Evidence map›Paper›PMID 39399402›Full record

ArticleHippokratia

An artificial neural network approach to diagnose and predict liver dysfunction and failure in the critical care setting.

S Pappada, B Sathelly, J Schmieder, A Javaid, M Owais, B Cameron, S Khuder, G Kostopanagiotou, R Smith, T Sparkle and 1 more

Abstract read
In one paragraph

Article in Hippokratia. 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

11 authors.

S PappadaDepartment of Anesthesiology, College of Medicine and Life Sciences, University of Toledo, Toledo, Ohio, USA.
B SathellyDepartment of Electrical Engineering and Computer Science, University of Toledo, Toledo, Ohio, USA.
J SchmiederCollege of Medicine and Life Sciences, University of Toledo, Toledo, Ohio, USA.
A JavaidDepartment of Electrical Engineering and Computer Science, University of Toledo, Toledo, Ohio, USA.
M OwaisDepartment of Electrical Engineering and Computer Science, University of Toledo, Toledo, Ohio, USA.
B CameronDepartment of Bioengineering, University of Toledo, Toledo, Ohio, USA.
S KhuderDepartment of Medicine, College of Medicine and Life Sciences, University of Toledo, Toledo, Ohio, USA.
G Kostopanagiotou2nd Department of Anesthesiology, National and Kapodistrian University of Athens, Attikon University Hospital, Athens, Greece.
R SmithDepartment of Psychiatry, University of Toledo, Toledo, Ohio, USA.
T SparkleDepartment of Anesthesiology, College of Medicine and Life Sciences, University of Toledo, Toledo, Ohio, USA.
T PapadimosDepartment of Anesthesiology, College of Medicine and Life Sciences, University of Toledo, Toledo, Ohio, USA.

Funding

Clinical and Translational Science Collaborative of Northern Ohio, Catalyzing Linkages to Equity in Health (CLE Health)UM1TR004528 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI GRACE A MCCOMSEY · 2023 to 2026
$32.1M
NCATS NIH HHS UM1 TR004528
6 · The paper itself

Abstract

Background: Detecting liver dysfunction/failure in the intensive care unit poses a challenge as individuals afflicted with these conditions often appear symptom-free, thereby complicating early diagnoses and contributing to unfavorable patient outcomes. The objective of this endeavor was to improve the chances of early diagnosis of liver dysfunction/failure by creating a predictive model for the critical care setting. This model has been designed to produce an index that reflects the probability of severe liver dysfunction/failure for patients in intensive care units, utilizing machine learning techniques. Materials and Methods: This effort used comprehensive open-access patient databases to build and validate machine learning-based models for predicting the likelihood of severe liver dysfunction/failure. Two artificial neural network model architectures that derived a novel 0-100 Liver Failure Risk Index were developed and validated using the comprehensive patient databases. Data used to train and develop the models included clinical (patient vital signs) and laboratory results related to liver function which included liver function test results. The performance of the developed models was compared in terms of sensitivity, specificity, and the mean lead time to diagnosis. Results: The best model performance demonstrated an 83.3 % sensitivity and a specificity of 77.5 % in diagnosing severe liver dysfunction/failure. This model accurately identified these patients a median of 17.5 hours before their clinical diagnosis, as documented in their electronic health records. The predictive diagnostic capability of the developed models is crucial to the intensive care unit setting, where treatment and preventative interventions can be made to avoid severe liver dysfunction/failure. Conclusion: Our machine learning approach facilitates early and timely intervention in the hepatic function of critically ill patients by their healthcare providers to prevent or minimize associated morbidity and mortality. HIPPOKRATIA 2024, 28 (1):1-10.

Indexed as

Clinical decision supportintelligent diagnosticsliver dysfunctionliver failuremachine learning

Identifiers

PMID39399402
PMCPMC11466107

What OpenQuestion holds

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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.