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Hepatitis B vaccination timing: results from demographic health surveys in 47 countries

OBJECTIVE: To examine the impact of hepatitis B vaccination schedules and types of vaccines on hepatitis B vaccination timing. METHODS: We used data for 211 643 children from demographic and health surveys in 47 low- and middle-income countries (median study year 2012). Data were from vaccination ca...

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Autores principales: Schweitzer, Aparna, Akmatov, Manas K, Krause, Gérard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: World Health Organization 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5328113/
https://www.ncbi.nlm.nih.gov/pubmed/28250533
http://dx.doi.org/10.2471/BLT.16.178822
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author Schweitzer, Aparna
Akmatov, Manas K
Krause, Gérard
author_facet Schweitzer, Aparna
Akmatov, Manas K
Krause, Gérard
author_sort Schweitzer, Aparna
collection PubMed
description OBJECTIVE: To examine the impact of hepatitis B vaccination schedules and types of vaccines on hepatitis B vaccination timing. METHODS: We used data for 211 643 children from demographic and health surveys in 47 low- and middle-income countries (median study year 2012). Data were from vaccination cards and maternal interviews. We grouped countries according to the vaccination schedule and type of vaccine used (monovalent or combination). For each country, we calculated hepatitis B vaccination coverage and timely receipt of vaccine doses. We used multivariable logistic regression models to study the effect of vaccination schedules and types on vaccination delay. FINDINGS: Substantial delays in vaccination were observed even in countries with fairly high coverage of all doses. Median delay was 1.0 week (interquartile range, IQR: 0.3 to 3.6) for the first dose (n = 108 626 children) and 3.7 weeks (IQR: 1.4 to 9.3) for the third dose (n = 101  542). We observed a tendency of lower odds of delays in vaccination schedules starting at 6 and at 9 weeks of age. For the first vaccine dose, we recorded lower odds of delays for combination vaccines than for monovalent vaccines (adjusted odds ratio, aOR: 0.76, 95% confidence interval, CI: 0.71 to 0.81). CONCLUSION: Wide variations in hepatitis B vaccination coverage and adherence to vaccination schedules across countries underscore the continued need to strengthen national immunization systems. Timely initiation of the vaccination process might lead to timely receipt of successive doses and improved overall coverage. We suggest incorporating vaccination timing as a performance indicator of vaccination programmes to complement coverage metrics.
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spelling pubmed-53281132017-03-02 Hepatitis B vaccination timing: results from demographic health surveys in 47 countries Schweitzer, Aparna Akmatov, Manas K Krause, Gérard Bull World Health Organ Research OBJECTIVE: To examine the impact of hepatitis B vaccination schedules and types of vaccines on hepatitis B vaccination timing. METHODS: We used data for 211 643 children from demographic and health surveys in 47 low- and middle-income countries (median study year 2012). Data were from vaccination cards and maternal interviews. We grouped countries according to the vaccination schedule and type of vaccine used (monovalent or combination). For each country, we calculated hepatitis B vaccination coverage and timely receipt of vaccine doses. We used multivariable logistic regression models to study the effect of vaccination schedules and types on vaccination delay. FINDINGS: Substantial delays in vaccination were observed even in countries with fairly high coverage of all doses. Median delay was 1.0 week (interquartile range, IQR: 0.3 to 3.6) for the first dose (n = 108 626 children) and 3.7 weeks (IQR: 1.4 to 9.3) for the third dose (n = 101  542). We observed a tendency of lower odds of delays in vaccination schedules starting at 6 and at 9 weeks of age. For the first vaccine dose, we recorded lower odds of delays for combination vaccines than for monovalent vaccines (adjusted odds ratio, aOR: 0.76, 95% confidence interval, CI: 0.71 to 0.81). CONCLUSION: Wide variations in hepatitis B vaccination coverage and adherence to vaccination schedules across countries underscore the continued need to strengthen national immunization systems. Timely initiation of the vaccination process might lead to timely receipt of successive doses and improved overall coverage. We suggest incorporating vaccination timing as a performance indicator of vaccination programmes to complement coverage metrics. World Health Organization 2017-03-01 2017-01-26 /pmc/articles/PMC5328113/ /pubmed/28250533 http://dx.doi.org/10.2471/BLT.16.178822 Text en (c) 2017 The authors; licensee World Health Organization. This is an open access article distributed under the terms of the Creative Commons Attribution IGO License (http://creativecommons.org/licenses/by/3.0/igo/legalcode), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. In any reproduction of this article there should not be any suggestion that WHO or this article endorse any specific organization or products. The use of the WHO logo is not permitted. This notice should be preserved along with the article's original URL.
spellingShingle Research
Schweitzer, Aparna
Akmatov, Manas K
Krause, Gérard
Hepatitis B vaccination timing: results from demographic health surveys in 47 countries
title Hepatitis B vaccination timing: results from demographic health surveys in 47 countries
title_full Hepatitis B vaccination timing: results from demographic health surveys in 47 countries
title_fullStr Hepatitis B vaccination timing: results from demographic health surveys in 47 countries
title_full_unstemmed Hepatitis B vaccination timing: results from demographic health surveys in 47 countries
title_short Hepatitis B vaccination timing: results from demographic health surveys in 47 countries
title_sort hepatitis b vaccination timing: results from demographic health surveys in 47 countries
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5328113/
https://www.ncbi.nlm.nih.gov/pubmed/28250533
http://dx.doi.org/10.2471/BLT.16.178822
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