From the Departments of Pathology (Shehabeldin, Rohra, Sellen, Zhao, Alqaidy, Aramin, Hameed, Perez, Lai, Tong, Edgerton, Fuller, Hansel, Prieto, Ballester, Aung) and Biostatistics (Milton), The University of Texas MD Anderson Cancer Center, Houston.
Arch Pathol Lab Med. 2024 Jun 1;148(6):715-721. doi: 10.5858/arpa.2023-0105-OA.
CONTEXT.—: In the United States, review of digital whole slide images (WSIs) using specific systems is approved for primary diagnosis but has not been implemented for intraoperative consultation.
OBJECTIVE.—: To evaluate the safety of review of WSIs and compare the efficiency of review of WSIs and glass slides (GSs) for intraoperative consultation.
DESIGN.—: Ninety-one cases previously submitted for frozen section evaluation were randomly selected from 8 different anatomic pathology subspecialties. GSs from these cases were scanned on a Leica Aperio AT2 scanner at ×20 magnification (0.25 μm/pixel). The slides were deidentified, and a short relevant clinical history was provided for each slide. Nine board-certified general pathologists who do not routinely establish primary diagnoses using WSIs reviewed the WSIs using Leica Aperio ImageScope viewing software. After a washout period of 2-3 weeks, the pathologists reviewed the corresponding GSs using a light microscope (Olympus BX43). The pathologists recorded the diagnosis and time to reach the diagnosis. Intraobserver concordance, time to diagnosis, and specificity and sensitivity compared to the original diagnosis were evaluated.
RESULTS.—: The rate of intraobserver concordance between GS results and WSI results was 93.7%. Mean time to diagnosis was 1.25 minutes for GSs and 1.76 minutes for WSIs (P < .001). Specificity was 91% for GSs and 90% for WSIs; sensitivity was 92% for GSs and 92% for WSIs.
CONCLUSIONS.—: Time to diagnosis was longer with WSIs than with GSs, and scanning GSs and uploading the data to whole slide imaging systems takes time. However, review of WSIs appears to be a safe alternative to review of GSs. Use of WSIs allows reporting from a remote site during a public health emergency such as the COVID-19 pandemic and facilitates subspecialty histopathology services.
在美国,使用特定系统对数字全切片图像(WSI)进行回顾性审查已被批准用于初步诊断,但尚未用于术中咨询。
评估 WSI 回顾性审查的安全性,并比较 WSI 和玻璃切片(GS)用于术中咨询的效率。
从 8 个不同的解剖病理学亚专科中随机选择了 91 例先前提交进行冷冻切片评估的病例。这些病例的 GS 被 Leica Aperio AT2 扫描仪以 20 倍放大率(0.25μm/像素)扫描。这些切片被去识别,并为每张切片提供简短的相关临床病史。9 位不常规使用 WSI 建立初步诊断的经过委员会认证的普通病理学家使用 Leica Aperio ImageScope 查看软件查看 WSI。在 2-3 周的洗脱期后,病理学家使用 Olympus BX43 显微镜查看相应的 GS。病理学家记录诊断和达到诊断的时间。评估了观察者内一致性、诊断时间以及与原始诊断的特异性和敏感性。
GS 结果与 WSI 结果之间观察者内一致性的比率为 93.7%。GS 的平均诊断时间为 1.25 分钟,WSI 的平均诊断时间为 1.76 分钟(P<0.001)。GS 的特异性为 91%,WSI 的特异性为 90%;GS 的敏感性为 92%,WSI 的敏感性为 92%。
与 GS 相比,WSI 的诊断时间更长,扫描 GS 并将数据上传到全切片成像系统需要时间。然而,WSI 的回顾性审查似乎是 GS 回顾性审查的一种安全替代方法。在 COVID-19 大流行等公共卫生紧急情况下,使用 WSI 可以允许从远程站点进行报告,并促进专科病理服务。