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Personalized teleprehabilitation in elective cardiac surgery: a study protocol of the Digital Cardiac Counselling randomized controlled trial
AIMS: Previous research has shown the possibility to use the pre-operative period to improve a patient’s tolerance for surgery. However, there is limited experience with prehabilitation in cardiac surgery. The aim of this study is to evaluate the effect of a comprehensive personalized teleprehabilit...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9708005/ https://www.ncbi.nlm.nih.gov/pubmed/36713609 http://dx.doi.org/10.1093/ehjdh/ztab041 |
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author | Scheenstra, Bart Mohansingh, Chanu Bongers, Bart C Dahmen, Sandra Wouters, Yvonne I M S Lenssen, Ton F Geerlings, Phil Knols, Henriette F M van Kuijk, Sander M J Kimman, Merel L Nieman, Maxime Maessen, Jos G van’t Hof, Arnoud W J Peyman, Sardari Nia |
author_facet | Scheenstra, Bart Mohansingh, Chanu Bongers, Bart C Dahmen, Sandra Wouters, Yvonne I M S Lenssen, Ton F Geerlings, Phil Knols, Henriette F M van Kuijk, Sander M J Kimman, Merel L Nieman, Maxime Maessen, Jos G van’t Hof, Arnoud W J Peyman, Sardari Nia |
author_sort | Scheenstra, Bart |
collection | PubMed |
description | AIMS: Previous research has shown the possibility to use the pre-operative period to improve a patient’s tolerance for surgery. However, there is limited experience with prehabilitation in cardiac surgery. The aim of this study is to evaluate the effect of a comprehensive personalized teleprehabilitation programme on major adverse cardiac events (MACE) in patients scheduled for elective cardiac surgery. Secondary outcomes are post-operative complications, cardiovascular risk factors, quality of life, and cost-effectiveness. METHODS AND RESULTS: In this single-centre randomized controlled trial, patients are eligible for inclusion when they are ≥18 years of age and cardiac surgery is scheduled at least 8 weeks from informed consent. Participants will be randomized to the teleprehabilitation group or the control group. After a digital baseline screening for perioperative risk factors, patients in the intervention arm can pre-operatively be referred to one or more of the prehabilitation modules (functional exercise training, inspiratory muscle training, psychological support, nutritional support, and/or smoking cessation). The programme is targeted at a duration of at least 6 weeks. It is executed by a multidisciplinary team using (video)calls and supported by a custom-made digital platform. During the pre-operative period, the platform is also used to inform patients about their upcoming surgery and for telemonitoring. CONCLUSION: Reducing perioperative risk factors might result in a reduction of MACE, post-operative complications, length of stay, and cardiovascular risk factors, as well as improved quality of life. Cost-effectiveness will be evaluated. |
format | Online Article Text |
id | pubmed-9708005 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-97080052023-01-27 Personalized teleprehabilitation in elective cardiac surgery: a study protocol of the Digital Cardiac Counselling randomized controlled trial Scheenstra, Bart Mohansingh, Chanu Bongers, Bart C Dahmen, Sandra Wouters, Yvonne I M S Lenssen, Ton F Geerlings, Phil Knols, Henriette F M van Kuijk, Sander M J Kimman, Merel L Nieman, Maxime Maessen, Jos G van’t Hof, Arnoud W J Peyman, Sardari Nia Eur Heart J Digit Health Original Articles AIMS: Previous research has shown the possibility to use the pre-operative period to improve a patient’s tolerance for surgery. However, there is limited experience with prehabilitation in cardiac surgery. The aim of this study is to evaluate the effect of a comprehensive personalized teleprehabilitation programme on major adverse cardiac events (MACE) in patients scheduled for elective cardiac surgery. Secondary outcomes are post-operative complications, cardiovascular risk factors, quality of life, and cost-effectiveness. METHODS AND RESULTS: In this single-centre randomized controlled trial, patients are eligible for inclusion when they are ≥18 years of age and cardiac surgery is scheduled at least 8 weeks from informed consent. Participants will be randomized to the teleprehabilitation group or the control group. After a digital baseline screening for perioperative risk factors, patients in the intervention arm can pre-operatively be referred to one or more of the prehabilitation modules (functional exercise training, inspiratory muscle training, psychological support, nutritional support, and/or smoking cessation). The programme is targeted at a duration of at least 6 weeks. It is executed by a multidisciplinary team using (video)calls and supported by a custom-made digital platform. During the pre-operative period, the platform is also used to inform patients about their upcoming surgery and for telemonitoring. CONCLUSION: Reducing perioperative risk factors might result in a reduction of MACE, post-operative complications, length of stay, and cardiovascular risk factors, as well as improved quality of life. Cost-effectiveness will be evaluated. Oxford University Press 2021-04-19 /pmc/articles/PMC9708005/ /pubmed/36713609 http://dx.doi.org/10.1093/ehjdh/ztab041 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the European Society of Cardiology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Articles Scheenstra, Bart Mohansingh, Chanu Bongers, Bart C Dahmen, Sandra Wouters, Yvonne I M S Lenssen, Ton F Geerlings, Phil Knols, Henriette F M van Kuijk, Sander M J Kimman, Merel L Nieman, Maxime Maessen, Jos G van’t Hof, Arnoud W J Peyman, Sardari Nia Personalized teleprehabilitation in elective cardiac surgery: a study protocol of the Digital Cardiac Counselling randomized controlled trial |
title | Personalized teleprehabilitation in elective cardiac surgery: a study protocol of the Digital Cardiac Counselling randomized controlled trial |
title_full | Personalized teleprehabilitation in elective cardiac surgery: a study protocol of the Digital Cardiac Counselling randomized controlled trial |
title_fullStr | Personalized teleprehabilitation in elective cardiac surgery: a study protocol of the Digital Cardiac Counselling randomized controlled trial |
title_full_unstemmed | Personalized teleprehabilitation in elective cardiac surgery: a study protocol of the Digital Cardiac Counselling randomized controlled trial |
title_short | Personalized teleprehabilitation in elective cardiac surgery: a study protocol of the Digital Cardiac Counselling randomized controlled trial |
title_sort | personalized teleprehabilitation in elective cardiac surgery: a study protocol of the digital cardiac counselling randomized controlled trial |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9708005/ https://www.ncbi.nlm.nih.gov/pubmed/36713609 http://dx.doi.org/10.1093/ehjdh/ztab041 |
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