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BiPAP autoSV Advanced System One
USER MANUAL

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Summary of Contents for PHILIPS Respironics BiPAP autoSV Advanced System One

  • Page 1 BiPAP autoSV Advanced System One USER MANUAL...
  • Page 2 © 2012 Koninklijke Philips Electronics N.V. All rights reserved.
  • Page 3: Table Of Contents

    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 Respironics .......................21 Specifications ................................22 EMC Information ..............................23 Limited Warranty ..........................Back Page User Manual...
  • Page 4: 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.
  • Page 5: Cautions

    • When DC power is obtained from a vehicle battery, the device should not be used while the vehicle’s engine is running. Damage to the device may occur. • Only use a Philips Respironics DC Power Cord and Battery Adapter Cable. Use of any other system may cause damage to the device.
  • Page 6: Symbol Key

    Symbol Key The following symbols may appear on the device and power supply: ymbol efinition Consult accompanying instructions for use. AC Power DC Power iP22 Drip Proof Equipment Caution, consult accompanying documents. ESD Warning symbol Class II (Double Insulated) Type BF Applied Part For Indoor Use Only.
  • Page 7: System Contents

    System overview The BiPAP autoSV Advanced System One device is intended to augment your breathing by supplying pressurized air through a circuit. It senses your breathing effort by monitoring airflow in the circuit and adjusts its output to assist in inhalation and exhalation.
  • Page 8: Control Buttons

    Control Buttons LCD Display Screen Humidifier Icon and Number Settings Control Wheel/Push Button Alarm Silence/Indicator Ramp Button Button This figure shows the primary control buttons on the device, described in the following table. eature eScription Display Screen Shows therapy settings, patient data, and other messages. The startup screen is shown temporarily when the unit is first powered.
  • Page 9: Installing The Air Filters

    1. Connect 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 Heated Tube is connected.
  • Page 10: Navigating The Device Screens

    1. Supply power to the device. 2. The first screen to display will be the Philips Respironics logo, followed by the screen showing the current software version number. The Blower hours screen will then appear, which shows the total blower hours for the device in hours and minutes.
  • Page 11: Monitor Pressure Screen

    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 •...
  • Page 12: Mask Fit Check Feature

    Mask Fit Check Feature The Mask Fit Check feature can be enabled or disabled by your home care provider. This feature allows you to check the fit of your mask prior to starting therapy. This is done by measuring the amount of leak. Put on your mask assembly.
  • Page 13: Setup Screen

    • 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 the Philips Respironics 22 mm tubing, or (15) for the Philips Respironics 15 mm tubing.
  • Page 14: Info Screen

    • Heated Tube humidification - This setting will only display if you are using the heated tube with the humidifier. You can enable or disable this feature. • Humidity level - This setting will only display if you are using the heated tube with the humidifier. This setting allows you to choose the desired humidity setting for the humidifier: 1, 2 or 3.
  • Page 15 • Oximetry - This screen displays the Oximetry parameters. note: This option is only shown when an optional Oximetry module is attached. • Status - This displays information sent from a peripheral (SD card , modem , etc.). If two peripherals are attached, two lines will appear with corresponding icons.
  • Page 16: Device Alerts

    • Periodic Breathing - During any given night, the device recognizes the percentage of time the patient was experiencing periodic breathing. This screen displays the nightly value of periodic breathing for the most recent 1 day time frame. It also displays the average of these individual nightly values of periodic breathing over a 7 day and a 30 day time frame (provided the device has at least 7 or 30 days of data respectively).
  • Page 17 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). •...
  • Page 18 Alarm / Priority Audible Visual Indicators Device Action User Action Alert Indicator High • • • • • Red flashing button; Operates This could be caused by an excessive Pressure “Low Pressure” leak or blockage or a device malfunction. Press the Alarm Silence/ Indicator button to silence the alarm.
  • Page 19 Alarm / Priority Audible Visual Indicators Device Action User Action Alert Indicator Patient High • • • • • Red flashing button; Operates This alarm occurs when the patient Disconnect “Patient Disconnect” circuit is disconnected or has a large leak. Press the Alarm Silence/Indicator button to silence the alarm.
  • Page 20: Troubleshooting

    Alarm / Priority Audible Visual Indicators Device Action User Action Alert Indicator SD Card: Info • “SD card inserted: Operates This info message will be present for 30 Prescription prescription accepted” seconds or until the user acknowledges Accepted it. No action needed. SD Card Info •...
  • Page 21 Make sure the Tubing type setting (22 or 15) matches the or too low. be incorrect. tubing that you are using (Philips Respironics 22 or 15 mm tubing). If you are using the Heated Tubing, this setting will be 15H and you cannot change it.
  • Page 22: Accessories

    SD Card The BiPAP autoSV Advanced System One comes with an SD card inserted in the SD card slot on the back of the device to record information for the home care provider. Your home care provider may ask you to periodically remove the SD card and send it to them for evaluation.
  • Page 23: Traveling With The System

    How to Contact Philips Respironics To have your device serviced, contact your home care provider. If you need to contact Philips Respironics directly, call the Philips Respironics Customer Service department at 1-800-345-6443 or 1-724-387-4000. You can also use the following address: Respironics, Inc.
  • Page 24: Specifications

    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”...
  • Page 25: Emc Information

    Maximum Flow Rate: (typical) Test pressures (cm H 14.5 20.0 25.0 22 mm Measured pressure at the patient 13.5 19.1 24.0 tubing connection port (cm H Average flow at the patient 90.5 145.9 158.5 151.6 133.0 connection port (LPM) 15 mm Measured pressure at the patient 13.5 19.0...
  • Page 26 Guidance and Manufacturer’s Declaration - Electromagnetic Immunity – This device is intended for use in the electromagnetic environment specified below. The user of this device should make sure it is used in such an environment. iec 60601 t mmunity evel ompliance evel lectromagnetic...
  • Page 27: Limited Warranty

    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.
  • Page 28 1103915 1103743 R00 JR 11/19/2012 EN-DOM...

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