Original article
Clinical endoscopy
Age- and sex-specific yield of Barrett's esophagus by endoscopy indication

https://doi.org/10.1016/j.gie.2009.06.035Get rights and content

Background

Barrett's esophagus is a precursor of esophageal adenocarcinoma, both of which are associated with GERD. Screening GERD patients for Barrett's esophagus has been suggested, but it is not known which patients should be screened and at what age.

Objective

To determine the age-specific yield of endoscopy for Barrett's esophagus stratified by sex and indication for endoscopy.

Design

Retrospective cross-sectional study.

Setting

National Endoscopic Database of the Clinical Outcomes Research Initiative (CORI).

Patients

A total of 155,641 patients undergoing their first endoscopy at one of the CORI sites for clinical indications.

Main Outcome Measurements

Age-specific yield of Barrett's esophagus.

Results

Among white men with GERD, the yield of Barrett's esophagus increases steeply from early adulthood (2.1% in the third decade of life) to middle adulthood (9.3% in the sixth decade) and then plateaus (the difference for the eighth decade minus the sixth decade is −1.1%; 95% CI, −3.9% to 1.7%). There is no difference in the yield of Barrett's esophagus between middle-aged white women with GERD and white men without GERD (difference is −0.46%; 95% CI, −1.23% to 0.31%).

Limitations

Possible bias by selection for endoscopy and the potential for misclassification of GERD status.

Conclusions

The yield of upper endoscopy for the diagnosis of Barrett's esophagus increases rapidly among white men with GERD until approximately age 50 and then reaches a plateau. White women with GERD are at no increased risk compared with white men without GERD.

Section snippets

CORI

CORI was established to study the use and outcomes of endoscopy in diverse practice settings. Sixty-five adult practice sites, representing 500 physicians, submit more than 250,000 reports annually to the CORI National Endoscopic Database, including 100,000 upper endoscopy reports. Practice sites include private practice (79% of reports), academic sites (10%), and Veterans Affairs sites (11%). All participating sites agree to use a standardized computerized report generator to create all

Results

The total study cohort comprised 155,641 unique patients undergoing a first documented upper endoscopy at one of 35 sites (Table 1). The majority were performed in the private practice setting on white non-Hispanics, with slightly more men than women. Overall, 48,476 (31.1%) were undergoing upper endoscopy for evaluation of GERD or screening for Barrett's esophagus (GERD screenees). Of the entire study cohort, 7804 (5.0%) were suspected by the endoscopist of having Barrett's esophagus, and

Discussion

From these retrospective analyses of a large, national endoscopic database, we found a substantially increased yield of Barrett's esophagus in middle adulthood compared with early adulthood among white men with GERD, with a plateau in yield after approximately age 50. It is therefore likely that the metaplastic event occurs at some point between the ages of 20 and 50 in most patients. Another important finding is the yield of endoscopy in women with GERD. In women younger than the age of 30, no

References (32)

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DISCLOSURE: The following authors received research support for this study: G. Eisen: Executive Codirector of CORI, a nonprofit organization that receives funding from federal and industry sources; CORI has received support from the following entities to support the infrastructure of the practice-based network: AstraZeneca, Bard International, Pentax USA, ProVation, Endosoft, GIVEN Imaging, and Ethicon. The commercial entities had no involvement in this research. This potential conflict of interest has been reviewed and managed by the Oregon Health and Science University Conflict of Interest in Research Committee. All other authors disclosed no financial relationships relevant to this publication. This project was supported with funding from NIDDK UO1 CA 89389-01 and R33-DK61778-01. J.H.R. is the Damon Runyon-Gordon Family Clinical Investigator and is supported in part by the Damon Runyon Cancer Research Foundation (CI-36-07), and was supported by NIDDK 1K23DK079291.

If you would like to chat with an author of this article, you may contact Dr. Rubenstein at [email protected].

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