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Clinical Aspects and Treatments for Pediatric Inflammatory Bowel Diseases

The incidence of pediatric inflammatory bowel disease (IBD) is increasing worldwide, especially in the developing countries. It differs from adult disease in clinical manifestations, especially with regard to genetic predisposition in monogenic IBD. Pediatric disease also have a tendency to show mor...

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Detalles Bibliográficos
Autor principal: Moon, Jin Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333592/
https://www.ncbi.nlm.nih.gov/pubmed/30671373
http://dx.doi.org/10.5223/pghn.2019.22.1.50
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author Moon, Jin Soo
author_facet Moon, Jin Soo
author_sort Moon, Jin Soo
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description The incidence of pediatric inflammatory bowel disease (IBD) is increasing worldwide, especially in the developing countries. It differs from adult disease in clinical manifestations, especially with regard to genetic predisposition in monogenic IBD. Pediatric disease also have a tendency to show more aggressive inflammation and greater extent of lesion. Newer drugs such as anti-tumor necrosis factor α have been known to make a difference in treating pediatric IBD. Recent studies suggested that the patients with high risk factors might have some benefits from earlier use of biologics. To achieve treatment goals such as relieving symptoms, optimizing growth, and improving quality of life while minimizing drug toxicity, more research is needed to develop tools for risk stratification in the use of biologics for pediatric IBD.
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spelling pubmed-63335922019-01-22 Clinical Aspects and Treatments for Pediatric Inflammatory Bowel Diseases Moon, Jin Soo Pediatr Gastroenterol Hepatol Nutr Review Article The incidence of pediatric inflammatory bowel disease (IBD) is increasing worldwide, especially in the developing countries. It differs from adult disease in clinical manifestations, especially with regard to genetic predisposition in monogenic IBD. Pediatric disease also have a tendency to show more aggressive inflammation and greater extent of lesion. Newer drugs such as anti-tumor necrosis factor α have been known to make a difference in treating pediatric IBD. Recent studies suggested that the patients with high risk factors might have some benefits from earlier use of biologics. To achieve treatment goals such as relieving symptoms, optimizing growth, and improving quality of life while minimizing drug toxicity, more research is needed to develop tools for risk stratification in the use of biologics for pediatric IBD. The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition 2019-01 2019-01-10 /pmc/articles/PMC6333592/ /pubmed/30671373 http://dx.doi.org/10.5223/pghn.2019.22.1.50 Text en Copyright © 2019 by The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Moon, Jin Soo
Clinical Aspects and Treatments for Pediatric Inflammatory Bowel Diseases
title Clinical Aspects and Treatments for Pediatric Inflammatory Bowel Diseases
title_full Clinical Aspects and Treatments for Pediatric Inflammatory Bowel Diseases
title_fullStr Clinical Aspects and Treatments for Pediatric Inflammatory Bowel Diseases
title_full_unstemmed Clinical Aspects and Treatments for Pediatric Inflammatory Bowel Diseases
title_short Clinical Aspects and Treatments for Pediatric Inflammatory Bowel Diseases
title_sort clinical aspects and treatments for pediatric inflammatory bowel diseases
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333592/
https://www.ncbi.nlm.nih.gov/pubmed/30671373
http://dx.doi.org/10.5223/pghn.2019.22.1.50
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