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dc.contributor.authorPin Vieito, Noel
dc.contributor.authorIglesias Varela, María José
dc.contributor.authorRemedios Espino, David Rafael 
dc.contributor.authorRodríguez-Alonso, Lorena
dc.contributor.authorRodriguez-Moranta, Francisco
dc.contributor.authorÁlvarez Sánchez, María Victoria 
dc.contributor.authorFernández-Bañares, Fernando
dc.contributor.authorBoadas, Jaume
dc.contributor.authorMartínez-Bauer, Eva
dc.contributor.authorCampo, Rafael
dc.contributor.authorBujanda, Luis
dc.contributor.authorFerrandez, Ángel
dc.contributor.authorPiñol, Virginia
dc.contributor.authorRodríguez-Alcalde, Daniel
dc.contributor.authorGuardiola, Jordi
dc.contributor.authorCubiella Fernández, Joaquín 
dc.date.accessioned2022-03-23T08:55:51Z
dc.date.available2022-03-23T08:55:51Z
dc.date.issued2020
dc.identifier.issn1007-9327
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pubmed/31933515es
dc.identifier.urihttp://hdl.handle.net/20.500.11940/16381
dc.description.abstractBACKGROUND: Faecal immunochemical test (FIT) has been recommended to assess symptomatic patients for colorectal cancer (CRC) detection. Nevertheless, some conditions could theoretically favour blood originating in proximal areas of the gastrointestinal tract passing through the colon unmetabolized. A positive FIT result could be related to other gastrointestinal cancers (GIC). AIM: To assess the risk of GIC detection and related death in FIT-positive symptomatic patients (threshold 10 mug Hb/g faeces) without CRC. METHODS: Post hoc cohort analysis performed within two prospective diagnostic test studies evaluating the diagnostic accuracy of different FIT analytical systems for CRC and significant colonic lesion detection. Ambulatory patients with gastrointestinal symptoms referred consecutively for colonoscopy from primary and secondary healthcare, underwent a quantitative FIT before undergoing a complete colonoscopy. Patients without CRC were divided into two groups (positive and negative FIT) using the threshold of 10 mug Hb/g of faeces and data from follow-up were retrieved from electronic medical records of the public hospitals involved in the research. We determined the cumulative risk of GIC, CRC and upper GIC. Hazard rate (HR) was calculated adjusted by age, sex and presence of significant colonic lesion. RESULTS: We included 2709 patients without CRC and a complete baseline colonoscopy, 730 (26.9%) with FIT >/= 10 microgr Hb/gr. During a mean time of 45.5 +/- 20.0 mo, a GIC was detected in 57 (2.1%) patients: An upper GIC in 35 (1.3%) and a CRC in 14 (0.5%). Thirty-six patients (1.3%) died due to GIC: 22 (0.8%) due to an upper GIC and 9 (0.3%) due to CRC. FIT-positive subjects showed a higher CRC risk (HR 3.8, 95%CI: 1.2-11.9) with no differences in GIC (HR 1.5, 95%CI: 0.8-2.7) or upper GIC risk (HR 1.0, 95%CI: 0.5-2.2). Patients with a positive FIT had only an increased risk of CRC-related death (HR 10.8, 95%CI: 2.1-57.1) and GIC-related death (HR 2.2, 95%CI: 1.1-4.3), with no differences in upper GIC-related death (HR 1.4, 95%CI: 0.6-3.3). An upper GIC was detected in 22 (0.8%) patients during the first year. Two variables were independently associated: anaemia (OR 5.6, 95%CI: 2.2-13.9) and age >/= 70 years (OR 2.7, 95%CI: 1.1-7.0). CONCLUSION: Symptomatic patients without CRC have a moderate risk increase in upper GIC, regardless of the FIT result. Patients with a positive FIT have an increased risk of post-colonoscopy CRC.es
dc.rightsAtribución-NoComercial 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subject.meshRisk Factors*
dc.subject.meshProportional Hazards Models*
dc.subject.meshGastrointestinal Neoplasms*
dc.subject.meshMiddle Aged*
dc.subject.meshColon*
dc.subject.meshSensitivity and Specificity*
dc.subject.meshColonoscopy*
dc.subject.meshPostoperative Period*
dc.subject.meshEarly Detection of Cancer*
dc.subject.meshPredictive Value of Tests*
dc.subject.meshHumans*
dc.subject.meshDiagnosis*
dc.subject.meshProspective Studies*
dc.subject.meshAged*
dc.titleRisk of gastrointestinal cancer in a symptomatic cohort after a complete colonoscopy: Role of faecal immunochemical test.en
dc.typeJournal Articlees
dc.contributor.authorcorpThe Colonpredict Study Investigators
dc.authorsophosPin-Vieito, Noel;Iglesias, María J;Remedios, David;Rodríguez-Alonso, Lorena;Rodriguez-Moranta, Francisco;Álvarez-Sánchez, Victoria;Fernández-Bañares, Fernando;Boadas, Jaume;Martínez-Bauer, Eva;Campo, Rafael;Bujanda, Luis;Ferrandez, Ángel;Piñol, Virginia;Rodríguez-Alcalde, Daniel;Guardiola, Jordi;Cubiella, Joaquín;Investigators, On Behalf Of The Colonpredict Study
dc.identifier.doi10.3748/wjg.v26.i1.70
dc.identifier.pmid31933515
dc.identifier.sophos36848
dc.issue.number1es
dc.journal.titleWORLD JOURNAL OF GASTROENTEROLOGYes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Ourense, Verín e O Barco de Valdeorras - Complexo Hospitalario Universitario de Ourense::Dixestivoes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Ourense, Verín e O Barco de Valdeorras - Hospital de Verínes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Pontevedra e O Salnés - Complexo Hospitalario Universitario de Pontevedra::Dixestivoes
dc.rights.accessRightsopenAccess
dc.subject.decssensibilidad y especificidad*
dc.subject.decsfactores de riesgo*
dc.subject.decsestudios prospectivos*
dc.subject.decscolon*
dc.subject.decspruebas de valores predictivos*
dc.subject.decsmediana edad*
dc.subject.decsneoplasias gastrointestinales*
dc.subject.decssíntomas*
dc.subject.decsperíodo postoperatorio*
dc.subject.decsanciano*
dc.subject.decsdiagnóstico*
dc.subject.decshumanos*
dc.subject.decscolonoscopia*
dc.subject.decsdetección precoz del cáncer*
dc.subject.decsmodelos de riesgos proporcionales*
dc.subject.keywordCHUOes
dc.subject.keywordHP Verínes
dc.subject.keywordCHUPes
dc.typefidesArtículo Originales
dc.typesophosArtículo Originales
dc.volume.number26es


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