Evidence map›Paper›PMID 42014557›Full record

ArticleHepatology international2026

Outcomes of first and further decompensation events in advanced chronic liver disease: a multi-centre competing risks analysis.

Angus W Jeffrey, Leon A Adams, Brendan Brew, Gary Jeffrey, Michael C Wallace, Marie Sinclair, Adam Testro, John D Chetwood, Ken Liu, Avik Majumdar

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Hepatology international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. 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

10 authors.

Angus W JeffreyMedical School, The University of Western Australia, Perth, Australia. angus.jeffrey@research.uwa.edu.au.ORCID http://orcid.org/0000-0002-9137-0204
Leon A AdamsMedical School, The University of Western Australia, Perth, Australia.
Brendan BrewVictorian Liver Transplant Unit, The Austin Hospital, Melbourne, Australia.
Gary JeffreyMedical School, The University of Western Australia, Perth, Australia.
Michael C WallaceMedical School, The University of Western Australia, Perth, Australia.
Marie SinclairVictorian Liver Transplant Unit, The Austin Hospital, Melbourne, Australia.
Adam TestroVictorian Liver Transplant Unit, The Austin Hospital, Melbourne, Australia.
John D ChetwoodAW Morrow Gastroenterology and Liver Centre, Royal Prince Alfred Hospital, New South Wales, Australia.
Ken LiuAW Morrow Gastroenterology and Liver Centre, Royal Prince Alfred Hospital, New South Wales, Australia.
Avik MajumdarVictorian Liver Transplant Unit, The Austin Hospital, Melbourne, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsDecompensated cirrhosis carries a significant health burden with high mortality. The aim of this study was to assess incidence of further decompensation and survival in patients with cirrhosis following hospitalization with initial decompensation.

methodsAdult patients with cirrhosis at three Australian state-wide liver transplant centres from 2006 to 2025, admitted to hospital with a first decompensating event (ascites, hepatic encephalopathy, variceal bleeding) and followed until further decompensation requiring hospitalisation, liver-related death (LRD), non-liver related death, or liver transplant (LT).

resultsA total of 542 patients were followed from first decompensation for a median of 24 (IQR 9-48) months, with alcohol-related liver disease the most common etiology (52%). Cumulative incidence of further decompensation at 5-years was 65.1% (95% CI 60.3-69.5), and incidence of LRD or LT was 39.2% (95% CI 34.1-44.2). Following further decompensation, cumulative incidence of LRD or LT was higher compared to first decompensation at 55.5% (sHR 3.45, 95% CI 2.31-5.16, p < 0.001). Ascites was the most common type of further decompensation (35.6%, 95% CI 31-40.2). Etiological treatment of the underlying CLD was protective for further decompensation and LRD/LT (sub hazard ratio [sHR] 0.58 and 0.65 respectively, p < 0.05), as was treatment with a non-selective beta blocker (sHR 0.40 and 0.60, p < 0.01).

conclusionsThis multi-centre study describes the trajectory of patients after a first episode of decompensation for the first time in the Australian context. It highlights high morbidity and poor prognosis associated with further decompensation with over 50% dying or requiring LT within 5 years.

Indexed as

AscitesEsophageal and Gastric VaricesGastrointestinal HemorrhageHepatic EncephalopathyLiver CirrhosisAgedAustraliaFemaleHospitalizationHumansIncidenceLiver TransplantationMaleMiddle AgedRisk AssessmentAscitescACLDCirrhosisCSPHEncephalopathyPrognosisVariceal bleeding

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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.