Paroxysmal atrial fibrillation ECG | Persistent atrial fibrillation ECG | Permanent atrial fibrillation ECG | Paroxysmal atrial fibrillation Holter Electrocardiography | Persistent atrial fibrillation Holter Electrocardiography | Permanent atrial fibrillation Holter Electrocardiography | Paroxysmal atrial fibrillation Chart | Persistent atrial fibrillation Chart | Permanent atrial fibrillation Chart | Blood pressure determination Quantity | Antihypertensive Agents
Item
unequivocal evidence (by ecg, holter ecg or medical charts) of aff (paroxysmal, persistent or permanent) in patients with blood pressure > 140/90 mmhg on at least 3 office measurements, or current use of anti-hypertensive drugs;
boolean
C0235480 (UMLS CUI [1,1])
C0013798 (UMLS CUI [1,2])
C2585653 (UMLS CUI [2,1])
C0013798 (UMLS CUI [2,2])
C2586056 (UMLS CUI [3,1])
C0013798 (UMLS CUI [3,2])
C0235480 (UMLS CUI [4,1])
C0013801 (UMLS CUI [4,2])
C2585653 (UMLS CUI [5,1])
C0013801 (UMLS CUI [5,2])
C2586056 (UMLS CUI [6,1])
C0013801 (UMLS CUI [6,2])
C0235480 (UMLS CUI [7,1])
C0007963 (UMLS CUI [7,2])
C2585653 (UMLS CUI [8,1])
C0007963 (UMLS CUI [8,2])
C2586056 (UMLS CUI [9,1])
C0007963 (UMLS CUI [9,2])
C0005824 (UMLS CUI [10,1])
C1265611 (UMLS CUI [10,2])
C0003364 (UMLS CUI [11])
Informed Consent
Item
written informed consent.
boolean
C0021430 (UMLS CUI [1])
Study Subject Participation Status | Refusal to Participate
Item
patient refusal to participate to the study;
boolean
C2348568 (UMLS CUI [1])
C1136454 (UMLS CUI [2])
Heart valve disease Moderate | Heart valve disease Severe | Congenital heart disease | Heart Disease Myocardial
Item
moderate-severe valvular or congenital or myocardial heart disease;
boolean
C0018824 (UMLS CUI [1,1])
C0205081 (UMLS CUI [1,2])
C0018824 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0152021 (UMLS CUI [3])
C0018799 (UMLS CUI [4,1])
C1522564 (UMLS CUI [4,2])
Thyroid function tests abnormal
Item
current abnormal thyroid function;
boolean
C0476414 (UMLS CUI [1])
Kidney Failure, Chronic | Creatinine measurement, serum | GFR estimation by MDRD
Item
chronic renal failure (screatinine > 200 μm or egfr < 40 ml/min, calculated with mdrd formula);
boolean
C0022661 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
C2170215 (UMLS CUI [3])
Hemochromatosis
Item
hemochromatosis;
boolean
C0018995 (UMLS CUI [1])
Alcohol abuse
Item
alcohol abuse;
boolean
C0085762 (UMLS CUI [1])
Acute Coronary Syndrome | Coronary Artery Bypass Surgery | PTCA With Stenting | PTCA Without Stenting | Myocardial Infarction
Item
acute coronary syndrome, or history of cabg, ptca with/without stenting, acute myocardial infarction;
boolean
C0948089 (UMLS CUI [1])
C0010055 (UMLS CUI [2])
C2936173 (UMLS CUI [3,1])
C0332287 (UMLS CUI [3,2])
C2348535 (UMLS CUI [3,3])
C2936173 (UMLS CUI [4,1])
C0332288 (UMLS CUI [4,2])
C2348535 (UMLS CUI [4,3])
C0027051 (UMLS CUI [5])
Hepatitis C | Hepatitis B | HIV Infection
Item
hepatitis c virus and/or b and/or hiv infection;
boolean
C0019196 (UMLS CUI [1])
C0019163 (UMLS CUI [2])
C0019693 (UMLS CUI [3])
Pheochromocytoma | Hypertensive disease Secondary
Item
pheochromocytoma and other known secondary forms of arterial hypertension;
boolean
C0031511 (UMLS CUI [1])
C0020538 (UMLS CUI [2,1])
C0175668 (UMLS CUI [2,2])
Hemodynamic instability Excludes Drug withdrawal | Adrenergic beta-1 Receptor Antagonists | Angiotensin II receptor antagonist | Angiotensin-Converting Enzyme Inhibitors | Diuretics | Hemodynamic instability Interferes with Plasma renin measurement | Hemodynamic instability Interferes with Direct renin measurement | Hemodynamic instability Interferes with Aldosterone measurement
Item
hemodynamic instability precluding withdrawal of drugs (e.g. β-blockers, arbs, ace-i, diuretics), interfering with pra (or dra) and aldosterone measurements.
boolean
C0948268 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,3])
C2349954 (UMLS CUI [1,4])
C0304516 (UMLS CUI [2])
C0521942 (UMLS CUI [3])
C0003015 (UMLS CUI [4])
C0012798 (UMLS CUI [5])
C0948268 (UMLS CUI [6,1])
C0521102 (UMLS CUI [6,2])
C2041375 (UMLS CUI [6,3])
C0948268 (UMLS CUI [7,1])
C0521102 (UMLS CUI [7,2])
C0373719 (UMLS CUI [7,3])
C0948268 (UMLS CUI [8,1])
C0521102 (UMLS CUI [8,2])
C0373535 (UMLS CUI [8,3])
Resistant hypertension
Item
patients with resistant hypertension in whom antihypertensive drug treatment withdrawal/modifications will be considered unsafe will be investigated on treatment and, if necessary, submitted to avs to exclude a lateralized cause of aldosterone excess. they will be analyzed as a separate group.
boolean
C0745130 (UMLS CUI [1])