Implantable Hemodynamic Monitor chronic | Implantable defibrillator chronic
Item
patients implanted with a chronicle ihm device (model 9520, model 9520b) or chronicle icd device (model 7286)
boolean
C4082936 (UMLS CUI [1,1])
C0021102 (UMLS CUI [1,2])
C0205191 (UMLS CUI [1,3])
C0162589 (UMLS CUI [2,1])
C0205191 (UMLS CUI [2,2])
Diuretic therapy Daily Heart failure
Item
patients who have been prescribed daily diuretic therapy for the management of heart failure
boolean
C0948575 (UMLS CUI [1,1])
C0332173 (UMLS CUI [1,2])
C0018801 (UMLS CUI [1,3])
Study Subject Participation Status | Heart failure Clinical Trial Specified
Item
patients currently participating in the compass-hf extension phase study (ide
boolean
C2348568 (UMLS CUI [1])
C0018801 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
C0205369 (UMLS CUI [2,3])
ID.4
Item
#g020304)
boolean
Informed Consent
Item
patients willing and able to give informed consent
boolean
C0021430 (UMLS CUI [1])
Right ventricular pressure Abnormal
Item
patients with non-physiologic right ventricular (rv) pressure values
boolean
C0456166 (UMLS CUI [1,1])
C0205161 (UMLS CUI [1,2])
Patients Resistant to Diuretics
Item
patients who have diuretic resistance
boolean
C0030705 (UMLS CUI [1,1])
C0332325 (UMLS CUI [1,2])
C0012798 (UMLS CUI [1,3])
Estimated Glomerular Filtration Rate
Item
patients who have an estimated glomerular filtration rate(egfr) <30 ml/min (recorded within the last six months)
boolean
C3811844 (UMLS CUI [1])
Implantable Hemodynamic Monitor chronic | Relationship Pulmonary arterial hypertension Clinical Trial
Item
patients who have a chronicle ihm device (model 9520) that was implanted as part of the pulmonary arterial hypertension (pah) pilot study (ide #g020303)
boolean
C4082936 (UMLS CUI [1,1])
C0021102 (UMLS CUI [1,2])
C0205191 (UMLS CUI [1,3])
C0439849 (UMLS CUI [2,1])
C2973725 (UMLS CUI [2,2])
C0008976 (UMLS CUI [2,3])
Heart failure Disease Management Unable
Item
patients who do not have the ability to actively participate in the management of their own heart failure care (determine by physician discretion)(e.g. patient does not have ability to operate study equipment, patient does not have a history of compliance to sending carelink transmissions)
boolean
C0018801 (UMLS CUI [1,1])
C0376636 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
Patient need for Replacement of device
Item
patients who have a reasonable probability of needing a device replacement during the study (approximately two months)
boolean
C0686904 (UMLS CUI [1,1])
C1446530 (UMLS CUI [1,2])
Study Subject Participation Status | Research study | Investigational New Drugs | Investigational Medical Device
Item
patients enrolled or planning to participate in a concurrent drug and/or device study during the course of this clinical trial
boolean
C2348568 (UMLS CUI [1])
C0681814 (UMLS CUI [2])
C0013230 (UMLS CUI [3])
C2346570 (UMLS CUI [4])
Pregnancy | Childbearing Potential Pregnancy test negative
Item
patient who are pregnant (all females of child-bearing potential must have a negative pregnancy test within 1 week of enrollment)
boolean
C0032961 (UMLS CUI [1])
C3831118 (UMLS CUI [2,1])
C0427780 (UMLS CUI [2,2])