Braverman Genna, Barbhaiya Medha, Nong Minerva, Bykerk Vivian P, Hupert Nathaniel, Lewis Colby, Mandl Lisa A
Hospital for Special Surgery and Weill Cornell Medicine, New York City, New York.
Hospital for Special Surgery, New York City, New York.
Arthritis Care Res (Hoboken). 2024 May;76(5):733-742. doi: 10.1002/acr.25288. Epub 2024 Feb 7.
We aimed to determine the association of COVID-19 vaccination with flares of systemic rheumatic disease (SRD).
Adults with systemic rheumatic disease (SRD) in a single-center COVID-19 Rheumatology Registry were invited to enroll in a study of flares. COVID-19 vaccine information from March 5, 2021, to September 6, 2022, was obtained from chart review and self-report. Participants self-reported periods of SRD flare and periods without SRD flare. "Hazard periods" were defined as the time before a self-report of flare and "control periods" as the time before a self-report of no flare. The association between flare and COVID-19 vaccination was evaluated during hazard and control periods through univariate conditional logistic regression stratified by participant, using lookback windows of 2, 7, and 14 days.
A total of 434 participants (mean ± SD age 59 ± 13 years, 84.1% female, 81.8% White, 64.5% with inflammatory arthritis, and 27.0% with connective tissue diseases) contributed to both the hazard and control periods and were included in analysis. A total of 1,316 COVID-19 vaccinations were identified (58.5% Pfizer-BioNTech, 39.5% Moderna, and 1.4% Johnson & Johnson); 96.1% of participants received at least one dose and 93.1% at least two doses. There was no association between COVID-19 vaccination and flares in the subsequent 2, 7, or 14 days (odds ratio [OR] 1.46, 95% confidence interval [CI] 0.86-2.46; OR 1.09, 95% CI 0.76-1.55; and OR 0.85, 95% CI 0.64-1.13, respectively). Analyses stratified on sex, age, SRD subtype, and vaccine manufacturer similarly showed no association between vaccination and flare.
COVID-19 vaccination was not associated with flares in this cohort of participants with SRD. These data are reassuring and can inform shared decision-making on COVID-19 immunization.
我们旨在确定2019冠状病毒病(COVID-19)疫苗接种与系统性风湿病(SRD)病情发作之间的关联。
邀请单中心COVID-19风湿病登记处的成年系统性风湿病患者参加一项关于病情发作的研究。通过病历审查和自我报告获取2021年3月5日至2022年9月6日的COVID-19疫苗接种信息。参与者自行报告系统性风湿病病情发作期和无病情发作期。“风险期”定义为自我报告病情发作前的时间段,“对照期”定义为自我报告无病情发作前的时间段。在风险期和对照期,通过按参与者分层的单变量条件逻辑回归,使用2天、7天和14天的回顾窗口,评估病情发作与COVID-19疫苗接种之间的关联。
共有434名参与者(平均年龄±标准差59±13岁,84.1%为女性,81.8%为白人,64.5%患有炎性关节炎,27.0%患有结缔组织病)同时参与了风险期和对照期研究并纳入分析。共识别出1316次COVID-19疫苗接种(58.5%为辉瑞 - 生物科技疫苗,39.5%为莫德纳疫苗,1.4%为强生疫苗);96.1%的参与者接种了至少一剂疫苗,93.1%接种了至少两剂疫苗。在随后的2天、7天或14天内,COVID-19疫苗接种与病情发作之间无关联(比值比[OR]分别为1.46,95%置信区间[CI]为0.86 - 2.46;OR为1.09,95%CI为0.76 - 1.55;OR为0.85,95%CI为0.64 - 1.13)。按性别、年龄、系统性风湿病亚型和疫苗制造商分层的分析同样显示疫苗接种与病情发作之间无关联。
在这组系统性风湿病参与者中COVID-19疫苗接种与病情发作无关。这些数据令人安心,可为COVID-19免疫接种的共同决策提供参考。