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Review article: NSAIDs, gastroprotection and cyclo-oxygenase-II-selective inhibitors
R Micklewright1, S Lane, W Linley
1National Prescribing Centre, Liverpool, UK. Ruth.Micklewright@npc.nhs.uk
Alimentary Pharmacology & Therapeutics
|February 4, 2003
Summary
For patients at high risk of NSAID-induced gastrointestinal issues, consider gastroprotection. Misoprostol is proven effective in reducing serious complications, while the role of H. pylori eradication remains uncertain.
Area of Science:
- Gastroenterology
- Pharmacology
Background:
- Non-steroidal anti-inflammatory drugs (NSAIDs) pose a risk of serious upper gastrointestinal complications.
- Gastroprotection strategies are crucial for high-risk individuals.
Purpose of the Study:
- To evaluate the efficacy of gastroprotective agents and the role of Helicobacter pylori eradication in mitigating NSAID-associated gastrointestinal toxicity.
- To assess the gastrointestinal safety profiles of newer NSAIDs compared to traditional ones.
Main Methods:
- Review of large clinical outcome trials assessing gastrointestinal complications.
- Analysis of data from trials like VIGOR and CLASS for newer NSAIDs (rofecoxib, celecoxib).
Main Results:
- Misoprostol (800 micro g/day) demonstrated a reduction in serious upper gastrointestinal complications in a major trial.
- Initial analyses of rofecoxib and celecoxib suggested gastrointestinal benefits over non-selective NSAIDs.
- Concerns regarding long-term gastrointestinal and cardiovascular safety profiles of rofecoxib and celecoxib have emerged.
Conclusions:
- Gastroprotection with misoprostol or proton pump inhibitors should be considered for high-risk NSAID users.
- Routine H. pylori testing and eradication are not currently recommended for NSAID users.
- The risk-benefit profiles of rofecoxib and celecoxib require further understanding before routine widespread use; their gastrointestinal safety compared to non-selective NSAIDs is not definitively established.
- Evidence supporting the use of meloxicam and etodolac over non-selective NSAIDs or coxibs is not robust due to inadequate trial data.