Evidence map›Paper›PMID 40211907›Full record

ArticleGut and liver2025

Predicting Mortality and Cirrhosis-Related Complications with MELD3.0: A Multicenter Cohort Analysis.

Jihye Lim, Ji Hoon Kim, Ahlim Lee, Ji Won Han, Soon Kyu Lee, Hyun Yang, Heechul Nam, Hae Lim Lee, Do Seon Song, Sung Won Lee and 12 more

Abstract readMulticenter Study
In one paragraph

Article in Gut and liver, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

22 authors.

Jihye LimThe Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0002-1878-0215
Ji Hoon KimThe Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0002-8701-942X
Ahlim LeeThe Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0002-1690-5280
Ji Won HanThe Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0003-1456-1450
Soon Kyu LeeThe Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0003-1865-8225
Hyun YangThe Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0001-6588-9806
Heechul NamThe Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0001-5421-6868
Hae Lim LeeThe Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0002-3242-8883
Do Seon SongThe Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0002-8278-4878
Sung Won LeeThe Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0002-5194-5130
Hee Yeon KimThe Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0002-9663-132X
Jung Hyun KwonThe Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0002-5484-5864
Chang Wook KimThe Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0003-1184-0358
U Im ChangThe Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0002-6937-2895
Soon Woo NamThe Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0001-5562-4775
Seok-Hwan KimThe Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0002-7625-7844
Pil Soo SungThe Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0002-5780-9607
Jeong Won JangThe Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0003-3255-8474
Si Hyun BaeThe Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0003-1727-7842
Jong Young ChoiThe Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0001-7833-0307
Seung Kew YoonThe Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0002-4476-4868
Myeong Jun SongThe Catholic University Liver Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0001-5244-0372

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: /Aims: This study aimed to evaluate the performance of the Model for End-Stage Liver Disease (MELD) 3.0 for predicting mortality and liver-related complications compared with the Child-Pugh classification, albumin-bilirubin (ALBI) grade, the MELD, and the MELD sodium (MELDNa) score. Methods: We evaluated a multicenter retrospective cohort of incorporated patients with cirrhosis between 2013 and 2019. We conducted comparisons of the area under the receiver operating characteristic curve (AUROC) of the MELD3.0 and other models for predicting 3-month mortality. Additionally, we assessed the risk of cirrhosis-related complications according to the MELD3.0 score. Results: A total of 3,314 patients were included. The mean age was 55.9±11.3 years, and 70.2% of the patients were male. Within the initial 3 months, 220 patients (6.6%) died, and the MELD3.0 had the best predictive performance among the tested models, with an AUROC of 0.851, outperforming the Child-Pugh classification, ALBI grade, MELD, and MELDNa. A high MELD3.0 score was associated with an increased risk of mortality. Compared with that of the group with a MELD3.0 score <10 points, the adjusted hazard ratio of the group with a score of 10-20 points was 2.176, and that for the group with a score of ≥20 points was 4.892. Each 1-point increase in the MELD3.0 score increased the risk of cirrhosis-related complications by 1.033-fold. The risk of hepatorenal syndrome showed the highest increase, with an adjusted hazard ratio of 1.149, followed by hepatic encephalopathy and ascites. Conclusions: The MELD3.0 demonstrated robust prognostic performance in predicting mortality in patients with cirrhosis. Moreover, the MELD3.0 score was linked to cirrhosis-related complications, particularly those involving kidney function, such as hepatorenal syndrome and ascites.

Indexed as

End Stage Liver DiseaseLiver CirrhosisSeverity of Illness IndexAdultAgedFemaleHumansMaleMiddle AgedPredictive Value of TestsPrognosisRetrospective StudiesRisk AssessmentROC CurveAscitesHepatic encephalopathyHepatorenal syndromeLiver cirrhosis

Identifiers

PMID40211907
PMCPMC12070204

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.