Early health technology assessments in pharmacogenomics: a case example in cardiovascular drugs

Joost W Geenen, Ekaterina V Baranova, Folkert W Asselbergs, Anthonius de Boer, Rick A Vreman, Colin Na Palmer, Anke H. Maitland-van der Zee, Anke M Hövels

Research output: Contribution to journalArticleAcademicpeer-review

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 languageEnglish
Pages (from-to)1143-1153
Number of pages11
JournalPharmacogenomics
Volume18
Issue number12
DOIs
Publication statusPublished - Aug 2017

Keywords

  • ACE inhibitor induced angioedema
  • ACE inhibitors
  • adverse drug reactions
  • angioedema
  • cardiovascular drugs
  • cost-effectiveness
  • health technology assessment
  • pharmacogenomic test

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