What is the recommended induction and maintenance therapy for Crohn’s disease, including options for mild ileocecal disease, steroid contraindications, and biologic‑sparing strategies?

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Last updated: February 17, 2026View editorial policy

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Crohn's Disease Treatment

Induction Therapy

Mild-to-Moderate Ileocecal Disease

For mild-to-moderate Crohn's disease limited to the ileum and/or ascending colon, use budesonide 9 mg once daily for 8 weeks as first-line therapy. 1

  • Budesonide achieves remission in 51% of patients versus 20% with placebo, with significantly fewer side effects than systemic corticosteroids 1, 2
  • This locally-acting steroid is as effective as prednisolone 40 mg (tapering to 5 mg) for ileocecal disease but with superior tolerability 1
  • Evaluate response between 4-8 weeks; patients not responding by week 8-14 are unlikely to benefit from continued dosing 1, 3
  • Critical pitfall: Budesonide has no efficacy for distal colonic disease—do not use for left-sided or extensive colonic involvement 1, 2

Active Colonic Crohn's Disease

For colonic Crohn's disease, initiate systemic corticosteroids (prednisolone 40 mg daily, tapering by 5 mg weekly over 8 weeks). 1

  • Systemic steroids achieve remission in 60-83% of patients with moderate-to-severe disease 2
  • Sulfasalazine 4 g daily is an alternative for colonic disease when steroids are contraindicated, though less preferred due to side effects 1
  • For hospitalized patients with severe disease, use intravenous methylprednisolone 40-60 mg/day with response assessment within 1 week 2

When Steroids Are Contraindicated

Use exclusive enteral nutrition (EEN) as an alternative induction strategy when corticosteroids are contraindicated or refused by the patient. 1

  • EEN is less effective than corticosteroids in adults but represents a reasonable steroid-sparing option 1
  • In pediatric patients, EEN achieves remission in 73% and is considered primary therapy 1
  • Important caveat: Recent data show EEN achieves only 30% clinical remission and 13% endoscopic remission in moderate-to-severe pediatric disease, suggesting biologics may be needed earlier 4

Moderate-to-Severe Disease

For moderate-to-severe Crohn's disease (CDAI >300), initiate biologic therapy (infliximab 5 mg/kg at weeks 0,2, and 6) rather than relying on corticosteroids alone. 5

  • Infliximab is indicated for patients with inadequate response to conventional therapy 5
  • Consider biologics at initial diagnosis for moderate-to-severe disease to prevent progression and complications 2
  • Critical principle: When prescribing systemic corticosteroids, simultaneously plan for advanced therapy (biologics or immunomodulators) to avoid steroid dependency 2

Maintenance Therapy

Steroid Tapering and Discontinuation

Taper budesonide over 1-2 weeks once remission is achieved; never use any corticosteroid (including budesonide) for maintenance therapy. 1, 3

  • Budesonide is no more effective than placebo for maintaining remission at 6 or 12 months 3
  • Prolonged corticosteroid use increases mortality risk, particularly above 3000 mg prednisolone equivalent per year 2
  • Major pitfall: Corticosteroid dependency indicates treatment failure—escalate to immunomodulators or biologics rather than continuing steroids 2

Biologic-Sparing Maintenance Strategies

For patients requiring maintenance after steroid-induced remission, use thiopurines (azathioprine 1.5-2.5 mg/kg/day or mercaptopurine 0.75-1.5 mg/kg/day) as a biologic-sparing option. 1

  • Thiopurines are appropriate for maintenance but ineffective as monotherapy for induction due to slow onset of action 1
  • Consider immunomodulators for patients requiring two or more steroid courses within a calendar year 2
  • Important limitation: Thiopurines have only low-quality evidence for maintenance and should not delay biologic therapy in moderate-to-severe disease 1

When to Avoid Biologic-Sparing Approaches

Do not attempt biologic-sparing strategies in patients with moderate-to-severe disease, fistulizing disease, or those who have failed conventional therapy. 5

  • Infliximab 5 mg/kg every 8 weeks is the standard maintenance regimen for moderate-to-severe disease 5
  • For fistulizing disease, use infliximab (three infusions at weeks 0,2, and 6) combined with immunomodulation and surgical drainage as needed 1
  • Patients losing response on 5 mg/kg may be escalated to 10 mg/kg, though this increases infection risk 5

5-ASA Has No Role

Do not use 5-aminosalicylic acid (mesalamine) for either induction or maintenance therapy in Crohn's disease. 1

  • Meta-analyses consistently show no benefit over placebo for clinical remission (RR 1.28,95% CI 0.97-1.69) 1
  • The only exception is sulfasalazine for colonic disease when steroids are contraindicated, though this is not first-line 1

Treatment Algorithm Summary

  1. Mild ileocecal disease: Budesonide 9 mg daily × 8 weeks → taper over 1-2 weeks → monitor closely or bridge to thiopurine if relapse risk is high 1, 3

  2. Mild colonic disease: Prednisolone 40 mg tapering over 8 weeks (or sulfasalazine if contraindication) → bridge to thiopurine if steroid-dependent 1, 2

  3. Moderate-to-severe disease: Initiate biologic therapy (infliximab) at diagnosis; use systemic steroids only as bridge therapy while biologics take effect 2, 5

  4. Steroid contraindication: EEN for induction → transition to thiopurine or biologic for maintenance 1

  5. Repeated steroid courses: Escalate to biologics immediately; avoid repeated steroid exposure 2

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Corticosteroid Use in Crohn's Disease Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Budesonide in Small Bowel Crohn's Disease Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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