Validation of digital pathology imaging for primary histopathological diagnosis

David Snead(University Hospitals Coventry and Warwickshire NHS Trust), Yee‐Wah Tsang(University Hospitals Coventry and Warwickshire NHS Trust), Aisha Meskiri(University Hospitals Coventry and Warwickshire NHS Trust), Peter Kimani(University of Warwick), R. H. S. Crossman(University of Warwick), Nasir Rajpoot(University Hospitals Coventry and Warwickshire NHS Trust), Elaine Blessing(University Hospitals Coventry and Warwickshire NHS Trust), Klaus Chen(University Hospitals Coventry and Warwickshire NHS Trust), Kishore Gopalakrishnan(University Hospitals Coventry and Warwickshire NHS Trust), P.N. Matthews(University Hospitals Coventry and Warwickshire NHS Trust), Navid Momtahan(Birmingham City Hospital), Sarah Louise Read-Jones(University Hospitals Coventry and Warwickshire NHS Trust), Shatrughan Prasad Sah(University Hospitals Coventry and Warwickshire NHS Trust), Emma Simmons(University Hospitals Coventry and Warwickshire NHS Trust), B. P. Sinha(University Hospitals Coventry and Warwickshire NHS Trust), Sari Suortamo(University Hospitals Coventry and Warwickshire NHS Trust), Yen Yeo(University Hospitals Coventry and Warwickshire NHS Trust), Hesham El Daly(University Hospitals Coventry and Warwickshire NHS Trust), Ian A. Cree(University Hospitals Coventry and Warwickshire NHS Trust)
Histopathology
September 26, 2015
Cited by 234Open Access
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Abstract

AIMS: Digital pathology (DP) offers advantages over glass slide microscopy (GS), but data demonstrating a statistically valid equivalent (i.e. non-inferior) performance of DP against GS are required to permit its use in diagnosis. The aim of this study is to provide evidence of non-inferiority. METHODS AND RESULTS: Seventeen pathologists re-reported 3017 cases by DP. Of these, 1009 were re-reported by the same pathologist, and 2008 by a different pathologist. Re-examination of 10 138 scanned slides (2.22 terabytes) produced 72 variances between GS and DP reports, including 21 clinically significant variances. Ground truth lay with GS in 12 cases and with DP in nine cases. These results are within the 95% confidence interval for existing intraobserver and interobserver variability, proving that DP is non-inferior to GS. In three cases, the digital platform was deemed to be responsible for the variance, including a gastric biopsy, where Helicobacter pylori only became visible on slides scanned at the ×60 setting, and a bronchial biopsy and penile biopsy, where dysplasia was reported on DP but was not present on GS. CONCLUSIONS: This is one of the largest studies proving that DP is equivalent to GS for the diagnosis of histopathology specimens. Error rates are similar in both platforms, although some problems e.g. detection of bacteria, are predictable.


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