Center for Infectious Disease Control, National Institute for Public Health and the Environment, PO Box 1, 3720 BA, Bilthoven, The Netherlands.
Netherlands Pharmocovigilance Centre Lareb, Goudsbloemvallei 7, 5237 MH, 's-Hertogenbosch, The Netherlands.
BMC Public Health. 2021 Sep 26;21(1):1752. doi: 10.1186/s12889-021-11767-9.
In 2018, meningococcal ACWY-TT vaccine (MenACWY-TT) was offered to adolescents in the Netherlands within the National Immunization Programme at 14 years of age. A questionnaire study assessed the tolerability of this vaccine.
Five thousand adolescents were invited to participate and to fill in two questionnaires about systemic events in the week before vaccination and local reactions and systemic events in the week after vaccination. Frequencies of local and systemic adverse events in the week after vaccination were calculated. Association between the occurrence of systemic symptoms in the week before and after the vaccination was tested by using generalized mixed models (GLMM).
Of all adolescents, 139 returned one or both questionnaires. Any local reaction within 7 days after vaccination was reported by 55.6% of the adolescents. Pain (50%) and reduced use of the injected arm (21.3%) were most often reported. Any systemic event was reported by 67.6% of the participants, with myalgia as the most often reported event (37.0%). Compared with the week before vaccination, there were no increased odds of experiencing systemic symptoms in the week after vaccination (OR 0.95; 95%CI 0.40-2.27).
After vaccination with MenACWY-TT vaccine, most adolescents reported one or more adverse events, which were mostly mild and transient. Systemic symptoms were not reported more often in the week after compared to the week before vaccination. Unfortunately, due to a low response rate we were not able to detect the absolute elevated risks the sample size calculation was based on. However, despite limited data, our results are in line with results from prelicensure data, and indicate that MenACWY-TT vaccination is well tolerated in adolescents.
2018 年,脑膜炎球菌 ACWY-TT 疫苗(MenACWY-TT)在荷兰国家免疫计划中向 14 岁的青少年提供。一项问卷调查研究评估了这种疫苗的耐受性。
邀请了 5000 名青少年参与,并填写了两份关于接种前一周全身事件和接种后一周局部反应和全身事件的问卷。计算了接种后一周局部和全身不良反应的频率。使用广义混合模型(GLMM)测试接种前和接种后全身症状发生的相关性。
所有青少年中,有 139 人返回了一份或两份问卷。55.6%的青少年在接种后 7 天内报告了任何局部反应。疼痛(50%)和注射手臂使用减少(21.3%)是最常报告的症状。67.6%的参与者报告了任何全身事件,其中肌肉疼痛是最常报告的事件(37.0%)。与接种前相比,接种后发生全身症状的几率没有增加(OR 0.95;95%CI 0.40-2.27)。
接种 MenACWY-TT 疫苗后,大多数青少年报告了一种或多种不良反应,大多数为轻度和短暂的。与接种前相比,接种后一周内没有更多的全身性症状报告。不幸的是,由于反应率低,我们无法检测到样本量计算所依据的绝对风险增加。然而,尽管数据有限,我们的结果与许可前数据的结果一致,表明 MenACWY-TT 疫苗在青少年中具有良好的耐受性。