Identifying the superior measure of rapid fibrosis for predicting premature cirrhosis after liver transplantation for hepatitis C. Issue 6 (13th September 2013)
- Record Type:
- Journal Article
- Title:
- Identifying the superior measure of rapid fibrosis for predicting premature cirrhosis after liver transplantation for hepatitis C. Issue 6 (13th September 2013)
- Main Title:
- Identifying the superior measure of rapid fibrosis for predicting premature cirrhosis after liver transplantation for hepatitis C
- Authors:
- Howell, J.
Sawhney, R.
Angus, P.
Fink, M.
Jones, R.
Wang, B.Z.
Visvanathan, K.
Crowley, P.
Gow, P. - Abstract:
- <abstract abstract-type="main" id="tid12134-abs-0001"> <title>Abstract</title> <sec id="tid12134-sec-0001" sec-type="section"> <title>Background</title> <p>Hepatitis C virus (HCV) recurrence post liver transplant is universal, with a subgroup of patients developing rapid hepatic fibrosis. Various clinical definitions of rapid fibrosis (RF) have been used to identify risks for rapid progression, but their comparability and efficacy at predicting adverse outcomes has not been determined.</p> </sec> <sec id="tid12134-sec-0002" sec-type="section"> <title>Methods</title> <p>Retrospective data analysis was conducted on 100 adult patients with HCV who underwent liver transplantation at a single center. We measured year 1 fibrosis progression (RF defined as METAVIR F score ≥1 at 1‐year liver biopsy), time to METAVIR F2‐stage fibrosis, and fibrosis rate (calculated using liver biopsies graded by METAVIR scoring F0–4; fibrosis rate = fibrosis stage/year post transplant). RF was defined as ≥0.5 units/year.</p> </sec> <sec id="tid12134-sec-0003" sec-type="section"> <title>Results</title> <p>Multivariate analysis revealed that donor age and peak HCV viral load were significant risks for RF, when fibrosis rate was used to define RF. Advanced donor age was a risk for rapid progression to F2‐stage fibrosis, whereas genotype 2 or 3 HCV infection was protective. Fibrosis rate had the strongest correlation with time to cirrhosis development (<italic>P</italic> &lt; 0.0001,<abstract abstract-type="main" id="tid12134-abs-0001"> <title>Abstract</title> <sec id="tid12134-sec-0001" sec-type="section"> <title>Background</title> <p>Hepatitis C virus (HCV) recurrence post liver transplant is universal, with a subgroup of patients developing rapid hepatic fibrosis. Various clinical definitions of rapid fibrosis (RF) have been used to identify risks for rapid progression, but their comparability and efficacy at predicting adverse outcomes has not been determined.</p> </sec> <sec id="tid12134-sec-0002" sec-type="section"> <title>Methods</title> <p>Retrospective data analysis was conducted on 100 adult patients with HCV who underwent liver transplantation at a single center. We measured year 1 fibrosis progression (RF defined as METAVIR F score ≥1 at 1‐year liver biopsy), time to METAVIR F2‐stage fibrosis, and fibrosis rate (calculated using liver biopsies graded by METAVIR scoring F0–4; fibrosis rate = fibrosis stage/year post transplant). RF was defined as ≥0.5 units/year.</p> </sec> <sec id="tid12134-sec-0003" sec-type="section"> <title>Results</title> <p>Multivariate analysis revealed that donor age and peak HCV viral load were significant risks for RF, when fibrosis rate was used to define RF. Advanced donor age was a risk for rapid progression to F2‐stage fibrosis, whereas genotype 2 or 3 HCV infection was protective. Fibrosis rate had the strongest correlation with time to cirrhosis development (<italic>P</italic> &lt; 0.0001, <italic>r</italic> = −0.76) and was the most accurate predictor of rapid graft cirrhosis (<italic>P</italic> &lt; 0.0001, area under the curve 0.979, sensitivity 100%, specificity 94%).</p> </sec> <sec id="tid12134-sec-0004" sec-type="section"> <title>Conclusion</title> <p>Different measures of RF progression identify different risks for RF and are not directly comparable. Fibrosis rate was the most accurate predictor of rapid graft cirrhosis.</p> </sec> </abstract> … (more)
- Is Part Of:
- Transplant infectious disease. Volume 15:Issue 6(2013)
- Journal:
- Transplant infectious disease
- Issue:
- Volume 15:Issue 6(2013)
- Issue Display:
- Volume 15, Issue 6 (2013)
- Year:
- 2013
- Volume:
- 15
- Issue:
- 6
- Issue Sort Value:
- 2013-0015-0006-0000
- Page Start:
- 588
- Page End:
- 599
- Publication Date:
- 2013-09-13
- Subjects:
- Transplantation of organs, tissues, etc -- Complications -- Periodicals
Communicable diseases -- Periodicals
Infection -- Periodicals
617.01 - Journal URLs:
- http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=mid ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/tid.12134 ↗
- Languages:
- English
- ISSNs:
- 1398-2273
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9024.988700
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4288.xml