Inclusion criteria | |
History of MI according to guidelines: | |
CHA2DS2-VASc score ≥ 4 in men/≥ 5 in women | |
LVEF > 35% as estimated within 6 months before enrollment but after conclusion of acute MI treatment | |
Patient accepts activation of home monitoring | |
Patient has provided written informed consent | |
Exclusion criteria | |
Platelet count < 90,000 per mm3 or patients with hemorrhagic diathesis | |
Permanent oral anticoagulation treatment for atrial fibrillation | |
Indication for chronic renal dialysis | |
Pacemaker or ICD implanted or indication for implantation | |
Parkinson’s disease | |
Life expectancy < 1 year | |
Participation in another interventional clinical investigation during the course of the study, i.e. the participation in a noninterventional clinical investigation is allowed. | |
Age < 18 years | |
Woman who are pregnant or breast feeding |