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The trialist’s perspective: what do you need to prove for remote monitoring devices to be approved?

Due to contrasting results from clinical trials, remote monitoring devices have so far rarely been approved for heart failure (HF) management in European countries. Implementation of telemedicine into clinical practice of heart failure outpatient care is still limited. As part of an expert meeting o...

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Detalles Bibliográficos
Autor principal: Angermann, Christiane E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6937513/
https://www.ncbi.nlm.nih.gov/pubmed/31908619
http://dx.doi.org/10.1093/eurheartj/suz214
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author Angermann, Christiane E
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description Due to contrasting results from clinical trials, remote monitoring devices have so far rarely been approved for heart failure (HF) management in European countries. Implementation of telemedicine into clinical practice of heart failure outpatient care is still limited. As part of an expert meeting on physiological monitoring in the complex mutimorbid HF patient, the needs to establish evidence supporting the use of devices in heart failure outpatient care was discussed according to a trialist’s perspective. This document reflects the key points debated by a multidisciplinary panel of leading international experts on this topic.
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spelling pubmed-69375132020-01-06 The trialist’s perspective: what do you need to prove for remote monitoring devices to be approved? Angermann, Christiane E Eur Heart J Suppl Articles Due to contrasting results from clinical trials, remote monitoring devices have so far rarely been approved for heart failure (HF) management in European countries. Implementation of telemedicine into clinical practice of heart failure outpatient care is still limited. As part of an expert meeting on physiological monitoring in the complex mutimorbid HF patient, the needs to establish evidence supporting the use of devices in heart failure outpatient care was discussed according to a trialist’s perspective. This document reflects the key points debated by a multidisciplinary panel of leading international experts on this topic. Oxford University Press 2019-12 2019-12-31 /pmc/articles/PMC6937513/ /pubmed/31908619 http://dx.doi.org/10.1093/eurheartj/suz214 Text en Published on behalf of the European Society of Cardiology. © The Author(s) 2019. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Articles
Angermann, Christiane E
The trialist’s perspective: what do you need to prove for remote monitoring devices to be approved?
title The trialist’s perspective: what do you need to prove for remote monitoring devices to be approved?
title_full The trialist’s perspective: what do you need to prove for remote monitoring devices to be approved?
title_fullStr The trialist’s perspective: what do you need to prove for remote monitoring devices to be approved?
title_full_unstemmed The trialist’s perspective: what do you need to prove for remote monitoring devices to be approved?
title_short The trialist’s perspective: what do you need to prove for remote monitoring devices to be approved?
title_sort trialist’s perspective: what do you need to prove for remote monitoring devices to be approved?
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6937513/
https://www.ncbi.nlm.nih.gov/pubmed/31908619
http://dx.doi.org/10.1093/eurheartj/suz214
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