Tsyruk Olga, Kaplan Gilaad G, Fortin Paul R, Hitchon Carol A, Chandran Vinod, Larché Maggie J, Avina-Zubieta Antonio, Boire Gilles, Colmegna Ines, Lacaille Diane, Lalonde Nadine, Proulx Laurie, Richards Dawn P, Boivin Natalie, DeBow Christopher, Kovalova-Wood Lucy, Paleczny Deborah, Wilhelm Linda, Lukusa Luck, Pereira Daniel, Lee Jennifer Lf, Bernatsky Sasha
Department of Medicine, McGill University, Montreal, QC H4A 3J1, Canada.
Division of Gastroenterology and Hepatology, Departments of Medicine and Community Health Sciences, University of Calgary, Calgary, AB T2N 4Z6, Canada.
Vaccines (Basel). 2024 Sep 8;12(9):1027. doi: 10.3390/vaccines12091027.
We were tasked by Canada's COVID-19 Immunity Task Force to describe severe adverse events (SAEs) associated with emergency department (ED) visits and/or hospitalizations in individuals with immune-mediated inflammatory diseases (IMIDs). At eight Canadian centres, data were collected from adults with rheumatoid arthritis (RA), axial spondyloarthritis (AxS), systemic lupus (SLE), psoriatic arthritis (PsA), and inflammatory bowel disease (IBD). We administered questionnaires, analyzing SAEs experienced within 31 days following SARS-CoV-2 vaccination. About two-thirds (63%) of 1556 participants were female; the mean age was 52.5 years. The BNT162b2 (Pfizer) vaccine was the most common, with mRNA-1273 (Moderna) being second. A total of 49% of participants had IBD, 27.4% had RA, 14.3% had PsA, 5.3% had SpA, and 4% had SLE. Twelve (0.77% of 1556 participants) SAEs leading to an ED visit or hospitalization were self-reported, occurring in 11 participants. SAEs included six (0.39% of 1556 participants) ED visits (including one due to Bell's Palsy 31 days after first vaccination) and six (0.39% of 1556 participants) hospitalizations (including one due to Guillain-Barré syndrome 15 days after the first vaccination). Two SAEs included pericarditis, one involved SLE (considered a serious disease flare), and one involved RA. Thus, in the 31 days after SARS-CoV-2 vaccination in our IMID sample, very few serious adverse events occurred. As SARS-CoV2 continues to be a common cause of death, our findings may help optimize vaccination acceptance.
加拿大新冠免疫工作组委托我们描述免疫介导性炎症疾病(IMID)患者因急诊就诊和/或住院而产生的严重不良事件(SAE)。在加拿大的八个中心,收集了类风湿关节炎(RA)、轴性脊柱关节炎(AxS)、系统性红斑狼疮(SLE)、银屑病关节炎(PsA)和炎症性肠病(IBD)成年患者的数据。我们发放了调查问卷,分析了在接种SARS-CoV-2疫苗后31天内经历的严重不良事件。1556名参与者中约三分之二(63%)为女性;平均年龄为52.5岁。BNT162b2(辉瑞)疫苗最为常用,其次是mRNA-1273(莫德纳)疫苗。共有49%的参与者患有IBD,27.4%患有RA,14.3%患有PsA,5.3%患有SpA,4%患有SLE。有12起(占1556名参与者的0.77%)导致急诊就诊或住院的严重不良事件是参与者自行报告的,涉及11名参与者。严重不良事件包括6起急诊就诊(占1556名参与者的0.39%,包括1例在首次接种疫苗31天后因贝尔麻痹就诊)和6起住院(占1556名参与者的0.39%,包括1例在首次接种疫苗15天后因吉兰-巴雷综合征住院)。两起严重不良事件包括心包炎,1起涉及SLE(被认为是严重疾病发作),1起涉及RA。因此,在我们的IMID样本中,接种SARS-CoV-2疫苗后的31天内,很少发生严重不良事件。由于SARS-CoV2仍然是常见的死亡原因,我们的研究结果可能有助于优化疫苗接种的接受度。