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Developing patient centric medicines for older people: reflections from the draft EMA paper on the pharmaceutical development of medicines for use in the older population

  • Medicines Evaluation Board (MEB), DVRN: International Collaboration Center. ADB: Chair of MEB, Utrecht, the Netherlands.
  • Swedish Medical Products Agency (MPA), Department of Pharmaceutics and Biotechnology, Uppsala, Sweden.
  • State Institute for Drug Control (SUKL), Department of Pharmaceutical Assessment of Chemical and Herbal Products, Prague, Czech Republic.

Research output: Contribution to journal › Review article › peer-review

Abstract

Increased global longevity requires a re-evaluation of current structures in society to adapt to the consequential demographic shift. As (very) old people are prone to impaired human organ and body functions resulting in e.g. multimorbidity, polypharmacy, hospitalisation, and problems in medication management, it is increasingly acknowledged that re-evaluations should include the suitability of pharmaceutical patient care as one of the cornerstones of public health. Following the 2011 European Medicines Agency (EMA) "Geriatric Strategy", in 2017, the EMA published the draft "Reflection paper on the pharmaceutical development of medicines for use in the older population". The draft paper was opened for public consultation and specific attention and feedback (either supportive or with a proposal for revision) was asked on three design aspects: tablet breaking, drug administration through enteral feeding tubes and medication management. Following publication, the draft paper was presented at two public conferences attended by participants from different disciplines. This manuscript is intended to draw the attention of different stakeholder parties on the urgency to collaborate on the emerging issues arising from increasing longevity and multimorbidity, and especially those associated with pharmaceutical patient care and the drug product design, including the need for collaborative research into existing or emerging knowledge gaps. The manuscript focuses on the three aforementioned aspects of pharmaceutical development (tablet breaking, drug administration through enteral feeding tubes and medication management) as these highly relate to medication safety and efficacy and constitute persistent and typical challenges for older people, caregivers and healthcare professionals in daily clinical practice.

Original languageEnglish
Pages (from-to)2008-2013
JournalBritish Journal of Clinical Pharmacology
Volume86
Early online date24 Aug 2020
DOIs
Publication statusPublished - 2020

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

  • aged 80 and over [MeSH]
  • clinical pharmacology
  • drug regulation
  • health policy
  • medication safety
  • drug development
  • drug delivery
  • European Medicines Agency (EMA)
  • medication errors [MeSH]
  • public health
  • regulations
  • technology pharmaceutical [MeSH]

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