Evidence map›Paper›PMID 41559603›Full record

ArticleBMC gastroenterology2026

Identifying patients at high risk of decompensated liver disease through unscheduled care attendance data: a retrospective cohort study.

R Swann, J Lewsey, D Jamieson, S Padmanabhan, J P Pell, D Mackay, R Dundas, J M Friday, T Q B Tran, D Brown and 8 more

Abstract read
In one paragraph

Article in BMC gastroenterology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

18 authors.

R SwannNHS Greater Glasgow and Clyde, Glasgow, UK. rachael.swann2@nhs.scot.
J LewseySchool of Health & Wellbeing, University of Glasgow, Glasgow, UK.
D JamiesonSchool of Cardiovascular & Metabolic Health, University of Glasgow, Glasgow, UK.
S PadmanabhanSchool of Cardiovascular & Metabolic Health, University of Glasgow, Glasgow, UK.
J P PellSchool of Health & Wellbeing, University of Glasgow, Glasgow, UK.
D MackaySchool of Health & Wellbeing, University of Glasgow, Glasgow, UK.
R DundasSchool of Health & Wellbeing, University of Glasgow, Glasgow, UK.
J M FridaySchool of Health & Wellbeing, University of Glasgow, Glasgow, UK.
T Q B TranSchool of Cardiovascular & Metabolic Health, University of Glasgow, Glasgow, UK.
D BrownSchool of Health & Wellbeing, University of Glasgow, Glasgow, UK.
F K HoSchool of Health & Wellbeing, University of Glasgow, Glasgow, UK.
C HastieSchool of Health & Wellbeing, University of Glasgow, Glasgow, UK.
M FlemingSchool of Health & Wellbeing, University of Glasgow, Glasgow, UK.
C GeueSchool of Health & Wellbeing, University of Glasgow, Glasgow, UK.
A StevensonSchool of Health & Wellbeing, University of Glasgow, Glasgow, UK.
C du ToitDigital Health Validation Lab, Living Laboratory, University of Glasgow, Glasgow, UK.
A FraserNHS Greater Glasgow and Clyde, Glasgow, UK.
E H ForrestNHS Greater Glasgow and Clyde, Glasgow, UK.

Funding

British Heart Foundation Centre of Research Excellence RE/18/6/34217Chief Scientist Office, Scottish Government Health and Social Care Directorate SPHSU17Medical Research Council MC_UU_00022/2UKRI Strength in Places Fund SIPF00007/1
6 · The paper itself

Abstract

backgroundLiver cirrhosis is one of the leading causes of mortality and morbidity in those of working age. Mortality from liver disease in the UK has continued to rise over the past decade. A significant proportion of patients presenting with decompensated liver disease have no prior diagnosis of liver disease despite multiple acute healthcare interactions providing opportunities for detection. We aimed to characterise patients presenting to unscheduled care with no known liver disease who subsequently had a liver related admission (DLD), and determine if a simple predictive score could identify those at high risk.

methodsAll patients attending unscheduled care in our health board between the beginning of 2018 and the end of 2020 were included with clinical follow up until end 2022. Exclusion criteria were known liver disease, early (< 6 months) presentation with DLD or missing key laboratory data. A predictive model was developed based on demographic and laboratory parameters.

resultsFollowing exclusions, a group of 173,486 patients were included in our analysis, of whom 1,609 (0.9%) went on to have a DLD-related admission in the 5 year-follow up period. A model to predict future admission was developed based on Fib4 score (using the common blood tests Aspartate aminotransferase (AST), Alanine Transaminase (ALT) and platelet count), geographical deprivation decile, and sex. This model had a Harrell’s C statistic of 0.78.

conclusionsUnscheduled care presentations provide an opportunity to identify those at high risk of advanced liver disease and decompensation. It is likely these patients have undiagnosed liver disease at the time of presentation, and a model using simple laboratory and demographic data may aid detection in this setting of those at risk of future liver-related admission. External validation of this model is required.

Indexed as

Liver CirrhosisLiver DiseasesAdultAgedAlanine TransaminaseAspartate AminotransferasesFemaleHospitalizationHumansMaleMiddle AgedPlatelet CountRetrospective StudiesRisk AssessmentRisk FactorsUnited KingdomAlanine TransaminaseAspartate AminotransferasesAlcohol related liver diseaseCirrhosisLiver disease

Identifiers

PMID41559603
PMCPMC12905958

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Registered trials

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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.