Tan Eng Hooi, Sena Anthony G, Prats-Uribe Albert, You Seng Chan, Ahmed Waheed-Ul-Rahman, Kostka Kristin, Reich Christian, Duvall Scott L, Lynch Kristine E, Matheny Michael E, Duarte-Salles Talita, Bertolin Sergio Fernandez, Hripcsak George, Natarajan Karthik, Falconer Thomas, Spotnitz Matthew, Ostropolets Anna, Blacketer Clair, Alshammari Thamir M, Alghoul Heba, Alser Osaid, Lane Jennifer C E, Dawoud Dalia M, Shah Karishma, Yang Yue, Zhang Lin, Areia Carlos, Golozar Asieh, Relcade Martina, Casajust Paula, Jonnagaddala Jitendra, Subbian Vignesh, Vizcaya David, Lai Lana Yh, Nyberg Fredrik, Morales Daniel R, Posada Jose D, Shah Nigam H, Gong Mengchun, Vivekanantham Arani, Abend Aaron, Minty Evan P, Suchard Marc, Rijnbeek Peter, Ryan Patrick B, Prieto-Alhambra Daniel
Centre for Statistics in Medicine, Nuffield Department of Orthopaedics, Rheumatology, and Musculoskeletal Sciences, University of Oxford, OX3 7LD, UK.
Janssen Research and Development, Titusville, NJ USA.
medRxiv. 2020 Nov 27:2020.11.24.20236802. doi: 10.1101/2020.11.24.20236802.
Patients with autoimmune diseases were advised to shield to avoid COVID-19, but information on their prognosis is lacking. We characterised 30-day outcomes and mortality after hospitalisation with COVID-19 among patients with prevalent autoimmune diseases, and compared outcomes after hospital admissions among similar patients with seasonal influenza.
Multinational network cohort study.
Electronic health records data from Columbia University Irving Medical Center (CUIMC) (NYC, United States [US]), Optum [US], Department of Veterans Affairs (VA) (US), Information System for Research in Primary Care-Hospitalisation Linked Data (SIDIAP-H) (Spain), and claims data from IQVIA Open Claims (US) and Health Insurance and Review Assessment (HIRA) (South Korea).
All patients with prevalent autoimmune diseases, diagnosed and/or hospitalised between January and June 2020 with COVID-19, and similar patients hospitalised with influenza in 2017-2018 were included.
30-day complications during hospitalisation and death.
We studied 133,589 patients diagnosed and 48,418 hospitalised with COVID-19 with prevalent autoimmune diseases. The majority of participants were female (60.5% to 65.9%) and aged ≥50 years. The most prevalent autoimmune conditions were psoriasis (3.5 to 32.5%), rheumatoid arthritis (3.9 to 18.9%), and vasculitis (3.3 to 17.6%). Amongst hospitalised patients, Type 1 diabetes was the most common autoimmune condition (4.8% to 7.5%) in US databases, rheumatoid arthritis in HIRA (18.9%), and psoriasis in SIDIAP-H (26.4%).Compared to 70,660 hospitalised with influenza, those admitted with COVID-19 had more respiratory complications including pneumonia and acute respiratory distress syndrome, and higher 30-day mortality (2.2% to 4.3% versus 6.3% to 24.6%).
Patients with autoimmune diseases had high rates of respiratory complications and 30-day mortality following a hospitalization with COVID-19. Compared to influenza, COVID-19 is a more severe disease, leading to more complications and higher mortality. Future studies should investigate predictors of poor outcomes in COVID-19 patients with autoimmune diseases.
Patients with autoimmune conditions may be at increased risk of COVID-19 infection andcomplications.There is a paucity of evidence characterising the outcomes of hospitalised COVID-19 patients with prevalent autoimmune conditions.
Most people with autoimmune diseases who required hospitalisation for COVID-19 were women, aged 50 years or older, and had substantial previous comorbidities.Patients who were hospitalised with COVID-19 and had prevalent autoimmune diseases had higher prevalence of hypertension, chronic kidney disease, heart disease, and Type 2 diabetes as compared to those with prevalent autoimmune diseases who were diagnosed with COVID-19.A variable proportion of 6% to 25% across data sources died within one month of hospitalisation with COVID-19 and prevalent autoimmune diseases.For people with autoimmune diseases, COVID-19 hospitalisation was associated with worse outcomes and 30-day mortality compared to admission with influenza in the 2017-2018 season.
自身免疫性疾病患者被建议进行防护以避免感染新冠病毒,但缺乏关于其预后的信息。我们对患有常见自身免疫性疾病的患者感染新冠病毒住院后的30天结局和死亡率进行了特征描述,并比较了类似的季节性流感患者住院后的结局。
跨国网络队列研究。
来自哥伦比亚大学欧文医学中心(CUIMC)(美国纽约)、Optum(美国)、退伍军人事务部(VA)(美国)、初级保健-住院关联数据研究信息系统(SIDIAP-H)(西班牙)的电子健康记录数据,以及来自IQVIA开放索赔数据库(美国)和健康保险审查评估机构(HIRA)(韩国)的索赔数据。
纳入2020年1月至6月期间确诊和/或因新冠病毒住院的所有患有常见自身免疫性疾病的患者,以及2017 - 2018年因流感住院的类似患者。
住院期间的30天并发症和死亡情况。
我们研究了133589例被诊断患有新冠病毒且患有常见自身免疫性疾病的患者以及48418例因新冠病毒住院的患者。大多数参与者为女性(60.5%至65.9%),年龄≥50岁。最常见的自身免疫性疾病为银屑病(3.5%至32.5%)、类风湿关节炎(3.9%至18.9%)和血管炎(3.3%至17.6%)。在住院患者中,1型糖尿病是美国数据库中最常见的自身免疫性疾病(4.8%至7.5%),类风湿关节炎在HIRA中最常见(18.9%),银屑病在SIDIAP-H中最常见(26.4%)。与70660例因流感住院的患者相比,因新冠病毒住院的患者有更多呼吸系统并发症,包括肺炎和急性呼吸窘迫综合征,且30天死亡率更高(2.2%至4.3%对比6.3%至24.6%)。
自身免疫性疾病患者感染新冠病毒住院后呼吸系统并发症发生率和30天死亡率较高。与流感相比,新冠病毒是一种更严重的疾病,会导致更多并发症和更高死亡率。未来研究应调查患有自身免疫性疾病的新冠病毒患者预后不良的预测因素。
自身免疫性疾病患者感染新冠病毒及出现并发症的风险可能增加。缺乏关于患有常见自身免疫性疾病的新冠病毒住院患者结局的证据。
大多数因新冠病毒需要住院治疗的自身免疫性疾病患者为50岁及以上女性,且既往有大量合并症。与被诊断患有新冠病毒的常见自身免疫性疾病患者相比,因新冠病毒住院的患者高血压、慢性肾病、心脏病和2型糖尿病的患病率更高。不同数据源中,6%至25%的因新冠病毒和常见自身免疫性疾病住院的患者在住院后一个月内死亡。对于自身免疫性疾病患者,与2017 - 2018年因流感住院相比,新冠病毒住院与更差的结局和30天死亡率相关。