Indication Cardiac Resynchronization Therapy Defibrillators
Item
patients who meet current indications for a bsc crt-d device with the smartdelay algorithm
boolean
C3146298 (UMLS CUI [1,1])
C1322646 (UMLS CUI [1,2])
Device implant Willing | Device implant Capability | Participation Testing
Item
patients who are willing and capable of undergoing a device implant and participating in all testing associated with the smart-av study
boolean
C0948629 (UMLS CUI [1,1])
C0600109 (UMLS CUI [1,2])
C0948629 (UMLS CUI [2,1])
C2698977 (UMLS CUI [2,2])
C0679823 (UMLS CUI [3,1])
C0039593 (UMLS CUI [3,2])
Pharmacotherapy Optimal Stable
Item
patients who are on optimal and stable pharmacologic therapy
boolean
C0013216 (UMLS CUI [1,1])
C2698651 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
Sinus rhythm
Item
patients who are expected to be in sinus rhythm at the time of implant
boolean
C0232201 (UMLS CUI [1])
Life Expectancy
Item
patients who have a life expectancy of more than 360 days, per physician's discretion
boolean
C0023671 (UMLS CUI [1])
Patient Geographic Stable | Compliance behavior Follow-up
Item
patients who are geographically stable and willing to comply with the required follow-up schedule
boolean
C0030705 (UMLS CUI [1,1])
C1517526 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C1321605 (UMLS CUI [2,1])
C3274571 (UMLS CUI [2,2])
Age | Age Legal | Informed Consent
Item
patients who are 18 years of age or above, or of legal age to give informed consent specific to state and national law
boolean
C0001779 (UMLS CUI [1])
C0001779 (UMLS CUI [2,1])
C1301860 (UMLS CUI [2,2])
C0021430 (UMLS CUI [3])
Complete atrioventricular block | Intolerant Pacing Specified
Item
patients who are in complete heart block, or who otherwise are unable to tolerate pacing at vvi-40 rv for up to 14 days
boolean
C0151517 (UMLS CUI [1])
C0231200 (UMLS CUI [2,1])
C0199640 (UMLS CUI [2,2])
C0205369 (UMLS CUI [2,3])
Upgrade Artificial cardiac pacemaker | Upgrade Implantable defibrillator | Intolerant Pacing Specified
Item
patients undergoing an upgrade of a pacemaker or implantable cardioverter-defibrillator who are unable to tolerate pacing at vvi-40 rv for up to 14 days
boolean
C3272274 (UMLS CUI [1,1])
C0030163 (UMLS CUI [1,2])
C3272274 (UMLS CUI [2,1])
C0162589 (UMLS CUI [2,2])
C0231200 (UMLS CUI [3,1])
C0199640 (UMLS CUI [3,2])
C0205369 (UMLS CUI [3,3])
Cardiac Resynchronization Therapy
Item
patients who have previously received cardiac resynchronization therapy
boolean
C1167956 (UMLS CUI [1])
Heart Transplantation Expected | Cardiac Surgery procedures Planned | Cardiac therapeutic procedures Planned
Item
patients who are expected to receive a heart transplant or have other cardiac surgeries or procedures planned during the course of the study
boolean
C0018823 (UMLS CUI [1,1])
C1517001 (UMLS CUI [1,2])
C0018821 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
C0876964 (UMLS CUI [3,1])
C1301732 (UMLS CUI [3,2])
Tricuspid valve prosthesis | Tricuspid valve prosthesis Receive Probably
Item
patients who currently have or who are likely to receive a tricuspid valve prosthesis
boolean
C3839627 (UMLS CUI [1])
C3839627 (UMLS CUI [2,1])
C1514756 (UMLS CUI [2,2])
C0750492 (UMLS CUI [2,3])
Neuromuscular Disease Preventing Walking | Orthopedic problem Preventing Walking | Condition Preventing Walking | Exception Heart condition
Item
patients who have a neuromuscular, orthopedic, or other non-cardiac condition that prevents normal, unsupported walking
boolean
C0027868 (UMLS CUI [1,1])
C1292733 (UMLS CUI [1,2])
C0080331 (UMLS CUI [1,3])
C0029354 (UMLS CUI [2,1])
C1292733 (UMLS CUI [2,2])
C0080331 (UMLS CUI [2,3])
C0348080 (UMLS CUI [3,1])
C1292733 (UMLS CUI [3,2])
C0080331 (UMLS CUI [3,3])
C1705847 (UMLS CUI [4,1])
C3842523 (UMLS CUI [4,2])
Pregnancy | Pregnancy, Planned
Item
patients who are pregnant or planning to become pregnant during the study
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
Study Subject Participation Status Impact Investigational Therapy | Study Subject Participation Status Impact Research results
Item
patients who are currently enrolled in another investigational study or registry that would directly impact the treatment or outcome of the current study
boolean
C2348568 (UMLS CUI [1,1])
C4049986 (UMLS CUI [1,2])
C0949266 (UMLS CUI [1,3])
C2348568 (UMLS CUI [2,1])
C4049986 (UMLS CUI [2,2])
C0683954 (UMLS CUI [2,3])