Evidence map›Paper›PMID 38832553›Full record

ArticleCardiology journal2024

Phenotype clustering of hospitalized high-risk patients with COVID-19 - a machine learning approach within the multicentre, multinational PCHF-COVICAV registry.

Mateusz Sokolski, Sander Trenson, Konrad Reszka, Szymon Urban, Justyna M Sokolska, Tor Biering-Sørensen, Mats C Højbjerg Lassen, Kristoffer Grundtvig Skaarup, Carmen Basic, Zacharias Mandalenakis and 9 more

Abstract readMulticenter Study
In one paragraph

Article in Cardiology journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

19 authors.

Mateusz SokolskiWroclaw Medical University, Faculty of Medicine, Institute of Heart Diseases, Wroclaw, Poland and Intitute of Heart Diseases, University Hospital, Wroclaw, Poland. matsok@gmail.com.ORCID 0000-0001-9925-3566
Sander TrensonDepartment of Cardiology, Sint-Jan Hospital Bruges, Bruges, Belgium.
Konrad ReszkaWroclaw Medical University, Faculty of Medicine, Institute of Heart Diseases, Wroclaw, Poland and Intitute of Heart Diseases, University Hospital, Wroclaw, Poland.
Szymon UrbanWroclaw Medical University, Faculty of Medicine, Institute of Heart Diseases, Wroclaw, Poland and Intitute of Heart Diseases, University Hospital, Wroclaw, Poland.
Justyna M SokolskaWroclaw Medical University, Faculty of Medicine, Institute of Heart Diseases, Wroclaw, Poland and Intitute of Heart Diseases, University Hospital, Wroclaw, Poland.
Tor Biering-SørensenDepartment of Cardiology, Copenhagen University Hospital - Herlev & Gentofte, Copenhagen, Denmark.
Mats C Højbjerg LassenDepartment of Cardiology, Copenhagen University Hospital - Herlev & Gentofte, Copenhagen, Denmark.
Kristoffer Grundtvig SkaarupDepartment of Cardiology, Copenhagen University Hospital - Herlev & Gentofte, Copenhagen, Denmark.
Carmen BasicDepartment of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Zacharias MandalenakisDepartment of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Klemens AblasserDivision of Cardiology, Medical University of Graz, Austria.
Peter P RainerDivision of Cardiology, Medical University of Graz, Austria.
Markus WallnerDivision of Cardiology, Medical University of Graz, Austria.
Valentina A RossiDepartment of Cardiology, University Heart Center, University Hospital, Zurich, Switzerland.
Marzia LilliuDivision of Infectious Diseases, Azienda ULSS 9, M. Magalini Hospital, Villafranca di Verona, Verona, Italy.
Goran LoncarInstitute for Cardiovascular Diseases Dedinje, Faculty of Medicine, University of Belgrade, Belgrade, Serbia.
Huseyin A CakmakDepartment of Cardiology, Mustafakemalpasa State Hospital, Bursa, Türkiye.
Frank RuschitzkaDepartment of Cardiology, University Heart Center, University Hospital, Zurich, Switzerland.
Andreas J FlammerDepartment of Cardiology, University Heart Center, University Hospital, Zurich, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

imtroductionThe high-risk population of patients with cardiovascular (CV) disease or risk factors (RF) suffering from COVID-19 is heterogeneous. Several predictors for impaired prognosis have been identified. However, with machine learning (ML) approaches, certain phenotypes may be confined to classify the affected population and to predict outcome. This study aimed to phenotype patients using unsupervised ML technique within the International Postgraduate Course Heart Failure Registry for patients hospitalized with COVID-19 and Cardiovascular disease and/or RF (PCHF-COVICAV). MATERIAL AND

methodsPatients from the eight centres with follow-up data available from the PCHF-COVICAV registry were included in this ML analysis (K-medoids algorithm).

resultsOut of 617 patients included into the prospective part of the registry, 458 [median age: 76 (IQR:65-84) years, 55% male] were analyzed and 46 baseline variables, including demographics, clinical status, comorbidities and biochemical characteristics were incorporated into the ML. Three clusters were extracted by this ML method. Cluster 1 (n = 181) represents mainly women with the least number of overall comorbidities and cardiovascular RF. Cluster 2 (n = 227) is characterized mainly by men with non-CV conditions and less severe symptoms of infection. Cluster 3 (n=50) mainly represents men with the highest prevalence of cardiac comorbidities and RF, more extensive inflammation and organ dysfunction with the highest 6-month all-cause mortality risk.

conclusionsThe ML process has identified three important clinical clusters from hospitalized COVID-19 CV and/or RF patients. The cluster of males with severe CV disease, particularly HF, and multiple RF presenting with increased inflammation had a particularly poor outcome.

Indexed as

Cardiovascular DiseasesCOVID-19HospitalizationMachine LearningPhenotypeRegistriesAgedAged, 80 and overCluster AnalysisFemaleHumansMalePrognosisProspective StudiesRisk AssessmentRisk Factorsartificial intelligencecardiovascular diseaseclusteringCOVID-19machine learningSARS-CoV2

Identifiers

PMID38832553
PMCPMC11374323

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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.