Abstract
Purpose
Methods
Results
Notes
Ethical statements
The study protocol was reviewed and approved by the Institutional Review Board of the Seoul National University Hospital (IRB No. 2205-034-1323). Informed consent was obtained.
Conflicts of interest
Seung-Ah Choe received research funding from SK Bioscience. Hee Gyung Kang is an editorial board member of the journal but was not involved in the peer reviewer selection, evaluation, or decision process of this article. No other potential conflicts of interest relevant to this article were reported.
Funding
This research was supported by a grant (22183MFDS433) from the Ministry of Food and Drug Safety in 2022-2025.
Author contributions
Conceptualization: SAC
Data curation: YHA, SHK, HGK
Formal analysis: SAC, YHA, YJC
Funding acquisition: SAC
Investigation: SAC, YHA, YJC
Methodology: SAC, JYS, NKC
Writing-original draft: SAC, NC
Writing-review & editing: SAC, YHA
All authors read and approved the final manuscript.
References
Table 1.
Variable | Study population |
---|---|
Age | |
5–11 yr | 11 (15.1) |
12–19 yr | 62 (84.9) |
Sex | |
Boys | 47 (64.4) |
Girls | 26 (35.6) |
Birth weight (kg) | 3.08±0.66 |
Preterm birth (<37 wk) | 9 (12.5) |
Completion of routine pediatric immunization | 72 (98.6) |
Parental age (yr) | |
Father | 47.3±4.66 |
Mother | 44.6±3.74 |
Parental highest education | |
Father | |
High school or lower | 22 (30.1) |
College/university or higher | 51 (69.7) |
Mother | |
High school or lower | 23 (31.5) |
College/university or higher | 50 (68.5) |
Underlying medical condition | |
Chronic kidney disease | 54 (74.0) |
Autoimmune disease | 10 (13.7) |
Other medical conditionsa) | 9 (12.3) |
Current medication | |
Immunosuppressant | 12 (16.4) |
Anti-inflammatory agent | 8 (11.0) |
Othersb) | 45 (61.6) |
No medication | 8 (11.0) |
Table 2.
Adverse events and management | Day 0 (n=73) | Day 21 (n=73) | Day 180 (n=57) |
---|---|---|---|
Adverse events | |||
Pain at injection site | 32 (43.8) | 11 (15.1) | 9 (15.8) |
Edema, redness at injection site | 12 (16.4) | 4 (5.48) | 6 (10.5) |
Fever | 23 (31.5) | 8 (11.0) | 11 (19.3) |
Nausea and vomiting | 4 (5.48) | 2 (2.74) | 5 (8.77) |
Headache, arthralgia, and myalgia | 24 (32.9) | 12 (16.4) | 11 (19.3) |
Fatigue | 25 (34.2) | 9 (12.3) | 10 (17.5) |
General allergic reaction (urticaria, rash, facial or hand edema, etc.) | 2 (2.74) | 1 (1.37) | 3 (5.26) |
Others | 5 (6.85) | 4 (5.48) | 8 (14.0) |
Any symptom | 48 (65.8) | 20 (27.4) | 14 (24.6) |
Management | |||
Outpatients visit due to adverse reaction | 5 (6.85) | 2 (2.74)a) | 7 (9.58)a) |
Hospitalization due to adverse reaction | 0 | 0 | 0 |
Table 3.
Outcome | Frequency (%) |
---|---|
COVID-19 immunization | |
First dose | 73 (100) |
Second dose | 72 (98.6) |
Third dose | 26 (36.1) |
SARS-CoV-2 infection after the 1st dose | 17 (23.3) |
Hospitalization from COVID-19 infection | 1 (5.88)a) |
ICU administration from COVID-19 infection | 0 |