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Diagnosis of dysplasia in upper gastro-intestinal tract biopsies through digital microscopy

机译:通过数字显微镜诊断上消化道活检增生异常

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Background:Whole slide digital imaging (WSDI) offers an alternative to glass slides for diagnostic interpretation. While prior work has concentrated on the use of whole slide digital imaging for routine diagnostic cases, this study focuses on diagnostic interpretation of digital images for a highly challenging area, upper gastro-intestinal (GI) dysplasia. The aim of this study is to study the accuracy and efficiency of WSDI in the diagnosis of upper GI tract dysplasia.Materials and Methods:Forty-two hematoxylin and eosin (H and E)-stained slides representing negative, indefinite, low grade and high grade dysplasia were selected and scanned at 20x (Aperio XT). Four attending GI pathologists reviewed the WSDI, then glass slides, with at least 3–4 weeks between each media; glass slides were re-reviewed 16–18 months later.Results:Intraobserver variability for three clinically relevant categories (negative, indefinite/low grade, high grade) was wider for WSDI to glass (kappa range 0.36–0.78) than glass to glass (kappa range 0.58–0.75). In comparison to glass slide review, WSDI review required more time and was associated with an unexpected trend toward downgrading dysplasia.Conclusions:Our results suggest: (1) upper GI dysplasia can be diagnosed using WSDI with similar intraobserver reproducibility as for glass slides; however, this is not true for all pathologists; (2) pathologists may have a tendency to downgrade dysplasia in digital images; and (3) pathologists who use WSDI for interpretation of GI dysplasia cases may benefit from regular, on-going, re-review of paired digital and glass images to ensure the most accurate utilization of digital technology, at least in the early stages of implementation.
机译:背景:全玻片数字成像(WSDI)提供了一种替代玻片的方法,以进行诊断解释。尽管先前的工作集中在对常规诊断病例使用整个幻灯片数字成像上,但本研究着重于对高度挑战性区域,上消化道(GI)异常增生的数字图像进行诊断解释。本研究的目的是研究WSDI在上消化道异型增生诊断中的准确性和效率。材料与方法:42份苏木精和曙红(H和E)染色的玻片代表阴性,不确定,低等级和高选择严重不典型增生并以20倍(Aperio XT)进行扫描。四名与会的GI病理学家对WSDI进行了回顾,然后对载玻片进行了回顾,每种媒介之间的间隔至少为3-4周。结果:16个临床相关类别(阴性,不确定/低等,高等)的观察者内部变异性比WSDI到玻璃(kappa范围为0.36-0.78)要大。卡伯值范围为0.58-0.75)。与载玻片检查相比,WSDI审查需要更多的时间,并且与异常增生降级的出乎意料的趋势有关。结论:我们的结果表明:(1)WSDI可以通过观察者内重复性与载玻片相似来诊断上消化道增生。然而,并非所有病理学家都如此。 (2)病理学家可能会降低数字图像中的异型增生; (3)使用WSDI解释胃肠道发育不良病例的病理学家可能会受益于定期的,正在进行的,重新检查成对的数字和玻璃图像,以确保至少在实施的早期就最准确地利用数字技术。

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