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Updated: Jul 16, 2025

Diagnosis of Neoplasia in Barrett’s Esophagus using Vital-dye Enhanced Fluorescence Imaging
Published on: May 11, 2014
Prevalence and Predictors of Barrett's Esophagus After Negative Initial Endoscopy: Analysis From Two National
Lovekirat Dhaliwal1, Amrit K Kamboj2, J Lucas Williams3
1Department of Internal Medicine, Louisiana State University Health, Shreveport, Louisiana.
Barrett's esophagus (BE) was found in 1.7%-3.4% of patients on repeat EGD, especially those with multiple risk factors. High-quality initial screening is crucial, with repeat screening considered for select high-risk patients.
Area of Science:
- Gastroenterology
- Endoscopy
- Oncology
Background:
- Current guidelines recommend a single screening esophagogastroduodenoscopy (EGD) for individuals with multiple risk factors for Barrett's esophagus (BE).
- The prevalence and predictors of BE on repeat EGD after a negative initial examination require further investigation.
Purpose of the Study:
- To determine the prevalence of BE on repeat EGD after a negative initial EGD.
- To identify predictors of BE detected on repeat EGD.
- To evaluate the utility of repeat EGD screening for BE.
Main Methods:
- Analysis of two large national databases (GIQuIC and TriNetX) including over 350,000 patients who underwent at least two EGDs.
- Exclusion of patients with BE or esophageal adenocarcinoma detected at their initial EGD.
- Multivariate logistic regression to identify independent risk factors for BE on repeat EGD.
Main Results:
- BE prevalence on repeat EGD was 1.7% in GIQuIC and 3.4% in TriNetX, representing 26%-45% of baseline prevalence.
- Most detected BE cases (89%) were nondysplastic.
- BE prevalence increased with the number of risk factors and was 3%-4% in high-risk populations (GERD + ≥1 risk factor).
Conclusions:
- Repeat EGD identified BE in 1.7%-3.4% of patients, with higher rates in those with multiple risk factors, suggesting potential missed diagnoses during initial screening.
- Routine repeat endoscopic BE screening is not recommended, but may be considered for carefully selected patients with GERD and multiple risk factors, potentially aided by non-endoscopic tools.
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