Genetic testing in patients with acute coronary syndrome undergoing percutaneous coronary intervention: a cost-effectiveness analysis

J Thromb Haemost. 2013 Jan;11(1):81-91. doi: 10.1111/jth.12059.

Abstract

Background: The CYP2C19 genotype is a predictor of adverse cardiovascular events in acute coronary syndrome (ACS) patients undergoing percutaneous coronary intervention (PCI) treated with clopidogrel.

Objectives: We aimed to evaluate the cost-effectiveness of a CYP2C19*2 genotype-guided strategy of antiplatelet therapy in ACS patients undergoing PCI, compared with two 'no testing' strategies (empiric clopidogrel or prasugrel).

Methods: We developed a Markov model to compare three strategies. The model captured adverse cardiovascular events and antiplatelet-related complications. Costs were expressed in 2010 US dollars and estimated using diagnosis-related group codes and Medicare reimbursement rates. The net wholesale price for prasugrel was estimated as $5.45 per day. A generic estimate for clopidogrel of $1.00 per day was used and genetic testing was assumed to cost $500.

Results: Base case analyses demonstrated little difference between treatment strategies. The genetic testing-guided strategy yielded the most QALYs and was the least costly. Over 15 months, total costs were $18 lower with a gain of 0.004 QALY in the genotype-guided strategy compared with empiric clopidogrel, and $899 lower with a gain of 0.0005 QALY compared with empiric prasugrel. The strongest predictor of the preferred strategy was the relative risk of thrombotic events in carriers compared with wild-type individuals treated with clopidogrel. Above a 47% increased risk, a genotype-guided strategy was the dominant strategy. Above a clopidogrel cost of $3.96 per day, genetic testing was no longer dominant but remained cost-effective.

Conclusions: Among ACS patients undergoing PCI, a genotype-guided strategy yields similar outcomes to empiric approaches to treatment, but is marginally less costly and more effective.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Coronary Syndrome / diagnosis
  • Acute Coronary Syndrome / economics*
  • Acute Coronary Syndrome / genetics
  • Acute Coronary Syndrome / mortality
  • Acute Coronary Syndrome / therapy*
  • Aryl Hydrocarbon Hydroxylases / genetics*
  • Aryl Hydrocarbon Hydroxylases / metabolism
  • Cerebrovascular Disorders / etiology
  • Clopidogrel
  • Computer Simulation
  • Cost-Benefit Analysis
  • Cytochrome P-450 CYP2C19
  • Decision Support Techniques
  • Disease-Free Survival
  • Drug Costs
  • Gene Frequency
  • Genetic Predisposition to Disease
  • Genetic Testing / economics*
  • Health Care Costs*
  • Hemorrhage / etiology
  • Humans
  • Insurance, Health, Reimbursement / economics
  • Kaplan-Meier Estimate
  • Markov Chains
  • Medicare / economics
  • Models, Economic
  • Myocardial Infarction / etiology
  • Percutaneous Coronary Intervention / adverse effects
  • Percutaneous Coronary Intervention / economics*
  • Percutaneous Coronary Intervention / mortality
  • Pharmacogenetics / economics
  • Phenotype
  • Piperazines / economics
  • Piperazines / metabolism
  • Piperazines / therapeutic use
  • Platelet Aggregation Inhibitors / economics
  • Platelet Aggregation Inhibitors / metabolism
  • Platelet Aggregation Inhibitors / therapeutic use
  • Prasugrel Hydrochloride
  • Predictive Value of Tests
  • Quality-Adjusted Life Years
  • Risk Assessment
  • Risk Factors
  • Thiophenes / economics
  • Thiophenes / metabolism
  • Thiophenes / therapeutic use
  • Thrombosis / economics
  • Thrombosis / genetics
  • Thrombosis / prevention & control
  • Ticlopidine / analogs & derivatives
  • Ticlopidine / economics
  • Ticlopidine / metabolism
  • Ticlopidine / therapeutic use
  • Time Factors
  • Treatment Outcome
  • United States

Substances

  • Piperazines
  • Platelet Aggregation Inhibitors
  • Thiophenes
  • Clopidogrel
  • Aryl Hydrocarbon Hydroxylases
  • CYP2C19 protein, human
  • Cytochrome P-450 CYP2C19
  • Prasugrel Hydrochloride
  • Ticlopidine