The purpose of this study is to study clinical factors and (blood) biomarkers related to progression of Atrial Fibrillation (AF) in patients diagnosed with self-terminating AF with special reference to hypercoagulability. All patients will be continuously monitored for their atrial rhythm to assess AF progression, either through an implantable loop recorder (Reveal LinQ) or via the atrial lead of a cardiac implantable electronic device (CIED), both in combination with the CareLink home monitoring system. Remote monitoring and interrogation will be installed and used on a daily basis.
Study Type
OBSERVATIONAL
Enrollment
750
Rijnstate Hospital
Arnhem, Gelderland, Netherlands
Maastricht University Medical Center
Maastricht, Limburg, Netherlands
Amsterdam University Medical Center - AMC
Amsterdam, Netherlands
Amsterdam University Medical Center - VU
Amsterdam, Netherlands
University Medical Center Groningen
Groningen, Netherlands
Martini Hospital
Groningen, Netherlands
Ommelander Ziekenhuis
Groningen, Netherlands
Laurentius Hospital
Roermond, Netherlands
Isala
Zwolle, Netherlands
Progression of AF burden
Time frame: 2.5 years
Major Adverse Cardiac and Cerebrovascular Events
Time frame: 2.5 years
Change in therapy due to continuous rhythm monitoring with the LinQ/Carelink system
Time frame: 2.5 years
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