Guest guest Posted October 6, 2004 Report Share Posted October 6, 2004 Liver Transpl. 2004 Oct;10 Suppl 10:S74. Evolving strategies to prevent HBV recurrence. Roche B, D. Centre Hepatobiliaire, Hopital Brousse, Villejuif, France. Key Points 1Long-term prophylaxis with hepatitis B immune globulin (HBIG) significantly reduces the risk for hepatitis B virus (HBV) recurrence and increases survival. Patients with HBV cirrhosis and / or positive HBV DNA at the time of transplantation have a high risk for recurrence despite HBIG prophylaxis.2Pre-orthotopic liver transplantation (OLT) antiviral treatment using lamivudine (LAM) can suppress HBV replication before transplantation and may induce clinical improvement in a subset of patients. Adefovir dipivoxil (ADV) may serve as " rescue " therapy for patients with LAM resistance; its place as first-line therapy requires further evaluation.3Combination prophylaxis with LAM and HBIG prevents HBV recurrence in 90% to 100% of patients who undergo transplantation for hepatitis B. The optimal HBIG protocol in the " nucleoside-nucleotide analog era " remains to be determined. The place of ADV or LAM as first-line posttransplant antiviral therapy in combination with HBIG requires further studies.4Future research should test new protocols using lower HBIG doses given intravenously (IV) or intramuscularly (IM) alone or in combination with antiviral agents and identify patients in whom HBIG prophylaxis can be stopped safely or replaced by antiviral agents or vaccination. (Liver Transpl 2004;10:S74-S85.) PMID: 15382222 [PubMed - in process] Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 6, 2004 Report Share Posted October 6, 2004 Liver Transpl. 2004 Oct;10 Suppl 10:S74. Evolving strategies to prevent HBV recurrence. Roche B, D. Centre Hepatobiliaire, Hopital Brousse, Villejuif, France. Key Points 1Long-term prophylaxis with hepatitis B immune globulin (HBIG) significantly reduces the risk for hepatitis B virus (HBV) recurrence and increases survival. Patients with HBV cirrhosis and / or positive HBV DNA at the time of transplantation have a high risk for recurrence despite HBIG prophylaxis.2Pre-orthotopic liver transplantation (OLT) antiviral treatment using lamivudine (LAM) can suppress HBV replication before transplantation and may induce clinical improvement in a subset of patients. Adefovir dipivoxil (ADV) may serve as " rescue " therapy for patients with LAM resistance; its place as first-line therapy requires further evaluation.3Combination prophylaxis with LAM and HBIG prevents HBV recurrence in 90% to 100% of patients who undergo transplantation for hepatitis B. The optimal HBIG protocol in the " nucleoside-nucleotide analog era " remains to be determined. The place of ADV or LAM as first-line posttransplant antiviral therapy in combination with HBIG requires further studies.4Future research should test new protocols using lower HBIG doses given intravenously (IV) or intramuscularly (IM) alone or in combination with antiviral agents and identify patients in whom HBIG prophylaxis can be stopped safely or replaced by antiviral agents or vaccination. (Liver Transpl 2004;10:S74-S85.) PMID: 15382222 [PubMed - in process] Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 6, 2004 Report Share Posted October 6, 2004 Liver Transpl. 2004 Oct;10 Suppl 10:S74. Evolving strategies to prevent HBV recurrence. Roche B, D. Centre Hepatobiliaire, Hopital Brousse, Villejuif, France. Key Points 1Long-term prophylaxis with hepatitis B immune globulin (HBIG) significantly reduces the risk for hepatitis B virus (HBV) recurrence and increases survival. Patients with HBV cirrhosis and / or positive HBV DNA at the time of transplantation have a high risk for recurrence despite HBIG prophylaxis.2Pre-orthotopic liver transplantation (OLT) antiviral treatment using lamivudine (LAM) can suppress HBV replication before transplantation and may induce clinical improvement in a subset of patients. Adefovir dipivoxil (ADV) may serve as " rescue " therapy for patients with LAM resistance; its place as first-line therapy requires further evaluation.3Combination prophylaxis with LAM and HBIG prevents HBV recurrence in 90% to 100% of patients who undergo transplantation for hepatitis B. The optimal HBIG protocol in the " nucleoside-nucleotide analog era " remains to be determined. The place of ADV or LAM as first-line posttransplant antiviral therapy in combination with HBIG requires further studies.4Future research should test new protocols using lower HBIG doses given intravenously (IV) or intramuscularly (IM) alone or in combination with antiviral agents and identify patients in whom HBIG prophylaxis can be stopped safely or replaced by antiviral agents or vaccination. (Liver Transpl 2004;10:S74-S85.) PMID: 15382222 [PubMed - in process] Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 6, 2004 Report Share Posted October 6, 2004 Liver Transpl. 2004 Oct;10 Suppl 10:S74. Evolving strategies to prevent HBV recurrence. Roche B, D. Centre Hepatobiliaire, Hopital Brousse, Villejuif, France. Key Points 1Long-term prophylaxis with hepatitis B immune globulin (HBIG) significantly reduces the risk for hepatitis B virus (HBV) recurrence and increases survival. Patients with HBV cirrhosis and / or positive HBV DNA at the time of transplantation have a high risk for recurrence despite HBIG prophylaxis.2Pre-orthotopic liver transplantation (OLT) antiviral treatment using lamivudine (LAM) can suppress HBV replication before transplantation and may induce clinical improvement in a subset of patients. Adefovir dipivoxil (ADV) may serve as " rescue " therapy for patients with LAM resistance; its place as first-line therapy requires further evaluation.3Combination prophylaxis with LAM and HBIG prevents HBV recurrence in 90% to 100% of patients who undergo transplantation for hepatitis B. The optimal HBIG protocol in the " nucleoside-nucleotide analog era " remains to be determined. The place of ADV or LAM as first-line posttransplant antiviral therapy in combination with HBIG requires further studies.4Future research should test new protocols using lower HBIG doses given intravenously (IV) or intramuscularly (IM) alone or in combination with antiviral agents and identify patients in whom HBIG prophylaxis can be stopped safely or replaced by antiviral agents or vaccination. (Liver Transpl 2004;10:S74-S85.) PMID: 15382222 [PubMed - in process] Quote Link to comment Share on other sites More sharing options...
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