14
7
To Remove the System from the Bed
Take the following steps to remove the system from the bed.
1. Ensure gloves are worn and all disinfection and occupational health and
safety protocols of the facility are adhered to.
2. If necessary clean and disinfect following instructions in previous
section.
3. Turn off the power switch on the side of the control unit and turn the
power off at the wall plug
4. Disconnect electrical cords from control unit and wall outlet. Also
disconnect the breakaway power cord from the head end of the
mattress and store in bag.
5. Disconnect CPR hose connector from side of pump and allow system to
deflate. It may be necessary to roll mattress from head end to squeeze
out any remaining air.
6. Once most air is removed, roll up mattress from head end to foot end
ensuring hose tube and electrical cord is tucked into the last roll.
7. Once rolled up - fit the mattress into the main compartment of the bag.
8. Lastly, remove the control unit from the foot board and place in the
special padded compartment at the front of the bag.
Storage
Store the system in its wheeled bag in a cool, dry area. Ensure that no
heavy items are placed on top of the bag during storage.
Mattress Removal
Safety Protocols
Important Recommendations for General Use of System
Mattress:
Do not place any layers of material between the patient and top cover
of the mattress! Doing so will compromise therapy!
This includes the following:
i) Hospital sheets - regular or fitted
ii) Sheepskins or equivalent
iii) Incontinence sheets
iv) Slide sheets
v) Electric heating blankets
The mattress top cover is fully sealed and designed for the patient to
lie directly on top. All that is required is an antibacterial wipe-down or
machine wash when necessary. See Care Section for more information.
Ensure the patient’s clothing does not cause skin damage due to ties,
buttons, creases, seams, objects in pockets and jewellery
Do not place any sharp items on or near the mattress such as syringes
or scalpels or any instrument that could hole the top cover
Do not place any solid item/s on top of the system besides the patient
Do not spill any liquids onto the control unit. If a spillage occurs then:
i) Turn off power to the control unit at the wall
ii) Disconnect the power cord from the control unit
iii) Wipe dry any excess moisture on the external casing
iv) Check that the interior of the power connector, plug and switch is dry
Failure to do the above may lead to component corrosion and or
electrical safety hazards to carers and patients
Do not use system in the presence of any flammable anaesthetic
mixture with air, nitrous oxide or oxygen or in the presence of smoking
materials or open flame - risk of explosion
Control Unit
Do not open the control unit as there is risk of electric shock. Control
units should only be opened by approved technicians or warranty will be
voided
Avoid blocking the air intake filter at the rear of the control unit
Ensure that the power leads are undamaged and properly connected
6
15
Recommended Usage
Indications
The Theraflow alternating mattress replacement standard model MRS-
TFW-001 is indicated for patients weighing between 40 and 180kg.
The system is designed for large area reperfusion therapy in patients
suffering from Stage 1 to Stage 4 pressure areas, or assessed at high risk of
exhibiting these conditions.
In addition - patients suffering from low blood flow or ischemia in the
extremities may also benefit from the application and release of pressure to
encourage blood flow in these areas.
Contra-Indications
Patient conditions for which the Theraflow alternating mattress
replacement would be contra-indicated would be the following.
• Non-stable spinal cord injury
• Cervical traction
• Any patient exhibiting unease or agitation on alternating surfaces
• Patients weighing under 40kg or over 200kg or otherwise too wide for a
standard single (<90cm) mattress width.
Intended Care Setting
The following care settings are recommended for the Theraflow alternating
mattress replacement system.
• Home care
• Aged care facilities
• Palliative care
• Long term or extended rehabilitation
• General hospital
• Intensive Care Units
Service Schedule
Service Schedule
The Theraflow alternating mattress replacement has been designed for
easy maintenance and service. The following schedule should be used as a
guide for maintaining the optimal performance of the system.
When Necessary and between Patient Use
• On site clean and disinfection of top cover, base and control unit casing.
see previous cleaning and disinfection instructions.
Do not use system without top cover attached.
• Inspection of top cover and base for any strike through or damage.
• Inspection of coverlet for soiling or contamination - clean or replace.
• Inspection of electrical cords for proper connection, damage and any
possible interference with moving bed parts
• Inspection of elastics. Between patient use or every 4 months -
turn mattress over and see through base windows the condition and
attachment of the elastics. If any are detached, re-attach. If any are
frayed or corrugated at the edges, replace those elastics.
Air Filter Replacement
To maintain optimal performance of the control unit,
it is recommended that the air filter, located at the
rear of the unit be checked, cleaned or replaced
every 6 to 12 months depending on the air quality
where the system is being used.
1. Using a paperclip wire or similar
insert in the edge notch and flip
the cover off the filter casing.
2. Remove the cover and turn upside down
and inspect - clean if discoloured.
3. To clean, remove the foam filter from inside
the cover. This filter can either be washed
or air cleaned and re-inserted after dry or
otherwise replaced.
