Are new models needed to optimize the utilization of new medicines to sustain healthcare systems?


Creative Commons License

Godman B., Malmström R. E., Diogene E., Gray A., Jayathissa S., Timoney A., ...More

Expert Review of Clinical Pharmacology, vol.8, no.1, pp.77-94, 2014 (SCI-Expanded, Scopus) identifier identifier identifier

  • Publication Type: Article / Review
  • Volume: 8 Issue: 1
  • Publication Date: 2014
  • Doi Number: 10.1586/17512433.2015.990380
  • Journal Name: Expert Review of Clinical Pharmacology
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.77-94
  • Keywords: clinical pharmacology, critical drug evaluation, dabigatran, differential pricing, ivacaftor, managed entry agreements, new models, rational use of medicines, sofosbuvir, trastuzumab emtansine, ORPHAN DRUGS, PRESCRIBING EFFICIENCY, ATRIAL-FIBRILLATION, COST-EFFECTIVENESS, UNITED-STATES, HEPATITIS-C, PHARMACEUTICAL COMPANIES, INSTITUTIONAL CORRUPTION, TECHNOLOGY-ASSESSMENT, RHEUMATOID-ARTHRITIS
  • Open Archive Collection: AVESIS Open Access Collection
  • Lokman Hekim University Affiliated: No

Abstract

© 2015 Informa UK, Ltd.Medicines have made an appreciable contribution to improving health. However, even high-income countries are struggling to fund new premium-priced medicines. This will grow necessitating the development of new models to optimize their use. The objective is to review case histories among health authorities to improve the utilization and expenditure on new medicines. Subsequently, use these to develop exemplar models and outline their implications. A number of issues and challenges were identified from the case histories. These included the low number of new medicines seen as innovative alongside increasing requested prices for their reimbursement, especially for oncology, orphan diseases, diabetes and HCV. Proposed models center on the three pillars of pre-, peri- and post-launch including critical drug evaluation, as well as multi-criteria models for valuing medicines for orphan diseases alongside potentially capping pharmaceutical expenditure. In conclusion, the proposed models involving all key stakeholder groups are critical for the sustainability of healthcare systems or enhancing universal access. The models should help stimulate debate as well as restore trust between key stakeholder groups.