Pantoprazole
Pantoprazole is a potent **proton pump inhibitor (PPI)** used to treat and prevent gastric acid-related pathologies, such as gastric ulcers, erosive esophagitis, and stress-related mucosal disease. While **omeprazole** is the most widely recognized oral PPI in veterinary medicine, pantoprazole is highly valued in clinical practice for its **intravenous (IV) formulation**. This makes it an excellent choice for hospitalized, critically ill patients (e.g., dogs or cats with severe pancreatitis, parvoviral enteritis, or active gastrointestinal bleeding) who cannot tolerate oral medications or have compromised GI absorption. * **Clinical Pearl:** Although its plasma half-life is very short (about 1 hour), its clinical effect lasts for 24 hours or more due to irreversible binding at the receptor site. * It has also been shown to directly reduce *in vitro* counts of *Helicobacter pylori* and is utilized in some eradication protocols.
กลไกการออกฤทธิ์: Pantoprazole is a substituted benzimidazole weak base. It accumulates in the highly acidic environment of the gastric parietal cell secretory canaliculi, where it is protonated and converted into its active sulfenamide form. * **Mechanism:** The active form binds **irreversibly via covalent disulfide bonds** to the **H+/K+ ATPase enzyme system** (the "proton pump") at the secretory surface of gastric parietal cells. * **Pathway:** Systemic circulation → Parietal cell → Acidic canaliculi → Active sulfenamide → **Irreversible inhibition of H+/K+ ATPase** → Profound suppression of both basal and stimulated gastric acid secretion. Because the binding is irreversible, acid secretion only resumes when new proton pump enzymes are synthesized by the parietal cell, explaining the prolonged duration of action despite rapid systemic clearance.
ขนาดยาตามชนิดสัตว์
- Gastric acid suppression · 0.5-1 mg/kg · IV · q24h · Administer over 15 minutes
- All uses (ulcers, oesophagitis, hypersecretory conditions) · 0.7-1.0 mg/kg · IV · q24h · Not specified · Administer over 15 min. Oral dose not established but likely similar to IV dose.
- Gastric acid suppression in neonatal foals · 1.5 mg/kg · IV · once daily · From an experimental study evaluating normal neonatal foals. Further studies required for critically ill patients.
- Intravenous treatment of stress-related mucosal disease · 0.7-1 mg/kg · IV · once daily
- Gastric acid suppression · 0.5-1 mg/kg · IV · q24h · Administer over 15 minutes
- All uses (ulcers, oesophagitis, hypersecretory conditions) · 0.7-1.0 mg/kg · IV · q24h · Not specified · Administer over 15 min. Oral dose not established but likely similar to IV dose.
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วิธีการให้ยา
ข้อห้ามใช้
- Known hypersensitivity to pantoprazole or other substituted benzimidazole PPIs
- Intramuscular (IM) or Subcutaneous (SQ) administration (parenteral form must be given IV)
- Intramuscular (IM) administration
- Subcutaneous (SC) administration
อาการไม่พึงประสงค์
- Diarrhea
- Headache (reported in humans)
- Hyperglycemia (rare, ~1% in humans)
- Injection site reactions (thrombophlebitis, abscess) with IV use
- Potential increased risk of community-acquired pneumonia (noted in human literature)
- Diarrhoea
- Headache
- Hyperglycaemia (rare)
- Increased risk of pneumonia
- Thrombophlebitis (associated with IV injection)
อันตรกิริยาระหว่างยา
- Ketoconazole, itraconazole, iron, ampicillin esters · Decreased drug absorption due to increased gastric pH (these drugs require an acidic environment for optimal absorption)
- Sucralfate · May decrease the bioavailability of orally administered pantoprazole
- Warfarin · Pantoprazole may increase the anticoagulant effect
- Itraconazole · Decreased absorption of itraconazole due to increased gastric pH · moderate
- Ketoconazole · Decreased absorption of ketoconazole due to increased gastric pH · moderate
การติดตาม
- Efficacy (resolution of clinical signs, improvement in gastric pH)
- Adverse effects (vomiting, diarrhea)
- Injection site reactions (thrombophlebitis, abscess) if used IV
- Resolution of clinical signs (vomiting, melena, regurgitation)
- Gastric pH (in critical care settings)
- IV catheter site for signs of thrombophlebitis
การได้รับยาเกินขนาด
Limited information available in veterinary species. A single oral dose of 887 mg/kg was lethal in dogs, causing acute toxic signs including ataxia, hypo-activity, and tremor. In humans, single oral overdoses up to 600 mg have been reported without adversity. In the event of a large overdose, contact an animal poison control center for guidance.
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