Telemedically Assisted Optimization for Heart Failure Patients Before Cardiac Surgery to Improve Perioperative Outcome

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMedical University Innsbruck

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:

Treatment groups

162 Participants
are divided into 2 treatment groups

Sponsors and collaborators