Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/11502
Title: Early-onset versus late-onset nonanastomotic biliary strictures post liver transplantation: risk factors reflect different pathogenesis.
Authors: Howell, Jessica A;Gow, Paul J;Angus, Peter W;Jones, Robert M;Wang, Bao-Zhong;Bailey, Michael J;Fink, Michael A
Affiliation: Liver Transplant Unit Victoria, Austin Hospital, Heidelberg, Australia. jess.howell@austin.org.au
Issue Date: 30-May-2012
Citation: Transplant International : Official Journal of the European Society For Organ Transplantation 2012; 25(7): 765-75
Abstract: Nonanastomotic 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.
Internal ID Number: 22643194
URI: http://ahro.austin.org.au/austinjspui/handle/1/11502
DOI: 10.1111/j.1432-2277.2012.01501.x
URL: http://www.ncbi.nlm.nih.gov/pubmed/22643194
Type: Journal Article
Subjects: Adult
Age of Onset
Biopsy
Cholangitis, Sclerosing.therapy
Cohort Studies
Constriction, Pathologic.etiology
Female
Humans
Liver.pathology
Liver Failure.complications.therapy
Liver Transplantation.adverse effects
Male
Middle Aged
Retrospective Studies
Risk Factors
Time Factors
Appears in Collections:Journal articles

Files in This Item:
There are no files associated with this item.


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.