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Implementation of coverage with evidence development schemes for medical devices: A decision tool for late technology adopter countries
Experiences with coverage with evidence development (CED) schemes are fairly limited in Central and Eastern European (CEE) countries, which are usually late adopters of new health technologies. Our aim was to put forward recommendations on how CEE health technology assessment bodies and payer organi...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9543994/ https://www.ncbi.nlm.nih.gov/pubmed/35322478 http://dx.doi.org/10.1002/hec.4504 |
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author | Kovács, Sandor Kaló, Zoltán Daubner‐Bendes, Rita Kolasa, Katarzyna Hren, Rok Tesar, Tomas Reckers‐Droog, Vivian Brouwer, Werner Federici, Carlo Drummond, Mike Zemplényi, Antal Tamás |
author_facet | Kovács, Sandor Kaló, Zoltán Daubner‐Bendes, Rita Kolasa, Katarzyna Hren, Rok Tesar, Tomas Reckers‐Droog, Vivian Brouwer, Werner Federici, Carlo Drummond, Mike Zemplényi, Antal Tamás |
author_sort | Kovács, Sandor |
collection | PubMed |
description | Experiences with coverage with evidence development (CED) schemes are fairly limited in Central and Eastern European (CEE) countries, which are usually late adopters of new health technologies. Our aim was to put forward recommendations on how CEE health technology assessment bodies and payer organizations can apply CED to reduce decision uncertainty on reimbursement of medical devices, with a particular focus on transferring the structure and data from CED schemes in early technology adopter countries in Western Europe. Structured interviews on the practices and feasibility of transferring CED schemes were conducted and subsequently, a draft tool for the systematic classification of decision alternatives and recommendations was developed. The decision tool was reviewed in a focus group discussion and validated within a wider group of CEE experts in a virtual workshop. Transferability assessment is needed in case of (1) joint implementation of a CED scheme; (2) transferring the structure of an existing CED scheme to a CEE country; (3) reimbursement decisions that are linked to outcomes of an ongoing CED scheme in another country and (4) real‐world evidence transferred from completed CED schemes. Efficient use of available resources may be improved by adequately transferring evidence and policy tools from early technology adopter countries. |
format | Online Article Text |
id | pubmed-9543994 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95439942022-10-14 Implementation of coverage with evidence development schemes for medical devices: A decision tool for late technology adopter countries Kovács, Sandor Kaló, Zoltán Daubner‐Bendes, Rita Kolasa, Katarzyna Hren, Rok Tesar, Tomas Reckers‐Droog, Vivian Brouwer, Werner Federici, Carlo Drummond, Mike Zemplényi, Antal Tamás Health Econ Supplement Papers Experiences with coverage with evidence development (CED) schemes are fairly limited in Central and Eastern European (CEE) countries, which are usually late adopters of new health technologies. Our aim was to put forward recommendations on how CEE health technology assessment bodies and payer organizations can apply CED to reduce decision uncertainty on reimbursement of medical devices, with a particular focus on transferring the structure and data from CED schemes in early technology adopter countries in Western Europe. Structured interviews on the practices and feasibility of transferring CED schemes were conducted and subsequently, a draft tool for the systematic classification of decision alternatives and recommendations was developed. The decision tool was reviewed in a focus group discussion and validated within a wider group of CEE experts in a virtual workshop. Transferability assessment is needed in case of (1) joint implementation of a CED scheme; (2) transferring the structure of an existing CED scheme to a CEE country; (3) reimbursement decisions that are linked to outcomes of an ongoing CED scheme in another country and (4) real‐world evidence transferred from completed CED schemes. Efficient use of available resources may be improved by adequately transferring evidence and policy tools from early technology adopter countries. John Wiley and Sons Inc. 2022-03-23 2022-09 /pmc/articles/PMC9543994/ /pubmed/35322478 http://dx.doi.org/10.1002/hec.4504 Text en © 2022 The Authors. Health Economics published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Supplement Papers Kovács, Sandor Kaló, Zoltán Daubner‐Bendes, Rita Kolasa, Katarzyna Hren, Rok Tesar, Tomas Reckers‐Droog, Vivian Brouwer, Werner Federici, Carlo Drummond, Mike Zemplényi, Antal Tamás Implementation of coverage with evidence development schemes for medical devices: A decision tool for late technology adopter countries |
title | Implementation of coverage with evidence development schemes for medical devices: A decision tool for late technology adopter countries |
title_full | Implementation of coverage with evidence development schemes for medical devices: A decision tool for late technology adopter countries |
title_fullStr | Implementation of coverage with evidence development schemes for medical devices: A decision tool for late technology adopter countries |
title_full_unstemmed | Implementation of coverage with evidence development schemes for medical devices: A decision tool for late technology adopter countries |
title_short | Implementation of coverage with evidence development schemes for medical devices: A decision tool for late technology adopter countries |
title_sort | implementation of coverage with evidence development schemes for medical devices: a decision tool for late technology adopter countries |
topic | Supplement Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9543994/ https://www.ncbi.nlm.nih.gov/pubmed/35322478 http://dx.doi.org/10.1002/hec.4504 |
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