Pantoprazole (Pantocid) Dosing in Hospitalized Patients
For hospitalized patients requiring stress ulcer prophylaxis or acid suppression, administer pantoprazole 40 mg intravenously once daily. 1
Standard Intravenous Dosing
- The FDA-approved dose is 40 mg IV once daily, administered over 15 minutes, for patients unable to take oral medication. 1, 2
- This dosing regimen effectively suppresses gastric acid secretion and maintains basal acid output below target levels for at least 24 hours. 1
- The 40 mg IV dose produces comparable antisecretory effects to 40 mg oral pantoprazole, with significant reduction in both maximum acid output and basal acid output compared to placebo. 1
Specific Clinical Scenarios
Stress Ulcer Prophylaxis in ICU Patients
- Administer 40 mg IV pantoprazole once daily during the ICU stay for patients at risk of gastrointestinal bleeding. 3
- This reduces clinically important gastrointestinal bleeding from 4.2% (placebo) to 2.5% (pantoprazole). 3
- However, mortality at 90 days is similar between pantoprazole and placebo (31.1% vs 30.4%), so the decision to use prophylaxis should weigh bleeding risk against potential adverse effects. 3
Pathological Hypersecretion (Zollinger-Ellison Syndrome)
- Start with 80 mg IV every 12 hours (total 160 mg/day) in divided doses. 1
- Doses of 160-240 mg daily in divided doses maintain basal acid secretion below target levels (≤10 mEq/h without prior gastric surgery; ≤5 mEq/h with prior surgery). 1
- Greater than 80% of patients achieve acid control with the 80 mg every 12 hours starting regimen. 1
Upper GI Bleeding with High-Risk Endoscopic Stigmata
- For patients with high-risk lesions after endoscopic hemostasis, use 80 mg IV bolus followed by 8 mg/hour continuous infusion for 72 hours. 4
- This high-dose regimen significantly reduces rebleeding rates and need for surgery compared to H2-receptor antagonists or placebo. 4
- The American College of Gastroenterology consensus supports this as a class effect achievable with either omeprazole or pantoprazole. 4
Transition to Oral Therapy
- Once the patient can tolerate oral intake, switch to pantoprazole 40 mg orally once daily, taken 30 minutes before breakfast on an empty stomach. 5
- The oral bioavailability is 77%, and switching from IV to oral maintains equivalent acid suppression. 1, 6
- For acute conditions like gastritis or esophagitis, continue treatment for 4-8 weeks. 5
Important Dosing Considerations
- Pantoprazole has lower relative potency than other PPIs (40 mg pantoprazole = 9 mg omeprazole equivalent). 7, 5
- No dose adjustment is needed for renal failure, as pharmacokinetics are unaltered. 6
- In severe liver cirrhosis, the half-life increases from 1.1 hours to 7-9 hours, but routine dose adjustment is typically not required. 6
- The elimination half-life is approximately 1.1 hours, with clearance of 0.1 L/h/kg. 6
Common Pitfalls to Avoid
- Do not administer pantoprazole with food or antacids, as this significantly reduces absorption and efficacy. 5
- Avoid empiric twice-daily dosing unless treating H. pylori infection or high-risk upper GI bleeding post-endoscopy, as this increases costs and adverse event risk without proven benefit for standard indications. 5
- Consider de-prescribing or dose reduction once acute symptoms resolve, as most hospitalized patients do not require long-term PPI therapy. 7
- Monitor for return of symptoms when transitioning from IV to oral or reducing dose, which would indicate need to return to higher dose. 7