Clinical Rheumatology, Ankara City Hospital, Cankaya, Turkey.
Division of Rheumatology, Department of Internal Medicine, Yıldırım Beyazıt University, Ankara City Hospital, Ankara, Türkiye.
Int J Rheum Dis. 2022 Sep;25(9):1068-1077. doi: 10.1111/1756-185X.14387. Epub 2022 Jul 18.
Vaccination represents a cornerstone in mastering the coronavirus disease 2019 (COVID-19) pandemic. There is a paucity of data regarding the safety of COVID-19 vaccines in patients with rheumatic diseases such as Behçet syndrome (BS). The present study aimed to investigate the side-effects and post-vaccine disease exacerbation rates of COVID-19 vaccines in a BS cohort.
We retrospectively evaluated 450 BS patients followed in our clinic who met the criteria of the International Study Group. COVID-19 vaccination status, type of vaccine received (Pfizer-BioNTech vs CoronaVac), post-vaccine side-effects and exacerbations were evaluated by interviewing patients over the phone or face to face. Behçet's Disease Current Activity Form (BDCAF) scores were calculated for BS symptoms before and after vaccination.
In all, 287 patients received at least one dose of the COVID-19 vaccine. Of the total number of COVID-19 vaccines (n = 639), 379 (59%) were Pfizer-BioNTech vaccines and 257 (41%) were CoronaVac vaccines. The number of side-effects after first, second, third and fourth vaccine doses were 151 (52.6%), 135 (49.4%), 29 (42.6%), and 3 (30%), respectively. BS exacerbation after first, second, third, and fourth vaccine doses were 151 (52.6%), 135 (49.4%), 16 (23.5%), and 3 (30%), respectively. Injection site pain/swelling was the most common side-effect at all vaccine doses followed by fatigue and arthralgia.
COVID-19 vaccines are well tolerated in patients with BS, and more side-effects develop after mRNA vaccines. Regardless of the vaccine type, exacerbations after the COVID-19 vaccine are common, predominantly mucocutaneous and articular involvement, and exacerbations in the form of other organ involvement are rare.
接种疫苗是控制 2019 年冠状病毒病(COVID-19)大流行的基石。关于 COVID-19 疫苗在贝切特综合征(BS)等风湿性疾病患者中的安全性数据很少。本研究旨在调查 BS 患者 COVID-19 疫苗的副作用和疫苗接种后疾病恶化率。
我们回顾性评估了在我们诊所接受治疗的符合国际研究组标准的 450 名 BS 患者。通过电话或面对面访谈评估 COVID-19 疫苗接种状况、接种疫苗类型(辉瑞-BioNTech 与科兴)、接种疫苗后副作用和疾病恶化情况。计算 BS 症状在接种疫苗前后的贝切特疾病活动评分(BDCAF)。
总共,287 名患者接种了至少一剂 COVID-19 疫苗。在总共 639 剂 COVID-19 疫苗中,379 剂(59%)为辉瑞-BioNTech 疫苗,257 剂(41%)为科兴疫苗。首次、第二次、第三次和第四次疫苗接种后出现副作用的数量分别为 151 例(52.6%)、135 例(49.4%)、29 例(42.6%)和 3 例(30%)。首次、第二次、第三次和第四次疫苗接种后 BS 恶化的数量分别为 151 例(52.6%)、135 例(49.4%)、16 例(23.5%)和 3 例(30%)。在所有疫苗剂量中,最常见的副作用是注射部位疼痛/肿胀,其次是疲劳和关节痛。
COVID-19 疫苗在 BS 患者中耐受良好,mRNA 疫苗接种后出现更多副作用。无论疫苗类型如何,COVID-19 疫苗接种后恶化都很常见,主要是黏膜和关节受累,其他器官受累的恶化很少见。