Indication Implantation of CRT-D | Therapeutic procedure Heart failure | Therapeutic procedure Ventricular Tachycardia Life Threatening
Item
approved indication per acc/aha/hrs guidelines for implantation of a crt-d system for treatment of heart failure or lifethreatening ventricular tachyarrhythmia(s)
boolean
C3146298 (UMLS CUI [1,1])
C1135480 (UMLS CUI [1,2])
C0087111 (UMLS CUI [2,1])
C0018801 (UMLS CUI [2,2])
C0087111 (UMLS CUI [3,1])
C0042514 (UMLS CUI [3,2])
C2826244 (UMLS CUI [3,3])
Implantable defibrillator insertion | Implantation of cardiac pacemaker | Upgrade Implantable defibrillator | Upgrade Artificial cardiac pacemaker | Implantation Lead Left ventricle Absent
Item
receiving a new implant or undergoing an upgrade from an existing icd or pacemaker implant with no prior lv lead placement.
boolean
C0877213 (UMLS CUI [1])
C0189842 (UMLS CUI [2])
C3272274 (UMLS CUI [3,1])
C0162589 (UMLS CUI [3,2])
C3272274 (UMLS CUI [4,1])
C0030163 (UMLS CUI [4,2])
C0021107 (UMLS CUI [5,1])
C0181586 (UMLS CUI [5,2])
C0225897 (UMLS CUI [5,3])
C0332197 (UMLS CUI [5,4])
Informed Consent | Protocol Compliance
Item
ability to provide informed consent for study participation and is willing and able to comply with the prescribed follow-up tests and schedule of evaluations
boolean
C0021430 (UMLS CUI [1])
C0525058 (UMLS CUI [2])
Cerebrovascular accident | Transient Ischemic Attack
Item
have had a recent cva or tia within three months of enrollment
boolean
C0038454 (UMLS CUI [1])
C0007787 (UMLS CUI [2])
Medical contraindication Emergency Thoracotomy
Item
have a contraindication for an emergency thoracotomy
boolean
C1301624 (UMLS CUI [1,1])
C0013956 (UMLS CUI [1,2])
C0039991 (UMLS CUI [1,3])
Hypersensitivity Dexamethasone sodium phosphate Dose | Heparin allergy
Item
have a hypersensitivity to a single 1.0mg dose of dexamethasone sodium phosphate or short term contact with heparin
boolean
C0020517 (UMLS CUI [1,1])
C0113286 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,3])
C0571776 (UMLS CUI [2])
Heart Transplantation Classification Status | Consideration Heart Transplantation
Item
have a classification of status 1 for cardiac transplantation or consideration for transplantation over the next 3 months
boolean
C0018823 (UMLS CUI [1,1])
C0008902 (UMLS CUI [1,2])
C0449438 (UMLS CUI [1,3])
C0518609 (UMLS CUI [2,1])
C0018823 (UMLS CUI [2,2])
Heart Transplantation
Item
have undergone a cardiac transplantation within 40 days of enrollment
boolean
C0018823 (UMLS CUI [1])
Myocardial Infarction | Angina, Unstable | Myocardial Revascularization | Percutaneous Transluminal Coronary Angioplasty | Stent | Coronary Artery Bypass Surgery
Item
have had a recent myocardial infarction, unstable angina or cardiac revascularization (ptca, stent or cabg) within 40 days of enrollment
boolean
C0027051 (UMLS CUI [1])
C0002965 (UMLS CUI [2])
C0027056 (UMLS CUI [3])
C2936173 (UMLS CUI [4])
C0038257 (UMLS CUI [5])
C0010055 (UMLS CUI [6])
Study Subject Participation Status | Clinical Trial Including Treatment Arm
Item
are currently participating in a clinical investigation that includes an active treatment arm
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2,1])
C0332257 (UMLS CUI [2,2])
C1522541 (UMLS CUI [2,3])
Pregnancy | Pregnancy, Planned
Item
are pregnant or planning to become pregnant during the duration of the study
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
Life Expectancy
Item
have a life expectancy of less than 6 months due to any condition
boolean
C0023671 (UMLS CUI [1])
Age
Item
are less than 18 years of age
boolean
C0001779 (UMLS CUI [1])
Follow-up Compliance behavior Unable
Item
are unable to comply with the follow up schedule
boolean
C3274571 (UMLS CUI [1,1])
C1321605 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])