Cyclooxygenase-2 (COX-2) inhibitors constitute a new group of non-steroidal
anti-inflammatory drugs (NSAIDs) which, at recommended doses, block prosta
glandin production by cyclooxygenase-2, but not by cyclooxygenase-1.
Two COX-2 inhibitors are currently available in Australia - celecoxib, whic
h is taken twice daily, and rofecoxib, which is taken once daily. Both drug
s act rapidly in providing pain relief and their antiinflammatory analgesic
effect in osteoarthritis and rheumatoid arthritis is equivalent to standar
d doses of non-selective NSAIDs.
Celecoxib and rofecoxib show significantly lower incidences of gastrotoxici
ty (as measured by endoscopic studies and gastrointestinal ulcers and bleed
s) than non-selective NSAIDs.
There is Level 2 evidence that COX-2 inhibitors:
reduce pain in classic pain models - third-molar extraction, dysmenorrhoea
and after orthopaedic surgery;
reduce pain and disability in osteoarthritis of the hip and knee; and
reduce pain and disability in rheumatoid arthritis.
Other adverse effects, such as interference with antihypertensive agents an
d the potential to produce renal dysfunction in patients with compromised r
enal function by COX-2 inhibitors, seem similar to those of non-selective N
SAIDs.