π©Ί Sucralfate is a mucosal protectant used in peptic ulcer disease and stress ulcer prophylaxis.
It acts locally, coating ulcerated mucosa and forming a physical barrier against acid, pepsin, and bile salts.
π‘ Best given on an empty stomach before meals and at bedtime.
π§ About
- Composed of aluminium hydroxide complexed with sulfated sucrose.
- Forms a viscous, sticky gel that adheres to ulcer bases and epithelial cells in acidic conditions (pH < 4).
- Provides a local βbandageβ effect rather than systemic acid suppression.
- Useful for gastric and duodenal ulcers, chronic gastritis, and stress ulcer prevention in critically ill patients.
βοΈ Mode of Action
- In acidic environments, sucralfate polymerises to form a viscous, negatively charged complex that binds to positively charged proteins at the ulcer base.
- This barrier protects mucosa from pepsin, acid, and bile reflux.
- Also stimulates prostaglandin synthesis and bicarbonate secretion, enhancing mucosal defence and repair.
- No significant systemic absorption β most of its action is local.
π― Indications
- Benign gastric or duodenal ulceration (acute or chronic).
- Chronic gastritis or erosive gastritis.
- Prophylaxis of stress-related mucosal damage (e.g. in ICU or ventilated patients).
- Alternative to proton pump inhibitors when acid suppression is contraindicated (e.g. risk of infection, C. difficile).
π Dose
- Benign gastric ulceration: 1 g QDS or 2 g BD before meals and at bedtime for 6β12 weeks.
- Duodenal ulceration: 1 g QDS or 2 g BD for 6β12 weeks.
- Chronic gastritis: 1 g QDS or 2 g BD for up to 12 weeks.
- Stress ulcer prophylaxis: 1 g every 4 hours (max 8 g/day) PO or via nasogastric tube.
Formulation | Typical Dose | Frequency | Route |
Sucralfate | 1β2 g | 2β4 times daily | Oral |
β οΈ Cautions
- Do not administer simultaneously with enteral feeds β risk of bezoar formation and feed occlusion.
- Space at least 2 hours apart from other oral medications (it can reduce absorption).
- Use with caution in renal impairment due to aluminium accumulation and potential toxicity.
- Monitor in elderly or immobile patients β constipation risk.
π« Contraindications
- Known hypersensitivity to sucralfate or its components.
- Severe renal failure (risk of aluminium accumulation).
- Previous bezoar formation or GI obstruction.
π Adverse Effects
- Common: constipation (from aluminium content).
- Occasional: dry mouth, nausea, back pain.
- Rare: bezoar formation (especially in enterally fed or debilitated patients).
- Very rare: hypophosphataemia, aluminium toxicity in renal failure.
π€° Pregnancy and Breastfeeding
- Generally considered safe in pregnancy β minimal systemic absorption.
- Compatible with breastfeeding (acts locally in the GI tract).
π©Ί Clinical Pearls
- Take on an empty stomach (1 hour before or 2 hours after food) for best mucosal adherence.
- Separate from other oral drugs by 2 hours β sucralfate can bind and impair their absorption (e.g. digoxin, ciprofloxacin, warfarin, phenytoin).
- Prefer liquid formulation if patient has difficulty swallowing or for nasogastric administration.
- Useful in ICU stress ulcer prophylaxis when acid suppression is contraindicated (e.g. pneumonia risk).
π‘ Teaching Tip
- Contrast with PPIs and Hβ blockers β sucralfate does not reduce acid secretion but rather protects mucosa.
- Mnemonic: βSUCralfate SUCks onto ulcersβ β sticks to the ulcer base to protect healing tissue.
- Bezoars form when sucralfate binds to enteral feed proteins β emphasise spacing doses.
π References
- BNF: Sucralfate
- NICE CKS: Dyspepsia and Peptic Ulcer (2024)
- Konturek SJ et al., J Physiol Pharmacol 2011;62(6):555β564 β Gastric protection mechanisms.