ID

12514

Beschrijving

GRACE is an international observational database of outcomes for patients who are hospitalized with an acute coronary syndrome (ACS). GRACE includes over 200 hospitals in 28 countries that enroll a total of more than 10,000 patients per year. Participating physicians receive confidential quarterly reports showing ther outcomes side-by-side with the aggregate outcomes of all participating hospitals. (http://www.outcomes-umassmed.org/GRACE/overview.aspx)

Link

http://www.outcomes-umassmed.org/GRACE/overview.aspx

Trefwoorden

  1. 15-04-15 15-04-15 -
  2. 25-11-15 25-11-15 -
Houder van rechten

Center for Outcomes Research, University of Massachusetts Medical School

Geüploaded op

25 november 2015

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY-NC 3.0

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Global registry of acute coronary events (GRACE)

GRACE Initial Form v3.5

General information
Beschrijving

General information

Patient initials
Beschrijving

Patient initials

Datatype

text

Alias
UMLS CUI-1
C2986440
Date of Birth
Beschrijving

Date of Birth (required)

Datatype

date

Alias
UMLS CUI-1
C0421451
A. Enrollment
Beschrijving

A. Enrollment

Confirmation of Eligibility per GRACE Protocol
Beschrijving

Confirmation of Eligibility per GRACE Protocol

Datatype

text

Alias
UMLS CUI [1]
C0013893
Pursuit Type
Beschrijving

Pursuit Type

Datatype

text

B. Demographics
Beschrijving

B. Demographics

Alias
UMLS CUI-1
C0011298
Postal Code (Patient Residence)
Beschrijving

Postal Code

Datatype

text

Alias
UMLS CUI-1
C0421454
Gender
Beschrijving

Gender

Datatype

text

Alias
UMLS CUI [1]
C0079399
Admission Weight
Beschrijving

Weight

Datatype

float

Alias
UMLS CUI-1
C0005910
Height
Beschrijving

Height

Datatype

float

Alias
UMLS CUI-1
C0005890
C. Medical History
Beschrijving

C. Medical History

Alias
UMLS CUI-1
C0262926
Angina
Beschrijving

Angina pectoris

Datatype

boolean

Alias
UMLS CUI [1]
C0455530
MI
Beschrijving

Myocardial Infarction

Datatype

boolean

Alias
UMLS CUI [1]
C1275835
CHF
Beschrijving

Congestive heart failure

Datatype

boolean

Alias
UMLS CUI [1]
C0455531
Coronary Angiogram Diagnostic for CAD
Beschrijving

Coronary Angiogram Diagnostic for Coronary artery disease

Datatype

boolean

Alias
UMLS CUI [1]
C1956346
UMLS CUI [2]
C0085532
PCI
Beschrijving

Percutaneous coronary intervention

Datatype

boolean

Alias
UMLS CUI [1]
C1320647
CABG
Beschrijving

Coronary Artery Bypass Surgery

Datatype

boolean

Alias
UMLS CUI [1]
C1275842
Valve Repair/Replacement
Beschrijving

Valve Repair/ Replacement

Datatype

boolean

Alias
UMLS CUI [1]
C0190112
UMLS CUI [2]
C0190173
Family History of CAD
Beschrijving

Family History of Coronary artery disease

Datatype

boolean

Alias
UMLS CUI-1
C0455404
Positive Stress Test
Beschrijving

Positive Stress Test

Datatype

boolean

Alias
UMLS CUI [1]
C3272313
Hypertension
Beschrijving

Hypertension

Datatype

boolean

Alias
UMLS CUI [1]
C0455527
Dyslipidemia
Beschrijving

Dyslipidemia

Datatype

boolean

Alias
UMLS CUI-1
C0242339
Peripheral Arterial Disease
Beschrijving

Peripheral Arterial Disease

Datatype

boolean

Alias
UMLS CUI [1]
C1881056
Atrial Fib
Beschrijving

Atrial Fibrillation

Datatype

boolean

Alias
UMLS CUI-1
C0004238
TIA/Stroke
Beschrijving

TIA/Stroke

Datatype

boolean

Alias
UMLS CUI [1]
C0559159
UMLS CUI [2]
C0007787
Smoker
Beschrijving

Smoker

Datatype

text

Alias
UMLS CUI [1]
C0543414
Diabetes
Beschrijving

Diabetes

Datatype

text

Alias
UMLS CUI-1
C0011849
Renal Insufficiency
Beschrijving

Renal Insufficiency

Datatype

text

Alias
UMLS CUI [1]
C1565489
Major Surgery
Beschrijving

Major Surgery

Datatype

boolean

Alias
UMLS CUI-1
C0679637
Major Bleeding
Beschrijving

Major Bleeding

Datatype

boolean

Alias
UMLS CUI [1]
C0019080
Internal Cardiac Defibrillator (ICD)
Beschrijving

Internal Cardiac Defibrillator (ICD)

Datatype

boolean

Alias
UMLS CUI-1
C1273352
History of Venous Thromboembolism
Beschrijving

History of Venous Thromboembolism

Datatype

boolean

Alias
UMLS CUI-1
C0340726
D. Presentation
Beschrijving

D. Presentation

Alias
UMLS CUI-1
C2708283
Symptom onset (Prompting Presentation to Hospital)
Beschrijving

Symptom onset

Datatype

datetime

Alias
UMLS CUI-1
C1320528
Hospital #1 Arrival
Beschrijving

Hospital Arrival

Datatype

datetime

Alias
UMLS CUI-1
C1320532
Systolic blood pressure
Beschrijving

Systolic blood pressure

Datatype

integer

Maateenheden
  • mmHg
Alias
UMLS CUI-1
C0871470
mmHg
Diastolic blood pressure
Beschrijving

Diastolic blood pressure

Datatype

integer

Alias
UMLS CUI-1
C0428883
Pulse
Beschrijving

Pulse

Datatype

integer

Maateenheden
  • bpm
Alias
UMLS CUI-1
C0232117
bpm
Cardiac arrest at presentation?
Beschrijving

Cardiac arrest

Datatype

boolean

Alias
UMLS CUI-1
C0018790
Killip Class
Beschrijving

Killip Class

Datatype

integer

Alias
UMLS CUI-1
C1881332
Presumptive Admission Diagnosis
Beschrijving

Presumptive Admission Diagnosis

Datatype

text

Alias
UMLS CUI [1]
C0332135
Was patient transferred from another hospital?
Beschrijving

Transfer from hospital

Datatype

boolean

Alias
UMLS CUI-1
C1579840
If Yes, Hospital #2 Arrival
Beschrijving

If Yes, Hospital #2 Arrival

Datatype

datetime

Reason for transfer
Beschrijving

Reason for transfer

Datatype

text

Alias
UMLS CUI-1
C1547731
ECG Findings
Beschrijving

ECG Findings

Alias
UMLS CUI-1
C0438154
Index ECG
Beschrijving

Index ECG

Datatype

datetime

Alias
UMLS CUI-1
C2826846
Was Index ECG done in pre-hospital setting?
Beschrijving

ECG in pre-hospital setting

Datatype

boolean

Alias
UMLS CUI [1]
N
Was Index ECG abnormal for Ischemia?
Beschrijving

ECG signs for ischemia

Datatype

boolean

Alias
UMLS CUI-1
C0474715
Other new abnormalities?
Beschrijving

Other new abnormalities

Datatype

text

Did the patient develop ST elevation or LBBB after the index ECG?
Beschrijving

Patient developed ST elevation or LBBB after the index ECG

Datatype

boolean

Alias
UMLS CUI [1]
C0520886
UMLS CUI [2]
C0023211
Anterior ST elevation in ECG
Beschrijving

Anterior ST elevation in ECG

Datatype

boolean

Alias
UMLS CUI [1]
C3874460
Inferior ST elevation in ECG
Beschrijving

Inferior ST elevation in ECG

Datatype

boolean

Alias
UMLS CUI [1]
C3874457
Lateral ST elevation in ECG
Beschrijving

Lateral ST elevation in ECG

Datatype

boolean

Alias
UMLS CUI [1]
C3874459
Anterior ST depression in ECG
Beschrijving

Anterior ST depression in ECG

Datatype

boolean

Alias
UMLS CUI [1]
C3874467
Inferior ST depression in ECG
Beschrijving

Inferior ST depression

Datatype

boolean

Alias
UMLS CUI [1]
C3874480
Lateral ST depression in ECG
Beschrijving

Lateral ST depression in ECG

Datatype

boolean

Alias
UMLS CUI [1]
C0743440
Significant Q Waves in anterior leads
Beschrijving

Significant Q Waves in anterior leads

Datatype

boolean

Alias
UMLS CUI [1]
C2242519
Significant Q Waves in inferior leads
Beschrijving

Significant Q Waves in inferior leads

Datatype

boolean

Alias
UMLS CUI [1]
C2242520
Significant Q Waves in lateral leads
Beschrijving

Significant Q Waves in lateral leads

Datatype

boolean

Alias
UMLS CUI [1]
C2242521
Left Bundle Branch Block
Beschrijving

Left Bundle Branch Block

Datatype

boolean

Alias
UMLS CUI-1
C0023211
Did the patient develop any of the following after the index ECG?
Beschrijving

Did the patient develop any of the following after the index ECG?

Datatype

text

Laboratory
Beschrijving

Laboratory

Alias
UMLS CUI-1
C0681902
Initial Creatinine
Beschrijving

Initial Creatinine

Datatype

float

Alias
UMLS CUI-1
C0201975
Preak Creatinine
Beschrijving

Preak Creatinine

Datatype

float

Alias
UMLS CUI [1,1]
C0444505
UMLS CUI [1,2]
C0201975
Initial WBC
Beschrijving

Inital White Blood Cell count

Datatype

float

Alias
UMLS CUI-1
C0023508
Serum Cholesterol
Beschrijving

Serum Cholesterol

Datatype

float

Alias
UMLS CUI-1
C1445957
LDL
Beschrijving

LDL

Datatype

float

Alias
UMLS CUI-1
C0428474
HDL
Beschrijving

HDL

Datatype

float

Alias
UMLS CUI-1
C0428472
Triglycerides
Beschrijving

Triglycerides

Datatype

float

Alias
UMLS CUI-1
C0202236
Initial Glucose
Beschrijving

Blood Glucose

Datatype

float

Alias
UMLS CUI-1
C0202042
Fasting Glucose
Beschrijving

Fasting Glucose

Datatype

float

Alias
UMLS CUI-1
C0202045
CPK
Beschrijving

Creatine Kinase

Datatype

float

Alias
UMLS CUI-1
C0201973
CPK maximum value
Beschrijving

Creatine kinase peak level

Datatype

float

Alias
UMLS CUI [1,1]
C0444505
UMLS CUI [1,2]
C0201973
CPK ULN
Beschrijving

CPK ULN

Datatype

float

Alias
UMLS CUI [1,1]
C0201973
UMLS CUI [1,2]
C1519815
Initial CK-MB
Beschrijving

CK-MB

Datatype

float

Alias
UMLS CUI-1
C0523584
CK-MB maximum value
Beschrijving

CK-MB peak level

Datatype

float

Alias
UMLS CUI [1,1]
C0444505
UMLS CUI [1,2]
C0523584
CK-MB ULN
Beschrijving

CK-MB ULN

Datatype

float

Alias
UMLS CUI [1,1]
C0523584
UMLS CUI [1,2]
C1519815
Troponin I
Beschrijving

Troponin I

Datatype

float

Alias
UMLS CUI-1
C0920210
Troponin I ULN
Beschrijving

Troponin I ULN

Datatype

float

Alias
UMLS CUI-1
C0920210
UMLS CUI-2
C1519815
Troponin T
Beschrijving

Troponin T

Datatype

float

Alias
UMLS CUI-1
C1141947
Troponin T ULN
Beschrijving

Troponin T ULN

Datatype

float

Alias
UMLS CUI [1,1]
C1141947
UMLS CUI [1,2]
C1519815
CRP
Beschrijving

CRP

Datatype

float

Alias
UMLS CUI-1
C0201657
BNP
Beschrijving

BNP

Datatype

float

Alias
UMLS CUI-1
C1095989
Homocysteine
Beschrijving

Homocysteine

Datatype

float

Alias
UMLS CUI-1
C2242817
Procedures
Beschrijving

Procedures

Alias
UMLS CUI-1
C2700391
Pacemaker
Beschrijving

Pacemaker

Datatype

text

Alias
UMLS CUI [1]
C0189842
Echocardiography
Beschrijving

Echocardiography

Datatype

boolean

Alias
UMLS CUI-1
C0013516
PA Catheter
Beschrijving

Pulmonary artery catheter

Datatype

boolean

Alias
UMLS CUI-1
C0190658
Ventilator
Beschrijving

Ventilator

Datatype

boolean

Alias
UMLS CUI [1]
C0087153
IABP
Beschrijving

Intra-Aortic Balloon Pumping

Datatype

boolean

Alias
UMLS CUI-1
C0021860
Stress test
Beschrijving

Stress test

Datatype

boolean

Alias
UMLS CUI-1
C1384495
Stress test pos/neg
Beschrijving

Stress test result

Datatype

boolean

Alias
UMLS CUI [1,1]
C1274040
UMLS CUI [1,2]
C1384495
Cardiac Cath/Interventions
Beschrijving

Cardiac Cath/Interventions

Patient/Family Refused Cardiac Cath
Beschrijving

Cardiac catheter refused

Datatype

boolean

Alias
UMLS CUI [1,1]
C3845227
UMLS CUI [1,2]
C0018795
Patient/Family Refused PCI
Beschrijving

PCI refused

Datatype

boolean

Alias
UMLS CUI [1,1]
C1532338
UMLS CUI [1,2]
C3845227
Patient/Family Refused CABG
Beschrijving

CABG refused

Datatype

boolean

Alias
UMLS CUI [1,1]
C0010055
UMLS CUI [1,2]
C3845227
Cardiac Cath
Beschrijving

Cardiac Catheterization

Datatype

boolean

Alias
UMLS CUI-1
C0018795
Total # of Cath Procedures
Beschrijving

Number of Cardiac Catheters

Datatype

integer

Alias
UMLS CUI-1
C0750480
UMLS CUI-2
C0018795
Stenosis > 50% in LM
Beschrijving

Left main coronary artery stenosis

Datatype

boolean

Alias
UMLS CUI-1
C2062905
Stenosis > 50% in LAD
Beschrijving

Left anterior descending coronary artery stenosis

Datatype

boolean

Alias
UMLS CUI-1
C3267165
Stenosis > 50% in LCX
Beschrijving

Circumflex branch of left coronary artery stenosis

Datatype

boolean

Alias
UMLS CUI-1
C0742837
Stenosis > 50% in RCA
Beschrijving

Right coronary artery stenosis

Datatype

boolean

Alias
UMLS CUI-1
C3267166
Stenosis > 50% in Bypass Graft(s)
Beschrijving

Coronary graft stenosis

Datatype

boolean

Alias
UMLS CUI-1
C0428830
Culprit Lesion Stenosis
Beschrijving

Culprit Lesion Stenosis

Datatype

integer

Maateenheden
  • %
Alias
UMLS CUI [1]
C1299364
%
Culprit Lesion Territory
Beschrijving

Culprit Lesion Territory

Datatype

text

Alias
UMLS CUI [1]
N
Culprit Artery TIMI Flow
Beschrijving

Culprit Artery TIMI Flow

Datatype

text

Alias
UMLS CUI [1]
C3272266
PCI
Beschrijving

PCI

Datatype

boolean

Alias
UMLS CUI-1
C1532338
Total # of PCI Procedures
Beschrijving

Total # of PCI Procedures

Datatype

integer

Alias
UMLS CUI [1,1]
C0750480
UMLS CUI [1,2]
C1532338
# of dilated vessels
Beschrijving

# of dilated vessels

Datatype

integer

Alias
UMLS CUI [1]
C0424830
# of Stents
Beschrijving

# of Stents

Datatype

integer

Alias
UMLS CUI-1
C2024081
PCI type
Beschrijving

PCI type

Datatype

text

Alias
UMLS CUI [1,1]
C1532338
UMLS CUI [1,2]
C0392360
PCI done with Brachytherapy
Beschrijving

PCI done with Brachytherapy

Datatype

boolean

Alias
UMLS CUI-1
C2145202
Insertion of Drug Coated Stent(s)
Beschrijving

Insertion of Drug Coated Stent(s)

Datatype

boolean

Alias
UMLS CUI-1
C1532966
Failed procedure
Beschrijving

Failed procedure

Datatype

boolean

Alias
UMLS CUI [1,1]
C0231175
UMLS CUI [1,2]
C1532338
CABG
Beschrijving

CABG

Datatype

boolean

Alias
UMLS CUI-1
C0010055
# of distal Graft(s)
Beschrijving

# of distal Graft(s)

Datatype

integer

Alias
UMLS CUI [1]
C1264697
Type of Graft(s)
Beschrijving

Type of Graft(s)

Datatype

text

Alias
UMLS CUI [1]
C0449494
LVEF
Beschrijving

LVEF

LVEF
Beschrijving

LVEF

Datatype

integer

Maateenheden
  • %
Alias
UMLS CUI-1
C0428772
%
LVEF Grade
Beschrijving

LVEF Grade

Datatype

text

LVEF how obtained
Beschrijving

LVEF how obtained

Datatype

text

Alias
UMLS CUI-1
C2708658
Thrombolytics
Beschrijving

Thrombolytics

Thrombolytics
Beschrijving

Thrombolytics

Datatype

boolean

Alias
UMLS CUI-1
C0040044
# of thrombolytics treatment
Beschrijving

# of thrombolytics treatment

Datatype

integer

Alias
UMLS CUI [1,1]
C0040044
UMLS CUI [1,2]
C0750480
Thrombolytics contraindicated
Beschrijving

Thrombolytics contraindicated

Datatype

boolean

Alias
UMLS CUI-1
C3260558
Name of First Thrombolytic Drug
Beschrijving

Name of First Thrombolytic Drug

Datatype

text

Alias
UMLS CUI [1]
C0016018
Thrombolytics Dose
Beschrijving

Thrombolytics Dose

Datatype

text

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0040044
Thrombolytic Initiation Site
Beschrijving

Thrombolytic Initiation Site

Datatype

text

Alias
UMLS CUI-1
N
Drugs administered simultaneously with thrombolytic
Beschrijving

Drugs administered simultaneously with thrombolytic

Datatype

text

Alias
UMLS CUI [1]
N
Antiplatelets/Antithrombins/Anticoagulants
Beschrijving

Antiplatelets/Antithrombins/Anticoagulants

Aspirin
Beschrijving

Aspirin

Datatype

text

Alias
UMLS CUI-1
C0004057
Aspirin dose
Beschrijving

Aspirin dose

Datatype

float

Maateenheden
  • mg/d
Alias
UMLS CUI [1,1]
C0004057
UMLS CUI [1,2]
C0178602
mg/d
Warfarin or other Vitamin K Antagonist
Beschrijving

Warfarin or other Vitamin K Antagonist

Datatype

text

Alias
UMLS CUI [1]
C0043031
UMLS CUI [2]
C2267235
Ticlopidine
Beschrijving

Ticlopidine

Datatype

text

Alias
UMLS CUI-1
C0040207
Clopidogrel
Beschrijving

Clopidogrel

Datatype

text

Alias
UMLS CUI-1
C0070166
Unfractionated Heparin
Beschrijving

Unfractionated Heparin

Datatype

text

Alias
UMLS CUI-1
C2825026
IV Enoxaparin
Beschrijving

IV Enoxaparin

Datatype

text

Alias
UMLS CUI-1
C0206460
SQ Enoxaparin
Beschrijving

SQ Enoxaparin

Datatype

text

Alias
UMLS CUI [1]
C0206460
Bivalirudin
Beschrijving

Bivalirudin

Datatype

text

Alias
UMLS CUI-1
C0168273
Fondaparinux
Beschrijving

Fondaparinux

Datatype

text

Alias
UMLS CUI-1
C1098510
Other Direct Thrombin Inhibitors
Beschrijving

Other Direct Thrombin Inhibitors

Datatype

text

Alias
UMLS CUI [1]
C3541936
Other LMW Heparin
Beschrijving

Other LMW Heparin

Datatype

text

Alias
UMLS CUI [1]
C3536766
Other Antiplatelet
Beschrijving

Antiplatelet

Datatype

text

Alias
UMLS CUI [1]
C1096021
Other Antithrombin
Beschrijving

Other Antithrombin

Datatype

text

IV GP llb/llla
Beschrijving

IV GP llb/llla

Datatype

text

Alias
UMLS CUI-1
C3640054
Reason for GP IIb/IIIa administration
Beschrijving

Reason for GP IIb/IIIa administration

Datatype

text

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0864559
Other Medications
Beschrijving

Other Medications

ACE Inhibitor
Beschrijving

ACE Inhibitor

Datatype

text

Alias
UMLS CUI-1
C0003015
Amiodarone
Beschrijving

Amiodarone

Datatype

text

Alias
UMLS CUI-1
C0002598
Angiotensin II Receptor Blocker (ARB)
Beschrijving

Angiotensin II Receptor Blocker (ARB)

Datatype

text

Alias
UMLS CUI-1
C0521942
Beta Blocker (IV)
Beschrijving

Beta Blocker (IV)

Datatype

text

Alias
UMLS CUI [1]
C0304516
Beta Blocker (Oral)
Beschrijving

Beta Blocker (Oral)

Datatype

text

Alias
UMLS CUI [1]
C0304516
Calcium Channel Blocker
Beschrijving

Calcium Channel Blocker

Datatype

text

Alias
UMLS CUI-1
C0006684
Digoxin
Beschrijving

Digoxin

Datatype

text

Alias
UMLS CUI-1
C0012265
Diuretic
Beschrijving

Diuretic

Datatype

text

Alias
UMLS CUI-1
C0012798
Glucose/Insulin/Potassium (GIK)
Beschrijving

Glucose/Insulin/Potassium (GIK)

Datatype

text

Alias
UMLS CUI-1
C0061420
Inotropic Agent (IV)
Beschrijving

Inotropic Agent (IV)

Datatype

text

Alias
UMLS CUI-1
C0304509
Insulin
Beschrijving

Insulin

Datatype

text

Alias
UMLS CUI-1
C0021641
Insulin Provider
Beschrijving

Insulin Provider

Datatype

text

Alias
UMLS CUI-1
C0935929
Insulin Sensitizer
Beschrijving

Insulin Sensitizer

Datatype

text

Alias
UMLS CUI-1
N
Magnesium (IV)
Beschrijving

Magnesium (IV)

Datatype

text

Alias
UMLS CUI-1
C3540792
Nitrate (IV)
Beschrijving

Nitrate (IV)

Datatype

text

Alias
UMLS CUI [1]
C0028125
Nitrate (Oral/Topical)
Beschrijving

Nitrate (Oral/Topical)

Datatype

text

Alias
UMLS CUI [1]
C0028125
Nicorandil
Beschrijving

Nicorandil

Datatype

text

Alias
UMLS CUI-1
C0068700
Omega-3 Fatty Acids
Beschrijving

Omega-3 Fatty Acids

Datatype

text

Alias
UMLS CUI-1
C0015689
Statin
Beschrijving

Statin

Datatype

text

Alias
UMLS CUI-1
C0360714
Other Lipid Lowering Agent
Beschrijving

Other Lipid Lowering Agent

Datatype

text

Medication Contraindications
Beschrijving

Medication Contraindications

ASA Contraindication
Beschrijving

ASA Contraindication

Datatype

boolean

Alias
UMLS CUI-1
C0729798
Beta Blockers Contraindication
Beschrijving

Beta Blockers Contraindication

Datatype

boolean

Alias
UMLS CUI-1
C1278474
ACE Inhibitors Contraindication
Beschrijving

ACE Inhibitors Contraindication

Datatype

boolean

Alias
UMLS CUI [1,1]
C0003015
UMLS CUI [1,2]
C0522473
ARB Contraindication
Beschrijving

ARB Contraindication

Datatype

boolean

Alias
UMLS CUI-1
C1273465
Statins Contraindication
Beschrijving

Statins Contraindication

Datatype

boolean

Alias
UMLS CUI-1
C1277178
LMWH Contraindication
Beschrijving

Low molecular weight heparin contraindication

Datatype

boolean

Alias
UMLS CUI [1,1]
C3536766
UMLS CUI [1,2]
C0522473
UFH Contraindication
Beschrijving

Unfractionated Heparin Contraindication

Datatype

boolean

Alias
UMLS CUI [1,1]
C2825026
UMLS CUI [1,2]
C0522473
Lifestyle interventions
Beschrijving

Lifestyle interventions

Alias
UMLS CUI-1
C2960841
If current cigarette smoker, was patient counseled to quit smoking by a health care professional?
Beschrijving

If current cigarette smoker, was patient counseled to quit smoking by a health care professional?

Datatype

text

Alias
UMLS CUI-1
C1273715
Was patient referred to a cardiac rehab program?
Beschrijving

Was patient referred to a cardiac rehab program?

Datatype

boolean

Alias
UMLS CUI-1
C0700431
In-hospital Events: After Presentation
Beschrijving

In-hospital Events: After Presentation

Recurrent Ischemic Symptoms
Beschrijving

Recurrent Ischemic Symptoms

Datatype

boolean

Alias
UMLS CUI-1
C1735908
CHF/Pulmonary Edema
Beschrijving

CHF/Pulmonary Edema

Datatype

boolean

Alias
UMLS CUI [1]
C0018802
UMLS CUI [2]
C0034063
Cardiogenic Shock
Beschrijving

Cardiogenic Shock

Datatype

boolean

Alias
UMLS CUI-1
C0036980
Cardiac Arrest/VF
Beschrijving

Cardiac Arrest/VF

Datatype

boolean

Alias
UMLS CUI [1]
C0018790
UMLS CUI [2]
C0042510
Date of cardiac arrest
Beschrijving

Date of cardiac arrest

Datatype

datetime

Alias
UMLS CUI-1
C2825160
Atrial Fib/Flutter
Beschrijving

Atrial Fib/Flutter

Datatype

boolean

Alias
UMLS CUI [1]
C0004238
UMLS CUI [2]
C0004239
Sustained VT
Beschrijving

Sustained VT

Datatype

boolean

Alias
UMLS CUI-1
C0750197
Thrombocytopenia
Beschrijving

Thrombocytopenia

Datatype

boolean

Alias
UMLS CUI-1
C0040034
HIT
Beschrijving

HIT

Datatype

boolean

Alias
UMLS CUI-1
C0272285
Venous Thromboembolism
Beschrijving

Venous Thromboembolism

Datatype

boolean

Alias
UMLS CUI-1
C1861172
Acute Renal Failure
Beschrijving

Acute Renal Failure

Datatype

boolean

Alias
UMLS CUI-1
C0022660
AV Block (Mobitz II, 3°)
Beschrijving

AV Block (Mobitz II, 3°)

Datatype

boolean

Alias
UMLS CUI [1]
C0004245
Mechanical Complication
Beschrijving

Mechanical Complication

Datatype

text

MI > 24 hrs after hospital presentation/Re-infarction
Beschrijving

MI > 24 hrs after hospital presentation/Re-infarction

Datatype

boolean

Alias
UMLS CUI [1]
C0948369
MI confirmed by
Beschrijving

MI confirmed by

Datatype

text

Alias
UMLS CUI [1,1]
C0521091
UMLS CUI [1,2]
C0027051
Stroke
Beschrijving

Stroke

Datatype

boolean

Alias
UMLS CUI-1
C0038454
Stroke date
Beschrijving

Stroke date

Datatype

date

Alias
UMLS CUI [1,1]
C0038454
UMLS CUI [1,2]
C0011008
Stroke confirmed by CT/MRI
Beschrijving

Stroke confirmed by CT/MRI

Datatype

boolean

Alias
UMLS CUI [1,1]
C0027051
UMLS CUI [1,2]
C0521091
Type of Stroke
Beschrijving

Type of Stroke

Datatype

text

Alias
UMLS CUI [1]
C3897486
Major bleeding
Beschrijving

Major bleeding

Datatype

boolean

Alias
UMLS CUI-1
C0019080
Date of major bleeding
Beschrijving

Date of major bleeding

Datatype

date

Alias
UMLS CUI [1,1]
C0019080
UMLS CUI [1,2]
C0011008
Bleeding location
Beschrijving

Bleeding location

Datatype

text

Alias
UMLS CUI [1,1]
C0019080
UMLS CUI [1,2]
C0450429
Bleeding treatment
Beschrijving

Bleeding treatment

Datatype

text

Alias
UMLS CUI-1
C0149533
Discharge status
Beschrijving

Discharge status

Was patient treated as part of a research protocol?
Beschrijving

Was patient treated as part of a research protocol?

Datatype

boolean

Alias
UMLS CUI-1
C0422739
Discharge Status
Beschrijving

Discharge Status

Datatype

text

Alias
UMLS CUI [1]
C2599747
Date of Discharge or Death
Beschrijving

Date of Discharge or Death

Datatype

date

Alias
UMLS CUI [1]
C2361123
UMLS CUI [2]
C1148348
Time of Death (if died)
Beschrijving

Time of Death (if died)

Datatype

time

Alias
UMLS CUI-1
C1301931
Primary Discharge Diagnosis
Beschrijving

Primary Discharge Diagnosis

Datatype

text

Alias
UMLS CUI-1
C0332144
Who was the primary physician who cared for the patient while in the hospital?
Beschrijving

Who was the primary physician who cared for the patient while in the hospital?

Datatype

text

Alias
UMLS CUI-1
C1508823

Similar models

GRACE Initial Form v3.5

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
General information
Patient initials
Item
Patient initials
text
C2986440 (UMLS CUI-1)
Date of Birth
Item
Date of Birth
date
C0421451 (UMLS CUI-1)
Item Group
A. Enrollment
Item
Confirmation of Eligibility per GRACE Protocol
text
C0013893 (UMLS CUI [1])
Code List
Confirmation of Eligibility per GRACE Protocol
CL Item
Symptoms of Ischemia (1)
CL Item
History of CAD (2)
CL Item
New Documentation of CAD (3)
CL Item
Qualifying ECG Changes (4)
CL Item
Positive Cardiac Enzymes (5)
Item
Pursuit Type
text
Code List
Pursuit Type
CL Item
Cold (1)
CL Item
Warm (2)
Item Group
B. Demographics
C0011298 (UMLS CUI-1)
Postal Code
Item
Postal Code (Patient Residence)
text
C0421454 (UMLS CUI-1)
Item
Gender
text
C0079399 (UMLS CUI [1])
Code List
Gender
CL Item
Male (1)
CL Item
Female (2)
Weight
Item
Admission Weight
float
C0005910 (UMLS CUI-1)
Height
Item
Height
float
C0005890 (UMLS CUI-1)
Item Group
C. Medical History
C0262926 (UMLS CUI-1)
History of Angina pectoris
Item
Angina
boolean
C0455530 (UMLS CUI [1])
History of myocardial infarction
Item
MI
boolean
C1275835 (UMLS CUI [1])
History of heart failure
Item
CHF
boolean
C0455531 (UMLS CUI [1])
Coronary artery disease
Item
Coronary Angiogram Diagnostic for CAD
boolean
C1956346 (UMLS CUI [1])
C0085532 (UMLS CUI [2])
Prior PCI
Item
PCI
boolean
C1320647 (UMLS CUI [1])
History of coronary artery bypass grafting
Item
CABG
boolean
C1275842 (UMLS CUI [1])
Valve Repair/ Replacement
Item
Valve Repair/Replacement
boolean
C0190112 (UMLS CUI [1])
C0190173 (UMLS CUI [2])
Family History of CAD
Item
Family History of CAD
boolean
C0455404 (UMLS CUI-1)
Cardiac Stress Test
Item
Positive Stress Test
boolean
C3272313 (UMLS CUI [1])
History of Hypertension
Item
Hypertension
boolean
C0455527 (UMLS CUI [1])
Dyslipidemia
Item
Dyslipidemia
boolean
C0242339 (UMLS CUI-1)
History of Peripheral Arterial Disease
Item
Peripheral Arterial Disease
boolean
C1881056 (UMLS CUI [1])
Atrial Fibrillation
Item
Atrial Fib
boolean
C0004238 (UMLS CUI-1)
TIA/Stroke
Item
TIA/Stroke
boolean
C0559159 (UMLS CUI [1])
C0007787 (UMLS CUI [2])
Item
Smoker
text
C0543414 (UMLS CUI [1])
Code List
Smoker
CL Item
Former Smoker (1)
CL Item
Current Smoker (2)
CL Item
Status not recorded (3)
Item
Diabetes
text
C0011849 (UMLS CUI-1)
Code List
Diabetes
CL Item
Diet controlled (1 )
CL Item
Oral hypoglycemics (2 )
CL Item
Insulin-dependent (3 )
CL Item
No treatment used (4 )
CL Item
Type not recorded (5 )
Item
Renal Insufficiency
text
C1565489 (UMLS CUI [1])
Code List
Renal Insufficiency
CL Item
No dialysis (1)
CL Item
Dialysis (2)
Major Surgery
Item
Major Surgery
boolean
C0679637 (UMLS CUI-1)
Hemorrhage
Item
Major Bleeding
boolean
C0019080 (UMLS CUI [1])
Internal Cardiac Defibrillator (ICD)
Item
Internal Cardiac Defibrillator (ICD)
boolean
C1273352 (UMLS CUI-1)
History of Venous Thromboembolism
Item
History of Venous Thromboembolism
boolean
C0340726 (UMLS CUI-1)
Item Group
D. Presentation
C2708283 (UMLS CUI-1)
Symptom onset
Item
Symptom onset (Prompting Presentation to Hospital)
datetime
C1320528 (UMLS CUI-1)
Hospital Arrival
Item
Hospital #1 Arrival
datetime
C1320532 (UMLS CUI-1)
Systolic blood pressure
Item
Systolic blood pressure
integer
C0871470 (UMLS CUI-1)
Diastolic blood pressure
Item
Diastolic blood pressure
integer
C0428883 (UMLS CUI-1)
Pulse
Item
Pulse
integer
C0232117 (UMLS CUI-1)
Cardiac arrest
Item
Cardiac arrest at presentation?
boolean
C0018790 (UMLS CUI-1)
Killip Class
Item
Killip Class
integer
C1881332 (UMLS CUI-1)
Item
Presumptive Admission Diagnosis
text
C0332135 (UMLS CUI [1])
Code List
Presumptive Admission Diagnosis
CL Item
Ml (1)
CL Item
Unstable Angina (2)
CL Item
Rule out Ml or suspected ACE/ACS (3)
CL Item
Chest Pain (4)
CL Item
Other Cardiac (5)
CL Item
Other (6)
Transfer from hospital
Item
Was patient transferred from another hospital?
boolean
C1579840 (UMLS CUI-1)
If Yes, Hospital #2 Arrival
Item
If Yes, Hospital #2 Arrival
datetime
Item
Reason for transfer
text
C1547731 (UMLS CUI-1)
Code List
Reason for transfer
CL Item
Acute Care (1)
CL Item
Cardiac Cath (2)
CL Item
PCI (3)
CL Item
CABG (4)
CL Item
Other (5)
Item Group
ECG Findings
C0438154 (UMLS CUI-1)
ECG Date
Item
Index ECG
datetime
C2826846 (UMLS CUI-1)
ECG in pre-hospital setting
Item
Was Index ECG done in pre-hospital setting?
boolean
N (UMLS CUI [1])
ECG signs for ischemia
Item
Was Index ECG abnormal for Ischemia?
boolean
C0474715 (UMLS CUI-1)
Item
Other new abnormalities?
text
Code List
Other new abnormalities?
CL Item
AV Block (Mobitz II, 3°)  (1)
C0004245 (UMLS CUI-1)
CL Item
Atrial Fib/Flutter (2)
C0004238 (UMLS CUI-1)
C0004239 (UMLS CUI-3)
CL Item
Posterior Infarction (3)
C0340319 (UMLS CUI-1)
CL Item
Nonspecific ST/T Change (4)
C0920117 (UMLS CUI-1)
CL Item
Left Ventricular Hypertrophy (5)
C0149721 (UMLS CUI-1)
CL Item
Vtach (6)
C0042514 (UMLS CUI-1)
CL Item
RBBB (7)
C0085615 (UMLS CUI-1)
CL Item
Paced Rhythm (8)
C2981711 (UMLS CUI-1)
ST elevation or LBBB
Item
Did the patient develop ST elevation or LBBB after the index ECG?
boolean
C0520886 (UMLS CUI [1])
C0023211 (UMLS CUI [2])
Anterior ST elevation in ECG
Item
Anterior ST elevation in ECG
boolean
C3874460 (UMLS CUI [1])
Inferior ST elevation in ECG
Item
Inferior ST elevation in ECG
boolean
C3874457 (UMLS CUI [1])
Lateral ST elevation in ECG
Item
Lateral ST elevation in ECG
boolean
C3874459 (UMLS CUI [1])
Anterior ST depression in ECG
Item
Anterior ST depression in ECG
boolean
C3874467 (UMLS CUI [1])
Inferior ST depression in ECG
Item
Inferior ST depression in ECG
boolean
C3874480 (UMLS CUI [1])
Lateral ST depression in ECG
Item
Lateral ST depression in ECG
boolean
C0743440 (UMLS CUI [1])
Q Waves in anterior leads
Item
Significant Q Waves in anterior leads
boolean
C2242519 (UMLS CUI [1])
Significant Q Waves in inferior leads
Item
Significant Q Waves in inferior leads
boolean
C2242520 (UMLS CUI [1])
Significant Q Waves in lateral leads
Item
Significant Q Waves in lateral leads
boolean
C2242521 (UMLS CUI [1])
Left Bundle Branch Block
Item
Left Bundle Branch Block
boolean
C0023211 (UMLS CUI-1)
Item
Did the patient develop any of the following after the index ECG?
text
Code List
Did the patient develop any of the following after the index ECG?
CL Item
Significant Q Waves or R>S in V1 (1)
C0429090 (UMLS CUI-1)
CL Item
ST Depressions (2)
C0520887 (UMLS CUI-1)
CL Item
T Wave Inversions (3)
C0520888 (UMLS CUI-1)
Item Group
Laboratory
C0681902 (UMLS CUI-1)
Initial Creatinine
Item
Initial Creatinine
float
C0201975 (UMLS CUI-1)
Preak Creatinine
Item
Preak Creatinine
float
C0444505 (UMLS CUI [1,1])
C0201975 (UMLS CUI [1,2])
White Blood Cell count
Item
Initial WBC
float
C0023508 (UMLS CUI-1)
Serum Cholesterol
Item
Serum Cholesterol
float
C1445957 (UMLS CUI-1)
LDL
Item
LDL
float
C0428474 (UMLS CUI-1)
HDL
Item
HDL
float
C0428472 (UMLS CUI-1)
Triglycerides
Item
Triglycerides
float
C0202236 (UMLS CUI-1)
Blood Glucose
Item
Initial Glucose
float
C0202042 (UMLS CUI-1)
Fasting Glucose
Item
Fasting Glucose
float
C0202045 (UMLS CUI-1)
Creatine Kinase
Item
CPK
float
C0201973 (UMLS CUI-1)
Creatine kinase peak level
Item
CPK maximum value
float
C0444505 (UMLS CUI [1,1])
C0201973 (UMLS CUI [1,2])
CPK ULN
Item
CPK ULN
float
C0201973 (UMLS CUI [1,1])
C1519815 (UMLS CUI [1,2])
CK-MB
Item
Initial CK-MB
float
C0523584 (UMLS CUI-1)
CK-MB peak level
Item
CK-MB maximum value
float
C0444505 (UMLS CUI [1,1])
C0523584 (UMLS CUI [1,2])
CK-MB ULN
Item
CK-MB ULN
float
C0523584 (UMLS CUI [1,1])
C1519815 (UMLS CUI [1,2])
Troponin I
Item
Troponin I
float
C0920210 (UMLS CUI-1)
Troponin I ULN
Item
Troponin I ULN
float
C0920210 (UMLS CUI-1)
C1519815 (UMLS CUI-2)
Troponin T
Item
Troponin T
float
C1141947 (UMLS CUI-1)
Troponin T ULN
Item
Troponin T ULN
float
C1141947 (UMLS CUI [1,1])
C1519815 (UMLS CUI [1,2])
CRP
Item
CRP
float
C0201657 (UMLS CUI-1)
BNP
Item
BNP
float
C1095989 (UMLS CUI-1)
Homocysteine
Item
Homocysteine
float
C2242817 (UMLS CUI-1)
Item Group
Procedures
C2700391 (UMLS CUI-1)
Item
Pacemaker
text
C0189842 (UMLS CUI [1])
Code List
Pacemaker
CL Item
Temporary Pacemaker (1)
CL Item
Permanent Pacemaker (2)
CL Item
ICD (3)
Echocardiography
Item
Echocardiography
boolean
C0013516 (UMLS CUI-1)
Pulmonary artery catheter
Item
PA Catheter
boolean
C0190658 (UMLS CUI-1)
Ventilator
Item
Ventilator
boolean
C0087153 (UMLS CUI [1])
Intra-Aortic Balloon Pumping
Item
IABP
boolean
C0021860 (UMLS CUI-1)
Stress test
Item
Stress test
boolean
C1384495 (UMLS CUI-1)
Stress test result
Item
Stress test pos/neg
boolean
C1274040 (UMLS CUI [1,1])
C1384495 (UMLS CUI [1,2])
Item Group
Cardiac Cath/Interventions
Cardiac catheter refused
Item
Patient/Family Refused Cardiac Cath
boolean
C3845227 (UMLS CUI [1,1])
C0018795 (UMLS CUI [1,2])
PCI refused
Item
Patient/Family Refused PCI
boolean
C1532338 (UMLS CUI [1,1])
C3845227 (UMLS CUI [1,2])
CABG refused
Item
Patient/Family Refused CABG
boolean
C0010055 (UMLS CUI [1,1])
C3845227 (UMLS CUI [1,2])
Cardiac Catheterization
Item
Cardiac Cath
boolean
C0018795 (UMLS CUI-1)
Number of Cardiac Catheters
Item
Total # of Cath Procedures
integer
C0750480 (UMLS CUI-1)
C0018795 (UMLS CUI-2)
Left main coronary artery stenosis
Item
Stenosis > 50% in LM
boolean
C2062905 (UMLS CUI-1)
Left anterior descending coronary artery stenosis
Item
Stenosis > 50% in LAD
boolean
C3267165 (UMLS CUI-1)
Circumflex branch of left coronary artery stenosis
Item
Stenosis > 50% in LCX
boolean
C0742837 (UMLS CUI-1)
Right coronary artery stenosis
Item
Stenosis > 50% in RCA
boolean
C3267166 (UMLS CUI-1)
Coronary graft stenosis
Item
Stenosis > 50% in Bypass Graft(s)
boolean
C0428830 (UMLS CUI-1)
Culprit Lesion Stenosis
Item
Culprit Lesion Stenosis
integer
C1299364 (UMLS CUI [1])
Item
Culprit Lesion Territory
text
N (UMLS CUI [1])
Code List
Culprit Lesion Territory
CL Item
LM (1)
CL Item
LAD (2)
CL Item
LCX (3)
CL Item
RCA (4)
CL Item
Vein Bypass Graft (5)
CL Item
Arterial Bypass Graft (6)
CL Item
Unknown (7)
Item
Culprit Artery TIMI Flow
text
C3272266 (UMLS CUI [1])
Code List
Culprit Artery TIMI Flow
CL Item
Occluded (TIMI 0/1) (1)
CL Item
Slow (TIMI 2) (2)
CL Item
Normal (TIMI 3) (3)
CL Item
Unknown (4)
PCI
Item
PCI
boolean
C1532338 (UMLS CUI-1)
Number of PCIs
Item
Total # of PCI Procedures
integer
C0750480 (UMLS CUI [1,1])
C1532338 (UMLS CUI [1,2])
Dilated vessels
Item
# of dilated vessels
integer
C0424830 (UMLS CUI [1])
Number of stents placed
Item
# of Stents
integer
C2024081 (UMLS CUI-1)
Item
PCI type
text
C1532338 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
Code List
PCI type
CL Item
Primary/direct (immediate mode of reperfusion in AMI) (1)
CL Item
Rescue (after failed thrombolysis, where failed refers to ongoing/recurrent ischemic discomfort and/or lack of ST segment elevation resolution or recurrent ST elevation) (2)
CL Item
Early PCI for cardiogenic shock (3)
CL Item
PCI for treatment of unstable angina (4)
CL Item
PCI for treatment of post AMI ischemia (5)
CL Item
Facilitated PCI (immediate PCI following successful thrombolysis, or in conjunction with thrombolysis) (6)
CL Item
Non-emergent adjunctive PCI of non-culprit lesion (stayed) (7)
CL Item
Other (including non-emergent elective PCI of suspected culprit lesion) (8)
PCI done with Brachytherapy
Item
PCI done with Brachytherapy
boolean
C2145202 (UMLS CUI-1)
Insertion of Drug Coated Stent
Item
Insertion of Drug Coated Stent(s)
boolean
C1532966 (UMLS CUI-1)
PCI failed
Item
Failed procedure
boolean
C0231175 (UMLS CUI [1,1])
C1532338 (UMLS CUI [1,2])
CABG
Item
CABG
boolean
C0010055 (UMLS CUI-1)
Number of distal Grafts
Item
# of distal Graft(s)
integer
C1264697 (UMLS CUI [1])
Item
Type of Graft(s)
text
C0449494 (UMLS CUI [1])
Code List
Type of Graft(s)
CL Item
Vein graft(s) (1)
CL Item
Arterial graft(s) (2)
CL Item
Both Vein and Arterial graft(s) (3)
Item Group
LVEF
LVEF
Item
LVEF
integer
C0428772 (UMLS CUI-1)
Item
LVEF Grade
text
Code List
LVEF Grade
CL Item
Normal (1)
C1535947 (UMLS CUI-1)
CL Item
Mildly Diminished (2)
C3274775 (UMLS CUI-1)
CL Item
Moderately Diminished (3)
C3274776 (UMLS CUI-1)
CL Item
Severely Diminished (4)
C3274777 (UMLS CUI-1)
Item
LVEF how obtained
text
C2708658 (UMLS CUI-1)
Code List
LVEF how obtained
CL Item
Ventriculogram (angiogram) (1)
C0596683 (UMLS CUI-1)
CL Item
Nuclear Imaging (2)
C0034606 (UMLS CUI-1)
CL Item
Echo (3)
C0013516 (UMLS CUI-1)
Item Group
Thrombolytics
Thrombolytics
Item
Thrombolytics
boolean
C0040044 (UMLS CUI-1)
Number of thrombolytics treatment
Item
# of thrombolytics treatment
integer
C0040044 (UMLS CUI [1,1])
C0750480 (UMLS CUI [1,2])
Thrombolytics contraindicated
Item
Thrombolytics contraindicated
boolean
C3260558 (UMLS CUI-1)
Item
Name of First Thrombolytic Drug
text
C0016018 (UMLS CUI [1])
Code List
Name of First Thrombolytic Drug
CL Item
Streptokinase (1)
CL Item
t-PA (2)
CL Item
r-PA (3)
CL Item
TNK-tPA (4)
CL Item
Other (5)
CL Item
Blinded Study Drug (6)
Item
Thrombolytics Dose
text
C0178602 (UMLS CUI [1,1])
C0040044 (UMLS CUI [1,2])
Code List
Thrombolytics Dose
CL Item
Half (1)
CL Item
Full (2)
Item
Thrombolytic Initiation Site
text
N (UMLS CUI-1)
Code List
Thrombolytic Initiation Site
CL Item
Pre-Hospital (1)
CL Item
In-Hospital (2)
Item
Drugs administered simultaneously with thrombolytic
text
N (UMLS CUI [1])
Code List
Drugs administered simultaneously with thrombolytic
CL Item
GP IIb/IIIa (1)
CL Item
LMWH (2)
CL Item
Unfractionated Heparin (3)
CL Item
Blinded Study Drug (4)
Item Group
Antiplatelets/Antithrombins/Anticoagulants
Item
Aspirin
text
C0004057 (UMLS CUI-1)
Code List
Aspirin
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Peri-PCI (6)
CL Item
Prescribed at Discharge (7)
CL Item
Not Prescribed (8)
Aspirin dose
Item
Aspirin dose
float
C0004057 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
Item
Warfarin or other Vitamin K Antagonist
text
C0043031 (UMLS CUI [1])
C2267235 (UMLS CUI [2])
Code List
Warfarin or other Vitamin K Antagonist
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Peri-PCI (6)
CL Item
Prescribed at Discharge (7)
CL Item
Not Prescribed (8)
Item
Ticlopidine
text
C0040207 (UMLS CUI-1)
Code List
Ticlopidine
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Peri-PCI (6)
CL Item
Prescribed at Discharge (7)
CL Item
Not Prescribed (8)
Item
Clopidogrel
text
C0070166 (UMLS CUI-1)
Code List
Clopidogrel
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Peri-PCI (6)
CL Item
Prescribed at Discharge (7)
CL Item
Not Prescribed (8)
Item
Unfractionated Heparin
text
C2825026 (UMLS CUI-1)
Code List
Unfractionated Heparin
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Peri-PCI (6)
CL Item
Prescribed at Discharge (7)
CL Item
Not Prescribed (8)
Item
IV Enoxaparin
text
C0206460 (UMLS CUI-1)
Code List
IV Enoxaparin
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Peri-PCI (6)
CL Item
Prescribed at Discharge (7)
CL Item
Not Prescribed (8)
Item
SQ Enoxaparin
text
C0206460 (UMLS CUI [1])
Code List
SQ Enoxaparin
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Peri-PCI (6)
CL Item
Prescribed at Discharge (7)
CL Item
Not Prescribed (8)
Item
Bivalirudin
text
C0168273 (UMLS CUI-1)
Code List
Bivalirudin
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Peri-PCI (6)
CL Item
Prescribed at Discharge (7)
CL Item
Not Prescribed (8)
Item
Fondaparinux
text
C1098510 (UMLS CUI-1)
Code List
Fondaparinux
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Peri-PCI (6)
CL Item
Prescribed at Discharge (7)
CL Item
Not Prescribed (8)
Item
Other Direct Thrombin Inhibitors
text
C3541936 (UMLS CUI [1])
Code List
Other Direct Thrombin Inhibitors
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Peri-PCI (6)
CL Item
Prescribed at Discharge (7)
CL Item
Not Prescribed (8)
Item
Other LMW Heparin
text
C3536766 (UMLS CUI [1])
Code List
Other LMW Heparin
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Peri-PCI (6)
CL Item
Prescribed at Discharge (7)
CL Item
Not Prescribed (8)
Item
Other Antiplatelet
text
C1096021 (UMLS CUI [1])
Code List
Other Antiplatelet
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Peri-PCI (6)
CL Item
Prescribed at Discharge (7)
CL Item
Not Prescribed (8)
Item
Other Antithrombin
text
Code List
Other Antithrombin
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Peri-PCI (6)
CL Item
Prescribed at Discharge (7)
CL Item
Not Prescribed (8)
Item
IV GP llb/llla
text
C3640054 (UMLS CUI-1)
Code List
IV GP llb/llla
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Peri-PCI (6)
CL Item
Prescribed at Discharge (7)
CL Item
Not Prescribed (8)
Item
Reason for GP IIb/IIIa administration
text
C0392360 (UMLS CUI [1,1])
C0864559 (UMLS CUI [1,2])
Code List
Reason for GP IIb/IIIa administration
CL Item
With PCI (started before PCI) (1)
CL Item
Without PCI (medical treatment) (2)
CL Item
Rescue (instituted after start of PCI. Sometimes referred to as bail-out use) (3)
Item Group
Other Medications
Item
ACE Inhibitor
text
C0003015 (UMLS CUI-1)
Code List
ACE Inhibitor
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Prescribed at Discharge/Transfer (6)
CL Item
Not Prescribed (7)
Item
Amiodarone
text
C0002598 (UMLS CUI-1)
Code List
Amiodarone
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Prescribed at Discharge/Transfer (6)
CL Item
Not Prescribed (7)
Item
Angiotensin II Receptor Blocker (ARB)
text
C0521942 (UMLS CUI-1)
Code List
Angiotensin II Receptor Blocker (ARB)
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Prescribed at Discharge/Transfer (6)
CL Item
Not Prescribed (7)
Item
Beta Blocker (IV)
text
C0304516 (UMLS CUI [1])
Code List
Beta Blocker (IV)
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Prescribed at Discharge/Transfer (6)
CL Item
Not Prescribed (7)
Item
Beta Blocker (Oral)
text
C0304516 (UMLS CUI [1])
Code List
Beta Blocker (Oral)
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Prescribed at Discharge/Transfer (6)
CL Item
Not Prescribed (7)
Item
Calcium Channel Blocker
text
C0006684 (UMLS CUI-1)
Code List
Calcium Channel Blocker
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Prescribed at Discharge/Transfer (6)
CL Item
Not Prescribed (7)
Item
Digoxin
text
C0012265 (UMLS CUI-1)
Code List
Digoxin
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Prescribed at Discharge/Transfer (6)
CL Item
Not Prescribed (7)
Item
Diuretic
text
C0012798 (UMLS CUI-1)
Code List
Diuretic
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Prescribed at Discharge/Transfer (6)
CL Item
Not Prescribed (7)
Item
Glucose/Insulin/Potassium (GIK)
text
C0061420 (UMLS CUI-1)
Code List
Glucose/Insulin/Potassium (GIK)
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Prescribed at Discharge/Transfer (6)
CL Item
Not Prescribed (7)
Item
Inotropic Agent (IV)
text
C0304509 (UMLS CUI-1)
Code List
Inotropic Agent (IV)
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Prescribed at Discharge/Transfer (6)
CL Item
Not Prescribed (7)
Item
Insulin
text
C0021641 (UMLS CUI-1)
Code List
Insulin
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Prescribed at Discharge/Transfer (6)
CL Item
Not Prescribed (7)
Item
Insulin Provider
text
C0935929 (UMLS CUI-1)
Code List
Insulin Provider
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Prescribed at Discharge/Transfer (6)
CL Item
Not Prescribed (7)
Item
Insulin Sensitizer
text
N (UMLS CUI-1)
Code List
Insulin Sensitizer
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Prescribed at Discharge/Transfer (6)
CL Item
Not Prescribed (7)
Item
Magnesium (IV)
text
C3540792 (UMLS CUI-1)
Code List
Magnesium (IV)
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Prescribed at Discharge/Transfer (6)
CL Item
Not Prescribed (7)
Item
Nitrate (IV)
text
C0028125 (UMLS CUI [1])
Code List
Nitrate (IV)
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Prescribed at Discharge/Transfer (6)
CL Item
Not Prescribed (7)
Item
Nitrate (Oral/Topical)
text
C0028125 (UMLS CUI [1])
Code List
Nitrate (Oral/Topical)
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Prescribed at Discharge/Transfer (6)
CL Item
Not Prescribed (7)
Item
Nicorandil
text
C0068700 (UMLS CUI-1)
Code List
Nicorandil
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Prescribed at Discharge/Transfer (6)
CL Item
Not Prescribed (7)
Item
Omega-3 Fatty Acids
text
C0015689 (UMLS CUI-1)
Code List
Omega-3 Fatty Acids
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Prescribed at Discharge/Transfer (6)
CL Item
Not Prescribed (7)
Item
Statin
text
C0360714 (UMLS CUI-1)
Code List
Statin
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Prescribed at Discharge/Transfer (6)
CL Item
Not Prescribed (7)
Item
Other Lipid Lowering Agent
text
Code List
Other Lipid Lowering Agent
CL Item
Blinded Study Drug (1)
CL Item
Chronic Use (2)
CL Item
Pre-Hospital Acute (3)
CL Item
Within 1st 24 hrs Hospital (4)
CL Item
After 1st 24 hrs Hospital (5)
CL Item
Prescribed at Discharge/Transfer (6)
CL Item
Not Prescribed (7)
Item Group
Medication Contraindications
Aspirin Contraindication
Item
ASA Contraindication
boolean
C0729798 (UMLS CUI-1)
Beta Blockers Contraindication
Item
Beta Blockers Contraindication
boolean
C1278474 (UMLS CUI-1)
ACE Inhibitors Contraindication
Item
ACE Inhibitors Contraindication
boolean
C0003015 (UMLS CUI [1,1])
C0522473 (UMLS CUI [1,2])
Angiotensin II Receptor Blocker Contraindication
Item
ARB Contraindication
boolean
C1273465 (UMLS CUI-1)
Statins Contraindication
Item
Statins Contraindication
boolean
C1277178 (UMLS CUI-1)
LMWH Contraindication
Item
LMWH Contraindication
boolean
C3536766 (UMLS CUI [1,1])
C0522473 (UMLS CUI [1,2])
UFH Contraindication
Item
UFH Contraindication
boolean
C2825026 (UMLS CUI [1,1])
C0522473 (UMLS CUI [1,2])
Item Group
Lifestyle interventions
C2960841 (UMLS CUI-1)
Item
If current cigarette smoker, was patient counseled to quit smoking by a health care professional?
text
C1273715 (UMLS CUI-1)
Code List
If current cigarette smoker, was patient counseled to quit smoking by a health care professional?
CL Item
No/Unknown (1)
CL Item
Yes (2)
CL Item
Does Not Apply (3)
Cardiac rehabilitation
Item
Was patient referred to a cardiac rehab program?
boolean
C0700431 (UMLS CUI-1)
Item Group
In-hospital Events: After Presentation
Recurrent Ischemic Symptoms
Item
Recurrent Ischemic Symptoms
boolean
C1735908 (UMLS CUI-1)
CHF/Pulmonary Edema
Item
CHF/Pulmonary Edema
boolean
C0018802 (UMLS CUI [1])
C0034063 (UMLS CUI [2])
Cardiogenic Shock
Item
Cardiogenic Shock
boolean
C0036980 (UMLS CUI-1)
Cardiac Arrest/VF
Item
Cardiac Arrest/VF
boolean
C0018790 (UMLS CUI [1])
C0042510 (UMLS CUI [2])
Date of cardiac arrest
Item
Date of cardiac arrest
datetime
C2825160 (UMLS CUI-1)
Atrial Fib/Flutter
Item
Atrial Fib/Flutter
boolean
C0004238 (UMLS CUI [1])
C0004239 (UMLS CUI [2])
Sustained ventricular tachycardia
Item
Sustained VT
boolean
C0750197 (UMLS CUI-1)
Thrombocytopenia
Item
Thrombocytopenia
boolean
C0040034 (UMLS CUI-1)
Heparin-induced thrombocytopenia
Item
HIT
boolean
C0272285 (UMLS CUI-1)
Venous Thromboembolism
Item
Venous Thromboembolism
boolean
C1861172 (UMLS CUI-1)
Acute Renal Failure
Item
Acute Renal Failure
boolean
C0022660 (UMLS CUI-1)
Severe AV Block
Item
AV Block (Mobitz II, 3°)
boolean
C0004245 (UMLS CUI [1])
Item
Mechanical Complication
text
Code List
Mechanical Complication
CL Item
Ventricular Septal Defect (1)
C0018818 (UMLS CUI-1)
CL Item
Mitral Regurgitation (2)
C0026266 (UMLS CUI-1)
CL Item
Free wall rupture (3)
C1959586 (UMLS CUI-1)
Myocardial Re-infarction
Item
MI > 24 hrs after hospital presentation/Re-infarction
boolean
C0948369 (UMLS CUI [1])
Item
MI confirmed by
text
C0521091 (UMLS CUI [1,1])
C0027051 (UMLS CUI [1,2])
Code List
MI confirmed by
CL Item
Cardiac Markers (1)
CL Item
ECG (2)
CL Item
Peri-procedural (3)
Stroke
Item
Stroke
boolean
C0038454 (UMLS CUI-1)
Stroke date
Item
Stroke date
date
C0038454 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Stroke confirmed by CT/MRI
Item
Stroke confirmed by CT/MRI
boolean
C0027051 (UMLS CUI [1,1])
C0521091 (UMLS CUI [1,2])
Item
Type of Stroke
text
C3897486 (UMLS CUI [1])
Code List
Type of Stroke
CL Item
Embolic/Ischemic (1)
CL Item
Embolic w/ Hemorrhagic Conversion (2)
CL Item
Hemorrhagic/Subdural (3)
CL Item
Hematoma (4)
CL Item
Other (5)
Major bleeding
Item
Major bleeding
boolean
C0019080 (UMLS CUI-1)
Date of major bleeding
Item
Date of major bleeding
date
C0019080 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Bleeding location
text
C0019080 (UMLS CUI [1,1])
C0450429 (UMLS CUI [1,2])
Code List
Bleeding location
CL Item
Vascular Access (1)
CL Item
Other Site (2)
Item
Bleeding treatment
text
C0149533 (UMLS CUI-1)
Code List
Bleeding treatment
CL Item
Surgery (1)
CL Item
Transfusion (2)
CL Item
Both Surgery and Transfusion (3)
CL Item
None (4)
Item Group
Discharge status
Patient in research protocol
Item
Was patient treated as part of a research protocol?
boolean
C0422739 (UMLS CUI-1)
Item
Discharge Status
text
C2599747 (UMLS CUI [1])
Code List
Discharge Status
CL Item
Death (1)
CL Item
Home (2)
CL Item
Transfer to Another Acute Facility (3)
CL Item
AMA/Self-Discharge (4)
CL Item
Other (5)
Date of Discharge
Item
Date of Discharge or Death
date
C2361123 (UMLS CUI [1])
C1148348 (UMLS CUI [2])
Time of Death
Item
Time of Death (if died)
time
C1301931 (UMLS CUI-1)
Item
Primary Discharge Diagnosis
text
C0332144 (UMLS CUI-1)
Code List
Primary Discharge Diagnosis
CL Item
ACS (1)
CL Item
Other Cardiac (2)
CL Item
Other (3)
Item
Who was the primary physician who cared for the patient while in the hospital?
text
C1508823 (UMLS CUI-1)
Code List
Who was the primary physician who cared for the patient while in the hospital?
CL Item
Cardiologist (1)
CL Item
Non-cardiologist (2)

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