Comparison of mortality risk in patients with cirrhosis and COVID-19 compared with patients with cirrhosis alone and COVID-19 alone: multicentre matched cohort.


Journal

Gut
ISSN: 1468-3288
Titre abrégé: Gut
Pays: England
ID NLM: 2985108R

Informations de publication

Date de publication:
03 2021
Historique:
received: 08 06 2020
revised: 18 06 2020
accepted: 24 06 2020
pubmed: 15 7 2020
medline: 12 2 2021
entrez: 15 7 2020
Statut: ppublish

Résumé

Comorbid conditions are associated with poor prognosis in COVID-19. Registry data show that patients with cirrhosis may be at high risk. However, outcome comparisons among patients with cirrhosis+COVID-19 versus patients with COVID-19 alone and cirrhosis alone are lacking. The aim of this study was to perform these comparisons. A multicentre study of inpatients with cirrhosis+COVID-19 compared with age/gender-matched patients with COVID-19 alone and cirrhosis alone was performed. COVID-19 and cirrhosis characteristics, development of organ failures and acute-on-chronic liver failure (ACLF) and mortality (inpatient death+hospice) were compared. 37 patients with cirrhosis+COVID-19 were matched with 108 patients with COVID-19 and 127 patients with cirrhosis from seven sites. Race/ethnicity were similar. Patients with cirrhosis+COVID-19 had higher mortality compared with patients with COVID-19 (30% vs 13%, p=0.03) but not between patients with cirrhosis+COVID-19 and patients with cirrhosis (30% vs 20%, p=0.16). Patients with cirrhosis+COVID-19 versus patients with COVID-19 alone had equivalent respiratory symptoms, chest findings and rates of intensive care unit transfer and ventilation. However, patients with cirrhosis+COVID-19 had worse Charlson Comorbidity Index (CCI 6.5±3.1 vs 3.3±2.5, p<0.001), lower presenting GI symptoms and higher lactate. Patients with cirrhosis alone had higher cirrhosis-related complications, maximum model for end-stage liver disease (MELD) score and lower BiPAP/ventilation requirement compared with patients with cirrhosis+COVID-19, but CCI and ACLF rates were similar. In the entire group, CCI (OR 1.23, 95% CI 1.11 to 1.37, p<0.0001) was the only variable predictive of mortality on multivariable regression. In this multicentre North American contemporaneously enrolled study, age/gender-matched patients with cirrhosis+COVID-19 had similar mortality compared with patients with cirrhosis alone but higher than patients with COVID-19 alone. CCI was the only independent mortality predictor in the entire matched cohort.

Identifiants

pubmed: 32660964
pii: gutjnl-2020-322118
doi: 10.1136/gutjnl-2020-322118
pmc: PMC7371484
doi:

Types de publication

Comparative Study Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

531-536

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

© Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Jasmohan S Bajaj (JS)

Gastroenterology, Hepatology and Nutrition, Virginia Commonwealth University Health System, Richmond, Virginia, USA jasmohan@gmail.com.
Department of Medicine, Gastroenterology, Hepatology and Nutrition, Virginia Commonwealth University and Central Virginia Health Care System, Richmond, Virginia, USA.

Guadalupe Garcia-Tsao (G)

Department of Medicine, Internal Medicine, Yale University, New Haven, Connecticut, USA.

Scott W Biggins (SW)

University of Washington, Seattle, Washington, USA.

Patrick S Kamath (PS)

Department of Medicine, Gastroenterology and Hepatology, Mayo Medical School, Rochester, Minnesota, USA.

Florence Wong (F)

Toronto General Hospital, Toronto, Ontario, Canada.

Sara McGeorge (S)

Department of Medicine, Gastroenterology, Hepatology and Nutrition, Virginia Commonwealth University and Central Virginia Health Care System, Richmond, Virginia, USA.

Jawaid Shaw (J)

Department of Medicine, Gastroenterology, Hepatology and Nutrition, Virginia Commonwealth University and Central Virginia Health Care System, Richmond, Virginia, USA.

Meredith Pearson (M)

University of Washington, Seattle, Washington, USA.

Micheal Chew (M)

Department of Medicine, Internal Medicine, Yale University, New Haven, Connecticut, USA.

Andrew Fagan (A)

Department of Medicine, Gastroenterology, Hepatology and Nutrition, Virginia Commonwealth University and Central Virginia Health Care System, Richmond, Virginia, USA.

Randolph de la Rosa Rodriguez (R)

Department of Medicine, Internal Medicine, Yale University, New Haven, Connecticut, USA.

Janelle Worthington (J)

Department of Medicine, Gastroenterology and Hepatology, Mayo Medical School, Rochester, Minnesota, USA.

Amy Olofson (A)

Department of Medicine, Gastroenterology and Hepatology, Mayo Medical School, Rochester, Minnesota, USA.

Vanessa Weir (V)

Department of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Calvin Trisolini (C)

Department of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Sarah Dwyer (S)

Department of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

K Rajender Reddy (KR)

Department of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Department of Medicine, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.

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