Vista AVS

TM

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USER MANUAL

Listening to LifeTM
TABLE OF CONTENTS

Section 1: Introduction 3

Section 2: Safety Information 4

Section 3: Description of Product and Controls 7

Section 4: Preparation for Use 12

Section 5: Menu Configuration and Set Up 14

Section 6: The Ankle Brachial Index (ABI) Exam 19

Section 7: The Toe Brachial Index (TBI) Exam 26

Section 8: The Seated ABI Exam 28

Section 9: Segmental Studies 31

Section 10: Individual Site Mode 33

Section 11: File Management 34

Section 12: Peripheral Arterial Waveform Interpretation 37

Section 13: Maintenance and Cleaning 40

Section 14: Battery Recharging and Replacement 42

Section 15: Specifications 44

Section 16: Accessories 49

Section 17: Troubleshooting, Service, and Warranty 50

Section 18: Clinical References 52

Section 19: AVS Report Software 53

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SECTION 1: Introduction

Thank you for choosing the Vista AVS from Summit Doppler Systems. We believe you
have purchased the finest arterial examination system available.

Your total satisfaction is our highest priority. We strive to continually improve our
products and services. Please contact us with any suggestions. We look forward to
enjoying a long-term relationship with you!

Summit Doppler Systems, Inc.

4680 Table Mountain Dr. #150
Golden, CO 80403 USA
Phone: 1-800-554-5090 or 1-303-423-7572
Fax: 1-303-940-7165
Email: [email protected]
Visit our website at www.summitdoppler.com

Important: Please read this manual carefully and become familiar with the
features, operation, care, and safety requirements of the Vista AVS prior to use.
Please note that while operating the Vista AVS, step-by-step instructions are shown
on the display to assist you through the examination.

Summit Doppler Systems, Inc. provides general reimbursement information related to the
diagnosis of peripheral arterial disease as an overview for our customers. It is important to
understand that reimbursement is a complex process and requirements are subject to change
without notice. It is the responsibility of the healthcare provider to determine and submit
appropriate codes, charges, and modifiers for services that are rendered. Prior to filing any
claims, customers are advised to contact their third-party payers for specific coverage, coding and
payment information. Summit Doppler Systems, Inc. makes no promise or guarantee of
reimbursement by Medicare or any other third-party payer.

© 2007, 2008, 2009, 2010, 2011 Summit Doppler Systems, Inc.

All rights reserved. No one is permitted to copy or reproduce, in any form, all or any portion of this manual without the
permission of Summit Doppler Systems, Inc.

Vista AVS, Vista TIP, AVS Report, and Listening to Life are trademarks of Summit Doppler Systems, Inc.

CPT is a registered trademark of the American Medical Association. Transeptic is a registered trademark of Parker
Laboratories, Inc. Precise is a registered trademark of Caltech Laboratories, Inc. Microsoft Word, Excel, and
Windows are registered trademarks of Microsoft Corporation in the United States and other countries. Adobe is a
registered trademark of Adobe Systems Incorporated.
Authorized Representative
NOVAMEDICA
Ign. Tsakalidis S.A. U.S. Patent Pending
6th klm. Thermi-Charilaou Str.
0470
Thessaloniki
GREECE
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SECTION 2: Safety Information

Intended Use:
This device is intended for detection of blood flow in veins and arteries and as an aid for
the diagnosis of peripheral vascular disease.

Contraindications:

WARNING: The ultrasound probes are not to be used on or near the eyes.

WARNING: This device is for use only on intact skin.

WARNING: This device is not intended for use with HF surgical equipment.

WARNING: This device is not intended for fetal use.

General Warnings:

WARNING: The Vista AVS is for use by qualified personnel only. Read the User’s
Manual before use.

WARNING: Carefully route all cables and tubing to reduce the possibility of patient
entanglement or strangulation.

WARNING: Do not allow the patient to operate any portion of the equipment, including
the hand-held controller.

WARNING: Do not place the equipment in any position that would allow it to roll, fall,
or collide with a user or patient.

WARNING: Do not use equipment that is damaged or malfunctioning. Seek

appropriate service when needed. Inspect equipment regularly for signs of damage. Use
alternate equipment if needed.

WARNING: Do not connect Luer fittings from Summit Doppler equipment into any
other equipment.

WARNING: Confirm the setting of the real-time clock prior to saving patient data.

WARNING: Any equipment connected to the USB data port must be configured to
comply with IEC 60601-1. By connecting additional equipment to the USB data port,
the user is configuring a medical system and the user is responsible for ensuring the
overall system compliance. Connected equipment must be certified to the applicable

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IEC standard (i.e. IEC 950 for data processing equipment, IEC 60601-1 for medical
equipment). Contact the technical service department for more information.

General Cautions:

CAUTION: Do not plug the probe cables into a telephone system, computer, or any
equipment other than the Vista AVS.

CAUTION: Read the Maintenance and Cleaning Section of this manual (Section 13)
before cleaning.

CAUTION: Federal law restricts this device to sale by or on the order of a licensed
practitioner.

CAUTION: Do not drop or mishandle the Vista AVS main unit, probes, hand controller
or other accessories. Damage may occur.

Limitations of Noninvasive Vascular Tests:

In Current Noninvasive Vascular Diagnosis (Chapter 13, Page 208), Ali F. AbuRahma and Edward B. Diethrich note
the following limitations of arterial leg Doppler examinations.

• Falsely high segmental pressure readings in areas with calcified arteries

• Artificially elevated high-thigh pressure in very large or obese patients

• Difficult interpretation of segmental pressures in patients with multilevel

occlusive disease

• Difficulty in interpretation of high-thigh readings

• False-negative results in patients with mild vascular occlusive disease who have
normal resting ankle pressures

Safety of Ultrasound:

The Vista AVS Doppler probes were designed to be safe and effective. However, the
risk from some hazards cannot be eliminated completely. Instead, they are reduced to a
level that is As Low As Reasonably Achievable (ALARA). Prudent use of this device in
accordance with the principle of ALARA includes minimizing the duration of the
patient’s exposure to ultrasound to the extent practical.

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 Clinical Safety
Approved by the American Institute of Ultrasound - March 1997, October 1982

Diagnostic ultrasound has been in use since the late 1950s. Given its known benefits and
recognized efficacy for medical diagnosis, including use during human pregnancy, the
American Institute of Ultrasound in Medicine herein addresses the clinical safety of such
use:

There are no confirmed biological effects on patients or instrument operators caused by

exposures from present diagnostic ultrasound instruments. Although the possibility exists
that such biological effects may be identified in the future, current data indicates that the
benefits to patients of the prudent use of diagnostic ultrasound outweigh the risks, if any,
that may be present.
Safety in Training and Research
Approved by the American Institute of Ultrasound - March 1997, March 1983
Diagnostic ultrasound has been in use since the late 1950s. There are no confirmed
adverse biological effects on patients resulting from this usage. Although no hazard has
been identified that would preclude the prudent and conservative use of diagnostic
ultrasound in education and research, experience from normal diagnostic practice may or
may not be relevant to extended exposure times and altered exposure conditions. It is
therefore considered appropriate to make the following recommendation:

In those special situations in which examinations are to be carried out for purposes other
than direct medical benefit to the individual being examined, the subject should be
informed of the anticipated exposure conditions, and of how these compare with
conditions for normal diagnostic practice.

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SECTION 3: Description of Product and Controls

Description of Unit

The Vista AVS is a physiologic exam system designed to aid the clinician in the
diagnosis of peripheral arterial disease (P.A.D.). The unit includes a sensitive, bi-
directional Doppler system, arterial photoplethysmograph (PPG), and a pressure system
that provides inflation, controlled deflation, and pulse volume recording (PVR)
capabilities.

The Vista AVS is well suited for the ankle brachial index (ABI) examination, the gold
standard for the diagnosis of P.A.D. The ABI compares the systolic blood pressure at the
ankles with the systolic pressure at the brachial arteries. A significantly reduced ankle
pressure results in a low (<0.9) ABI value, which indicates P.A.D. Systolic ankle
pressures are obtained with a pressure cuff and audio Doppler probe. ABI measurements
are discussed in detail in Section 6 of this manual.

A single level, lower extremity arterial exam (CPT® 93922) includes the ABI pressures,
calculated index, and arterial physiologic waveforms. Two types of waveform modalities
are provided on the Vista AVS: continuous-wave (CW), bi-directional Doppler and PVR.
Both of these waveform modalities meet the requirements of CPT 93922. Although both
modalities have significant clinical utility, it is generally not necessary to include both
PVR and Doppler waveforms in reimbursement documentation for CPT 93922 - either
one is sufficient. Waveform analysis is discussed in Section 12 of this manual.

The Vista AVS is designed to perform segmental studies to compare three or more lower
limb pressures to the brachial pressures. This procedure is reimbursable under CPT code
93923 as a non-invasive, physiologic study of upper or lower extremity arteries, multiple
levels or with provocative functional maneuvers, complete bilateral study.

The Doppler waveform is a graph with a vertical axis (Doppler frequency shift, or pitch)
proportional to the velocity of arterial blood flow. Flow toward the probe is indicated
above the baseline. Flow away from the probe is indicated below the baseline. The 8
MHz, bi-directional probe is best for superficial vessels and all-around use. The optional
5 MHz, bi-directional probe is used for deeper vessels and with some obese patients.

Pulse Volume Recording (PVR) is a form of plethysmography, which is an indirect

method of limb volume measurement. A pressure cuff is applied to the limb and inflated
to 65 mmHg to detect the minute fluctuations in limb volume that occur with each heart
beat. The PVR waveform’s contour is a qualitative indicator of presence or absence of
peripheral arterial disease. This type of PVR does not permit calibration by injection of a
known air volume and is used for arterial waveform analysis.
Photoplethysmography (PPG) is an optoelectronic technique for detecting the small
changes of blood volume that occur in the capillary bed. Infrared (IR) light is emitted by

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the PPG probe into the skin. Light reflected from the under-lying tissue is received by a
detector and converted to an electrical signal. Since blood attenuates IR light at a higher
level than the surrounding tissue, the signal’s pulse contours are determined by the
arterial blood supply.

This type of PPG system is primarily for arterial pulse detection. In conjunction with a
digit cuff, arterial PPG is quite useful for toe pressure measurement, which is an
additional diagnostic tool when the arteries at the ankle are noncompressible (ABI >
1.30) due to calcification. Calcified arteries are prevalent among patients with diabetes or
kidney disease, but the small arteries of the toes seldom become calcified. When the
Vista AVS is configured for PPG, the system automatically calculates the toe brachial
index (TBI). A low TBI (<0.65) indicates an arterial obstruction. The TBI is discussed
in Section 7 of this manual.

The Vista AVS includes everything that is needed to conduct fast, efficient peripheral
arterial examinations including display, printer, Doppler probes, PPG probe, pressure
hose, limb pressure cuffs, and a digit cuff. The instrument operates from either its
internal battery pack or from an external medical grade power supply at 100-240VAC.

Controls and Indicators:

Main Unit

ON/OFF - Turns the unit on or off with momentary actuation

FEED - Printer feeds paper while pressed

CHARGING
- On: Charging
- Flashing: Charging complete (trickle charging while flashing)

LOW BATT - Flashing: Low battery

PAPER RELEASE
- Blue button under paper dispenser: Opens printer cover

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Display Screen - Protocol Location and Markers

Pressure Gauge (mmHg)

Right & Left ABI

Right & Left Brachial Sites

Waveform Sites (Right & Left PT or DP)

Right & Left Ankle Sites (PT or DP)

(Toe Sites when in PPG Mode)

Date and Time

Step-By-Step ABI Instructions

Hand-Held Controller

PUMP Pump runs while pressed

PUMP

SAVE During deflation- Stores current cuff pressure and deflates

SAVE Active waveform- Stores waveform data
Frozen waveform- Stores the frozen waveform
2nd button press- Confirms the stored pressure or waveform

FREEZE Active waveform- Freezes the displayed waveform

FREEZE Frozen waveform- Starts new waveform acquisition

SITE Moves the protocol marker to the next location

SITE Saves data before leaving old protocol location

SCALE Changes the waveform scaling

SCALE

MUTE MUTE Enables/disables Doppler speaker output

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 PRINT Prints out the waveform on adhesive-backed label paper
PRINT

ENTER/MENU Enters the displayed value or makes a menu selection

ENTER/MENU - also used to open the OPTIONS screen

UP Navigates through the menu in the up direction & Moves

UP the caliper tool to adjust the pressure values

DOWN Navigates through the menu in the down direction & Moves
DOWN the caliper tool to adjust the pressure values

Numeral Mode Character Mode

1 Numeral 1

2 Numeral 2 A, B, C

3 Numeral 3 D, E, F

4 Numeral 4 G, H, I

5 Numeral 5 J, K, L

6 Numeral 6 M, N, O

7 Numeral 7 P, Q, R

8 Numeral 8 S, T, U

9 Numeral 9 V, W, X

0 Numeral 0 Y, Z

Space Space
SPACE
Hyphen Hyphen
-
See Section 5 for information on how to change between Character and Numeral Modes.

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Package Contents

The Vista AVS unit includes all of the following.

- Manual - Vista AVS ABI Report Forms

- ABI Chart - Stand with Basket & Knobs
- Hand Controller - Training Video
- Digit Cuff - Ultrasound Gel
- 10 cm Cuffs (2) - PPG
- 12 cm Cuffs (4) - Doppler Cable
- 17 cm Cuffs (2) - 8 MHz Bi-Directional Probe
- Printer Paper - AVS Report Software
- Tape Measure - USB Cable
- Hose Set - Power Supply (+7VDC) & Cable

The following are optional and sold separately from the Vista AVS.

- 5 MHz Bi-Directional Probe

- Carrying case

Connectors

Doppler PPG Hand USB + 7VDC (Power) Cuff

Controller

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SECTION 4: Preparation for Use

Tools required: Phillips head screwdriver

1. Unpack the Vista AVS and inspect the unit for external damage.

2. Verify that you have received each of the contents listed on the packing list.

3. Assemble the rolling stand (if applicable) using the instructions provided.

4. Use a Phillips head screwdriver to attach the Vista AVS mounting bracket to
the end of the rolling stand’s pole. Be sure to fit the pole’s alignment pin
through the alignment hole on the bracket.

5. Use the two stand mounting knobs to attach the mounting bracket to the Vista
AVS.

6. Review the unit and locate each of the controls and connectors (see Section 3
of this manual).

7. Plug the external power supply into the + 7VDC (Power) connector.

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 VISTA TIPTM:
o For first time use, allow the unit to charge for at least one hour before
operating the Vista AVS from its battery.

8. Plug the power cord into the external power supply and then into a properly
grounded wall outlet.

9. Plug the Doppler cable into the Doppler probe.

10. Plug the Doppler cable into the Doppler connector. (Blue port)

11. Plug the PPG probe into the PPG connector. (Black port)

VISTA TIP:
o The Doppler and PPG connectors are color coded and physically
interchangeable. If you fail to connect the proper probe, no damage
will occur.

12. Attach a cuff to the Luer style hose fitting.

13. Plug the hose quick connect style fitting into the CUFF connector on the
connector panel.

14. Plug the hand-held controller into the HAND CONTROLLER connector.

VISTA TIP:
o To maintain patient safety, it is not possible to conduct an examination
while the Vista AVS is connected to a PC via the USB port.

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SECTION 5: Menu Configuration and Set Up
Loading Paper:

The Vista AVS is shipped with paper pre-loaded. To load a new roll of paper, press the
printer release button. Remove any remaining paper from the old roll and drop in the
new roll as shown below. Close the paper door and push firmly enough to latch the door
into position. Press the FEED button to ensure proper paper alignment.

WARNING: Printer components become hot during printing. Do not touch the metal
pieces inside the paper holder immediately after printing. After loading paper, press the
ON/OFF switch to begin using the instrument.

Configuring the Examination

The Vista AVS can be configured to perform P.A.D. testing in four different automated
modes. Pressure can be obtained using either the Doppler at the ankle for typical ABI
testing described in Section 6 or using a PPG at the toes for TBI testing described in
Section 7. Additionally, waveforms used to complete the physiologic study can be
performed with either a Doppler or the Pulse Volume Recording (PVR) mode.

1. Press the ENTER/MENU key to open the OPTIONS menu.

2. Press the number 1 key to select the CONFIGURE EXAMINATION.

3. Select the desired configuration for the examination by pressing the

appropriate number:

1 – ABI with PVR Waveform

2 – ABI with Doppler Waveform
3 – TBI with PVR Waveform
4 – TBI with Doppler Waveform
5 – Segmental with PVR Waveform
6 – Segmental with Doppler Waveform

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VISTA TIP
° The current configuration mode will be displayed at the bottom of the
waveform upon returning to the main screen.

Setting the Date and Time

1. Press ENTER/MENU to open the OPTIONS menu.

2. Press the number 2 key to select SYSTEM SETTINGS.

3. Press the number 1 key to set the clock.

4. The clock setting format is:

MM DD YY HH MM SS (Month-Day-Year-Hours-Minutes-Seconds)

5. Use the UP key to move the * cursor over the field that needs to be changed.

6. Use the numerals on the hand-held controller to set the date and time.

7. Press ENTER/MENU or move the * cursor to the end to exit the CLOCK menu.

8. Press the ENTER/MENU key to exit the OPTIONS menu.

Contrast Adjust

To modify the contrast level on the Vista AVS screen:

1. Press the ENTER/MENU key to open the menu.

2. Press the number 2 key to select the SYSTEM SETTINGS.

3. Press the number 2 key to increase CONTRAST ADJUST LEVEL one level.

4. Continue to press the number 2 key until desired level is reached.

VISTA TIP
•° If there is flickering or shadowing on the text, the contrast is adjusted too
high. Readjust contrast level by pressing the number 2 key until contrast level
starts over at 1 and slowly increase the contrast level.

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Setting the Power Down Status

The Vista AVS can be set to turn off automatically to save battery power. If the
automatic power down is set to ON, the unit will turn off after 20 minutes automatically
after the last key press. If the automatic power down is set to OFF, the unit will not turn
off until either the user presses the ON/OFF button or the battery becomes low.
1. Press ENTER/MENU to open the OPTIONS menu.

2. Press the number 2 key to select SYSTEM SETTINGS.

3. Press the number 3 key to toggle the power down value to ON and OFF.

4. After setting the desired value, press ENTER/MENU to exit the OPTIONS menu.

Setting the Ankle Protocol

The Vista AVS can be set to accommodate protocols that use either one pressure
measurement or two pressure measurements from each ankle. The DUAL ANKLE
PRESSURE mode will be set to OFF for a single ankle pressure. For protocols that use
measurements from both the dorsalis pedis (DP) and the posterior tibia (PT) arteries,
select HIGH or LOW to select the desired protocol with second ankle pressure.

1. Press ENTER/MENU to open the OPTIONS menu.

2. Press the number 2 key to select SYSTEM SETTINGS.

3. Press the number 5 key to toggle the ankle value between OFF, HIGH or LOW.

4. After setting the desired value, press ENTER/MENU to exit the OPTIONS menu.

File Annotation

The File Management SAVE function can use either alpha or numeric characters for
saving a patient filename. To configure the system to the desired function:

1. Press the ENTER/MENU key to open the OPTIONS menu.

2. Press the number 2 key to select the SYSTEM SETTINGS.

3. Press the number 4 key to toggle between NAME or NUMBER modes.

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 4. To enter a filename, use the alphanumeric keys on the hand-held controller.
Use the DOWN key to backspace and the UP key to move between different
letters on the same button.

5. Press the SAVE key to save the filename and begin the exam.

Selecting a Modality for Obtaining Pressures

Choose between the Doppler probe or the photoplethysmography (PPG) probe to obtain
pressure values for ankle brachial index (ABI) exams, toe brachial index (TBI) exams or
segmental studies:

1. Press the ENTER/MENU key to open the OPTIONS menu.

2. Press the number 2 key to select the SYSTEM SETTINGS.

3. Press the number 6 key to toggle between DOPPLER or PPG.

The selected pressure modality is indicated in the lower right corner of the display (DOP
or PPG will appear depending on which is selected) as shown below.

Modality –
Doppler probe

VISTA TIP
• If you’re trying to obtain pressures or waveforms using the Doppler probe but
it is not audible when rubbing the probe tip, the system is probably set in PPG
mode. To change the setting, go to the System Settings menu and select
Doppler for obtaining pressures and waveforms.

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Entering a Filename Prior to Beginning an Exam

If beginning a new exam by pressing the number 6 key for NEW EXAM – CLEAR ALL
under the OPTIONS screen, the system will display the ENTER FILENAME message.
This message ensures that the user is aware that the patient data will not be automatically
saved. After completing the exam, the user can save the data by following the
instructions provided in the “Saving a File” paragraph of Section 11.

If a current exam is not saved and the user selects either NEW EXAM - CLEAR ALL or
NEW EXAM – KEEP BRACHIALS under the OPTIONS screen, the system will display
the UNSAVED DATA message below to let the user know they have not saved the
previous data.

Press the ENTER/MENU key to ignore this message and start a new exam (the ENTER
FILENAME will appear), or press the SAVE key to save the data and the SAVE FILE
menu will appear.

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SECTION 6: The Ankle Brachial Index (ABI) Examination

Preparing the Patient

In a warm room, have the patient take off their shoes and socks and rest in a supine
position for approximately 5 minutes prior to taking pressures. The patient should wear
thin, loose fitting clothing. Avoid rolling up sleeves or pant cuffs in such a manner that it
obstructs blood flow. Bulky items such as sweaters should be removed.

Wrap the cuffs snuggly around the arms and ankles as shown below. The edge of the
cuff should be placed approximately 1 to 2 inches above the site of examination. Select
the proper cuff width, equivalent to 40% of the patient’s limb circumference. In general,
average sized adults use 10 cm cuffs, while larger adults use 12 cm cuffs. The most
efficient way to conduct the exam is to wrap all four limbs prior to taking any pressures.

Arm Cuff Leg Cuff

While applying the cuffs, it may be a good time to explain the examination to the patient
and answer any questions.

NOTE: It is very important that the patient remain still and in a supine position for the
duration of the exam.

VISTA TIP:
o The Vista AVS performs the ABI exam in the following order: Right Brachial
Pressure (R-BRA), Right Ankle Waveform (R-WAV), Right Ankle Pressure (R-
ANK), Left Ankle Waveform (L-WAV), Left Ankle Pressure (L-ANK), and Left
Brachial Pressure (L-BRA). You may override this order by using the SITE key
to move between protocol locations.
o Notice that the patient’s right hand side is shown on the left side of the Vista
AVS's screen in order to match what you see when you face the patient.

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Getting Started

Press the ENTER/MENU key to open the OPTIONS menu. Press the number 6 key to start
a new exam. You may enter a filename at this time by using the keypad. Refer to
Section 5 of this manual for File Annotation instructions.

VISTA TIP:
To start a new study on the current patient, press the number 5 key to clear the
° data except for brachial pressures. This is useful when it is determined a TBI will
be required following an ABI with noncompressible arteries.

Obtaining the Right Brachial Pressure

Connect the pressure hose to the fitting on the right brachial cuff. Apply a small amount
of gel over the right brachial artery and place the Doppler probe at approximately 45
degrees, pointing in the direction toward the shoulder as shown below. Slide the probe
laterally across the arm to find the brachial artery and obtain the best signal possible.
Adjust the volume knob to acquire a proper audio level. Once the best signal is obtained,
brace the hand holding the probe against the patient’s arm to ensure a stable position. Be
careful not to apply too much pressure against the skin. Excessive pressure could
occlude the artery.

Next, press and hold the PUMP key to inflate the cuff. Release the key once the pressure
reaches about 20 mmHg above the occlusion pressure. After the pump stops the Vista
AVS automatically bleeds the cuff at the correct rate.

Press the SAVE key at the moment flow returns. This will store the brachial pressure
value in the R BRA protocol location. This is the systolic pressure. In general, the
audible Doppler signal is a slightly more sensitive indicator of the systolic pressure than
the Doppler waveform display.

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 Doppler Waveform
During Acquisition
of Systolic Pressure

The cuff deflates automatically when SAVE is pressed. If needed, press PUMP again to
repeat the measurement, or use the arrow keys or numeric keypad to adjust the pressure
value before confirming the value by pressing the SAVE or SITE key.

Press SITE or SAVE again to confirm the right brachial pressure and move to the next
protocol location.

VISTA TIP:
o Once a satisfactory pressure has been obtained, pressing SAVE or SITE will
confirm the stored value and move to the next protocol location.
o During deflation, pressing PUMP again will re-inflate the cuff and allow a new
pressure to be taken.

OBTAINING PRESSURES USING THE PPG PROBE:

In the supine position, ABI pressures can also be obtained using the PPG probe. For
obtaining pressures, apply the PPG probe to an index finger for brachial pressures or the
great toe for ankle pressures. It is important the patient is still and the fingers and toes
are reasonably warm. To obtain brachial pressures, wrap the cuffs around the arms at the
brachial artery site. Place the PPG on the index finger with the blue side of the probe
against the skin. It should be snug to ensure contact, but not too tight to occlude blood
flow as shown below.

It will take a few seconds for the waveform to stabilize on the display after applying the
probe. You may want to consider changing the scale of the display to get a better view of
the waveform by pressing the SCALE key. Once the waveform is stable, press the PUMP

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key to inflate the cuff to a pressure approximately 20 mmHg above the pressure until the
PPG pulsations disappear. The arm cuff will begin to deflate automatically once the
pump stops.

After the first, consistent pulsation returns press the FREEZE key to freeze the waveform
on the display. Use the caliper tool by pressing the UP or DOWN arrow keys to adjust the
pressure reading. Move the caliper to the beginning of the first upward slope at the start
of the pulsation as shown below. This is the systolic pressure. Press the SAVE key to
save the pressure and move to the next site to be measured.

Refer to Section 7 for instructions for using the PPG probe to obtain toe pressures.

Right Ankle Waveform

Verify that the protocol marker is on R WAV.

VISTA TIP:
o A single level lower extremity arterial examination normally consists of the ABI
value and either bi-directional Doppler waveforms or PVR waveforms. The
following shows how to set the waveform mode. See Section 12 of this manual for
information on waveform interpretation. Note that arterial tests documented with
PPG waveforms are not reimbursable as opposed to Doppler or PVR waveforms.

The Vista AVS can acquire bi-directional Doppler waveforms, pulse volume recording
(PVR) waveforms and photoplethysmography (PPG) waveforms. See Section 5 of this
manual for configuring the desired waveform mode.

OBTAINING DOPPLER WAVEFORMS:

Apply a small amount of coupling gel over the site of the artery, either the PT or DP
artery. Place the probe over the artery at an angle of approximately 45 degrees, pointing
the probe tip in the direction toward the calf and knee. Slide the probe slowly across the
artery until the best signal is obtained.

PT DP

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Once the waveform is optimized, press the SCALE button one or more times as needed to
adjust the vertical scaling to obtain a waveform as large as possible without clipping at
the top. If the probe is pointed in the correct direction (approximately 45 degrees
“upstream”) the majority of the waveform will be above the baseline. Press PRINT to
print the waveform or FREEZE to freeze or pause the waveform. When frozen, the UP or
DOWN keys will scroll the waveform. Press SAVE to store the waveform, and then use
the UP key to adjust the site label (PT, DP, TOE, BRA, ***). Press SITE or SAVE again
to store these values and move to the R-ANK (right ankle) location.

OBTAINING PVR WAVEFORMS:

VISTA TIP:
• If you pump over 75 mmHg pressure, the unit will automatically deflate to 65
mmHg. Note that the audio will be off or muted while in the PVR mode.
• You may want to consider setting the scale to PVR x 2 to view the waveform.
This is done by pressing SCALE on the hand-held controller to change the
view of the display.

To obtain the PVR waveform from the ankle, wrap the proper size cuff (see Section 7 for
Preparing the Patient for proper cuff selection) around the ankle. Move the cursor to the
Right WAV site and use the PUMP control to inflate the ankle cuff to 65 mmHg or
slightly higher. It will take several seconds for the position of the waveform to “settle
out” and return to the center of the display. After the waveform stabilizes, press the
FREEZE key. Here, you have two options: if the waveform is acceptable, press SAVE to
record it. Or, you can use the UP or DOWN key to scroll to the optimum waveform. Press
SITE or SAVE again to move to the R ANK (right ankle) location.

PVR Waveform

Right Ankle Pressure

Verify that the protocol marker is on the R ANK location.

VISTA TIP:
• The system can be configured for exam protocols that use either one or two
(DP and PT) ankle pressure measurements. See Section 5 of this manual for
information on how to set the Ankle Protocol.

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Ensure that the pressure hose is connected to the fitting on the right ankle cuff. Position
the Doppler probe over the PT or DP artery. Be sure to use ample gel. Obtain an
adequate signal, then press and hold the PUMP key to inflate the cuff. Release the key
once the pressure reaches about 20 mmHg above the occlusion pressure.
After releasing the PUMP key, the Vista AVS automatically deflates or bleeds the cuff at
the correct rate. Press the SAVE key at the moment flow returns to store ankle pressure
value in the R-ANK location.

The cuff fully deflates automatically when the pressure is saved. If needed, press PUMP
again to repeat the measurement, or use the UP or DOWN keys or numeric keypad to
adjust the pressure value before confirming the value by pressing the SAVE or SITE key.

Protocol for Two Ankle Pressures

If the protocol configuration is set to HIGH or LOW, press SAVE while deflating to the
PT pressure. Press SAVE again to confirm this pressure.

The site will change to DP. Press PUMP to repeat the pressure cycle. Both pressures will
be stored and displayed. The displayed ABI will be either the higher or the lower value,
depending on the user setting.

VISTA TIP
• When conducting the ABI exam on an amputee, use the SITE key to select the
appropriate pressure/waveform locations.

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Left Ankle Waveform

Repeat the procedure described previously for the right ankle waveform. When the left
ankle waveform is stored in the L WAV site, the site cursor moves to L ANK (left ankle
pressure) site.

Left Ankle Pressure

Move the cuff hose to the left ankle cuff and repeat the procedure described for the right
ankle on the left ankle. When the left ankle pressure is stored in the L ANK site, the site
cursor moves to L BRA (left brachial pressure) site.

Left Brachial Pressure

Move the cuff hose to the left arm cuff and repeat the procedure described for the right
brachial on the left brachial. The greater of the two arm pressures will be used to
calculate the ABI. A difference of 20 mmHg or more between the two brachial pressures
is a possible indication of upper extremity stenosis. In this case, the arm pressures should
be repeated and if the result still indicates a difference of 20 mmHg or more, upper
extremity testing should be considered.

After the left brachial pressure is stored in the L BRA site, the site cursor moves to R
BRA (right brachial pressure) site. At this point, the exam data is ready for saving,
printing and/or downloading.

Assessment of the Ankle Brachial Index (ABI)

The Vista AVS automatically calculates the ankle brachial index (ABI) for both sides.
The right and left ABI are both calculated using the higher of the two brachial pressures.

ABI Assessment

Above 1.30 Noncompressible Artery

1.00 to 1.29 Normal
0.91 to 0.99 Borderline (equivocal)
0.41 to 0.90 Moderate Disease
0.00 to 0.40 Severe Disease

See Section 11 of this manual for File Management information including saving,
printing, recalling patient data, & for information on how to reset for new patient data.

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SECTION 7: The Toe Brachial Index (TBI) Examination
Toe pressures are useful in the assessment of diabetic patients with noncompressible arteries
(ABI > 1.30), and patients with Raynaud’s syndrome, or with advanced peripheral arterial
occlusive disease including the smaller distal vessels. Most clinicians do not perform toe
pressures on patients with normal ABI results.

Preparing the Patient

Patient preparation for the TBI exam is similar to preparation for the ABI exam, however the
need to obtain PPG signals from the toes requires consideration of patient temperature. It
may be more difficult to obtain PPG waveforms if the patient is cold. If needed, consider
laying a blanket over the patient or wrapping a warm towel around the patient’s foot. Some
clinicians prefer to leave the patient’s socks on until they are ready to take the toe pressures.

Brachial Pressures

Brachial pressures are conducted in the manner described in Section 6 of this manual for the
ABI examination.

Ankle Waveforms

Either Doppler or PVR waveforms may be used accurately on patients with noncompressible
arteries. In some cases, calcification may result in reduced ultrasound penetration and weak
Doppler signals. Refer to Section 5 for details on switching to Doppler or PVR waveforms.
Obtaining ankle waveforms are described in Section 6 of this manual.

Toe Pressures

Refer to Section 5 of this manual for details on configuring the system for TBI using PPG.

Wrap the great toe with a 2.5 cm or 1.9 cm digit cuff and attach the pressure hose. The cuff
should be 40% of the toe circumference. Place the cuff at the base of the toe and attach the
PPG probe to the distal phalanx with the blue side of the probe against the skin as shown in
the photos below. NOTE: The ankle cuff is not used while taking toe pressures.

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Wait a few seconds for the PPG waveform to stabilize after applying the probe. Once a
stable PPG waveform is obtained, press the PUMP key to inflate the digit cuff. Continue to
inflate to a pressure approximately 20 mmHg above the pressure where the PPG pulsations
disappear. The digit cuff will begin to deflate automatically once the pump stops. To get a
better view of the waveform on the display, press the SCALE key.

After the first pulsation returns press the FREEZE key to freeze the waveform on the display.
Use the caliper tool by pressing the UP or DOWN arrow keys to adjust the pressure reading.
Move the caliper to the beginning of the first upward slope at the start of the pulsation as
shown below. This is the toe systolic pressure. Press the SAVE key to save the pressure and
move to the next site to be measured.

Systolic Pulse Reappearance

NOTE: A substantial shift in the baseline may occur when blood flow returns. This is a
useful indicator of pulse reappearance.

Press SAVE or SITE to confirm the value and move to the next exam location.

Assessment of the Toe Brachial Index

The Vista AVS automatically calculates the toe brachial index (TBI) for both sides. The
right and left TBI are both calculated using the higher of the two brachial pressures.

TBI Assessment

Above 0.70 Normal

0.64-0.70 Borderline
Below 0.64 Abnormal

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SECTION 8: The Seated ABI

Performing the ABI in the seated position makes it possible to assess patients who are not
able to lay in the supine position for ABI determination. These patients may be
physically disabled or wheel chair bound, patients with degenerative disease of the spine
or severe back pain, patients with advanced cardiopulmonary disease and orthopnea.

The Vista AVS is able to calculate ABI values for seated patients by compensating for
the effects of gravity on the lower extremity pressures based on the vertical distance
between the arm and ankle cuffs.

To begin the exam, have the patient sit erect in a chair with knees at a 90-degree angle.
Their feet should rest flat on the floor or on an elevated platform - feet should not be
dangling. Wrap the cuffs around the arms and ankles.

To determine the difference in height between the two cuffs, use a tape measure or
yardstick, measure the distance in centimeters between the middle of the arm cuff to the
floor and the middle of the ankle cuff to the floor as shown below. Next, subtract the
ankle distance from the arm distance to get the vertical distance to be entered for the
hydrostatic correction.

Press the ENTER/MENU key on the hand-held controller to open the OPTIONS menu.
Press the number 1 key to CONFIGURE EXAMINATION. You will press the number 1
key to select “ABI with PVR Waveform”. Press the ENTER/MENU key to open the
OPTIONS menu again and press number 2 key for SYSTEM SETTINGS.

Press the number 6 key to use the Doppler probe for obtaining pressures. Press the
ENTER/MENU key to exit. Press the ENTER/MENU key again to open the OPTIONS
menu. You will then press the number 7 key for HYDROSTATIC CORRECTION and
using the keypad, enter the vertical height between the cuffs in centimeters. Press the
SAVE key when finished.

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Start at the right brachial by applying the gel and placing the Doppler probe over the
artery site to listen to the blood flow. While holding the probe steady on the artery, press
and hold the PUMP key to about 20 mmHg above the occlusion pressure. Release the
PUMP key and the cuff will automatically start to deflate.

Press the SAVE key when you hear the first pulsation return. If you were late pressing the
SAVE key, you can adjust the pressure reading by using the UP or DOWN key. You will
then press the SAVE key again to record the systolic pressure and the marker will move to
the next protocol location.

Move the hose to the from the arm cuff to the ankle cuff to obtain the ankle waveform
using PVR. Press and hold the PUMP key to inflate the cuff to 75 mmHg and release the
key when the inflation automatically stops. Pressure will deflate to 65 mmHg for
optimum PVR. Wait for the “cuff deflating” message on the display to disappear. If
needed, use the scale key to optimize the waveform.

After the waveform stabilizes, press the FREEZE key and if the waveform is acceptable,
press the SAVE key to record. Or, use the UP or DOWN key to scroll to the optimum
waveform and press the SAVE key to record it. Press the SAVE key again to move to the
next protocol location.

Now, obtain the ankle pressure. The hose should be connected to the ankle cuff. Apply
gel to either the dorsalis pedis artery or the posterior tibia artery and use the Doppler
probe to listen to the blood flow. While holding the probe steady on the artery, press and
hold the PUMP key to about 20 mmHg above the occlusion pressure. Release the PUMP
key and the cuff will automatically start to deflate.

Press the SAVE key when you hear the first pulsation return. If you were late pressing the
SAVE key, adjust the pressure reading by using the UP or DOWN key. Press the SAVE key
again to record the systolic pressure and the marker will move to the next protocol
location. Continue these steps for the remaining sites to complete the exam. The Vista
AVS makes the hydrostatic correction based on the vertical distance entered prior to
obtaining pressures.

The corrected pressure

values will be displayed.

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VISTA TIP:
• If the calculation for the hydrostatic correction factor results in an ankle
pressure that is equal to or less than zero, the result is displayed as "---" and
the associated Seated Index (SI) is "0.0".
• The PPG probe is not suitable for obtaining pressures in the seated position.
The Doppler probe is available and recommended.
• The two pressure modes, high or low, are not available while performing the
Seated ABI.

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SECTION 9: Segmental Studies

Segmental studies are usually performed on patients diagnosed with P.A.D. to localize
the occlusion in the lower limbs. A segmental study is an extension of the ABI exam,
comparing three or more lower limb pressures to the brachial pressures. It is possible to
obtain pressures and waveforms from five lower-limb, arterial sites using the Vista AVS.

For a complete segmental study, you must obtain at least three pressures and waveforms
from the lower extremity. A difference of 20 mmHg or greater from one cuff site to the
next distal cuff site suggests P.A.D. at the area just proximal to the distal cuff.

To begin, press the ENTER/MENU key to open the OPTIONS menu and press the number
1 key to CONFIGURE EXAMINATION. Here, you have two options: press the number
5 key to select “Segmental with PVR Waveform” or press the number 6 key to select
“Segmental with Doppler Waveform”.

Once you have made your selection, the SEGMENTAL EXAMINATION

CONFIGURATION screen will be displayed. Press number 1 through 5 keys toggle
through the various arterial sites to assess. Press the number 6 key to choose between
performing the exam “In-Line” down the leg or “Laterally” moving from one side of the
patient to the other. When finished, press the ENTER/MENU key.

Now that you’ve configured the segmental exam, press the ENTER/MENU key to open the
OPTIONS menu again and then press the number 2 key for SYSTEM SETTING. Press
the number 6 key to choose a modality for obtaining pressures (either PPG or
DOPPLER).

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After making your selection, press the ENTER/MENU key to exit the SYSTEM SETTING
menu and the screen should look like the example below.

Wrap a cuff at each site as the patient lays supine to prepare for the exam. Commonly, a
10 cm cuff is used at the ankle, a 12 cm cuff is used at the calf and a special, 17 cm-
contoured, thigh cuff is used at the thigh. Be sure to connect the hose to the cuff of the
site to be measured. Proceed with obtaining pressures and waveforms from the desired
sites. Refer to Sections 6 and 7 for more details for using a Doppler probe, PVR and PPG.

Segmental Interpretation:

Normal
• All segmental pressures, including the thigh pressure, should be equal to or slightly greater
than the brachial pressure.

Abnormal
• A 20 mmHg or greater drop in pressure generally is considered positive for hemodynamically
significant stenosis (> 60% diameter) in the segment(s) leading into the cuff or under the cuff.
It may be helpful to compare pressures in one limb to the other, and to consider the PVR (or
Doppler) waveforms in addition to the pressures.

Caution: It is necessary that an appropriately sized cuff be used for thigh pressures – typically 12
cm, 17 cm or 22 cm in diameter. If the patient is too large for the available cuff, the girth of the
limb may cause an artificially high pressure, known as the “high thigh cuff artifact”. In this
situation, the following exceptions apply:

Normal
• High Thigh Exception: The pressure should be at least 20 mmHg above the brachial pressure.
Abnormal
• High Thigh Exception: A pressure drop of 30 mmHg from the high thigh to above knee is
suggestive of disease.

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SECTION 10: Individual Site Mode

If you would like to quickly obtain a pressure or waveform from an arterial site (NOT
following the standard protocol sequence of the exam calculation), use the INDIVIDUAL
SITE MODE by pressing the ENTER/MENU key to open the OPTIONS screen and
pressing the number 4 key. You can use this mode while in the middle of performing the
ABI, TBI and segmental study and it will not interrupt the order of the exam. When you
exit the INDIVIDUAL SITE MODE, you will return to the exact site where you left off
to complete the exam.

There are three modality options in this mode: Doppler, PVR or PPG. Use the UP or
DOWN keys to move the menu cursor to select a modality option.

NOTE: Pressures and waveforms obtained using the INDIVIDUAL SITE MODE can be
printed but the data is only temporarily stored on the display screen and cannot be saved
or downloaded. Temporarily storing or freezing a waveform enables you to change to
another modality to obtain the next pressure.

Use the SITE key to select the desired arterial site. There are several site options to
choose from:

RIGHT BRACHIA (brachial) LEFT BRACHIA (brachial)

RIGHT FINGER LEFT FINGER
RIGHT THIGH LEFT THIGH
RIGHT HI KNEE (above the knee) LEFT HI KNEE (above the knee)
RIGHT LO KNEE (below the knee) LEFT LO KNEE (below the knee)
RIGHT CALF LEFT CALF
RIGHT ANKLE LEFT ANKLE
RIGHT PT (posterior tibia) LEFT PT (posterior tibia)
RIGHT DP (dorsalis pedis) LEFT DP (dorsalis pedis)
RIGHT TOE LEFT TOE
PENIS

To obtain a pressure, use the PUMP key to inflate the cuff then use the SAVE key to
record the pressure and deflate remaining pressure in the cuff. If system is set to digit
(i.e. finger, toe or penis), the cuff will pump slowly. Otherwise, pump is set at normal
speed. To obtain a waveform, press the SAVE or FREEZE keys to freeze the waveform on
the display screen. Use the PRINT key to print out the waveform, including site and
pressure information. To restore waveform activity, press the SAVE or FREEZE key
again. Please refer to Sections 6 and 7 for a more detailed explanation of obtaining
pressures and waveforms using a Doppler, PVR or PPG.

To exit the INDIVIDUAL SITE MODE, use the UP or DOWN keys to select EXIT and
press the ENTER/MENU key.

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SECTION 11: File Management

VISTA TIP:
o Exam reports can be configured for either numeric or alpha character
filenames. To change the filename configuration, use the SYSTEM SETTINGS
option (see Section 5 for details).
o It is not possible to alter exam data after a file is saved.

Saving a File

To save an exam, press the ENTER/MENU key to open the OPTIONS screen. Press the
number 3 key to select FILE MANAGEMENT. Press the number 1 key to save the
current exam. There are 10 storage locations that retain data if all power is lost. Select
the number of an unused file storage location (this location will be highlighted). Use the
alphanumeric keys on the hand-held controller to enter a patient filename. Use the DOWN
key to backspace. Use the UP key to move between different letters on the same button.
Press SAVE to save the file. After saving, the system returns to the main screen.

If the system was powered down prior to saving data, the FILE RESTORE message will
appear on the display upon power up (see image below). Pressing the ENTER/MENU key
will remove the message and allow the user to start a new exam or recall the previous
unsaved patient data by accessing “Restore Data”. Powering down a second time will not
repeat the message even if the restored file is still stored.

NOTE: When saving an exam, the SAVE and ENTER/MENU keys perform the same
function. Either key can be pressed to save an exam file.

If the user saves an exam under FILE MANAGEMENT by entering a patient name or ID
and turns off the power before pressing the SAVE or ENTER/MENU key, the system will
automatically complete the save function before the power is turned off.

NOTE: Powering off by unplugging the system will not activate this feature.

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Recalling a File

To recall an exam, press the ENTER/MENU key to open OPTIONS screen. Press the
number 3 key to select FILE MANAGEMENT. Press the number 3 key to recall an
exam from a file storage location. Select the number of the file to be recalled using the
numeric keypad. To return to the existing file without recalling one of the saved files,
press the ENTER/MENU key to exit FILE MANAGEMENT.

The Vista AVS automatically stores a backup copy of patient data in the “Restore Data”
each time a new name, pressure or waveform is saved. The exam stored in the “Restore
Data” is purged upon entering patient data (name, pressure or waveform) for a new exam.
In other words, once new patient data is entered for a new exam, the previous exam in the
“Restore Data” is deleted and the new exam is stored in the “Restore Data”. It is
important to note that the power down and clear exam functions do not erase the
previously stored exam in the “Restore Data”.

To access the exam stored in the “Restore Data”, press the ENTER/MENU key to open the
OPTIONS screen. Press the number 3 key to open FILE MANAGEMENT and press the
number 3 key again to open RECALL EXAM FROM FILE. Next, press the UP key to
highlight RESTORE DATA and press the ENTER/MENU key to open the exam.

Printing a File

The PRINT key prints the patient data in the exam screen. Use the RECALL function
described above to recall a saved file if needed. When only one waveform has been
saved, the saved pressures, ABI’s, and one waveform will print. If no waveform has
been saved, only the pressures and ABI’s will print. The printout will show 4 seconds of
recorded waveform data although the display only shows 3 seconds. NOTE: It is not
possible to print directly from the FILE menu.

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Deleting a File

To delete an exam, press the ENTER/MENU key to open the OPTIONS screen. Press the
number 3 key to select FILE MANAGEMENT. Press the number 2 key to delete an
exam from a file storage location. Select the file number on the numeric keypad to delete
the file, which will be highlighted. Press that number again to confirm or press any other
key to cancel. To return to the exam screen, press the ENTER/MENU key to exit. To
delete all files, use the UP or DOWN keys to navigate to DELETE ALL and press
ENTER/MENU. Press the ENTER/MENU key again to confirm deletion or press any other
key to cancel.

Downloading a File to a PC (current exam has NOT been saved)

To download patient data to a PC, open the OPTIONS screen using the ENTER/MENU
key. Press the number 3 key to select FILE MANAGEMENT. Press the number 5 key
to download the current exam. Current patient data will be transferred automatically, or
press the ENTER/MENU key to cancel.

See Section 19 of this manual for more information about the AVS Report software.

VISTA TIP:
o When downloading data, the current exam screen is transferred to the PC.
o Downloading is only possible if the USB cable is connected between the Vista
AVS and the PC.
o AVS Report software must be installed on the PC in order to transfer data.

Downloading Exam from File (current exam has been saved)

To download patient data to a PC, open the OPTIONS screen using the ENTER/MENU
key. Press the number 3 key to select FILE MANAGEMENT. Press the number 4 key
to download an exam that has been previously saved. Using the numeric keypad, select
the number of the file to recall and download. Saved patient data will be transferred
automatically or press the ENTER/MENU key to cancel. You may also download all of the
saved exams at once by using the UP or DOWN arrow keys to select DOWNLOAD ALL
and pressing the ENTER/MENU key.

VISTA TIP
° This mode is useful to help expedite downloads of saved files by eliminating the
need to recall the file first.

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SECTION 12: Peripheral Arterial Waveform Interpretation

Bi-Directional Waveform Interpretation:

Continuous-wave, bi-directional Doppler waveforms are useful for assessment of lower

extremity P.A.D. severity and progression and are a valuable addition to the ABI
particularly for patients with noncompressible arteries.

The normal Doppler signal is pulsatile and multi-phasic. Below is a normal waveform
from the PT artery. The systolic acceleration and deceleration are rapid. These
waveforms are tri-phasic with two diastolic components.

The waveform’s rise and fall times lengthen as disease progresses. A long deceleration
is a sensitive indicator of P.A.D. As disease progresses, the diastolic components are
lost and the waveform becomes mono-phasic. In addition, the weak signals associated
with diminished flow produce waveforms that are often more jagged in appearance.

Above is a waveform with the characteristics of abnormal PT flow. The acceleration and
deceleration times are slow, the diastolic components are absent, and the waveforms have
a somewhat diminished height. These waveforms are typical of a patient with mild to
moderate arterial disease.

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The characteristics of waveforms acquired at the DP are similar. Below is an example of
normal DP waveforms. This is a bi-phasic waveform from a normal patient. The signal
is pulsatile with a pronounced diastolic component. Absence of the second diastolic
component without additional evidence is not an indication of disease.

Continuous-wave, Doppler waveforms are often considered to be the most useful type of
physiological waveform for detecting P.A.D. Doppler waveforms are given a
Recommendation of Class I in the ACC/AHA P.A.D. Guidelines (Hirsch, 2005).

Pulse Volume Recording (PVR) Waveform Interpretation:

PVR serves as a qualitative aid in the assessment of peripheral hemodynamics. The

waveform contour is useful to confirm the results of the ABI and is a valuable diagnostic
tool for patients with noncompressible vessels (ABI > 1.30). Additionally, the PVR can
be used to monitor limb perfusion after revascularization.

Normal plethysmographic waveforms resemble the arterial pressure pulse. The normal
PVR waveform (shown below) has a sharp systolic upstroke, and a somewhat narrow
peak. After peaking, the waveform drops quickly during diastole with its slope bowing in
toward the baseline. Normal waveforms usually have a dicrotic notch between the peak
and baseline. However, the dicrotic notch may become less noticeable with vasodilation
or may become more pronounced during vasoconstriction.

Distal to an arterial occlusion, the waveform becomes more rounded with a more gradual
up slope, and the down slope may bow away from the baseline. Amplitude of the

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abnormal waveform (shown below) is usually diminished, but this condition is not
sufficient for diagnosis because amplitude is influenced by additional factors such as
blood pressure, arrhythmia, vasomotor tone, and limb position.

Dicrotic notch is
missing – bows
away from the
baseline.

Again, note that the waveform contour may be altered during vasodilation or
vasoconstriction. Improper cuff size, over- or under-inflation, low cardiac stroke volume,
and improper cuff application may affect the waveform contour.

PVR waveforms are given a Recommendation of Class IIb in the ACC/AHA P.A.D.
Guidelines (Hirsch, 2005).

NOTE: Although Doppler waveforms are given a higher recommendation than PVR
waveforms, PVR waveforms may be easier to obtain.

PPG Waveforms:

PPG waveforms are made available on the Vista AVS as an aid for obtaining systolic
pressures at the toe. PPG waveform contour interpretation is similar to the interpretation
of PVR waveforms. However, because the PPG waveform is obtained at a digit,
distortion of the PPG contour due to vasoconstriction or vasodilation is more common.

PPG waveforms are not acceptable for meeting reimbursement criteria for the lower
extremity arterial exam, however PPG is useful for obtaining pressures as described in
Section 7 of this manual. Toe pressures obtained with PPG meet reimbursement criteria
if accompanied by either Doppler or PVR waveforms.

For these reasons, Summit Doppler Systems recommends using PVR and Doppler modes
for waveform analysis.

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SECTION 13: Maintenance and Cleaning

Cleaning Precautions:

WARNING: The Vista AVS is not designed for liquid immersion. Do not soak or
drop the probes or main unit in liquids. Do not use solvent cleaners. Use only the
recommended spray or wipe cleaners and disinfectants (see “Cleaning and Disinfection”
below).

WARNING: The Vista AVS is not designed for sterilization processes such as
autoclaving or irradiation.

WARNING: The Vista AVS is not intended for use on open skin. If there is evidence
of open wound contamination, disinfect the probes before using again as described
below.

Cleaning and Disinfection:

Excess gel should be wiped off the ultrasound probes after every examination. Probes
and main unit should be cleaned with a cloth dampened by warm water or with pre-
saturated isopropyl alcohol wipes or spray such as Transceptic® from Parker
Laboratories, Inc. Be sure to clean carefully along any seams, but do not allow liquids to
enter the unit through connectors or speaker grill.

To disinfect the unit, use commercially available spray or wipe disinfectants that are
registered with the U.S. Environmental Protection Agency (EPA), such as Precise® QTB
from Caltech Industries, Inc. Follow the instructions provided with the disinfectant and
be sure to wipe the unit dry when finished.

Vista AVS users should wash hands and change gloves after every exam. Refer to local
and hospital policies regarding cleaning and disinfection.

Store the unit in a clean area free of dust and debris. Follow the temperature and
humidity storage requirements as specified in Section 15 of this manual.

Maintenance:

CAUTION: If the unit is to be stored for longer than 90 days without use, remove the
battery pack prior to storage.

Replace the battery pack annually or when its capacity is noticeably diminished.

A qualified technician must verify the accuracy of the pressure readout annually. Return

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the unit to Summit Doppler Systems for calibration if needed. See Section 15 of this
manual for applicable pressure specifications.

Periodically -- not less than annually -- inspect the main unit and probes for signs of
cracks or breakage. Inspect cables, tubing, and connectors for signs of wear or failure.
Inspect labels for damage. The user should discontinue use of the unit or probes if any
loss of housing integrity is detected.

Check the tightness of the screw that attaches the mounting bracket to the rolling stand’s
pole (if applicable) at least annually.

In order to preserve, protect and improve the quality of the

environment, protect human health and utilize natural resources
prudently and rationally – do not dispose of waste electrical or
electronic equipment (WEEE) as unsorted municipal waste. Contact
local WEEE disposal sites or Summit Doppler Systems to dispose of
equipment.

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SECTION 14: Battery Recharging and Replacement

The external power supply (Summit Catalog #B200) becomes the power source when the
Vista AVS is operated while the supply is connected. When the external power supply
is connected while Vista AVS is off, the supply provides power for recharging. Plug
the supply into the + 7VDC (POWER) connector.

The green CHARGING indicator is held ON during charging. The indicator flashes
during trickle charge. The CHARGING indicator will turn off when charging is
complete.

The Vista AVS uses a 7.2V six-cell Nickel Medal Hydride (NiMH) battery pack. This
battery pack has sufficient capacity to allow the product to be used for 12 ABI exams.
The system charges a fully depleted battery in 3 hours. After the charging is completed, a
maintenance charge (sometimes called a “trickle charge”) is applied.

When the remaining battery life is less than 15 minutes, the yellow LOW BATT indicator
on the front panel will flash. When the battery life is severely depleted, the flashing rate
will increase. At this point, plug in the external power supply immediately to avoid
losing any unsaved exam data.

NOTE: The Vista AVS will not print when the battery is low to ensure that there is no
loss of data.

VISTA TIP:
o Once the LOW BATT indicator begins to flash, the battery may become depleted
rapidly if a mode that requires additional power is selected such as PUMP. Plug
in the external power supply as soon as possible once the LOW BATT indicator
begins to flash.

When operating from the external power supply, the Vista AVS will switch over to
battery power automatically if there is a power outage.

NOTE: Charging will not begin if the battery temperature is less than 0°C (32°F).

NOTE: It is important not to unplug the Vista AVS from the wall during an exam. This
may result in system reset.

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Replacing the battery:

Tool required: Philips head screwdriver

To replace the battery, use a Philips head screwdriver to remove the battery compartment
screw. Press the latch on the side of the battery connector and unplug the old battery.
Plug in the new battery and close the battery door. Tighten the screw firmly but do not
over tighten. Charge the new battery for 2 hours before use.

CAUTION: The battery pack contains a temperature measurement component that is

matched to the cell type and to the product requirements. Use only replacement battery
packs as specified by Summit Doppler Systems, Inc.

CAUTION: Unauthorized battery substitutions will void the warranty and may cause
overheating.

CAUTION: Used NiMH batteries must be recycled or disposed of properly. Do not

incinerate.

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SECTION 15: Specifications
Note: Unless otherwise indicated, all specifications are subject to change without notice.

System Functionality:

Ankle Brachial Index

o Ankle and Arm Systolic Pressures
o Automatic ABI Calculation
o Automatic Selection of Arm Pressure (higher of the two)
o Configurable for one or two Ankle Pressures
Toe Brachial Index
o Arm and Toe Systolic Pressures
o Automatic TBI Calculation
o Automatic Selection of Arm Pressure (higher of the two)

Seated ABI
o Ankle and Arm Systolic Pressures
o Automatic Hydrostatic Correction and ABI Calculation
o Automatic Selection of Arm Pressure (higher of the two)
o Configurable for one or two Ankle Pressures

Segmental Studies
o Arm and 5 Lower Limb Systolic Pressures
o Automatic Index Calculation
o Automatic Selection of Arm Pressure (higher of the two)
o Ability to customize study by selecting the number and location of arterial sites
Waveforms
o Bi-Directional Doppler
o Pulse Volume Recording (PVR)
o Photoplethysmography (PPG)
Reporting
o Index and Waveform Printing on Summit Label Paper
o Optional Download Capability to PC
o Ten patient examination storage locations

Doppler:

Doppler Type: Bi-Directional, Continuous-Wave (CW)

Audio Bandwidth: >4 KHz
Waveform Display: Digital Mean Frequency Estimator
Separate Forward and Reverse Flow Waveforms

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Available Probe Frequencies: 8.43MHz, 5.5 MHz
Displayed Waveform Amplitude Accuracy: +/-10%
Speaker Output: > 0.25 W
Speaker Type: 2 inch, 5 W
Cable length: 6.5 ft
Volume Control: Continuously variable with mute

Photoplethysmography (PPG):

Wavelength: 940 nm
Artifact Rejection: Synchronous demodulation, AC coupled output
Operating Frequency: 1KHz
Cable length: 6.5 ft

Pressure:

Range: 0 – 265 mmHg

Accuracy: +/-3 mmHg 0 – 200 mmHg, +/-2% above 200mmHg
Safety: Pressure released if greater than 280 mmHg
Pressure released if held above 100 mmHg beyond 3 minutes
Pressure released if held between 30-100 mmHg beyond 5 minutes*
(*Operator may over-ride for exam purposes)
Redundant Control
Bleed Rate: 2.5 mmHg/sec nominal
PVR: 0.16 to 12.5 Hz bandwidth, AC Coupled

Display:

Size: 5.7 inch, ¼ VGA (320 x 240 dot)

Backlight: LED Backlight
Type: Transflective Monochrome

Printer:

Type: High Speed Thermal Array

Paper Width: 58 mm
Print Width: 48 mm
Resolution: 8 dots/mm
Paper Type: Thermal, K180 Adhesive Backed Label or Thermal, Archival, 58mm

CAUTION: Use only the specified paper. Use of improper paper may damage the print
mechanism.

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Data Storage and Transfer:

Storage: 10 storage locations, 16 numeric or 24 alpha character length filenames

Type: USB 2.0
Connector: Peripheral
Output: AVS Report Software – Adobe PDF or comma delimited files

Power (External Supply):

Type: Medical Grade Supply

Rated Mains Supply Voltage: 100-240VAC, 50-60Hz, 1.2A
Output: +7V, 5A

Battery:

Type: 6-cell NiMH pack

Rating: 7.2V, 2000 maHr
Replacement Part No: B200
Battery Life: 3 hours continuous use or minimum of 12 ABI Exams
Replacement Interval: 1 year
Charge Time: 3 hours

Mechanical and Environmental:

Dimensions: 10” H x 12” W x 3.6” D

Weight: 4.75 lbs.
Stand height: 47”
Operating Conditions: Temp. 10 to 30°C, Humidity 30 to 75% non -condensing
Transport & Storage Conditions: Temp. –20 to 50°C, Humidity 5 to 90% non-condensing

Safety

Degree of protection against electric shock:

Type B Applied part

Classification:

Class II Equipment - when externally connected

Internally Powered Equipment - when not externally connected (battery powered)

Degree of protection against ingress of water: Ordinary (not rated)

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Designed and tested to meet:
IEC601-1, IEC60601-1-2, IEC60601-1-4, IEC60601-2-37. EMC Classification: Class A
This equipment was tested to applicable standards for electromagnetic interference. If
interference occurs, attempt to eliminate the source of the interference or increase the
distance between the Vista AVS and the source of the interference.

WARNING: Connect the Vista AVS only to equipment that meets the appropriate
standards. The Vista AVS and its External Power Supply are a medical system. The
External Power Supply must meet IEC60601-1 construction requirements for Reinforced
Insulation at minimum in order for the system to comply with the appropriate safety
standards.

Attention: Consult Accompanying Documents

Additional technical information is available upon customer request.

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Transducer Model: LifeDopTM 5 MHz Bi-Dir Operating Mode: Continuous-Wave (cw)
Application(s): Peripheral Vascular
ACOUSTIC OUTPUT MI ISPTA.3 ISPPA.3
2 2
(mW/cm ) (W/cm )
Global Maximum Value 0.05 500 0.5
Pr.3 (Mpa) 0.12
wo (mW) 32.7 32.7
Associated fc (MHz) 5.50 5.50 5.50
Acoustic zsp (cm) 0.85 0.85 0.85
Parameter x-6 (cm) 0.4 0.4
Beam Dimensions y-6 (cm) 0.6 0.6
Az (cm) 0.4
EBD Ele. (cm) 0.8

Transducer Model: LifeDopTM 8 MHz Bi-Dir Operating Mode: Continuous-Wave (cw)

Application(s): Peripheral Vascular
ACOUSTIC OUTPUT MI ISPTA.3 ISPPA.3
2 2
(mW/cm ) (W/cm )
Global Maximum Value 0.04 365 0.37
Pr.3 (Mpa) 0.116
wo (mW) 15.7 15.7
Associated fc (MHz) 8.43 8.43 8.43
Acoustic zsp (cm) 0.63 0.63 0.63
Parameter x-6 (cm) 0.42 0.42
Beam Dimensions y-6 (cm) 0.14 0.14
Az (cm) 0.6
EBD Ele. (cm) 0.3

ISPTA.3 the derated spatial-peak temporal-average intensity (mwatts per cm2).

ISPPA.3 the derated spatial-peak pulse-average intensity (watts per cm2).
MI the Mechanical Index.
Pr.3 the peak rarefactional pressure (megapascals) associated with the transmit pattern giving rise to the value reported for MI.
Wo the total time-average ultrasonic power (mwatts).
fc the probe center frequency (MHz).
zsp the axial distance at which the reported parameter is measured (cm).
x-6, y-6 are the –6dB beam dim. in the x-y plane where zsp is found (cm).
EBD the entrance beam dimensions (cm). These dimensions are the same as the dimensions of the transmit crystal.

Measurement Uncertainties: Power: +34, -42%

Pressure: +11, -16%
Intensity (ISPTA): +23, -26%
Frequency: +/- 5%

Acoustic Output Parameters are measured in water. Derated values, denoted by the subscript “.3”, take into account a conservative level of attenuation
that would be encountered in the human body. The derated intensity values (I.3) are obtained from water values of intensity (Iw) at a depth of z calculated
by:
I.3 = exp(-0.23*0.3*f*z)*Iw
(where f is the probe frequency in MHz and z is the depth in centimeters)

The derated peak rarefactional pressure is calculated from the value of measure water (pr) by:
Pr.3 = exp(-0.115*0.3*f*z)*pr
(where pressure is given in megapascals)

Additional Output Reporting Information for IEC 61157

8 MHz: Iob < 112 mW/cm2

Note that parameter zsp (in the probe reporting tables) is the same parameter as Ip in IEC 61157.
Operating Conditions: There are no user controls, which affect the ultrasound output.

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SECTION 16: Accessories

The following accessories and replacement items are available from Summit Doppler
Systems. Contact us at 1-800-554-5090 or (303) 423-7572, or order on-line at
www.summitdoppler.com

Cuffs and Tubing:

Cuff, 10 cm CUF0002
Cuff, 12 cm CUF0003
Cuff, 17 cm CUF0008
Cuff, 1.9 cm CUF0004
Cuff, 2.5 cm CUF0005
Cuff, 1.9 cm CUF0009
Hose Set, Vista AVS ASY0008

Cables: (serial numbers required)

Doppler, Vista AVS CBL0018

USB, 6 ft CBL0024

Printer Paper:

ABI Printer Label Paper, Box of 5 rolls K180

Gel:

Ultrasound Gel, 250 g G155

Ultrasound Gel, 60 g G150

Probes: (serial numbers required)

Bi-Directional Probe, 8MHz (for L250AB/L250AC) SD8B

Bi-Directional Probe, 5MHz (for L250AB/L250AC) SD5B
Bi-Directional Probe, 8 MHz (for Vista AVS/Vista ABI) SD8V
Bi-Directional Probe, 5 MHz (for Vista AVS/Vista ABI) SD5V
PPG SPPG

Battery Pack:

Battery, Vista AVS, 7.2V B200

Roll-stand with Basket K270

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 SECTION 17: Troubleshooting, Service, and Warranty
Troubleshooting:

WARNING: Use alternate equipment in case of unit failure. Call Summit Doppler
Systems’ Service Department if the unit or probes malfunction.

WARNING: Risk of Electric Shock - the Vista AVS contains no user serviceable
components. Only qualified personnel should attempt to service the unit.

CAUTION: Do not drop or mishandle the Vista AVS probes. Damage may occur.

Vista AVS Troubleshooting Guide

Symptom: Check for:
Doppler is not audible when user rubs Doppler mode is not selected (see pg. 17 for selecting modalities)
probe tip Mute is selected
Probe cable is not plugged into the main unit or plugged into an
incorrect part
USB cable is connected to PC
Cannot obtain PPG signal at toe TBI mode is not selected
Probe cable is not plugged into main unit
Verify PPG signal can be obtained on a finger – if yes, try warming
the foot
Unit will not print Printer out of paper
Paper coming off roll too loosely – tighten roll
Incorrect paper type
Paper roll inserted improperly
Unit will not pump Verify that the site cursor is at a BRA or ANK position or at WAV
with PVR (i.e. not in Doppler waveform mode) – also ensure that
the hose connection is secure
Pump runs but cuff does not inflate Verify that both ends of the cuff hose is plugged in correctly to
Vista AVS and the cuff
Unit will not download Verify that Host PC is running AVS Report Software, Software
key has been entered properly, USB cable is connected
Cannot save 2nd ankle pressure Verify that DUAL ANKLE PRESSURES is not set to OFF.
Unit shuts off Power Down is set to ON or battery is low
Faint Doppler signal audible, but There is normally a slight noise threshold that must be overcome
waveform is not displayed prior to a waveform being displayed
Printed waveform differs from The printed waveform always includes two additional seconds of
displayed waveform waveform data
Doppler Audio cuts out when Verify proper exam configuration.
attempting to take an ankle pressure or
waveform
Unit pumps too slow PPG using digit cuffs automatically inflate slowly – switch to a
digit cuff
If you press “ENTER/MENU” during If you did not want to go to the Main Menu, press
a segmental study, you will return to “ENTER/MENU” again to return to the segmental study.
the Main Menu

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Warranty and Service Information:

Summit Doppler Systems, Inc. is pleased to offer our customers with a 30-day, no hassle
evaluation return policy in the event that you are not satisfied with our product.

The Vista AVS is warranted against defects in material and workmanship for 12 months
from the original sale of the device. This includes all parts and labor required to repair or
replace the unit to original specifications and shipping costs associated with sending the
product back to the customer. The customer is responsible for providing adequate
packaging materials and shipping costs to Summit Doppler Systems. Products shall be
repaired or replaced in a reasonable amount of time.

Summit Doppler Systems’ liability for any claim is limited to materials and labor
associated with repair or replacement. In no event shall Summit Doppler Systems be
liable for incidental or consequential losses or damages in connection with the purchase
of this product.

Summit Doppler Systems disclaims all expressed or implied warranties, agreements or

arrangements other than issued in this warranty unless specified in writing and signed by
the President of Summit Doppler Systems.

Summit Doppler Systems is not responsible for damages to the device that occur as a
result of the inadequate shipping to Summit Doppler Systems, improper maintenance or
cleaning as described in the user manual, misuse, abuse, alteration of the equipment from
its original specifications, or dismantling the unit (other than by Summit Doppler
Systems approved service technicians).

If you need to return the Vista AVS or one of its components or accessories for repair:

1) Call Summit Doppler Systems at 1-800-554-5090 to obtain a Return

Authorization (RA) and any special instructions prior to shipping.
2) Clean the product before shipping.
3) Ensure the product is well packaged and suitable for shipment.

Note: The customer is responsible for any damage incurred during return shipment
associated with improper packaging.

After contacting Summit Doppler, send the product to:

Service Department
Summit Doppler Systems, Inc.
4680 Table Mountain Dr., Unit 150
Golden, CO 80403

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SECTION 18: Clinical References

Clinical References:

Aburahma AF, Diethrich, EB (eds): Current Noninvasive Vascular Diagnosis. Littleton

MA, PSG Publishing, 1988.

American Diabetes Association: Peripheral Arterial Disease in People with Diabetes

(Consensus Statement). Diabetes Care 26:3333-3341, 2003.

American Heart Association: Human Blood Pressure Determination by

Sphygmomanometry, 2001.

Daigle RJ: Techniques in Noninvasive Vascular Diagnosis – an Encyclopedia of

Vascular Testing. Littleton, CO: Summer Publishing, 2002:137-153.

Gerlock AJ, Giyanani VL, Krebs C: Applications of Noninvasive Vascular Techniques.

Philadelphia, W.B. Saunders, 1988:299-332,413-434.

Hirsch AT, Haskal ZJ, Hertzer NR, Bakal CW, Creager MA, Halperin JL, Hiratzka LF,
Murphy WRC, Olin JW, Puschett JB, Rosenfield KA, Sacks D, Stanley JC, Taylor LM Jr,
White CJ, White J, White RA. ACC/AHA Guidelines for the Management of Patients
with Peripheral Arterial Disease (Lower Extremity, Renal, Mesenteric, and Abdominal
Aortic): A Collaborative Report from the American Association for Vascular
Surgery/Society for Vascular Surgery, Society for Cardiovascular Angiography and
Interventions, Society of Interventional Radiology, Society for Vascular Medicine and
Biology, and the American College of Cardiology/American Heart Association Task
Force on Practice Guidelines, 2005.

Olin JW. Clinical Evaluation and Office-Based Detection of Peripheral Arterial Disease,
Contained in: Hirsch, AT (Ed). Primary Care Series: Peripheral Arterial Disease and
Intermittant Claudication, Hillsborough, NJ: Excerpta Medica, Inc., A Reed Elsevier Co.

General Information about P.A.D:

National Institute of Health (NIH) Stay in Circulation Campaign: www.aboutpad.org

P.A.D. Coalition: www.padcoalition.org

The Vascular Disease Foundation (VDF): www.vdf.org

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SECTION 19: AVS ReportTM – Report Generation Software

NOTE: If the software is not purchased with the Vista ABI (model # L450VA), 5 trial
downloads will be included so you can try it out prior to purchase.

The AVS Report software allows a clinician to download examination results from the
Vista AVS and annotate patient data, add clinician interpretation and comments, store
and print a patient examination report.

WARNING: User supplied external hardware used to operate the AVS Report
software should conform to recognized standards for safety such as IEC601-1,
IEC60065, UL2601-1 or UL544.

WARNING: The Vista AVS shall not be connected to the user supplied external
hardware during an examination.

WARNING: The Vista AVS and AVS Report software shall be operated by
trained personnel who have read all manufacturer supplied labeling.

WARNING: The AVS Report software does not provide an interpretation of the
examination results. Results should be verified prior to performing additional
procedures on the patient.

CAUTION: In the event of AVS Report software transmission error, the data is
invalid and shall be re-transmitted.

CAUTION: To ensure integrity of data on the user supplied external hardware, the
equipment should be backed up frequently.

CAUTION: To ensure proper operation of the user supplied external hardware, the
equipment should run virus checking software and system diagnostics frequently.

CAUTION: When the AVS Report application is running the Windows® Standby
and Hibernate functions are disabled.

Getting Started:

Minimum Requirements:
Operating system supported only with a 64 or 32-bit Windows® 7 Home Premium or
better, a 32-bit Windows® XP Professional, and a 32-bit Windows® Vista Home Premium
or better.

Installation instructions:
Insert AVS Report installing disk into CD ROM Drive. Installation will start
automatically and the following screen will appear:

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NOTE: The standard installation does not include DICOM formatted file option. To
install the DICOM feature, contact Summit Doppler.

1. When you begin to install the AVS

Report software, this screen will appear.

2. Select “Next” to continue the installation.

3. Select “Install” to load to the AVS Report

software program to your computer.

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 4. This screen will appear as the installation
is in process.

5. This screen will be displayed briefly just

before the Installshield Wizard is complete.

6. When this screen appears, the AVS Report

software has been successfully installed.
Select “Finish” to complete the installation
process.

Connecting to Vista AVS:

Using the USB cable provided, connect the equipment end of the cable to the Vista
AVS and the computer end of the cable to an unused USB Port on the PC. Once the
cable is connected to both devices, turn on the Vista AVS. When the computer
successfully recognizes the device, the following message will appear:

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Starting AVS Report:
If the installation was completed properly, an application icon is already on your
computer desktop. Double click on the icon to start the software.

Generating a Report:

USB Communication:
When the Vista AVS is on and connected to the computer while the AVS
Report software is running, the bottom of the screen will indicate “Connected”.
The “Read Success” indicates that the communication channel is open and
operating properly.

If the indication is “Disconnected” then the software was started without the Vista
AVS connected. PLEASE NOTE: The software can be operated without the device
connected for opening previously generated files, printing or importing as described
below.

If the indication is “Write Call Failed” then the AVS Report has lost communication
with the Vista AVS. Check to ensure the cables are connected at both ends and
ensure the unit is on.

Data Download:
On the Vista AVS OPTIONS menu, select FILE and DOWNLOAD to transfer data
that is currently active. The AVS Report software will briefly indicate “Upload
Success” to verify that the data was accepted.

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 If a transmission error occurs, the report software screen will indicate that the data
verification failed. Check to ensure the USB cable is securely connected on both
ends and download the file again. Contact Summit Doppler Systems if the error
continues to occur.

Report data is segmented into 4 Sections of the software and separated by tabs at the top
of the application. Select the appropriate tab to access or enter information.

Patient Info – User editable information regarding the patient, general comments and the
examiner identification.
Pressures/Waveforms – Non-editable pressure, waveform and ABI information from the
Vista AVS downloaded file.
CPT-ICD9 Codes – User editable billing information to appear on the report.

Patient Information (“Patient Info” Tab):

Patient Name or ID will be transferred from the Vantage ABI file information and are
shown in the Patient Info Tab. Other information can be annotated at this time such
as:

Patient Name -
Date of Birth -
Age -
Sex -
I.D. Number –
Date/Time –
Referring Physician –
Interpreting Physician –
 

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Patient Name or Patient ID will be downloaded directly from the Vista AVS file
information if it was saved on the device.

Risk Factors –
Check the appropriate boxes to enter
the patient’s P.A.D. risk factors. The
“Other” section can be used for extra
details such as pack years of smoking
or date of previous CV event.

Current Symptoms –
Check appropriate boxes to enter the
patient’s P.A.D. symptoms and the
location of the symptoms. The
“Other” section can be used for extra
details such as when or how often
symptoms occur.

Examiner Comments –

General comments and interpretation sections are provided for extended comments
from the interpreting clinician or from the examiner.

Pressures, Waveforms and ABI Values (“Pressures/Waveforms” Tab):

The ankle and brachial pressures download from the Vista AVS are included in the
Pressure/ABI Tab along with the modality used to take the pressures, Doppler or
PPG. A reference table is also displayed for either ABI or TBI clinically accepted
values as an aid for the clinician in determining a diagnosis.

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 ABI Exam

Arm and Ankle Pressures

Reference ABI Table

ABI Value
Modality

Seated ABI Exam

Arm and Ankle Pressures

Reference ABI Table

Hydrostatic Correction

Modality

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 Segmental Study

Arm and Lower Extremity

Pressures
Arm and Lower Extremity
Index Values

Time and Date

Modality

CPT - ICD-9 Codes (“CPT - ICD-9 Codes” Tab):

The CPT and ICD-9 Codes Tab allows the user to select a billing option to be displayed
on the report. Select the tabs at the bottom of the page to choose either CPT or ICD-9.
Select the appropriate code on each screen or type a code in the “Other” section if the
desired code is not available. Only one selection can be valid on any given report.

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Managing a Report:

File Menu:

Open:
Allows the user to open a previously
saved report.

Save/Save As:
Allows the user to select the report name
and location for later recovery and backup.

Close:

Allows the user to close out of the currently opened file.

Export:
Allows user to generate an Adobe® PDF file, DICOM file or Comma Delimited file for
export. See below for further explanation on exporting files.

Print:
Allows the user to print the report on the selected printer.

Print Preview:
Allows the user to view the completed report prior to printing. Zoom in and out, scroll
pages or print directly from the preview window.

Printer Select:
Allows the user to change the default printer.

Exit:
Allows the user to exit the application.

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Preferences Menu:

Allows the user to enter facility information that will be included in the report such as
facility name and address. This information will be stored in the application and used
on each subsequent report that is generated until the information is changed.

The File Paths menu allows the user to select a default directory for each file format
to save exams.

The screen above allows the user to enter

The File Paths menu allows the user to
facility information that will be included in
select a default directory for each file
the report such as the facility name and
format to save exams.
address. This information will be stored in
the application and used on each subsequent
report that is generated until the information
is changed.

The screen above allows the user to enter Enter the information in the fields and click “OK”.
physician names to be used for referring or
interpreting physician on the patient
information tab. Select “Add” to enter a
new name.

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 The screen to the left allows a user to
customize the severity table shown in the
report. The default is from the ACC/AHA
guidelines. To customize, select “Custom”.

To edit the text line, double-click the

text line. To delete the text line, right-
click the text line. To add a new line,
click on “New Line” and left-click and
drag to a new location. Press “OK”
when editing a line of text.

The screen to the left will appear.

Click “OK” when complete.

Exporting a Report:

There are three file export types that are supported: Adobe PDF, DICOM and Comma
Delimited files (CSV). NOTE: The saved files will default directly into the folder
initially created in the File Path menu to store the AVS Report software.

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Adobe PDF (2 Options):

1. Select File>Export>Adobe Acrobat (.pdf)>Export and Launch Acrobat to

immediately view the PDF file on your computer screen.

2. Select File>Export>Adobe Acrobat (.pdf)>Export Report File Only to

save/store the file to view at a later time.

- Enter a file name and save it to convert the current file to this format and the
Adobe application (if it is currently loaded on the PC) will automatically start.

- If the application is not loaded, a free reader version can be downloaded from
the website: www.adobe.com

- Once the file has been converted and opened into the Adobe application, all
features and functions of that application are supported. The file can be
saved, printed, e-mailed, etc.

Comma Delimited Files:

Select File>Export>Comma Delimited (.csv). Enter a file name and save it to convert the
current file to a delimited format that can be read using any software application for
viewing text files, such as Microsoft Word®, Microsoft Excel® and Notepad. These
applications do not automatically open once the file has been saved. This file can be used
to configure data into EMR systems. Special programming may be required by the system
administrator.

DICOM (Digital Imaging and Communications in Medicine)

Select File>Export>DICOM (.dcm). Enter a file name and save it to convert the current
file to a DICOM format that can be connected to a DICOM system (i.e. PACS). A DICOM
viewer must be used to open and review these files.

AVS ReportTM DICOM Conformance Statement: The DICOM portions of the AVS
Report application were developed using software tools supplied by Lead Technologies,
Inc., a leading supplier of industrial medical imaging applications. DICOM files created
by AVS Report use the Secondary Capture Image Storage SOP Class. These files have
been evaluated using the conformance test supplied by Lead Technologies and meet all
applicable criteria of this SOP Class. Additionally, AVS Report files have been
successfully evaluated using several independent DICOM viewing applications. As these
standards are constantly evolving, all efforts have been made to verify the DICOM files
and data elements conform to the latest published DICOM standards for this SOP Class.

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Completed Sample ABI Report in PDF File Format

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Completed Sample Seated ABI Report in PDF File Format

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Completed Sample Segmental Study Report in PDF File Format

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Example of data from a comma-delimited file:

SubTitle Ankle Brachial Index Assessment Form

PatientName John Smith
PatientID 123-45-6789
Severity ABI Severity
Severity1 0.90 - 1.30 - Normal
Severity2 0.70 - 0.89 - Mild
Severity3 0.40 - 0.69 - Moderate
Severity4 0.0 - 0.39 - Severe
Results ABI Results
Comments Right side P.A.D. Spoke to patient re: life style modifications
Recommend further evaluation
CPTCode 93922 Non-invasive physiologic studies of upper or lower extremity
arteries, single level, bilateral
ICD9Code 440.21 Atherosclerosis of native arteries of the extremities with
intermittent claudication
RightSite PT
LeftSite PT
RightProbe 8 MHZ
LeftProbe 8 MHZ
ABIRightArm 154
ABILeftArm 148
ABIRightToeAnkle Right Ankle
ABIRightTA 96
ABILeftToeAnkle Left Ankle
ABILeftTA 158
LeftTAP Left Ankle Pressure
RightTAP Right Ankle Pressure
LeftTAPVal 158
RightTAPVal 96
HAPValue1 154
HAPValue2 154
LeftABIValue 1.02
RightABIValue 0.62
PatientAge 67
Date 12/27/06 10:02:54
RiskOther 2 pack per day smoker
SymptomOther Max walking distance - 1 block
HospitalName St. Joseph
HospitalAddr 1234 Main Golden
SummitAddr 4680 Table Mountain Drive #150 Golden, CO 80403
Phone: 303.423.7572
Fax: 303.940.7165
Toll Free: 800.554.5090
Examiner Kathy C. - RVT
Modality Pressures – Doppler

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