Impact of a national external quality assessment scheme for breast pathology in the UK

Ian O. Ellis(Nottingham City Hospital), D Coleman(Institute of Cancer Research), Clive Wells(St Bartholomew's Hospital), S Kodikara(Institute of Cancer Research), EC Paish(Nottingham City Hospital), S Moss(Institute of Cancer Research), S. Al‐Sam(Broomfield Hospital), Neil Anderson(University of Ulster), Lynda G. Bobrow(Addenbrooke's Hospital), I Buley(John Radcliffe Hospital), Cathy Connolly(University Hospital Galway), N S Dallimore(University Hospital Llandough), S Hales(University of Liverpool), A M Hanby(St James's University Hospital), S Humphreys(Medical Solutions), Fiona Knox(Wythenshawe Hospital), James Lowe(University Hospital of North Tees), J Macartney(University Hospitals Coventry and Warwickshire NHS Trust), Robert J. Nash(St George's Hospital), David M. Parham(Royal Bournemouth Hospital), Julietta Patnick(Macmillan Cancer Support), Sarah E. Pinder(Addenbrooke's Hospital), Cecily Quinn(St. Vincent's University Hospital), A J Robertson(University of Dundee), J Shrimankar(University Hospital of North Tees), R A Walker(University of Leicester), Ronald L. Winder
Journal of Clinical Pathology
January 27, 2006
Cited by 107Open Access
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Abstract

BACKGROUND: This article presents the results and observed effects of the UK National Health Service Breast Screening Programme (NHSBSP) external quality assurance scheme in breast histopathology. AIMS/METHODS: The major objectives were to monitor and improve the consistency of diagnoses made by pathologists and the quality of prognostic information in pathology reports. The scheme is based on a twice yearly circulation of 12 cases to over 600 registered participants. The level of agreement was generally measured using kappa statistics. RESULTS: Four main situations were encountered with respect to diagnostic consistency, namely: (1) where consistency is naturally very high-this included diagnosing in situ and invasive carcinomas (and certain distinctive subtypes) and uncomplicated benign lesions; (2) where the level of consistency was low but could be improved by making guidelines more detailed and explicit-this included histological grading; (3) where consistency could be improved but only by changing the system of classification-this included classification of ductal carcinoma in situ; and (4) where no improvement in consistency could be achieved-this included diagnosing atypical hyperplasia and reporting vascular invasion. Size measurements were more consistent for invasive than in situ carcinomas. Even in cases where there is a high level of agreement on tumour size, a few widely outlying measurements were encountered, for which no explanation is readily forthcoming. CONCLUSIONS: These results broadly confirm the robustness of the systems of breast disease diagnosis and classification adopted by the NHSBSP, and also identify areas where improvement or new approaches are required.


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