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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...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
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
Descripción
Sumario: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.