{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T07:11:55Z","timestamp":1791270715031,"version":"4.1.0"},"reference-count":27,"publisher":"BMJ","issue":"12","content-domain":{"domain":["bmj.com"],"crossmark-restriction":true},"short-container-title":["J Clin Pathol"],"accepted":{"date-parts":[[2022,9,14]]},"published-print":{"date-parts":[[2023,12]]},"abstract":"<jats:sec>\n                  <jats:title>Aims<\/jats:title>\n                  <jats:p>Barrett\u2019s oesophagus with indefinite for dysplasia (IDD) carries a risk of prevalent and incident dysplasia and oesophageal adenocarcinoma. This study seeks to determine the risk of neoplasia in a multicentre prospective IDD cohort, along with determining adherence to British Society of Gastroenterology (BSG) guidelines for management and histology reporting.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Methods<\/jats:title>\n                  <jats:p>This was a cohort study using prospectively collected data from pathology databases from two centres in the North West of England (UK). Cases with IDD were identified over a 10-year period. Data were obtained on patient demographics, Barrett\u2019s endoscopy findings and histology, outcomes and histological reporting.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Results<\/jats:title>\n                  <jats:p>102 biopsies with IDD diagnosis in 88 patients were identified. Endoscopy was repeated in 78\/88 (88%) patients. 12\/78 progressed to low-grade dysplasia (15% or 2.6 per 100 person years), 6\/78 (7.7%, 1.3 per 100 person years) progressed to high-grade dysplasia and 6\/78 (7.7%, 1.3 per 100 person years) progressed to oesophageal adenocarcinoma. The overall incidence rate for progression to any type of dysplasia was 5.1 per 100 person years. Cox regression analysis identified longer Barrett\u2019s segment, multifocal and persistent IDD as predictors of progression to dysplasia. Histology reporting did not meet 100% adherence to the BSG histology reporting minimum dataset prior to or after the introduction of the guidelines.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Conclusions<\/jats:title>\n                  <jats:p>IDD carries significant risk of progression to dysplasia or neoplasia. Therefore, careful diagnosis and management aided by clear histological reporting of these cases is required to diagnose prevalent and incident neoplasia.<\/jats:p>\n               <\/jats:sec>","DOI":"10.1136\/jcp-2022-208524","type":"journal-article","created":{"date-parts":[[2022,9,23]],"date-time":"2022-09-23T14:08:07Z","timestamp":1663942087000},"page":"847-854","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":5,"title":["Barrett\u2019s oesophagus with indefinite for dysplasia shows high rates of prevalent and incident neoplasia in a UK multicentre cohort"],"prefix":"10.1136","volume":"76","author":[{"given":"Maja","family":"Kopczynska","sequence":"first","affiliation":[{"name":"Gastroenterology Department, Northern Care Alliance NHS Foundation Trust, Salford, Manchester, UK"},{"name":"Faculty of Medical and Human Sciences, The University of Manchester, Manchester, 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