Who Requires Gastrointestinal Prophylaxis?
Critically ill patients at high risk (>4%) of clinically important gastrointestinal bleeding should receive GI prophylaxis, while those at lower risk (≤4%) generally do not require prophylaxis. 1
High-Risk Patients Requiring Prophylaxis
The following patients meet criteria for GI prophylaxis:
Definite High-Risk Criteria
- Mechanical ventilation for >48 hours (strongest predictor) 2, 3
- Coagulopathy (OR = 4.3 for GI bleeding; one of the strongest clinical predictors) 2, 3
- Acute liver failure requiring ICU admission 2
- Severe liver disease (e.g., MELD ≥35) 3
Additional High-Risk Criteria (≥2 factors increase risk significantly)
- Sepsis or septic shock 3, 1
- Acute kidney injury 3
- Shock states (particularly hypovolemic shock causing gastric hypoperfusion) 3
- Multiple organ failure 3
- History of GI bleeding or peptic ulcer disease 3
- Mechanical ventilation WITHOUT enteral nutrition 1
Moderate-Risk Criteria
- Chronic liver disease 1
- Burns >35% body surface area 4
- Traumatic brain injury or spinal cord injury 5
- Major surgery (vascular, abdominal) 3
Patients Who Do NOT Require Prophylaxis
- Critically ill patients without the above risk factors (bleeding risk ≤4%) 1
- General medical ward patients without critical illness 1
- Patients receiving adequate enteral nutrition (provides natural mucosal protection) 3
Preferred Prophylactic Agents
First-Line Recommendation
Proton pump inhibitors (PPIs) are preferred over H2-receptor antagonists (H2RAs) for stress ulcer prophylaxis in high-risk patients. 3, 1
- Intravenous pantoprazole 40 mg daily is the preferred agent for critically ill patients unable to take oral medications, particularly those with severe liver disease 3
- PPIs provide superior acid suppression and probably reduce bleeding risk more than H2RAs (moderate certainty evidence) 1
- Both PPIs and H2RAs are acceptable options when prophylaxis is indicated, though PPIs are generally preferred 3, 1
Second-Line Options
- H2-receptor antagonists (e.g., ranitidine) are effective but may be associated with drug interactions and encephalopathy in neurocritical patients 2, 5
- Sucralfate should NOT be used (strong recommendation against) due to inferior efficacy 1
Timing and Duration
- Initiate prophylaxis immediately upon ICU admission for high-risk patients 3
- Continue prophylaxis as long as risk factors persist and critical illness continues 3
- Discontinue when sepsis resolves and patient tolerates enteral nutrition 3
- Reevaluate daily for continued need based on risk factor resolution 3
Important Caveats
Potential Harms to Consider
- PPIs and H2RAs might increase pneumonia risk (low certainty evidence), though this remains controversial 1, 5
- No mortality benefit has been demonstrated with prophylaxis (moderate certainty) 1
- Clostridioides difficile infection risk may be increased with acid suppression 6
Special Populations
- Acute liver failure patients should receive PPIs or H2RAs (or sucralfate as second-line) given their high bleeding risk from coagulopathy 2
- Neurocritical care patients should preferentially receive PPIs over H2RAs to avoid encephalopathy and anticonvulsant drug interactions 5
- Cancer patients with neutropenia do not require routine prophylaxis for infectious diarrhea, only for stress ulcers if other high-risk criteria are met 2