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Laboratory variation in the grading of dysplasia of duodenal adenomas in familial adenomatous polyposis patients

To prevent duodenal and ampullary cancer in familial adenomatous polyposis (FAP) patients, a diagnosis of high grade dysplasia (HGD) plays an important role in the clinical management. Previous research showed that FAP patients are both over- and undertreated after a misdiagnosis of HGD, indicating...

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Autores principales: Soons, E., Siersema, P. D., van Lierop, L. M. A., Bisseling, T. M., van Kouwen, M. C. A., Nagtegaal, I. D., van der Post, R. S., Atsma, F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10020317/
https://www.ncbi.nlm.nih.gov/pubmed/36401146
http://dx.doi.org/10.1007/s10689-022-00320-1
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author Soons, E.
Siersema, P. D.
van Lierop, L. M. A.
Bisseling, T. M.
van Kouwen, M. C. A.
Nagtegaal, I. D.
van der Post, R. S.
Atsma, F.
author_facet Soons, E.
Siersema, P. D.
van Lierop, L. M. A.
Bisseling, T. M.
van Kouwen, M. C. A.
Nagtegaal, I. D.
van der Post, R. S.
Atsma, F.
author_sort Soons, E.
collection PubMed
description To prevent duodenal and ampullary cancer in familial adenomatous polyposis (FAP) patients, a diagnosis of high grade dysplasia (HGD) plays an important role in the clinical management. Previous research showed that FAP patients are both over- and undertreated after a misdiagnosis of HGD, indicating unwarranted variation. We aimed to investigate the laboratory variation in dysplasia grading of duodenal adenomas and explore possible explanations for this variation. We included data from all Dutch pathology laboratories between 1991 and 2020 by retrieving histology reports from upper endoscopy specimens of FAP patients from the Dutch nationwide pathology databank (PALGA). Laboratory variation was investigated by comparing standardized proportions of HGD. To describe the degree of variation between the laboratories a factor score was calculated. A funnel plot was used to identify outliers. A total of 3050 specimens from 25 laboratories were included in the final analyses. The mean observed HGD proportion was 9.4%. The top three HGD-diagnosing laboratories diagnosed HGD 3.9 times more often than the lowest three laboratories, even after correcting for case-mix. No outliers were identified. Moderate laboratory variation was found in HGD diagnoses of duodenal tissue of FAP patients after adjusting for case-mix. Despite the fact that no outliers were observed, there may well be room for quality improvement. Concentration of these patients in expertise centers may decrease variation. To further reduce unwarranted variation, we recommend (inter)national guidelines to become more uniform in their recommendations regarding duodenal tissue sampling and consequences of HGD diagnoses. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10689-022-00320-1.
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spelling pubmed-100203172023-03-18 Laboratory variation in the grading of dysplasia of duodenal adenomas in familial adenomatous polyposis patients Soons, E. Siersema, P. D. van Lierop, L. M. A. Bisseling, T. M. van Kouwen, M. C. A. Nagtegaal, I. D. van der Post, R. S. Atsma, F. Fam Cancer Original Article To prevent duodenal and ampullary cancer in familial adenomatous polyposis (FAP) patients, a diagnosis of high grade dysplasia (HGD) plays an important role in the clinical management. Previous research showed that FAP patients are both over- and undertreated after a misdiagnosis of HGD, indicating unwarranted variation. We aimed to investigate the laboratory variation in dysplasia grading of duodenal adenomas and explore possible explanations for this variation. We included data from all Dutch pathology laboratories between 1991 and 2020 by retrieving histology reports from upper endoscopy specimens of FAP patients from the Dutch nationwide pathology databank (PALGA). Laboratory variation was investigated by comparing standardized proportions of HGD. To describe the degree of variation between the laboratories a factor score was calculated. A funnel plot was used to identify outliers. A total of 3050 specimens from 25 laboratories were included in the final analyses. The mean observed HGD proportion was 9.4%. The top three HGD-diagnosing laboratories diagnosed HGD 3.9 times more often than the lowest three laboratories, even after correcting for case-mix. No outliers were identified. Moderate laboratory variation was found in HGD diagnoses of duodenal tissue of FAP patients after adjusting for case-mix. Despite the fact that no outliers were observed, there may well be room for quality improvement. Concentration of these patients in expertise centers may decrease variation. To further reduce unwarranted variation, we recommend (inter)national guidelines to become more uniform in their recommendations regarding duodenal tissue sampling and consequences of HGD diagnoses. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10689-022-00320-1. Springer Netherlands 2022-11-19 2023 /pmc/articles/PMC10020317/ /pubmed/36401146 http://dx.doi.org/10.1007/s10689-022-00320-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Soons, E.
Siersema, P. D.
van Lierop, L. M. A.
Bisseling, T. M.
van Kouwen, M. C. A.
Nagtegaal, I. D.
van der Post, R. S.
Atsma, F.
Laboratory variation in the grading of dysplasia of duodenal adenomas in familial adenomatous polyposis patients
title Laboratory variation in the grading of dysplasia of duodenal adenomas in familial adenomatous polyposis patients
title_full Laboratory variation in the grading of dysplasia of duodenal adenomas in familial adenomatous polyposis patients
title_fullStr Laboratory variation in the grading of dysplasia of duodenal adenomas in familial adenomatous polyposis patients
title_full_unstemmed Laboratory variation in the grading of dysplasia of duodenal adenomas in familial adenomatous polyposis patients
title_short Laboratory variation in the grading of dysplasia of duodenal adenomas in familial adenomatous polyposis patients
title_sort laboratory variation in the grading of dysplasia of duodenal adenomas in familial adenomatous polyposis patients
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10020317/
https://www.ncbi.nlm.nih.gov/pubmed/36401146
http://dx.doi.org/10.1007/s10689-022-00320-1
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