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1.
Appl Health Econ Health Policy ; 15(2): 119-126, 2017 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-27766548

RESUMO

With finite resources, healthcare payers must make difficult choices regarding spending and the ethical distribution of funds. Here, we describe some of the ethical issues surrounding inequity in healthcare in nine major European countries, using cancer care as an example. To identify relevant studies, we conducted a systematic literature search. The results of the literature review suggest that although prevention, access to early diagnosis, and radiotherapy are key factors associated with good outcomes in oncology, public and political attention often focusses on the availability of pharmacological treatments. In some countries this focus may divert funding towards cancer drugs, for example through specific cancer drugs funds, leading to reduced expenditure on other areas of cancer care, including prevention, and potentially on other diseases. In addition, as highly effective, expensive agents are developed, the use of value-based approaches may lead to unacceptable impacts on health budgets, leading to a potential need to re-evaluate current cost-effectiveness thresholds. We anticipate that the question of how to fund new therapies equitably will become even more challenging in the future, with the advent of expensive, innovative, breakthrough treatments in other therapeutic areas.


Assuntos
Prioridades em Saúde/ética , Oncologia/ética , Antineoplásicos/uso terapêutico , Europa (Continente) , Financiamento da Assistência à Saúde/ética , Humanos , Oncologia/economia , Neoplasias/tratamento farmacológico , Neoplasias/economia , Neoplasias/terapia , Mecanismo de Reembolso , Alocação de Recursos/ética
2.
Health Policy ; 119(5): 569-76, 2015 May.
Artigo em Inglês | MEDLINE | ID: mdl-25703539

RESUMO

OBJECTIVE: The objective of this study is to identify the possible barriers and critical success factors for the implementation of European collaboration in the field of relative effectiveness assessment (REA) of drugs. METHODS: Data were gathered through semi-structured interviews with representatives from eight European health technology assessment (HTA) organisations involved in assessment of drugs for coverage decision-making (AAZ, AIFA, AHTAPol, HAS, HVB, IQWIG, NICE and ZiN). RESULTS: Potential barriers identified mainly relate to methodology, resources and challenges with implementation in the respective national processes (e.g. legal restrictions). The most critical success factors for production of cross-border assessments were the continuous cooperation of competent partners, and the quality and timely availability of the assessment. CONCLUSION: Further adaptation of the process and methods is required for optimal collaboration. In the near future it can be expected that cross-border assessments will meet in particular the needs of smaller/middle-sized European countries and also European countries with less developed HTA systems as the potential efficiency/quality gains are the highest for these countries. Therefore, national implementation of cross-border assessments is especially likely in these countries in the coming years. Once more experience is gained with cross-border assessments, and successes become more evident, efficiency/quality gains may also be likely for some larger countries with well established processes.


Assuntos
Pesquisa Comparativa da Efetividade , Avaliação de Medicamentos , Cooperação Internacional , Estudos Transversais , Avaliação de Medicamentos/métodos , Europa (Continente) , Humanos , Modelos Organizacionais , Preparações Farmacêuticas/normas , Proibitinas , Pesquisa Qualitativa , Inquéritos e Questionários
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