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1Introduction
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Introduction
The VPAP
TM
Auto 25, VPAP
TM
ST and the VPAP
TM
S are indicated for the treatment
of obstructive sleep apnea (OSA) in patients weighing more than 66 lb (30 kg). They
are 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.
!
WARNING
Read the entire manual before using these VPAP devices.
!
CAUTION (USA ONLY)
Federal law restricts these devices to sale by or on the order of a physician.
The VPAP System
The VPAP Auto 25, VPAP ST and the VPAP S comprise the following elements:
• VPAP device
• 6’6” (2 m) air tubing
• Power cord
• Travel bag
• ResScan™ Data Card.
Optional components include:
• 9’9” (3 m ) air tubing
• DC/DC converter 24V/50W
• ResMed Oxygen Connector Port.