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Balancing Evidence and Uncertainty when Considering Rubella Vaccine Introduction

BACKGROUND: Despite a safe and effective vaccine, rubella vaccination programs with inadequate coverage can raise the average age of rubella infection; thereby increasing rubella cases among pregnant women and the resulting congenital rubella syndrome (CRS) in their newborns. The vaccination coverag...

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Autores principales: Lessler, Justin, Metcalf, C. Jessica E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3702572/
https://www.ncbi.nlm.nih.gov/pubmed/23861777
http://dx.doi.org/10.1371/journal.pone.0067639
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author Lessler, Justin
Metcalf, C. Jessica E.
author_facet Lessler, Justin
Metcalf, C. Jessica E.
author_sort Lessler, Justin
collection PubMed
description BACKGROUND: Despite a safe and effective vaccine, rubella vaccination programs with inadequate coverage can raise the average age of rubella infection; thereby increasing rubella cases among pregnant women and the resulting congenital rubella syndrome (CRS) in their newborns. The vaccination coverage necessary to reduce CRS depends on the birthrate in a country and the reproductive number, R(0), a measure of how efficiently a disease transmits. While the birthrate within a country can be known with some accuracy, R(0) varies between settings and can be difficult to measure. Here we aim to provide guidance on the safe introduction of rubella vaccine into countries in the face of substantial uncertainty in R(0). METHODS: We estimated the distribution of R(0) in African countries based on the age distribution of rubella infection using Bayesian hierarchical models. We developed an age specific model of rubella transmission to predict the level of R(0) that would result in an increase in CRS burden for specific birth rates and coverage levels. Combining these results, we summarize the safety of introducing rubella vaccine across demographic and coverage contexts. FINDINGS: The median R(0) of rubella in the African region is 5.2, with 90% of countries expected to have an R(0) between 4.0 and 6.7. Overall, we predict that countries maintaining routine vaccination coverage of 80% or higher are can be confident in seeing a reduction in CRS over a 30 year time horizon. CONCLUSIONS: Under realistic assumptions about human contact, our results suggest that even in low birth rate settings high vaccine coverage must be maintained to avoid an increase in CRS. These results lend further support to the WHO recommendation that countries reach 80% coverage for measles vaccine before introducing rubella vaccination, and highlight the importance of maintaining high levels of vaccination coverage once the vaccine is introduced.
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spelling pubmed-37025722013-07-16 Balancing Evidence and Uncertainty when Considering Rubella Vaccine Introduction Lessler, Justin Metcalf, C. Jessica E. PLoS One Research Article BACKGROUND: Despite a safe and effective vaccine, rubella vaccination programs with inadequate coverage can raise the average age of rubella infection; thereby increasing rubella cases among pregnant women and the resulting congenital rubella syndrome (CRS) in their newborns. The vaccination coverage necessary to reduce CRS depends on the birthrate in a country and the reproductive number, R(0), a measure of how efficiently a disease transmits. While the birthrate within a country can be known with some accuracy, R(0) varies between settings and can be difficult to measure. Here we aim to provide guidance on the safe introduction of rubella vaccine into countries in the face of substantial uncertainty in R(0). METHODS: We estimated the distribution of R(0) in African countries based on the age distribution of rubella infection using Bayesian hierarchical models. We developed an age specific model of rubella transmission to predict the level of R(0) that would result in an increase in CRS burden for specific birth rates and coverage levels. Combining these results, we summarize the safety of introducing rubella vaccine across demographic and coverage contexts. FINDINGS: The median R(0) of rubella in the African region is 5.2, with 90% of countries expected to have an R(0) between 4.0 and 6.7. Overall, we predict that countries maintaining routine vaccination coverage of 80% or higher are can be confident in seeing a reduction in CRS over a 30 year time horizon. CONCLUSIONS: Under realistic assumptions about human contact, our results suggest that even in low birth rate settings high vaccine coverage must be maintained to avoid an increase in CRS. These results lend further support to the WHO recommendation that countries reach 80% coverage for measles vaccine before introducing rubella vaccination, and highlight the importance of maintaining high levels of vaccination coverage once the vaccine is introduced. Public Library of Science 2013-07-05 /pmc/articles/PMC3702572/ /pubmed/23861777 http://dx.doi.org/10.1371/journal.pone.0067639 Text en © 2013 Lessler, Metcalf http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lessler, Justin
Metcalf, C. Jessica E.
Balancing Evidence and Uncertainty when Considering Rubella Vaccine Introduction
title Balancing Evidence and Uncertainty when Considering Rubella Vaccine Introduction
title_full Balancing Evidence and Uncertainty when Considering Rubella Vaccine Introduction
title_fullStr Balancing Evidence and Uncertainty when Considering Rubella Vaccine Introduction
title_full_unstemmed Balancing Evidence and Uncertainty when Considering Rubella Vaccine Introduction
title_short Balancing Evidence and Uncertainty when Considering Rubella Vaccine Introduction
title_sort balancing evidence and uncertainty when considering rubella vaccine introduction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3702572/
https://www.ncbi.nlm.nih.gov/pubmed/23861777
http://dx.doi.org/10.1371/journal.pone.0067639
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