Evidence map›Paper›PMID 35471179›Full record

ArticleBiomedica : revista del Instituto Nacional de Salud2022

Deep learning representations to support COVID-19 diagnosis on CT slices.

Josué Ruano, John Arcila, David Romo-Bucheli, Carlos Vargas, Jefferson Rodríguez, Óscar Mendoza, Miguel Plazas, Lola Bautista, Jorge Villamizar, Gabriel Pedraza and 7 more

Abstract read
In one paragraph

Article in Biomedica : revista del Instituto Nacional de Salud, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

17 authors.

Josué RuanoBIVL2ab Biomedical Imaging, Vision and Learning Laboratory, Escuela de Ingeniería de Sistemas e Informática, Universidad Industrial de Santander, Bucaramanga, Colombia. jaruanob@unal.edu.co.
John ArcilaBIVL2ab Biomedical Imaging, Vision and Learning Laboratory, Escuela de Ingeniería de Sistemas e Informática, Universidad Industrial de Santander, Bucaramanga, Colombia. john.archila.valderrama@gmail.com.
David Romo-BucheliBIVL2ab Biomedical Imaging, Vision and Learning Laboratory, Escuela de Ingeniería de Sistemas e Informática, Universidad Industrial de Santander, Bucaramanga, Colombia. deromob@uis.edu.co.
Carlos VargasBIVL2ab Biomedical Imaging, Vision and Learning Laboratory, Escuela de Ingeniería de Sistemas e Informática, Universidad Industrial de Santander, Bucaramanga, Colombia. cavargasp@unal.edu.co.
Jefferson RodríguezBIVL2ab Biomedical Imaging, Vision and Learning Laboratory, Escuela de Ingeniería de Sistemas e Informática, Universidad Industrial de Santander, Bucaramanga, Colombia. jefferson.rodriguez2@saber.uis.edu.co.
Óscar MendozaBIVL2ab Biomedical Imaging, Vision and Learning Laboratory, Escuela de Ingeniería de Sistemas e Informática, Universidad Industrial de Santander, Bucaramanga, Colombia. oscar.mendoza2@saber.uis.edu.co.
Miguel PlazasBIVL2ab Biomedical Imaging, Vision and Learning Laboratory, Escuela de Ingeniería de Sistemas e Informática, Universidad Industrial de Santander, Bucaramanga, Colombia. miguel.plazas@saber.uis.edu.co.
Lola BautistaBIVL2ab Biomedical Imaging, Vision and Learning Laboratory, Escuela de Ingeniería de Sistemas e Informática, Universidad Industrial de Santander, Bucaramanga, Colombia. lxbautis@uis.edu.co.
Jorge VillamizarBIVL2ab Biomedical Imaging, Vision and Learning Laboratory, Escuela de Ingeniería de Sistemas e Informática, Universidad Industrial de Santander, Bucaramanga, Colombia; Facultad de Ingeniería, Universidad de Los Andes, Mérida, Venezuela. jorge@uis.edu.co.
Gabriel PedrazaBIVL2ab Biomedical Imaging, Vision and Learning Laboratory, Escuela de Ingeniería de Sistemas e Informática, Universidad Industrial de Santander, Bucaramanga, Colombia. gpedraza@uis.edu.co.
Alejandra MorenoBIVL2ab Biomedical Imaging, Vision and Learning Laboratory, Escuela de Ingeniería de Sistemas e Informática, Universidad Industrial de Santander, Bucaramanga, Colombia. alejandra.moreno@saber.uis.edu.co.
Diana ValenzuelaClínica FOSCAL, Fundación Oftalmológica de Santander, Bucaramanga, Colombia. dimavasa2424@gmail.com.
Lina VázquezClínica FOSCAL, Fundación Oftalmológica de Santander, Bucaramanga, Colombia. lina22.maria@gmail.com.
Carolina Valenzuela-SantosClínica FOSCAL, Fundación Oftalmológica de Santander, Bucaramanga, Colombia. carolvasa@gmail.com.
Paul CamachoClínica FOSCAL, Fundación Oftalmológica de Santander, Bucaramanga, Colombia. paul.camacho@foscal.com.co.
Daniel MantillaClínica FOSCAL, Fundación Oftalmológica de Santander, Bucaramanga, Colombia. daniel.mantilla@foscal.com.co.
Fabio Martínez CarrilloBIVL2ab Biomedical Imaging, Vision and Learning Laboratory, Escuela de Ingeniería de Sistemas e Informática, Universidad Industrial de Santander, Bucaramanga, Colombia. famarcar@uis.edu.co.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe coronavirus disease 2019 (COVID-19) has become a significant public health problem worldwide. In this context, CT-scan automatic analysis has emerged as a COVID-19 complementary diagnosis tool allowing for radiological finding characterization, patient categorization, and disease follow-up. However, this analysis depends on the radiologist's expertise, which may result in subjective evaluations.

objectiveTo explore deep learning representations, trained from thoracic CT-slices, to automatically distinguish COVID-19 disease from control samples. MATERIALS AND

methodsTwo datasets were used: SARS-CoV-2 CT Scan (Set-1) and FOSCAL clinic's dataset (Set-2). The deep representations took advantage of supervised learning models previously trained on the natural image domain, which were adjusted following a transfer learning scheme. The deep classification was carried out: (a) via an end-to-end deep learning approach and (b) via random forest and support vector machine classifiers by feeding the deep representation embedding vectors into these classifiers.

resultsThe end-to-end classification achieved an average accuracy of 92.33% (89.70% precision) for Set-1 and 96.99% (96.62% precision) for Set-2. The deep feature embedding with a support vector machine achieved an average accuracy of 91.40% (95.77% precision) and 96.00% (94.74% precision) for Set-1 and Set-2, respectively.

conclusionDeep representations have achieved outstanding performance in the identification of COVID-19 cases on CT scans demonstrating good characterization of the COVID-19 radiological patterns. These representations could potentially support the COVID-19 diagnosis in clinical settings.

Indexed as

COVID-19Deep LearningCOVID-19 TestingHumansNeural Networks, ComputerSARS-CoV-2Tomography, X-Ray ComputedCoronavirus infections/diagnosisdeep learningtomographyX-ray computed

Identifiers

PMID35471179
PMCPMC9071798

What OpenQuestion holds

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LicenceCC BY
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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.