Shi Wangpan, Georgiou Petros, Akram Aqsa, Proute Matthew C, Serhiyenia Tatsiana, Kerolos Mina E, Pradeep Roshini, Kothur Nageshwar R, Khan Safeera
Pathology, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Internal Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.
Cureus. 2021 Aug 12;13(8):e17116. doi: 10.7759/cureus.17116. eCollection 2021 Aug.
Digital microscopy (DM) is one of the cutting-edge advances in pathology, which entails improved efficiency, diagnostic advantages, and potential application in virtual diagnosis, particularly in the current era of the coronavirus disease (COVID-19) pandemic. However, the diagnostic challenges are the remaining concerns for its wider adoption by pathologists, and these concerns should be addressed in a specific subspecialty. We aim to identify the common diagnostic pitfalls of whole slide imaging (WSI), one modality of DM, in gastrointestinal (GI) pathology. From validating studies of primary diagnosis performance, we included 16 records with features on GI cases involved, at least two weeks wash-out periods, and more than 60 case study designs. A tailored quality appraisal assessment was utilized to evaluate the risks of bias for these diagnostic accuracy studies. Furthermore, due to the highly heterogeneous studies and unstandardized definition of discordance, we extract the discordant cases in GI pathology and calculate the discrepant rate, resulting from 0.5% to 64.28%. Targeting discrepancy cases between digital microscopy and light microscopy, we demonstrate five main diagnostic pitfalls regarding WSI as follows: additional time to review slides in WSI, hard to identify dysplasia nucleus, missed organisms like (), specific cell recognitions, and technical issues. After detailed reviews and analysis, we generate two essential suggestions for further GI cases signing out by DM. One is to use systematized 20x scans for diagnostic workouts and requesting 40x or even 60x scans for challenging cases; another is that a high-volume slides training should be set before the real clinical application of WSI for primary diagnosis, particularly in GI pathology.
数字显微镜检查(DM)是病理学领域的前沿进展之一,它提高了效率,具有诊断优势,并在虚拟诊断中具有潜在应用价值,尤其是在当前冠状病毒病(COVID-19)大流行的时代。然而,诊断挑战仍然是病理学家更广泛采用它的担忧所在,这些担忧应在特定亚专业中得到解决。我们旨在确定数字显微镜检查的一种模式——全玻片成像(WSI)在胃肠道(GI)病理学中的常见诊断陷阱。从对初步诊断性能的验证研究中,我们纳入了16份记录,这些记录涉及GI病例的特征、至少两周的洗脱期以及超过60个病例研究设计。采用量身定制的质量评估来评估这些诊断准确性研究的偏倚风险。此外,由于研究高度异质性以及不一致性的定义不标准化,我们提取了GI病理学中的不一致病例并计算差异率,结果为0.5%至64.28%。针对数字显微镜检查和光学显微镜检查之间的差异病例,我们展示了关于WSI的五个主要诊断陷阱如下:WSI中查看玻片的额外时间、难以识别发育异常细胞核、遗漏如()的生物体、特定细胞识别以及技术问题。经过详细审查和分析,我们针对DM进一步签署GI病例提出了两条重要建议。一是使用系统化的20倍扫描进行诊断工作,并对具有挑战性的病例要求40倍甚至60倍扫描;另一个是在WSI实际临床应用于初步诊断之前,尤其是在GI病理学中,应进行大量玻片训练。