Assessment of a computerized quantitative quality control tool for whole slide images of kidney biopsies

Inconsistencies in the preparation of histology slides and whole‐slide images (WSIs) may lead to challenges with subsequent image analysis and machine learning approaches for interrogating the WSI. These variabilities are especially pronounced in multicenter cohorts, where batch effects (i.e. system...

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Veröffentlicht in:The Journal of pathology 2021-03, Vol.253 (3), p.268-278
Hauptverfasser: Chen, Yijiang, Zee, Jarcy, Smith, Abigail, Jayapandian, Catherine, Hodgin, Jeffrey, Howell, David, Palmer, Matthew, Thomas, David, Cassol, Clarissa, Farris, Alton B, Perkinson, Kathryn, Madabhushi, Anant, Barisoni, Laura, Janowczyk, Andrew
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Sprache:eng
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Zusammenfassung:Inconsistencies in the preparation of histology slides and whole‐slide images (WSIs) may lead to challenges with subsequent image analysis and machine learning approaches for interrogating the WSI. These variabilities are especially pronounced in multicenter cohorts, where batch effects (i.e. systematic technical artifacts unrelated to biological variability) may introduce biases to machine learning algorithms. To date, manual quality control (QC) has been the de facto standard for dataset curation, but remains highly subjective and is too laborious in light of the increasing scale of tissue slide digitization efforts. This study aimed to evaluate a computer‐aided QC pipeline for facilitating a reproducible QC process of WSI datasets. An open source tool, HistoQC, was employed to identify image artifacts and compute quantitative metrics describing visual attributes of WSIs to the Nephrotic Syndrome Study Network (NEPTUNE) digital pathology repository. A comparison in inter‐reader concordance between HistoQC aided and unaided curation was performed to quantify improvements in curation reproducibility. HistoQC metrics were additionally employed to quantify the presence of batch effects within NEPTUNE WSIs. Of the 1814 WSIs (458 H&E, 470 PAS, 438 silver, 448 trichrome) from n = 512 cases considered in this study, approximately 9% (163) were identified as unsuitable for subsequent computational analysis. The concordance in the identification of these WSIs among computational pathologists rose from moderate (Gwet's AC1 range 0.43 to 0.59 across stains) to excellent (Gwet's AC1 range 0.79 to 0.93 across stains) agreement when aided by HistoQC. Furthermore, statistically significant batch effects (p
ISSN:0022-3417
1096-9896
DOI:10.1002/path.5590