Comparative safety of monovalent and bivalent mRNA COVID-19 booster vaccines in adolescents aged 12 to 17 years in the Republic of Korea.

IF 2.1 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Osong Public Health and Research Perspectives Pub Date : 2024-08-01 Epub Date: 2024-07-09 DOI:10.24171/j.phrp.2024.0081
Mijeong Ko, Seontae Kim, Seok-Kyoung Choi, Seung Hwan Shin, Yeon-Kyeng Lee, Yunhyung Kwon
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Abstract

Background: This study analyzed the safety of coronavirus disease 2019 (COVID-19) bivalent and monovalent booster vaccines, including the frequency of adverse events (AEs) such as myocarditis and pericarditis, in adolescents aged 12 to 17 years in the Republic of Korea. We aimed to share the safety profile of the COVID-19 bivalent vaccine booster doses.

Methods: We analyzed the frequencies of AEs reported to the COVID-19 vaccination management system (CVMS) or self-reported through the text message survey (TMS). Diagnostic eligibility and causality with vaccines were compared using odds ratios (ORs) by vaccine type, and incidence rates per 100,000 person-days were calculated for confirmed cases of myocarditis and pericarditis following monovalent and bivalent booster doses.

Results: In the CVMS, the AE reporting rate (per 100,000 doses) was lower after the bivalent booster (66.5) than after the monovalent booster (264.6). Among the AEs reported for both monovalent and bivalent vaccines 98.3% were non-serious and 1.7% were serious. According to the TMS, both local and systemic AEs were reported less frequently after the bivalent vaccination than after the monovalent vaccination in adolescents aged 12 to 17 years (p<0.001). The incidence rates per 100,000 person-days for confirmed myocarditis/pericarditis following monovalent and bivalent booster doses were 0.03 and 0.05, respectively; this difference was not statistically significant (OR, 1.797; 95% confidence interval, 0.210-15.386).

Conclusion: AEs in 12- to 17-year-olds following the bivalent booster were less frequent than those following the monovalent booster in the Republic of Korea, and no major safety issues were identified. However, the reporting rates for AEs were low.

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大韩民国 12 至 17 岁青少年接种单价和双价 mRNA COVID-19 强化疫苗的安全性比较。
研究目的本研究分析了大韩民国12至17岁青少年接种冠状病毒病2019(COVID-19)二价和一价加强型疫苗的安全性,包括心肌炎和心包炎等不良事件(AEs)的发生频率。我们旨在分享 COVID-19 二价疫苗加强剂量的安全性概况:我们分析了向 COVID-19 疫苗接种管理系统 (CVMS) 报告或通过短信调查 (TMS) 自我报告的 AEs 频率。使用疫苗类型的几率比 (OR) 比较了诊断资格和与疫苗的因果关系,并计算了单价和二价强化剂接种后每 10 万人天心肌炎和心包炎确诊病例的发病率:在CVMS中,二价加强剂后的AE报告率(每10万剂)(66.5)低于单价加强剂后的AE报告率(264.6)。在单价和二价疫苗报告的不良反应中,98.2%为非严重不良反应,1.8%为严重不良反应。TMS显示,在12至17岁的青少年中,接种二价疫苗后发生局部和全身不良反应的频率低于接种一价疫苗(p结论:在12至17岁的青少年中,接种二价疫苗后发生局部和全身不良反应的频率低于接种一价疫苗:在大韩民国,12 至 17 岁青少年接种二价强化疫苗后的不良反应发生率低于接种一价强化疫苗后的不良反应发生率,未发现重大安全问题。然而,AEs 的报告率较低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Osong Public Health and Research Perspectives
Osong Public Health and Research Perspectives Medicine-Public Health, Environmental and Occupational Health
CiteScore
10.30
自引率
2.30%
发文量
44
审稿时长
16 weeks
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