The present invention relates to a cushioning device, such as an overlay for a mattress, which includes an integrated restraint structure.
Flick et al. disclose in U.S. Pat. No. 6,739,001 a mattress system 10 having a fluid cushion 12 connected to a first restraint 14 and a second restraint 16 positioned on a patient support device 17 (i.e., a bed frame) with railings 18 as illustrated in
The fluid cushion 12 has a head end 20, a foot end 22, a middle area 24, a right side 26, a left side 28, a top surface 30 and a bottom surface 32. The fluid cushion can be a plurality of air bladders, an air bladder with interior welds, low loss air bladders with or without interior welds, or any other conventional fluid cushion material. Examples of such cushions include and are not limited to Gaymar Industries, Inc.'s Airflo pad, Paradise pad, and Aire-Twin mattress bladders.
The first restraint 14 is positioned on the cushion's right side 26 and the second restraint 16 is positioned on the cushion's left side 28. Respectively, the restraints 14, 16 can (a) extend the entire length of the right side 26 and left side 28 as illustrated in
The restraints 14, 16 have a top surface 50, a bottom surface 52, an interior surface 54 and an exterior surface 56. The restraints 14, 16 can be fluid bladders, foam, foam beads, gels, batting, or other suitable materials for inhibiting and/or restraining a user from rolling (a) off the long term support device 17 and/or (b) into the area between the fluid cushion 12 and the railing 18. What ever the restraint material, the restraints 14, 16 are attached and/or interconnected to the cushion 12 to ensure the restraints perform as a restraint.
Where the cushion attaches and/or interconnects to the restraints is a critical issue. Flick et al. explicitly disclose the cushion's top surface 30 is always below the restraint's top surface 50.
Gaymar Industries, Inc. has learned that a restraint makes it difficult to transfer a patient. Many individuals complain about lifting a patient over the restraint member.
For a number of years, Gaymar has been manufacturing its Sof-Matt RSM Low-Air-Loss Mattress System as illustrated in
The air pump provides air to the air bladder at least at two different inflation modes. The first inflation mode is referred to as maximum volume. At maximum volume, the air bladder's top surface 66 is planar to the crib's top surface 64 as illustrated in
A cushioning device having a first deep cell inflatable bladder, a first restraint structure, a pump and an attachment. The first deep cell inflatable bladder has a first side, a second side, an upper surface and a lower surface. The first restraint structure has a top surface and a bottom surface. The pump has (a) a maximum inflation mode that inflates the first deep cell inflatable bladder so the bladder's upper surface and the first restraint's top surface are in or approximately in the same plane and (b) a normal operating inflation mode that provides sufficient inflation to (A) prevent the first bladder's upper surface from contacting the first bladder's lower surface, (B) decrease (i) the formation of debuticus ulcers on a patient and (ii) the patient's tissue interface pressure, and (C) allow the restraint structure to inhibit and/or restrain the patient from rolling off the first deep cell inflatable bladder. The attachment attaches at least a portion of the first bladder's first side to the first restraint structure at a predetermined distance below the first restraint's top surface so (A) the first restraint during the normal operating mode inhibits and/or restrains the patient from rolling off the first deep cell inflatable bladder, and (B) the first restraint and first deep cell inflatable bladder provide lateral stability to allow the patient to get in and out of the cushioning device and facilitating patient transfers during the maximum inflate mode.
a is a top view of a second prior art mattress system of a crib surrounding air bladders at maximum inflation mode.
b is a cross-sectional view of
The cushioning section 120 has at least one inflatable bladder 122. Each inflatable bladder 122 has a top surface 124, a bottom surface 126, a left side 128, a right side 130, a head side 132, and a foot side 134. There can be one bladder (
The inflatable bladder 122 is a deep cell inflatable bladder. A deep cell inflatable bladder is preferably at a minimum five inches in height.
The first restraint 110 is positioned adjacent to and attached 99a to the cushioning section's right side 144 and the second restraint 112 is positioned adjacent to and attached 99b to the cushion's left side 146, as best seen at
The restraints 110, 120 extend the entire length of the right side 144 and left side 146 as illustrated in
The bladder 122 and the restraints 110, 112 are attached 99 (a) directly to each other through heat welding, sonic welding, stitching or other conventional attachment methods used in the mattress industry or (b) indirectly to each other for example through a strap. The strap has a first end and a second end. The first end attaches to the bladder 122 and the second end attaches to the respective restraints 110, 120. The straps are attached to the bladder or restraints through heat welding, sonic welding, stitching, other conventional attachment methods used in the mattress industry or combinations thereof. The attachment 99 should be sufficient to withstand the pressures applied by a patient positioned on the restraint/cushioning system 100 and the internal pressure provided by the fluid pump 114.
The fluid pump 114 inflates the bladders through at least two inflation modes. The first inflation mode is maximum inflate. Maximum inflate means every bladder 122 is fully inflated which results in every bladder's top surface 124 being on or within approximate area of the same plane as the restraint's top surface 150 as illustrated in
The second inflation mode is the normal operating mode. The normal operating mode provides sufficient inflation to prevent the patient from bottoming out and sufficient pressure to decrease (a) the formation of debuticus ulcers and (b) the tissue interface pressure. The tissue interface pressure decreases because the hammock effect is avoided.
The hammock effect is avoided and the restraints perform as restraints when the pump is in the normal operating mode, which involves attaching 99 the bladder 122 to each restraint's 110, 112 interior surface 154 at a first predetermined distance (x) below the restraint's top surface 150 and a second predetermined distance (y) above the restraint's bottom surface 152.
The first predetermined distance x is the distance below the restraint's top surface 150 wherein the restraint 110, 120 during the normal operating mode performs as a restraint as illustrated in
That first predetermined distance x is not near or at the restraint's top surface 150 because that creates a hammock effect which is undesired for reasons set forth in the background of the invention and inhibits the restraint from performing as a restraint. The first predetermined distance x is also not near the restraint's bottom surface 152 because then the desired lateral stability is not obtained for patient transfer. That means the first predetermined distance x ranges from about three inches below the restraint's top surface 150 and the first predetermined distance x does not enter into the range of the second predetermined distance y.
The second predetermined distance y is an area in which if the attachment 99 is positioned the bladders 122 and the restraint 110, 120 do not provide the desired lateral stability in the maximum inflation mode. There is a balance between lateral stability during maximum inflation mode and restraint capabilities during normal operating mode. Balancing those two issues have not been addressed in the past until now.
The restraint capability has to be obtained. It has been determined that about 3 inches is a minimum length for the first predetermined distance x. The minimum about three inches allows the restraint 110, 120 to provide the desired restraint characteristics during normal operating mode—inhibiting a patient from rolling off the cushion 120 (and possibly falling off the bed configuration and/or falling between the cushion and the bed configuration's railings 18 (item 18a illustrates an embodiment when the railing 18 is lowered.)
When the restraint is 5 inches high, the cushion 120 is the minimum 5 inches high and the first predetermined distance x for the attachment 99 between the cushion and the restraint is at a minimum about three inches; the restraint and the cushion provides the desired stability for transferring a patient during maximum inflate mode; and the restraint provides the desired restraint characteristics during normal operating mode.
In an alternative embodiment, the cushioning section 120 may be comprised of multiple side-by-side bladders 122 as illustrated in
In another embodiment of the present invention, the cushioning section 120 may include a plurality of pin holes or micro-vents in its top surface 124 to produce a gentle flow of air beneath the user and to minimize moisture build-up.
In yet another alternative embodiment of the present invention, the cushioning section 120 may be of the alternating pressure type, i.e., it has at least two series of alternating cells, which are alternately inflated and deflated, one series of cells being inflated while the other series of cells is deflated. Such alternating pressure type cushions are disclosed, for example, in U.S. Pat. Nos. 5,794,289 and 5,901,393, which are hereby incorporated by reference in their entirety.
There have also been provided cushion and pump combinations in which alternate air chambers are alternately inflated and deflated to relieve excess pressure on patients at risk of developing pressure ulcers or to relieve excess pressure on patients with pressure ulcers (e.g., the Airflo Alternating Pressure System from Gaymar Industries, Inc.). Micro-vents and/or low air loss tubes may also provided to produce a gentle flow of air beneath the patient to help minimize moisture build-up.
In a further embodiment of the present invention, the cushioning section 120 may include a device for measuring the internal pressure of the cushioning section 120. Typically, such devices activate a light when the internal pressure of the cushioning section 120 is below a certain level, indicating a bottoming condition. The device may be integrated into the valve through which fluid is being fed into the cushioning section 120. Such devices are well known in the art and are described, for example, in U.S. Pat. No. 5,140,309, which is hereby incorporated by reference in its entirety.
Rotating the patient on an inflatable mattress is also a well known method to avoid bed sores on immobile patients. Such a method is disclosed, for example, in U.S. Pat. Nos. 5,794,289 and 6,079,070which are commonly assigned and incorporated by reference.
Although preferred embodiments have been depicted and described in detail herein, it will be apparent to those skilled in the relevant art that various modifications, additions, substitutions, and the like can be made without departing from the spirit of the invention and these are therefore considered to be within the scope of the invention as defined in the claims which follow.
This application claims priority to U.S. provisional patent application Ser. No. 60/927,577, filed on May 4, 2007.
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