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Corticosteroid Dosing in Pediatric Acute Severe Ulcerative Colitis: A Propensity Score Analysis
Sapir Choshen1, Helen Finnamore, Marcus K H Auth
1*The Juliet Keidan Institute of Pediatric Gastroenterology and Nutrition, Shaare Zedek Medical Center†The Hebrew University of Jerusalem, Jerusalem, Israel‡Alder Hey Children's NHS Foundation Trust, Liverpool, UK§Children's Hospital of Eastern Ontario IBD Centre and Department of Pediatrics, University of Ottawa, Ottawa, Canada||Connecticut Children's Medical Center, Hartford, CT¶Hasbro Chidren's Hospital/Rhode Island Hospital, Alpert School of Medicine at Brown University, Providence#SickKids Hospital, University of Toronto, Toronto, Canada.
Optimal intravenous corticosteroid (IVCS) dosing for acute severe colitis in children suggests higher doses are not necessary. Doses exceeding 1 to 1.5 mg/kg/day (max 40-60 mg/day) are not justified for pediatric ulcerative colitis treatment.
Area of Science:
- Pediatric Gastroenterology
- Clinical Pharmacology
- Inflammatory Bowel Disease Research
Background:
- Acute severe colitis in children requires effective treatment with intravenous corticosteroids (IVCS).
- Determining optimal IVCS dosing is crucial for maximizing efficacy while minimizing potential side effects.
- Previous studies have not definitively established the ideal IVCS dosage for pediatric ulcerative colitis.
Purpose of the Study:
- To investigate the optimal dosing strategy for IVCS in pediatric patients with acute severe colitis.
- To utilize a robust statistical method on the largest available pediatric cohort to date.
- To compare outcomes associated with different IVCS dosage levels.
Main Methods:
- A retrospective analysis of 283 children treated with IVCS for ulcerative colitis over one year.
- Propensity score matching was employed to address confounding by indication, comparing high- and low-IVCS dose groups.
- Three distinct IVCS dosage cutoffs were analyzed: 1 mg·kg⁻¹·day⁻¹, 1.25 mg·kg⁻¹·day⁻¹, and 2 mg·kg⁻¹·day⁻¹.
Main Results:
- No significant differences in clinical outcomes were observed between lower IVCS dosage groups (up to 1.25 mg·kg⁻¹·day⁻¹).
- Higher IVCS doses (2 mg·kg⁻¹·day⁻¹) showed a potential benefit that was not sustained in sensitivity analyses or regression models.
- Successful matching was confirmed by the absence of significant differences in 25 baseline variables across dosage cutoffs.
Conclusions:
- Current guidelines supporting IVCS doses up to 1 to 1.5 mg·kg⁻¹·day⁻¹ (max 40-60 mg/day) are supported by this study's findings.
- Doses exceeding 1.5 mg·kg⁻¹·day⁻¹ are not statistically justified for treating acute severe colitis in children.
- This research provides evidence-based recommendations for IVCS dosing in pediatric ulcerative colitis.
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