Efficacy of the newest COX-2 selective inhibitors in rheumatic disease

Curr Pharm Des. 2007;13(22):2228-36. doi: 10.2174/138161207781368819.

Abstract

Non-steroidal antiinflammatory drugs (NSAIDs) are standard treatment for the pain and inflammation associated with arthritis. Traditional NSAIDs and cyclooxygenase-2 (COX-2) selective inhibitors exhibit comparable efficacy, with different safety profiles. Traditional NSAIDs are associated with an increased risk of serious gastrointestinal (GI) adverse events versus COX-2 selective inhibitors, and chronic use frequently necessitates adjunctive therapy with gastroprotective agents. COX-2 selective inhibitors are often used in preference to avoid these GI adverse events. Recent studies have raised the concern that COX-2 selective inhibitors and traditional NSAIDs appear to be associated with a higher incidence of thrombotic cardiovascular events versus placebo. The key in prescribing these agents is for the physician to take a proactive approach to patient management and evaluation of GI and cardiovascular risk factors. This review examines the role of the newest COX-2 selective inhibitors, etoricoxib and lumiracoxib, in treating rheumatic disease.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Anti-Inflammatory Agents, Non-Steroidal / adverse effects
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use*
  • Arthritis, Gouty / drug therapy
  • Arthritis, Gouty / enzymology
  • Arthritis, Rheumatoid / drug therapy
  • Arthritis, Rheumatoid / enzymology
  • Cardiovascular Diseases / chemically induced
  • Cyclooxygenase 2 / metabolism*
  • Cyclooxygenase 2 Inhibitors / adverse effects
  • Cyclooxygenase 2 Inhibitors / therapeutic use*
  • Diclofenac / adverse effects
  • Diclofenac / analogs & derivatives*
  • Diclofenac / therapeutic use
  • Etoricoxib
  • Gastrointestinal Hemorrhage / chemically induced
  • Humans
  • Membrane Proteins / metabolism*
  • Osteoarthritis / drug therapy
  • Osteoarthritis / enzymology
  • Patient Selection
  • Pyridines / adverse effects
  • Pyridines / therapeutic use*
  • Rheumatic Diseases / drug therapy*
  • Rheumatic Diseases / enzymology
  • Risk Assessment
  • Risk Factors
  • Spondylitis, Ankylosing / drug therapy
  • Spondylitis, Ankylosing / enzymology
  • Sulfones / adverse effects
  • Sulfones / therapeutic use*

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Cyclooxygenase 2 Inhibitors
  • Membrane Proteins
  • Pyridines
  • Sulfones
  • Diclofenac
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • lumiracoxib
  • Etoricoxib