Patient ID; Centre Number
Item
Patient ID, Centre No.
text
C1269815 (UMLS CUI [1,1])
C2825181 (UMLS CUI [1,2])
C1300638 (UMLS CUI [1,3])
Patient ID; Envelope Number
Item
Patient ID, Envelope No.
text
C1269815 (UMLS CUI [1,1])
C2348585 (UMLS CUI [1,2])
Patient Initials
Item
Patient Initials
text
C2986440 (UMLS CUI [1])
Hemorrhage; date of onset
Item
Onset of bleeding - date
date
C0019080 (UMLS CUI [1,1])
C0574845 (UMLS CUI [1,2])
Hemorrhage; start time
Item
Onset of bleeding - time
time
C0019080 (UMLS CUI [1,1])
C1301880 (UMLS CUI [1,2])
Hemorrhage; AE report number
Item
Onset of bleeding - related AE report #
integer
C0019080 (UMLS CUI [1,1])
C0877248 (UMLS CUI [1,2])
C0684224 (UMLS CUI [1,3])
C0237753 (UMLS CUI [1,4])
Hemorrhage, end date
Item
Cessation of bleeding - date
date
C0019080 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Hemorrhage, end time
Item
Cessation of bleeding - time
time
C0019080 (UMLS CUI [1,1])
C1522314 (UMLS CUI [1,2])
Item
Clinically overt bleeding meeting criteria for major bleed
text
C3160769 (UMLS CUI [1])
Code List
Clinically overt bleeding meeting criteria for major bleed
CL Item
Yes - Fatal bleed (Yes - Fatal bleed)
CL Item
Yes- Symptomatic intracranial hemorrhage (Yes- Symptomatic intracranial hemorrhage)
CL Item
Yes - Drop in hemoglobin of at least 3 g/dL (with each unit counting for 1.0 g/dL) (Yes - Drop in hemoglobin of at least 3 g/dL (with each unit counting for 1.0 g/dL))
CL Item
Yes - Requiring transfusion of 2 or more units of blood (Yes - Requiring transfusion of 2 or more units of blood)
CL Item
Yes - Retroperitoneal hemorrhage (Yes - Retroperitoneal hemorrhage)
CL Item
Yes - Intraocular bleeding leading to significant vision loss (Yes - Intraocular bleeding leading to significant vision loss)
Minor bleeding
Item
Minor bleeding: any other clinically overt bleeding not meeting major bleeding definition
boolean
C0019080 (UMLS CUI [1,1])
C0205165 (UMLS CUI [1,2])
Item
Was this bleeding event associated with any of the following?
text
C1560575 (UMLS CUI [1])
Code List
Was this bleeding event associated with any of the following?
CL Item
Index PCI (Index PCI)
CL Item
Repeat PCI (Repeat PCI)
CL Item
CABG surgery (CABG surgery)
CL Item
Coronary angiography (Coronary angiography)
CL Item
Other surgery (Other surgery)
CL Item
Other (specify) (Other (specify))
Item
Site/source
text
C0019080 (UMLS CUI [1,1])
C1515974 (UMLS CUI [1,2])
C0019080 (UMLS CUI [2,1])
C0449416 (UMLS CUI [2,2])
CL Item
Hematuria (Hematuria)
CL Item
Hemoptysis (Hemoptysis)
CL Item
Puncture site (Puncture site)
CL Item
Epistaxis (Epistaxis)
CL Item
Gastrointestinal (Gastrointestinal)
CL Item
Injection site (Injection site)
CL Item
Cardiac tamponade (Cardiac tamponade)
CL Item
Other (specify) (Other (specify))
Item
Was blood transfusion required?
text
C0019080 (UMLS CUI [1,1])
C0005841 (UMLS CUI [1,2])
Code List
Was blood transfusion required?
CL Item
Yes (give number of units) (Yes (give number of units))
Hemorrhage; Hemoglobin Before; Collection of blood specimen for laboratory procedure, Date in time
Item
Hemoglobin drop associated with bleeding episode - prior to bleeding episode - date of sample
date
C0019080 (UMLS CUI [1,1])
C0019046 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,3])
C0005834 (UMLS CUI [1,4])
C0011008 (UMLS CUI [1,5])
Hemorrhage; Hemoglobin Before; Collection of blood specimen for laboratory procedure, time
Item
Hemoglobin drop associated with bleeding episode - prior to bleeding episode - time of sample
time
C0019080 (UMLS CUI [1,1])
C0019046 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,3])
C0005834 (UMLS CUI [1,4])
C0040223 (UMLS CUI [1,5])
Hemorrhage; Hemoglobin Before
Item
Hemoglobin drop associated with bleeding episode - prior to bleeding episode
float
C0019080 (UMLS CUI [1,1])
C0019046 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,3])
Hemorrhage; hematocrit Before
Item
Hemoglobin drop associated with bleeding episode - prior to bleeding episode - hematocrit
integer
C0019080 (UMLS CUI [1,1])
C0518014 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,3])
Hemorrhage; Hemoglobin minimum; Collection of blood specimen for laboratory procedure, Date in time
Item
Hemoglobin drop associated with bleeding episode - lowest value - date of sample
date
C0019080 (UMLS CUI [1,1])
C0019046 (UMLS CUI [1,2])
C1524031 (UMLS CUI [1,3])
C0005834 (UMLS CUI [1,4])
C0011008 (UMLS CUI [1,5])
Hemorrhage; Hemoglobin minimum; Collection of blood specimen for laboratory procedure, time
Item
Hemoglobin drop associated with bleeding episode - lowest value - time of sample
time
C0019080 (UMLS CUI [1,1])
C0019046 (UMLS CUI [1,2])
C1524031 (UMLS CUI [1,3])
C0005834 (UMLS CUI [1,4])
C0040223 (UMLS CUI [1,5])
Hemorrhage; Hemoglobin minimum; Collection of blood specimen for laboratory procedure, time
Item
Hemoglobin drop associated with bleeding episode - lowest value - time of sample
time
C0019080 (UMLS CUI [1,1])
C0019046 (UMLS CUI [1,2])
C1524031 (UMLS CUI [1,3])
C0005834 (UMLS CUI [1,4])
C0040223 (UMLS CUI [1,5])
Hemorrhage; Hemoglobin minimum
Item
Hemoglobin drop associated with bleeding episode - lowest value
float
C0019080 (UMLS CUI [1,1])
C0019046 (UMLS CUI [1,2])
C1524031 (UMLS CUI [1,3])
Hemorrhage; hemoglobin minimum; hematocrit
Item
Hemoglobin drop associated with bleeding episode - lowest value
integer
C0019080 (UMLS CUI [1,1])
C0019046 (UMLS CUI [1,2])
C1524031 (UMLS CUI [1,3])
C0518014 (UMLS CUI [1,4])
Item
Were any of the following investigations performed?
text
C0019080 (UMLS CUI [1,1])
C0841577 (UMLS CUI [1,2])
Code List
Were any of the following investigations performed?
CL Item
CT Scan (CT Scan)
CL Item
Ultrasound (Ultrasound)
CL Item
Endoscopy (Endoscopy)
Item
Indicate whether any of the following medications were taken by the patient within 24 hrs of this bleeding event?
text
C0019080 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C4035156 (UMLS CUI [1,3])
Code List
Indicate whether any of the following medications were taken by the patient within 24 hrs of this bleeding event?
CL Item
GPIIb/IIIa antagonists (GPIIb/IIIa antagonists)
CL Item
Oral anticoagulants (Oral anticoagulants)
CL Item
Hirudin (Hirudin)
CL Item
Bivalirudin (Bivalirudin)
CL Item
open label UFH (open label UFH)
CL Item
Study drug (Study drug)
Item
Indicate whether any of the following medications were taken by the patient within 5 days of this bleeding event?
text
C0019080 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
Code List
Indicate whether any of the following medications were taken by the patient within 5 days of this bleeding event?
CL Item
Clopidogrel (Clopidogrel)
CL Item
Ticlopidine (Ticlopidine)