The cost-effectiveness of cyclooxygenase-2 selective inhibitors in the management of chronic arthritis

Ann Intern Med. 2003 May 20;138(10):795-806. doi: 10.7326/0003-4819-138-10-200305200-00007.

Abstract

Background: Rofecoxib and celecoxib (coxibs) effectively treat chronic arthritis pain and reduce ulcer complications by 50% compared with nonselective nonsteroidal anti-inflammatory drugs (NSAIDs). However, their absolute risk reduction is small and the cost-effectiveness of treatment is uncertain.

Objective: To determine whether the degree of risk reduction in gastrointestinal complications by coxibs offsets their increased cost compared with a generic nonselective NSAID.

Design: Cost-utility analysis.

Data sources: Systematic review of MEDLINE and published abstracts.

Target population: Patients with osteoarthritis or rheumatoid arthritis who are not taking aspirin and who require long-term NSAID therapy for moderate to severe arthritis pain.

Perspective: Third-party payer.

Interventions: Naproxen, 500 mg twice daily, and coxib, once daily. Patients intolerant of naproxen were switched to a coxib.

Time horizon: Lifetime.

Outcome measures: Incremental cost per quality-adjusted life-year (QALY) gained.

Results of base-case analysis: Using a coxib instead of a nonselective NSAID in average-risk patients cost an incremental 275 809 dollars per year to gain 1 additional QALY.

Results of sensitivity analysis: The incremental cost per QALY gained decreased to 55 803 dollars when the analysis was limited to the subset of patients with a history of bleeding ulcers. The coxib strategy became dominant when the cost of coxibs was reduced by 90% of the current average wholesale price. In probabilistic sensitivity analysis, if a third-party payer was willing to pay 150 000 dollars per QALY gained, then 4.3% of average-risk patients would fall within the budget.

Conclusions: The risk reduction seen with coxibs does not offset their increased costs compared with nonselective NSAIDs in the management of average-risk patients with chronic arthritis. However, coxibs may provide an acceptable incremental cost-effectiveness ratio in the subgroup of patients with a history of bleeding ulcers.

Publication types

  • Meta-Analysis
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.
  • Review
  • Systematic Review

MeSH terms

  • Anti-Inflammatory Agents, Non-Steroidal / adverse effects
  • Anti-Inflammatory Agents, Non-Steroidal / economics*
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use
  • Arthritis, Rheumatoid / drug therapy*
  • Cardiovascular Diseases / chemically induced
  • Celecoxib
  • Chronic Disease
  • Cost-Benefit Analysis
  • Cyclooxygenase 2
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors / adverse effects
  • Cyclooxygenase Inhibitors / economics*
  • Cyclooxygenase Inhibitors / therapeutic use
  • Decision Support Techniques
  • Humans
  • Isoenzymes / antagonists & inhibitors*
  • Lactones / adverse effects
  • Lactones / economics*
  • Lactones / therapeutic use
  • Membrane Proteins
  • Osteoarthritis / drug therapy*
  • Peptic Ulcer / chemically induced
  • Peptic Ulcer / prevention & control
  • Prostaglandin-Endoperoxide Synthases
  • Pyrazoles
  • Quality-Adjusted Life Years
  • Recurrence
  • Risk Factors
  • Sensitivity and Specificity
  • Sulfonamides / adverse effects
  • Sulfonamides / economics*
  • Sulfonamides / therapeutic use
  • Sulfones

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors
  • Isoenzymes
  • Lactones
  • Membrane Proteins
  • Pyrazoles
  • Sulfonamides
  • Sulfones
  • rofecoxib
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Prostaglandin-Endoperoxide Synthases
  • Celecoxib