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Dynamic transmission modelling to address infant pneumococcal conjugate vaccine schedule modifications in the UK

The 13-valent pneumococcal conjugate vaccine (PCV) has been part of routine immunisation in a 2 + 1 schedule (two primary infant doses and one booster during the second year of life) in the UK since 2010. Recently, the UK's Joint Committee on Vaccination and Immunisation recommended changing to...

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Autores principales: Wasserman, M., Lucas, A., Jones, D., Wilson, M., Hilton, B., Vyse, A., Madhava, H., Brogan, A., Slack, M., Farkouh, R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9506701/
https://www.ncbi.nlm.nih.gov/pubmed/30012224
http://dx.doi.org/10.1017/S095026881800198X
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author Wasserman, M.
Lucas, A.
Jones, D.
Wilson, M.
Hilton, B.
Vyse, A.
Madhava, H.
Brogan, A.
Slack, M.
Farkouh, R.
author_facet Wasserman, M.
Lucas, A.
Jones, D.
Wilson, M.
Hilton, B.
Vyse, A.
Madhava, H.
Brogan, A.
Slack, M.
Farkouh, R.
author_sort Wasserman, M.
collection PubMed
description The 13-valent pneumococcal conjugate vaccine (PCV) has been part of routine immunisation in a 2 + 1 schedule (two primary infant doses and one booster during the second year of life) in the UK since 2010. Recently, the UK's Joint Committee on Vaccination and Immunisation recommended changing to a 1 + 1 schedule while conceding that this will increase disease burden; however, uncertainty remains on how much pneumococcal burden – including invasive pneumococcal disease (IPD) and non-invasive disease – will increase. We built a dynamic transmission model to investigate this question. The model predicted that a 1 + 1 schedule would incur 8777–27 807 additional cases of disease and 241–743 more deaths over 5 years. Serotype 19A caused 55–71% of incremental IPD cases. Scenario analyses showed that booster dose adherence, effectiveness against carriage and waning in a 1 + 1 schedule had the most influence on resurgence of disease. Based on the model assumptions, switching to a 1 + 1 schedule will substantially increase disease burden. The results likely are conservative since they are based on relatively low vaccine-type pneumococcal transmission, a paradigm that has been called into question by data demonstrating an increase of IPD due to several vaccine serotypes during the last surveillance year available.
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spelling pubmed-95067012022-10-07 Dynamic transmission modelling to address infant pneumococcal conjugate vaccine schedule modifications in the UK Wasserman, M. Lucas, A. Jones, D. Wilson, M. Hilton, B. Vyse, A. Madhava, H. Brogan, A. Slack, M. Farkouh, R. Epidemiol Infect Original Paper The 13-valent pneumococcal conjugate vaccine (PCV) has been part of routine immunisation in a 2 + 1 schedule (two primary infant doses and one booster during the second year of life) in the UK since 2010. Recently, the UK's Joint Committee on Vaccination and Immunisation recommended changing to a 1 + 1 schedule while conceding that this will increase disease burden; however, uncertainty remains on how much pneumococcal burden – including invasive pneumococcal disease (IPD) and non-invasive disease – will increase. We built a dynamic transmission model to investigate this question. The model predicted that a 1 + 1 schedule would incur 8777–27 807 additional cases of disease and 241–743 more deaths over 5 years. Serotype 19A caused 55–71% of incremental IPD cases. Scenario analyses showed that booster dose adherence, effectiveness against carriage and waning in a 1 + 1 schedule had the most influence on resurgence of disease. Based on the model assumptions, switching to a 1 + 1 schedule will substantially increase disease burden. The results likely are conservative since they are based on relatively low vaccine-type pneumococcal transmission, a paradigm that has been called into question by data demonstrating an increase of IPD due to several vaccine serotypes during the last surveillance year available. Cambridge University Press 2018-10 2018-07-17 /pmc/articles/PMC9506701/ /pubmed/30012224 http://dx.doi.org/10.1017/S095026881800198X Text en © Cambridge University Press 2018 https://creativecommons.org/licenses/by-nc-sa/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike licence (http://creativecommons.org/licenses/by-nc-sa/4.0/ (https://creativecommons.org/licenses/by-nc-sa/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the same Creative Commons licence is included and the original work is properly cited. The written permission of Cambridge University Press must be obtained for commercial re-use.
spellingShingle Original Paper
Wasserman, M.
Lucas, A.
Jones, D.
Wilson, M.
Hilton, B.
Vyse, A.
Madhava, H.
Brogan, A.
Slack, M.
Farkouh, R.
Dynamic transmission modelling to address infant pneumococcal conjugate vaccine schedule modifications in the UK
title Dynamic transmission modelling to address infant pneumococcal conjugate vaccine schedule modifications in the UK
title_full Dynamic transmission modelling to address infant pneumococcal conjugate vaccine schedule modifications in the UK
title_fullStr Dynamic transmission modelling to address infant pneumococcal conjugate vaccine schedule modifications in the UK
title_full_unstemmed Dynamic transmission modelling to address infant pneumococcal conjugate vaccine schedule modifications in the UK
title_short Dynamic transmission modelling to address infant pneumococcal conjugate vaccine schedule modifications in the UK
title_sort dynamic transmission modelling to address infant pneumococcal conjugate vaccine schedule modifications in the uk
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9506701/
https://www.ncbi.nlm.nih.gov/pubmed/30012224
http://dx.doi.org/10.1017/S095026881800198X
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