Sa1844 Erosive Esophagitis As a Potential Precursor of Barrett's Esophagus -Findings From a Population Based Cohort

2014 ◽  
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pp. S-310
Author(s):  
Milli Gupta ◽  
Cathy D. Schleck ◽  
Alan R. Zinsmeister ◽  
David A. Katzka ◽  
Kelly T. Dunagan ◽  
...  
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Oscar Gutierrez ◽  
J. Becerra ◽  
William Otero ◽  
Antonia Sepulveda ◽  
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Author(s):  
Matthew G. Bell ◽  
Siddharth Agarwal ◽  
Ramona Lansing ◽  
Rachel E. Rhody ◽  
Cadman L. Leggett ◽  
...  

2015 ◽  
Vol 61 (1) ◽  
pp. 158-167 ◽  
Author(s):  
Kavel Visrodia ◽  
Prasad G. Iyer ◽  
Cathy D. Schleck ◽  
Alan R. Zinsmeister ◽  
David A. Katzka

2011 ◽  
Vol 140 (5) ◽  
pp. S-667 ◽  
Author(s):  
Romy E. Verbeek ◽  
Martijn G. van Oijen ◽  
Fiebo J. ten Kate ◽  
Frank P. Vleggaar ◽  
Marguerite E. Schipper ◽  
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2011 ◽  
Vol 140 (5) ◽  
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Helen G. Mulholland ◽  
Damian T. McManus ◽  
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...  

2020 ◽  
Vol 33 (10) ◽  
Author(s):  
Lisa M O’Byrne ◽  
Jolene Witherspoon ◽  
Roy J J Verhage ◽  
Marie O’Brien ◽  
Cian Muldoon ◽  
...  

Summary Barrett’s esophagus (BE) is the main pathological precursor of esophageal adenocarcinoma (EAC). Progression to high-grade dysplasia (HGD) or EAC from nondysplastic BE (NDBE), low-grade dysplasia (LGD) and indefinite for dysplasia (IND) varies widely between population-based studies and specialized centers for many reasons, principally the rigor of the biopsy protocol and the accuracy of pathologic definition. In the Republic of Ireland, a multicenter prospective registry and bioresource (RIBBON) was established in 2011 involving six academic medical centers, and this paper represents the first report from this network. A detailed clinical, endoscopic and pathologic database registered 3,557 patients. BE was defined strictly by both endoscopic evidence of Barrett’s epithelium and the presence of specialized intestinal metaplasia (SIM). A prospective web-based database was used to gather information with initial and follow-up data abstracted by a data manager at each site. A total of 2,244 patients, 1,925 with no dysplasia, were included with complete follow-up. The median age at diagnosis was 60.5 with a 2.1:1 male to female ratio and a median follow-up time of 2.7 years (IQR 1.19–4.04), and 6609.25 person years. In this time period, 125 (5.57%) progressed to HGD/EAC, with 74 (3.3%) after 1 year of follow-up and 38 (1.69%) developed EAC, with 20 (0.89%) beyond 1 year. The overall incidence of HGD/EAC was 1.89% per year; 1.16% if the first year is excluded. The risk of progression to EAC alone overall was 0.57% per year, 0.31% excluding the first year, and 0.21% in the 1,925 patients who had SIM alone at diagnosis. Low-grade dysplasia (LGD) progressed to HGD/EAC in 31% of patients, a progression rate of 12.96% per year, 6.71% with the first year excluded. In a national collaboration of academic centers in Ireland, the progression rate for NDBE was similar to recent population studies. Almost one in two who progressed was evident within 1 year. Crucially, LGD diagnosed and confirmed by specialist gastrointestinal pathologists represents truly high-risk disease, highlighting the importance of expertise in diagnosis and management, and providing indirect support for ablative therapies in this context.


2009 ◽  
Vol 136 (5) ◽  
pp. A-628 ◽  
Author(s):  
P.J. de Jonge ◽  
Mark van Blankenstein ◽  
Caspar W. Looman ◽  
M.K. Casparie ◽  
Gerrit A. Meijer ◽  
...  

2003 ◽  
Vol 124 (4) ◽  
pp. A638
Author(s):  
Roy Dekel ◽  
Isaac B. Malagon ◽  
Harinder S. Garewal ◽  
Ronnie Fass

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