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 OCT scans
Item
1) Date of OCT scans
date
C0011008 (UMLS CUI [1,1])
C0920367 (UMLS CUI [1,2])
Date Clinical Visit
Item
2) Date of Clinical Visit coinciding with scans
date
C0011008 (UMLS CUI [1,1])
C2174682 (UMLS CUI [1,2])
Item
3) Was time-domain OCT (Stratus-Zeiss) performed?
text
C4052697 (UMLS CUI [1])
Code List
3) Was time-domain OCT (Stratus-Zeiss) performed?
Item
4) Was spectral-domain OCT (Cirrus-Zeiss) performed?
text
C3876157 (UMLS CUI [1])
Code List
4) Was spectral-domain OCT (Cirrus-Zeiss) performed?
Item
5) Was spectral-domain OCT (Spectralis-Heidelberg) performed?
text
C3876157 (UMLS CUI [1])
Code List
5) Was spectral-domain OCT (Spectralis-Heidelberg) performed?
Item
6) Was ganglion cell layer thickness (segmentation) OCT (Cirrus-Zeiss) performed?
text
C0920367 (UMLS CUI [1,1])
C2697664 (UMLS CUI [1,2])
Code List
6) Was ganglion cell layer thickness (segmentation) OCT (Cirrus-Zeiss) performed?
Item
7) Was scan-based QA/QC performed?
text
C0178932 (UMLS CUI [1])
Code List
7) Was scan-based QA/QC performed?
Item
a. If Yes, indicate QA/QC results:
text
C1274040 (UMLS CUI [1,1])
C0178932 (UMLS CUI [1,2])
Code List
a. If Yes, indicate QA/QC results:
CL Item
fail (Explain) (2)
Result quality assurance
Item
If fail, explain:
text
C1274040 (UMLS CUI [1,1])
C0178932 (UMLS CUI [1,2])
Ocular Refraction right
Item
8) Refraction right eye (OD):
text
C1261472 (UMLS CUI [1,1])
C0205090 (UMLS CUI [1,2])
Ocular Refraction left
Item
9) Refraction left eye (OS):
text
C1261472 (UMLS CUI [1,1])
C0205091 (UMLS CUI [1,2])