Gastroprotective strategies in chronic NSAID users: a cost-effectiveness analysis comparing single-tablet formulations with individual components

Value Health. 2013 Jul-Aug;16(5):769-77. doi: 10.1016/j.jval.2013.05.002. Epub 2013 Jul 11.

Abstract

Objectives: To evaluate the cost-effectiveness of competing gastroprotective strategies, including single-tablet formulations, in the prevention of gastrointestinal (GI) complications in patients with chronic arthritis taking nonsteroidal anti-inflammatory drugs (NSAIDs).

Methods: We performed a cost-utility analysis to compare eight gastroprotective strategies including NSAIDs, cyclooxygenase-2 inhibitors, proton pump inhibitors (PPIs), histamine-2 receptor antagonists, misoprostol, and single-tablet formulations. We derived estimates for outcomes and costs from medical literature. The primary outcome was incremental cost per quality-adjusted life-year gained. We performed sensitivity analyses to assess the effect of GI complications, compliance rates, and drug costs.

Results: For average-risk patients, NSAID + PPI cotherapy was most cost-effective. The NSAID/PPI single-tablet formulation became cost-effective only when its price decreased from €0.78 to €0.56 per tablet, or when PPI compliance fell below 51% in the NSAID + PPI strategy. All other strategies were more costly and less effective. The model was highly sensitive to the GI complication risk, costs of PPI and NSAID/PPI single-tablet formulation, and compliance to PPI. In patients with a threefold higher risk of GI complications, both NSAID + PPI cotherapy and single-tablet formulation were cost-effective.

Conclusions: NSAID + PPI cotherapy is the most cost-effective strategy in all patients with chronic arthritis irrespective of their risk for GI complications. For patients with increased GI risk, the NSAID/PPI single-tablet formulation is also cost-effective.

Keywords: compliance; cost-effectiveness; cost-utility; dyspepsia; gastrointestinal bleeding; nonsteroidal anti-inflammatory drugs; proton pump inhibitors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Inflammatory Agents, Non-Steroidal / administration & dosage
  • Anti-Inflammatory Agents, Non-Steroidal / adverse effects
  • Anti-Inflammatory Agents, Non-Steroidal / economics*
  • Anti-Ulcer Agents / administration & dosage
  • Anti-Ulcer Agents / economics*
  • Arthritis / drug therapy*
  • Assessment of Medication Adherence
  • Cost-Benefit Analysis
  • Costs and Cost Analysis
  • Cyclooxygenase 2 Inhibitors / administration & dosage
  • Cyclooxygenase 2 Inhibitors / adverse effects
  • Cyclooxygenase 2 Inhibitors / economics
  • Decision Support Techniques
  • Drug Combinations
  • Drug Therapy, Combination
  • Gastrointestinal Diseases / prevention & control*
  • Histamine H2 Antagonists / administration & dosage
  • Histamine H2 Antagonists / economics
  • Humans
  • Markov Chains
  • Misoprostol / administration & dosage
  • Misoprostol / economics
  • Models, Economic
  • Proton Pump Inhibitors / administration & dosage
  • Proton Pump Inhibitors / economics
  • Quality-Adjusted Life Years

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Anti-Ulcer Agents
  • Cyclooxygenase 2 Inhibitors
  • Drug Combinations
  • Histamine H2 Antagonists
  • Proton Pump Inhibitors
  • Misoprostol