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User Manual

CauTion: 

U. S. federal law restricts this device to sale by or on the order of a physician.

intended use

The BiPAP autoSV Advanced System One is intended to provide non-invasive ventilatory support to treat adult patients (>30 kg/66 lbs) 
with Obstructive Sleep Apnea and Respiratory Insufficiency caused by central and/or mixed apneas and periodic breathing. This device 
may be used in the hospital or home.

Warnings

A warning indicates the possibility of injury to the user or the operator.

•   This manual serves as a reference. The instructions in this manual are not intended to supersede the health care professional’s 

instructions regarding the use of the device.

•   The operator should read and understand this entire manual before using the device.
•  This device is not intended for life support.
•   The device should be used only with masks and connectors recommended by Philips Respironics or with those recommended 

by the health care professional or respiratory therapist. A mask should not be used unless the device is turned on and operating 
properly. The exhalation port(s) or entrainment valve associated with the mask should never be blocked. 

Explanation of the 

Warning:

 The device is intended to be used with special masks or connectors that have exhalation ports to allow continuous 

flow of air out of the mask. When the device is turned on and functioning properly, new air from the device flushes the exhaled 
air out through the mask exhalation port or entrainment valve. However, when the device is not operating, enough fresh air will 
not be provided through the mask, and exhaled air may be rebreathed.

•   If you are using a full face mask (a mask covering both your mouth and your nose), the mask must be equipped with a safety 

(entrainment) valve.

•   When using oxygen with this system, a Philips Respironics Pressure Valve must be placed in-line with the patient circuit between 

the device and the oxygen source. The pressure valve helps prevent the backflow of oxygen from the patient circuit into the 
device when the unit is off. Failure to use the pressure valve could result in a fire hazard.

•   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.

•   Oxygen supports combustion. Oxygen should not be used while smoking or in the presence of an open flame.
•   When using oxygen with this system, the oxygen supply must comply with local regulations for medical oxygen.
•   Do not connect the device to an unregulated or high pressure oxygen source.
•   Do not use the device near a source of toxic or harmful vapors.
•   Do not use the device in the presence of a flammable anaesthetic mixture in combination with oxygen or air, or in the presence 

of nitrous oxide.

•   Do not use this device if the room temperature is warmer than 35° C (95° F). If the device is used at room temperatures warmer 

than 35° C (95° F), the temperature of the airflow may exceed 43° C (109° F). This could cause irritation or injury to your airway.

•   Do not operate the device in direct sunlight or near a heating appliance because these conditions can increase the temperature of 

the air coming out of the device.

•   If you notice any unexplained changes in the performance of this device, if it is making unusual or harsh sounds, if it has been 

dropped or mishandled, if water is spilled into the enclosure, or if the enclosure is broken, disconnect the power cord and 
discontinue use. Contact your home care provider.

•   Periodically inspect electrical cords and cables for damage or signs of wear.  Discontinue use and replace if damaged. 
•   To avoid electrical shock, always unplug the power cord from the wall outlet before cleaning the device. DO NOT immerse the 

device in any fluids. 

•   If the device is used by multiple persons (such as rental devices), a low-resistance, main flow bacteria filter should be installed in-

line between the device and the circuit tubing to prevent contamination.

•   Be sure to 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.

•   This device is activated when the power cord is connected.
•   For safe operation when using a humidifier, the humidifier must always be positioned below the breathing circuit connection at 

the mask and the air outlet on the device. The humidifier must be level for proper operation.

•   The BiPAP autoSV Advanced System One device can deliver pressures up to 25 cm H

2

O. In the unlikely event of certain fault 

conditions, pressures of up to 35 cm H

2

O are possible.

•   The data obtained when using an Oximetry module accessory is not considered to be diagnostic and is not to be used in the 

diagnosis of a patient’s condition.

•   Repairs and adjustments must be performed by Philips Respironics-authorized service personnel only. Unauthorized service could 

cause injury, invalidate the warranty, or result in costly damage.

  note: 

Please see the “Limited Warranty” section of this manual for information on warranty coverage.

Содержание BiPAP autoSV Advanced System One

Страница 1: ...BiPAP autoSV Advanced System One USER MANUAL ...

Страница 2: ... 2012 Koninklijke Philips Electronics N V All rights reserved ...

Страница 3: ...o Place the Device 7 Supplying AC Power to the Device 7 Navigating the Device Screens 8 Starting the Device 8 Monitor Pressure Screen 9 Ramp Feature 9 Mask Fit Check Feature 10 Humidifier Preheat 10 Bi Flex Rise time Screen 10 Setup Screen 11 Info Screen 12 Device Alerts 14 Troubleshooting 18 Accessories 20 Service 20 Traveling with the System 21 Home Cleaning 21 Disposal 21 How to Contact Philips...

Страница 4: ...ire Oxygen supports combustion Oxygen should not be used while smoking or in the presence of an open flame When using oxygen with this system the oxygen supply must comply with local regulations for medical oxygen Do not connect the device to an unregulated or high pressure oxygen source Do not use the device near a source of toxic or harmful vapors Do not use the device in the presence of a flamm...

Страница 5: ...ar build up within the device which may result in the device malfunctioning Dirty inlet filters may cause high operating temperatures that may affect device performance Regularly examine the inlet filters as needed for integrity and cleanliness Never install a wet filter into the device You must ensure sufficient drying time for the cleaned filter Always ensure that the DC power cord securely fits...

Страница 6: ...symbol Class II Double Insulated Type BF Applied Part For Indoor Use Only Do not disassemble ForAirline Use Complies with RTCA DO 160F section 21 category M Separate collection for electrical and electronic equipment per EC Directive 2002 96 EC Use only with the standard 60W power supply 1091398 not for use with Heated Tubing Use only with the Heated Tubing compatible 80W power supply 1091399 can ...

Страница 7: ...The air pressure will gradually increase until the prescription pressure is reached Additionally the Bi Flex comfort feature provides increased pressure relief during the expiratory phase of breathing Several accessories are also available for use with the device Contact your home care provider to purchase any accessories not included with your system Air Outlet Port Power Inlet Filter Area SD Car...

Страница 8: ...activate the Mask Fit Check This button lights up when therapy is active or during specific alerts Alarm Silence Indicator Button Silences the audible portion of the alarm for a period of time and indicates an alarm condition Available Therapy Features If prescribed for you the device provides the following therapy features Bi Flex Comfort Feature If enabled the device provides a comfort feature c...

Страница 9: ...ct the flexible tubing to the air outlet on the side of the device Note Make sure the Tubing type setting 15 or 22 matches the tubing you are using Philips Respironics 15 or 22 mm tubing Make sure the Tubing type setting is 15 or 15H when the HeatedTube is connected Note If required connect a bacteria filter to the device air outlet and then connect the flexible tubing to the outlet of the bacteri...

Страница 10: ...either display a blank screen or it will show Bi Flex or Rise time depending on how the provider set up the device Note The SD card icon will display next to Info if the SD card is inserted 3 Put on your mask assembly Note If you are having trouble with your mask refer to the instructions supplied with the mask 4 Turn the wheel to toggle between the options Highlight Therapy Press the wheel to tur...

Страница 11: ...displays during a machine triggered breath when the Breath Rate setting is not Off I or E I is displayed above the pressure setting during IPAP Inspiratory Positive Airway Pressure and E is displayed during EPAP Expiratory Positive Airway Pressure The Ramp symbol displays while the Ramp function is active The bottom section of the display shows additional measured parameters which may include Resp...

Страница 12: ...is time During the 30 minute preheat you will still be able to use the control wheel to select other menu options from the Home screen If you press the wheel while Therapy is highlighted on the Home screen preheat mode will end and the blower will turn on to begin therapy The humidifier number selected in the setup menu 0 1 2 3 4 or 5 will now take effect Bi Flex Rise time Screen From the Home scr...

Страница 13: ...you with the most comfort A setting of 0 is the fastest Rise time while 3 is the slowest This setting will not display if your provider has not enabled Rise time on your device Note This same setting is also available under the Flex Rise time screen Ramp time This enables you to modify the Ramp time setting in 5 minute increments The range for this setting is 0 to 45 minutes Ramp start This displa...

Страница 14: ... or C5 for these settings This will only display if the humidifier is attached Please refer to the humidifier manual if using a humidifier Auto on You can enable this feature if you want the device to automatically turn the airflow on whenever you apply the interface mask to your airway You can also disable this feature Humidifier LED Backlight Ramp Backlight You can enable or disable the LED back...

Страница 15: ...e the patient is actually receiving therapy on the device for the most recent 1 day time frame It also displays the average amount of time the patient is actually receiving therapy on the device over a 7 day and a 30 day time frame provided the device has at least 7 or 30 days of data respectively If the device has only 5 days of data to use for the calculation the 5 day average value will be seen...

Страница 16: ...calculation the 5 day average value will be seen under the 7 day display Average PS Pressure Support is the difference between IPAP Inspiratory Positive Airway Pressure and EPAP Expiratory Positive Airway Pressure This screen displays the average of the Pressure Support values over a 1 day 7 day and 30 day time frame provided the device has at least 7 or 30 days of data respectively If the device ...

Страница 17: ...n the device detects that a certain action has been completed for example when an SD card is inserted or removed from the device a brief 1 beep audible indicator sounds The descriptions later in this manual display this indicator as Silencing an Alarm You can silence an alarm by pressing the Alarm Silence Indicator button This will silence the alarm for one minute If another alarm occurs while the...

Страница 18: ...unctioning device Press the Alarm Silence Indicator button to silence the alarm Remove your mask Remove power from the device Restore power If the alarm continues contact your home care provider for service Low Pressure Support High Red flashing button Low Pressure Support Operates This could be caused by an excessive leak or blockage or a device malfunction Press the Alarm Silence Indicator butto...

Страница 19: ...s contact your home care provider for service SD Card Corrupted Low Solid yellow button SD card corrupted Reformat card Operates This alarm occurs when a problem exists with the SD card The data may be corrupted Press the Alarm Silence Indicator button to silence the alarm Choose yes to reformat the card If you choose no the card will not be reformatted Note Any information on the card will be los...

Страница 20: ...onds then return to solid blue Only displayed when incorrect power supply is used with the heated tube Using wrong power supply Alert is present for 30 seconds or until the condition is fixed You must use the 80W power supply when using the heated tube If the alert continues to occur contact your home care provider Heated Tube Error Alert Info none Humidifier LED icon will slowly flash orange for ...

Страница 21: ...pressure setting on the Monitor Pressure screen If it is set to the minimum setting 4 0 cm H2 O or the starting pressure is the same as the prescribed pressure the Ramp feature will not work The airflow is much warmer than usual The air filters may be dirty The device may be operating in direct sunlight or near a heater Clean or replace the air filters The temperature of the air may vary somewhat ...

Страница 22: ...s about the SD card Adding Supplemental Oxygen Oxygen may be added at the mask connection Please note the warnings listed below when using oxygen with the device WARNINGS When using oxygen with this system a Philips Respironics Pressure Valve must be placed in line with the patient circuit between the device and the oxygen source The pressure valve helps prevent the backflow of oxygen from the pat...

Страница 23: ...ed after 30 nights of use or sooner if it appears dirty DO NOT clean the ultra fine filter CAUTION Dirty inlet filters may cause high operating temperatures that may affect device performance Regularly examine the inlet filters as needed for integrity and cleanliness 1 If the device is operating stop the airflow Disconnect the device from the power source 2 Remove the filter s from the enclosure b...

Страница 24: ...C 6 67 A Fuses There are no user replaceable fuses Noise Minimum Alarm Sound Level 45 dB A Declared Dual Number Noise Emissions Values In accordance with ISO 4871 The measured A weighted emission sound pressure level is 27 dB A with an uncertainty of 2 dB A The measured A weighted sound power level is 35 dB A with an uncertainty of 2 dB A Note These measurements apply to this device with an option...

Страница 25: ...ure it is used in such an environment Immunity Test IEC 60601 Test Level Compliance Level Electromagnetic Environment Guidance 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...

Страница 26: ... 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 device is used exceeds the applicable RF compliance level above the device should be observed to verify normal operation If abnormal performance is observed additional measures may be necessary such as re orienting or relocati...

Страница 27: ...rized distributors of Respironics Inc products and Respironics Inc reserves the right to charge dealers for warranty service of failed product not purchased directly from Respironics Inc or authorized distributors Respironics Inc disclaims all liability for economic loss loss of profits overhead or consequential damages which may be claimed to arise from any sale or use of this product Some states...

Страница 28: ...1103915 1103743 R00 JR 11 19 2012 EN DOM ...

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