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Published on: November 30, 2022
Coxibs Refocus Attention on the Cardiovascular Risks of Non-Aspirin NSAIDs.
Dixon Thomas1, Zoya Ali2, Seeba Zachariah2
1College of Pharmacy, Gulf Medical University, Post Box: 4184, Ajman, United Arab Emirates. dixon.thomas@gmail.com.
Non-steroidal anti-inflammatory drugs (NSAIDs), including traditional and COX-2 specific drugs, carry cardiovascular risks. Clinical focus has shifted to balancing gastrointestinal and heart health when prescribing NSAIDs.
Area of Science:
- Pharmacology
- Cardiovascular Medicine
- Gastroenterology
Background:
- Non-steroidal anti-inflammatory drugs (NSAIDs) were developed as safer alternatives to steroids.
- Cyclooxygenase (COX)-2 inhibitors (coxibs) emerged, offering potentially reduced gastrointestinal risks compared to traditional NSAIDs.
- Market withdrawal of rofecoxib highlighted significant cardiovascular risks associated with coxibs, shifting clinical focus.
Purpose of the Study:
- To explain how coxibs influenced the understanding of NSAID cardiovascular safety.
- To discuss the implications of COX-2 inhibition on cardiovascular risk.
- To review the current landscape of NSAID safety, considering both gastrointestinal and cardiovascular aspects.
Main Methods:
- Review of clinical practice and market trends concerning NSAIDs and coxibs.
- Analysis of the relationship between COX-2 specificity and cardiovascular risk.
- Examination of current recommendations for NSAID selection.
Main Results:
- All NSAIDs, including traditional and coxibs, are associated with cardiovascular risks.
- COX-2 activity/specificity is a factor in cardiovascular risk, but not the sole determinant.
- Naproxen and ibuprofen show less COX-2 specificity than some traditional NSAIDs.
Conclusions:
- NSAIDs should be viewed as a single class regarding cardiovascular risk, distinct from aspirin.
- Clinicians must balance immediate gastrointestinal benefits against long-term cardiovascular risks.
- Ibuprofen and naproxen are preferred NSAIDs; coxibs are suitable for specific patient profiles with high GI risk and low CV risk.
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