Clinica Medicine, Universidade Federal de Pernambuco, Recife, Brazil.
Musculoskeletal System Department, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil
RMD Open. 2021 Jan;7(1). doi: 10.1136/rmdopen-2020-001461.
To evaluate risk factors associated with unfavourable outcomes: emergency care, hospitalisation, admission to intensive care unit (ICU), mechanical ventilation and death in patients with immune-mediated rheumatic disease (IMRD) and COVID-19.
Analysis of the first 8 weeks of observational multicentre prospective cohort study (ReumaCoV Brasil register). Patients with IMRD and COVID-19 according to the Ministry of Health criteria were classified as eligible for the study.
334 participants were enrolled, a majority of them women, with a median age of 45 years; systemic lupus erythematosus (32.9%) was the most frequent IMRD. Emergency care was required in 160 patients, 33.0% were hospitalised, 15.0% were admitted to the ICU and 10.5% underwent mechanical ventilation; 28 patients (8.4%) died. In the multivariate adjustment model for emergency care, diabetes (prevalence ratio, PR 1.38; 95% CI 1.11 to 1.73; p=0.004), kidney disease (PR 1.36; 95% CI 1.05 to 1.77; p=0.020), oral glucocorticoids (GC) (PR 1.49; 95% CI 1.21 to 1.85; p<0.001) and pulse therapy with methylprednisolone (PR 1.38; 95% CI 1.14 to 1.67; p=0.001) remained significant; for hospitalisation, age >50 years (PR 1.89; 95% CI 1.26 to 2.85; p=0.002), no use of tumour necrosis factor inhibitor (TNFi) (PR 2.51;95% CI 1.16 to 5.45; p=0.004) and methylprednisolone pulse therapy (PR 2.50; 95% CI 1.59 to 3.92; p<0.001); for ICU admission, oral GC (PR 2.24; 95% CI 1.36 to 3.71; p<0.001) and pulse therapy with methylprednisolone (PR 1.65; 95% CI 1.00 to 2.68; p<0.043); the two variables associated with death were pulse therapy with methylprednisolone or cyclophosphamide (PR 2.86; 95% CI 1.59 to 5.14; p<0.018).
Age >50 years and immunosuppression with GC and cyclophosphamide were associated with unfavourable outcomes of COVID-19. Treatment with TNFi may have been protective, perhaps leading to the COVID-19 inflammatory process.
评估与不良结局相关的危险因素:患有免疫介导性风湿病(IMRD)和 COVID-19 的患者需要紧急护理、住院、入住重症监护病房(ICU)、机械通气和死亡。
对观察性多中心前瞻性队列研究(ReumaCoV Brasil 登记处)的前 8 周进行分析。根据卫生部的标准,将患有 IMRD 和 COVID-19 的患者分类为符合研究条件。
共纳入 334 名参与者,大多数为女性,中位年龄为 45 岁;系统性红斑狼疮(SLE)(32.9%)是最常见的 IMRD。160 名患者需要紧急护理,33.0%住院,15.0%入住 ICU,10.5%接受机械通气;28 名患者(8.4%)死亡。在紧急护理的多变量调整模型中,糖尿病(患病率比,PR 1.38;95%CI 1.11 至 1.73;p=0.004)、肾脏疾病(PR 1.36;95%CI 1.05 至 1.77;p=0.020)、口服糖皮质激素(GC)(PR 1.49;95%CI 1.21 至 1.85;p<0.001)和甲基强的松龙脉冲疗法(PR 1.38;95%CI 1.14 至 1.67;p=0.001)仍然显著;对于住院治疗,年龄>50 岁(PR 1.89;95%CI 1.26 至 2.85;p=0.002)、未使用肿瘤坏死因子抑制剂(TNFi)(PR 2.51;95%CI 1.16 至 5.45;p=0.004)和甲基强的松龙脉冲疗法(PR 2.50;95%CI 1.59 至 3.92;p<0.001);对于 ICU 入院,口服 GC(PR 2.24;95%CI 1.36 至 3.71;p<0.001)和甲基强的松龙脉冲疗法(PR 1.65;95%CI 1.00 至 2.68;p<0.043);与死亡相关的两个变量是甲基强的松龙或环磷酰胺脉冲疗法(PR 2.86;95%CI 1.59 至 5.14;p<0.018)。
年龄>50 岁和 GC 和环磷酰胺的免疫抑制与 COVID-19 的不良结局相关。TNFi 的治疗可能具有保护作用,可能导致 COVID-19 的炎症过程。