Said Kamaleldin B, Al-Otaibi Amal, Aljaloud Luluh, Al-Anazi Basmah, Alsolami Ahmed, Alreshidi Fayez Saud
Department of Pathology and Microbiology, College of Medicine, University of Ha'il, Ha'il 55476, Saudi Arabia.
Genomics, Bioinformatics and Systems Biology, Carleton University, 1125 Colonel-By Drive, Ottawa, ON K1S 5B6, Canada.
Vaccines (Basel). 2022 Jun 24;10(7):1015. doi: 10.3390/vaccines10071015.
Vaccination is the most promising approach for ending or containing the SARS-CoV-2 pandemic. However, serious post-COVID-19 vaccine reactions, including immunocytopenia (ITP) syndrome, have been increasingly reported. Several factors cause increased risks including multiple doses, age-dependent heterogeneity in immune-responses, platelet cross-reactions with microbial components, and Long-COVID syndrome. Thus, in the absence of widely available specific therapeutics, vigilance is important while more studies are needed. Using a structured questionnaire sent to different regions in Saudi Arabia, we conducted a comprehensive investigation on the frequency, rates, disease patterns, and patient demographics of post-COVID-19 vaccine side effects on febrile patients after administration three major vaccines. Results indicated that the majority of respondents administered Pfizer BioNtech vaccine (81%, = 809); followed by AstraZeneca (16%, = 155); and Moderna (3%, = 34). Overall 998 participants, 74% ( = 737) showed no serious symptoms; however, 26.2% ( = 261) revealed typical syndromes. In a focused group of 722 participants, the following rates were identified: shortness of breath (20%), bruises or bleeding (18%), inattention (18%), GIT symptoms (17.6%), skin irritation (8.6%), and anosmia and ageusia (8%) were the most prominent among those who showed typical symptoms. The onset time was mostly between 1-3 days in 49% ( = 128), followed by 4-7 days in 21.8% ( = 57), 8-14 days in 16.5% ( = 43), and more than a month in 12.6% ( = 33). The onsets occurred mostly after the first, second, or both doses, 9%, 10%, and 7% of participants, respectively. The frequency of symptoms was significantly higher after Moderna vaccine (-value = 0.00006) and it was significantly lower in participants who received Pfizer (-value = 0.00231). We did not find significant difference in symptoms related to differences in regions. Similarly, the region, age, sex, education, and nationality had no influence on the dose and onset timings. The findings of this study have significant clinical implications in disease management strategies, preventive measures, and vaccine development. Future vertical studies would reveal more insights into the mechanisms of post-COVID-19 vaccine syndrome.
接种疫苗是终结或控制新冠疫情最具前景的方法。然而,越来越多的报告称出现了严重的新冠疫苗接种后反应,包括免疫性血小板减少症(ITP)综合征。多种因素导致风险增加,包括多剂接种、免疫反应中与年龄相关的异质性、血小板与微生物成分的交叉反应以及新冠后综合征。因此,在缺乏广泛可用的特效疗法的情况下,保持警惕很重要,同时还需要更多的研究。我们通过向沙特阿拉伯不同地区发送结构化问卷,对三种主要疫苗接种后发热患者的新冠疫苗副作用的频率、发生率、疾病模式和患者人口统计学特征进行了全面调查。结果表明,大多数受访者接种的是辉瑞 - 生物科技疫苗(81%,n = 809);其次是阿斯利康疫苗(16%,n = 155);以及莫德纳疫苗(3%,n = 34)。在总共998名参与者中,74%(n = 737)没有出现严重症状;然而,26.2%(n = 261)出现了典型症状。在722名参与者的重点组中,确定了以下发生率:呼吸急促(20%)、瘀伤或出血(18%)、注意力不集中(18%)、胃肠道症状(17.6%)、皮肤刺激(8.6%)以及嗅觉减退和味觉减退(8%)是出现典型症状者中最突出的症状。发病时间大多在1 - 3天,占49%(n = 128),其次是4 - 7天,占21.8%(n = 57),8 - 14天,占16.5%(n = 43),超过一个月,占12.6%(n = 33)。发病大多发生在第一剂、第二剂或两剂之后,分别占参与者的9%、10%和7%。莫德纳疫苗接种后症状出现频率显著更高(p值 = 0.00006),而接种辉瑞疫苗的参与者症状出现频率显著更低(p值 = 0.00231)。我们没有发现与地区差异相关的症状有显著差异。同样,地区、年龄、性别、教育程度和国籍对剂量和发病时间没有影响。本研究结果在疾病管理策略、预防措施和疫苗研发方面具有重要的临床意义。未来的纵向研究将揭示更多关于新冠疫苗接种后综合征机制的见解。