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Adverse events following immunization with pentavalent vaccine: experiences of newly introduced vaccine in Iran
BACKGROUND: The most important factors that affect the incidence of vaccine-related complications are the constituent biological components of the vaccine, injection site reactions, age and sex. The aim of this study is to determine the incidence rate of adverse events following immunization with pe...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5569531/ https://www.ncbi.nlm.nih.gov/pubmed/28835207 http://dx.doi.org/10.1186/s12865-017-0226-8 |
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author | Karami, Manoochehr Ameri, Pegah Bathaei, Jalal Berangi, Zeinab Pashaei, Tahereh Zahiri, Ali Zahraei, Seyed Mohsen Erfani, Hussein Ponnet, Koen |
author_facet | Karami, Manoochehr Ameri, Pegah Bathaei, Jalal Berangi, Zeinab Pashaei, Tahereh Zahiri, Ali Zahraei, Seyed Mohsen Erfani, Hussein Ponnet, Koen |
author_sort | Karami, Manoochehr |
collection | PubMed |
description | BACKGROUND: The most important factors that affect the incidence of vaccine-related complications are the constituent biological components of the vaccine, injection site reactions, age and sex. The aim of this study is to determine the incidence rate of adverse events following immunization with pentavalent vaccine (DTPw-Hep B-Hib (PRP-T) vaccine (pentavac) (adsorbed) is manufactured by Serum Institute of India ltd), which was introduced in Iran in November 2014. It is important to monitor vaccine-related adverse events because of the role of vaccine safety in immunization program success. METHODS: This study was a mixed cohort study that included 1119 children less than 1 year of age. In 2015, the children were referred to Hamadan health centers to receive pentavalent vaccine at 2, 4 and 6 months of age. The data were collected from the parents of the children using a questionnaire that was administered either face-to-face or by telephone. The cumulative incidence of side effects and risk ratio was reported with 95% confidence intervals (CI). Chi-squared tests and logistic regressions were used to investigate the association between the variables. RESULTS: The cumulative incidence rate of pentavalent-related adverse events during 48 h following immunization was estimated to be 15.8% for swelling, 10.9% for redness, 44.2% for pain, 12.6% for mild fever, 0.1% for high fever, 20.0% for drowsiness, 15.0% for loss of appetite, 32.9% for irritability, 4.6% for vomiting and 5.5% for persistent crying. There is no evidence for the occurrence of convulsion and encephalopathy among children who receive pentavalent vaccines. CONCLUSION: Further large studies with long time follow up are required to address rare events include convulsions, encephalopathy or persistent crying. However, Findings urge immunization programs to use pentavalent vaccinations and to continue implementing the current immunization program in children under 1 year of age. |
format | Online Article Text |
id | pubmed-5569531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55695312017-08-29 Adverse events following immunization with pentavalent vaccine: experiences of newly introduced vaccine in Iran Karami, Manoochehr Ameri, Pegah Bathaei, Jalal Berangi, Zeinab Pashaei, Tahereh Zahiri, Ali Zahraei, Seyed Mohsen Erfani, Hussein Ponnet, Koen BMC Immunol Research Article BACKGROUND: The most important factors that affect the incidence of vaccine-related complications are the constituent biological components of the vaccine, injection site reactions, age and sex. The aim of this study is to determine the incidence rate of adverse events following immunization with pentavalent vaccine (DTPw-Hep B-Hib (PRP-T) vaccine (pentavac) (adsorbed) is manufactured by Serum Institute of India ltd), which was introduced in Iran in November 2014. It is important to monitor vaccine-related adverse events because of the role of vaccine safety in immunization program success. METHODS: This study was a mixed cohort study that included 1119 children less than 1 year of age. In 2015, the children were referred to Hamadan health centers to receive pentavalent vaccine at 2, 4 and 6 months of age. The data were collected from the parents of the children using a questionnaire that was administered either face-to-face or by telephone. The cumulative incidence of side effects and risk ratio was reported with 95% confidence intervals (CI). Chi-squared tests and logistic regressions were used to investigate the association between the variables. RESULTS: The cumulative incidence rate of pentavalent-related adverse events during 48 h following immunization was estimated to be 15.8% for swelling, 10.9% for redness, 44.2% for pain, 12.6% for mild fever, 0.1% for high fever, 20.0% for drowsiness, 15.0% for loss of appetite, 32.9% for irritability, 4.6% for vomiting and 5.5% for persistent crying. There is no evidence for the occurrence of convulsion and encephalopathy among children who receive pentavalent vaccines. CONCLUSION: Further large studies with long time follow up are required to address rare events include convulsions, encephalopathy or persistent crying. However, Findings urge immunization programs to use pentavalent vaccinations and to continue implementing the current immunization program in children under 1 year of age. BioMed Central 2017-08-23 /pmc/articles/PMC5569531/ /pubmed/28835207 http://dx.doi.org/10.1186/s12865-017-0226-8 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Karami, Manoochehr Ameri, Pegah Bathaei, Jalal Berangi, Zeinab Pashaei, Tahereh Zahiri, Ali Zahraei, Seyed Mohsen Erfani, Hussein Ponnet, Koen Adverse events following immunization with pentavalent vaccine: experiences of newly introduced vaccine in Iran |
title | Adverse events following immunization with pentavalent vaccine: experiences of newly introduced vaccine in Iran |
title_full | Adverse events following immunization with pentavalent vaccine: experiences of newly introduced vaccine in Iran |
title_fullStr | Adverse events following immunization with pentavalent vaccine: experiences of newly introduced vaccine in Iran |
title_full_unstemmed | Adverse events following immunization with pentavalent vaccine: experiences of newly introduced vaccine in Iran |
title_short | Adverse events following immunization with pentavalent vaccine: experiences of newly introduced vaccine in Iran |
title_sort | adverse events following immunization with pentavalent vaccine: experiences of newly introduced vaccine in iran |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5569531/ https://www.ncbi.nlm.nih.gov/pubmed/28835207 http://dx.doi.org/10.1186/s12865-017-0226-8 |
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