Endoscopic factors in the diagnosis of colorectal dysplasia in chronic inflammatory bowel disease
Background: Surveillance colonoscopy in inflammatory bowel diseases (IBDs) is advocated for early diagnosis of neoplasia but is imperfect because some patients develop cancer despite surveillance. We sought to determine if any endoscopic factors during surveillance colonoscopy were associated with t...
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Veröffentlicht in: | Inflammatory bowel diseases 2005-05, Vol.11 (5), p.428-434 |
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description | Background: Surveillance colonoscopy in inflammatory bowel diseases (IBDs) is advocated for early diagnosis of neoplasia but is imperfect because some patients develop cancer despite surveillance. We sought to determine if any endoscopic factors during surveillance colonoscopy were associated with the diagnosis of colorectal dysplasia before the development of cancer.
Methods: We reviewed the Mayo Clinic endoscopic database and medical records of patients with IBD who underwent surveillance colonoscopy between January 2002 and November 2003. Associations were sought between endoscopic factors and the diagnosis of dysplasia. Among 635 IBD patients, 24 (3.8%) had flat dysplasia and 12 (1.9%) had IBD‐related polypoid dysplasia. In 28 patients (4.4%), sporadic tubular adenoma was identified. Colonoscopies in which flat dysplasia was identified varied in duration from 7 to 81 minutes (median, 24.5 min) compared with 3 to 70 minutes (median, 22 min) for those in which dysplasia was not found.
Results: Using logistic regression analysis, we found that every additional minute in total colonoscopy time increased the flat dysplasia diagnosis rate by 3.5% (P = 0.0157). There was a significant correlation between median surveillance colonoscopy duration per endoscopist and flat dysplasia diagnosis rate (P = 0.0066). The number of biopsies taken during the procedures with flat dysplasia ranged from 6 to 36 (median, 28) compared with 2 to 54 (median, 25) in those without flat dysplasia. There was no significant effect of biopsy number of dysplasia diagnosis.
Conclusions: Our results show that the practice of surveillance colonoscopy varies greatly among endoscopists, and longer procedure duration is significantly associated with the likelihood of dysplasia diagnosis. |
doi_str_mv | 10.1097/01.MIB.0000158951.54388.3a |
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Methods: We reviewed the Mayo Clinic endoscopic database and medical records of patients with IBD who underwent surveillance colonoscopy between January 2002 and November 2003. Associations were sought between endoscopic factors and the diagnosis of dysplasia. Among 635 IBD patients, 24 (3.8%) had flat dysplasia and 12 (1.9%) had IBD‐related polypoid dysplasia. In 28 patients (4.4%), sporadic tubular adenoma was identified. Colonoscopies in which flat dysplasia was identified varied in duration from 7 to 81 minutes (median, 24.5 min) compared with 3 to 70 minutes (median, 22 min) for those in which dysplasia was not found.
Results: Using logistic regression analysis, we found that every additional minute in total colonoscopy time increased the flat dysplasia diagnosis rate by 3.5% (P = 0.0157). There was a significant correlation between median surveillance colonoscopy duration per endoscopist and flat dysplasia diagnosis rate (P = 0.0066). The number of biopsies taken during the procedures with flat dysplasia ranged from 6 to 36 (median, 28) compared with 2 to 54 (median, 25) in those without flat dysplasia. There was no significant effect of biopsy number of dysplasia diagnosis.
Conclusions: Our results show that the practice of surveillance colonoscopy varies greatly among endoscopists, and longer procedure duration is significantly associated with the likelihood of dysplasia diagnosis.</description><identifier>ISSN: 1078-0998</identifier><identifier>EISSN: 1536-4844</identifier><identifier>DOI: 10.1097/01.MIB.0000158951.54388.3a</identifier><identifier>PMID: 15867581</identifier><language>eng</language><publisher>Philadelphia: Lippincott Williams & Wilkins, Inc</publisher><subject>Adenoma ; Adult ; Aged ; Aged, 80 and over ; Biopsy ; Cholangitis, Sclerosing - complications ; Cholangitis, Sclerosing - pathology ; Colon ; Colon - pathology ; Colonoscopy ; Colorectal Neoplasms - etiology ; Dysplasia ; Female ; Humans ; inflammatory bowel disease ; Inflammatory bowel diseases ; Inflammatory Bowel Diseases - complications ; Inflammatory Bowel Diseases - pathology ; Male ; medical records ; Middle Aged ; Neoplasia ; Predictive Value of Tests ; Regression analysis ; Retrospective Studies ; Risk Factors ; surveillance colonoscopy ; Time Factors</subject><ispartof>Inflammatory bowel diseases, 2005-05, Vol.11 (5), p.428-434</ispartof><rights>Copyright © 2005 Crohn's & Colitis Foundation of America, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4632-798eea795df53411d606e0d95cee5ca61b16e6e6dfd157f01dcbd7692d8c56bf3</citedby><cites>FETCH-LOGICAL-c4632-798eea795df53411d606e0d95cee5ca61b16e6e6dfd157f01dcbd7692d8c56bf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1097%2F01.MIB.0000158951.54388.3a$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1097%2F01.MIB.0000158951.54388.3a$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15867581$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Toruner, Murat</creatorcontrib><creatorcontrib>Harewood, Gavin C</creatorcontrib><creatorcontrib>Loftus, Edward V</creatorcontrib><creatorcontrib>Sandborn, William J</creatorcontrib><creatorcontrib>Tremaine, William J</creatorcontrib><creatorcontrib>Faubion, William A</creatorcontrib><creatorcontrib>Schroeder, Kenneth W</creatorcontrib><creatorcontrib>Egan, Laurence J</creatorcontrib><title>Endoscopic factors in the diagnosis of colorectal dysplasia in chronic inflammatory bowel disease</title><title>Inflammatory bowel diseases</title><addtitle>Inflamm Bowel Dis</addtitle><description>Background: Surveillance colonoscopy in inflammatory bowel diseases (IBDs) is advocated for early diagnosis of neoplasia but is imperfect because some patients develop cancer despite surveillance. We sought to determine if any endoscopic factors during surveillance colonoscopy were associated with the diagnosis of colorectal dysplasia before the development of cancer.
Methods: We reviewed the Mayo Clinic endoscopic database and medical records of patients with IBD who underwent surveillance colonoscopy between January 2002 and November 2003. Associations were sought between endoscopic factors and the diagnosis of dysplasia. Among 635 IBD patients, 24 (3.8%) had flat dysplasia and 12 (1.9%) had IBD‐related polypoid dysplasia. In 28 patients (4.4%), sporadic tubular adenoma was identified. Colonoscopies in which flat dysplasia was identified varied in duration from 7 to 81 minutes (median, 24.5 min) compared with 3 to 70 minutes (median, 22 min) for those in which dysplasia was not found.
Results: Using logistic regression analysis, we found that every additional minute in total colonoscopy time increased the flat dysplasia diagnosis rate by 3.5% (P = 0.0157). There was a significant correlation between median surveillance colonoscopy duration per endoscopist and flat dysplasia diagnosis rate (P = 0.0066). The number of biopsies taken during the procedures with flat dysplasia ranged from 6 to 36 (median, 28) compared with 2 to 54 (median, 25) in those without flat dysplasia. There was no significant effect of biopsy number of dysplasia diagnosis.
Conclusions: Our results show that the practice of surveillance colonoscopy varies greatly among endoscopists, and longer procedure duration is significantly associated with the likelihood of dysplasia diagnosis.</description><subject>Adenoma</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biopsy</subject><subject>Cholangitis, Sclerosing - complications</subject><subject>Cholangitis, Sclerosing - pathology</subject><subject>Colon</subject><subject>Colon - pathology</subject><subject>Colonoscopy</subject><subject>Colorectal Neoplasms - etiology</subject><subject>Dysplasia</subject><subject>Female</subject><subject>Humans</subject><subject>inflammatory bowel disease</subject><subject>Inflammatory bowel diseases</subject><subject>Inflammatory Bowel Diseases - complications</subject><subject>Inflammatory Bowel Diseases - pathology</subject><subject>Male</subject><subject>medical records</subject><subject>Middle Aged</subject><subject>Neoplasia</subject><subject>Predictive Value of Tests</subject><subject>Regression analysis</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>surveillance colonoscopy</subject><subject>Time Factors</subject><issn>1078-0998</issn><issn>1536-4844</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkU9v1DAQxS0EoqXwFVDEgZ4SZuL4Hzdalnalol7K2XLsCTVK4iXeVbXfHpddqbdK9TvYh997o_Fj7BNCg2DUF8Dm5_qigXJQaCOwER3XuuHuFTtFwWXd6a57Xd6gdA3G6BP2Luc_AG2RectOik0qofGUudUcUvZpE301OL9NS67iXG3vqQrR_Z5TjrlKQ-XTmBbyWzdWYZ83o8vRPYL-fklz8cZ5GN00uRKwr_r0QIWLmVym9-zN4MZMH473Gfv1Y3V3eV3f3F6tL7_d1L6TvK2V0UROGREGwTvEIEESBCM8kfBOYo-SisIQUKgBMPg-KGnaoL2Q_cDP2Pkhd7OkvzvKWzvF7Gkc3Uxpl62BlnMJqi3k52dJqZRG6LoCfj2Afkk5LzTYzRInt-wtgn2swgLaUoV9qsL-r8JyV8wfj1N2_UThyXr8-wKsDsBDHGn_gmi7vvjOlQZEEGWpfzhOmqI</recordid><startdate>200505</startdate><enddate>200505</enddate><creator>Toruner, Murat</creator><creator>Harewood, Gavin C</creator><creator>Loftus, Edward V</creator><creator>Sandborn, William J</creator><creator>Tremaine, William J</creator><creator>Faubion, William A</creator><creator>Schroeder, Kenneth W</creator><creator>Egan, Laurence J</creator><general>Lippincott Williams & Wilkins, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7T5</scope><scope>H94</scope></search><sort><creationdate>200505</creationdate><title>Endoscopic factors in the diagnosis of colorectal dysplasia in chronic inflammatory bowel disease</title><author>Toruner, Murat ; Harewood, Gavin C ; Loftus, Edward V ; Sandborn, William J ; Tremaine, William J ; Faubion, William A ; Schroeder, Kenneth W ; Egan, Laurence J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4632-798eea795df53411d606e0d95cee5ca61b16e6e6dfd157f01dcbd7692d8c56bf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adenoma</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biopsy</topic><topic>Cholangitis, Sclerosing - complications</topic><topic>Cholangitis, Sclerosing - pathology</topic><topic>Colon</topic><topic>Colon - pathology</topic><topic>Colonoscopy</topic><topic>Colorectal Neoplasms - etiology</topic><topic>Dysplasia</topic><topic>Female</topic><topic>Humans</topic><topic>inflammatory bowel disease</topic><topic>Inflammatory bowel diseases</topic><topic>Inflammatory Bowel Diseases - complications</topic><topic>Inflammatory Bowel Diseases - pathology</topic><topic>Male</topic><topic>medical records</topic><topic>Middle Aged</topic><topic>Neoplasia</topic><topic>Predictive Value of Tests</topic><topic>Regression analysis</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>surveillance colonoscopy</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Toruner, Murat</creatorcontrib><creatorcontrib>Harewood, Gavin C</creatorcontrib><creatorcontrib>Loftus, Edward V</creatorcontrib><creatorcontrib>Sandborn, William J</creatorcontrib><creatorcontrib>Tremaine, William J</creatorcontrib><creatorcontrib>Faubion, William A</creatorcontrib><creatorcontrib>Schroeder, Kenneth W</creatorcontrib><creatorcontrib>Egan, Laurence J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Inflammatory bowel diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Toruner, Murat</au><au>Harewood, Gavin C</au><au>Loftus, Edward V</au><au>Sandborn, William J</au><au>Tremaine, William J</au><au>Faubion, William A</au><au>Schroeder, Kenneth W</au><au>Egan, Laurence J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Endoscopic factors in the diagnosis of colorectal dysplasia in chronic inflammatory bowel disease</atitle><jtitle>Inflammatory bowel diseases</jtitle><addtitle>Inflamm Bowel Dis</addtitle><date>2005-05</date><risdate>2005</risdate><volume>11</volume><issue>5</issue><spage>428</spage><epage>434</epage><pages>428-434</pages><issn>1078-0998</issn><eissn>1536-4844</eissn><abstract>Background: Surveillance colonoscopy in inflammatory bowel diseases (IBDs) is advocated for early diagnosis of neoplasia but is imperfect because some patients develop cancer despite surveillance. We sought to determine if any endoscopic factors during surveillance colonoscopy were associated with the diagnosis of colorectal dysplasia before the development of cancer.
Methods: We reviewed the Mayo Clinic endoscopic database and medical records of patients with IBD who underwent surveillance colonoscopy between January 2002 and November 2003. Associations were sought between endoscopic factors and the diagnosis of dysplasia. Among 635 IBD patients, 24 (3.8%) had flat dysplasia and 12 (1.9%) had IBD‐related polypoid dysplasia. In 28 patients (4.4%), sporadic tubular adenoma was identified. Colonoscopies in which flat dysplasia was identified varied in duration from 7 to 81 minutes (median, 24.5 min) compared with 3 to 70 minutes (median, 22 min) for those in which dysplasia was not found.
Results: Using logistic regression analysis, we found that every additional minute in total colonoscopy time increased the flat dysplasia diagnosis rate by 3.5% (P = 0.0157). There was a significant correlation between median surveillance colonoscopy duration per endoscopist and flat dysplasia diagnosis rate (P = 0.0066). The number of biopsies taken during the procedures with flat dysplasia ranged from 6 to 36 (median, 28) compared with 2 to 54 (median, 25) in those without flat dysplasia. There was no significant effect of biopsy number of dysplasia diagnosis.
Conclusions: Our results show that the practice of surveillance colonoscopy varies greatly among endoscopists, and longer procedure duration is significantly associated with the likelihood of dysplasia diagnosis.</abstract><cop>Philadelphia</cop><pub>Lippincott Williams & Wilkins, Inc</pub><pmid>15867581</pmid><doi>10.1097/01.MIB.0000158951.54388.3a</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Wiley Online Library Journals Frontfile Complete; Oxford University Press Journals All Titles (1996-Current) |
subjects | Adenoma Adult Aged Aged, 80 and over Biopsy Cholangitis, Sclerosing - complications Cholangitis, Sclerosing - pathology Colon Colon - pathology Colonoscopy Colorectal Neoplasms - etiology Dysplasia Female Humans inflammatory bowel disease Inflammatory bowel diseases Inflammatory Bowel Diseases - complications Inflammatory Bowel Diseases - pathology Male medical records Middle Aged Neoplasia Predictive Value of Tests Regression analysis Retrospective Studies Risk Factors surveillance colonoscopy Time Factors |
title | Endoscopic factors in the diagnosis of colorectal dysplasia in chronic inflammatory bowel disease |
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