Abstract
Background and Objectives
Temporal and spectral fluorescence spectroscopy can identify adenomatous colonic polyps accurately. In this study, these techniques were examined as a potential means of improving the surveillance of high grade dysplasia (HGD) in Barrett's esophagus (BE).
Study Design/Materials and Methods
Using excitation wavelengths of 337 and 400 nm, 148 fluorescence spectra, and 108 transient decay profiles (at 550 ± 20 nm) were obtained endoscopically in 37 patients. Corresponding biopsies were collected and classified as carcinoma, HGD, or low risk tissue (LRT) [non‐dysplastic BE, indefinite for dysplasia (IFD), and low grade dysplasia (LGD)]. Diagnostic algorithms were developed retrospectively using linear discriminant analysis (LDA) to separate LRT from HGD.
Results
LDA produced diagnostic algorithms based solely on spectral data. Moderate levels of sensitivity (Se) and specificity (Sp) were obtained for both 337 nm (Se = 74%, Sp = 67%) and 400 nm (Se = 74%, Sp = 85%) excitation.
Conclusions
In the diagnosis of HGD in BE, steady‐state fluorescence was more effective than time‐resolved data, and excitation at 400 nm excitation was more effective than 337 nm. While fluorescence‐targeted biopsy is approaching clinical usefulness, increased sensitivity to dysplastic changes—possibly through modification of system parameters—is needed to improve accuracy levels. Lasers Surg. Med. 32:10–16,2003. © 2003 Wiley‐Liss, Inc.