Observer variability in the histopathologic diagnosis of microscopic colitis and subgroups
Summary The diagnosis of microscopic colitis (MC) is based on histologic findings and includes collagenous colitis (CC) and lymphocytic colitis (LC). Incomplete MC (MCi) denotes patients with chronic diarrhea and a normal endoscopy and morphological changes that do not completely meet the histologic...
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Veröffentlicht in: | Human pathology 2013-11, Vol.44 (11), p.2461-2466 |
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description | Summary The diagnosis of microscopic colitis (MC) is based on histologic findings and includes collagenous colitis (CC) and lymphocytic colitis (LC). Incomplete MC (MCi) denotes patients with chronic diarrhea and a normal endoscopy and morphological changes that do not completely meet the histologic criteria of LC or CC. The aim of this study was to investigate the intraobserver and interobserver agreement on the MC subtypes of CC, LC, and MCi and the ability to discriminate MCi from normal and inflammatory bowel disease/nonspecific reactive changes. A single hematoxylin and eosin–stained specimen from biopsies of the following 5 groups were randomly selected and blinded: CC, LC, MCi, inflammatory bowel disease, and normal. Three pathologists independently reviewed the specimens. The specimens were relabeled and reinterpreted 4 months later. Intraobserver and interobserver agreement was evaluated by κ statistics. κ values for intraobserver agreement were good for 5 diagnostic groups varying from 0.70 to 0.83 and very good when simplifying to only 3 diagnostic groups varying from 0.88 to 0.96, separating MC/MCi from non-MC. κ values for interobserver agreement varied from 0.60 to 0.75 for 5 diagnostic groups and 0.81 to 0.89 for 3 diagnostic groups. The study shows that the intraobserver and interobserver agreement is high for discriminating between MC/MCi and non-MC, whereas the ability to discriminate MCi from CC and LC is lower. A revision and consensus on the histologic criteria of the MC subtypes seem warranted. |
doi_str_mv | 10.1016/j.humpath.2013.06.004 |
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Incomplete MC (MCi) denotes patients with chronic diarrhea and a normal endoscopy and morphological changes that do not completely meet the histologic criteria of LC or CC. The aim of this study was to investigate the intraobserver and interobserver agreement on the MC subtypes of CC, LC, and MCi and the ability to discriminate MCi from normal and inflammatory bowel disease/nonspecific reactive changes. A single hematoxylin and eosin–stained specimen from biopsies of the following 5 groups were randomly selected and blinded: CC, LC, MCi, inflammatory bowel disease, and normal. Three pathologists independently reviewed the specimens. The specimens were relabeled and reinterpreted 4 months later. Intraobserver and interobserver agreement was evaluated by κ statistics. κ values for intraobserver agreement were good for 5 diagnostic groups varying from 0.70 to 0.83 and very good when simplifying to only 3 diagnostic groups varying from 0.88 to 0.96, separating MC/MCi from non-MC. κ values for interobserver agreement varied from 0.60 to 0.75 for 5 diagnostic groups and 0.81 to 0.89 for 3 diagnostic groups. The study shows that the intraobserver and interobserver agreement is high for discriminating between MC/MCi and non-MC, whereas the ability to discriminate MCi from CC and LC is lower. A revision and consensus on the histologic criteria of the MC subtypes seem warranted.</description><identifier>ISSN: 0046-8177</identifier><identifier>EISSN: 1532-8392</identifier><identifier>DOI: 10.1016/j.humpath.2013.06.004</identifier><identifier>PMID: 24029708</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Aged ; Agreements ; Biopsy ; Colitis, Collagenous - classification ; Colitis, Collagenous - pathology ; Colitis, Lymphocytic - classification ; Colitis, Lymphocytic - pathology ; Colitis, Microscopic - classification ; Colitis, Microscopic - pathology ; Collagenous colitis ; Colonoscopy ; Confidence intervals ; Diagnosis, Differential ; Diarrhea ; Female ; Histology ; Humans ; Inflammatory bowel disease ; Interobserver variability ; Intraobserver variability ; Lymphocytic colitis ; Male ; Microscopic colitis ; Microscopic colitis incomplete ; Middle Aged ; Observer Variation ; Pathology ; Reproducibility ; Reproducibility of Results</subject><ispartof>Human pathology, 2013-11, Vol.44 (11), p.2461-2466</ispartof><rights>Elsevier Inc.</rights><rights>2013 Elsevier Inc.</rights><rights>2013.</rights><rights>Copyright Elsevier Limited Nov 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-ad07cff10ddda4c187e2bc4b87918d357e261252fe0fed4825a8933d5702c05b3</citedby><cites>FETCH-LOGICAL-c448t-ad07cff10ddda4c187e2bc4b87918d357e261252fe0fed4825a8933d5702c05b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S004681771300258X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24029708$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fiehn, Anne-Marie Kanstrup, MD</creatorcontrib><creatorcontrib>Bjørnbak, Camilla, MD</creatorcontrib><creatorcontrib>Warnecke, Mads, MD</creatorcontrib><creatorcontrib>Engel, Peter Johan Heiberg, MD</creatorcontrib><creatorcontrib>Munck, Lars Kristian, MD, Sci</creatorcontrib><title>Observer variability in the histopathologic diagnosis of microscopic colitis and subgroups</title><title>Human pathology</title><addtitle>Hum Pathol</addtitle><description>Summary The diagnosis of microscopic colitis (MC) is based on histologic findings and includes collagenous colitis (CC) and lymphocytic colitis (LC). Incomplete MC (MCi) denotes patients with chronic diarrhea and a normal endoscopy and morphological changes that do not completely meet the histologic criteria of LC or CC. The aim of this study was to investigate the intraobserver and interobserver agreement on the MC subtypes of CC, LC, and MCi and the ability to discriminate MCi from normal and inflammatory bowel disease/nonspecific reactive changes. A single hematoxylin and eosin–stained specimen from biopsies of the following 5 groups were randomly selected and blinded: CC, LC, MCi, inflammatory bowel disease, and normal. Three pathologists independently reviewed the specimens. The specimens were relabeled and reinterpreted 4 months later. Intraobserver and interobserver agreement was evaluated by κ statistics. κ values for intraobserver agreement were good for 5 diagnostic groups varying from 0.70 to 0.83 and very good when simplifying to only 3 diagnostic groups varying from 0.88 to 0.96, separating MC/MCi from non-MC. κ values for interobserver agreement varied from 0.60 to 0.75 for 5 diagnostic groups and 0.81 to 0.89 for 3 diagnostic groups. The study shows that the intraobserver and interobserver agreement is high for discriminating between MC/MCi and non-MC, whereas the ability to discriminate MCi from CC and LC is lower. A revision and consensus on the histologic criteria of the MC subtypes seem warranted.</description><subject>Adult</subject><subject>Aged</subject><subject>Agreements</subject><subject>Biopsy</subject><subject>Colitis, Collagenous - classification</subject><subject>Colitis, Collagenous - pathology</subject><subject>Colitis, Lymphocytic - classification</subject><subject>Colitis, Lymphocytic - pathology</subject><subject>Colitis, Microscopic - classification</subject><subject>Colitis, Microscopic - pathology</subject><subject>Collagenous colitis</subject><subject>Colonoscopy</subject><subject>Confidence intervals</subject><subject>Diagnosis, Differential</subject><subject>Diarrhea</subject><subject>Female</subject><subject>Histology</subject><subject>Humans</subject><subject>Inflammatory bowel disease</subject><subject>Interobserver variability</subject><subject>Intraobserver variability</subject><subject>Lymphocytic colitis</subject><subject>Male</subject><subject>Microscopic colitis</subject><subject>Microscopic colitis incomplete</subject><subject>Middle Aged</subject><subject>Observer Variation</subject><subject>Pathology</subject><subject>Reproducibility</subject><subject>Reproducibility of Results</subject><issn>0046-8177</issn><issn>1532-8392</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkl2r1DAQhoMonvXoT1AK3njTOvlqszeKHPyCA-dCBfEmpMl0N2vb1KRd2H9vyq4K50YIhEyeeWfmZQh5TqGiQOvXh2q_DJOZ9xUDyiuoKwDxgGyo5KxUfMsekk2O1KWiTXNFnqR0AKBUCvmYXDEBbNuA2pAfd23CeMRYHE30pvW9n0-FH4t5j8XepzmsNUIfdt4WzpvdGJJPReiKwdsYkg1T_rAhp-WwGV2RlnYXwzKlp-RRZ_qEzy73Nfn24f3Xm0_l7d3HzzfvbksrhJpL46CxXUfBOWeEpapB1lrRqmZLleMyP2vKJOsQOnRCMWnUlnMnG2AWZMuvyauz7hTDrwXTrAefLPa9GTEsSVMhuICtEHVGX95DD2GJY-5upfKBul4peabWAVPETk_RDyaeNAW9mq8P-mK-Xs3XUOtsdc57cVFf2gHd36w_bmfg7RnAbMfRY9TJehwtOh_RztoF_98Sb-4p2N6P3pr-J54w_ZtGJ6ZBf1k3YF0AygGYVN_5b7rRrho</recordid><startdate>20131101</startdate><enddate>20131101</enddate><creator>Fiehn, Anne-Marie Kanstrup, MD</creator><creator>Bjørnbak, Camilla, MD</creator><creator>Warnecke, Mads, MD</creator><creator>Engel, Peter Johan Heiberg, MD</creator><creator>Munck, Lars Kristian, MD, Sci</creator><general>Elsevier Inc</general><general>Elsevier Limited</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>K9.</scope><scope>7X8</scope></search><sort><creationdate>20131101</creationdate><title>Observer variability in the histopathologic diagnosis of microscopic colitis and subgroups</title><author>Fiehn, Anne-Marie Kanstrup, MD ; Bjørnbak, Camilla, MD ; Warnecke, Mads, MD ; Engel, Peter Johan Heiberg, MD ; Munck, Lars Kristian, MD, Sci</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-ad07cff10ddda4c187e2bc4b87918d357e261252fe0fed4825a8933d5702c05b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Agreements</topic><topic>Biopsy</topic><topic>Colitis, Collagenous - classification</topic><topic>Colitis, Collagenous - pathology</topic><topic>Colitis, Lymphocytic - classification</topic><topic>Colitis, Lymphocytic - pathology</topic><topic>Colitis, Microscopic - classification</topic><topic>Colitis, Microscopic - pathology</topic><topic>Collagenous colitis</topic><topic>Colonoscopy</topic><topic>Confidence intervals</topic><topic>Diagnosis, Differential</topic><topic>Diarrhea</topic><topic>Female</topic><topic>Histology</topic><topic>Humans</topic><topic>Inflammatory bowel disease</topic><topic>Interobserver variability</topic><topic>Intraobserver variability</topic><topic>Lymphocytic colitis</topic><topic>Male</topic><topic>Microscopic colitis</topic><topic>Microscopic colitis incomplete</topic><topic>Middle Aged</topic><topic>Observer Variation</topic><topic>Pathology</topic><topic>Reproducibility</topic><topic>Reproducibility of Results</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fiehn, Anne-Marie Kanstrup, MD</creatorcontrib><creatorcontrib>Bjørnbak, Camilla, MD</creatorcontrib><creatorcontrib>Warnecke, Mads, MD</creatorcontrib><creatorcontrib>Engel, Peter Johan Heiberg, MD</creatorcontrib><creatorcontrib>Munck, Lars Kristian, MD, Sci</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Human pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fiehn, Anne-Marie Kanstrup, MD</au><au>Bjørnbak, Camilla, MD</au><au>Warnecke, Mads, MD</au><au>Engel, Peter Johan Heiberg, MD</au><au>Munck, Lars Kristian, MD, Sci</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Observer variability in the histopathologic diagnosis of microscopic colitis and subgroups</atitle><jtitle>Human pathology</jtitle><addtitle>Hum Pathol</addtitle><date>2013-11-01</date><risdate>2013</risdate><volume>44</volume><issue>11</issue><spage>2461</spage><epage>2466</epage><pages>2461-2466</pages><issn>0046-8177</issn><eissn>1532-8392</eissn><abstract>Summary The diagnosis of microscopic colitis (MC) is based on histologic findings and includes collagenous colitis (CC) and lymphocytic colitis (LC). Incomplete MC (MCi) denotes patients with chronic diarrhea and a normal endoscopy and morphological changes that do not completely meet the histologic criteria of LC or CC. The aim of this study was to investigate the intraobserver and interobserver agreement on the MC subtypes of CC, LC, and MCi and the ability to discriminate MCi from normal and inflammatory bowel disease/nonspecific reactive changes. A single hematoxylin and eosin–stained specimen from biopsies of the following 5 groups were randomly selected and blinded: CC, LC, MCi, inflammatory bowel disease, and normal. Three pathologists independently reviewed the specimens. The specimens were relabeled and reinterpreted 4 months later. Intraobserver and interobserver agreement was evaluated by κ statistics. κ values for intraobserver agreement were good for 5 diagnostic groups varying from 0.70 to 0.83 and very good when simplifying to only 3 diagnostic groups varying from 0.88 to 0.96, separating MC/MCi from non-MC. κ values for interobserver agreement varied from 0.60 to 0.75 for 5 diagnostic groups and 0.81 to 0.89 for 3 diagnostic groups. The study shows that the intraobserver and interobserver agreement is high for discriminating between MC/MCi and non-MC, whereas the ability to discriminate MCi from CC and LC is lower. A revision and consensus on the histologic criteria of the MC subtypes seem warranted.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>24029708</pmid><doi>10.1016/j.humpath.2013.06.004</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Aged Agreements Biopsy Colitis, Collagenous - classification Colitis, Collagenous - pathology Colitis, Lymphocytic - classification Colitis, Lymphocytic - pathology Colitis, Microscopic - classification Colitis, Microscopic - pathology Collagenous colitis Colonoscopy Confidence intervals Diagnosis, Differential Diarrhea Female Histology Humans Inflammatory bowel disease Interobserver variability Intraobserver variability Lymphocytic colitis Male Microscopic colitis Microscopic colitis incomplete Middle Aged Observer Variation Pathology Reproducibility Reproducibility of Results |
title | Observer variability in the histopathologic diagnosis of microscopic colitis and subgroups |
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