Treatment of Type 2 Gastric Ulcer in Older Adults
For an older adult with a Type 2 gastric ulcer, immediately discontinue all NSAIDs, initiate a proton pump inhibitor (PPI) at standard dosing (e.g., omeprazole 20-40 mg daily), and test for H. pylori with subsequent eradication therapy if positive. 1, 2
Immediate Management Steps
NSAID Discontinuation
- Stop all NSAIDs immediately as they significantly increase the risk of ulcer recurrence and complications, even with concurrent PPI therapy 3
- Substitute with acetaminophen for pain relief, which does not cause gastric injury 3
- If NSAIDs are absolutely necessary, use a COX-2 selective inhibitor (celecoxib) combined with a PPI for gastroprotection 1, 4
Acid Suppression Therapy
- Start a PPI immediately for ulcer healing—PPIs are superior to H2-receptor antagonists for healing NSAID-associated gastric ulcers 2
- Standard dosing: omeprazole 20-40 mg once daily or equivalent PPI 2, 3
- Continue treatment for a full 8 weeks to ensure complete healing 2, 3
- After healing, consider maintenance PPI therapy if NSAIDs must be continued indefinitely 2
H. pylori Testing and Eradication
Testing Strategy
- Test all patients with gastric ulcers for H. pylori infection using either urea breath test or stool antigen test 2, 5
- H. pylori infection increases the risk of NSAID-related complications by 2-4 fold 1, 3
- Testing during acute bleeding may yield false-negatives, so repeat testing if initially negative 2
Eradication Therapy (if H. pylori positive)
- Triple therapy regimen: PPI + amoxicillin 1000 mg twice daily + clarithromycin 500 mg twice daily for 14 days 2, 6
- Alternative: Bismuth quadruple therapy or concomitant therapy (non-bismuth quadruple therapy) due to increasing clarithromycin resistance 5
- H. pylori eradication reduces the likelihood of peptic ulcers by one-half in NSAID users 5
- Eradication before starting NSAIDs reduces subsequent ulcer risk (from 26% to 7% over 8 weeks) 1
Risk Stratification and Long-Term Management
Patient Risk Assessment
- Very high risk category: History of ulcer complications—avoid all NSAIDs if possible 1
- High risk category: Multiple risk factors (age >60, cardiovascular disease, concomitant aspirin/anticoagulants/steroids) 1
- Older adults are at particularly high risk for NSAID-associated adverse events, which increase in frequency and severity with age 1
Long-Term Prevention Strategy
- If NSAIDs cannot be avoided: Use COX-2 selective inhibitor plus PPI for maximum gastroprotection 1, 4
- The combination of COX-2 inhibitor and PPI provides superior protection compared to either agent alone 4
- For patients on warfarin: COX-2 inhibitor plus misoprostol 1
- For patients on low-dose aspirin: COX-2 inhibitor plus PPI or misoprostol 1
Critical Warnings and Common Pitfalls
Medication Considerations
- H2-receptor antagonists are inadequate for NSAID-associated gastric ulcers—they only protect against duodenal ulcers, not gastric ulcers 2
- Standard-dose misoprostol (800 mg/day) is superior to PPIs for preventing gastric ulcers in H. pylori-negative NSAID users, but has significant side effects limiting tolerability 7, 8
- Poor compliance with gastroprotective agents increases the risk of NSAID-induced adverse events 4-6 fold 1, 3
H. pylori Eradication Nuances
- Among patients already on long-term NSAIDs, H. pylori eradication is less effective for preventing NSAID ulcers compared to NSAID-naïve patients 1, 9
- H. pylori eradication is most beneficial for primary prophylaxis (before starting NSAIDs) rather than secondary prevention (after ulcer has occurred) 7
- Despite reduced effectiveness in chronic NSAID users, all H. pylori-infected patients with peptic ulcers should receive eradication therapy regardless of NSAID use 7
Cardiovascular Considerations
- COX-2 inhibitors carry increased cardiovascular risk—avoid in patients where CV risk exceeds GI bleeding risk 1
- Some traditional NSAIDs (particularly ibuprofen) may interfere with the antiplatelet effect of aspirin 1
- Diclofenac has been identified as having potentially higher risk for adverse cardiovascular events 1