Atrial Fibrillation
Item
every newly diagnosed af patient.
boolean
C0004238 (UMLS CUI [1])
Atrial Fibrillation | Seen by cardiologist Lacking
Item
every af patient who is not seen by a cardiologist or electrophysiologist in the past 2 years before inclusion.
boolean
C0004238 (UMLS CUI [1])
C0583557 (UMLS CUI [2,1])
C0332268 (UMLS CUI [2,2])
Atrial Fibrillation Electrocardiogram
Item
af must be confirmed on electrocardiogram.
boolean
C0004238 (UMLS CUI [1,1])
C1623258 (UMLS CUI [1,2])
Informed Consent
Item
capable of providing written informed consent.
boolean
C0021430 (UMLS CUI [1])
Able to speak Dutch Language | Impaired cognition Absent
Item
dutch speaking and verbally testable, without cognitive impairment.
boolean
C0564215 (UMLS CUI [1,1])
C0376241 (UMLS CUI [1,2])
C0338656 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Atrial Fibrillation | Consult Arrhythmia Received
Item
af patients who once received an arrhythmologic consult about af prior to the start of the study.
boolean
C0004238 (UMLS CUI [1])
C0009818 (UMLS CUI [2,1])
C0003811 (UMLS CUI [2,2])
C1514756 (UMLS CUI [2,3])
Atrial Fibrillation | Follow-up systematic Cardiologist
Item
af patients who have a systematic follow-up at a cardiologist prior to the start of the study.
boolean
C0004238 (UMLS CUI [1])
C1522577 (UMLS CUI [2,1])
C0220922 (UMLS CUI [2,2])
C0175906 (UMLS CUI [2,3])
Atrial Fibrillation Terminal illness
Item
terminally ill af patients
boolean
C0004238 (UMLS CUI [1,1])
C0679247 (UMLS CUI [1,2])
Study Subject Participation Status
Item
participation in another clinical trial
boolean
C2348568 (UMLS CUI [1])