Abstract
Objectives:
Celecoxib for the treatment of pain resulting from osteoarthritis (OA) was reviewed by the Tandvårds- och läkemedelsförmånsverket–Dental and Pharmaceutical Benefits Board (TLV) in Sweden in late 2010. This study aimed to evaluate the incremental cost-effectiveness ratio (ICER) of celecoxib plus a proton pump inhibitor (PPI) compared to diclofenac plus a PPI in a Swedish setting.
Methods:
The National Institute for Health and Care Excellence (NICE) in the UK developed a health economic model as part of their 2008 assessment of treatments for OA. In this analysis, the model was reconstructed and adapted to a Swedish perspective. Drug costs were updated using the TLV database. Adverse event costs were calculated using the regional price list of Southern Sweden and the standard treatment guidelines from the county council of Stockholm. Costs for treating cardiovascular (CV) events were taken from the Swedish DRG codes and the literature.
Results:
Over a patient’s lifetime treatment with celecoxib plus a PPI was associated with a quality-adjusted life year (QALY) gain of 0.006 per patient when compared to diclofenac plus a PPI. There was an increase in discounted costs of 529kr per patient, which resulted in an incremental cost-effectiveness ratio (ICER) of 82,313kr ($12,141). Sensitivity analysis showed that treatment was more cost effective in patients with an increased risk of bleeding or gastrointestinal (GI) complications.
Conclusions:
The results suggest that celecoxib plus a PPI is a cost effective treatment for OA when compared to diclofenac plus a PPI. Treatment is shown to be more cost effective in Sweden for patients with a high risk of bleeding or GI complications. It was in this population that the TLV gave a positive recommendation. There are known limitations on efficacy in the original NICE model.
Transparency
Declaration of funding
This study was sponsored by Pfizer Inc.; however, the publication of study results was not contingent on the sponsor’s approval or censorship of the manuscript.
Declaration of financial/other relationships
NB and BP have disclosed that they received funding from Pfizer to conduct this study. RA has disclosed that he received funding from Pfizer as a consultant. ME has disclosed that he is a current employee of Pfizer and holds stock in the company. NB and BP are employees of BresMed, ME is an employee of Pfizer, and RA is an employee of ScHARR, University of Sheffield, Sheffield, UK, who were paid consultants to Pfizer in connection with the development of this manuscript. JME peer reviewers on this manuscript have no relevant financial or other relationships to disclose.
Acknowledgments
The authors would like to thank Pfizer for giving full permission to use their clinical data and the University of Sheffield for giving full permission to use their economic model.
Notes
*Celebrex is a registered trademark of Pfizer Inc.