Understanding interobserver variability of pathologists to improve oral epithelial dysplasia grading

Author:

Ng Grace Tze Ern1,Phang Sarah Carmen1,Yu Kae Shyang1,Tiwari Lalima1ORCID,Khurram Syed Ali2ORCID,Sloan Philip345,Kujan Omar1ORCID

Affiliation:

1. UWA Dental School, The University of Western Australia Nedlands Western Australia Australia

2. Unit of Oral & Maxillofacial Pathology School of Clinical Dentistry, University of Sheffield Sheffield UK

3. School of Dental Sciences, Faculty of Medical Sciences Newcastle University Newcastle upon Tyne UK

4. Department of Cellular Pathology Newcastle upon Tyne Hospitals NHS Foundation Trust Newcastle upon Tyne UK

5. AMLo Biosciences Newcastle upon Tyne UK

Abstract

AbstractObjectiveThis study aimed to understand reasons for interobserver variability in the grading of oral epithelial dysplasia (OED) through a survey of pathologists to provide insight for improvements in the reliability and reproducibility of OED diagnoses.MethodsThe study design included quantitative and qualitative methodology. A pre‐validated 31‐item questionnaire was distributed to general, head and neck, and oral and maxillofacial histopathology specialists worldwide.ResultsA total of 132 pathologists participated and completed the questionnaire. Over two‐thirds used the three‐tier grading system for OED, while about a third used both binary and three‐tier systems. Regular reporters of OED preferred the three‐tier system and grading architectural features. Continuing education significantly aided recognition of architectural and cytological changes. Irregular epithelial stratification and drop‐shaped rete ridges had the lowest prognostic value and recognition scores, while loss of epithelial cell cohesion had the highest. Most participants used clinical information and often sought a second opinion when grading OED.ConclusionOur study has found that frequency of OED reporting and attendance of CME/CPD can play an important role in grading OED. Variations in the prognostic value of individual histological features and the use of clinical information may further contribute to interobserver variability.

Publisher

Wiley

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