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Interprovider variation of celiac disease testing in childhood chronic abdominal pain
BACKGROUND: To determine within one tertiary care center: 1) the variation between providers in testing for celiac disease in children with chronic abdominal pain; 2) the characteristics of those children who were more likely to be tested, and 3) the prevalence of celiac disease in those evaluated....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852708/ https://www.ncbi.nlm.nih.gov/pubmed/24124697 http://dx.doi.org/10.1186/1471-230X-13-150 |
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author | Chumpitazi, Bruno Pedro Mysore, Krupa Tsai, Cynthia Man-Wai Shulman, Robert Jay |
author_facet | Chumpitazi, Bruno Pedro Mysore, Krupa Tsai, Cynthia Man-Wai Shulman, Robert Jay |
author_sort | Chumpitazi, Bruno Pedro |
collection | PubMed |
description | BACKGROUND: To determine within one tertiary care center: 1) the variation between providers in testing for celiac disease in children with chronic abdominal pain; 2) the characteristics of those children who were more likely to be tested, and 3) the prevalence of celiac disease in those evaluated. METHODS: Retrospective review of children with a primary complaint of chronic abdominal pain referred to a tertiary care children’s hospital for pediatric gastroenterology evaluation over a 2-year period was conducted. Children with at least two visits and without an identified organic etiology for the pain were included. RESULTS: 160 children were evaluated by 16 pediatric gastroenterologists and one nurse practitioner. Celiac serologic testing was completed in 63 (39.4%) children. There was no significant variance in the frequency of celiac serologic testing between providers. Child age, gender, body mass index, and baseline gastrointestinal symptoms did not predict whether celiac serologic testing occurred, though Caucasians (P < 0.01) were more likely to be tested. Eighty-two (51.3%) children underwent either serologic testing and/or esophagogastroduodenoscopy. Four (4.9%, 95% CI: 1.6-11.3%) of the 82 tested were diagnosed with celiac disease. CONCLUSIONS: Though interprovider variation for celiac disease testing in children with chronic abdominal pain did not occur, a large number of these children were not evaluated for celiac disease. Children’s race/ethnicity but not their associated gastrointestinal symptoms predicted whether celiac testing was undertaken. In those tested, celiac disease was identified in a higher percentage than that expected in the general population. |
format | Online Article Text |
id | pubmed-3852708 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38527082013-12-06 Interprovider variation of celiac disease testing in childhood chronic abdominal pain Chumpitazi, Bruno Pedro Mysore, Krupa Tsai, Cynthia Man-Wai Shulman, Robert Jay BMC Gastroenterol Research Article BACKGROUND: To determine within one tertiary care center: 1) the variation between providers in testing for celiac disease in children with chronic abdominal pain; 2) the characteristics of those children who were more likely to be tested, and 3) the prevalence of celiac disease in those evaluated. METHODS: Retrospective review of children with a primary complaint of chronic abdominal pain referred to a tertiary care children’s hospital for pediatric gastroenterology evaluation over a 2-year period was conducted. Children with at least two visits and without an identified organic etiology for the pain were included. RESULTS: 160 children were evaluated by 16 pediatric gastroenterologists and one nurse practitioner. Celiac serologic testing was completed in 63 (39.4%) children. There was no significant variance in the frequency of celiac serologic testing between providers. Child age, gender, body mass index, and baseline gastrointestinal symptoms did not predict whether celiac serologic testing occurred, though Caucasians (P < 0.01) were more likely to be tested. Eighty-two (51.3%) children underwent either serologic testing and/or esophagogastroduodenoscopy. Four (4.9%, 95% CI: 1.6-11.3%) of the 82 tested were diagnosed with celiac disease. CONCLUSIONS: Though interprovider variation for celiac disease testing in children with chronic abdominal pain did not occur, a large number of these children were not evaluated for celiac disease. Children’s race/ethnicity but not their associated gastrointestinal symptoms predicted whether celiac testing was undertaken. In those tested, celiac disease was identified in a higher percentage than that expected in the general population. BioMed Central 2013-10-14 /pmc/articles/PMC3852708/ /pubmed/24124697 http://dx.doi.org/10.1186/1471-230X-13-150 Text en Copyright © 2013 Chumpitazi et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Chumpitazi, Bruno Pedro Mysore, Krupa Tsai, Cynthia Man-Wai Shulman, Robert Jay Interprovider variation of celiac disease testing in childhood chronic abdominal pain |
title | Interprovider variation of celiac disease testing in childhood chronic abdominal pain |
title_full | Interprovider variation of celiac disease testing in childhood chronic abdominal pain |
title_fullStr | Interprovider variation of celiac disease testing in childhood chronic abdominal pain |
title_full_unstemmed | Interprovider variation of celiac disease testing in childhood chronic abdominal pain |
title_short | Interprovider variation of celiac disease testing in childhood chronic abdominal pain |
title_sort | interprovider variation of celiac disease testing in childhood chronic abdominal pain |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852708/ https://www.ncbi.nlm.nih.gov/pubmed/24124697 http://dx.doi.org/10.1186/1471-230X-13-150 |
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