Thonginnetra Saraiorn, Tawinprai Kriangkrai, Niemsorn Krongkwan, Promsena Pathariya, Tandhansakul Manunya, Kasemlawan Naruporn, Ruangkijpaisal Natthanan, Banomyong Narin, Phattraprayoon Nanthida, Rangkakulnuwat Pisuttikan, Vanichsetakul Preeda, Ungtrakul Teerapat, Wittayasak Kasiruck, Thonwirak Nawarat, Soonklang Kamonwan, Mahanonda Nithi
Department of Pediatrics, Chulabhorn Hospital, Chulabhorn Royal Academy, Bangkok 10210, Thailand.
Department of Medicine, Chulabhorn Hospital, Chulabhorn Royal Academy, Bangkok 10210, Thailand.
Vaccines (Basel). 2022 Oct 21;10(10):1765. doi: 10.3390/vaccines10101765.
Coronavirus disease 2019 affected child health and impacted learning because of the resulting onsite school closures. This prospective cohort study included children aged 10-17 who received two 4 µg doses of BBIBP-CorV administered intramuscularly 21-28 days apart. To assess vaccine safety, 36,808 participants were then followed with paper- and web-based online questionnaire surveys that captured local and systemic reactogenicities following vaccine administration on days 1, 7, and 30. Among participants, 76% (27,880) reported reactogenicity within the first 24 h and 7 days following the first dose. Half (51.41%) of participants experienced pain at the injection site; the majority of cases were mild in severity. Injection site tenderness (37.93%) was another common local reaction. Fatigue (37.89%), myalgia (33.56%), and headache (26.76%) were the most common systemic reactions. On days 2-7 after the first dose, 25.85% of participants experienced adverse reactions. Following the second dose, reactogenicity was 7.6% and 1.09% within 24 h and between days 2-7. The majority of reactions were of mild to moderate severity. We report that two doses of the BBIBP-CorV caused mild to moderate side effects in adolescents in Thailand. The findings confirm the vaccine's safety profile in this age group.
2019冠状病毒病影响了儿童健康,并因学校现场关闭而影响了学习。这项前瞻性队列研究纳入了10至17岁的儿童,他们接受了两剂4μg的BBIBP-CorV,间隔21至28天进行肌肉注射。为了评估疫苗安全性,随后对36,808名参与者进行了纸质和网络在线问卷调查,以收集接种疫苗后第1天、第7天和第30天的局部和全身反应原性。在参与者中,76%(27,880人)报告在第一剂接种后的前24小时和7天内出现反应原性。一半(51.41%)的参与者在注射部位出现疼痛;大多数病例症状较轻。注射部位压痛(37.93%)是另一种常见的局部反应。疲劳(37.89%)、肌痛(33.56%)和头痛(26.76%)是最常见的全身反应。在第一剂接种后的第2至7天,25.85%的参与者出现不良反应。在接种第二剂后,24小时内和第2至7天的反应原性分别为7.6%和1.09%。大多数反应为轻度至中度。我们报告,两剂BBIBP-CorV在泰国青少年中引起了轻度至中度的副作用。这些发现证实了该疫苗在这个年龄组的安全性。