Outcomes of Vaccination Against SARS-CoV-2 in Patients with Rheumatic Diseases in Latvia

I. Buliņa, J. Zepa
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Abstract

The retrospective study for rheumatic disease patients was conducted between 27 December 2020 and 31 August 2021 at Pauls Stradiņš Clinical University Hospital, in the largest centre of Rheumatology in Latvia with the aim of assessing the impact of vaccination against SARS-CoV-2 for rheumatic disease patients. From the hospital’s local medical electronic system, we collected demographic data, disease activity, comorbidities, data regarding vaccines and their side effects for 422 rheumatic disease patients. Most of them, 377 (89.3%), had inflammatory arthritis or a rare rheumatic disease and the most common disease was rheumatoid arthritis 30.1%; 26.5% of all patients were in remission. csDMARDs (conventional synthetic disease modified antirheumatic drugs) were used in 47.2%, biological DMARDs in 51%, and immunosuppressive medicines in 4.2% cases. The most commonly used vaccine was BNT162b2, for 49.05% patients. The main side effect after vaccination was pain in the injection site, for 16.1% patients. 36.7% of patients had no side effects after vaccination. 8.7% of patients had a flare of disease after the vaccination process. The most common comorbidity was cardiovascular diseases, for 38.7% of patients. Mild side effects, and a small percentage of flare-up of a rheumatic disease demonstrated the safety of vaccination against SARS-CoV-2 in the rheumatic disease patient group.
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拉脱维亚风湿病患者接种 SARS-CoV-2 疫苗的结果
这项针对风湿病患者的回顾性研究于 2020 年 12 月 27 日至 2021 年 8 月 31 日在拉脱维亚最大的风湿病中心保尔斯-斯特拉季林斯临床大学医院进行,目的是评估风湿病患者接种 SARS-CoV-2 疫苗的影响。我们从医院的本地医疗电子系统中收集了 422 名风湿病患者的人口统计学数据、疾病活动、合并症、疫苗数据及其副作用。其中,377 人(89.3%)患有炎症性关节炎或罕见的风湿病,最常见的疾病是类风湿性关节炎,占 30.1%;26.5% 的患者处于缓解期。47.2% 的患者使用了 csDMARDs(常规合成疾病修饰抗风湿药),51% 的患者使用了生物 DMARDs,4.2% 的患者使用了免疫抑制剂。最常用的疫苗是 BNT162b2,占 49.05% 的患者。接种疫苗后的主要副作用是注射部位疼痛,占 16.1%。36.7%的患者在接种后无任何副作用。8.7%的患者在接种疫苗后疾病复发。最常见的合并症是心血管疾病,占患者总数的 38.7%。轻微的副作用和小比例的风湿病复发表明,在风湿病患者群体中接种 SARS-CoV-2 疫苗是安全的。
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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
61
审稿时长
20 weeks
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