The impact of COVID‐19 on the clinical course and outcome of patients with cirrhosis: An observational study

Background and Aims Severe outcomes of COVID‐19 are associated with advancing age and comorbidities. The specific aim of our study was to determine the impact of COVID‐19 on the clinical course and outcome of patients with cirrhosis. Methods We retrieved data from VA national repository and identifi...

Full description

Saved in:
Bibliographic Details
Published inHealth science reports Vol. 7; no. 6; pp. e2207 - n/a
Main Authors Shaikh, Obaid S., Yan, Peng, Rogal, Shari, Butt, Adeel A.
Format Journal Article
LanguageEnglish
Published United States John Wiley & Sons, Inc 01.06.2024
John Wiley and Sons Inc
Subjects
Online AccessGet full text
ISSN2398-8835
2398-8835
DOI10.1002/hsr2.2207

Cover

Abstract Background and Aims Severe outcomes of COVID‐19 are associated with advancing age and comorbidities. The specific aim of our study was to determine the impact of COVID‐19 on the clinical course and outcome of patients with cirrhosis. Methods We retrieved data from VA national repository and identified patients tested for SARS‐CoV‐2 RNA who had cirrhosis. Each virus positive patient was propensity‐matched with virus negative subjects by demographics and comorbidities. Primary endpoint was death within 30 days of COVID‐19 diagnosis and secondary endpoint was hospitalization within 14 days. Results Among 1,115,037 individuals tested for SARS‐CoV‐2 RNA, 31,680 had cirrhosis. Of those patients, 4456 virus positive patients were propensity‐matched with 8752 virus negative subjects. In this cohort of 13,208, median age was 67 years and 95% were male. Most had multiple comorbidities. Alcohol use, hepatitis C and MASH were the dominant etiologies of cirrhosis. At baseline, median MELD was 6% and 21% had hepatic decompensation. Advanced age was the most significant determinant of hospitalization and mortality. Comorbidities, alcohol use and MELD increased the likelihood of hospitalization whereas SARS‐CoV‐2 positivity had lower Day‐14 hospitalization hazard. MELD was associated with higher mortality hazard whereas vaccination reduced the hazard of hospitalization and death. SARS‐CoV‐2 positivity increased the hazard of death at Day‐30 by 72% and at Day‐90 by 26%. Conclusion Although patients with cirrhosis who developed COVID‐19 were less likely to be hospitalized, they were more likely to die within 30 days compared to their virus negative counterparts. Vaccination was effective in reducing both hospitalization and death. Lay summary Patients with cirrhosis who develop COVID‐19, in particular aged 65 years or older, are at increased risk of death which may be prevented by vaccination. Key points BACKGROUND: Using data from Veterans Affairs national repository, we identified patients with cirrhosis who were tested for SARS‐CoV‐2, to determine the impact of COVID‐19 on the outcome of such patients. FINDINGS: In the study cohort of 13,208 patients with 4456 SARS‐CoV‐2 positive patients propensity matched to virus negative subjects, SARS‐CoV‐2 infection was associated with 9% lower hazard of 14‐day hospitalization but 72% increased hazard of 30‐day mortality. IMPLICATIONS FOR PATIENT CARE: The study confirmed prior observations that COVID‐19 increased the mortality risk of patients with cirrhosis. It also validated the effectiveness of vaccination in reducing both hospitalization and death among patients with cirrhosis.
AbstractList Background and Aims Severe outcomes of COVID‐19 are associated with advancing age and comorbidities. The specific aim of our study was to determine the impact of COVID‐19 on the clinical course and outcome of patients with cirrhosis. Methods We retrieved data from VA national repository and identified patients tested for SARS‐CoV‐2 RNA who had cirrhosis. Each virus positive patient was propensity‐matched with virus negative subjects by demographics and comorbidities. Primary endpoint was death within 30 days of COVID‐19 diagnosis and secondary endpoint was hospitalization within 14 days. Results Among 1,115,037 individuals tested for SARS‐CoV‐2 RNA, 31,680 had cirrhosis. Of those patients, 4456 virus positive patients were propensity‐matched with 8752 virus negative subjects. In this cohort of 13,208, median age was 67 years and 95% were male. Most had multiple comorbidities. Alcohol use, hepatitis C and MASH were the dominant etiologies of cirrhosis. At baseline, median MELD was 6% and 21% had hepatic decompensation. Advanced age was the most significant determinant of hospitalization and mortality. Comorbidities, alcohol use and MELD increased the likelihood of hospitalization whereas SARS‐CoV‐2 positivity had lower Day‐14 hospitalization hazard. MELD was associated with higher mortality hazard whereas vaccination reduced the hazard of hospitalization and death. SARS‐CoV‐2 positivity increased the hazard of death at Day‐30 by 72% and at Day‐90 by 26%. Conclusion Although patients with cirrhosis who developed COVID‐19 were less likely to be hospitalized, they were more likely to die within 30 days compared to their virus negative counterparts. Vaccination was effective in reducing both hospitalization and death. Lay summary Patients with cirrhosis who develop COVID‐19, in particular aged 65 years or older, are at increased risk of death which may be prevented by vaccination. Key points BACKGROUND: Using data from Veterans Affairs national repository, we identified patients with cirrhosis who were tested for SARS‐CoV‐2, to determine the impact of COVID‐19 on the outcome of such patients. FINDINGS: In the study cohort of 13,208 patients with 4456 SARS‐CoV‐2 positive patients propensity matched to virus negative subjects, SARS‐CoV‐2 infection was associated with 9% lower hazard of 14‐day hospitalization but 72% increased hazard of 30‐day mortality. IMPLICATIONS FOR PATIENT CARE: The study confirmed prior observations that COVID‐19 increased the mortality risk of patients with cirrhosis. It also validated the effectiveness of vaccination in reducing both hospitalization and death among patients with cirrhosis.
Severe outcomes of COVID-19 are associated with advancing age and comorbidities. The specific aim of our study was to determine the impact of COVID-19 on the clinical course and outcome of patients with cirrhosis. We retrieved data from VA national repository and identified patients tested for SARS-CoV-2 RNA who had cirrhosis. Each virus positive patient was propensity-matched with virus negative subjects by demographics and comorbidities. Primary endpoint was death within 30 days of COVID-19 diagnosis and secondary endpoint was hospitalization within 14 days. Among 1,115,037 individuals tested for SARS-CoV-2 RNA, 31,680 had cirrhosis. Of those patients, 4456 virus positive patients were propensity-matched with 8752 virus negative subjects. In this cohort of 13,208, median age was 67 years and 95% were male. Most had multiple comorbidities. Alcohol use, hepatitis C and MASH were the dominant etiologies of cirrhosis. At baseline, median MELD was 6% and 21% had hepatic decompensation. Advanced age was the most significant determinant of hospitalization and mortality. Comorbidities, alcohol use and MELD increased the likelihood of hospitalization whereas SARS-CoV-2 positivity had lower Day-14 hospitalization hazard. MELD was associated with higher mortality hazard whereas vaccination reduced the hazard of hospitalization and death. SARS-CoV-2 positivity increased the hazard of death at Day-30 by 72% and at Day-90 by 26%. Although patients with cirrhosis who developed COVID-19 were less likely to be hospitalized, they were more likely to die within 30 days compared to their virus negative counterparts. Vaccination was effective in reducing both hospitalization and death.
Severe outcomes of COVID-19 are associated with advancing age and comorbidities. The specific aim of our study was to determine the impact of COVID-19 on the clinical course and outcome of patients with cirrhosis.Background and AimsSevere outcomes of COVID-19 are associated with advancing age and comorbidities. The specific aim of our study was to determine the impact of COVID-19 on the clinical course and outcome of patients with cirrhosis.We retrieved data from VA national repository and identified patients tested for SARS-CoV-2 RNA who had cirrhosis. Each virus positive patient was propensity-matched with virus negative subjects by demographics and comorbidities. Primary endpoint was death within 30 days of COVID-19 diagnosis and secondary endpoint was hospitalization within 14 days.MethodsWe retrieved data from VA national repository and identified patients tested for SARS-CoV-2 RNA who had cirrhosis. Each virus positive patient was propensity-matched with virus negative subjects by demographics and comorbidities. Primary endpoint was death within 30 days of COVID-19 diagnosis and secondary endpoint was hospitalization within 14 days.Among 1,115,037 individuals tested for SARS-CoV-2 RNA, 31,680 had cirrhosis. Of those patients, 4456 virus positive patients were propensity-matched with 8752 virus negative subjects. In this cohort of 13,208, median age was 67 years and 95% were male. Most had multiple comorbidities. Alcohol use, hepatitis C and MASH were the dominant etiologies of cirrhosis. At baseline, median MELD was 6% and 21% had hepatic decompensation. Advanced age was the most significant determinant of hospitalization and mortality. Comorbidities, alcohol use and MELD increased the likelihood of hospitalization whereas SARS-CoV-2 positivity had lower Day-14 hospitalization hazard. MELD was associated with higher mortality hazard whereas vaccination reduced the hazard of hospitalization and death. SARS-CoV-2 positivity increased the hazard of death at Day-30 by 72% and at Day-90 by 26%.ResultsAmong 1,115,037 individuals tested for SARS-CoV-2 RNA, 31,680 had cirrhosis. Of those patients, 4456 virus positive patients were propensity-matched with 8752 virus negative subjects. In this cohort of 13,208, median age was 67 years and 95% were male. Most had multiple comorbidities. Alcohol use, hepatitis C and MASH were the dominant etiologies of cirrhosis. At baseline, median MELD was 6% and 21% had hepatic decompensation. Advanced age was the most significant determinant of hospitalization and mortality. Comorbidities, alcohol use and MELD increased the likelihood of hospitalization whereas SARS-CoV-2 positivity had lower Day-14 hospitalization hazard. MELD was associated with higher mortality hazard whereas vaccination reduced the hazard of hospitalization and death. SARS-CoV-2 positivity increased the hazard of death at Day-30 by 72% and at Day-90 by 26%.Although patients with cirrhosis who developed COVID-19 were less likely to be hospitalized, they were more likely to die within 30 days compared to their virus negative counterparts. Vaccination was effective in reducing both hospitalization and death.ConclusionAlthough patients with cirrhosis who developed COVID-19 were less likely to be hospitalized, they were more likely to die within 30 days compared to their virus negative counterparts. Vaccination was effective in reducing both hospitalization and death.
Patients with cirrhosis who develop COVID‐19, in particular aged 65 years or older, are at increased risk of death which may be prevented by vaccination. BACKGROUND: Using data from Veterans Affairs national repository, we identified patients with cirrhosis who were tested for SARS‐CoV‐2, to determine the impact of COVID‐19 on the outcome of such patients. FINDINGS: In the study cohort of 13,208 patients with 4456 SARS‐CoV‐2 positive patients propensity matched to virus negative subjects, SARS‐CoV‐2 infection was associated with 9% lower hazard of 14‐day hospitalization but 72% increased hazard of 30‐day mortality. IMPLICATIONS FOR PATIENT CARE: The study confirmed prior observations that COVID‐19 increased the mortality risk of patients with cirrhosis. It also validated the effectiveness of vaccination in reducing both hospitalization and death among patients with cirrhosis.
Background and AimsSevere outcomes of COVID-19 are associated with advancing age and comorbidities. The specific aim of our study was to determine the impact of COVID-19 on the clinical course and outcome of patients with cirrhosis.MethodsWe retrieved data from VA national repository and identified patients tested for SARS-CoV-2 RNA who had cirrhosis. Each virus positive patient was propensity-matched with virus negative subjects by demographics and comorbidities. Primary endpoint was death within 30 days of COVID-19 diagnosis and secondary endpoint was hospitalization within 14 days.ResultsAmong 1,115,037 individuals tested for SARS-CoV-2 RNA, 31,680 had cirrhosis. Of those patients, 4456 virus positive patients were propensity-matched with 8752 virus negative subjects. In this cohort of 13,208, median age was 67 years and 95% were male. Most had multiple comorbidities. Alcohol use, hepatitis C and MASH were the dominant etiologies of cirrhosis. At baseline, median MELD was 6% and 21% had hepatic decompensation. Advanced age was the most significant determinant of hospitalization and mortality. Comorbidities, alcohol use and MELD increased the likelihood of hospitalization whereas SARS-CoV-2 positivity had lower Day-14 hospitalization hazard. MELD was associated with higher mortality hazard whereas vaccination reduced the hazard of hospitalization and death. SARS-CoV-2 positivity increased the hazard of death at Day-30 by 72% and at Day-90 by 26%.ConclusionAlthough patients with cirrhosis who developed COVID-19 were less likely to be hospitalized, they were more likely to die within 30 days compared to their virus negative counterparts. Vaccination was effective in reducing both hospitalization and death.
Author Yan, Peng
Butt, Adeel A.
Rogal, Shari
Shaikh, Obaid S.
AuthorAffiliation 3 Weill Cornell Medicine Doha Qatar
4 Hamad Medical Corporation Doha Qatar
1 Veterans Affairs Pittsburgh Healthcare System Pittsburgh Pennsylvania USA
2 University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA
AuthorAffiliation_xml – name: 3 Weill Cornell Medicine Doha Qatar
– name: 1 Veterans Affairs Pittsburgh Healthcare System Pittsburgh Pennsylvania USA
– name: 2 University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA
– name: 4 Hamad Medical Corporation Doha Qatar
Author_xml – sequence: 1
  givenname: Obaid S.
  orcidid: 0000-0002-4955-9222
  surname: Shaikh
  fullname: Shaikh, Obaid S.
  email: obaid@pitt.edu
  organization: University of Pittsburgh School of Medicine
– sequence: 2
  givenname: Peng
  surname: Yan
  fullname: Yan, Peng
  organization: Veterans Affairs Pittsburgh Healthcare System
– sequence: 3
  givenname: Shari
  surname: Rogal
  fullname: Rogal, Shari
  organization: University of Pittsburgh School of Medicine
– sequence: 4
  givenname: Adeel A.
  surname: Butt
  fullname: Butt, Adeel A.
  organization: Hamad Medical Corporation
BackLink https://www.ncbi.nlm.nih.gov/pubmed/38915355$$D View this record in MEDLINE/PubMed
BookMark eNp9kc9OFTEYxRuDEUQWvoBp4gYXF_pvZlo3hlxESEhIFN02nbbjlMy017YDuTsfwWf0SehckCCJrtrk-52T73znJdjywVsAXmN0gBEih32K5IAQ1DwDO4QKvuCcVluP_ttgL6UrVFhEWMXFC7BNucAVraod4C97C924UjrD0MHlxbez498_f2EBg4e5zPTgvNNqgDpMMVmovIFhyjqMdhasVHbW5wRvXO6hdjH2Ibn0Hh55GNpk43UBgi_6lCezfgWed2pIdu_-3QVfTz5eLk8X5xefzpZH5wvNGGsWBHNTdx03LVaKmobXyPDGoJa1RlcYK6aqkg-1mHWN6YxpbIspVryrasuqju6CD3e-q6kdrdFlxagGuYpuVHEtg3Ly74l3vfweriXGWDAicHHYv3eI4cdkU5ajS9oOg_I2TElS1GAhRI3rgr59gl6VW5XMG4rQplx9NnzzeKWHXf50UYB3d4COIaVouwcEIzlXLeeq5Vx1YQ-fsNrlzaVLGjf8T3HjBrv-t7U8_fKZbBS3Awm7iA
CitedBy_id crossref_primary_10_2169_internalmedicine_4856_24
Cites_doi 10.1097/MD.0000000000024369
10.1037/adb0000796
10.1002/hep.31742
10.1053/j.gastro.2021.07.010
10.1053/j.gastro.2020.04.064
10.1053/jhep.2001.22172
10.1002/hep.31649
10.7326/M21-1577
10.1001/jama.2020.2648
10.1093/gerona/glac087
10.1016/S2213-8587(21)00244-8
10.1038/s41577-021-00656-2
10.1001/jamainternmed.2021.4325
10.1093/gerona/glaa320
10.15585/mmwr.mm6924e2
10.1002/hep4.1802
10.1001/jamanetworkopen.2023.11098
10.1001/jamanetworkopen.2019.6412
10.1001/jamanetworkopen.2020.22942
10.1136/gutjnl-2020-322118
10.1016/0021-9681(87)90171-8
10.1016/S0140-6736(22)00462-7
10.1002/hsr2.657
10.1002/hep.31404
ContentType Journal Article
Copyright 2024 The Authors. published by Wiley Periodicals LLC.
2024 The Authors. Health Science Reports published by Wiley Periodicals LLC.
2024. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Copyright_xml – notice: 2024 The Authors. published by Wiley Periodicals LLC.
– notice: 2024 The Authors. Health Science Reports published by Wiley Periodicals LLC.
– notice: 2024. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
DBID 24P
AAYXX
CITATION
NPM
3V.
7X7
7XB
8FI
8FJ
8FK
ABUWG
AFKRA
AZQEC
BENPR
CCPQU
COVID
DWQXO
FYUFA
GHDGH
K9.
M0S
PHGZM
PHGZT
PIMPY
PKEHL
PQEST
PQQKQ
PQUKI
PRINS
7X8
5PM
DOI 10.1002/hsr2.2207
DatabaseName Wiley Online Library Open Access
CrossRef
PubMed
ProQuest Central (Corporate)
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
ProQuest Hospital Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest Central Essentials
ProQuest Central
ProQuest One Community College
Coronavirus Research Database
ProQuest Central
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Health & Medical Complete (Alumni)
ProQuest Health & Medical Collection
ProQuest Central Premium
ProQuest One Academic
Publicly Available Content Database
ProQuest One Academic Middle East (New)
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
PubMed
Publicly Available Content Database
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
ProQuest One Academic Eastern Edition
ProQuest Health & Medical Complete (Alumni)
Coronavirus Research Database
ProQuest Central (Alumni Edition)
ProQuest One Community College
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
ProQuest Central China
ProQuest Hospital Collection (Alumni)
ProQuest Central
ProQuest Health & Medical Complete
Health Research Premium Collection
ProQuest One Academic UKI Edition
Health and Medicine Complete (Alumni Edition)
ProQuest Central Korea
ProQuest Central (New)
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList
PubMed
MEDLINE - Academic

Publicly Available Content Database
CrossRef
Database_xml – sequence: 1
  dbid: 24P
  name: Wiley Online Library Open Access
  url: https://authorservices.wiley.com/open-science/open-access/browse-journals.html
  sourceTypes: Publisher
– sequence: 2
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 3
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
DocumentTitleAlternate SHAIKH et al
EISSN 2398-8835
EndPage n/a
ExternalDocumentID PMC11194291
38915355
10_1002_hsr2_2207
HSR22207
Genre researchArticle
Journal Article
GeographicLocations United States--US
GeographicLocations_xml – name: United States--US
GroupedDBID 0R~
1OC
24P
53G
7X7
8FI
8FJ
AAHHS
ABUWG
ACCFJ
ACCMX
ACXQS
ADBBV
ADKYN
ADZMN
ADZOD
AEEZP
AEQDE
AFKRA
AIWBW
AJBDE
ALIPV
ALMA_UNASSIGNED_HOLDINGS
ALUQN
AOIJS
AVUZU
BCNDV
BENPR
BPHCQ
BVXVI
CCPQU
EBS
EJD
EMOBN
FYUFA
GROUPED_DOAJ
HMCUK
HYE
IAO
IHR
INH
ITC
M~E
OK1
PIMPY
PQQKQ
PROAC
RPM
UKHRP
WIN
AAYXX
CITATION
PHGZM
PHGZT
NPM
3V.
7XB
8FK
AAMMB
AEFGJ
AGXDD
AIDQK
AIDYY
AZQEC
COVID
DWQXO
K9.
PKEHL
PQEST
PQUKI
PRINS
7X8
PUEGO
5PM
ID FETCH-LOGICAL-c4447-218d6ff8db1aa3d7860d87d0b4bdc511a4a52390b14f7dfdd7eb131a8f56e45f3
IEDL.DBID 7X7
ISSN 2398-8835
IngestDate Thu Aug 21 18:33:11 EDT 2025
Thu Sep 04 17:07:42 EDT 2025
Wed Aug 13 09:38:33 EDT 2025
Wed Feb 19 02:05:39 EST 2025
Tue Jul 01 02:50:16 EDT 2025
Thu Apr 24 23:06:46 EDT 2025
Wed Jan 22 17:18:16 EST 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 6
Keywords veterans
COVID vaccination
data analysis
SARS‐CoV‐2
Language English
License Attribution-NonCommercial-NoDerivs
2024 The Authors. Health Science Reports published by Wiley Periodicals LLC.
This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c4447-218d6ff8db1aa3d7860d87d0b4bdc511a4a52390b14f7dfdd7eb131a8f56e45f3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ORCID 0000-0002-4955-9222
OpenAccessLink https://www.proquest.com/docview/3072374581?pq-origsite=%requestingapplication%
PMID 38915355
PQID 3072374581
PQPubID 4370312
PageCount 11
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_11194291
proquest_miscellaneous_3071999616
proquest_journals_3072374581
pubmed_primary_38915355
crossref_primary_10_1002_hsr2_2207
crossref_citationtrail_10_1002_hsr2_2207
wiley_primary_10_1002_hsr2_2207_HSR22207
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate June 2024
PublicationDateYYYYMMDD 2024-06-01
PublicationDate_xml – month: 06
  year: 2024
  text: June 2024
PublicationDecade 2020
PublicationPlace United States
PublicationPlace_xml – name: United States
– name: Hoboken
PublicationTitle Health science reports
PublicationTitleAlternate Health Sci Rep
PublicationYear 2024
Publisher John Wiley & Sons, Inc
John Wiley and Sons Inc
Publisher_xml – name: John Wiley & Sons, Inc
– name: John Wiley and Sons Inc
References 2021; 9
2020; 3
1987; 40
2023; 78
2023
2019; 2
2022; 5
2023; 6
2020; 72
2022; 6
2020; 159
2021; 181
2022; 36
2020; 69
2021; 161
2021; 174
2020; 323
2021; 100
2022; 77
2022; 22
2001; 33
2021; 74
2022; 399
2021; 70
e_1_2_9_11_1
e_1_2_9_10_1
e_1_2_9_13_1
e_1_2_9_12_1
e_1_2_9_15_1
e_1_2_9_14_1
e_1_2_9_17_1
e_1_2_9_16_1
e_1_2_9_19_1
e_1_2_9_18_1
e_1_2_9_20_1
e_1_2_9_22_1
e_1_2_9_21_1
e_1_2_9_24_1
e_1_2_9_23_1
e_1_2_9_8_1
e_1_2_9_7_1
e_1_2_9_6_1
e_1_2_9_5_1
e_1_2_9_4_1
e_1_2_9_3_1
e_1_2_9_2_1
e_1_2_9_9_1
e_1_2_9_26_1
e_1_2_9_25_1
e_1_2_9_27_1
References_xml – volume: 74
  start-page: 926
  year: 2021
  end-page: 936
  article-title: Black patients with cirrhosis have higher mortality and lower transplant rates: results from a metropolitan cohort study
  publication-title: Hepatology
– volume: 399
  start-page: 1303
  year: 2022
  end-page: 1312
  article-title: Comparative analysis of the risks of hospitalisation and death associated with SARS‐CoV‐2 omicron (B.1.1.529) and delta (B.1.617.2) variants in England: a cohort study
  publication-title: The Lancet
– volume: 74
  start-page: 322
  year: 2021
  end-page: 335
  article-title: Cirrhosis and severe acute respiratory syndrome coronavirus 2 infection in US veterans: risk of infection, hospitalization, ventilation, and mortality
  publication-title: Hepatology
– volume: 77
  start-page: 872
  year: 2022
  end-page: 878
  article-title: Age, multiple chronic conditions, and COVID‐19: a literature review
  publication-title: J Gerontol A Biol Sci Med Sci
– volume: 22
  start-page: 47
  year: 2022
  end-page: 56
  article-title: Immune dysregulation and immunopathology induced by SARS‐CoV‐2 and related coronaviruses—are we our own worst enemy?
  publication-title: Nat Rev Immunol
– volume: 323
  start-page: 1239
  year: 2020
  end-page: 1242
  article-title: Characteristics of and important lessons from the coronavirus disease 2019 (COVID‐19) outbreak in China: summary of a report of 72314 cases from the Chinese center for disease control and prevention
  publication-title: JAMA
– volume: 100
  year: 2021
  article-title: The impact of coronavirus disease 2019 (COVID‐19) on liver injury in China: a systematic review and meta‐analysis
  publication-title: Medicine
– volume: 161
  start-page: 1487
  year: 2021
  end-page: 1501.e5
  article-title: Outcomes of SARS‐CoV‐2 infection in patients with chronic liver disease and cirrhosis: a national COVID cohort collaborative study
  publication-title: Gastroenterology
– volume: 181
  start-page: 1306
  year: 2021
  end-page: 1314
  article-title: Association of BNT162b2 mRNA and mRNA‐1273 vaccines with COVID‐19 infection and hospitalization among patients with cirrhosis
  publication-title: JAMA Intern Med
– volume: 159
  start-page: 768
  year: 2020
  end-page: 771.e3
  article-title: Clinical characteristics and outcomes of coronavirus disease 2019 among patients with preexisting liver disease in the United States: a multicenter research network study
  publication-title: Gastroenterology
– volume: 78
  start-page: 365
  year: 2023
  end-page: 372
  article-title: National norms for the elixhauser and charlson comorbidity indexes among hospitalized adults
  publication-title: J Gerontol A Biol Sci Med Sci
– volume: 5
  year: 2022
  article-title: COVID‐19 mortality and its predictors in the elderly: a systematic review
  publication-title: Health Sci Rep
– volume: 33
  start-page: 464
  year: 2001
  end-page: 470
  article-title: A model to predict survival in patients with end‐stage liver disease
  publication-title: Hepatology
– volume: 3
  year: 2020
  article-title: Changes in adult alcohol use and consequences during the COVID‐19 pandemic in the US
  publication-title: JAMA Netw Open
– volume: 72
  start-page: 807
  year: 2020
  end-page: 817
  article-title: Acute liver injury in COVID‐19: prevalence and association with clinical outcomes in a large U.S. cohort
  publication-title: Hepatology
– volume: 69
  start-page: 759
  year: 2020
  end-page: 765
  article-title: Coronavirus disease 2019 case surveillance‐‐United States, January 22–May 30, 2020
  publication-title: MMWR Morb Mortal Wkly Rep
– volume: 6
  start-page: 3062
  year: 2022
  end-page: 3072
  article-title: Independent predictors of mortality among patients with NAFLD hospitalized with COVID‐19 infection
  publication-title: Hepatol Commun
– volume: 40
  start-page: 373
  year: 1987
  end-page: 383
  article-title: A new method of classifying prognostic comorbidity in longitudinal studies: development and validation
  publication-title: J Chronic Dis
– year: 2023
– volume: 174
  start-page: 1404
  year: 2021
  end-page: 1408
  article-title: SARS‐CoV‐2 vaccine effectiveness in a high‐risk national population in a real‐world setting
  publication-title: Ann Intern Med
– volume: 36
  start-page: 1
  year: 2022
  end-page: 19
  article-title: Changes in alcohol use during COVID‐19 and associations with contextual and individual difference variables: a systematic review and meta‐analysis
  publication-title: Psychol Addict Behav
– volume: 9
  start-page: 786
  year: 2021
  end-page: 798
  article-title: COVID‐19 and metabolic disease: mechanisms and clinical management
  publication-title: Lancet Diabetes Endocrinol
– volume: 2
  year: 2019
  article-title: Trends in characteristics, mortality, and other outcomes of patients with newly diagnosed cirrhosis
  publication-title: JAMA Netw Open
– volume: 70
  start-page: 531
  year: 2021
  end-page: 536
  article-title: Comparison of mortality risk in patients with cirrhosis and COVID‐19 compared with patients with cirrhosis alone and COVID‐19 alone: multicentre matched cohort
  publication-title: Gut
– volume: 6
  issue: 5
  year: 2023
  article-title: COVID‐19 mortality by race and ethnicity in US metropolitan and nonmetropolitan areas, March 2020 to February 2022
  publication-title: JAMA Netw Open
– ident: e_1_2_9_6_1
  doi: 10.1097/MD.0000000000024369
– ident: e_1_2_9_22_1
  doi: 10.1037/adb0000796
– ident: e_1_2_9_25_1
  doi: 10.1002/hep.31742
– ident: e_1_2_9_9_1
  doi: 10.1053/j.gastro.2021.07.010
– ident: e_1_2_9_11_1
  doi: 10.1053/j.gastro.2020.04.064
– ident: e_1_2_9_26_1
  doi: 10.1053/jhep.2001.22172
– ident: e_1_2_9_8_1
  doi: 10.1002/hep.31649
– ident: e_1_2_9_17_1
– ident: e_1_2_9_14_1
  doi: 10.7326/M21-1577
– ident: e_1_2_9_2_1
  doi: 10.1001/jama.2020.2648
– ident: e_1_2_9_18_1
  doi: 10.1093/gerona/glac087
– ident: e_1_2_9_19_1
  doi: 10.1016/S2213-8587(21)00244-8
– ident: e_1_2_9_27_1
  doi: 10.1038/s41577-021-00656-2
– ident: e_1_2_9_13_1
  doi: 10.1001/jamainternmed.2021.4325
– ident: e_1_2_9_5_1
  doi: 10.1093/gerona/glaa320
– ident: e_1_2_9_4_1
  doi: 10.15585/mmwr.mm6924e2
– ident: e_1_2_9_20_1
  doi: 10.1002/hep4.1802
– ident: e_1_2_9_24_1
  doi: 10.1001/jamanetworkopen.2023.11098
– ident: e_1_2_9_12_1
– ident: e_1_2_9_16_1
  doi: 10.1001/jamanetworkopen.2019.6412
– ident: e_1_2_9_21_1
  doi: 10.1001/jamanetworkopen.2020.22942
– ident: e_1_2_9_10_1
  doi: 10.1136/gutjnl-2020-322118
– ident: e_1_2_9_15_1
  doi: 10.1016/0021-9681(87)90171-8
– ident: e_1_2_9_3_1
  doi: 10.1016/S0140-6736(22)00462-7
– ident: e_1_2_9_23_1
  doi: 10.1002/hsr2.657
– ident: e_1_2_9_7_1
  doi: 10.1002/hep.31404
SSID ssj0002024589
Score 2.2645855
Snippet Background and Aims Severe outcomes of COVID‐19 are associated with advancing age and comorbidities. The specific aim of our study was to determine the impact...
Patients with cirrhosis who develop COVID‐19, in particular aged 65 years or older, are at increased risk of death which may be prevented by vaccination....
Severe outcomes of COVID-19 are associated with advancing age and comorbidities. The specific aim of our study was to determine the impact of COVID-19 on the...
Background and AimsSevere outcomes of COVID-19 are associated with advancing age and comorbidities. The specific aim of our study was to determine the impact...
SourceID pubmedcentral
proquest
pubmed
crossref
wiley
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage e2207
SubjectTerms Alcohol use
Body mass index
Cardiovascular disease
Comorbidity
COVID vaccination
COVID-19 vaccines
Creatinine
data analysis
Demographics
Diabetes
Endocrinology and Metabolic Disorders
Epidemiology
Etiology
Gastroenterology/Hepatology
General Medicine
Genetics and Genomics
Hepatitis
Hospitalization
Hypertension
Illnesses
Immunology
Infections
Infectious Diseases
Kidney diseases
Laboratories
Liver cirrhosis
Liver diseases
Medical prognosis
Metabolic disorders
Mortality
Observational studies
Original Research
Pandemics
Patients
SARS‐CoV‐2
Severe acute respiratory syndrome coronavirus 2
Transplantation
Veterans
SummonAdditionalLinks – databaseName: Wiley Online Library Open Access
  dbid: 24P
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3LbtQwFLWqIiE2qLyHFmQQCzahseM4DqyqQjUg8RBQ1F3kp2Yk5FSTmX0_od_YL-Fe5wGjgsQukq_lJMfX9_hxjwl5UQLGtZEsq0KuMhF8nmlhZaa8sVVucsFMOm3xSc5PxYez8myHvBlzYXp9iGnBDT0jjdfo4Np0h79FQxfdir_iHDPJb2BqLd7bwMWXaYGF46ZiugIPJe4yBVRjVBbK-eFUezseXSOZ189K_slhUxA62SO3B_ZIj3q475AdH--Smx-H_fF7JALqtE98pG2gx59_vH97dXHJatpGClSPjomQ1LZ4eoPq6Gi7WcO3e6wwqKx2FJdnqV2uVou2W3av6VGkrZkWcKF-kqW9T05P3n0_nmfDjQqZFQIlGZhyMgTlDNO6cJWSuVOVy40wzgL10kLDxLTODROhcsG5CobygmkVSulFGYoHZDe20T8iVGsHzNLIWhVWeGZVGeoQBEzXQiVqz2bk5fhfGzvIjeOtFz-bXiiZNwhBgxDMyPPJ9LzX2Pib0cEITjO4WdfAAMWLCmCG5p5NxeAguOuho283yQalFiSTM_Kwx3JqBTdpS2BcM6K2UJ4MUHx7uyQuF0mEG2JEDbEcvzN1iH-_eTP_9pXjw-P_N90nt7D_9mfSDsjuerXxT4D9rM3T1Mt_AYD8Aas
  priority: 102
  providerName: Wiley-Blackwell
Title The impact of COVID‐19 on the clinical course and outcome of patients with cirrhosis: An observational study
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fhsr2.2207
https://www.ncbi.nlm.nih.gov/pubmed/38915355
https://www.proquest.com/docview/3072374581
https://www.proquest.com/docview/3071999616
https://pubmed.ncbi.nlm.nih.gov/PMC11194291
Volume 7
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1Lb9QwEB7RVkJcEO-mLSuDOHAJjRMndrigPrUgUapC0d4iP7UrVUnZ7P5_PM6jrUq5RfJEifONPZOZ8TcAH3KPcakKGnOXiJg5m8SS6SIWVmmeqIRRFaotzorpJfs2y2d9wK3tyyqHPTFs1KbRGCPf97qYZpzlgn65_hNj1yjMrvYtNDZgK1CXeX3mMz7GWFLMK4pyIBRK0v15u0w_pSk2j71thu75lvdLJG-7rsH2nD6Dp73TSA46lJ_DI1u_gMff-7T4S7jyYJPuvCNpHDn68fvrcUxL0tTE-3dkOP1IdIMlG0TWhjTrlZ-3RfGeWrUlGJMlerFczpt20X4mBzVp1Bi19fcHLtpXcHl68utoGvdtFGLNGPIwUGEK54RRVMrMcFEkRnCTKKaM9v6WZNL_jZaJosxx44zhfv_OqBQuLyzLXfYaNuumtttApDTenVRFKTLNLNUid6VzzP-jOc5KSyP4OHzVSvcc49jq4qrq2JHTCgGoEIAI3o-i1x2xxr-E9gZoqn5ttdWNJkTwbhz2qwJTHbK2zTrIIL9CQYsI3nRIjk_BzGzu3awIxB2MRwFk3L47Ui_mgXnbG4bSG3CcZ1CHh9-8mv68SPFi5_9T2IUnqKVd8dkebK6Wa_vWuzkrNYGNlJ1PgkZPYOvw5Oz8YhJCBn8BcEkBOg
linkProvider ProQuest
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Zb9QwEB6VrQS8IG4WChgEEi9pY8dJHCSESg_t0nZBpUV9Cz61K1VJ2ewK8af4jXhy0arAW98iZXLYM7Y_z4y_AXgVex1nKqFB6kIRcGfDQHKdBMIqnYYq5FTV2RaTZHTMP57EJyvwqzsLg2mV3ZxYT9Sm1Ogj3_C2yKKUx4K-P_seYNUojK52JTQas9izP3_4LVv1brzt9fuasd2do61R0FYVCDTnSEtAhUmcE0ZRKSOTiiQ0IjWh4spoDz8kl35zloWKcpcaZ0zqp7OISuHixPLYRf6912CV44nWAax-2Jl8Puy9OgwjmSLrKIxCtjGt5mydMSxXe37hu4RmLydlngfL9Wq3extutTCVbDZ2dQdWbHEXrh-0gfh7cOrNizQnLEnpyNanr-PtgGakLIhHlKQ7b0l0iUkiRBaGlMuF72mL4i2Za0XQC0z0bD6fltWseks2C1Kq3k_sn6_Zb-_D8ZV08QMYFGVhHwGR0ngAq5JMRJpbqkXsMue43xW6lGeWDuFN16u5blnNsbjGad7wMbMcFZCjAobwshc9a6g8_ia01qkmb0dzlf-xvSG86G_7cYjBFVnYclnLIKNDQpMhPGw02X8FY8GxB3ZDEBd03Asgx_fFO8VsWnN9-6Uo85AB21mbw7__PB99OWR48fj_TXgON0ZHB_v5_niy9wRuosU2qW9rMFjMl_apB1kL9ay1bALfrnow_QaGFDzb
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9QwELZKkSouiDeBAgaBxCVs7Dixg4RQ1WW1S6EgoGhvIX5pV6qSstkV4q_x65jJi1YFbr1FyuRhz4z92TP-hpCnCeg40ykLpY9UKLyLwkKYNFROGxnpSDDdZFscptMj8XaezLfIr_4sDKZV9mNiM1DbyuAe-QhskcdSJIqNfJcW8XE8eX3yPcQKUhhp7ctptCZy4H7-gOVb_Wo2Bl0_43zy5sv-NOwqDIRGCKQoYMqm3iurWVHEVqo0skraSAttDUCRQhSwUMsizYSX1lsrYWiLWaF8kjqR-Bjee4lcljGgKvAlOZfD_g7HmKbKejKjiI8W9Yq_4BwL156eAs_h2vPpmadhczPvTa6Rqx1gpXuthV0nW668QXbedyH5m-QYDI22Zy1p5en-h6-zccgyWpUUsCXtT15SU2G6CC1KS6vNGvrcoXhH61pT3A-mZrlaLap6Wb-keyWt9LBjDM83PLi3yNGFdPBtsl1WpbtLaFFYgLI6zVRshGNGJT7zXsD60EuRORaQ532v5qbjN8cyG8d5y8zMc1RAjgoIyJNB9KQl9fib0G6vmrzz6zr_Y4UBeTzcBo_EMEtRumrTyCC3Q8rSgNxpNTl8BaPCCUC8gKgzOh4EkO377J1yuWhYv2FSygA8YDsbc_j3n-fTz584Xtz7fxMekR1wofzd7PDgPrmCBtvmwO2S7fVq4x4A2lrrh41ZU_Ltov3oN4ZqP6I
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=The+impact+of+COVID-19+on+the+clinical+course+and+outcome+of+patients+with+cirrhosis%3A+An+observational+study&rft.jtitle=Health+science+reports&rft.au=Shaikh%2C+Obaid+S&rft.au=Yan%2C+Peng&rft.au=Rogal%2C+Shari&rft.au=Butt%2C+Adeel+A&rft.date=2024-06-01&rft.eissn=2398-8835&rft.volume=7&rft.issue=6&rft.spage=e2207&rft_id=info:doi/10.1002%2Fhsr2.2207&rft_id=info%3Apmid%2F38915355&rft.externalDocID=38915355
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2398-8835&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2398-8835&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2398-8835&client=summon