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Are supplemental appraisal/reimbursement processes needed for rare disease treatments? An international comparison of country approaches

BACKGROUND: There is increasing recognition that conventional appraisal approaches may be unsuitable for assessing the value rare disease treatments (RDTs). This research examines what supplemental appraisal/reimbursement processes for RDTs are used internationally and how they can be characterised....

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Autores principales: Nicod, Elena, Whittal, Amanda, Drummond, Michael, Facey, Karen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7370450/
https://www.ncbi.nlm.nih.gov/pubmed/32690107
http://dx.doi.org/10.1186/s13023-020-01462-0
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author Nicod, Elena
Whittal, Amanda
Drummond, Michael
Facey, Karen
author_facet Nicod, Elena
Whittal, Amanda
Drummond, Michael
Facey, Karen
author_sort Nicod, Elena
collection PubMed
description BACKGROUND: There is increasing recognition that conventional appraisal approaches may be unsuitable for assessing the value rare disease treatments (RDTs). This research examines what supplemental appraisal/reimbursement processes for RDTs are used internationally and how they can be characterised. A qualitative research design was used that included (1) documentation of country appraisal/reimbursement processes for RDTs via questionnaires, desk research and iterative interactions with country experts to produce country vignettes, and (2) a cross-country analysis of these processes to identify and characterise features in supplemental processes for RDTs, and compare them to countries without supplemental processes. RESULTS: Thirty-two of the 37 invited countries participated in this research. Forty-one percent (13/32) use supplemental processes for RDTs. Their level of integration within standard processes ranged from low to high, characterised by whether they are separate or partially separate from the standard process, adapted or accelerated standard processes, or standard processes that may be applied to RDTs. They are characterised by features implemented throughout the appraisal process. These features are mechanisms that allow application of different standards to assess the value of the medicine, support to the appraisal/decision-making process, overcome the issues of lack of cost-effectiveness, or exempt from part of/the full appraisal/reimbursement process. They increase the likelihood of reimbursement by adjusting and/or foregoing part of the assessment process, or accepting to pay more for the same added benefit as for common conditions. A large proportion of countries with standard processes include one or more of these features (formally or informally) or are discussing potential changes in their systems. CONCLUSIONS: Results suggest revealed preferences to treat RDTs differently than conventional medicines. Some of the challenges around uncertainty and high price remain, but supplemental process features can support decision-making that is more flexible and consistent. Many of these processes are new and countries continue to adjust as they gain experience.
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spelling pubmed-73704502020-07-21 Are supplemental appraisal/reimbursement processes needed for rare disease treatments? An international comparison of country approaches Nicod, Elena Whittal, Amanda Drummond, Michael Facey, Karen Orphanet J Rare Dis Research BACKGROUND: There is increasing recognition that conventional appraisal approaches may be unsuitable for assessing the value rare disease treatments (RDTs). This research examines what supplemental appraisal/reimbursement processes for RDTs are used internationally and how they can be characterised. A qualitative research design was used that included (1) documentation of country appraisal/reimbursement processes for RDTs via questionnaires, desk research and iterative interactions with country experts to produce country vignettes, and (2) a cross-country analysis of these processes to identify and characterise features in supplemental processes for RDTs, and compare them to countries without supplemental processes. RESULTS: Thirty-two of the 37 invited countries participated in this research. Forty-one percent (13/32) use supplemental processes for RDTs. Their level of integration within standard processes ranged from low to high, characterised by whether they are separate or partially separate from the standard process, adapted or accelerated standard processes, or standard processes that may be applied to RDTs. They are characterised by features implemented throughout the appraisal process. These features are mechanisms that allow application of different standards to assess the value of the medicine, support to the appraisal/decision-making process, overcome the issues of lack of cost-effectiveness, or exempt from part of/the full appraisal/reimbursement process. They increase the likelihood of reimbursement by adjusting and/or foregoing part of the assessment process, or accepting to pay more for the same added benefit as for common conditions. A large proportion of countries with standard processes include one or more of these features (formally or informally) or are discussing potential changes in their systems. CONCLUSIONS: Results suggest revealed preferences to treat RDTs differently than conventional medicines. Some of the challenges around uncertainty and high price remain, but supplemental process features can support decision-making that is more flexible and consistent. Many of these processes are new and countries continue to adjust as they gain experience. BioMed Central 2020-07-20 /pmc/articles/PMC7370450/ /pubmed/32690107 http://dx.doi.org/10.1186/s13023-020-01462-0 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits 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/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Nicod, Elena
Whittal, Amanda
Drummond, Michael
Facey, Karen
Are supplemental appraisal/reimbursement processes needed for rare disease treatments? An international comparison of country approaches
title Are supplemental appraisal/reimbursement processes needed for rare disease treatments? An international comparison of country approaches
title_full Are supplemental appraisal/reimbursement processes needed for rare disease treatments? An international comparison of country approaches
title_fullStr Are supplemental appraisal/reimbursement processes needed for rare disease treatments? An international comparison of country approaches
title_full_unstemmed Are supplemental appraisal/reimbursement processes needed for rare disease treatments? An international comparison of country approaches
title_short Are supplemental appraisal/reimbursement processes needed for rare disease treatments? An international comparison of country approaches
title_sort are supplemental appraisal/reimbursement processes needed for rare disease treatments? an international comparison of country approaches
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7370450/
https://www.ncbi.nlm.nih.gov/pubmed/32690107
http://dx.doi.org/10.1186/s13023-020-01462-0
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