Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Department of Paediatrics, Örebro University Hospital, Örebro, Sweden.
United European Gastroenterol J. 2021 Mar;9(2):177-192. doi: 10.1002/ueg2.12049. Epub 2021 Mar 11.
There are concerns that individuals with chronic immune-mediated diseases are at increased risk of COVID-19 and related severe adverse outcome, including intensive care admission or death. We aimed to explore the absolute and relative risk of severe COVID-19 in inflammatory bowel disease (IBD).
This population-based cohort study used nationwide registers in Sweden, with 67,292 individuals with a diagnosis of IBD 1969-2017 (Crohn's disease, n = 21,599; ulcerative colitis: n = 43,622; IBD-unclassified: n = 2071) and alive on 1 February 2020. Patients with IBD were matched to up to five controls from the general population (n = 297,910). Cox regression estimated hazard ratios (HRs) for (i) hospital admission with laboratory-confirmed COVID-19 as the primary diagnosis, and (ii) severe COVID-19 (composite outcome consisting of (a) COVID-19 intensive care admission, or (b) death from COVID-19 or (c) death within 30 days of COVID-19 hospital admission), were calculated. Analyses were conditioned on age, sex, calendar period, and county and adjusted for other comorbidities.
Between 1 February and 31 July 2020, 179 (0.27%) IBD patients and 500 (0.17%) general population controls were admitted to hospital with COVID-19 (adjusted HR [aHR] = 1.43; 95% CI = 1.19-1.72). The corresponding numbers for severe COVID-19 was 65 (0.10%) and 183 (0.06%; aHR = 1.11; 95% CI = 0.81-1.52). Adjusted HRs were similar in Crohn's disease and ulcerative colitis. In a propensity score-matched model taking comorbidity into account until 2016, the increased risk for COVID-19 hospital admission remained (aHR = 1.32; 1.12-1.56), but there was no increased risk of severe COVID-19 (aHR = 1.12; 0.85-1.47).
While individuals with IBD were more likely to be admitted to hospital for COVID-19 than the general population, the risk of severe COVID-19 was not higher.
人们担心患有慢性免疫介导性疾病的个体患 COVID-19 及相关严重不良结局(包括入住重症监护病房或死亡)的风险增加。本研究旨在探讨炎症性肠病(IBD)患者发生严重 COVID-19 的绝对风险和相对风险。
本基于人群的队列研究使用了瑞典全国登记处的数据,纳入了 1969 年至 2017 年间诊断为 IBD 的 67292 例患者(克罗恩病,n=21599 例;溃疡性结肠炎,n=43622 例;IBD 未分类,n=2071 例),并要求这些患者在 2020 年 2 月 1 日时存活。将 IBD 患者与一般人群中最多 5 名对照者(n=297910 例)相匹配。采用 Cox 回归估计了(i)以实验室确诊 COVID-19 为主要诊断的住院患者,和(ii)严重 COVID-19(由(a)COVID-19 重症监护病房入院、(b)COVID-19 死亡或(c)COVID-19 入院后 30 天内死亡组成的复合结局)的风险比(HR)。分析基于年龄、性别、日历时间、县和其他合并症进行了条件化,并对其他合并症进行了调整。
在 2020 年 2 月 1 日至 7 月 31 日期间,179 例(0.27%)IBD 患者和 500 例(0.17%)一般人群对照者因 COVID-19 住院(调整后的 HR[aHR]为 1.43;95%CI 为 1.19-1.72)。严重 COVID-19 的相应数字为 65 例(0.10%)和 183 例(0.06%;aHR 为 1.11;95%CI 为 0.81-1.52)。克罗恩病和溃疡性结肠炎的调整 HR 相似。在考虑到合并症的倾向评分匹配模型中,直到 2016 年,COVID-19 住院的风险仍有所增加(aHR 为 1.32;1.12-1.56),但严重 COVID-19 的风险没有增加(aHR 为 1.12;0.85-1.47)。
虽然 IBD 患者因 COVID-19 住院的可能性高于一般人群,但发生严重 COVID-19 的风险并不更高。