ID
44783
Description
The ACTION Registry®–GWTG™ is a risk-adjusted, outcomes-based quality improvement program that focuses exclusively on high-risk STEMI/NSTEMI patients. It helps hospitals apply ACC/AHA clinical guideline recommendations in their facilities and provides invaluable tools to measure care and achieve quality improvement goals. (http://cvquality.acc.org/NCDR-Home/Registries/Hospital-Registries.aspx)
Link
http://cvquality.acc.org/NCDR-Home/Registries/Hospital-Registries.aspx
Keywords
Versions (5)
- 4/15/15 4/15/15 -
- 11/25/15 11/25/15 -
- 4/14/21 4/14/21 - Ahmed Rafee, MD
- 9/20/21 9/20/21 -
- 11/18/21 11/18/21 -
Copyright Holder
American College of Cardiology Foundation
Uploaded on
November 18, 2021
DOI
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License
Creative Commons BY 4.0
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ACTION Registry®-GWTG™
ACTION Registry
- StudyEvent: ODM
Description
Admission
Alias
- UMLS CUI [1]
- C0030673
Description
Indicate the means of transportation to the facility where the patient first received treatment
Data type
text
Alias
- UMLS CUI [1]
- C3258270
Description
Indicate the date when the patient was first evaluated by emergency medical services (EMS) prior to arrival at your facility. Indicate the date of first medical contact only for patients who were transported by ambulance or air. This is NOT the date of arrival to your facility.
Data type
datetime
Alias
- UMLS CUI-1
- C1320531
Description
Indicate the date and time the responding unit was notified by dispatch.
Data type
datetime
Alias
- UMLS CUI [1,1]
- C3261085
- UMLS CUI [1,2]
- C1264639
Description
Indicate the date when the patient was first evaluated by a healthcare professional prior to arrival at your facility. This is NOT the time of arrival to your facility. Indicate the date of first medical contact with a medical professional, prior to arrival at your hospital.
Data type
datetime
Alias
- UMLS CUI [1,1]
- C1518384
- UMLS CUI [1,2]
- C1279901
- UMLS CUI [1,3]
- C1521801
- UMLS CUI [1,4]
- C0011008
Description
Indicate the date and time the responding unit left the scene with a patient (started moving).
Data type
datetime
Alias
- UMLS CUI [1,1]
- C3261085
- UMLS CUI [1,2]
- C1264639
Description
Indicate the emergency medical services agency number.
Data type
integer
Alias
- UMLS CUI [1,1]
- C4037969
- UMLS CUI [1,2]
- C1301943
- UMLS CUI [1,3]
- C0805701
Description
Indicate the emergency medical services run number.
Data type
integer
Alias
- UMLS CUI [1,1]
- C4037969
- UMLS CUI [1,2]
- C2348184
Description
Indicate the date and time the Cath Lab was activated.
Data type
datetime
Alias
- UMLS CUI [1,1]
- C0018795
- UMLS CUI [1,2]
- C1879547
- UMLS CUI [1,3]
- C0011008
Description
Transferred from Outside Facility
Data type
boolean
Alias
- UMLS CUI-1
- C1546432
Description
Means of Transfer from outside facility
Data type
text
Alias
- UMLS CUI [1]
- C0449375
Description
Indicate the date and time the patient arrived at the outside facility.
Data type
datetime
Alias
- UMLS CUI-1
- C1320532
Description
Transfer from Outside Facility Date/Time
Data type
datetime
Alias
- UMLS CUI [1,1]
- C1546432
- UMLS CUI [1,2]
- C0011008
Description
Name of Transferring Facility/AHA Number
Data type
text
Alias
- UMLS CUI [1,1]
- C0018704
- UMLS CUI [1,2]
- C0600091
Description
Indicate the date and time the patient arrived at your facility.
Data type
datetime
Alias
- UMLS CUI-1
- C1320532
Description
Indicate the date the patient was admitted as an inpatient to your facility for the current episode of care.
Data type
date
Alias
- UMLS CUI-1
- C1302393
Description
Indicate the location the patient was first evaluated at your facility.
Data type
text
Alias
- UMLS CUI [1]
- C0450429
Description
Indicate the date the patient was moved out of the emergency department, either to another location within your facility or to another acute care center.
Data type
datetime
Alias
- UMLS CUI [1,1]
- C3495034
- UMLS CUI [1,2]
- C0011008
Description
Insurance Payors
Data type
text
Alias
- UMLS CUI [1]
- C0021672
Description
Indicate the admitting primary provider's last name.
Data type
text
Alias
- UMLS CUI-1
- C0807500
Description
Indicate the primary providers National Provider Identifier. NPIs, assigned by the Center for Medicare and Medicaid Services (CMS), are used to uniquely identify physicians for Medicare billing purposes.
Data type
text
Alias
- UMLS CUI [1,1]
- C1549728
- UMLS CUI [1,2]
- C1547428
Description
Indicate the patient's Health Insurance Claim (HIC) number.
Data type
integer
Alias
- UMLS CUI [1,1]
- C0021682
- UMLS CUI [1,2]
- C0237753
Description
Cardiac status on first medical contact
Alias
- UMLS CUI [1]
- C1999091
Description
Indicate the date the patient first noted ischemic symptoms lasting greater than or equal to 10 minutes. If the patient had intermittent ischemic symptoms, record the date and time of the most recent ischemic symptoms prior to hospital presentation. Symptoms may include jaw pain, arm pain, shortness of breath, nausea, vomiting, fatigue/malaise, or other equivalent discomfort suggestive of a myocardial infarction. In the event of stuttering symptoms, Acute Coronary Syndrome (ACS) symptom onset is the time at which symptoms became constant in quality or intensity.
Data type
datetime
Alias
- UMLS CUI-1
- C1320528
Description
Symptom Onset Time Estimated
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1320528
- UMLS CUI [1,2]
- C0750572
Description
Indicate if the symptom onset time was not available.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1320528
- UMLS CUI [1,2]
- C0439673
Description
Indicate when the first 12-lead electrocardiogram (ECG) was obtained.
Data type
text
Alias
- UMLS CUI [1]
- C2826640
Description
Indicate the date and time of the first 12-lead electrocardiogram (ECG).
Data type
datetime
Alias
- UMLS CUI [1]
- C2826846
Description
Indicate if there is a non system reason for the delay in the first ECG.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1623258
- UMLS CUI [1,2]
- C0205421
- UMLS CUI [1,3]
- C0566251
Description
Indicate if the ECG findings demonstrated a STEMI or STEMI equivalent. STEMI or STEMI equivalent must be noted prior to any procedures and not more than 24 hours after arrival at first facility. Arrival at first facility refers to either the time of arrival at your facility or the time of arrival at the transferring facility.
Data type
boolean
Alias
- UMLS CUI-1
- C3538872
Description
Indicate if the ECG findings demonstrated either new or presumed new ST-segment elevation, new left bundle branch block, or isolated posterior myocardial infarction prior to any procedures and not more than 24 hours after arrival at first facility.
Data type
text
Alias
- UMLS CUI-1
- C0438154
Description
STEMI or STEMI Equivalent First Noted
Data type
text
Alias
- UMLS CUI [1,1]
- C3538872
- UMLS CUI [1,2]
- C2348792
Description
Subsequent ECG with STEMI or STEMI Equivalent Date/Time
Data type
datetime
Alias
- UMLS CUI [1,1]
- C3538872
- UMLS CUI [1,2]
- C0011008
Description
Indicate if other findings from the electrocardiogram were demonstrated within 24 hours of arrival at first facility. If more than one present, code the findings on which treatment was based.
Data type
text
Alias
- UMLS CUI [1,1]
- C0438154
- UMLS CUI [1,2]
- C0205394
Description
Indicate if there is physician documentation or report of heart failure on first medical contact.
Data type
boolean
Alias
- UMLS CUI-1
- C0018801
Description
Indicate if the patient was in a state of cardiogenic shock on first medical contact.
Data type
boolean
Alias
- UMLS CUI-1
- C0036980
Description
Indicate the first measurement or earliest record of heart rate (in beats per minute).
Data type
integer
Measurement units
- bpm
Alias
- UMLS CUI-1
- C0018810
Description
Systolic BP
Data type
integer
Measurement units
- mmHg
Alias
- UMLS CUI-1
- C0871470
Description
Indicate if the patient was in cardiac arrest when first evaluated by EMS or ED personnel.
Data type
boolean
Alias
- UMLS CUI-1
- C0018790
Description
Indicate if the patient's cardiac arrest was prior to arrival at the outside facility and/or occurred during transfer from the outside facility to this facility.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0018790
- UMLS CUI [1,2]
- C3272300
Description
Indicate if the patient's cardiac arrest occurred during the hospitalization at the first facility.
Data type
boolean
Alias
- UMLS CUI-1
- C2936490
Description
History and Risk Factors
Alias
- UMLS CUI-1
- C0035648
Description
Indicate the patient's height in centimeters.
Data type
integer
Measurement units
- cm
Alias
- UMLS CUI-1
- C0005890
Description
Indicate the patient's weight in kilograms.
Data type
float
Measurement units
- kg
Alias
- UMLS CUI-1
- C0005910
Description
Current/Recent Smoker (w/in 1 year)
Data type
boolean
Alias
- UMLS CUI [1]
- C0543414
Description
Indicate if the patient has been diagnosed previously with hypertension.
Data type
boolean
Alias
- UMLS CUI-1
- C0455527
Description
Indicate if the patient has a history of dyslipidemia diagnosed and/or treated by a physician.
Data type
boolean
Alias
- UMLS CUI-1
- C0242339
Description
Indicate if the patient is currently undergoing either hemodialysis or peritoneal dialysis on an ongoing basis as a result of renal failure.
Data type
boolean
Alias
- UMLS CUI [1]
- C0011946
Description
Indicate if the patient has a history of diabetes mellitus, regardless of duration of disease or need for antidiabetic agents.
Data type
boolean
Alias
- UMLS CUI-1
- C0011849
Description
Indicate the therapy method the patient presented with. Choose the most aggressive therapy.
Data type
text
Alias
- UMLS CUI [1]
- C3274787
Description
Indicate if the patient has had at least one documented previous myocardial infarction.
Data type
boolean
Alias
- UMLS CUI-1
- C1275835
Description
Indicate if the patient has a history of cancer.
Data type
boolean
Alias
- UMLS CUI-1
- C0006826
Description
Indicate the type of cancer if the patient has a history of cancer.
Data type
text
Alias
- UMLS CUI [1]
- C0872066
Description
Indicate if there is a previous history of heart failure.
Data type
boolean
Alias
- UMLS CUI-1
- C0455531
Description
Indicate if the patient had a previous percutaneous coronary intervention (PCI) of any type (balloon angioplasty, stent or other).
Data type
boolean
Alias
- UMLS CUI-1
- C1320647
Description
Most Recent PCI Date
Data type
date
Alias
- UMLS CUI [1,1]
- C1532338
- UMLS CUI [1,2]
- C1264639
Description
Indicate whether the patient had a coronary artery bypass graft (CABG).
Data type
boolean
Alias
- UMLS CUI-1
- C1275842
Description
If the patient had a previous coronary artery bypass graft (CABG), indicate the date.
Data type
date
Alias
- UMLS CUI [1,1]
- C0010055
- UMLS CUI [1,2]
- C0011008
Description
Atrial Fibrillation or Flutter
Data type
boolean
Alias
- UMLS CUI [1]
- C0004238
- UMLS CUI [2]
- C0004239
Description
Indicate if the patient has a history of cerebrovascular disease.
Data type
boolean
Alias
- UMLS CUI-1
- C0007820
Description
Indicate if the patient has had a stroke.
Data type
boolean
Alias
- UMLS CUI-1
- C0559159
Description
Indicate if the patient has a history of TIAs.
Data type
boolean
Alias
- UMLS CUI [1]
- C0007787
Description
Indicate the level of assistance the patient required with ambulation.
Data type
text
Alias
- UMLS CUI [1]
- C0080331
Description
Indicate the patients level of cognition.
Data type
text
Alias
- UMLS CUI [1]
- C0009240
Description
Indicate the level of assistance the patient required with acitivities of daily living.
Data type
text
Alias
- UMLS CUI [1]
- C0001288
Description
Medications
Alias
- UMLS CUI [1]
- C0013227
Description
Aspirin
Data type
text
Alias
- UMLS CUI [1]
- C0004057
Description
Aspirin contraindicated
Data type
boolean
Alias
- UMLS CUI-1
- C0729798
Description
Clopidogrel
Data type
text
Alias
- UMLS CUI-1
- C0070166
Description
Clopidogrel dose
Data type
float
Measurement units
- mg
Alias
- UMLS CUI [1,1]
- C0070166
- UMLS CUI [1,2]
- C0178602
Description
Clopidogrel contraindicated
Data type
boolean
Alias
- UMLS CUI-1
- C1319916
Description
Ticlopidine
Data type
text
Alias
- UMLS CUI [1]
- C0040207
Description
Ticlodipine dose
Data type
float
Measurement units
- mg
Alias
- UMLS CUI [1,1]
- C0040207
- UMLS CUI [1,2]
- C0178602
Description
Ticlopidine contraindicated
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0040207
- UMLS CUI [1,2]
- C0522473
Description
Prasugrel
Data type
text
Alias
- UMLS CUI-1
- C1620287
Description
Prasugrel Dose
Data type
float
Measurement units
- mg
Alias
- UMLS CUI [1,1]
- C1620287
- UMLS CUI [1,2]
- C0178602
Description
Prasugrel contraindicated
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1620287
- UMLS CUI [1,2]
- C0522473
Description
Ticagrelor
Data type
text
Alias
- UMLS CUI-1
- C1999375
Description
Ticagrelor Contraindicated
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1999375
- UMLS CUI [1,2]
- C0522473
Description
Warfarin
Data type
text
Alias
- UMLS CUI-1
- C0043031
Description
Warfarin contraindicated
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0043031
- UMLS CUI [1,2]
- C0522473
Description
Dabigatran
Data type
text
Alias
- UMLS CUI-1
- C2348066
Description
Dabigatran contraindicated
Data type
boolean
Alias
- UMLS CUI-1
- C2348066
- UMLS CUI-2
- C0522473
Description
Rivaroxaban
Data type
text
Alias
- UMLS CUI-1
- C1739768
Description
Rivaroxaban contraindicated
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1739768
- UMLS CUI [1,2]
- C0522473
Description
Apixiban
Data type
text
Alias
- UMLS CUI [1]
- C1831808
Description
Apixiban Contraindicated
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1831808
- UMLS CUI [1,2]
- C0522473
Description
Beta Blocker
Data type
text
Alias
- UMLS CUI-1
- C0304516
Description
Beta Blocker Contraindicated
Data type
boolean
Alias
- UMLS CUI-1
- C1278474
Description
ACE Inhibitor
Data type
text
Alias
- UMLS CUI-1
- C0003015
Description
ACE inhibitor contraindicated
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0003015
- UMLS CUI [1,2]
- C0522473
Description
Angiotensin Receptor Blocker
Data type
text
Alias
- UMLS CUI-1
- C0521942
Description
Angiotensin Receptor Blocker contraindiacted
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0521942
- UMLS CUI [1,2]
- C0522473
Description
Aldosterone Blocking Agent
Data type
text
Alias
- UMLS CUI-1
- C0002007
Description
Aldosterone blocking agent contraindicated
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0002007
- UMLS CUI [1,2]
- C0522473
Description
Statin
Data type
text
Alias
- UMLS CUI-1
- C0360714
Description
Statin dose
Data type
text
Alias
- UMLS CUI [1,1]
- C0360714
- UMLS CUI [1,2]
- C0178602
Description
Statin contraindicated
Data type
boolean
Alias
- UMLS CUI-1
- C1277178
Description
Non-Statin Lipid-Lowering Agent
Data type
text
Alias
- UMLS CUI [1]
- C0086440
Description
Indicate if a GP IIb/IIIa inhibitor was administered.
Data type
text
Alias
- UMLS CUI [1]
- C3640054
Description
Indicate the dose of GP IIb/IIIa administered.
Data type
text
Alias
- UMLS CUI [1,1]
- C3640054
- UMLS CUI [1,2]
- C0178602
Description
GP IIb/IIIa inhibitor start date/time
Data type
datetime
Alias
- UMLS CUI [1,1]
- C1301880
- UMLS CUI [1,2]
- C3640054
Description
Indicate if an anticoagulant was administered.
Data type
boolean
Alias
- UMLS CUI-1
- C0003280
Description
Anticoagulant contraindicated
Data type
boolean
Alias
- UMLS CUI-1
- C1531588
Description
Indicate if unfractionated heparin was administered.
Data type
boolean
Alias
- UMLS CUI-1
- C2825026
Description
Indicate if an initial bolus of unfractionated heparin was administered.
Data type
integer
Measurement units
- units
Alias
- UMLS CUI [1,1]
- C2825026
- UMLS CUI [1,2]
- C0178602
Description
Unfractionated Heparin Start Date/Time
Data type
datetime
Alias
- UMLS CUI [1,1]
- C1301880
- UMLS CUI [1,2]
- C2825026
Description
Enoxaparin (LMWH)
Data type
boolean
Alias
- UMLS CUI-1
- C3536766
Description
LMWH Start Date/Time
Data type
datetime
Alias
- UMLS CUI [1,1]
- C3536766
- UMLS CUI [1,2]
- C1301880
Description
LMWH injection frequency
Data type
text
Alias
- UMLS CUI [1,1]
- C3536766
- UMLS CUI [1,2]
- C3476109
Description
LMWH dose
Data type
float
Measurement units
- mg
Alias
- UMLS CUI [1,1]
- C3536766
- UMLS CUI [1,2]
- C0178602
Description
Indicate if bivalirudin (Angiomax) was administered.
Data type
boolean
Alias
- UMLS CUI-1
- C0168273
Description
Bivalirudin Start Date/Time
Data type
datetime
Alias
- UMLS CUI [1,1]
- C1301880
- UMLS CUI [1,2]
- C0168273
Description
Indicate if an anticoagulant was given that is not listed.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0003280
- UMLS CUI [1,2]
- C1518896
- UMLS CUI [1,3]
- C0205394
Description
Procedures and Tests
Alias
- UMLS CUI [1,1]
- C0392366
- UMLS CUI [1,2]
- C0184661
Description
Indicate if the patient underwent exercise or pharmacologic stress testing with or without echocardiographic or nuclear imaging.
Data type
boolean
Alias
- UMLS CUI-1
- C3272313
Description
Indicate the date of exercise or pharmacologic stress testing with or without echocardiographic or nuclear imaging.
Data type
datetime
Alias
- UMLS CUI [1,1]
- C3272313
- UMLS CUI [1,2]
- C0011008
Description
Code the best estimate of the current left ventricular ejection fraction closest to discharge.
Data type
float
Measurement units
- %
Alias
- UMLS CUI-1
- C0428772
Description
Indicate whether the left ventricular ejection fraction was assessed.
Data type
boolean
Alias
- UMLS CUI-1
- C3248481
Description
Indicate if the LVEF assessment is planned for after discharge.
Data type
boolean
Alias
- UMLS CUI-1
- C3248276
Description
Indicate if the patient had a diagnostic coronary angiography procedure.
Data type
boolean
Alias
- UMLS CUI-1
- C0085532
Description
Indicate the date the patient had diagnostic coronary angiography
Data type
date
Alias
- UMLS CUI [1,1]
- C0085532
- UMLS CUI [1,2]
- C0011008
Description
Indicate the number of diseased vessels found during the diagnostic catheterization.
Data type
text
Alias
- UMLS CUI [1]
- C3275120
Description
Indicate whether or not the left main coronary artery is 50 percent or more stenotic.
Data type
boolean
Alias
- UMLS CUI-1
- C2825221
Description
Indicate if a graft is present when the left main stenosis is greater than or equal to 50 percent.
Data type
text
Alias
- UMLS CUI [1]
- C2062905
Description
Indicate if the left anterior descending coronary artery is greater than or equal to 70 percent stenotic.
Data type
boolean
Alias
- UMLS CUI-1
- C2825222
Description
Indicate if a graft is present when the proximal LAD is greater than or equal to 70 percent stenotic.
Data type
text
Alias
- UMLS CUI [1]
- C2825222
Description
Indicate if a catheterization was not performed because it was contraindicated.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1532338
- UMLS CUI [1,2]
- C0522473
Description
Indicate if the patient had a percutaneous coronary intervention (PCI).
Data type
boolean
Alias
- UMLS CUI-1
- C1532338
Description
Indicate the date and time the patient arrived to the cath lab where the PCI was being performed, as documented in the medical record.
Data type
datetime
Alias
- UMLS CUI-1
- C3838354
Description
Indicate the date and time the first device was activated regardless of type of device used.
Data type
datetime
Alias
- UMLS CUI [1,1]
- C0025080
- UMLS CUI [1,2]
- C1879547
- UMLS CUI [1,3]
- C0011008
Description
Indicate the primary location of percutaneous entry. Code the site used to perform the majority of the procedure if more than one site was used.
Data type
text
Alias
- UMLS CUI-1
- C3272298
Description
Indicate if a stent or stents were placed in the affected coronary artery.
Data type
boolean
Alias
- UMLS CUI-1
- C3272316
Description
Stent Type(s)
Data type
text
Alias
- UMLS CUI [1,1]
- C0687568
- UMLS CUI [1,2]
- C0332307
Description
Indicate the primary reason PCI was performed or attempted.
Data type
text
Alias
- UMLS CUI [1,1]
- C1532338
- UMLS CUI [1,2]
- C0392360
Description
Indicate if there is documentation of a non-system reason for a delay in doing the first percutaneous coronary intervention (PCI) after hospital arrival by a physician/advanced practice nurse/physician assistant (physician/APN/PA).
Data type
text
Alias
- UMLS CUI [1]
- C3640267
Description
Indicate if the patient had a CABG (coronary artery bypass graft surgery).
Data type
boolean
Alias
- UMLS CUI-1
- C0010055
Description
Indicate the date of the coronary artery bypass graft (CABG) surgery.
Data type
datetime
Alias
- UMLS CUI [1,1]
- C0010055
- UMLS CUI [1,2]
- C0011008
Description
Indicate if an in-hospital hypothermia protocol was initiated.
Data type
boolean
Alias
- UMLS CUI-1
- C0150255
Description
Indicate the location where the hypothermia protocol was initiated.
Data type
text
Alias
- UMLS CUI [1,1]
- C0150255
- UMLS CUI [1,2]
- C0450429
Description
Reperfusion Strategy
Alias
- UMLS CUI [1]
- C0035124
Description
Indicate if the STEMI patient is a reperfusion candidate for primary PCI or Thrombolytic therapy.
Data type
boolean
Alias
- UMLS CUI-1
- C0035124
Description
Indicate the one primary reason, documented in the medical record, that reperfusion therapy (thrombolytic therapy or primary PCI) was not indicated.
Data type
text
Alias
- UMLS CUI [1,1]
- C1549995
- UMLS CUI [1,2]
- C0035124
- UMLS CUI [1,3]
- C0040809
Description
Indicate if the patient received primary PCI as an urgent treatment for STEMI.
Data type
boolean
Alias
- UMLS CUI-1
- C3275089
Description
Indicate if the patient received thrombolytic therapy as an urgent treatment for STEMI.
Data type
boolean
Alias
- UMLS CUI-1
- C0040044
Description
Indicate the strength of dose of the thrombolytic.
Data type
text
Alias
- UMLS CUI [1,1]
- C0178602
- UMLS CUI [1,2]
- C0040044
Description
Indicate the type of thrombolytic first administered.
Data type
text
Alias
- UMLS CUI [1]
- C0040044
Description
Thrombolytic Therapy Start Date/Time
Data type
datetime
Alias
- UMLS CUI [1,1]
- C0040044
- UMLS CUI [1,2]
- C1301880
Description
Indicate if there is documentation of a non-system reason for delay in initiating thrombolytic therapy greater than 30 minutes from the time of first facility arrival (including an ambulance capable of administering thrombolytic therapy).
Data type
boolean
Alias
- UMLS CUI [1]
- C3640267
Description
Indicate if the patient was Lytic ineligible and required prolonged transfer time for primary PCI.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0040044
- UMLS CUI [1,2]
- C1301624
- UMLS CUI [2,1]
- C3275089
- UMLS CUI [2,2]
- C0040223
Description
Indicate the one primary reason, documented in the medical record, that primary PCI was not performed as reperfusion therapy.
Data type
text
Alias
- UMLS CUI [1,1]
- C0522473
- UMLS CUI [1,2]
- C1532338
Description
Indicate the one primary reason, documented in the medical record, that thrombolytics were not administered as reperfusion therapy.
Data type
text
Alias
- UMLS CUI-1
- C3260558
Description
In-Hospital clinical events
Alias
- UMLS CUI [1,1]
- C0205210
- UMLS CUI [1,2]
- C0441471
- UMLS CUI [1,3]
- C0019994
Description
Indicate if there are clinical signs and symptoms of a new infarction or repeat infarction.
Data type
boolean
Alias
- UMLS CUI [1]
- C0948369
Description
Indicate the date when the clinical signs and symptoms of the new myocardial infarction first occurred.
Data type
date
Alias
- UMLS CUI [1,1]
- C0948369
- UMLS CUI [1,2]
- C0011008
Description
Indicate if the patient had a new onset or acute recurrence of cardiogenic shock in your facility.
Data type
boolean
Alias
- UMLS CUI-1
- C0036980
Description
Indicate the date when a diagnosis of cardiogenic shock was made.
Data type
date
Alias
- UMLS CUI [1,1]
- C0036980
- UMLS CUI [1,2]
- C0011008
Description
Indicate if there is physician documentation or report of either new onset or acute reoccurrence of heart failure.
Data type
boolean
Alias
- UMLS CUI-1
- C0018801
Description
Indicate the date of the new onset or acute reoccurrence of heart failure.
Data type
date
Alias
- UMLS CUI-1
- C2984177
Description
Indicate if the patient experienced a stroke or cerebrovascular accident (CVA) in your facility.
Data type
boolean
Alias
- UMLS CUI-1
- C0038454
Description
Indicate the date of onset of stroke or cerebrovascular accident (CVA) symptoms. If a stroke occurs during sleep, last awake time may be used.
Data type
date
Alias
- UMLS CUI [1,1]
- C0038454
- UMLS CUI [1,2]
- C0011008
Description
Indicate if the patient experienced a hemorrhagic stroke with documentation on imaging.
Data type
boolean
Alias
- UMLS CUI-1
- C0553692
Description
Indicate if the patient experienced atrial fibrillation during the current admission.
Data type
boolean
Alias
- UMLS CUI-1
- C0004238
Description
Indicate the date the patient experienced episode of atrial fibrillation.
Data type
date
Alias
- UMLS CUI [1,1]
- C0004238
- UMLS CUI [1,2]
- C0011008
Description
Indicate if the patient experienced VTach and/or VFib during the current admission.
Data type
boolean
Alias
- UMLS CUI [1]
- C0042514
- UMLS CUI [2]
- C0042510
Description
Indicate the date the patient experienced VTach and/or VFib.
Data type
date
Alias
- UMLS CUI [1,1]
- C0042514
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [2,1]
- C0042510
- UMLS CUI [2,2]
- C0011008
Description
Indicate if the patient experienced an episode of cardiac arrest in your facility.
Data type
boolean
Alias
- UMLS CUI-1
- C0018790
Description
Indicate the date of the cardiac arrest.
Data type
date
Alias
- UMLS CUI-1
- C2825160
Description
Indicate if there was a suspected or confirmed bleeding event observed and documented in the medical record that was associated with any of the following: 1. Hemoglobin drop of >=3 g/dL; 2. Transfusion of whole blood or packed red blood cells; 3. Procedural intervention/surgery at the bleeding site to reverse/stop or correct the bleeding (such as surgical closures/exploration of the arteriotomy site, balloon angioplasty to seal an arterial tear, endoscopy with cautery of a GI bleed).
Data type
boolean
Alias
- UMLS CUI-1
- C0019080
Description
Indicate the date of the suspected bleeding event.
Data type
date
Alias
- UMLS CUI [1,1]
- C0019080
- UMLS CUI [1,2]
- C0011008
Description
Suspected Bleeding Event Location
Data type
text
Alias
- UMLS CUI [1,1]
- C0019080
- UMLS CUI [1,2]
- C0450429
Description
Indicate if the suspected bleeding event observed required procedural intervention or surgery at the bleeding site to reverse, stop or correct the bleeding (e.g. surgical closures, exploration of the arteriotomy site, balloon angioplasty to seal an arterial tear, or endoscopy with cautery of a GI bleed).
Data type
boolean
Alias
- UMLS CUI-1
- C3841143
Description
Indicate if there was a transfusion of either whole blood or packed red blood cells.
Data type
boolean
Alias
- UMLS CUI [1]
- C0086252
Description
Indicate the date of the first whole blood or red blood cell transfusion.
Data type
date
Alias
- UMLS CUI-1
- C0808300
Description
Indicate if any red blood cell/whole blood transfusion was related to CABG.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0086252
- UMLS CUI [1,2]
- C0010055
Description
Indicate if the patient experienced acute or worsening renal failure necessitating renal dialysis.
Data type
boolean
Alias
- UMLS CUI-1
- C0011946
Description
Indicate the date of acute or worsening renal failure leading to a new requirement for dialysis.
Data type
date
Alias
- UMLS CUI [1]
- C0011946
Description
Indicate if the patient required the use of other mechanical ventricular support. This includes use of cardiopulmonary bypass, left ventricular assist device (LVAD) and/or extracorporeal membrane oxygenation (ECMO).
Data type
text
Alias
- UMLS CUI [1]
- C0457617
Similar models
ACTION Registry
- StudyEvent: ODM
C0205394 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,2])
C1279901 (UMLS CUI [1,2])
C1521801 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
C1264639 (UMLS CUI [1,2])
C1301943 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,3])
C2348184 (UMLS CUI [1,2])
C1879547 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C1547428 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,2])
C0750572 (UMLS CUI [1,2])
C0439673 (UMLS CUI [1,2])
C0205421 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C2348792 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C3272300 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0004239 (UMLS CUI [2])
C0178602 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,2])
C0522473 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,2])
C0522473 (UMLS CUI [1,2])
C0522473 (UMLS CUI [1,2])
C0522473 (UMLS CUI [1,2])
C0522473 (UMLS CUI-2)
C0522473 (UMLS CUI [1,2])
C0522473 (UMLS CUI [1,2])
C0522473 (UMLS CUI [1,2])
C0522473 (UMLS CUI [1,2])
C0522473 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,2])
C3640054 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,2])
C2825026 (UMLS CUI [1,2])
C1301880 (UMLS CUI [1,2])
C3476109 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,2])
C0168273 (UMLS CUI [1,2])
C1518896 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C0184661 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0522473 (UMLS CUI [1,2])
C1879547 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C0450429 (UMLS CUI [1,2])
C0035124 (UMLS CUI [1,2])
C0040809 (UMLS CUI [1,3])
C0040044 (UMLS CUI [1,2])
C1301880 (UMLS CUI [1,2])
C1301624 (UMLS CUI [1,2])
C3275089 (UMLS CUI [2,1])
C0040223 (UMLS CUI [2,2])
C1532338 (UMLS CUI [1,2])
C0441471 (UMLS CUI [1,2])
C0019994 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0042510 (UMLS CUI [2])
C0011008 (UMLS CUI [1,2])
C0042510 (UMLS CUI [2,1])
C0011008 (UMLS CUI [2,2])
C0011008 (UMLS CUI [1,2])
C0450429 (UMLS CUI [1,2])
C0010055 (UMLS CUI [1,2])
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