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Surveillance of Barrett’s esophagus using wide-area transepithelial sampling: systematic review and meta-analysis

Background and study aims  Wide-area transepithelial sampling (WATS) is an emerging technique that may increase dysplasia detection in Barrett’s esophagus (BE). We conducted a systematic review and meta-analysis of patients who underwent surveillance for BE assessing the additional yield of WATS to...

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Autores principales: Qumseya, Bashar, Bukannan, Aymen, Rosasco, Robyn, Liu, Xiuli, Qumseya, Amira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Georg Thieme Verlag KG 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9010089/
https://www.ncbi.nlm.nih.gov/pubmed/35433217
http://dx.doi.org/10.1055/a-1783-9015
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author Qumseya, Bashar
Bukannan, Aymen
Rosasco, Robyn
Liu, Xiuli
Qumseya, Amira
author_facet Qumseya, Bashar
Bukannan, Aymen
Rosasco, Robyn
Liu, Xiuli
Qumseya, Amira
author_sort Qumseya, Bashar
collection PubMed
description Background and study aims  Wide-area transepithelial sampling (WATS) is an emerging technique that may increase dysplasia detection in Barrett’s esophagus (BE). We conducted a systematic review and meta-analysis of patients who underwent surveillance for BE assessing the additional yield of WATS to forceps biopsy (FB). Methods  We searched Pubmed, Embase, Web of science, and the Cochrane library, ending in January 2021. The primary outcomes of interest were the relative and absolute increase in dysplasia detection when adding WATS to FB. Heterogeneity was assessed using I (2) and Q statistic. Publication bias was assessed using funnel plots and classic fail-safe test. Results  A total of seven studies were included totaling 2,816 patients. FB identified 158 dysplasia cases, whereas WATS resulted in an additional 114 cases. The pooled risk ratio (RR) of all dysplasia detection was 1.7 (1.43–2.03), P  < 0.001, I (2)  = 0. For high-grade dysplasia (HGD), the pooled RR was 1.88 (1.28–2.77), P  = 0.001, I (2)  = 33 %. The yield of WATS was dependent on the prevalence of dysplasia in the study population. Among studies with high rates of dysplasia, the absolute increase in dysplasia detection (risk difference, RD) was 13 % (8 %-18 %, P  < 0.0001, number needed to treat [NNT] = 8). The pooled RD in HGD was 9 % (2 %-16 %), P  < 0.001, NNT = 11. For studies with a low prevalence of dysplasia, RD for all dysplasia was 2 % (1 %-3 %), P  = 0.001, NNT = 50. For HGD, the RD was 0.6 % (0.2 %-1.3 %), P  = 0.019, NNT = 166. Conclusions  In populations with a high prevalence of dysplasia, adding WATS to FB results in a significant increase in dysplasia detection.
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spelling pubmed-90100892022-04-15 Surveillance of Barrett’s esophagus using wide-area transepithelial sampling: systematic review and meta-analysis Qumseya, Bashar Bukannan, Aymen Rosasco, Robyn Liu, Xiuli Qumseya, Amira Endosc Int Open Background and study aims  Wide-area transepithelial sampling (WATS) is an emerging technique that may increase dysplasia detection in Barrett’s esophagus (BE). We conducted a systematic review and meta-analysis of patients who underwent surveillance for BE assessing the additional yield of WATS to forceps biopsy (FB). Methods  We searched Pubmed, Embase, Web of science, and the Cochrane library, ending in January 2021. The primary outcomes of interest were the relative and absolute increase in dysplasia detection when adding WATS to FB. Heterogeneity was assessed using I (2) and Q statistic. Publication bias was assessed using funnel plots and classic fail-safe test. Results  A total of seven studies were included totaling 2,816 patients. FB identified 158 dysplasia cases, whereas WATS resulted in an additional 114 cases. The pooled risk ratio (RR) of all dysplasia detection was 1.7 (1.43–2.03), P  < 0.001, I (2)  = 0. For high-grade dysplasia (HGD), the pooled RR was 1.88 (1.28–2.77), P  = 0.001, I (2)  = 33 %. The yield of WATS was dependent on the prevalence of dysplasia in the study population. Among studies with high rates of dysplasia, the absolute increase in dysplasia detection (risk difference, RD) was 13 % (8 %-18 %, P  < 0.0001, number needed to treat [NNT] = 8). The pooled RD in HGD was 9 % (2 %-16 %), P  < 0.001, NNT = 11. For studies with a low prevalence of dysplasia, RD for all dysplasia was 2 % (1 %-3 %), P  = 0.001, NNT = 50. For HGD, the RD was 0.6 % (0.2 %-1.3 %), P  = 0.019, NNT = 166. Conclusions  In populations with a high prevalence of dysplasia, adding WATS to FB results in a significant increase in dysplasia detection. Georg Thieme Verlag KG 2022-04-14 /pmc/articles/PMC9010089/ /pubmed/35433217 http://dx.doi.org/10.1055/a-1783-9015 Text en The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited.
spellingShingle Qumseya, Bashar
Bukannan, Aymen
Rosasco, Robyn
Liu, Xiuli
Qumseya, Amira
Surveillance of Barrett’s esophagus using wide-area transepithelial sampling: systematic review and meta-analysis
title Surveillance of Barrett’s esophagus using wide-area transepithelial sampling: systematic review and meta-analysis
title_full Surveillance of Barrett’s esophagus using wide-area transepithelial sampling: systematic review and meta-analysis
title_fullStr Surveillance of Barrett’s esophagus using wide-area transepithelial sampling: systematic review and meta-analysis
title_full_unstemmed Surveillance of Barrett’s esophagus using wide-area transepithelial sampling: systematic review and meta-analysis
title_short Surveillance of Barrett’s esophagus using wide-area transepithelial sampling: systematic review and meta-analysis
title_sort surveillance of barrett’s esophagus using wide-area transepithelial sampling: systematic review and meta-analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9010089/
https://www.ncbi.nlm.nih.gov/pubmed/35433217
http://dx.doi.org/10.1055/a-1783-9015
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