NZ728499B2 - Mattress - Google Patents
Mattress Download PDFInfo
- Publication number
- NZ728499B2 NZ728499B2 NZ728499A NZ72849915A NZ728499B2 NZ 728499 B2 NZ728499 B2 NZ 728499B2 NZ 728499 A NZ728499 A NZ 728499A NZ 72849915 A NZ72849915 A NZ 72849915A NZ 728499 B2 NZ728499 B2 NZ 728499B2
- Authority
- NZ
- New Zealand
- Prior art keywords
- air
- holding portion
- mattress
- chambers
- way
- Prior art date
Links
- 239000012530 fluid Substances 0.000 claims abstract description 9
- 239000000463 material Substances 0.000 claims description 26
- 238000005086 pumping Methods 0.000 claims description 3
- 208000004210 Pressure Ulcer Diseases 0.000 abstract description 12
- 206010011985 Decubitus ulcer Diseases 0.000 abstract description 11
- 230000002265 prevention Effects 0.000 abstract description 3
- 210000000474 Heel Anatomy 0.000 description 24
- 238000007906 compression Methods 0.000 description 14
- 210000002683 Foot Anatomy 0.000 description 12
- 150000002500 ions Chemical class 0.000 description 10
- 239000006260 foam Substances 0.000 description 9
- 210000002414 Leg Anatomy 0.000 description 8
- 210000004197 Pelvis Anatomy 0.000 description 3
- 210000001699 lower leg Anatomy 0.000 description 3
- 210000003491 Skin Anatomy 0.000 description 2
- 229920002803 Thermoplastic polyurethane Polymers 0.000 description 2
- 239000004433 Thermoplastic polyurethane Substances 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 210000001519 tissues Anatomy 0.000 description 2
- 210000003423 Ankle Anatomy 0.000 description 1
- 210000004369 Blood Anatomy 0.000 description 1
- 210000000988 Bone and Bones Anatomy 0.000 description 1
- 210000001217 Buttocks Anatomy 0.000 description 1
- 210000001513 Elbow Anatomy 0.000 description 1
- 210000001624 Hip Anatomy 0.000 description 1
- 210000003205 Muscles Anatomy 0.000 description 1
- 229940116542 OTHER NUTRIENTS in ATC Drugs 0.000 description 1
- 206010031252 Osteomyelitis Diseases 0.000 description 1
- 210000002832 Shoulder Anatomy 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000003247 decreasing Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000006261 foam material Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 230000000607 poisoning Effects 0.000 description 1
- 231100000572 poisoning Toxicity 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 230000002035 prolonged Effects 0.000 description 1
- 230000003068 static Effects 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61G—TRANSPORT, PERSONAL CONVEYANCES, OR ACCOMMODATION SPECIALLY ADAPTED FOR PATIENTS OR DISABLED PERSONS; OPERATING TABLES OR CHAIRS; CHAIRS FOR DENTISTRY; FUNERAL DEVICES
- A61G7/00—Beds specially adapted for nursing; Devices for lifting patients or disabled persons
- A61G7/05—Parts, details or accessories of beds
- A61G7/057—Arrangements for preventing bed-sores or for supporting patients with burns, e.g. mattresses specially adapted therefor
- A61G7/05769—Arrangements for preventing bed-sores or for supporting patients with burns, e.g. mattresses specially adapted therefor with inflatable chambers
- A61G7/05776—Arrangements for preventing bed-sores or for supporting patients with burns, e.g. mattresses specially adapted therefor with inflatable chambers with at least two groups of alternately inflated chambers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61G—TRANSPORT, PERSONAL CONVEYANCES, OR ACCOMMODATION SPECIALLY ADAPTED FOR PATIENTS OR DISABLED PERSONS; OPERATING TABLES OR CHAIRS; CHAIRS FOR DENTISTRY; FUNERAL DEVICES
- A61G7/00—Beds specially adapted for nursing; Devices for lifting patients or disabled persons
- A61G7/05—Parts, details or accessories of beds
- A61G7/065—Rests specially adapted therefor
- A61G7/075—Rests specially adapted therefor for the limbs
- A61G7/0755—Rests specially adapted therefor for the limbs for the legs or feet
Abstract
mattress (100) comprises a first air-holding portion (102) and a second air-holding portion (104). The first air-holding portion comprises the approximate middle section of the mattress and the second air-holding portion comprises the foot portion of the mattress. The second air-holding portion further comprises a plurality of interconnected chambers wherein at least one of the chambers is larger than the other chambers and located closer to the middle section of the mattress than the other chambers, the chambers being in fluid communication such that air may flow in only one direction between the plurality of chambers. The first air-holding portion is connected to the second air-holding portion via a connecting portion (106) arranged with a one-way valve (108) to allow only one-way airflow from the first air-holding portion to the second air-holding portion. The first air-holding portion includes a one-way air inlet valve (112) and the second air-holding portion includes a one-way air outlet valve (114). The mattress assists in the prevention of pressure sores that can develop from external forces on a patient, resulting from direct pressure, shear and friction. This is achieved by relieving pressure on vulnerable areas by changing the patient position without requiring significant carer time or disturbing the patient. rther comprises a plurality of interconnected chambers wherein at least one of the chambers is larger than the other chambers and located closer to the middle section of the mattress than the other chambers, the chambers being in fluid communication such that air may flow in only one direction between the plurality of chambers. The first air-holding portion is connected to the second air-holding portion via a connecting portion (106) arranged with a one-way valve (108) to allow only one-way airflow from the first air-holding portion to the second air-holding portion. The first air-holding portion includes a one-way air inlet valve (112) and the second air-holding portion includes a one-way air outlet valve (114). The mattress assists in the prevention of pressure sores that can develop from external forces on a patient, resulting from direct pressure, shear and friction. This is achieved by relieving pressure on vulnerable areas by changing the patient position without requiring significant carer time or disturbing the patient.
Description
Mattress
Field of the Invention
The present invention concerns a ss arrangement
and mattress. More particularly, but not exclusively, this
ion concerns a mattress to assist in the prevention of
re sores, and a method of reducing pressure sores.
Background of the Invention
In hospitals and other care nments, patients who
are bed—bound or spend a long period of time confined to bed
can suffer from pressure sores, which are also known as
pressure ulcers. These are painful and attending to
pressure sores also diverts nurses and carers from other
tasks. The cost of attending to re sores can also be
high causing a strain on healthcare budgets.
Pressure sores develop as a result of external forces
on a patient, resulting from direct pressure, shear, and
friction, causing stresses and strain on the tissue. This
inhibits circulation and may prevent oxygen and other
nutrients from reaching the tissue. Common places for
pressure sores include bony protuberances, such as the
heels, ankles, hips, bottom, shoulders, elbows, back, and
back of the head of a patient. Prolonged pressure n
these pressure points and a mattress may result in red skin
which, in time, forms a blister, followed by an open sore.
The re sore can be painful for a patient, and also
destroy or damage the muscle and/or bone under the skin.
These may also become infected and cause potentially life—
threatening blood poisoning or bone infections.
The heels of a patient are particularly vulnerable to
pressure sores because of the small amount of flesh present
at the heels.
One way to prevent pressure sores is to reduce or
relieve the pressure on vulnerable areas. This may be by
moving the t and changing the patient position. One
way in which this can be achieved, t requiring
significant nurse or carer time, and without disturbing the
patient more than necessary, is by using special mattresses.
Conventional pressure relief sses include specialised
foam mattresses comprising a foam base and a lly
contoured foam insert on which the patient body is
ted. These mattresses may be known as static
mattresses. Although such mattresses may be effective at
preventing the development of pressure sores, some ts
may require more assistance to keep moving. Alternative
mattresses may be provided, such as an inflatable mattress.
These mattresses maybe known as dynamic mattresses. This
type of mattress comprises a series of inflated sections.
Such mattresses may be permanently inflated or the
inflatable sections may be partially or wholly
inflated/deflated using motorised pumps. Where a pump is
used, each inflatable section is in fluid communication with
the pump, the pump selectively inflating and deflating each
inflatable section thereby gently moving the patient
supported on the mattress. However, it is not practical to
supply every bed in a hospital or care home with an
inflatable mattress with a pump due to the significant costs
involved.
The present invention seeks to mitigate the above—
mentioned problems. atively or additionally, the
2015/050471
present ion seeks to provide an improved mattress and
mattress system for use in a hospital and/or care
environment.
Summary of the Invention
The present invention provides, according to a first
aspect, a mattress comprising:
a first air—holding portion;
a second air—holding n;
wherein the first air—holding portion comprises the
approximate middle section of the mattress and the second
air—holding portion comprises the foot portion of the
mattress;
the first air—holding portion connected to the second
air—holding portion via a connecting portion arranged to
allow only y airflow from the first air—holding
portion to the second air-holding portion;
wherein the first air—holding portion includes a one—
way air inlet valve and the second air—holding n
includes a one—way air outlet valve.
The skilled person will appreciate that the middle
portion of a mattress is the section in which the pelvis of
a user lying or sitting on a mattress would usually be
placed on, and the foot portion of the ss is the
section in which the feet of a user lying or g on a
mattress would y be placed on.
Preferably, the mattress is configured to allow passage
of air through the mattress in one direction only. The
first air—holding portion may take air in through the one—
way air inlet valve and push air into the second air—holding
2015/050471
portion, via the connecting portion. The second air—holding
portion may take air in from the first air—holding portion
and push air out of the one—way air outlet valve.
The one—way air inlet valve may be open to the
atmosphere. The one—way air outlet valve may be open to the
atmosphere. The mattress may be an “open” system, in that
air may be taken into the mattress from the atmosphere and
leave the mattress arrangement to the atmosphere.
The connecting portion may comprise a tube and a one—
way valve.
The first lding portion and second air—holding
portion may be made of an air impermeable material.
Advantageously, the first air—holding portion may be
compressible, for example in response to a patient g
or lying on the ss. Such compression may increase the
pressure within the first air—holding portion and cause the
first air—holding portion to pump air into the second air-
holding portion. Therefore, airflow through the mattress
may be tated using only the movement of a patient,
with no motorised pump required.
The first air—holding portion may comprise a r.
The first air-holding portion may comprise a ity of
interconnected chambers. The chambers may be interconnected
such that the chambers are in fluid communication with each
other. The interconnection may be such that air may flow in
any direction between the plurality of chambers.
atively, the interconnection may be such that air may
flow in only one direction between the plurality of
chambers. The chamber(s) comprising the first air—holding
portion may comprise an air—retaining material. The air—
retaining material may be a foam. The air—retaining
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material may be surrounded by an air impermeable material,
such as polyurethane or PVC. The first air—holding portion
may be resiliently deformable. The air—retaining material
may be resilient, such that under compression the material
is biased to return to an uncompressed position. The volume
of the first air—holding portion may be reduced under
ssion. The volume of the first air—holding portion
may be reduced under compression as air is pushed into the
second lding portion. The air—retaining material may
act to return the first air—holding portion to an
uncompressed volume on removal of the compression. The
first air—holding portion may take air in through the one-
way air inlet valve On removal of ssion.
The second air-holding portion may comprise a chamber.
The second air—holding portion may comprise a plurality of
interconnected chambers. At least one of the ity of
interconnected chambers may be larger than the other
interconnected chambers. The at least one larger
interconnected chamber may be located closer to the middle
n of the mattress than the other interconnected
The chambers may be interconnected such that the
chambers are in fluid communication with each other. The
interconnection may be such that the air may flow in only
one direction between the plurality of chambers. The
plurality of interconnected chambers may be interconnected
such that air may flow only in one direction between the
plurality of chambers, from the smaller chamber or chambers
to the larger chamber. The one-way air outlet valve may be
ated with the larger chamber.
The direction of airflow in the first air—retaining
portion may be opposite to the direction of airflow in the
second air—retaining portion. The second air—holding
portion may be deformable. The chamber(s) may be
substantially free of any air—retaining material. On
compression, the volume of the second air—holding n
may be reduced. The volume of the second air—holding
portion may be reduced under compression as air is pushed
out of the one—way air outlet valve. The volume of the
second lding portion may remain reduced on removal of
the compressive force. The re within the second air-
holding portion may reduce to substantially zero pressure
under compression. The volume of the second air-holding
portion may remain reduced on removal of the compressive
force until additional air is moved into the second air—
g portion by compression of the first air—holding
portion.
The middle section of a mattress may be the n of
the mattress which experiences the greatest pressure when
the mattress is used on an adjustable bed in a seating
position. The foot sectiOn of a mattress is the area of a
mattress in which a user of the mattress places their feet
in usual stances. As a patient sits or lies on the
first air—holding n they may compress the first air-
g portion such that air is pushed into the second air—
holding portion. The air pushed into the second air—holding
portion may increase the pressure within the second air—
holding portion. When the pressure within the second air—
holding portion increases to a certain level, air passes out
of the second air—holding portion via the one—way air output
valve. The pressure may increase to such a level due to the
passage of air from the first air—holding portion to the
second air—holding portion. Alternatively or additionally,
the pressure may increase to such a level due to the user
adjusting their position on the second air-holding portion
or simply the weight of the user acting on the second air—
holding portion. The pressure at which air passes out of
the second lding portion via the one-way air output
value may be in the range from 1mm Hg (millimetre of
mercury) to 25mm Hg. The pressure at which air passes out
of the second air—holding portion via the one—way air output
value may be in the range from 3mm Hg to 10mm Hg. The
pressure at which air passes out of the second air—holding
portion via the one—way air output valve may be 6mm Hg. The
pressure at which the air passes out of the second air—
holding portion via the one—way air output valve may be
determined by the rating of the air output valve. The one—
way air output valve may be rated according to any of the
ranges or valves described above.
According to a second aspect, there is provided a method of
2O pumping air through a mattress, the mattress according to
the first aspect of the invention, comprising the steps of:
compressing the first air—holding portion, y pushing
air into the second air—holding portion, and compressing the
second air—holding portion, thereby pushing air out of the
second air—holding portion into the atmosphere.
According to a third aspect, the invention provides a
method of reducing the pressure on the heels of a bed user,
the method sing the steps of providing a ss
according to the first aspect of the ion, a user lying
or sitting on the mattress, with their pelvis d on the
first air-holding n and their heels located on the
second air—holding portion, nt of the user compressing
the first air-holding portion, thereby pusing air into the
second air—holding portion, and pressure d by the user
on the second air—holding portion compressing the second
lding portion,.thereby pushing air out of the second
air holding portion into the atmosphere.
The second air—retaining portion may comprise a
plurality of interconnected chambers, with a larger chamber
located towards the middle of the mattress. The larger
chamber may be arranged to support the leg of the user above
their heels, for example, around their mid—calf. Supporting
the leg of the user above their heels may act to reduce the
pressure experienced by the heels of the user, thereby
helping to reduce pressure sores on the heels of a user.
The plurality of interconnected chambers may be arranged
such that pressure d by the heels of a user on the
second air—retaining portion pushes air from the smaller of
‘the interconnected chambers to the larger interconnected
chamber. Therefore, the heels of the user may initially
sink into the smaller of the interconnected chambers, and
the larger of the interconnected chambers may increase in
size to support the lower leg of the user. The heels of the
user may end up in t with the smaller of the
interconnected chambers, but essentially experiencing little
or no pressure as a result of the contact, due to the lower
leg support offered by the larger of the interconnected
chambers. The pressure d on the larger chamber by the
lower legs of the user may increase as the volume of air in
the larger chamber increases, causing the air outlet valve
ated with the larger chamber to release a ty of
air. The volume of the larger chamber will then reduce, and
the support provided to the lower legs se. As the
user moves, more air will be pumped from the first air—
retaining portion to the second air—retaining portion. This
will increase the pressure in the chamber or chambers
supporting the heels of the user. The heels of the user
will rise, and the cycle begins again, with the pressure on
the heels initially being raised and then reduced as air is
pumped into the larger of the interconnected chambers. The
ion in pressure on the heels of the user, together
with the gentle movement provided by the pumping action, may
significantly reduce the risk of re sores developing.
According to a fourth , the invention provides a
hospital bed, the hospital bed comprising a mattress as
described with s to the first aspect of the invention.
It will of course be appreciated that features
described in relation to one aspect of the present invention
may be incorporated into other aspects of the present
invention. For example, the method of the invention may
incorporate any of the es described with reference to
the mattress of the invention and vice versa.
Description of the Drawings
Embodiments of the present invention will now be
bed by way of example only with reference to the
accompanying schematic drawings of which:
Figure 1 shows a schematic View of a mattress arrangement
according to a first embodiment of the
invention;
_lO_
Figure 2 shows a schematic view of a mattress arrangement
according to a second embodiment of the
invention;
Figure 3 shows a mattress according to a third embodiment
of the invention comprising a mattress
arrangement according to the second embodiment
of the ion;
Figure 4 shows a cross—sectional view of the first air—
holding portion according to the first
embodiment of the invention;
Figure 5 shows a mattress ing to a fourth
embodiment of the invention, and
Figure 6 shows a cross-sectional view of the second air—
ing portion of the fourth embodiment of
the invention.
Detailed Description
Figure 1 shows a mattress comprising a ss
arrangement 100. The mattress arrangement 100 comprises a
first air—holding n 102 and a second air—holding
portion 104. The first air holding portion 102 is in fluid
communication with the second air—holding portion 104 via a
connecting portion comprising a tube 106, which includes a
one-way valve 108. The one way valve 108 allows air to flow
from the first air—holding portion 102 to the second air—
holding portion 104 via the tube 106, but does not allow air
flow in the reverse ion. Both the first air—holding
portion 102 and second air—holding portion 104 are made of
an air impermeable material, in this case thermoplastic
polyurethane (TPU) film. Alternative suitable materials may
2015/050471
-11..
be used, as will be appreciated by the skilled person, and
may include a number of plastics and/or rubber materials
provided the materials are suitably strong, resilient, and
air impermeable. The first air-holding portion 102 includes
an air—retaining material 110 in the form of a foam
material. An example air—retaining al is tion
modified high-resilience (CMHR) foam. The air—retaining
material 110 is porous and resiliently deformable. When
compressed, the air—retaining material 110 is reduced in
volume, but when the compressive force is removed, the air—
retaining material 110 returns to the al volume.
Figure 4 shows a potential cross—sectional profile of the
taining material 110. The profile of the cross—section
may be ed depending on the required physicalr
teristics for the foam.
The first air—holding portion 102 comprises a one—way
air intake valve 112. The oneeway air intake valve 112 is
open to the atmosphere and allows air to be drawn into the
first air—holding portion 102, but does not allow air to
leave the first air—holding portion 102. When the first
air—holding portion 102 is compressed, air passes via the
tube 106, through the valve 108, and into the second air-
holding portion 104. When the compressive force is removed
or reduced, the air retaining material 110 decompresses and
draws air into the first lding means 102 Via the one-
way air inlet valve 112.
The second air-holding portion 104 does not include any
air-retaining al. Other than the air impermeable
material and any air held within the second air—holding
portion 104, the second air—holding portion 104 is
substantially empty. If the pressure within the second air—
_12_
g n 104 s a n value, in this
embodiment 6mm Hg, air will begin to pass through the one—
way air outlet valve 114. The pressure within the second
air-holding means 104 may be increased due to either the
volume of the second air—holding means 104 being reduced by
compression, or due to the ingress of air which has been
pumped from the first air—holding portion 102. If the
second lding portion 104 is compressed, resulting in
the egress of air from the second air—holding portion 104,
the pressure within the second air—holding portion 104 may
reduce to substantially zero. Once compressed, the volume
and pressure within the second air—holding portion 104 will
not increase until air is pumped into the second lding
portion 104 from the first air—holding portion 102.
Figure 2 shows a schematic view of a second embodiment
of the invention. A mattress arrangement 200 comprises a
first air-holding n 202 and a second air—holding
portion 204. The first air—holding portion 202 comprises
three chambers 206, 208, and 210. Each of the chambers,
206, 208, 210, comprises a foam air—retaining material as
described for the air—holding portion 102 in relation to
figure 1. To improve clarity, the foam air—retaining
material is not shown in figure 2. The chamber 206 is
connected to a one—way air inlet valve 212 arranged to allow
air to flow into the chamber 206 but not out of the chamber
206. The chambers 206, 208, 210 are in fluid communication
with each other via tubes 214, 216, such that air may flow
between the chambers 206, 208, 210, in any ion. The
second air—holding means comprises three chambers 218, 220,
and 222. The chambers are connected to each other via tubes
224 and 226 which include one way valves. The one—way
_l3_
valves are arranged such that air may flow from chamber 218
to chamber 220, but not from chamber 220 to chamber 218.
Also air may flow from chamber 220 to chamber 222, but not
chamber 222 to r 220. Chamber 222 is connected to a
one—way outlet valve 230 which allows air to flow out of
chamber 222 but not into chamber 222. Therefore, airflow
through the second lding portion 204 is allowed in one
ion only. The chambers 218, 220, and 222, are
substantially empty apart from air, as described in relation
to the second air—holding portion 104 with reference to
figure 1. The first air—holding portion 202 and second air—
holding n 204 are connected via a connecting portion
comprising a tube 226 running between the chamber 210 and
chamber 218. The tube 226 includes a one—way valve 228
which allows air to pass from the first air—holding n
202 to the second air—holding portion 204, but not from the
second air—holding pdrtion 204 to the first air—holding
portion 202.
Figure 3 shows a mattress according to a third
embodiment of the invention. The mattress 300 comprises a
foam body 302, into which the mattress arrangement 200 has
been integrated. Not all of the features of the mattress
arrangement have been shown in figure 3 to e clarity.
The first air—holding portion 202 is located in the
approximate middle of the mattress 300. This is where the
buttocks of a patient will be d when the patient is
lying on the mattress 300. The second air—holding portion
204 is located at the foot of the ss 300. This will
be where the heels and feet of a patient will be located
when the patient is lying on the mattress 300. The mattress
300 may be placed on an adjustable bed, where the bed is
-14—
e of being laid fully flat, or in one or more
ted sitting positions. Whether the patient is in a
fully flat lying position or in a supported position, the
principles of operation of the mattress assembly 200 remain
the same.
The mattress may be covered by a stretchable fabric
cover to t the mattress. The stretchable fabric cover
may be chosen to be easily cleaned n patient
changeovers.
A significant portion of the weight of a patient will
be supported by the first air—holding portion 202. When a
patient moves, the first air—holding portion 202 may be
compressed. This compression of the first air—holding
portion 202 will increase the pressure within the rs
206, 208 and 210 until the one—way valve 228 is opened, and
air is pushed into the second air—holding portion 204. When
the patient moves again, the compression of the first air—
holding portion 202 may be reduced, and the chambers 206,
208, and 210 increase in volume under the action of the air—
ing material, drawing air in from the atmosphere via
the one—way air inlet valve 212.
The air pushed through the valve 228 enters the chamber
218 of the second air—holding n 204. If and when the
pressure inside the chamber 218 increases to the point of
g the valve in the tube 224, air will be pushed into
the chamber 220. Such a pressure increase may be as a
result of the movement of air from the first air—holding
portion 202. Alternatively or additionally, the pressure
increase may be caused by compression of the chamber 218 via
the movement of the feet of a patient, the feet being
supported by the second air—holding portion, or simply the
WO 16602
_15_
weight of the feet on chamber 218. This compression and
resultant w into chamber 220 may reduce the pressure
inside the r 218 to substantially nothing. Therefore,
the pressure on the heels and feet of a patient may be
significantly reduced. The amount of air within the chamber
218 will only increase if the first air—holding portion 202
pushes air through the tube 226. The amount of air within
the chamber 220 may be reduced in a similar way, such that
air may flow from the chamber 220 to the chamber 222. The
amount of air within-the chamber 224 is only reduced by
passage of air out of the chamber via the outlet valve 230,
open to the atmosphere. Therefore, it can be seen that the
first lding portion 202, acts, under the movement of a
patient, to pump air into the second air holding portion
204. The movement of a patient then acts to pump air out of
the second lding portion 204 into the atmosphere. The
movement of a patient over time results in the second air—
holding portion being increased and decreased in pressure
and volume in a similar way to that found in dynamic
pressure relief mattresses, but without requiring a powered
pump to be present.
Figure 5 shows a mattress ing to a fourth
embodiment of the invention. The mattress 500 ses a
first air-retaining portion 502 comprising a plurality of
interconnected rs 506, 508, 510, located in the
approximate middle of the mattress 500. An air inlet valve
is associated with the chamber 506, and each of the chambers
506, 508, and 510, include an air—retaining material as
described for the chambers 206, 208, and 210, of figure 3.
The ss 500 also comprises a second air—retaining
portion 504 which comprises a plurality of interconnected
-16...
chambers 518, 520, and 522. The chamber 510 is connected to
the chamber 522 via a tube and a one way valve, such that
compression of the chambers 506, 508, and 510, pumps air
into the chamber 522: The chamber 522 is fluidly connected
to the chamber 520 by a one way valve, arranged to allow air
to flow from the chamber 522 to the chamber 520. The
chamber 520 is connected to the chamber 518 by a one way
valve, ed to allow air to flow from the chamber 520 to
the chamber 518. The chamber 518 includes a one—way air
outlet valve, which is open to the atmosphere. As can be
seen in figure 6, the chamber 518 is larger than the chamber
520 and 522. This allows a user to rest their legs on the
second air—retaining portion 504 with their heels in contact
with one or both of the chambers 520, and also a part of
their lower leg, in this case mid—calf, in contact with the
r 518. A user may sit or lie on the mattress 500 with
their pelvis located over the first air—retaining portion
502. In this position, their heels will be located over the
second air—retaining n, as described with reference to
figure 6. When a user shifts position, they will ss
the first taining portion 502, causing air to be
pumped from the chambers 506, 508, and 510, into the chamber
522 of the second air—retaining portion 504. When the
pressure in the chamber 522 builds to the required level,
air will pass into the chamber 520 via the one-way valve
connecting the two chambers. The pressure within the
chamber 520 will increase accordingly. The weight of the
user’s heels on the r 520 will act to ss the
chamber 520, causing air to be pumped from the chamber 520
into the chamber 518 via the one—way valve connecting the
two chambers. This will lift the lower legs of the user,
-17—
reducing pressure on the feels, which with the reduction of
re in the r 520 means that the pressure
experienced by the heels of the user is much reduced,
tending to zero. Once the pressure within chamber 518
increases to a certain level, air will escape through the
air outlet valve. Movement of the user will pump air from
the first air—retaining portion 502 into the chamber 522,
and the cycle will begin again, with the lower legs and
heels of the user being moved and the pressure experienced
by the heels and lower legs of the user being varied
accordingly.
Whilst the present invention has been described and
illustrated with reference to particular embodiments, it
will be appreciated by those of ordinary skill in the art
that the invention lends itself to many different variations
not specifically illustrated herein. By way of example
only, certain possible ions will now be described. In
the description above, the second air—holding portion is
located at the foot of the mattress. In alternative
embodiments, the second air—holding n may be d
at any area in which reduced pressure is required or
desired. For example, the second air—holding portion may be
located at the head of a mattress.
In an alternative ment, the mattress arrangement
may be a modular arrangement, thereby allowing the
configuration of the mattress to be adjusted according to
the ular needs of a patient for which the mattress
arrangement is intended. The modular arrangement may
provide a ss system which is configurable in
dependence on the weight and/or size of a patient. The
modular arrangement may comprise a number of connectable and
-18—
disconnectable tubes, chambers, and valves. The
configuration may se adjusting the size or position of
the mattress elements in relation to a patient.
Alternatively or additionally, the pressures required to
pump air through the mattress arrangement may be adjusted by
selection of the als from the first air—holding
portion and/or second air holding portion may be made, and
the ratings of the valves and tubes included in the ss
arrangement.
Where in the foregoing description, integers or
ts are mentioned which have known, obvious or
foreseeable equivalents, then such equivalents are herein
incorporated as if individually set forth. Reference should
be made to the claims for determining the true scope of the
present invention, which should be construed so as to
encompass any such equivalents. It will also be appreciated
by the reader that rs or features of the ion
that are described as preferable, advantageous, convenient
or the like are optional and do not limit the scope of the
independent claims. Moreover, it is to be understood that
such optional integers or features, whilst of possible
benefit in some embodiments of the invention, may not be
desirable, and may ore be absent, in other
embodiments.
Claims (11)
1. A mattress comprising: a first air-holding portion; a second air-holding portion; wherein the first air-holding portion comprises the approximate middle section of the mattress and the second air-holding portion comprises the foot portion of the ss, the first air-holding portion connected to the second air-holding portion via a connecting portion ed to allow only one-way airflow from the first air-holding portion to the second air-holding portion; wherein the first air-holding portion includes a one- way air inlet valve and the second air-holding portion includes a one-way air outlet valve, wherein the second air-holding portion comprises a plurality of interconnected chambers, n at least one of the plurality of interconnected chambers is larger than the other interconnected chambers and the at least one larger chamber is located closer to the middle portion of the mattress than the other interconnected chambers, the chambers being interconnected such that the rs are in fluid communication with each other, and the interconnection is such that the air may flow in only one direction between the plurality of
2. A mattress as claimed in claim 1, wherein the one-way air inlet valve is open to the here.
3. A mattress as claimed in claim 1 or claim 2, wherein the one-way air outlet valve is open to the atmosphere.
4. A mattress as claimed in any preceding claim, wherein the first air-holding portion comprises a plurality of interconnected chambers.
5. A mattress as claimed in claim 4, n the chambers are interconnected such that the chambers are in fluid communication with each other.
6. A mattress as claimed in claim 4 or claim 5, wherein the chambers sing the first lding portion comprise an air-retaining material.
7. A mattress as claimed in claim 1, wherein the chambers are interconnected such that air may flow only in one direction between the ity of chambers, from the smaller chamber or chambers to the larger chamber.
8. A mattress as claimed in claim 7, wherein the one-way air outlet valve is associated with the larger chamber.
9. A mattress as claimed in any preceding claim, n the second air-holding portion is substantially free of any air retaining material.
10. A method of pumping air through a mattress arrangement, the mattress arrangement according to any of claims 1 to 9, sing the steps of: compressing the first lding portion, thereby pushing air into the second airholding n, and compressing the second air-holding portion, thereby pushing air out of the second airholding portion into the atmosphere.
11. A hospital bed comprising a mattress as claimed in any of claims 1 to 9. WO 16602
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1413414.2 | 2014-07-29 | ||
GBGB1413414.2A GB201413414D0 (en) | 2014-07-29 | 2014-07-29 | Mattress |
PCT/GB2015/050471 WO2016016602A1 (en) | 2014-07-29 | 2015-02-18 | Mattress |
Publications (2)
Publication Number | Publication Date |
---|---|
NZ728499A NZ728499A (en) | 2021-01-29 |
NZ728499B2 true NZ728499B2 (en) | 2021-04-30 |
Family
ID=
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