Improving patient access to novel medical technologies in Europe
Improving patient access to novel medical technologies in Europe
The European Society of Cardiology (ESC) organized a one-day workshop with clinicians, health economic experts, and health technology appraisal experts to discuss the equity of patient access to novel medical technologies in Europe. Two index technologies were considered: implantable cardioverter defibrillators (ICDs) and drug-eluting stents (DES). The use of ICDs range from 35 implants/million population in Portugal to 166 implants/million population in Germany, whereas for implants of DES (as percentage of total stents) it is lowest in Germany at 14% and high in Portugal at 65%. These differences can in part be explained by a lack of structured implementation of guidelines, the direct cost in relation to the overall healthcare budget, and to differences in procedures and models applied by Health Technology Assessment (HTA) agencies in Europe. The workshop participants concluded that physicians need to be involved in a more structured way in HTA and need to become better acquainted with its methods and terminology. Clinical guidelines should be systematically translated, explained, disseminated, updated, and adopted by cardiologists in Europe. Clinically appropriate, consistent and transparent health economic models need to be developed and high-quality international outcome and cost data should be used. A process for funding of a technology should be developed after a positive recommendation from HTA agencies. Both the ESC and the national cardiac societies should build-up health economic expertise and engage more actively in discussions with stakeholders involved in the provision of healthcare.
health technology assessment, des, drug eluting stents, icd, iplantable cardioverter defibrillators, health economics, esc guidelines, funding
882-885
Kearney, Peter
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Stokoe, Graham
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Breithardt, Günter
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Longson, Carole
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Marco, Jean
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Morgan, John
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Priori, Silvia
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Ruether, Alric
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Taylor, Rod
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Hertog, Michaël
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April 2006
Kearney, Peter
155e868c-236a-4838-88de-d4da36207282
Stokoe, Graham
8a5066a6-08b8-4b04-9b78-fc67dc49ce8f
Breithardt, Günter
b733b43c-dc8b-4052-b268-2d7b4140602e
Longson, Carole
faf52ddd-4f35-4518-8441-7c56e08fbd0f
Marco, Jean
b7c7e6fa-40a5-46c9-8b1a-ccf87d928126
Morgan, John
b9446d5b-771e-4065-a84d-d05050c7bbe4
Priori, Silvia
c2b3eb47-2034-4781-92dd-5602ec270e33
Ruether, Alric
c8663e38-7f4a-4649-b862-1b1a0b0ba262
Taylor, Rod
12fb1379-fab8-4713-9c5d-2662b5b6ca14
Hertog, Michaël
9e55f833-aceb-4f99-ba7c-82af2a681105
Kearney, Peter, Stokoe, Graham, Breithardt, Günter, Longson, Carole, Marco, Jean, Morgan, John, Priori, Silvia, Ruether, Alric, Taylor, Rod and Hertog, Michaël
(2006)
Improving patient access to novel medical technologies in Europe.
European Heart Journal, 27 (7), .
(doi:10.1093/eurheartj/ehi794).
Abstract
The European Society of Cardiology (ESC) organized a one-day workshop with clinicians, health economic experts, and health technology appraisal experts to discuss the equity of patient access to novel medical technologies in Europe. Two index technologies were considered: implantable cardioverter defibrillators (ICDs) and drug-eluting stents (DES). The use of ICDs range from 35 implants/million population in Portugal to 166 implants/million population in Germany, whereas for implants of DES (as percentage of total stents) it is lowest in Germany at 14% and high in Portugal at 65%. These differences can in part be explained by a lack of structured implementation of guidelines, the direct cost in relation to the overall healthcare budget, and to differences in procedures and models applied by Health Technology Assessment (HTA) agencies in Europe. The workshop participants concluded that physicians need to be involved in a more structured way in HTA and need to become better acquainted with its methods and terminology. Clinical guidelines should be systematically translated, explained, disseminated, updated, and adopted by cardiologists in Europe. Clinically appropriate, consistent and transparent health economic models need to be developed and high-quality international outcome and cost data should be used. A process for funding of a technology should be developed after a positive recommendation from HTA agencies. Both the ESC and the national cardiac societies should build-up health economic expertise and engage more actively in discussions with stakeholders involved in the provision of healthcare.
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Published date: April 2006
Keywords:
health technology assessment, des, drug eluting stents, icd, iplantable cardioverter defibrillators, health economics, esc guidelines, funding
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Local EPrints ID: 61281
URI: http://eprints.soton.ac.uk/id/eprint/61281
ISSN: 0195-668X
PURE UUID: 2b54cf87-8f54-4e5e-9df2-8ac86b136e07
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Date deposited: 29 Sep 2008
Last modified: 15 Mar 2024 11:25
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Contributors
Author:
Peter Kearney
Author:
Graham Stokoe
Author:
Günter Breithardt
Author:
Carole Longson
Author:
Jean Marco
Author:
John Morgan
Author:
Silvia Priori
Author:
Alric Ruether
Author:
Rod Taylor
Author:
Michaël Hertog
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