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Development of benchmark quality criteria for assessing whole-endoscopy Barrett's esophagus biopsy cases

BACKGROUND: Dysplasia in Barrett's esophagus (BE) biopsies is associated with low observer agreement among general pathologists. Therefore, expert review is advised. We are developing a web-based, national expert review panel for histological review of BE biopsies. OBJECTIVE: The aim of this st...

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Autores principales: van der Wel, MJ, Duits, LC, Klaver, E, Pouw, RE, Seldenrijk, CA, Offerhaus, GJA, Visser, M, ten Kate, FJW, Tijssen, JG, Bergman, JJGHM, Meijer, SL
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6047285/
https://www.ncbi.nlm.nih.gov/pubmed/30023060
http://dx.doi.org/10.1177/2050640618764710
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author van der Wel, MJ
Duits, LC
Klaver, E
Pouw, RE
Seldenrijk, CA
Offerhaus, GJA
Visser, M
ten Kate, FJW
Tijssen, JG
Bergman, JJGHM
Meijer, SL
author_facet van der Wel, MJ
Duits, LC
Klaver, E
Pouw, RE
Seldenrijk, CA
Offerhaus, GJA
Visser, M
ten Kate, FJW
Tijssen, JG
Bergman, JJGHM
Meijer, SL
author_sort van der Wel, MJ
collection PubMed
description BACKGROUND: Dysplasia in Barrett's esophagus (BE) biopsies is associated with low observer agreement among general pathologists. Therefore, expert review is advised. We are developing a web-based, national expert review panel for histological review of BE biopsies. OBJECTIVE: The aim of this study was to create benchmark quality criteria for future members. METHODS: Five expert BE pathologists, with 10–30 years of BE experience, weekly handling 5–10 cases (25% dysplastic), assessed a case set of 60 digitalized cases, enriched for dysplasia. Each case contained all slides from one endoscopy (non-dysplastic BE (NDBE), n = 21; low-grade dysplasia (LGD), n = 20; high-grade dysplasia (HGD), n = 19). All cases were randomized and assessed twice followed by group discussions to create a consensus diagnosis. Outcome measures: percentage of ‘indefinite for dysplasia’ (IND) diagnoses, intra-observer agreement, and agreement with the consensus ‘gold standard’ diagnosis. RESULTS: Mean percentage of IND diagnoses was 8% (3–14%) and mean intra-observer agreement was 0.84 (0.66–1.02). Mean agreement with the consensus diagnosis was 90% (95% prediction interval (PI) 82–98%). CONCLUSION: Expert pathology review of BE requires the scoring of a limited number of IND cases, consistency of assessment and a high agreement with a consensus gold standard diagnosis. These benchmark quality criteria will be used to assess the performance of other pathologists joining our panel.
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spelling pubmed-60472852018-07-18 Development of benchmark quality criteria for assessing whole-endoscopy Barrett's esophagus biopsy cases van der Wel, MJ Duits, LC Klaver, E Pouw, RE Seldenrijk, CA Offerhaus, GJA Visser, M ten Kate, FJW Tijssen, JG Bergman, JJGHM Meijer, SL United European Gastroenterol J Original Articles BACKGROUND: Dysplasia in Barrett's esophagus (BE) biopsies is associated with low observer agreement among general pathologists. Therefore, expert review is advised. We are developing a web-based, national expert review panel for histological review of BE biopsies. OBJECTIVE: The aim of this study was to create benchmark quality criteria for future members. METHODS: Five expert BE pathologists, with 10–30 years of BE experience, weekly handling 5–10 cases (25% dysplastic), assessed a case set of 60 digitalized cases, enriched for dysplasia. Each case contained all slides from one endoscopy (non-dysplastic BE (NDBE), n = 21; low-grade dysplasia (LGD), n = 20; high-grade dysplasia (HGD), n = 19). All cases were randomized and assessed twice followed by group discussions to create a consensus diagnosis. Outcome measures: percentage of ‘indefinite for dysplasia’ (IND) diagnoses, intra-observer agreement, and agreement with the consensus ‘gold standard’ diagnosis. RESULTS: Mean percentage of IND diagnoses was 8% (3–14%) and mean intra-observer agreement was 0.84 (0.66–1.02). Mean agreement with the consensus diagnosis was 90% (95% prediction interval (PI) 82–98%). CONCLUSION: Expert pathology review of BE requires the scoring of a limited number of IND cases, consistency of assessment and a high agreement with a consensus gold standard diagnosis. These benchmark quality criteria will be used to assess the performance of other pathologists joining our panel. SAGE Publications 2018-03-07 2018-07 /pmc/articles/PMC6047285/ /pubmed/30023060 http://dx.doi.org/10.1177/2050640618764710 Text en © Author(s) 2018 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
van der Wel, MJ
Duits, LC
Klaver, E
Pouw, RE
Seldenrijk, CA
Offerhaus, GJA
Visser, M
ten Kate, FJW
Tijssen, JG
Bergman, JJGHM
Meijer, SL
Development of benchmark quality criteria for assessing whole-endoscopy Barrett's esophagus biopsy cases
title Development of benchmark quality criteria for assessing whole-endoscopy Barrett's esophagus biopsy cases
title_full Development of benchmark quality criteria for assessing whole-endoscopy Barrett's esophagus biopsy cases
title_fullStr Development of benchmark quality criteria for assessing whole-endoscopy Barrett's esophagus biopsy cases
title_full_unstemmed Development of benchmark quality criteria for assessing whole-endoscopy Barrett's esophagus biopsy cases
title_short Development of benchmark quality criteria for assessing whole-endoscopy Barrett's esophagus biopsy cases
title_sort development of benchmark quality criteria for assessing whole-endoscopy barrett's esophagus biopsy cases
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6047285/
https://www.ncbi.nlm.nih.gov/pubmed/30023060
http://dx.doi.org/10.1177/2050640618764710
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