THE CARDIOVASCULAR PREVENTION MODEL (CPM), A GENERICALLY APPLICABLE MODEL FOR UNDERTAKING COST-EFFECTIVENESS ANALYSES OF PREVENTIVE INTERVENTIONS

Author(s)

Kate Webb, BA, Director1, Danny Liew, FRACP, PhD, Associate Professor2, Shane Nanayakkara, MBBS, Research Assistant3, Mendel Grobler, BPharm, MBA, Director4, Philippa J Delahoy, BSc, (Hons), Outcomes Research Statistical Lead5, Dianna J Magliano, BAppSc, MPH, PhD, Senior Epidemiologist61Pfizer Inc, Tadworth, Surrey, United Kingdom; 2 The University of Melbourne, Melbourne, Victoria, Australia; 3 Monash University, Melbourne, Victoria, Australia; 4 Pfizer Australia Pty Ltd, Sydney, NSW, Australia; 5 Pfizer Australia Pty Ltd, West Ryde, NSW, Australia; 6 International Diabetes Institute, Melbourne, Victoria, Australia

OBJECTIVES: To develop an epidemiological and economic model of cardiovascular disease (CVD, comprising coronary heart disease and stroke) that can be used to predict the future incidence of CVD in a given population (with representative cross-sectional data on cardiovascular risk factors) and undertake cost-effectiveness analyses of primary preventive strategies. METHODS: The CPM is a Markov model comprising four health states: ‘Alive without CVD’, ‘Alive with CVD’, ‘Dead from CVD’ and ‘Dead from non-CVD causes’. Individual subjects’ risks of CVD are derived from Framingham and UKPDS risk equations for non-diabetic and diabetic individuals, respectively. The risks of non-CVD death are drawn from local mortality data. To illustrate the function of the CPM, it was populated with 1335 Australian subjects from the nationally-representative 1999-2000 Australian Diabetes, Obesity and Lifestyle study who were: aged 35-74 years; free of CVD; and met current criteria for reimbursed access to statin treatment. Follow-up was simulated until death or age 75 years. The cost-effectiveness of atorvastatin for the primary prevention of CVD was modelled via decision analysis, using efficacy data from a recent meta-analysis of randomized trials and Australian cost and utility data. A 5% annual discount rate was applied. RESULTS: The CPM predicted that of Australians currently aged 35-74 years who were CVD-free but met criteria for lipid-lowering treatment, 23.3% would develop CVD and 24.3% would be dead by age 75 years without statin treatment. Atorvastatin would reduce these figures to 16.5% and 22.2%, representing numbers needed to treat of 14.7 and 46.2 to prevent CVD and death, respectively. The estimated ICERs were AUD$54,100/YoLS and AUD$35,600/QALY. CONCLUSIONS: The CPM allows for the prediction of future incidences of CVD in a population where representative cross-sectional data on cardiovascular risk factors are available. It can also be applied to cost-effectiveness analyses of primary preventive interventions for that population.

Conference/Value in Health Info

2008-11, ISPOR Europe 2008, Athens, Greece

Value in Health, Vol. 11, No. 6 (November 2008)

Code

PCV123

Topic

Clinical Outcomes, Economic Evaluation, Methodological & Statistical Research

Topic Subcategory

Clinical Outcomes Assessment, Cost/Cost of Illness/Resource Use Studies, Modeling and simulation

Disease

Cardiovascular Disorders

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