Gender | Whole Ultrasound screening of breast Scheduled | Full field digital mammogram Scheduled
Item
women scheduled for screening wbus and a screening ffdm on the same day or within the following 30 days of each other
boolean
C0079399 (UMLS CUI [1])
C2367051 (UMLS CUI [2,1])
C0439751 (UMLS CUI [2,2])
C0205539 (UMLS CUI [2,3])
C3862913 (UMLS CUI [3,1])
C0205539 (UMLS CUI [3,2])
Gender | Contrast enhanced digital mammography Scheduled
Item
women scheduled for screening cedm alone
boolean
C0079399 (UMLS CUI [1])
C4511913 (UMLS CUI [2,1])
C0205539 (UMLS CUI [2,2])
Gender | Whole Ultrasound screening of breast Scheduled | Contrast enhanced digital mammography Scheduled
Item
women scheduled for wbus and screening cedm on the same day or within 30 days of one another
boolean
C0079399 (UMLS CUI [1])
C2367051 (UMLS CUI [2,1])
C0439751 (UMLS CUI [2,2])
C0205539 (UMLS CUI [2,3])
C4511913 (UMLS CUI [3,1])
C0205539 (UMLS CUI [3,2])
Age
Item
age < 30 years old
boolean
C0001779 (UMLS CUI [1])
Gender
Item
male patients
boolean
C0079399 (UMLS CUI [1])
Breast symptoms | Palpable mass | Nipple discharge
Item
patients with any clinical breast symptoms (palpable mass, nipple discharge, etc)
boolean
C2220038 (UMLS CUI [1])
C0746412 (UMLS CUI [2])
C0149741 (UMLS CUI [3])
Breast Carcinoma
Item
patients with known diagnosis of breast cancer
boolean
C0678222 (UMLS CUI [1])
Operation on breast | Biopsy of breast
Item
patients with any breast surgery or biopsy within 90 days prior to the study
boolean
C3714726 (UMLS CUI [1])
C0405352 (UMLS CUI [2])
Segmental Mastectomy Breast Carcinoma
Item
patients who have had a lumpectomy for breast cancer within 3 years prior to the study
boolean
C0024885 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
Magnetic resonance imaging of breast
Item
patients who are thought to have a breast mri within 3 years prior to the study
boolean
C0344104 (UMLS CUI [1])
Breast implants | Breast Imaging
Item
patients with breast implants on the breast that is being imaged
boolean
C0179412 (UMLS CUI [1])
C0006141 (UMLS CUI [2,1])
C0011923 (UMLS CUI [2,2])
Medical contraindication Iodinated contrast agent Intravenous use | Hypersensitivity Iodinated contrast media | Renal Insufficiency Severe | Creatinine measurement, serum
Item
patients with contraindication to the intravenous use of iodinated contrast agent (i.e. allergy to iodinated contrast or severely impaired renal function with a creatinine level ≥1.3)
boolean
C1301624 (UMLS CUI [1,1])
C0879373 (UMLS CUI [1,2])
C1522726 (UMLS CUI [1,3])
C0020517 (UMLS CUI [2,1])
C1960405 (UMLS CUI [2,2])
C1565489 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0201976 (UMLS CUI [4])