期刊
GASTROINTESTINAL ENDOSCOPY
卷 70, 期 4, 页码 645-654出版社
MOSBY-ELSEVIER
DOI: 10.1016/j.gie.2009.02.009
关键词
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资金
- NCRR NIH HHS [K12 RR023266, K12 RR023266-02] Funding Source: Medline
Background: The detection of high-grade dysplasia and cancer in Barrett's esophagus (BE) can be challenging. Confocal laser endomicroscopy (CLE) allows in vivo visualization of mucosal histology during endoscopy. Objective: To determine whether CLE with optical biopsy and targeted mucosal biopsy improves the diagnostic yield of endoscopically inapparent, BE-associated neoplasia compared to standard endoscopy with a 4-quadrant, random biopsy protocol. Design: Prospective, double-blind, randomized, crossover study. Setting: Single, tertiary-care academic center. Patients: This study involved patients with BE undergoing routine surveillance or referred for treatment of non-localized, endoscopically inapparent, BE-associated neoplasia. Intervention: All participants underwent both a confocal endomicroscopy with a targeted biopsy procedure and standard endoscopy with a 4-quadrant biopsy procedure in a randomized order. Main Outcome Measurements: Increase in diagnostic yield for neoplasia, reduction in mucosal biopsy number, final pathologic diagnosis. Results: CLE with targeted biopsy almost doubled the diagnostic yield for neoplasia and was equivalent to the standard protocol for the final diagnosis of neoplasia. Two thirds of patients in the surveillance group did not need any mucosal biopsies at all. Limitation: Single-center study. Conclusion: CLE with targeted biopsy significantly improves the diagnostic yield for endoscopically inapparent BE neoplasia compared to a standard endoscopy with a random-biopsy protocol. CLE with targeted biopsy also greatly reduces the number of biopsies needed per patient and allows some patients without neoplasia to completely forgo mucosal biopsy. (This trial was registered at www.clinicaltrials.gov, ID number NCT00487695.) (Gastrointest Endosc 2009;70:645-54.)
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