24764-7 |
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