Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/11502
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dc.contributor.authorHowell, Jessica A-
dc.contributor.authorGow, Paul J-
dc.contributor.authorAngus, Peter W-
dc.contributor.authorJones, Robert M-
dc.contributor.authorWang, Bao-Zhong-
dc.contributor.authorBailey, Michael J-
dc.contributor.authorFink, Michael A-
dc.date.accessioned2015-05-16T01:06:56Z
dc.date.available2015-05-16T01:06:56Z
dc.date.issued2012-05-30-
dc.identifier.citationTransplant International : Official Journal of the European Society For Organ Transplantation 2012; 25(7): 765-75en_US
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/11502en
dc.description.abstractNonanastomotic biliary strictures (NAS) cause significant morbidity post liver transplantation. Timing of stricture development varies considerably, but the relationship between timing of stricture onset and aetiology has not been fully elucidated. Database analysis was performed on all adult patients undergoing liver transplantation between 1st January 1990 and 31st May 2008. Diagnosis of NAS required demonstration on at least two radiological studies. Early NAS were defined as developing <1 year post transplant (minimum 1-year follow-up) and late NAS developing >1 year post transplant (minimum 10-year follow-up). Ninety-six of 397 patients developed NAS (24%); 54 were early-onset NAS (56%) and 42 late-onset NAS (44%). Primary sclerosing cholangitis (PSC) was the only risk factor for NAS overall (P = 0.001). However, when patients with PSC were excluded, older donor age was a significant risk for NAS (P = 0.003). Early-onset NAS were associated with advanced donor age (P = 0.02), high MELD score (P = 0.001) and ABO-identical grafts (P = 0.02), whereas late-onset NAS were associated with PSC (P = 0.0008), bilio-enteric anastomosis (P = 0.006) and tacrolimus (P = 0.0001). Advanced donor age is a significant risk for NAS in patients without PSC. Importantly, aetiology of NAS varies depending on time to stricture development, suggesting early-onset and late-onset NAS may have different pathogenesis.en_US
dc.language.isoenen
dc.subject.otherAdulten
dc.subject.otherAge of Onseten
dc.subject.otherBiopsyen
dc.subject.otherCholangitis, Sclerosing.therapyen
dc.subject.otherCohort Studiesen
dc.subject.otherConstriction, Pathologic.etiologyen
dc.subject.otherFemaleen
dc.subject.otherHumansen
dc.subject.otherLiver.pathologyen
dc.subject.otherLiver Failure.complications.therapyen
dc.subject.otherLiver Transplantation.adverse effectsen
dc.subject.otherMaleen
dc.subject.otherMiddle Ageden
dc.subject.otherRetrospective Studiesen
dc.subject.otherRisk Factorsen
dc.subject.otherTime Factorsen
dc.titleEarly-onset versus late-onset nonanastomotic biliary strictures post liver transplantation: risk factors reflect different pathogenesis.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleTransplant International : Official Journal of the European Society For Organ Transplantationen_US
dc.identifier.affiliationVictorian Liver Transplant Uniten_US
dc.identifier.doi10.1111/j.1432-2277.2012.01501.xen_US
dc.description.pages765-75en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/22643194en
dc.type.contentTexten_US
dc.type.austinJournal Articleen
local.name.researcherAngus, Peter W
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
crisitem.author.deptVictorian Liver Transplant Unit-
crisitem.author.deptGastroenterology and Hepatology-
crisitem.author.deptVictorian Liver Transplant Unit-
crisitem.author.deptGastroenterology and Hepatology-
crisitem.author.deptVictorian Liver Transplant Unit-
crisitem.author.deptSurgery (University of Melbourne)-
crisitem.author.deptHepatopancreatobiliary Surgery-
crisitem.author.deptGastroenterology and Hepatology-
crisitem.author.deptVictorian Liver Transplant Unit-
crisitem.author.deptSurgery-
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