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dc.contributor.authorUnanue Arza, Saloa ORCID
dc.contributor.authorIdigoras Rubio, Isabel
dc.contributor.authorFernández Landa, María José
dc.contributor.authorBilbao-Iturribarria, Isabel
dc.contributor.authorBujanda Fernández de Pierola, Luis ORCID
dc.contributor.authorPortillo Villares, María Isabel
dc.date.accessioned2021-10-27T11:38:47Z
dc.date.available2021-10-27T11:38:47Z
dc.date.issued2021-10-12
dc.identifier.citationCancers 13(20) : (2021) // Article ID 5105es_ES
dc.identifier.issn2072-6694
dc.identifier.urihttp://hdl.handle.net/10810/53656
dc.description.abstractUsing the algorithm of the World Endoscopy Organisation (WEO), we have studied retrospectively all colorectal cancers, both detected and non-detected by the Basque Country screening programme from 2009 to 2017. In the screening programme 61,335 colonoscopies were performed following a positive Faecal Immunochemical test (FIT) (≥20 µg Hb/g faeces) and the 128 cases of post-colonoscopy colorectal cancer (PCCRC) detected were analysed. Among them, 50 interval type PCCRCs were diagnosed (before the recommended surveillance), 0.8 cases per 1000 colonoscopies performed, and 78 non-interval type PCCRCs (in the surveillance carried out at the recommended time or delayed), 1.3 per 1000 colonoscopies. Among the non-interval type PCCRCs, 61 cases were detected in the surveillance carried out at the recommended time (type A) and 17 when the surveillance was delayed (type B), 1 case per 1000 colonoscopies performed and 0.28 cases per 1000 colonoscopies performed, respectively. Interval type PCCRC is less frequent than non-interval type PCCRC. In interval type PCCRCs, CRCs detected in advanced stages (stages III–IV) were significantly more frequent than those detected in early stages, compared to those of non-interval type PCCRCs (OR = 3.057; 95% CI, 1.410–6.625; p < 0.005). Non-interval type B PCCRCs are less frequent than non-interval type A PCCRCs, but the frequency of advanced stages is higher in interval type B PCCRCs.es_ES
dc.description.sponsorshipS.U.-A. have received funding from the Department of Education of the Basque Government through the Consolidated Research Group MATHMODE (IT1294-19).es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/
dc.subjectcolorectal neoplasmses_ES
dc.subjectearly detection of canceres_ES
dc.subjectcolonoscopyes_ES
dc.subjectinterval canceres_ES
dc.subjectadverse effectses_ES
dc.subjectrisk factorses_ES
dc.titleAnalysis of Post-Colonoscopy Colorectal Cancer and Its Subtypes in a Screening Programmees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.date.updated2021-10-22T13:56:16Z
dc.rights.holder2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).es_ES
dc.relation.publisherversionhttps://www.mdpi.com/2072-6694/13/20/5105/htmes_ES
dc.identifier.doi10.3390/cancers13205105
dc.departamentoesEnfermería
dc.departamentoeuErizaintza


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2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's license is described as 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).