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Value of biopsy in a cohort of children with high-titer celiac serologies: observation of dynamic policy differences between Europe and North America
BACKGROUND: Healthcare systems implement change at different rates because of differences in incentives, organizational processes, key influencers, and management styles. A comparable set of forces may play out at the national and international levels as demonstrated in significant differences in th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7576777/ https://www.ncbi.nlm.nih.gov/pubmed/33081760 http://dx.doi.org/10.1186/s12913-020-05815-0 |
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author | Badizadegan, Kamran Vanlandingham, David M. Hampton, Wesley Thompson, Kimberly M. |
author_facet | Badizadegan, Kamran Vanlandingham, David M. Hampton, Wesley Thompson, Kimberly M. |
author_sort | Badizadegan, Kamran |
collection | PubMed |
description | BACKGROUND: Healthcare systems implement change at different rates because of differences in incentives, organizational processes, key influencers, and management styles. A comparable set of forces may play out at the national and international levels as demonstrated in significant differences in the diagnostic management of pediatric Celiac Disease (CD) between European and North American practitioners. METHODS: We use retrospective clinical cohorts of 27,868 serum tissue transglutaminase (tTG) immunoglobulin A levels and 7907 upper gastrointestinal endoscopy pathology reports to create a dataset of 793 pathology reports with matching tTG results between July 1 of 2014 and July 1 of 2018. We use this dataset to characterize histopathological findings in the duodenum, stomach and esophagus of patients as a function of serum tTG levels. In addition, we use the dataset to estimate the local and national cost of endoscopies performed in patients with serum tTG levels greater than 10 times the upper limit of normal. RESULTS: Using evidence from a US tertiary care center, we show that in the cohort of pediatric patients with high pre-test probability of CD as determined by serum tTG levels, biopsy provides no additional diagnostic value for CD, and that it counter-intuitively introduces diagnostic uncertainty in a number of patients. We estimate that using the European diagnostic algorithms could avoid between 4891 and 7738 pediatric endoscopies per year in the US for evaluation of CD. CONCLUSIONS: This study considers the North American and European management guidelines for the diagnosis of pediatric CD and highlights the slow adoption in North America of evidence-based algorithms developed and applied in Europe for triage of endoscopy and biopsy. We suggest that system dynamics influences that help maintain the status quo in North America include a variety of social and economic factors in addition to medical evidence. This work contributes to the growing body of evidence that the dynamics that largely favor maintaining status quo management policies in a variety of systems extend to clinical medicine and potentially influence clinical decisions at the level of individual patients and the population. SUPPLEMENTARY INFORMATION: Supplementary information accompanies this paper at 10.1186/s12913-020-05815-0. |
format | Online Article Text |
id | pubmed-7576777 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-75767772020-10-21 Value of biopsy in a cohort of children with high-titer celiac serologies: observation of dynamic policy differences between Europe and North America Badizadegan, Kamran Vanlandingham, David M. Hampton, Wesley Thompson, Kimberly M. BMC Health Serv Res Research Article BACKGROUND: Healthcare systems implement change at different rates because of differences in incentives, organizational processes, key influencers, and management styles. A comparable set of forces may play out at the national and international levels as demonstrated in significant differences in the diagnostic management of pediatric Celiac Disease (CD) between European and North American practitioners. METHODS: We use retrospective clinical cohorts of 27,868 serum tissue transglutaminase (tTG) immunoglobulin A levels and 7907 upper gastrointestinal endoscopy pathology reports to create a dataset of 793 pathology reports with matching tTG results between July 1 of 2014 and July 1 of 2018. We use this dataset to characterize histopathological findings in the duodenum, stomach and esophagus of patients as a function of serum tTG levels. In addition, we use the dataset to estimate the local and national cost of endoscopies performed in patients with serum tTG levels greater than 10 times the upper limit of normal. RESULTS: Using evidence from a US tertiary care center, we show that in the cohort of pediatric patients with high pre-test probability of CD as determined by serum tTG levels, biopsy provides no additional diagnostic value for CD, and that it counter-intuitively introduces diagnostic uncertainty in a number of patients. We estimate that using the European diagnostic algorithms could avoid between 4891 and 7738 pediatric endoscopies per year in the US for evaluation of CD. CONCLUSIONS: This study considers the North American and European management guidelines for the diagnosis of pediatric CD and highlights the slow adoption in North America of evidence-based algorithms developed and applied in Europe for triage of endoscopy and biopsy. We suggest that system dynamics influences that help maintain the status quo in North America include a variety of social and economic factors in addition to medical evidence. This work contributes to the growing body of evidence that the dynamics that largely favor maintaining status quo management policies in a variety of systems extend to clinical medicine and potentially influence clinical decisions at the level of individual patients and the population. SUPPLEMENTARY INFORMATION: Supplementary information accompanies this paper at 10.1186/s12913-020-05815-0. BioMed Central 2020-10-20 /pmc/articles/PMC7576777/ /pubmed/33081760 http://dx.doi.org/10.1186/s12913-020-05815-0 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Badizadegan, Kamran Vanlandingham, David M. Hampton, Wesley Thompson, Kimberly M. Value of biopsy in a cohort of children with high-titer celiac serologies: observation of dynamic policy differences between Europe and North America |
title | Value of biopsy in a cohort of children with high-titer celiac serologies: observation of dynamic policy differences between Europe and North America |
title_full | Value of biopsy in a cohort of children with high-titer celiac serologies: observation of dynamic policy differences between Europe and North America |
title_fullStr | Value of biopsy in a cohort of children with high-titer celiac serologies: observation of dynamic policy differences between Europe and North America |
title_full_unstemmed | Value of biopsy in a cohort of children with high-titer celiac serologies: observation of dynamic policy differences between Europe and North America |
title_short | Value of biopsy in a cohort of children with high-titer celiac serologies: observation of dynamic policy differences between Europe and North America |
title_sort | value of biopsy in a cohort of children with high-titer celiac serologies: observation of dynamic policy differences between europe and north america |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7576777/ https://www.ncbi.nlm.nih.gov/pubmed/33081760 http://dx.doi.org/10.1186/s12913-020-05815-0 |
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