ResMed VPAP ST Technisches Handbuch

English

VPAP™ST / VPAP™S

POSITIVE AIRWAY PRESSURE DEVICE

Information Guide

English • Deutsch • Français • Italiano

English

Please read the entire Information and Welcome Guides before using your device.

VPAP ST indications for use

The VPAP ST is intended to provide non-invasive ventilation to patients weighing more than 13 kg

with respiratory insufficiency or obstructive sleep apnoea (OSA). The VPAP ST is intended for home

and hospital use.

VPAP S indications for use

The VPAP S is intended to provide non-invasive ventilation to patients weighing more than 13 kg with

respiratory insufficiency or obstructive sleep apnoea (OSA). The VPAP S is intended for home and

hospital use.

Contraindications

Positive airway pressure therapy may be contraindicated in some patients with the following pre-

existing conditions:

•severe bullous lung disease

•pneumothorax or pneumomediastinum

•pathologically low blood pressure, particularly if associated with intravascular volume depletion

•dehydration

•cerebrospinal fluid leak, recent cranial surgery, or trauma.

Adverse effects

Patients should report unusual chest pain, severe headache, or increased breathlessness to their

prescribing physician. An acute upper respiratory tract infection may require temporary

discontinuation of treatment.

The following side effects may arise during the course of therapy with the device:

•drying of the nose, mouth, or throat

•nosebleed

•bloating

•ear or sinus discomfort

•eye irritation

•skin rashes.

Troubleshooting

If there is a problem, try the following suggestions. If the problem cannot be solved, contact your

equipment supplier or ResMed. Do not attempt to open the device(s).

Problem/possible cause Solution

No display

Power is not connected. Ensure the power cable is connected and the power outlet

(if available) is on.

The DC plug is partially inserted into

the back of the device or inserted too

slowly.

Fully insert the DC plug.

Insufficient air delivered from the VPAP device

Ramp time is in use. Wait for air pressure to build up or change ramp time.

Air filter is dirty. Replace air filter.

Air tubing is not connected properly. Check air tubing.

Air tubing is blocked, pinched or

punctured.

Unblock or free the air tubing. Check the air tubing for

punctures.

Mask and headgear are not positioned

correctly.

Adjust position of mask and headgear.

Incorrect air tubing selected. If you are using the SlimLine, Standard or 3m air tubing

ensure that you have the correct air tubing selected via the

menu.

Device does not start when you breathe into the mask

Breath is not deep enough to trigger

SmartStart/Stop.

Take a deep breath in and out through the mask.

English

Problem/possible cause Solution

There is excessive leak.

Note: If Leak Alert is enabled, an

audible alert is activated and a high

leak message is displayed.

Adjust position of mask and headgear.

Air tubing not connected properly. Connect firmly at both

ends.

SmartStart/Stop is disabled.

Note: SmartStart/Stop is not available

if Leak Alert is enabled.

Enable SmartStart/Stop.

Device does not stop when you remove your mask

SmartStart/Stop is disabled.

Note: SmartStart/Stop is not available

if Leak Alert is enabled.

Enable SmartStart/Stop.

SmartStart/Stop is enabled but the device does not stop automatically when you remove your

mask

Incompatible mask system being

used.

Only use equipment recommended by ResMed.

The patient is using a nasal pillows

mask or pediatric mask with a set

pressure less than 7 cm H2O.

Disable SmartStart/Stop.

Pressure rises inappropriately

Talking, coughing or breathing in an

unusual manner.

Avoid talking with a nasal mask on, and breathe as normally

as possible.

Mask cushion is buzzing against the

skin.

Adjust the headgear.

Cushion seated incorrectly causing

excessive leak.

Adjust headgear or re-fit cushion.

Displays error message: High temperature fault, refer to user manual

Device has been left in a hot

environment.

Allow to cool before re-use. Disconnect the power cord and

then reconnect it to restart the device.

Problem/possible cause Solution

Air filter is blocked. Replace your air filter. Disconnect the power cord and then

reconnect it to restart the device.

Air tubing is blocked. Check your air tubing and remove any blockages. Disconnect

the power cord and then reconnect it to restart the device.

Humidifier setting is too high,

resulting in accumulation of water in

the air tubing.

Turn the humidifier setting down and empty the water from

the air tubing.

Displays error message: Check ResMed Power Supply Unit and fully insert the connector

The DC plug is partially inserted into

the back of the device or inserted too

slowly.

Fully insert the DC plug.

A non-ResMed power supply unit is

connected to the device.

Remove the power supply unit and replace with a ResMed

power supply unit.

The power supply unit is being

covered by bedding.

Make sure that the power supply unit is free from bedding,

clothes or other objects that could cover it.

Displays error message: Tube blocked, please check your tube

Air tubing is blocked. Check your air tubing and remove any blockages. Disconnect

the power cord and then reconnect it to restart the device.

Displays error message: High leak, please check system setup and all connections

There is excessive leak. Adjust position of mask and headgear.

Air tubing is not connected properly. Connect firmly at both

ends.

The following message is displayed on the LCD after you try to update settings or copy data to

the SD card: Card error, please remove SD card and contact service provider

SD card is not inserted correctly. Ensure that the SD card is inserted correctly.

You may have removed the SD card

before settings were copied to the

VPAP device.

Reinsert the SD card and wait for the Home screen or the

“Settings updated successfully, press any key”message

to appear on the LCD.

Note: This message only appears once. If you re-insert the

SD card after you have updated your settings, the message

will not be re-displayed.

English

Problem/possible cause Solution

The following message is NOT displayed on the LCD after you try to update the settings using

the SD card: Settings updated successfully, press any key

The settings were not updated. Contact your clinician/service provider immediately.

General technical specifications

Power supply

90W power supply unit

Input range: 100–240V, 50–60Hz, 110V, 400Hz nominal for aircraft use

Typical power consumption: 70W (80VA)

Maximum power consumption: 110W (120VA)

30W power supply unit

Input range: 100–240V, 50–60Hz, 110V, 400Hz nominal for aircraft use

Typical power consumption: 20W (30VA)

Maximum power consumption: 36W (75VA)

90W DC/DC converter

Nominal inputs: 12V, 24V

Typical power consumption: 70W (80VA)

Maximum power consumption: 110W (120VA)

Environmental

conditions

Operating temperature: +5°C to +35°C

Operating humidity: 10 to 95% non-condensing

Operating altitude: Sea level to 2,591m

Storage and transport temperature: -20°C to +60°C

Storage and transport humidity: 10 to 95% non-condensing

Aircraft use ResMed confirms that the device/s meets the Federal Aviation Administration

(FAA) requirements (RTCA/DO-160F, section 21, category M) for all phases of air

travel.

Electromagnetic

compatibility

Product complies with all applicable electromagnetic compatibility requirements

(EMC) according to IEC60601-1-2, for residential, commercial and light industry

environments. Information regarding the electromagnetic emissions and

immunity of this ResMed device can be found on www.resmed.com,on the

Products page under Service and Support. Click on the PDF file for your

language.

IEC 60601-1

classification

Class II (double insulation), Type BF

VPAP technical specifications

Pressure and

flow state

Operating pressure range (measured at the mask): 4–20 cm H2O (CPAP),

2–25 cm H2O (VPAP)

Maximum single fault steady state pressure: 30 cm H2O (CPAP) - if pressure

exceeded for > 6 sec; 40 cm H2O (VPAP) - if pressure exceeded for >1 sec

Pressure measurement tolerance: ±0.5 cm H2O ± 4% of the measured reading

Flow measurement tolerance: ±6 L/min or 10% of reading, whichever is greater,

at 0 to 150 L/min positive flow

Mode reading CPAP mode

Set Pressure: 4 to 20 cm H2O

S, ST and T modes

IPAP: 4 to 25 cm H

O; EPAP: 2 to 25 cm H

Physical Nominal dimensions (L x W x H): 153 mm x 140 mm x 86 mm

Weight: 835 g

Housing construction: Flame retardant engineering thermoplastic

Air outlet: 22 mm conical air outlet (complies with ISO 5356-1:2004)

Air filter Hypoallergenic air filter: Acrylic and polypropylene fibers in a polypropylene

carrier

Standard air filter: Polyester non-woven fiber

Sound

DECLARED

DUAL-NUMBER

NOISE EMISSION

VALUES in

accordance with

ISO 4871: 1996

Pressure level (CPAP mode)

With SlimLine tube: 24 dBA as measured according to ISO 17510-1:2002

26 dBA with uncertainty of 2 dBA as measured according

to ISO 17510-1:2007

With Standard tube: 24 dBA as measured according to ISO 17510-1:2002

27 dBA with uncertainty of 2 dBA as measured according

to ISO 17510-1:2007

With either SlimLine

or Standard tube and

H5i:

27 dBA as measured according to ISO 17510-1:2002

28 dBA with uncertainty of 2 dBA as measured according

to ISO 17510-1:2007

English

Power level (CPAP mode)

With SlimLine tube: 34 dBA with uncertainty of 2 dBA as measured according

to ISO 17510-1:2007

With Standard tube: 35 dBA with uncertainty of 2 dBA as measured according

to ISO 17510-1:2007

With either SlimLine

or Standard tube and

H5i:

36 dBA with uncertainty of 2 dBA as measured according

to ISO 17510-1:2007

Supplemental

oxygen

Recommended maximum supplemental oxygen flow: 15 L/min

Air tubing technical specifications

ClimateLine SlimLine ClimateLineMAX Standard 3 m

Maximum

recommended

pressure

25 cm H2O 25 cm H2O 25 cm H2O 25 cm H2O 25 cm H2O

Inner diameter

15 mm

19 mm

Length 1.98 m 1.8 m 1.91 m 2.0 m 3.0 m

Material Flexible

plastic and

electrical

components

Flexible plastic Flexible plastic

and electrical

components

Flexible

plastic

Flexible

plastic

Heated tubing

temperature cut-

out

≤41°C ≤41°C

Notes:

•The manufacturer reserves the right to change these specifications without notice.

•The temperature and relative humidity settings displayed for ClimateLine / ClimateLineMAX are not

measured values.

•Check with your clinician/service provider before using the SlimLine air tubing with devices other

than the S9 or H5i.

•The electrical connector end of the heated air tubing is only compatible with the H5i air outlet and

should not be fitted to the device or mask.

•When using the SlimLine or ClimateLine above 20 cm H2O, the device optimum performance may

not be reached if used with an antibacterial filter. The device performance must be checked prior

to prescribing the SlimLine or ClimateLine for use with an antibacterial filter.

Humidifier performance

The following settings have been tested at 22°C, 40% RH ambient conditions:

Mask pressure

cm H2O

RH output % Nominal system output AH

, BTPS

Setting 3 Setting 6 Setting 3 Setting 6

100

10 95 100 11.5 21

20 95 100 11 18

25 100 100 12 13.5

a. AH - Absolute Humidity in mg/L.

b. BTPS - Body Temperature Pressure Saturated.

Pneumatic flow path

1. Inlet filter

2. Blower

3. Tube

4. Mask

Flow (maximum) at set pressures

The following are measured at the end of the specified tubing:

Pressure, cm H2OVPAP and

Standard air

tube, L/min

VPAP and

SlimLine air tube,

L/min

VPAP, H5i and

ClimateLine

heated air tube,

L/min

VPAP, H5i and

Standard air

tube, L/min

4 200 195 170 170

200

190

170

12 200 184 170 170

16 200 175 170 170

20 190 168 161 170

180

144

125

161

English

Displayed values

Value Range Accuracy Display resolution

Pressure sensor at air outlet

Pressure 2 to 25 cm H2O ±0.5 cm H2O (±4% of

measured value)

0.2 cm H2O

Flow derived values

Leak 0–120 L/min b1 L/min

Tidal volume 0–4000 mL ±10% 0.02 L

Respiratory rate 0–50 BPM ±0.5 BPM

1 BPM

Minute ventilation 0–30 L/min ±10% 0.1 L/min

Ti Avg 0.1–4.0 sec ±10% 0.1 sec

a. Results may be inaccurate in the presence of leaks or supplemental oxygen.

b. The displayed values are estimates. They are provided for trending purposes only.

c. Results may be inaccurate if the tidal volume is below 50 mL.

Pressure accuracy

Maximum static pressure variation at 10 cm H2O according to ISO 17510-1:2007

Without humidifier (SlimLine tube) 9.76 cm H

O to 9.87 cm H

With H5i humidifier (SlimLine tube) 9.78 cm H

O to 9.88 cm H

Maximum dynamic pressure variation according to ISO 17510-1:2007

Pressure (cm H2O)

10 BPM

15 BPM

20 BPM

VPAP and SlimLine tube without H5i / VPAP and SlimLine tube with H5i

4 0.22 / 0.20 0.28 / 0.29 0.47 / 0.53

8 0.23 / 0.19 0.32 / 0.29 0.41 / 0.42

12 0.22 / 0.21 0.35 / 0.29 0.41 / 0.45

0.22 / 0.23

0.41 / 0.33

0.44 / 0.50

20 0.24 / 0.27 0.37 / 0.34 0.48 / 0.50

25 0.31 / 0.31 0.50 / 0.54 0.78 / 0.84

Symbols

The following symbols may appear on your product or packaging.

Caution; Read instructions before use; Drip proof; Not drip proof;

Type BF equipment; Class II equipment; Start/Stop; Manufacturer;

European RoHS; Lot number; Part number; Serial number;

Direct current; Lock/unlock; China pollution control logo 1;

China pollution control logo 2.

Environmental information

WEEE 2002/96/EC is a European Directive that requires the proper disposal of electrical and electronic

equipment. This device should be disposed of separately, not as unsorted municipal waste. To

dispose of your device, you should use appropriate collection, reuse and recycling systems available

in your region. The use of these collection, reuse and recycling systems is designed to reduce

pressure on natural resources and prevent hazardous substances from damaging the environment.

If you need information on these disposal systems, please contact your local waste administration.

The crossed-bin symbol invites you to use these disposal systems. If you require information on

collection and disposal of your ResMed device please contact your ResMed office, local distributor or

go to www.resmed.com/environment.

Servicing

The VPAP device is intended to provide safe and reliable operation when operated in accordance with

the instructions provided by ResMed. ResMed recommends that the VPAP device be inspected and

serviced by an authorised ResMed Service Centre if there is any sign of wear or concern with device

function. Otherwise, service and inspection of the devices generally should not be required during the

five year design life of the device.

Andere Handbücher für VPAP ST

Dieses Handbuch passt für folgende Modelle

Inhaltsverzeichnis

Sprachen:

Andere ResMed Medizinische Geräte Handbücher

ResMed

ResMed AirFit N30 Bedienungsanleitung

ResMed

ResMed VPAP IV ST Betriebsanleitung

ResMed

ResMed Mirage SoftGel Bedienungsanleitung

ResMed

ResMed Mirage Activa LT Bedienungsanleitung

ResMed

ResMed VPAP III ST-A Bedienungsanleitung

ResMed

ResMed NV Elbow F20 Bedienungsanleitung

ResMed

ResMed AirSense 11 Bedienungsanleitung

ResMed

ResMed Airtouch F20 Bedienungsanleitung

ResMed

ResMed Mirage SoftGel Bedienungsanleitung

ResMed

ResMed Swift FX Nano Montageanleitung

ResMed

ResMed AutoSet CS-A Bedienungs- und Sicherheitshinweise

ResMed

ResMed Lumis 100 VPAP S Bedienungsanleitung

ResMed

ResMed S8 AutoSet Spirit II Bedienungsanleitung

ResMed

ResMed S8 ESCAPE S8 Bedienungsanleitung

ResMed

ResMed ResScan Bedienungsanleitung

ResMed

ResMed AirSense 11 Bedienungsanleitung

ResMed

ResMed H5i Technisches Handbuch

ResMed

ResMed AirSense 10 Bedienungsanleitung

ResMed

ResMed Swift FX Nano Bedienungsanleitung

ResMed

ResMed H5i Bedienungsanleitung

ResMed

ResMed AirFit N20 Bedienungsanleitung

ResMed

ResMed ApneaLink Bedienungsanleitung

ResMed

ResMed AirFit F30 Bedienungsanleitung

ResMed

ResMed stellar series Bedienungsanleitung

Beliebte Medizinische Geräte Handbücher anderer Marken

TekTone

TekTone Tek-CARE160 Bedienungsanleitung

NeuroMetrix

NeuroMetrix Quell 2.0 Bedienungsanleitung

AMT

AMT XLR8 Bedienungsanleitung

EDAN

EDAN SONOTRAX Pro Bedienungsanleitung

Restorative Therapies

Restorative Therapies RT300 Bedienungsanleitung

Gendex

Gendex Expert DC Bedienungsanleitung

Dexcowin

Dexcowin ADX4000W Bedienungsanleitung

Libelium

Libelium MySignals Bedienungsanleitung

Acelity

Acelity V.A.C.ULTA 4 Bedienungsanleitung

Caputron

Caputron ActivaDose II tDCS Bedienungsanleitung

Plinth 2000

Plinth 2000 93CDT Bedienungsanleitung

GE SENOGRAPHE 800T Bedienungsanleitung

GE Definium 5000 Bedienungsanleitung

Kanmed

Kanmed GE-1380 Bedienungsanleitung

Huntleigh

Huntleigh FD1 Bedienungsanleitung

Stryker

Stryker SPR Plus Bedienungsanleitung

Tobii Dynavox

Tobii Dynavox I-Series Bedienungsanleitung

S-Capepod

S-Capepod Evac Cocoon Bedienungsanleitung