The cost of clopidogrel use in atrial fibrillation in the ACTIVE-A trial

Andre Lamy1, Wesley Tong, Peggy Gao

  • 1CADENCE Research Group, Hamilton Health Sciences, Hamilton, Ontario, Canada. lamya@mcmaster.ca

Insights

Adding clopidogrel to aspirin (C+A) for atrial fibrillation patients unsuitable for vitamin K antagonist therapy is cost-neutral. Stroke prevention savings offset medication costs, supporting C+A use in this population.

Area of Science:

  • Cardiovascular Medicine
  • Health Economics
  • Clinical Trial Analysis

Background:

  • The ACTIVE-A trial showed clopidogrel plus aspirin (C+A) reduced stroke risk but increased bleeding in atrial fibrillation patients ineligible for vitamin K antagonists (VKAs).
  • This study evaluated the economic impact of C+A in this specific patient group.

Purpose of the Study:

  • To determine the cost-effectiveness of adding clopidogrel to aspirin therapy for patients with atrial fibrillation who cannot use VKA therapy.
  • To analyze the direct healthcare costs associated with C+A versus aspirin alone.

Main Methods:

  • Extracted healthcare utilization data, focusing on direct costs and hospitalizations.
  • Utilized Canadian unit costs and the Canadian list price for clopidogrel.
  • Applied a 3% annual discount rate to costs in 2008 Canadian dollars.

Main Results:

  • C+A demonstrated cost savings in healthcare utilization components, excluding the study medication itself.
  • Cost savings from stroke prevention effectively balanced the expense of clopidogrel.
  • Total costs per patient were $14,132 for C+A versus $13,756 for aspirin alone, an incremental cost of $376, with sensitivity analyses indicating potential cost savings or increases depending on clopidogrel pricing.

Conclusions:

  • Combination therapy with clopidogrel and aspirin is cost-neutral for atrial fibrillation patients unsuitable for VKA therapy under the study's conditions.
  • The cost of clopidogrel is offset by the prevention of expensive stroke-related healthcare events.
  • Findings support the use of C+A in ACTIVE-A patients for whom VKA therapy is not a suitable option.
Abstract

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