COVID-19 Outcomes in Patients With Systemic Autoimmune Rheumatic Diseases Compared to the General Population: A US Multicenter, Comparative Cohort Study.
COVID-19 Outcomes in Patients With Systemic Autoimmune Rheumatic Diseases Compared to the General Population: A US Multicenter, Comparative Cohort Study.
复制标题
DOI:
10.1002/art.41619
复制
发表时间:
2021-06
期刊:
影响因子:
--
通讯作者:
Choi HK
中科院分区:
文献类型:
--
作者:
D'Silva KM;Jorge A;Cohen A;McCormick N;Zhang Y;Wallace ZS;Choi HK
Patients living with systemic autoimmune rheumatic diseases (SARDs) continue to be concerned about risks of severe COVID-19 outcomes. Using a large multi-center electronic health record network, we conducted a comparative cohort study of patients with SARDs diagnosed with COVID-19 (identified by diagnostic code or positive molecular test) versus non-SARD comparators with COVID-19, matched by age, sex, race/ethnicity, and body mass index (primary model) and comorbidities and health care utilization (extended model). Thirty-day outcomes were assessed, including hospitalization, intensive care unit (ICU) admission, mechanical ventilation, acute renal failure requiring renal replacement therapy (ARF), ischemic stroke, venous thromboembolism (VTE), and death. We initially identified 2,379 SARD patients with COVID-19 (mean age 58 years, 79% female) and 142,750 comparators (mean age 47 years, 54% female). In the primary matched model (2,379 SARD patients and 2,379 matched non-SARD comparators with COVID-19), SARD patients had significantly higher risks of hospitalization (RR 1.14, 95% CI: 1.03 to 1.26), ICU admission (RR 1.32, 95% CI: 1.03 to 1.68), ARF (RR 1.81, 95% CI: 1.07 to 3.07), and VTE (RR 1.74, 95% CI: 1.23 to 2.45) versus comparators but did not have significantly higher risks of mechanical ventilation or death. In the extended model, all risks were largely attenuated except risk of VTE (RR 1.60, 95% CI: 1.14 to 2.25). SARD patients with COVID-19 may be at higher risk of hospitalization, ICU admission, ARF, and VTE versus matched comparators. These risks may be largely mediated by comorbidities, except for risk of VTE.
登录
查看更多内容
影响因子:
27.4
作者:
Ye, Cong;Cai, Shaozhe;Dong, Lingli
通讯作者:
Dong, Lingli
影响因子:
8.9
作者:
Alkhouli, Mohamad;Nanjundappa, Aravinda;Bhatt, Deepak L.
通讯作者:
Bhatt, Deepak L.
DOI:
10.1038/nrrheum.2014.36
发表时间:
2014-07
期刊:
Nature reviews. Rheumatology
影响因子:
--
作者:
通讯作者:
--
影响因子:
3.9
作者:
Bernatsky, Sasha;Linehan, Tina;Hanly, John G.
通讯作者:
Hanly, John G.
影响因子:
27.4
作者:
Pablos, Jose L.;Abasolo, Lydia;Seijas-Lopez, Alvaro
通讯作者:
Seijas-Lopez, Alvaro