Eaden J, Abrams K, McKay H, Denley H, Mayberry J
Gastrointestinal Research Unit and Department of Pathology, Leicester General Hospital, Gwendolen Road, Leicester, LE5 4PW, UK.
J Pathol. 2001 Jun;194(2):152-7. doi: 10.1002/path.876.
Histological dysplasia is the cornerstone of colorectal cancer surveillance in ulcerative colitis (UC). Recently, pathologists have received unfavourable media attention concerning other cancer screening programmes. The aim of this study was to determine whether colonic biopsy specimens should be examined by gastrointestinal pathologists as opposed to generalists, by examining inter-observer variation between the two groups. Fifty-one coded slides showing varying degrees of dysplasia were mailed to seven gastrointestinal and six general histopathologists. Pathologists allocated each biopsy into one of four categories without the benefit of a clinical history or an opportunity to use the 'indefinite' category that is included in the Riddell classification. The responses were analysed using kappa statistics. The overall kappa statistic for gastrointestinal pathologists was 0.30 [95% confidence interval (CI)=0.26-0.34] and for general pathologists 0.28 (95% CI=0.23-0.32). Agreement was best for high-grade dysplasia (kappa of 0.54 and 0.61 for GI and general pathologists, respectively). There was total concordance of the 13 pathologists in only four of the 51 slides (7.8%) (95% CI=0.4-15.2%). It is concluded from these results that gastrointestinal pathologists are no better than generalists when grading dysplasia in UC and that agreement is poor in both groups. There is therefore no evidence that there would be any benefit in having specialist histopathology centres concentrating specifically on the interpretation of all surveillance colonoscopy biopsies from around the UK. It must be made clear to the public that surveillance and screening programmes carry a significant rate of histological error and that perfection cannot be expected or achieved with present methods.
组织学发育异常是溃疡性结肠炎(UC)结直肠癌监测的基石。最近,病理学家在其他癌症筛查项目方面受到了媒体的负面关注。本研究的目的是通过检查两组之间的观察者间差异,确定结肠活检标本应由胃肠病理学家而非普通病理学家进行检查。将51张显示不同程度发育异常的编码玻片邮寄给7名胃肠病理学家和6名普通组织病理学家。病理学家在没有临床病史且没有机会使用Riddell分类中包含的“不确定”类别的情况下,将每个活检标本分为四类之一。使用kappa统计分析结果。胃肠病理学家的总体kappa统计值为0.30 [95%置信区间(CI)=0.26 - 0.34],普通病理学家为0.28(95% CI = 0.23 - 0.32)。对于高级别发育异常,一致性最佳(胃肠病理学家和普通病理学家的kappa值分别为0.54和0.61)。51张玻片中只有4张(7.8%)(95% CI = 0.4 - 15.2%)的13名病理学家完全一致。从这些结果可以得出结论,在对UC发育异常进行分级时,胃肠病理学家并不比普通病理学家更好,且两组的一致性都很差。因此,没有证据表明专门设立专注于解读来自英国各地所有监测结肠镜活检的专科组织病理学中心会有任何益处。必须向公众明确说明,监测和筛查项目存在显著的组织学误差率,并且不能期望或通过现有方法实现完美。