Safety of Ketorolac Before Dermal Procedures
Ketorolac should not be taken 12 hours before a dermal procedure due to its significant antiplatelet effects and increased risk of bleeding complications. 1
Mechanism of Concern
Ketorolac is a potent non-steroidal anti-inflammatory drug (NSAID) that:
- Inhibits both COX-1 and COX-2 enzymes
- Affects platelet aggregation, which can significantly impair hemostasis 1
- Has a half-life of 4-6 hours, but its antiplatelet effects may persist longer 2
Recommended Timing for Discontinuation
For patients undergoing dermal procedures:
Discontinuation timing:
- Stop ketorolac at least 24 hours before any dermal procedure
- For patients with renal impairment, consider stopping 36-48 hours before the procedure 1
Risk stratification:
Evidence Supporting Recommendation
The FDA drug label for ketorolac explicitly warns about:
- Increased risk of bleeding complications when used perioperatively
- Postoperative hematomas and wound bleeding reported with perioperative use 1
- The drug label specifically states: "peri-operative use of ketorolac tromethamine should be avoided and postoperative use be undertaken with caution when hemostasis is critical" 1
Alternative Pain Management Options
If pain management is needed before a dermal procedure:
Selective COX-2 inhibitors (like celecoxib) have minimal effects on platelet function and may be safer alternatives for perioperative pain management 3
Acetaminophen can be considered as it does not affect coagulation 4
Important Caveats
- Even short-term therapy with ketorolac is not without risk 1
- The American College of Chest Physicians guidelines recommend continuing certain antiplatelet drugs for minor dermatologic procedures, but this recommendation does not extend to ketorolac, which has more potent antiplatelet effects 4
- There is a documented case of a lethal idiosyncratic reaction to ketorolac in a patient with mastocytosis, highlighting its potential for serious adverse effects 4
Conclusion
The evidence strongly supports avoiding ketorolac 12 hours before dermal procedures due to bleeding risk. The FDA drug label provides the most definitive guidance on this issue, explicitly cautioning against perioperative use when hemostasis is critical.