VPAP™ Adapt SV
User Guide
English
228234-Eng/3 08 10
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Introduction
VPAP™ Adapt SV
The VPAP Adapt SV flow generator has been designed to be reliable, comfortable
and easy to use. You can observe your treatment and make adjustments to
settings using a keypad and LCD screen.
CAUTION
!
USA federal law restricts this device to sale by or on the order of a
physician.
User/Owner Responsibility
The user or owner of this system shall have sole responsibility and liability for any
injury to persons or damage to property resulting from:
•
•
operation which is not in accordance with the operating instructions supplied
maintenance or modifications carried out unless in accordance with
authorized instructions and by authorized persons.
Please read this manual carefully before use.
Definitions
WARNING
!
!
Alerts you to possible injury.
CAUTION
Explains special measures for the safe and effective use of the device.
Medical Information
Intended Use
The VPAP Adapt SV system is intended to provide non-invasive ventilatory
support to treat adult patients with obstructive sleep apnea (OSA) and respiratory
insufficiency caused by central and/or mixed apneas and periodic breathing. This
device is intended for use in the hospital or home.
Contraindications
The VPAP Adapt SV is not a life support ventilator and may stop operating with
power failure or in the unlikely event of certain fault conditions.
Before using the VPAP Adapt SV tell your doctor if you have any of the following
conditions:
•
•
•
•
hypotension or significant intravascular volume depletion
acute sinusitis or otitis media
epistaxis (severe nosebleeds) causing a risk of pulmonary aspiration
conditions predisposing to a risk of vomiting into mask
Introduction
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•
•
•
•
impaired ability to clear secretions
pneumothorax or pneumomediastinum
recent cranial trauma or surgery
chronic hypoventilation.
Below are general warnings and cautions. Further specific warnings,
cautions and notes appear next to the relevant instructions in the manual.
WARNINGS
!
•
•
•
The VPAP Adapt SV is NOT a life support ventilator.
The entire manual should be read before using the VPAP Adapt SV.
Advice contained in this manual should not supersede instructions given by
the prescribing physician.
•
The VPAP Adapt SV should be used with masks and accessories
recommended by ResMed or the prescribing physician. Use of incorrect
masks and accessories may adversely affect the function of the
VPAP Adapt SV.
•
The VPAP Adapt SV is designed for use with masks that allow exhaled gases
to be flushed out through vent holes. Exhaled gases will be rebreathed if the
mask is worn with the machine turned off, or the vent holes are occluded. If
this occurs over prolonged periods, suffocation may occur.
In the event of power failure or machine malfunction, remove the mask.
•
•
º
The air flow for breathing produced by this device can be as much as 11 F
º
(6 C ) higher than the temperature of the room. Caution should be exercised
º
º
if the room temperature is warmer than 90 F (32 C).
•
The VPAP Adapt SV can be set to deliver pressures up to 25 cm H O. In the
2
unlikely event of certain fault conditions, pressures of up to 40 cm H O for
2
less than one second are possible.
•
•
The VPAP Adapt SV is not suitable for use in the vicinity of flammable
anesthetics.
If oxygen is used with the VPAP Adapt SV, the oxygen flow should be
stopped when the device is not operating. If oxygen flow continues when
the device is not operating, oxygen may accumulate within the device and
create a risk of fire.
•
•
Do not use the VPAP Adapt SV if there are obvious external defects or
unexplained changes in performance.
Do not open the VPAP Adapt SV case. There are no user serviceable parts
inside. Repairs and internal servicing should only be performed by an
authorized service agent.
CAUTIONS
!
You should report unusual chest pain, severe headache or increased
breathlessness to your physician. An acute upper respiratory tract infection may
require temporary discontinuation of treatment.
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The following side effects may arise during a course of therapy with the
VPAP Adapt SV:
•
•
•
•
•
•
drying of the nose, mouth, or throat
bloating
ear or sinus discomfort
eye irritation
skin rashes
chest discomfort.
Quick Setup Guide
1
Attach the air tubing and pressure sensor tube to the VPAP Adapt SV and mask
(page 9).
Attach a humidifier if required (page 10).
2
3
4
5
Switch on the VPAP Adapt SV. Make sure the mask is unblocked.
Select the mask setting (page 21).
Perform the Air Circuit Learn function (page 21) at first-time use, or if you are
adding or removing a component of the system (eg, a humidifier or anti-bacterial
filter).
Fit the mask and commence breathing into it. The SmartStart™ function should
trigger treatment to commence within the first couple of breaths. If not, press
the Start/Stop key once to commence treatment (page 16).
6
Note: You can observe treatment progress (eg, mask leak) via the Treatment
screens (page 24).
Quick Setup Guide
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Remove your mask to stop treatment. If SmartStop is enabled, treatment will
stop automatically. If the SmartStop function has been disabled, press the
Start/Stop key once.
7
VPAP Adapt SV System
VPAP Adapt SV Components
The VPAP Adapt SV flow generator is supplied with air tubing and a power cord.
Masks are supplied separately, as you and your clinician have to decide which
mask is best for you.
Some people experience dryness of the nose, mouth and throat while using the
VPAP Adapt SV system, especially during winter. Others may experience
sneezing and/or a runny or blocked nose during the first few weeks of VPAP
treatment. In many cases, these symptoms of nasal irritation can be resolved
with a humidifier. See page 10 to connect a humidifier to the VPAP Adapt SV.
LCD screen
Control panel
Carry handle
Removable
Pressure sensor
front cover
tube connector
Air tubing connector
Figure 1: VPAP Adapt SV flow generator
The control panel allows you to adjust settings on the flow generator, and the
LCD screen displays information about your treatment. See “Control Panel
Functions” on page 17.
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ResLink attachment point
Air filter
Power cord
Figure 2: Rear of VPAP Adapt SV
See page 14 to connect a ResLink™. See page 30 to replace the air filter.
Proximal cuff
Luer connector
Tube clip
Pressure sensor tube
Connect this end to
the flow generator
Connect this end
to the mask
Air tubing
Figure 3: Air tubing fully assembled
All necessary air tubing components are packed with the VPAP Adapt SV:
•
•
a 6’6" (2 m) length of air tubing
a pressure sensor tube (to measure pressure at the mask) with Luer
connectors
•
•
tube clips (to hold the pressure sensor tube onto the air tubing)
a proximal cuff (a special connector that attaches the pressure sensor tube
into the main air tubing so you only need to make one attachment to the
mask).
The air tubing is supplied with the proximal cuff connected. Attach the tube clips
evenly along the air tubing. Press the pressure sensor tube into the tube clips,
and screw the Luer connectors together at the proximal cuff. Make sure the
pressure sensor tube is not kinked, obstructed or twisted.
Note: ResMed recommends the following tubing products for use with the
VPAP Adapt SV: replacement air hose (only) PN14986; replacement air delivery
system (hose, sensor line, clips, proximal cuff) PN26923.
Masks
You will also need a ResMed mask system (supplied separately). For the latest
set up your mask correctly for use with the VPAP Adapt SV. Your clinician can
explain the features of the masks available and will discuss the mask that best
suits your needs.
VPAP Adapt SV System
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Assembling the VPAP Adapt SV System
Complete the following steps to assemble the VPAP Adapt SV system. Make
sure the area around the unit is clean (dust free) and clear of bedding, clothes and
any other potential blockages.
To add a humidifier see page 10.
WARNING
!
Use only the air tubing system supplied with the VPAP Adapt SV system.
Connect the power cord
1
There are two sockets at the rear of the flow generator—the top one for an AC
(standard mains electricity) and the lower one for a DC power cord (see “Using
DC Power to Run the VPAP Adapt SV” on page 15). ResMed recommends using
the AC power cord supplied with the unit.
The customized ResMed power cord can be held in place with the locking clips.
To insert the locking clip, pinch the free ends together and fit the pins into the
holes on both sides of the socket. Insert the power cord into the socket. Push
the locking clip down so that the groove holds the power cord in place. Plug one
end of the power cord into the power socket at the rear of the unit, and the other
end into a power outlet.
Power switch
AC locking clip
AC power cord
Plug the free end of the power cord into a power outlet.
CAUTIONS
!
!
•
Do not connect both AC and DC power cords to the VPAP Adapt SV at
the same time.
•
Be careful not to place the device where it can be bumped or where
someone is likely to trip over the power cord.
WARNING
Make sure the power cord and plug are in good condition and the
equipment is not damaged.
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Connect air tubing
2
Connect the air tube firmly onto the air outlet at the front of the unit.
Air tubing connector
Pressure sensor tube
connector
Figure 4: Front view of VPAP Adapt SV
To attach the pressure sensor tube to the unit, screw the Luer connector onto
the socket on the side of the unit.
Figure 5: Twisting the Luer lock connectors together
WARNING
!
Use care when handling the air tubing. Be particularly careful when
attaching the Luer connector to the VPAP Adapt SV. If you kink or
excessively twist the sensor tube it may affect the protection offered by the
mask pressure alarm system.
Attach the mask to the air tubing.
3
The mask system should already be assembled. If it is not, please refer to the
user instructions supplied with the mask.
Connect the mask system to the free end of the air tubing.
Proximal cuff
Figure 6: Assembling the VPAP Adapt SV system
VPAP Adapt SV System
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Humidifiers
A humidifier may be required if you are experiencing dryness of the nose, throat,
or mouth. The following ResMed humidifiers are compatible with the
VPAP Adapt SV:
HumidAire 2i
heated humidifier
HumidAire
heated humidifier
Humidifier accessory (HumidAire only)
Medium air tubing
21" (52 cm)
Figure 7: Humidifiers compatible with the VPAP Adapt SV
When using a humidifier, stop the VPAP Adapt SV by using the Start/Stop key or
by removing the mask to trigger the SmartStop function. Do not switch the
VPAP Adapt SV off at the power switch or the power source while it is running, as
this could result in condensation in the motor.
Please refer to the relevant humidifier user manual for detailed instructions and
warnings.
CAUTIONS
!
• Be very careful not to allow water to enter the VPAP Adapt SV
as this could affect therapy and/or damage the device.
• Do not tip the humidifier while it is connected to the
VPAP Adapt SV. If water enters the VPAP Adapt SV device, turn off the
main power switch at the back of the unit and unplug it from the power
outlet. Return the unit to your equipment supplier for checking.
Connecting a Humidifier
Note: After connecting or removing a humidifier, always perform the Air Circuit
Learn function (see page 21).
WARNING
!
When using a humidifier, position it so that it is lower than your head will
be during sleep, and at the same level or lower than the VPAP Adapt SV.
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HumidAire 2i™
The HumidAire 2i provides heated humidification for the VPAP Adapt SV.
To attach the HumidAire 2i, remove the VPAP Adapt SV front cover and attach
the humidifier docking station and water chamber. No other accessories are
required for use. Please refer to the HumidAire 2i User’s Manual for details.
Once you have performed the Air Circuit Learn function the VPAP Adapt SV is
ready for use. See “Starting Treatment” on page 16.
VPAP Adapt SV
HumidAire 2i
docking station
HumidAire 2i
water chamber
Figure 8: HumidAire 2i attached to the VPAP Adapt SV
Figure 9: HumidAire 2i attached to VPAP Adapt SV and mask
WARNING
!
•
Make sure that the water chamber is empty and thoroughly dried before
transporting the HumidAire 2i.
•
When using the carry bag, always separate the VPAP Adapt SV unit and
the Humidaire 2i before placing in their respective compartments.
VPAP Adapt SV System
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HumidAire™
You will need a medium size 21" (52 cm) air tube to connect the VPAP Adapt SV
unit to the HumidAire™ (see Figure 7).
1
Make sure both the HumidAire and the VPAP Adapt SV are turned off.
Fill the HumidAire with water as described in the humidifier manual. Place the
filled water chamber inside the HumidAire.
Gently detach enough of the tube clips to release the end of the pressure sensor
tube from the VPAP Adapt SV air tubing.
2
Connect the VPAP Adapt SV air tubing to the left connector port on the humidifier,
and the medium 21" (52 cm) air tubing to the right connector port. Close the
HumidAire lid.
Medium air tubing
HumidAire
Pressure sensor tube
VPAP Adapt SV air tubing
Place the VPAP Adapt SV on top of the HumidAire. Never place the
VPAP Adapt SV unit underneath the humidifier. (This is to avoid water spilling into
the unit.)
3
Connect the free end of the medium air tubing to the VPAP Adapt SV.
Connect the pressure sensor tube by twisting the Luer lock onto the
VPAP Adapt SV (see page 9).
4
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Connect the mask system to the free end of the long air tubing. The final
assembly should look like this:
5
Switch on the HumidAire and the VPAP Adapt SV.
6
WARNING
!
Make sure that the power cords and plugs are in good condition and the
equipment is not damaged.
Perform the Air Circuit Learn function (see page 21).
For information about filling and maintaining your humidifier, refer to the
7
HumidAire User’s Manual.
The VPAP Adapt SV is now ready for use with the HumidAire. See “Starting
Treatment” on page 16.
CAUTION
•
!
Set up the HumidAire and the VPAP Adapt SV unit so that the tubing to
the mask runs higher than the machines. This will prevent condensation
build-up.
•
If condensation appears in the mask, turn the humidifier settings down.
VPAP Adapt SV System
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ResLink™
The ResLink is a device that records data onto a SmartMedia™ card during your
therapy. The card can be returned to your clinician so that they can observe your
progress and adjust flow generator parameters if necessary. The ResLink
connects to the back of VPAP Adapt SV as shown. For full details on using the
ResLink, please refer to the ResLink User’s Manual.
Anti-bacterial Filter
Your clinician may recommend that you use an anti-bacterial filter. A filter should
be placed in the air tubing between the mask and the flow generator. If using a
humidifier, place the filter between it and the flow generator (see Figure 10
below).
Typically, the filter should be replaced daily. Check the filter instructions for full
details.
Whenever a filter is added, removed or replaced you must run the Air Circuit
Learn function (see “Learn Circuit” on page 21).
Note: Only hydrophobic anti-bacterial filters should be used with a
HumidAire 2i.
Anti-bacterial filters
Figure 10: Inserting anti-bacterial filters
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Using DC Power to Run the VPAP Adapt SV
The VPAP Adapt SV can be run on DC in case of power failure. ResMed supplies
separately a converter that allows a 12V or 24V battery to be connected to the
DC input of the VPAP Adapt SV. When using a DC power supply, the power is
turned on and off via the switch on the converter, and not the power switch at
the back of the VPAP Adapt SV. The DC converter is a separate accessory that
can be purchased through your ResMed distributor.
The humidifier heater will be automatically disabled when the VPAP Adapt SV is
operating from the DC supply.
Power consumption of the VPAP Adapt SV varies with treatment settings.
Adequate battery type and sizing is required before operation on DC, and it is
recommended that you contact ResMed’s Technical Services division or see
ResMed's website for information on your specific application.
CAUTION
!
The VPAP Adapt SV uses 30V DC power. Only connect the VPAP Adapt SV
to DC power using the VPAP Adapt SV DC Converter (P/N 26928) specified
for this application.
Supplemental Oxygen
The VPAP Adapt SV is designed to be compatible with the use of low flow
oxygen therapy provided from an external source and supplied at a fixed rate of
up to 15 L/min. At a fixed flow rate of supplemental oxygen flow, the inhaled
oxygen concentration will vary, depending on the pressure settings, patient
breathing pattern, mask selection, and the leak rate. This warning applies to most
types of bilevel machines.
WARNING
!
•
If oxygen is used with this device, the oxygen flow must be turned off
when the device is not operating.
Explanation: When the device is not in operation, and the oxygen flow is
left on, oxygen delivered into the ventilator tubing may accumulate
within the device enclosure and create a risk of fire.
Always begin VPAP Adapt SV therapy before the oxygen supply is
turned on.
Always turn the oxygen supply off before stopping VPAP Adapt SV
therapy.
Oxygen supports combustion. Oxygen should not be used while
smoking or in the presence of an open flame.
•
•
•
VPAP Adapt SV System
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Using the VPAP Adapt SV
WARNING
!
Before starting therapy with a new mask, select the correct mask type in the
Settings menu (page 21). When adding or removing a new component,
such as a mask, humidifier, or anti-bacterial filter, perform the Air Circuit
Learn function (page 21).
Starting Treatment
When the system is fully assembled press the power switch at the back of the
VPAP Adapt SV to ON. The Welcome screen will be displayed while the flow
generator is warming up. Allow the unit to warm up for approximately 30
seconds before placing the mask on your face.
WELCOME
Figure 11: Welcome screen
Once the VPAP Adapt SV has warmed up, breathing into the mask should start
therapy immediately. If not, press the Start/Stop key once to commence
treatment.
The VPAP Adapt SV restarts in the mode in which it stopped.
Stopping Treatment
If SmartStop is enabled, treatment will stop automatically when you remove your
mask. If the SmartStop function has been disabled, press the Start/Stop key.
Standby Mode
VPAP ADAPT SV
menu
Figure 12: Standby screen
Once you have stopped treatment, the VPAP Adapt SV will be in standby mode.
In standby you can:
•
•
press the power switch at the back to OFF to turn off the flow generator
commence treatment again by breathing into the mask or pressing the
Start/Stop key
•
enter any of the menus by pressing the Left key.
When in standby mode, a gentle (non-therapeutic) flow of air will still be present.
Note: If the SMART DATA - AUTO APPEAR option is set to ON the screens
available under the Results menu will be displayed automatically for
approximately 20 minutes after your session is completed.
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Control Panel Functions
The control panel of the VPAP Adapt SV has a keypad that allows you to:
•
•
•
•
start or stop treatment
adjust settings on the flow generator
mute or stop alarms
view treatment data.
LCD display
QuickView key
Alarm LEDs
Alarm mute key
Start/Stop Left
key key
Up/Down Right
key key
Figure 13: The VPAP Adapt SV control panel
LCD screen
Displays information about flow generator settings, alarms and treatment. The
LCD screen is backlit whenever any key is pressed. The lighting will turn off
automatically when no button has been pressed for two minutes, or can be set
to stay on (see “Options Menu” on page 23).
An alarm message will overwrite any other message on the screen. The original
screen will reappear when any key is pressed.
Start/Stop key
•
Press the key once to start or stop treatment.
Up/Down key
•
•
Moves backwards and forwards within a menu and between menus.
Increases and decreases values of parameters—press once to adjust in
single increments; hold down to move quickly through the values.
Using the VPAP Adapt SV
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Left key (green)
•
•
•
Enters a menu.
Confirms and applies settings.
Performs the function indicated by the text above it in the LCD (eg, ’enter’,
’change’).
Right key (red)
•
•
•
Performs the function indicated by the text above it in the LCD (eg, ’exit’).
Cancels operations.
Extended hold: exits to the top level of the menu.
QuickView key
Takes you immediately to the Treatment screens, with information on your
current therapy. See “Treatment Screens” on page 24.
Alarm LEDs and Alarm mute
The Alarm LEDs are lights that indicate that an alarm has been triggered. Alarms
can be muted by pressing the Alarm mute key once. The Alarm LEDs will
remain lit for as long as the alarm is being triggered. See “Alarms” on page 25.
Adjusting Settings
By using the Left, Right and Up/Down keys you can adjust some aspects of
your treatment. The settings can be seen in the LCD display.
To change a setting, press the Up/Down key until you arrive at the menu you
require.
•
•
•
•
Press the Left key to enter the menu, then use the Up/Down key again to
scroll through the options.
Once you find the option you require press the Left key to select the function
that is displayed in the bottom left of the screen eg, ’change’, ’yes’.
Use the Up/Down key to alter the parameters and press the Left key when
you have the setting you require.
Press the Right key to exit from the menu.
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Example
You wish to change the setting for the mask you are using.
VPAP Adapt SV
menu
Press ’down’ arrow on Up/Down key
to move to next menu
Press Left key to enter menu options
SETTINGS
enter
exit
ꢀ
(ASV MODE)
MASK: FULL FACE
1. Press Left key to select ’change’.
2. Press Up/Down key to reach setting.
3. Press Left key to enter setting.
4. Press Right key to exit.
change exit
ꢀ
LEARN CIRCUIT?
yes exit
ꢁ
SMARTSTOP: OFF
change exit
ꢁ
SOUND LEVEL: LOW
change exit
ꢂ
RESULTS
enter
exit
exit
exit
ꢁ
OPTIONS
enter
ꢁ
SERVICING
enter
ꢂ
Figure 14: Using the keys to adjust settings
Using the VPAP Adapt SV
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Menus
The options available in the Settings menu will depend on the therapy you are
receiving (either ASV or CPAP), as set by your clinician.
VPAP ADAPT SV
menu
SETTINGS
enter
exit
ꢀ
CPAP MODE
exit
ASV MODE
MASK: FULL FACE
change exit
RAMP: 20min
change
ꢀ
ꢀ
MASK: FULL FACE
change exit
LEARN CIRCUIT?
yes exit
ꢁ
ꢁ
LEARN CIRCUIT?
yes exit
SMARTSTOP: OFF
change exit
ꢁ
ꢁ
SMARTSTOP: OFF
change exit
SOUND LEVEL: LOW
change exit
ꢁ
ꢂ
SOUND LEVEL: LOW
change exit
ꢂ
RESULTS
enter
exit
ꢁ
- -
MASK FIT: ***
good
exit
ꢀ
These menus appear
only if at least one
Smart Data option
has been enabled by
the clinician.
AVG PRESS: 10.4
exit
ꢁ
USAGE: 4.56hrs
exit
ꢂ
SERVICING
enter
exit
ꢂ
SN: 1234567890123
4567 exit
ꢀ
PCB: 123456789012
exit
exit
ꢁ
SW: SX432-0201
ꢂ
Figure 15: Navigating the Patient menu.
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Settings Menu
You will only see the options relevant to your therapy. In CPAP (Continuous
Positive Airway Pressure) mode, the clinician sets a pressure that will be
constant throughout treatment. In ASV mode, the VPAP Adapt SV continually
measures your breathing and regulates the air pressure accordingly.
Mask
Select the type of mask that you will be using (you will only need to adjust this if
you have more than one mask). The following table shows the setting that
should be selected for each mask type. If your mask type is not mentioned
below, please contact your clinician. Not all mask types can be used with the
VPAP Adapt SV.
Option in Settings menu
Use setting with:
Vista
Vista™
Ultra
Ultra Mirage™
Full Face
Mirage™ Full Face Mask Series II
Ultra Mirage™ Full Face Mask
Mirage Quattro™ Full Face Mask
Activa
Activa™
Selecting mask options in the Settings menu
Learn Circuit
The Air Circuit Learn function takes approximately 20 seconds to run. It allows
the unit to ’learn’ what pressure it needs to build in to its calculations, based on
the components in the system. Select LEARN CIRCUIT every time you add or
remove a component (eg, mask, humidifier) or move to a significantly different
altitude.
To run this function:
1. Set up the entire VPAP Adapt SV system (flow generator, mask, humidifier
etc) as you wish to use it.
2. Make sure that the mask is unobstructed so air can flow from the mask to
the flow generator.
3. Turn on the VPAP Adapt SV at the power switch.
4. Move through the menus until you reach LEARN CIRCUIT and select ’yes’ by
pressing the Left key.
5. A message will remind you to check that the airflow from the mask is clear.
Select ’start’ with the Left key.
6. A progress screen is displayed while the Air Circuit Learn function is running.
LEARNING CIRCUIT
Using the VPAP Adapt SV
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7. When the function is complete, a screen will appear saying that the circuit
has been learned successfully. The next menu item is then displayed.
Commence treatment as described in “Starting Treatment” on page 16.
If there is a problem with the circuit a screen saying ’Invalid circuit’ will be
displayed instead of the progress screen. Check that all the connections
between the pieces of equipment are secure. You may need to return to the
previous chapter of this manual to check that you have set up the system
correctly.
SmartStop
Turn the SmartStop function on or off. When SmartStop is on, the
VPAP Adapt SV will automatically stop therapy when the mask is removed.
Note: The unit will automatically ’SmartStart’ whenever you start to breathe
into the mask.
Leak Alert
If your clinician has enabled Leak Alert, you will hear an alert tone sound when
you have a high leak from your mask. You can then adjust the mask on your face
to remove the leak. If Leak Alert is turned off, an extra leak alert message will be
displayed at the end of a session if high leak occurred. The message will be
displayed until a key is pressed.
Ramp (CPAP mode only)
Ramp time is the length of time taken for the air pressure to build up to the
maximum pressure set by your clinician. This setting allows you to increase or
decrease the ramp time in 5-minute intervals.
If you find that you are still awake when the air pressure starts to build you may
wish to increase the Ramp time.
Results Menu
This menu has a series of screens showing information about your most recent
treatment session. If enabled by your clinician the following data may be viewed:
•
•
•
Mask-fit
Average Pressure
Usage.
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Mask-fit
Gives a rating of how well the mask was fitting during your last session on the
VPAP Adapt SV. The stars indicate how good the fit was (more stars = better fit).
Star rating
Definition
*****
****-
***--
Excellent
Very good
Good
**---
Adjust mask
Adjust mask
Adjust mask
*----
HIGH LEAK
Average Pressure
Provides information on the average air pressure during your most recent
session on the VPAP Adapt SV.
Usage
Tells you how long the VPAP Adapt SV was in use during your most recent
session.
Options Menu
The Options menu allows you to change:
•
•
•
Smart Data (Auto Appear)
Backlight
Language.
Smart Data
If the SMART DATA - AUTO APPEAR option is set to ON, the screens available
under the Results menu will be displayed automatically for approximately 20
minutes after your session is completed. After this time the data will still be
available in the Results menu.
If you want to turn off AUTO APPEAR, select ’enter’ in the SMART DATA screen
by pressing the Left key. The AUTO APPEAR screen will be displayed. Select
’change’ by pressing the Left key and you will switch from ON to OFF (similarly,
you can turn it from OFF to ON). Your clinician may also turn off AUTO APPEAR.
Backlight
On: Display a permanent backlight for the LCD.
Auto: Backlight turns off if no button has been pressed for two minutes.
Language
Change the language of the LCD display. Languages available are: English,
French, Spanish and Portuguese.
Using the VPAP Adapt SV
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Servicing Menu
This menu displays the following information:
•
•
•
SN—the flow generator’s serial number
PCB—the flow generator’s PCB number (PCB—printed circuit board)
SW—the version of software currently installed on the flow generator.
Treatment Screens
There are three Treatment screens displayed in the VPAP Adapt SV LCD. The
LCD will display the Treatment screens when treatment commences, and during
treatment if no key is pressed for 20 minutes.
Press the QuickView key at any point within a menu to display
Treatment Screen 1. You can return to your original screen if you press
the QuickView key again within 20 minutes.
Press the Right key to move from a Treatment screen to the Standby screen.
If an alarm is triggered while you are in the Treatment screens, the arrow will
flash. Press the Down key until you reach the alarm message.
Scroll through the screens in the usual way, using the Up/Down key.
Treatment mode Pressure
ASV
5.0--15.0
exit
Figure 16: Treatment Screen 1
Leak
Respiratory rate
LK:18L/min
RR:12
VT: 428
Tidal volume
Figure 17: Treatment Screen 2
Minute ventilation
MV:6.2
Target ventilation
TARG:5.8
exit
Figure 18: Treatment Screen 3
Note: TARG is not a relevant parameter in CPAP mode.
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Alarms
The VPAP Adapt SV unit is fitted with alarms to alert you to changes that will
affect your treatment. The most common reason for an alarm to sound is
because the system has not been properly assembled. Check that the air tubing
and pressure sensor tube have been properly attached to the flow generator and
mask (and humidifier if used).
You can mute an alarm by pressing the Alarm Mute key once. Unless the alarm
requires you to turn the power off, you can press any key again to remove the
alarm message from the LCD screen and to access all menus. If the problem is
still present, the alarm will sound and display again after one minute. The Alarm
LED will remain lit for as long as the problem is present.
We recommend that you test the audible alarm once a week. To do this, hold
down the Mute key while the VPAP Adapt is starting up. If the alarm is
functioning correctly it will beep twice.
LCD message
Alarm type
Action
LOW PRESSURE!
Check circuit
Low mask pressure
alarm
Check tube connections.
LCD turns off
Power fail alarm
Turn off VPAP Adapt SV at power switch.
Turn off VPAP Adapt SV at power switch.
HIGH PRESSURE!
Turn power off
High pressure alarm
HIGH AVG PRESS!
High pressure alarm
High mask leak alert
Turn off VPAP Adapt SV at power switch.
Adjust the mask.
HIGH LEAK!
Check circuit
LOW PS!
Check circuit
Insufficient pressure
Support alarm
Check tubing.
Run LEARN CIRCUIT.
FLOW BLOCKED!
Turn power off
Flow blocked alarm
Turn off VPAP Adapt SV. Check air
circuit. Turn on VPAP Adapt SV.
Low Mask Pressure Alarm
Triggered by:
•
•
•
pressure sensor line is blocked or disconnected
air pressure at the mask has fallen below a set level
mask is removed and SmartStop has been disabled.
If a low pressure alarm sounds:
1. Check that the air tube and sensor tube are connected properly.
2. Turn the VPAP Adapt SV off and on again at the power switch. If the alarm
persists, return the unit to ResMed for servicing.
Alarms
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Will clear when:
•
the low pressure condition is fixed
•
treatment is stopped by pressing the Start/Stop key.
Power Fail Alarm
Triggered by:
•
power failure
•
machine is disconnected or switched off while delivering treatment.
If a power fail alarm sounds:
the flow generator stops delivering air pressure.
Will stop:
•
•
•
•
when the Alarm Mute key is pressed, or
after two minutes, or
when power is restored.
CAUTION
!
Remove the mask from your face if the power fails.
High Pressure / High Average Pressure Alarms
Triggered by:
•
High Pressure Alarm: the mask pressure exceeds the set trigger level (30
cm H O) for more than 700 milliseconds.
2
•
High Average Pressure Alarm: the mask pressure exceeds the set trigger
level (22 cm H O), averaged over approximately one minute.
2
If a high pressure alarm sounds:
1. The treatment will stop.
2. Turn power off.
3. Check that the air tube and sensor tube are connected properly.
4. Turn power back on.
5. Remove mask and perform Air Circuit Learn function.
6. Try using the flow generator one more time.
7. If the high pressure alarm activates repeatedly, discontinue use and return to
ResMed for servicing. If the alarm does not recur, then continue to use as
normal.
Note: The alarm system is designed to ignore coughing. However, if a cough is
especially intense and prolonged, it may trigger the high pressure alarm.
Will stop when:
•
the VPAP Adapt SV is turned off.
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High Leak Alert
Triggered by:
•
high mask leak (greater than 30 L/min) for more than 20 seconds
•
the mask being removed while SmartStop is disabled.
If a high leak alert sounds:
•
adjust the mask to minimize leak
•
check that the air tube and sensor tube are connected properly.
Will stop when:
the mask leak has been rectified.
•
Note: The High Leak alert can be turned off in the Leak Alert option in the
Settings menu.
Insufficient Pressure Support Alarm
Triggered by:
•
air pressure at the mask has failed to reach an expected level for 3 breaths
the Air Circuit Learn function (page 21) has not been run after adding a new
component (eg, new mask, humidifier) to the system.
•
If an insufficient pressure support alarm sounds:
•
•
•
check that the pressure sensor tubing is not kinked
check that the pressure sensor tubing is properly connected
run LEARN CIRCUIT.
Will stop when:
•
the pressure sensor tubing is unobstructed and properly connected to the
flow generator and mask
•
•
treatment is stopped (Start/Stop key or SmartStop)
the VPAP Adapt SV is turned off.
Flow Blocked Alarm
Triggered by:
•
blockage in air circuit.
If a flow blocked alarm sounds:
1. The treatment will stop.
2. Turn power off.
3. Check whether there is a blockage in the air circuit.
4. Remove blockage.
5. Turn power back on.
6. If the flow blocked alarm activates repeatedly, discontinue use and return to
ResMed for servicing. If the alarm does not recur, then continue to use as
normal.
Alarms
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Will stop when:
blockage is removed.
•
Cleaning and Maintenance
You should regularly carry out the cleaning and maintenance described in this
manual.
CAUTION
!
Do not wash the pressure sensor tube. If fluid enters the pressure sensor
tube allow it to dry completely by hanging it in a clean place out of direct
sunlight. If the pressure sensor tube cannot be dried completely it should be
replaced.
Daily
1. Disconnect the air tubing and pressure sensor tube and hang them in a clean,
dry place until next use. Do not hang the air tubing in direct sunlight as it may
harden and crack over time.
2. Clean the mask according to the mask user instructions.
3. If you are using a humidifier, clean it according to the instructions in the
manual.
Weekly
1. Remove the air tubing and pressure sensor tube from the VPAP Adapt unit
and the mask.
2. Remove the pressure sensor tube and proximal cuff from the air tubing.
3. Wash the mask system according to the instructions supplied with it.
4. Wash the air tubing and proximal cuff in warm water using mild liquid soap.
Rinse thoroughly, hang, and allow to dry.
5. Before next use, assemble the mask and headgear according to the mask
user instructions.
6. Reconnect the pressure sensor tube to the air tubing, then connect both to
the proximal cuff. Attach the proximal cuff to the mask.
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Air tubing
Remove proximal cuff
Remove the pressure sensor tube
from air tubing
Tubing clips
Figure 19: Air tubing assembly removed for cleaning
CAUTION
•
!
Do not use bleach, chlorine-, alcohol-, or aromatic-based solutions
(including all scented oils), moisturising or antibacterial soaps to clean
the cushion, mask, air tubing, or the VPAP Adapt SV. These solutions
may cause hardening and reduce the life of the product.
º
º
•
•
Do not wash or dry the mask frame at a temperature above 176 F (80 C).
Exposure to higher temperatures may reduce the life of the product.
Do not hang the air tubing and pressure sensor tube in direct sunlight as
the tubing may harden over time and eventually crack.
Periodically
1. The mask and air tubing are subject to normal wear and tear. Inspect them
regularly for damage.
2. Remove the power cord. Clean the exterior of the flow generator with a
damp cloth and mild liquid soap.
3. Inspect the air filter to check if it is blocked by dirt or contains holes. See full
instructions below.
WARNING
!
!
Beware of electric shock. Do not immerse the flow generator or power cord
in water. Always unplug the flow generator before cleaning and be sure that
it is dry before reconnecting.
CAUTION
Do not attempt to open the VPAP Adapt SV. There are no user serviceable
parts inside. Repairs and internal servicing should only be performed by an
authorized service agent.
Cleaning and Maintenance
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Air Filter
Inspect the air filter every month and check if it is blocked by dirt or contains
holes.
Air filter cover
The filter should be replaced every six months, or more often if the flow
generator is operating in a dusty environment.
WARNING
!
Do not wash the air filter once it has become soiled. The air filter is not
washable or reusable.
Fitting the filter
•
•
•
Remove the filter cover at the back of the flow generator.
Remove and discard the old air filter.
Insert a new filter, the blue tinted side facing towards you.
Note: Match the cut corner of the filter with the shape of the casing.
•
Replace the air filter cover. The blue tinted side of the filter should be facing
out.
Hypoallergenic Air Filter
The ResMed hypo-allergenic filter is a standard filter to which an electrostatic
filter has been bonded to capture very small particles. The filter is intended for
those users of ResMed flow generators who will benefit from enhanced filtering
of the air delivered during treatment.
Inspect the air filter every month and check if it is blocked by dirt or contains
holes.
The filter should be replaced every three months, or more often if the flow
generator is operating in a dusty environment.
Fit as described above in “Air Filter”.
Servicing
This product (VPAP Adapt SV) should be inspected by an authorised ResMed
Service Centre five years from the date of manufacture. Prior to this, the device
is intended to provide safe and reliable operation provided that it is operated and
maintained in accordance with the instructions provided by ResMed.
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Applicable ResMed warranty details are provided with the device at the time of
original supply. Of course, as with all electrical devices, if any irregularity
becomes apparent, you should exercise caution and have the device inspected
by an authorized ResMed service center.
If you feel the unit is not performing properly, see “Troubleshooting” on page 31.
Servicing (Australia and New Zealand)
This device is intended to provide safe and reliable operation when operated and
maintained in accordance with the instructions provided by ResMed. To ensure
that your device continues to provide optimum performance it is recommended
that this product (VPAP Adapt SV) be inspected by an authorised ResMed
Service Centre five years from the date of purchase.
CAUTION
!
Inspection and repair should only be performed by an authorized service
agent. Under no circumstances should you attempt to service or repair the
unit yourself.
Troubleshooting
If there is a problem, try the following suggestions. If the problem cannot be
solved, contact your equipment supplier or ResMed. Do not attempt to open the
flow generator.
Problem
Possible cause
Solution
Insufficient air delivered
from flow generator
Air filter is dirty.
Replace air filter.
Air tubing is kinked or
punctured.
Straighten or replace tubing.
Flow generator operating
erratically, ie, switching on
and off, pressure varying at
random
Water may have entered the
air tubing.
Remove the water from the
air tubing.
Pressure rises
inappropriately
You are talking, coughing,
voluntarily breath-holding
(eg, while rolling over in bed),
or intentionally breathing in
an unusual manner.
Avoid talking with the mask
on, and breathe as normally
as possible.
Severe mask leak or mouth
leak (greater than 30 L/min).
Correct your leak condition.
Alarm stays on continuously
Blockage in air circuit.
Ensure there is no barrier to
the passage of air.
Internal malfunction.
Return the device to your
equipment supplier for
service.
Troubleshooting
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Problem
Possible cause
Solution
No LCD display
Power not connected or
switch at back is not on.
Ensure the power cable is
connected, and that the
switch at the back of the unit
is in the ’on’ position.
FAULT message displayed
on LCD
Internal malfunction.
Return the device to your
equipment supplier for
service.
System Error 7 message
Device power-on has been
interrupted by breathing into
the mask during warm up.
Turn the flow generator off
and on again. Do not place
mask on face during warm
up (30 seconds). Select
LEARN CIRCUIT (page 21).
If the error is not cleared,
contact your equipment
supplier for service.
Internal malfunction.
Return the device to your
equipment supplier for
service.
Glossary
Alarms
When more than one alarm is activated at the one time, the highest priority
alarm will be displayed.
Backlight
The backlight turns off if no button has been pressed for two minutes. It can
also be kept permanently on by selecting On in the Backlight screen of the
Options menu.
bpm
breaths per minute
L/min
liters per minute
Mean
The average value of the monitored parameter.
Minute ventilation
A measure of the respiratory rate x tidal volume.
Proximal cuff
A connector between the air tubing and the mask. The pressure sensor tub-
ing attaches to the proximal cuff so that pressure at the mask can be
detected and monitored.
SmartStart
A feature that starts the VPAP Adapt SV automatically when you breathe into
the mask.
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SmartStop
A feature that stops the VPAP Adapt SV automatically when you remove the
mask. You can turn SmartStop on or off in the Settings menu.
Tidal volume
The volume of air, in liters, breathed in or out in one breath.
Technical Specifications
Dimensions (H x W x D)
5.6" x 9.8" x 11.5" (142 mm x 248 mm x 293 mm)
Weight
Flow generator with cover: 8.14 lbs (3.7 kg)
Flow generator with HumidAire 2i (empty): 9.24 lbs (4.2 kg)
Environmental conditions
Operating temperature: 41 F to 95 F (+5 C to +35 C)
Storage and transport temperature: -4 F to +140 F (-20 C to +60 C)
º
º
º
º
º
º
º
º
Humidity—operating, storage and transportation: 10%–95% non-condensing
Housing construction
Injection moulded plastic
Air tubing
1 x 6’6” (2 m)
Air filter
Synthetic fiber
Patient connection port
22 mm taper, compatible with ISO 5356-1:2004 Anaesthetic & Respiratory
Equipment—Conical Connectors
Power supply
AC Input range: 110–120V and 220–240V; 50–60Hz; 60VA
DC Input range (if using DC Converter: 12–13.8V DC
Performance
Operating pressure range: 4–25 cm H O
2
Sound pressure level
<30 dBA (tested in accordance with the requirements of ISO 17510-1)
Battery type
Lithium
Technical Specifications
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Alarm specifications
•
High maximum mask pressure alarm
Stops air delivery at 30 cm H O >700 msec.
2
•
High mean mask pressure alarm
Stops air delivery when mean mask pressure exceeds 22 cm H O (averaged
2
over approx 1 minute).
•
•
Low mask pressure alarm
Mask pressure is less than 3 cm H O for longer than 5 seconds while the
patient is using the VPAP Adapt SV.
Insufficient pressure support alarm
2
Is triggered if for 3 breaths in a row the maximum mask pressure achieved at
inspiratory to expiratory transition is either <87.5% of the absolute mask
pressure targeted at that point, or < absolute mask pressure targeted minus
1 cm H O, whichever is the lower.
2
•
•
High leak alarm
Leak exceeds 30 L/min for more than 20 seconds.
Flow blocked alarm
Flow is less than 6 L/min for more than 20 seconds.
IEC 601-1 classifications
Class II, Type CF
Class II medical electrical equipment provides protection against electric shock
either by double insulation or reinforced insulation and does not require a
protective earth.
Inspiratory Trigger Characteristics
The inspiratory trigger occurs at a flow greater than 0 LPM when tested with
EPAP=5 cm H O, IPAP=15 cm H O, sinisoidal breath shape. The inspiratory
2
2
trigger response time is <600 ms when tested with EPAP=5 cm H O,
2
IPAP=15 cm H O, 0.67 L/sec inspiratory and expiratory flow rate. The time is
2
measured from the beginning of inspiratory flow to the beginning of pressure
rise to IPAP.
Note: The ASV algorithm is designed to treat a patient with essentially normal
lungs. Hence, trigger response is less sensitive and pressure ramp-up is more
gentle than typical non-invasive ventilators.
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Displayed values
Value
Display
Resolution
Range
Accuracy
Proximal cuff
Pressure
-3 to 40 cm H2O
0.5 cm H2O
0.1 cm H2O
Mass flow sensor
Leak
0–99 liters per minute
8–30 breaths per minute
0–4500 milliliters
+/- 12 L/min
+/- 10%
1 liter per breath
1 breath per minute
1 milliliter
Respiratory rate
Tidal volume
Minute ventilation
Target MV
+/- 10%
0–40 liters per minute
0–40 liters per minute
+/- 10%
0.1 liters per minute
0.1 liters per minute
+/- 10%
Maximum low impedance flow at stated pressures
Pressure (cm H O)
Flow (L/min)
2
4.2
217
218
219
8.6
13.0
Glossary of symbols
Read the relevant operating manual before using
Type CF equipment
AC switch
Class II
Drip proof
IPX1
Technical Specifications
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Guidance and Manufacturer’s Declaration — Electromagnetic
Emissions and Immunity
Guidance and manufacturer’s declaration – electromagnetic emissions
The VPAP Adapt SV is intended for use in the electromagnetic environment specified below. The
customer or the user of the VPAP Adapt SV should assure that it is used in such an environment.
Electromagnetic environment -
guidance
Emissions test
Compliance
RF emissions CISPR 11
Group 1
The VPAP Adapt SV uses RF energy
only for its internal function.
Therefore, its RF emissions are very
low and are not likely to cause any
interference in nearby electronic
equipment.
RF emissions CISPR 11
Class B
Class A
The VPAP Adapt SV is suitable for use
in all establishments, including
domestic establishments and those
directly connected to the public low-
voltage network that supplies
Harmonic Emissions
IEC 61000-3-2
Voltage Fluctuations/Flicker
Emissions IEC 61000-3-3
Complies
buildings used for domestic purposes.
Medical Electrical Equipment needs special precautions regarding EMC and needs to be installed
and put into service according to EMC information provided in this document.
Warnings: The VPAP Adapt SV should not be used adjacent to or stacked with other equipment.
If adjacent or stacked use is necessary, the VPAP Adapt SV should be observed to verify normal
operation in the configuration in which it will be used.
The use of accessories (eg Humidifiers) other than those specified in this manual is not
recommended. They may result in increased emissions or immunity of the VPAP Adapt SV.
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Guidance and manufacturer’s declaration – electromagnetic immunity
The VPAP Adapt SV is intended for use in the electromagnetic environment specified below. The
customer or the user of the VPAP Adapt SV should assure that it is used in such an environment.
Electromagnetic
environment –
guidance
IEC60601-1-2
test level
Compliance
level
Immunity test
Electrostatic
discharge (ESD)
IEC 61000-4-2
6 kV contact
8 kV air
6 kV contact
8 kV air
Floors should be wood,
concrete or ceramic tile. If
floors are covered with
synthetic material, the
relative humidity should be
at least 30%.
Electrical fast
transient/burst
IEC 61000-4-4
2 kV for power
supply lines
2 kV
Mains power quality should
be that of a typical
commercial or hospital
environment.
1 kV for input/
output lines
Not Applicable
Surge
IEC 61000-4-5
1 kV differential
mode
1 kV differential
mode
Mains power quality should
be that of a typical
commercial or hospital
environment.
2 kV common
mode
2 kV common
mode
Voltage dips, short
interruptions and
voltage variations on
power supply input
lines.
<5% Ut
(>95% dip in Ut)
for 0.5 cycle
< 12V
(>95% dip in 240V)
for 0.5 cycle
Mains power quality should
be that of a typical
commercial or hospital
environment.
40% Ut
(60% dip in Ut)
for 5 cycles
96V
If the user of the
IEC 61000-4-11
(60% dip in 240V)
for 5 cycles
VPAP Adapt SV requires
continued operation during
power mains interruptions,
it is recommended that the
VPAP Adapt SV be powered
from an uninterruptible
power source.
70% Ut
(30% dip in Ut)
for 25 cycles
168V
(30% dip in 240V)
for 25 cycles
<5% Ut
<12V
(>95%dip in Ut)
for 5 sec
(>95%dip in 240V)
for 5 sec
Power frequency
(50/60 Hz)
magnetic field
IEC 61000-4-8
3 A/m
3 A/m
Power frequency magnetic
fields should be at levels
characteristic of a typical
location in a typical
commercial or hospital
environment
NOTE: Ut is the AC mains voltage prior to application of the test level.
(Continued next page)
Technical Specifications
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Guidance and manufacturer’s declaration – electromagnetic immunity (continued)
The VPAP Adapt SV is intended for use in the electromagnetic environment specified below. The customer
or the user of the VPAP Adapt SV should assure that it is used in such an environment.
Immunity
test
IEC60601-1-2
test level
Complianc
e level
Electromagnetic environment –
guidance
Portable and mobile RF communications
equipment should be used no closer to any
part of the VPAP Adapt SV, including cables,
than the recommended separation distance
calculated from the equation applicable to the
frequency of the transmitter.
Recommended separation distance
Conducted RF
IEC 61000-4-6
3 Vrms
150 kHz to 80 MHz
3 Vrms
10 V/m
d = 1.17 √P
Radiated RF
IEC 61000-4-3
10 V/m
80 MHz to 2.5 GHz
d = 0.35 √P 80 MHz to 800 MHz
d = 0.70 √P 800 MHz to 2.5 GHz
where P is the maximum output power rating
of the transmitter in watts (W) according to the
transmitter manufacturer and d is the
recommended separation distance in meters
(m).
Field strengths from fixed RF transmitters, as
determined by an electromagnetic site
a
survey, should be less than the compliance
b
level in each frequency range.
Interference may occur in the vicinity of
equipment marked with the following symbol:
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.
a
Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and
land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted
theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an
electromagnetic site survey should be considered. If the measured field strength in the location in which
the VPAP Adapt SV is used exceeds the applicable RF compliance level above, the VPAP Adapt SV should
be observed to verify normal operation. If abnormal performance is observed, additional measures may be
necessary, such as reorienting or relocating the VPAP Adapt SV.
b
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 10 V/m.
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Recommended separation distances between portable and mobile RF communications
equipment and the VPAP Adapt SV
The VPAP Adapt SV is intended for use in an environment in which radiated RF disturbances are controlled.
The customer or the user of the VPAP Adapt SV can help prevent electromagnetic interference by
maintaining a minimum distance between portable and mobile RF communications equipment
(transmitters) and the VPAP Adapt SV as recommended below, according to the maximum output power of
the communications equipment.
Separation distance according to frequency of transmitter
m
Rated maximum output
power of transmitter
W
150 kHz to 80 MHz
80 MHz to 800 MHz
800 MHz to 2.5 GHz
d = 1.17 √P
d = 0.35 √P
d = 0.7 √P
0.01
0.1
1
0.17
0.37
1.17
0.04
0.11
0.35
1.11
0.07
0.22
0.70
2.21
7.00
10
3.69
11.70
100
3.50
For transmitters rated at a maximum output power not listed above, the recommended separation distance
d in metres (m) can be determined using the equation applicable to the frequency of the transmitter, where
P is the maximum output power rating of the transmitter in watts (W) according to the transmitter
manufacturer.
NOTE 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.
Technical Specifications
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Limited Warranty
ResMed warrants that your ResMed product shall be free from defects in
material and workmanship for the period specified below from the date of
purchase by the initial consumer. This warranty is not transferable.
Product
Warranty Period
ResMed humidifiers, ResControl™, ResLink™, ResTraxx™
ResMed flow generators
1 Year
2 Years
90 Days
Accessories, mask systems (including mask frame, cushion,
headgear and tubing). Excludes single-use devices.
Note: Some models are not available in all regions.
If the product fails under conditions of normal use, ResMed will repair or replace,
at its option, the defective product or any of its components. This Limited
Warranty does not cover:
a) any damage caused as a result of improper use, abuse, modification or
alteration of the product;
b) repairs carried out by any service organization that has not been expressly
authorized by ResMed to perform such repairs;
c) any damage or contamination due to cigarette, pipe, cigar or other smoke;
d) any damage caused by water being spilled on or into a flow generator.
Warranty is void on product sold, or resold, outside the region of original
purchase. Warranty claims on defective product must be made by the initial
consumer at the point of purchase.
This warranty is in lieu of all other express or implied warranties, including any
implied warranty of merchantability or fitness for a particular purpose. Some
regions or states do not allow limitations on how long an implied warranty lasts,
so the above limitation may not apply to you.
ResMed shall not be responsible for any incidental or consequential damages
claimed to have occurred as a result of the sale, installation or use of any ResMed
product. Some regions or states do not allow the exclusion or limitation of
incidental or consequential damages, so the above limitation may not apply to
you. This warranty gives you specific legal rights, and you may also have other
rights which vary from region to region.
For further information on your warranty rights, contact your local ResMed dealer
or ResMed office.
40
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Index
right 18
A
start/stop 17
up/down 17
air circuit learn function 21
air filter 30
hypoallergenic 30
air pressure
monitoring 23
air tubing
L
language
change setting 23
LCD display 31
leak alert 22
attaching to mask 9
cleaning 28
learn circuit 21
Luer connector 9
connecting 9
air tubing system 6, 7, 9
alarm
M
mask
flow blocked 27
high leak 27
connection 9
indication of fit 23
recommended 7
select from menu 21
medical information 3
menus
high pressure 26
low mask pressure 25
power fail 26
alarm LED 18
anti-bacterial filter 14
how to use 19
navigation 20
B
backlight
change setting 23
O
Options menu 23
oxygen
C
cautions 4
supplemental 15
contraindications 3
CPAP mode 21
P
power cord
D
connection 8
pressure sensor tube
connecting 9
proximal cuff 7
DC converter 15
F
fault message 31
Q
H
quick setup guide 5
HumidAire
connection 12
HumidAire 2i 11
humidifier
connecting 10
types 10
R
Ramp 21, 22
ResLink 14
Results menu 22
S
K
Settings menu 20
Smart data 23
SmartStop 22
key
alarm mute 18, 25
left 18
Index
41
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standby mode 16
starting treatment 16
stopping treatment 16
Supplemental oxygen 15
System Error 7 message 32
T
Treatment screens 24
U
user/owner responsibility 3
V
VPAP Adapt SV
usage 23
VPAP Adapt SV Components 6
42
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