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...
Saved in:
Published in | Health science reports Vol. 7; no. 6; pp. e2207 - n/a |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
United States
John Wiley & Sons, Inc
01.06.2024
John Wiley and Sons Inc |
Subjects | |
Online Access | Get full text |
ISSN | 2398-8835 2398-8835 |
DOI | 10.1002/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 |