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

  • Joost W. Geenen (Lead / Corresponding author)
  • , Ekaterina V. Baranova
  • , Folkert W. Asselbergs
  • , Anthonius de Boer
  • , Rick A. Vreman
  • , Colin N. A. Palmer
  • , Anke Hilse Maitland-van der Zee
  • , Anke M. Hövels
  • , PREDICTION-ADR Consortium

    Research output: Contribution to journalArticlepeer-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
    JournalPharmacogenomics
    Volume18
    Issue number12
    Early online date26 Jul 2017
    DOIs
    Publication statusPublished - Aug 2017

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • Journal article
    • Adverse drug reactions
    • Angioedema
    • ACE inhibitors ACE inhibitor induced angioedema
    • Cardiovascular drugs
    • Cost–effectiveness
    • Health technology assessment
    • Pharmacogenomic test

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