Evidence map›Paper›PMID 42860771›Full record

SynthesisLiver international : official journal of the International Association for the Study of the Liver2026

Network Meta-Analysis: Treatments for Acute Alcohol-Associated Hepatitis.

Charles Gallaher, Guruprasad P Aithal, Ashwin Dhanda, Ewan Forrest, James O'Beirne, Ken Liu, Mark Thursz, Richard Parker

Abstract readNetwork Meta-AnalysisSystematic Review
In one paragraph

Synthesis in Liver international : official journal of the International Association for the Study of the Liver, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Network Meta-Analysis: Treatments for Acute Alcohol-Associated Hepatitis.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Pooled it
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

8 authors.

Charles GallaherDepartment of Gastroenterology, University Hospital Lewisham, London, UK.ORCID https://orcid.org/0000-0002-6153-4933
Guruprasad P AithalDepartment of Hepatology, Nottingham University Hospitals NHS Trust, Nottingham, UK.ORCID https://orcid.org/0000-0003-3924-4830
Ashwin DhandaDepartment of Hepatology, University Hospitals Plymouth NHS Trust, Plymouth, UK.ORCID https://orcid.org/0000-0002-0523-0193
Ewan ForrestDepartment of Gastroenterology, NHS Greater Glasgow and Clyde, Glasgow, UK.ORCID https://orcid.org/0000-0002-7293-2574
James O'BeirneUniversity of the Sunshine Coast, Brisbane, Australia.ORCID https://orcid.org/0000-0003-3400-2816
Ken LiuDepartment of Gastroenterology and Hepatology, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia.ORCID https://orcid.org/0000-0002-0453-3168
Mark ThurszNIHR Imperial Biomedical Research Centre, London, UK.ORCID https://orcid.org/0000-0002-8218-192X
Richard ParkerLeeds Liver Unit, St James's University Hospital, Leeds, UK.ORCID https://orcid.org/0000-0003-4888-8670

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlcohol-related hepatitis (AH) is an acute form of liver disease with a high short-term mortality. A variety of treatments have been explored in randomised studies. Recent consensus on study outcomes has identified 90-day survival as the primary outcome metric.

aimsThis systematic review and network meta-analysis is to update understanding of the comparative efficacy of treatments for AH, based on 90-day survival, to inform future Phase III studies.

methodsPubMed, Ovid-Medline and Embase were searched for randomised studies of treatments of AH. The risk of bias in included papers was measured using the Cochrane risk of bias 2 tool. Data were synthesised with network meta-analysis to estimate risk ratio (RR) of survival at 90 days after randomisation. Heterogeneity was assessed with the magnitude of the between-study variance (tau

resultsThirty five studies including 5045 participants were identified that examined 24 treatments for AH. Twenty-three studies were considered to be at low risk of bias. In network meta-analysis considering placebo as the reference treatment, only granulocyte colony stimulating factor (GCSF) showed a statistically significant benefit on 90-day mortality (RR 0.49, 95% CI 0.28-0.84; p = 0.009). In subgroup analysis of studies at low risk of bias, no treatments showed a significant effect on mortality at 90 days.

conclusionsIndividual studies are small and heterogeneity is marked; however, some agents show promise to improve survival at 90 days in people with AH. This information should inform adequately powered studies to explore potential treatments for AH.

Indexed as

Hepatitis, AlcoholicAcute DiseaseGranulocyte Colony-Stimulating FactorHumansRandomized Controlled Trials as TopicTreatment OutcomeGranulocyte Colony-Stimulating Factoralcohol‐related hepatitisnetwork meta‐analysistreatment

Identifiers

PMID42860771
PMCPMC13655491

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.