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Measuring Costs of Cardiovascular Disease Prevention for Patients with Familial Hypercholesterolemia in
Lauren E Passero1, Megan C Roberts2
1Division of Pharmaceutical Outcomes and Policy, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA. laurl4@email.unc.edu.
Insights
Familial hypercholesterolemia screening and treatment incur significant real-world costs for lipid testing and medications. These estimates are crucial for improving cost-effectiveness models for cardiovascular disease prevention.
Area of Science:
- Pharmacoeconomics
- Cardiovascular Disease Prevention
- Genetic Lipid Disorders
Background:
- Familial hypercholesterolemia (FH) is a prevalent genetic disorder significantly increasing cardiovascular event risk.
- FH is a prime candidate for population-wide screening, yet cost data for interventions is scarce.
- Accurate real-world cost estimates are vital for economic analyses of FH screening and management.
Purpose of the Study:
- To estimate the real-world costs of lipid panel testing for hyperlipidemia.
- To determine the costs of statins, ezetimibe, and PCSK9 inhibitors for familial hypercholesterolemia treatment.
- To provide data for improving cost-effectiveness models of FH screening and care.
Main Methods:
- Utilized a commercial claims database to analyze costs.
- Calculated costs per lipid panel and per prescription by days' supply.
- Focused on patients with hyperlipidemia and familial hypercholesterolemia.
Main Results:
- Mean cost for a 90-day statin supply was $183.33, over double the 30-day supply cost ($79.35).
- PCSK9 inhibitors represented the highest mean medication costs for FH patients.
- Lipid testing and lipid-lowering therapies incur substantial real-world expenditures.
Conclusions:
- Lipid testing and medications for cardiovascular disease prevention in FH are associated with significant real-world costs.
- These cost data are essential for refining economic models of FH screening and management.
- Improved cost-effectiveness analyses can guide resource allocation for FH care.
Introduction:
Familial hypercholesterolemia is a common genetic condition that significantly increases an individual's risk of cardiovascular events such as heart attack, stroke, and cardiac death and is a candidate for population-wide screening programs. Economic analyses of strategies to identify and treat familial hypercholesterolemia are limited by a lack of real-world cost estimates for screening services and medications for reducing cardiovascular risk in this population.
Methods:
We estimated the cost of lipid panel testing in patients with hyperlipidemia and the cost of statins, ezetimibe, and PCKS9 inhibitors in patients with familial hypercholesterolemia from a commercial claims database and report costs and charges per panel and prescription by days' supply.
Results:
The mean cost for a 90-day supply for statins was $183.33, 2.3 times the mean cost for a 30-day supply at $79.35. PCSK9 inhibitors generated the highest mean costs among medications used by patients with familial hypercholesterolemia.
Conclusions:
Lipid testing and lipid-lowering medications for cardiovascular disease prevention generate substantial real-world costs which can be used to improve cost-effectiveness models of familial hypercholesterolemia screening and care management.
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