Evidence map›Paper›PMID 11544420›Full record

ArticleTransplantation2001

Liver transplantation for alcoholic cirrhosis: long term follow-up and impact of disease recurrence.

C O Bellamy, A M DiMartini, K Ruppert, A Jain, F Dodson, M Torbenson, T E Starzl, J J Fung, A J Demetris

Open access · greenAbstract read
In one paragraph

Article in Transplantation, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 5 pooled it
5.4field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 5 syntheses or guidelines pooled it, 177 citations in OpenAlex.

  1. Guideline
  2. World journal of gastroenterology · 2019
    Pooled it
  3. Pooled it
  4. Pooled it
  5. Pooled it
  6. Article
  7. Review
  8. Review
  9. Review
  10. Post-transplant malignancies in alcoholic liver disease.Translational gastroenterology and hepatology · 2020
    Review
  11. Superior Wait-List Outcomes in Patients with Alcohol-Associated Liver Disease Compared With Other Indications for Liver Transplantation.Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society · 2019
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Observational
  18. Article
  19. Lower relapse rates with good post-transplant outcome in alcoholic liver disease: Experience from a living donor liver transplant center.Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology · 2016
    Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 2 countries.

C O BellamyDepartment of Pathology, Edinburgh University Medical School, Scotland.
A M DiMartini
K Ruppert
A Jain
F Dodson
M Torbenson
T E Starzl
J J Fung
A J Demetris
University of Pittsburgh Medical Center · USUniversity of Edinburgh · GB

Funding

INTERLEUKIN 6 AND HUMAN BILIARY EPITHELIAL PROLIFERATIONR01DK049615 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DEMETRIS, ANTHONY J · 1996 to 2006
$1.4M
COMBINED BONE MARROW AND ORGAN TRANSPLANTATION IN HUMANSR01AI040329 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FUNG, JOHN J · 1996 to 2000
$314k
NIAID NIH HHS R01AI40329-05NIDDK NIH HHS 1R01 DK49615-01A1NIDDK NIH HHS R01 DK049615
6 · The paper itself

Abstract

backgroundAlcoholic liver disease has emerged as a leading indication for hepatic transplantation, although it is a controversial use of resources. We aimed to examine all aspects of liver transplantation associated with alcohol abuse.

methodsRetrospective cohort analysis of 123 alcoholic patients with a median of 7 years follow-up at one center.

resultsIn addition to alcohol, 43 (35%) patients had another possible factor contributing to cirrhosis. Actuarial patient and graft survival rates were, respectively, 84% and 81% (1 year); 72% and 66% (5 years); and 63% and 59% (7 years). After transplantation, 18 patients (15%) manifested 21 noncutaneous de novo malignancies, which is significantly more than controls (P=0.0001); upper aerodigestive squamous carcinomas were overrepresented (P=0.03). Thirteen patients had definitely relapsed and three others were suspected to have relapsed. Relapse was predicted by daily ethanol consumption (P=0.0314), but not by duration of pretransplant sobriety or explant histology. No patient had alcoholic hepatitis after transplantation and neither late onset acute nor chronic rejection was significantly increased. Multiple regression analyses for predictors of graft failure identified major biliary/vascular complications (P=0.01), chronic bile duct injury on biopsy (P=0.002), and pericellular fibrosis on biopsy (P=0.05); graft viral hepatitis was marginally significant (P=0.07) on univariate analysis.

conclusionsAlcoholic liver disease is an excellent indication for liver transplantation in those without coexistent conditions. Recurrent alcoholic liver disease alone is not an important cause of graft pathology or failure. Potential recipients should be heavily screened before transplantation for coexistent conditions (e.g., hepatitis C, metabolic diseases) and other target-organ damage, especially aerodigestive malignancy, which are greater causes of morbidity and mortality than is recurrent alcohol liver disease.

Indexed as

Liver TransplantationAdultAgedAlcoholismCohort StudiesFemaleFollow-Up StudiesGraft SurvivalHumansIncidenceLiverLiver Cirrhosis, AlcoholicMaleMiddle AgedNeoplasmsPostoperative Complications

Identifiers

PMID11544420
PMCPMC2963946
OpenAlexW2159254384

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.