age; gender; informed consent
Item
male or non-pregnant female equal or greater than the age of 18 years old and is able to provide informed consent.
boolean
C0001779 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
C0021430 (UMLS CUI [3])
Catheterization elective
Item
subject is scheduled to undergo an elective catheterization procedure
boolean
C0007430 (UMLS CUI [1,1])
C0439608 (UMLS CUI [1,2])
hemodynamically stable
Item
hemodynamically stable
boolean
C0578150 (UMLS CUI [1])
Contrast Induced Nephropathy
Item
at increased risk of developing cin
boolean
C0748300 (UMLS CUI [1])
testing follow-up
Item
subject has agreed to all follow-up testing.
boolean
C0039593 (UMLS CUI [1,1])
C1522577 (UMLS CUI [1,2])
congestive heart failure
Item
class 3 or 4 congestive heart failure (chf)
boolean
C0018802 (UMLS CUI [1])
renal replacement therapy; foley catheter
Item
is anuric or has undergone renal replacement therapy within the past month, or has a known inability to have a foley catheter placed.
boolean
C0206074 (UMLS CUI [1])
C0179804 (UMLS CUI [2])
hospitalization; dialysis; renal function
Item
subject has been hospitalized or treated medically for any change in renal function over the past week (i.e. dialysis, etc.), or a significant change in renal function is noted at time of screening.
boolean
C0019993 (UMLS CUI [1])
C0011946 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
severe aortic stenosis; Replacement of aortic valve
Item
has documented severe aortic stenosis.(note: subjects who have undergone successful replacement or repair of their aortic valve are not excluded.)
boolean
C3806272 (UMLS CUI [1])
C0003506 (UMLS CUI [2])
Hemodynamics; electrolyte imbalance; Cardiac Arrhythmia
Item
currently has a known clinically significant electrolyte imbalance or clinically significant arrhythmias which compromise subject's hemodynamic state.
boolean
C0019010 (UMLS CUI [1])
C0342579 (UMLS CUI [2])
C0003811 (UMLS CUI [3])
severe anemia; Hematocrit level
Item
patient has moderate to severe anemia (hematocrit < 27%) at screening
boolean
C0238644 (UMLS CUI [1])
C0518014 (UMLS CUI [2])
major surgical procedure
Item
has received contrast within 10 days of procedure or has a planned additional cardiac or renal or other major surgical procedure within the7 day follow-up period.
boolean
C0038894 (UMLS CUI [1])
heart attack
Item
has ruled in for an serious heart attack within 48 hours of the planned procedure
boolean
C0027051 (UMLS CUI [1])
respiratory insufficiency; Oxygen saturation measurement
Item
has documented respiratory insufficiency as evidenced by an oxygen saturation of < 90% on room air assessed on day of procedure.
boolean
C0035229 (UMLS CUI [1])
C0523807 (UMLS CUI [2])
dose adjustment; drug nephrotoxic
Item
planned addition, discontinuation or dose adjustment of the nephrotoxic drugs
boolean
C2826232 (UMLS CUI [1])
C0013227 (UMLS CUI [2,1])
C1514118 (UMLS CUI [2,2])
hypersensitivity furosemide
Item
subject has a known hypersensitivity to furosemide and/or the contrast agent being used.
boolean
C0020517 (UMLS CUI [1,1])
C0016860 (UMLS CUI [1,2])
Study Subject Participation Status
Item
subject is currently, plans, or has been enrolled in another clinical study involving use of an investigational drug or device within the prior 30 days.
boolean
C2348568 (UMLS CUI [1])
lactating; pregnant
Item
subject is pregnant or breastfeeding.
boolean
C2828358 (UMLS CUI [1])
C0549206 (UMLS CUI [2])
informed consent
Item
subject is unable to provide informed consent.
boolean
C0021430 (UMLS CUI [1])