Economic analysis of pharmacogenomic-guided clopidogrel treatment in Serbian patients with myocardial infarction undergoing primary percutaneous coronary intervention

Author:

Mitropoulou Christina1,Fragoulakis Vasilios23,Rakicevic Ljiljana B4,Novkovic Mirjana M4,Vozikis Athanassios5,Matic Dragan M6,Antonijevic Nebojsa M78,Radojkovic Dragica P4,van Schaik Ron H1,Patrinos George P2

Affiliation:

1. Department of Clinical Chemistry, Erasmus University Medical Center, Rotterdam, The Netherlands

2. Department of Pharmacy, School of Health Sciences, University of Patras, Patras, Greece

3. National School of Public Health, Athens, Greece

4. Institute for Molecular Genetics & Genetic Engineering, University of Belgrade, Belgrade, Serbia

5. Economics Department, University of Piraeus, Piraeus, Greece

6. Emergency Department, Clinic for Cardiology, Clinical Center of Serbia, Belgrade, Serbia

7. Faculty of Medicine, University of Belgrade, Belgrade, Serbia

8. Clinic for Cardiology, Clinical Center of Serbia, Belgrade, Serbia

Abstract

Introduction: Clopidogrel, which is activated by the CYP2C19 enzyme, is among the drugs for which all major regulatory agencies recommend genetic testing to be performed to identify a patient's CYP2C19 genotype in order to determine the optimal antiplatelet therapeutic scheme. The CYP2C19*2 and CYP2C19*3 variants are loss-of-function alleles, leading to abolished CYP2C19 function and thus have the risk of thrombotic events for carriers of these alleles on standard dosages, while the CYP2C19*17 allele results in CYP2C19 hyperactivity. Aims: Here, we report our findings from a retrospective study to assess whether genotyping for the CYP2C19*2 allele was cost effective for myocardial infarction patients receiving clopidogrel treatment in the Serbian population compared with the nongenotype-guided treatment. Results: We found that 59.3% of the CYP2C19*1/*1 patients had a minor or major bleeding event versus 42.85% of the CYP2C19*1/*2 and *2/*2, while a reinfarction event occurred only in 2.3% of the CYP21C9*1/*1 patients, compared with 11.2% of the CYP2C19*1/*2 and CYP2C19*2/*2 patients. There were subtle differences between the two patient groups, as far as the duration of hospitalization and rehabilitation is concerned, in favor of the CYP2C19*1/*1 group. The mean cost for the CYP2C19*1/*1 patients was estimated at €2547 versus €2799 in the CYP2C19*1/*2 and CYP2C19*2/*2 patients. Furthermore, based on the overall CYP2C19*1/*2 genotype frequencies in the Serbian population, a break-even point analysis indicated that performing the genetic test prior to drug prescription represents a cost-saving option, saving €13 per person on average. Conclusion: Overall, our data demonstrate that pharmacogenomics-guided clopidogrel treatment may represent a cost-saving approach for the management of myocardial infarction patients undergoing primary percutaneous coronary intervention in Serbia.

Publisher

Future Medicine Ltd

Subject

Pharmacology,Genetics,Molecular Medicine

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