Gasparotto Michela, Bindoli Sara, Padoan Roberto, Cozzi Giacomo, Depascale Roberto, Zanatta Elisabetta, Giollo Alessandro, Gatto Mariele, Zen Margherita, Schiavon Franco, Ramonda Roberta, Sfriso Paolo, Doria Andrea, Iaccarino Luca
Rheumatology Unit, Department of Medicine, University of Padova, Italy.
Clin Exp Rheumatol. 2023 Mar;41(3):642-648. doi: 10.55563/clinexprheumatol/vx44zn. Epub 2022 Aug 5.
Anti-COVID-19 vaccines have proved to be effective and well tolerated. Great attention is now being paid to the characterisation of possible adverse events associated to their administration. We report a case series of suspected rheumatic diseases (RDs) following anti-COVID-19 vaccination.
We included patients evaluated at first-aid rheumatologic consultancy and at rheumatologic outpatient and inpatient clinic at Padova University Hospital between May and September 2021 presenting with a RD within 30 days after an anti-COVID-19 vaccine dose. Our selection was in accordance with the World Health Organisation guidelines for adverse event following immunisation (AEFI) surveillance. Patients were regularly re-evaluated by telemedicine or face-to-face visit.
We identified 30 cases of RD following vaccination: 24 (80.0%) new onsets and 6 (20.0%) flares. Most of patients (76.6%) received the BNT162b2 vaccine. The mean time to RD onset/flare was 12±9 days. The most common manifestations were inflammatory arthritis (40.0%), rheumatic polymyalgia (33.3%) and adult-onset Still's disease (13.3%). At the last FU visit (9.6±2.2 months), 83.3% of patients showed complete response to first- or second-line therapy, 13.3% a partial response and one patient (3.3%) was still experiencing an active disease.
Considering the amount of vaccine doses administered during the evaluation period we overall detected a limited number of cases. We noted a clear prevalence of autoinflammatory conditions and seronegative manifestations. The great majority of patients had mild features and showed a good response to therapy.
抗新冠病毒疫苗已被证明有效且耐受性良好。目前,人们高度关注与疫苗接种相关的可能不良事件的特征。我们报告了一系列抗新冠病毒疫苗接种后疑似风湿性疾病(RD)的病例。
我们纳入了2021年5月至9月期间在帕多瓦大学医院急救风湿科咨询门诊以及风湿科门诊和住院部就诊的患者,这些患者在接种一剂抗新冠病毒疫苗后30天内出现了RD。我们的选择符合世界卫生组织免疫接种后不良事件(AEFI)监测指南。患者通过远程医疗或面对面就诊进行定期重新评估。
我们确定了30例接种疫苗后发生的RD病例:24例(80.0%)为新发病例,6例(20.0%)为病情复发。大多数患者(76.6%)接种的是BNT162b2疫苗。RD发病/复发的平均时间为12±9天。最常见的表现为炎性关节炎(40.0%)、风湿性多肌痛(33.3%)和成人斯蒂尔病(13.3%)。在最后一次随访(9.6±2.2个月)时,83.3%的患者对一线或二线治疗显示完全缓解,13.3%部分缓解,1例患者(3.3%)仍患有活动性疾病。
考虑到评估期间接种的疫苗剂量数量,我们总体上检测到的病例数量有限。我们注意到自身炎症性疾病和血清阴性表现明显占优势。绝大多数患者症状轻微,对治疗反应良好。