Evidence map›Paper›PMID 39014101›Full record

ArticleDigestive diseases and sciences2024

Etiology-Specific Effects of Impaired Functional Status on Liver Transplant Outcomes.

David Uihwan Lee, Kuntal Bhowmick, Aldanah Althwanay, Sarah Sandlow, Michal Wiseman, Ki Jung Lee, Gregory Hongyuan Fan, Hannah Chou, Harrison Chou, Kimberly Schuster and 2 more

Abstract read
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In one paragraph

Article in Digestive diseases and sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Clinical Outcomes and Non-Invasive Testing in Metabolic Dysfunction-Associated Steatohepatitis With Cirrhosis: A Systematic Review.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Pooled it
  2. Article
  3. Article
  4. Article
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

12 authors.

David Uihwan LeeDivision of Gastroenterology and Hepatology, Department of Medicine, University of Maryland School of Medicine, 22 S Greene St, Baltimore, MD, 21201, USA. dvleeman@gmail.com.
Kuntal BhowmickDepartment of Medicine, Warren Alpert Medical School of Brown University, Providence, RI, USA.
Aldanah AlthwanayDivision of Gastroenterology and Hepatology, Department of Medicine, University of Maryland School of Medicine, 22 S Greene St, Baltimore, MD, 21201, USA.
Sarah SandlowDepartment of Medicine, Tufts University School of Medicine, Washington St, Boston, MA, 02111, USA.
Michal WisemanDivision of Gastroenterology and Hepatology, Department of Medicine, University of Maryland School of Medicine, 22 S Greene St, Baltimore, MD, 21201, USA.
Ki Jung LeeDepartment of Medicine, Tufts University School of Medicine, Washington St, Boston, MA, 02111, USA.
Gregory Hongyuan FanDepartment of Medicine, Tufts University School of Medicine, Washington St, Boston, MA, 02111, USA.
Hannah ChouDepartment of Medicine, Tufts University School of Medicine, Washington St, Boston, MA, 02111, USA.
Harrison ChouDepartment of Medicine, Tufts University School of Medicine, Washington St, Boston, MA, 02111, USA.
Kimberly SchusterDepartment of Medicine, Tufts University School of Medicine, Washington St, Boston, MA, 02111, USA.
KeeSeok LeeDepartment of Medicine, Tufts University School of Medicine, Washington St, Boston, MA, 02111, USA.
Zurabi LominadzeDivision of Gastroenterology and Hepatology, Department of Medicine, University of Maryland School of Medicine, 22 S Greene St, Baltimore, MD, 21201, USA.

Funding

Research Training in Gastroenterology and HepatologyT32DK067872 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI RAUFMAN, JEAN-PIERRE · 2005 to 2024
$7.2M
NIH NIDDK T32 DK067872-17
6 · The paper itself

Abstract

BACKGROUND AND

aimsPre-liver transplant (LT) functional status is an important determinant of prognosis post LT. There is insufficient data on how functional status affects outcomes of transplant recipients based on the specific etiology of liver disease. We stratified LT recipients by etiology of liver disease to evaluate the effects of functional status on post-LT prognosis in each subgroup.

methods2005-2019 United Network for Organ Sharing (UNOS) Standard Transplant Analysis and Research (STAR) was used to select patients with liver transplant. A total of 14,290 patients were included in the analysis. These patients were stratified by functional status according to Karnofsky Performance Scale (KPS) score: no assistance, some assistance, or total assistance. They were then further divided into six diagnosis categories: metabolic dysfunction-associated steatotic liver disease (MASLD), hereditary disorders, hepatitis C, hepatitis B, autoimmune disease (AID), and alcoholic liver disease (ALD). Primary endpoints included all-cause mortality and graft failure, while secondary endpoints included organ-specific causes of death. Those under the age of 18 and those with non-whole liver or prior liver transplantation were excluded.

resultsPatients with MASLD requiring some assistance (aHR: 1.57, 95% CI 1.03-2.39, p = 0.04) and those requiring total assistance (aHR: 2.32, 95% CI 1.48-3.64, p < 0.001) had higher incidences of graft failure compared to those requiring no assistance. Those with MASLD requiring total assistance had a higher all-cause mortality rate than those needing no assistance (aHR: 1.62, 95% CI 1.38-1.89, p < 0.001). Patients with hereditary causes of liver disease showed a lower incidence of all-cause mortality in recipients needing some assistance compared with those needing no assistance (aHR: 0.52, 95% CI 0.34-0.80, p = 0.003). LT recipients with hepatitis C, AID, and ALD all showed higher incidences of all-cause mortality in the total assistance cohort when compared to the no assistance cohort. For the secondary endpoints of specific cause of death, transplant recipients with MASLD needing total assistance had higher rates of death due to general cardiac causes, graft rejection, general infectious causes, sepsis, general renal causes, and general respiratory causes.

conclusionPatients with MASLD cirrhosis demonstrated the worst overall outcomes, suggesting that this population may be particularly vulnerable. Poor functional status in patients with end-stage liver disease from hepatitis B or hereditary disease was not associated with a significantly increased rate of adverse outcomes, suggesting that the KPS score may not be broadly applicable to all patients awaiting LT.

Indexed as

Liver TransplantationAdultAgedFemaleFunctional StatusHumansKarnofsky Performance StatusLiver DiseasesMaleMiddle AgedRetrospective StudiesTreatment OutcomeAlcoholic liver diseaseAutoimmune hepatitisFunctional statusHepatitis BHepatitis CLiver transplantMetabolic dysfunction-associated steatotic liver diseaseNon-alcoholic steatohepatitisUNOS-STAR

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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.