Evidence map›Paper›PMID 41648842›Full record

ArticleiGIE : innovation, investigation and insights2022

Utility of wide-area transepithelial sampling with 3-dimensional computer-assisted analysis as an adjunct to forceps biopsy sampling in the surveillance of patients with Barrett's esophagus after endoscopic eradication therapy.

F Scott Corbett, Robert D Odze, Matthew J McKinley

Abstract read
In one paragraph

Article in iGIE : innovation, investigation and insights, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

3 authors.

F Scott CorbettDepartment of Medicine, Florida State University College of Medicine, Sarasota, Florida, USA.
Robert D OdzeDepartment of Pathology, Tufts University School of Medicine, Boston, Massachusetts, USA.
Matthew J McKinleyDepartment of Medicine, NYU Grossman School of Medicine, New York, New York, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aims: Recurrence of Barrett's esophagus (BE) and associated dysplasia is not uncommon after endoscopic eradication therapy (EET). However, the most optimal method for detection of residual/recurrent disease remains unknown. This study evaluated the utility of wide-area transepithelial sampling with 3-dimensional computer-assisted analysis (WATS-3D) as an adjunct to standard forceps biopsy (FB) sampling for detection of BE and dysplasia after EET. Methods: Data were examined from 2 large commercial registries of community practices that prospectively evaluated BE surveillance using both standard FB sampling combined with WATS-3D. Comprising the study cohort were 1114 consecutive BE patients (mean age, 68.9; men 68.1%, women 31.9%) who had EET. The adjunctive (and absolute) increased yield of WATS-3D for detection of intestinal metaplasia (IM) and dysplasia was evaluated according to the extent of endoscopic residual BE. Results: The WATS-3D adjunctive yield for detection of residual/recurrent IM or dysplasia was 52.5% and 91.5%, respectively. The highest adjunctive yield for detection of IM (260%) occurred in patients without any gross endoscopic evidence of residual or recurrent BE. The absolute yield for IM and dysplasia detection was 16% and 4.4%, respectively, and dysplasia detection was significantly greater in patients with visible BE compared with those with no endoscopic evidence of residual BE. Of 29 patients with high-grade dysplasia or esophageal adenocarcinoma detected by WATS-3D, FB sampling missed 11, including 7 where FB sampling did not detect any IM. The number of patients needed to test for detection of residual/recurrent BE was 6.2 and for detection of dysplasia was 22.9. Conclusions: WATS-3D is effective at increasing the diagnostic yield of IM and dysplasia in BE patients after EET when used as an adjunct to FB sampling.

Identifiers

PMID41648842
PMCPMC12850876

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.