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Single dose oral celecoxib for postoperative pain
J Barden1, J E Edwards, H J McQuay
1Pain Research Unit, University of Oxford, Churchill Hospital, Old Road, Oxford, UK, OX3 7LJ. jodie.barden@pru.ox.ac.uk
The Cochrane Database of Systematic Reviews
|June 14, 2003
Summary
Single-dose oral celecoxib effectively manages moderate to severe postoperative pain, offering relief comparable to aspirin and paracetamol. Further research is needed to confirm efficacy at recommended doses and quantify adverse effects.
Area of Science:
- Pharmacology
- Pain Management
- Clinical Trials
Background:
- Celecoxib, a selective cyclooxygenase-2 (COX-2) inhibitor, is used for chronic pain in osteoarthritis and rheumatoid arthritis.
- It is presumed to have fewer adverse effects than traditional non-steroidal anti-inflammatory drugs (NSAIDs).
- The efficacy of celecoxib for acute pain has not been systematically reviewed.
Purpose of the Study:
- To evaluate the analgesic efficacy of a single oral dose of celecoxib for moderate to severe postoperative pain.
- To assess the adverse effects associated with single-dose oral celecoxib in postoperative pain management.
Main Methods:
- Systematic review of randomized controlled trials (RCTs) comparing oral celecoxib to placebo for acute postoperative pain.
- Searched databases including Cochrane Library, MEDLINE, Biological Abstracts, PubMed, and Oxford Pain database (up to May 2002).
- Extracted data on pain relief (at least 50% over 4-6 hours) to calculate relative benefit (RB) and number-needed-to-treat (NNT).
Main Results:
- The number-needed-to-treat (NNT) for celecoxib 200 mg was 4.5 (CI 3.3 to 7.2), indicating one additional patient achieved significant pain relief compared to placebo.
- The median time to remedication was 5.1 hours with celecoxib 200 mg versus 1.5 hours with placebo.
- No serious or unexpected adverse effects were reported, though quantitative analysis was not possible.
Conclusions:
- Single-dose oral celecoxib is effective for postoperative pain relief, with efficacy similar to aspirin and paracetamol.
- The reviewed trials used a 200 mg dose, which is 50% less than recommended for acute pain.
- Further trials are necessary to assess the efficacy of the recommended 400 mg dose and to gather pooled data on adverse effects.