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Real-world implementation of non-endoscopic triage testing for Barrett’s oesophagus during COVID-19
BACKGROUND: The Coronavirus pandemic (COVID-19) curtailed endoscopy services, adding to diagnostic backlogs. Building on trial evidence for a non-endoscopic oesophageal cell collection device coupled with biomarkers (Cytosponge), an implementation pilot was launched for patients on waiting lists for...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10497181/ https://www.ncbi.nlm.nih.gov/pubmed/37220898 http://dx.doi.org/10.1093/qjmed/hcad093 |
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author | Landy, R Killcoyne, S Tang, C Juniat, S O’Donovan, M Goel, N Gehrung, M Fitzgerald, R C |
author_facet | Landy, R Killcoyne, S Tang, C Juniat, S O’Donovan, M Goel, N Gehrung, M Fitzgerald, R C |
author_sort | Landy, R |
collection | PubMed |
description | BACKGROUND: The Coronavirus pandemic (COVID-19) curtailed endoscopy services, adding to diagnostic backlogs. Building on trial evidence for a non-endoscopic oesophageal cell collection device coupled with biomarkers (Cytosponge), an implementation pilot was launched for patients on waiting lists for reflux and Barrett’s oesophagus surveillance. AIMS: (i) To review reflux referral patterns and Barrett’s surveillance practices. (ii) To evaluate the range of Cytosponge findings and impact on endoscopy services. DESIGN AND METHODS: Cytosponge data from centralized laboratory processing (trefoil factor 3 (TFF3) for intestinal metaplasia (IM), haematoxylin & eosin for cellular atypia and p53 for dysplasia) over a 2-year period were included. RESULTS: A total of 10 577 procedures were performed in 61 hospitals in England and Scotland, of which 92.5% (N = 9784/10 577) were sufficient for analysis. In the reflux cohort (N = 4074 with gastro-oesophageal junction sampling), 14.7% had one or more positive biomarkers (TFF3: 13.6% (N = 550/4056), p53: 0.5% (21/3974), atypia: 1.5% (N = 63/4071)), requiring endoscopy. Among samples from individuals undergoing Barrett’s surveillance (N = 5710 with sufficient gland groups), TFF3-positivity increased with segment length (odds ratio = 1.37 per cm (95% confidence interval: 1.33–1.41, P < 0.001)). Some surveillance referrals (21.5%, N = 1175/5471) had ≤1 cm segment length, of which 65.9% (707/1073) were TFF3 negative. Of all surveillance procedures, 8.3% had dysplastic biomarkers (4.0% (N = 225/5630) for p53 and 7.6% (N = 430/5694) for atypia), increasing to 11.8% (N = 420/3552) in TFF3+ cases with confirmed IM and 19.7% (N = 58/294) in ultra-long segments. CONCLUSIONS: Cytosponge-biomarker tests enabled targeting of endoscopy services to higher-risk individuals, whereas those with TFF3 negative ultra-short segments could be reconsidered regarding their Barrett’s oesophagus status and surveillance requirements. Long-term follow-up will be important in these cohorts. |
format | Online Article Text |
id | pubmed-10497181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-104971812023-09-13 Real-world implementation of non-endoscopic triage testing for Barrett’s oesophagus during COVID-19 Landy, R Killcoyne, S Tang, C Juniat, S O’Donovan, M Goel, N Gehrung, M Fitzgerald, R C QJM Original Paper BACKGROUND: The Coronavirus pandemic (COVID-19) curtailed endoscopy services, adding to diagnostic backlogs. Building on trial evidence for a non-endoscopic oesophageal cell collection device coupled with biomarkers (Cytosponge), an implementation pilot was launched for patients on waiting lists for reflux and Barrett’s oesophagus surveillance. AIMS: (i) To review reflux referral patterns and Barrett’s surveillance practices. (ii) To evaluate the range of Cytosponge findings and impact on endoscopy services. DESIGN AND METHODS: Cytosponge data from centralized laboratory processing (trefoil factor 3 (TFF3) for intestinal metaplasia (IM), haematoxylin & eosin for cellular atypia and p53 for dysplasia) over a 2-year period were included. RESULTS: A total of 10 577 procedures were performed in 61 hospitals in England and Scotland, of which 92.5% (N = 9784/10 577) were sufficient for analysis. In the reflux cohort (N = 4074 with gastro-oesophageal junction sampling), 14.7% had one or more positive biomarkers (TFF3: 13.6% (N = 550/4056), p53: 0.5% (21/3974), atypia: 1.5% (N = 63/4071)), requiring endoscopy. Among samples from individuals undergoing Barrett’s surveillance (N = 5710 with sufficient gland groups), TFF3-positivity increased with segment length (odds ratio = 1.37 per cm (95% confidence interval: 1.33–1.41, P < 0.001)). Some surveillance referrals (21.5%, N = 1175/5471) had ≤1 cm segment length, of which 65.9% (707/1073) were TFF3 negative. Of all surveillance procedures, 8.3% had dysplastic biomarkers (4.0% (N = 225/5630) for p53 and 7.6% (N = 430/5694) for atypia), increasing to 11.8% (N = 420/3552) in TFF3+ cases with confirmed IM and 19.7% (N = 58/294) in ultra-long segments. CONCLUSIONS: Cytosponge-biomarker tests enabled targeting of endoscopy services to higher-risk individuals, whereas those with TFF3 negative ultra-short segments could be reconsidered regarding their Barrett’s oesophagus status and surveillance requirements. Long-term follow-up will be important in these cohorts. Oxford University Press 2023-05-23 /pmc/articles/PMC10497181/ /pubmed/37220898 http://dx.doi.org/10.1093/qjmed/hcad093 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Association of Physicians. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Paper Landy, R Killcoyne, S Tang, C Juniat, S O’Donovan, M Goel, N Gehrung, M Fitzgerald, R C Real-world implementation of non-endoscopic triage testing for Barrett’s oesophagus during COVID-19 |
title | Real-world implementation of non-endoscopic triage testing for Barrett’s oesophagus during COVID-19 |
title_full | Real-world implementation of non-endoscopic triage testing for Barrett’s oesophagus during COVID-19 |
title_fullStr | Real-world implementation of non-endoscopic triage testing for Barrett’s oesophagus during COVID-19 |
title_full_unstemmed | Real-world implementation of non-endoscopic triage testing for Barrett’s oesophagus during COVID-19 |
title_short | Real-world implementation of non-endoscopic triage testing for Barrett’s oesophagus during COVID-19 |
title_sort | real-world implementation of non-endoscopic triage testing for barrett’s oesophagus during covid-19 |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10497181/ https://www.ncbi.nlm.nih.gov/pubmed/37220898 http://dx.doi.org/10.1093/qjmed/hcad093 |
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