BiPAP autoSV Advanced System One USER MANUAL
© 2010 Koninklijke Philips Electronics N.V. All rights reserved.
Table of Contents Intended Use............................................................................................................................................................ 2 Warnings................................................................................................................................................................... 2 Cautions.............................................................................................................................................
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.
• Before operating the device, ensure that the SD card cover is replaced whenever any of the accessories such as the Link Module or Modem are not installed. Refer to the instructions that came with your accessory. • Condensation may damage the device. If this device has been exposed to either very hot or very cold temperatures, allow it to adjust to room temperature (operating temperature) before starting therapy.
System Contents Your BiPAP autoSV Advanced System One includes the following items: • Device • Flexible tubing, 22 mm (optional 15 mm tubing is also available) • User manual • Power cord and power supply (Part# 1058190) • Carrying case • Side cover panel • Reusable gray foam filter • SD card • Disposable ultra-fine filter • Humidifier (optional) Note: If any of these items are missing, contact your home care provider.
Control Buttons LCD Display Screen Humidifier Icon and Number Settings Control Wheel/Push Button Alarm Silence/Indicator Button Ramp Button This figure shows the primary control buttons on the device, described in the following table. Feature Description Display Screen Shows therapy settings, patient data, and other messages. The startup screen is shown temporarily when the unit is first powered.
Installing the Air Filters CAUTION: A properly installed, undamaged gray foam filter is required for proper operation. The device uses a gray foam filter that is washable and reusable, and an optional white ultra-fine filter that is disposable. The reusable filter screens out normal household dust and pollens, while the ultra-fine filter provides more complete filtration of very fine particles. The reusable gray foam filter and the optional disposable ultra-fine filter are supplied with the device.
Navigating the Device Screens Turn the wheel to toggle between options and settings on the screen. Press the wheel to choose an option or setting that is highlighted. If you choose “Back” on any screen, it will take you back to the previous screen. Note: The screens shown throughout this manual are examples only. Actual screens may vary slightly. Examples are for reference only. Starting the Device 1. Supply power to the device. 2. The Home screen will appear, shown below.
Monitor Pressure Screen From the Main Menu, if you select Therapy and then press the Wheel, the following Monitor Pressure screen appears. Example shown here. The Monitor Pressure screen displays the following items: • Pressure • Timed Breath Indication • I/E State Indication • Ramp Indication • Icon Bar • Therapy Parameters Note: Additional icons may appear if optional accessories are being used (such as the oximetry module). Refer to the manual that accompanies the accessory for more information.
Bi-Flex/Rise time Screen From the Home screen, highlight “Bi-Flex” or “Rise time” and press the wheel. The following screen will appear. Note: This screen will be blank on the Home screen if your provider has not enabled Bi-Flex or Rise time on your device. Back Bi-Flex Rise time Back 1 0 2 1 3 2 3 Flex Screen • Bi-Flex - The Bi-Flex comfort feature allows you to adjust the level of air pressure relief that you feel when you exhale during therapy.
• Tubing Type - This setting allows you to select the correct size diameter tubing that you are using with the device.You can choose either “22” for any Respironics 22 mm tubing, or “15” for the optional Respironics 15 mm tubing. If you are using the optional Respironics 15 mm tubing, the device tubing type setting must be set to 15. Note: If the provider has locked this feature, this setting will not display. • Ramp start - This displays the Ramp starting pressure.
Note: The screen will only show a few lines at a time. As you rotate the wheel to toggle over different options the screen will slide up and down accordingly. If the text is too long to completely fit on the screen, it will scroll horizontally across the screen when highlighted. • Oximetry - This screen displays the Oximetry parameters. Note: This option is only shown when an optional Oximetry module is attached.
• AHI - The device accumulates individual Apnea/Hypopnea indices (AHI) for each session the patient used the device. This screen displays the average of these individual nightly AHI values over a 7 day and 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 under the 7 day display. This screen only displays if your home care provider has enabled it.
Alert Audible Indicators An audible indicator sounds whenever a power failure or a high, medium, or low priority alarm is detected. Additionally, an audible indicator sounds for informational messages and to confirm that certain actions have occurred (for example, when an SD card is inserted or removed from the device). • Device Inoperative - When a device inoperative alarm occurs, a continuous audible indicator sounds.
Alarm Priority Audible Indicator Visual Indicators Device Action User Action Low Pressure Alarm High ••• •• Red flashing button; “Low Pressure” Operates This could be caused by an excessive leak or blockage or a device malfunction. Press the Alarm Silence/Indicator button to silence the alarm. Remove your mask. Check for the following: dirty inlet filters, blocked air intake, excessive leak in the patient circuit. If the alarm continues, contact your home care provider.
Alarm Low Input Voltage Priority Medium Audible Indicator ••• Visual Indicators Device Action User Action Yellow flashing button; “Low Voltage” Device Operates; Humidifier shuts down The alarm is caused when input power at the device, either from an AC outlet or battery, falls below the acceptable limit for 10 seconds. Press the Alarm Silence/Indicator button to silence the alarm. If the device is plugged into a wall outlet, unplug the device and then plug it back in.
Troubleshooting The table below lists some of the problems you may experience with your device and possible solutions to those problems. Problem Nothing happens when you apply power to the device. The backlights on the buttons do not light. Why It Happened There is no power at the outlet or the device is unplugged. What to Do If you are using AC power, check the outlet and verify that the device is properly plugged in. Make sure there is power available at the outlet.
Accessories There are several accessories available for your BiPAP autoSV Advanced System One device such as a humidifier, Oximetry module or a modem. Contact your home care provider for additional information on the available accessories. When using optional accessories, always follow the instructions enclosed with the accessories. Caution: Pins of connectors should not be touched. Connections should not be made to these connectors unless ESD precautionary procedures are used.
Traveling with the System When traveling, the carrying case is for carry-on luggage only. The carrying case will not protect the system if it is put through checked baggage. For your convenience at security stations, there is a note on the bottom of the device stating that it is medical equipment and is suitable for airline use. It may be helpful to bring this manual along with you to help security personnel understand the BiPAP autoSV Advanced System One device.
Specifications Environmental Operating Temperature: 5° to 35° C (41° to 95° F) Storage Temperature: -20° to 60° C (-4° to 140° F) Relative Humidity (operating & storage): 15 to 95% (non-condensing) Atmospheric Pressure: 101 to 77 kPa (0 - 2286 m / 0 - 7500 ft) Physical Dimensions: 18 x 14 x 10 cm (7” L x 5.5” W x 4” H) Weight (Device with power supply): Approximately 1.53 kg (3.
Disposal Dispose of this device in accordance with local regulations. How to Contact Respironics To have your device serviced, contact your home care provider. If you need to contact Respironics directly, call the Respironics Customer Service department at 1-800-345-6443 or 1-724-387-4000.You can also use the following addresses: Respironics, Inc.
Limited Warranty Respironics, Inc. warrants that the system shall be free from defects of workmanship and materials and will perform in accordance with the product specifications for a period of two (2) years from the date of sale by Respironics, Inc. to the dealer. If the product fails to perform in accordance with the product specifications, Respironics, Inc. will repair or replace – at its option – the defective material or part. Respironics, Inc. will pay customary freight charges from Respironics, Inc.
1071073 1070900 R00 JR 12/20/2010 EN-DOM
