Dysplasia Surveillance in Inflammatory Bowel Disease: A Cohort Study
Main Author: | |
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Publication Date: | 2021 |
Other Authors: | , , , , |
Format: | Article |
Language: | eng |
Source: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Download full: | http://scielo.pt/scielo.php?script=sci_arttext&pid=S2341-45452021000200097 |
Summary: | Abstract: Introduction: Patients with colonic inflammatory bowel disease (IBD) are at an increased risk for colorectal cancer (CRC), whereby surveillance colonoscopy is recommended. Aim: To study the clinical and endoscopic variables associated with dysplasia in IBD patients. Methods: A cohort study was conducted on IBD patients who were part of a colonoscopy surveillance program between 2011 and 2016. Results: A total of 342 colonoscopies were performed on 162 patients (105 with ulcerative colitis [UC] and 57 with Crohn’s disease). Random biopsies were performed at least once on 81.5% of patients; 33.3% of the patients underwent chromoendoscopy (CE) at least once. Endoscopically resectable lesions were detected in 55 patients (34%), and visible lesions deemed unfit for endoscopic resection were found in 5 patients (3.1%). Overall, 62 dysplastic visible lesions (58 with lowgrade dysplasia and 3 with high-grade dysplasia) and 1 adenocarcinoma were found in 34 patients. Dysplasia in random biopsies was present in 3 patients, the yield of random biopsies for dysplasia being 1.85%/patient (3/162), 1.75%/ colonoscopy (6/342), and 0.25%/biopsy (9/3,637). Dysplasia detected in random biopsies was significantly associated with a personal history of visible dysplasia (p = 0.006). Upon univariate analysis, dysplasia was significantly associated with the type of IBD, the performance of random biopsies, and CE (p = 0.016/0.009/0.05, respectively). On multivariate analysis, dysplasia was associated with duration of disease. Conclusion: Our data confirm that patients with long-standing IBD, in particular UC, should be enrolled in dysplasia surveillance programs, and that performing CE and random biopsies seems to help in the detection of colonic neoplastic lesions. |
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Dysplasia Surveillance in Inflammatory Bowel Disease: A Cohort StudyInflammatory bowel disease (IBD)Ulcerative colitisCrohn’s diseaseDysplasiaSurveillanceAbstract: Introduction: Patients with colonic inflammatory bowel disease (IBD) are at an increased risk for colorectal cancer (CRC), whereby surveillance colonoscopy is recommended. Aim: To study the clinical and endoscopic variables associated with dysplasia in IBD patients. Methods: A cohort study was conducted on IBD patients who were part of a colonoscopy surveillance program between 2011 and 2016. Results: A total of 342 colonoscopies were performed on 162 patients (105 with ulcerative colitis [UC] and 57 with Crohn’s disease). Random biopsies were performed at least once on 81.5% of patients; 33.3% of the patients underwent chromoendoscopy (CE) at least once. Endoscopically resectable lesions were detected in 55 patients (34%), and visible lesions deemed unfit for endoscopic resection were found in 5 patients (3.1%). Overall, 62 dysplastic visible lesions (58 with lowgrade dysplasia and 3 with high-grade dysplasia) and 1 adenocarcinoma were found in 34 patients. Dysplasia in random biopsies was present in 3 patients, the yield of random biopsies for dysplasia being 1.85%/patient (3/162), 1.75%/ colonoscopy (6/342), and 0.25%/biopsy (9/3,637). Dysplasia detected in random biopsies was significantly associated with a personal history of visible dysplasia (p = 0.006). Upon univariate analysis, dysplasia was significantly associated with the type of IBD, the performance of random biopsies, and CE (p = 0.016/0.009/0.05, respectively). On multivariate analysis, dysplasia was associated with duration of disease. Conclusion: Our data confirm that patients with long-standing IBD, in particular UC, should be enrolled in dysplasia surveillance programs, and that performing CE and random biopsies seems to help in the detection of colonic neoplastic lesions.Sociedade Portuguesa de Gastrenterologia2021-04-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articletext/htmlhttp://scielo.pt/scielo.php?script=sci_arttext&pid=S2341-45452021000200097GE-Portuguese Journal of Gastroenterology v.28 n.2 2021reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAPenghttp://scielo.pt/scielo.php?script=sci_arttext&pid=S2341-45452021000200097Saraiva,SofiaRosa,IsadoraMoleiro,JoanaSilva,João Pereira daFonseca,RicardoPereira,António Diasinfo:eu-repo/semantics/openAccess2024-02-06T17:34:09Zoai:scielo:S2341-45452021000200097Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T13:21:04.793048Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
Dysplasia Surveillance in Inflammatory Bowel Disease: A Cohort Study |
title |
Dysplasia Surveillance in Inflammatory Bowel Disease: A Cohort Study |
spellingShingle |
Dysplasia Surveillance in Inflammatory Bowel Disease: A Cohort Study Saraiva,Sofia Inflammatory bowel disease (IBD) Ulcerative colitis Crohn’s disease Dysplasia Surveillance |
title_short |
Dysplasia Surveillance in Inflammatory Bowel Disease: A Cohort Study |
title_full |
Dysplasia Surveillance in Inflammatory Bowel Disease: A Cohort Study |
title_fullStr |
Dysplasia Surveillance in Inflammatory Bowel Disease: A Cohort Study |
title_full_unstemmed |
Dysplasia Surveillance in Inflammatory Bowel Disease: A Cohort Study |
title_sort |
Dysplasia Surveillance in Inflammatory Bowel Disease: A Cohort Study |
author |
Saraiva,Sofia |
author_facet |
Saraiva,Sofia Rosa,Isadora Moleiro,Joana Silva,João Pereira da Fonseca,Ricardo Pereira,António Dias |
author_role |
author |
author2 |
Rosa,Isadora Moleiro,Joana Silva,João Pereira da Fonseca,Ricardo Pereira,António Dias |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Saraiva,Sofia Rosa,Isadora Moleiro,Joana Silva,João Pereira da Fonseca,Ricardo Pereira,António Dias |
dc.subject.por.fl_str_mv |
Inflammatory bowel disease (IBD) Ulcerative colitis Crohn’s disease Dysplasia Surveillance |
topic |
Inflammatory bowel disease (IBD) Ulcerative colitis Crohn’s disease Dysplasia Surveillance |
description |
Abstract: Introduction: Patients with colonic inflammatory bowel disease (IBD) are at an increased risk for colorectal cancer (CRC), whereby surveillance colonoscopy is recommended. Aim: To study the clinical and endoscopic variables associated with dysplasia in IBD patients. Methods: A cohort study was conducted on IBD patients who were part of a colonoscopy surveillance program between 2011 and 2016. Results: A total of 342 colonoscopies were performed on 162 patients (105 with ulcerative colitis [UC] and 57 with Crohn’s disease). Random biopsies were performed at least once on 81.5% of patients; 33.3% of the patients underwent chromoendoscopy (CE) at least once. Endoscopically resectable lesions were detected in 55 patients (34%), and visible lesions deemed unfit for endoscopic resection were found in 5 patients (3.1%). Overall, 62 dysplastic visible lesions (58 with lowgrade dysplasia and 3 with high-grade dysplasia) and 1 adenocarcinoma were found in 34 patients. Dysplasia in random biopsies was present in 3 patients, the yield of random biopsies for dysplasia being 1.85%/patient (3/162), 1.75%/ colonoscopy (6/342), and 0.25%/biopsy (9/3,637). Dysplasia detected in random biopsies was significantly associated with a personal history of visible dysplasia (p = 0.006). Upon univariate analysis, dysplasia was significantly associated with the type of IBD, the performance of random biopsies, and CE (p = 0.016/0.009/0.05, respectively). On multivariate analysis, dysplasia was associated with duration of disease. Conclusion: Our data confirm that patients with long-standing IBD, in particular UC, should be enrolled in dysplasia surveillance programs, and that performing CE and random biopsies seems to help in the detection of colonic neoplastic lesions. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-04-01 |
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info:eu-repo/semantics/publishedVersion |
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http://scielo.pt/scielo.php?script=sci_arttext&pid=S2341-45452021000200097 |
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http://scielo.pt/scielo.php?script=sci_arttext&pid=S2341-45452021000200097 |
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eng |
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eng |
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http://scielo.pt/scielo.php?script=sci_arttext&pid=S2341-45452021000200097 |
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openAccess |
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Sociedade Portuguesa de Gastrenterologia |
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Sociedade Portuguesa de Gastrenterologia |
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