Abstract
AIM: To assess the required characteristics (cost, sensitivity and specificity) of a pharmacogenomic test for being a cost-effective prevention of angiotensin-converting enzyme inhibitors induced angioedema. Furthermore, we assessed the influence of only testing high-risk populations.
MATERIALS & METHODS: A decision tree was used.
RESULTS: With a willingness-to-pay threshold of €20,000 and €80,000 per quality adjusted life year, a 100% sensitive and specific test may have a maximum cost of €1.30 and €1.95, respectively. When only genotyping high-risk populations, the maximum test price would be €5.03 and €7.55, respectively.
CONCLUSION: This theoretical pharmacogenomic test is only cost-effective at high specificity, high sensitivity and a low price. Only testing high-risk populations yields more realistic maximum test prices for cost-effectiveness of the intervention.
| Original language | English |
|---|---|
| Pages (from-to) | 1143-1153 |
| Number of pages | 11 |
| Journal | Pharmacogenomics |
| Volume | 18 |
| Issue number | 12 |
| DOIs | |
| Publication status | Published - Aug 2017 |
Keywords
- ACE inhibitor induced angioedema
- ACE inhibitors
- adverse drug reactions
- angioedema
- cardiovascular drugs
- cost-effectiveness
- health technology assessment
- pharmacogenomic test