VA Nebraska-Western Iowa Health Care System and University of Nebraska Medical Center, Omaha.
University of Nebraska Medical Center, Omaha.
Arthritis Rheumatol. 2021 Dec;73(12):2179-2188. doi: 10.1002/art.41800. Epub 2021 Oct 19.
Rheumatoid arthritis (RA) and its treatments are associated with an increased risk of infection, but it remains unclear whether these factors have an impact on the risk or severity of COVID-19. The present study was undertaken to assess the risk and severity of COVID-19 in a US Department of Veterans Affairs (VA) cohort of patients with RA and those without RA.
A matched cohort study using national VA data was conducted. Patients diagnosed as having RA were identified among nondeceased individuals who were active in the VA health care system as of January 1, 2020 and who had received care in a VA medical center in 2019; patients for whom no RA diagnostic code was indicated were matched to the RA patients (1:1) by age, sex, and VA site (non-RA controls). Patients diagnosed as having COVID-19 and those with severe COVID-19 (defined as requiring hospitalization or leading to death) were ascertained from a national VA COVID-19 surveillance database through December 10, 2020. Multivariable Cox models were used to compare the risk of COVID-19 and COVID-19 hospitalization or death between RA patients and non-RA controls, after adjusting for demographic characteristics, comorbidities, health care utilization and access, and county-level COVID-19 incidence rates.
This VA cohort of RA patients and non-RA controls (n = 33,886 subjects per group) predominantly comprised male patients (84.5%), and the mean age was 67.8 years. During follow-up, 1,503 patients in the cohort were diagnosed as having COVID-19; among them, 388 patients had severe COVID-19 (hospitalization or death), while in 228 patients, the deaths were not related to COVID-19. In the multivariable model, RA was associated with a higher risk of COVID-19 (adjusted hazard ratio [HR] 1.25 [95% confidence interval (95% CI) 1.13-1.39]) and a higher risk of COVID-19 hospitalization or death (adjusted HR 1.35 [95% CI 1.10-1.66]) as compared to non-RA controls. Use of disease-modifying antirheumatic drugs and prednisone, as well as self-reported Black race, self-reported Hispanic ethnicity, and presence of several chronic conditions, but not seropositivity for RA autoantibodies, were each associated with risk of COVID-19 and severe COVID-19 (hospitalization or death).
Patients with RA are at higher risk of developing COVID-19 and severe COVID-19 (leading to hospitalization or death) compared to those without RA. With a risk of COVID-19 that approaches that of other recognized chronic conditions, these findings suggest that RA patients should be prioritized for COVID-19 prevention and management strategies.
类风湿关节炎(RA)及其治疗与感染风险增加有关,但尚不清楚这些因素是否会影响 COVID-19 的风险或严重程度。本研究旨在评估美国退伍军人事务部(VA)RA 患者和非 RA 患者队列中 COVID-19 的风险和严重程度。
使用全国 VA 数据进行匹配队列研究。于 2020 年 1 月 1 日确定在 VA 医疗保健系统中活跃且在 2019 年在 VA 医疗中心接受过治疗的非死亡个体中诊断为 RA 的患者;对于没有 RA 诊断代码的患者,通过年龄、性别和 VA 地点(非 RA 对照组)与 RA 患者进行匹配(1:1)。通过全国 VA COVID-19 监测数据库,于 2020 年 12 月 10 日确定诊断为 COVID-19 以及 COVID-19 住院或死亡的患者(定义为需要住院或导致死亡)。使用多变量 Cox 模型,在调整人口统计学特征、合并症、医疗保健利用和获得情况以及县级 COVID-19 发病率后,比较 RA 患者和非 RA 对照组之间 COVID-19 和 COVID-19 住院或死亡的风险。
本项 VA 队列研究中的 RA 患者和非 RA 对照组(每组 33886 名患者)主要由男性患者(84.5%)组成,平均年龄为 67.8 岁。在随访期间,队列中有 1503 名患者被诊断为 COVID-19;其中 388 名患者患有严重 COVID-19(住院或死亡),而在 228 名患者中,死亡与 COVID-19 无关。在多变量模型中,与非 RA 对照组相比,RA 与 COVID-19 风险增加(调整后的危险比[HR]1.25[95%置信区间(95%CI)1.13-1.39])和 COVID-19 住院或死亡风险增加(调整后的 HR 1.35[95%CI 1.10-1.66])相关。使用疾病修饰抗风湿药物和泼尼松、自我报告的黑种人、自我报告的西班牙裔以及存在多种慢性疾病,但不包括 RA 自身抗体的血清阳性,均与 COVID-19 和严重 COVID-19(导致住院或死亡)的风险相关。
与非 RA 患者相比,RA 患者发生 COVID-19 和严重 COVID-19(导致住院或死亡)的风险更高。鉴于 COVID-19 的风险接近其他公认的慢性疾病,这些发现表明应优先考虑 RA 患者实施 COVID-19 预防和管理策略。