Eligibility Heart Failure NCT02282683

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StudyEvent: Eligibility
1. Eligibility Heart Failure NCT02282683

Name

Tipo

Description | Question | Decode (Coded Value)

Tipo de dados

Alias

Inclusion Criteria

Item Group

C1512693 (UMLS CUI)

Hospitalization Due to Heart Failure Quantity | Emergency department patient visit Quantity Heart failure

Item

repeated (>2) hospitalizations or ed visits for hf in the past year

boolean

C3898876 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0586082 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0018801 (UMLS CUI [2,3])

Exercise Unable | Including Exertion Limited | Including Intolerance Exertion | Including Resting Symptoms | Including Dependence Inotropic agent

Item

inability to exercise including exertion limited, exertion intolerance, resting symptoms or inotrope dependent

boolean

C0015259 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0332257 (UMLS CUI [2,1])
C0031807 (UMLS CUI [2,2])
C0439801 (UMLS CUI [2,3])
C0332257 (UMLS CUI [3,1])
C0231199 (UMLS CUI [3,2])
C0031807 (UMLS CUI [3,3])
C0332257 (UMLS CUI [4,1])
C0035253 (UMLS CUI [4,2])
C1457887 (UMLS CUI [4,3])
C0332257 (UMLS CUI [5,1])
C0439857 (UMLS CUI [5,2])
C0304509 (UMLS CUI [5,3])

Left ventricular ejection fraction

Item

left ventricular ejection fraction ≤35%

boolean

C0428772 (UMLS CUI [1])

Serum uric acid measurement

Item

serum uric acid level ≥500μmol/l

boolean

C0455272 (UMLS CUI [1])

Prednisone

Item

received prednisone treatment during hospitalization period and and more 5 of the followings

boolean

C0032952 (UMLS CUI [1])

Renal function Deterioration Progressive | Blood urea increased | Serum creatinine raised

Item

1. progressive deterioration in renal function (e.g., rise in bun and creatinine)

boolean

C0232804 (UMLS CUI [1,1])
C0868945 (UMLS CUI [1,2])
C0205329 (UMLS CUI [1,3])
C0151539 (UMLS CUI [2])
C0700225 (UMLS CUI [3])

Weight loss | Independent of Cardiac cachexia

Item

2. weight loss without other cause (e.g., cardiac cachexia)

boolean

C1262477 (UMLS CUI [1])
C0332291 (UMLS CUI [2,1])
C0562491 (UMLS CUI [2,2])

Intolerance to Angiotensin-Converting Enzyme Inhibitors | Etiology Hypotension | Etiology Renal function Worsening

Item

3. intolerance to ace inhibitors due to hypotension and/or worsening renal function

boolean

C1744706 (UMLS CUI [1,1])
C0003015 (UMLS CUI [1,2])
C0015127 (UMLS CUI [2,1])
C0020649 (UMLS CUI [2,2])
C0015127 (UMLS CUI [3,1])
C0232804 (UMLS CUI [3,2])
C0332271 (UMLS CUI [3,3])

Intolerance to Adrenergic beta-1 Receptor Antagonists | Etiology Heart failure Worsening | Etiology Hypotension

Item

4. intolerance to beta blockers due to worsening hf or hypotension

boolean

C1744706 (UMLS CUI [1,1])
C0304516 (UMLS CUI [1,2])
C0015127 (UMLS CUI [2,1])
C0018801 (UMLS CUI [2,2])
C0332271 (UMLS CUI [2,3])
C0015127 (UMLS CUI [3,1])
C0020649 (UMLS CUI [3,2])

Systolic Pressure Frequent

Item

5. frequent systolic blood pressure <90 mm hg

boolean

C0871470 (UMLS CUI [1,1])
C0332183 (UMLS CUI [1,2])

Patient need for Diuretics Dose Escalation | Furosemide Equivalent Dose | Thiazide Diuretics Supplemental

Item

6. recent need to escalate diuretics to maintain volume status, often reaching daily furosemide equivalent dose >160 mg/d and/or use of supplemental thizide therapy

boolean

C0686904 (UMLS CUI [1,1])
C0012798 (UMLS CUI [1,2])
C3816728 (UMLS CUI [1,3])
C0016860 (UMLS CUI [2,1])
C0205163 (UMLS CUI [2,2])
C0178602 (UMLS CUI [2,3])
C0012802 (UMLS CUI [3,1])
C2348609 (UMLS CUI [3,2])

Serum sodium decreased Progressive

Item

7. progressive decline in serum sodium, usually to <133 meq/l

boolean

C4048754 (UMLS CUI [1,1])
C0205329 (UMLS CUI [1,2])

Item

8. gastrointestinal symptoms (abdominal discomfort, nausea, poor appetite), disabling ascites, or severe lower-extremity edema

boolean

C0426576 (UMLS CUI [1])
C0232487 (UMLS CUI [2])
C0027497 (UMLS CUI [3])
C0232462 (UMLS CUI [4])
C0003962 (UMLS CUI [5,1])
C4061999 (UMLS CUI [5,2])
C0239340 (UMLS CUI [6,1])
C0205082 (UMLS CUI [6,2])

Exclusion Criteria

Item Group

C0680251 (UMLS CUI)

Condition Limiting Use of Prednisone | Exception Heart failure

Item

any condition (other than heart failure) that could limit the use of prednisone

boolean

C0348080 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C1524063 (UMLS CUI [1,3])
C0032952 (UMLS CUI [1,4])
C1705847 (UMLS CUI [2,1])
C0018801 (UMLS CUI [2,2])

Comorbidity Limiting Life Expectancy

Item

any concurrent disease that likely limits life expectancy;

boolean

C0009488 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0023671 (UMLS CUI [1,3])

Myocarditis | Hypertrophic Cardiomyopathy | Restrictive cardiomyopathy

Item

active myocarditis, or an hypertrophic obstructive or restrictive cardiomyopathy;

boolean

C0027059 (UMLS CUI [1])
C0007194 (UMLS CUI [2])
C0007196 (UMLS CUI [3])

Myocardial Infarction | Cerebrovascular accident | Angina, Unstable | Cardiac Surgery

Item

myocardial infarction, stroke, unstable angina, or cardiac surgery within the previous 3 months;

boolean

C0027051 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
C0002965 (UMLS CUI [3])
C0018821 (UMLS CUI [4])

Indication Hemodialysis

Item

indication for hemodialysis

boolean

C3146298 (UMLS CUI [1,1])
C0019004 (UMLS CUI [1,2])

Systolic Pressure Uncontrolled

Item

uncontrolled systolic blood pressure > 160 mmhg

boolean

C0871470 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])

Complex congenital heart disease

Item

complex congenital heart disease

boolean

C0744669 (UMLS CUI [1])

Poorly controlled diabetes mellitus

Item

poorly controlled diabetes

boolean

C0554876 (UMLS CUI [1])

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Eligibility Heart Failure NCT02282683