Detection of dysplasia at colonoscopy using laser-induced fluorescence: a blinded study☆,☆☆,★,★★
Section snippets
METHODS
During a 14-month period, adult patients of either gender referred for colonoscopic removal of previously identified polyps or for surveillance colonoscopy because of a history of adenomatous polyps were invited to participate in the study. The study protocol was approved by the Institutional Review Board of The Cleveland Clinic Foundation and The Committee on Use of Humans as Experimental Subjects of the Massachusetts Institute of Technology. Informed consent was obtained from each patient
RESULTS
Fluorescence emission spectra were collected from 103 polypoid and 104 endoscopically normal-appearing mucosal sites in the colons of 57 patients (38 men, 19 women). Data from several polyps were eliminated because melanosis coli (2), intramucosal adenocarcinoma (1), ganglioneuroma (1), or lipoma (1) was detected on histologic examination, or histologic diagnosis was impossible because of electrocautery artifact or an absence of sufficient tissue (4). Benign lymphoid aggregates (5), which
DISCUSSION
This study evaluated the accuracy of laser-induced fluorescence spectroscopy for the detection of gastrointestinal dysplasia in patients with colonic polyps. Two spectral regions containing specific information were identified, each of these being described by a pair of parameters. From an analysis of the probability distributions of these parameters, a decision algorithm was constructed that could easily be visualized. This approach forms the basis of a method that detects colonic dysplasia
Acknowledgements
The authors thank Michael Feldstein, Irving Itzkan, and George Zonios for helpful discussions.
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Cited by (0)
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From the Departments of Biomedical Engineering, Gastroenterology, and Anatomic Pathology, The Cleveland Clinic Foundation, Cleveland, Ohio, the Division of Gastroenterology and the Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, and the Laser Biomedical Research Center, George R. Harrison Spectroscopy Laboratory, Massachusetts Institute of Technology, Cambridge, Massachusetts.
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This work was supported by the National Institutes of Health grant #CA53717, and #RR02594 through the administration of the MIT Laser Biomedical Research Center. The authors also gratefully acknowledge a generous educational grant from Albert Reidy, Chairman, Wilmington Arena Authority, which supports in part Dr. Van Dam's efforts.
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Reprint requests: Robert Cothren, PhD, Biomedical Engineering/Wb3, The Cleveland Clinic Foundation, 9500 Euclid Ave., Cleveland, OH 44195.
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