STATIN therapy prior to randomisation
Item
1. Was the subject regularly taking STATIN therapy for 8 weeks or more prior to randomisation?
boolean
C0360714 (UMLS CUI [1])
STATIN therapy at randomisation
Item
2. Was the subject taking STATIN therapy at the time of randomisation?
boolean
C0360714 (UMLS CUI [1,1])
C0034656 (UMLS CUI [1,2])
Item
If no, indicate reason
text
C0360714 (UMLS CUI [1])
Code List
If no, indicate reason
CL Item
Subject is intolerant or clinically contraindicated (1)
no STATIN therapy at randomisation other reason
Item
If other reason, specify:
text
C0746919 (UMLS CUI [1,1])
C3840932 (UMLS CUI [1,2])
ASPIRIN therapy prior to randomisation
Item
3. Was the subject regularly taking ASPIRIN therapy for 8 weeks or more prior to randomisation?
boolean
C4303556 (UMLS CUI [1])
ASPIRIN at randomisation
Item
4. Was the subject taking ASPIRIN at the time of randomisation?
boolean
C0004057 (UMLS CUI [1])
Item
If no, indicate reason:
text
C0004057 (UMLS CUI [1])
Code List
If no, indicate reason:
CL Item
Subject is intolerant or clinically contraindicated (1)
no ASPIRIN at randomisation other reason
Item
If other reason, specify:
integer
C0746919 (UMLS CUI [1,1])
C3840932 (UMLS CUI [1,2])
C0004057 (UMLS CUI [1,3])
P2Y12 inhibitors
Item
5. Is the subject regularly taking any P2Y12 inhibitors (i.e. thienopyridines)?
boolean
C2936585 (UMLS CUI [1])
Item
If no, indicate reason:
text
C2936585 (UMLS CUI [1])
Code List
If no, indicate reason:
CL Item
Subject is intolerant or clinically contraindicated (1)
CL Item
Not clinically indicated (2)
no P2Y12 inhibitors other reason
Item
If other reason, specify:
text
C2936585 (UMLS CUI [1])
beta-blocker
Item
6. Is the subject taking a beta-blocker?
boolean
C0001645 (UMLS CUI [1])
Item
If no, indicate reason:
text
C0001645 (UMLS CUI [1])
Code List
If no, indicate reason:
CL Item
Subject is intolerant or clinically contraindicated (1)
CL Item
Not clinically indicated (2)
no beta-blocker other reason
Item
If other reason, specify:
text
C0001645 (UMLS CUI [1])
ACE inhibitor
Item
7. Is the subject taking an ACE inhibitor?
boolean
C0003015 (UMLS CUI [1])
Item
If no, indicate reason:
text
C0003015 (UMLS CUI [1])
Code List
If no, indicate reason:
CL Item
Subject is intolerant or clinically contraindicated (1)
CL Item
Not clinically indicated (2)
no ACE inhibitors other reason
Item
If other reason, specify:
text
C0003015 (UMLS CUI [1])
ARB
Item
8. Is the subject taking an ARB?
boolean
C0521942 (UMLS CUI [1])
Item
If no, indicate reason:
text
C0521942 (UMLS CUI [1])
Code List
If no, indicate reason:
CL Item
Subject is intolerant or clinically contraindicated (1)
CL Item
Not clinically indicated (2)
no ARB other reason
Item
If other reason, specify:
text
C0746919 (UMLS CUI [1,1])
C3840932 (UMLS CUI [1,2])
C0521942 (UMLS CUI [1,3])
renin-angiotensin-aldosterone system-targeted medication
Item
9. Is the subject taking any other renin-angiotensin-aldosterone system-targeted medication?
boolean
C3653735 (UMLS CUI [1])
Item
If no, indicate reason:
text
C3653735 (UMLS CUI [1])
Code List
If no, indicate reason:
CL Item
Subject is intolerant or clinically contraindicated (1)
CL Item
Not clinically indicated (2)
no renin-angiotensin-aldosterone system-targeted medication other reason
Item
If other reason, specify:
text
C3653735 (UMLS CUI [1])
