The purpose of this research is to learn more about the normal care of patients with a new or pre-existing diagnosis of atrial fibrillation (AF). These abnormal and irregular heartbeats place patients at increased risk of developing clots in their bloodstream that could potentially lead to stroke. Normal care is designed to help prevent this from happening and to lessen or eliminate the symptoms patients may have. There are many different types of AF as well as numerous ways in which a variety of patients are treated. The investigators are interested in gathering more information to better keep track of patient treatment patterns (trends) that may differ from physician to physician, hospital to hospital, medication to medication, patient to patient and if necessary, procedure to procedure.
The objective of this research is to establish a contemporary and simple to construct AF management registry that expands progressively over the continuum of care for each individual patient. The registry will be used to determine the course and progression of AF management in preventing thrombo-embolic events using rhythm and rate control interventions. Primary endpoints: 1. Atrial fibrillation natural history 2. Thrombo-embolic event 3. Death Secondary endpoints: 1. Bleeding 2. Pro-arrhythmia 3. Patient adherence 4. Treatment complication
Study Type
OBSERVATIONAL
Enrollment
1,000
CorVita Science Foundation (NFP)
Chicago, Illinois, United States
RECRUITINGRecurrence of Atrial fibrillation
The natural progression of the condition will be assessed per medical record review
Time frame: From enrollment to 10- year study completion
Number of participants who had thrombo-embolic event
All strokes, transient ischemic and systemic thrombo-embolic events
Time frame: From enrollment to 10- year study completion
Mortality
All cause death will be noted
Time frame: From enrollment to 10- year study completion
Number of participants who have experienced bleeding
All bleeding events events will be will be assessed throughout the duration of the study per medical record review
Time frame: From enrollment to 10- year study completion
Number of patients who have had pro-arrhythmia events
All pro-arrhythmic events will be documented and assessed
Time frame: From enrollment to 10- year study completion
Number of patients who have had patient adherence events
Events relating to subject non-compliance of medications will be documented for the duration of the study per medical record review
Time frame: From enrollment to 10- year study completion
Treatment complication
All adverse outcomes/events related to routine standard of care treatments will be noted and assessed for the duration of the study per medical record review
Time frame: From enrollment to 10- year study completion
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