Estimated Glomerular Filtration Rate
Item
• screening egfr between 20 and 59 ml/min/1.73m2
boolean
C3811844 (UMLS CUI [1])
Hydration Therapy | Blood specimen Available | Administration Contrast Media
Item
baseline scr obtained within 72 hours and before hydration or, if obtained after hydration started, had the screening blood sample obtained within 72 hours of contrast administration
boolean
C1881074 (UMLS CUI [1])
C0178913 (UMLS CUI [2,1])
C0470187 (UMLS CUI [2,2])
C1533734 (UMLS CUI [3,1])
C0009924 (UMLS CUI [3,2])
Blood specimen Post-dose Quantity Available
Item
at least one post dose blood sample available
boolean
C0178913 (UMLS CUI [1,1])
C0439568 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0470187 (UMLS CUI [1,4])
Contrast Media Randomized Received
Item
received randomized contrast agent
boolean
C0009924 (UMLS CUI [1,1])
C0034656 (UMLS CUI [1,2])
C1514756 (UMLS CUI [1,3])
Angiocardiography Quantity | Percutaneous Coronary Intervention
Item
underwent only one cardiac angiography procedure (diagnostic cardiac angiography followed by pci was considered as one procedure if confirmed by investigator and total duration does not exceed 12 hours), then for this study
boolean
C0002971 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C1532338 (UMLS CUI [2])
Informed Consent | Protocol Compliance
Item
provides written informed consent and is willing to comply with protocol requirements;
boolean
C0021430 (UMLS CUI [1])
C0525058 (UMLS CUI [2])
Study Subject Participation Status | List Company Specified
Item
was included in the patient list provided by bracco;
boolean
C2348568 (UMLS CUI [1])
C0745732 (UMLS CUI [2,1])
C0683757 (UMLS CUI [2,2])
C0205369 (UMLS CUI [2,3])
Study Subject Participation Status | Clinical Trial Previous
Item
at least 1 year has passed since the patient's participation ended in the original care trial, as determined from the list provided by bracco
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2,1])
C0205156 (UMLS CUI [2,2])
Estimated Glomerular Filtration Rate
Item
• screening egfr outside the range of 20 and 59 ml/min/1.73m2
boolean
C3811844 (UMLS CUI [1])
Kidney Disease Unstable | Kidney Disease Requirement Dialysis
Item
unstable kidney disease or requiring dialysis upon enrollment
boolean
C0022658 (UMLS CUI [1,1])
C0443343 (UMLS CUI [1,2])
C0022658 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
C0011946 (UMLS CUI [2,3])
Blood draw Post-dose | Event Clinical Affecting Measurement of renal function
Item
prior to the post-dose blood draw, suffered a critical clinical event that would affect the reliability of serological measurement of renal function
boolean
C0005834 (UMLS CUI [1,1])
C0439568 (UMLS CUI [1,2])
C0441471 (UMLS CUI [2,1])
C0205210 (UMLS CUI [2,2])
C0392760 (UMLS CUI [2,3])
C2711919 (UMLS CUI [2,4])
Contrast Media Randomized Lacking
Item
did not receive randomized contrast agent per care protocol
boolean
C0009924 (UMLS CUI [1,1])
C0034656 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
Angiocardiography Lacking
Item
did not undergo a cardiac angiography procedure per care protocol
boolean
C0002971 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])