Gender criteria Fulfill
Item
women who satisfy the following conditions are the only subjects who will be eligible for this study:
boolean
C0079399 (UMLS CUI [1,1])
C0243161 (UMLS CUI [1,2])
C1550543 (UMLS CUI [1,3])
Normal Volunteers
Item
normal volunteers
boolean
C3661466 (UMLS CUI [1])
Breast Disease | Breast Disease Suspected
Item
subjects with known or suspected breast disease
boolean
C0006145 (UMLS CUI [1])
C0006145 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
Informed Consent
Item
subjects must have signed an approved consent form.
boolean
C0021430 (UMLS CUI [1])
Age
Item
subjects must be ≥ 18 years old.
boolean
C0001779 (UMLS CUI [1])
Kidney Disease Absent
Item
the protocol nurse will check with the patient that there is no h/o kidney disease
boolean
C0022658 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Creatinine normal | Estimated Glomerular Filtration Rate
Item
normal creatinine and estimated gfr* within 30 days under the following circumstances
boolean
C0860945 (UMLS CUI [1])
C3811844 (UMLS CUI [2])
Serum creatinine abnormal
Item
had abnormal creatinine in the last 60 days
boolean
C0438243 (UMLS CUI [1])
Age
Item
are over 60 years of age
boolean
C0001779 (UMLS CUI [1])
Chemotherapy
Item
has received chemotherapy within the past 30 days
boolean
C0392920 (UMLS CUI [1])
Diabetes Mellitus | HIV Infection | Kidney Disease | Renal carcinoma
Item
has diabetes, hiv, renal disease or hx of renal cancer
boolean
C0011849 (UMLS CUI [1])
C0019693 (UMLS CUI [2])
C0022658 (UMLS CUI [3])
C1378703 (UMLS CUI [4])
Estimated Glomerular Filtration Rate
Item
* gfr will be calculated using: http://www.kidney.org/professionals/kdoqi/gfr_calculator.cfm
boolean
C3811844 (UMLS CUI [1])
Estimated Glomerular Filtration Rate | Chemotherapy deteriorating Renal function | Therapeutic procedure deteriorating Renal function | Condition deteriorating Renal function | Gadolinium Agent
Item
patients with an egfr>90ml/min reported within 30 days, and who have not had intervening chemotherapy or other treatment or condition that might deteriorate renal function, may receive any gadolinium agent.
boolean
C3811844 (UMLS CUI [1])
C0392920 (UMLS CUI [2,1])
C1457868 (UMLS CUI [2,2])
C0232804 (UMLS CUI [2,3])
C0087111 (UMLS CUI [3,1])
C1457868 (UMLS CUI [3,2])
C0232804 (UMLS CUI [3,3])
C0348080 (UMLS CUI [4,1])
C1457868 (UMLS CUI [4,2])
C0232804 (UMLS CUI [4,3])
C0016911 (UMLS CUI [5,1])
C1254351 (UMLS CUI [5,2])
Children
Item
children will be excluded from this study.
boolean
C0008059 (UMLS CUI [1])
Pregnancy | Breast Feeding | Premenopausal state Urine pregnancy test | Premenopausal state Serum Beta-HCG Test
Item
pregnant women and women who are breast feeding will be excluded from this study. (the vanderbilt university medical center radiology "mri procedure screening form" will be used to identify and exclude subjects who are pregnant or breastfeeding. a urine pregnancy test/or serum beta hcg will also be performed for each pre-menopausal subject.)
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0232969 (UMLS CUI [3,1])
C0430056 (UMLS CUI [3,2])
C0232969 (UMLS CUI [4,1])
C1255526 (UMLS CUI [4,2])
Materials Inappropriate Magnetic Resonance
Item
subjects found to have any constitutionally present non-mr compatible ferromagnetic materials will be excluded from this study.
boolean
C0520510 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
C0917874 (UMLS CUI [1,3])
Illness Ineligibility Clinical Trial
Item
patients who are acutely ill who are deemed by their treating physician as not suitable candidates for this study
boolean
C0221423 (UMLS CUI [1,1])
C1512714 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
Magnetic Resonance Imaging | Patient unsuitable for procedure Due to Breast Volume | Patient unsuitable for procedure Due to Obesity
Item
subjects for whom an mri is technically not feasible (e.g. breast volume, obesity)
boolean
C0024485 (UMLS CUI [1])
C3839996 (UMLS CUI [2,1])
C0678226 (UMLS CUI [2,2])
C0006141 (UMLS CUI [2,3])
C0449468 (UMLS CUI [2,4])
C3839996 (UMLS CUI [3,1])
C0678226 (UMLS CUI [3,2])
C0028754 (UMLS CUI [3,3])
Vascular Access Ports Safety of devices Problem | Implants Safety of devices Problem
Item
subjects who have vascular access ports or other implanted devices rated as anything other than "safe" or "conditional 6"
boolean
C1608324 (UMLS CUI [1,1])
C0086139 (UMLS CUI [1,2])
C0033213 (UMLS CUI [1,3])
C0021102 (UMLS CUI [2,1])
C0086139 (UMLS CUI [2,2])
C0033213 (UMLS CUI [2,3])