Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/10693
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dc.contributor.authorAngus, Peter Wen
dc.contributor.authorPatterson, Scott Jen
dc.contributor.authorStrasser, Simone Ien
dc.contributor.authorMcCaughan, Geoffrey Wen
dc.contributor.authorGane, Edwarden
dc.date.accessioned2015-05-16T00:13:38Z
dc.date.available2015-05-16T00:13:38Z
dc.date.issued2008-11-01en
dc.identifier.citationHepatology (baltimore, Md.); 48(5): 1460-6en
dc.identifier.govdoc18925641en
dc.identifier.otherPUBMEDen
dc.identifier.urihttp://ahro.austin.org.au/austinjspui/handle/1/10693en
dc.description.abstractPrior to effective prophylaxis, liver transplantation for hepatitis B virus (HBV)-related disease was frequently complicated by recurrence, which could be severe and rapidly progressive. Combination hepatitis B immunoglobulin (HBIG) and lamivudine prophylaxis reduces this rate of recurrence to <5% at 5 years; however, HBIG administration is costly and inconvenient. We conducted a multicenter randomized study of adefovir dipivoxil substitution for low-dose intramuscular (IM) HBIG in patients without HBV recurrence at least 12 months posttransplantation for HBV-related disease. Thirty-four patients were randomized, 16 to adefovir (1 patient withdrew consent at 3 months and is not considered in the results) and 18 to continue HBIG. All continued lamivudine. Groups were well matched by age, sex, and time since transplantation (median, 4.5 years), and background virological risk for HBV recurrence (30% of patients in the adefovir group, 24% in the HBIG group having detectable HBV DNA at transplantation). All patients were alive at study completion without recurrence. One patient in the adefovir group became hepatitis B surface antigen-positive at 5 months but was persistently HBV DNA undetectable via polymerase chain reaction (sensitivity 14 IU/mL) over the following 20 months. Median creatinine was not significantly changed over the course of the study in either group. One patient in the adefovir group with a background of diabetic and hypertensive nephropathy (baseline creatinine 150 micromol/L) developed increased creatinine leading to dose reduction and ultimately cessation of adefovir at 15 months. Yearly cost of combination adefovir/lamivudine prophylaxis was $8,290 versus $13,718 IM HBIG/lamivudine.Compared with combination HBIG plus lamivudine prophylaxis, combination adefovir plus lamivudine provides equivalent protection against recurrent HBV infection but with better tolerability and less cost.en
dc.language.isoenen
dc.subject.otherAdenine.analogs & derivatives.therapeutic useen
dc.subject.otherAdulten
dc.subject.otherAgeden
dc.subject.otherAntiviral Agents.therapeutic useen
dc.subject.otherDNA, Viral.blooden
dc.subject.otherFemaleen
dc.subject.otherHepatitis B.immunology.prevention & controlen
dc.subject.otherHumansen
dc.subject.otherImmunization, Passiveen
dc.subject.otherImmunoglobulins.therapeutic useen
dc.subject.otherLamivudine.therapeutic useen
dc.subject.otherLiver Transplantation.adverse effectsen
dc.subject.otherMaleen
dc.subject.otherMiddle Ageden
dc.subject.otherOrganophosphonates.therapeutic useen
dc.subject.otherPatient Selectionen
dc.subject.otherPostoperative Complications.prevention & controlen
dc.subject.otherViral Loaden
dc.titleA randomized study of adefovir dipivoxil in place of HBIG in combination with lamivudine as post-liver transplantation hepatitis B prophylaxis.en
dc.typeJournal Articleen
dc.identifier.journaltitleHepatology (Baltimore, Md.)en
dc.identifier.affiliationVictorian Liver Transplant Unit, Austin Health, Victoria, Australiaen
dc.identifier.doi10.1002/hep.22524en
dc.description.pages1460-6en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/18925641en
dc.type.austinJournal Articleen
item.languageiso639-1en-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
crisitem.author.deptVictorian Liver Transplant Unit-
crisitem.author.deptGastroenterology and Hepatology-
crisitem.author.deptGastroenterology and Hepatology-
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