Atrial Fibrillation Clinical Trial
Official title:
Remote Heart Rhythm Monitoring Using Photoplethysmography-based Smartphone Technology for the Early Detection of Atrial Fibrillation and Adverse Events After Cardiac Surgery
The objective of the study is to evaluate the clinical consequences following the detection of postoperative atrial fibrillation or flutter (POAF) using a remote heart rhythm monitoring strategy with a photoplethysmography based smartphone technology in the early postoperative period after discharge.
A predefined subgroup analysis of the outcomes described below will be performed in the following subgroups: - Subjects not on anticoagulation drug therapy (for a planned duration of >45 days) at discharge. - Subjects with no history of AF prior to surgery and no POAF lasting >24h in hospital. - Subjects with a CHADSVASC score ≥ 4 or a CHADSVASC score ≥ 2 with at least one additional risk factor associated with the risk of developing POAF. additional risk factors include: - chronic obstructive pulmonary disease - sleep apnea - impaired renal function - left atrial enlargement - elevated body mass index - combined CABG with valve repair or replacement ;
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