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dc.contributor.authorLizancos Vidal, Plácido Francisco
dc.contributor.authorde Moura Ramos, Jose Joaquim
dc.contributor.authorNovo Buján, Jorge
dc.contributor.authorOrtega Hortas, Marcos
dc.date.accessioned2024-01-02T10:02:08Z
dc.date.available2024-01-02T10:02:08Z
dc.date.issued2021
dc.identifier.issn0957-4174
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pubmed/33612998es
dc.identifier.urihttp://hdl.handle.net/20.500.11940/18429
dc.description.abstractOne of the main challenges in times of sanitary emergency is to quickly develop computer aided diagnosis systems with a limited number of available samples due to the novelty, complexity of the case and the urgency of its implementation. This is the case during the current pandemic of COVID-19. This pathogen primarily infects the respiratory system of the afflicted, resulting in pneumonia and in a severe case of acute respiratory distress syndrome. This results in the formation of different pathological structures in the lungs that can be detected by the use of chest X-rays. Due to the overload of the health services, portable X-ray devices are recommended during the pandemic, preventing the spread of the disease. However, these devices entail different complications (such as capture quality) that, together with the subjectivity of the clinician, make the diagnostic process more difficult and suggest the necessity for computer-aided diagnosis methodologies despite the scarcity of samples available to do so. To solve this problem, we propose a methodology that allows to adapt the knowledge from a well-known domain with a high number of samples to a new domain with a significantly reduced number and greater complexity. We took advantage of a pre-trained segmentation model from brain magnetic resonance imaging of a unrelated pathology and performed two stages of knowledge transfer to obtain a robust system able to segment lung regions from portable X-ray devices despite the scarcity of samples and lesser quality. This way, our methodology obtained a satisfactory accuracy of 0.9761 +/- 0.0100 for patients with COVID-19, 0.9801 +/- 0.0104 for normal patients and 0.9769 +/- 0.0111 for patients with pulmonary diseases with similar characteristics as COVID-19 (such as pneumonia) but not genuine COVID-19.
dc.language.isoen
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleMulti-stage transfer learning for lung segmentation using portable X-ray devices for patients with COVID-19
dc.typeJournal Articlees
dc.authorsophosLizancos Vidal, Plácido;de Moura, Joaquim;Novo, Jorge;Ortega, Marcos
dc.identifier.doi10.1016/j.eswa.2021.114677
dc.identifier.pmid33612998
dc.identifier.sophos46366
dc.issue.number173.
dc.journal.titleEXPERT SYSTEMS WITH APPLICATIONS
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.)::Instituto de Investigación Biomédica de A Coruña (INIBIC)
dc.rights.accessRightsopenAccess
dc.subject.keywordINIBICes
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)es
dc.typesophosArtículo Originales


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