Esophagus to Small Intestine

Gut. 2025;74(4):539-546

Adler J, Gadepalli S, Rahman M, Kim S

Early tumour necrosis factor antagonist treatment prevents perianal fistula development in children with Crohn’s disease: Post-hoc analysis of the RISK study


Background: One in 3 children with Crohn’s disease develop perianal fistula complications (PFCs), among the most disturbing and difficult-to-treat disease-related complications. Retrospective evidence suggests PFCs may be preventable.
Objective: The aim of this study was to determine if early anti-tumour necrosis factor-alpha (anti-TNFα) therapy prevents PFC development in a well-characterised prospective cohort of paediatric patients with Crohn’s disease who were free from PFC at enrolment.
Design: RISK was a multicentre inception cohort of children newly diagnosed with Crohn’s disease. The authors included all patients who had never experienced PFCs 30 days after study enrolment. They conducted nearest-neighbour propensity score-matched triad analyses. Matching was performed to balance patient characteristics across 3 mutually exclusive treatment groups based on therapy prior to either PFC development or the end of the observation period.
Results: Among 873 patients without perianal fistula, 447 matched patients were included (149 per treatment group). The presence of non-penetrating perianal lesions (large skin tags, ulcers and/or fissures) was significantly associated with PFC development, with 4-fold greater odds of PFC (odds ratio [OR] = 4.08, 95% confidence interval [CI]: 1.70–9.78; p = 0.0016). Early anti-TNFα therapy was associated with an 82% decrease in the odds of PFC (OR = 0.18, 95% CI: 0.05–0.66; p = 0.01). Among those with perianal lesions, anti-TNFα therapy was associated with 94% reduced odds of PFC development (OR = 0.055, 95% CI: 0.006–0.50; p = 0.010). No other treatment group was associated with reduced risk of PFC.

Conclusion: Early anti-TNF therapy prevents perianal fistula development, especially among patients at increased risk.

J. Adler, Pediatric Gastroenterology, University of Michigan, Michigan Medicine, Ann Arbor, MI, USA, E-Mail: jeradler@umich.edu

DOI:  10.1136/gutjnl-2024-333280

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