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Risk of severe COVID-19 and mortality in patients with established chronic liver disease: a nationwide matched cohort study
BACKGROUND AND AIMS: Some, but not all, prior studies have suggested that patients with chronic liver disease are at increased risk of contracting COVID-19 and developing more severe disease. However, nationwide data are lacking from well-phenotyped cohorts with liver histology and comparisons to ma...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8609512/ https://www.ncbi.nlm.nih.gov/pubmed/34814851 http://dx.doi.org/10.1186/s12876-021-02017-8 |
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author | Simon, Tracey G. Hagström, Hannes Sharma, Rajani Söderling, Jonas Roelstraete, Bjorn Larsson, Emma Ludvigsson, Jonas F. |
author_facet | Simon, Tracey G. Hagström, Hannes Sharma, Rajani Söderling, Jonas Roelstraete, Bjorn Larsson, Emma Ludvigsson, Jonas F. |
author_sort | Simon, Tracey G. |
collection | PubMed |
description | BACKGROUND AND AIMS: Some, but not all, prior studies have suggested that patients with chronic liver disease are at increased risk of contracting COVID-19 and developing more severe disease. However, nationwide data are lacking from well-phenotyped cohorts with liver histology and comparisons to matched general population controls. METHODS: We conducted a nationwide cohort study of all Swedish adults with chronic liver disease (CLD) confirmed by liver biopsy between 1966 and 2017 (n = 42,320), who were alive on February 1, 2020. CLD cases were matched to ≤ 5 population comparators by age, sex, calendar year and county (n = 182,147). Using Cox regression, we estimated multivariable-adjusted hazard ratios (aHRs) and 95% confidence intervals (CIs) for COVID-19 hospitalization and severe COVID-19 (intensive care admission or death due to COVID-19). RESULTS: Between February 1 and July 31, 2020, 161 (0.38%) CLD patients and 435 (0.24%) general population controls were hospitalized with COVID-19 (aHR = 1.36, 95% CI = 1.11–1.66), while 65 (0.15%) CLD patients and 191 (0.10%) controls developed severe COVID-19 (aHR = 1.08, 95% CI = 0.79–1.48). Results were similar in patients with CLD due to alcohol use, nonalcoholic fatty liver disease, viral hepatitis, autoimmune hepatitis, and other etiologies. Among patients with cirrhosis (n = 2549), the aHRs for COVID-19 hospitalization and for severe COVID-19 were 1.08 (95% CI 0.48–2.40) and 1.23 (95% CI = 0.37–4.04), respectively, compared to controls. Moreover, among all patients diagnosed with COVID-19, the presence of underlying CLD was not associated with increased mortality (aHR = 0.85, 95% CI = 0.61–1.19). CONCLUSIONS: In this nationwide cohort, patients with CLD had a higher risk of hospitalization for COVID-19 compared to the general population, but they did not have an increased risk of developing severe COVID-19. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12876-021-02017-8. |
format | Online Article Text |
id | pubmed-8609512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-86095122021-11-23 Risk of severe COVID-19 and mortality in patients with established chronic liver disease: a nationwide matched cohort study Simon, Tracey G. Hagström, Hannes Sharma, Rajani Söderling, Jonas Roelstraete, Bjorn Larsson, Emma Ludvigsson, Jonas F. BMC Gastroenterol Research BACKGROUND AND AIMS: Some, but not all, prior studies have suggested that patients with chronic liver disease are at increased risk of contracting COVID-19 and developing more severe disease. However, nationwide data are lacking from well-phenotyped cohorts with liver histology and comparisons to matched general population controls. METHODS: We conducted a nationwide cohort study of all Swedish adults with chronic liver disease (CLD) confirmed by liver biopsy between 1966 and 2017 (n = 42,320), who were alive on February 1, 2020. CLD cases were matched to ≤ 5 population comparators by age, sex, calendar year and county (n = 182,147). Using Cox regression, we estimated multivariable-adjusted hazard ratios (aHRs) and 95% confidence intervals (CIs) for COVID-19 hospitalization and severe COVID-19 (intensive care admission or death due to COVID-19). RESULTS: Between February 1 and July 31, 2020, 161 (0.38%) CLD patients and 435 (0.24%) general population controls were hospitalized with COVID-19 (aHR = 1.36, 95% CI = 1.11–1.66), while 65 (0.15%) CLD patients and 191 (0.10%) controls developed severe COVID-19 (aHR = 1.08, 95% CI = 0.79–1.48). Results were similar in patients with CLD due to alcohol use, nonalcoholic fatty liver disease, viral hepatitis, autoimmune hepatitis, and other etiologies. Among patients with cirrhosis (n = 2549), the aHRs for COVID-19 hospitalization and for severe COVID-19 were 1.08 (95% CI 0.48–2.40) and 1.23 (95% CI = 0.37–4.04), respectively, compared to controls. Moreover, among all patients diagnosed with COVID-19, the presence of underlying CLD was not associated with increased mortality (aHR = 0.85, 95% CI = 0.61–1.19). CONCLUSIONS: In this nationwide cohort, patients with CLD had a higher risk of hospitalization for COVID-19 compared to the general population, but they did not have an increased risk of developing severe COVID-19. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12876-021-02017-8. BioMed Central 2021-11-23 /pmc/articles/PMC8609512/ /pubmed/34814851 http://dx.doi.org/10.1186/s12876-021-02017-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Simon, Tracey G. Hagström, Hannes Sharma, Rajani Söderling, Jonas Roelstraete, Bjorn Larsson, Emma Ludvigsson, Jonas F. Risk of severe COVID-19 and mortality in patients with established chronic liver disease: a nationwide matched cohort study |
title | Risk of severe COVID-19 and mortality in patients with established chronic liver disease: a nationwide matched cohort study |
title_full | Risk of severe COVID-19 and mortality in patients with established chronic liver disease: a nationwide matched cohort study |
title_fullStr | Risk of severe COVID-19 and mortality in patients with established chronic liver disease: a nationwide matched cohort study |
title_full_unstemmed | Risk of severe COVID-19 and mortality in patients with established chronic liver disease: a nationwide matched cohort study |
title_short | Risk of severe COVID-19 and mortality in patients with established chronic liver disease: a nationwide matched cohort study |
title_sort | risk of severe covid-19 and mortality in patients with established chronic liver disease: a nationwide matched cohort study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8609512/ https://www.ncbi.nlm.nih.gov/pubmed/34814851 http://dx.doi.org/10.1186/s12876-021-02017-8 |
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