Faculty of Pharmaceutical and Allied Health Sciences, Institute of Pharmacy, Lahore College for Women University, Lahore, Pakistan.
Institute of Pharmaceutical Sciences, University of Veterinary and Animal Sciences, Lahore, Pakistan.
Front Public Health. 2023 Jan 17;10:1084017. doi: 10.3389/fpubh.2022.1084017. eCollection 2022.
The elevated risk of serious complications like myocarditis and pericarditis after COVID-19 vaccination, especially in adolescent has been reported in some instances that need to be tested in regional populations and different ethnicity groups. The purpose of the study was to evaluate the side effects, hesitancy, and effectiveness outcomes following COVID-19 vaccination among children in Pakistan.
The study was planned using a cross-sectional design and data from Children and Adolescents (CA) was collected through a convenient sampling method using a validated questionnaire between February to July 2022. A total of 1,108 CA between the age of 12-18 years who received one or two doses of vaccine were selected and data were collected through direct interviews with respondents.
The results showed that among 99.8% of respondents who received the Pfizer COVID-19 vaccine, 72.3% of respondents were partially vaccinated (with one dose) while 27.7% were fully vaccinated (with two doses). COVID vaccination regime had a favorable safety profile in children as compared to adults. Vaccine hesitancy in children was reported to be 52.4% and the most common reasons for hesitance were the assumption that the vaccine is not safe (23.7%), the vaccine is not required (19.6%) and the vaccine is not effective (10.4%). The reported side effects were mainly mild (88.5%) followed by moderate (10.6%) and only 0.8% were of severe intensity. Post-vaccination local side effects of mild intensity were common with an onset of an average of 24 h (68%) and a duration of 2-3 days (60.6%). The reported side effects were significantly associated with gender ( = 0.00) while age had no significant effect on the occurrence of side effects. Overall, the vaccine was well tolerated by children and adolescents and was effective in preventing the reoccurrence of COVID-19 infection in 99.9% of participants.
COVID-19 vaccine by Pfizer approved by the FDA for use in CA 12-18 years of age was well tolerated with a good safety profile and no serious adverse drug reactions were reported. The vaccine side effects were mild (88.5%) and lasted for an average of 2-3 days only (60.4%). The vaccine was effective in safeguarding Children against COVID-19 infection.
在某些情况下,已经报道了 COVID-19 疫苗接种后出现心肌炎和心包炎等严重并发症的风险增加,尤其是在青少年中,这需要在区域人群和不同种族群体中进行测试。本研究的目的是评估 COVID-19 疫苗接种在巴基斯坦儿童中的副作用、犹豫和有效性结果。
本研究采用横断面设计,于 2022 年 2 月至 7 月期间通过便利抽样法,使用经过验证的问卷收集儿童(CA)的数据。共选择了 1108 名年龄在 12-18 岁之间的 CA,通过受访者直接访谈收集数据。
结果显示,在接受辉瑞 COVID-19 疫苗的 99.8%的受访者中,72.3%的受访者部分接种(一剂),27.7%的受访者完全接种(两剂)。与成年人相比,COVID 疫苗接种方案在儿童中具有良好的安全性。儿童疫苗犹豫率报告为 52.4%,最常见的犹豫原因是假设疫苗不安全(23.7%)、疫苗不必要(19.6%)和疫苗无效(10.4%)。报告的副作用主要为轻度(88.5%),其次为中度(10.6%),只有 0.8%为重度。接种后,轻度局部副作用常见,平均发病时间为 24 小时(68%),持续时间为 2-3 天(60.6%)。报告的副作用与性别显著相关( = 0.00),而年龄对副作用的发生没有显著影响。总体而言,儿童和青少年对 COVID-19 疫苗耐受性良好,在 99.9%的参与者中有效预防了 COVID-19 感染的再次发生。
FDA 批准用于 12-18 岁 CA 的辉瑞 COVID-19 疫苗耐受性良好,安全性良好,无严重药物不良反应报告。疫苗副作用轻微(88.5%),平均持续时间仅为 2-3 天(60.4%)。该疫苗有效保护儿童免受 COVID-19 感染。