Identification of predictive factors for early neoplasia in Barrett's esophagus after autofluorescence imaging: a stepwise multicenter structured assessment

Background Autofluorescence imaging is a novel imaging technique that may improve the detection of early neoplasia in Barrett's esophagus. Autofluorescence imaging is, however, associated with a 40% to 81% false-positive rate. Objective Our purpose was to identify endoscopic features that may p...

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Veröffentlicht in:Gastrointestinal endoscopy 2009-07, Vol.70 (1), p.9-17
Hauptverfasser: Curvers, Wouter L., MD, Singh, Rajvinder, MD, Wallace, Michael B., MD, PhD, Wong Kee Song, Louis-Michel, MD, Ragunath, Krish, MD, Wolfsen, Herbert C., MD, ten Kate, Fiebo J., MD, PhD, Fockens, Paul, MD, PhD, Bergman, Jacques J.G.H.M., MD, PhD
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Sprache:eng
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Zusammenfassung:Background Autofluorescence imaging is a novel imaging technique that may improve the detection of early neoplasia in Barrett's esophagus. Autofluorescence imaging is, however, associated with a 40% to 81% false-positive rate. Objective Our purpose was to identify endoscopic features that may predict the presence of early neoplasia in autofluorescence-positive areas. Design Descriptive and prospective cohort study. Setting Tertiary referral centers for the detection and treatment of early Barrett's neoplasia. Patients and Methods Patients undergoing autofluorescence endoscopy. High-quality images with autofluorescence imaging and white-light endoscopy were obtained with corresponding histologic study. A systematic image evaluation process was performed, including an unblinded orientation phase (10 areas), a blinded derivation phase, and a blinded validation phase by 5 international experts in autofluorescence imaging (80 areas). Subsequently the identified features were validated in a prospective pilot study. Main Outcome Measurements Association between endoscopic features and presence of early neoplasia in autofluorescence-positive areas. Results Autofluorescence intensity, proximity of gastric folds
ISSN:0016-5107
1097-6779
DOI:10.1016/j.gie.2008.10.026