IMPROV-ED trial: eHealth programme for faster recovery and reduced healthcare utilisation after CABG

• Published in: Netherlands heart journal 2021-02, Vol.29 (2), p.80-87
• Main Authors: van Steenbergen, G. J., van Veghel, D., ter Woorst, J., van Lieshout, D., Dekker, L.
• Format: Article
• Language: English
• Subjects: Anxiety; Cardiology; Clinical outcomes; Coronary vessels; Educational films; Emergency medical care; Family physicians; Health services utilization; Heart surgery; Hospitals; Informed consent; Internet access; Intervention; Medical Education; Medical personnel; Medicine; Medicine & Public Health; Nurse practitioners; Original Article – Study Design Article; Original – Study Design; Outpatient care facilities; Patient satisfaction; Psychologists; Quality of life; Questionnaires; Recovery (Medical); Telemedicine; Veins & arteries
• ISSN: 1568-5888; 1876-6250
• DOI: 10.1007/s12471-020-01508-9

Background After coronary artery bypass grafting (CABG), healthcare utilisation is high and is partly unplanned. eHealth applications have been proposed to reduce healthcare consumption and to enable patients to get actively involved in their recovery. This way, healthcare expenses can be reduced and the quality of care can be improved. Objectives We aim to evaluate whether the use of an eHealth programme can reduce unplanned healthcare utilisation and improve mental and physical health in the first 6 weeks after discharge in patients who underwent CABG. In addition, patient satisfaction and use of the eHealth programme will be evaluated. Methods For this single-centre randomised controlled trial, at least 280 patients referred for CABG will be included at the preoperative outpatient clinic and randomised to an intervention or control group. The intervention group will have access to an eHealth programme, which consists of online educational videos developed by the Dutch Heart Foundation and postoperative video consultations with a physician. The control group will receive standard care and will not have access to the eHealth programme. The primary endpoint is healthcare utilisation; other endpoints include anxiety, duration of recovery, quality of life and patient satisfaction. Participants will complete several questionnaires at 6 time points during the study. Results Patient enrolment started in February 2020 and completion of the follow-up period is expected in August 2021. Conclusion This randomised trial was initiated to test the hypothesis that patients who are partaking in our eHealth programme use less unplanned care and experience a better quality of life, less anxiety and a faster recovery than controls.