Congestive heart failure | Status post Myocardial Infarction | Status post Dilated Cardiomyopathy
Item
congestive heart failure after myocardial infarction or dilated cardiomyopathy with:
boolean
C0018802 (UMLS CUI [1])
C0231290 (UMLS CUI [2,1])
C0027051 (UMLS CUI [2,2])
C0231290 (UMLS CUI [3,1])
C0007193 (UMLS CUI [3,2])
Left ventricular ejection fraction
Item
lvef < 0.35,
boolean
C0428772 (UMLS CUI [1])
New York Heart Association Classification
Item
nyha class ii - iii,
boolean
C1275491 (UMLS CUI [1])
Stable status | Worsening pattern Absent
Item
stable without any signs of worsening for at least 6 weeks,
boolean
C0205360 (UMLS CUI [1])
C0332271 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Therapy Optimal
Item
minimum 3 months of optimal medical treatment,
boolean
C0087111 (UMLS CUI [1,1])
C2698651 (UMLS CUI [1,2])
Revascularization Previous | Cardiac Resynchronization Therapy Previous
Item
previous revascularisation or crt should be more than 6 months before inclusion.
boolean
C0581603 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C1167956 (UMLS CUI [2,1])
C0205156 (UMLS CUI [2,2])
Comorbidity Significant
Item
significant intercurrent illness last 6 weeks,
boolean
C0009488 (UMLS CUI [1,1])
C0750502 (UMLS CUI [1,2])
Ventricular arrhythmia Severe
Item
known severe ventricular arrhythmia with functional or prognostic significance unless protected with icd,
boolean
C0085612 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Ischemia
Item
significant ischemia,
boolean
C0022116 (UMLS CUI [1])
Hemodynamics deterioration | Cardiac Arrhythmia Exercise induced
Item
hemodynamic deterioration or exercise-induced arrhythmia at baseline testing,
boolean
C0019010 (UMLS CUI [1,1])
C0868945 (UMLS CUI [1,2])
C0003811 (UMLS CUI [2,1])
C0239313 (UMLS CUI [2,2])
Heart Disease Limiting Exercise Tolerance | Valvular disease | Hypertrophic Cardiomyopathy
Item
other heart disease that limits exercise tolerance (valve disease with significant hemodynamic consequences, hypertrophic cardiomyopathy etc.,
boolean
C0018799 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0162521 (UMLS CUI [1,3])
C3258293 (UMLS CUI [2])
C0007194 (UMLS CUI [3])
Comorbidity Influence Prognosis
Item
co-morbidity that may significantly influence one-year prognosis,
boolean
C0009488 (UMLS CUI [1,1])
C4054723 (UMLS CUI [1,2])
C0033325 (UMLS CUI [1,3])
Functional disability Limiting Exercise | Mental handicap Limiting Exercise
Item
functional or mental disability that may limit exercise,
boolean
C0872173 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0015259 (UMLS CUI [1,3])
C1306341 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
C0015259 (UMLS CUI [2,3])
Heart Transplantation Scheduled
Item
patients scheduled for heart transplant at time of inclusion,
boolean
C0018823 (UMLS CUI [1,1])
C0205539 (UMLS CUI [1,2])
Vigorous physical activity | Exercise Training | Study Subject Participation Status | Clinical Trial
Item
a habit of regular vigorous exercise or participation in a program of exercise training less than 6 months before inclusion, or participation in another clinical trial,
boolean
C4267713 (UMLS CUI [1])
C4279936 (UMLS CUI [2])
C2348568 (UMLS CUI [3])
C0008976 (UMLS CUI [4])
Chronic Obstructive Airway Disease | Percent predicted FEV1
Item
patients with copd with fev1 below 50% of expected values are excluded,
boolean
C0024117 (UMLS CUI [1])
C0730561 (UMLS CUI [2])
Adrenal Cortex Hormones Oral
Item
patients taking oral corticosteroids are excluded in all cases.
boolean
C0001617 (UMLS CUI [1,1])
C1527415 (UMLS CUI [1,2])