Atrial Fibrillation
Conditions
Brief summary
The purpose of the Heidelberg Registry of Atrial Fibrillation (HERA-FIB) is to collect data on the prevalence and clinical significance of elevated cardiac troponin in a large registry of unselected patients with atrial fibrillation presenting to an emergency department in the era of novel oral anticoagulants (NOACs).
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
* documented atrial fibrillation * availability of at least one hsTnT measurement
Exclusion criteria
* none
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Nonfatal myocardial infarction | Follow up after at least 6 months |
| Vascular and non-vascular death | Follow up after at least 6 months |
| Stroke/systemic embolism | Follow up after at least 6 months |
Secondary
| Measure | Time frame |
|---|---|
| Stroke, systemic embolism, myocardial infarction, vascular death, non-vascular death, composite endpoint of vascular and non-vascular death, nonfatal MI, stroke/systemic embolism | Follow up after at least 6 months |
Other
| Measure | Time frame |
|---|---|
| Major bleeding by definition of International Society on Thrombosis and Haemostasis (ISTH) | Follow up after at least 6 months |
Countries
Germany