Herbert C Wolfsen1, Prateek Sharma2, Michael B Wallace1, Cadman Leggett3, Guillermo Tearney4, Kenneth K Wang3. 1. Department of Gastroenterology, Mayo Clinic, Jacksonville, Florida. 2. Gastroenterology, Hepatology, and Motility, Kansas City Veterans Administration Medical Center, Kansas City, Missouri. 3. Department of Gastroenterology, Mayo Clinic Rochester, Rochester, Minnesota. 4. Department of Pathology, Massachusetts General Hospital, Boston, Massachusetts.
Abstract
BACKGROUND: Volumetric laser endomicroscopy (VLE) produces high-resolution, cross-sectional surface, and subsurface images for detecting neoplasia, targeting biopsies, and guiding real-time treatment. OBJECTIVE: To evaluate the safety and feasibility of the Nvision VLE system. DESIGN: Prospective, multicenter study. SETTING: Tertiary-care medical centers. PATIENTS: One hundred patients with suspected Barrett's esophagus, including 52 patients with prior endotherapy. INTERVENTIONS: The first-generation Nvision VLE Imaging System, a balloon-centered, rotating optical probe provided images of the mucosa and submucosa through a 6-cm segment length and 360° scan of the distal esophagus. MAIN OUTCOME MEASUREMENTS: Acquisition of a complete, 6-cm scan from the distal esophagus, demographic and procedural data, and final histologic diagnosis. RESULTS: VLE imaging was successfully performed in 87 cases. After VLE imaging, biopsy specimens were obtained in 77 patients and mucosal resection was performed in 20 patients. The final pathologic diagnoses of the patients studied were adenocarcinoma (4 patients), high-grade dysplasia (10 patients), low-grade dysplasia (11 patients), indefinite (5 patients), intestinal metaplasia (29 patients), and normal squamous cells (18 patients). VLE was not completed in 13 of 100 (13%) because of optical probe and console issues. There were 2 minor adverse events (mucosal lacerations not requiring therapy). LIMITATIONS: This was a feasibility study with a first-generation device. There was no direct histopathologic correlation with the VLE images or any comparative analysis with white-light endoscopy or narrow-band imaging findings. CONCLUSION: VLE is a safe procedure for patients with suspected or confirmed Barrett's esophagus. Real-time VLE images enabled visualization of the mucosa and submucosa in 87% of cases. Further studies are needed to evaluate the in vivo diagnostic accuracy and clinical utility of VLE.
BACKGROUND: Volumetric laser endomicroscopy (VLE) produces high-resolution, cross-sectional surface, and subsurface images for detecting neoplasia, targeting biopsies, and guiding real-time treatment. OBJECTIVE: To evaluate the safety and feasibility of the Nvision VLE system. DESIGN: Prospective, multicenter study. SETTING: Tertiary-care medical centers. PATIENTS: One hundred patients with suspected Barrett's esophagus, including 52 patients with prior endotherapy. INTERVENTIONS: The first-generation Nvision VLE Imaging System, a balloon-centered, rotating optical probe provided images of the mucosa and submucosa through a 6-cm segment length and 360° scan of the distal esophagus. MAIN OUTCOME MEASUREMENTS: Acquisition of a complete, 6-cm scan from the distal esophagus, demographic and procedural data, and final histologic diagnosis. RESULTS: VLE imaging was successfully performed in 87 cases. After VLE imaging, biopsy specimens were obtained in 77 patients and mucosal resection was performed in 20 patients. The final pathologic diagnoses of the patients studied were adenocarcinoma (4 patients), high-grade dysplasia (10 patients), low-grade dysplasia (11 patients), indefinite (5 patients), intestinal metaplasia (29 patients), and normal squamous cells (18 patients). VLE was not completed in 13 of 100 (13%) because of optical probe and console issues. There were 2 minor adverse events (mucosal lacerations not requiring therapy). LIMITATIONS: This was a feasibility study with a first-generation device. There was no direct histopathologic correlation with the VLE images or any comparative analysis with white-light endoscopy or narrow-band imaging findings. CONCLUSION: VLE is a safe procedure for patients with suspected or confirmed Barrett's esophagus. Real-time VLE images enabled visualization of the mucosa and submucosa in 87% of cases. Further studies are needed to evaluate the in vivo diagnostic accuracy and clinical utility of VLE.
Authors: Neel Sharma; Supriya Srivastava; Florian Kern; Wa Xian; Teh Ming; Frank McKeon; Khek Yu Ho Journal: United European Gastroenterol J Date: 2015-12-15 Impact factor: 4.623
Authors: Osman O Ahsen; Kaicheng Liang; Hsiang-Chieh Lee; Michael G Giacomelli; Zhao Wang; Benjamin Potsaid; Marisa Figueiredo; Qin Huang; Vijaysekhar Jayaraman; James G Fujimoto; Hiroshi Mashimo Journal: Endoscopy Date: 2018-09-27 Impact factor: 10.093