Bpap-A 40
Bpap-A 40
Bpap-A 40
Support System
BY
AHMAD YOUNES
Warnings
Warnings
• Prior to placing a patient on the ventilator, a clinical
assessment should be performed to determine:
••The device alarm settings
••Needed alternative ventilation equipment
••If an alternative monitor (i.e., an alarming Pulse Oximeter or
Respiratory Monitor) should be used
• BiPAP A40 is a restricted medical device designed for use
by Respiratory Therapists or other trained and qualified
caregivers under the supervision of a physician
• The prescription and other device settings should only be
changed on the order of the supervising physician.
Warnings
• The ventilator has a two-stage low battery alarm. The
medium priority alarm indicates that approximately 20
minutes of operation remain, and the high priority alarm
indicates that less than 10 minutes of operation remain.
• Immediately seek an alternate power source when the
“Low Battery” alarm appears. Complete power failure
and loss of power is imminent.
• Do not use this device if the room temperature is
warmer than 35˚ C because the temperature of the
airflow may exceed 43˚ C. This could cause thermal
irritation or injury to the patient’s airway.
• Do not use the device while positioned in a warm place,
such as direct sunlight.
Warnings
• Always verify that the audible tone sounds and the
alarm LEDs light red then yellow momentarily.
• Philips Respironics recommends that a main line outlet
bacteria filter be used whenever the device is used on
multiple patients.
• The AVAPS-AE mode is for non-invasive use on adult
patients only.
• The ventilator should only be used with patient
interfaces (e.g., masks, circuits and exhalation ports)
recommended by Philips Respironics.
• Do not block the exhalation port. This can reduce
airflow and result in rebreathing of exhaled air.
Warnings
• At low expiratory pressures, the flow through the
exhalation port may be inadequate to clear all exhaled
gas from the tubing – some rebreathing may occur.
• When using a patient circuit with a full face mask, the
mask must be equipped with a safety (entrainment)
valve. Make sure that the safety (entrainment) valve is
functioning properly with the ventilator.
• If you notice any unexplained changes in the
performance of the device, if it is making unusual
sounds, if the device or detachable battery are dropped,
if water is spilled into the enclosure, or if the enclosure
is cracked or broken, discontinue use and contact
Philips Respironics or an authorized service center for
service.
Warnings
• Route the power cord to the outlet in a way that will
prevent the cord from being tripped over or interfered
with by chairs or other furniture.
• Use of power cords and cables not supplied by Philips
Respironics may cause overheating or damage to the
device.
• The inspired oxygen concentration will vary, depending
on the pressures, patient flows and circuit leak.
• When using oxygen with this system, a Philips
Respironics Pressure Valve must be placed at the
device outlet. Failure to use the pressure valve could
result in a fire hazard.
• Appropriate patient monitoring should be used, as
medically indicated, such as an alarming pulse
oximeter.
Warnings
• Oxygen supports combustion. Oxygen should not be
used while smoking or in the presence of an open flame.
• When using oxygen with this system, turn the device on
before turning on the oxygen. Turn the oxygen off
before turning the device off. This will prevent oxygen
accumulation in the device.
• Explanation of the Warning: When the device is not in
operation and the oxygen flow is left on, oxygen
delivered into the tubing may accumulate within the
device’s enclosure. Oxygen accumulated in the device
enclosure will create a risk of fire.
• Portable and Mobile RF Communications Equipment can
affect Medical Electrical Equipment.
Warnings
• To avoid electrical shock, always unplug the power cord
from the wall outlet before cleaning the device.
• Never operate the device if any parts are damaged or if it
is not working properly.
• Repairs and adjustments must be performed by Philips
Respironics-authorized service personnel only.
• A properly installed, undamaged gray foam filter is
required for proper operation. Wash periodically and
replace when damaged for proper operation.
• Do not use extension cords with this device.
• Do not place the device in or on any container that can
collect or hold water.
• Do not place the device directly onto carpet, fabric, or
other flammable materials.
Warnings
• The heated humidifier can only be used when the ventilator
is connected to AC power. It cannot be used with a battery.
• Do not use the same external battery to operate both the
ventilator and any other equipment such as power chairs.
• An external battery should only be connected to the
ventilator using the Philips Respironics External Battery
Cable. This cable is fused, pre-wired, and properly
terminated to ensure safe connection to a standard deep
cycle lead acid battery. Use of any other adapter or cable
may cause improper operation of the ventilator
• Do not immerse the device or allow any liquid to enter the
enclosure or the inlet filter.
• Do not use harsh detergents, abrasive cleaners, or brushes
to clean the ventilator system.
Contraindications
• The BiPAP A40 ventilator is not a life support device.
• The device is contraindicated for both invasive use and
pediatric use when in AVAPS-AE mode.
• If the patient has any of the following conditions, avoid
using the device in a non-invasive mode:
1- Inability to adequately clear secretions
2-At risk for aspiration of gastric contents
4-Diagnosed with acute sinusitis or otitis media
5- Epistaxis, causing pulmonary aspiration of blood
6-Hypotension
Patient Precautions
• If skin irritation or breakdown develops from the
use of the mask, refer to the mask instructions
for appropriate action.
• The following are potential side effects of non-
invasive positive pressure therapy:
––Ear discomfort
––Conjunctivitis
––Skin abrasions due to non-invasive interfaces
––Gastric distention (aerophagia)
System Overview
Finger tip pulse oximeter with adapter
Detachable Battery ,Detachable
Battery Module and roll stand
Carrying Case. The bag is designed
to attach the ventilator to a wheelchair
Control Buttons
The figure below shows the display screen and
primary control buttons on the device.
Full and Limited Menu Access Modes
• The ventilator has two levels of menu access :
1- Full Menu Access allows you to alter all
available settings.
2- Limited Menu access permits the user to alter
only those prescription settings that affect
patient comfort, such as Rise Time or Flex, if
they are available as part of the prescription.
Turning the Lock settings off in Full Menu
Access mode allows users to modify them.
Use the following key sequence to enter Full Menu
Access mode:
1. From the Standby or Monitor screen, press the Down
button and the Alarm Indicator/Audio Pause button
simultaneously for several seconds. This temporarily
places the device in Full Menu Access mode.
2. If you perform this key sequence from the Monitor
screen, the Main Menu appears. If you perform it from
the Standby screen, the Setup screen appears.
3. An audible indicator sounds indicating you are now in
Full Menu Access mode.
4. You can access the Options menu and permanently
change the Menu Access setting to Full. Otherwise, the
device will return to Limited mode once you exit the
menu screens or if one minute passes without pressing
any device buttons.
AVAPS
• Average Volume Assured Pressure Support (AVAPS) is
a feature available in the S, S/T, PC, and T modes. (In
AVAPS-AE mode, the AVAPS feature is always enabled.)
• AVAPS helps patients maintain a tidal volume (VT) equal
to or greater than the target tidal volume (Tidal Volume
setting) by automatically controlling the pressure
support (PS) provided to the patient.
• The AVAPS feature adjusts PS by varying the IPAP level
between the IPAP Min and IPAP Max settings (or
Pressure Support Min and Pressure Support Max in
AVAPS-AE mode).
• AVAPS will retain the learned PS for the patient so that
each time therapy is started the PS will start at the
learned PS.
AVAPS
• The muscle effort of a spontaneous breath
typically results in a larger tidal volume than a
machine breath delivered at the same pressure.
• The new AVAPS algorithm will adjust the
pressure slightly on machine delivered breaths
to compensate for this difference, and
throughout the night, the algorithm will “learn”
the correct amount of pressure adjustment to
apply to machine triggered breaths.
• If IPAP Max is reached and the target tidal
volume is not achieved, the Low Tidal Volume
alarm activates (if enabled).
AVAPS Rate
• The AVAPS Rate setting allows you to adjust the
maximum rate at which the pressure support
automatically changes to achieve the target tidal
volume.
• The actual rate may be less than this maximum setting
depending on how far the current estimated tidal volume
is from the target tidal volume.
• A higher rate allows the AVAPS algorithm to change
pressure support faster to meet the target tidal volume.
• It can be set from 0.5 cmH2O per minute to 5.0 cmH2O
per minute in increments of 0.5 cmH2O per minute.
Bi-Flex Comfort Feature
• If enabled, the device provides a comfort feature
called Bi-Flex in S mode only.
• The Bi-Flex attribute adjusts therapy by
inserting a small amount of pressure relief
during the latter stages of inspiration and
during active exhalation (the beginning part of
exhalation).
• Bi-Flex levels of 1, 2, or 3 progressively reflect
increased pressure relief that will take place at
the end of inspiration and the beginning part of
exhalation
Bi-Flex Comfort Feature
Ramp
• The ramp feature is designed to offer lower pressures when
activated and then gradually increase to allow the patient to
fall asleep.
• If ramp is activated with AVAPS enabled or in AVAPS-AE
mode, it will reduce the maximum pressure support
capability to IPAP Min or Pressure Support Min and ramp to
the IPAP Max or Pressure Support Max.
• In AVAPS-AE mode, the EPAP will reduce to the EPAP Min
setting but is not ramped, and Auto-EPAP adjusts the
pressure according to the patient’s needs. During the ramp
period, the IPAP or pressure support applied will be
adjusted by the AVAPS algorithm but will be constrained by
the current maximum ramp pressure set point. The
pressures (with exception of EPAP in AVAPS-AE mode) will
then ramp up to the original prescribed settings over the
ramp time period.
Ramp
Rise Time
• If enabled, the device provides a feature called Rise
Time in S, S/T, T, PC, and AVAPS-AE modes.
• Rise time is the amount of time it takes the device to
change from the expiratory pressure setting to the
inspiratory pressure setting.
• Rise time levels of 1, 2, 3, 4, 5, or 6 progressively reflect
slowed response of the pressure increase that will take
place at the beginning of inspiration.
• A setting of 1 is the fastest rise time while a setting of 6
is the slowest.
• Adjust the rise time to find the most comfortable setting
for the patient.
• Rise time cannot be adjusted when Bi-Flex is enabled.
Rise Time
Digital Auto-Trak
• An important characteristic of the device is its ability to
recognize and compensate for unintentional leaks in the
system and to automatically adjust its trigger and cycle
algorithms to maintain optimum performance in the
presence of leaks. This feature is known as Digital Auto-
Trak.
• The device continuously monitors flow and adjusts the
estimate of patient flow as circuit leak changes. The
compensation provides a better estimate of patient flow to
be used to track patient breathing patterns and calculate
flow-based parameters, such as exhaled tidal volume.
Digital Auto-Trak
• The device continually tracks breathing patterns
and automatically adjusts sensitivity thresholds
to ensure optimum patient and machine
synchrony as breathing patterns change or as
circuit leak varies.
• Sensitive Auto-Trak is an enhancement to the
Auto-Trak algorithm that improves patient and
machine synchrony for patients with minimal
respiratory effort. Sensitive Auto-Trak refines
the baseline trigger and cycle sensitivity
thresholds.
Event Detection in Modes with a Back-up Rate
- Patient Pressure
- Exhaled Tidal Volume
- Leak
- Minute Ventilation
- Respiratory Rate - I:E Ratio
-When an oximeter is connected, the current SpO2 and
Heart Rate readings will only display on the Patient
Accessory panel if Detailed View is turned on.
-When Detailed View is turned off, only a heart icon
displays to indicate that the oximeter is connected and
show the data status. The data values will not display.
Changing Settings in Provider Menu Access Mode
1. Press the Up key to enter the Menu screens from the
Standby or Monitor screens. The Main Menu screen
appears.
2. Choose from the following selections on the Main Menu
screen:
- Safely Remove SD Card: This option will appear if an SD
card is inserted in the ventilator. Select this option when
you want to remove the SD card. When the “Remove SD
Card” confirmation message appears, remove the card.
If you press the left (cancel) button or don’t remove the
card within 30 seconds, the confirmation message will
close and the ventilator will continue writing to the card.
- Settings and Alarms: View and change prescription
settings and alarms.
Changing Settings in Provider Menu Access Mode