Study ID
Item
Study ID
text
C2826693 (UMLS CUI [1])
Study site
Item
Study site name
text
C2825164 (UMLS CUI [1])
Subject ID
Item
Subject ID
text
C2348585 (UMLS CUI [1])
Item
Classify the subject using the ACC/AHA Stage of Heart Failure
integer
C0002458 (UMLS CUI [1,1])
C0018801 (UMLS CUI [1,2])
Code List
Classify the subject using the ACC/AHA Stage of Heart Failure
CL Item
(A) Patients at high risk of developing HF because of the presence of conditions that are strongly associated with the development of HF; such patients have no identified structural or functional abnormalities of the pericardium, myocardium, or cardiac valves and have never shown signs or symptoms of HF (1)
CL Item
(B) Patients who have developed structural heart disease that is strongly associated with the development of HF but who have never shown signs or symptoms of HF (2)
CL Item
(C) Patients who have current or prior symptoms of HF associated with underlying structural heart disease (3)
CL Item
(D) Patients with advanced structural heart disease and marked symptoms of HF at rest despite maximal medical therapy and who require specialized interventions (4)
Number of hospitalizations
Item
Indicate the number of hospitalizations the participant had in the past year
integer
C0750480 (UMLS CUI [1,1])
C0019993 (UMLS CUI [1,2])
Start date hospitalization
Item
Indicate the start date of participants hospitalization
date
C0019993 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Item
Indicate cause for hospitalization
integer
C1830395 (UMLS CUI [1])
Code List
Indicate cause for hospitalization
CL Item
Cardiovascular (1)
CL Item
Other, specify (2)
Reason for hospitalization
Item
Reason for hospitalization:please specify if other reason than cardiovascular
text
C1830395 (UMLS CUI [1])