Fisher & Paykel MyAIRVO 2 Tracheostomy Direct Interface

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Optiflow Tracheostomy Interface offers a humidified high flow therapy for tracheostomy patients. This patient interface is mainly used to deliver humidified respiratory gases.

Features:

• Evaqua technology - designed to reduce the formation of condensation
• 93% less condensate - connects to our AirSpiral™ breathing tube for 93% less condensate
• Stable Easy to use - re-designed sputum guard provides stability and ease of use
• Optimally humidified gas is delivered directly into the tracheostomy, minimising discomfort around the tracheostomy site
• Lightweight and extremely flexible interface tube
• Lanyard designed to take the weight of the circuit off the tracheostomy tube

Suggested Use:

• To ensure loading and movement on tracheostomy tube is kept to a minimum, make sure the lanyard is secured properly
• Lanyard position is not suitable for patients with damaged skin
• Connect to the humidification system
• Make sure all connections are secure
• If using an MR850, attach the tubing clip to the breathing circuit but ensure probe cable is not crushed by tubing clip
• Orientate the sputum guard so that sputum drains downwards
• The sputum guard can be removed if required

Warning:

• Appropriate patient monitoring must be used at all times
• Failure to monitor the patient may result in loss of therapy, serious injury or death
• Do not obstruct and or modify any part of the interface to avoid hypoxia from loss of therapy
• Do not use with an air entrainer, to avoid over-pressure
• Do not use near a naked flame, to avoid fires
• Do not crush or stretch tube, to prevent loss of therapy
• For single patient use only. Reuse may result in transmission of infectious substances
• Attempting to reprocess will result in degradation of materials and render the product defective
• The lanyard poses a potential risk of strangulation to vulnerable patients (e.g. children)
• The lanyard is designed to minimize loading and movement of the tracheostomy tube
• Secure the lanyard properly to avoid accidental decannulation or airway damage
• The sputum guard is intended to be detachable which may pose a choking risk

Caution:

• Failure to use the set-up described above can compromise performance and affect patient safety
• Before connecting the interface, check for adequate gas flow and ensure that the system has warmed up
• Check for condensate regularly
• Drain as required
• Do not use if packaging is not sealed

Hospital Use:

• This product is intended to be used for a maximum of 14 days
• Do not soak, wash or sterilise

Home Use: This product is intended to be used for a maximum of 30 days providing daily and weekly cleaning instructions are followed(Please see myAIRVO 2 User Manual).