Risk factors and outcomes for acute-on-chronic liver failure in COVID-19: a large multi-center observational cohort study

被引:10
|
作者
Satapathy, Sanjaya K. [1 ,5 ,6 ]
Roth, Nitzan C. [1 ]
Kvasnovsky, Charlotte [1 ]
Hirsch, Jamie S. [1 ,3 ,4 ]
Trindade, Arvind J. [1 ]
Molmenti, Ernesto [1 ,3 ]
Barish, Matthew [1 ,2 ,3 ]
Hirschwerk, David [1 ]
Da, Ben L. [1 ]
Bernstein, David [1 ]
机构
[1] Northwell Hlth, Donald & Barbara Zucker Sch Med Hofstra Northwell, 500 Hofstra Blvd, Hempstead, NY 11549 USA
[2] Northwell Hlth, North Shore Univ Hosp, Radiol Informat, Imaging Serv Line, 300 Community Dr, Manhasset, NY USA
[3] Northwell Hlth, Feinstein Inst Med Res, Inst Hlth Innovat & Outcomes Res, 350 Community Dr, Manhasset, NY 11030 USA
[4] Northwell Hlth, Dept Informat Serv, New Hyde Pk, NY USA
[5] Northwell Hlth, Barbara & Zucker Sch Med, Div Hepatol, 400 Community Dr, Manhasset, NY 11030 USA
[6] Northwell Hlth, Barbara & Zucker Sch Med, Sandra Atlas Bass Ctr Liver Dis & Transplantat, 400 Community Dr, Manhasset, NY 11030 USA
基金
美国国家卫生研究院;
关键词
Acute-on-chronic liver failure; COVID-19; Chronic liver disease; Cirrhosis; Liver chemistries; Mortality; Organ failure; CXC CHEMOKINES; INJURY; MORTALITY; DISEASE;
D O I
10.1007/s12072-021-10181-y
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objective Coronavirus disease 2019 [COVID-19] infection in patients with chronic liver disease [CLD] may precipitate acute-on-chronic liver failure [ACLF]. In a large multi-center cohort of COVID-19-infected patients, we aim to analyze (1) the outcomes of patients with underlying CLD [with and without cirrhosis] and (2) the development and impact of ACLF on in-hospital mortality. Design We identified 192 adults with CLD from among 10,859 patients with confirmed COVID-19 infection (admitted to any of 12 hospitals in a New York health care system between March 1, 2020 and April 27, 2020). ACLF was defined using the EASL-CLIF Consortium definition. Patient follow-up was through April 30, 2020, or until the date of discharge, transfer, or death. Results Of the 84 patients with cirrhosis, 32 [38%] developed ACLF, with respiratory failure [39%] and renal failure [26%] being the most common. Hispanic/Latino ethnicity was particularly at higher risk of in-hospital mortality [adjusted HR 4.92, 95% 1.27-19.09, p < 0.02] in cirrhosis despite having lower risk of development of ACLF [HR 0.26, 95% CI 0.08-0.89, p = 0.03]. Hypertension on admission predicted development of ACLF [HR 3.46, 95% CI 1.12-10.75, p = 0.03]. In-hospital mortality was not different between CLD patients with or without cirrhosis [p = 0.24] but was higher in those with cirrhosis who developed ACLF [adjusted HR 9.06, 95% CI 2.63-31.12, p < 0.001] with a trend for increased mortality by grade of ACLF [p = 0.002]. There was no difference in in-hospital mortality between the CLD cohort compared to matched control without CLD (log rank, p = 0.98) and between the cirrhosis cohort compared to matched control without cirrhosis (log rank, p = 0.51). Conclusion Development of ACLF is the main driver of increased in-hospital mortality in hospitalized patients with COVID-19 infection and cirrhosis.
引用
收藏
页码:766 / 779
页数:14
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