乳糜泻的窄带放大内镜成像:一项前瞻性单中心研究的结果

Diagnostic and Therapeutic Endoscopy Pub Date : 2013-01-01 Epub Date: 2013-08-06 DOI:10.1155/2013/580526
L De Luca, L Ricciardiello, M B L Rocchi, M T Fabi, M L Bianchi, A de Leone, S Fiori, D Baroncini
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引用次数: 21

摘要

在乳糜泻(CD)中,肠道病变可能是斑片状的,部分绒毛萎缩可能在标准内窥镜(SE)中无法检测到。窄带成像(NBI)系统结合放大内窥镜(ME)是一种简单的工具,能够获得目标活检标本。该研究的目的是评估NBI-ME与CD诊断组织学之间的相关性,并比较NBI-ME和SE在检测CD绒毛异常方面的诊断准确性。44名连续接受上消化道内窥镜检查的疑似CD患者进行了前瞻性评估。使用SE和NBI-ME,观察到的表面模式使用k-Cohen一致系数从活检标本获得的组织学结果进行比较。在SE正常的12例患者中,NBI-ME鉴定出部分绒毛萎缩,其敏感性、特异性和准确性分别为100%、92.6%和95%。与SE和组织学相比,NBI-ME和组织学之间的总体一致性显著更高(kappa评分:0.90比0.46;P = 0.001)。NBI-ME可以在常规内镜检查中帮助识别部分粘膜萎缩,潜在地减少盲活检的需要。NBI-ME优于SE,能可靠地预测CD的体内绒毛变化。
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Narrow band imaging with magnification endoscopy for celiac disease: results from a prospective, single-center study.

In celiac disease (CD), the intestinal lesions can be patchy and partial villous atrophy may elude detection at standard endoscopy (SE). Narrow Band Imaging (NBI) system in combination with a magnifying endoscope (ME) is a simple tool able to obtain targeted biopsy specimens. The aim of the study was to assess the correlation between NBI-ME and histology in CD diagnosis and to compare diagnostic accuracy between NBI-ME and SE in detecting villous abnormalities in CD. Forty-four consecutive patients with suspected CD undergoing upper gastrointestinal endoscopy have been prospectively evaluated. Utilizing both SE and NBI-ME, observed surface patterns were compared with histological results obtained from biopsy specimens using the k-Cohen agreement coefficient. NBI-ME identified partial villous atrophy in 12 patients in whom SE was normal, with sensitivity, specificity, and accuracy of 100%, 92.6%, and 95%, respectively. The overall agreement between NBI-ME and histology was significantly higher when compared with SE and histology (kappa score: 0.90 versus 0.46; P = 0.001) in diagnosing CD. NBI-ME could help identify partial mucosal atrophy in the routine endoscopic practice, potentially reducing the need for blind biopsies. NBI-ME was superior to SE and can reliably predict in vivo the villous changes of CD.

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