Survival after COVID-19-associated organ failure among inpatients with systemic lupus erythematosus in France: a nationwide study
Survival after COVID-19-associated organ failure among inpatients with systemic lupus erythematosus in France: a nationwide study
复制标题
DOI:
10.1136/annrheumdis-2021-221599
复制
发表时间:
2021-12-09
影响因子:
27.4
通讯作者:
Timsit, Jean-Francois
中科院分区:
文献类型:
--
作者:
Mageau, Arthur;Papo, Thomas;Timsit, Jean-Francois
Objective We analysed the incidence of, the specific outcomes and factors associated with COVID-19-associated organ failure (AOF) in patients with systemic lupus erythematosus (SLE) in France. Methods We performed a cohort study using the French national medical/administrative hospital database for the January 2011-November 2020 period. Each patient with SLE diagnosed in a French hospital with a COVID-19-AOF until November 2020 was randomly matched with five non-SLE patients with COVID-19-AOF. We performed an exact matching procedure taking age +/- 2 years, gender and comorbidities as matching variables. COVID-19-AOF was defined as the combination of at least one code of COVID-19 diagnosis with one code referring to an organ failure diagnosis. Results From March to November 2020, 127 380 hospital stays in France matched the definition of COVID-19-AOF, out of which 196 corresponded with patients diagnosed with SLE. Based on the presence of comorbidities, we matched 908 non-SLE patients with COVID-19-AOF with 190 SLE patients with COVID-19-AOF. On day 30, 43 in-hospital deaths (22.6%) occurred in SLE patients with COVID-19-AOF vs 198 (21.8%) in matched non-SLE patients with COVID-19-AOF: HR 0.98 (0.71-1.34). Seventy-five patients in the SLE COVID-19-AOF group and 299 in the matched control group were followed up from day 30 to day 90. During this period, 19 in-hospital deaths occurred in the SLE group (25.3%) vs 46 (15.4%) in the matched control group; the HR associated with death occurring after COVID-19-AOF among patients with SLE was 1.83 (1.05-3.20). Conclusions COVID-19-AOF is associated with a poor late-onset prognosis among patients with SLE.