the European Union’s Horizon 2020 research and innovation programme(825162)
Patients' perspectives are important to identify preferences, estimate values and
appreciate unmet medical needs in the process of research and development and subsequent
assessment of new health technologies. Patient and public involvement in health technology
assessment (HTA) is essential in understanding and assessing wider implications of
coverage and reimbursement decisions for patients, their relatives, caregivers, and
the general population. There are two approaches to incorporating the patients' voice
in HTA, preferably used in a mix. In the first one, patients, caregivers and/or their
representatives directly participate at discussions in different stages of the HTA
process, often at the same table with other stakeholders. Secondly, patient involvement
activities can be supported by evidence on patient value and experience collected
directly from patients, caregivers and/or their representatives often by patient groups
Patient involvement practices, however, are limited in Central and Eastern European
(CEE) countries without clear methodology or regulatory mechanisms to guide patient
involvement in the HTA process. This poses the question of transferability of practices
used in other countries, and might call for the development of new CEE-specific guidelines
and methods. In this study we aim to map potential barriers of patient involvement
in HTA in countries of the CEE region.