Sucralfate
Sucralfate is a locally-acting **gastroprotectant** primarily used in the treatment and management of oral, esophageal, gastric, and duodenal ulcers. It is also occasionally employed to prevent drug-induced (e.g., NSAID or aspirin) gastric erosions, though its efficacy for prophylaxis is considered sporadic. > **Clinical Pearl:** Sucralfate is often described in veterinary medicine as a "liquid band-aid" for the gastrointestinal tract. Because it requires an acidic environment to properly polymerize and coat ulcers, the timing of administration relative to feeding and other antacids (like H2-receptor antagonists or proton pump inhibitors) is critical. While it has been used in human medicine as a phosphate binder for patients with hyperphosphatemia secondary to renal failure, veterinary studies (such as in healthy cats) have shown mixed or insignificant results regarding its ability to lower serum phosphorus levels.
Mecanismo: Sucralfate exerts a **local, non-systemic effect** on the gastrointestinal mucosa. * **Polymerization:** After oral administration, sucralfate reacts with hydrochloric acid (HCl) in the stomach → undergoes cross-linking → forms a highly viscous, paste-like complex. * **Barrier Formation:** This complex carries a strong negative charge and binds tightly to the positively charged **proteinaceous exudates** (like albumin and fibrinogen) found at ulcer sites. This forms an insoluble physical barrier that protects the ulcerated tissue from further degradation by **pepsin**, acid, and bile salts. * **Enzyme & Bile Acid Inactivation:** Sucralfate directly inactivates **pepsin** and binds to bile acids, reducing their mucosal toxicity. * **Cytoprotection:** It exhibits cytoprotective properties, likely mediated through the local stimulation and release of **prostaglandin E2 (PGE2)** and **prostaglandin I2 (PGI2)**, which enhance mucosal blood flow and mucus/bicarbonate secretion. *Note: Sucralfate does not significantly alter gastric acid output or pancreatic enzyme activity.*
Dosificación por especie
- General dosing · 0.25-0.5 grams PO q8-12h · PO · q8-12h
- Empirical dosage · ¼ of a 1 gram tablet per cat PO three to four times a day. · PO · TID-QID
- For gastric ulcers, esophagitis · 0.25-0.5 grams PO per cat PO q8-12h · PO · q8-12h
- General dosing · 75 mg/kg PO q4-6h; give 10 minutes prior to feeding · PO · q4-6h
- For adjunctive treatment (used with acid suppressive drugs) for preventing stress-induced ulcers in foals · 10-20 mg/kg PO q6-8h · PO · q6-8h
- For treating equine gastric ulcer syndrome · 20-40 mg/kg PO q8h · PO · q8h
- Right dorsal colitis (colonic ulcers) · 22 mg/kg PO q6-8h · PO · q6-8h · Sucralfate alone may not be beneficial in treatment of equine gastric ulcer syndrome, but can be used in conjunction with acid-suppressive therapy and may be more suited for treatment of right dorsal colitis.
- For esophagitis · 0.5-1 gram PO three times a day. Suspensions are more therapeutic than intact tablets. · PO · TID
- General dosing · For large dogs: 1 gram PO q8; for smaller dogs: 0.5 gram PO q8h · PO · q8h
Vías de administración
Contraindicaciones
- No absolute contraindications
- Use with caution in patients with decreased gastrointestinal transit times (e.g., megacolon, ileus) due to the risk of constipation
- Known hypersensitivity to sucralfate
Efectos adversos
- Constipation (most common in dogs and humans)
- Vomiting (reported primarily in cats)
- Constipation (most common)
- Hypophosphatemia (rare, with prolonged use)
Interacciones farmacológicas
- Azithromycin · Decreased oral absorption; separate dosing by at least 2 hours
- Ciprofloxacin / Enrofloxacin (and other oral fluoroquinolones) · Decreased oral absorption; separate dosing by at least 2 hours
- Diclofenac · Decreased oral absorption; separate dosing by at least 2 hours
- Digoxin · Decreased oral absorption; separate dosing by at least 2 hours · moderate
- Doxycycline · Decreased oral absorption; separate dosing by at least 2 hours
- Erythromycin · Decreased oral absorption; separate dosing by at least 2 hours
- Ketoconazole · Decreased oral absorption; separate dosing by at least 2 hours
- Levothyroxine · Decreased oral absorption; separate dosing by at least 2 hours
- Penicillamine · Decreased oral absorption; separate dosing by at least 2 hours
- Tetracycline · Decreased oral absorption; separate dosing by at least 2 hours
- Theophylline · Decreased oral absorption; separate dosing by at least 2 hours
- Vitamins (fat soluble) · Decreased oral absorption; separate dosing by at least 2 hours
Monitoreo
- Clinical efficacy (resolution of vomiting, melena, anorexia, or abdominal pain)
- Endoscopic examination of ulcer healing
- Fecal occult blood
- Resolution of clinical signs of GI ulceration (e.g., vomiting, melena, anorexia)
- Fecal consistency (monitor for constipation)
Sobredosis
Overdosage is highly unlikely to cause any significant systemic problems due to minimal absorption. Laboratory animals receiving massive doses up to 12 grams/kg orally demonstrated no incidence of mortality. The primary concern with a massive overdose would be constipation.
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