ID
44131
Beschrijving
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.
Trefwoorden
Versies (3)
- 15-04-15 15-04-15 -
- 10-04-21 10-04-21 - Ahmed Rafee, MD
- 20-09-21 20-09-21 -
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Copyright Irish Department of Health and Children/European Society of Cardiology
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20 september 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
- StudyEvent: ODM
Beschrijving
Past History relevant to Coronary Artery Disease
Beschrijving
Indicate if the patient had at least one previous myocardial infarction before this admission.
Datatype
text
Alias
- UMLS CUI-1
- C1275835
Beschrijving
Indicate if the patient has a history of angina and / or has been treated previously for angina by a physician.
Datatype
text
Alias
- UMLS CUI-1
- C0455530
Beschrijving
Indicate if the patient has a history of congestive heart failure and/or has previously been treated for congestive heart failure by a physician.
Datatype
text
Alias
- UMLS CUI-1
- C0455531
Beschrijving
Indicate if the patient has a history of cerebrovascular accident (CVA) / stroke, as evidenced by a persistent neurological deficit due to ischaemia.
Datatype
text
Alias
- UMLS CUI-1
- C0559159
Beschrijving
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%.
Datatype
text
Alias
- UMLS CUI-1
- C1881056
Beschrijving
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
Datatype
text
Alias
- UMLS CUI-1
- C1533077
Beschrijving
Indicate if the patient has a history of chronic lung disease and/or has previously been treated for chronic lung disease by a physician.
Datatype
text
Alias
- UMLS CUI-1
- C1533075
Beschrijving
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).
Datatype
text
Alias
- UMLS CUI-1
- C1320647
Beschrijving
Indicate if the patient had coronary artery bypass graft (CABG) done prior to this admission
Datatype
text
Alias
- UMLS CUI-1
- C1275842
Beschrijving
Indicate if the patient has a history confirming any form of tobacco use in the past. This includes cigarettes/cigar/pipe.
Datatype
text
Alias
- UMLS CUI-1
- C0543414
Beschrijving
Indicate if the patient has a history of diabetes mellitus diagnosed prior to the current admission.
Datatype
text
Alias
- UMLS CUI-1
- C0011849
Beschrijving
Indicate if the patient has a history of hypertension diagnosed and/or treated by a physician.
Datatype
text
Alias
- UMLS CUI-1
- C0455527
Beschrijving
Indicate if the patient has a documented history of hypercholesterolemia diagnosed and/or treated by a physician.
Datatype
text
Alias
- UMLS CUI-1
- C1533076
Beschrijving
Medication: pre hospital
Beschrijving
Indicate if the patient was taking aspirin regularly prior to this admission to hospital.
Datatype
text
Alias
- UMLS CUI-1
- C0004057
Beschrijving
Indicate if the patient was taking antiplatelet medication (other than aspirin) regularly prior to this admission to hospital.
Datatype
text
Beschrijving
Indicate if the patient was taking anticoagulant medication before this hospital admission.
Datatype
text
Alias
- UMLS CUI-1
- C0003280
Beschrijving
Indicate if the patient was taking Beta-blockers regularly prior to this admission to hospital
Datatype
text
Alias
- UMLS CUI-1
- C0304516
Beschrijving
Indicate if the patient was taking ACE inhibitors regularly prior to this admission to hospital.
Datatype
text
Alias
- UMLS CUI-1
- C0003015
Beschrijving
Indicate if the patient was taking angiotensin II receptorblockers regularly prior to this admission to hospital.
Datatype
text
Alias
- UMLS CUI-1
- C0521942
Beschrijving
Indicate the main method of diabetic treatment the patient has been receiving.
Datatype
text
Alias
- UMLS CUI-1
- C3274787
Beschrijving
Indicate if the patient was taking statins regularly prior to this admission to hospital.
Datatype
text
Alias
- UMLS CUI-1
- C0360714
Beschrijving
Indicate if the patient was taking non-statin lipid lowering agents regularly prior to this admission to hospital.
Datatype
text
Alias
- UMLS CUI-1
- C0086440
Beschrijving
Working Diagnosis
Alias
- UMLS CUI-1
- C0332135
Beschrijving
Indicate the predominant symptom /reason why patient presented for medical attention.
Datatype
text
Alias
- UMLS CUI-1
- C3177142
Beschrijving
Indicate the date and time of onset of symptom / reason that prompted the patient's presentation for medical attention.
Datatype
datetime
Alias
- UMLS CUI-1
- C1320528
Beschrijving
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.
Datatype
integer
Maateenheden
- bpm
Alias
- UMLS CUI-1
- C0018810
Beschrijving
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.
Datatype
integer
Maateenheden
- mmHg
Alias
- UMLS CUI-1
- C0871470
Beschrijving
Indicate the date and time the patient first presented to the hospital for this admission.
Datatype
datetime
Alias
- UMLS CUI-1
- C1320532
Beschrijving
Indicate the Killip class of the patient at the time of hospital admission.
Datatype
text
Alias
- UMLS CUI-1
- C1881332
Beschrijving
Indicate the rhythm on the first admission ECG.
Datatype
text
Alias
- UMLS CUI-1
- C0232187
Beschrijving
Indicate if first admission ECG has any QRS abnormalities.
Datatype
text
Alias
- UMLS CUI-1
- C2983649
Beschrijving
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.
Datatype
text
Alias
- UMLS CUI-1
- C0232326
Beschrijving
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).
Datatype
text
Alias
- UMLS CUI [1,1]
- C1271630
- UMLS CUI [1,2]
- C07022401
Beschrijving
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.
Datatype
text
Alias
- UMLS CUI-1
- C1271630
Beschrijving
Indicate the first total serum cholesterol level in mmol/l [ideally taken within 24 hours of this admission].
Datatype
float
Maateenheden
- mmol/l
Alias
- UMLS CUI-1
- C1445957
Beschrijving
Indicate the level of the serum creatinine (first) during this admission in mg/dl or umol/l.
Datatype
float
Alias
- UMLS CUI-1
- C0201975
Beschrijving
After initial assessment of the patient, indicate the diagnosis on which further management of the patient is based.
Datatype
text
Alias
- UMLS CUI-1
- C0332135
Beschrijving
Investigations and Treatment
Alias
- UMLS CUI-1
- C0808232
Beschrijving
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).
Datatype
text
Alias
- UMLS CUI-1
- C0040044
Beschrijving
Indicate the date and time thrombolysis was commenced. This is defined as the time the infusion was commenced and/or time of bolus injection.
Datatype
datetime
Alias
- UMLS CUI [1,1]
- C0040044
- UMLS CUI [1,2]
- C1301880
Beschrijving
Reason why thrombolysis not administered
Datatype
text
Alias
- UMLS CUI-1
- C3260558
Beschrijving
If the patient underwent a percutaneous coronary intervention indicate the type.
Datatype
text
Alias
- UMLS CUI-1
- C0027054
Beschrijving
Indicate the date and time of percutaneous coronary intervention [PCI].
Datatype
datetime
Alias
- UMLS CUI-1
- C1532338
- UMLS CUI-2
- C1264639
- UMLS CUI-3
- P
Beschrijving
If the patient underwent a stress test during hospital stay indicate the type of stress test.
Datatype
text
Alias
- UMLS CUI-1
- C1384495
Beschrijving
Indicate if signs of ischaemia were present on the stress test used (as determined by the clinician).
Datatype
text
Alias
- UMLS CUI-1
- C1274040
- UMLS CUI-2
- C1384495
- UMLS CUI-3
- P
Beschrijving
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.
Datatype
text
Alias
- UMLS CUI-1
- C0428772
Beschrijving
Indicate if the patient underwent diagnostic coronary angiography during this admission episode.
Datatype
text
Alias
- UMLS CUI-1
- C0085532
Beschrijving
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.
Datatype
text
Alias
- UMLS CUI-1
- C3275120
Beschrijving
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'.
Datatype
text
Alias
- UMLS CUI-1
- C1532338
Beschrijving
Indicate the date the PCI was performed if performed during this admission episode.
Datatype
datetime
Alias
- UMLS CUI [1,1]
- C1532338
- UMLS CUI [1,2]
- C1264639
Beschrijving
Indicate if the patient underwent CABG during this admission episode.
Datatype
text
Alias
- UMLS CUI-1
- C0010055
Beschrijving
Indicate the date the CABG was performed if performed during this admission episode.
Datatype
datetime
Alias
- UMLS CUI [1,1]
- C0010055
- UMLS CUI [1,2]
- C0011008
Beschrijving
Indicate if the patient had any of the following electrical devices implanted during this admission episode.
Datatype
text
Alias
- UMLS CUI-1
- C0018831
Beschrijving
Medication during hospital stay
Beschrijving
Indicate if aspirin was administered in the treatment of ACS.
Datatype
text
Alias
- UMLS CUI-1
- C0004057
Beschrijving
Indicate if heparin/low molecular weight heparin [LMWH] was administered in the treatment of ACS .
Datatype
text
Beschrijving
Indicate the use of IV Glycoprotein IIb/IIIa inhibitors and type in the treatment of ACS.
Datatype
text
Alias
- UMLS CUI-1
- C3640054
Beschrijving
Indicate if ACE inhibitors were administered in the treatment of ACS.
Datatype
text
Alias
- UMLS CUI-1
- C0003015
Beschrijving
Indicate if Beta-blockers were administered in the treatment of ACS.
Datatype
text
Alias
- UMLS CUI-1
- C0304516
Beschrijving
Indicate if diuretics were administered in the treatment of ACS.
Datatype
text
Alias
- UMLS CUI-1
- C0012798
Beschrijving
Indicate if inotropes were administered in the treatment of ACS.
Datatype
text
Alias
- UMLS CUI-1
- C0304509
Beschrijving
Outcome
Beschrijving
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)
Datatype
text
Alias
- UMLS CUI-1
- C2882123
Beschrijving
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).
Datatype
text
Alias
- UMLS CUI-1
- C0019080
Beschrijving
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.
Datatype
text
Alias
- UMLS CUI-1
- C0038454
Beschrijving
Indicate if the patient had a cardiac arrest during hospital admission and was successfully resuscitated.
Datatype
text
Alias
- UMLS CUI-1
- C0018790
- UMLS CUI-2
- C1882942
Beschrijving
Indicate the date and time of cardiac arrest
Datatype
datetime
Alias
- UMLS CUI-1
- C2825160
Beschrijving
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.
Datatype
text
Beschrijving
Indicate the patients discharge ECG rhythm.
Datatype
text
Alias
- UMLS CUI-1
- C0232187
Beschrijving
Indicate the discharge diagnosis.
Datatype
text
Alias
- UMLS CUI-1
- C0332144
Beschrijving
Indicate vital status at discharge.
Datatype
text
Alias
- UMLS CUI-1
- C0586514
Beschrijving
Indicate the date the patient was discharged from hospital or if patient died record the date of death.
Datatype
datetime
Alias
- UMLS CUI-1
- C2361123
- UMLS CUI-2
- C1148348
Beschrijving
Medication at discharge
Beschrijving
Indicate if the patient was prescribed aspirin on discharge from hospital.
Datatype
text
Beschrijving
Indicate if the patient was prescribed antiplatelet medication (other than aspirin) on discharge from hospital.
Datatype
text
Beschrijving
Indicate if the patient was prescribed anticoagulant medication on discharge from hospital.
Datatype
text
Beschrijving
Indicate if the patient was prescribed Beta-Blockers on discharge from hospital.
Datatype
text
Beschrijving
Indicate if the patient was prescribed ACE inhibitors on discharge from hospital.
Datatype
text
Beschrijving
Indicate if the patient was prescribed angiotensin II receptor blockers on discharge from hospital.
Datatype
text
Beschrijving
Indicate the main method of diabetic treatment the patient was prescribed on discharge from hospital.
Datatype
text
Beschrijving
Indicate if the patient was prescribed statins on discharge.
Datatype
text
Beschrijving
Indicate if the patient was prescribed non-statin lipid lowering agents on discharge.
Datatype
text
Beschrijving
Follow up
Beschrijving
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.
Datatype
date
Alias
- UMLS CUI-1
- C3694716
Beschrijving
Indicate vital status at follow up.
Datatype
text
Beschrijving
If the patient died indicate the date of death.
Datatype
date
Alias
- UMLS CUI-1
- C1148348
Beschrijving
Indicate the primary cause of death.
Datatype
text
Alias
- UMLS CUI-1
- C0007465
Beschrijving
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.
Datatype
text
Alias
- UMLS CUI-1
- C1277207
Beschrijving
Grade breathing status using the New York Heart Association (NYHA) functional classification.
Datatype
text
Alias
- UMLS CUI-1
- C1275491
Beschrijving
If the patient was readmitted to hospital indicate the date.
Datatype
date
Alias
- UMLS CUI [1,1]
- C0030700
- UMLS CUI [1,2]
- C0011008
Beschrijving
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.
Datatype
text
Alias
- UMLS CUI-1
- C0027051
Beschrijving
Indicate the date of the myocardial infarction.
Datatype
date
Alias
- UMLS CUI-1
- C2924287
Beschrijving
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.
Datatype
text
Beschrijving
Indicate the date of the stroke. Date
Datatype
date
Beschrijving
Indicate if the patient had a percutaneous coronary intervention since the date of discharge.
Datatype
text
Beschrijving
Indicate the date of percutaneous coronary intervention [PCI].
Datatype
date
Beschrijving
Indicate if the patient had coronary artery bypass graft [CABG] since the date of discharge.
Datatype
text
Beschrijving
Indicate the date of coronary artery bypass graft [CABG].
Datatype
date
Beschrijving
Indicate if the patient attended or is attending a cardiac rehabilitation programme since discharge.
Datatype
text
Alias
- UMLS CUI-1
- C0700431
Beschrijving
Medication at follow up
Beschrijving
On follow up indicate if the patient is taking aspirin regularly.
Datatype
text
Beschrijving
On follow-up indicate if the patient is taking antiplatelet medication (other than aspirin) regularly.
Datatype
text
Beschrijving
On follow-up indicate if the patient is taking anticoagulant medication regularly.
Datatype
text
Beschrijving
On follow-up indicate if the patient is taking Beta-Blockers regularly.
Datatype
text
Beschrijving
On follow-up indicate if the patient is taking ACE inhibitors regularly.
Datatype
text
Beschrijving
On follow-up indicate if the patient is taking angiotensin II receptor blockers regularly.
Datatype
text
Beschrijving
On follow-up indicate the main method of diabetic control the patient is regularly receiving.
Datatype
text
Beschrijving
On follow-up indicate if the patient is taking statins regularly.
Datatype
text
Beschrijving
On follow-up indicate if the patient is taking non-statin lipid lowering agents regularly.
Datatype
text
Similar models
CCU/ACS Data Standards
- StudyEvent: ODM
C0019994 (UMLS CUI [1,2])
C0070166 (UMLS CUI-2)
C0085298 (UMLS CUI-2)
C07022401 (UMLS CUI [1,2])
C1141947 (UMLS CUI-2)
C1301880 (UMLS CUI [1,2])
C1264639 (UMLS CUI-2)
P (UMLS CUI-3)
C1384495 (UMLS CUI-2)
P (UMLS CUI-3)
C1264639 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C1522726 (UMLS CUI-2)
P (UMLS CUI-3)
C0304516 (UMLS CUI-2)
P (UMLS CUI-3)
C1882942 (UMLS CUI-2)
C1148348 (UMLS CUI-2)
C0011008 (UMLS CUI [1,2])
C0070166 (UMLS CUI-2)