ID

27738

Description

BREAST CANCER DATA COLLECTION Version 2.0.3 Revised: April 5th, 2017, International Consortium for Health Outcomes Measurement (ICHOM), Source: http://www.ichom.org/ Conditions: Asymptomatic Coronary Artery Disease | Stable Angina | Acute Coronary Syndrome (Includes AMI) Treatment Approaches: Lifestyle Modification | Drug Therapy | Percutaneous Coronary Intervention (PCI) | Coronary Artery Bypass Grafting (CABG)

Link

http://www.ichom.org/

Keywords

Versions (7)
  1. 11/27/17 11/27/17 -
  2. 11/27/17 11/27/17 -
  3. 12/4/17 12/4/17 -
  4. 12/7/17 12/7/17 -
  5. 12/8/17 12/8/17 -
  6. 11/22/18 11/22/18 - Sarah Riepenhausen
  7. 4/30/20 4/30/20 - Sarah Riepenhausen
Copyright Holder

ICHOM

Uploaded on

November 27, 2017

DOI

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License

Creative Commons BY-NC 3.0
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ICHOM Coronary Artery Disease

English

ICHOM Coronary Artery Disease

1 forms  
Coronary Artery Disease
Description

Coronary Artery Disease

Indicate the patient's medical record number
Description

This number will not be shared with ICHOM. In the case patient-level data is submitted to ICHOM for benchmarking or research purposes, a separate ICHOM Patient Identifier will be created and cross-linking between the ICHOM Patient Identifier and the medical record number will only be known at the treating institution INCLUSION CRITERIA: All patients TIMING: On all forms REPORTING SOURCE: Administrative or clinical RESPONSE OPTIONS: According to institution

Data type

integer

Alias
UMLS CUI [1]
C1269815
Demographic factors
Description

Demographic factors

What is your date of birth?
Description

INCLUSION CRITERIA: All patients TIMING: At time of diagnosis REPORTING SOURCE: Patient-reported, clinical, or administrative data

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1]
C0421451
DD/MM/YYYY
Please indicate your sex at birth
Description

INCLUSION CRITERIA: All patients TIMING: At time of diagnosis REPORTING SOURCE: Patient-reported, clinical, or administrative data TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0079399
Baseline health status
Description

Baseline health status

Indicate if the patient has had at least one documented previous myocardial infarction at any point in their history
Description

INCLUSION CRITERIA: All patients TIMING: At time of diagnosis REPORTING SOURCE: Clinical* TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0027051
Indicate if the patient has a documented history of heart failure
Description

Heart failure is defined as physician documentation or report of any of the following clinical symptoms of heart failure described as unusual dyspnea on light exertion, recurrent dyspnea occurring in the supine position, fluid retention; or the description of rales, jugular venous distension, pulmonary edema on physical exam, or pulmonary edema on chest x-ray presumed to be cardiac dysfunction. A low ejection fraction alone, without clinical evidence of heart failure does not qualify as heart failure INCLUSION CRITERIA: All patients TIMING: At time of diagnosis REPORTING SOURCE: Clinical* TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0018802
Indicate whether the patient has a documented history of hypertension diagnosed and treated with medication and/or diet and/or exercise
Description

INCLUSION CRITERIA: All patients TIMING: At time of diagnosis REPORTING SOURCE: Clinical* TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0020538
Indicate whether the patient has a documented history of stroke
Description

Stroke is defined as any confirmed neurological deficit of abrupt onset caused by a disturbance in blood supply to the brain that did not resolve within 24 hours INCLUSION CRITERIA: All patients TIMING: At time of diagnosis REPORTING SOURCE: Clinical* TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0038454
Indicate if the patient has a documented history of diabetes mellitus (regardless of duration of disease or need for anti-diabetic agents)
Description

INCLUSION CRITERIA: All patients TIMING: At time of diagnosis REPORTING SOURCE: Clinical* TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0011849
Indicate if the patient is insulin dependent
Description

INCLUSION CRITERIA: All patients If answered 'yes' to patient having a documented history of diabetes mellitus (DIAB) TIMING: At time of diagnosis REPORTING SOURCE: Clinical* TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0011854
Indicate whether the patient has a history of peripheral arterial disease
Description

Includes upper and lower extremity, renal, mesenteric, and abdominal aortic systems evidenced by a documented history of 1. Peripheral arterial disease and/or 2. Claudication, either with exertion or at rest, and/or 3. Amputation for arterial vascular insufficiency, and/or 4. Vascular reconstruction, bypass surgery, or percutaneous intervention to the extremities (excluding dialysis fistulas and vein stripping), and/or 5. Documented aortic aneurysm with or without repair. Peripheral arterial disease excludes disease in the carotid or cerebrovascular arteries INCLUSION CRITERIA: All patients TIMING: At time of diagnosis REPORTING SOURCE: Clinical* TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1]
C1881056
Indicate whether the patient is dialysis dependent
Description

INCLUSION CRITERIA: All patients TIMING: At time of diagnosis REPORTING SOURCE: Clinical* TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0524376
Indicate the patient’s baseline creatinine level
Description

INCLUSION CRITERIA: All patients TIMING: At time of diagnosis REPORTING SOURCE: Clinical RESPONSE OPTIONS: Absolute numerical value of baseline creatinine level (include units)

Data type

integer

Alias
UMLS CUI [1]
C0201975
Indicate units of baseline creatinine level
Description

INCLUSION CRITERIA: All patients TIMING: At time of diagnosis REPORTING SOURCE: Clinical* TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0201975
UMLS CUI [1,2]
C1519795
Indicate whether the patient has a chronic lung disease
Description

Including but not limited to COPD and asthma INCLUSION CRITERIA: All patients TIMING: At time of diagnosis REPORTING SOURCE: Clinical* TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1]
C1533075
Indicate if the patient is oxygen dependent
Description

INCLUSION CRITERIA: All patients If answered 'yes' to patient having a chronic lung disease (CHRONLD) TIMING: At time of diagnosis REPORTING SOURCE: Clinical* TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0030054
UMLS CUI [1,3]
C0439857
Indicate whether the patient has a history of cirrhosis
Description

INCLUSION CRITERIA: All patients TIMING: At time of diagnosis REPORTING SOURCE: Clinical* TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0023890
Indicate whether the patient has a history of dementia
Description

Including but not limited to, Alzheimer’s disease, vascular dementia, lewy body dementia and frontotemporal dementia INCLUSION CRITERIA: All patients TIMING: At time of diagnosis REPORTING SOURCE: Clinical* TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0497327
Indicate the patient's height
Description

Height and weight are used to calculate BMI INCLUSION CRITERIA: All patients TIMING: Index hospitalization REPORTING SOURCE: Clinical RESPONSE OPTIONS: Numerical value of height in centimeters or inches

Data type

integer

Alias
UMLS CUI [1]
C0005890
Indicate units of height
Description

INCLUSION CRITERIA: All patients TIMING: Index hospitalization REPORTING SOURCE: Clinical TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0005890
UMLS CUI [1,2]
C1519795
Indicate the patient's weight
Description

Height and weight are used to calculate BMI INCLUSION CRITERIA: All patients TIMING: Index hospitalization REPORTING SOURCE: Clinical RESPONSE OPTIONS: Numerical value of weight in kilograms or pounds

Data type

integer

Alias
UMLS CUI [1]
C0005910
Indicate units of weight
Description

INCLUSION CRITERIA: All patients TIMING: Index hospitalization REPORTING SOURCE: Clinical TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1,1]
C0005910
UMLS CUI [1,2]
C1519795
Indicate whether troponin T or I
Description

INCLUSION CRITERIA: ACS patients TIMING: Index hospitalization REPORTING SOURCE: Clinical TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C0523952
Indicate the peak level reached
Description

INCLUSION CRITERIA: ACS patients TIMING: Index hospitalization REPORTING SOURCE: Clinical RESPONSE OPTIONS: Numerical value of peak level

Data type

integer

Alias
UMLS CUI [1,1]
C0523952
UMLS CUI [1,2]
C0444505
Give the lab’s upper limit of normal
Description

INCLUSION CRITERIA: ACS patients TIMING: Index hospitalization REPORTING SOURCE: Clinical RESPONSE OPTIONS: Numerical value of upper limit of normal

Data type

integer

Alias
UMLS CUI [1,1]
C0523952
UMLS CUI [1,2]
C1519815
Indicate the first measurement or earliest record of heart rate (in beats per minute) for this episode of care
Description

Measurement from the transferring facility is acceptable INCLUSION CRITERIA: ACS patients TIMING: Index hospitalization REPORTING SOURCE: Clinical RESPONSE OPTIONS: Numerical value of heart rate in beats per minute

Data type

integer

Alias
UMLS CUI [1]
C0018810
Indicate the first measurement or earliest record of systolic blood pressure (mm Hg) for this episode of care
Description

Measurement from the transferring facility is acceptable INCLUSION CRITERIA: ACS patients TIMING: Index hospitalization REPORTING SOURCE: Clinical RESPONSE OPTIONS: Numerical value of systolic blood pressure in mm Hg

Data type

integer

Alias
UMLS CUI [1]
C0871470
Indicate whether the patient has a documented discharge diagnosis of NSTEMI or STEMI
Description

INCLUSION CRITERIA: ACS patients TIMING: Index hospitalization REPORTING SOURCE: Clinical TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C1555319
Indicate whether the patient has had an episode of cardiogenic shock at first medical contact
Description

Cardiogenic shock is defined as a sustained (>30 minutes) episode of systolic blood pressure <90 mm Hg, and/or cardiac index, 2.2 L/min/m2 determined to be secondary to cardiac dysfunction, and/or the requirement for parenteral inotropic or vasopressor agents or mechanical support (e.g., IABP, extracorporeal circulation, ventricular assist devices) to maintain blood pressure and cardiac index above those specified levels. Note: Transient episodes of hypotension reversed with IV fluid or atropine do not constitute cardiogenic shock. The hemodynamic compromise (with or without extraordinary supportive therapy) must persist for at least 30 minutes INCLUSION CRITERIA: ACS patients, PCI and CABG patients TIMING: Index hospitalization REPORTING SOURCE: Clinical TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C0036980
Indicate if the patient has had an episode of cardiac arrest evaluated by pre- hospital emergency services or emergency department personnel
Description

Cardiac arrest means the patient either 1. received attempts at external defibrillation (by lay responders or emergency personnel) or chest compressions by organized pre-hospital emergency services or emergency department personnel or 2. was pulseless but did not receive attempts to defibrillate or cardiopulmonary resuscitation (CPR) by emergency personnel. ‘Sudden’ cardiac arrest is the sudden cessation of cardiac activity so that the victim becomes unresponsive, with no normal breathing and no signs of circulation. If corrective measures are not taken rapidly, this condition progresses to sudden death. Cardiac arrest should be used to signify an event as described above that is reversed, usually by CPR, and/or defibrillation or cardioversion, or cardiac pacing. Sudden cardiac arrest is not the same as sudden cardiac death. Sudden cardiac death describes a fatal event INCLUSION CRITERIA: ACS patients, PCI and CABG patients TIMING: Index hospitalization REPORTING SOURCE: Clinical TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C0018790
Indicate units of presenting creatinine level
Description

INCLUSION CRITERIA: ACS patients, PCI and CABG patients TIMING: At time of diagnosis REPORTING SOURCE: Clinical TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1,1]
C0201976
UMLS CUI [1,2]
C1519795
Indicate units of presenting creatinine level
Description

INCLUSION CRITERIA: All patients TIMING: At time of diagnosis REPORTING SOURCE: Clinical TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1,1]
C0201976
UMLS CUI [1,2]
C1519795
Indicate the clinical status of the patient prior to entering the operating room
Description

Elective: The patient’s cardiac function has been stable in the days or weeks prior to the operation. The procedure could be deferred without increased risk of compromised cardiac outcome Urgent: Procedure required during same hospitalization in order to minimize chance of further clinical deterioration. Examples include but are not limited to: Worsening chest pain, sudden chest pain, CHF, acute myocardial infarction (AMI), anatomy, IABP, unstable angina (USA) with intravenous (IV) nitroglycerin (NTG) or rest angina Emergent: Patients requiring emergency operations will have ongoing, refractory (difficult, complicated, and/or unmanageable) unrelenting cardiac compromise, with or without hemodynamic instability, and not responsive to any form of therapy except cardiac surgery. An emergency operation is one in which there should be no delay in providing operative intervention Emergent Salvage: The patient is undergoing CPR en route to the operating room or prior to anesthesia induction or has ongoing ECMO to maintain life INCLUSION CRITERIA: CABG patients only TIMING: Index hospitalization REPORTING SOURCE: Clinical TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C0010055
Indicate the clinical status of the patient prior to entering the operating room
Description

Elective: The patient’s cardiac function has been stable in the days or weeks prior to the operation. The procedure could be deferred without increased risk of compromised cardiac outcome Not elective: Urgent, emergent, or emergent salvage (see above) INCLUSION CRITERIA: PCI patients only TIMING: Index hospitalization REPORTING SOURCE: Clinical TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C1320647
Indicate whether the patient has Left Main Coronary Disease
Description

Elective: The patient’s cardiac function has been stable in the days or weeks prior to the operation. The procedure could be deferred without increased risk of compromised cardiac outcome Not elective: Urgent, emergent, or emergent salvage (see above) INCLUSION CRITERIA: PCI and CABG patients only TIMING: Index hospitalization REPORTING SOURCE: Clinical TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C1299433
Indicate the number of diseased major native coronary vessel systems: LAD system, Circumflex system, and/or Right system with ≥50 percent narrowing of any vessel preoperatively
Description

Left main disease (≥50 percent) is counted as TWO vessels (LAD and Circumflex, which may include a Ramus Intermedius). For example, left main and RCA would count as three total INCLUSION CRITERIA: PCI and CABG patients only TIMING: Index hospitalization REPORTING SOURCE: Clinical RESPONSE OPTIONS: Numerical value of diseased vessels

Data type

integer

Alias
UMLS CUI [1]
C3275120
Indicate the patient’s pre-procedural creatinine level
Description

INCLUSION CRITERIA: PCI and CABG patients only TIMING: Index hospitalization REPORTING SOURCE: Clinical RESPONSE OPTIONS: Absolute numerical value of pre-procedural creatinine level in mg/dl

Data type

integer

Alias
UMLS CUI [1,1]
C0201976
UMLS CUI [1,2]
C0332152
UMLS CUI [1,3]
C0087111
Indicate the patient’s pre-procedural creatinine level
Description

INCLUSION CRITERIA: PCI and CABG patients only TIMING: Index hospitalization REPORTING SOURCE: Clinical RESPONSE OPTIONS: Absolute numerical value of pre-procedural creatinine level in mg/dl

Data type

integer

Alias
UMLS CUI [1,1]
C0201976
UMLS CUI [1,2]
C0332152
UMLS CUI [1,3]
C0087111
Prior Treatments
Description

Prior Treatments

Indicate if the patient has had a previous CABG
Description

Includes CABG + other heart surgery e.g. CABG + Valve INCLUSION CRITERIA: ACS patients, PCI and CABG patients TIMING: Index hospitalization REPORTING SOURCE: Clinical TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0010055
Indicate date of CABG
Description

INCLUSION CRITERIA: ACS patients, PCI and CABG patients TIMING: Index hospitalization REPORTING SOURCE: Clinical

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0010055
UMLS CUI [1,2]
C0011008
DD/MM/YYYY
Indicate if the patient had a previous percutaneous coronary intervention (PCI) of any type (balloon angioplasty, stent or other)
Description

A percutaneous coronary intervention (PCI) is the placement of an angioplasty guide wire, balloon, or other device (e.g. stent, atherectomy, brachytherapy, or thrombectomy catheter) into a native coronary artery or coronary artery bypass graft for the purpose of mechanical coronary revascularization INCLUSION CRITERIA: ACS patients, PCI and CABG patients TIMING: Index hospitalization REPORTING SOURCE: Clinical TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1]
C1320647
Indicate date of PCI
Description

INCLUSION CRITERIA: ACS patients, PCI and CABG patients TIMING: Index hospitalization REPORTING SOURCE: Clinical

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C1532338
UMLS CUI [1,2]
C0011008
DD/MM/YYYY
TREATMENT VARIABLES
Description

TREATMENT VARIABLES

Indicate the PCI procedure type
Description

PCI + other includes but is not limited to: right heart caths, EtOH ablations, septal closures, and other angiograms and/or endovascular interventions INCLUSION CRITERIA: Patients receiving percutaneous coronary interventions TIMING: During index visit or hospitalization for procedure REPORTING SOURCE: Clinical TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C1532338
UMLS CUI [1,2]
C0332307
Indicate the cardiac surgery procedure type
Description

CABG + other includes but is not limited to: placement of ventricular assist devices, non-cardiac procedures INCLUSION CRITERIA: Patients receiving cardiac surgery TIMING: During index visit or hospitalization for procedure REPORTING SOURCE: Clinical TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0018821
UMLS CUI [1,2]
C0332307
Indicate the episode type
Description

INCLUSION CRITERIA: All patients undergoing interventional treatment for coronary disease TIMING: During index visit or hospitalization for procedure REPORTING SOURCE: Clinical TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0741923
Acute complications of treatment
Description

Acute complications of treatment

Indicate if the patient has died, regardless of cause
Description

Any death, regardless of cause occurring (1) within 30 days after surgery in or out of the hospital, and (2) after 30 days during the same hospitalization subsequent to the operation INCLUSION CRITERIA: PCI and CABG patients TIMING: Within 30 days of procedure REPORTING SOURCE: Clinical or administrative data TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0011065
Indicate the date the patient was declared dead
Description

INCLUSION CRITERIA: PCI and CABG patients If answered 'yes' that patient has died (DEATH) TIMING: Within 30 days of procedure REPORTING SOURCE: Clinical or administrative data

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1]
C1148348
DD/MM/YYYY
Indicate where the patient died
Description

INCLUSION CRITERIA: PCI and CABG patients If answered 'yes' that patient has died (DEATH) TIMING: Within 30 days of procedure REPORTING SOURCE: Clinical or administrative data TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1]
C2924451
Indicate whether the patient had a stroke
Description

Stroke is defined as any confirmed neurological deficit of abrupt onset caused by a disturbance in blood supply to the brain that did not resolve within 24 hours INCLUSION CRITERIA: PCI and CABG patients TIMING: Within 30 days of procedure REPORTING SOURCE: Clinical or administrative data TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0038454
Indicate type of stroke if documented on imaging, or via lumbar puncture, neurosurgery, or autopsy
Description

INCLUSION CRITERIA: PCI and CABG patients If answered 'yes' that patient had a stroke (STROKE) TIMING: Within 30 days of procedure REPORTING SOURCE: Clinical or administrative data TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1]
C3897486
Indicate whether the patient has a diagnosis of acute renal failure
Description

Acute renal failure is the documented history of AKI and/or Increase in serum creatinine by ≥ 0.3 mg/dl (≥ 26.5 l mol/l) within 48 hours; and/or increase in serum creatinine to ≥ 1.5 times baseline, which is known or presumed to have occurred within the prior 7 days; and/or urine volume < 0.5 ml/kg/h for 6 hours; and/or new requirement for dialysis INCLUSION CRITERIA: PCI and CABG patients TIMING: Within 30 days of procedure REPORTING SOURCE: Clinical or administrative data TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0022660
Indicate the date the patient first arrived
Description

Date used to calculate total length of stay and post-procedure length of stay INCLUSION CRITERIA: PCI and CABG patients TIMING: Within 30 days of procedure REPORTING SOURCE: Clinical or administrative data

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1]
C1302393
DD/MM/YYYY
Indicate the date the patient was discharged
Description

Date used to calculate total length of stay INCLUSION CRITERIA: PCI and CABG patients TIMING: Within index hospitalization REPORTING SOURCE: Administrative data

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1]
C2361123
DD/MM/YYYY
Indicate the date of intervention
Description

Date used to calculate post-procedure length of stay INCLUSION CRITERIA: PCI and CABG patients TIMING: Within index hospitalization REPORTING SOURCE: Administrative data

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1]
C2584899
DD/MM/YYYY
Major surgery complications
Description

Major surgery complications

Indicate whether the patient had prolonged pulmonary ventilator >24 hours after CABG
Description

Includes (but not limited to) causes such as ARDS, pulmonary edema, and/or any patient requiring mechanical ventilation > 24 hours postoperatively INCLUSION CRITERIA: CABG patients TIMING: Within index hospitalization REPORTING SOURCE: Clinical TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0199470
UMLS CUI [1,2]
C0439590
Indicate whether the patient had a deep sternal infection involving muscle, bone, and/or mediastinum REQUIRING OPERATIVE INTERVENTION
Description

Must have ALL of the following conditions: 1. Wound opened with excision of tissue (I&D) or re-exploration of mediastinum 2. Positive culture unless patient on antibiotics at time of culture or no culture obtained 3. Treatment with antibiotics beyond perioperative prophylaxis INCLUSION CRITERIA: CABG patients TIMING: Within 30 days of procedure REPORTING SOURCE: Clinical TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0043241
UMLS CUI [1,2]
C1411231
Indicate if the patient required a return to the operating room for bleeding with or without tamponade, graft occlusion, valve dysfunction, or other cardiac reason
Description

INCLUSION CRITERIA: CABG patients TIMING: Within 30 days of procedure REPORTING SOURCE: Clinical TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0558347
Major interventional cardiology complications
Description

Major interventional cardiology complications

Indicate if a significant dissection was observed at the time of PCI
Description

Typically, dissections described as type A or B are not considered significant dissections because there is no impairment of flow. Significant dissections are grade C dissections in the presence of ischemia, or grade D-F dissections, all of which are further described as: Type C: persisting contrast medium extravasations; Type D: spital filling defect with delayed but complete distal flow; Type E: persistent filling defect with delayed antegrade flow; Type F: filling defect with impaired flow and total occlusion INCLUSION CRITERIA: PCI patients TIMING: Within index hospitalization REPORTING SOURCE: Clinical TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C1532338
UMLS CUI [1,2]
C0012737
Indicate if angiographic or clinical evidence of perforation was observed at the time of the PCI procedure
Description

A coronary artery perforation occurs when there is angiographic or clinical evidence of a dissection or intimal tear that extends through the full thickness of the arterial wall INCLUSION CRITERIA: PCI patients TIMING: Within index hospitalization REPORTING SOURCE: Clinical TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C1532338
UMLS CUI [1,2]
C0340664
Indicate the occurrence of any emergency cardiothoracic surgical procedure (whether or not this actually involves the placing of bypass grafts)
Description

The surgery should be: a. Cardio-thoracic (rather than for peripheral vascular complications at access sites) b. Prompted and indicated by a need to - Perform emergency revascularization to a coronary distribution that has been the subject of a PCI or attempted PCI and/or - To correct as an emergency a complication of PCI such as abrupt vessel closure, cardiac or vessel perforation, dissection of a thoracic great vessel etc. INCLUSION CRITERIA: PCI patients TIMING: Within index hospitalization REPORTING SOURCE: Clinical TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0010055
UMLS CUI [1,2]
C0184893
Indicate if the patient experienced any non-cardiac vascular complications (excluding external bleeding or hematomas) at the percutaneous entry site that required treatment or intervention
Description

Vascular complications can include, but are not limited to, access site occlusions, peripheral embolizations, dissections, pseudoaneurysms and/or AV fistulas. Any noted vascular complication must have had an intervention such as a fibrin injection, angioplasty, or surgical repair to qualify. Prolonged pressure does not qualify as an intervention, but ultrasonic guided compression after making a diagnosis of pseudoaneurysm does qualify. A retroperitoneal bleed or hematoma requiring transfusion is not a vascular complication under this data element. To qualify, this adverse outcome should be attributable to this procedure and not related to a previous or subsequent procedure INCLUSION CRITERIA: PCI patients TIMING: Within 30 days of procedure REPORTING SOURCE: Clinical TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C1393529
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C0184661
Indicate if the patient experienced a suspected or confirmed bleeding event
Description

A bleeding event is 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) INCLUSION CRITERIA: PCI patients TIMING: Within 72 hours of procedure REPORTING SOURCE: Clinical TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0019080
Patient-Reported Health Status
Description

Patient-Reported Health Status

Do you get out of breath in the following situations? When hurrying on ground level or walking up a slight hill
Description

INCLUSION CRITERIA: All patients TIMING: Baseline 30 days + annually up to 5 years after index event REPORTING SOURCE: Patient-reported TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1]
C4288225
When walking with other people your age on level ground
Description

INCLUSION CRITERIA: All patients TIMING: Baseline 30 days + annually up to 5 years after index event REPORTING SOURCE: Patient-reported TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1]
C2183407
When walking your own pace on level ground
Description

INCLUSION CRITERIA: All patients TIMING: Baseline 30 days + annually up to 5 years after index event REPORTING SOURCE: Patient-reported TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C2183407
UMLS CUI [1,2]
C3173662
When washing or dressing
Description

INCLUSION CRITERIA: All patients TIMING: Baseline 30 days + annually up to 5 years after index event REPORTING SOURCE: Patient-reported TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0013404
UMLS CUI [1,2]
C3827978
Over the past 2 weeks, how often have you been bothered by any of the following problems? Little interest or pleasure in doing things
Description

INCLUSION CRITERIA: All patients TIMING: Baseline 30 days + annually up to 5 years after index event REPORTING SOURCE: Patient-reported TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1]
C2707451
Feeling down, depressed or hopeless
Description

INCLUSION CRITERIA: All patients TIMING: Baseline 30 days + annually up to 5 years after index event REPORTING SOURCE: Patient-reported TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1]
C2707455
Cardiovascular disease progression
Description

Cardiovascular disease progression

Indicate if the patient was admitted due to an AMI
Description

INCLUSION CRITERIA: All patients TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding) TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0155626
Indicate the date of each admission for AMI during the defined interval
Description

Date used to calculate total length of stay due to AMI INCLUSION CRITERIA: All patients If answered 'yes' to the patient being admitted for an AMI (AMI) TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding)

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0155626
UMLS CUI [1,2]
C1302393
DD/MM/YYYY
Indicate the date of each discharge for AMI during the defined interval
Description

Date used to calculate total length of stay due to AMI INCLUSION CRITERIA: All patients If answered 'yes' to the patient being admitted for an AMI (AMI) TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding)

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0155626
UMLS CUI [1,2]
C2361123
DD/MM/YYYY
Indicate if the patient was admitted due to a hemorrhagic stoke
Description

INCLUSION CRITERIA: All patients TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding) TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1]
C1096400
Indicate the date of each admission for hemorrhagic stroke during the defined interval
Description

Date used to calculate total length of stay due to hemorrhagic stroke INCLUSION CRITERIA: All patients If answered 'yes' to the patient being admitted for a hemorrhagic stroke (HSTROKE) TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding)

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C1096400
UMLS CUI [1,2]
C1302393
DD/MM/YYYY
Indicate the date of each discharge for hemorrhagic stroke during the defined interval
Description

Date used to calculate total length of stay due to hemorrhagic stroke INCLUSION CRITERIA: All patients If answered 'yes' to the patient being admitted for a hemorrhagic stroke (HSTROKE) TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding)

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C1096400
UMLS CUI [1,2]
C2361123
DD/MM/YYYY
Indicate if the patient was admitted due to an ischemic stoke
Description

INCLUSION CRITERIA: All patients TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding) TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0948008
Indicate the date of each admission for ischemic stroke during the defined interval
Description

Date used to calculate total length of stay due to ischemic stroke INCLUSION CRITERIA: All patients If answered 'yes' to the patient being admitted for an ischemic stroke (ISTROKE) TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding)

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0948008
UMLS CUI [1,2]
C1302393
DD/MM/YYYY
Indicate the date of each discharge for ischemic stroke during the defined interval
Description

Date used to calculate total length of stay due to ischemic stroke INCLUSION CRITERIA: All patients If answered 'yes' to the patient being admitted for an ischemic stroke (ISTROKE) TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding)

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0948008
UMLS CUI [1,2]
C2361123
DD/MM/YYYY
Indicate if the patient was admitted due to an unknown stoke
Description

INCLUSION CRITERIA: All patients TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding) TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0038454
Indicate the date of each admission for unknown stroke during the defined interval
Description

Date used to calculate total length of stay due to unknown stroke INCLUSION CRITERIA: All patients If answered 'yes' to the patient being admitted for an unknown stroke (USTROKE) TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding)

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0038454
UMLS CUI [1,2]
C2316983
DD/MM/YYYY
Indicate the date of each discharge for unknown stroke during the defined interval
Description

Date used to calculate total length of stay due to unknown stroke INCLUSION CRITERIA: All patients If answered 'yes' to the patient being admitted for an unknown stroke (USTROKE) TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding)

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0038454
UMLS CUI [1,2]
C2361123
DD/MM/YYYY
Indicate if the patient was admitted due to heart failure
Description

Heart failure is defined as physician documentation or report of any of the following clinical symptoms of heart failure described as unusual dyspnea on light exertion, recurrent dyspnea occurring in the supine position, fluid retention; or the description of rales, jugular venous distension, pulmonary edema on physical exam, or pulmonary edema on chest x-ray presumed to be cardiac dysfunction. A low ejection fraction alone, without clinical evidence of heart failure does not qualify as heart failure INCLUSION CRITERIA: All patients TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding) TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0018801
Indicate the date of each admission for heart failure during the defined interval
Description

Date used to calculate total length of stay due to heart failure INCLUSION CRITERIA: All patients If answered 'yes' to the patient being admitted for heart failure (HF) TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding)

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C1302393
DD/MM/YYYY
Indicate the date of each discharge for unknown stroke during the defined interval
Description

Date used to calculate total length of stay due to heart failure INCLUSION CRITERIA: All patients If answered 'yes' to the patient being admitted for heart failure (HF) TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding)

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C2361123
DD/MM/YYYY
Indicate if a PCI was performed
Description

INCLUSION CRITERIA: All patients TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding) TYPE: Multiple answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C1532338
Indicate the date of the PCI
Description

Restricted to PCI, CABG INCLUSION CRITERIA: All patients TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding)

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0189573
UMLS CUI [1,2]
C2584899
DD/MM/YYYY
Indicate the date of the PCI
Description

Restricted to PCI, CABG INCLUSION CRITERIA: All patients TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding)

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0189573
UMLS CUI [1,2]
C2584899
DD/MM/YYYY
Indicate if a CABG was performed
Description

INCLUSION CRITERIA: All patients TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding) TYPE: Multiple answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0010055
Indicate the date of the CABG
Description

Restricted to PCI, CABG INCLUSION CRITERIA: All patients TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding)

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0010055
UMLS CUI [1,2]
C2584899
DD/MM/YYYY
Indicate the date of the CABG
Description

Restricted to PCI, CABG INCLUSION CRITERIA: All patients TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding)

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0010055
UMLS CUI [1,2]
C2584899
DD/MM/YYYY
Indicate if the patient has a new requirement for dialysis
Description

INCLUSION CRITERIA: All patients TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding) TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0011946
UMLS CUI [1,2]
C1514873
Indicate the date the patient first began dialysis treatment
Description

INCLUSION CRITERIA: All patients If answered 'yes' that the began dialysis treatment TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding)

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0011946
UMLS CUI [1,2]
C2584899
DD/MM/YYYY
Survival
Description

Survival

Indicate if the patient has died, regardless of cause
Description

INCLUSION CRITERIA: All patients TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding) TYPE: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0011065
Indicate the date the patient was declared dead
Description

INCLUSION CRITERIA: All patients If answered 'yes' on Mortality: Patient died regardless of cause (DEATHADMIN) TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding)

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1]
C1148348
DD/MM/YYYY
Indicate where the patient died
Description

INCLUSION CRITERIA: All patients If answered 'yes' on Mortality: Patient died regardless of cause (DEATHADMIN) TIMING: Tracked ongoing Reported at 1 year + 5 years after index event REPORTING SOURCE: Administrative data (diagnosis coding) TYPE: Single answer

Data type

integer

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1]
C2924451
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Similar models

ICHOM Coronary Artery Disease

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Coronary Artery Disease
Patient ID
Item
Indicate the patient's medical record number
integer
C1269815 (UMLS CUI [1])
Item Group
Demographic factors
Age
Item
What is your date of birth?
date
C0421451 (UMLS CUI [1])
Item
Please indicate your sex at birth
integer
C0079399 (UMLS CUI [1])
Sex
Code List
Please indicate your sex at birth
CL Item
Male (1)
CL Item
Female (2)
Item Group
Baseline health status
Item
Indicate if the patient has had at least one documented previous myocardial infarction at any point in their history
integer
C0262926 (UMLS CUI [1,1])
C0027051 (UMLS CUI [1,2])
Past medical history: Previous AMI
Code List
Indicate if the patient has had at least one documented previous myocardial infarction at any point in their history
CL Item
No (0)
CL Item
Yes (1)
Item
Indicate if the patient has a documented history of heart failure
integer
C0262926 (UMLS CUI [1,1])
C0018802 (UMLS CUI [1,2])
Past medical history: Previous AMI
Code List
Indicate if the patient has a documented history of heart failure
CL Item
No (0)
CL Item
Yes (1)
Item
Indicate whether the patient has a documented history of hypertension diagnosed and treated with medication and/or diet and/or exercise
integer
C0262926 (UMLS CUI [1,1])
C0020538 (UMLS CUI [1,2])
Past medical history: Previous AMI
Code List
Indicate whether the patient has a documented history of hypertension diagnosed and treated with medication and/or diet and/or exercise
CL Item
No (0)
CL Item
Yes (1)
Item
Indicate whether the patient has a documented history of stroke
integer
C0262926 (UMLS CUI [1,1])
C0038454 (UMLS CUI [1,2])
Past medical history: Previous AMI
Code List
Indicate whether the patient has a documented history of stroke
CL Item
No (0)
CL Item
Yes (1)
Item
Indicate if the patient has a documented history of diabetes mellitus (regardless of duration of disease or need for anti-diabetic agents)
integer
C0262926 (UMLS CUI [1,1])
C0011849 (UMLS CUI [1,2])
Past medical history: Previous AMI
Code List
Indicate if the patient has a documented history of diabetes mellitus (regardless of duration of disease or need for anti-diabetic agents)
CL Item
No (0)
CL Item
Yes (1)
Item
Indicate if the patient is insulin dependent
integer
C0262926 (UMLS CUI [1,1])
C0011854 (UMLS CUI [1,2])
Past medical history: Previous AMI
Code List
Indicate if the patient is insulin dependent
CL Item
No (0)
CL Item
Yes (1)
Item
Indicate whether the patient has a history of peripheral arterial disease
integer
C1881056 (UMLS CUI [1])
Past medical history: Previous AMI
Code List
Indicate whether the patient has a history of peripheral arterial disease
CL Item
No (0)
CL Item
Yes (1)
Item
Indicate whether the patient is dialysis dependent
integer
C0524376 (UMLS CUI [1])
Past medical history: Previous AMI
Code List
Indicate whether the patient is dialysis dependent
CL Item
No (0)
CL Item
Yes (1)
Laboratory values: Baseline creatinine level
Item
Indicate the patient’s baseline creatinine level
integer
C0201975 (UMLS CUI [1])
Item
Indicate units of baseline creatinine level
integer
C0201975 (UMLS CUI [1,1])
C1519795 (UMLS CUI [1,2])
Past medical history: Previous AMI
Code List
Indicate units of baseline creatinine level
CL Item
µmol/l (1)
CL Item
mg/dl (2)
Item
Indicate whether the patient has a chronic lung disease
integer
C1533075 (UMLS CUI [1])
Past medical history: Previous AMI
Code List
Indicate whether the patient has a chronic lung disease
CL Item
No (0)
CL Item
Yes (1)
Item
Indicate if the patient is oxygen dependent
integer
C0262926 (UMLS CUI [1,1])
C0030054 (UMLS CUI [1,2])
C0439857 (UMLS CUI [1,3])
Past medical history: Previous AMI
Code List
Indicate if the patient is oxygen dependent
CL Item
No (0)
CL Item
Yes (1)
Item
Indicate whether the patient has a history of cirrhosis
integer
C0262926 (UMLS CUI [1,1])
C0023890 (UMLS CUI [1,2])
Past medical history: Previous AMI
Code List
Indicate whether the patient has a history of cirrhosis
CL Item
No (0)
CL Item
Yes (1)
Item
Indicate whether the patient has a history of dementia
integer
C0262926 (UMLS CUI [1,1])
C0497327 (UMLS CUI [1,2])
Past medical history: Previous AMI
Code List
Indicate whether the patient has a history of dementia
CL Item
No (0)
CL Item
Yes (1)
Item
Indicate the patient's height
integer
C0005890 (UMLS CUI [1])
Past medical history: Previous AMI
Code List
Indicate the patient's height
CL Item
No (0)
CL Item
Yes (1)
Item
Indicate units of height
integer
C0005890 (UMLS CUI [1,1])
C1519795 (UMLS CUI [1,2])
Past medical history: Previous AMI
Code List
Indicate units of height
CL Item
centimeters (1)
CL Item
inches (2)
Weight
Item
Indicate the patient's weight
integer
C0005910 (UMLS CUI [1])
Item
Indicate units of weight
integer
C0005910 (UMLS CUI [1,1])
C1519795 (UMLS CUI [1,2])
Weight units
Code List
Indicate units of weight
CL Item
kilograms (1)
CL Item
pounds (2)
Item
Indicate whether troponin T or I
integer
C0523952 (UMLS CUI [1])
Weight units
Code List
Indicate whether troponin T or I
CL Item
Troponin T (1)
CL Item
Troponin I (2)
Question 2 of peak troponin elevation (Absolute value)
Item
Indicate the peak level reached
integer
C0523952 (UMLS CUI [1,1])
C0444505 (UMLS CUI [1,2])
Question 3 of peak troponin elevation (Lab's upper limit of normal)
Item
Give the lab’s upper limit of normal
integer
C0523952 (UMLS CUI [1,1])
C1519815 (UMLS CUI [1,2])
Physiologic variables at first medical contact: Heart rate
Item
Indicate the first measurement or earliest record of heart rate (in beats per minute) for this episode of care
integer
C0018810 (UMLS CUI [1])
Physiologic variables at first medical contact: Systolic blood pressure
Item
Indicate the first measurement or earliest record of systolic blood pressure (mm Hg) for this episode of care
integer
C0871470 (UMLS CUI [1])
Item
Indicate whether the patient has a documented discharge diagnosis of NSTEMI or STEMI
integer
C1555319 (UMLS CUI [1])
Discharge diagnosis
Code List
Indicate whether the patient has a documented discharge diagnosis of NSTEMI or STEMI
CL Item
NSTEMI (1)
CL Item
STEMI (2)
Item
Indicate whether the patient has had an episode of cardiogenic shock at first medical contact
integer
C0036980 (UMLS CUI [1])
Past medical history: Previous AMI
Code List
Indicate whether the patient has had an episode of cardiogenic shock at first medical contact
CL Item
No (0)
CL Item
Yes (1)
Item
Indicate if the patient has had an episode of cardiac arrest evaluated by pre- hospital emergency services or emergency department personnel
integer
C0018790 (UMLS CUI [1])
Past medical history: Previous AMI
Code List
Indicate if the patient has had an episode of cardiac arrest evaluated by pre- hospital emergency services or emergency department personnel
CL Item
No (0)
CL Item
Yes (1)
Item
Indicate units of presenting creatinine level
integer
C0201976 (UMLS CUI [1,1])
C1519795 (UMLS CUI [1,2])
Past medical history: Previous AMI
Code List
Indicate units of presenting creatinine level
CL Item
µmol/l (1)
CL Item
mg/dl (2)
Item
Indicate units of presenting creatinine level
integer
C0201976 (UMLS CUI [1,1])
C1519795 (UMLS CUI [1,2])
Past medical history: Previous AMI
Code List
Indicate units of presenting creatinine level
CL Item
µmol/l (1)
CL Item
mg/dl (2)
Item
Indicate the clinical status of the patient prior to entering the operating room
integer
C0010055 (UMLS CUI [1])
Past medical history: Previous AMI
Code List
Indicate the clinical status of the patient prior to entering the operating room
CL Item
Elective (1)
CL Item
Urgent (2)
CL Item
Emergent (3)
CL Item
Emergent Salvage (4)
Item
Indicate the clinical status of the patient prior to entering the operating room
integer
C1320647 (UMLS CUI [1])
Past medical history: Previous AMI
Code List
Indicate the clinical status of the patient prior to entering the operating room
CL Item
Elective (1)
CL Item
Not elective (2)
Item
Indicate whether the patient has Left Main Coronary Disease
integer
C1299433 (UMLS CUI [1])
Past medical history: Previous AMI
Code List
Indicate whether the patient has Left Main Coronary Disease
CL Item
No (0)
CL Item
Yes (1)
Number of major diseased vessels
Item
Indicate the number of diseased major native coronary vessel systems: LAD system, Circumflex system, and/or Right system with ≥50 percent narrowing of any vessel preoperatively
integer
C3275120 (UMLS CUI [1])
Laboratory values: Pre-procedural creatinine
Item
Indicate the patient’s pre-procedural creatinine level
integer
C0201976 (UMLS CUI [1,1])
C0332152 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
Laboratory values: Pre-procedural creatinine
Item
Indicate the patient’s pre-procedural creatinine level
integer
C0201976 (UMLS CUI [1,1])
C0332152 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
Item Group
Prior Treatments
Item
Indicate if the patient has had a previous CABG
integer
C0262926 (UMLS CUI [1,1])
C0010055 (UMLS CUI [1,2])
Past medical history: Previous AMI
Code List
Indicate if the patient has had a previous CABG
CL Item
No (0)
CL Item
Yes (1)
Date of previous CABG
Item
Indicate date of CABG
date
C0010055 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Indicate if the patient had a previous percutaneous coronary intervention (PCI) of any type (balloon angioplasty, stent or other)
integer
C1320647 (UMLS CUI [1])
Past medical history: Previous AMI
Code List
Indicate if the patient had a previous percutaneous coronary intervention (PCI) of any type (balloon angioplasty, stent or other)
CL Item
No (0)
CL Item
Yes (1)
Date of previous PCI
Item
Indicate date of PCI
date
C1532338 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item Group
TREATMENT VARIABLES
Item
Indicate the PCI procedure type
integer
C1532338 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
PCI procedure type
Code List
Indicate the PCI procedure type
CL Item
PCI only (1)
CL Item
PCI + other (2)
Item
Indicate the cardiac surgery procedure type
integer
C0018821 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
PCI procedure type
Code List
Indicate the cardiac surgery procedure type
CL Item
CABG only (1)
CL Item
CABG + valve (2)
CL Item
CABG + other (3)
Item
Indicate the episode type
integer
C0741923 (UMLS CUI [1])
PCI procedure type
Code List
Indicate the episode type
CL Item
Acute myocardial infarction, without PCI or CABG (1)
CL Item
PCI, with or without acute myocardial infarction (2)
CL Item
CABG, with or without acute myocardial infarction (3)
Item Group
Acute complications of treatment
Item
Indicate if the patient has died, regardless of cause
integer
C0011065 (UMLS CUI [1])
Patient died, regardless of cause
Code List
Indicate if the patient has died, regardless of cause
CL Item
No (0)
CL Item
Yes, during index hospitalization (1)
CL Item
Yes, after discharge but within 30 days of procedure (2)
Date of death
Item
Indicate the date the patient was declared dead
date
C1148348 (UMLS CUI [1])
Item
Indicate where the patient died
integer
C2924451 (UMLS CUI [1])
Location of death (if patient died after discharge)
Code List
Indicate where the patient died
CL Item
Home (1)
CL Item
Acute care hospital or rehab (2)
CL Item
Nursing home or hospice (3)
CL Item
Other (888)
Item
Indicate whether the patient had a stroke
integer
C0038454 (UMLS CUI [1])
Location of death (if patient died after discharge)
Code List
Indicate whether the patient had a stroke
CL Item
Yes, during index hospitalization (1)
CL Item
Yes, after discharge but within 30 days of procedure (2)
CL Item
No (0)
Item
Indicate type of stroke if documented on imaging, or via lumbar puncture, neurosurgery, or autopsy
integer
C3897486 (UMLS CUI [1])
Location of death (if patient died after discharge)
Code List
Indicate type of stroke if documented on imaging, or via lumbar puncture, neurosurgery, or autopsy
CL Item
Ischemic (1)
CL Item
Hemorrhagic (2)
CL Item
Unknown (999)
Item
Indicate whether the patient has a diagnosis of acute renal failure
integer
C0022660 (UMLS CUI [1])
Location of death (if patient died after discharge)
Code List
Indicate whether the patient has a diagnosis of acute renal failure
CL Item
Yes, during index hospitalization (1)
CL Item
Yes, after discharge but within 30 days of procedure (2)
CL Item
No (0)
Date of arrival
Item
Indicate the date the patient first arrived
date
C1302393 (UMLS CUI [1])
Date of discharge
Item
Indicate the date the patient was discharged
date
C2361123 (UMLS CUI [1])
Date of procedure
Item
Indicate the date of intervention
date
C2584899 (UMLS CUI [1])
Item Group
Major surgery complications
Item
Indicate whether the patient had prolonged pulmonary ventilator >24 hours after CABG
integer
C0199470 (UMLS CUI [1,1])
C0439590 (UMLS CUI [1,2])
Prolonged ventilation
Code List
Indicate whether the patient had prolonged pulmonary ventilator >24 hours after CABG
CL Item
No (0)
CL Item
Yes, during index hospitalization (1)
CL Item
Yes, after discharge but within 30 days of procedure (2)
Item
Indicate whether the patient had a deep sternal infection involving muscle, bone, and/or mediastinum REQUIRING OPERATIVE INTERVENTION
integer
C0043241 (UMLS CUI [1,1])
C1411231 (UMLS CUI [1,2])
Prolonged ventilation
Code List
Indicate whether the patient had a deep sternal infection involving muscle, bone, and/or mediastinum REQUIRING OPERATIVE INTERVENTION
CL Item
No (0)
CL Item
Yes, during index hospitalization (1)
CL Item
Yes, after discharge but within 30 days of procedure (2)
Item
Indicate if the patient required a return to the operating room for bleeding with or without tamponade, graft occlusion, valve dysfunction, or other cardiac reason
integer
C0558347 (UMLS CUI [1])
Prolonged ventilation
Code List
Indicate if the patient required a return to the operating room for bleeding with or without tamponade, graft occlusion, valve dysfunction, or other cardiac reason
CL Item
No (0)
CL Item
Yes, during index hospitalization (1)
CL Item
Yes, after discharge but within 30 days of procedure (2)
Item Group
Major interventional cardiology complications
Item
Indicate if a significant dissection was observed at the time of PCI
integer
C1532338 (UMLS CUI [1,1])
C0012737 (UMLS CUI [1,2])
Past medical history: Previous AMI
Code List
Indicate if a significant dissection was observed at the time of PCI
CL Item
No (0)
CL Item
Yes (1)
Item
Indicate if angiographic or clinical evidence of perforation was observed at the time of the PCI procedure
integer
C1532338 (UMLS CUI [1,1])
C0340664 (UMLS CUI [1,2])
Past medical history: Previous AMI
Code List
Indicate if angiographic or clinical evidence of perforation was observed at the time of the PCI procedure
CL Item
No (0)
CL Item
Yes (1)
Item
Indicate the occurrence of any emergency cardiothoracic surgical procedure (whether or not this actually involves the placing of bypass grafts)
integer
C0010055 (UMLS CUI [1,1])
C0184893 (UMLS CUI [1,2])
Past medical history: Previous AMI
Code List
Indicate the occurrence of any emergency cardiothoracic surgical procedure (whether or not this actually involves the placing of bypass grafts)
CL Item
No (0)
CL Item
Yes (1)
Item
Indicate if the patient experienced any non-cardiac vascular complications (excluding external bleeding or hematomas) at the percutaneous entry site that required treatment or intervention
integer
C1393529 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0184661 (UMLS CUI [1,3])
Past medical history: Previous AMI
Code List
Indicate if the patient experienced any non-cardiac vascular complications (excluding external bleeding or hematomas) at the percutaneous entry site that required treatment or intervention
CL Item
No (0)
CL Item
Yes, during index hospitalization (1)
CL Item
Yes, after discharge but within 30 days of procedure (2)
Item
Indicate if the patient experienced a suspected or confirmed bleeding event
integer
C0019080 (UMLS CUI [1])
Past medical history: Previous AMI
Code List
Indicate if the patient experienced a suspected or confirmed bleeding event
CL Item
No (0)
CL Item
Yes, during index hospitalization (1)
CL Item
Yes, after discharge but within 72 hours of procedure (2)
Item Group
Patient-Reported Health Status
Item
Do you get out of breath in the following situations? When hurrying on ground level or walking up a slight hill
integer
C4288225 (UMLS CUI [1])
Past medical history: Previous AMI
Code List
Do you get out of breath in the following situations? When hurrying on ground level or walking up a slight hill
CL Item
No (0)
CL Item
Yes (1)
Item
When walking with other people your age on level ground
integer
C2183407 (UMLS CUI [1])
Past medical history: Previous AMI
Code List
When walking with other people your age on level ground
CL Item
No (0)
CL Item
Yes (1)
Item
When walking your own pace on level ground
integer
C2183407 (UMLS CUI [1,1])
C3173662 (UMLS CUI [1,2])
Past medical history: Previous AMI
Code List
When walking your own pace on level ground
CL Item
No (0)
CL Item
Yes (1)
Item
When washing or dressing
integer
C0013404 (UMLS CUI [1,1])
C3827978 (UMLS CUI [1,2])
Past medical history: Previous AMI
Code List
When washing or dressing
CL Item
No (0)
CL Item
Yes (1)
Item
Over the past 2 weeks, how often have you been bothered by any of the following problems? Little interest or pleasure in doing things
integer
C2707451 (UMLS CUI [1])
Past medical history: Previous AMI
Code List
Over the past 2 weeks, how often have you been bothered by any of the following problems? Little interest or pleasure in doing things
CL Item
Not at all (1)
CL Item
Several days (2)
CL Item
More than half the days (3)
CL Item
Nearly every day (4)
Item
Feeling down, depressed or hopeless
integer
C2707455 (UMLS CUI [1])
Past medical history: Previous AMI
Code List
Feeling down, depressed or hopeless
CL Item
Not at all (1)
CL Item
Several days (2)
CL Item
More than half the days (3)
CL Item
Nearly every day (4)
Item Group
Cardiovascular disease progression
Item
Indicate if the patient was admitted due to an AMI
integer
C0155626 (UMLS CUI [1])
Past medical history: Previous AMI
Code List
Indicate if the patient was admitted due to an AMI
CL Item
No (0)
CL Item
Yes (1)
Admission for acute myocardial infarction (AMI)
Item
Indicate the date of each admission for AMI during the defined interval
date
C0155626 (UMLS CUI [1,1])
C1302393 (UMLS CUI [1,2])
Discharge for acute myocardial infarction (AMI)
Item
Indicate the date of each discharge for AMI during the defined interval
date
C0155626 (UMLS CUI [1,1])
C2361123 (UMLS CUI [1,2])
Item
Indicate if the patient was admitted due to a hemorrhagic stoke
integer
C1096400 (UMLS CUI [1])
Past medical history: Previous AMI
Code List
Indicate if the patient was admitted due to a hemorrhagic stoke
CL Item
No (0)
CL Item
Yes (1)
Admission for hemorrhagic stroke
Item
Indicate the date of each admission for hemorrhagic stroke during the defined interval
date
C1096400 (UMLS CUI [1,1])
C1302393 (UMLS CUI [1,2])
Discharge for hemorrhagic stroke
Item
Indicate the date of each discharge for hemorrhagic stroke during the defined interval
date
C1096400 (UMLS CUI [1,1])
C2361123 (UMLS CUI [1,2])
Item
Indicate if the patient was admitted due to an ischemic stoke
integer
C0948008 (UMLS CUI [1])
Past medical history: Previous AMI
Code List
Indicate if the patient was admitted due to an ischemic stoke
CL Item
No (0)
CL Item
Yes (1)
Admission for ischemic stroke
Item
Indicate the date of each admission for ischemic stroke during the defined interval
date
C0948008 (UMLS CUI [1,1])
C1302393 (UMLS CUI [1,2])
Discharge for ischemic stroke
Item
Indicate the date of each discharge for ischemic stroke during the defined interval
date
C0948008 (UMLS CUI [1,1])
C2361123 (UMLS CUI [1,2])
Item
Indicate if the patient was admitted due to an unknown stoke
integer
C0038454 (UMLS CUI [1])
Past medical history: Previous AMI
Code List
Indicate if the patient was admitted due to an unknown stoke
CL Item
No (0)
CL Item
Yes (1)
Admission for unknown stroke
Item
Indicate the date of each admission for unknown stroke during the defined interval
date
C0038454 (UMLS CUI [1,1])
C2316983 (UMLS CUI [1,2])
Discharge for unknown stroke
Item
Indicate the date of each discharge for unknown stroke during the defined interval
date
C0038454 (UMLS CUI [1,1])
C2361123 (UMLS CUI [1,2])
Item
Indicate if the patient was admitted due to heart failure
integer
C0018801 (UMLS CUI [1])
Past medical history: Previous AMI
Code List
Indicate if the patient was admitted due to heart failure
CL Item
No (0)
CL Item
Yes (1)
Admission for heart failure
Item
Indicate the date of each admission for heart failure during the defined interval
date
C0018801 (UMLS CUI [1,1])
C1302393 (UMLS CUI [1,2])
Discharge for unknown stroke
Item
Indicate the date of each discharge for unknown stroke during the defined interval
date
C0018801 (UMLS CUI [1,1])
C2361123 (UMLS CUI [1,2])
Item
Indicate if a PCI was performed
integer
C0262926 (UMLS CUI [1,1])
C1532338 (UMLS CUI [1,2])
Previous revascularization procedures: PCI
Code List
Indicate if a PCI was performed
CL Item
No additional procedure (0)
CL Item
PCI (1)
Date of intervention #1
Item
Indicate the date of the PCI
date
C0189573 (UMLS CUI [1,1])
C2584899 (UMLS CUI [1,2])
Date of intervention #2
Item
Indicate the date of the PCI
date
C0189573 (UMLS CUI [1,1])
C2584899 (UMLS CUI [1,2])
Item
Indicate if a CABG was performed
integer
C0262926 (UMLS CUI [1,1])
C0010055 (UMLS CUI [1,2])
Previous revascularization procedures: CABG
Code List
Indicate if a CABG was performed
CL Item
No additional procedure (0)
CL Item
CABG (1)
Date of intervention #1
Item
Indicate the date of the CABG
date
C0010055 (UMLS CUI [1,1])
C2584899 (UMLS CUI [1,2])
Date of intervention #2
Item
Indicate the date of the CABG
date
C0010055 (UMLS CUI [1,1])
C2584899 (UMLS CUI [1,2])
Item
Indicate if the patient has a new requirement for dialysis
integer
C0011946 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
Past medical history: Previous AMI
Code List
Indicate if the patient has a new requirement for dialysis
CL Item
No (0)
CL Item
Yes (1)
Date of documented first dialysis
Item
Indicate the date the patient first began dialysis treatment
date
C0011946 (UMLS CUI [1,1])
C2584899 (UMLS CUI [1,2])
Item Group
Survival
Item
Indicate if the patient has died, regardless of cause
integer
C0011065 (UMLS CUI [1])
Past medical history: Previous AMI
Code List
Indicate if the patient has died, regardless of cause
CL Item
No (0)
CL Item
Yes (1)
Death: Date of death
Item
Indicate the date the patient was declared dead
date
C1148348 (UMLS CUI [1])
Item
Indicate where the patient died
integer
C2924451 (UMLS CUI [1])
Death: Location of death (from death certificate)
Code List
Indicate where the patient died
CL Item
Home (1)
CL Item
Acute care hospital or rehab (2)
CL Item
Nursing home or hospice (3)
CL Item
Other (888)
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