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Qualitative Analysis of the Design and Implementation of Benefit-Sharing Programs for Biologics Across Europe

BACKGROUND: To encourage the rational prescribing of biologics, payers across Europe have experimented with the implementation of benefit-sharing programs. Benefit-sharing programs are incentive programs that promote the use of ‘best-value’ off-patent biologics and biosimilars by driving changes in...

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Autores principales: Barcina Lacosta, Teresa, Vulto, Arnold G., Turcu-Stiolica, Adina, Huys, Isabelle, Simoens, Steven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8986662/
https://www.ncbi.nlm.nih.gov/pubmed/35303281
http://dx.doi.org/10.1007/s40259-022-00523-z
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author Barcina Lacosta, Teresa
Vulto, Arnold G.
Turcu-Stiolica, Adina
Huys, Isabelle
Simoens, Steven
author_facet Barcina Lacosta, Teresa
Vulto, Arnold G.
Turcu-Stiolica, Adina
Huys, Isabelle
Simoens, Steven
author_sort Barcina Lacosta, Teresa
collection PubMed
description BACKGROUND: To encourage the rational prescribing of biologics, payers across Europe have experimented with the implementation of benefit-sharing programs. Benefit-sharing programs are incentive programs that promote the use of ‘best-value’ off-patent biologics and biosimilars by driving changes in prescribing practices. The aim of these programs is to generate savings that can be shared among stakeholders involved (e.g. health authorities/payers, health care professionals, hospital managers/administration) and are generally used to improve the quality of health care and to increase patients’ access to innovative services and medicines. However, the scarcity of information concerning the design, implementation and outcomes of benefit-sharing programs limits the transfer of knowledge to institutions aiming to adopt these types of incentive schemes in the future. OBJECTIVE: The aim of our study was to map benefit-sharing experiences across Europe, to compare their design and implementation characteristics and to assess the impact of the different benefit-sharing strategies on the use of ‘best-value’ biologics. METHOD: Our approach was based on a literature review and on semi-structured interviews with payers/insurers, regulators, health care professionals and industry representatives. RESULTS: Our analysis revealed variable design characteristics for benefit-sharing programs, depending on the organization of the health care system, the specific timeframe, the care setting and the policy environment. All these aspects can influence the robustness of benefit-sharing initiatives and their potential to stay in effect over time. We also noted a generalized lack of transparency regarding the distribution of savings and how they are reinvested. This lack of transparency has raised questions on how to optimally implement benefit-sharing in the future. CONCLUSIONS: To realize the full potential of benefit-sharing programs, we identify the importance of (i) setting up and timely monitoring success indicators for these programs; (ii) including quality of care and access to care parameters as success indicators; (iii) establishing clear pathways for the transparent redistribution/reinvestment of savings and (iv) transparently communicating with patients about the outcomes of benefit-sharing programs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40259-022-00523-z.
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spelling pubmed-89866622022-04-22 Qualitative Analysis of the Design and Implementation of Benefit-Sharing Programs for Biologics Across Europe Barcina Lacosta, Teresa Vulto, Arnold G. Turcu-Stiolica, Adina Huys, Isabelle Simoens, Steven BioDrugs Original Research Article BACKGROUND: To encourage the rational prescribing of biologics, payers across Europe have experimented with the implementation of benefit-sharing programs. Benefit-sharing programs are incentive programs that promote the use of ‘best-value’ off-patent biologics and biosimilars by driving changes in prescribing practices. The aim of these programs is to generate savings that can be shared among stakeholders involved (e.g. health authorities/payers, health care professionals, hospital managers/administration) and are generally used to improve the quality of health care and to increase patients’ access to innovative services and medicines. However, the scarcity of information concerning the design, implementation and outcomes of benefit-sharing programs limits the transfer of knowledge to institutions aiming to adopt these types of incentive schemes in the future. OBJECTIVE: The aim of our study was to map benefit-sharing experiences across Europe, to compare their design and implementation characteristics and to assess the impact of the different benefit-sharing strategies on the use of ‘best-value’ biologics. METHOD: Our approach was based on a literature review and on semi-structured interviews with payers/insurers, regulators, health care professionals and industry representatives. RESULTS: Our analysis revealed variable design characteristics for benefit-sharing programs, depending on the organization of the health care system, the specific timeframe, the care setting and the policy environment. All these aspects can influence the robustness of benefit-sharing initiatives and their potential to stay in effect over time. We also noted a generalized lack of transparency regarding the distribution of savings and how they are reinvested. This lack of transparency has raised questions on how to optimally implement benefit-sharing in the future. CONCLUSIONS: To realize the full potential of benefit-sharing programs, we identify the importance of (i) setting up and timely monitoring success indicators for these programs; (ii) including quality of care and access to care parameters as success indicators; (iii) establishing clear pathways for the transparent redistribution/reinvestment of savings and (iv) transparently communicating with patients about the outcomes of benefit-sharing programs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40259-022-00523-z. Springer International Publishing 2022-03-18 2022 /pmc/articles/PMC8986662/ /pubmed/35303281 http://dx.doi.org/10.1007/s40259-022-00523-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Research Article
Barcina Lacosta, Teresa
Vulto, Arnold G.
Turcu-Stiolica, Adina
Huys, Isabelle
Simoens, Steven
Qualitative Analysis of the Design and Implementation of Benefit-Sharing Programs for Biologics Across Europe
title Qualitative Analysis of the Design and Implementation of Benefit-Sharing Programs for Biologics Across Europe
title_full Qualitative Analysis of the Design and Implementation of Benefit-Sharing Programs for Biologics Across Europe
title_fullStr Qualitative Analysis of the Design and Implementation of Benefit-Sharing Programs for Biologics Across Europe
title_full_unstemmed Qualitative Analysis of the Design and Implementation of Benefit-Sharing Programs for Biologics Across Europe
title_short Qualitative Analysis of the Design and Implementation of Benefit-Sharing Programs for Biologics Across Europe
title_sort qualitative analysis of the design and implementation of benefit-sharing programs for biologics across europe
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8986662/
https://www.ncbi.nlm.nih.gov/pubmed/35303281
http://dx.doi.org/10.1007/s40259-022-00523-z
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