Peripheral Atherosclerotic Vascular Disease EHR key data elements

Beschrijving

Sex

Datatype

integer

Alias

UMLS CUI-1

C0079399

Beschrijving

Date of Birth

Datatype

date

Alias

UMLS CUI-1

C0421451

Beschrijving

Race

Datatype

integer

Alias

UMLS CUI-1

C0034510

Beschrijving

Hispanic ethnicity

Datatype

boolean

Beschrijving

Patient ZIP code

Datatype

text

Beschrijving

Healthcare facility

Datatype

text

Alias

UMLS CUI-1

C0018704

Beschrijving

Insurance payer

Datatype

integer

Beschrijving

Date and time of presentation to healthcare facility

Datatype

datetime

Beschrijving

Type of encounter

Datatype

integer

Alias

UMLS CUI-1

C1512346

Beschrijving

Primary reason for encounter

Datatype

integer

Beschrijving

Admission location

Datatype

integer

Beschrijving

Means of transport

Datatype

integer

Alias

UMLS CUI-1

C0150390

Beschrijving

Location of encounter

Datatype

integer

Beschrijving

Indicate if the patient has a current or previous diagnosis of hypertension as defined by any of the following: - History of hypertension diagnosed and treated with medication, diet, and/or exercise - On at least 2 occasions, documented blood pressure >140 mm Hg systolic and/or 90 mm Hg diastolic in patients without diabetes or chronic kidney disease; >130 mm Hg systolic or 80 mm Hg diastolic in patients with diabetes or chronic kidney disease - Currently on pharmacological therapy for treatment of hypertension More than 1 of the above may apply. The year of onset (first diagnosis) may be helpful.

Datatype

text

Alias

UMLS CUI-1

C0455527

Beschrijving

History of diabetes diagnosed and/or treated by a physician. The American Diabetes Association criteria include documentation of the following - Hemoglobin A1c >6.5%; or - Fasting plasma glucose >126 mg/dL (7.0 mmol/L); or - Two-hour plasma glucose >200 mg/dL (11.1 mmol/L) during an oral glucose tolerance test; or - In a patient with classic symptoms of hyperglycemia or hyperglycemic crisis, a random plasma glucose >200 mg/dL (11.1 mmol/L). This does not include gestational diabetes. Indicate the following: 1. Type 1 or type 2 diabetes 2. Year of onset (if known)

Datatype

text

Alias

UMLS CUI-1

C0455488

Beschrijving

Current or previous diagnosis of dyslipidemia per the National Cholesterol Education Program criteria, defined as any 1 of the following: - Total cholesterol >200 mg/dL (5.18 mmol/L) - LDL >=130 mg/dL (3.37 mmol/L) - HDL <40 mg/dL (1.04 mmol/L) in men and <50 mg/dL (1.30 mmol/L) in women Treatment is also initiated if LDL is >100 mg/dL (2.59 mmol/L) in patients with known coronary artery disease or CHD equivalent, and this would qualify as hypercholesterolemia.

Datatype

text

Alias

UMLS CUI-1

C0242339

UMLS CUI-2

C0332119

Beschrijving

History confirming cigarette smoking in the past.

Datatype

integer

Alias

UMLS CUI-1

C1519384

Beschrijving

Specify the patient’s history of alcohol consumption. Choose from the following categories: - None - <=1 alcoholic drinks/wk - 2–7 alcoholic drinks/wk - 8–13 alcoholic drinks/wk - 14–20 alcoholic drinks/wk - >=21 alcoholic drinks/wk Specify alcohol-dependency history. Choose all that apply: Documented alcohol dependency Medical sequelae of alcohol consumption (alcoholic hepatitis, cirrhosis, alcohol neuropathy, Wernicke-Korsakoff syndrome) Treatment for alcohol dependency For patients with alcohol dependency, note treatment for dependency, cessation of use, or continued use.

Datatype

text

Alias

UMLS CUI-1

C0552479

Beschrijving

Indicate history of current, recent, or remote abuse of any illicit drug (eg, cocaine, methamphetamine, marijuana) or controlled substance.

Datatype

boolean

Alias

UMLS CUI-1

C2239127

Beschrijving

The term myocardial infarction should be used when there is evidence of myocardial necrosis in a clinical setting consistent with myocardial ischemia. Under these conditions, any 1 of the following criteria meets the diagnosis for MI: 1) Detection of rise and/or fall of cardiac biomarkers (preferably troponin) with at least 1 value above the 99th percentile of URL together with evidence of myocardial ischemia with at least 1 of the following: — Symptoms of ischemia — Electrocardiographic changes indicative of new ischemia (new ST-T changes or new LBBB) — Development of pathological Q waves in the ECG — Imaging evidence of new loss of viable myocardium or new regional wall motion abnormality 2) Sudden unexpected cardiac death, involving cardiac arrest, often with symptoms suggestive of myocardial ischemia, and accompanied by presumably new ST elevation or new LBBB and/or evidence of fresh thrombus by coronary angiography a time before the appearance of cardiac biomarkers in the blood. 3) For PCI in patients with normal baseline indicative of periprocedural myocardial necrosis. By convention, increases of biomarkers >3x99th percentile URL have been designated as PCI-related MI. A subtype related to a documented stent thrombosis is recognized. 4) For CABG in patients with normal baseline troponin values, elevations of cardiac biomarkers above the 99th percentile URL are indicative of periprocedural myocardial necrosis. By convention, increases of biomarkers >5x99th percentile URL plus either new pathological Q waves or new or imaging evidence of new loss of viable myocardium have been designated as defining CABG-related MI. 5) Pathological findings of an acute MI.

Datatype

text

Alias

UMLS CUI-1

C1275835

Beschrijving

Indicate if the patient had an MI within 6 wk prior to the index procedure as evidenced by the following: 1.) Acute MI (<=7 d) manifested as a rise and fall of cardiac biomarkers (preferably troponin) with at least 1 value above the range of normal for your laboratory (above the 99th percentile of the URL) together with evidence of myocardial ischemia with at least 1 of the following: a. Ischemic symptoms b. Electrocardiographic changes indicative of new ischemia (new ST-T and/or T-wave changes or new LBBB) c. Development of pathological Q waves on the ECG d. Imaging evidence of new loss of viable myocardium or new regional wall motion abnormality 2.) Recent MI (>7 d) manifested by a. An MI meeting the criteria for an acute MI as documented in the medical record, or b. By any 1 of the following: 1. Development of new pathological Q waves with or without symptoms 2. Imaging evidence of a region of loss of viable myocardium that is thinned and fails to contract 3. In the absence of a nonischemic cause

Datatype

boolean

Beschrijving

History of angina - Stable angina (CCS class, date of onset) - Unstable angina (date of onset) - Prior angina (currently asymptomatic)

Datatype

text

Alias

UMLS CUI-1

C0455530

Beschrijving

Indicate history of prior Coronary Artery Bypass Graft (CABG) surgery, including the date or year of surgery. The total number of CABG procedures and the year of the most recent procedure may be helpful.

Datatype

text

Alias

UMLS CUI-1

C1842251

Beschrijving

Prior PCI of any type (balloon angioplasty, atherectomy, stent, or other). Total number of PCI procedures and dates (years)

Datatype

text

Alias

UMLS CUI-1

C1320647

Beschrijving

Indicate if the patient has a history of lower extremity PAD (from iliac to tibials). Excludes renal, coronary, cerebral, and mesenteric vessels and aneurysm. Major symptoms can include - Asymptomatic (confirmed by noninvasive diagnostic test) - Claudication relieved by rest - Ischemic rest pain - Tissue loss (including ischemic ulcer and/or gangrene) - Amputation for critical limb ischemia - Vascular reconstruction, bypass surgery, or percutaneous revascularization in the arteries of the lower extremities - Positive noninvasive test (eg, ABI <=0.90, ultrasound, MR or CT imaging demonstrating >50% diameter stenosis in any peripheral artery, ie, aorta, iliac, femoral, popliteal, tibial, peroneal)

Datatype

boolean

Alias

UMLS CUI-1

C1881056

Beschrijving

Indicate if the patient has a history of aortic aneurysm. This can include - Thoracic aneurysm - Thoracoabdominal aneurysm - AAA Confirmed by ultrasound, CT, and/or MR imaging.

Datatype

boolean

Alias

UMLS CUI-1

C0459854

Beschrijving

Indicate if the patient has a history of renal or mesenteric artery disease. This can include an abnormal imaging study such as duplex ultrasonography, MRA, CTA, or catheter-based contrast angiography demonstrating >50% diameter stenosis in the renal artery, celiac trunk, SMA, or IMA.

Datatype

boolean

Beschrijving

Indicate if the patient has a documented history of TIA consisting of a transient episode of neurological dysfunction caused by focal brain, spinal cord, or retinal ischemia without acute infarction. Note the following: - Right retinal - Right hemispheric - Left retinal - Left hemispheric - Vertebrobasilar - Unknown distribution

Datatype

text

Alias

UMLS CUI-1

C0455536

Beschrijving

Indicate whether the patient has a history of stroke, which is defined as an acute episode of neurological dysfunction caused by focal or global brain, spinal cord, or retinal vascular injury as a result of hemorrhage or infarction. If present, record the type of stroke: - Ischemic - Intracerebral hemorrhage - Subarachnoid hemorrhage - Unknown If ischemic, list the most likely etiologies: - Large-artery atherosclerosis of the extracranial vessels (eg, carotid) - Large-artery atherosclerosis of the intracranial vessels (eg, middle cerebral artery stenosis) - Cardioembolism - Small-vessel occlusion (lacunar) - Ischemic stroke of other determined etiology (eg, arterial dissection) - Ischemic stroke of undetermined etiology

Datatype

text

Alias

UMLS CUI-1

C0559159

Beschrijving

Indicate if the patient has a previous history of Congestive Heart Failure (CHF). This includes a previous hospital admission with a principal diagnosis of CHF. CHF is defined as documentation or report of any 2 of the following Framingham major criteria of heart failure: orthopnea/paroxysmal nocturnal dyspnea; or the description of rales, jugular venous distention, hepatojugular reflux, S3 gallop, or pulmonary edema on chest x-ray; or 1 of the major criteria plus 2 Framingham minor criteria, including dyspnea on exertion, nocturnal cough, ankle edema, pleural effusion, or tachycardia. A low ejection fraction without clinical evidence of heart failure does not qualify as heart failure. Include the year of onset if known.

Datatype

text

Alias

UMLS CUI-1

C0455531

Beschrijving

NYHA classification scale

Datatype

text

Alias

UMLS CUI-1

C1275491

Beschrijving

Indicate if the patient has a history of pulmonary insufficiency. Pulmonary insufficiency is defined as PaO2 of <60 mm Hg while breathing air or PaCO2 of >50 mm Hg.

Datatype

boolean

Alias

UMLS CUI-1

C0340398

UMLS CUI-2

C0332119

Beschrijving

Current or previous history of chronic kidney disease. Chronic kidney disease is defined as either kidney damage or GFR <60 mL/min/1.73 m2 for >=3 mo. Kidney damage is defined as pathologic abnormalities or markers of damage, including abnormalities in blood or urine tests or imaging studies. Indicate the patient’s stage of disease: - Stage 0: No known kidney disease - Stage 1: Kidney damage with normal or high GFR >=90 mL/min/1.73 m2 - Stage 2: Kidney damage with mildly decreased GFR—60–89 mL/min/1.73 m2 - Stage 3: Moderately decreased GFR—30–59 mL/min/1.73 m2 - Stage 4: Severely decreased GFR—15–29 mL/min/1.73 m2 - Stage 5: Kidney failure—GFR <15 mL/min/1.73 m2 or on dialysis Year of onset (first diagnosis) may be helpful.

Datatype

text

Alias

UMLS CUI-1

C3532472

Beschrijving

Height

Datatype

float

Maateenheden

• cm

Alias

UMLS CUI [1]

C0005890

Beschrijving

Body weight

Datatype

float

Maateenheden

• kg

Alias

UMLS CUI [1]

C0005910

Beschrijving

Body Mass Index

Datatype

float

Maateenheden

• kg/m2

Alias

UMLS CUI [1]

C1305855

Beschrijving

Systolic

Datatype

integer

Maateenheden

• mmHg

Alias

UMLS CUI [1]

C0871470

Beschrijving

Diastolic

Datatype

integer

Maateenheden

• mmHg

Alias

UMLS CUI [1]

C0428883

Beschrijving

Heart rate

Datatype

integer

Maateenheden

• bpm

Alias

UMLS CUI [1]

C0018810

Beschrijving

Cardiac rhythm

Datatype

integer

Alias

UMLS CUI-1

C0232187

Beschrijving

Complete vascular examination: Carotid, upper, lower extremity pulses, auscultation of the neck for carotid bruits, auscultation of the abdomen and femoral arteries for bruits, palpation of the abdomen and popliteal fossa for aneurysms

Datatype

text

Alias

UMLS CUI-1

C2053830

Beschrijving

Complete cardiac examination: Palpation and auscultation of the heart, assessing rate, rhythm, presence of murmur, presence of gallop (eg, S3 suggesting left ventricular dysfunction; S4 suggesting noncompliant left ventricle), notation of location of point of maximal intensity

Datatype

text

Beschrijving

Limb edema. Note the presence/absence of lower extremity (less commonly, upper extremity) edema, including location, extent, and pitting versus nonpitting.

Datatype

text

Alias

UMLS CUI-1

C0085649

Beschrijving

Include RBC, WBC, and platelet counts: 1) value, 2) unit of measurement, 3) date, and 4) normal range (upper limit of normal when appropriate)

Datatype

text

Alias

UMLS CUI-1

C0009555

Beschrijving

Hemoglobin

Datatype

float

Maateenheden

• g/dL

Alias

UMLS CUI [1]

C0019046

Beschrijving

Hematocrit

Datatype

float

Maateenheden

• %

Alias

UMLS CUI [1]

C0518014

Beschrijving

Glucose

Datatype

float

Maateenheden

• mg/dl

Alias

UMLS CUI [1]

C0202042

Beschrijving

BUN

Datatype

float

Maateenheden

• mg/dL

Alias

UMLS CUI [1]

C0005845

Beschrijving

Creatinine

Datatype

float

Maateenheden

• mg/dL

Alias

UMLS CUI [1]

C0201976

Beschrijving

Indicate estimated or actual GFR in milliliters per minute per 1.73 meters squared.

Datatype

float

Maateenheden

• ml/(min*1,73m2)

Alias

UMLS CUI-1

C0017654

Beschrijving

Sodium

Datatype

float

Maateenheden

• mmol/L

Alias

UMLS CUI [1]

C0337443

Beschrijving

Potassium

Datatype

float

Maateenheden

• mmol/l

Alias

UMLS CUI [1]

C0202194

Beschrijving

Hemogloblin A1C

Datatype

float

Maateenheden

• %

Alias

UMLS CUI [1]

C0019018

Beschrijving

Prothrombin time Measured in seconds. Report INR as ratio.

Datatype

float

Maateenheden

• s

Alias

UMLS CUI-1

C0033707

Beschrijving

Partial thromboplastin time Indicate whether activators used (aPTT) or not (PTT). Measured in seconds.

Datatype

float

Maateenheden

• s

Alias

UMLS CUI-1

C0030605

Beschrijving

Total cholesterol 1) value, 2) unit of measurement, 3) date, and 4) normal range (upper limit of normal when appropriate)

Datatype

float

Maateenheden

• mg/dL

Alias

UMLS CUI [1]

C1445957

Beschrijving

LDL

Datatype

float

Maateenheden

• mg/dL

Alias

UMLS CUI [1]

C0428474

Beschrijving

HDL

Datatype

float

Maateenheden

• mg/dL

Alias

UMLS CUI [1]

C0428472

Beschrijving

Triglycerides

Datatype

float

Maateenheden

• mg/dL

Alias

UMLS CUI [1]

C0202236

Beschrijving

hs-CRP 1) value, 2) unit of measurement, 3) date, and 4) normal range (upper limit of normal when appropriate)

Datatype

float

Alias

UMLS CUI-1

C0201657

Beschrijving

ESR 1) value, 2) unit of measurement, 3) date, and 4) normal range (upper limit of normal when appropriate)

Datatype

float

Alias

UMLS CUI-1

C0086250

Beschrijving

Calcium

Datatype

float

Maateenheden

• mmol/l

Alias

UMLS CUI [1]

C0201925

Beschrijving

Phosphorus 1) value, 2) unit of measurement, 3) date, and 4) normal range (upper and lower limit of normal when appropriate)

Datatype

float

Alias

UMLS CUI-1

C0523826

Beschrijving

Magnesium 1) value, 2) unit of measurement, 3) date, and 4) normal range (upper and lower limit of normal when appropriate)

Datatype

float

Alias

UMLS CUI-1

C0373675

Beschrijving

TSH 1) value, 2) unit of measurement, 3) date, and 4) normal range (upper limit of normal when appropriate)

Datatype

float

Alias

UMLS CUI-1

C0202230

Beschrijving

BNP or N-terminal BNP 1) value, 2) unit of measurement, 3) date, and 4) normal range (upper limit of normal when appropriate)

Datatype

float

Alias

UMLS CUI-1

C1095989

Beschrijving

AST (SGOT)

Datatype

float

Maateenheden

• U/L

Alias

UMLS CUI [1]

C0201899

Beschrijving

ALT (SGPT)

Datatype

float

Maateenheden

• U/L

Alias

UMLS CUI [1]

C0201836

Beschrijving

The upper limit of normal of total CK as defined by individual hospital laboratory standards. Units of CK and type of units should be noted (eg, IU, ng/dL, kCat/L). All CK values during hospitalization should be noted; include units, date, and time.

Datatype

float

Alias

UMLS CUI-1

C0201973

Beschrijving

Indicate the upper limit of normal (usually the 99th percentile of a normal population) and units (eg, ng/dL). All troponin T values during hospitalization should be noted; include units, date, and time.

Datatype

float

Alias

UMLS CUI-1

C1141947

Beschrijving

Indicate the upper limit of normal (usually the 99th percentile of a normal population) and units (eg, ng/dL). All troponin I values during hospitalization should be noted; include units, date, and time.

Datatype

float

Alias

UMLS CUI-1

C0920210

Beschrijving

Homocysteine 1) value, 2) unit of measurement, 3) date, and 4) normal range (upper limit of normal when appropriate)

Datatype

float

Alias

UMLS CUI-1

C2242817

Beschrijving

Vitamin B12 1) value, 2) unit of measurement, 3) date, and 4) normal range (upper limit of normal when appropriate)

Datatype

float

Alias

UMLS CUI-1

C0202252

Beschrijving

Folate 1) value, 2) unit of measurement, 3) date, and 4) normal range (upper limit of normal when appropriate)

Datatype

float

Alias

UMLS CUI-1

C0523631

Beschrijving

Prothrombin 20210 gene mutation 1) value, 2) unit of measurement, 3) date, and 4) normal range (upper limit of normal when appropriate)

Datatype

float

Alias

UMLS CUI-1

C1273306

Beschrijving

Protein C activity 1) value, 2) unit of measurement, 3) date, and 4) normal range (upper limit of normal when appropriate)

Datatype

float

Alias

UMLS CUI-1

C1255234

Beschrijving

Protein S activity 1) value, 2) unit of measurement, 3) date, and 4) normal range (upper limit of normal when appropriate)

Datatype

float

Alias

UMLS CUI-1

C0919678

Beschrijving

Antithrombin III 1) value, 2) unit of measurement, 3) date, and 4) normal range (upper limit of normal when appropriate)

Datatype

float

Alias

UMLS CUI-1

C2825854

Beschrijving

Anticardiolipin antibody 1) value, 2) unit of measurement, 3) date, and 4) normal range (upper limit of normal when appropriate)

Datatype

float

Alias

UMLS CUI-1

C0201535

Beschrijving

Lupus anticoagulant 1) value, 2) unit of measurement, 3) date, and 4) normal range (upper limit of normal when appropriate)

Datatype

float

Alias

UMLS CUI-1

C1142517

Beschrijving

Aspirin. Note specific dose.

Datatype

integer

Alias

UMLS CUI-1

C0004057

Beschrijving

Clopidogrel. Note specific dose.

Datatype

integer

Alias

UMLS CUI-1

C0070166

Beschrijving

Prasugrel. Note specific dose.

Datatype

integer

Alias

UMLS CUI-1

C1620287

Beschrijving

Other P2Y12 antagonists (Purinergic P2Y12 Receptor Antagonists). Note specific drug and dose.

Datatype

integer

Alias

UMLS CUI-1

C2936585

Beschrijving

Dipyridamole. Note specific dose.

Datatype

integer

Alias

UMLS CUI-1

C0012582

Beschrijving

Other antiplatelet drugs. Note specific drug and dose.

Datatype

text

Beschrijving

Unfractionated heparin. Note specific dose.

Datatype

integer

Alias

UMLS CUI-1

C2825026

Beschrijving

Low–molecular-weight heparin. Note specific drug and dose.

Datatype

integer

Alias

UMLS CUI-1

C0019139

Beschrijving

Fondaparinux. Note specific dose.

Datatype

integer

Alias

UMLS CUI-1

C1098510

Beschrijving

Other factor Xa inhibitor. Note specific drug and dose.

Datatype

text

Alias

UMLS CUI-1

C2825027

Beschrijving

Direct thrombin inhibitor. Note specific drug and dose.

Datatype

text

Alias

UMLS CUI-1

C3536847

Beschrijving

Warfarin. Indicate whether this drug has been prescribed; note INR.

Datatype

text

Alias

UMLS CUI-1

C0043031

Beschrijving

Other anticoagulant drug. Note specific drug and dose.

Datatype

text

Alias

UMLS CUI-1

C0003280

Beschrijving

Antihypertensive drugs. Note specific drug and dose.

Datatype

text

Alias

UMLS CUI-1

C0003364

Beschrijving

Statins and lipid-control agents. Note specific drug and dose.

Datatype

text

Alias

UMLS CUI-1

C0360714

Beschrijving

Drugs for diabetes. Note specific drug and dose.

Datatype

text

Alias

UMLS CUI-1

C3653344

Beschrijving

Drugs to aid in smoking cessation. Note specific drug and dose.

Datatype

text

Alias

UMLS CUI-1

C1095963

Beschrijving

Antiarrhythmic drugs. Note specific drug and dose.

Datatype

text

Alias

UMLS CUI-1

C0003195

Beschrijving

Heart failure medications. Note specific drug and dose.

Datatype

text

Alias

UMLS CUI-1

C0018801

UMLS CUI-2

C0013227

Beschrijving

Drugs for symptoms of PAD. Note specific drug and dose.

Datatype

text

Beschrijving

Noncardiovascular medications. Note the specific drug and dose.

Datatype

text

Beschrijving

Medication allergy. Specify the medication and type of reaction

Datatype

text

Alias

UMLS CUI-1

C0013182

Beschrijving

Medication side effect. Describe the side effect and whether the medication was stopped.

Datatype

text

Alias

UMLS CUI-1

C0041755