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Pregled bibliografske jedinice broj: 583512

Disease phenotype at diagnosis in pediatric Crohn's disease : 5-year analyses of the EUROKIDS registry


de Bie, C.I.; Paerregaard, A.; Kolaček, Sanja; Ruemmele, F.M.; Koletzko, S.; Fell, J.M.; Escher, J.C.
Disease phenotype at diagnosis in pediatric Crohn's disease : 5-year analyses of the EUROKIDS registry // Inflammatory bowel diseases, 19 (2013), 2; 378-85 doi:10.1002/ibd.23008 (međunarodna recenzija, članak, znanstveni)


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Naslov
Disease phenotype at diagnosis in pediatric Crohn's disease : 5-year analyses of the EUROKIDS registry

Autori
De Bie, C.I. ; Paerregaard, A. ; Kolaček, Sanja ; Ruemmele, F.M. ; Koletzko, S. ; Fell, J.M. ; Escher, J.C.

Izvornik
Inflammatory bowel diseases (1078-0998) 19 (2013), 2; 378-85

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
disease phenotype; Crohn's disease

Sažetak
It has been speculated that pediatric Crohn's disease (CD) is a distinct disease entity, with probably different disease subtypes. We therefore aimed to accurately phenotype newly diagnosed pediatric CD by using the pediatric modification of the Montreal classification, the Paris classification. Information was collected from the EUROKIDS registry, a prospective, web-based registry of new-onset pediatric IBD patients in 17 European countries and Israel. When a complete diagnostic workup was performed (ileocolonoscopy, upper gastrointestinal [GI] endoscopy, small bowel imaging), CD patients were evaluated for ileocolonic disease extent, esophagogastroduodenal involvement, and jejunal/proximal ileal involvement. Disease behavior and the occurrence of granulomas were also analyzed. In all, 582 pediatric CD patients could be classified according to the Paris classification. Isolated terminal ileal disease (±limited cecal disease) was seen at presentation in 16%, isolated colonic disease in 27%, ileocolonic disease in 53%, and isolated upper GI disease in 4% of patients. In total, 30% had esophagogastroduodenal involvement and 24% jejunal/proximal ileal disease. Patients with L2 disease were less likely to have esophagogastroduodenal involvement or stricturing disease than patients with L1 or L3 disease. Terminal ileal disease and stricturing disease behavior were more common in children diagnosed after 10 years of age than in younger patients. Granulomas were identified in 43% of patients. Accurate phenotyping is essential in pediatric CD, as this affects the management of individual patients. Disease phenotypes differ according to age at disease onset. The Paris classification is a useful tool to capture the variety of phenotypic characteristics of pediatric CD. (Inflamm Bowel Dis 2012 ; ).

Izvorni jezik
Engleski

Znanstvena područja
Kliničke medicinske znanosti



POVEZANOST RADA


Projekti:
072-1083107-2054 - Celijakija u djece: primarna prevencija i patogeneza kromosomske nestabilnosti (Kolaček, Sanja, MZOS ) ( CroRIS)

Ustanove:
Klinika za dječje bolesti Medicinskog fakulteta

Profili:

Avatar Url Sanja Kolaček (autor)

Poveznice na cjeloviti tekst rada:

doi journals.lww.com

Citiraj ovu publikaciju:

de Bie, C.I.; Paerregaard, A.; Kolaček, Sanja; Ruemmele, F.M.; Koletzko, S.; Fell, J.M.; Escher, J.C.
Disease phenotype at diagnosis in pediatric Crohn's disease : 5-year analyses of the EUROKIDS registry // Inflammatory bowel diseases, 19 (2013), 2; 378-85 doi:10.1002/ibd.23008 (međunarodna recenzija, članak, znanstveni)
De Bie, C., Paerregaard, A., Kolaček, S., Ruemmele, F., Koletzko, S., Fell, J. & Escher, J. (2013) Disease phenotype at diagnosis in pediatric Crohn's disease : 5-year analyses of the EUROKIDS registry. Inflammatory bowel diseases, 19 (2), 378-85 doi:10.1002/ibd.23008.
@article{article, author = {de Bie, C.I. and Paerregaard, A. and Kola\v{c}ek, Sanja and Ruemmele, F.M. and Koletzko, S. and Fell, J.M. and Escher, J.C.}, year = {2013}, pages = {378-85}, DOI = {10.1002/ibd.23008}, keywords = {disease phenotype, Crohn's disease}, journal = {Inflammatory bowel diseases}, doi = {10.1002/ibd.23008}, volume = {19}, number = {2}, issn = {1078-0998}, title = {Disease phenotype at diagnosis in pediatric Crohn's disease : 5-year analyses of the EUROKIDS registry}, keyword = {disease phenotype, Crohn's disease} }
@article{article, author = {de Bie, C.I. and Paerregaard, A. and Kola\v{c}ek, Sanja and Ruemmele, F.M. and Koletzko, S. and Fell, J.M. and Escher, J.C.}, year = {2013}, pages = {378-85}, DOI = {10.1002/ibd.23008}, keywords = {disease phenotype, Crohn's disease}, journal = {Inflammatory bowel diseases}, doi = {10.1002/ibd.23008}, volume = {19}, number = {2}, issn = {1078-0998}, title = {Disease phenotype at diagnosis in pediatric Crohn's disease : 5-year analyses of the EUROKIDS registry}, keyword = {disease phenotype, Crohn's disease} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


Citati:





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