Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
TriNetX, Cambridge.
Arthritis Rheumatol. 2021 Jun;73(6):914-920. doi: 10.1002/art.41619. Epub 2021 May 1.
Patients with systemic autoimmune rheumatic diseases (ARDs) continue to be concerned about risks of severe coronavirus disease 2019 (COVID-19) outcomes. This study was undertaken to evaluate the risks of severe outcomes in COVID-19 patients with systemic ARDs compared to COVID-19 patients without systemic ARDs.
Using a large multicenter electronic health record network, we conducted a comparative cohort study of patients with systemic ARDs diagnosed as having COVID-19 (identified by diagnostic code or positive molecular test result) compared to patients with COVID-19 who did not have systemic ARDs, matched for age, sex, race/ethnicity, and body mass index (primary matched model) and additionally matched for comorbidities and health care utilization (extended matched model). Thirty-day outcomes were assessed, including hospitalization, intensive care unit (ICU) admission, mechanical ventilation, acute renal failure requiring renal replacement therapy, ischemic stroke, venous thromboembolism, and death.
We initially identified 2,379 COVID-19 patients with systemic ARDs (mean age 58 years; 79% female) and 142,750 comparators (mean age 47 years; 54% female). In the primary matched model (2,379 patients with systemic ARDs and 2,379 matched comparators with COVID-19 without systemic ARDs), patients with systemic ARDs had a significantly higher risk of hospitalization (relative risk [RR] 1.14 [95% confidence interval (95% CI) 1.03-1.26]), ICU admission (RR 1.32 [95% CI 1.03-1.68]), acute renal failure (RR 1.81 [95% CI 1.07-3.07]), and venous thromboembolism (RR 1.74 [95% CI 1.23-2.45]) versus comparators but did not have a significantly higher risk of mechanical ventilation or death. In the extended model, all risks were largely attenuated, except for the risk of venous thromboembolism (RR 1.60 [95% CI 1.14-2.25]).
Our findings indicate that COVID-19 patients with systemic ARDs may be at a higher risk of hospitalization, ICU admission, acute renal failure, and venous thromboembolism when compared to COVID-19 patients without systemic ARDs. These risks may be largely mediated by comorbidities, except for the risk of venous thromboembolism.
患有系统性自身免疫性风湿病(ARDs)的患者仍然担心 COVID-19 重症结局的风险。本研究旨在评估与 COVID-19 无系统性 ARD 患者相比,COVID-19 伴系统性 ARD 患者发生重症结局的风险。
使用大型多中心电子健康记录网络,我们对诊断为 COVID-19(通过诊断代码或阳性分子检测结果确定)的系统性 ARD 患者进行了比较队列研究,并与 COVID-19 无系统性 ARD 患者进行了比较,这些患者在年龄、性别、种族/民族和体重指数(主要匹配模型)方面进行了匹配,并且在合并症和医疗保健利用方面进行了匹配(扩展匹配模型)。评估了 30 天结局,包括住院、入住重症监护病房(ICU)、机械通气、需要肾脏替代治疗的急性肾功能衰竭、缺血性卒中、静脉血栓栓塞和死亡。
我们最初确定了 2379 例 COVID-19 伴系统性 ARD 患者(平均年龄 58 岁;79%为女性)和 142750 例对照者(平均年龄 47 岁;54%为女性)。在主要匹配模型(2379 例 COVID-19 伴系统性 ARD 患者和 2379 例 COVID-19 无系统性 ARD 对照者)中,与对照者相比,患有系统性 ARD 的患者住院(相对风险 [RR] 1.14 [95%置信区间 95%CI 1.03-1.26])、入住 ICU(RR 1.32 [95%CI 1.03-1.68])、急性肾功能衰竭(RR 1.81 [95%CI 1.07-3.07])和静脉血栓栓塞(RR 1.74 [95%CI 1.23-2.45])的风险明显更高,但机械通气或死亡的风险无显著差异。在扩展模型中,除静脉血栓栓塞(RR 1.60 [95%CI 1.14-2.25])风险外,所有风险均明显降低。
我们的研究结果表明,与 COVID-19 无系统性 ARD 患者相比,COVID-19 伴系统性 ARD 患者的住院、入住 ICU、急性肾功能衰竭和静脉血栓栓塞风险可能更高。这些风险可能主要由合并症介导,除静脉血栓栓塞风险外。