Atrial Fibrillation Duration Electrocardiography | Atrial Fibrillation Duration Holter Electrocardiography | Atrial Fibrillation Duration Cardiac event recording
Item
1. patients with newly diagnosed af detected on electrocardiogram (ecg), holder recordings or event recorder with a duration > 30 seconds, in the 3 months before inclusion or
boolean
C0004238 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C1623258 (UMLS CUI [1,3])
C0004238 (UMLS CUI [2,1])
C0449238 (UMLS CUI [2,2])
C0013801 (UMLS CUI [2,3])
C0004238 (UMLS CUI [3,1])
C0449238 (UMLS CUI [3,2])
C1273297 (UMLS CUI [3,3])
Atrial Fibrillation | Control Regular Lacking | Referral for Diagnostic procedure New | Referral for Problem Therapeutic
Item
2. patients with a history of diagnosed af, with no regular control at a cardiologist for af in the last 2 years and referred by a (non-)cardiologic medical specialist for new diagnostics or therapeutic issue;
boolean
C0004238 (UMLS CUI [1])
C2587213 (UMLS CUI [2,1])
C0205272 (UMLS CUI [2,2])
C0332268 (UMLS CUI [2,3])
C2585524 (UMLS CUI [3,1])
C0086143 (UMLS CUI [3,2])
C0205314 (UMLS CUI [3,3])
C2585524 (UMLS CUI [4,1])
C0033213 (UMLS CUI [4,2])
C0302350 (UMLS CUI [4,3])
Age
Item
3. age ≥18 years.
boolean
C0001779 (UMLS CUI [1])
Electrocardiography Lacking Atrial Fibrillation
Item
1. no electrocardiographic objectified af;
boolean
C1623258 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
C0004238 (UMLS CUI [1,3])
Heart failure Unstable New York Heart Association Classification | Heart failure Hospitalization Required
Item
2. unstable heart failure defined as nyha iv or heart failure necessitating hospital admission < 3 months before inclusion;
boolean
C0018801 (UMLS CUI [1,1])
C0443343 (UMLS CUI [1,2])
C1275491 (UMLS CUI [1,3])
C0018801 (UMLS CUI [2,1])
C1708385 (UMLS CUI [2,2])
Acute Coronary Syndrome | Myocardial Infarction | Angina, Unstable | Chest Pain | Electrocardiographic changes Ischemic | Cardiac enzymes increased
Item
3. acute coronary syndrome (acute myocardial infarction or instable angina pectoris, with two of the following characteristics: chest pain and/ or ischemic electrocardiographic changes, and/ or cardiac enzyme rise) < 3 months before inclusion;
boolean
C0948089 (UMLS CUI [1])
C0027051 (UMLS CUI [2])
C0002965 (UMLS CUI [3])
C0008031 (UMLS CUI [4])
C0855329 (UMLS CUI [5,1])
C0475224 (UMLS CUI [5,2])
C0741921 (UMLS CUI [6])
Hyperthyroidism Untreated | Euthyroidism
Item
4. untreated hyperthyroidism or < 3 months euthyroidism before inclusion;
boolean
C0020550 (UMLS CUI [1,1])
C0332155 (UMLS CUI [1,2])
C1848783 (UMLS CUI [2])
Artificial cardiac pacemaker | Implantable defibrillator | Cardiac Resynchronization Therapy | Artificial cardiac pacemaker Planned | Implantable defibrillator Planned | Cardiac Resynchronization Therapy Planned
Item
5. current or foreseen pacemaker, internal cardioverter defibrillator, and/ or cardiac resynchronization therapy;
boolean
C0030163 (UMLS CUI [1])
C0162589 (UMLS CUI [2])
C1167956 (UMLS CUI [3])
C0030163 (UMLS CUI [4,1])
C1301732 (UMLS CUI [4,2])
C0162589 (UMLS CUI [5,1])
C1301732 (UMLS CUI [5,2])
C1167956 (UMLS CUI [6,1])
C1301732 (UMLS CUI [6,2])
Cardiac Surgery
Item
6. cardiac surgery ≤ 3 months before inclusion;
boolean
C0018821 (UMLS CUI [1])
Cardiac Surgery Planned
Item
7. planned cardiac surgery;
boolean
C0018821 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
Control Regular | Treatment Regular | Control Regular Atrial Fibrillation; | Treatment Regular Atrial Fibrillation
Item
8. regular control and treatment, also for af, at another specialized outpatient cardiac clinic;
boolean
C2587213 (UMLS CUI [1,1])
C0205272 (UMLS CUI [1,2])
C0087111 (UMLS CUI [2,1])
C0205272 (UMLS CUI [2,2])
C2587213 (UMLS CUI [3,1])
C0205272 (UMLS CUI [3,2])
C0004238 (UMLS CUI [3,3])
C0087111 (UMLS CUI [4,1])
C0205272 (UMLS CUI [4,2])
C0004238 (UMLS CUI [4,3])
Questionnaires Completion Unable
Item
9. patient is not able to fill in the questionnaires;
boolean
C0034394 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
Study Subject Participation Status
Item
10. participation in other clinical study.
boolean
C2348568 (UMLS CUI [1])