What is the typical hospital treatment for a Crohn's disease flare?

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Last updated: November 15, 2025View editorial policy

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Hospital Treatment for Crohn's Disease Flare

For patients with Crohn's disease requiring hospitalization due to severe disease activity, intravenous corticosteroids (methylprednisolone 40-60 mg/day) should be initiated immediately to induce symptomatic remission. 1

Initial Assessment Upon Admission

  • Rule out complications that require specific interventions rather than medical therapy alone, including intra-abdominal abscess, intestinal stricture with obstruction, or superimposed infection (such as Clostridium difficile). 2
  • Confirm active inflammation using biomarkers such as C-reactive protein (CRP) and fecal calprotectin to distinguish true inflammatory flares from functional symptoms. 2
  • Assess disease location and extent as this influences both immediate and subsequent treatment decisions. 1

Induction Therapy in Hospital

Intravenous Corticosteroids (First-Line)

  • Administer methylprednisolone 40-60 mg/day intravenously as the standard approach for severe Crohn's disease requiring hospitalization. 1
  • Evaluate clinical response within 1 week to determine whether therapy modification is needed—patients who fail to respond require escalation to biologic therapy. 1
  • The evidence supporting IV corticosteroids is conditional with low-quality data, but this remains standard practice for hospitalized patients. 1

Early Biologic Consideration

  • For patients with moderate-to-severe disease and risk factors for poor prognosis (young age at diagnosis, extensive disease, perianal involvement, deep ulcerations, prior surgery), consider initiating anti-TNF therapy during hospitalization rather than waiting for corticosteroid response. 1
  • Infliximab is preferred in the hospital setting due to its intravenous administration and rapid onset of action, dosed at 5 mg/kg at weeks 0,2, and 6. 1, 3
  • Combination therapy with infliximab plus a thiopurine (azathioprine or 6-mercaptopurine) is more effective than monotherapy for inducing and maintaining remission. 1

Monitoring Response and Treatment Modification

Corticosteroid Response Assessment

  • If no symptomatic improvement within 1 week of IV corticosteroids, escalate to biologic therapy immediately rather than continuing ineffective steroid treatment. 1
  • Once clinical improvement occurs, transition from IV to oral corticosteroids (prednisone 40-60 mg/day) and plan for discharge with outpatient taper. 1

Planning Maintenance Therapy

  • Initiate maintenance therapy before discharge to prevent relapse after corticosteroid taper—corticosteroids must never be used for maintenance. 1, 2
  • Options for maintenance include:
    • Anti-TNF biologics (infliximab or adalimumab) with or without thiopurine combination therapy 1
    • Ustekinumab for patients with inadequate response to or contraindications to anti-TNF therapy 1
    • Thiopurines (azathioprine 2-2.5 mg/kg/day or 6-mercaptopurine 1-1.5 mg/kg/day) for selected patients who achieved remission on corticosteroids 1
    • Parenteral methotrexate (15-25 mg subcutaneously weekly) as an alternative immunosuppressant 1

Important Contraindications and Cautions

What NOT to Use

  • Do NOT use 5-ASA/mesalazine for induction or maintenance of remission in Crohn's disease—it is ineffective regardless of disease severity or location. 1, 4, 2
  • Do NOT use oral budesonide for hospitalized patients with severe disease—it is only appropriate for mild-to-moderate ileal/right colonic disease in outpatients. 1, 4
  • Do NOT continue corticosteroids for maintenance—they carry significant risks including infections, metabolic complications, osteoporosis, and increased intra-abdominal abscess formation without preventing relapse. 1, 2

Corticosteroid-Related Complications

  • Monitor for steroid-related adverse effects including increased risk of abdominal/pelvic abscesses (particularly concerning in Crohn's disease), Cushing syndrome, hyperglycemia, hypertension, and osteoporosis. 2
  • Screen for latent tuberculosis before initiating biologic therapy, as the combination of corticosteroids and biologics significantly increases infection risk. 3

Treatment Algorithm for Hospitalized Patients

  1. Day 1-7: IV methylprednisolone 40-60 mg/day + rule out complications + assess for poor prognostic factors 1, 2

  2. If high-risk features present: Add infliximab 5 mg/kg IV (with thiopurine if not contraindicated) during hospitalization 1

  3. If standard risk and responding to steroids by day 7: Transition to oral prednisone, discharge with outpatient follow-up, and initiate maintenance therapy (thiopurine or biologic) 1, 4

  4. If no response by day 7: Escalate to anti-TNF therapy (infliximab preferred) or ustekinumab if anti-TNF contraindicated 1

  5. Before discharge: Ensure maintenance therapy initiated, corticosteroid taper plan established, and follow-up scheduled within 2-4 weeks 1, 4

Post-Discharge Monitoring

  • Evaluate response to anti-TNF induction between 8-12 weeks after initiation—if no response by week 14, discontinue and switch to alternative biologic. 4, 5
  • Taper prednisone over 8-12 weeks while monitoring for symptom recurrence that would indicate need for maintenance therapy optimization. 4
  • Assess for steroid dependency—patients requiring repeated courses or unable to taper below 10 mg/day require escalation to biologic or immunomodulator therapy. 2

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Treatment of Crohn's Disease Flares

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Treatment of Crohn's Disease Flare

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Treatment of Moderate Crohn's Disease

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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