Evaluation of current treatment recommendations for chronic hepatitis B: A 2011 update
Background and Aim: Guidelines for the treatment of chronic hepatitis B have been recently updated in the 2009 European Association for the Study of the Liver consensus statement, the 2008 US Panel, the 2008 Asian–Pacific consensus statement, and the 2009 American Association for the Study of Liver...
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description | Background and Aim: Guidelines for the treatment of chronic hepatitis B have been recently updated in the 2009 European Association for the Study of the Liver consensus statement, the 2008 US Panel, the 2008 Asian–Pacific consensus statement, and the 2009 American Association for the Study of Liver Disease practice guidelines. We sought to determine whether these guidelines identified patients who developed hepatocellular carcinoma (HCC) or who died of non‐HCC liver‐related deaths for antiviral therapy.
Methods: The criteria described in the new treatment guidelines were matched to the database of 369 hepatitis B surface antigen‐positive patients, in whom 30 developed HCC and 37 died of non‐HCC liver‐related deaths during a mean follow up of 84 months.
Results: Using criteria for antiviral therapy as stated by the four current guidelines, 19–30% of patients who died of non‐HCC liver‐related complications, and 23–53% of patients who developed HCC, would have been excluded for antiviral therapy. If baseline serum albumin levels of ≤ 3.5 g/dL or platelet counts of ≤ 130 000 mm3 were included into the treatment criteria, then 85–94% of patients who developed liver‐related complications would have been recommended for antiviral therapy. Also, the addition of precore A1896 mutants and basal core promoter T1762/A1764 mutants would have identified 98.5–100% of these patients.
Conclusion: The updated treatment guidelines for hepatitis B still excluded patients who developed serious liver‐related complications. The inclusion of baseline serum albumin and platelet counts to current criteria would have identified a majority of these patients for antiviral therapy. These tests should be included into hepatitis B treatment strategies. |
doi_str_mv | 10.1111/j.1440-1746.2011.06623.x |
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Methods: The criteria described in the new treatment guidelines were matched to the database of 369 hepatitis B surface antigen‐positive patients, in whom 30 developed HCC and 37 died of non‐HCC liver‐related deaths during a mean follow up of 84 months.
Results: Using criteria for antiviral therapy as stated by the four current guidelines, 19–30% of patients who died of non‐HCC liver‐related complications, and 23–53% of patients who developed HCC, would have been excluded for antiviral therapy. If baseline serum albumin levels of ≤ 3.5 g/dL or platelet counts of ≤ 130 000 mm3 were included into the treatment criteria, then 85–94% of patients who developed liver‐related complications would have been recommended for antiviral therapy. Also, the addition of precore A1896 mutants and basal core promoter T1762/A1764 mutants would have identified 98.5–100% of these patients.
Conclusion: The updated treatment guidelines for hepatitis B still excluded patients who developed serious liver‐related complications. The inclusion of baseline serum albumin and platelet counts to current criteria would have identified a majority of these patients for antiviral therapy. These tests should be included into hepatitis B treatment strategies.</description><identifier>ISSN: 0815-9319</identifier><identifier>EISSN: 1440-1746</identifier><identifier>DOI: 10.1111/j.1440-1746.2011.06623.x</identifier><identifier>PMID: 21214888</identifier><language>eng</language><publisher>Melbourne, Australia: Blackwell Publishing Asia</publisher><subject>Albumin ; Antiviral Agents - therapeutic use ; antiviral therapy ; basal core promoter mutant ; Biological and medical sciences ; Biomarkers - blood ; California ; Carcinoma, Hepatocellular - mortality ; Carcinoma, Hepatocellular - virology ; Disease Progression ; DNA Mutational Analysis ; DNA, Viral - blood ; Female ; Follow-Up Studies ; Gastroenterology. Liver. Pancreas. Abdomen ; Genotype ; Guideline Adherence ; Hepatitis B ; Hepatitis B Surface Antigens - blood ; Hepatitis B virus - genetics ; Hepatitis B virus - immunology ; Hepatitis B, Chronic - complications ; Hepatitis B, Chronic - diagnosis ; Hepatitis B, Chronic - drug therapy ; Hepatitis B, Chronic - mortality ; Hepatocellular carcinoma ; Human viral diseases ; Humans ; Infectious diseases ; Liver diseases ; Liver Neoplasms - mortality ; Liver Neoplasms - virology ; liver-related death ; Male ; Medical sciences ; Mutation ; Patient Selection ; platelet ; Platelet Count ; Platelets ; Practice Guidelines as Topic ; precore mutant ; Predictive Value of Tests ; Promoters ; Serum Albumin - analysis ; Time Factors ; Treatment Outcome ; Viral diseases ; Viral hepatitis</subject><ispartof>Journal of gastroenterology and hepatology, 2011-05, Vol.26 (5), p.829-835</ispartof><rights>2011 Journal of Gastroenterology and Hepatology Foundation and Blackwell Publishing Asia Pty Ltd</rights><rights>2015 INIST-CNRS</rights><rights>2011 Journal of Gastroenterology and Hepatology Foundation and Blackwell Publishing Asia Pty Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4693-f09501090a9c837d2674b17dd060b4ec4449683da15612f159158a895ff75a533</citedby><cites>FETCH-LOGICAL-c4693-f09501090a9c837d2674b17dd060b4ec4449683da15612f159158a895ff75a533</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1440-1746.2011.06623.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1440-1746.2011.06623.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24105064$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21214888$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tong, Myron John</creatorcontrib><creatorcontrib>Hsu, Leeyen</creatorcontrib><creatorcontrib>Chang, Patrick W</creatorcontrib><creatorcontrib>Blatt, Lawrence Mitchell</creatorcontrib><title>Evaluation of current treatment recommendations for chronic hepatitis B: A 2011 update</title><title>Journal of gastroenterology and hepatology</title><addtitle>J Gastroenterol Hepatol</addtitle><description>Background and Aim: Guidelines for the treatment of chronic hepatitis B have been recently updated in the 2009 European Association for the Study of the Liver consensus statement, the 2008 US Panel, the 2008 Asian–Pacific consensus statement, and the 2009 American Association for the Study of Liver Disease practice guidelines. We sought to determine whether these guidelines identified patients who developed hepatocellular carcinoma (HCC) or who died of non‐HCC liver‐related deaths for antiviral therapy.
Methods: The criteria described in the new treatment guidelines were matched to the database of 369 hepatitis B surface antigen‐positive patients, in whom 30 developed HCC and 37 died of non‐HCC liver‐related deaths during a mean follow up of 84 months.
Results: Using criteria for antiviral therapy as stated by the four current guidelines, 19–30% of patients who died of non‐HCC liver‐related complications, and 23–53% of patients who developed HCC, would have been excluded for antiviral therapy. If baseline serum albumin levels of ≤ 3.5 g/dL or platelet counts of ≤ 130 000 mm3 were included into the treatment criteria, then 85–94% of patients who developed liver‐related complications would have been recommended for antiviral therapy. Also, the addition of precore A1896 mutants and basal core promoter T1762/A1764 mutants would have identified 98.5–100% of these patients.
Conclusion: The updated treatment guidelines for hepatitis B still excluded patients who developed serious liver‐related complications. The inclusion of baseline serum albumin and platelet counts to current criteria would have identified a majority of these patients for antiviral therapy. These tests should be included into hepatitis B treatment strategies.</description><subject>Albumin</subject><subject>Antiviral Agents - therapeutic use</subject><subject>antiviral therapy</subject><subject>basal core promoter mutant</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - blood</subject><subject>California</subject><subject>Carcinoma, Hepatocellular - mortality</subject><subject>Carcinoma, Hepatocellular - virology</subject><subject>Disease Progression</subject><subject>DNA Mutational Analysis</subject><subject>DNA, Viral - blood</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Genotype</subject><subject>Guideline Adherence</subject><subject>Hepatitis B</subject><subject>Hepatitis B Surface Antigens - blood</subject><subject>Hepatitis B virus - genetics</subject><subject>Hepatitis B virus - immunology</subject><subject>Hepatitis B, Chronic - complications</subject><subject>Hepatitis B, Chronic - diagnosis</subject><subject>Hepatitis B, Chronic - drug therapy</subject><subject>Hepatitis B, Chronic - mortality</subject><subject>Hepatocellular carcinoma</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Liver diseases</subject><subject>Liver Neoplasms - mortality</subject><subject>Liver Neoplasms - virology</subject><subject>liver-related death</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mutation</subject><subject>Patient Selection</subject><subject>platelet</subject><subject>Platelet Count</subject><subject>Platelets</subject><subject>Practice Guidelines as Topic</subject><subject>precore mutant</subject><subject>Predictive Value of Tests</subject><subject>Promoters</subject><subject>Serum Albumin - analysis</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Viral diseases</subject><subject>Viral hepatitis</subject><issn>0815-9319</issn><issn>1440-1746</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkEtvEzEUhS0EoqHwF5A3CDYzXD_HRmLRViUBVbAprcTGcjy2OmEewZ6B9N_jaULYIbzxke93ru89CGECJcnn7aYknENBKi5LCoSUICVl5e4RWhwLj9ECFBGFZkSfoGcpbQCAQyWeohNKKOFKqQW6ufxp28mOzdDjIWA3xej7EY_R27GbVfRu6LKqH5iEwxCxu4tD3zh857f5dWwSPn-Hz_A8CZ62mfTP0ZNg2-RfHO5T9PXD5fXFqrj6svx4cXZVOC41KwJoAQQ0WO0Uq2oqK74mVV2DhDX3jnOupWK1JUISGojQRCirtAihElYwdope7_tu4_Bj8mk0XZOcb1vb-2FKRkmaeyo6k2_-SRKgoLhUVGRU7VEXh5SiD2Ybm87G-wyZOX-zMXPMZo7ZzFubh_zNLltfHn6Z1p2vj8Y_gWfg1QGwydk2RNu7Jv3lOAEBkmfu_Z771bT-_r8HMJ-Wq1llf7H3N2n0u6Pfxu9GVqwS5vbz0qy-na84vb02N-w3vj6tGw</recordid><startdate>201105</startdate><enddate>201105</enddate><creator>Tong, Myron John</creator><creator>Hsu, Leeyen</creator><creator>Chang, Patrick W</creator><creator>Blatt, Lawrence Mitchell</creator><general>Blackwell Publishing Asia</general><general>Wiley-Blackwell</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>201105</creationdate><title>Evaluation of current treatment recommendations for chronic hepatitis B: A 2011 update</title><author>Tong, Myron John ; Hsu, Leeyen ; Chang, Patrick W ; Blatt, Lawrence Mitchell</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4693-f09501090a9c837d2674b17dd060b4ec4449683da15612f159158a895ff75a533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Albumin</topic><topic>Antiviral Agents - therapeutic use</topic><topic>antiviral therapy</topic><topic>basal core promoter mutant</topic><topic>Biological and medical sciences</topic><topic>Biomarkers - blood</topic><topic>California</topic><topic>Carcinoma, Hepatocellular - mortality</topic><topic>Carcinoma, Hepatocellular - virology</topic><topic>Disease Progression</topic><topic>DNA Mutational Analysis</topic><topic>DNA, Viral - blood</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Genotype</topic><topic>Guideline Adherence</topic><topic>Hepatitis B</topic><topic>Hepatitis B Surface Antigens - blood</topic><topic>Hepatitis B virus - genetics</topic><topic>Hepatitis B virus - immunology</topic><topic>Hepatitis B, Chronic - complications</topic><topic>Hepatitis B, Chronic - diagnosis</topic><topic>Hepatitis B, Chronic - drug therapy</topic><topic>Hepatitis B, Chronic - mortality</topic><topic>Hepatocellular carcinoma</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Liver diseases</topic><topic>Liver Neoplasms - mortality</topic><topic>Liver Neoplasms - virology</topic><topic>liver-related death</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mutation</topic><topic>Patient Selection</topic><topic>platelet</topic><topic>Platelet Count</topic><topic>Platelets</topic><topic>Practice Guidelines as Topic</topic><topic>precore mutant</topic><topic>Predictive Value of Tests</topic><topic>Promoters</topic><topic>Serum Albumin - analysis</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Viral diseases</topic><topic>Viral hepatitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tong, Myron John</creatorcontrib><creatorcontrib>Hsu, Leeyen</creatorcontrib><creatorcontrib>Chang, Patrick W</creatorcontrib><creatorcontrib>Blatt, Lawrence Mitchell</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of gastroenterology and hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tong, Myron John</au><au>Hsu, Leeyen</au><au>Chang, Patrick W</au><au>Blatt, Lawrence Mitchell</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of current treatment recommendations for chronic hepatitis B: A 2011 update</atitle><jtitle>Journal of gastroenterology and hepatology</jtitle><addtitle>J Gastroenterol Hepatol</addtitle><date>2011-05</date><risdate>2011</risdate><volume>26</volume><issue>5</issue><spage>829</spage><epage>835</epage><pages>829-835</pages><issn>0815-9319</issn><eissn>1440-1746</eissn><abstract>Background and Aim: Guidelines for the treatment of chronic hepatitis B have been recently updated in the 2009 European Association for the Study of the Liver consensus statement, the 2008 US Panel, the 2008 Asian–Pacific consensus statement, and the 2009 American Association for the Study of Liver Disease practice guidelines. We sought to determine whether these guidelines identified patients who developed hepatocellular carcinoma (HCC) or who died of non‐HCC liver‐related deaths for antiviral therapy.
Methods: The criteria described in the new treatment guidelines were matched to the database of 369 hepatitis B surface antigen‐positive patients, in whom 30 developed HCC and 37 died of non‐HCC liver‐related deaths during a mean follow up of 84 months.
Results: Using criteria for antiviral therapy as stated by the four current guidelines, 19–30% of patients who died of non‐HCC liver‐related complications, and 23–53% of patients who developed HCC, would have been excluded for antiviral therapy. If baseline serum albumin levels of ≤ 3.5 g/dL or platelet counts of ≤ 130 000 mm3 were included into the treatment criteria, then 85–94% of patients who developed liver‐related complications would have been recommended for antiviral therapy. Also, the addition of precore A1896 mutants and basal core promoter T1762/A1764 mutants would have identified 98.5–100% of these patients.
Conclusion: The updated treatment guidelines for hepatitis B still excluded patients who developed serious liver‐related complications. The inclusion of baseline serum albumin and platelet counts to current criteria would have identified a majority of these patients for antiviral therapy. These tests should be included into hepatitis B treatment strategies.</abstract><cop>Melbourne, Australia</cop><pub>Blackwell Publishing Asia</pub><pmid>21214888</pmid><doi>10.1111/j.1440-1746.2011.06623.x</doi><tpages>7</tpages></addata></record> |
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subjects | Albumin Antiviral Agents - therapeutic use antiviral therapy basal core promoter mutant Biological and medical sciences Biomarkers - blood California Carcinoma, Hepatocellular - mortality Carcinoma, Hepatocellular - virology Disease Progression DNA Mutational Analysis DNA, Viral - blood Female Follow-Up Studies Gastroenterology. Liver. Pancreas. Abdomen Genotype Guideline Adherence Hepatitis B Hepatitis B Surface Antigens - blood Hepatitis B virus - genetics Hepatitis B virus - immunology Hepatitis B, Chronic - complications Hepatitis B, Chronic - diagnosis Hepatitis B, Chronic - drug therapy Hepatitis B, Chronic - mortality Hepatocellular carcinoma Human viral diseases Humans Infectious diseases Liver diseases Liver Neoplasms - mortality Liver Neoplasms - virology liver-related death Male Medical sciences Mutation Patient Selection platelet Platelet Count Platelets Practice Guidelines as Topic precore mutant Predictive Value of Tests Promoters Serum Albumin - analysis Time Factors Treatment Outcome Viral diseases Viral hepatitis |
title | Evaluation of current treatment recommendations for chronic hepatitis B: A 2011 update |
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