Abstract
AIM: To investigate the cost-effectiveness of pharmacogenetic-guided phenprocoumon dosing versus standard anticoagulation care in Dutch patients with atrial fibrillation.
MATERIALS & METHODS: Using a decision-analytic Markov model, cost-effectiveness of pharmacogenetic-guided therapy versus standard care was estimated.
RESULTS: Compared with standard care, the pharmacogenetic-guided dosing strategy increased quality-adjusted life-years (QALYs) only very slightly and increased costs by €15. The incremental cost-effectiveness ratio was €2658 per QALY gained. In sensitivity analyses, the cost of genotyping had the largest influence on the cost-effectiveness ratio. In a probabilistic sensitivity analysis, the incremental costs of genotype-guided dosing were less than €20,000 per QALY gained in 75.6% of the simulations.
CONCLUSION: Pharmacogenetic-guided dosing of phenprocoumon has the potential to increase health slightly and may be able to achieve this in a cost-effective way. Owing to the many uncertainties it is too early to conclude whether or not patients starting phenprocoumon should be genotyped.
Original language | English |
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Pages (from-to) | 869-83 |
Number of pages | 15 |
Journal | Pharmacogenomics |
Volume | 14 |
Issue number | 8 |
DOIs | |
Publication status | Published - Jun 2013 |
Keywords
- Anticoagulants
- Aryl Hydrocarbon Hydroxylases
- Atrial Fibrillation
- Cost-Benefit Analysis
- Cytochrome P-450 CYP2C9
- Decision Support Techniques
- Genotype
- Humans
- Markov Chains
- Pharmacogenetics
- Phenprocoumon
- Warfarin