School of Public Health, The University of Sydney, Sydney, New South Wales, Australia
National Centre for Immunisation Research and Surveillance, The Children's Hospital at Westmead, Westmead, New South Wales, Australia.
BMJ Open. 2021 Mar 25;11(3):e043880. doi: 10.1136/bmjopen-2020-043880.
To assess the safety of live attenuated herpes zoster vaccine live (ZVL) through cumulative analysis of near real-time, participant-based active surveillance from Australia's AusVaxSafety system.
ZVL was funded in Australia for adults aged 70 years from November 2016, with a time-limited catch up programme for those up to 79 years. This cohort study monitored safety in the first two programme years through active surveillance at 246 sentinel surveillance immunisation sites.
Adults aged 70-79 years vaccinated with ZVL who responded to an opt-out survey sent via automated short message service (SMS) 3 days following vaccination (n=17 458) or contributed supplementary data through a separate, opt-in online survey at 16 and 24 days following vaccination (n=346).
Rates of overall and prespecified adverse events following immunisation (AEFI) by sex, concomitant vaccination and underlying medical condition. Signal detection methods (fast initial response cumulative summation and Bayesian updating analyses) were applied to reports of medical attendance.
The median age of participants was 72 years; 53% were female. The response rate following automated SMS was high (73% within 7 days of vaccination). Females were more likely than males to report any adverse event within 7 days of vaccination (RR 2.07, 95% CI 1.86 to 2.31); injection site reaction was the most commonly reported (2.3%, n=377). Concomitant vaccination was not associated with higher adverse event rates (RR 1.05, 95% CI 0.93 to 1.18). Rates of medical attendance were low (0.3%) with no safety signals identified. Supplementary opt-in survey data on later onset adverse events did not identify any difference in AEFI rates between those with and without underlying medical conditions.
ZVL has a very good safety profile in the first week after vaccination in older adults. Active, participant-based surveillance in this primary care cohort is an effective method to monitor vaccine safety among older adults and will be used as a key component of COVID-19 vaccine safety surveillance in Australia.
通过从澳大利亚 AusVaxSafety 系统中实时收集基于参与者的主动监测数据,对减毒活带状疱疹疫苗(ZVL)的安全性进行累积分析。
ZVL 于 2016 年 11 月在澳大利亚为 70 岁以上成年人提供资金,为 70-79 岁人群提供有限的补种计划。这项队列研究通过 246 个监测点的主动监测,在项目的头两年监测安全性。
接种 ZVL 并通过自动短信服务(SMS)在接种后 3 天回复退出调查(n=17458)或在接种后 16 和 24 天通过单独的、选择加入的在线调查提供补充数据的 70-79 岁成年人(n=346)。
按性别、同时接种疫苗和潜在医疗状况划分的接种后总体和特定不良事件(AEFI)发生率。应用快速初始反应累积总和和贝叶斯更新分析方法对医疗就诊报告进行信号检测。
参与者的中位年龄为 72 岁,53%为女性。接种后自动 SMS 的回复率很高(接种后 7 天内为 73%)。女性在接种后 7 天内报告任何不良事件的可能性高于男性(RR 2.07,95%CI 1.86 至 2.31);最常见的报告是注射部位反应(2.3%,n=377)。同时接种疫苗与更高的不良事件发生率无关(RR 1.05,95%CI 0.93 至 1.18)。就诊率较低(0.3%),未发现安全信号。关于后期不良事件的补充选择加入调查数据未发现有潜在医疗条件的人与无潜在医疗条件的人之间 AEFI 发生率有差异。
在老年人接种后第一周,ZVL 的安全性非常好。在这个初级保健队列中进行的主动、基于参与者的监测是监测老年人疫苗安全性的有效方法,也将作为澳大利亚 COVID-19 疫苗安全性监测的关键组成部分。