<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang L</submitter><funding>Natural Science Foundation of China</funding><funding>the National major science and technology project for the prevention and treatment of AIDS and viral hepatitis</funding><funding>Sun Yat-Sen University Clinical Research 5010 Program</funding><funding>Guangzhou Municipal Science and Technology Project</funding><funding>Research project on degree and postgraduate education reform in Guangdong province</funding><funding>Young teacher training program of Sun Yat-Sen university</funding><funding>the Five-Year Plan of Third Affiliated Hospital of Sun Yat-Sen University</funding><pagination>162</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8976971</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>22(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The long-term prognosis of patients with hepatitis B virus-related acute-on-chronic liver failure (HBV-ACLF) is not well characterised. We assessed long-term outcomes and the associated risk factors of HBV-ACLF patients in southern China.&lt;h4>Methods&lt;/h4>We retrospectively analysed clinical data, adverse events, and clinical endpoint events of HBV-ACLF patients treated at our department between January 2014 and December 2018.&lt;h4>Results&lt;/h4>A total of 616 (52.3%) patients with cirrhosis and 561 (47.7%) patients without cirrhosis were included. In 973 (83%) patients, the disease was associated only with HBV, while 204 (17%) patients had two or more aetiological factors. The proportion of patients receiving antiviral treatment for HBV was low (20.3%). Further analyses indicated that patients without cirrhosis had a significantly lower 90-day liver transplantation-free mortality and higher 5-year survival rate than those with cirrhosis (59.5% vs. 27.6%; 62% vs. 36%; P &lt; 0.05). Remarkably, self-withdrawal of nucleos(t)ide analog (NA) was an independent risk factor for short-term prognosis. Age, cirrhosis at admission, and platelet level were closely related to long-term prognosis of HBV-ACLF patients.&lt;h4>Conclusion&lt;/h4>The proportion of HBV-ACLF patients receiving antiviral treatment is very low in south China. Cirrhosis at admission has a significant effect on both short-term and long-term prognosis. No significant improvement in the short-term prognosis of HBV-ACLF patients was observed compared with previous studies. More comprehensive access to antiviral treatment and long-term surveillance of HBV patients are key imperatives to reduce the incidence of HBV-ACLF and improve the prognosis. Trial Registration The trial was registered at ClinicalTrials.gov (CT.gov identifier: NCT04231565) on May 13, 2020: https://register.&lt;h4>Clinicaltrials&lt;/h4>gov/prs/app/action/SelectProtocol?sid=S0009OZY&amp;selectaction=Edit&amp;uid=U00036P1&amp;ts=2&amp;cx=27seqt.</pubmed_abstract><journal>BMC gastroenterology</journal><pubmed_title>Long-term prognosis of patients with hepatitis B virus-related acute-on-chronic liver failure: a retrospective study.</pubmed_title><pmcid>PMC8976971</pmcid><funding_grant_id>2018009 to CX, 2020007 to LP</funding_grant_id><funding_grant_id>16ykpy40 to CX</funding_grant_id><funding_grant_id>2018JGXM04 to CX</funding_grant_id><funding_grant_id>K00006 to LP</funding_grant_id><funding_grant_id>No. 81873572 to LP , 82070611 to LP</funding_grant_id><funding_grant_id>201904010442 to CX, 202102010204 to LP</funding_grant_id><funding_grant_id>2018ZX10302204-002 to LP, 2018ZX10302205-002 to CX</funding_grant_id><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Luo Q</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Peng L</pubmed_authors><pubmed_authors>Xu W</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Xie C</pubmed_authors><pubmed_authors>Wang L</pubmed_authors><pubmed_authors>Chen D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Long-term prognosis of patients with hepatitis B virus-related acute-on-chronic liver failure: a retrospective study.</name><description>&lt;h4>Background&lt;/h4>The long-term prognosis of patients with hepatitis B virus-related acute-on-chronic liver failure (HBV-ACLF) is not well characterised. We assessed long-term outcomes and the associated risk factors of HBV-ACLF patients in southern China.&lt;h4>Methods&lt;/h4>We retrospectively analysed clinical data, adverse events, and clinical endpoint events of HBV-ACLF patients treated at our department between January 2014 and December 2018.&lt;h4>Results&lt;/h4>A total of 616 (52.3%) patients with cirrhosis and 561 (47.7%) patients without cirrhosis were included. In 973 (83%) patients, the disease was associated only with HBV, while 204 (17%) patients had two or more aetiological factors. The proportion of patients receiving antiviral treatment for HBV was low (20.3%). Further analyses indicated that patients without cirrhosis had a significantly lower 90-day liver transplantation-free mortality and higher 5-year survival rate than those with cirrhosis (59.5% vs. 27.6%; 62% vs. 36%; P &lt; 0.05). Remarkably, self-withdrawal of nucleos(t)ide analog (NA) was an independent risk factor for short-term prognosis. Age, cirrhosis at admission, and platelet level were closely related to long-term prognosis of HBV-ACLF patients.&lt;h4>Conclusion&lt;/h4>The proportion of HBV-ACLF patients receiving antiviral treatment is very low in south China. Cirrhosis at admission has a significant effect on both short-term and long-term prognosis. No significant improvement in the short-term prognosis of HBV-ACLF patients was observed compared with previous studies. More comprehensive access to antiviral treatment and long-term surveillance of HBV patients are key imperatives to reduce the incidence of HBV-ACLF and improve the prognosis. Trial Registration The trial was registered at ClinicalTrials.gov (CT.gov identifier: NCT04231565) on May 13, 2020: https://register.&lt;h4>Clinicaltrials&lt;/h4>gov/prs/app/action/SelectProtocol?sid=S0009OZY&amp;selectaction=Edit&amp;uid=U00036P1&amp;ts=2&amp;cx=27seqt.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-05-29T19:47:18.462Z</modification><creation>2025-05-29T19:47:18.462Z</creation></dates><accession>S-EPMC8976971</accession><cross_references><pubmed>35366805</pubmed><doi>10.1186/s12876-022-02239-4</doi></cross_references></HashMap>