[Cost-benefit analysis of new lipid-lowering agents]

Christopher Blaum1, Natalie Arnold1,2, Christoph Waldeyer3,4

  • 1Klinik für Kardiologie, Universitäres Herz- und Gefäßzentrum Hamburg, Universitätsklinikum Hamburg-Eppendorf, Martinistr. 52, 20246, Hamburg, Deutschland.

Herz
|April 25, 2022
PubMed

Insights

New lipid-lowering drugs address residual cardiovascular risk in patients with atherosclerotic cardiovascular disease. Cost-effectiveness analyses show PCSK9 inhibitors, bempedoic acid, and eicosapentaenoic acid offer value, particularly for high-risk individuals or those with statin intolerance.

Area of Science:

  • Cardiology
  • Pharmacoeconomics
  • Internal Medicine

Background:

  • Patients with atherosclerotic cardiovascular disease (ASCVD) face high risks of recurrent cardiovascular events, even with optimal statin and ezetimibe therapy.
  • Dyslipidemia is a primary driver of this residual risk, often failing to meet guideline-recommended target values.
  • Emerging lipid-lowering agents offer new options for managing this unmet need.

Purpose of the Study:

  • To evaluate the cost-effectiveness of novel lipid-lowering therapies for managing residual cardiovascular risk in patients with ASCVD.
  • To identify patient subgroups and clinical criteria that support the economic justification of these new treatments.

Main Methods:

  • Analysis of cost-effectiveness using key pharmacoeconomic variables such as Quality-Adjusted Life Years (QALY) and Incremental Cost-Effectiveness Ratio (ICER).
  • Review of clinical data and cost-effectiveness thresholds across different healthcare systems.
  • Assessment of specific agents including proprotein convertase subtilisin-kexin type 9 (PCSK9) inhibitors (alirocumab, evolocumab), PCSK9 small interfering RNA (siRNA) (inclisiran), bempedoic acid, and eicosapentaenoic acid.

Main Results:

  • PCSK9 inhibitors (alirocumab, evolocumab) and PCSK9 siRNA (inclisiran) are cost-effective, especially for patients with high baseline low-density lipoprotein cholesterol (LDL-C) or significant cardiovascular risk.
  • Bempedoic acid demonstrates cost-effectiveness primarily in patients with statin intolerance.
  • Eicosapentaenoic acid is generally cost-effective, though conclusive placebo-controlled efficacy data are pending.

Conclusions:

  • Novel lipid-lowering therapies offer valuable options for managing residual cardiovascular risk in ASCVD patients.
  • Cost-effectiveness varies by drug, patient profile (e.g., baseline LDL-C, cardiovascular risk, statin tolerance), and healthcare system thresholds.
  • Economic evaluations are crucial for guiding the optimal integration of these advanced treatments into clinical practice.

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