Wan Eric Yuk Fai, Chui Celine Sze Ling, Wang Yuan, Ng Vanessa Wai Sei, Yan Vincent Ka Chun, Lai Francisco Tsz Tsun, Li Xue, Wong Carlos King Ho, Chan Esther Wai Yin, Wong Christina Sze Man, Leung Kathy Sze Man, Ni Michael Yuxuan, Valkenburg Sophie Alessandra, Peiris Joseph Sriyal Malik, Wu Joseph Tsz Kei, Cowling Benjamin John, Ashcroft Darren M, Hung Ivan Fan Ngai, Leung Gabriel Matthew, Wong Ian Chi Kei
Centre for Safe Medication Practice and Research, Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, China.
Department of Family Medicine and Primary Care, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, China.
Lancet Reg Health West Pac. 2022 Apr;21:100393. doi: 10.1016/j.lanwpc.2022.100393. Epub 2022 Feb 2.
Stimulation of immunity by vaccination may elicit adverse events. There is currently inconclusive evidence on the relationship between herpes zoster related hospitalization and COVID-19 vaccination. This study aimed to evaluate the effect of inactivated virus (CoronaVac, Sinovac) and mRNA (BNT162b2, BioNTech/Fosun Pharma) COVID-19 vaccine on the risk of herpes zoster related hospitalization.
Self-controlled case series (SCCS) analysis was conducted using the data from the electronic health records in Hospital Authority and COVID-19 vaccination records in the Department of Health in Hong Kong. We conducted the SCCS analysis including patients with a first primary diagnosis of herpes zoster in the hospital inpatient setting between February 23 and July 31, 2021. A confirmatory analysis by nested case-control method was also conducted. Each herpes zoster case was randomly matched with ten controls according to sex, age, Charlson comorbidity index, and date of hospital admission. Conditional Poisson regression and logistic regression models were used to assess the potential excess rates of herpes zoster after vaccination.
From February 23 to July 31, 2021, a total of 16 and 27 patients were identified with a first primary hospital diagnosis of herpes zoster within 28 days after CoronaVac and BNT162b2 vaccinations. The incidence of herpes zoster was 7.9 (95% Confidence interval [CI]: 5.2-11.5) for CoronaVac and 7.1 (95% CI: 4.1-11.5) for BNT162b2 per 1,000,000 doses administered. In SCCS analysis, CoronaVac vaccination was associated with significantly higher risk of herpes zoster within 14 days after first dose (adjusted incidence rate ratio [aIRR]=2.67, 95% CI: 1.08-6.59) but not in other periods afterwards compared to the baseline period. Regarding BNT162b2 vaccination, a significantly increased risk of herpes zoster was observed after first dose up to 14 days after second dose (0-13 days after first dose: aIRR=5.23, 95% CI: 1.61-17.03; 14-27 days after first dose: aIRR=5.82, 95% CI: 1.62-20.91; 0-13 days after second dose: aIRR=5.14, 95% CI: 1.29-20.47). Using these relative rates, we estimated that there has been an excess of approximately 5 and 7 cases of hospitalization as a result of herpes zoster after every 1,000,000 doses of CoronaVac and BNT162b2 vaccination, respectively. The findings in the nested case control analysis showed similar results.
We identified an increased risk of herpes zoster related hospitalization after CoronaVac and BNT162b2 vaccinations. However, the absolute risks of such adverse event after CoronaVac and BNT162b2 vaccinations were very low. In locations where COVID-19 is prevalent, the protective effects on COVID-19 from vaccinations will greatly outweigh the potential side effects of vaccination.
The project was funded by Research Grant from the Food and Health Bureau, The Government of the Hong Kong Special Administrative Region (Ref. No.COVID19F01). FTTL (Francisco Tsz Tsun Lai) and ICKW (Ian Chi Kei Wong)'s posts were partly funded by D4H; hence this work was partly supported by AIR@InnoHK administered by Innovation and Technology Commission.
疫苗接种刺激免疫系统可能引发不良事件。目前,关于带状疱疹相关住院与新冠病毒疫苗接种之间的关系,证据尚无定论。本研究旨在评估灭活病毒(科兴新冠疫苗)和信使核糖核酸(复必泰疫苗)新冠病毒疫苗对带状疱疹相关住院风险的影响。
利用香港医院管理局电子健康记录数据和香港卫生署新冠病毒疫苗接种记录进行自我对照病例系列(SCCS)分析。我们对2021年2月23日至7月31日期间在医院住院环境中首次被初步诊断为带状疱疹的患者进行了SCCS分析。还采用巢式病例对照法进行了验证性分析。根据性别、年龄、查尔森合并症指数和住院日期,将每例带状疱疹病例与十名对照进行随机匹配。使用条件泊松回归和逻辑回归模型评估接种疫苗后带状疱疹的潜在超额发生率。
2021年2月23日至7月31日期间,共有16例和27例患者在接种科兴新冠疫苗和复必泰疫苗后28天内首次被医院初步诊断为带状疱疹。科兴新冠疫苗每接种100万剂,带状疱疹发病率为7.9(95%置信区间[CI]:5.2 - 11.5);复必泰疫苗每接种100万剂,带状疱疹发病率为7.1(95%CI:4.1 - 11.5)。在SCCS分析中,与基线期相比,接种科兴新冠疫苗后14天内带状疱疹风险显著更高(调整发病率比[aIRR]=2.67,95%CI:1.08 - 6.59),但在之后的其他时间段并非如此。对于复必泰疫苗接种,在首剂后直至第二剂后14天内观察到带状疱疹风险显著增加(首剂后0 - 13天:aIRR=5.23,95%CI:1.61 - 17.03;首剂后14 - 27天:aIRR=5.82,95%CI:1.62 - 20.91;第二剂后0 - 13天:aIRR=5.14,95%CI:1.29 - 20.47)。根据这些相对发生率,我们估计每接种100万科兴新冠疫苗和复必泰疫苗后,分别因带状疱疹导致住院的病例约多出5例和7例。巢式病例对照分析的结果显示出相似的结果。
我们发现接种科兴新冠疫苗和复必泰疫苗后,带状疱疹相关住院风险增加。然而,接种科兴新冠疫苗和复必泰疫苗后此类不良事件的绝对风险非常低。在新冠病毒流行地区,疫苗接种对新冠病毒的保护作用将大大超过接种疫苗的潜在副作用。
本项目由香港特别行政区政府食物及卫生局研究资助(编号:COVID19F01)资助。黎梓俊(FTTL)和黄智奇(ICKW)的职位部分由D4H资助;因此,本研究部分得到创新科技署管理的InnoHK AIR的支持。