TY - JOUR
T1 - Predicting Outcomes in Pediatric Crohn's Disease for Management Optimization
T2 - Systematic Review and Consensus Statements From the Pediatric Inflammatory Bowel Disease–Ahead Program
AU - Pediatric Inflammatory Bowel Disease–Ahead Steering Committee
AU - Ricciuto, Amanda
AU - Aardoom, Martine
AU - Orlanski-Meyer, Esther
AU - Navon, Dan
AU - Carman, Nicholas
AU - Aloi, Marina
AU - Bronsky, Jiri
AU - Däbritz, Jan
AU - Dubinsky, Marla
AU - Hussey, Séamus
AU - Lewindon, Peter
AU - Martín De Carpi, Javier
AU - Navas-López, Víctor Manuel
AU - Orsi, Marina
AU - Ruemmele, Frank M.
AU - Russell, Richard K.
AU - Veres, Gabor
AU - Walters, Thomas D.
AU - Wilson, David C.
AU - Kaiser, Thomas
AU - de Ridder, Lissy
AU - Turner, Dan
AU - Griffiths, Anne M.
N1 - Publisher Copyright:
© 2021 The Authors
PY - 2021/1
Y1 - 2021/1
N2 - Background & Aims: A better understanding of prognostic factors within the heterogeneous spectrum of pediatric Crohn's disease (CD) should improve patient management and reduce complications. We aimed to identify evidence-based predictors of outcomes with the goal of optimizing individual patient management. Methods: A survey of 202 experts in pediatric CD identified and prioritized adverse outcomes to be avoided. A systematic review of the literature with meta-analysis, when possible, was performed to identify clinical studies that investigated predictors of these outcomes. Multiple national and international face-to-face meetings were held to draft consensus statements based on the published evidence. Results: Consensus was reached on 27 statements regarding prognostic factors for surgery, complications, chronically active pediatric CD, and hospitalization. Prognostic factors for surgery included CD diagnosis during adolescence, growth impairment, NOD2/CARD15 polymorphisms, disease behavior, and positive anti-Saccharomyces cerevisiae antibody status. Isolated colonic disease was associated with fewer surgeries. Older age at presentation, small bowel disease, serology (anti-Saccharomyces cerevisiae antibody, antiflagellin, and OmpC), NOD2/CARD15 polymorphisms, perianal disease, and ethnicity were risk factors for penetrating (B3) and/or stenotic disease (B2). Male sex, young age at onset, small bowel disease, more active disease, and diagnostic delay may be associated with growth impairment. Malnutrition and higher disease activity were associated with reduced bone density. Conclusions: These evidence-based consensus statements offer insight into predictors of poor outcomes in pediatric CD and are valuable when developing treatment algorithms and planning future studies. Targeted longitudinal studies are needed to further characterize prognostic factors in pediatric CD and to evaluate the impact of treatment algorithms tailored to individual patient risk.
AB - Background & Aims: A better understanding of prognostic factors within the heterogeneous spectrum of pediatric Crohn's disease (CD) should improve patient management and reduce complications. We aimed to identify evidence-based predictors of outcomes with the goal of optimizing individual patient management. Methods: A survey of 202 experts in pediatric CD identified and prioritized adverse outcomes to be avoided. A systematic review of the literature with meta-analysis, when possible, was performed to identify clinical studies that investigated predictors of these outcomes. Multiple national and international face-to-face meetings were held to draft consensus statements based on the published evidence. Results: Consensus was reached on 27 statements regarding prognostic factors for surgery, complications, chronically active pediatric CD, and hospitalization. Prognostic factors for surgery included CD diagnosis during adolescence, growth impairment, NOD2/CARD15 polymorphisms, disease behavior, and positive anti-Saccharomyces cerevisiae antibody status. Isolated colonic disease was associated with fewer surgeries. Older age at presentation, small bowel disease, serology (anti-Saccharomyces cerevisiae antibody, antiflagellin, and OmpC), NOD2/CARD15 polymorphisms, perianal disease, and ethnicity were risk factors for penetrating (B3) and/or stenotic disease (B2). Male sex, young age at onset, small bowel disease, more active disease, and diagnostic delay may be associated with growth impairment. Malnutrition and higher disease activity were associated with reduced bone density. Conclusions: These evidence-based consensus statements offer insight into predictors of poor outcomes in pediatric CD and are valuable when developing treatment algorithms and planning future studies. Targeted longitudinal studies are needed to further characterize prognostic factors in pediatric CD and to evaluate the impact of treatment algorithms tailored to individual patient risk.
KW - ASCA
KW - Complications
KW - Growth Impairment
KW - NOD2/CARD15
KW - Polymorphism
KW - Prognostic Factors
KW - Serology
KW - Structuring or Penetrating Disease
UR - http://www.scopus.com/inward/record.url?scp=85097481115&partnerID=8YFLogxK
U2 - 10.1053/j.gastro.2020.07.065
DO - 10.1053/j.gastro.2020.07.065
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C2 - 32979356
AN - SCOPUS:85097481115
SN - 0016-5085
VL - 160
SP - 403-436.e26
JO - Gastroenterology
JF - Gastroenterology
IS - 1
ER -