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The ImproveCareNow Registry: Prediction of remission rates in paediatric Crohn's disease

Jonathan Van Hecke1, Gigi Veereman2, Koen Huysentruyt2

  • 1Geneeskunde en Farmacie, Vrije Universiteit Brussel (VUB), Brussels, Belgium.

Insights

Female sex, younger age, and higher BMI predict poor outcomes in pediatric Crohn's disease (CD). Early or late use of biologics also impacts remission time, guiding future therapeutic strategies for pediatric CD patients.

Area of Science:

  • Pediatric Gastroenterology
  • Inflammatory Bowel Disease Research
  • Clinical Trial Analysis

Background:

  • Identifying predictors of poor outcomes (POPO) in pediatric Crohn's disease (CD) is crucial for optimizing treatment strategies.
  • Previous studies have explored various factors, but a comprehensive analysis of predictors for both short-term and long-term remission is needed.

Purpose of the Study:

  • To assess predictors of 2-year non-remission in pediatric CD patients.
  • To evaluate factors influencing time to first remission (TFR), corticosteroid-free remission (TCSFR), and sustained remission (TSR).

Main Methods:

  • Retrospective analysis of prospectively collected data from 6959 pediatric CD patients (2007-2023) from the ImproveCareNow Registry.
  • Remission defined as Pediatric CD Activity Index <10. Logistic and Cox regression models were used with multiple imputation to identify predictors.

Main Results:

  • Female sex and later ustekinumab use predicted non-remission at 2 years.
  • Female sex and infliximab (IFX) use at the first visit predicted longer TFR.
  • Female sex, white race, and IFX treatment were associated with longer TCSFR, while Asian race and CS/immunomodulator use were linked to longer TCSFR.
  • Older age at diagnosis and higher BMI predicted longer TSR.

Conclusions:

  • Clinical factors like female sex, younger age, and higher BMI are associated with poor outcomes in pediatric CD.
  • Therapeutic strategies, including the timing of biologic use, significantly influence remission.
  • These findings can guide personalized treatment approaches for pediatric CD.
Abstract

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