Asiri Ashwag, Alotaibi Hend M, Alotaibi Nouf Ali, Alsaleem Alfahdah Abdullah
Department of Child Health, College of Medicine, King Khalid University, Abha, Saudi Arabia.
Department of Dermatology, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Int J Gen Med. 2025 Jun 17;18:3227-3237. doi: 10.2147/IJGM.S520084. eCollection 2025.
To investigate the incidence, characteristics, and associated factors of cutaneous adverse reactions to COVID-19 vaccines among adult patients with pre-existing urticaria in Saudi Arabia.
A cross-sectional study enrolled 190 adult patients (≥18 years) with urticaria attending allergy/dermatology clinics at King Khalid University Hospital, Riyadh (November 2021-April 2022). Data on demographics, urticaria characteristics, vaccination status, cutaneous reactions, and comorbidities were collected via questionnaire. Statistical analyses included descriptive statistics, Chi-square/Fisher exact tests, Cochran's test, and binary logistic regression.
Participants were predominantly female (87.4%), with chronic spontaneous urticaria (97.9%); 78.9% used regular antihistamines. Reactions occurred after dose 1 (22.7%), dose 2 (26.2%), and dose 3 (31.0%). Among symptomatic individuals, onset was typically <24h, resolving in 1-3 days for ~50%. Common reactions included injection site reactions (13.1-16.3%), pruritus (7.8-10.5%), and urticaria exacerbation (3.9-9.1%). Urticaria exacerbation decreased significantly after dose 3 (p=0.030). Regular antihistamine use was associated with fewer reactions after dose 1 (adjusted OR 0.4, p=0.028). Female gender, asthma/atopy, and autoimmune disease were associated with specific reactions. Adjusted vaccine type showed no significant association.
Cutaneous reactions post-COVID-19 vaccination in urticaria patients are relatively common but generally mild and transient. Decreasing urticaria exacerbations after dose 3 is reassuring. Regular antihistamine use may offer some protection, particularly after the first dose. Findings support vaccine safety and aid patient counseling.
调查沙特阿拉伯成年慢性荨麻疹患者中新型冠状病毒肺炎(COVID-19)疫苗皮肤不良反应的发生率、特征及相关因素。
一项横断面研究纳入了190例年龄≥18岁的慢性荨麻疹成年患者,这些患者于2021年11月至2022年4月在利雅得的哈立德国王大学医院过敏/皮肤科门诊就诊。通过问卷调查收集患者的人口统计学数据、荨麻疹特征、疫苗接种状况、皮肤反应及合并症信息。统计分析包括描述性统计、卡方检验/费舍尔精确检验、 Cochr an检验及二元逻辑回归。
参与者以女性为主(87.4%),患有慢性自发性荨麻疹(97.9%);78.9%的患者使用常规抗组胺药。不良反应发生在第1剂(22.7%)、第2剂(26.2%)和第3剂(31.0%)之后。在出现症状的个体中,症状通常在<24小时内出现,约50%的患者在1 - 3天内消退。常见反应包括注射部位反应(13.1 - 16.3%)、瘙痒(7.8 - 10.5%)和荨麻疹加重(3.9 - 9.1%)。第3剂后荨麻疹加重情况显著减少(p = 0.030)。常规使用抗组胺药与第1剂后较少的不良反应相关(调整后的比值比为0.4,p = 0.028)。女性、哮喘/特应性疾病和自身免疫性疾病与特定反应相关。调整后的疫苗类型无显著关联。
慢性荨麻疹患者接种COVID-19疫苗后的皮肤反应相对常见,但通常较轻且为一过性。第3剂后荨麻疹加重情况减少令人安心。常规使用抗组胺药可能提供一定保护,尤其是在第1剂之后。研究结果支持疫苗安全性并有助于患者咨询。