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A universal infant rotavirus vaccine program in two delivery models: Effectiveness and adverse events following immunization

Rotavirus is the most common cause of diarrhea leading to hospitalization in young children. Rotavirus vaccines are available in Canada but have not been introduced in all provinces. In a controlled trial, 2 study sites (Prince Edward Island and the Capital District Health Authority (District 9, Nov...

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Autores principales: Sanford, Carolyn, Langley, Joanne M, Halperin, Scott A, Zelman, Mitchell, Maritime Universal Rotavirus Vaccination Program, MURVP
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4514393/
https://www.ncbi.nlm.nih.gov/pubmed/25746110
http://dx.doi.org/10.1080/21645515.2015.1012028
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author Sanford, Carolyn
Langley, Joanne M
Halperin, Scott A
Zelman, Mitchell
Maritime Universal Rotavirus Vaccination Program, MURVP
author_facet Sanford, Carolyn
Langley, Joanne M
Halperin, Scott A
Zelman, Mitchell
Maritime Universal Rotavirus Vaccination Program, MURVP
author_sort Sanford, Carolyn
collection PubMed
description Rotavirus is the most common cause of diarrhea leading to hospitalization in young children. Rotavirus vaccines are available in Canada but have not been introduced in all provinces. In a controlled trial, 2 study sites (Prince Edward Island and the Capital District Health Authority (District 9, Nova Scotia) introduced universal rotavirus vaccine programs for infants at 2 and 4 months of age beginning 1 December 2010, using public health nurse or general practitioner-delivery models, respectively. A third site (Saint John, NB) served as the non-intervention control setting. Vaccine coverage, rotavirus hospitalizations, intussusception and all-cause diarrhea were monitored. A universal rotavirus vaccine program with >90% coverage was associated with reductions in rotavirus-associated hospitalizations (from a peak of 52.8 hospitalizations/100,000 population to 0 hospitalizations) in infants < 12 months and 1 to < 2 y of age 12 months after program implementation. No apparent reduction occurred in the site with vaccine coverage of < 40%, or in the non-intervention control site. No cases of intussusception were associated with vaccine receipt, and no increase in all-cause diarrhea was observed. A universal infant rotavirus vaccine program with high coverage was associated with reductions in rotavirus and no safety signals; no reduction was observed in settings with low vaccine coverage.
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spelling pubmed-45143932016-02-03 A universal infant rotavirus vaccine program in two delivery models: Effectiveness and adverse events following immunization Sanford, Carolyn Langley, Joanne M Halperin, Scott A Zelman, Mitchell Maritime Universal Rotavirus Vaccination Program, MURVP Hum Vaccin Immunother Research Paper Rotavirus is the most common cause of diarrhea leading to hospitalization in young children. Rotavirus vaccines are available in Canada but have not been introduced in all provinces. In a controlled trial, 2 study sites (Prince Edward Island and the Capital District Health Authority (District 9, Nova Scotia) introduced universal rotavirus vaccine programs for infants at 2 and 4 months of age beginning 1 December 2010, using public health nurse or general practitioner-delivery models, respectively. A third site (Saint John, NB) served as the non-intervention control setting. Vaccine coverage, rotavirus hospitalizations, intussusception and all-cause diarrhea were monitored. A universal rotavirus vaccine program with >90% coverage was associated with reductions in rotavirus-associated hospitalizations (from a peak of 52.8 hospitalizations/100,000 population to 0 hospitalizations) in infants < 12 months and 1 to < 2 y of age 12 months after program implementation. No apparent reduction occurred in the site with vaccine coverage of < 40%, or in the non-intervention control site. No cases of intussusception were associated with vaccine receipt, and no increase in all-cause diarrhea was observed. A universal infant rotavirus vaccine program with high coverage was associated with reductions in rotavirus and no safety signals; no reduction was observed in settings with low vaccine coverage. Taylor & Francis 2015-03-06 /pmc/articles/PMC4514393/ /pubmed/25746110 http://dx.doi.org/10.1080/21645515.2015.1012028 Text en © 2015 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Research Paper
Sanford, Carolyn
Langley, Joanne M
Halperin, Scott A
Zelman, Mitchell
Maritime Universal Rotavirus Vaccination Program, MURVP
A universal infant rotavirus vaccine program in two delivery models: Effectiveness and adverse events following immunization
title A universal infant rotavirus vaccine program in two delivery models: Effectiveness and adverse events following immunization
title_full A universal infant rotavirus vaccine program in two delivery models: Effectiveness and adverse events following immunization
title_fullStr A universal infant rotavirus vaccine program in two delivery models: Effectiveness and adverse events following immunization
title_full_unstemmed A universal infant rotavirus vaccine program in two delivery models: Effectiveness and adverse events following immunization
title_short A universal infant rotavirus vaccine program in two delivery models: Effectiveness and adverse events following immunization
title_sort universal infant rotavirus vaccine program in two delivery models: effectiveness and adverse events following immunization
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4514393/
https://www.ncbi.nlm.nih.gov/pubmed/25746110
http://dx.doi.org/10.1080/21645515.2015.1012028
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