ID

44131

Description

The main objective of each of the Expert Committees was to produce standardised data sets limited to less than 100 variables. The variables derived had to reflect current treatment guidelines, and also were to be of use for clinical audit, clinical care of patients, service planning and epidemiology. The process involved regular meetings of the Expert Committees, electronic communication between members, and consultation with specialist groups and cardiac societies represented by the European Society of Cardiology. The development of the draft data standards for the three modules was completed in April 2004.

Keywords

  1. 4/15/15 4/15/15 -
  2. 4/10/21 4/10/21 - Ahmed Rafee, MD
  3. 9/20/21 9/20/21 -
Copyright Holder

Copyright Irish Department of Health and Children/European Society of Cardiology

Uploaded on

September 20, 2021

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Creative Commons BY-NC 4.0

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Cardiology Audit and Registration Data Standards for Coronary Care Unit [CCU]/Acute Coronary Syndrome [ACS] admissions.

CCU/ACS Data Standards

  1. StudyEvent: ODM
    1. CCU/ACS Data Standards
Demographics
Description

Demographics

Alias
UMLS CUI-1
C0011298
Hospital identification number
Description

Hospital identification number

Data type

integer

Alias
UMLS CUI [1,1]
C0600091
UMLS CUI [1,2]
C0019994
Patient identification number
Description

Patient identification number

Data type

integer

Alias
UMLS CUI-1
C2348585
Date of birth
Description

The date the patient was born as recorded on their birth certificate.

Data type

date

Alias
UMLS CUI-1
C0421451
Sex
Description

The sex of the patient.

Data type

text

Alias
UMLS CUI-1
C0079399
Height
Description

Height in cms.

Data type

integer

Measurement units
  • cm
Alias
UMLS CUI-1
C0005890
cm
Weight
Description

Weight in kgs.

Data type

integer

Alias
UMLS CUI-1
C0005910
Transferred from another hosptial
Description

Indicate if the patient was transferred from another hospital for this admission

Data type

text

Alias
UMLS CUI-1
C1546432
Past History relevant to Coronary Artery Disease
Description

Past History relevant to Coronary Artery Disease

History of previous myocardial infarction (MI)
Description

Indicate if the patient had at least one previous myocardial infarction before this admission.

Data type

text

Alias
UMLS CUI-1
C1275835
Prior angina
Description

Indicate if the patient has a history of angina and / or has been treated previously for angina by a physician.

Data type

text

Alias
UMLS CUI-1
C0455530
History of congestive heart failure (CHF)
Description

Indicate if the patient has a history of congestive heart failure and/or has previously been treated for congestive heart failure by a physician.

Data type

text

Alias
UMLS CUI-1
C0455531
History of stroke
Description

Indicate if the patient has a history of cerebrovascular accident (CVA) / stroke, as evidenced by a persistent neurological deficit due to ischaemia.

Data type

text

Alias
UMLS CUI-1
C0559159
History of peripheral vascular disease
Description

History or evidence of aneurysm or occlusive peripheral Code vascular disease or carotid disease, including aortic aneurysm, previous aorto-iliac or peripheral vascular surgery, or reduced or absent peripheral pulses and / or angiographic stenosis of more than 50%.

Data type

text

Alias
UMLS CUI-1
C1881056
History of chronic renal failure
Description

Indicate if the patient has a history of chronic renal failure documented by any one of the following: (a) Serum creatinine greater than 2.0 mg/dl or 200 umol/l in the past (b) On dialysis (c) Has had a renal transplantation

Data type

text

Alias
UMLS CUI-1
C1533077
Chronic lung disease
Description

Indicate if the patient has a history of chronic lung disease and/or has previously been treated for chronic lung disease by a physician.

Data type

text

Alias
UMLS CUI-1
C1533075
Previous percutaneous coronary intervention (PCI)
Description

Indicate if the patient has had a previous PCI of any type before the current admission (e.g. balloon angioplasty, implantation of intra coronary stent or other catheter devices for treating coronary atheroma, atherectomy, laser angioplasty or other).

Data type

text

Alias
UMLS CUI-1
C1320647
Coronary artery bypass graft [CABG]
Description

Indicate if the patient had coronary artery bypass graft (CABG) done prior to this admission

Data type

text

Alias
UMLS CUI-1
C1275842
Smoking status
Description

Indicate if the patient has a history confirming any form of tobacco use in the past. This includes cigarettes/cigar/pipe.

Data type

text

Alias
UMLS CUI-1
C0543414
Diabetes mellitus
Description

Indicate if the patient has a history of diabetes mellitus diagnosed prior to the current admission.

Data type

text

Alias
UMLS CUI-1
C0011849
History of hypertension
Description

Indicate if the patient has a history of hypertension diagnosed and/or treated by a physician.

Data type

text

Alias
UMLS CUI-1
C0455527
History of hypercholesterolemia
Description

Indicate if the patient has a documented history of hypercholesterolemia diagnosed and/or treated by a physician.

Data type

text

Alias
UMLS CUI-1
C1533076
Medication: pre hospital
Description

Medication: pre hospital

Aspirin
Description

Indicate if the patient was taking aspirin regularly prior to this admission to hospital.

Data type

text

Alias
UMLS CUI-1
C0004057
Other antiplatelet
Description

Indicate if the patient was taking antiplatelet medication (other than aspirin) regularly prior to this admission to hospital.

Data type

text

Anticoagulants
Description

Indicate if the patient was taking anticoagulant medication before this hospital admission.

Data type

text

Alias
UMLS CUI-1
C0003280
Beta-blockers
Description

Indicate if the patient was taking Beta-blockers regularly prior to this admission to hospital

Data type

text

Alias
UMLS CUI-1
C0304516
ACE inhibitors
Description

Indicate if the patient was taking ACE inhibitors regularly prior to this admission to hospital.

Data type

text

Alias
UMLS CUI-1
C0003015
Angiotensin II receptor blockers
Description

Indicate if the patient was taking angiotensin II receptorblockers regularly prior to this admission to hospital.

Data type

text

Alias
UMLS CUI-1
C0521942
Diabetic control
Description

Indicate the main method of diabetic treatment the patient has been receiving.

Data type

text

Alias
UMLS CUI-1
C3274787
Statins
Description

Indicate if the patient was taking statins regularly prior to this admission to hospital.

Data type

text

Alias
UMLS CUI-1
C0360714
Non-statin lipid lowering agents
Description

Indicate if the patient was taking non-statin lipid lowering agents regularly prior to this admission to hospital.

Data type

text

Alias
UMLS CUI-1
C0086440
Working Diagnosis
Description

Working Diagnosis

Alias
UMLS CUI-1
C0332135
Predominant presenting symptom
Description

Indicate the predominant symptom /reason why patient presented for medical attention.

Data type

text

Alias
UMLS CUI-1
C3177142
Symptom onset date and time
Description

Indicate the date and time of onset of symptom / reason that prompted the patient's presentation for medical attention.

Data type

datetime

Alias
UMLS CUI-1
C1320528
Heart rate
Description

Indicate the patient's heart rate (beats per minute) reading. This should be the first heart rate recorded by a health care provider (GP/ ambulance staff/A&E staff) AND when the patient is in a stable cardiac rhythm.

Data type

integer

Measurement units
  • bpm
Alias
UMLS CUI-1
C0018810
bpm
Systolic blood pressure
Description

Indicate the patient's systolic blood pressure reading (mm Hg). This should be the first blood pressure recorded by a health care provider (GP/ ambulance staff/A&E staff) AND when the patient is in a stable cardiac rhythm.

Data type

integer

Measurement units
  • mmHg
Alias
UMLS CUI-1
C0871470
mmHg
Date and time of admission/arrival at hospital
Description

Indicate the date and time the patient first presented to the hospital for this admission.

Data type

datetime

Alias
UMLS CUI-1
C1320532
Killip class
Description

Indicate the Killip class of the patient at the time of hospital admission.

Data type

text

Alias
UMLS CUI-1
C1881332
ECG rhythm
Description

Indicate the rhythm on the first admission ECG.

Data type

text

Alias
UMLS CUI-1
C0232187
ECG QRS annotation
Description

Indicate if first admission ECG has any QRS abnormalities.

Data type

text

Alias
UMLS CUI-1
C2983649
ECG STT changes
Description

Indicate if the first admission ECG has any STT changes. Note: if more than one of these options are applicable to a patient then the most severe should be coded. For example if the patient has 2,3,and 4 then 2 should be coded. Options 2, 3, 4 and 88 are ranked in order.

Data type

text

Alias
UMLS CUI-1
C0232326
Elevated biochemical marker
Description

Indicate if biochemical markers were raised above the levels recognised in guidelines for diagnosis of acute myocardial infarction (NB these levels may vary between laboratories).

Data type

text

Alias
UMLS CUI [1,1]
C1271630
UMLS CUI [1,2]
C07022401
Biochemical marker type
Description

Indicate which biochemical marker was tested to indicate the presence/absence of an acute MI Note: these options are ranked in order so if all three biochemical markers were tested code option one, if option 2 and 3 were raised code option 2 etc.

Data type

text

Alias
UMLS CUI-1
C1271630
Cholesterol [total]
Description

Indicate the first total serum cholesterol level in mmol/l [ideally taken within 24 hours of this admission].

Data type

float

Measurement units
  • mmol/l
Alias
UMLS CUI-1
C1445957
mmol/l
Serum creatinine
Description

Indicate the level of the serum creatinine (first) during this admission in mg/dl or umol/l.

Data type

float

Alias
UMLS CUI-1
C0201975
Working diagnosis (this will determine the patients treatment)
Description

After initial assessment of the patient, indicate the diagnosis on which further management of the patient is based.

Data type

text

Alias
UMLS CUI-1
C0332135
Investigations and Treatment
Description

Investigations and Treatment

Alias
UMLS CUI-1
C0808232
Thrombolysis therapy administered
Description

Indicate the type of thrombolysis therapy administered. NB if in field ACS 6.04 option 'facilitated' is ticked the type of thrombolysis used should also be indicated in this field (6.01).

Data type

text

Alias
UMLS CUI-1
C0040044
Date and time of thrombolysis
Description

Indicate the date and time thrombolysis was commenced. This is defined as the time the infusion was commenced and/or time of bolus injection.

Data type

datetime

Alias
UMLS CUI [1,1]
C0040044
UMLS CUI [1,2]
C1301880
Reason why thrombolysis not administered
Description

Reason why thrombolysis not administered

Data type

text

Alias
UMLS CUI-1
C3260558
Reperfusion by PCI
Description

If the patient underwent a percutaneous coronary intervention indicate the type.

Data type

text

Alias
UMLS CUI-1
C0027054
Date and time of percutaneous coronary intervention (PCI)
Description

Indicate the date and time of percutaneous coronary intervention [PCI].

Data type

datetime

Alias
UMLS CUI-1
C1532338
UMLS CUI-2
C1264639
UMLS CUI-3
P
Type of stress test
Description

If the patient underwent a stress test during hospital stay indicate the type of stress test.

Data type

text

Alias
UMLS CUI-1
C1384495
Stress test result
Description

Indicate if signs of ischaemia were present on the stress test used (as determined by the clinician).

Data type

text

Alias
UMLS CUI-1
C1274040
UMLS CUI-2
C1384495
UMLS CUI-3
P
Left ventricular (LV) function
Description

Indicate the patients estimated or calculated left ventricular [LV] function This categorises the percentage of the blood emptied from the left ventricle at the end of the contraction. Data may have been derived from angiography, echocardiography, nuclear imaging, magnetic resonance imaging etc.

Data type

text

Alias
UMLS CUI-1
C0428772
Coronary angiogram
Description

Indicate if the patient underwent diagnostic coronary angiography during this admission episode.

Data type

text

Alias
UMLS CUI-1
C0085532
Number of vessels diseased
Description

Indicate from the coronary angiogram performed the number of vessels with significant reduction in luminal diameter due to coronary atheroma (I.e. with stenosis greater than 50%) Significant disease is indicated if the luminal diameter of the coronary artery is reduced by > 50% due to coronary arteromatous disease.

Data type

text

Alias
UMLS CUI-1
C3275120
Percutaneous coronary intervention (PCI)
Description

Indicate if the patient underwent a PCI during this admission episode. This is for patients who had PCI during this admission that was not for primary reperfusion. Patients who had PCI for primary reperfusion and who had no subsequent PCI during this admission are coded as 'no'.

Data type

text

Alias
UMLS CUI-1
C1532338
Date and time of percutaneous coronary intervention (PCI)
Description

Indicate the date the PCI was performed if performed during this admission episode.

Data type

datetime

Alias
UMLS CUI [1,1]
C1532338
UMLS CUI [1,2]
C1264639
Coronary artery bypass graft (CABG)
Description

Indicate if the patient underwent CABG during this admission episode.

Data type

text

Alias
UMLS CUI-1
C0010055
Coronary artery bypass graft (CABG) date
Description

Indicate the date the CABG was performed if performed during this admission episode.

Data type

datetime

Alias
UMLS CUI [1,1]
C0010055
UMLS CUI [1,2]
C0011008
Electrical devices
Description

Indicate if the patient had any of the following electrical devices implanted during this admission episode.

Data type

text

Alias
UMLS CUI-1
C0018831
Medication during hospital stay
Description

Medication during hospital stay

Aspirin
Description

Indicate if aspirin was administered in the treatment of ACS.

Data type

text

Alias
UMLS CUI-1
C0004057
Heparin/low molecular weight heparin
Description

Indicate if heparin/low molecular weight heparin [LMWH] was administered in the treatment of ACS .

Data type

text

IV Glycoprotein (GP) IIb/IIIa
Description

Indicate the use of IV Glycoprotein IIb/IIIa inhibitors and type in the treatment of ACS.

Data type

text

Alias
UMLS CUI-1
C3640054
ACE inhibitors
Description

Indicate if ACE inhibitors were administered in the treatment of ACS.

Data type

text

Alias
UMLS CUI-1
C0003015
Beta- blockers
Description

Indicate if Beta-blockers were administered in the treatment of ACS.

Data type

text

Alias
UMLS CUI-1
C0304516
Diuretics
Description

Indicate if diuretics were administered in the treatment of ACS.

Data type

text

Alias
UMLS CUI-1
C0012798
Inotropes
Description

Indicate if inotropes were administered in the treatment of ACS.

Data type

text

Alias
UMLS CUI-1
C0304509
Outcome
Description

Outcome

Myocardial reinfarction during hospital stay
Description

Indicate if the patient had a myocardial reinfarction during this hospital stay. To meet the criteria as a post admission event, an MI must be distinct from the index event at the time of admission. See ESC/ACC definition of MI (appendix 1)

Data type

text

Alias
UMLS CUI-1
C2882123
Bleeding during hospital stay
Description

Indicate if there was an episode of bleeding during the hospital stay that required close monitoring and/ or specific treatment, e.g. transfusion (blood or blood products).

Data type

text

Alias
UMLS CUI-1
C0019080
Stroke during hospital stay
Description

Indicate if the patient was diagnosed as having a stroke during hospital stay, as evidenced by persistent loss of neurological function caused by an ischaemic event.

Data type

text

Alias
UMLS CUI-1
C0038454
Resuscitated cardiac arrest
Description

Indicate if the patient had a cardiac arrest during hospital admission and was successfully resuscitated.

Data type

text

Alias
UMLS CUI-1
C0018790
UMLS CUI-2
C1882942
Date and time of cardiac arrest
Description

Indicate the date and time of cardiac arrest

Data type

datetime

Alias
UMLS CUI-1
C2825160
Mechanical complications
Description

Indicate if the patient developed any of the following mechanical complications during this admission. If more than one occurred indicate the most life threatening complications - i.e. 2>3>4.

Data type

text

Discharge ECG rhythm
Description

Indicate the patients discharge ECG rhythm.

Data type

text

Alias
UMLS CUI-1
C0232187
Discharge diagnosis
Description

Indicate the discharge diagnosis.

Data type

text

Alias
UMLS CUI-1
C0332144
Survival status at discharge
Description

Indicate vital status at discharge.

Data type

text

Alias
UMLS CUI-1
C0586514
Date of discharge/death
Description

Indicate the date the patient was discharged from hospital or if patient died record the date of death.

Data type

datetime

Alias
UMLS CUI-1
C2361123
UMLS CUI-2
C1148348
Medication at discharge
Description

Medication at discharge

Aspirin
Description

Indicate if the patient was prescribed aspirin on discharge from hospital.

Data type

text

Antiplatelet
Description

Indicate if the patient was prescribed antiplatelet medication (other than aspirin) on discharge from hospital.

Data type

text

Anticoagulants
Description

Indicate if the patient was prescribed anticoagulant medication on discharge from hospital.

Data type

text

Beta-blockers
Description

Indicate if the patient was prescribed Beta-Blockers on discharge from hospital.

Data type

text

ACE inhibitors
Description

Indicate if the patient was prescribed ACE inhibitors on discharge from hospital.

Data type

text

Angiotensin II receptor blockers
Description

Indicate if the patient was prescribed angiotensin II receptor blockers on discharge from hospital.

Data type

text

Diabetic control
Description

Indicate the main method of diabetic treatment the patient was prescribed on discharge from hospital.

Data type

text

Statins
Description

Indicate if the patient was prescribed statins on discharge.

Data type

text

Non-statin lipid lowering agents
Description

Indicate if the patient was prescribed non-statin lipid lowering agents on discharge.

Data type

text

Follow up
Description

Follow up

Date of follow up
Description

Indicate the date of last follow up alive. This may be the date of follow up or the date the patient is last seen alive by verifiable sources.

Data type

date

Alias
UMLS CUI-1
C3694716
Survival status at follow up
Description

Indicate vital status at follow up.

Data type

text

Date of death
Description

If the patient died indicate the date of death.

Data type

date

Alias
UMLS CUI-1
C1148348
Primary cause of death
Description

Indicate the primary cause of death.

Data type

text

Alias
UMLS CUI-1
C0007465
Anginal status
Description

Indicate the patients anginal status at the time of followup using the Canadian Cardiovascular Society (CCS) grading system NB: there are eight blocks to a mile.

Data type

text

Alias
UMLS CUI-1
C1277207
Dyspnoea
Description

Grade breathing status using the New York Heart Association (NYHA) functional classification.

Data type

text

Alias
UMLS CUI-1
C1275491
Date of first hospital readmission since discharge
Description

If the patient was readmitted to hospital indicate the date.

Data type

date

Alias
UMLS CUI [1,1]
C0030700
UMLS CUI [1,2]
C0011008
Myocardial infarction [MI]
Description

Indicate if the patient was diagnosed as having an myocardial infarction since the date of discharge. See Appendix 1 for ESC/ACC definition of MI.

Data type

text

Alias
UMLS CUI-1
C0027051
Myocardial infarction [MI] date
Description

Indicate the date of the myocardial infarction.

Data type

date

Alias
UMLS CUI-1
C2924287
Stroke
Description

Indicate if the patient was diagnosed as having a stroke since discharge from hospital, as evidenced by persistent loss of neurological function caused by an ischaemic event.

Data type

text

Stroke date
Description

Indicate the date of the stroke. Date

Data type

date

Percutaneous coronary intervention [PCI]
Description

Indicate if the patient had a percutaneous coronary intervention since the date of discharge.

Data type

text

Percutaneous coronary intervention [PCI] date
Description

Indicate the date of percutaneous coronary intervention [PCI].

Data type

date

Coronary artery bypass graft [CABG]
Description

Indicate if the patient had coronary artery bypass graft [CABG] since the date of discharge.

Data type

text

Coronary artery bypass graft [CABG] date
Description

Indicate the date of coronary artery bypass graft [CABG].

Data type

date

Cardiac rehabilitation program
Description

Indicate if the patient attended or is attending a cardiac rehabilitation programme since discharge.

Data type

text

Alias
UMLS CUI-1
C0700431
Medication at follow up
Description

Medication at follow up

Aspirin
Description

On follow up indicate if the patient is taking aspirin regularly.

Data type

text

Antiplatelet
Description

On follow-up indicate if the patient is taking antiplatelet medication (other than aspirin) regularly.

Data type

text

Anticoagulants
Description

On follow-up indicate if the patient is taking anticoagulant medication regularly.

Data type

text

Beta-blockers
Description

On follow-up indicate if the patient is taking Beta-Blockers regularly.

Data type

text

ACE inhibitors
Description

On follow-up indicate if the patient is taking ACE inhibitors regularly.

Data type

text

Angiotensin II receptor blockers
Description

On follow-up indicate if the patient is taking angiotensin II receptor blockers regularly.

Data type

text

Diabetic control
Description

On follow-up indicate the main method of diabetic control the patient is regularly receiving.

Data type

text

Statins
Description

On follow-up indicate if the patient is taking statins regularly.

Data type

text

Non-statin lipid lowering agents
Description

On follow-up indicate if the patient is taking non-statin lipid lowering agents regularly.

Data type

text

Similar models

CCU/ACS Data Standards

  1. StudyEvent: ODM
    1. CCU/ACS Data Standards
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Demographics
C0011298 (UMLS CUI-1)
Hospital id
Item
Hospital identification number
integer
C0600091 (UMLS CUI [1,1])
C0019994 (UMLS CUI [1,2])
patient id
Item
Patient identification number
integer
C2348585 (UMLS CUI-1)
Date of birth
Item
Date of birth
date
C0421451 (UMLS CUI-1)
Item
Sex
text
C0079399 (UMLS CUI-1)
Code List
Sex
CL Item
Male (1)
C0086582 (UMLS CUI-1)
CL Item
Female (2)
C0086287 (UMLS CUI-1)
CL Item
Unknown (3)
C0421467 (UMLS CUI-1)
Height
Item
Height
integer
C0005890 (UMLS CUI-1)
Weight
Item
Weight
integer
C0005910 (UMLS CUI-1)
Item
Transferred from another hosptial
text
C1546432 (UMLS CUI-1)
Code List
Transferred from another hosptial
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item Group
Past History relevant to Coronary Artery Disease
Item
History of previous myocardial infarction (MI)
text
C1275835 (UMLS CUI-1)
Code List
History of previous myocardial infarction (MI)
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Prior angina
text
C0455530 (UMLS CUI-1)
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
History of congestive heart failure (CHF)
text
C0455531 (UMLS CUI-1)
Code List
History of congestive heart failure (CHF)
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
History of stroke
text
C0559159 (UMLS CUI-1)
Code List
History of stroke
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
History of peripheral vascular disease
text
C1881056 (UMLS CUI-1)
Code List
History of peripheral vascular disease
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
History of chronic renal failure
text
C1533077 (UMLS CUI-1)
Code List
History of chronic renal failure
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Chronic lung disease
text
C1533075 (UMLS CUI-1)
Code List
Chronic lung disease
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Previous percutaneous coronary intervention (PCI)
text
C1320647 (UMLS CUI-1)
Code List
Previous percutaneous coronary intervention (PCI)
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Coronary artery bypass graft [CABG]
text
C1275842 (UMLS CUI-1)
Code List
Coronary artery bypass graft [CABG]
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Smoking status
text
C0543414 (UMLS CUI-1)
Code List
Smoking status
CL Item
Never (1)
C0337672 (UMLS CUI-1)
CL Item
Current (2)
C3241966 (UMLS CUI-1)
CL Item
Former (3)
C0337671 (UMLS CUI-1)
CL Item
Unknown (4)
C0425306 (UMLS CUI-1)
Item
Diabetes mellitus
text
C0011849 (UMLS CUI-1)
Code List
Diabetes mellitus
CL Item
Non-diabetic (1)
CL Item
Diabetic (dietary control) (2)
C0421246 (UMLS CUI-1)
CL Item
Diabetic (oral medication) (3)
C0421247 (UMLS CUI-1)
CL Item
Diabetic (insulin) (4)
C0421248 (UMLS CUI-1)
CL Item
Newly diagnosed diabetic (5)
C3275118 (UMLS CUI-1)
CL Item
Unknown (6)
Item
History of hypertension
text
C0455527 (UMLS CUI-1)
Code List
History of hypertension
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
History of hypercholesterolemia
text
C1533076 (UMLS CUI-1)
Code List
History of hypercholesterolemia
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item Group
Medication: pre hospital
Item
Aspirin
text
C0004057 (UMLS CUI-1)
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Other antiplatelet
text
Code List
Other antiplatelet
CL Item
No (1)
CL Item
Ticlopidine/Clopidogrel (2)
C0040207 (UMLS CUI-1)
C0070166 (UMLS CUI-2)
CL Item
Other antiplatelet agent (3)
CL Item
Unknown (4)
Item
Anticoagulants
text
C0003280 (UMLS CUI-1)
Code List
Anticoagulants
CL Item
No (1)
CL Item
Vitamin K antagonist (2)
C2267235 (UMLS CUI-1)
CL Item
Oral thrombin inhibitors (3)
CL Item
Other (4)
CL Item
Unknown (5)
Item
Beta-blockers
text
C0304516 (UMLS CUI-1)
Code List
Beta-blockers
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
ACE inhibitors
text
C0003015 (UMLS CUI-1)
Code List
ACE inhibitors
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Angiotensin II receptor blockers
text
C0521942 (UMLS CUI-1)
Code List
Angiotensin II receptor blockers
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Diabetic control
text
C3274787 (UMLS CUI-1)
Code List
Diabetic control
CL Item
None (1)
C3275118 (UMLS CUI-1)
CL Item
Insulin and oral agent (2)
C1272306 (UMLS CUI-1)
CL Item
Insulin (3)
C0421248 (UMLS CUI-1)
CL Item
Oral agent (4)
C0421247 (UMLS CUI-1)
CL Item
Diet alone (5)
C0421246 (UMLS CUI-1)
CL Item
Unknown (6)
Item
Statins
text
C0360714 (UMLS CUI-1)
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Non-statin lipid lowering agents
text
C0086440 (UMLS CUI-1)
Code List
Non-statin lipid lowering agents
CL Item
None (1)
CL Item
Ezetimibe (2)
C1142985 (UMLS CUI-1)
CL Item
Fibrates (3)
C1449704 (UMLS CUI-1)
CL Item
Other non-statin (4)
CL Item
Unknown (5)
Item Group
Working Diagnosis
C0332135 (UMLS CUI-1)
Item
Predominant presenting symptom
text
C3177142 (UMLS CUI-1)
Code List
Predominant presenting symptom
CL Item
Asymptomatic (1)
C0231221 (UMLS CUI-1)
CL Item
Chest Pain (2)
C0008031 (UMLS CUI-1)
CL Item
Dyspnoea (3)
C0013404 (UMLS CUI-1)
CL Item
Fatigue (4)
C0015672 (UMLS CUI-1)
CL Item
Syncope (5)
C0039070 (UMLS CUI-1)
CL Item
Cardiac arrest/aborted sudden death (6)
C0018790 (UMLS CUI-1)
C0085298 (UMLS CUI-2)
CL Item
Other symptoms (7)
CL Item
Unknown (8)
Symptom onset date and time
Item
Symptom onset date and time
datetime
C1320528 (UMLS CUI-1)
Heart rate
Item
Heart rate
integer
C0018810 (UMLS CUI-1)
Systolic blood pressure
Item
Systolic blood pressure
integer
C0871470 (UMLS CUI-1)
Date and time of admission/arrival at hospital
Item
Date and time of admission/arrival at hospital
datetime
C1320532 (UMLS CUI-1)
Item
Killip class
text
C1881332 (UMLS CUI-1)
Code List
Killip class
CL Item
Class I (1)
C2697844 (UMLS CUI-1)
CL Item
Class II (2)
C2697845 (UMLS CUI-1)
CL Item
Class III (3)
C2697846 (UMLS CUI-1)
CL Item
Class IV (4)
C2697847 (UMLS CUI-1)
CL Item
Unknown (5)
Item
ECG rhythm
text
C0232187 (UMLS CUI-1)
Code List
ECG rhythm
CL Item
Sinus rhythm (1)
C0232201 (UMLS CUI-1)
CL Item
Atrial fibrillation (2)
C0004238 (UMLS CUI-1)
CL Item
Pacemaker (3)
C2981711 (UMLS CUI-1)
CL Item
Other (4)
CL Item
Unknown (5)
Item
ECG QRS annotation
text
C2983649 (UMLS CUI-1)
Code List
ECG QRS annotation
CL Item
Normal (1)
C0438172 (UMLS CUI-1)
CL Item
LBBB (2)
C0023211 (UMLS CUI-1)
CL Item
RBBB (3)
C0085615 (UMLS CUI-1)
CL Item
Other (4)
CL Item
Unknown (5)
Item
ECG STT changes
text
C0232326 (UMLS CUI-1)
Code List
ECG STT changes
CL Item
Normal (1)
C0855336 (UMLS CUI-1)
CL Item
ST elevation (2)
C0520886 (UMLS CUI-1)
CL Item
ST depression (3)
C0520887 (UMLS CUI-1)
CL Item
Pathological T-inversion (absence of ST deviation) (4)
C0520888 (UMLS CUI-1)
CL Item
Other (5)
CL Item
Unknown (6)
Item
Elevated biochemical marker
text
C1271630 (UMLS CUI [1,1])
C07022401 (UMLS CUI [1,2])
Code List
Elevated biochemical marker
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Biochemical marker type
text
C1271630 (UMLS CUI-1)
Code List
Biochemical marker type
CL Item
Troponin T and/or I (1)
C0920210 (UMLS CUI-1)
C1141947 (UMLS CUI-2)
CL Item
CK-MB (2)
C0523584 (UMLS CUI-1)
CL Item
CK (3)
C0201973 (UMLS CUI-1)
CL Item
Unknown (4)
Total Cholesterol
Item
Cholesterol [total]
float
C1445957 (UMLS CUI-1)
Serum creatinine
Item
Serum creatinine
float
C0201975 (UMLS CUI-1)
Item
Working diagnosis (this will determine the patients treatment)
text
C0332135 (UMLS CUI-1)
Code List
Working diagnosis (this will determine the patients treatment)
CL Item
STEMI/LBBB MI (1)
C1536220 (UMLS CUI-1)
CL Item
NSTEMI (2)
C3537184 (UMLS CUI-1)
CL Item
Unstable Angina (3)
C0002965 (UMLS CUI-1)
CL Item
Unknown (4)
Item Group
Investigations and Treatment
C0808232 (UMLS CUI-1)
Item
Thrombolysis therapy administered
text
C0040044 (UMLS CUI-1)
Code List
Thrombolysis therapy administered
CL Item
None (1)
CL Item
Streptokinase (2)
C0038418 (UMLS CUI-1)
CL Item
tPA agents (3)
C0032144 (UMLS CUI-1)
CL Item
Other (4)
CL Item
Unknown (5)
Date and time of thrombolysis
Item
Date and time of thrombolysis
datetime
C0040044 (UMLS CUI [1,1])
C1301880 (UMLS CUI [1,2])
Item
Reason why thrombolysis not administered
text
C3260558 (UMLS CUI-1)
Code List
Reason why thrombolysis not administered
CL Item
Primary PCI (1)
CL Item
No ECG criteria (2)
CL Item
Too late (3)
CL Item
Other known contraindications (4)
CL Item
Unknown (5)
Item
Reperfusion by PCI
text
C0027054 (UMLS CUI-1)
Code List
Reperfusion by PCI
CL Item
No (1)
CL Item
Primary (2)
CL Item
Facilitated (3)
CL Item
Rescue (4)
CL Item
Unknown (5)
PCI date/time
Item
Date and time of percutaneous coronary intervention (PCI)
datetime
C1532338 (UMLS CUI-1)
C1264639 (UMLS CUI-2)
P (UMLS CUI-3)
Item
Type of stress test
text
C1384495 (UMLS CUI-1)
Code List
Type of stress test
CL Item
None (1)
CL Item
Exercise ECG (2)
C1304755 (UMLS CUI-1)
CL Item
Stress echocardiogram (3)
C0920208 (UMLS CUI-1)
CL Item
Scintigraphy (4)
C2350391 (UMLS CUI-1)
CL Item
Other (5)
CL Item
Unknown (6)
Item
Stress test result
text
C1274040 (UMLS CUI-1)
C1384495 (UMLS CUI-2)
P (UMLS CUI-3)
Code List
Stress test result
CL Item
No ischaemia (1)
C1096370 (UMLS CUI-1)
CL Item
Signs of ischaemia (2)
C1096350 (UMLS CUI-1)
CL Item
Indeterminate (3)
CL Item
Unknown (4)
Item
Left ventricular (LV) function
text
C0428772 (UMLS CUI-1)
Code List
Left ventricular (LV) function
CL Item
Normal (>50%) (1)
C1535947 (UMLS CUI-1)
CL Item
Slightly reduced (41-50%) (2)
C3274775 (UMLS CUI-1)
CL Item
Moderately reduced (31-40%) (3)
C3274776 (UMLS CUI-1)
CL Item
Severely reduced (<30%) (4)
C3274777 (UMLS CUI-1)
CL Item
LV function not assessed (5)
C3248481 (UMLS CUI-1)
CL Item
Unknown (6)
Item
Coronary angiogram
text
C0085532 (UMLS CUI-1)
Code List
Coronary angiogram
CL Item
No (1)
CL Item
Yes (2)
CL Item
Transferred/Planned (3)
CL Item
Unknown (4)
Item
Number of vessels diseased
text
C3275120 (UMLS CUI-1)
Code List
Number of vessels diseased
CL Item
0 (1)
CL Item
1 (2)
C3275121 (UMLS CUI-1)
CL Item
2 (3)
C0581375 (UMLS CUI-1)
CL Item
3 (4)
C3272265 (UMLS CUI-1)
CL Item
Left Main Stem (LMD) only (5)
CL Item
Left Main Stem (LMD) and Right Coronary Artery (6)
CL Item
Unkown (7)
Item
Percutaneous coronary intervention (PCI)
text
C1532338 (UMLS CUI-1)
Code List
Percutaneous coronary intervention (PCI)
CL Item
No (1)
CL Item
Yes (2)
CL Item
Transferred/Planned (3)
CL Item
Unknown (4)
Date and time of percutaneous coronary intervention (PCI)
Item
Date and time of percutaneous coronary intervention (PCI)
datetime
C1532338 (UMLS CUI [1,1])
C1264639 (UMLS CUI [1,2])
Item
Coronary artery bypass graft (CABG)
text
C0010055 (UMLS CUI-1)
Code List
Coronary artery bypass graft (CABG)
CL Item
No (1)
CL Item
Yes (2)
CL Item
Transferred/Planned (3)
CL Item
Unknown (4)
Coronary artery bypass graft (CABG) date
Item
Coronary artery bypass graft (CABG) date
datetime
C0010055 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Electrical devices
text
C0018831 (UMLS CUI-1)
Code List
Electrical devices
CL Item
None (1)
CL Item
Pacemaker (permanent) (2)
C0030163 (UMLS CUI-1)
CL Item
ICD (3)
C2825184 (UMLS CUI-1)
CL Item
ICD and Pacemaker (4)
C1998005 (UMLS CUI-1)
CL Item
Unknown (5)
Item Group
Medication during hospital stay
Item
Aspirin
text
C0004057 (UMLS CUI-1)
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Heparin/low molecular weight heparin
text
Code List
Heparin/low molecular weight heparin
CL Item
No (1)
CL Item
Unfractionated heparin (2)
C2825026 (UMLS CUI-1)
CL Item
LMWH (3)
C3536766 (UMLS CUI-1)
CL Item
LMWH + Unfractionated heparin (4)
CL Item
Unknown (5)
Item
IV Glycoprotein (GP) IIb/IIIa
text
C3640054 (UMLS CUI-1)
Code List
IV Glycoprotein (GP) IIb/IIIa
CL Item
No (1)
CL Item
Abciximab (2)
C0288672 (UMLS CUI-1)
CL Item
Tirofiban (3)
C0247025 (UMLS CUI-1)
CL Item
Eptifibatide (4)
C0253563 (UMLS CUI-1)
CL Item
Unknown (5)
Item
ACE inhibitors
text
C0003015 (UMLS CUI-1)
Code List
ACE inhibitors
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Beta- blockers
text
C0304516 (UMLS CUI-1)
Code List
Beta- blockers
CL Item
No (1)
CL Item
Intravenous (2)
C0304516 (UMLS CUI-1)
C1522726 (UMLS CUI-2)
P (UMLS CUI-3)
CL Item
Oral (3)
C1527415 (UMLS CUI-1)
C0304516 (UMLS CUI-2)
P (UMLS CUI-3)
CL Item
Intravenous and oral (4)
CL Item
Unknown (5)
Item
Diuretics
text
C0012798 (UMLS CUI-1)
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Inotropes
text
C0304509 (UMLS CUI-1)
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item Group
Outcome
Item
Myocardial reinfarction during hospital stay
text
C2882123 (UMLS CUI-1)
Code List
Myocardial reinfarction during hospital stay
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Bleeding during hospital stay
text
C0019080 (UMLS CUI-1)
Code List
Bleeding during hospital stay
CL Item
No (1)
CL Item
Intracranial bleed (2)
C0151699 (UMLS CUI-1)
CL Item
Retroperitoneal bleed (major) (3)
C0151705 (UMLS CUI-1)
CL Item
Any other spontaneous bleed (major) (4)
CL Item
Unknown (5)
Item
Stroke during hospital stay
text
C0038454 (UMLS CUI-1)
Code List
Stroke during hospital stay
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Resuscitated cardiac arrest
text
C0018790 (UMLS CUI-1)
C1882942 (UMLS CUI-2)
Code List
Resuscitated cardiac arrest
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Date and time of cardiac arrest
Item
Date and time of cardiac arrest
datetime
C2825160 (UMLS CUI-1)
Item
Mechanical complications
text
Code List
Mechanical complications
CL Item
None (1)
CL Item
Free wall rupture (2)
C1959586 (UMLS CUI-1)
CL Item
Ventricular septal defect (3)
C0018818 (UMLS CUI-1)
CL Item
Mitral regurgitation (4)
C0026266 (UMLS CUI-1)
CL Item
Tamponade (5)
C0007177 (UMLS CUI-1)
CL Item
Unknown (6)
Item
Discharge ECG rhythm
text
C0232187 (UMLS CUI-1)
Code List
Discharge ECG rhythm
CL Item
Sinus rhythm (1)
C0232201 (UMLS CUI-1)
CL Item
Atrial fibrillation (2)
C0004238 (UMLS CUI-1)
CL Item
Pacemaker (3)
C2981711 (UMLS CUI-1)
CL Item
Other (4)
CL Item
Unknown (5)
Item
Discharge diagnosis
text
C0332144 (UMLS CUI-1)
Code List
Discharge diagnosis
CL Item
STEMI/LBBB MI (1)
C1536220 (UMLS CUI-1)
CL Item
NSTEMI (2)
C3537184 (UMLS CUI-1)
CL Item
Unstable Angina (3)
C0002965 (UMLS CUI-1)
CL Item
Stable Angina (4)
C0340288 (UMLS CUI-1)
CL Item
Other (5)
CL Item
Unknown (6)
Item
Survival status at discharge
text
C0586514 (UMLS CUI-1)
Code List
Survival status at discharge
CL Item
Alive (1)
C1299454 (UMLS CUI-1)
CL Item
Dead (2)
C1299455 (UMLS CUI-1)
CL Item
Unknown (3)
Date of discharge/death
Item
Date of discharge/death
datetime
C2361123 (UMLS CUI-1)
C1148348 (UMLS CUI-2)
Item Group
Medication at discharge
Item
Aspirin
text
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Antiplatelet
text
Code List
Antiplatelet
CL Item
No (1)
CL Item
Ticlopidine/Clopidogrel (2)
CL Item
Other antiplatelet agent (3)
CL Item
Unknown (4)
Item
Anticoagulants
text
Code List
Anticoagulants
CL Item
No (1)
CL Item
Vit. K antagonists (2)
CL Item
Oral thrombin inhibitors (3)
CL Item
Other (4)
CL Item
Unknown (5)
Item
Beta-blockers
text
Code List
Beta-blockers
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
ACE inhibitors
text
Code List
ACE inhibitors
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Angiotensin II receptor blockers
text
Code List
Angiotensin II receptor blockers
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Diabetic control
text
Code List
Diabetic control
CL Item
None (1)
CL Item
Insulin and oral agent (2)
CL Item
Insulin (3)
CL Item
Oral agent (4)
CL Item
Diet only (5)
CL Item
Unknown (6)
Item
Statins
text
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Non-statin lipid lowering agents
text
Code List
Non-statin lipid lowering agents
CL Item
None (1)
CL Item
Ezetimibe (2)
CL Item
Fibrates (3)
CL Item
Other non-statin (4)
CL Item
Unknown (5)
Item Group
Follow up
Date of follow up
Item
Date of follow up
date
C3694716 (UMLS CUI-1)
Item
Survival status at follow up
text
Code List
Survival status at follow up
CL Item
Alive (1)
CL Item
Dead (2)
CL Item
Unknown (3)
Date of death
Item
Date of death
date
C1148348 (UMLS CUI-1)
Item
Primary cause of death
text
C0007465 (UMLS CUI-1)
Code List
Primary cause of death
CL Item
Cardiovascular (1)
C2924466 (UMLS CUI-1)
CL Item
Non-Cardiovascular (2)
CL Item
Unknown (3)
Item
Anginal status
text
C1277207 (UMLS CUI-1)
Code List
Anginal status
CL Item
None (1)
CL Item
CCS I (2)
C2698967 (UMLS CUI-1)
CL Item
CCS II (3)
C2698968 (UMLS CUI-1)
CL Item
CCS III (4)
C2698969 (UMLS CUI-1)
CL Item
CCS IV (5)
C2698970 (UMLS CUI-1)
CL Item
Unknown (6)
Item
Dyspnoea
text
C1275491 (UMLS CUI-1)
Code List
Dyspnoea
CL Item
NYHA I (1)
C1319793 (UMLS CUI-1)
CL Item
NYHA II (2)
C1319794 (UMLS CUI-1)
CL Item
NYHA III (3)
C1319795 (UMLS CUI-1)
CL Item
NYHA IV (4)
C1319796 (UMLS CUI-1)
CL Item
Unknown (5)
Date of first hospital readmission since discharge
Item
Date of first hospital readmission since discharge
date
C0030700 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Myocardial infarction [MI]
text
C0027051 (UMLS CUI-1)
Code List
Myocardial infarction [MI]
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Myocardial infarction [MI] date
Item
Myocardial infarction [MI] date
date
C2924287 (UMLS CUI-1)
Item
Stroke
text
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Stroke date
Item
Stroke date
date
Item
Percutaneous coronary intervention [PCI]
text
Code List
Percutaneous coronary intervention [PCI]
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Percutaneous coronary intervention [PCI] date
Item
Percutaneous coronary intervention [PCI] date
date
Item
Coronary artery bypass graft [CABG]
text
Code List
Coronary artery bypass graft [CABG]
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Coronary artery bypass graft [CABG] date
Item
Coronary artery bypass graft [CABG] date
date
Item
Cardiac rehabilitation program
text
C0700431 (UMLS CUI-1)
Code List
Cardiac rehabilitation program
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Aspirin
text
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Antiplatelet
text
Code List
Antiplatelet
CL Item
No (1)
CL Item
Ticlopidine/Clopidogrel (2)
C0040207 (UMLS CUI-1)
C0070166 (UMLS CUI-2)
CL Item
Other antiplatelet agent (3)
CL Item
Unknown (4)
Item
Anticoagulants
text
Code List
Anticoagulants
CL Item
No (1)
CL Item
Vitamin K antagonist (2)
C2267235 (UMLS CUI-1)
CL Item
Oral thrombin inhibitors (3)
CL Item
Other (4)
CL Item
Unknown (5)
Item
Beta-blockers
text
Code List
Beta-blockers
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
ACE inhibitors
text
Code List
ACE inhibitors
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Angiotensin II receptor blockers
text
Code List
Angiotensin II receptor blockers
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Diabetic control
text
Code List
Diabetic control
CL Item
None (1)
C3275118 (UMLS CUI-1)
CL Item
Insulin and oral agent (2)
C1272306 (UMLS CUI-1)
CL Item
Insulin (3)
C0421248 (UMLS CUI-1)
CL Item
Oral agent (4)
C0421247 (UMLS CUI-1)
CL Item
Diet alone (5)
C0421246 (UMLS CUI-1)
CL Item
Unknown (6)
Item
Statins
text
CL Item
No (1)
CL Item
Yes (2)
CL Item
Unknown (3)
Item
Non-statin lipid lowering agents
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Code List
Non-statin lipid lowering agents
CL Item
None (1)
CL Item
Ezetimibe (2)
C1142985 (UMLS CUI-1)
CL Item
Fibrates (3)
C1449704 (UMLS CUI-1)
CL Item
Other non-statin (4)
CL Item
Unknown (5)

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