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Implementation of a universal rotavirus vaccination program: comparison of two delivery systems
BACKGROUND: Rotavirus vaccine is recommended for all infants in Canada. To evaluate the logistics of implementing a universal rotavirus vaccination program, we compared the effectiveness of program implementation in jurisdictions with either a physician-administered or public health nurse-administer...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4165993/ https://www.ncbi.nlm.nih.gov/pubmed/25182067 http://dx.doi.org/10.1186/1471-2458-14-908 |
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author | Zelman, Mitchell Sanford, Carolyn Neatby, Anne Halperin, Beth A MacDougall, Donna Rowswell, Corinne Langley, Joanne M Halperin, Scott A |
author_facet | Zelman, Mitchell Sanford, Carolyn Neatby, Anne Halperin, Beth A MacDougall, Donna Rowswell, Corinne Langley, Joanne M Halperin, Scott A |
author_sort | Zelman, Mitchell |
collection | PubMed |
description | BACKGROUND: Rotavirus vaccine is recommended for all infants in Canada. To evaluate the logistics of implementing a universal rotavirus vaccination program, we compared the effectiveness of program implementation in jurisdictions with either a physician-administered or public health nurse-administered program. METHODS: All infants born between October 1, 2010 and September 30, 2012 in Prince Edward Island and Nova Scotia’s Capital District Health Authority were eligible for the vaccination program. A universal rotavirus vaccination program was implemented and delivered in public health clinics in Prince Edward Island and in physicians’ offices in Nova Scotia. RESULTS: Engagement of vaccinators in delivery of the universal vaccination program was more successful in Prince Edward Island than in Nova Scotia. Vaccine coverage rates rose rapidly in Prince Edward Island, exceeding 90% for both doses within 3 months and remaining at those levels over the two-year program. In contrast, coverage rates in Nova Scotia rose more slowly and never exceeded 40% during the two years. Access to coverage data was more timely and accurate in Prince Edward Island than Nova Scotia. CONCLUSION: A universal rotavirus vaccination program delivered through public health clinics achieved more rapid and higher levels of coverage than a program administered through physicians’ offices. TRIAL REGISTRATION: NCT01273077. |
format | Online Article Text |
id | pubmed-4165993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41659932014-09-18 Implementation of a universal rotavirus vaccination program: comparison of two delivery systems Zelman, Mitchell Sanford, Carolyn Neatby, Anne Halperin, Beth A MacDougall, Donna Rowswell, Corinne Langley, Joanne M Halperin, Scott A BMC Public Health Research Article BACKGROUND: Rotavirus vaccine is recommended for all infants in Canada. To evaluate the logistics of implementing a universal rotavirus vaccination program, we compared the effectiveness of program implementation in jurisdictions with either a physician-administered or public health nurse-administered program. METHODS: All infants born between October 1, 2010 and September 30, 2012 in Prince Edward Island and Nova Scotia’s Capital District Health Authority were eligible for the vaccination program. A universal rotavirus vaccination program was implemented and delivered in public health clinics in Prince Edward Island and in physicians’ offices in Nova Scotia. RESULTS: Engagement of vaccinators in delivery of the universal vaccination program was more successful in Prince Edward Island than in Nova Scotia. Vaccine coverage rates rose rapidly in Prince Edward Island, exceeding 90% for both doses within 3 months and remaining at those levels over the two-year program. In contrast, coverage rates in Nova Scotia rose more slowly and never exceeded 40% during the two years. Access to coverage data was more timely and accurate in Prince Edward Island than Nova Scotia. CONCLUSION: A universal rotavirus vaccination program delivered through public health clinics achieved more rapid and higher levels of coverage than a program administered through physicians’ offices. TRIAL REGISTRATION: NCT01273077. BioMed Central 2014-09-02 /pmc/articles/PMC4165993/ /pubmed/25182067 http://dx.doi.org/10.1186/1471-2458-14-908 Text en © Zelman et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Zelman, Mitchell Sanford, Carolyn Neatby, Anne Halperin, Beth A MacDougall, Donna Rowswell, Corinne Langley, Joanne M Halperin, Scott A Implementation of a universal rotavirus vaccination program: comparison of two delivery systems |
title | Implementation of a universal rotavirus vaccination program: comparison of two delivery systems |
title_full | Implementation of a universal rotavirus vaccination program: comparison of two delivery systems |
title_fullStr | Implementation of a universal rotavirus vaccination program: comparison of two delivery systems |
title_full_unstemmed | Implementation of a universal rotavirus vaccination program: comparison of two delivery systems |
title_short | Implementation of a universal rotavirus vaccination program: comparison of two delivery systems |
title_sort | implementation of a universal rotavirus vaccination program: comparison of two delivery systems |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4165993/ https://www.ncbi.nlm.nih.gov/pubmed/25182067 http://dx.doi.org/10.1186/1471-2458-14-908 |
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