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Evaluating Therapeutic Interventions in the SHIP-deficient Mouse Model of Crohn Disease-like Ileitis and Fibrosis
Published on: October 14, 2025
Current therapy of inflammatory bowel disease in children
1Center for Inflammatory Bowel Diseases, Combined Program in Gastroenterology and Nutrition, Children's Hospital, Boston, Massachusetts 02115, USA. paul.rufo@childrens.harvard.edu
Insights
This review covers managing pediatric inflammatory bowel disease (IBD), including ulcerative colitis (UC) and Crohn disease (CD). It highlights unique challenges in children and adolescents, focusing on optimizing treatment for growth and development.
Area of Science:
- Gastroenterology
- Pediatric Medicine
- Immunology
Background:
- Ulcerative colitis (UC) and Crohn disease (CD) are chronic inflammatory bowel diseases (IBD) affecting the gastrointestinal tract.
- Approximately 20% of IBD cases present in childhood or adolescence, posing unique developmental, psychosocial, and physiological challenges.
- These challenges include growth delays, altered drug dosing, and psychosocial adjustments during critical developmental stages.
Purpose of the Study:
- To review current management strategies for UC and CD in pediatric patients.
- To highlight treatment considerations specific to children and adolescents with IBD.
- To emphasize the importance of a multidisciplinary approach involving pharmacologic therapies, nutritional support, psychologic care, and timely surgery.
Main Methods:
- Review of current medical literature and clinical guidelines for IBD management.
- Analysis of therapeutic options for inducing and maintaining remission in UC and CD.
- Discussion of surgical considerations and long-term monitoring for pediatric IBD patients.
Main Results:
- UC management involves aminosalicylates, corticosteroids, and cyclosporine for induction, with aminosalicylates, mercaptopurine, and azathioprine for maintenance. Colectomy with J-pouch is a standard for refractory cases.
- CD treatment is complex, depending on disease location and behavior. Induction therapies include aminosalicylates, antibiotics, nutritional therapy, corticosteroids, and infliximab. Maintenance involves similar agents plus methotrexate.
- Both UC and CD patients require nutritional monitoring for deficiencies and colonoscopy surveillance due to increased colon cancer risk.
Conclusions:
- Optimal management of pediatric IBD requires balancing disease control with minimizing adverse effects on growth and development.
- Individualized treatment plans integrating medical, nutritional, psychologic, and surgical interventions are crucial for long-term outcomes.
- Close monitoring for nutritional deficiencies and cancer risk is essential for children and adolescents with IBD.
Abstract:
Ulcerative colitis (UC) and Crohn disease (CD) are chronic intestinal inflammatory diseases that can present as bloody diarrhea, abdominal pain, and malnutrition. Collectively, these disorders are referred to as inflammatory bowel disease (IBD). All patients with IBD share a common pathophysiology. However, there are a number of developmental, psychosocial, and physiologic issues that are unique to the approximate, equals 20% of patients that present during childhood or adolescence. These include the possibility of disease-induced delays in linear growth or physical development, differences in drug dosing, and the changes in social and cognitive development that occur as children move from school-age years into adolescence and early adulthood. Gastroenterologists caring for these children must therefore develop an optimal regimen of pharmacologic therapies, nutritional management, psychologic support, and properly timed surgery (when necessary) that will maintain disease remission, minimize disease and drug-induced adverse effects, and optimize growth and development. This article reviews current approaches to the management of patients with UC and CD and highlights issues specific to the treatment of children with IBD. The principal medical therapies used to induce disease remission in patients with UC are aminosalicylates (for mild disease), corticosteroids (for moderate disease), and cyclosporine (ciclosporin) (for severe disease). If a patient responds to the induction regimen, maintenance therapies that are used to prevent disease relapse include aminosalicylates, mercaptopurine, and azathioprine. Colectomy with creation of an ileal pouch anal anastomosis (J pouch) has become the standard of care for patients with severe or refractory colitis and results in an improved quality of life in most patients. Therefore, the risks associated with using increasingly potent immunosuppressant agents must be balanced in each case against a patient's desire to retain their colon and avoid a temporary or potentially permanent ileostomy. Decisions about drug therapy in the management of patients with CD are more complex and depend on both the location (e.g. gastroduodenal vs small intestinal vs colonic), as well as the behavior of the disease (inflammatory/mucosal vs stricturing vs perforating) in a given patient. Induction therapies for CD typically include aminosalicylates and antibiotics (for mild mucosal disease), nutritional therapy (including elemental or polymeric formulas), corticosteroids (for moderate disease), and infliximab (for corticosteroid-resistant or fistulizing disease). Aminosalicylates, mercaptopurine, azathioprine, methotrexate, and infliximab can be used as maintenance therapies. Because surgical treatment of CD is not curative, it is typically reserved for those patients either with persistent symptoms and disease limited to a small section of the intestine (e.g. the terminal ileum and cecum) or for the management of complications of the disease including stricture or abdominal abscess. When surgery is necessary, maintenance medications administered postoperatively will postpone recurrence. Patients with UC and CD are at risk for the development of micronutrient deficiencies (including folate, iron, and vitamin D deficiencies) and require close nutritional monitoring. In addition, patients with UC and CD involving the colon are at increased risk of developing colon cancer, and should be enrolled into a colonoscopy surveillance program after 8-10 years of disease duration.
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