Thatsawatpagorn Salase. Adverse Events After the Third Dose of COVID-19 Vaccine: A Case Study of Healthcare Workers at Buntharik Hospital, Thailand. (). Mae Fah Luang University. Learning Resources and Educational Media Center. : , .
Adverse Events After the Third Dose of COVID-19 Vaccine: A Case Study of Healthcare Workers at Buntharik Hospital, Thailand
Abstract:
Introduction: COVID-19 vaccine is currently being developed then the
information regarding the unfavorable adverse events of vaccines is not clearly
known.
Objective: The purpose of this study was to estimate the prevalence of and to
determine factor adverse events after receiving the third dose of COVID-19 vaccine
among healthcare workers who were working at Buntharik hospital in
Ubon Ratchathani Province.
Methods: A cross-sectional study was conducted for data collection among
healthcare workers who received the third dose of the AstraZeneca vaccine in July
2021. Data were collected from LINE group which was specific design to monitor
the adverse events following immunization (AEFI) among people who received the
3
rddose of the COVID-19 vaccine. Independent t-test and logistic regression were
used to detect mean differences and factors associated between variables at the
significance level of =0.05.
Results: A total of 74 participants were recruited into the study; 21.6% of
vaccine-related adverse events without any severe symptoms were reported.
More than half were females (62.2%), an average age was 37.2±10.5 years, and
18.8% were presented with chronic illness at the time of immunization. Fever was
reported as the highest adverse event after getting the 3rddose (81.3%), myalgia
(75.0%), and pain and edema at the injection site (56.3%). Two variables were
found to be associated with having adverse events after getting the 3rddose of
COVID-19 vaccination. Those who had body mass index (BMI) 23 kg/m2 had a
5.3 time (95%CI=1.34-20.95) greater chance to have adverse events than those who
were normal BMI. Those who received the 3rddose after the 2ndfor 56 days had a
3.4 time (95%CI=1.02-11.49) greater chance to have an adverse event than those
who received their 3rddose after 28-41days of the 2nddose.
Conclusion: Individuals BMI and time interval between the 2
nddose and 3
rddose
are presented as factors associated with presenting adverse event who receive
COVID-19 vaccine. All people who are planning to receive COVID-19 vaccine
should be informed in concerning their BMI and time between the doses to avoid
adverse events.
Mae Fah Luang University. Learning Resources and Educational Media Center
Address:
CHIANG RAI
Email:
library@mfu.ac.th
Modified:
2023-01-13
Issued:
2023-01-13
บทความ/Article
application/pdf
Journal of Health Science and Alternative Medicine (2022) Vol.4 (3): 1-5