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Aminosalicylates, steroids and immunomodulators in IBD

Essential points for quick revision.

Synopsis

Use conventional IBD medicines for their correct induction or maintenance role, prevent cumulative corticosteroid harm, and apply reliable laboratory, infection and reproductive safeguards.

  • Mesalazine is effective for inducing and maintaining mild to moderate ulcerative colitis when formulation and route match extent; it has little general role in active Crohn disease.
  • Rectal 5-ASA is an active treatment, not an optional extra, for proctitis and left-sided disease; combined oral and topical delivery can outperform either route alone.
  • Systemic and locally acting corticosteroids induce remission but do not maintain it; steroid dependence, excess or refractoriness is a treatment outcome that demands a new strategy.

Key red flags

Fever, sepsis physiology, severe sore throat, spontaneous bleeding or mouth ulceration on thiopurine or methotrexate needs urgent blood count and infection assessment before another dose.

Investigation priorities

01
Baseline full blood count, liver and renal profileFirst step

Identify contraindications and create a safety comparator before conventional immunomodulation.

Management branches

5-ASAOptimise aminosalicylate treatment

Mild to moderate ulcerative colitis is suitable for a mucosal first-line strategy.

  1. Map proctitis, left-sided or extensive disease and choose suppository, enema and oral delivery that physically reaches the inflamed segment.
  2. Explain formulation, daily routine and adherence, obtain baseline renal function and check for salicylate, sulfasalazine or excipient-specific risk.
STEROIDUse induction without creating dependence

Objective activity needs faster control than optimised first-line or maintenance therapy provides.

Key medicines

MesalazinePreparation-specific oral or rectal induction followed by a licensed maintenance regimen.
Prednisolone or budesonide formulationTime-limited induction course with formulation, taper and duration specified explicitly.
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Sources and review status6 sources · checked 27 Aug 2026 · clinical review pending
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 27 Aug 2026; clinical approval remains outstanding.

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom