Study ID
Item
Study ID
integer
C2826693 (UMLS CUI [1])
Study site name
Item
Study site name
text
C2825164 (UMLS CUI [1])
Subject ID
Item
Subject ID
integer
C2348585 (UMLS CUI [1])
Date MRI
Item
1. Date of MRI:
date
C0011008 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
Date Clinical Visit
Item
2. Date of Clinical Visit coinciding with scan:
date
C0011008 (UMLS CUI [1,1])
C2174682 (UMLS CUI [1,2])
Item
3. Clinical Visit type coinciding with scan (choose only one):
text
C2174682 (UMLS CUI [1])
Code List
3. Clinical Visit type coinciding with scan (choose only one):
CL Item
End of treatment (2)
Item
4. Scanner Manufacturer (choose only one):
text
C0947322 (UMLS CUI [1])
Code List
4. Scanner Manufacturer (choose only one):
Other
Item
Other specify
text
C0205394 (UMLS CUI [1])
Item
5. Field Strength of Scanner Used (choose only one):
text
C3896987 (UMLS CUI [1,1])
C3898570 (UMLS CUI [1,2])
Code List
5. Field Strength of Scanner Used (choose only one):
Other
Item
Other specify
text
C0205394 (UMLS CUI [1])
MRI Software
Item
6. MRI Software Version Number:
text
C3204107 (UMLS CUI [1])
Item
7. Was Gadolinium administered in the protocol window?
text
C0016911 (UMLS CUI [1])
Code List
7. Was Gadolinium administered in the protocol window?
Gadolinium
Item
a. If No, explain:
text
C0016911 (UMLS CUI [1])
Magnetic Resonance Imaging Gadolinium
Item
8. What was the delay in time from injection to start of post-Gd T1-weighted sequence?
text
C0024485 (UMLS CUI [1,1])
C0016911 (UMLS CUI [1,2])
date estimated glomerular filtration rate
Item
9. Date estimated glomerular filtration rate (eGFR) was performed:
date
C0011008 (UMLS CUI [1,1])
C3811844 (UMLS CUI [1,2])
Estimated glomerular filtration rate
Item
10. Estimated glomerular filtration rate (eGFR) result (note a caution warning if <55 and an exclusion for Gd administration if <45):
float
C3811844 (UMLS CUI [1])
Item
11. Was scan-based QA/QC performed?
text
C0178932 (UMLS CUI [1])
Code List
11. Was scan-based QA/QC performed?
Item
12. If Yes, indicate QA/QC results:
text
C0178932 (UMLS CUI [1])
Code List
12. If Yes, indicate QA/QC results:
CL Item
Fail, explain: (2)
Explanation
Item
If fail, explain:
text
C0681841 (UMLS CUI [1])