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1Introduction
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Introduction
The VPAP
TM
IV and the VPAP
TM
IV ST are intended to provide non-invasive ventilation
for patients with respiratory insufficiency or obstructive sleep apnoea (OSA), in the
hospital or home.
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.
!
WARNING
Read the entire manual before using these VPAP devices.
The VPAP System
Both the VPAP IV and the VPAP IV ST systems comprise the following elements:
• VPAP device
• 2 m air tubing
• Power cord
• Travel bag
• ResScan™ Data Card
• ResMed Oxygen Connector Port.
Optional components include:
• 3 m air tubing
• DC/DC Converter 24V/50W.