Prevention and management of hyperphosphatemia with sevelamer in Canada: Health and economic consequences

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Abstract

Background: Sevelamer hydrochloride (Renagel) binds phosphate in patients with end-stage renal disease without the use of exogenous calcium and may reduce the progression of coronary vascular calcification. This intervention was shown to be cost-effective in the United States. This paper presents the Canadian adaptation. Methods: A discrete event simulation of the long-term cardiovascular implications of 1 year of phosphate binding in a prevalent hemodialysis population was used to estimate the cost-effectiveness of sevelamer use in Canada based on the demographics, comorbidities, physiological and renal characteristics. Initial calcification score and expected changes over 1 year were derived using regression equations developed from a clinical trial and translated to cardiovascular disease risk based on equations developed from a long-term cohort study. Direct medical costs from a Canadian Medicare perspective were taken from Ontario data. Ten replications of 10,000 patients over 13 years (discounting at 3%) were done for the base case and extensive sensitivity analyses were conducted. Results: The cardioprotective effect of sevelamer over 1 year is estimated to prevent 10 cardiovascular events and gain 18 life-years compared with calcium carbonate in 100 patients over a lifetime. These benefits are obtained at a net cost of CAD$2,096; an incremental cost-effectiveness ratio of CAD$12,384 per discounted life-year gained. Sensitivity analyses showed that the time horizon and efficacy were the most important factors. Conclusion: The results of this study provide evidence that use of sevelamer in Canada would be economically sound. © 2008, International Society for Pharmacoeconomics and Outcomes Research (ISPOR).

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Huybrechts, K. F., Caro, J. J., & O’Brien, J. A. (2009). Prevention and management of hyperphosphatemia with sevelamer in Canada: Health and economic consequences. Value in Health, 12(1), 16–19. https://doi.org/10.1111/j.1524-4733.2008.00408.x

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