ID
44232
Beschreibung
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
Stichworte
Versionen (5)
- 15.04.15 15.04.15 -
- 25.11.15 25.11.15 -
- 14.04.21 14.04.21 - Ahmed Rafee, MD
- 20.09.21 20.09.21 -
- 18.11.21 18.11.21 -
Rechteinhaber
American College of Cardiology Foundation
Hochgeladen am
20. September 2021
DOI
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Lizenz
Creative Commons BY 4.0
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ACTION Registry®-GWTG™
ACTION Registry
- StudyEvent: ODM
Beschreibung
Admission
Beschreibung
Indicate the means of transportation to the facility where the patient first received treatment
Datentyp
text
Alias
- UMLS CUI [1]
- C3258270
Beschreibung
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.
Datentyp
datetime
Alias
- UMLS CUI-1
- C1320531
Beschreibung
Indicate the date and time the responding unit was notified by dispatch.
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C3261085
- UMLS CUI [1,2]
- C1264639
Beschreibung
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.
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C1518384
- UMLS CUI [1,2]
- C1279901
- UMLS CUI [1,3]
- C1521801
- UMLS CUI [1,4]
- C0011008
Beschreibung
Indicate the date and time the responding unit left the scene with a patient (started moving).
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C3261085
- UMLS CUI [1,2]
- C1264639
Beschreibung
Indicate the emergency medical services agency number.
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C4037969
- UMLS CUI [1,2]
- C1301943
- UMLS CUI [1,3]
- C0805701
Beschreibung
Indicate the emergency medical services run number.
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C4037969
- UMLS CUI [1,2]
- C2348184
Beschreibung
Indicate the date and time the Cath Lab was activated.
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C0018795
- UMLS CUI [1,2]
- C1879547
- UMLS CUI [1,3]
- C0011008
Beschreibung
Transferred from Outside Facility
Datentyp
boolean
Alias
- UMLS CUI-1
- C1546432
Beschreibung
Means of Transfer from outside facility
Datentyp
text
Alias
- UMLS CUI [1]
- C0449375
Beschreibung
Indicate the date and time the patient arrived at the outside facility.
Datentyp
datetime
Alias
- UMLS CUI-1
- C1320532
Beschreibung
Transfer from Outside Facility Date/Time
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C1546432
- UMLS CUI [1,2]
- C0011008
Beschreibung
Name of Transferring Facility/AHA Number
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0018704
- UMLS CUI [1,2]
- C0600091
Beschreibung
Indicate the date and time the patient arrived at your facility.
Datentyp
datetime
Alias
- UMLS CUI-1
- C1320532
Beschreibung
Indicate the date the patient was admitted as an inpatient to your facility for the current episode of care.
Datentyp
date
Alias
- UMLS CUI-1
- C1302393
Beschreibung
Indicate the location the patient was first evaluated at your facility.
Datentyp
text
Alias
- UMLS CUI [1]
- C0450429
Beschreibung
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.
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C3495034
- UMLS CUI [1,2]
- C0011008
Beschreibung
Insurance Payors
Datentyp
text
Alias
- UMLS CUI [1]
- C0021672
Beschreibung
Indicate the admitting primary provider's last name.
Datentyp
text
Alias
- UMLS CUI-1
- C0807500
Beschreibung
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.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1549728
- UMLS CUI [1,2]
- C1547428
Beschreibung
Indicate the patient's Health Insurance Claim (HIC) number.
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0021682
- UMLS CUI [1,2]
- C0237753
Beschreibung
Cardiac status on first medical contact
Beschreibung
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.
Datentyp
datetime
Alias
- UMLS CUI-1
- C1320528
Beschreibung
Symptom Onset Time Estimated
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1320528
- UMLS CUI [1,2]
- C0750572
Beschreibung
Indicate if the symptom onset time was not available.
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1320528
- UMLS CUI [1,2]
- C0439673
Beschreibung
Indicate when the first 12-lead electrocardiogram (ECG) was obtained.
Datentyp
text
Alias
- UMLS CUI [1]
- C2826640
Beschreibung
Indicate the date and time of the first 12-lead electrocardiogram (ECG).
Datentyp
datetime
Alias
- UMLS CUI [1]
- C2826846
Beschreibung
Indicate if there is a non system reason for the delay in the first ECG.
Datentyp
boolean
Alias
- UMLS CUI-1
- N
Beschreibung
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.
Datentyp
boolean
Alias
- UMLS CUI-1
- C3538872
Beschreibung
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.
Datentyp
text
Alias
- UMLS CUI-1
- C0438154
Beschreibung
STEMI or STEMI Equivalent First Noted
Datentyp
text
Alias
- UMLS CUI [1,1]
- C3538872
- UMLS CUI [1,2]
- C0011008
Beschreibung
Subsequent ECG with STEMI or STEMI Equivalent Date/Time
Datentyp
datetime
Alias
- UMLS CUI-1
- N
Beschreibung
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.
Datentyp
text
Beschreibung
Indicate if there is physician documentation or report of heart failure on first medical contact.
Datentyp
boolean
Alias
- UMLS CUI-1
- C0018801
Beschreibung
Indicate if the patient was in a state of cardiogenic shock on first medical contact.
Datentyp
boolean
Alias
- UMLS CUI-1
- C0036980
Beschreibung
Indicate the first measurement or earliest record of heart rate (in beats per minute).
Datentyp
integer
Maßeinheiten
- bpm
Alias
- UMLS CUI-1
- C0018810
Beschreibung
Systolic BP
Datentyp
integer
Maßeinheiten
- mmHg
Alias
- UMLS CUI-1
- C0871470
Beschreibung
Indicate if the patient was in cardiac arrest when first evaluated by EMS or ED personnel.
Datentyp
boolean
Alias
- UMLS CUI-1
- C0018790
Beschreibung
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.
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0018790
- UMLS CUI [1,2]
- C3272300
Beschreibung
Indicate if the patient's cardiac arrest occurred during the hospitalization at the first facility.
Datentyp
boolean
Alias
- UMLS CUI-1
- C2936490
Beschreibung
History and Risk Factors
Alias
- UMLS CUI-1
- C0035648
Beschreibung
Indicate the patient's height in centimeters.
Datentyp
integer
Maßeinheiten
- cm
Alias
- UMLS CUI-1
- C0005890
Beschreibung
Indicate the patient's weight in kilograms.
Datentyp
float
Maßeinheiten
- kg
Alias
- UMLS CUI-1
- C0005910
Beschreibung
Current/Recent Smoker (w/in 1 year)
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0543414
Beschreibung
Indicate if the patient has been diagnosed previously with hypertension.
Datentyp
boolean
Alias
- UMLS CUI-1
- C0455527
Beschreibung
Indicate if the patient has a history of dyslipidemia diagnosed and/or treated by a physician.
Datentyp
boolean
Alias
- UMLS CUI-1
- C0242339
Beschreibung
Indicate if the patient is currently undergoing either hemodialysis or peritoneal dialysis on an ongoing basis as a result of renal failure.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0011946
Beschreibung
Indicate if the patient has a history of diabetes mellitus, regardless of duration of disease or need for antidiabetic agents.
Datentyp
boolean
Alias
- UMLS CUI-1
- C0011849
Beschreibung
Indicate the therapy method the patient presented with. Choose the most aggressive therapy.
Datentyp
text
Alias
- UMLS CUI [1]
- C3274787
Beschreibung
Indicate if the patient has had at least one documented previous myocardial infarction.
Datentyp
boolean
Alias
- UMLS CUI-1
- C1275835
Beschreibung
Indicate if the patient has a history of cancer.
Datentyp
boolean
Alias
- UMLS CUI-1
- C0006826
Beschreibung
Indicate the type of cancer if the patient has a history of cancer.
Datentyp
text
Alias
- UMLS CUI [1]
- C0872066
Beschreibung
Indicate if there is a previous history of heart failure.
Datentyp
boolean
Alias
- UMLS CUI-1
- C0455531
Beschreibung
Indicate if the patient had a previous percutaneous coronary intervention (PCI) of any type (balloon angioplasty, stent or other).
Datentyp
boolean
Alias
- UMLS CUI-1
- C1320647
Beschreibung
Most Recent PCI Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1532338
- UMLS CUI [1,2]
- C1264639
Beschreibung
Indicate whether the patient had a coronary artery bypass graft (CABG).
Datentyp
boolean
Alias
- UMLS CUI-1
- C1275842
Beschreibung
If the patient had a previous coronary artery bypass graft (CABG), indicate the date.
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0010055
- UMLS CUI [1,2]
- C0011008
Beschreibung
Atrial Fibrillation or Flutter
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0004238
- UMLS CUI [2]
- C0004239
Beschreibung
Indicate if the patient has a history of cerebrovascular disease.
Datentyp
boolean
Alias
- UMLS CUI-1
- C0007820
Beschreibung
Indicate if the patient has had a stroke.
Datentyp
boolean
Alias
- UMLS CUI-1
- C0559159
Beschreibung
Indicate if the patient has a history of TIAs.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0007787
Beschreibung
Indicate the level of assistance the patient required with ambulation.
Datentyp
text
Alias
- UMLS CUI [1]
- C0080331
Beschreibung
Indicate the patients level of cognition.
Datentyp
text
Alias
- UMLS CUI [1]
- C0009240
Beschreibung
Indicate the level of assistance the patient required with acitivities of daily living.
Datentyp
text
Alias
- UMLS CUI [1]
- C0001288
Beschreibung
Medications
Beschreibung
Aspirin
Datentyp
text
Alias
- UMLS CUI [1]
- C0004057
Beschreibung
Aspirin contraindicated
Datentyp
boolean
Alias
- UMLS CUI-1
- C0729798
Beschreibung
Clopidogrel
Datentyp
text
Alias
- UMLS CUI-1
- C0070166
Beschreibung
Clopidogrel dose
Datentyp
float
Maßeinheiten
- mg
Alias
- UMLS CUI [1,1]
- C0070166
- UMLS CUI [1,2]
- C0178602
Beschreibung
Clopidogrel contraindicated
Datentyp
boolean
Alias
- UMLS CUI-1
- C1319916
Beschreibung
Ticlopidine
Datentyp
text
Alias
- UMLS CUI [1]
- C0040207
Beschreibung
Ticlodipine dose
Datentyp
float
Maßeinheiten
- mg
Alias
- UMLS CUI [1,1]
- C0040207
- UMLS CUI [1,2]
- C0178602
Beschreibung
Ticlopidine contraindicated
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0040207
- UMLS CUI [1,2]
- C0522473
Beschreibung
Prasugrel
Datentyp
text
Alias
- UMLS CUI-1
- C1620287
Beschreibung
Prasugrel Dose
Datentyp
float
Maßeinheiten
- mg
Alias
- UMLS CUI [1,1]
- C1620287
- UMLS CUI [1,2]
- C0178602
Beschreibung
Prasugrel contraindicated
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1620287
- UMLS CUI [1,2]
- C0522473
Beschreibung
Ticagrelor
Datentyp
text
Alias
- UMLS CUI-1
- C1999375
Beschreibung
Ticagrelor Contraindicated
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1999375
- UMLS CUI [1,2]
- C0522473
Beschreibung
Warfarin
Datentyp
text
Alias
- UMLS CUI-1
- C0043031
Beschreibung
Warfarin contraindicated
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0043031
- UMLS CUI [1,2]
- C0522473
Beschreibung
Dabigatran
Datentyp
text
Alias
- UMLS CUI-1
- C2348066
Beschreibung
Dabigatran contraindicated
Datentyp
boolean
Alias
- UMLS CUI-1
- C2348066
- UMLS CUI-2
- C0522473
Beschreibung
Rivaroxaban
Datentyp
text
Alias
- UMLS CUI-1
- C1739768
Beschreibung
Rivaroxaban contraindicated
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1739768
- UMLS CUI [1,2]
- C0522473
Beschreibung
Apixiban
Datentyp
text
Alias
- UMLS CUI [1]
- C1831808
Beschreibung
Apixiban Contraindicated
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1831808
- UMLS CUI [1,2]
- C0522473
Beschreibung
Beta Blocker
Datentyp
text
Alias
- UMLS CUI-1
- C0304516
Beschreibung
Beta Blocker Contraindicated
Datentyp
boolean
Alias
- UMLS CUI-1
- C1278474
Beschreibung
ACE Inhibitor
Datentyp
text
Alias
- UMLS CUI-1
- C0003015
Beschreibung
ACE inhibitor contraindicated
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0003015
- UMLS CUI [1,2]
- C0522473
Beschreibung
Angiotensin Receptor Blocker
Datentyp
text
Alias
- UMLS CUI-1
- C0521942
Beschreibung
Angiotensin Receptor Blocker contraindiacted
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0521942
- UMLS CUI [1,2]
- C0522473
Beschreibung
Aldosterone Blocking Agent
Datentyp
text
Alias
- UMLS CUI-1
- C0002007
Beschreibung
Aldosterone blocking agent contraindicated
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0002007
- UMLS CUI [1,2]
- C0522473
Beschreibung
Statin
Datentyp
text
Alias
- UMLS CUI-1
- C0360714
Beschreibung
Statin dose
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0360714
- UMLS CUI [1,2]
- C0178602
Beschreibung
Statin contraindicated
Datentyp
boolean
Alias
- UMLS CUI-1
- C1277178
Beschreibung
Non-Statin Lipid-Lowering Agent
Datentyp
text
Alias
- UMLS CUI [1]
- C0086440
Beschreibung
Indicate if a GP IIb/IIIa inhibitor was administered.
Datentyp
text
Alias
- UMLS CUI [1]
- C3640054
Beschreibung
Indicate the dose of GP IIb/IIIa administered.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C3640054
- UMLS CUI [1,2]
- C0178602
Beschreibung
GP IIb/IIIa inhibitor start date/time
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C1301880
- UMLS CUI [1,2]
- C3640054
Beschreibung
Indicate if an anticoagulant was administered.
Datentyp
boolean
Alias
- UMLS CUI-1
- C0003280
Beschreibung
Anticoagulant contraindicated
Datentyp
boolean
Alias
- UMLS CUI-1
- C1531588
Beschreibung
Indicate if unfractionated heparin was administered.
Datentyp
boolean
Alias
- UMLS CUI-1
- C2825026
Beschreibung
Indicate if an initial bolus of unfractionated heparin was administered.
Datentyp
integer
Maßeinheiten
- units
Alias
- UMLS CUI [1,1]
- C2825026
- UMLS CUI [1,2]
- C0178602
Beschreibung
Unfractionated Heparin Start Date/Time
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C1301880
- UMLS CUI [1,2]
- C2825026
Beschreibung
Enoxaparin (LMWH)
Datentyp
boolean
Alias
- UMLS CUI-1
- C3536766
Beschreibung
LMWH Start Date/Time
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C3536766
- UMLS CUI [1,2]
- C1301880
Beschreibung
LMWH injection frequency
Datentyp
text
Alias
- UMLS CUI [1,1]
- C3536766
- UMLS CUI [1,2]
- C3476109
Beschreibung
LMWH dose
Datentyp
float
Maßeinheiten
- mg
Alias
- UMLS CUI [1,1]
- C3536766
- UMLS CUI [1,2]
- C0178602
Beschreibung
Indicate if bivalirudin (Angiomax) was administered.
Datentyp
boolean
Alias
- UMLS CUI-1
- C0168273
Beschreibung
Bivalirudin Start Date/Time
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C1301880
- UMLS CUI [1,2]
- C0168273
Beschreibung
Indicate if an anticoagulant was given that is not listed.
Datentyp
boolean
Beschreibung
Procedures and Tests
Beschreibung
Indicate if the patient underwent exercise or pharmacologic stress testing with or without echocardiographic or nuclear imaging.
Datentyp
boolean
Alias
- UMLS CUI-1
- C3272313
Beschreibung
Indicate the date of exercise or pharmacologic stress testing with or without echocardiographic or nuclear imaging.
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C3272313
- UMLS CUI [1,2]
- C0011008
Beschreibung
Code the best estimate of the current left ventricular ejection fraction closest to discharge.
Datentyp
float
Maßeinheiten
- %
Alias
- UMLS CUI-1
- C0428772
Beschreibung
Indicate whether the left ventricular ejection fraction was assessed.
Datentyp
boolean
Alias
- UMLS CUI-1
- C3248481
Beschreibung
Indicate if the LVEF assessment is planned for after discharge.
Datentyp
boolean
Alias
- UMLS CUI-1
- C3248276
Beschreibung
Indicate if the patient had a diagnostic coronary angiography procedure.
Datentyp
boolean
Alias
- UMLS CUI-1
- C0085532
Beschreibung
Indicate the date the patient had diagnostic coronary angiography
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0085532
- UMLS CUI [1,2]
- C0011008
Beschreibung
Indicate the number of diseased vessels found during the diagnostic catheterization.
Datentyp
text
Alias
- UMLS CUI [1]
- C3275120
Beschreibung
Indicate whether or not the left main coronary artery is 50 percent or more stenotic.
Datentyp
boolean
Alias
- UMLS CUI-1
- C2825221
Beschreibung
Indicate if a graft is present when the left main stenosis is greater than or equal to 50 percent.
Datentyp
text
Alias
- UMLS CUI [1]
- C2062905
Beschreibung
Indicate if the left anterior descending coronary artery is greater than or equal to 70 percent stenotic.
Datentyp
boolean
Alias
- UMLS CUI-1
- C2825222
Beschreibung
Indicate if a graft is present when the proximal LAD is greater than or equal to 70 percent stenotic.
Datentyp
text
Alias
- UMLS CUI [1]
- C2825222
Beschreibung
Indicate if a catheterization was not performed because it was contraindicated.
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1532338
- UMLS CUI [1,2]
- C0522473
Beschreibung
Indicate if the patient had a percutaneous coronary intervention (PCI).
Datentyp
boolean
Alias
- UMLS CUI-1
- C1532338
Beschreibung
Indicate the date and time the patient arrived to the cath lab where the PCI was being performed, as documented in the medical record.
Datentyp
datetime
Alias
- UMLS CUI-1
- C3838354
Beschreibung
Indicate the date and time the first device was activated regardless of type of device used.
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C0025080
- UMLS CUI [1,2]
- C1879547
- UMLS CUI [1,3]
- C0011008
Beschreibung
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.
Datentyp
text
Alias
- UMLS CUI-1
- C3272298
Beschreibung
Indicate if a stent or stents were placed in the affected coronary artery.
Datentyp
boolean
Alias
- UMLS CUI-1
- C3272316
Beschreibung
Stent Type(s)
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0687568
- UMLS CUI [1,2]
- C0332307
Beschreibung
Indicate the primary reason PCI was performed or attempted.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1532338
- UMLS CUI [1,2]
- C0392360
Beschreibung
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).
Datentyp
text
Alias
- UMLS CUI [1]
- C3640267
Beschreibung
Indicate if the patient had a CABG (coronary artery bypass graft surgery).
Datentyp
boolean
Alias
- UMLS CUI-1
- C0010055
Beschreibung
Indicate the date of the coronary artery bypass graft (CABG) surgery.
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C0010055
- UMLS CUI [1,2]
- C0011008
Beschreibung
Indicate if an in-hospital hypothermia protocol was initiated.
Datentyp
boolean
Alias
- UMLS CUI-1
- C0150255
Beschreibung
Indicate the location where the hypothermia protocol was initiated.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0150255
- UMLS CUI [1,2]
- C0450429
Beschreibung
Reperfusion Strategy
Beschreibung
Indicate if the STEMI patient is a reperfusion candidate for primary PCI or Thrombolytic therapy.
Datentyp
boolean
Alias
- UMLS CUI-1
- C0035124
Beschreibung
Indicate the one primary reason, documented in the medical record, that reperfusion therapy (thrombolytic therapy or primary PCI) was not indicated.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1549995
- UMLS CUI [1,2]
- C0035124
- UMLS CUI [1,3]
- C0040809
Beschreibung
Indicate if the patient received primary PCI as an urgent treatment for STEMI.
Datentyp
boolean
Alias
- UMLS CUI-1
- C3275089
Beschreibung
Indicate if the patient received thrombolytic therapy as an urgent treatment for STEMI.
Datentyp
boolean
Alias
- UMLS CUI-1
- C0040044
Beschreibung
Indicate the strength of dose of the thrombolytic.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0178602
- UMLS CUI [1,2]
- C0040044
Beschreibung
Indicate the type of thrombolytic first administered.
Datentyp
text
Alias
- UMLS CUI [1]
- C0040044
Beschreibung
Thrombolytic Therapy Start Date/Time
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C0040044
- UMLS CUI [1,2]
- C1301880
Beschreibung
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).
Datentyp
boolean
Alias
- UMLS CUI [1]
- C3640267
Beschreibung
Indicate if the patient was Lytic ineligible and required prolonged transfer time for primary PCI.
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0040044
- UMLS CUI [1,2]
- C1301624
- UMLS CUI [2,1]
- C3275089
- UMLS CUI [2,2]
- C0040223
Beschreibung
Indicate the one primary reason, documented in the medical record, that primary PCI was not performed as reperfusion therapy.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0522473
- UMLS CUI [1,2]
- C1532338
Beschreibung
Indicate the one primary reason, documented in the medical record, that thrombolytics were not administered as reperfusion therapy.
Datentyp
text
Alias
- UMLS CUI-1
- C3260558
Beschreibung
In-Hospital clinical events
Beschreibung
Indicate if there are clinical signs and symptoms of a new infarction or repeat infarction.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0948369
Beschreibung
Indicate the date when the clinical signs and symptoms of the new myocardial infarction first occurred.
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0948369
- UMLS CUI [1,2]
- C0011008
Beschreibung
Indicate if the patient had a new onset or acute recurrence of cardiogenic shock in your facility.
Datentyp
boolean
Alias
- UMLS CUI-1
- C0036980
Beschreibung
Indicate the date when a diagnosis of cardiogenic shock was made.
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0036980
- UMLS CUI [1,2]
- C0011008
Beschreibung
Indicate if there is physician documentation or report of either new onset or acute reoccurrence of heart failure.
Datentyp
boolean
Alias
- UMLS CUI-1
- C0018801
Beschreibung
Indicate the date of the new onset or acute reoccurrence of heart failure.
Datentyp
date
Alias
- UMLS CUI-1
- C2984177
Beschreibung
Indicate if the patient experienced a stroke or cerebrovascular accident (CVA) in your facility.
Datentyp
boolean
Alias
- UMLS CUI-1
- C0038454
Beschreibung
Indicate the date of onset of stroke or cerebrovascular accident (CVA) symptoms. If a stroke occurs during sleep, last awake time may be used.
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0038454
- UMLS CUI [1,2]
- C0011008
Beschreibung
Indicate if the patient experienced a hemorrhagic stroke with documentation on imaging.
Datentyp
boolean
Alias
- UMLS CUI-1
- C0553692
Beschreibung
Indicate if the patient experienced atrial fibrillation during the current admission.
Datentyp
boolean
Alias
- UMLS CUI-1
- C0004238
Beschreibung
Indicate the date the patient experienced episode of atrial fibrillation.
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0004238
- UMLS CUI [1,2]
- C0011008
Beschreibung
Indicate if the patient experienced VTach and/or VFib during the current admission.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0042514
- UMLS CUI [2]
- C0042510
Beschreibung
Indicate the date the patient experienced VTach and/or VFib.
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0042514
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [2,1]
- C0042510
- UMLS CUI [2,2]
- C0011008
Beschreibung
Indicate if the patient experienced an episode of cardiac arrest in your facility.
Datentyp
boolean
Alias
- UMLS CUI-1
- C0018790
Beschreibung
Indicate the date of the cardiac arrest.
Datentyp
date
Alias
- UMLS CUI-1
- C2825160
Beschreibung
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).
Datentyp
boolean
Alias
- UMLS CUI-1
- C0019080
Beschreibung
Indicate the date of the suspected bleeding event.
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0019080
- UMLS CUI [1,2]
- C0011008
Beschreibung
Suspected Bleeding Event Location
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0019080
- UMLS CUI [1,2]
- C0450429
Beschreibung
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).
Datentyp
boolean
Alias
- UMLS CUI-1
- C3841143
Beschreibung
Indicate if there was a transfusion of either whole blood or packed red blood cells.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0086252
Beschreibung
Indicate the date of the first whole blood or red blood cell transfusion.
Datentyp
date
Alias
- UMLS CUI-1
- C0808300
Beschreibung
Indicate if any red blood cell/whole blood transfusion was related to CABG.
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0086252
- UMLS CUI [1,2]
- C0010055
Beschreibung
Indicate if the patient experienced acute or worsening renal failure necessitating renal dialysis.
Datentyp
boolean
Alias
- UMLS CUI-1
- C0011946
Beschreibung
Indicate the date of acute or worsening renal failure leading to a new requirement for dialysis.
Datentyp
date
Alias
- UMLS CUI [1]
- C0011946
Beschreibung
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).
Datentyp
text
Alias
- UMLS CUI [1]
- C0457617
Ähnliche Modelle
ACTION Registry
- StudyEvent: ODM
C0205394 (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])
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])
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])
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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