Department of Epidemiology and Public Health, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.
Avenier, Centre of Vaccination and Travel Medicine, Ostrava, Czech Republic.
Cent Eur J Public Health. 2024 Sep;32(3):147-154. doi: 10.21101/cejph.a8170.
Allergic patients may be concerned about more frequent and/or more severe adverse events following vaccination, which may lead to the refusal of vaccines among these patients. The aim of this study is to assess whether allergic patients have more frequent adverse events (AEs) after vaccination than healthy individuals.
Study participants (N = 591) underwent vaccination of their choice at a selected Vaccination and Travel Medicine Centre. At a 10 to 14-day interval, they were contacted for a telephone questionnaire survey on the occurrence of AEs after vaccination. A group of allergic patients (n = 188) and healthy controls (n = 403) were followed in the study.
No significant difference was found in the occurrence of AEs between study and control group. Only in redness and swelling, which was more common in allergic patients, but only in a few individuals. All side effects were minor, such as pain at the injection site or fatigue. No participant experienced a serious or life-threatening adverse event. In the studied group, no statistically significant differences were found even in the occurrence of AEs after singular vs. simultaneous administration of vaccines (p = 0.094), nor after vaccination with inactivated vs. attenuated vaccines (p = 0.655), or after vaccination against bacterial vs. viral infections (p = 0.140).
Vaccination of allergic patients did not cause more frequent and/or more serious adverse events in our study compared to healthy people. If general contraindications are observed, then vaccination of allergic patients is considered safe.
过敏患者可能会担心接种疫苗后出现更频繁和/或更严重的不良反应,这可能导致这些患者拒绝接种疫苗。本研究旨在评估过敏患者接种疫苗后是否比健康个体更频繁发生不良反应(AE)。
研究参与者(N=591)在选定的疫苗接种和旅行医学中心接种他们选择的疫苗。在 10 到 14 天的间隔内,通过电话问卷对他们进行了接种后 AE 发生情况的调查。研究中随访了一组过敏患者(n=188)和健康对照组(n=403)。
研究组和对照组之间 AE 的发生无显著差异。只有在过敏患者中更常见的红肿中发现了差异,但仅在少数个体中发现了差异。所有的副作用都是轻微的,如注射部位疼痛或疲劳。没有参与者经历严重或危及生命的不良事件。在研究组中,即使在单次与同时接种疫苗(p=0.094)、接种灭活与减毒疫苗(p=0.655)或接种细菌性与病毒性感染疫苗(p=0.140)后,AE 的发生也没有统计学上的显著差异。
与健康人群相比,我们的研究中过敏患者接种疫苗并未导致更频繁和/或更严重的不良反应。如果观察到一般禁忌症,那么过敏患者接种疫苗被认为是安全的。