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Quo Vadis HTA for Medical Devices in Central and Eastern Europe? Recommendations to Address Methodological Challenges
Objectives: Methodological challenges in the evaluation of medical devices (MDs) may be different for early and late technology adopter countries, as well as the potential health technology assessment (HTA) solutions to tackle them. This study aims to provide guidance to Central and Eastern European...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820783/ https://www.ncbi.nlm.nih.gov/pubmed/33490024 http://dx.doi.org/10.3389/fpubh.2020.612410 |
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author | Daubner-Bendes, Rita Kovács, Sándor Niewada, Maciej Huic, Mirjana Drummond, Michael Ciani, Oriana Blankart, Carl Rudolf Mandrik, Olena Torbica, Aleksandra Yfantopoulos, John Petrova, Guenka Holownia-Voloskova, Malwina Taylor, Rod S. Al, Maiwenn Piniazhko, Oresta Lorenzovici, László Tarricone, Rosanna Zemplényi, Antal Kaló, Zoltán |
author_facet | Daubner-Bendes, Rita Kovács, Sándor Niewada, Maciej Huic, Mirjana Drummond, Michael Ciani, Oriana Blankart, Carl Rudolf Mandrik, Olena Torbica, Aleksandra Yfantopoulos, John Petrova, Guenka Holownia-Voloskova, Malwina Taylor, Rod S. Al, Maiwenn Piniazhko, Oresta Lorenzovici, László Tarricone, Rosanna Zemplényi, Antal Kaló, Zoltán |
author_sort | Daubner-Bendes, Rita |
collection | PubMed |
description | Objectives: Methodological challenges in the evaluation of medical devices (MDs) may be different for early and late technology adopter countries, as well as the potential health technology assessment (HTA) solutions to tackle them. This study aims to provide guidance to Central and Eastern European (CEE) countries on how to address key challenges of HTA for MDs with special focus on the transferability of scientific evidence. Methods: As part of the COMED Horizon 2020 project, a comprehensive list of issues related to MD HTA were identified based on a targeted literature review. Health technology assessment issues which pose a greater challenge or require different solutions in late technology adopter countries were selected. Draught recommendations to address these issues were developed and discussed in a focus group. The recommendations were then validated with a wider group of experts, including HTA and reimbursement decision makers from CEE countries in May and June 2020. Results: A consolidated list of 11 recommendations were developed in 3 major areas: (1) clinical value assessment, focusing on the use of joint EU work, relying on real-world evidence, use of coverage with evidence development schemes, transferring evidence from foreign countries and addressing the challenges of learning curve and centre effect; (2) economic value assessment, covering cost calculation of complex medical devices and transferability of economic evaluations of MDs; (3) HTA processes, related to the frequent product modifications and various indications of MDs. Conclusions: Central and Eastern European countries with limited resources for conducting HTA, can benefit from HTA methods and evidence generated in early technology adopter countries. Considering the appropriate reuse of international HTA materials, late technology adopter countries can still implement HTA, even for MDs, which have a more limited evidence base compared with pharmaceuticals. |
format | Online Article Text |
id | pubmed-7820783 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78207832021-01-23 Quo Vadis HTA for Medical Devices in Central and Eastern Europe? Recommendations to Address Methodological Challenges Daubner-Bendes, Rita Kovács, Sándor Niewada, Maciej Huic, Mirjana Drummond, Michael Ciani, Oriana Blankart, Carl Rudolf Mandrik, Olena Torbica, Aleksandra Yfantopoulos, John Petrova, Guenka Holownia-Voloskova, Malwina Taylor, Rod S. Al, Maiwenn Piniazhko, Oresta Lorenzovici, László Tarricone, Rosanna Zemplényi, Antal Kaló, Zoltán Front Public Health Public Health Objectives: Methodological challenges in the evaluation of medical devices (MDs) may be different for early and late technology adopter countries, as well as the potential health technology assessment (HTA) solutions to tackle them. This study aims to provide guidance to Central and Eastern European (CEE) countries on how to address key challenges of HTA for MDs with special focus on the transferability of scientific evidence. Methods: As part of the COMED Horizon 2020 project, a comprehensive list of issues related to MD HTA were identified based on a targeted literature review. Health technology assessment issues which pose a greater challenge or require different solutions in late technology adopter countries were selected. Draught recommendations to address these issues were developed and discussed in a focus group. The recommendations were then validated with a wider group of experts, including HTA and reimbursement decision makers from CEE countries in May and June 2020. Results: A consolidated list of 11 recommendations were developed in 3 major areas: (1) clinical value assessment, focusing on the use of joint EU work, relying on real-world evidence, use of coverage with evidence development schemes, transferring evidence from foreign countries and addressing the challenges of learning curve and centre effect; (2) economic value assessment, covering cost calculation of complex medical devices and transferability of economic evaluations of MDs; (3) HTA processes, related to the frequent product modifications and various indications of MDs. Conclusions: Central and Eastern European countries with limited resources for conducting HTA, can benefit from HTA methods and evidence generated in early technology adopter countries. Considering the appropriate reuse of international HTA materials, late technology adopter countries can still implement HTA, even for MDs, which have a more limited evidence base compared with pharmaceuticals. Frontiers Media S.A. 2021-01-08 /pmc/articles/PMC7820783/ /pubmed/33490024 http://dx.doi.org/10.3389/fpubh.2020.612410 Text en Copyright © 2021 Daubner-Bendes, Kovács, Niewada, Huic, Drummond, Ciani, Blankart, Mandrik, Torbica, Yfantopoulos, Petrova, Holownia-Voloskova, Taylor, Al, Piniazhko, Lorenzovici, Tarricone, Zemplényi and Kaló. 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) and the copyright owner(s) 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 | Public Health Daubner-Bendes, Rita Kovács, Sándor Niewada, Maciej Huic, Mirjana Drummond, Michael Ciani, Oriana Blankart, Carl Rudolf Mandrik, Olena Torbica, Aleksandra Yfantopoulos, John Petrova, Guenka Holownia-Voloskova, Malwina Taylor, Rod S. Al, Maiwenn Piniazhko, Oresta Lorenzovici, László Tarricone, Rosanna Zemplényi, Antal Kaló, Zoltán Quo Vadis HTA for Medical Devices in Central and Eastern Europe? Recommendations to Address Methodological Challenges |
title | Quo Vadis HTA for Medical Devices in Central and Eastern Europe? Recommendations to Address Methodological Challenges |
title_full | Quo Vadis HTA for Medical Devices in Central and Eastern Europe? Recommendations to Address Methodological Challenges |
title_fullStr | Quo Vadis HTA for Medical Devices in Central and Eastern Europe? Recommendations to Address Methodological Challenges |
title_full_unstemmed | Quo Vadis HTA for Medical Devices in Central and Eastern Europe? Recommendations to Address Methodological Challenges |
title_short | Quo Vadis HTA for Medical Devices in Central and Eastern Europe? Recommendations to Address Methodological Challenges |
title_sort | quo vadis hta for medical devices in central and eastern europe? recommendations to address methodological challenges |
topic | Public Health |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820783/ https://www.ncbi.nlm.nih.gov/pubmed/33490024 http://dx.doi.org/10.3389/fpubh.2020.612410 |
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