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ResMed lumis series User Manual

ResMed lumis series
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English 1
ENGLISH
Welcome
The Lumis
VPAP ST-A is a bilevel positive airway pressure device.
WARNING
Read this entire guide before using the device.
Use the device according to the intended use provided in this guide.
The advice provided by your prescribing doctor should be followed ahead of the
information provided in this guide.
This device is not suitable for ventilator-dependent patients.
Indications for use
Lumis 150 VPAP ST-A
The Lumis 150 ST-A device is indicated to provide non-invasive ventilation for patients weighing
more than 13 kg or more than 30 kg in iVAPS mode with respiratory insufficiency or obstructive
sleep apnoea (OSA). It is intended for home and hospital use.
Lumis 100 VPAP ST-A
The Lumis 100 ST-A device is indicated to provide non-invasive ventilation for patients weighing
more than 13 kg with respiratory insufficiency or obstructive sleep apnoea (OSA). It is intended for
home and hospital use.
The humidifier is intended for single patient use in the home environment and re-use in a
hospital/institutional environment.
Clinical benefits
The clinical benefit of CPAP and bilevel PAP therapy for the treatment of OSA is a reduction in
apnoeas, hypopnoeas and sleepiness, as well as improved quality of life.
The clinical benefits of bilevel therapy for the treatment of respiratory insufficiency may include;
improvement in overall survival, daytime symptoms, blood gases, health-related quality of life and
sleep quality, and a decrease in hospitalisations and dyspnoea.
The clinical benefit of humidification is the reduction of positive airway pressure related side effects.
Intended patient population/medical conditions
Obstructive pulmonary diseases (eg, Chronic Obstructive Pulmonary Disease), restrictive pulmonary
diseases (eg, diseases of the lung parenchyma, diseases of the chest wall, neuromuscular
diseases), central respiratory regulation diseases, obstructive sleep apnoea (OSA) and obesity
hypoventilation syndrome (OHS).
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.

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ResMed lumis series Specifications

General IconGeneral
Device TypeNon-invasive ventilator
Pressure Range4-25 cm H2O
ModesCPAP, S, ST, T, iVAPS
Ramp Time0-45 minutes
HumidificationIntegrated heated humidifier
Data StorageSD card
Power SupplyAC 100-240V, 50-60Hz
Weight1.3 kg
Operating AltitudeUp to 2, 591 m
Heated TubingCompatible with ClimateLineAir heated tubing
ConnectivityBluetooth
DisplayLCD

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