- | Acute coronary syndrome clinical event cluster |
|
| |
- | Date of acute coronary syndrome related clinical event | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | Conditional obligation: If a clinical event has occurred, record the date when it was experienced by the person.
DSS specific information: The date is to be provided for each clinical event experienced during this hospital presentation. |
- | Time of acute coronary syndrome related clinical event | Date/Time
[4]
| hhmm
A valid time measured as hours and minutes using a 24 hour clock. | Conditional obligation: If a clinical event has occurred, record the time when it was experienced by the person.
DSS specific information: The time is to be provided for each clinical event experienced during this hospital presentation. |
- | Acute coronary syndrome related clinical event type | Number
[2]
| 1 | Cardiogenic shock | 2 | Cardiac rupture | 3 | Cardiac arrest | 4 | New or recurrent myocardial infarction | 5 | Stroke | 6 | Acute pulmonary oedema | 7 | Recurrent rest angina with electrocardiogram changes | 8 | Recurrent rest angina without electrocardiogram changes | 9 | New onset arrhythmia: atrial | 10 | New onset arrhythmia: ventricular | 11 | New onset arrhythmia: heart block (1,2,3) | 12 | Unplanned revascularisation | 13 | Acute renal failure | 14 | Thrombocytopaenia | 99 | Not stated/inadequately described |
| Conditional obligation: If a clinical event has occurred, record the clinical event type. DSS specific information: Codes are to be provided for each clinical event prescribed during this hospital presentation. |
- | Acute coronary syndrome pharmacotherapy data cluster |
|
| |
- | Pharmacotherapy type prescribed for acute coronary syndrome in hospital | Number
[2]
| 1 | Aspirin | 2 | Angiotensin converting enzyme (ACE) inhibitor | 3 | Angiotensin II receptor blocker | 4 | Antithrombin | 5 | Beta-blocker | 6 | Clopidogrel | 7 | Fibrinolytic | 8 | Glycoprotein IIb/IIIa receptor antagonist | 9 | Statin | 99 | Not stated/inadequately described |
| DSS specific information: Codes provided for each of those prescribed during this hospital presentation. |
- | Pharmacotherapy type taken for acute coronary syndrome post discharge | Number
[2]
| 1 | Aspirin | 2 | Angiotensin converting enzyme (ACE) inhibitor | 3 | Angiotensin II receptor blocker | 4 | Beta-blocker | 5 | Clopidogrel | 6 | Statin | 99 | Not stated/inadequately described |
| DSS specific information: To be provided at the follow-up visit following discharge from the hospital for each of the relevant pharmacotherapy types prescribed. |
- | Fibrinolytic drug used | Number
[1]
| 1 | Streptokinase | 2 | t-PA (Tissue Plasminogen Activator) (Alteplase) | 3 | r-PA (Reteplase) | 4 | TNK t-PA (Tenecteplase) | 9 | Not stated/inadequately described |
| Conditional obligation: If prescribed, provide the fibrinolytic drug administered. |
- | Date of intravenous fibrinolytic therapy | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | Conditional obligation: If prescribed, provide the date when the fibrinolytic therapy is administered. |
- | Time of intravenous fibrinolytic therapy | Date/Time
[4]
| hhmm
A valid time measured as hours and minutes using a 24 hour clock. | Conditional obligation: If prescribed, provide the time when the fibrinolytic therapy is administered.
|
- | Reason for non prescription of pharmacotherapy | Number
[1]
| 1 | Not indicated | 2 | Contraindicated | 9 | Not stated/inadequately described |
| Conditional obligation: To be provided for each of the pharmacotherapies listed in the data element 'Pharmacotherapy type prescribed for acute coronary syndrome in hospital' not prescribed. |
- | Timing of ACE-inhibitor prescription | Number
[1]
| 1 | Prior to presentation at hospital | 2 | First 24 hours of presentation | 3 | After 24 hours and before discharge | 4 | At discharge | 9 | Not stated/inadequately described |
| Conditional obligation: If prescribed, provide a phase for each time ACE-inhibitor therapy is prescribed. |
- | Timing of angiotensin II receptor blocker prescription | Number
[1]
| 1 | Prior to presentation at hospital | 2 | First 24 hours of presentation | 3 | After 24 hours and before discharge | 4 | At discharge | 9 | Not stated/inadequately described |
| Conditional obligation: If prescribed, provide a phase for each time angiotensin II receptor blocker therapy is prescribed. |
- | Timing of antithrombin therapy prescription | Number
[1]
| 1 | Initial medical management: preceding reperfusion therapy | 2 | During reperfusion therapy | 3 | Following reperfusion therapy | 9 | Not stated/inadequately described |
| Conditional obligation: If prescribed, provide a phase for each time antithrombin therapy is prescribed |
- | Timing of aspirin prescription | Number
[1]
| 1 | Prior to presentation at hospital | 2 | First 24 hours of presentation | 3 | After 24 hours and before discharge | 4 | At discharge | 9 | Not stated/inadequately described |
| Conditional obligation: If prescribed, provide a phase for each time aspirin therapy is prescribed. |
- | Timing of beta-blocker prescription | Number
[1]
| 1 | Prior to presentation at hospital | 2 | First 24 hours of presentation | 3 | After 24 hours and before discharge | 4 | At discharge | 9 | Not stated/inadequately described |
| Conditional obligation: If prescribed, provide a phase for each time beta-blocker therapy is prescribed. |
- | Timing of clopidogrel prescription | Number
[1]
| 1 | Prior to presentation at hospital | 2 | First 24 hours of presentation | 3 | After 24 hours and before discharge | 4 | At discharge | 9 | Not stated/inadequately described |
| Conditional obligation: If prescribed, provide a phase for each time clopidogrel therapy is prescribed. |
- | Timing of glycoprotein IIb/IIIa inhibitor prescription | Number
[1]
| 1 | Initial medical management: preceding invasive management | 2 | During invasive management | 3 | Following invasive management | 9 | Not stated/inadequately described |
| Conditional obligation: If prescribed, provide a phase for each time glycoprotein IIb/IIIa inhibitor therapy is prescribed. |
- | Timing of statin prescription | Number
[1]
| 1 | Prior to presentation at hospital | 2 | First 24 hours of presentation | 3 | After 24 hours and before discharge | 4 | At discharge | 9 | Not stated/inadequately described |
| Conditional obligation: If prescribed, provide a phase for each time statin therapy is prescribed. |
- | Coronary artery cluster |
|
| |
- | Date of coronary artery bypass graft | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | Conditional obligation: Record when a coronary artery bypass graft is performed. |
- | Coronary artery bypass graft location | Number
[1]
| 1 | Left anterior descending artery (LAD) | 2 | Diagonal artery | 3 | Left circumflex artery (LCx) | 4 | Inferior surface artery | 5 | Posterior descending artery | 6 | Right coronary artery | 8 | Other artery | 9 | Not stated/inadequately described |
| Conditional obligation: Record when a coronary artery bypass graft is performed. DSS specific information: Codes provided for each location where a graft is performed during this hospital presentation. |
- | Coronary artery stenosis location | Number
[1]
| 1 | Left anterior descending artery (LAD) | 2 | Diagonal artery | 3 | Left circumflex artery (LCx) | 4 | Left main coronary artery | 5 | Inferior surface artery | 6 | Posterior descending artery | 7 | Right coronary artery | 9 | Not stated/inadequately described |
| |
- | Number of coronary artery lesions attempted | Number
[2]
| 99 | Not stated/inadequately described |
| Conditional obligation: Record when a percutaneous coronary intervention is performed. |
- | Number of coronary artery lesions successfully dilated | Number
[2]
| 99 | Not stated/inadequately described |
| Conditional obligation: Record when a percutaneous coronary intervention is performed.
|
- | Number of coronary artery stents | Number
[2]
| 99 | Not stated/inadequately described |
| Conditional obligation: Record when a percutaneous coronary intervention with stent implantation (bare metal stent or drug eluting stent) is performed. |
- | Maximum stenosis coronary artery | Number
[3]
| 999 | Not stated/inadequately described |
| |
- | Percutaneous coronary intervention procedure type | String | 1 | Balloon angioplasty only | 2 | Bare metal stent implantation | 3 | Drug-eluting stent implantation | 99 | Not stated/inadequately described |
| Conditional obligation: Record when a percutaneous coronary intervention is performed. This includes those performed for primary, rescue or revascularisation reasons. |
- | Date of primary percutaneous coronary intervention | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | Conditional obligation: Record when a primary percutaneous coronary intervention is performed. |
- | Time of primary percutaneous coronary intervention | Date/Time
[4]
| hhmm
A valid time measured as hours and minutes using a 24 hour clock. | Conditional obligation: Record when a primary percutaneous coronary intervention is performed.
|
- | Date of rescue percutaneous coronary intervention | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | Conditional obligation: Record when a rescue percutaneous coronary intervention is performed. |
- | Time of rescue percutaneous coronary intervention | Date/Time
[4]
| hhmm
A valid time measured as hours and minutes using a 24 hour clock. | Conditional obligation: Record when a rescue percutaneous coronary intervention is performed. |
- | Date of revascularisation percutaneous coronary intervention | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | Conditional obligation: Record when a percutaneous coronary intervention is performed for revascularisation. |
- | Time of revascularisation percutaneous coronary intervention | Date/Time
[4]
| hhmm
A valid time measured as hours and minutes using a 24 hour clock. | Conditional obligation: Record when a percutaneous coronary intervention is performed for revascularisation. |
- | Electrocardiogram cluster |
|
| |
- | Bundle-branch block status | Number
[1]
| 1 | New | 2 | Pre-existing | 3 | Uncertain timing | 9 | Not stated/inadequately described |
| Conditional obligation: Record if a bundle-branch block has been detected on an electrocardiogram. |
- | Electrocardiogram change location | Number
[1]
| 1 | Inferior leads: II, III, aVF | 2 | Anterior leads: V1 to V4 | 3 | Lateral leads: I, aVL, V5 to V6 | 4 | True posterior: V1 V2 | 9 | Not stated/inadequately described |
| DSS specific information: To be provided each time an ECG is performed.
|
- | Electrocardiogram change type | Number
[2]
| 10 | ST-segment-elevation >= 1 mm (0.1 mV) in >= 2 contiguous limb leads | 11 | ST-segment-elevation >= 2 mm (0.2 mV) in >= 2 contiguous chest leads | 12 | ST-segment depression >= 0.5 mm (0.05 mV) in >= 2 contiguous leads (includes reciprocal changes) | 20 | T-wave inversion >= 2 mm (0.1 mV) | 30 | Significant Q waves | 40 | Left bundle-branch block (BBB) | 41 | Right bundle-branch block (BBB) | 42 | Indeterminate bundle-branch block (BBB) | 90 | Non specific | 99 | Not stated/inadequately described |
| DSS specific information: To be provided each time an ECG is performed.
|
- | Date of electrocardiogram | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | DSS specific information: To be provided each time an ECG is performed. |
- | Time of electrocardiogram | Date/Time
[4]
| hhmm
A valid time measured as hours and minutes using a 24 hour clock. | DSS specific information: To be provided each time an ECG is performed. |
- | Heart rhythm type | String
[2]
| 1 | Sinus rhythm | 2 | Atrial fibrillation | 3 | Atrial flutter | 4 | Second degree heart block | 5 | Complete heart block | 6 | Supraventricular tachycardia | 7 | Idioventricular rhythm | 8 | Ventricular tachycardia | 9 | Ventricular fibrillation | 10 | Paced | 11 | Other rhythm | 99 | Not stated/inadequately described |
| DSS specific information: To be provided each time an ECG is performed.
|
- | Electrocardiogram - lead V4R presence indicator | Boolean
[1]
| 1 | Yes | 2 | No | 9 | Not stated/inadequately described |
| DSS specific information: To be provided each time an ECG is performed. |
- | Electrocardiogram - new Q waves indicator | Boolean
[1]
| 1 | Yes | 2 | No | 9 | Not stated/inadequately described |
| Conditional obligation: Record if Q waves are present on the follow up electrocardiogram. |
- | Electrocardiogram - ST-segment-elevation in lead V4R | Boolean
[1]
| 1 | Yes | 2 | No | 9 | Not stated/inadequately described |
| Conditional obligation: Record when lead V4R was performed on the electrocardiogram. |
- | ECG - Q waves indicator | Boolean
[1]
| 1 | Yes | 2 | No | 9 | Not stated/inadequately described |
| Conditional obligation: Record for all follow up electrocardiograms performed after the initial electrocardiogram. |
- | Functional stress test cluster |
|
| |
- | Functional stress test assessment of cardiac perfusion | Number
[1]
| 1 | Exercise tolerance | 2 | Pharmacological | 9 | Not stated/inadequately described |
| Conditional obligation: To be provided when a functional stress test is performed. |
- | Functional stress ischaemic and perfusion outcome result | Number
[1]
| 1 | No abnormal outcome | 2 | Ischaemic discomfort and/or ST shift | 3 | Fixed perfusion or wall motion defects only | 4 | Reversible perfusion or wall motion defects only | 5 | Fixed and reversible perfusion and wall motion defects | 6 | Equivocal | 9 | Not stated/inadequately described |
| Conditional obligation: To be provided when a functional stress test is performed. |
- | Functional stress test element | Number
[1]
| 1 | ECG monitoring | 2 | Echocardiography | 3 | Radionuclide (perfusion) imaging (e.g. Thallium, Sestamibi) | 4 | Positron Emission Tomography (PET) | 5 | Magnetic Resonance Imaging (MRI) | 9 | Not stated/inadequately described |
| Conditional obligation: To be provided when a functional stress test is performed.
|
- | Functional stress test intensity | Number
[1]
| 1 | Maximal (symptom limited) | 2 | Submaximal | 3 | Rest / distribution study | 9 | Not stated/inadequately described |
| Conditional obligation: To be provided when a functional stress test is performed. |
- | Date of functional stress test | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | Conditional obligation: To be provided when a functional stress test is performed. |
- | Functional stress test performed indicator | Boolean
[1]
| 1 | Yes | 2 | No | 9 | Not stated/inadequately described |
| |
- | Ventricular ejection fraction cluster |
|
| |
- | Ventricular ejection fraction measurement indicator | Boolean
[1]
| 1 | Yes | 2 | No | 9 | Not stated/inadequately described |
| |
- | Date of ventricular ejection fraction test | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | Conditional obligation: To be provided when the ventricular ejection fraction is measured. |
- | Time of ventricular ejection fraction test | Date/Time
[4]
| hhmm
A valid time measured as hours and minutes using a 24 hour clock. | Conditional obligation: To be provided when the ventricular ejection fraction is measured. |
- | Ventricular ejection fraction test type | Number
[1]
| 1 | Echocardiography | 2 | Angiography | 3 | Gated blood pool scan | 4 | Magnetic resonance imaging (MRI) | 9 | Not stated/inadequately described |
| Conditional obligation: To be provided when the ventricular ejection fraction is measured. |
- | Ventricular ejection fraction test result (code) | Number
[1]
| 1 | Normal | 2 | Mild | 3 | Moderate | 4 | Severe | 9 | Not stated/inadequately described |
| Conditional obligation: To be provided when the ventricular ejection fraction is measured. |
- | Ventricular ejection fraction test result (percentage) | Number
[3]
| 99.9 | Not stated/inadequately described |
| Conditional obligation: To be provided when the ventricular ejection fraction is measured. |
- | Emergency department arrival mode - transport | Number
[1]
| 1 | Ambulance, air ambulance or helicopter rescue service | 2 | Police/correctional services vehicle | 8 | Other | 9 | Not stated/unknown |
| Conditional obligation: This data element should only be collected for patients who presented to the emergency department for treatment related to acute coronary syndromes. DSS specific information: This data element should only be collected for patients who presented to the emergency department for treatment related to acute coronary syndromes. |
- | Admission date | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | |
- | Admission time | Date/Time
[4]
| hhmm
A valid time measured as hours and minutes using a 24 hour clock. | |
- | Separation date | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | |
- | Mode of separation | Number
[1]
| 1 | Discharge/transfer to (an)other acute hospital | 2 | Discharge/transfer to a residential aged care service, unless this is the usual place of residence | 3 | Discharge/transfer to (an)other psychiatric hospital | 4 | Discharge/transfer to other health care accommodation (includes mothercraft hospitals) | 5 | Statistical discharge - type change | 6 | Left against medical advice/discharge at own risk | 7 | Statistical discharge from leave | 8 | Died | 9 | Other (includes discharge to usual residence, own accommodation/welfare institution (includes prisons, hostels and group homes providing primarily welfare services)) |
| |
- | Principal diagnosis—episode of care | String
[6]
| ANN{.N[N]} The ICD-10-AM (8th edition) code set representing diagnoses. | |
- | Funding source for hospital patient | String
[2]
| 01 | Australian Health Care Agreements | 02 | Private health insurance | 03 | Self-funded | 04 | Worker's compensation | 05 | Motor vehicle third party personal claim | 06 | Other compensation (e.g. public liability, common law, medical negligence) | 07 | Department of Veterans' Affairs | 08 | Department of Defence | 09 | Correctional facility | 10 | Other hospital or public authority (contracted care) | 11 | Reciprocal health care agreements (with other countries) | 12 | Other | 13 | No charge raised | 99 | Not known |
| |
- | Establishment identifier | String
[9]
| NNX[X]NNNNN A combination of numeric and alphanumeric characters that identify an entity. | |
- | Date patient presents | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | DSS specific information: This data element should only be collected for patients who presented to the emergency department for treatment related to acute coronary syndromes. |
- | Time patient presents | Date/Time
[4]
| hhmm
A valid time measured as hours and minutes using a 24 hour clock. | DSS specific information: This data element should only be collected for patients who presented to the emergency department for treatment related to acute coronary syndromes. |
- | Date of referral to rehabilitation | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | DSS specific information: Required to derive those referred to a rehabilitation service from those eligible to attend and who actually attend. This metadata item can be used to determine the time lag between referral and commencement of rehabilitation. |
- | Creatine kinase isoenzyme—upper limit of normal range (U/L) | Number
[4]
| 9998 | Not measured | 9999 | Not stated/inadequately described |
| |
- | Creatine kinase MB isoenzyme—upper limit of normal range (micrograms per litre) | Number
[4]
| 9998 | Not measured | 9999 | Not stated/inadequately described |
| |
- | Creatine kinase MB isoenzyme—upper limit of normal range (units per litre) | Number
[4]
| 9998 | Not measured | 9999 | Not stated/inadequately described |
| |
- | Troponin assay—upper limit of normal range (micrograms per litre) | Number
[4]
| 9998 | Not measured | 9999 | Not stated/inadequately described |
| |
- | Glycosylated haemoglobin—upper limit of normal range (percentage) | Number
[3]
| 99.9 | Not stated/inadequately described |
| |
- | Triage category | Number
[1]
| 1 | Resuscitation: immediate (within seconds) | 2 | Emergency: within 10 minutes | 3 | Urgent: within 30 minutes | 4 | Semi-urgent: within 60 minutes | 5 | Non-urgent: within 120 minutes |
| Conditional obligation: This data element should only be collected for patients who presented to the emergency department for treatment related to acute coronary syndromes. |
- | Date of triage | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | DSS specific information: This data element should only be collected for patients who presented to the emergency department for treatment related to acute coronary syndromes. |
- | Time of triage | Date/Time
[4]
| hhmm
A valid time measured as hours and minutes using a 24 hour clock. | DSS specific information: This data element should only be collected for patients who presented to the emergency department for treatment related to acute coronary syndromes. |
- | Type of visit to emergency department | Number
[1]
| 1 | Emergency presentation: attendance for an actual or suspected condition which is sufficiently serious to require acute unscheduled care. | 2 | Return visit, planned: presentation is planned and is a result of a previous emergency department presentation or return visit. | 3 | Pre-arranged admission: a patient who presents at the emergency department for either clerical, nursing or medical processes to be undertaken, and admission has been pre-arranged by the referring medical officer and a bed allocated. | 4 | Patient in transit: the emergency department is responsible for care and treatment of a patient awaiting transport to another facility. | 5 | Dead on arrival: a patient who is dead on arrival at the emergency department. |
| DSS specific information: This data element should only be collected for patients who presented to the emergency department for treatment related to acute coronary syndromes. |
- | Instrumented bleeding location | Number
[2]
| 1 | Percutaneous coronary procedure arterial access site | 2 | Coronary artery bypass graft site | 3 | Gastrointestinal site | 4 | Genitourinary site | 5 | Intracranial site | 6 | Pulmonary site | 7 | Pericardial site | 8 | Other site(s) | 9 | Unidentified site | 99 | Not stated/inadequately described |
| |
- | Non-instrumented bleeding location | Number
[2]
| 1 | Gastrointestinal site | 2 | Genitourinary site | 3 | Intracranial site | 4 | Pulmonary site | 5 | Pericardial site | 6 | Other site(s) | 7 | Unidentified site | 99 | Not stated/inadequately described |
| |
- | Lifestyle counselling type | Number
[1]
| 1 | Diet | 2 | Physical activity | 3 | Smoking cessation | 4 | Weight management | 9 | Not stated/inadequately described |
| |
- | Other/Underlying cause of acute coronary syndrome | Number
[9]
| 1 | Anaemia | 2 | Severe valvular disease | 3 | Thyrotoxicosis | 4 | Fever | 5 | Hypoxaemia | 6 | Trauma | 7 | Surgery | 88 | Other | 99 | Not stated/inadequately described |
| |
- | Acute coronary syndrome procedure type | String
[2]
| 01 | Coronary artery bypass graft (CABG) | 05 | Reperfusion: fibrinolytic therapy | 06 | Reperfusion: primary percutaneous coronary intervention (PCI) | 07 | Reperfusion: rescue percutaneous coronary intervention (PCI) | 08 | Vascular reconstruction, bypass surgery, or percutaneous intervention to the extremities or for aortic aneurysm | 09 | Amputation for arterial vascular insufficiency | 10 | Diagnostic cardiac catheterisation/angiography | 11 | Blood transfusion | 12 | Insertion of pacemaker | 13 | Implantable cardiac defibrillator | 14 | Intra-aortic balloon pump (IABP) | 15 | Non-invasive ventilation (CPAP) | 16 | Invasive ventilation | 17 | Defibrillation | 18 | Revascularisation: percutaneous coronary intervention (PCI) | 19 | Pulmonary artery (Swan Ganz) catheter | 88 | Other | 99 | Not stated/inadequately described |
| |
- | Acute coronary syndrome related medical history | Number
[2]
| 11 | Angina (excluding unstable angina): prior existing | 12 | Angina (excluding unstable angina): new onset | 13 | Unstable angina | 21 | Chronic lung disease | 31 | Heart failure | 41 | Hypertension | 51 | Ischaemic: non-haemorrhagic cerebral infarction | 52 | Haemorrhagic: intracerebral haemorrhage | 61 | Peripheral artery disease | 62 | Aortic aneurysm | 63 | Renal artery stenosis | 71 | Sleep apnoea | 81 | Previous myocardial infarction | 91 | Atrial fibrillation | 92 | Other dysrhythmia or conductive disorder | 93 | Left ventricular hypertrophy | 99 | Not stated/inadequately described |
| |
- | Acute coronary syndrome stratum | Number
[1]
| 1 | ST-segment-elevation (myocardial infarction) | 2 | Non-ST-segment-elevation ACS with high-risk features | 3 | Non-ST-segment-elevation ACS with intermediate-risk features | 4 | Non-ST-segment-elevation ACS with low-risk features | 9 | Not stated/inadequately described |
| |
- | Date of onset of acute coronary syndrome symptoms | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | |
- | Time of onset of acute coronary syndrome symptoms | Date/Time
[4]
| hhmm
A valid time measured as hours and minutes using a 24 hour clock. | |
- | Number of episodes of angina in last 24 hours | Number
[3]
| 999 | Not stated/inadequately described |
| |
- | Angina status | Number
[1]
| 1 | No angina with ordinary physical activity | 2 | Slight limitation of ordinary physical activity | 3 | Marked limitation of ordinary physical activity | 4 | Inability for any physical activity without anginal symptoms | 9 | Not stated/inadequately described |
| DSS specific information: This is the status of angina that a person experiences following discharge from hospital. |
- | Bleeding episode using TIMI criteria (status) | Number
[1]
| 1 | Major | 2 | Minor | 3 | Non TIMI bleeding | 9 | Not stated/inadequately described |
| |
- | C-reactive protein level (measured) | Number
[4]
| 999.9 | Not stated/inadequately described |
| DSS specific information: The C-reactive protein (CRP) level should be measured as early as possible following presentation to the hospital. |
- | Date C-reactive protein level measured | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | DSS specific information: The date of C-reactive protein (CRP) measurement recorded should be after or the same as the date of onset of ACS symptoms. |
- | Time C-reactive protein level measured | Date/Time
[4]
| hhmm
A valid time measured as hours and minutes using a 24 hour clock. | |
- | Chest pain pattern category | Number
[1]
| 1 | Atypical chest pain | 2 | Stable chest pain pattern | 3 | Unstable chest pain pattern: rest &/or prolonged | 4 | Unstable chest pain pattern: new & severe | 5 | Unstable chest pain pattern: accelerated & severe | 9 | Not stated/inadequately described |
| DSS specific information: The Canadian Cardiovascular Society classes of angina can be used to support categorisation of chest pain patterns. Canadian Cardiovascular Society (CCS) classes of angina (Campeau L. Grading of angina pectoris. Circulation 1976; 54:522.) - Ordinary physical activity (for example, walking or climbing stairs) does not cause angina; angina occurs with strenuous or rapid or prolonged exertion at work or recreation.
- Slight limitation of ordinary activity (for example, angina occurs walking or stair climbing after meals, in cold, in wind, under emotional stress, or only during the few hours after awakening; walking more than 2 blocks on the level or climbing more than 1 flight of ordinary stairs at a normal pace; and in normal conditions).
- Marked limitation of ordinary activity (for example, angina occurs with walking 1 or 2 blocks on the level or climbing 1 flight of stairs in normal conditions and at a normal pace).
- Inability to perform any physical activity without discomfort; angina syndrome may be present at rest.
|
- | Cholesterol—total (measured) | Number
[3]
| 99.9 | Not stated/inadequately described. |
| |
- | Clinical evidence of acute coronary syndrome related medical history | Boolean
[1]
| 1 | Yes | 2 | No | 9 | Not stated/inadequately described |
| |
- | Clinical procedure timing (status) | Number
[1]
| 1 | Procedure performed prior to this hospital presentation | 2 | Procedure performed during this hospital presentation |
| |
- | Country of birth | Number
[4]
| NNNN
The Standard Australian Classification of Countries (SACC 2011) code set representing a country. | |
- | Creatine kinase level (U/L) | Number
[4]
| 9998 | Not measured | 9999 | Not stated/inadequately described |
| DSS specific information: The measured CK isoenzyme levels and the timing of these measurements are important to the diagnosis of myocardial infarction. |
- | Date creatine kinase MB isoenzyme measured | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | DSS specific information: The measured CK isoenzyme levels and the timing of these measurements are important to the diagnosis of myocardial infarction. |
- | Time creatine kinase MB isoenzyme measured | Date/Time
[4]
| hhmm
A valid time measured as hours and minutes using a 24 hour clock. | DSS specific information: The measured CK isoenzyme levels and the timing of these measurements are important to the diagnosis of myocardial infarction. |
- | Creatine kinase MB isoenzyme level (micrograms per litre) | Number
[4]
| 9998 | Not measured | 9999 | Not stated/inadequately described |
| |
- | Creatine kinase MB isoenzyme level (units per litre) | Number
[4]
| 9998 | Not measured | 9999 | Not stated/inadequately described |
| DSS specific information: For Acute coronary syndrome (ACS) reporting, can be used to determine diagnostic strata. |
- | Date creatinine serum level measured | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | DSS specific information: In settings where the monitoring of a person's health is ongoing and where a measure can change over time (such as general practice), the Service contact—service contact date, DDMMYYYY should be recorded. Record absolute result of the most recent serum creatinine measurement in the last 12 months to the nearest µmol/L (micromoles per litre). |
- | Creatinine serum level (measured) | String
[4]
| NN[NN] Number of micromoles per litre (µmol/L) | |
- | Date of birth | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | |
- | Date of death | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | DSS specific information: If a date of death is recorded, the cause of death must also be recorded. These data are recorded regardless of the cause of death. |
- | Diabetes status | String
[2]
| 01 | Type 1 diabetes | 02 | Type 2 diabetes | 03 | Gestational diabetes mellitus (GDM) | 04 | Other (secondary diabetes) | 05 | Previous gestational diabetes mellitus (GDM) | 06 | Impaired fasting glucose (IFG) | 07 | Impaired glucose tolerance (IGT) | 08 | Not diagnosed with diabetes | 09 | Not assessed | 99 | Not stated/inadequately described |
| |
- | Diabetes therapy type | String
[2]
| 01 | Diet and exercise only | 02 | Oral hypoglycaemic - sulphonylurea only | 03 | Oral hypoglycaemic - biguanide (eg metformin) only | 04 | Oral hypoglycaemic - alpha-glucosidase inhibitor only | 05 | Oral hypoglycaemic - thiazolidinedione only | 06 | Oral hypoglycaemic - meglitinide only | 07 | Oral hypoglycaemic - combination (eg biguanide & sulphonylurea) | 08 | Oral hypoglycaemic - other | 09 | Insulin only | 10 | Insulin plus oral hypoglycaemic | 98 | Nil - not currently receiving diabetes treatment | 99 | Not stated/inadequately described |
| |
- | Date of diagnostic cardiac catheterisation | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | |
- | Time of diagnostic cardiac catheterisation | Date/Time
[4]
| hhmm
A valid time measured as hours and minutes using a 24 hour clock. | |
- | Dyslipidaemia treatment indicator | Boolean
[1]
| 1 | Yes | 2 | No | 9 | Not stated/inadequately described |
| |
- | Glycosylated haemoglobin level (measured) | Number
[3]
| 99.9 | Not stated/inadequately described |
| |
- | Height (measured) | Number
[4]
| | |
- | Cholesterol—HDL (measured) | Number
[3]
| 9.99 | Not measured/inadequately described |
| |
- | Hypertension - treatment | Boolean
[1]
| 1 | Yes | 2 | No | 9 | Not stated/inadequately described |
| |
- | Date of implantable cardiac defibrillator procedure | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | |
- | Time of implantable cardiac defibrillator procedure | Date/Time
[4]
| hhmm
A valid time measured as hours and minutes using a 24 hour clock. | |
- | Indigenous status | Number
[1]
| 1 | Aboriginal but not Torres Strait Islander origin | 2 | Torres Strait Islander but not Aboriginal origin | 3 | Both Aboriginal and Torres Strait Islander origin | 4 | Neither Aboriginal nor Torres Strait Islander origin | 9 | Not stated/inadequately described |
| |
- | Date of intra-aortic balloon pump procedure | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | |
- | Time of intra-aortic balloon pump procedure | Date/Time
[4]
| hhmm
A valid time measured as hours and minutes using a 24 hour clock. | |
- | Killip classification code | Number
[1]
| 1 | Class 1 | 2 | Class 2 | 3 | Class 3 | 4 | Class 4 | 8 | Other | 9 | Not stated/inadequately described |
| DSS specific information: For Acute Coronary Syndrome (ACS) reporting, this data element describes the objective evidence of haemodynamic compromise by clinical examination at the time of presentation. Rales or crepitations represent evidence of pulmonary interstitial oedema on lung auscultation and an S3 is an audible extra heart sound by cardiac auscultation. |
- | Cholesterol—LDL (calculated) | Number
[3]
| 99.9 | Not stated/inadequately described |
| |
- | Date of most recent stroke | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | DSS specific information: Record the date of the most recent stroke that preceded presentation to the hospital. |
- | Date of non-invasive ventilation administration | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | |
- | Time of non-invasive ventilation administration | Date/Time
[4]
| hhmm
A valid time measured as hours and minutes using a 24 hour clock. | |
- | Date of pacemaker insertion | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | |
- | Time of pacemaker insertion | Date/Time
[4]
| hhmm
A valid time measured as hours and minutes using a 24 hour clock. | |
- | Person identifier | String
[20]
| XXXXXX[X(14)]
A logical combination of valid alphanumeric characters that identify an entity. | |
- | Premature cardiovascular disease family history (status) | Number
[1]
| 1 | Yes | 2 | No | 3 | Family history status not known | 9 | Not recorded |
| |
- | Reason for readmission—acute coronary syndrome | Number
[2]
| 1 | ST-segment-elevation myocardial infarction | 2 | non-ST-segment-elevation ACS with high-risk features | 3 | non-ST-segment-elevation ACS with intermediate-risk features | 4 | non-ST-segment-elevation ACS with low-risk features | 5 | Percutaneous coronary intervention (PCI) | 6 | Coronary artery bypass graft (CABG) | 7 | Heart Failure (without MI) | 8 | Arrhythmia (without MI) | 99 | Not stated/inadequately described |
| |
- | Sex | Number
[1]
| 1 | Male | 2 | Female | 3 | Intersex or indeterminate | 9 | Not stated/inadequately described |
| |
- | Tobacco smoking status | Number
[1]
| 1 | Daily smoker | 2 | Weekly smoker | 3 | Irregular smoker | 4 | Ex-smoker | 5 | Never smoked |
| DSS specific information: Smoker type is used to define sub-populations of adults (age 18+ years) based on their smoking behaviour. Smoking has long been known as a health risk factor. Population studies indicate a relationship between smoking and increased mortality/morbidity. This metadata item can be used to estimate smoking prevalence. Other uses are: - To evaluate health promotion and disease prevention programs (assessment of interventions)
- To monitor health risk factors and progress towards National Health Goals and Targets
|
- | Triglyceride level (measured) | Number
[3]
| 99.9 | Not stated/inadequately described. |
| |
- | Troponin assay type | Number
[1]
| 1 | Cardiac troponin T (cTnT) | 2 | Cardiac troponin I (cTnI) | 9 | Not stated/inadequately described |
| DSS specific information: For Acute coronary syndrome (ACS) reporting, record the type of troponin assay (I or T) used to assess troponin levels during this presentation. |
- | Troponin level (measured) | Number
[4]
| 88.88 | Not measured | 99.99 | Not stated/inadequately described |
| DSS specific information: For Acute coronary syndrome (ACS ) reporting, can be used to determine diagnostic strata. |
- | Date troponin measured | Date/Time
[8]
| DDMMYYYY
The day of a particular month and year. | |
- | Time troponin measured | Date/Time
[4]
| hhmm
A valid time measured as hours and minutes using a 24 hour clock. | |
- | Underlying cause of death | String
[7]
| ANN-ANN
The ICD-10 code set representing the disease or injury which initiated the train of morbid events leading directly to death or the circumstances of the accident or violence which produced the fatal injury (WHO 2004). | Conditional obligation: If a date of death is recorded, the cause of death must also be recorded. These data are recorded regardless of the cause of death. |
- | Total blood units transfused | Number
[4]
| 9999 | Not stated/inadequately described |
| Conditional obligation: Record the total number of blood units (either whole blood or packed red blood cells) that the person has received following a haemorrhagic event. |
- | Vascular history | String
[2]
| 01 | Myocardial infarction | 02 | Unstable angina pectoris | 03 | Angina | 04 | Heart failure | 05 | Atrial fibrillation | 06 | Other dysrhythmia or conductive disorder | 07 | Rheumatic heart disease | 08 | Non-rheumatic valvular heart disease | 09 | Left ventricular hypertrophy | 10 | Stroke | 11 | Transient ischaemic attack | 12 | Hypertension | 13 | Peripheral vascular disease (includes abdominal aortic aneurism) | 14 | Deep vein thrombosis | 15 | Other atherosclerotic disease | 16 | Carotid stenosis | 17 | Vascular renal disease | 18 | Vascular retinopathy (hypertensive) | 19 | Vascular retinopathy (diabetic) | 97 | Other vascular | 98 | No vascular history | 99 | Unknown/not stated /not specified |
| |
- | Weight in kilograms (measured) | Number
[4]
| | |