Age
Item
20-70 years old
boolean
C0001779 (UMLS CUI [1])
Chronic heart failure Disease length | Symptoms Heart failure | Episode of Chronic heart failure
Item
more than 3 months of chronic heart failure history or clinical symptoms of heart failure last for more than 3 months (including acute episode of chronic heart failure), chronic heart failure diagnostic criteria refer to 2012esc guidelines for the diagnosis and treatment of acute and chronic heart failure
boolean
C0264716 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
C1457887 (UMLS CUI [2,1])
C0018801 (UMLS CUI [2,2])
C0332189 (UMLS CUI [3,1])
C0264716 (UMLS CUI [3,2])
New York Heart Association Classification | Cardiac ejection fraction
Item
nyha functional class iii-iv, ejection fraction ≤45%
boolean
C1275491 (UMLS CUI [1])
C0232174 (UMLS CUI [2])
N-Terminal ProB-type Natriuretic Peptide Measurement
Item
nt-probnp>400ng/l
boolean
C3272900 (UMLS CUI [1])
First episode Heart failure
Item
first episode of acute heart failure
boolean
C0439615 (UMLS CUI [1,1])
C0018801 (UMLS CUI [1,2])
Heart valve disease | Resolution Lacking | Change Hemodynamic
Item
unrepaired valvular heart disease accompanied with hemodynamic changes
boolean
C0018824 (UMLS CUI [1])
C1514893 (UMLS CUI [2,1])
C0332268 (UMLS CUI [2,2])
C0392747 (UMLS CUI [3,1])
C0019010 (UMLS CUI [3,2])
Hypertrophic Cardiomyopathy | Disorder of pericardium | Congenital heart disease | Pulmonary Hypertension Severe
Item
hypertrophic cardiomyopathy, pericardial disease, congenital heart disease, severe pulmonary hypertension
boolean
C0007194 (UMLS CUI [1])
C0265122 (UMLS CUI [2])
C0152021 (UMLS CUI [3])
C0020542 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
Second degree sinoatrial block Type | Second degree atrioventricular block | Pacemaker Procedure Absent
Item
second-degree type 2 or worse sinoatrial or atrioventricular block without pacemaker therapy
boolean
C3854674 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
C0264906 (UMLS CUI [2])
C3275122 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
Right-Sided Heart Failure caused by Disease | Respiratory Failure | Right-Sided Heart Failure Chronic Obstructive Airway Disease Induced
Item
right heart failure caused by various diseases, respiratory failure or right heart failure induced by chronic obstructive pulmonary disease
boolean
C0235527 (UMLS CUI [1,1])
C0015127 (UMLS CUI [1,2])
C0012634 (UMLS CUI [1,3])
C1145670 (UMLS CUI [2])
C0235527 (UMLS CUI [3,1])
C0024117 (UMLS CUI [3,2])
C0205263 (UMLS CUI [3,3])
Renal decompensation | Creatinine measurement, serum
Item
overt renal decompensation: serum creatinine>2.1mg/dl(186umol/l)
boolean
C0748288 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
Liver Dysfunction Severe | Transaminases increased | Alkaline phosphatase raised
Item
severe hepatic dysfunction, transaminase or alkaline phosphatase > 3 times the upper limit of normal
boolean
C0086565 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0438717 (UMLS CUI [2])
C0151849 (UMLS CUI [3])
Cerebrovascular accident | Cerebral Infarction | Cerebral Embolism | Cerebral Hemorrhage
Item
cerebral vascular accident in three months( cerebral infarction, cerebral embolism, cerebral hemorrhage,etc)
boolean
C0038454 (UMLS CUI [1])
C0007785 (UMLS CUI [2])
C0007780 (UMLS CUI [3])
C2937358 (UMLS CUI [4])
Life Expectancy
Item
life expectancy shorter than 6 months
boolean
C0023671 (UMLS CUI [1])
Malignant Neoplasms | Precancerous lesions
Item
patients with a previous or present history of tumour or precancerous lesions confirmed by pathological examination
boolean
C0006826 (UMLS CUI [1])
C0940937 (UMLS CUI [2])
Deformity of spine Puncture Site | Skin infection Puncture Site
Item
spine deformity or skin infection at puncture site
boolean
C0575157 (UMLS CUI [1,1])
C0034117 (UMLS CUI [1,2])
C1515974 (UMLS CUI [1,3])
C0037278 (UMLS CUI [2,1])
C0034117 (UMLS CUI [2,2])
C1515974 (UMLS CUI [2,3])
Study Subject Participation Status
Item
participate in any clinical drug trials in the three months
boolean
C2348568 (UMLS CUI [1])
Informed Consent Absent | Protocol Compliance Unable | Protocol Compliance Unwilling | Study Subject Participation Status Inappropriate
Item
the patients who do not sign the informed consent, unable or unwilling to comply with the requirements of the protocol or unsuitable for the study
boolean
C0021430 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
C0525058 (UMLS CUI [3,1])
C0558080 (UMLS CUI [3,2])
C2348568 (UMLS CUI [4,1])
C1548788 (UMLS CUI [4,2])