Clinical outcomes in pediatric inflammatory bowel disease patients: a systematic review of prospective studies

Abstract

AbstractBackground and AimWe studied response and remission rates in children and adolescents with inflammatory bowel disease whose real‐world data were collected prospectively.MethodsA systematic literature search was performed in MEDLINE, Embase, and the Improve Care Now registry from inception until March 17, 2022. Inclusion criteria were prospective studies with patients < 18 years at diagnosis (M0) and minimum follow‐up of 1 year (M12) mentioning disease phenotype and disease activity. Exclusion criteria were (i) reporting disease activity only at diagnosis, (ii) retrospective studies, and (iii) outcome limited to steroid‐free remission. The Preferred Reporting Items for Systematic Reviews and Meta‐Analyses Protocols guidelines and the Newcastle‐Ottawa scale were applied. Proportions between groups were compared using a chi‐square test (α = 0.05).ResultsThe search yielded 394 records and 7 inclusions with a sample size ranging from 33 to 390 patients (total population: 888) and a median follow‐up of 1–5 years. Proportions of disease activity differed between M0 and M12 (P < 0.0001) with more inactive (χ2 = 5.5) and less moderate‐to‐severe disease (χ2 = 23) at M12. Interestingly, disease activity after 1 year did not differ globally (P = 0.53). Proportions of disease activity in Crohn's disease only and limited to Belgium significantly differed from baseline after 5 years (P < 0.0001 for evolution) but not between 1‐ and 5‐year follow‐up (P = 0.94).ConclusionsThe few available prospective cohorts reported a significant decrease in disease activity after 1 year, with no global differences. Proportions of disease activity did not differ between 1‐ and 5‐year follow‐up in the Belgian Crohn's disease cohort, suggesting stable disease activity.