Philips Respironics DreamStation Auto CPAP Manual

Philips Ikke kategoriseret Respironics DreamStation Auto CPAP

Læs gratis den danske manual til Philips Respironics DreamStation Auto CPAP (32 sider) i kategorien Ikke kategoriseret. Denne vejledning er vurderet som hjælpsom af 38 personer og har en gennemsnitlig bedømmelse på 3.5 stjerner ud af 19.5 anmeldelser. Har du et spørgsmål om Philips Respironics DreamStation Auto CPAP, eller vil du spørge andre brugere om produktet?

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User manual
DreamStation CPAP
DreamStation CPAP Pro
DreamStation Auto CPAP
© 2015 Koninklijke Philips N.V. All rights reserved.
Table of Contents
Intended Use ........................................................................................................................................................... 1
Important ................................................................................................................................................................. 1
Warnings .................................................................................................................................................................. 1
Cautions ................................................................................................................................................................... 2
Contraindications .................................................................................................................................................. 2
Symbol Key ..............................................................................................................................................................3
System Contents .................................................................................................................................................... 3
How to Contact Philips Respironics ................................................................................................................. 3
System Overview ................................................................................................................................................... 4
Installing/Replacing the Air Filters ......................................................................................................................5
Where to Place the Device .................................................................................................................................6
Supplying AC Power to the Device .................................................................................................................... 6
Connecting the Breathing Circuit ...................................................................................................................... 7
Navigating the Device Screens ............................................................................................................................8
Starting the Device ................................................................................................................................................8
Menu Navigation (Therapy ON) and Optional Humidication Settings ...................................................9
Ramp Feature .......................................................................................................................................................... 9
Menu Navigation (Therapy OFF) ......................................................................................................................10
Bluetooth® Wireless Technology .........................................................................................................................14
Check Mask Fit .....................................................................................................................................................15
Sleep Progress ......................................................................................................................................................15
Altitude Compensation ......................................................................................................................................15
Device Alerts ........................................................................................................................................................16
Troubleshooting ...................................................................................................................................................20
Accessories ...........................................................................................................................................................22
Traveling with the System ..................................................................................................................................23
Cleaning the Device ............................................................................................................................................24
Cleaning or Replacing the Filters .....................................................................................................................24
Cleaning the Tubing ..............................................................................................................................................24
Service ....................................................................................................................................................................24
Additional Notices ...............................................................................................................................................25
Specications ........................................................................................................................................................26
Disposal ..................................................................................................................................................................27
EMC Information .................................................................................................................................................27
Limited Warranty ...................................................................................................................................Back Page
1User Manual
Caution: U. S. federal law restricts this device to sale by or on the order of a physician.
Intended Use
The Philips Respironics DreamStation systems deliver positive airway pressure therapy for the treatment of Obstructive Sleep Apnea in
spontaneously breathing patients weighing over 30 kg (66 lbs). It is for use in the home or hospital/institutional environment.
Important
The device is to be used only on the instruction of a licensed physician. Your home care provider will make the correct pressure
settings and device congurations including accessories according to your health care proessionals prescription
Several accessories are available to make your OSA treatment with the DreamStation system as convenient and comfortable as
possile To ensure that you receive the sae eective therapy prescried or you use only hilips espironics accessories
Warnings
A warning indicates the possibility of injury to the user or the operator.
This manual serves as a reerence The instructions in this manual are not intended to supersede the health care proessionals
instructions regarding the use of the device.
The operator should read and understand this entire manual eore using the device
This device is not intended or lie support
ended y hilips espironics or ith those recommended y the The device should e used only ith mass and connectors recomm
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) associated with the mask should never be blocked. The device is intended Explanation of the Warning:
to e used ith special mass or connectors that have ehalation ports to allo continuouso o air out o the mas hen
the device is turned on and unctioning properly ne air rom the device ushes the ehaled air out through the mas ehalation
port Hoever hen the device is not operating enough resh air ill not e provided through the mas and ehaled air may e
rebreathed. Rebreathing of exhaled air for longer than several minutes can in some circumstances lead to suffocation.
 you are using a ull ace mas (a mas covering oth your mouth and your nose) the mas must e euipped ith a saety
(entrainment) valve.
hen using oygen ith this system the oygen supply must comply ith local regulations or medical oygen
Oygen supports comustion Oygen should not e used hile smoing or in the presence o an open ame
hen using oygen ith this system turn the device on eore turning on the oygen Turn the oygen o eore turning the
device off. This will prevent oxygen accumulation in the device. Explanation of the Warning: hen the device is not in
operation and the oygen o is let on oygen delivered into the tuing may accumulate ithin the devices enclosure Oygen
accumulated in the device enclosure ill create a ris o re
hen using oygen ith this system a hilips espironics ressure alve must e placed inline ith the patient circuit eteen
the device and the oygen source The pressure valve helps prevent the aco o oygen rom the patient circuit into the
device hen the unit is o ailure to use the pressure valve could result in a re haard
o not connect the device to an unregulated or high pressure oygen source
o not use the device in the presence o a ammale anaesthetic miture in comination ith oygen or air or in the presence
of nitrous oxide.
o not use the device near a source o toic or harmul vapors
  ( )  the device is used at room temperaturesarmer o not use this device i the room temperature is armer than 
than ( ) the temperature o the airo may eceed   ( ) This could cause irritation or inury to your airay
o not operate the device in direct sunlight or near a heating appliance ecause these conditions can increase the temperature o
the air coming out of the device.
ontact your health care proessional i symptoms o sleep apnea recur
 you notice any uneplained changes in the perormance o this device i it is maing unusual or harsh sounds i it has een
dropped or mishandled i ater is spilled into the enclosure or i the enclosure is roen disconnect the poer cord and
discontinue use ontact your home care provider
epairs and adustments must e perormed y hilips espironicsauthoried service personnel only nauthoried service could
cause inury invalidate the arranty or result in costly damage
o not use any accessories detachale parts and materials not recommended y hilips espironics ncompatile parts or
accessories can result in degraded performance.
se only approved cales and accessories Misuse may aect M perormance and should e avoided
The Health ndustry Manuacturers ssociation recommends that a minimum separation o si inches e maintained eteen
a ireless phone and a pacemaer to avoid potential intererence ith the pacemaer The reamStation onoard Bluetooth
communication should be considered a wireless phone in this regard.
ay cause se only poer cords supplied y hilips espironics or this devicese opoer cords not suppliedy hilips espironics m
overheating or damage to the device and may result in increased emissions or decreased immunity o the euipment or system
The device should not e used hile staced or in close approimation to other nonapproved devices
o not pull or stretch the tuing This could result in circuit leas
2User Manual
nspect the tuing or damage or ear iscard and replace the tuing as necessary
eriodically inspect electrical cords and cales or damage or signs o ear iscontinue use and replace i damaged
To avoid electrical shoc alays unplug the poer cord rom the all outlet eore cleaning the device O NOT immerse the
device in any uids
 the device is used y multiple persons (such as rental devices) a loresistance main o acteria lter should e installed in
line between the device and the circuit tubing to prevent contamination.
e sure to route the poer cord to the outlet in a ay that ill prevent the cord rom eing tripped over or interered ith y
chairs or other furniture.
This device is activated hen the poer cord is connected
or sae operation hen using a humidier the humidier must alays e positioned elo the reathing circuit connection at
the mas The humidier must e level or proper operation
Note: lease see the imited arranty section o this manual or inormation on arranty coverage
Cautions
A Caution indicates the possibility of damage to the device.
Medical electrical euipment needs special precautions regarding M and needs to e installed according to M inormation
ontact your home care provider regarding M installation inormation
Moile  communications euipment can aect medical electrical euipment
ins o connectors mared ith the S arning symol shall not e touched and connections shall not e made ithout
special precautions recautionary procedures include methods to prevent uildup o electrostatic charge (eg air conditioning
humidication conductive oor coverings nonsynthetic clothing) discharging ones ody to the rame o the euipment or
system or to earth. It is recommended that all individuals that will handle this device understand these precautionary procedures
at a minimum as part of their training.
ss door and the modem access door are oth closed henever any eore operating the device ensure that the S cardlter acce
o the accessories such as the in Module or Modem are not installed eer to the instructions that came ith your accessory
ondensation may damage the device  this device has een eposed to either very hot or very cold temperatures allo it to
adust to room temperature (operating temperature) eore starting therapy o not operate the device outside o the operating
temperature range shon in the Specications
o not use etension cords ith this device
Mae sure the lter area on the side o the device is not loced y edding curtains or other items ir must o reely around
the device for the system to work properly.
o not place the device directly onto carpet aric or other ammale materials
o not place the device in or on any container that can collect or hold ater
 properly installed undamaged hilips espironics lue pollen lter is reuired or proper operation
Toacco smoe may cause tar uildup ithin the device hich may result in the device malunctioning
irty inlet lters may cause high operating temperatures that may aect device perormance egularly eamine the inlet lters as
needed for integrity and cleanliness.
Never install a et lter into the device ou must ensure sucient drying time or the cleaned lter
lays ensure that the  poer cord securely ts into your therapy device prior to use ontact your home care provider or
hilips espironics to determine i you have the appropriate  cord or your specic therapy device
hen  poer is otained rom a vehicle attery the device should not e used hile the vehicles engine is running amage
to the device may occur.
Only use a hilips espironicsoerord andattery dapteralese o any other system may cause damage to the device
Contraindications
hen assessing the relative riss and enets o using this euipment the clinician should understand that this device can deliver
pressures up to 20 cm H2O n the event o certain ault conditions a maimum pressure o  cm H2O is possible. Studies have
shon that the olloing preeisting conditions may contraindicate the use o  therapy or some patients
ullous ung isease
athologically o lood ressure
ypassed pper iray
neumothora
neumocephalus has een reported in a patient using nasal ontinuous ositive iray ressure aution should e used hen
prescriing  or susceptile patients such as those ith cereral spinal uid (S) leas anormalities o the cririorm
plate prior history o head trauma andor pneumocephalus (hest  )
The use of positive airway pressure therapy may be temporarily contraindicated if you exhibit signs of a sinus or middle ear
inection Not or use ith patients hose upper airays are ypassed ontact your health care proessional i you have any
uestions concerning your therapy
3User Manual
Symbol Key
The olloing symols may appear on the device poer supply and accessories
Symbol Symbolenition enition
onsult accompanying instructions or
use.
or irline seomplies ith TO
 section category M
 oer
Separate collection for electrical and
electronic euipment per  irective

 oer Bluetooth® symbol
IP22 rip roo uipment This device contains an RF transmitter.
aution consult accompanying
documents. Oimeter onnection
S arning symol Serial onnection
lass  (oule nsulated) Avoid ultraviolet radiation
Type  pplied art
aution  S ederal la restricts this
device to sale by or on the order of a
physician.
For Indoor Use Only. Do not disassemble.
System Contents
our reamStation system may include the olloing items
 evice  S card
 ser manual  leile tuing
 arrying case  eusale lue pollen lter
 oer cord  isposale lightlue ultrane lter (optional)
 oer supply ( )  Humidier (optional)
Note:  any o these items are missing contact your home care provider
How to Contact Philips Respironics
Should you eperience troule ith this euipment or reuire assistance setting up using or maintaining the device
or accessories please contact your home care provider  you need to contact hilips espironics directly call
the hilips espironics ustomer Service department at  or  ou can also use the
olloing address
espironics nc
 Murry idge ane
Murrysville  
User Manual
Installing/Replacing the Air Filters
Caution:  properly installed undamaged hilips espironics lue pollen lter is reuired or proper operation
The device uses a lue pollen lter that is ashale and reusale and a lightlue ultrane lter that is disposale
The reusale lue lter screens out normal household dust and pollens hile the lightlue ultrane lter provides
more complete ltration o very ne particles The reusale lue lter must e in place at all times hen the device is
operating The ultrane lter is recommended or people ho are sensitive to toacco smoe or other small particles
The reusale lue lter is supplied ith the device  disposale lightlue ultrane lter may also e included  your
lter is not already installed hen you receive your device you must at least install the reusale lter eore using the
device.
This device has an automatic air lter reminder very  days the device ill display a message reminding you to
chec your lters and replace them as directed
Note: This message is a reminder only The device does not detect the perormance o the lters nor does it
recognie hen a lter has een cleaned or replaced
 it up on the lter access door and sing open  replacing pull out the old lter assemly
  applicale place a clean reusale lue pollen lter () on top o a ne optional disposale lightlue ultrane
lter () and rmly snap them together
 lace the ne lter assemly ac in the side o the therapy device Sing the door closed


Produkt Specifikationer

Mærke: Philips
Kategori: Ikke kategoriseret
Model: Respironics DreamStation Auto CPAP

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