Evidence map›Paper›PMID 36376577›Full record

ArticleDigestive diseases and sciences2023

MELD-Lactate Predicts Poor Outcome in Variceal Bleeding in Cirrhosis.

Thomas Horvatits, Nadim Mahmud, Marina Serper, Oliver Seiz, Dominik Reher, Andreas Drolz, Naveed Sarnast, Wenyi Gu, Hans Peter Erasmus, Gabriel Allo and 13 more

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in Digestive diseases and sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.2field-weighted citation impact, top 11% of its field
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

9 citing papers in PubMed, 18 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 5 institutions in 2 countries.

Thomas HorvatitsI. Department of Medicine, Gastroenterology and Hepatology, University Medical Center Hamburg-Eppendorf, Martinistr. 42, 20246, Hamburg, Germany. t.horvatits@uke.de.ORCID http://orcid.org/0000-0003-0682-4476
Nadim MahmudDivision of Gastroenterology and Hepatology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, USA.
Marina SerperDivision of Gastroenterology and Hepatology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, USA.
Oliver SeizI. Department of Medicine, Gastroenterology and Hepatology, University Medical Center Hamburg-Eppendorf, Martinistr. 42, 20246, Hamburg, Germany.
Dominik ReherI. Department of Medicine, Gastroenterology and Hepatology, University Medical Center Hamburg-Eppendorf, Martinistr. 42, 20246, Hamburg, Germany.
Andreas DrolzI. Department of Medicine, Gastroenterology and Hepatology, University Medical Center Hamburg-Eppendorf, Martinistr. 42, 20246, Hamburg, Germany.
Naveed SarnastBaylor Scott and White, Baylor University Medical Center, Dallas, TX, USA.
Wenyi GuDepartment of Internal Medicine I, University of Frankfurt, Frankfurt, Germany.
Hans Peter ErasmusDepartment of Internal Medicine I, University of Frankfurt, Frankfurt, Germany.
Gabriel AlloDepartment of Gastroenterology and Hepatology, University Hospital Cologne, Cologne, Germany.
Phillip FerstlDepartment of Internal Medicine I, University of Frankfurt, Frankfurt, Germany.
Sebastian WittmannI. Department of Medicine, Gastroenterology and Hepatology, University Medical Center Hamburg-Eppendorf, Martinistr. 42, 20246, Hamburg, Germany.
Felix PiechaI. Department of Medicine, Gastroenterology and Hepatology, University Medical Center Hamburg-Eppendorf, Martinistr. 42, 20246, Hamburg, Germany.
Stefan GrothDepartment of Interdisciplinary Endoscopy, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Stefan ZeuzemDepartment of Internal Medicine I, University of Frankfurt, Frankfurt, Germany.
Christoph SchrammDepartment of Gastroenterology and Hepatology, University Hospital Cologne, Cologne, Germany.
Samuel HuberI. Department of Medicine, Gastroenterology and Hepatology, University Medical Center Hamburg-Eppendorf, Martinistr. 42, 20246, Hamburg, Germany.
Thomas RöschDepartment of Interdisciplinary Endoscopy, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Ansgar W LohseI. Department of Medicine, Gastroenterology and Hepatology, University Medical Center Hamburg-Eppendorf, Martinistr. 42, 20246, Hamburg, Germany.
Jonel TrebickaDepartment of Internal Medicine I, University of Frankfurt, Frankfurt, Germany.
Gerald OgolaBaylor Scott and White, Baylor University Medical Center, Dallas, TX, USA.
Sumeet K AsraniBaylor Scott and White, Baylor University Medical Center, Dallas, TX, USA.
Johannes KluweI. Department of Medicine, Gastroenterology and Hepatology, University Medical Center Hamburg-Eppendorf, Martinistr. 42, 20246, Hamburg, Germany.
Universität Hamburg · DEGoethe University Frankfurt · DEBaylor University Medical Center · USPhiladelphia VA Medical Center · USUniversity Hospital Cologne · DE

Funding

Improving Surgical Risk Prediction and Decision Making among Patients with CirrhosisK08DK124577 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI MAHMUD, NADIM · 2021 to 2025
$835k
NIDDK NIH HHS K08 DK124577
6 · The paper itself

Abstract

backgroundPredictors of poor outcome associated with variceal bleeding remain suboptimal. In patients with cirrhosis, serum lactate combined with Model for End-Stage Liver Disease (MELD-LA) improved prediction across heterogeneous populations. However, prognostic properties have not yet been assessed in the context of variceal bleeding.

aimsWe aimed to evaluate the predictive performance of MELD-LA compared to MELD, lactate, and nadir hemoglobin in cirrhosis patients with variceal bleeding.

methodsIn this multicenter study, we identified 472 patients with variceal bleeding from a German primary cohort (University Hospitals Hamburg/Frankfurt/Cologne), and two independent external validation cohorts [Veterans Affairs (VA), Baylor University]. Discrimination for 30-day mortality was analyzed and scores were compared. MELD-LA was evaluated separately in validation cohorts to ensure consistency of findings.

resultsIn contrast to nadir hemoglobin, MELD and peak-lactate at time of bleeding were significantly higher in 30-day non-survivors in the primary cohort (p = 0.708; p < 0.001). MELD-LA had excellent discrimination for 30-day mortality (AUROC 0.82, 95% CI 0.76-0.88), better than MELD and peak-lactate (AUROC 0.78, 95% CI 0.71-0.84; AUROC 0.73, 95% CI 0.66-0.81). MELD-LA predicted 30-day mortality independently of age, sex, severity of liver disease and vasopressor support (HR 1.29 per 1-point-increase of MELD-LA; 95% CI 1.19-1.41; p < 0.001). Similarly, MELD-LA demonstrated excellent discrimination for 30-day mortality in the VA (AUROC = 0.86, 95% CI 0.79-0.93) and Baylor cohort (AUROC = 0.85, 95% CI 0.74-0.95).

conclusionsMELD-LA significantly improves discrimination of short-term mortality associated with variceal bleeding, compared to MELD, peak-lactate and nadir hemoglobin. Thus, MELD-LA might represent a useful and objective marker for risk assessment and therapeutic intervention in patients with variceal bleeding.

Indexed as

End Stage Liver DiseaseEsophageal and Gastric VaricesGastrointestinal HemorrhageHumansLactic AcidLiver CirrhosisPrognosisRetrospective StudiesSeverity of Illness IndexLactic AcidCirrhosisGI bleedingMELD-lactateVariceal bleeding

Identifiers

PMID36376577
PMCPMC10023372
OpenAlexW4309028492

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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.