Evidence map›Paper›PMID 39776102›Full record

ArticleAcademic emergency medicine : official journal of the Society for Academic Emergency Medicine2025

Clinical decision instruments for predicting mortality in patients with cirrhosis seeking emergency department care.

Swetha Parvataneni, Michelle Haugh, Yara Sarkis, Brittany Baker, Lauren D Nephew, Marwan S Ghabril, Raj Vuppalanchi, Eric S Orman, Naga P Chalasani, Archita P Desai and 1 more

Abstract read
In one paragraph

Article in Academic emergency medicine : official journal of the Society for Academic Emergency Medicine, 2025. 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. Clinical decision instruments for predicting mortality in patients with cirrhosis seeking emergency department care.Academic emergency medicine : official journal of the Society for Academic Emergency Medicine · 2025
    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

11 authors.

Swetha ParvataneniDivision of Gastroenterology and Hepatology, Indiana University, Indianapolis, Indiana, USA.
Michelle HaughDivision of Gastroenterology and Hepatology, Indiana University, Indianapolis, Indiana, USA.
Yara SarkisDepartment of Medicine, Indiana University, Indianapolis, Indiana, USA.
Brittany BakerDepartment of Medicine, Indiana University, Indianapolis, Indiana, USA.
Lauren D NephewDivision of Gastroenterology and Hepatology, Indiana University, Indianapolis, Indiana, USA.
Marwan S GhabrilDivision of Gastroenterology and Hepatology, Indiana University, Indianapolis, Indiana, USA.
Raj VuppalanchiDivision of Gastroenterology and Hepatology, Indiana University, Indianapolis, Indiana, USA.ORCID 0000-0003-0637-1577
Eric S OrmanDivision of Gastroenterology and Hepatology, Indiana University, Indianapolis, Indiana, USA.
Naga P ChalasaniDivision of Gastroenterology and Hepatology, Indiana University, Indianapolis, Indiana, USA.
Archita P DesaiDivision of Gastroenterology and Hepatology, Indiana University, Indianapolis, Indiana, USA.
Nicholas Eric HarrisonDepartment of Emergency Medicine, Indiana University, Indianapolis, Indiana, USA.ORCID 0000-0002-8331-7833

Funding

Quality Assurance and Quality Control Project Management: Improving Submissions and Study Conduct in the Human Subjects Research Prior Approval ProcessUL1TR002529 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI MOE, SHARON M, WIEHE, SARAH ELIZABETH · 2018 to 2022
$27.2M
Translating Measures of Visual Experience to Children with Autism and Down SyndromeKL2TR002530 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI ROBB, SHERI L · 2018 to 2022
$4.8M
CTSA K12 Program at Indiana UniversityK12TR004415 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI SAMIR KUMAR GUPTA · 2023 to 2026
$3.4M
The Intersection of Personalized Medicine and Implementation Science to Improve Healthcare Utilization in CirrhosisK23DK123408 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI DESAI, ARCHITA P. · 2020 to 2024
$903k
NCATS NIH HHS K12 TR004415NCATS NIH HHS KL2 TR002530NCATS NIH HHS UL1 TR002529NIDDK NIH HHS K23 DK123408
6 · The paper itself

Abstract

objectiveClinical decision instruments (CDIs) could be useful to aid risk stratification and disposition of emergency department (ED) patients with cirrhosis. Our primary objective was to derive and internally validate a novel Cirrhosis Risk Instrument for Stratifying Post-Emergency department mortality (CRISPE) for the outcomes of 14- and 30-day post-ED mortality. Secondarily, we externally validated the existing Model for End-Stage Liver Disease (MELD) scores for explicit use in ED patients and prediction of the same outcomes.

methodsA cohort of 2093 adults with cirrhosis, at 16 sites in a statewide health system, was analyzed for 119 candidate variables available at ED disposition. LASSO with 10-fold cross-validation was used in variable selection for 14-day (CRISPE-14) and 30-day (CRISPE-30) logistic regression models. Area under the receiver operating characteristic curve (AUROC) was calculated for each variant of the CRISPE and MELD scores and compared via Delong's test. Predictions were compared to actual ED disposition for predictive value and reclassification statistics.

resultsMedian (interquartile range [IQR]) characteristics of the cohort were age 62 (53-70) years and MELD 3.0 13.0 (8.0-20.0). Mortality was 4.3% and 8.5% at 14 and 30 days, respectively. CRISPE-14 and CRISPE-30 outperformed each MELD variant, achieving AUROC of 0.824 (95% CI: 0.781-0.866) and 0.829 (0.796-0.861), respectively. MELD 3.0 AUROCs were 0.724 (0.667-0.781) and 0.715 (0.672-0.781), respectively. Compared to ED disposition, CRISPE-14, CRISPE-30, and MELD 3.0 significantly improved positive and negative predictive value and net reclassification index at multiple cutoffs. Applying CRISPE-30 (cutoff 4.5) favorably reclassified one net ED disposition for mortality for every 12 patients, while MELD 3.0 net reclassified one disposition per 84 patients.

conclusionsCDIs may be useful in risk-stratifying ED patients with cirrhosis and aiding disposition decision making. The novel CRISPE CDI showed powerful performance and requires external validation, while the existing MELD 3.0 score has moderate performance and is now externally-validated in an ED population for short-term mortality.

Indexed as

Emergency Service, HospitalLiver CirrhosisAgedFemaleHospital MortalityHumansLogistic ModelsMaleMiddle AgedPredictive Value of TestsRisk AssessmentROC CurveSeverity of Illness Indexcirrhosisclinical decision instrumentemergency department

Identifiers

PMID39776102
PMCPMC12171671

What OpenQuestion holds

Textmetadata
LicenceTDM
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.