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Histopathological changes in anatomical distribution of inflammatory bowel disease in children: a retrospective cohort study

BACKGROUND: Anatomical progression of pediatric inflammatory bowel disease is under-reported. The aim of this work was to examine possible changes in the anatomical distribution of IBD in pediatric patients at diagnosis and at follow up. METHODS: In a retrospective cohort study, the medical records...

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Autores principales: Tsang, Jessica, Sikora, Sheena, Spady, Donald, El-Matary, Wael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3508883/
https://www.ncbi.nlm.nih.gov/pubmed/23061647
http://dx.doi.org/10.1186/1471-2431-12-162
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author Tsang, Jessica
Sikora, Sheena
Spady, Donald
El-Matary, Wael
author_facet Tsang, Jessica
Sikora, Sheena
Spady, Donald
El-Matary, Wael
author_sort Tsang, Jessica
collection PubMed
description BACKGROUND: Anatomical progression of pediatric inflammatory bowel disease is under-reported. The aim of this work was to examine possible changes in the anatomical distribution of IBD in pediatric patients at diagnosis and at follow up. METHODS: In a retrospective cohort study, the medical records of children with inflammatory bowel disease were examined. Patients who had at least 2 endoscopic/colonoscopic examinations were included. Primary outcome was histopathological progression based on histopathological examination of biopsies taken during endoscopic and colonoscopic bowel examination. Factors predictive of disease progression were also examined. RESULTS: A total of 98 patients fulfilled inclusion criteria (49 female, 54 with ulcerative colitis, range 2 – 17 years, mean age at diagnosis was 10.6 years, SD ± 3.67), the mean duration of follow up was 32.9 months (range 0.1 – 60 months, SD ± 8.54). In the ulcerative colitis group, 41% had disease progression and none of the examined variables (age, gender, laboratory markers, growth and disease activity at diagnosis) appeared to effect disease progression. In the Crohn’s disease group, 75% had disease progression. Girls (OR = 0.13, 95% CI 0.02 – 0.79) and patients with high erythrocytic sedimentation rate (OR=0.942, 95% CI 0.894 – 0.99) were predictive for disease progression. CONCLUSIONS: Despite maximum therapy, the majority of children with Crohn’s disease appeared to have histopathological disease progression. Female sex and high erythrocytic sedimentation rate seemed to be predictive for disease progression. None of the factors analyzed seemed predictive of disease progression in ulcerative colitis.
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spelling pubmed-35088832012-11-29 Histopathological changes in anatomical distribution of inflammatory bowel disease in children: a retrospective cohort study Tsang, Jessica Sikora, Sheena Spady, Donald El-Matary, Wael BMC Pediatr Research Article BACKGROUND: Anatomical progression of pediatric inflammatory bowel disease is under-reported. The aim of this work was to examine possible changes in the anatomical distribution of IBD in pediatric patients at diagnosis and at follow up. METHODS: In a retrospective cohort study, the medical records of children with inflammatory bowel disease were examined. Patients who had at least 2 endoscopic/colonoscopic examinations were included. Primary outcome was histopathological progression based on histopathological examination of biopsies taken during endoscopic and colonoscopic bowel examination. Factors predictive of disease progression were also examined. RESULTS: A total of 98 patients fulfilled inclusion criteria (49 female, 54 with ulcerative colitis, range 2 – 17 years, mean age at diagnosis was 10.6 years, SD ± 3.67), the mean duration of follow up was 32.9 months (range 0.1 – 60 months, SD ± 8.54). In the ulcerative colitis group, 41% had disease progression and none of the examined variables (age, gender, laboratory markers, growth and disease activity at diagnosis) appeared to effect disease progression. In the Crohn’s disease group, 75% had disease progression. Girls (OR = 0.13, 95% CI 0.02 – 0.79) and patients with high erythrocytic sedimentation rate (OR=0.942, 95% CI 0.894 – 0.99) were predictive for disease progression. CONCLUSIONS: Despite maximum therapy, the majority of children with Crohn’s disease appeared to have histopathological disease progression. Female sex and high erythrocytic sedimentation rate seemed to be predictive for disease progression. None of the factors analyzed seemed predictive of disease progression in ulcerative colitis. BioMed Central 2012-10-13 /pmc/articles/PMC3508883/ /pubmed/23061647 http://dx.doi.org/10.1186/1471-2431-12-162 Text en Copyright ©2012 Tsang 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
Tsang, Jessica
Sikora, Sheena
Spady, Donald
El-Matary, Wael
Histopathological changes in anatomical distribution of inflammatory bowel disease in children: a retrospective cohort study
title Histopathological changes in anatomical distribution of inflammatory bowel disease in children: a retrospective cohort study
title_full Histopathological changes in anatomical distribution of inflammatory bowel disease in children: a retrospective cohort study
title_fullStr Histopathological changes in anatomical distribution of inflammatory bowel disease in children: a retrospective cohort study
title_full_unstemmed Histopathological changes in anatomical distribution of inflammatory bowel disease in children: a retrospective cohort study
title_short Histopathological changes in anatomical distribution of inflammatory bowel disease in children: a retrospective cohort study
title_sort histopathological changes in anatomical distribution of inflammatory bowel disease in children: a retrospective cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3508883/
https://www.ncbi.nlm.nih.gov/pubmed/23061647
http://dx.doi.org/10.1186/1471-2431-12-162
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