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The Impact of Biologic Therapies on Rate of Colectomy in Paediatric-onset Ulcerative Colitis - A Population-Based
Emma Hope1, Cameron Kuronen-Stewart1, David C Wilson2
1Department of Paediatric Surgery, Royal Hospital for Children and Young People, Edinburgh, 50 Little France Crescent, Edinburgh, EH16 4TJ, UK.
Insights
Biologic therapies did not reduce colectomy rates in pediatric ulcerative colitis (UC) patients. Those receiving biologics showed a higher risk of colectomy, possibly due to increased disease severity.
Area of Science:
- Pediatric Gastroenterology
- Inflammatory Bowel Disease Research
- Clinical Outcomes Analysis
Background:
- Limited data exist on colectomy rates in pediatric-onset ulcerative colitis (UC).
- Biologic therapies are used in adult UC but their impact on pediatric colectomy rates is unclear.
- Understanding colectomy trends in pediatric UC is crucial for long-term management.
Purpose of the Study:
- To determine colectomy rates in pediatric-onset UC.
- To evaluate the effect of biologic therapies on colectomy risk in this population.
- To analyze colectomy rates over time, including transition to adult care.
Main Methods:
- Population-based cohort study of prevalent pediatric-onset UC patients in South-East Scotland (2000-2021).
- Data collected from a prospectively accrued database and health records.
- Kaplan-Meier analysis used to calculate cumulative colectomy risk.
Main Results:
- 145 patients identified; 16% underwent colectomy over a median follow-up of 7.9 years.
- 34% received biologic therapy; 57% of those who had colectomy received biologics.
- Biologic-exposed patients had higher 5- and 10-year colectomy rates (22% and 34%).
Conclusions:
- Defined 1-, 5-, and 10-year colectomy rates for pediatric-onset UC.
- Biologic therapy was associated with a significantly increased colectomy risk.
- Increased disease severity in biologic-treated patients may explain the higher colectomy risk.
Aim:
Biologic therapies have been associated with reduced rate of colectomy in ulcerative colitis (UC) in adults, but data are limited in paediatric-onset UC. Our aim was to define the rate of colectomy in paediatric-onset UC, including post-transition into adult care, and to evaluate the impact of biologic therapies on rate of colectomy.
Method:
All prevalent patients diagnosed with paediatric-onset UC in South-East Scotland were identified from a prospectively accrued database at our regional tertiary centre. Patients exposed to biologics or surgery were identified and further data collected from health records. Kaplan-Meier analysis was used to calculate cumulative risk of colectomy over time.
Results:
145 prevalent patients were identified between 2000 and 2021. Median follow-up was 7.9 years (IQR 4.1-13.1). 23 patients (16 %) underwent a colectomy. 50/145 (34 %) patients received biologic therapy, and 13/23 (57 %) patients who underwent colectomy received biologics. The cumulative risk of colectomy across the whole cohort at 1, 5, and 10 years was 3 %, 13 % and 16 %, respectively. Patients exposed to biologics had a higher colectomy rate at 5 and 10 years (22 % and 34 %). Patients in the pre-biologic era (2000-2008) had non-significantly reduced time from diagnosis to colectomy (2.4 vs 3.7 years, p = 0.204).
Conclusion:
We have defined the 1-, 5-, and 10-year colectomy rate in a population-based cohort of Paediatric-onset UC patients. Patients who received biologic therapy had a significantly increased risk of colectomy. Increased severity of disease in these patients may account for the greater colectomy risk.
Level Of Evidence:
Level 1.
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