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A Comparison of Reimbursement Recommendations by European HTA Agencies: Is There Opportunity for Further Alignment?

Introduction: In Europe and beyond, the rising costs of healthcare and limited healthcare resources have resulted in the implementation of health technology assessment (HTA) to inform health policy and reimbursement decision-making. European legislation has provided a harmonized route for the regula...

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Autores principales: Allen, Nicola, Liberti, Lawrence, Walker, Stuart R., Salek, Sam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5491965/
https://www.ncbi.nlm.nih.gov/pubmed/28713265
http://dx.doi.org/10.3389/fphar.2017.00384
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author Allen, Nicola
Liberti, Lawrence
Walker, Stuart R.
Salek, Sam
author_facet Allen, Nicola
Liberti, Lawrence
Walker, Stuart R.
Salek, Sam
author_sort Allen, Nicola
collection PubMed
description Introduction: In Europe and beyond, the rising costs of healthcare and limited healthcare resources have resulted in the implementation of health technology assessment (HTA) to inform health policy and reimbursement decision-making. European legislation has provided a harmonized route for the regulatory process with the European Medicines Agency, but reimbursement decision-making still remains the responsibility of each country. There is a recognized need to move toward a more objective and collaborative reimbursement environment for new medicines in Europe. Therefore, the aim of this study was to objectively assess and compare the national reimbursement recommendations of 9 European jurisdictions following European Medicines Agency (EMA) recommendation for centralized marketing authorization. Methods: Using publicly available data and newly developed classification tools, this study appraised 9 European reimbursement systems by assessing HTA processes and the relationship between the regulatory, HTA and decision-making organizations. Each national HTA agency was classified according to two novel taxonomies. The System taxonomy, focuses on the position of the HTA agency within the national reimbursement system according to the relationship between the regulator, the HTA-performing agency, and the reimbursement decision-making coverage body. The HTA Process taxonomy distinguishes between the individual HTA agency's approach to economic and therapeutic evaluation and the inclusion of an independent appraisal step. The taxonomic groups were subsequently compared with national HTA recommendations. Results: This study identified European national reimbursement recommendations for 102 new active substances (NASs) approved by the EMA from 2008 to 2012. These reimbursement recommendations were compared using a novel classification tool and identified alignment between the organizational structure of reimbursement systems (System taxonomy) and HTA recommendations. However, there was less alignment between the HTA processes and recommendations. Conclusions: In order to move forward to a more harmonized HTA environment within Europe, it is first necessary to understand the variation in HTA practices within Europe. This study has identified alignment between HTA recommendations and the System taxonomy and one of the major implications of this study is that such alignment could support a more collaborative HTA environment in Europe.
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spelling pubmed-54919652017-07-14 A Comparison of Reimbursement Recommendations by European HTA Agencies: Is There Opportunity for Further Alignment? Allen, Nicola Liberti, Lawrence Walker, Stuart R. Salek, Sam Front Pharmacol Pharmacology Introduction: In Europe and beyond, the rising costs of healthcare and limited healthcare resources have resulted in the implementation of health technology assessment (HTA) to inform health policy and reimbursement decision-making. European legislation has provided a harmonized route for the regulatory process with the European Medicines Agency, but reimbursement decision-making still remains the responsibility of each country. There is a recognized need to move toward a more objective and collaborative reimbursement environment for new medicines in Europe. Therefore, the aim of this study was to objectively assess and compare the national reimbursement recommendations of 9 European jurisdictions following European Medicines Agency (EMA) recommendation for centralized marketing authorization. Methods: Using publicly available data and newly developed classification tools, this study appraised 9 European reimbursement systems by assessing HTA processes and the relationship between the regulatory, HTA and decision-making organizations. Each national HTA agency was classified according to two novel taxonomies. The System taxonomy, focuses on the position of the HTA agency within the national reimbursement system according to the relationship between the regulator, the HTA-performing agency, and the reimbursement decision-making coverage body. The HTA Process taxonomy distinguishes between the individual HTA agency's approach to economic and therapeutic evaluation and the inclusion of an independent appraisal step. The taxonomic groups were subsequently compared with national HTA recommendations. Results: This study identified European national reimbursement recommendations for 102 new active substances (NASs) approved by the EMA from 2008 to 2012. These reimbursement recommendations were compared using a novel classification tool and identified alignment between the organizational structure of reimbursement systems (System taxonomy) and HTA recommendations. However, there was less alignment between the HTA processes and recommendations. Conclusions: In order to move forward to a more harmonized HTA environment within Europe, it is first necessary to understand the variation in HTA practices within Europe. This study has identified alignment between HTA recommendations and the System taxonomy and one of the major implications of this study is that such alignment could support a more collaborative HTA environment in Europe. Frontiers Media S.A. 2017-06-30 /pmc/articles/PMC5491965/ /pubmed/28713265 http://dx.doi.org/10.3389/fphar.2017.00384 Text en Copyright © 2017 Allen, Liberti, Walker and Salek. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Allen, Nicola
Liberti, Lawrence
Walker, Stuart R.
Salek, Sam
A Comparison of Reimbursement Recommendations by European HTA Agencies: Is There Opportunity for Further Alignment?
title A Comparison of Reimbursement Recommendations by European HTA Agencies: Is There Opportunity for Further Alignment?
title_full A Comparison of Reimbursement Recommendations by European HTA Agencies: Is There Opportunity for Further Alignment?
title_fullStr A Comparison of Reimbursement Recommendations by European HTA Agencies: Is There Opportunity for Further Alignment?
title_full_unstemmed A Comparison of Reimbursement Recommendations by European HTA Agencies: Is There Opportunity for Further Alignment?
title_short A Comparison of Reimbursement Recommendations by European HTA Agencies: Is There Opportunity for Further Alignment?
title_sort comparison of reimbursement recommendations by european hta agencies: is there opportunity for further alignment?
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5491965/
https://www.ncbi.nlm.nih.gov/pubmed/28713265
http://dx.doi.org/10.3389/fphar.2017.00384
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