ID
42216
Description
2012 ACCF / AHA Data Standard Peripheral Atherosclerotic Disease (PAD) Lower Extremity data elements see http://www.ncbi.nlm.nih.gov/pubmed/22144570
Link
http://www.ncbi.nlm.nih.gov/pubmed/22144570
Keywords
Versions (4)
- 11/1/14 11/1/14 - Martin Dugas
- 11/1/14 11/1/14 - Martin Dugas
- 11/1/14 11/1/14 - Martin Dugas
- 4/13/21 4/13/21 - Dr. rer. medic Philipp Neuhaus
Uploaded on
April 13, 2021
DOI
To request one please log in.
License
Creative Commons BY-NC 3.0 Legacy
Model comments :
You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.
Itemgroup comments for :
Item comments for :
In order to download data models you must be logged in. Please log in or register for free.
Peripheral Atherosclerotic Disease (PAD) - Lower Extremity data elements
Peripheral Atherosclerotic Disease (PAD) - Lower Extremity data elements
- StudyEvent: ODM-Test
Description
Patient Assessment: Physical evaluation
Alias
- UMLS CUI-1
- C0031809
Description
Pulses. Indicate the characteristics of pulses in the following locations: - Femoral - Popliteal - Dorsalis pedis - Posterior tibial Indicate if pulses are: 0: Absent 1: Diminished 2: Normal 3: Bounding
Data type
text
Alias
- UMLS CUI-1
- C0232139
Description
Bruits. Indicate the presence or absence of bruits on auscultation in the following: - Carotid - Abdominal - Femoral - Subclavian
Data type
text
Alias
- UMLS CUI-1
- C0006318
Description
Elevation pallor. Indicate the presence of pallor of the forefoot after elevating the leg 60° for 1 min.
Data type
boolean
Alias
- UMLS CUI-1
- C2216288
Description
Reperfusion delay (>40 s)
Data type
boolean
Alias
- UMLS CUI-1
- C2609254
Description
Dependent rubor. Indicate if rubor of the foot is present when held in dependence after an elevation pallor maneuver.
Data type
boolean
Alias
- UMLS CUI-1
- C2242631
Description
Acute limb ischemia is characterized by - Pallor - Pulselessness - Poikilothermia - Paralysis One of the following categories should be assigned: I: Viable—Limb is not immediately threatened; no sensory loss; no muscle weakness; audible arterial and venous Doppler II: Threatened—Mild to moderate sensory or motor loss; inaudible arterial Doppler; audible venous Doppler III: Irreversible—Major tissue loss or permanent nerve damage inevitable; profound sensory loss, anesthetic; profound muscle weakness or paralysis (rigor); inaudible arterial and venous Doppler
Data type
text
Alias
- UMLS CUI-1
- C2945695
- UMLS CUI-2
- C0205178
Description
Tissue loss (ischemic wound or gangrene): characteristics Tissue loss is characterized by - Dryness - Necrosis - Granulation
Data type
text
Alias
- UMLS CUI-1
- C0750433
Description
Tissue loss (ischemic wound or gangrene): affected limb
Data type
integer
Description
Tissue loss (ischemic wound or gangrene): location Specify the location of tissue loss. Choose all that apply: - Distal aspect of leg or foot - Over bony prominence - Toe - Others
Data type
text
Description
Tissue loss (ischemic wound or gangrene): wound area Indicate the measured area of the wound in centimeters.
Data type
float
Measurement units
- cm
Alias
- UMLS CUI-1
- C3534343
Description
Tissue loss (ischemic wound or gangrene): infection
Data type
boolean
Description
Tissue loss (ischemic wound or gangrene): type
Data type
integer
Description
Tissue loss (ischemic wound or gangrene): depth/Wagner grade
Data type
text
Description
Diagnostic Testing: Noninvasive Procedures
Alias
- UMLS CUI-1
- C0259832
Description
Ankle Brachial Index/Toe Brachial Index Date of procedure Indicate the date the procedure was performed. Ankle systolic pressure Indicate the ankle systolic pressure of the right and left legs and whether it is recorded from the posterior tibial or dorsalis pedis arteries. ABI value Indicate the ABI value for each leg. Choose 1 of the following: - Normal (ABI 1.00–1.40) - Abnormal (ABI <0.90) - Borderline (ABI 0.91–0.99) - Noncompressible arteries (ABI >1.40) Great toe systolic pressure: Indicate the right and left great toe systolic pressures. TBI value: Indicate the TBI value for each leg. A TBI value of <=0.7 is abnormal.
Data type
text
Description
Exercise Testing: Treadmill Exercise Date of procedure Indicate the date exercise testing was performed. Protocol Specify the symptom-limited exercise protocol used (constant load/graded). Postexercise ankle pressure and/or ABI Indicate if immediate postexercise ankle pressure and/or ABI measurement were performed. Choose 1 of the following: - Yes. If so, indicate value. - No Walking time Indicate the following walking time in minutes: - Claudication onset time - Peak walking time Distance: Indicate the walking distance in meters or feet: - Claudication-onset walking distance - Peak walking distance METS 1 MET is defined as 3.5 mL O2*kg^-1*min^-1. Indicate METS at peak exercise. Alternative method A 6-min walk is the distance walked in 6 min on flat surface using standardized measurement procedures. It is reported in meters or feet.
Data type
text
Alias
- UMLS CUI-1
- C0430507
Description
Segmental Pressure Examination Date of examination Segmental pressure measurements - Right and left brachial pressures - Right and left thigh pressures - Right and left low thigh pressures - Right and left thigh calf pressures - Right and left dorsalis pedis pressures - Right and left posterior tibial pressures Indicate if there is a >20 mm Hg drop between the contiguous segments of the same leg, which can suggest the location of stenosis.
Data type
text
Alias
- UMLS CUI-1
- C3665822
Description
Pulse Volume Recording (PVR) Date of recording Amplitude reduction - Indicate the leg and location of PVR: - Right/left high thigh - Right/left low thigh - Right/left calf - Right/left ankle - Right/left metatarsal Choose 1 of the following to describe pulse wave amplitude: - Normal - Abnormal - Mildly reduced - Moderately reduced - Severely reduced
Data type
text
Description
Transcutaneous Oxygen Pressure Date of measurement TcPO2 measured: Measurement of the pressure of oxygen on the surface of the skin. Indicate the TcPO2 value in the right foot and left foot.
Data type
text
Alias
- UMLS CUI-1
- C1261152
Description
Duplex Ultrasound Date of procedure Artery imaged: - Aorta - Right/left CIA - Right/left EIA - Right/left common femoral artery - Right/left proximal profunda femoris artery - Right/left superficial femoral artery - Right/left popliteal artery - Right/left tibioperoneal trunk - Right/left anterior tibial artery - Right/left posterior tibial artery - Right/left peroneal artery
Data type
text
Alias
- UMLS CUI-1
- C0242845
Description
Peak systolic velocity. Specify for - Aorta - Right/left CIA - Right/left EIA - Right/left common femoral artery - Right/left proximal profunda femoris artery - Right/left superficial femoral artery - Right/left popliteal artery - Right/left tibioperoneal trunk - Right/left anterior tibial artery - Right/left posterior tibial artery - Right/left peroneal artery
Data type
text
Description
Category of stenosis. Specify for - Aorta - Right/left CIA - Right/left EIA - Right/left common femoral artery - Right/left proximal profunda femoris artery - Right/left superficial femoral artery - Right/left popliteal artery - Right/left tibioperoneal trunk - Right/left anterior tibial artery - Right/left posterior tibial artery - Right/left peroneal artery Indicate the category of stenosis: - Normal - 1%–49% - 50%–99% - Occlusion
Data type
text
Description
Bypass graft. Indicate location of proximal and distal anastomosis and type (eg, in situ saphenous vein, reverse saphenous vein, PTFE).
Data type
text
Alias
- UMLS CUI-1
- C0185098
Description
Peak systolic velocity of bypass graft Indicate peak systolic velocity at proximal anastomosis, along conduit, and at distal anastomosis.
Data type
float
Description
Ratios of peak systolic velocities along bypass graft Indicate ratio of peak systolic velocity of 2 contiguous segments at proximal anastomosis, along conduit, and at distal anastomosis
Data type
float
Description
Category of bypass graft stenosis
Data type
integer
Description
Magnetic Resonance Angiography Date of procedure Indicate if gadolinium was used Indicate the artery imaged. Choose all that apply: - Abdominal aorta - Right/left iliac (common, internal, external) artery - Right/left femoral (common, superficial, deep) artery - Right/left popliteal (above knee, below knee, both) artery - Right/left tibial/peroneal (anterior tibial, posterior tibial, peroneal) arteries Specify the location of the lesion. Indicate the severity of stenosis by quantitative analysis using the formula 100x(1-minimum lumen diameter)/maximum diameter of reference segment Indicate if reconstitution was seen (yes/no)
Data type
text
Alias
- UMLS CUI-1
- C0243032
Description
CT Angiography: Date of procedure. Type of contrast: Ionic contrast, Nonionic contrast (specify: Monomer, Dimer). Indicate the volume of contrast used in milliliters. Indicate the slice thickness in millimeters. Indicate if raw images were reviewed: yes/no Indicate if reconstructed images were reviewed: - Yes (specify: Shaded surface images or Maximum intensity projection) - No Indicate the artery imaged. Choose all that apply: - Abdominal aorta - Right/left iliac (common, internal, external) artery - Right/left femoral (common, superficial, deep) artery - Right/left popliteal (above knee, below knee, both) artery - Right/left tibial/peroneal (anterior tibial, posterior tibial peroneal) arteries Specify the location of the lesion. Indicate if calcification is present: None / Mild / Moderate / Severe If present, specify the location Indicate the severity of stenosis by quantitative analysis using the formula 100x(1-minimum lumen diameter)/maximum diameter of reference segment Indicate if reconstitution was seen (yes/no)
Data type
text
Alias
- UMLS CUI-1
- C1536105
Description
Diagnostic Testing: Invasive procedures
Alias
- UMLS CUI-1
- C0430022
- UMLS CUI-2
- C0205281
Description
Catheter Angiography Date of procedure Operator name Type of anesthesia: - General - Local, sedation yes/no - Regional, sedation yes/no Specify the vascular access site. Indicate the contrast agent used: - Iodinated: Ionic / Nonionic (Monomer / Dimer) - Noniodinated (CO2) Specify the contrast volume given. Indicate the field size in centimeters or inches. Indicate the Frame rate [FPS]. Indicate the image type: Cine / Digital images Digital subtraction: yes/no Indicate total fluoroscopy time recorded to the nearest 0.10 min. The time recorded should include the total time for the procedure. Indicate the artery imaged. Choose all that apply: - Abdominal aorta - Right/left iliac (common, internal, external) artery - Right/left femoral (common, deep, superficial) artery - Right/left popliteal (above knee, below knee, or both) artery - Right/left tibial/peroneal (anterior tibial, posterior tibial, peroneal) arteries Specify the location of the lesion (ostial, proximal third, middle third, and distal third). Indicate if calcification is present: None / Mild / Moderate / Severe If present, specify the location. Indicate the severity of stenosis by quantitative analysis using the formula 100x(1-minimum lumen diameter)/maximum diameter of reference segment Indicate if the artery is reconstituted by collaterals: Yes (If yes, indicate level) / No Translesional pressure gradient: Indicate the pressure measured proximal to the stenosis minus the pressure measured distal to the stenosis. Also indicate the following: - Baseline pressure gradient: Systolic, Mean, Diastolic - Enhanced (hyperemic, postvasodilator) pressure gradient: Systolic, Mean, Diastolic - Measurement timing: Simultaneous / Pullback Indicate any technical complications encountered during the diagnostic procedure: Choose all that apply: - Pseudoaneurysm - Atrioventricular fistula - Hematoma - Dissection - Vessel thrombosis - Vessel perforation - Atheromatous embolization - Contrast nephropathy - Contrast hypersensitivity - Requirement of intervention to prevent permanent impairment/damage
Data type
text
Alias
- UMLS CUI-1
- C0002979
Description
Pharmacological Therapy for Symptoms of Claudication
Description
Indicate if cilostazol has been prescribed for the patient: - Yes (If yes, indicate Dose and Duration of treatment) - No
Data type
text
Alias
- UMLS CUI-1
- C0055729
Description
Indicate if pentoxifylline has been prescribed for the patient: - Yes (If yes, indicate Dose and Duration of treatment) - No
Data type
text
Alias
- UMLS CUI-1
- C0030899
Description
Exercise Rehabilitation for Intermittent Claudication
Description
Exercise Program Assessment Functional status/quality of life: Document functional ability at initiation and completion of the exercise program based on the following: - Claudication onset walking distance - Peak walking distance - METS achieved at peak exercise - 6-min walking test - Questionnaires Document the total exercise time during the exercise session at initiation and completion of the exercise program. Document the total rest time spent during the exercise session at initiation and completion of the exercise program. Document the duration of walking time at initiation and completion of the exercise program.
Data type
text
Description
Exercise Prescription Indicate the place where exercise is done: Supervised facility / Home based Indicate the mode of exercise prescribed: - Treadmill: Indicate initial speed and grade, final speed and grade - Track walking: Indicate initial speed, final speed - Cycling: Indicate initial speed and watts, final speed and watts Indicate the recommendation for progression of exercise. Intensity level: Indicate the recommended claudication pain intensity level before resting. Indicate the recommended range of RPE. Indicate the duration of the exercise session in minutes. Frequency of session: Indicate the number of days of exercise session per week Duration of prescription: Indicate how long the exercise prescription should be performed in number of sessions or number of weeks
Data type
text
Description
Therapeutic Procedures: Endovascular and Open Surgical Revascularization
Alias
- UMLS CUI-1
- C0087111
Description
Endovascular Revascularization Date of procedure Operator name Limb revascularized: Right / Left / Both Procedure: - Balloon angioplasty - Cutting balloon - Stent (drug eluting yes/no, type of drug-eluting stent) - Stent graft - Atherectomy - Laser - Cryoplasty Indicate the target vessel for revascularization. Choose all that apply: - Aorta - CIA - EIA - IIA - Common femoral artery - Superficial femoral artery - Deep femoral artery - Popliteal (above the knee) - Popliteal (below the knee) - Anterior tibial artery - Posterior tibial artery - Peroneal artery - Pedal arteries Indicate the manufacturer of the device. Indicate the model number of the device. Indicate the maximum diameter of the device in millimeters. Indicate the maximum length of the device in millimeters. Indicate the time of patient arrival in the catheterization lab in hours:minutes. Last catheter removed: Indicate the date and time the last catheter was removed. Indicate the thrombolytic agent used. Specify the following: - Specific thrombolytic agent used - Route of delivery - Dosage - Duration of infusion Indicate the antithrombotic agent used. Specify the following: - Specific antithrombotic agent used: Unfractionated heparin / Low–molecular-weight heparin / Fondaparinux / Direct thrombin inhibitor - Route of delivery - Dosage - Duration of infusion Antiplatelet agent Indicate the antiplatelet agent used. Specify Dosage Indicate if a closure device was used: yes (specify Manufacturer and Model) / no Indicate type of contrast used: - Iodinated: Ionic / Nonionic / Monomer / Dimer / Noniodinated (CO2) Indicate the devices used for the procedure. Choose all that apply: - Guidewires - Guiding catheters - Intravascular ultrasound - Angioplasty balloons - Cutting balloon - Infusion catheter - Laser catheter - Thrombectomy device - Atherectomy device - Reentry device - Thermal balloon - EPD - Stent - Drug-eluting stent - Stent graft Indicate the technical outcome of the procedure. Specify the following: - Postprocedure translesional gradient - Residual percent stenosis Indicate any technical complications encountered during the procedure: Choose all that apply: - Vessel perforation - Embolization (loss of runoff vessel) - Dissection - Vasospasm - Access site bleeding
Data type
text
Alias
- UMLS CUI-1
- C2939280
Description
Open Surgery Date of procedure Operator name Indicate which limb the procedure was done: Right / Left / Both Indicate the type of procedure performed. Choose 1 of the following: - Primary/secondary - Bypass -- Inflow/outflow -- Anatomic/extra-anatomic - Endarterectomy - Thrombectomy - Graft revision Indicate the proximal anastomotic site and side. Choose 1 of the following: - Thoracic aorta - Abdominal aorta - CIA - EIA - Common femoral artery - Proximal superficial femoral artery - Distal superficial femoral artery - Profunda femoral artery - Proximal popliteal artery - Distal popliteal artery - Tibioperoneal artery - Proximal anterior tibial artery - Distal anterior tibial artery - Proximal posterior tibial artery - Distal posterior tibial artery - Proximal peroneal artery - Distal peroneal artery - Dorsalis pedis/tarsal artery Indicate the distal anastomotic site. Choose 1 of the following: - CIA - EIA - Common femoral artery - Proximal superficial femoral artery - Distal superficial femoral artery - Profunda femoral artery - Proximal popliteal artery - Distal popliteal artery - Tibioperoneal artery - Proximal anterior tibial artery - Distal anterior tibial artery - Proximal posterior tibial artery - Distal posterior tibial artery - Proximal peroneal artery - Distal peroneal artery - Dorsalis pedis/tarsal artery Graft material Indicate the type of graft material used for the procedure. Choose 1 of the following: - Autogenous -- Harvest site Left / Right -- Specify the vein used: --- Great saphenous vein, in situ --- Great saphenous vein, nonreversed --- Great saphenous vein, reversed --- Arm vein --- Small saphenous vein --- Composite vein --- Vein patch - Autogenous-prosthetic composite - Prosthetic -- Specify the type. Choose 1 of the following: --- PTFE --- Heparin-coated PTFE --- Dacron --- Other (specify) Specify graft diameter: - Prosthetic - Vein Indicate type of anesthesia used. Choose 1 of the following: - General - Local, sedation yes/no - Regional, sedation yes/no -- Epidural -- Spinal Indicate the technical outcome of the procedure. Specify the following: - Postprocedure translesional gradient - Residual percent stenosis Indicate the type of study performed after the procedure. Choose 1 of the following: - Angiogram - Duplex ultrasound Estimated blood loss in milliliters. Indicate the blood products transfused to the patient. Choose all that apply: - Auto transfused blood (specify volume used) - Packed RBCs - Fresh frozen plasma - Platelets - Other (specify) Indicate the total time of the procedure in hours:minutes.
Data type
text
Alias
- UMLS CUI-1
- C0348025
Description
Outcomes of Endovascular/Open Surgery Procedures
Alias
- UMLS CUI-1
- C0184661
- UMLS CUI-2
- C0184788
Description
Indicate the period at which outcome measures are assessed
Data type
integer
Alias
- UMLS CUI-1
- C2986292
Description
Indicate major clinical complications arising from the management or treatment of the disease.
Data type
text
Alias
- UMLS CUI-1
- C1519255
Description
Indicate postoperative clinical events or conditions associated with the endovascular procedure
Data type
integer
Alias
- UMLS CUI-1
- C0009566
- UMLS CUI-2
- C2936204
Description
Complications of open surgery
Data type
integer
Alias
- UMLS CUI-1
- C0009566
- UMLS CUI-2
- C0348025
Description
Clinical Outcomes: Limb-Related Outcomes
Description
Indicate the period at which outcome measures are assessed
Data type
integer
Alias
- UMLS CUI-1
- C2986292
Description
Limb-related outcomes: symptoms - Claudication -- None -- Unchanged -- Improved -- Worsened - Ischemic rest pain - Ischemic tissue loss - Amputation
Data type
text
Description
Walking ability - Pain-free walking distance (in meters) or time (in minutes) - Maximum walking distance (in meters) or time (in minutes) Functional status/quality of life - Questionnaire assessment -- Community-based walking (PAD specific): Walking Impairment Questionnaire, others -- Generic health status: SF-36, Nottingham Health Profile, EuroQol, Sickness Impact Profile, and others -- PAD-specific quality of life: VascuQOL Questionnaire, PADQOL, and others - Patient anecdote
Data type
text
Description
Noninvasive assessment of outcome - Limb perfusion pressure and/or ABI - Graft scan - Other imaging (CTA or MRA)
Data type
text
Description
Procedure-related outcomes: Patency
Data type
integer
Alias
- UMLS CUI-1
- C0042377
Description
Wound healing characteristics - Description of dressing - 1-wk change in area - 4-wk change in area - Presence and amount of granulation tissue - Presence of reepithelialization - Presence of fibrin slough
Data type
text
Description
Cardiovascular outcomes
Description
New cardiovascular ischemic event
Data type
integer
Similar models
Peripheral Atherosclerotic Disease (PAD) - Lower Extremity data elements
- StudyEvent: ODM-Test
C1521970 (UMLS CUI-2)
C0678257 (UMLS CUI-2)
C1515974 (UMLS CUI-2)
C0080331 (UMLS CUI-2)
C0475224 (UMLS CUI-2)
C0205178 (UMLS CUI-2)
C0205178 (UMLS CUI-2)
C0205281 (UMLS CUI-2)
C0184788 (UMLS CUI-2)
C2936204 (UMLS CUI-2)
C0348025 (UMLS CUI-2)