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数字病理学(全切片成像)用于原发性组织病理学诊断的验证与确认:全威尔士经验

Verification and Validation of Digital Pathology (Whole Slide Imaging) for Primary Histopathological Diagnosis: All Wales Experience.

作者信息

Babawale M, Gunavardhan A, Walker J, Corfield T, Huey P, Savage A, Bansal A, Atkinson M, Abdelsalam H, Raweily E, Christian A, Evangelou I, Thomas D, Shannon J, Youd E, Brumwell P, Harrison J, Thompson I, Rashid M, Leopold G, Finall A, Roberts S, Housa D, Nedeva P, Davies A, Fletcher D, Aslam Muhammad

机构信息

Department of Cellular Pathology, Glan Clwyd Hospital, Betsi Cadwaladr University Health Board, Bodelwyddan, Wales.

Department of Anaesthetics, Gwynedd Hospital, Betsi Cadwaladr University Health Board, Bangor, Wales.

出版信息

J Pathol Inform. 2021 Jan 23;12:4. doi: 10.4103/jpi.jpi_55_20. eCollection 2021.

Abstract

AIMS

The study is aimed to verify Aperio AT2 scanner for reporting on the digital pathology platform (DP) and to validate the cohort of pathologists in the interpretation of DP for routine diagnostic histopathological services in Wales, United Kingdom.

MATERIALS METHODS AND RESULTS

This was a large multicenter study involving seven hospitals across Wales and unique with 22 (largest number) pathologists participating. 7491 slides from 3001 cases were scanned on Leica Aperio AT2 scanner and reported on digital workstations with Leica software of e-slide manager. A senior pathology fellow compared DP reports with authorized reports on glass slide (GS). A panel of expert pathologists reviewed the discrepant cases under multiheader microscope to establish ground truth. 2745 out of 3001 (91%) cases showed complete concordance between DP and GS reports. Two hundred and fifty-six cases showed discrepancies in diagnosis, of which 170 (5.6%) were deemed of no clinical significance by the review panel. There were 86 (2.9%) clinically significant discrepancies in the diagnosis between DP and GS. The concordance was raised to 97.1% after discounting clinically insignificant discrepancies. Ground truth lay with DP in 28 out of 86 clinically significant discrepancies and with GS in 58 cases. Sensitivity of DP was 98.07% (confidence interval [CI] 97.57-98.56%); for GS was 99.07% (CI 98.72-99.41%).

CONCLUSIONS

We concluded that Leica Aperio AT2 scanner produces adequate quality of images for routine histopathologic diagnosis. Pathologists were able to diagnose in DP with good concordance as with GS.

STRENGTHS AND LIMITATIONS OF THIS STUDY

Strengths of this study - This was a prospective blind study. Different pathologists reported digital and glass arms at different times giving an ambience of real-time reporting. There was standardized use of software and hardware across Wales. A strong managerial support from efficiency through the technology group was a key factor for the implementation of the study.

LIMITATIONS

This study did not include Cytopathology and hybridization slides. Difficulty in achieving surgical pathology practise standardization across the whole country contributed to intra-observer variations.

摘要

目的

本研究旨在验证Aperio AT2扫描仪在数字病理平台(DP)上的报告情况,并验证病理学家团队对DP的解读,以用于英国威尔士的常规诊断组织病理学服务。

材料、方法与结果:这是一项大型多中心研究,涉及威尔士的七家医院,有22位(数量最多)病理学家参与,颇具独特性。对来自3001例病例的7491张玻片在徕卡Aperio AT2扫描仪上进行扫描,并在配备徕卡电子玻片管理器软件的数字工作站上进行报告。一位资深病理学研究员将DP报告与玻片(GS)上的授权报告进行比较。一组专家病理学家在多头显微镜下对存在差异的病例进行审查,以确定真实情况。3001例病例中有2745例(91%)在DP报告和GS报告之间显示出完全一致。256例病例在诊断上存在差异,其中170例(5.6%)被审查小组认为无临床意义。DP和GS在诊断上有86例(2.9%)具有临床意义的差异。在排除无临床意义的差异后,一致性提高到97.1%。在86例具有临床意义的差异中,28例的真实情况与DP一致,58例与GS一致。DP的敏感性为98.07%(置信区间[CI] 97.57 - 98.56%);GS的敏感性为99.07%(CI 98.72 - 99.41%)。

结论

我们得出结论,徕卡Aperio AT2扫描仪生成的图像质量足以用于常规组织病理学诊断。病理学家能够在DP上进行诊断,与在GS上的诊断具有良好的一致性。

本研究的优势与局限性

本研究的优势——这是一项前瞻性盲法研究。不同的病理学家在不同时间报告数字和玻片结果,营造出实时报告的氛围。威尔士各地对软件和硬件的使用是标准化的。通过技术团队从效率方面给予的有力管理支持是本研究得以实施的关键因素。

局限性

本研究未包括细胞病理学和杂交玻片。在全国范围内难以实现外科病理学实践标准化导致了观察者内部的差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/765d/8112347/f0160fc87d3f/JPI-12-4-g001.jpg

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