Evidence map›Paper›PMID 30509300›Full record

ArticleJournal of translational medicine2018

Machine-learned models using hematological inflammation markers in the prediction of short-term acute coronary syndrome outcomes.

Konrad Pieszko, Jarosław Hiczkiewicz, Paweł Budzianowski, Janusz Rzeźniczak, Jan Budzianowski, Jerzy Błaszczyński, Roman Słowiński, Paweł Burchardt

Abstract read
In one paragraph

Article in Journal of translational medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 3 pooled it
–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

16 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
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  4. Observational
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  10. Artificial Intelligence Technologies in Cardiology.Journal of cardiovascular development and disease · 2023
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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

8 authors.

Konrad PieszkoFaculty of Medicine and Health Sciences, University of Zielona Gora, Zielona Gora, Poland. konrad.pieszko@gmail.com.ORCID 0000-0002-5514-7750
Jarosław HiczkiewiczFaculty of Medicine and Health Sciences, University of Zielona Gora, Zielona Gora, Poland.
Paweł BudzianowskiDepartment of Engineering, University of Cambridge, Cambridge, UK.
Janusz RzeźniczakDepartment of Cardiology, J Strus Hospital, Poznan, Poland.
Jan BudzianowskiFaculty of Medicine and Health Sciences, University of Zielona Gora, Zielona Gora, Poland.ORCID 0000-0001-5660-1268
Jerzy BłaszczyńskiLaboratory of Intelligent Decision Support Systems, Poznań University of Technology, Poznan, Poland.
Roman SłowińskiLaboratory of Intelligent Decision Support Systems, Poznań University of Technology, Poznan, Poland.
Paweł BurchardtBiology of Lipid Disorders Department, Poznan University of Medical Sciences, Poznan, Poland.ORCID 0000-0003-0353-3470

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIncreased systemic and local inflammation play a vital role in the pathophysiology of acute coronary syndrome. This study aimed to assess the usefulness of selected machine learning methods and hematological markers of inflammation in predicting short-term outcomes of acute coronary syndrome (ACS).

methodsWe analyzed the predictive importance of laboratory and clinical features in 6769 hospitalizations of patients with ACS. Two binary classifications were considered: significant coronary lesion (SCL) or lack of SCL, and in-hospital death or survival. SCL was observed in 73% of patients. In-hospital mortality was observed in 1.4% of patients and it was higher in the case of patients with SCL. Ensembles of decision trees and decision rule models were trained to predict these classifications.

resultsThe best performing model for in-hospital mortality was based on the dominance-based rough set approach and the full set of laboratory as well as clinical features. This model achieved 81 ± 2.4% sensitivity and 81.1 ± 0.5% specificity in the detection of in-hospital mortality. The models trained for SCL performed considerably worse. The best performing model for detecting SCL achieved 56.9 ± 0.2% sensitivity and 66.9 ± 0.2% specificity. Dominance rough set approach classifier operating on the full set of clinical and laboratory features identifies presence or absence of diabetes, systolic and diastolic blood pressure and prothrombin time as having the highest confirmation measures (best predictive value) in the detection of in-hospital mortality. When we used the limited set of variables, neutrophil count, age, systolic and diastolic pressure and heart rate (taken at admission) achieved the high feature importance scores (provided by the gradient boosted trees classifier) as well as the positive confirmation measures (provided by the dominance-based rough set approach classifier).

conclusionsMachine learned models can rely on the association between the elevated inflammatory markers and the short-term ACS outcomes to provide accurate predictions. Moreover, such models can help assess the usefulness of laboratory and clinical features in predicting the in-hospital mortality of ACS patients.

Indexed as

Machine LearningModels, TheoreticalAcute Coronary SyndromeAgedBiomarkersHospital MortalityHumansInflammationLogistic ModelsReproducibility of ResultsROC CurveTime FactorsTreatment OutcomeBiomarkersAcute coronary syndromeBiomarkersInflammationMachine learningOutcomes researchRisk assessment

Identifiers

PMID30509300
PMCPMC6276170

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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.