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μμ© κΈ°μ : Sucralfate exerts a **local, non-systemic effect** on the gastrointestinal mucosa. * **Polymerization:** After oral administration, sucralfate reacts with hydrochloric acid (HCl) in the stomach β undergoes cross-linking β 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.*
λλ¬Ό μ’ λ³ μ©λ
- General dosing Β· 0.25-0.5 grams PO q8-12h Β· PO Β· q8-12h
- Empirical dosage Β· ΒΌ of a 1 gram tablet per cat PO three to four times a day. Β· PO Β· TID-QID
- For gastric ulcers, esophagitis Β· 0.25-0.5 grams PO per cat PO q8-12h Β· PO Β· q8-12h
- General dosing Β· 75 mg/kg PO q4-6h; give 10 minutes prior to feeding Β· PO Β· q4-6h
- For adjunctive treatment (used with acid suppressive drugs) for preventing stress-induced ulcers in foals Β· 10-20 mg/kg PO q6-8h Β· PO Β· q6-8h
- For treating equine gastric ulcer syndrome Β· 20-40 mg/kg PO q8h Β· PO Β· q8h
- Right dorsal colitis (colonic ulcers) Β· 22 mg/kg PO q6-8h Β· PO Β· q6-8h Β· 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 Β· 0.5-1 gram PO three times a day. Suspensions are more therapeutic than intact tablets. Β· PO Β· TID
- General dosing Β· For large dogs: 1 gram PO q8; for smaller dogs: 0.5 gram PO q8h Β· PO Β· q8h
ν¬μ¬ κ²½λ‘
κΈκΈ°
- 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
μ΄μλ°μ
- Constipation (most common in dogs and humans)
- Vomiting (reported primarily in cats)
- Constipation (most common)
- Hypophosphatemia (rare, with prolonged use)
μ½λ¬Ό μνΈμμ©
- Azithromycin Β· Decreased oral absorption; separate dosing by at least 2 hours
- Ciprofloxacin / Enrofloxacin (and other oral fluoroquinolones) Β· Decreased oral absorption; separate dosing by at least 2 hours
- Diclofenac Β· Decreased oral absorption; separate dosing by at least 2 hours
- Digoxin Β· Decreased oral absorption; separate dosing by at least 2 hours Β· moderate
- Doxycycline Β· Decreased oral absorption; separate dosing by at least 2 hours
- Erythromycin Β· Decreased oral absorption; separate dosing by at least 2 hours
- Ketoconazole Β· Decreased oral absorption; separate dosing by at least 2 hours
- Levothyroxine Β· Decreased oral absorption; separate dosing by at least 2 hours
- Penicillamine Β· Decreased oral absorption; separate dosing by at least 2 hours
- Tetracycline Β· Decreased oral absorption; separate dosing by at least 2 hours
- Theophylline Β· Decreased oral absorption; separate dosing by at least 2 hours
- Vitamins (fat soluble) Β· Decreased oral absorption; separate dosing by at least 2 hours
- Warfarin Β· Decreased oral absorption; separate dosing by at least 2 hours
λͺ¨λν°λ§
- 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)
κ³Όμ©λ
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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