ID

42247

Beschreibung

Ticagrelor is a new, reversible binding, anti-platelet medication. Anti-platelet medications work to prevent the formation of blood clots. Ticagrelor is being developed as a treatment for patients with acute coronary syndrome (ACS). ACS is a term that is used to describe both heart attacks in progress or the imminent threat of a heart attack. ACS is usually caused by the formation of a blood clot in an artery that partially or totally blocks the blood supply to a portion of the heart muscle. Ticagrelor will be compared with clopidogrel to determine which drug, when either is used in conjunction with aspirin, is better at reducing deaths from vascular causes, future heart attacks and/or strokes in patients with ACS. https://clinicaltrials.gov/ct2/show/NCT00391872

Link

https://clinicaltrials.gov/ct2/show/NCT00391872

Stichworte

Versionen (3)
  1. 28.11.15 28.11.15 -
  2. 14.04.21 14.04.21 - Ahmed Rafee, MD
  3. 15.04.21 15.04.21 - Ahmed Rafee, MD
Rechteinhaber

AstraZeneca

Hochgeladen am

15. April 2021

DOI

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Lizenz

Creative Commons BY 4.0
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Excerpt PLATO Acute coronary Syndrome NCT00391872

Englisch

Section Event Forms

14 Formulare  
Death
Beschreibung

Death

Alias
UMLS CUI-1
C1306577
Event tracking number
Beschreibung

Event tracking number

Datentyp

text

Alias
UMLS CUI [1,1]
C0441471
UMLS CUI [1,2]
C0600091
Date of death
Beschreibung

Date of death

Datentyp

date

Alias
UMLS CUI [1]
C1148348
Time of death
Beschreibung

Time of death

Datentyp

time

Alias
UMLS CUI [1]
C1301931
Autopsy performed
Beschreibung

Autopsy performed

Datentyp

boolean

Alias
UMLS CUI [1]
C0004398
Death witnessed
Beschreibung

Death witnessed

Datentyp

boolean

Alias
UMLS CUI [1]
C2924291
Death category
Beschreibung

Cause of Death

Datentyp

text

Alias
UMLS CUI [1]
C0007465
If Vascular death, Sub-classification
Beschreibung

Cause of vascular death

Datentyp

text

Alias
UMLS CUI [1]
C0007465
If Non-vascular death, Sub-classification
Beschreibung

Cause of non-vascular death

Datentyp

text

Alias
UMLS CUI [1]
C0007465
Myocardial Infarction, Silent
Beschreibung

Myocardial Infarction, Silent

Alias
UMLS CUI-1
C0340324
Event tracking number
Beschreibung

Event tracking number

Datentyp

text

Alias
UMLS CUI [1,1]
C0441471
UMLS CUI [1,2]
C0600091
Date of ECG
Beschreibung

Date of ECG

Datentyp

date

Alias
UMLS CUI [1]
C2826640
Any other supportive data
Beschreibung

Supportive data

Datentyp

boolean

Alias
UMLS CUI [1]
C1320722
Cardiac Ischaemic Event
Beschreibung

Cardiac Ischaemic Event

Alias
UMLS CUI-1
C0151744
Event tracking number
Beschreibung

Event tracking number

Datentyp

text

Alias
UMLS CUI [1,1]
C0441471
UMLS CUI [1,2]
C0600091
Event text
Beschreibung

Event text

Datentyp

text

Alias
UMLS CUI [1,1]
C1527021
UMLS CUI [1,2]
C0441471
Event started date and time
Beschreibung

Event started date and time

Datentyp

datetime

Alias
UMLS CUI [1,1]
C2585732
UMLS CUI [1,2]
C0151744
Duration of symptoms
Beschreibung

Duration of symptoms

Datentyp

text

Alias
UMLS CUI [1]
C0436359
Ischaemic symptoms at rest
Beschreibung

Ischaemic symptoms at rest

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0745417
UMLS CUI [1,2]
C0443144
Related to a procedure/surgery
Beschreibung

Related to a procedure/ surgery

Datentyp

boolean

Alias
UMLS CUI [1]
C2924519
Event resulted in an urgent revascularization
Beschreibung

Urgent cardiac revascularization

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0027056
UMLS CUI [1,2]
C0439609
Specify main reason urgent revascularization not performed
Beschreibung

Main reason urgent revascularization not performed

Datentyp

text

Alias
UMLS CUI [1,1]
C0027056
UMLS CUI [1,2]
C0439609
UMLS CUI [1,3]
C0445106
UMLS CUI [1,4]
C0566251
Event prolonged an ongoing hospitalization
Beschreibung

Event prolonged an ongoing hospitalization

Datentyp

boolean

Alias
UMLS CUI [1]
C0745041
Event resulted in a hospitalization
Beschreibung

Event resulted in a hospitalization

Datentyp

boolean

Alias
UMLS CUI [1]
C0019993
Event did not result in or prolong an ongoing hospitalization
Beschreibung

Event did not result in or prolong an ongoing hospitalization

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1519255
UMLS CUI [1,2]
C3640791
UMLS CUI [1,3]
C1518422
New Q waves (> 0.03 sec in width and > 1 mm in depth)
Beschreibung

Q waves

Datentyp

boolean

Alias
UMLS CUI [1]
C1305738
New ST depression (> 0.5 mm)
Beschreibung

ST depression

Datentyp

boolean

Alias
UMLS CUI [1]
C0520887
New pathological T wave inversion (> 1 mm)
Beschreibung

T wave inversion

Datentyp

boolean

Alias
UMLS CUI [1]
C0520888
New ST elevation (> 1 mm)
Beschreibung

ST elevation

Datentyp

boolean

Alias
UMLS CUI [1]
C0520886
New left bundle branch block
Beschreibung

left bundle branch block

Datentyp

boolean

Alias
UMLS CUI [1]
C0023211
Local cardiac biomarker measurements
Beschreibung

Cardiac biomarker measurements

Datentyp

text

Alias
UMLS CUI [1]
C1271630
Did this event result in death
Beschreibung

Death

Datentyp

boolean

Alias
UMLS CUI [1]
C1306577
Final diagnosis
Beschreibung

Final diagnosis

Datentyp

text

Alias
UMLS CUI [1]
C0332144
Did the Subject experience any additional cardiac ischaemic events since previous visit
Beschreibung

Additional cardiac ischaemic events

Datentyp

boolean

Alias
UMLS CUI [1]
C0151744
Stroke/TIA
Beschreibung

Stroke/TIA

Alias
UMLS CUI-1
C0038454
Event tracking number
Beschreibung

Event tracking number

Datentyp

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0600091
Event text
Beschreibung

Event text

Datentyp

text

Alias
UMLS CUI [1,1]
C1527021
UMLS CUI [1,2]
C0877248
Event started date and time
Beschreibung

Event started date and time

Datentyp

date

Alias
UMLS CUI [1,1]
C2585732
UMLS CUI [1,2]
C0038454
Type of event
Beschreibung

Type of event

Datentyp

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0332307
Symptoms of stroke/TIA
Beschreibung

Symptoms of stroke/TIA

Datentyp

text

Alias
UMLS CUI [1,1]
C1457887
UMLS CUI [1,2]
C0038454
Duration of symptoms
Beschreibung

Duration of symptoms

Datentyp

integer

Alias
UMLS CUI [1]
C0436359
Event prolonged an ongoing hospitalization
Beschreibung

hospitalization prolonged

Datentyp

boolean

Alias
UMLS CUI [1]
C0745041
Event resulted in a hospitalization
Beschreibung

Hospitalization

Datentyp

boolean

Alias
UMLS CUI [1]
C0019993
Event did not result in or prolong an ongoing hospitalization
Beschreibung

Event did not result in or prolong an ongoing hospitalization

Datentyp

boolean

Alias
UMLS CUI [1]
C0745041
Stroke/TIA verified by
Beschreibung

Stroke/TIA verified

Datentyp

text

Alias
UMLS CUI [1,1]
C1711411
UMLS CUI [1,2]
C0038454
Bleeding Event
Beschreibung

Bleeding Event

Alias
UMLS CUI-1
C0019080
Event tracking number
Beschreibung

Event tracking number

Datentyp

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0600091
Event text
Beschreibung

Event text

Datentyp

text

Alias
UMLS CUI [1,1]
C1527021
UMLS CUI [1,2]
C0877248
Type of bleed
Beschreibung

Type of bleed

Datentyp

text

Alias
UMLS CUI [1,1]
C0019080
UMLS CUI [1,2]
C0332307
Primary location of bleed
Beschreibung

Primary location of bleed

Datentyp

text

Alias
UMLS CUI [1,1]
C0019080
UMLS CUI [1,2]
C0450429
Nature of bleed
Beschreibung

Nature of bleed

Datentyp

text

Alias
UMLS CUI [1,1]
C0019080
UMLS CUI [1,2]
C0332307
Administration of pressors
Beschreibung

Administration of pressors

Datentyp

boolean

Alias
UMLS CUI [1]
C0237795
Haemodynamic compromise
Beschreibung

Haemodynamic compromise

Datentyp

boolean

Alias
UMLS CUI [1]
C0948268
Surgical intervention required to stop or treat bleeding
Beschreibung

Surgical intervention required to stop or treat bleeding

Datentyp

boolean

Alias
UMLS CUI [1]
C0149533
Haemoglobin measurements relevant to event
Beschreibung

Haemoglobin measurements

Datentyp

text

Alias
UMLS CUI [1]
C0518015
Haemoglobin measurements not available preceding event
Beschreibung

Haemoglobin measurements not available preceding event

Datentyp

boolean

Alias
UMLS CUI [1]
C0149533
Arterial Thrombotic Event
Beschreibung

Arterial Thrombotic Event

Alias
UMLS CUI-1
C0151942
Event tracking number
Beschreibung

Event tracking number

Datentyp

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0600091
Event text
Beschreibung

Event text

Datentyp

text

Alias
UMLS CUI [1,1]
C1527021
UMLS CUI [1,2]
C0877248
Event started date and time
Beschreibung

Event started date and time

Datentyp

datetime

Alias
UMLS CUI [1,1]
C2585732
UMLS CUI [1,2]
C0151942
Clinical symptoms
Beschreibung

Clinical symptoms

Datentyp

text

Alias
UMLS CUI [1,1]
C1457887
UMLS CUI [1,2]
C0151942
Diagnostic study(s) performed
Beschreibung

Diagnostics performed

Datentyp

text

Alias
UMLS CUI [1]
C3259360
Event prolonged an ongoing hospitalization
Beschreibung

hospitalization prolonged

Datentyp

boolean

Alias
UMLS CUI [1]
C0745041
Event resulted in a hospitalization
Beschreibung

Hospitalization

Datentyp

boolean

Alias
UMLS CUI [1]
C0019993
Event did not result in or prolong an ongoing hospitalization
Beschreibung

Event did not result in or prolong an ongoing hospitalization

Datentyp

boolean

Alias
UMLS CUI [1]
C0745041
Final diagnosis
Beschreibung

Final diagnosis

Datentyp

text

Alias
UMLS CUI [1]
C0332144
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Ähnliche Modelle

Section Event Forms

14 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Death
C1306577 (UMLS CUI-1)
Event tracking number
Item
Event tracking number
text
C0441471 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Date of death
Item
Date of death
date
C1148348 (UMLS CUI [1])
Time of death
Item
Time of death
time
C1301931 (UMLS CUI [1])
Autopsy performed
Item
Autopsy performed
boolean
C0004398 (UMLS CUI [1])
Death witnessed
Item
Death witnessed
boolean
C2924291 (UMLS CUI [1])
Item
Death category
text
C0007465 (UMLS CUI [1])
Cause of Death
Code List
Death category
CL Item
Vascular (Vascular)
I (UMLS CUI-1)
CL Item
Non-vascular (Non-vascular)
I (UMLS CUI-1)
CL Item
Unknown (Unknown)
I (UMLS CUI-1)
Item
If Vascular death, Sub-classification
text
C0007465 (UMLS CUI [1])
Cause of vascular death
Code List
If Vascular death, Sub-classification
CL Item
Sudden death (Sudden death)
CL Item
Myocardial infarction (Myocardial infarction)
CL Item
Unstable angina (Unstable angina)
CL Item
Other coronary artery disease (Other coronary artery disease)
CL Item
Stroke (Stroke)
CL Item
Arterial embolism (Arterial embolism)
CL Item
Pulmonary embolism (Pulmonary embolism)
CL Item
Ruptured aortic aneurysm (Ruptured aortic aneurysm)
CL Item
Aortic dissection (Aortic dissection)
CL Item
Heart failure (Heart failure)
CL Item
Cardiac arrhythmia (Cardiac arrhythmia)
CL Item
Death from bleeding (not related to trauma) (Death from bleeding (not related to trauma))
CL Item
Endocarditis (Endocarditis)
CL Item
Valvular disease (Valvular disease)
CL Item
Other (Other)
Item
If Non-vascular death, Sub-classification
text
C0007465 (UMLS CUI [1])
Cause of non-vascular death
Code List
If Non-vascular death, Sub-classification
CL Item
Respiratory failure (Respiratory failure)
CL Item
Pneumonia (Pneumonia)
CL Item
Cancer (Cancer)
CL Item
Trauma (Trauma)
CL Item
Suicide (Suicide)
CL Item
Liver failure (Liver failure)
CL Item
Renal failure (Renal failure)
CL Item
Sepsis (Sepsis)
CL Item
Multiorgan failure (Multiorgan failure)
CL Item
Other (Other)
Item Group
Myocardial Infarction, Silent
C0340324 (UMLS CUI-1)
Event tracking number
Item
Event tracking number
text
C0441471 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Date of ECG
Item
Date of ECG
date
C2826640 (UMLS CUI [1])
Supportive data
Item
Any other supportive data
boolean
C1320722 (UMLS CUI [1])
Item Group
Cardiac Ischaemic Event
C0151744 (UMLS CUI-1)
Event tracking number
Item
Event tracking number
text
C0441471 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Event text
Item
Event text
text
C1527021 (UMLS CUI [1,1])
C0441471 (UMLS CUI [1,2])
Event started date and time
Item
Event started date and time
datetime
C2585732 (UMLS CUI [1,1])
C0151744 (UMLS CUI [1,2])
Item
Duration of symptoms
text
C0436359 (UMLS CUI [1])
Duration of symptoms
Code List
Duration of symptoms
CL Item
≥10-<20 mins (≥10-<20 mins)
CL Item
≥20 mins (≥20 mins)
Ischaemic symptoms at rest
Item
Ischaemic symptoms at rest
boolean
C0745417 (UMLS CUI [1,1])
C0443144 (UMLS CUI [1,2])
Related to a procedure/ surgery
Item
Related to a procedure/surgery
boolean
C2924519 (UMLS CUI [1])
Urgent cardiac revascularization
Item
Event resulted in an urgent revascularization
boolean
C0027056 (UMLS CUI [1,1])
C0439609 (UMLS CUI [1,2])
Item
Specify main reason urgent revascularization not performed
text
C0027056 (UMLS CUI [1,1])
C0439609 (UMLS CUI [1,2])
C0445106 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,4])
Main reason urgent revascularization not performed
Code List
Specify main reason urgent revascularization not performed
CL Item
Subject refusal (Subject refusal)
CL Item
No significant coronary lesion (No significant coronary lesion)
CL Item
Vascular anatomy not suitable (Vascular anatomy not suitable)
CL Item
Subject’s condition not suitable (Subject’s condition not suitable)
CL Item
PCI planned within 30 days (PCI planned within 30 days)
CL Item
PCI planned after 30 days (PCI planned after 30 days)
CL Item
CABG planned within 30 days (CABG planned within 30 days)
CL Item
CABG planned after 30 days (CABG planned after 30 days)
CL Item
Other (Other)
Event prolonged an ongoing hospitalization
Item
Event prolonged an ongoing hospitalization
boolean
C0745041 (UMLS CUI [1])
Event resulted in a hospitalization
Item
Event resulted in a hospitalization
boolean
C0019993 (UMLS CUI [1])
Event did not result in or prolong an ongoing hospitalization
Item
Event did not result in or prolong an ongoing hospitalization
boolean
C1519255 (UMLS CUI [1,1])
C3640791 (UMLS CUI [1,2])
C1518422 (UMLS CUI [1,3])
Q waves
Item
New Q waves (> 0.03 sec in width and > 1 mm in depth)
boolean
C1305738 (UMLS CUI [1])
ST depression
Item
New ST depression (> 0.5 mm)
boolean
C0520887 (UMLS CUI [1])
T wave inversion
Item
New pathological T wave inversion (> 1 mm)
boolean
C0520888 (UMLS CUI [1])
ST elevation
Item
New ST elevation (> 1 mm)
boolean
C0520886 (UMLS CUI [1])
left bundle branch block
Item
New left bundle branch block
boolean
C0023211 (UMLS CUI [1])
Cardiac biomarker measurements
Item
Local cardiac biomarker measurements
text
C1271630 (UMLS CUI [1])
Death
Item
Did this event result in death
boolean
C1306577 (UMLS CUI [1])
Item
Final diagnosis
text
C0332144 (UMLS CUI [1])
Final diagnosis
Code List
Final diagnosis
CL Item
STEMI (STEMI)
I (UMLS CUI-1)
CL Item
NSTEMI (NSTEMI)
I (UMLS CUI-1)
CL Item
Unstable angina (Unstable angina)
I (UMLS CUI-1)
CL Item
Stable angina (Stable angina)
I (UMLS CUI-1)
CL Item
Other (Other)
I (UMLS CUI-1)
Additional cardiac ischaemic events
Item
Did the Subject experience any additional cardiac ischaemic events since previous visit
boolean
C0151744 (UMLS CUI [1])
Item Group
Stroke/TIA
C0038454 (UMLS CUI-1)
Event tracking number
Item
Event tracking number
text
C0877248 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Event text
Item
Event text
text
C1527021 (UMLS CUI [1,1])
C0877248 (UMLS CUI [1,2])
Event started date and time
Item
Event started date and time
date
C2585732 (UMLS CUI [1,1])
C0038454 (UMLS CUI [1,2])
Item
Type of event
text
C0877248 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Type of event
Code List
Type of event
CL Item
Stroke (Stroke)
C0038454 (UMLS CUI-1)
CL Item
TIA (TIA)
C0007787 (UMLS CUI-1)
Item
Symptoms of stroke/TIA
text
C1457887 (UMLS CUI [1,1])
C0038454 (UMLS CUI [1,2])
Symptoms of stroke/TIA
Code List
Symptoms of stroke/TIA
CL Item
Hemiplegia/paresis (Hemiplegia/paresis)
CL Item
Hemianaesthesia/sensory deficit (Hemianaesthesia/sensory deficit)
CL Item
Hemianopsia (Hemianopsia)
CL Item
Neglect (Neglect)
CL Item
Isolated facial weakness/droop (Isolated facial weakness/droop)
CL Item
Ataxia/dysmetria (Ataxia/dysmetria)
CL Item
Dysarthria/speech impairment (Dysarthria/speech impairment)
CL Item
Aphasia (expressive and/or (Aphasia (expressive and/or)
CL Item
receptive (receptive)
CL Item
Other (Other)
Item
Duration of symptoms
integer
C0436359 (UMLS CUI [1])
Duration of symptoms
Code List
Duration of symptoms
CL Item
<24 hrs (1)
I (UMLS CUI-1)
CL Item
>24 hrs (2)
I (UMLS CUI-1)
CL Item
Persistent (3)
I (UMLS CUI-1)
hospitalization prolonged
Item
Event prolonged an ongoing hospitalization
boolean
C0745041 (UMLS CUI [1])
Hospitalization
Item
Event resulted in a hospitalization
boolean
C0019993 (UMLS CUI [1])
Event did not result in or prolong an ongoing hospitalization
Item
Event did not result in or prolong an ongoing hospitalization
boolean
C0745041 (UMLS CUI [1])
Item
Stroke/TIA verified by
text
C1711411 (UMLS CUI [1,1])
C0038454 (UMLS CUI [1,2])
Stroke/TIA verified
Code List
Stroke/TIA verified by
CL Item
Autopsy (Autopsy)
I (UMLS CUI-1)
CL Item
Clinical diagnosis (Clinical diagnosis)
I (UMLS CUI-1)
CL Item
CT scan (CT scan)
I (UMLS CUI-1)
CL Item
MRI (MRI)
I (UMLS CUI-1)
CL Item
Lumbar puncture (Lumbar puncture)
I (UMLS CUI-1)
CL Item
Neurosurgery (Neurosurgery)
I (UMLS CUI-1)
CL Item
Other (Other)
I (UMLS CUI-1)
Item Group
Bleeding Event
C0019080 (UMLS CUI-1)
Event tracking number
Item
Event tracking number
text
C0877248 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Event text
Item
Event text
text
C1527021 (UMLS CUI [1,1])
C0877248 (UMLS CUI [1,2])
Item
Type of bleed
text
C0019080 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Type of bleed
Code List
Type of bleed
CL Item
Major bleed, fatal/life-threatening (Major bleed, fatal/life-threatening)
C3160769 (UMLS CUI-1)
CL Item
Major bleed, other (Major bleed, other)
C3160769 (UMLS CUI-1)
CL Item
Minor bleed (Minor bleed)
C3160770 (UMLS CUI-1)
CL Item
Minimal bleed (Minimal bleed)
N (UMLS CUI-1)
Item
Primary location of bleed
text
C0019080 (UMLS CUI [1,1])
C0450429 (UMLS CUI [1,2])
Primary location of bleed
Code List
Primary location of bleed
CL Item
Subcutaneous/dermal (Subcutaneous/dermal)
I (UMLS CUI-1)
CL Item
Cardiac cath/PCI access site (Cardiac cath/PCI access site)
I (UMLS CUI-1)
CL Item
Epistaxis (Epistaxis)
I (UMLS CUI-1)
CL Item
Gastrointestinal (Gastrointestinal)
I (UMLS CUI-1)
CL Item
Urinary (Urinary)
I (UMLS CUI-1)
CL Item
Retroperitoneal (Retroperitoneal)
I (UMLS CUI-1)
CL Item
Pericardial (Pericardial)
I (UMLS CUI-1)
CL Item
Intracranial (Intracranial)
I (UMLS CUI-1)
CL Item
Hemoptysis (Hemoptysis)
I (UMLS CUI-1)
CL Item
Intraocular (Intraocular)
I (UMLS CUI-1)
CL Item
Intraspinal (Intraspinal)
I (UMLS CUI-1)
CL Item
Intra-articular (Intra-articular)
I (UMLS CUI-1)
CL Item
Other bleeding site (Other bleeding site)
I (UMLS CUI-1)
Item
Nature of bleed
text
C0019080 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Nature of bleed
Code List
Nature of bleed
CL Item
Spontaneous bleed (Spontaneous bleed)
C1321132 (UMLS CUI-1)
CL Item
Related to procedure (Related to procedure)
C0032788 (UMLS CUI-1)
Administration of pressors
Item
Administration of pressors
boolean
C0237795 (UMLS CUI [1])
Haemodynamic compromise
Item
Haemodynamic compromise
boolean
C0948268 (UMLS CUI [1])
Surgical intervention required to stop or treat bleeding
Item
Surgical intervention required to stop or treat bleeding
boolean
C0149533 (UMLS CUI [1])
Haemoglobin measurements
Item
Haemoglobin measurements relevant to event
text
C0518015 (UMLS CUI [1])
Haemoglobin measurements not available preceding event
Item
Haemoglobin measurements not available preceding event
boolean
C0149533 (UMLS CUI [1])
Item Group
Arterial Thrombotic Event
C0151942 (UMLS CUI-1)
Event tracking number
Item
Event tracking number
text
C0877248 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Event text
Item
Event text
text
C1527021 (UMLS CUI [1,1])
C0877248 (UMLS CUI [1,2])
Event started date and time
Item
Event started date and time
datetime
C2585732 (UMLS CUI [1,1])
C0151942 (UMLS CUI [1,2])
Item
Clinical symptoms
text
C1457887 (UMLS CUI [1,1])
C0151942 (UMLS CUI [1,2])
Clinical symptoms
Code List
Clinical symptoms
CL Item
Abrupt development of pain in an extremity (Abrupt development of pain in an extremity)
I (UMLS CUI-1)
CL Item
Abrupt development of flank pain (Abrupt development of flank pain)
I (UMLS CUI-1)
CL Item
Abrupt development of abdominal pain (Abrupt development of abdominal pain)
I (UMLS CUI-1)
CL Item
Absent pulses, pallor, and/or paresis (Absent pulses, pallor, and/or paresis)
I (UMLS CUI-1)
CL Item
in an extremity (at least an entire digit) (in an extremity (at least an entire digit))
I (UMLS CUI-1)
CL Item
Change in laboratory values (Change in laboratory values)
I (UMLS CUI-1)
CL Item
Abrupt loss in vision (Abrupt loss in vision)
I (UMLS CUI-1)
CL Item
Other (Other)
I (UMLS CUI-1)
Item
Diagnostic study(s) performed
text
C3259360 (UMLS CUI [1])
Diagnostics performed
Code List
Diagnostic study(s) performed
CL Item
Angiography (Angiography)
I (UMLS CUI-1)
CL Item
CT scan (CT scan)
I (UMLS CUI-1)
CL Item
MRI (MRI)
I (UMLS CUI-1)
CL Item
Ultrasound (Ultrasound)
I (UMLS CUI-1)
CL Item
Colonoscopy (Colonoscopy)
I (UMLS CUI-1)
CL Item
Other (Other)
I (UMLS CUI-1)
hospitalization prolonged
Item
Event prolonged an ongoing hospitalization
boolean
C0745041 (UMLS CUI [1])
Hospitalization
Item
Event resulted in a hospitalization
boolean
C0019993 (UMLS CUI [1])
Event did not result in or prolong an ongoing hospitalization
Item
Event did not result in or prolong an ongoing hospitalization
boolean
C0745041 (UMLS CUI [1])
Item
Final diagnosis
text
C0332144 (UMLS CUI [1])
Final diagnosis
Code List
Final diagnosis
CL Item
Renal infarction (Renal infarction)
I (UMLS CUI-1)
CL Item
Retinal infarction (Retinal infarction)
I (UMLS CUI-1)
CL Item
Bowel infarction (Bowel infarction)
I (UMLS CUI-1)
CL Item
Peripheral ischaemia (Peripheral ischaemia)
I (UMLS CUI-1)
CL Item
Other (Other)
I (UMLS CUI-1)
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