ResMed AirFit N20 Mode d'emploi

Nasal mask

User guide

English | Français

Español | Português

638088 Geelong Covers WITH VENT option 2_Mul2.indd 2 18/10/2016 1:15:58 PM

i

1 2

3 4

5

76

Fitting / Mise en place / Colocación / Colocação

638088 Geelong Covers WITH VENT option 2_Mul2.indd 1 18/10/2016 1:16:00 PM

ii

Removal

11 22

Adjustment / Ajustement / Ajuste / Ajuste

Removal / Retrait / Remoción / Remoção

638088 Geelong Covers WITH VENT option 2_Mul2.indd 2 18/10/2016 1:16:03 PM

iii

1 2

3

Disassembly / Démontage / Desensamblado /

Desmontagem

638088 Geelong Covers WITH VENT option 2_Mul2.indd 3 18/10/2016 1:16:03 PM

iv

1 2

Reassembly / Remontage / Reensamblado / Remontagem

638088 Geelong Covers WITH VENT option 2_Mul2.indd 4 18/10/2016 1:16:03 PM

v

86°F / 30°C

1 2

3 4

5

Cleaning your mask at home / Nettoyage de votre

masque à domicile / Limpieza de la mascarilla en el

domicilio / Limpeza da máscara em casa

638088 Geelong Covers WITH VENT option 2_Mul2.indd 5 18/10/2016 1:16:04 PM

English 1

ENGLISH

Nasal Mask

Thank you for choosing the AirFit N20. This document provides the user

instructions for the AirFit N20 and AirFit N20 for Her masks referred to

collectively as AirFit N20 throughout this manual.

Using this guide

Please read the entire guide before use. When following instructions,

refer to the images at the front of the guide.

Intended use

The AirFit N20 channels airflow non-invasively to a patient from a positive

airway pressure (PAP) device such as a continuous positive airway

pressure (CPAP) or bilevel device.

The AirFit N20 is:

• to be used by patients weighing more than 66 lb (30 kg) for whom

positive airway pressure has been prescribed

• intended for single-patient re-use in the home environment and

multi-patient re-use in the hospital/institutional environment.

WARNING

Magnets are used in the lower headgear straps and the frame of the

AirFit N20. Ensure the headgear and frame is kept at least 2" (50 mm)

away from any active medical implant (eg, pacemaker or

defibrillator) to avoid possible effects from localized magnetic fields.

The magnetic field strength is less than 400 mT.

Contraindications

Use of masks with magnetic components is contraindicated in patients

with the following pre-existing conditions:

• a metallic hemostatic clip implanted in your head to repair an

aneurysm

• metallic splinters in one or both eyes following a penetrating eye

injury.

2

GENERAL WARNINGS

• The vent holes must be kept clear.

• The mask should only be used with CPAP or bilevel devices

recommended by a physician or respiratory therapist.

• The mask should not be used unless the device is turned on. Once

the mask is fitted, ensure the device is blowing air. Explanation:

CPAP and bilevel devices are intended to be used with special

masks (or connectors) which have vent holes 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 vent holes. However, when the device is

not operating, insufficient fresh air will be provided through the

mask, and the exhaled air may be rebreathed. Rebreathing of

exhaled air for longer than several minutes can, in some

circumstances, lead to suffocation. This applies to most models of

CPAP or bilevel devices.

• Follow all precautions when using supplemental oxygen.

• Oxygen flow must be turned off when the CPAP or bilevel device

is not operating, so that unused oxygen does not accumulate

within the device enclosure and create a risk of fire.

• Oxygen supports combustion. Oxygen must not be used while

smoking or in the presence of an open flame. Only use oxygen in

well ventilated rooms.

• At a fixed rate of supplemental oxygen flow, the inhaled oxygen

concentration varies, depending on the pressure settings, patient

breathing pattern, mask, point of application and leak rate. This

warning applies to most types of CPAP or bilevel devices.

• The technical specifications of the mask are provided for your

clinician to check that they are compatible with the CPAP or

bilevel device. If used outside specification or if used with

incompatible devices, the seal and comfort of the mask may not

be effective, optimum therapy may not be achieved, and leak, or

variation in the rate of leak, may affect the CPAP or bilevel device

function.

• Discontinue using this mask if you have ANY adverse reaction to

the use of the mask, and consult your physician or sleep therapist.

• Using a mask may cause tooth, gum or jaw soreness or aggravate

an existing dental condition. If symptoms occur, consult your

physician or dentist.

English 3

• As with all masks, some rebreathing may occur at low CPAP

pressures.

• Refer to your CPAP or bilevel device manual for details on

settings and operational information.

• Remove all packaging before using the mask.

• The mask must be used under qualified supervision for users who

are unable to remove the mask by themselves.

• This mask is not for use on patients with impaired laryngeal

reflexes or other conditions predisposing to aspiration in the

event of regurgitation or vomiting.

• Avoid connecting flexible PVC products (eg, PVC tubing) directly

to any part of the mask. Flexible PVC contains elements that can

be damaging to the materials of the mask, and may cause the

components to crack or break.3

• N20 line of nasal CPAP masks are not intended to be used

simultaneously with nebulizer medications that are in the air path

of the mask/tube.

• The mask contains an exhaust port safety feature to enable

normal breathing. The mask should not be worn if this safety

feature is damaged or missing.

Using your mask

When using your mask with ResMed CPAP or bilevel devices that have

mask setting options, refer to the Technical specifications section in this

user guide for the correct setting.

For a full list of compatible devices for this mask, see the Mask/Device

Compatibility List on www.resmed.com/downloads/masks. If you do not

have internet access, please contact your ResMed representative.

Fitting

1. Twist and pull both magnetic clips away from the frame.

2. With both lower headgear straps released, hold the mask against your

face and pull the headgear over your head.

Headgear check:

Ensure that the ResMed logo on the headgear is facing outwards and

is upright when the headgear is put on.

3. Bring the lower straps below your ears, and attach the magnetic clip

to the frame.

4

4. Undo the fastening tabs on the upper headgear straps. Adjust the

straps evenly until the mask sits comfortably just over the nose.

Reattach the fastening tabs.

5. Undo the fastening tabs on the lower headgear straps. Adjust the

straps evenly until the mask is stable. Reattach the fastening tabs.

6. Connect the device air tubing to the short tube. Attach the elbow to

the mask by pressing the side buttons and pushing the elbow into the

mask, ensuring it clicks in on both sides.

7. Your mask and headgear should be positioned as shown in the

illustration.

Adjustment

If necessary, slightly adjust the position of the mask for the most

comfortable fit. Ensure that the cushion is not creased and the headgear

is not twisted.

1. Turn on your device so that it is blowing air.

Adjustment tips:

 To resolve any leaks at the upper part of the mask, adjust the

upper headgear straps. For the lower part, adjust the lower

headgear straps. Adjust only enough for a comfortable seal.

 The upper strap adjustment is the key to seal and comfort.

 Do not overtighten the lower straps because they mainly serve to

keep the cushion in position.

Removal

1. Twist and pull both magnetic clips away from the frame.

2. Pull the mask away from your face and back over your head.

English 5

Disassembly

If the mask is connected to your device, disconnect the device air tubing

from the short tube.

1. Undo the fastening tabs on the upper headgear straps. Pull the straps

out of the frame.

Tip: Keep the magnetic clips attached to the lower headgear straps to

easily distinguish the upper and lower straps when reassembling.

2. Remove the elbow from the mask by pressing the side button and

pulling the elbow away.

3. Hold the frame by placing your thumb over the side slot. Pull the

cushion away from the frame.

Reassembly

1. Push the cushion into the frame. The frame has a shape that allows

you to insert the cushion only one way.

2. With the ResMed logo on the headgear facing outside and upright,

thread the upper headgear straps into the frame slots from the inside.

Fold them over to secure.

Cleaning your mask at home

It is important to follow the steps below to get the best performance out

of your mask.

WARNING

• As part of good hygiene, always follow cleaning instructions and

use a mild liquid detergent. Some cleaning products may damage

the mask, its parts and their function, or leave harmful residual

vapours that could be inhaled if not rinsed thoroughly.

• Regularly clean your mask and its components to maintain the

quality of your mask and to prevent the growth of germs that can

adversely affect your health.

CAUTION

If any visible deterioration of a system component is apparent

(cracking, crazing, tears etc), the component should be discarded and

replaced.

6

Daily/After each use:

Before cleaning, take the mask components apart according to the

disassembly instructions.

1. Soak and agitate the cushion, elbow and short tube in warm water

(approximately 86°F/30°C) using a mild liquid detergent for up to

10 minutes.

2. Clean the components with a soft bristle brush, paying particular

attention to the small vent holes on the elbow.

3. Thoroughly rinse the components under warm flowing drinking quality

water.

4. Inspect each component to ensure that they are visually clean and

free of detergent residue. If required, repeat washing.

5. Allow the components to dry out of direct sunlight before assembling.

Weekly:

The magnetic clips can be left on for washing.

1. Soak and agitate the separated headgear and frame in warm water

(approximately 86°F/30°C) using a mild liquid detergent for up to

10 minutes.

2. To rinse the components, repeatedly squeeze them under warm

flowing drinking quality water until it is free of detergent residue.

3. Squeeze the components to remove excess water.

4. Allow the components to dry out of direct sunlight before assembling.

Reprocessing the mask between patients

Only Sleep Lab Mask (SLM) variants of the mask are intended for

multi-patient re-use. When using between patients, these masks must be

reprocessed according to cleaning and disinfection instructions available

on ResMed.com/downloads/masks.

English 7

Troubleshooting

Problem/possible cause

Solution

Mask is too noisy.

Vent is dirty. Clean the vent according to the instructions.

Mask is incorrectly assembled. Disassemble the mask, then reassemble

according to the instructions.

Mask is leaking. Refit or reposition your mask.

Readjust the headgear straps to bring the mask

closer to the face and improve your seal.

Check that your mask is assembled correctly.

Mask leaks around face.

Mask is not positioned correctly. Check that the mask size indicator is facing

downward on the bottom of the cushion along

the bottom of your nose.

Mask may have been fitted

incorrectly.

Pull the mask away from your face and

reposition, ensuring that the lower corners of the

mask fully enclose your nose. If necessary,

readjust the headgear straps to keep the mask in

the right place.

Cushion may be dirty. Clean the cushion according to the instructions.

Cushion membrane is creased or

folded.

Remove and refit your mask according to the

fitting instructions. Ensure that you position the

cushion correctly over your nose before pulling

the headgear over your head. Do not slide the

mask down your face during fitting as this may

lead to folding or curling of the cushion.

Mask is not tightened correctly. Ensure that the headgear straps are not

overtightened or too loose. You may find that this

mask does not need to be tightened as much as

other nasal masks.

Check that the headgear is not twisted.

Mask may be the wrong size. Talk to your clinician.

Mask does not fit properly.

Mask is incorrectly assembled. Disassemble the mask, then reassemble

according to the instructions.

Mask may be the wrong size. Talk to your clinician.

8

Technical specifications

Pressure-flow

curve

The mask contains passive venting to protect against rebreathing.

As a result of manufacturing variations, the vent flow rate may vary.

Pressure

(cm H

2

O)

Flow

(L/min)

4

20

7

27

11

35

14

40

17

44

20

49

24

54

27

58

30

61

Dead space

information

Physical dead space is the empty volume of the mask to the end of

the swivel. Using the large cushions it is 103.3 mL.

Therapy

pressure

4 to 30 cm H

2

O

Resistance

Drop in pressure measured (nominal)

at 50 L/min: 0.3 cm H

2

O

at 100 L/min: 1.3 cm H

2

O

Environmental

conditions

Operating temperature: 41°F to +104°F (5°C to 40°C)

Operating humidity: 15% to 95% non-condensing

Storage and transport temperature: -4°F to +140°F (-20°C to +60°C)

Storage and transport humidity: up to 95% non-condensing

Sound

DECLARED DUAL-NUMBER NOISE EMISSION VALUES in accordance

with ISO 4871. The A-weighted sound power level of the mask is

24 dBA, with uncertainty of 3 dBA. The A-weighted sound pressure

level of the mask at a distance of 1 m is 16 dBA, with uncertainty of

3 dBA.

Gross

dimensions

13.3" (H) x 11.4" (W) x 6.4" (D)

(339 mm (H) x 291 mm (W) x 162 mm (D))

Mask fully assembled with the short tube assembly and swivel,

excluding the headgear

English 9

International

Commission on

Non-Ionizing

Radiation

Protection

(ICNIRP)

Magnets used in this mask are within ICNIRP guidelines for general

public use.

Service life

The service life of the AirFit N20 mask system is dependent on the

intensity of usage, maintenance, and environmental conditions to

which the mask is used or stored. As this mask system and its

components are modular in nature, it is recommended that the user

maintain and inspect it on a regular basis, and replace the mask

system or any components if deemed necessary or according to the

‘visual criteria for product inspection’ in the ‘Cleaning your mask at

home’ section of this guide. Refer to the ‘Mask components’ section

of this guide for information of how to order replacement parts.

Mask setting

options

For AirSense, AirCurve and S9: Select 'Pillows'.

For other devices: Select 'SWIFT' (if available), otherwise select

'MIRAGE' as the mask option.

Notes:

• This product is not made with PVC, DEHP, DBP or BBP.

• This product is not made with natural rubber latex.

• The manufacturer reserves the right to change these specifications

without notice.

Storage

Ensure that the mask is thoroughly clean and dry before storing it for any

length of time. Store the mask in a dry place out of direct sunlight.

Disposal

This mask does not contain any hazardous substances and may be

disposed of with your normal household refuse.

10

Symbols

The following symbols may appear on your product or packaging:

Catalog number

Batch code

Humidity limitation

Temperature limitation

Manufacturer

European Authorized

Representative

Keep away from rain

This way up

Nasal mask

Device setting - Pillows

Size - small

Size - medium

Size - large

Fragile, handle with care

Indicates a Warning or Caution and alerts you to a possible injury or explains

special measures for the safe and effective use of the device

Caution, consult accompanying documents

Prescription only (In the US, Federal law restricts these devices to sale by or on

the order of a physician)

English 11

Limited warranty

ResMed Pty Ltd (ResMed) warrants that your ResMed mask system

(including mask frame, cushion, headgear and tubing) will be free from

defects in material and workmanship from the date of purchase for 90

days, or in the case of disposable masks and disposable mask

components for 7 days. This warranty is only available to the initial

consumer. It is not transferable. If the product fails under conditions of

normal use, ResMed will repair or replace, at its option, the defective

product or any of its components. This limited warranty does not cover: a)

any damage caused as a result of improper use, abuse, modification or

alteration of the product; b) repairs carried out by any service organization

that has not been expressly authorized by ResMed to perform such

repairs; and c) any damage or contamination due to cigarette, pipe, cigar

or other smoke. Warranty is void on product sold, or resold, outside the

region of original purchase.

Warranty claims on defective product must be made by the initial

consumer at the point of purchase.

This warranty replaces all other expressed or implied warranties, including

any implied warranty of merchantability or fitness for a particular purpose.

Some regions or states do not allow limitations on how long an implied

warranty lasts, so the above limitation may not apply to you.

ResMed will not be responsible for any incidental or consequential

damages claimed to have resulted from the sale, installation or use of any

ResMed product. Some regions or states do not allow the exclusion or

limitation of incidental or consequential damages, so the above limitation

may not apply to you. This warranty gives you specific legal rights, and

you may also have other rights which vary from region to region. For

further information on your warranty rights, contact your local ResMed

dealer or ResMed office.

Français 1

FRANÇAIS

Masque nasal

Merci d'avoir choisi l'AirFit N20. Ce document indique comment utiliser

les masques AirFit N20 et AirFit N20 for Her, désignés par AirFit N20

dans le présent manuel.

Utilisation de ce guide

Veuillez lire le guide entièrement avant d’utiliser ce masque. Les

instructions doivent être lues en consultant les illustrations au début de

ce manuel.

Usage prévu

L'AirFit N20 achemine au patient de façon non-invasive le débit d'air

produit par un appareil à pression positive tel qu'un appareil de PPC ou à

deux niveaux de pression.

L'AirFit N20 est prévu pour :

• une utilisation par des patients (> 66 lb (30 kg)) à qui une pression

positive a été prescrite;

• un usage multiple par un seul patient à domicile ou pour un usage

multiple par plusieurs patients en milieu médical.

AVERTISSEMENT

Des aimants sont utilisés dans les sangles inférieures du harnais et

dans l'entourage rigide de l'AirFit N20. Vérifiez que le harnais et

l'entourage rigide soient maintenus à une distance minimale de

50 mm (2 pouces) de tout implant médical actif (p. ex. un pacemaker

ou un défribillateur) pour éviter les effets possibles des champs

magnétiques localisés. La force du champ magnétique est inférieure

à 400 mT.

2

Contre-indications

L'utilisation des masques avec des composants magnétiques est

contre-indiqué chez les patients présentant les caractéristiques

pré-existantes suivantes :

• dispositif hémostatique métallique implanté dans le crâne suite à un

anévrisme;

• éclats métalliques dans un œil ou dans les deux yeux suite à un

traumatisme oculaire pénétrant.

AVERTISSEMENTS D’ORDRE GÉNÉRAL

• Les orifices de ventilation ne doivent jamais être obstrués.

• Le masque doit être utilisé uniquement avec les appareils de PPC

ou à deux niveaux de pression recommandés par un médecin ou

un kinésithérapeute respiratoire.

• Le masque ne doit être porté que si l'appareil est sous tension.

Une fois le masque en place, s'assurer que l'appareil produit un

débit d'air. Explication : Les appareils de PPC et d’aide inspiratoire

avec PEP sont conçus pour une utilisation avec des masques (ou

raccords) spéciaux possédant des orifices de ventilation qui

permettent l’écoulement continu de l’air hors du masque. Lorsque

l'appareil est sous tension et qu'il fonctionne correctement, l'air

neuf provenant de l'appareil expulse l'air vicié par les orifices de

ventilation du masque. Cependant, lorsque l'appareil ne

fonctionne pas, le débit d'air propre délivré dans le masque est

insuffisant et une réinhalation de l'air expiré peut se produire. Si

la réinhalation d'air expiré dure plus de quelques minutes, elle

peut, dans certains cas, entraîner une suffocation. Cela s’applique

à la plupart des modèles d’appareils de PPC ou à deux niveaux de

pression.

• Prendre toutes les précautions applicables lors de l'adjonction

d'oxygène.

• L'arrivée d'oxygène doit être fermée lorsque l'appareil de PPC ou

à deux niveaux de pression n'est pas en marche afin d'empêcher

l'oxygène inutilisé de s'accumuler dans le boîtier de l'appareil et

de créer un risque d'incendie.

Français 3

• L'oxygène est combustible. Veiller à ne pas fumer ni approcher de

flamme nue près de l'appareil lors de l'utilisation d'oxygène.

L’adjonction d’oxygène ne doit avoir lieu que dans des salles bien

aérées.

• Lorsque l'adjonction d'oxygène est délivrée à un débit fixe, la

concentration de l'oxygène inhalé varie en fonction des réglages

de pression, de la respiration du patient, du masque, du point

d'arrivée de l'oxygène et du niveau de fuite. Cet avertissement

s'applique à la plupart des types d'appareils de PPC ou à deux

niveaux de pression.

• Les caractéristiques techniques de votre masque sont fournies

afin que votre prestataire de soins puisse vérifier que celui-ci est

compatible avec votre appareil de PPC ou à deux niveaux de

pression. L’utilisation du masque en dehors de ses

caractéristiques ou avec des appareils incompatibles peut

compromettre son étanchéité et son confort ainsi que l’efficacité

du traitement, et les fuites ou la variation du niveau de fuites

peuvent affecter le fonctionnement de l’appareil de PPC ou à deux

niveaux de pression.

• En cas de réaction indésirable QUELCONQUE au masque, cesser

de l'utiliser et consulter un médecin ou un spécialiste du sommeil.

• L’utilisation d’un masque peut provoquer des douleurs dans les

dents, les gencives ou la mâchoire ou aggraver un problème

dentaire existant. Si ces symptômes apparaissent, consulter un

médecin ou un dentiste.

• Comme c’est le cas avec tous les masques, une réinhalation peut

se produire à une pression PPC basse.

• Consulter le guide d'utilisation de l'appareil de PPC ou à deux

niveaux de pression pour davantage d'informations sur les

réglages et le fonctionnement.

• Retirer l'intégralité de l'emballage avant d'utiliser le masque.

• Le masque doit être utilisé sous le contrôle d'une personne

qualifiée si le patient n'est pas en mesure de l'enlever de

lui-même.

• Ce masque ne doit pas être utilisé chez les patients présentant

une altération du réflexe laryngé ou d'autres pathologies les

prédisposant à une aspiration en cas de régurgitation ou de

vomissement.

La page charge ...

ResMed AirFit N20 Mode d'emploi

Ce manuel convient également à

ResMed AirFit N20 Mode d'emploi

dans d''autres langues

Documents connexes

Autres documents