Study of Severe Adverse Events Following Immunisation in Patients of Jamnagar District and their Follow-up at Tertiary Care Hospital
Introduction: The World Health Organisation (WHO) defines Adverse Effects Following Immunisation (AEFI) as a medical incident that takes place after an immunisation, causes concern, and believed to be caused by immunization. Aim: To study the patterns of serious adverse events following immunis...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
JCDR Research and Publications Pvt. Ltd.
2021-01-01
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Series: | Indian Journal of Neonatal Medicine and Research |
Subjects: | |
Online Access: | http://www.ijnmr.net/articles/PDF/2291/44241_F(SHU)_PF1(ShG_SHU)_PFA(SHU)_PN(SHU).pdf |
Summary: | Introduction: The World Health Organisation (WHO) defines
Adverse Effects Following Immunisation (AEFI) as a medical
incident that takes place after an immunisation, causes
concern, and believed to be caused by immunization.
Aim: To study the patterns of serious adverse events following
immunisation among children in Jamnagar district in tertiary
care centre.
Materials and Methods: The study was conducted at pediatrics
department at Shree MP Shah medical college Jamnagar
along with two primary health centers, one community health
centre and four private clinics of Jamnagar district. There were
26 children included in the study that lasted for one year, from
April 2013 to April 2014.The numbers of adverse event reports
were calculated in five age groups: 0-1 month (neonates), 1-12
months (infants), 1-3 years (toddler), 3-6 year (pre- school) and
6-14 years (school going). Vaccination details had been taken
from place of immunisation. The variables were assessed for
normality using the Kolmogorov-Smirnov test. Descriptive
statistics were calculated.
Results: From the one year of events reported of AEFI,
most commonly AEFI noted was due to immunisation of
Pentavalent vaccine. Most serious adverse events found
were swelling, pain and tenderness, redness and persistent
crying. Remaining were local requiring primary support in the
hospital. The numbers of adverse event reports had been
calculated in five age groups: 0-1 month (neonates), 1-12
months (infants), 1-3 years (toddler), 3-6 year (pre- school)
and 6-14 years (school going).
Conclusion: The most common age affected group
was infants. Regular follow-up should be done for all
participants,so that focus should be done in this population
for reducing AEFI. |
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ISSN: | 2277-8527 2455-6890 |