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Brief Report

Impact of chondroitin sulphate on health utility in patients with knee osteoarthritis: towards economic analysis

, , , , &
Pages 356-360 | Published online: 10 Nov 2009
 

Abstract

Abstract

Objectives: The first objective was to assess the effect of the chondroitin 4 and 6 sulphate (CS) on health-related quality of life using utility values in patients with knee osteoarthritis (OA) during a 24-month treatment course. The second objective was, using these data, to conduct economic analyses.

Methods: Data from the STOPP study was used. This study was a randomised, double-blind, placebo (PL) -controlled trial of 2-year duration. In the STOPP study, authors assessed quality of life using the Western Ontario and McMaster Osteoarthritis Index (WOMAC). WOMAC scores were translated into Health Utility Index (HUI) scores using a specific formula. Incremental cost effectiveness ratio (ICER) was calculated taking into account the cost of CS and its effect on HUI scores, compared to PL.

Results: At baseline, the mean (SD) HUI scores were 0.59 (0.17), and 0.59 (0.18) for the PL and CS groups, respectively (p=0.31 between the two groups). The mean (SD) HUI scores changes from baseline to 6 months were 0.02 (0.02), and 0.05 (0.01) for the PL and CS groups, respectively (p=0.03). After 24 months of follow-up, HUI score increases by 0.04 (0.02) in the PL group and by 0.05 (0.02) in the CS group (p=0.37). Using the price bracket of CS in Europe, ICER assessment always resulted in a cost below €30,000 per QALY gained, after 6, 12 and 24 months of treatment.

Conclusion: CS treatment increases health utilities in patients with knee OA compared to PL over the first 6 months of treatment. Economic evaluation based on these data suggests that CS treatment could be considered as cost-effective in patients with knee OA up to a period of 24 months. A limitation in this study is the absence of direct utility assessment as well as the absence of effective treatment as comparator.

Acknowledgement

Declaration of interest: This study was funded by a grants from the European Society for Clinical and Economical Aspect of Osteoarthritis and Osteoporosis (ESCEO)-Amgen and IBSA Institut Biochimique SA, Lugano, Switzerland. O.B. has disclosed that he has received lecture fees from IBSA. JYR has received consulting fees and lecture fees from IBSA. SS, AN, MH, and AA have disclosed they have no relevant financial relationships. The funding agencies had no role in the design and conduct of the study, in the collection, management, analysis, and interpretation of the data, in the preparation or approval of the manuscript or in the decision to submit the manuscript for publication.

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