Oxford Liver Unit, Translational Gastroenterology Unit, Oxford University Hospitals NHS Foundation Trust, University of Oxford, Oxford, UK.
Division of Gastroenterology and Hepatology, University of North Carolina, North Carolina, USA.
J Hepatol. 2021 Mar;74(3):567-577. doi: 10.1016/j.jhep.2020.09.024. Epub 2020 Oct 6.
BACKGROUND & AIMS: Chronic liver disease (CLD) and cirrhosis are associated with immune dysregulation, leading to concerns that affected patients may be at risk of adverse outcomes following SARS-CoV-2 infection. We aimed to determine the impact of COVID-19 on patients with pre-existing liver disease, which currently remains ill-defined.
Between 25th March and 8th July 2020, data on 745 patients with CLD and SARS-CoV-2 (including 386 with and 359 without cirrhosis) were collected by 2 international registries and compared to data on non-CLD patients with SARS-CoV-2 from a UK hospital network.
Mortality was 32% in patients with cirrhosis compared to 8% in those without (p <0.001). Mortality in patients with cirrhosis increased according to Child-Pugh class (A [19%], B [35%], C [51%]) and the main cause of death was from respiratory failure (71%). After adjusting for baseline characteristics, factors associated with death in the total CLD cohort were age (odds ratio [OR] 1.02; 1.01-1.04), Child-Pugh A (OR 1.90; 1.03-3.52), B (OR 4.14; 2.4-7.65), or C (OR 9.32; 4.80-18.08) cirrhosis and alcohol-related liver disease (OR 1.79; 1.03-3.13). Compared to patients without CLD (n = 620), propensity-score-matched analysis revealed significant increases in mortality in those with Child-Pugh B (+20.0% [8.8%-31.3%]) and C (+38.1% [27.1%-49.2%]) cirrhosis. Acute hepatic decompensation occurred in 46% of patients with cirrhosis, of whom 21% had no respiratory symptoms. Half of those with hepatic decompensation had acute-on-chronic liver failure.
In the largest such cohort to date, we demonstrate that baseline liver disease stage and alcohol-related liver disease are independent risk factors for death from COVID-19. These data have important implications for the risk stratification of patients with CLD across the globe during the COVID-19 pandemic.
This international registry study demonstrates that patients with cirrhosis are at increased risk of death from COVID-19. Mortality from COVID-19 was particularly high among patients with more advanced cirrhosis and those with alcohol-related liver disease.
慢性肝脏疾病(CLD)和肝硬化与免疫失调有关,这导致人们担心受影响的患者在感染 SARS-CoV-2 后可能面临不良后果。我们旨在确定 COVID-19 对患有先前存在的肝脏疾病的患者的影响,而目前这方面的情况仍不明确。
在 2020 年 3 月 25 日至 7 月 8 日期间,两个国际注册中心收集了 745 名患有 CLD 和 SARS-CoV-2 的患者(包括 386 名患有肝硬化和 359 名无肝硬化的患者)的数据,并与来自英国医院网络的患有 SARS-CoV-2 的非 CLD 患者的数据进行了比较。
肝硬化患者的死亡率为 32%,而无肝硬化患者的死亡率为 8%(p<0.001)。肝硬化患者的死亡率根据 Child-Pugh 分级(A[19%]、B[35%]、C[51%])而增加,主要死亡原因是呼吸衰竭(71%)。在调整了基线特征后,在整个 CLD 队列中与死亡相关的因素是年龄(优势比[OR]1.02;1.01-1.04)、Child-Pugh A(OR 1.90;1.03-3.52)、B(OR 4.14;2.4-7.65)或 C(OR 9.32;4.80-18.08)肝硬化和酒精性肝病(OR 1.79;1.03-3.13)。与没有 CLD 的患者(n=620)相比,经过倾向评分匹配分析,Child-Pugh B(+20.0%[8.8%-31.3%])和 C(+38.1%[27.1%-49.2%])肝硬化患者的死亡率显著增加。46%的肝硬化患者发生急性肝失代偿,其中 21%没有呼吸症状。肝失代偿的一半患者发生慢加急性肝衰竭。
在迄今为止最大的此类队列中,我们证明了基线肝脏疾病分期和酒精性肝病是 COVID-19 死亡的独立危险因素。这些数据对 COVID-19 大流行期间全球 CLD 患者的风险分层具有重要意义。
这项国际注册研究表明,肝硬化患者死于 COVID-19 的风险增加。COVID-19 死亡率在更晚期肝硬化和酒精性肝病患者中特别高。