ID

10152

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)

Lien

http://cvquality.acc.org/NCDR-Home/Registries/Hospital-Registries.aspx

Mots-clés

Versions (5)
  1. 15/04/2015 15/04/2015 -
  2. 25/11/2015 25/11/2015 -
  3. 14/04/2021 14/04/2021 - Ahmed Rafee, MD
  4. 20/09/2021 20/09/2021 -
  5. 18/11/2021 18/11/2021 -
Détendeur de droits

Copyright National Cardiovascular Data Registry

Téléchargé le

15 avril 2015

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC-ND 3.0
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ACTION Registry®-GWTG™

Anglais

ACTION Registry

1 Formulaires  
  1. StudyEvent: ODM
    1. ACTION Registry
Demographics
Description

Demographics

Alias
UMLS CUI-1
C0011298
Indicate the patient's last name. Hyphenated names should be recorded with a hyphen.
Description

Indicate the patient's last name. Hyphenated names should be recorded with a hyphen.

Type de données

text

Alias
UMLS CUI-1
C1301584
First name
Description

Indicate the patient's first name.

Type de données

text

Alias
UMLS CUI-1
C1443235
Middle Name
Description

Indicate the patient's middle name.

Type de données

text

Alias
UMLS CUI-1
C2598119
SSN
Description

Indicate the patient's United States Social Security Number (SSN).

Type de données

text

Alias
UMLS CUI-1
C1301821
SSNA N/A
Description

Indicate if the patient does not have a United States Social Security Number.

Type de données

boolean

Alias
UMLS CUI-1
C1547437
Patient ID
Description

Indicate the number created and automatically inserted by the software that uniquely identifies this patient. Once assigned to a patient at the participating facility, this number will never be changed or reassigned to a different patient. If the patient returns to the same participating facility or for followup, they will receive this same unique patient identifier.

Type de données

integer

Alias
UMLS CUI-1
C2348585
Other ID
Description

An optional patient identifier, such as Medical Record Number, that can be associated with the patient.

Type de données

integer

Birth Date
Description

Indicate the patient's date of birth.

Type de données

date

Alias
UMLS CUI-1
C0421451
Sex
Description

Indicate the patient's sex at birth.

Type de données

text

Alias
UMLS CUI-1
C0079399
Patient Zip Code
Description

Indicate the patient's United States Postal Service zip code of their primary residence. If the patient does not have a U.S. residence, or is homeless, leave blank and check 'Zip Code NA'.

Type de données

text

Alias
UMLS CUI-1
C0421454
ZIP Code N/A
Description

Indicate if the patient does not have a United States Postal Service zip code. This includes patients who do not have a US residence or are homeless.

Type de données

boolean

Alias
UMLS CUI-1
C2600019
Race
Description

Race

Type de données

text

Alias
UMLS CUI-1
C0034510
If Asian, specify:
Description

If Asian, specify:

Type de données

text

If Native Hawaiian/Pacific Islander, specify:
Description

If Native Hawaiian/Pacific Islander, specify:

Type de données

text

Hispanic or Latino Ethnicity
Description

Indicate if the patient is of Hispanic or Latino ethnicity as determined by the patient/family.

Type de données

text

Alias
UMLS CUI-1
C0015031
Admission
Description

Admission

Means of Transport to First Facility
Description

Indicate the means of transportation to the facility where the patient first received treatment

Type de données

text

Alias
UMLS CUI-1
C3258270
EMS 1st Med. Contact Date/Time
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.

Type de données

datetime

Alias
UMLS CUI-1
C1320531
EMS Dispatch Date/Time
Description

Indicate the date and time the responding unit was notified by dispatch.

Type de données

datetime

Alias
UMLS CUI-1
C3261085
UMLS CUI-2
C1264639
UMLS CUI-3
P
Non-EMS 1st Med. Contact Date/Time
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.

Type de données

datetime

Alias
UMLS CUI-1
N
EMS Leaving Scene Date/Time
Description

Indicate the date and time the responding unit left the scene with a patient (started moving).

Type de données

datetime

Alias
UMLS CUI-1
N
EMS Agency Number
Description

Indicate the emergency medical services agency number.

Type de données

integer

Alias
UMLS CUI-1
N
EMS Run Number
Description

Indicate the emergency medical services run number.

Type de données

integer

Alias
UMLS CUI-1
N
Cath Lab Activation Date/Time
Description

Indicate the date and time the Cath Lab was activated.

Type de données

datetime

Alias
UMLS CUI-1
N
Transferred from Outside Facility
Description

Transferred from Outside Facility

Type de données

boolean

Alias
UMLS CUI-1
C1546432
Means of Transfer from outside facility
Description

Means of Transfer from outside facility

Type de données

text

Alias
UMLS CUI-1
C0449375
Arrival at Outside Facility Date/Time
Description

Indicate the date and time the patient arrived at the outside facility.

Type de données

datetime

Alias
UMLS CUI-1
C1320532
Transfer from Outside Facility Date/Time
Description

Transfer from Outside Facility Date/Time

Type de données

datetime

Alias
UMLS CUI-1
C1546432
UMLS CUI-2
C0011008
UMLS CUI-3
P
Name of Transferring Facility/AHA Number
Description

Name of Transferring Facility/AHA Number

Type de données

text

Alias
UMLS CUI-1
N
Arrival Date/Time
Description

Indicate the date and time the patient arrived at your facility.

Type de données

datetime

Alias
UMLS CUI-1
C1320532
Admission Date
Description

Indicate the date the patient was admitted as an inpatient to your facility for the current episode of care.

Type de données

date

Alias
UMLS CUI-1
C1302393
Location of First Evaluation
Description

Indicate the location the patient was first evaluated at your facility.

Type de données

text

Alias
UMLS CUI-1
N
ED Transfer Out Date/Time
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.

Type de données

datetime

Alias
UMLS CUI-1
C3495034
UMLS CUI-2
C0011008
UMLS CUI-3
P
Insurance Payors
Description

Insurance Payors

Type de données

text

Alias
UMLS CUI-1
C0021672
Provider Name
Description

Indicate the admitting primary provider's last name.

Type de données

text

Alias
UMLS CUI-1
C0807500
Admitting Provider NPI
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.

Type de données

text

Alias
UMLS CUI-1
C1549728
UMLS CUI-2
C1547428
UMLS CUI-3
P
HIC #
Description

Indicate the patient's Health Insurance Claim (HIC) number.

Type de données

integer

Alias
UMLS CUI-1
N
Cardiac status on first medical contact
Description

Cardiac status on first medical contact

Symptom Onset Date/Time
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.

Type de données

datetime

Alias
UMLS CUI-1
C1320528
Symptom Onset Time Estimated
Description

Symptom Onset Time Estimated

Type de données

boolean

Alias
UMLS CUI-1
C1320528
UMLS CUI-2
C0750572
UMLS CUI-3
P
Symptom Onset Time Not Available
Description

Indicate if the symptom onset time was not available.

Type de données

boolean

Alias
UMLS CUI-1
C1320528
UMLS CUI-2
C0439673
UMLS CUI-3
P
First ECG Obtained
Description

Indicate when the first 12-lead electrocardiogram (ECG) was obtained.

Type de données

text

Alias
UMLS CUI-1
N
First ECG Date/Time
Description

Indicate the date and time of the first 12-lead electrocardiogram (ECG).

Type de données

datetime

Alias
UMLS CUI-1
N
First ECG Non-System Reason For Delay
Description

Indicate if there is a non system reason for the delay in the first ECG.

Type de données

boolean

Alias
UMLS CUI-1
N
STEMI or STEMI Equivalent
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.

Type de données

boolean

Alias
UMLS CUI-1
C3538872
ECG Findings
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.

Type de données

text

Alias
UMLS CUI-1
C0438154
STEMI or STEMI Equivalent First Noted
Description

STEMI or STEMI Equivalent First Noted

Type de données

text

Alias
UMLS CUI-1
N
Subsequent ECG with STEMI or STEMI Equivalent Date/Time
Description

Subsequent ECG with STEMI or STEMI Equivalent Date/Time

Type de données

datetime

Alias
UMLS CUI-1
N
Other ECG Findings
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.

Type de données

text

Alias
UMLS CUI-1
C0438154
Heart failure
Description

Indicate if there is physician documentation or report of heart failure on first medical contact.

Type de données

boolean

Alias
UMLS CUI-1
C0018801
Cardiogenic Shock
Description

Indicate if the patient was in a state of cardiogenic shock on first medical contact.

Type de données

boolean

Alias
UMLS CUI-1
C0036980
Heart Rate
Description

Indicate the first measurement or earliest record of heart rate (in beats per minute).

Type de données

integer

Unités de mesure
  • bpm
Alias
UMLS CUI-1
C0018810
bpm
Systolic BP
Description

Systolic BP

Type de données

integer

Unités de mesure
  • mmHg
Alias
UMLS CUI-1
C0871470
mmHg
Cardiac Arrest
Description

Indicate if the patient was in cardiac arrest when first evaluated by EMS or ED personnel.

Type de données

boolean

Alias
UMLS CUI-1
C0018790
Cardiac Arrest Pre-Hospital
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.

Type de données

boolean

Alias
UMLS CUI-1
N
Cardiac Arrest Outside Facility
Description

Indicate if the patient's cardiac arrest occurred during the hospitalization at the first facility.

Type de données

boolean

Alias
UMLS CUI-1
C2936490
History and Risk Factors
Description

History and Risk Factors

Alias
UMLS CUI-1
C0035648
Height
Description

Indicate the patient's height in centimeters.

Type de données

integer

Unités de mesure
  • cm
Alias
UMLS CUI-1
C0005890
cm
Weight
Description

Indicate the patient's weight in kilograms.

Type de données

float

Unités de mesure
  • kg
Alias
UMLS CUI-1
C0005910
kg
Current/Recent Smoker (w/in 1 year)
Description

Current/Recent Smoker (w/in 1 year)

Type de données

boolean

Alias
UMLS CUI-1
C3241966
UMLS CUI-2
C0337671
Hypertension
Description

Indicate if the patient has been diagnosed previously with hypertension.

Type de données

boolean

Alias
UMLS CUI-1
C0455527
Dyslipidemia
Description

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

Type de données

boolean

Alias
UMLS CUI-1
C0242339
Currently on Dialysis
Description

Indicate if the patient is currently undergoing either hemodialysis or peritoneal dialysis on an ongoing basis as a result of renal failure.

Type de données

boolean

Alias
UMLS CUI-1
C0455667
Diabetes Mellitus
Description

Indicate if the patient has a history of diabetes mellitus, regardless of duration of disease or need for antidiabetic agents.

Type de données

boolean

Alias
UMLS CUI-1
C0011849
Diabetes Therapy
Description

Indicate the therapy method the patient presented with. Choose the most aggressive therapy.

Type de données

text

Alias
UMLS CUI-1
C3274787
Prior MI
Description

Indicate if the patient has had at least one documented previous myocardial infarction.

Type de données

boolean

Alias
UMLS CUI-1
C1275835
Cancer
Description

Indicate if the patient has a history of cancer.

Type de données

boolean

Alias
UMLS CUI-1
C0006826
Cancer Type
Description

Indicate the type of cancer if the patient has a history of cancer.

Type de données

text

Alias
UMLS CUI-1
C0872066
Prior Heart Failure
Description

Indicate if there is a previous history of heart failure.

Type de données

boolean

Alias
UMLS CUI-1
C0455531
Prior PCI
Description

Indicate if the patient had a previous percutaneous coronary intervention (PCI) of any type (balloon angioplasty, stent or other).

Type de données

boolean

Alias
UMLS CUI-1
C1320647
Most Recent PCI Date
Description

Most Recent PCI Date

Type de données

date

Alias
UMLS CUI-1
C1532338
UMLS CUI-2
C1264639
UMLS CUI-3
P
Prior CABG
Description

Indicate whether the patient had a coronary artery bypass graft (CABG).

Type de données

boolean

Alias
UMLS CUI-1
C1275842
Most Recent CABG Date
Description

If the patient had a previous coronary artery bypass graft (CABG), indicate the date.

Type de données

date

Alias
UMLS CUI-1
C2164190
Atrial Fibrillation or Flutter
Description

Atrial Fibrillation or Flutter

Type de données

boolean

Alias
UMLS CUI-1
C0004238
UMLS CUI-2
C0004239
Cerebrovascular Disease
Description

Indicate if the patient has a history of cerebrovascular disease.

Type de données

boolean

Alias
UMLS CUI-1
C0007820
Prior Stroke
Description

Indicate if the patient has had a stroke.

Type de données

boolean

Alias
UMLS CUI-1
C0559159
Prior TIA
Description

Indicate if the patient has a history of TIAs.

Type de données

boolean

Alias
UMLS CUI-1
C0007787
UMLS CUI-2
C0455536
Walking
Description

Indicate the level of assistance the patient required with ambulation.

Type de données

text

Alias
UMLS CUI-1
C0080331
Cognition
Description

Indicate the patients level of cognition.

Type de données

text

Alias
UMLS CUI-1
C0009240
Basic ADLs
Description

Indicate the level of assistance the patient required with acitivities of daily living.

Type de données

text

Alias
UMLS CUI-1
C0001288
Medications
Description

Medications

Aspirin
Description

Aspirin

Type de données

text

Alias
UMLS CUI-1
C0004057
Aspirin contraindicated
Description

Aspirin contraindicated

Type de données

boolean

Alias
UMLS CUI-1
C0729798
Clopidogrel
Description

Clopidogrel

Type de données

text

Alias
UMLS CUI-1
C0070166
Clopidogrel dose
Description

Clopidogrel dose

Type de données

float

Unités de mesure
  • mg
Alias
UMLS CUI-1
C0070166
UMLS CUI-2
C0178602
UMLS CUI-3
P
mg
Clopidogrel contraindicated
Description

Clopidogrel contraindicated

Type de données

boolean

Alias
UMLS CUI-1
C1319916
Ticlopidine
Description

Ticlopidine

Type de données

text

Alias
UMLS CUI-1
C0749510
Ticlodipine dose
Description

Ticlodipine dose

Type de données

float

Unités de mesure
  • mg
Alias
UMLS CUI-1
C0749510
UMLS CUI-2
C0178602
UMLS CUI-3
P
mg
Ticlopidine contraindicated
Description

Ticlopidine contraindicated

Type de données

boolean

Alias
UMLS CUI-1
C0749510
UMLS CUI-2
C0522473
UMLS CUI-3
P
Prasugrel
Description

Prasugrel

Type de données

text

Alias
UMLS CUI-1
C1620287
Prasugrel Dose
Description

Prasugrel Dose

Type de données

float

Unités de mesure
  • mg
Alias
UMLS CUI-1
C1620287
UMLS CUI-2
C0178602
UMLS CUI-3
P
mg
Prasugrel contraindicated
Description

Prasugrel contraindicated

Type de données

boolean

Alias
UMLS CUI-1
C1620287
UMLS CUI-2
C0522473
UMLS CUI-3
P
Ticagrelor
Description

Ticagrelor

Type de données

text

Alias
UMLS CUI-1
C1999375
Ticagrelor Contraindicated
Description

Ticagrelor Contraindicated

Type de données

boolean

Alias
UMLS CUI-1
C1999375
UMLS CUI-2
C0522473
UMLS CUI-3
P
Warfarin
Description

Warfarin

Type de données

text

Alias
UMLS CUI-1
C0043031
Warfarin contraindicated
Description

Warfarin contraindicated

Type de données

boolean

Alias
UMLS CUI-1
C0043031
UMLS CUI-2
C0522473
UMLS CUI-3
P
Dabigatran
Description

Dabigatran

Type de données

text

Alias
UMLS CUI-1
C2348066
Dabigatran contraindicated
Description

Dabigatran contraindicated

Type de données

boolean

Alias
UMLS CUI-1
C2348066
UMLS CUI-2
C0522473
Rivaroxaban
Description

Rivaroxaban

Type de données

text

Alias
UMLS CUI-1
C1739768
Rivaroxaban contraindicated
Description

Rivaroxaban contraindicated

Type de données

boolean

Alias
UMLS CUI-1
C1739768
UMLS CUI-2
C0522473
UMLS CUI-3
P
Apixiban
Description

Apixiban

Type de données

text

Alias
UMLS CUI-1
N
Apixiban Contraindicated
Description

Apixiban Contraindicated

Type de données

boolean

Alias
UMLS CUI-1
N
Beta Blocker
Description

Beta Blocker

Type de données

text

Alias
UMLS CUI-1
C0304516
Beta Blocker Contraindicated
Description

Beta Blocker Contraindicated

Type de données

boolean

Alias
UMLS CUI-1
C1278474
ACE Inhibitor
Description

ACE Inhibitor

Type de données

text

Alias
UMLS CUI-1
C0003015
ACE inhibitor contraindicated
Description

ACE inhibitor contraindicated

Type de données

boolean

Alias
UMLS CUI-1
C0003015
UMLS CUI-2
C0522473
UMLS CUI-3
P
Angiotensin Receptor Blocker
Description

Angiotensin Receptor Blocker

Type de données

text

Alias
UMLS CUI-1
C0521942
Angiotensin Receptor Blocker contraindiacted
Description

Angiotensin Receptor Blocker contraindiacted

Type de données

boolean

Alias
UMLS CUI-1
C0521942
UMLS CUI-2
C0522473
UMLS CUI-3
P
Aldosterone Blocking Agent
Description

Aldosterone Blocking Agent

Type de données

text

Alias
UMLS CUI-1
C0002007
Aldosterone blocking agent contraindicated
Description

Aldosterone blocking agent contraindicated

Type de données

boolean

Alias
UMLS CUI-1
C0002007
UMLS CUI-2
C0522473
UMLS CUI-3
P
Statin
Description

Statin

Type de données

text

Alias
UMLS CUI-1
C0360714
Statin dose
Description

Statin dose

Type de données

text

Alias
UMLS CUI-1
C0360714
UMLS CUI-2
C0178602
UMLS CUI-3
P
Statin contraindicated
Description

Statin contraindicated

Type de données

boolean

Alias
UMLS CUI-1
C1277178
Non-Statin Lipid-Lowering Agent
Description

Non-Statin Lipid-Lowering Agent

Type de données

text

GP IIb/IIIa Inhibitor
Description

Indicate if a GP IIb/IIIa inhibitor was administered.

Type de données

text

Alias
UMLS CUI-1
C3640054
GP IIb/IIIa blocker dosage
Description

Indicate the dose of GP IIb/IIIa administered.

Type de données

text

Alias
UMLS CUI-1
C3640054
UMLS CUI-2
C0178602
UMLS CUI-3
P
GP IIb/IIIa inhibitor start date/time
Description

GP IIb/IIIa inhibitor start date/time

Type de données

datetime

Alias
UMLS CUI-1
C1301880
UMLS CUI-2
C1301880
UMLS CUI-3
P
Anticoagulant
Description

Indicate if an anticoagulant was administered.

Type de données

boolean

Alias
UMLS CUI-1
C0003280
Anticoagulant contraindicated
Description

Anticoagulant contraindicated

Type de données

boolean

Alias
UMLS CUI-1
C1531588
Unfractionated Heparin
Description

Indicate if unfractionated heparin was administered.

Type de données

boolean

Alias
UMLS CUI-1
C2825026
Unfractionated Heparin Dose
Description

Indicate if an initial bolus of unfractionated heparin was administered.

Type de données

integer

Unités de mesure
  • units
Alias
UMLS CUI-1
C2825026
UMLS CUI-2
C0178602
UMLS CUI-3
P
units
Unfractionated Heparin Start Date/Time
Description

Unfractionated Heparin Start Date/Time

Type de données

datetime

Alias
UMLS CUI-1
C1301880
UMLS CUI-2
C2825026
UMLS CUI-3
P
Enoxaparin (LMWH)
Description

Enoxaparin (LMWH)

Type de données

boolean

Alias
UMLS CUI-1
C3536766
LMWH Start Date/Time
Description

LMWH Start Date/Time

Type de données

datetime

Alias
UMLS CUI-1
C3536766
UMLS CUI-2
C1301880
UMLS CUI-3
P
LMWH injection frequency
Description

LMWH injection frequency

Type de données

text

Alias
UMLS CUI-1
N
LMWH dose
Description

LMWH dose

Type de données

float

Unités de mesure
  • mg
Alias
UMLS CUI-1
C3536766
UMLS CUI-2
C0178602
UMLS CUI-3
P
mg
Bivalirudin
Description

Indicate if bivalirudin (Angiomax) was administered.

Type de données

boolean

Alias
UMLS CUI-1
C0168273
Bivalirudin Start Date/Time
Description

Bivalirudin Start Date/Time

Type de données

datetime

Alias
UMLS CUI-1
C1301880
UMLS CUI-2
C0168273
UMLS CUI-3
P
Other parenteral anticoagulants given
Description

Indicate if an anticoagulant was given that is not listed.

Type de données

boolean

Procedures and Tests
Description

Procedures and Tests

Non-invasive Stress Testing
Description

Indicate if the patient underwent exercise or pharmacologic stress testing with or without echocardiographic or nuclear imaging.

Type de données

boolean

Alias
UMLS CUI-1
C3272313
Noninvasive stress testing Date
Description

Indicate the date of exercise or pharmacologic stress testing with or without echocardiographic or nuclear imaging.

Type de données

datetime

Alias
UMLS CUI-1
C3272313
UMLS CUI-2
C0011008
UMLS CUI-3
P
LVEF
Description

Code the best estimate of the current left ventricular ejection fraction closest to discharge.

Type de données

float

Unités de mesure
  • %
Alias
UMLS CUI-1
C0428772
%
LVEF not assessed
Description

Indicate whether the left ventricular ejection fraction was assessed.

Type de données

boolean

Alias
UMLS CUI-1
C3248481
LVEF planned for after discharge
Description

Indicate if the LVEF assessment is planned for after discharge.

Type de données

boolean

Alias
UMLS CUI-1
C3248276
Diagnostic Coronary Angiography
Description

Indicate if the patient had a diagnostic coronary angiography procedure.

Type de données

boolean

Alias
UMLS CUI-1
C0085532
Diagnostic Coronary Angiography Date
Description

Indicate the date the patient had diagnostic coronary angiography

Type de données

date

Alias
UMLS CUI-1
C0085532
UMLS CUI-2
C0011008
UMLS CUI-3
P
Number of Diseased Vessels
Description

Indicate the number of diseased vessels found during the diagnostic catheterization.

Type de données

text

Alias
UMLS CUI-1
C3275120
Left Main Stenosis >=50%
Description

Indicate whether or not the left main coronary artery is 50 percent or more stenotic.

Type de données

boolean

Alias
UMLS CUI-1
C2825221
Left Main Stenosis Graft is Present
Description

Indicate if a graft is present when the left main stenosis is greater than or equal to 50 percent.

Type de données

text

Alias
UMLS CUI-1
N
Proximal LAD Stenosis >= 70%
Description

Indicate if the left anterior descending coronary artery is greater than or equal to 70 percent stenotic.

Type de données

boolean

Alias
UMLS CUI-1
C2825222
Proximal LAD Graft is Present
Description

Indicate if a graft is present when the proximal LAD is greater than or equal to 70 percent stenotic.

Type de données

text

Alias
UMLS CUI-1
N
Diagnostic Cath Contraindication
Description

Indicate if a catheterization was not performed because it was contraindicated.

Type de données

boolean

Alias
UMLS CUI-1
C1532338
UMLS CUI-2
C0522473
UMLS CUI-3
P
PCI
Description

Indicate if the patient had a percutaneous coronary intervention (PCI).

Type de données

boolean

Alias
UMLS CUI-1
C1532338
Cath Lab Arrival Date/Time
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.

Type de données

datetime

Alias
UMLS CUI-1
C3838354
First Device Activation Date/Time
Description

Indicate the date and time the first device was activated regardless of type of device used.

Type de données

datetime

Alias
UMLS CUI-1
N
Arterial Access Site
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.

Type de données

text

Alias
UMLS CUI-1
C3272298
Stent(s) Placed
Description

Indicate if a stent or stents were placed in the affected coronary artery.

Type de données

boolean

Alias
UMLS CUI-1
C3272316
Stent Type(s)
Description

Stent Type(s)

Type de données

text

PCI Indication
Description

Indicate the primary reason PCI was performed or attempted.

Type de données

text

Alias
UMLS CUI-1
C1532338
UMLS CUI-2
C0392360
UMLS CUI-3
P
Non-system Reason for Delay in PCI
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).

Type de données

text

Alias
UMLS CUI-1
C3640267
CABG
Description

Indicate if the patient had a CABG (coronary artery bypass graft surgery).

Type de données

boolean

Alias
UMLS CUI-1
C0010055
CABG Date
Description

Indicate the date of the coronary artery bypass graft (CABG) surgery.

Type de données

datetime

Alias
UMLS CUI-1
C0010055
UMLS CUI-2
C0011008
UMLS CUI-3
P
Patient treated with an in-hospital hypothermia protocol
Description

Indicate if an in-hospital hypothermia protocol was initiated.

Type de données

boolean

Alias
UMLS CUI-1
C0150255
In-Hospital hypothermia protocol initiated Location
Description

Indicate the location where the hypothermia protocol was initiated.

Type de données

text

Alias
UMLS CUI-1
N
Reperfusion Strategy
Description

Reperfusion Strategy

Reperfusion Candidate
Description

Indicate if the STEMI patient is a reperfusion candidate for primary PCI or Thrombolytic therapy.

Type de données

boolean

Alias
UMLS CUI-1
C0035124
Primary Reason No Reperfusion
Description

Indicate the one primary reason, documented in the medical record, that reperfusion therapy (thrombolytic therapy or primary PCI) was not indicated.

Type de données

text

Alias
UMLS CUI-1
N
Primary PCI
Description

Indicate if the patient received primary PCI as an urgent treatment for STEMI.

Type de données

boolean

Alias
UMLS CUI-1
C3275089
Thrombolytics
Description

Indicate if the patient received thrombolytic therapy as an urgent treatment for STEMI.

Type de données

boolean

Alias
UMLS CUI-1
C0040044
Strength of Thrombolytic Dose
Description

Indicate the strength of dose of the thrombolytic.

Type de données

text

Alias
UMLS CUI-1
C0178602
UMLS CUI-2
C0040044
UMLS CUI-3
P
Type of Thrombolytics
Description

Indicate the type of thrombolytic first administered.

Type de données

text

Alias
UMLS CUI-1
C0040044
Thrombolytic Therapy Start Date/Time
Description

Thrombolytic Therapy Start Date/Time

Type de données

datetime

Alias
UMLS CUI-1
C0040044
UMLS CUI-2
C1301880
UMLS CUI-3
P
Non-System Reason for Delay
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).

Type de données

boolean

Alias
UMLS CUI-1
N
Lytic Ineligible and require prolonged transfer for Primary PCI
Description

Indicate if the patient was Lytic ineligible and required prolonged transfer time for primary PCI.

Type de données

boolean

Alias
UMLS CUI-1
N
Reason Primary PCI Not Performed
Description

Indicate the one primary reason, documented in the medical record, that primary PCI was not performed as reperfusion therapy.

Type de données

text

Alias
UMLS CUI-1
C0522473
UMLS CUI-2
C1532338
UMLS CUI-3
P
Reason Thrombolytics Not Administered
Description

Indicate the one primary reason, documented in the medical record, that thrombolytics were not administered as reperfusion therapy.

Type de données

text

Alias
UMLS CUI-1
C3260558
In-Hospital clinical events
Description

In-Hospital clinical events

Reinfarction
Description

Indicate if there are clinical signs and symptoms of a new infarction or repeat infarction.

Type de données

boolean

Alias
UMLS CUI-1
C2882123
Reinfarction date
Description

Indicate the date when the clinical signs and symptoms of the new myocardial infarction first occurred.

Type de données

date

Alias
UMLS CUI-1
C2882123
UMLS CUI-2
C0011008
UMLS CUI-3
P
Cardiogenic Shock
Description

Indicate if the patient had a new onset or acute recurrence of cardiogenic shock in your facility.

Type de données

boolean

Alias
UMLS CUI-1
C0036980
Cardiogenic Shock Date
Description

Indicate the date when a diagnosis of cardiogenic shock was made.

Type de données

date

Alias
UMLS CUI-1
C0036980
UMLS CUI-2
C0011008
UMLS CUI-3
P
Heart failure
Description

Indicate if there is physician documentation or report of either new onset or acute reoccurrence of heart failure.

Type de données

boolean

Alias
UMLS CUI-1
C0018801
Heart failure date
Description

Indicate the date of the new onset or acute reoccurrence of heart failure.

Type de données

date

Alias
UMLS CUI-1
C2984177
CVA/Stroke
Description

Indicate if the patient experienced a stroke or cerebrovascular accident (CVA) in your facility.

Type de données

boolean

Alias
UMLS CUI-1
C0038454
CVA/Stroke Date
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.

Type de données

date

Alias
UMLS CUI-1
C0038454
UMLS CUI-2
C0011008
UMLS CUI-3
P
Hemorrhagic Stroke
Description

Indicate if the patient experienced a hemorrhagic stroke with documentation on imaging.

Type de données

boolean

Alias
UMLS CUI-1
C0553692
Atrial Fibrillation
Description

Indicate if the patient experienced atrial fibrillation during the current admission.

Type de données

boolean

Alias
UMLS CUI-1
C0004238
Atrial Fibrillation Date
Description

Indicate the date the patient experienced episode of atrial fibrillation.

Type de données

date

Alias
UMLS CUI-1
C0004238
UMLS CUI-2
C0011008
UMLS CUI-3
P
VTach/VFib
Description

Indicate if the patient experienced VTach and/or VFib during the current admission.

Type de données

boolean

Alias
UMLS CUI-1
C0042514
UMLS CUI-2
C0042510
VTach/VFib Date
Description

Indicate the date the patient experienced VTach and/or VFib.

Type de données

date

Alias
UMLS CUI-1
C0042514
UMLS CUI-2
C0011008
UMLS CUI-3
P
UMLS CUI-4
C0042510
UMLS CUI-5
C0011008
UMLS CUI-6
P
Cardiac arrest
Description

Indicate if the patient experienced an episode of cardiac arrest in your facility.

Type de données

boolean

Alias
UMLS CUI-1
C0018790
Cardiac Arrest Date
Description

Indicate the date of the cardiac arrest.

Type de données

date

Alias
UMLS CUI-1
C2825160
Suspected bleeding event
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).

Type de données

boolean

Alias
UMLS CUI-1
C0019080
Suspected Bleeding Event Date
Description

Indicate the date of the suspected bleeding event.

Type de données

date

Alias
UMLS CUI-1
C0019080
UMLS CUI-2
C0011008
UMLS CUI-3
P
Suspected Bleeding Event Location
Description

Suspected Bleeding Event Location

Type de données

text

Alias
UMLS CUI-1
C0019080
UMLS CUI-2
C0450429
UMLS CUI-3
P
Surgical Procedure or Intervention Required
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).

Type de données

boolean

Alias
UMLS CUI-1
C3841143
RBC/Whole Blood Transfusion
Description

Indicate if there was a transfusion of either whole blood or packed red blood cells.

Type de données

boolean

Alias
UMLS CUI-1
C1879316
UMLS CUI-2
C0086252
First Transfusion Date
Description

Indicate the date of the first whole blood or red blood cell transfusion.

Type de données

date

Alias
UMLS CUI-1
C0808300
Transfusion Related to CABG
Description

Indicate if any red blood cell/whole blood transfusion was related to CABG.

Type de données

boolean

Alias
UMLS CUI-1
N
New Requirement for Dialysis
Description

Indicate if the patient experienced acute or worsening renal failure necessitating renal dialysis.

Type de données

boolean

Alias
UMLS CUI-1
C0011946
New Requirement for Dialysis Date
Description

Indicate the date of acute or worsening renal failure leading to a new requirement for dialysis.

Type de données

date

Alias
UMLS CUI-1
N
Mechanical Support
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).

Type de données

text

Alias
UMLS CUI-1
C0457617
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Similar models

ACTION Registry

1 Formulaires
  1. StudyEvent: ODM
    1. ACTION Registry
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Demographics
C0011298 (UMLS CUI-1)
Last Name
Item
Indicate the patient's last name. Hyphenated names should be recorded with a hyphen.
text
C1301584 (UMLS CUI-1)
First name
Item
First name
text
C1443235 (UMLS CUI-1)
Middle Name
Item
Middle Name
text
C2598119 (UMLS CUI-1)
Social security number
Item
SSN
text
C1301821 (UMLS CUI-1)
Social security number not availiable
Item
SSNA N/A
boolean
C1547437 (UMLS CUI-1)
Patient ID
Item
Patient ID
integer
C2348585 (UMLS CUI-1)
Other ID
Item
Other ID
integer
Date of birth
Item
Birth Date
date
C0421451 (UMLS CUI-1)
Item
Sex
text
C0079399 (UMLS CUI-1)
Sex
Code List
Sex
CL Item
Male (1)
C0024554 (UMLS CUI-1)
CL Item
Female (2)
C0015780 (UMLS CUI-1)
Postal code
Item
Patient Zip Code
text
C0421454 (UMLS CUI-1)
Postal code not availiable
Item
ZIP Code N/A
boolean
C2600019 (UMLS CUI-1)
Item
Race
text
C0034510 (UMLS CUI-1)
Race
Code List
Race
CL Item
White (1)
C0007457 (UMLS CUI-1)
CL Item
Black/African American (2)
C0085756 (UMLS CUI-1)
CL Item
American Indian/Alaskan Native (3)
C0002460 (UMLS CUI-1)
C0597091 (UMLS CUI-2)
CL Item
Asian (4)
C0078988 (UMLS CUI-1)
CL Item
Native Hawaiian/Pacific Islander (5)
C0337920 (UMLS CUI-1)
C0242191 (UMLS CUI-2)
Item
If Asian, specify:
text
Asian Race
Code List
If Asian, specify:
CL Item
Indian (1)
C1524069 (UMLS CUI-1)
CL Item
Chinese (2)
C0152035 (UMLS CUI-1)
CL Item
Filipino (3)
C1556093 (UMLS CUI-1)
CL Item
Japanese (4)
C1556094 (UMLS CUI-1)
CL Item
Korean (5)
C1556095 (UMLS CUI-1)
CL Item
Vietnamese (6)
C1561452 (UMLS CUI-1)
CL Item
Other (7)
C0438971 (UMLS CUI-1)
Item
If Native Hawaiian/Pacific Islander, specify:
text
Native Hawaiian/Pacific Islander Race
Code List
If Native Hawaiian/Pacific Islander, specify:
CL Item
Native Hawaiian (1)
C0337920 (UMLS CUI-1)
CL Item
Guamanian or Chamorro (2)
C1553342 (UMLS CUI-1)
CL Item
Samoan (3)
C1556103 (UMLS CUI-1)
CL Item
Other Island (4)
C1553351 (UMLS CUI-1)
Item
Hispanic or Latino Ethnicity
text
C0015031 (UMLS CUI-1)
Ethnicity
Code List
Hispanic or Latino Ethnicity
CL Item
Mexican, Mexican-American, Chicano (1)
C3829110 (UMLS CUI-1)
CL Item
Puerto Rican (2)
C0034043 (UMLS CUI-1)
CL Item
Cuban (3)
C1553379 (UMLS CUI-1)
CL Item
Other Hispanic, Latino or Spanish Origin (4)
C3844642 (UMLS CUI-1)
Item Group
Admission
Item
Means of Transport to First Facility
text
C3258270 (UMLS CUI-1)
Means of Transport
Code List
Means of Transport to First Facility
CL Item
Self/Family (1)
C0497714 (UMLS CUI-1)
CL Item
Ambulance (2)
C1699601 (UMLS CUI-1)
CL Item
Air (3)
C3841560 (UMLS CUI-1)
Time of emergency service contact
Item
EMS 1st Med. Contact Date/Time
datetime
C1320531 (UMLS CUI-1)
EMS Dispatch Date/Time
Item
EMS Dispatch Date/Time
datetime
C3261085 (UMLS CUI-1)
C1264639 (UMLS CUI-2)
P (UMLS CUI-3)
Non-EMS first medical contact date/time
Item
Non-EMS 1st Med. Contact Date/Time
datetime
N (UMLS CUI-1)
EMS Leaving Scene Date/Time
Item
EMS Leaving Scene Date/Time
datetime
N (UMLS CUI-1)
EMS Agency Number
Item
EMS Agency Number
integer
N (UMLS CUI-1)
EMS Run Number
Item
EMS Run Number
integer
N (UMLS CUI-1)
Catheterization lab activation date/time
Item
Cath Lab Activation Date/Time
datetime
N (UMLS CUI-1)
Transfer patient
Item
Transferred from Outside Facility
boolean
C1546432 (UMLS CUI-1)
Item
Means of Transfer from outside facility
text
C0449375 (UMLS CUI-1)
Means of transport of transfer patient
Code List
Means of Transfer from outside facility
CL Item
Ambulance (1)
C1699601 (UMLS CUI-1)
CL Item
Air (2)
C3841560 (UMLS CUI-1)
Arrival at Outside Facility Date/Time
Item
Arrival at Outside Facility Date/Time
datetime
C1320532 (UMLS CUI-1)
Transfer from outside hospital date/time
Item
Transfer from Outside Facility Date/Time
datetime
C1546432 (UMLS CUI-1)
C0011008 (UMLS CUI-2)
P (UMLS CUI-3)
Name of Transferring Facility/AHA Number
Item
Name of Transferring Facility/AHA Number
text
N (UMLS CUI-1)
Arrival Date/Time
Item
Arrival Date/Time
datetime
C1320532 (UMLS CUI-1)
Admission Date
Item
Admission Date
date
C1302393 (UMLS CUI-1)
Item
Location of First Evaluation
text
N (UMLS CUI-1)
Location of First Evaluation
Code List
Location of First Evaluation
CL Item
ED (1)
CL Item
Cath Lab (2)
CL Item
Other (3)
Transfer out of ED date/time
Item
ED Transfer Out Date/Time
datetime
C3495034 (UMLS CUI-1)
C0011008 (UMLS CUI-2)
P (UMLS CUI-3)
Item
Insurance Payors
text
C0021672 (UMLS CUI-1)
Insurance Payors
Code List
Insurance Payors
CL Item
Private Health Insurance (1)
C2347682 (UMLS CUI-1)
CL Item
Medicare (2)
C0018717 (UMLS CUI-1)
CL Item
Medicaid (3)
C0025071 (UMLS CUI-1)
CL Item
Military Health Care (4)
C3242021 (UMLS CUI-1)
CL Item
State-Specific Plan (non-Medicaid) (5)
CL Item
Indian Health Service (6)
C0085141 (UMLS CUI-1)
CL Item
Non-US Insurance (7)
C0027453 (UMLS CUI-1)
CL Item
Non (8)
C3530214 (UMLS CUI-1)
Primary practitioner name
Item
Provider Name
text
C0807500 (UMLS CUI-1)
Admitting Provider NPI
Item
Admitting Provider NPI
text
C1549728 (UMLS CUI-1)
C1547428 (UMLS CUI-2)
P (UMLS CUI-3)
Health Insurance Claim Number
Item
HIC #
integer
N (UMLS CUI-1)
Item Group
Cardiac status on first medical contact
Symptom Onset Date/Time
Item
Symptom Onset Date/Time
datetime
C1320528 (UMLS CUI-1)
Symptom Onset Time Estimated
Item
Symptom Onset Time Estimated
boolean
C1320528 (UMLS CUI-1)
C0750572 (UMLS CUI-2)
P (UMLS CUI-3)
Symptom Onset Time Not Available
Item
Symptom Onset Time Not Available
boolean
C1320528 (UMLS CUI-1)
C0439673 (UMLS CUI-2)
P (UMLS CUI-3)
Item
First ECG Obtained
text
N (UMLS CUI-1)
Location of first ECG
Code List
First ECG Obtained
CL Item
Pre-Hospital (e.g. ambulance) (1)
CL Item
After 1st hosp. arrival (2)
First ECG Date/Time
Item
First ECG Date/Time
datetime
N (UMLS CUI-1)
First ECG Reason For Delay
Item
First ECG Non-System Reason For Delay
boolean
N (UMLS CUI-1)
STEMI or STEMI Equivalent
Item
STEMI or STEMI Equivalent
boolean
C3538872 (UMLS CUI-1)
Item
ECG Findings
text
C0438154 (UMLS CUI-1)
ECG evidence for STEMI or STEMI equivalent
Code List
ECG Findings
CL Item
ST elevation (1)
C0520886 (UMLS CUI-1)
CL Item
LBBB (2)
C0023211 (UMLS CUI-1)
CL Item
Isolated posterior MI (3)
C3642316 (UMLS CUI-1)
Item
STEMI or STEMI Equivalent First Noted
text
N (UMLS CUI-1)
ECG STEMI or STEMI equivalent noted
Code List
STEMI or STEMI Equivalent First Noted
CL Item
First ECG (1)
CL Item
Subsequent ECG (2)
Subsequent ECG with STEMI or STEMI Equivalent Date/Time
Item
Subsequent ECG with STEMI or STEMI Equivalent Date/Time
datetime
N (UMLS CUI-1)
Item
Other ECG Findings
text
C0438154 (UMLS CUI-1)
Other ECG Findings
Code List
Other ECG Findings
CL Item
New or presumed new ST depression (1)
C0520887 (UMLS CUI-1)
CL Item
New or presumed new T-Wave inversion (2)
C0520888 (UMLS CUI-1)
CL Item
Transient ST elevation lasting < 20 minutes (3)
C0520886 (UMLS CUI-1)
CL Item
Old LBBB (4)
C0023211 (UMLS CUI-1)
CL Item
None (5)
CL Item
Other (6)
Heart failure
Item
Heart failure
boolean
C0018801 (UMLS CUI-1)
Cardiogenic Shock
Item
Cardiogenic Shock
boolean
C0036980 (UMLS CUI-1)
Heart Rate
Item
Heart Rate
integer
C0018810 (UMLS CUI-1)
Systolic Blood Pressure
Item
Systolic BP
integer
C0871470 (UMLS CUI-1)
Cardiac Arrest
Item
Cardiac Arrest
boolean
C0018790 (UMLS CUI-1)
Cardiac Arrest Pre-Hospital
Item
Cardiac Arrest Pre-Hospital
boolean
N (UMLS CUI-1)
Cardiac Arrest Outside Facility
Item
Cardiac Arrest Outside Facility
boolean
C2936490 (UMLS CUI-1)
Item Group
History and Risk Factors
C0035648 (UMLS CUI-1)
Height
Item
Height
integer
C0005890 (UMLS CUI-1)
Weight
Item
Weight
float
C0005910 (UMLS CUI-1)
Current/Recent Smoker
Item
Current/Recent Smoker (w/in 1 year)
boolean
C3241966 (UMLS CUI-1)
C0337671 (UMLS CUI-2)
History of Hypertension
Item
Hypertension
boolean
C0455527 (UMLS CUI-1)
Dyslipidemia
Item
Dyslipidemia
boolean
C0242339 (UMLS CUI-1)
Currently on Dialysis
Item
Currently on Dialysis
boolean
C0455667 (UMLS CUI-1)
Diabetes Mellitus
Item
Diabetes Mellitus
boolean
C0011849 (UMLS CUI-1)
Item
Diabetes Therapy
text
C3274787 (UMLS CUI-1)
Diabetes Therapy
Code List
Diabetes Therapy
CL Item
None (1)
C3275118 (UMLS CUI-1)
CL Item
Diet (2)
C0421246 (UMLS CUI-1)
CL Item
Oral (3)
C0421247 (UMLS CUI-1)
CL Item
Insulin (4)
C0421248 (UMLS CUI-1)
CL Item
Other (5)
Prior MI
Item
Prior MI
boolean
C1275835 (UMLS CUI-1)
Cancer
Item
Cancer
boolean
C0006826 (UMLS CUI-1)
Item
Cancer Type
text
C0872066 (UMLS CUI-1)
Cancer Type
Code List
Cancer Type
CL Item
Solid Organ (1)
C0280100 (UMLS CUI-1)
CL Item
Hematologic (2)
C0376545 (UMLS CUI-1)
Prior Heart Failure
Item
Prior Heart Failure
boolean
C0455531 (UMLS CUI-1)
Prior PCI
Item
Prior PCI
boolean
C1320647 (UMLS CUI-1)
Most Recent PCI Date
Item
Most Recent PCI Date
date
C1532338 (UMLS CUI-1)
C1264639 (UMLS CUI-2)
P (UMLS CUI-3)
Prior CABG
Item
Prior CABG
boolean
C1275842 (UMLS CUI-1)
Most Recent CABG Date
Item
Most Recent CABG Date
date
C2164190 (UMLS CUI-1)
Atrial Fibrillation or Flutter
Item
Atrial Fibrillation or Flutter
boolean
C0004238 (UMLS CUI-1)
C0004239 (UMLS CUI-2)
Cerebrovascular Disease
Item
Cerebrovascular Disease
boolean
C0007820 (UMLS CUI-1)
Prior Stroke
Item
Prior Stroke
boolean
C0559159 (UMLS CUI-1)
Prior Transient Ischemic Attack
Item
Prior TIA
boolean
C0007787 (UMLS CUI-1)
C0455536 (UMLS CUI-2)
Item
Walking
text
C0080331 (UMLS CUI-1)
Walking
Code List
Walking
CL Item
Unassisted (1)
C0429988 (UMLS CUI-1)
CL Item
Assisted (2)
C1286783 (UMLS CUI-1)
CL Item
Wheelchair (3)
C0429977 (UMLS CUI-1)
CL Item
Unknown (4)
Item
Cognition
text
C0009240 (UMLS CUI-1)
Cognition
Code List
Cognition
CL Item
Normal (1)
C1846595 (UMLS CUI-1)
CL Item
Mildly impaired (2)
C1291708 (UMLS CUI-1)
CL Item
Mod/Severely impaired (3)
C1291708 (UMLS CUI-1)
C1291708 (UMLS CUI-2)
CL Item
Unknown (4)
Item
Basic ADLs
text
C0001288 (UMLS CUI-1)
acitivities of daily living
Code List
Basic ADLs
CL Item
Independent of all ADLs (1)
C3840941 (UMLS CUI-1)
CL Item
Partial assist > (2)
CL Item
Full assist > (3)
C2732873 (UMLS CUI-1)
CL Item
Unknown (4)
Item Group
Medications
Item
Aspirin
text
C0004057 (UMLS CUI-1)
Aspirin
Code List
Aspirin
CL Item
Home Medication (1)
C1964151 (UMLS CUI-1)
CL Item
Administered in first 24 hours (2)
CL Item
Prescribed at discharge (3)
Aspirin contraindicated
Item
Aspirin contraindicated
boolean
C0729798 (UMLS CUI-1)
Item
Clopidogrel
text
C0070166 (UMLS CUI-1)
Aspirin
Code List
Clopidogrel
CL Item
Home Medication (1)
C1964151 (UMLS CUI-1)
CL Item
Administered in first 24 hours (2)
CL Item
Prescribed at discharge (3)
Clopidogrel dose
Item
Clopidogrel dose
float
C0070166 (UMLS CUI-1)
C0178602 (UMLS CUI-2)
P (UMLS CUI-3)
Clopidogrel contraindicated
Item
Clopidogrel contraindicated
boolean
C1319916 (UMLS CUI-1)
Item
Ticlopidine
text
C0749510 (UMLS CUI-1)
Aspirin
Code List
Ticlopidine
CL Item
Home Medication (1)
C1964151 (UMLS CUI-1)
CL Item
Administered in first 24 hours (2)
CL Item
Prescribed at discharge (3)
Ticlodipine dose
Item
Ticlodipine dose
float
C0749510 (UMLS CUI-1)
C0178602 (UMLS CUI-2)
P (UMLS CUI-3)
Ticlopidine contraindicated
Item
Ticlopidine contraindicated
boolean
C0749510 (UMLS CUI-1)
C0522473 (UMLS CUI-2)
P (UMLS CUI-3)
Item
Prasugrel
text
C1620287 (UMLS CUI-1)
Aspirin
Code List
Prasugrel
CL Item
Home Medication (1)
C1964151 (UMLS CUI-1)
CL Item
Administered in first 24 hours (2)
CL Item
Prescribed at discharge (3)
Prasugrel Dose
Item
Prasugrel Dose
float
C1620287 (UMLS CUI-1)
C0178602 (UMLS CUI-2)
P (UMLS CUI-3)
Prasugrel contraindicated
Item
Prasugrel contraindicated
boolean
C1620287 (UMLS CUI-1)
C0522473 (UMLS CUI-2)
P (UMLS CUI-3)
Item
Ticagrelor
text
C1999375 (UMLS CUI-1)
Aspirin
Code List
Ticagrelor
CL Item
Home Medication (1)
C1964151 (UMLS CUI-1)
CL Item
Administered in first 24 hours (2)
CL Item
Prescribed at discharge (3)
Ticagrelor Contraindicated
Item
Ticagrelor Contraindicated
boolean
C1999375 (UMLS CUI-1)
C0522473 (UMLS CUI-2)
P (UMLS CUI-3)
Item
Warfarin
text
C0043031 (UMLS CUI-1)
Aspirin
Code List
Warfarin
CL Item
Home Medication (1)
C1964151 (UMLS CUI-1)
CL Item
Administered in first 24 hours (2)
CL Item
Prescribed at discharge (3)
Warfarin contraindicated
Item
Warfarin contraindicated
boolean
C0043031 (UMLS CUI-1)
C0522473 (UMLS CUI-2)
P (UMLS CUI-3)
Item
Dabigatran
text
C2348066 (UMLS CUI-1)
Aspirin
Code List
Dabigatran
CL Item
Home Medication (1)
C1964151 (UMLS CUI-1)
CL Item
Administered in first 24 hours (2)
CL Item
Prescribed at discharge (3)
Dabigatran contraindicated
Item
Dabigatran contraindicated
boolean
C2348066 (UMLS CUI-1)
C0522473 (UMLS CUI-2)
Item
Rivaroxaban
text
C1739768 (UMLS CUI-1)
Aspirin
Code List
Rivaroxaban
CL Item
Home Medication (1)
C1964151 (UMLS CUI-1)
CL Item
Administered in first 24 hours (2)
CL Item
Prescribed at discharge (3)
Rivaroxaban contraindicated
Item
Rivaroxaban contraindicated
boolean
C1739768 (UMLS CUI-1)
C0522473 (UMLS CUI-2)
P (UMLS CUI-3)
Item
Apixiban
text
N (UMLS CUI-1)
Aspirin
Code List
Apixiban
CL Item
Home Medication (1)
C1964151 (UMLS CUI-1)
CL Item
Administered in first 24 hours (2)
CL Item
Prescribed at discharge (3)
Apixiban Contraindicated
Item
Apixiban Contraindicated
boolean
N (UMLS CUI-1)
Item
Beta Blocker
text
C0304516 (UMLS CUI-1)
Aspirin
Code List
Beta Blocker
CL Item
Home Medication (1)
C1964151 (UMLS CUI-1)
CL Item
Administered in first 24 hours (2)
CL Item
Prescribed at discharge (3)
Beta Blocker Contraindicated
Item
Beta Blocker Contraindicated
boolean
C1278474 (UMLS CUI-1)
Item
ACE Inhibitor
text
C0003015 (UMLS CUI-1)
Aspirin
Code List
ACE Inhibitor
CL Item
Home Medication (1)
C1964151 (UMLS CUI-1)
CL Item
Administered in first 24 hours (2)
CL Item
Prescribed at discharge (3)
ACE inhibitor contraindicated
Item
ACE inhibitor contraindicated
boolean
C0003015 (UMLS CUI-1)
C0522473 (UMLS CUI-2)
P (UMLS CUI-3)
Item
Angiotensin Receptor Blocker
text
C0521942 (UMLS CUI-1)
Aspirin
Code List
Angiotensin Receptor Blocker
CL Item
Home Medication (1)
C1964151 (UMLS CUI-1)
CL Item
Administered in first 24 hours (2)
CL Item
Prescribed at discharge (3)
ARB contraindiacted
Item
Angiotensin Receptor Blocker contraindiacted
boolean
C0521942 (UMLS CUI-1)
C0522473 (UMLS CUI-2)
P (UMLS CUI-3)
Item
Aldosterone Blocking Agent
text
C0002007 (UMLS CUI-1)
Aspirin
Code List
Aldosterone Blocking Agent
CL Item
Home Medication (1)
C1964151 (UMLS CUI-1)
CL Item
Administered in first 24 hours (2)
CL Item
Prescribed at discharge (3)
Aldosterone blocking agent contraindicated
Item
Aldosterone blocking agent contraindicated
boolean
C0002007 (UMLS CUI-1)
C0522473 (UMLS CUI-2)
P (UMLS CUI-3)
Item
Statin
text
C0360714 (UMLS CUI-1)
Aspirin
Code List
Statin
CL Item
Home Medication (1)
C1964151 (UMLS CUI-1)
CL Item
Administered in first 24 hours (2)
CL Item
Prescribed at discharge (3)
Statin dose
Item
Statin dose
text
C0360714 (UMLS CUI-1)
C0178602 (UMLS CUI-2)
P (UMLS CUI-3)
Statin contraindicated
Item
Statin contraindicated
boolean
C1277178 (UMLS CUI-1)
Item
Non-Statin Lipid-Lowering Agent
text
Aspirin
Code List
Non-Statin Lipid-Lowering Agent
CL Item
Home Medication (1)
C1964151 (UMLS CUI-1)
CL Item
Administered in first 24 hours (2)
CL Item
Prescribed at discharge (3)
Item
GP IIb/IIIa Inhibitor
text
C3640054 (UMLS CUI-1)
GP IIb/IIIa blocker
Code List
GP IIb/IIIa Inhibitor
CL Item
Eptifibatide (1)
C0253563 (UMLS CUI-1)
CL Item
Tirofiban (2)
C0247025 (UMLS CUI-1)
CL Item
Abciximab (3)
C0288672 (UMLS CUI-1)
Item
GP IIb/IIIa blocker dosage
text
C3640054 (UMLS CUI-1)
C0178602 (UMLS CUI-2)
P (UMLS CUI-3)
GP IIb/IIIa blocker dosage
Code List
GP IIb/IIIa blocker dosage
CL Item
Full (1)
CL Item
Reduced (2)
CL Item
Other (3)
GP IIb/IIIa inhibitor administered start date/time
Item
GP IIb/IIIa inhibitor start date/time
datetime
C1301880 (UMLS CUI-1)
C1301880 (UMLS CUI-2)
P (UMLS CUI-3)
Anticoagulant
Item
Anticoagulant
boolean
C0003280 (UMLS CUI-1)
Anticoagulant contraindicated
Item
Anticoagulant contraindicated
boolean
C1531588 (UMLS CUI-1)
Unfractionated Heparin
Item
Unfractionated Heparin
boolean
C2825026 (UMLS CUI-1)
Unfractionated Heparin Dose
Item
Unfractionated Heparin Dose
integer
C2825026 (UMLS CUI-1)
C0178602 (UMLS CUI-2)
P (UMLS CUI-3)
Unfractionated Heparin Start Date/Time
Item
Unfractionated Heparin Start Date/Time
datetime
C1301880 (UMLS CUI-1)
C2825026 (UMLS CUI-2)
P (UMLS CUI-3)
LMWH
Item
Enoxaparin (LMWH)
boolean
C3536766 (UMLS CUI-1)
LMWH Start Date/Time
Item
LMWH Start Date/Time
datetime
C3536766 (UMLS CUI-1)
C1301880 (UMLS CUI-2)
P (UMLS CUI-3)
Item
LMWH injection frequency
text
N (UMLS CUI-1)
LMWH injection frequency
Code List
LMWH injection frequency
CL Item
12hr (1)
CL Item
24hr (2)
CL Item
None (3)
LMWH dose
Item
LMWH dose
float
C3536766 (UMLS CUI-1)
C0178602 (UMLS CUI-2)
P (UMLS CUI-3)
Bivalirudin
Item
Bivalirudin
boolean
C0168273 (UMLS CUI-1)
Bivalirudin Start Date/Time
Item
Bivalirudin Start Date/Time
datetime
C1301880 (UMLS CUI-1)
C0168273 (UMLS CUI-2)
P (UMLS CUI-3)
Other parenteral anticoagulants given
Item
Other parenteral anticoagulants given
boolean
Item Group
Procedures and Tests
Noninvasive Stress Testing
Item
Non-invasive Stress Testing
boolean
C3272313 (UMLS CUI-1)
Date of noninvasive stress testing
Item
Noninvasive stress testing Date
datetime
C3272313 (UMLS CUI-1)
C0011008 (UMLS CUI-2)
P (UMLS CUI-3)
LVEF
Item
LVEF
float
C0428772 (UMLS CUI-1)
LVEF not assessed
Item
LVEF not assessed
boolean
C3248481 (UMLS CUI-1)
LVEF planned for after discharge
Item
LVEF planned for after discharge
boolean
C3248276 (UMLS CUI-1)
Diagnostic Coronary Angiography
Item
Diagnostic Coronary Angiography
boolean
C0085532 (UMLS CUI-1)
Diagnostic Coronary Angiography Date
Item
Diagnostic Coronary Angiography Date
date
C0085532 (UMLS CUI-1)
C0011008 (UMLS CUI-2)
P (UMLS CUI-3)
Item
Number of Diseased Vessels
text
C3275120 (UMLS CUI-1)
Number of Diseased Vessels
Code List
Number of Diseased Vessels
CL Item
None (1)
CL Item
1 (2)
C3275121 (UMLS CUI-1)
CL Item
2 (3)
C0581375 (UMLS CUI-1)
CL Item
3 (4)
C3272265 (UMLS CUI-1)
Left Main Stenosis >=50%
Item
Left Main Stenosis >=50%
boolean
C2825221 (UMLS CUI-1)
Item
Left Main Stenosis Graft is Present
text
N (UMLS CUI-1)
Left Main Stenosis Graft is Present
Code List
Left Main Stenosis Graft is Present
CL Item
No (1)
CL Item
Yes - graft patent (2)
C0428829 (UMLS CUI-1)
CL Item
Yes - graft not patent (3)
C0428830 (UMLS CUI-1)
Proximal LAD Stenosis
Item
Proximal LAD Stenosis >= 70%
boolean
C2825222 (UMLS CUI-1)
Item
Proximal LAD Graft is Present
text
N (UMLS CUI-1)
Left Main Stenosis Graft is Present
Code List
Proximal LAD Graft is Present
CL Item
No (1)
CL Item
Yes - graft patent (2)
C0428829 (UMLS CUI-1)
CL Item
Yes - graft not patent (3)
C0428830 (UMLS CUI-1)
Diagnostic Cath Contraindication
Item
Diagnostic Cath Contraindication
boolean
C1532338 (UMLS CUI-1)
C0522473 (UMLS CUI-2)
P (UMLS CUI-3)
PCI
Item
PCI
boolean
C1532338 (UMLS CUI-1)
Cath Lab Arrival Date/Time
Item
Cath Lab Arrival Date/Time
datetime
C3838354 (UMLS CUI-1)
First Device Activation Date/Time
Item
First Device Activation Date/Time
datetime
N (UMLS CUI-1)
Item
Arterial Access Site
text
C3272298 (UMLS CUI-1)
Arterial Access Site
Code List
Arterial Access Site
CL Item
Femoral (1)
CL Item
Brachial (2)
CL Item
Radial (3)
CL Item
Other (4)
Stent(s) Placed
Item
Stent(s) Placed
boolean
C3272316 (UMLS CUI-1)
Item
Stent Type(s)
text
Stent type
Code List
Stent Type(s)
CL Item
Bare metal stent (1)
C2825200 (UMLS CUI-1)
CL Item
Drug eluting stent (2)
C1322815 (UMLS CUI-1)
CL Item
Other (3)
Item
PCI Indication
text
C1532338 (UMLS CUI-1)
C0392360 (UMLS CUI-2)
P (UMLS CUI-3)
PCI Indication
Code List
PCI Indication
CL Item
Primary PCI for STEMI (1)
C3275089 (UMLS CUI-1)
CL Item
Rescue PCI for STEMI (after failed full-dose lytic) (2)
C3272253 (UMLS CUI-1)
CL Item
PCI for NSTEMI (3)
C3275123 (UMLS CUI-1)
CL Item
PCI for STEMI (stable after successful full-dose lytic) (4)
C3272246 (UMLS CUI-1)
CL Item
PCI for STEMI (unstable, >12 hr from sx onset) (5)
C3272247 (UMLS CUI-1)
CL Item
PCI for STEMI (stable, >12 hr from sx onset) (6)
C3272245 (UMLS CUI-1)
CL Item
Other (7)
Item
Non-system Reason for Delay in PCI
text
C3640267 (UMLS CUI-1)
Non-system Reason for Delay in PCI
Code List
Non-system Reason for Delay in PCI
CL Item
Difficult vascular access (1)
C3275076 (UMLS CUI-1)
CL Item
Cardiac arrest and/or need for intubation before PCI (2)
C3275053 (UMLS CUI-1)
CL Item
Patient delays in providing consent for the procedure O Difficulty crossing the culprit lesion during the PCI procedure (3)
C3272261 (UMLS CUI-1)
CL Item
Other (4)
CL Item
None (5)
CABG
Item
CABG
boolean
C0010055 (UMLS CUI-1)
CABG surgery date/time
Item
CABG Date
datetime
C0010055 (UMLS CUI-1)
C0011008 (UMLS CUI-2)
P (UMLS CUI-3)
Patient treated with an in-hospital hypothermia protocoI
Item
Patient treated with an in-hospital hypothermia protocol
boolean
C0150255 (UMLS CUI-1)
Item
In-Hospital hypothermia protocol initiated Location
text
N (UMLS CUI-1)
In-Hospital hypothermia protocol initiated Location
Code List
In-Hospital hypothermia protocol initiated Location
CL Item
Pre-Hospital (1)
CL Item
ER (2)
CL Item
Cath Lab (3)
CL Item
ICU/CCU (4)
Item Group
Reperfusion Strategy
Reperfusion Candidate
Item
Reperfusion Candidate
boolean
C0035124 (UMLS CUI-1)
Item
Primary Reason No Reperfusion
text
N (UMLS CUI-1)
Primary Reason Not Indicated
Code List
Primary Reason No Reperfusion
CL Item
No ST elevation/LBBB (1)
CL Item
MI diagnosis unclear (2)
CL Item
Chest pain resolved (3)
CL Item
ST elevation resolved (4)
CL Item
MI symptoms onset >12 hours (5)
CL Item
No chest pain (6)
CL Item
Other (7)
Primary PCI
Item
Primary PCI
boolean
C3275089 (UMLS CUI-1)
Thrombolytics
Item
Thrombolytics
boolean
C0040044 (UMLS CUI-1)
Item
Strength of Thrombolytic Dose
text
C0178602 (UMLS CUI-1)
C0040044 (UMLS CUI-2)
P (UMLS CUI-3)
Strength of Thrombolytic Dose
Code List
Strength of Thrombolytic Dose
CL Item
Full dose (1)
CL Item
Reduced dose (2)
Item
Type of Thrombolytics
text
C0040044 (UMLS CUI-1)
Type of Thrombolytics
Code List
Type of Thrombolytics
CL Item
Tenecteplase (1)
C0872913 (UMLS CUI-1)
CL Item
Reteplase (2)
C0256103 (UMLS CUI-1)
CL Item
Other (3)
Thrombolytics start date/time
Item
Thrombolytic Therapy Start Date/Time
datetime
C0040044 (UMLS CUI-1)
C1301880 (UMLS CUI-2)
P (UMLS CUI-3)
Non-System Reason for Thrombolytics Delay
Item
Non-System Reason for Delay
boolean
N (UMLS CUI-1)
Lytic Ineligible and require prolonged transfer for Primary PCI
Item
Lytic Ineligible and require prolonged transfer for Primary PCI
boolean
N (UMLS CUI-1)
Item
Reason Primary PCI Not Performed
text
C0522473 (UMLS CUI-1)
C1532338 (UMLS CUI-2)
P (UMLS CUI-3)
Reason Primary PCI Not Performed
Code List
Reason Primary PCI Not Performed
CL Item
Non-compressible vascular puncture(s) (1)
CL Item
Spontaneous reperfusion (documented by cath only) (2)
CL Item
Other (3)
CL Item
Active bleeding on arrival or within 24 hours (4)
CL Item
Patient/family refusal (5)
CL Item
Not performed (not a PCI center) (6)
CL Item
Quality of life decision (7)
CL Item
DNR at time of treatment decision (8)
CL Item
No reason documented (9)
CL Item
Anatomy not suitable to primary PCI (10)
CL Item
Prior allergic reaction to IV contrast (11)
CL Item
Thrombolytic Administered (12)
Item
Reason Thrombolytics Not Administered
text
C3260558 (UMLS CUI-1)
Reason Thrombolytics Not Administered
Code List
Reason Thrombolytics Not Administered
CL Item
Known bleeding diathesis (1)
CL Item
Ischemic stroke w/in 3 months except acute ischemic stroke within 3 hours (2)
CL Item
Recent bleeding within 4 weeks (3)
CL Item
Any prior intracranial hemorrhage (4)
CL Item
Recent surgery/trauma (5)
CL Item
Pregnancy (6)
CL Item
Intracranial neoplasm, AV malformation, or aneurysm (7)
CL Item
Prior allergic reaction to thrombolytics (8)
CL Item
Severe uncontrolled hypertension (9)
CL Item
DNR at time of treatment decision (10)
CL Item
Suspected aortic dissection O Other (11)
CL Item
Significant close head or facial trauma within previous 3 months (12)
CL Item
Expected DTB < 90 minutes (13)
CL Item
Active peptic ulcer (14)
CL Item
No reason documented (15)
CL Item
Traumatic CPR that precludes thrombolytics (16)
Item Group
In-Hospital clinical events
Reinfarction
Item
Reinfarction
boolean
C2882123 (UMLS CUI-1)
Reinfarction date
Item
Reinfarction date
date
C2882123 (UMLS CUI-1)
C0011008 (UMLS CUI-2)
P (UMLS CUI-3)
Cardiogenic Shock
Item
Cardiogenic Shock
boolean
C0036980 (UMLS CUI-1)
Cardiogenic Shock Date
Item
Cardiogenic Shock Date
date
C0036980 (UMLS CUI-1)
C0011008 (UMLS CUI-2)
P (UMLS CUI-3)
Heart failure
Item
Heart failure
boolean
C0018801 (UMLS CUI-1)
Heart failure date
Item
Heart failure date
date
C2984177 (UMLS CUI-1)
CVA/Stroke
Item
CVA/Stroke
boolean
C0038454 (UMLS CUI-1)
Stroke date
Item
CVA/Stroke Date
date
C0038454 (UMLS CUI-1)
C0011008 (UMLS CUI-2)
P (UMLS CUI-3)
Hemorrhagic Stroke
Item
Hemorrhagic Stroke
boolean
C0553692 (UMLS CUI-1)
Atrial Fibrillation
Item
Atrial Fibrillation
boolean
C0004238 (UMLS CUI-1)
Atrial Fibrillation Date
Item
Atrial Fibrillation Date
date
C0004238 (UMLS CUI-1)
C0011008 (UMLS CUI-2)
P (UMLS CUI-3)
Ventricular tachycardia/fibrillation
Item
VTach/VFib
boolean
C0042514 (UMLS CUI-1)
C0042510 (UMLS CUI-2)
VTach/VFib Date
Item
VTach/VFib Date
date
C0042514 (UMLS CUI-1)
C0011008 (UMLS CUI-2)
P (UMLS CUI-3)
C0042510 (UMLS CUI-4)
C0011008 (UMLS CUI-5)
P (UMLS CUI-6)
Cardiac arrest
Item
Cardiac arrest
boolean
C0018790 (UMLS CUI-1)
Cardiac Arrest Date
Item
Cardiac Arrest Date
date
C2825160 (UMLS CUI-1)
Suspected bleeding event
Item
Suspected bleeding event
boolean
C0019080 (UMLS CUI-1)
Suspected Bleeding Event Date
Item
Suspected Bleeding Event Date
date
C0019080 (UMLS CUI-1)
C0011008 (UMLS CUI-2)
P (UMLS CUI-3)
Item
Suspected Bleeding Event Location
text
C0019080 (UMLS CUI-1)
C0450429 (UMLS CUI-2)
P (UMLS CUI-3)
Suspected Bleeding Event Location
Code List
Suspected Bleeding Event Location
CL Item
Access site (1)
CL Item
Retroperitoneal (2)
CL Item
GI (3)
CL Item
GU (4)
CL Item
Other (5)
Surgical Procedure or Intervention Required
Item
Surgical Procedure or Intervention Required
boolean
C3841143 (UMLS CUI-1)
RBC/Whole Blood Transfusion
Item
RBC/Whole Blood Transfusion
boolean
C1879316 (UMLS CUI-1)
C0086252 (UMLS CUI-2)
First Transfusion Date
Item
First Transfusion Date
date
C0808300 (UMLS CUI-1)
Transfusion Related to CABG
Item
Transfusion Related to CABG
boolean
N (UMLS CUI-1)
New Requirement for Dialysis
Item
New Requirement for Dialysis
boolean
C0011946 (UMLS CUI-1)
New Requirement for Dialysis Date
Item
New Requirement for Dialysis Date
date
N (UMLS CUI-1)
Item
Mechanical Support
text
C0457617 (UMLS CUI-1)
Mechanical Support
Code List
Mechanical Support
CL Item
IABP (1)
C0021860 (UMLS CUI-1)
CL Item
Tandem Heart (2)
C3509480 (UMLS CUI-1)
CL Item
Impella (3)
C2944703 (UMLS CUI-1)
CL Item
ECMO (4)
C0015357 (UMLS CUI-1)
CL Item
LVAD (5)
C0181598 (UMLS CUI-1)
CL Item
BiVAD (6)
C0179322 (UMLS CUI-1)
CL Item
Other (7)
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