4.4 Article

Yield of Repeat Endoscopy in Barrett's Esophagus with No Dysplasia and Low-Grade Dysplasia: A Population-Based Study

期刊

DIGESTIVE DISEASES AND SCIENCES
卷 61, 期 1, 页码 158-167

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SPRINGER
DOI: 10.1007/s10620-015-3697-6

关键词

Barrett's esophagus; Repeat endoscopy; Missed dysplasia; Prevalent dysplasia

资金

  1. National Institutes of Health [RC4DK 090413]
  2. Mayo Center for Clinical and Translational Sciences from the National Center for Advancing Translational Sciences (NCATS), a component of the National Institutes of Health] [UL1 TR000135]
  3. Rochester Epidemiology project - National Institute on Aging of the National Institutes of Health [R01AG034676]

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The yield of early repeat endoscopy in patients with Barrett's esophagus (BE) is not well established. To determine how often early repeat endoscopy detected missed dysplasia or esophageal adenocarcinoma (EAC) in a population-based cohort of patients with BE. Secondary aims were to identify risk factors for missed dysplasia/EAC and compare detection of prevalent versus incident HGD/EAC. A population-based cohort of BE subjects in Olmsted County, MN, was studied. Patients with initial non-dysplastic BE or low-grade dysplasia (LGD) who underwent repeat endoscopy within 24 months were included. Those with a worse histologic diagnosis on repeat endoscopy were considered to have missed dysplasia/EAC. Baseline characteristics among patients with and without missed dysplasia/EAC were compared. The absolute numbers of asymptomatic prevalent or missed, and incident HGD/EAC in the entire cohort were ascertained. Of 488 BE cases, 210 were included for the primary aim of this study. Repeat endoscopy revealed four HGD/EAC (1.9 %) and 16 LGD (8.8 %) for a combined miss rate of 9.5 %. Long-segment BE (LSBE) and lack of PPI use were predictors of missed dysplasia/EAC (P = 0.008), but adherence to biopsy protocol was not. Increased prevalent HGD/EAC (n = 30) rather than incident HGD/EAC (n = 22) was identified during a median 4.8 years of follow-up in this cohort. Dysplasia/EAC is commonly missed at initial BE diagnosis, particularly in patients with LSBE and no PPI use. Efforts should be made to enhance the sensitivity of detecting dysplasia/neoplasia around the time of initial BE diagnosis.

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