Evidence map›Paper›PMID 33219546›Full record

ArticleHepatology (Baltimore, Md.)2021

Cirrhosis and Severe Acute Respiratory Syndrome Coronavirus 2 Infection in US Veterans: Risk of Infection, Hospitalization, Ventilation, and Mortality.

George N Ioannou, Peter S Liang, Emily Locke, Pamela Green, Kristin Berry, Ann M O'Hare, Javeed A Shah, Kristina Crothers, McKenna C Eastment, Vincent S Fan and 1 more

Open access · greenAbstract read
In one paragraph

Article in Hepatology (Baltimore, Md.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 2 pooled it
5.5field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

56 citing papers in PubMed, 2 syntheses or guidelines pooled it, 83 citations in OpenAlex.

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  6. Decreasing Case Fatality Rates for Patients With Cirrhosis Infected With SARS-CoV-2: A National COVID Cohort Collaborative Study.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

George N IoannouDivision of Gastroenterology, Veterans Affairs Puget Sound Healthcare System and University of Washington, Seattle, WA.ORCID 0000-0003-1796-8977
Peter S LiangDivision of Gastroenterology, Veterans Affairs New York Harbor Health Care System and NYU Langone Health, New York, NY.
Emily LockeResearch and Development, Veterans Affairs Puget Sound Health Care System, Seattle, WA.
Pamela GreenResearch and Development, Veterans Affairs Puget Sound Health Care System, Seattle, WA.
Kristin BerryResearch and Development, Veterans Affairs Puget Sound Health Care System, Seattle, WA.
Ann M O'HareDivision of Nephrology, Veterans Affairs Puget Sound Healthcare System and University of Washington, Seattle, WA.
Javeed A ShahDivision of Allergy and Infectious Disease, Veterans Affairs Puget Sound Healthcare System and University of Washington, Seattle, WA.
Kristina CrothersDivision of Pulmonary and Critical Care, Veterans Affairs Puget Sound Healthcare System and University of Washington, Seattle, WA.
McKenna C EastmentDivision of Allergy and Infectious Disease, Veterans Affairs Puget Sound Healthcare System and University of Washington, Seattle, WA.
Vincent S FanDivision of Pulmonary and Critical Care, Veterans Affairs Puget Sound Healthcare System and University of Washington, Seattle, WA.
Jason A DominitzDivision of Gastroenterology, Veterans Affairs Puget Sound Healthcare System and University of Washington, Seattle, WA.
University of Washington · USVA Puget Sound Health Care System · USVA NY Harbor Healthcare System · US

Funding

VENEREAL DISEASET32AI007140 · NIAID · UNIVERSITY OF WASHINGTON · PI Julia Cook Dombrowski · 1985 to 2026
$19.4M
TOLLIP Deficiency, Immune Dysregulation, and Tuberculosis SusceptibilityR01AI136921 · NIAID · UNIVERSITY OF WASHINGTON · PI SHAH, JAVEED ALI · 2018 to 2022
$2.5M
Longitudinal Adherence to Colorectal Cancer Screening in the VAK08CA230162 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI LIANG, PETER SHUANG · 2019 to 2023
$1.1M
CSRD VA COVID19-8900-11NCI NIH HHS K08 CA230162NIAID NIH HHS R01 AI136921NIAID NIH HHS T32 AI007140
6 · The paper itself

Abstract

BACKGROUND AND

aimsWhether patients with cirrhosis have increased risk of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and the extent to which infection and cirrhosis increase the risk of adverse patient outcomes remain unclear. APPROACH AND

resultsWe identified 88,747 patients tested for SARS-CoV-2 between March 1, 2020, and May 14, 2020, in the Veterans Affairs (VA) national health care system, including 75,315 with no cirrhosis-SARS-CoV-2-negative (C0-S0), 9,826 with no cirrhosis-SARS-CoV-2-positive (C0-S1), 3,301 with cirrhosis-SARS-CoV-2-negative (C1-S0), and 305 with cirrhosis-SARS-CoV-2-positive (C1-S1). Patients were followed through June 22, 2020. Hospitalization, mechanical ventilation, and death were modeled in time-to-event analyses using Cox proportional hazards regression. Patients with cirrhosis were less likely to test positive than patients without cirrhosis (8.5% vs. 11.5%; adjusted odds ratio, 0.83; 95% CI, 0.69-0.99). Thirty-day mortality and ventilation rates increased progressively from C0-S0 (2.3% and 1.6%) to C1-S0 (5.2% and 3.6%) to C0-S1 (10.6% and 6.5%) and to C1-S1 (17.1% and 13.0%). Among patients with cirrhosis, those who tested positive for SARS-CoV-2 were 4.1 times more likely to undergo mechanical ventilation (adjusted hazard ratio [aHR], 4.12; 95% CI, 2.79-6.10) and 3.5 times more likely to die (aHR, 3.54; 95% CI, 2.55-4.90) than those who tested negative. Among patients with SARS-CoV-2 infection, those with cirrhosis were more likely to be hospitalized (aHR, 1.37; 95% CI, 1.12-1.66), undergo ventilation (aHR, 1.61; 95% CI, 1.05-2.46) or die (aHR, 1.65; 95% CI, 1.18-2.30) than patients without cirrhosis. Among patients with cirrhosis and SARS-CoV-2 infection, the most important predictors of mortality were advanced age, cirrhosis decompensation, and high Model for End-Stage Liver Disease score.

conclusionsSARS-CoV-2 infection was associated with a 3.5-fold increase in mortality in patients with cirrhosis. Cirrhosis was associated with a 1.7-fold increase in mortality in patients with SARS-CoV-2 infection.

Indexed as

SARS-CoV-2AdolescentAdultAgedAged, 80 and overCOVID-19FemaleHospitalizationHumansLiver CirrhosisMaleMiddle AgedProportional Hazards ModelsRespiration, ArtificialRisk FactorsUnited States

Identifiers

PMID33219546
PMCPMC7753324
OpenAlexW3101609987

What OpenQuestion holds

Textmetadata
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.