The Natural History of Crohn’s Disease Leading to Intestinal Failure: A Longitudinal Cohort Study from 1973 to 2018

Abstract

Abstract Background and Aims The natural history of Crohn’s disease leading to intestinal failure is not well characterised. This study aims to describe the clinical course of Crohn’s disease preceding intestinal failure and to compare disease course and burden between Crohn’s disease patients with and without intestinal failure. Methods Patients with Crohn’s disease complicated by intestinal failure from Rigshospitalet, Copenhagen [n = 182] and a nationwide Danish Crohn’s disease cohort without intestinal failure [n = 22,845] were included. Using nationwide registries in Denmark, disease course was determined from hospitalisations, surgeries, and outpatient medications, and disease burden was determined from employment and mortality data. Results The 10-year cumulative incidence of intestinal failure following Crohn’s disease diagnosis declined from 2.7% prior to 1980 to 0.2% after 2000. Compared with Crohn’s disease patients without intestinal failure, those with intestinal failure experienced significantly longer duration of severe disease [50 vs 19 years per 100 patient-years, p < 0.01], secondary to greater corticosteroid use [71% vs 60%, p = 0.02], inpatient contacts [98% vs 55%, p < 0.01], and abdominal surgeries [99% vs 48%, p < 0.01]. However, exposure to biologics was not different between the two groups [20.4% vs 21%, p = 0.95], and duration on biologics was shorter in Crohn’s disease patients with intestinal failure [2068 vs 4126 days per 100 patient-years, p = 0.02]. Standard mortality ratio in Crohn’s disease patients with intestinal failure was 3.66 (97.5% confidence interval [CI] 2.79, 4.72]. Conclusion Patients with Crohn’s disease complicated by intestinal failure experienced a more persistently severe preceding course of Crohn’s disease but were not more likely to be treated with biological therapy.