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Prophylaxis and treatment of recurrent viral hepatitis after liver transplantation
Chronic hepatitis B or C can cause severe liver diseases such as liver cirrhosis and hepatocellular carcinoma (HCC). Both viral infections together especially hepatitis c virus infection (HCV) are the mayor indication for liver transplantation in Western Europe and the United States. Recurrence of h...
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Published in: | Nephrology, dialysis, transplantation dialysis, transplantation, 2007-09, Vol.22 (suppl-8), p.viii37-viii46 |
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container_start_page | viii37 |
container_title | Nephrology, dialysis, transplantation |
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creator | Riediger, Carina Berberat, Pascal O. Sauer, Peter Gotthardt, Daniel Weiss, Karl Heinz Mehrabi, Arianeb Merle, Uta Stremmel, Wolfgang Encke, Jens |
description | Chronic hepatitis B or C can cause severe liver diseases such as liver cirrhosis and hepatocellular carcinoma (HCC). Both viral infections together especially hepatitis c virus infection (HCV) are the mayor indication for liver transplantation in Western Europe and the United States. Recurrence of hepatitis B virus (HBV) or HCV infection after orthotopic liver transplantation (OLT) plays a key role for the outcome after liver transplantation concerning patient and graft survival rates. Allograft dysfunctions, cirrhosis of the allograft and graft failure are major complications after recurrent viral hepatitis. The survival after liver transplantation for HBV-related liver disease changed dramatically during the last two decades with results today comparable with non-HBV-related liver transplantations. Availability of immunoprophylaxis with hepatitis B immunoglobulin (HBIG) as well as nucleoside/nucleotide analogues like lamivudine or adefovir in the pre- and post-transplant setting conferred to significant better results due to an efficient prophylaxis and the possibility of therapy of HBV reinfection of the allograft. New drugs such as entecavir, tenofovir and telbivudine for the treatment of chronic hepatitis B infections may offer even more opportunities in the transplant setting. In contrast, despite recent achievements in the treatment of HCV infection with pegylated interferons and ribavirin, patients with HCV cirrhosis or after liver transplantation are difficult to treat. Sustained virological response (SVR) rates in prophylactic and therapeutic approaches of HCV reinfection after OLT are only low compared to the pre-cirrhotic HCV infection. Moreover, best treatment duration and dosage of recurrent HCV infection with pegylated interferon in combination with ribavirin remains to be defined. |
doi_str_mv | 10.1093/ndt/gfm655 |
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Both viral infections together especially hepatitis c virus infection (HCV) are the mayor indication for liver transplantation in Western Europe and the United States. Recurrence of hepatitis B virus (HBV) or HCV infection after orthotopic liver transplantation (OLT) plays a key role for the outcome after liver transplantation concerning patient and graft survival rates. Allograft dysfunctions, cirrhosis of the allograft and graft failure are major complications after recurrent viral hepatitis. The survival after liver transplantation for HBV-related liver disease changed dramatically during the last two decades with results today comparable with non-HBV-related liver transplantations. Availability of immunoprophylaxis with hepatitis B immunoglobulin (HBIG) as well as nucleoside/nucleotide analogues like lamivudine or adefovir in the pre- and post-transplant setting conferred to significant better results due to an efficient prophylaxis and the possibility of therapy of HBV reinfection of the allograft. New drugs such as entecavir, tenofovir and telbivudine for the treatment of chronic hepatitis B infections may offer even more opportunities in the transplant setting. In contrast, despite recent achievements in the treatment of HCV infection with pegylated interferons and ribavirin, patients with HCV cirrhosis or after liver transplantation are difficult to treat. Sustained virological response (SVR) rates in prophylactic and therapeutic approaches of HCV reinfection after OLT are only low compared to the pre-cirrhotic HCV infection. Moreover, best treatment duration and dosage of recurrent HCV infection with pegylated interferon in combination with ribavirin remains to be defined.</description><identifier>ISSN: 0931-0509</identifier><identifier>EISSN: 1460-2385</identifier><identifier>DOI: 10.1093/ndt/gfm655</identifier><identifier>PMID: 17890261</identifier><identifier>CODEN: NDTREA</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Antiviral Agents - pharmacology ; Biological and medical sciences ; Emergency and intensive care: renal failure. Dialysis management ; Fibrosis - therapy ; Fibrosis - virology ; hepatitis B ; Hepatitis B virus ; Hepatitis B, Chronic - immunology ; hepatitis C ; Hepatitis C virus ; Hepatitis, Chronic - diagnosis ; Hepatitis, Chronic - prevention & control ; Hepatitis, Chronic - therapy ; Hepatitis, Chronic - virology ; Human viral diseases ; Humans ; Immunoglobulins - chemistry ; Infectious diseases ; Intensive care medicine ; Interferons - pharmacology ; liver transplantation ; Liver Transplantation - methods ; Medical sciences ; Polyethylene Glycols - chemistry ; Recurrence ; recurrent viral hepatitis ; Ribavirin - pharmacology ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Surgery of the urinary system ; Treatment Outcome ; Viral diseases ; Viral hepatitis</subject><ispartof>Nephrology, dialysis, transplantation, 2007-09, Vol.22 (suppl-8), p.viii37-viii46</ispartof><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-92c5d54249efe3afa6b4bf75670d55c96ee9d1036bed534b2e67b5765845da233</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>309,310,314,780,784,789,790,23930,23931,25140,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19225340$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17890261$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Riediger, Carina</creatorcontrib><creatorcontrib>Berberat, Pascal O.</creatorcontrib><creatorcontrib>Sauer, Peter</creatorcontrib><creatorcontrib>Gotthardt, Daniel</creatorcontrib><creatorcontrib>Weiss, Karl Heinz</creatorcontrib><creatorcontrib>Mehrabi, Arianeb</creatorcontrib><creatorcontrib>Merle, Uta</creatorcontrib><creatorcontrib>Stremmel, Wolfgang</creatorcontrib><creatorcontrib>Encke, Jens</creatorcontrib><title>Prophylaxis and treatment of recurrent viral hepatitis after liver transplantation</title><title>Nephrology, dialysis, transplantation</title><addtitle>Nephrol Dial Transplant</addtitle><description>Chronic hepatitis B or C can cause severe liver diseases such as liver cirrhosis and hepatocellular carcinoma (HCC). Both viral infections together especially hepatitis c virus infection (HCV) are the mayor indication for liver transplantation in Western Europe and the United States. Recurrence of hepatitis B virus (HBV) or HCV infection after orthotopic liver transplantation (OLT) plays a key role for the outcome after liver transplantation concerning patient and graft survival rates. Allograft dysfunctions, cirrhosis of the allograft and graft failure are major complications after recurrent viral hepatitis. The survival after liver transplantation for HBV-related liver disease changed dramatically during the last two decades with results today comparable with non-HBV-related liver transplantations. Availability of immunoprophylaxis with hepatitis B immunoglobulin (HBIG) as well as nucleoside/nucleotide analogues like lamivudine or adefovir in the pre- and post-transplant setting conferred to significant better results due to an efficient prophylaxis and the possibility of therapy of HBV reinfection of the allograft. New drugs such as entecavir, tenofovir and telbivudine for the treatment of chronic hepatitis B infections may offer even more opportunities in the transplant setting. In contrast, despite recent achievements in the treatment of HCV infection with pegylated interferons and ribavirin, patients with HCV cirrhosis or after liver transplantation are difficult to treat. Sustained virological response (SVR) rates in prophylactic and therapeutic approaches of HCV reinfection after OLT are only low compared to the pre-cirrhotic HCV infection. Moreover, best treatment duration and dosage of recurrent HCV infection with pegylated interferon in combination with ribavirin remains to be defined.</description><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Antiviral Agents - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Emergency and intensive care: renal failure. Dialysis management</subject><subject>Fibrosis - therapy</subject><subject>Fibrosis - virology</subject><subject>hepatitis B</subject><subject>Hepatitis B virus</subject><subject>Hepatitis B, Chronic - immunology</subject><subject>hepatitis C</subject><subject>Hepatitis C virus</subject><subject>Hepatitis, Chronic - diagnosis</subject><subject>Hepatitis, Chronic - prevention & control</subject><subject>Hepatitis, Chronic - therapy</subject><subject>Hepatitis, Chronic - virology</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Immunoglobulins - chemistry</subject><subject>Infectious diseases</subject><subject>Intensive care medicine</subject><subject>Interferons - pharmacology</subject><subject>liver transplantation</subject><subject>Liver Transplantation - methods</subject><subject>Medical sciences</subject><subject>Polyethylene Glycols - chemistry</subject><subject>Recurrence</subject><subject>recurrent viral hepatitis</subject><subject>Ribavirin - pharmacology</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Surgery of the urinary system</subject><subject>Treatment Outcome</subject><subject>Viral diseases</subject><subject>Viral hepatitis</subject><issn>0931-0509</issn><issn>1460-2385</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqF0E1LwzAYB_AgipvTix9AetGDUJcmTdIcZb5MERSZMryEtH2i1b6ZZOK-vRkbevSQhPD_8ZD8ETpM8FmCJR23pR-_moYztoWGScpxTGjGttEwhEmMGZYDtOfcO8ZYEiF20SARmcSEJ0P0-GC7_m1Z6-_KRbotI29B-wZaH3UmslAsrF1dviqr6-gNeu0rv6LGg43q6ivs3urW9bVufQi7dh_tGF07ONicI_R0dTmbTOO7--ubyfldXKQE-1iSgpUsJakEA1QbzfM0N4JxgUvGCskBZJlgynMoGU1zAlzkTHCWpazUhNIROlnP7W33uQDnVVO5AurwEOgWTvGM4rCyfyHBJMuI5AGermFhO-csGNXbqtF2qRKsVlWrULVaVx3w0WbqIm-g_KObbgM43gDtCl2b0FJRuT8nCQn_wsHFa1c5D9-_ubYfigsqmJrOX9QzmV7MKblVM_oDAriYCg</recordid><startdate>20070901</startdate><enddate>20070901</enddate><creator>Riediger, Carina</creator><creator>Berberat, Pascal O.</creator><creator>Sauer, Peter</creator><creator>Gotthardt, Daniel</creator><creator>Weiss, Karl Heinz</creator><creator>Mehrabi, Arianeb</creator><creator>Merle, Uta</creator><creator>Stremmel, Wolfgang</creator><creator>Encke, Jens</creator><general>Oxford University Press</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>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20070901</creationdate><title>Prophylaxis and treatment of recurrent viral hepatitis after liver transplantation</title><author>Riediger, Carina ; Berberat, Pascal O. ; Sauer, Peter ; Gotthardt, Daniel ; Weiss, Karl Heinz ; Mehrabi, Arianeb ; Merle, Uta ; Stremmel, Wolfgang ; Encke, Jens</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-92c5d54249efe3afa6b4bf75670d55c96ee9d1036bed534b2e67b5765845da233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Antiviral Agents - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Emergency and intensive care: renal failure. Dialysis management</topic><topic>Fibrosis - therapy</topic><topic>Fibrosis - virology</topic><topic>hepatitis B</topic><topic>Hepatitis B virus</topic><topic>Hepatitis B, Chronic - immunology</topic><topic>hepatitis C</topic><topic>Hepatitis C virus</topic><topic>Hepatitis, Chronic - diagnosis</topic><topic>Hepatitis, Chronic - prevention & control</topic><topic>Hepatitis, Chronic - therapy</topic><topic>Hepatitis, Chronic - virology</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Immunoglobulins - chemistry</topic><topic>Infectious diseases</topic><topic>Intensive care medicine</topic><topic>Interferons - pharmacology</topic><topic>liver transplantation</topic><topic>Liver Transplantation - methods</topic><topic>Medical sciences</topic><topic>Polyethylene Glycols - chemistry</topic><topic>Recurrence</topic><topic>recurrent viral hepatitis</topic><topic>Ribavirin - pharmacology</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the urinary system</topic><topic>Treatment Outcome</topic><topic>Viral diseases</topic><topic>Viral hepatitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Riediger, Carina</creatorcontrib><creatorcontrib>Berberat, Pascal O.</creatorcontrib><creatorcontrib>Sauer, Peter</creatorcontrib><creatorcontrib>Gotthardt, Daniel</creatorcontrib><creatorcontrib>Weiss, Karl Heinz</creatorcontrib><creatorcontrib>Mehrabi, Arianeb</creatorcontrib><creatorcontrib>Merle, Uta</creatorcontrib><creatorcontrib>Stremmel, Wolfgang</creatorcontrib><creatorcontrib>Encke, Jens</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>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Nephrology, dialysis, transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Riediger, Carina</au><au>Berberat, Pascal O.</au><au>Sauer, Peter</au><au>Gotthardt, Daniel</au><au>Weiss, Karl Heinz</au><au>Mehrabi, Arianeb</au><au>Merle, Uta</au><au>Stremmel, Wolfgang</au><au>Encke, Jens</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prophylaxis and treatment of recurrent viral hepatitis after liver transplantation</atitle><jtitle>Nephrology, dialysis, transplantation</jtitle><addtitle>Nephrol Dial Transplant</addtitle><date>2007-09-01</date><risdate>2007</risdate><volume>22</volume><issue>suppl-8</issue><spage>viii37</spage><epage>viii46</epage><pages>viii37-viii46</pages><issn>0931-0509</issn><eissn>1460-2385</eissn><coden>NDTREA</coden><abstract>Chronic hepatitis B or C can cause severe liver diseases such as liver cirrhosis and hepatocellular carcinoma (HCC). Both viral infections together especially hepatitis c virus infection (HCV) are the mayor indication for liver transplantation in Western Europe and the United States. Recurrence of hepatitis B virus (HBV) or HCV infection after orthotopic liver transplantation (OLT) plays a key role for the outcome after liver transplantation concerning patient and graft survival rates. Allograft dysfunctions, cirrhosis of the allograft and graft failure are major complications after recurrent viral hepatitis. The survival after liver transplantation for HBV-related liver disease changed dramatically during the last two decades with results today comparable with non-HBV-related liver transplantations. Availability of immunoprophylaxis with hepatitis B immunoglobulin (HBIG) as well as nucleoside/nucleotide analogues like lamivudine or adefovir in the pre- and post-transplant setting conferred to significant better results due to an efficient prophylaxis and the possibility of therapy of HBV reinfection of the allograft. New drugs such as entecavir, tenofovir and telbivudine for the treatment of chronic hepatitis B infections may offer even more opportunities in the transplant setting. In contrast, despite recent achievements in the treatment of HCV infection with pegylated interferons and ribavirin, patients with HCV cirrhosis or after liver transplantation are difficult to treat. Sustained virological response (SVR) rates in prophylactic and therapeutic approaches of HCV reinfection after OLT are only low compared to the pre-cirrhotic HCV infection. Moreover, best treatment duration and dosage of recurrent HCV infection with pegylated interferon in combination with ribavirin remains to be defined.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>17890261</pmid><doi>10.1093/ndt/gfm655</doi><oa>free_for_read</oa></addata></record> |
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subjects | Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Antiviral Agents - pharmacology Biological and medical sciences Emergency and intensive care: renal failure. Dialysis management Fibrosis - therapy Fibrosis - virology hepatitis B Hepatitis B virus Hepatitis B, Chronic - immunology hepatitis C Hepatitis C virus Hepatitis, Chronic - diagnosis Hepatitis, Chronic - prevention & control Hepatitis, Chronic - therapy Hepatitis, Chronic - virology Human viral diseases Humans Immunoglobulins - chemistry Infectious diseases Intensive care medicine Interferons - pharmacology liver transplantation Liver Transplantation - methods Medical sciences Polyethylene Glycols - chemistry Recurrence recurrent viral hepatitis Ribavirin - pharmacology Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the urinary system Treatment Outcome Viral diseases Viral hepatitis |
title | Prophylaxis and treatment of recurrent viral hepatitis after liver transplantation |
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