About this trial
Patients with heart failure undergoing cardiac surgery face a significantly increased perioperative risk, yet no standardized strategy exists to mitigate this risk effectively. Current preoperative management relies on optimization of medical therapy without a structured prehabilitation approach. Given the strong association between eleveated preoperative N-terminal pro-B-type natriuretic peptide levels and postoperative outcomes, patients at increased risk could be identified using this biomarker. Telemedical disease management programs have demonstrated efficacy in outpatient heart failure care, but their role in preoperative optimization remains underexplored. This study aims to assess whether a structured, multidisciplinary, telemedicine-assisted prehabilitation program can reduce perioperative complications, and improve surgical outcomes.
Eligibility criteria
Qualifiers
Indication for elective cardiac surgery in the Heart team
NTproBNP ≥ 1500 ng/L
≥ 18 years willing to participate in trial
Written informed consent
Disqualifiers
Neuropsychiatric disorders / illnesses (e.g. drug addiction, alcohol abuse) that do not allow adherent participation in the study
No sufficient ability to measure and transfer data or existing support in the social environment
no sufficient ability to communicate (language skills, eyesight, hearing)
Pregnancy
Trial design
Treatments tested in this trial
- PREPARE-HF disease management program, which includes: