The present disclosure relates to support slings, lifting apparatus, and methods of repositioning a human bed occupant, particularly a patient confined to a bed for extended time period(s) with limited mobility.
Prolonged bed rest without adequate mobilization is often associated with increased risk of pressure ulcers and/or injuries, pulmonary complications including hypoxia and atelectasis, and hospital-acquired infections such as ventilator-associated pneumonia. Pressure ulcers are a type of injury that breaks down the skin and underlying tissue when an area of skin is placed under constant pressure (either shear, compression or a combination of the two) for a certain period, causing tissue ischemia, cessation of nutrition and oxygen supply to the tissues and eventually tissue necrosis. In short, distortion or deformation damage results from pressure sustained over an extended time period. Pressure ulcers caused by pressure due to excessive duration of little or no movement can take an exceedingly long time to heal as well as add significant cost to the provider. To reduce the risk of these ailments for patients unable to mobilize themselves sufficiently, treatment has often included caregivers manually repositioning patients at regular intervals. In other cases, automated components such as powered articulating frames and inflatable bladders have been integrated into patient support apparatus to vary pressure over areas of a patient's body.
Present treatment options for pressure ulcers include various approaches of cleaning the wound, debridement, optimized dressings, role of antibiotics and reconstructive surgery. The newer treatment options such as negative pressure wound therapy, hyperbaric oxygen therapy, cell therapy have been discussed, and the advantages and disadvantages of current and newer methods have also been described.
However, replacing an existing bed with such apparatus can be expensive and labor intensive. In addition, an apparatus that merely varies pressure from under a patient's body may fail to provide certain benefits associated with a caregiver manually turning the patient, such as increased airflow, improved fluid drainage, increased blood flow, and reduced temperature and maceration at areas of a patient's body that are shifted entirely away from contact with a mattress or other support surface when the patient is turned.
According to an aspect of the disclosure [ACCORD claim 1 UPON APPROVAL OF CLAIMS]
Although the characteristic features of this disclosure will be particularly pointed out in the claims, the disclosed method and system, and how it may be made and used, may be better understood by referring to the following description taken in connection with the accompanying drawings forming a part hereof, wherein like reference numerals refer to like parts throughout the several views and in which:
A person of ordinary skill in the art will appreciate that elements of the figures above are illustrated for simplicity and clarity and are not necessarily drawn to scale. The dimensions of some elements in the figures may have been exaggerated relative to other elements to help to understand the present teachings. Furthermore, a particular order in which certain elements, parts, components, modules, steps, actions, events and/or processes are described or illustrated may not be required. A person of ordinary skills in the art will appreciate that, for simplicity and clarity of illustration, some commonly known and well-understood elements that are useful and/or necessary in a commercially feasible embodiment may not be depicted to provide a clear view of various embodiments per the present teachings.
In the following description of various non-limiting examples of embodiments of the disclosed systems and methods, reference is made to the accompanying drawings, which form a part hereof, and in which are shown by way of illustration various example devices, systems, and environments in which aspects of the disclosed systems and methods can be practiced. Other specific arrangements of parts, example devices, systems, and environments can be used, and structural modifications and functional modifications can be made without departing from the scope of the disclosed systems and methods.
As illustrated in the accompanying drawings and described herein, the present disclosure provides a patient repositioning system for shifting the weight of a patient on prolonged bed rest bed with limited self-mobility. The system includes a support assembly and a lifter apparatus, the support assembly being disposed between the patient and a mattress on the bed, and the lifter apparatus being operative to lift at least a portion of the support assembly so as to shift the patient's weight from the mattress to the support assembly. More particularly, the support assembly includes a frame and a sling attached to the frame. The frame can include an assembly of interconnected frame members that is movably connected to a fixed base. For example, such interconnected frame members can be frame poles and a headboard as described herein, the frame poles being connected between a headboard, and the base. A footboard can be adjustably connected to the frame, such as by connecting to the frame poles at a selected position along their lengths, illustrated here as being selected from a continuous range of available positions, but which in other embodiments could be a finite number of positions distributed along the lengths of the frame poles. The sling, headboard, base, and footboard, can constitute (sub)assemblies unto themselves, being constructed from multiple parts as in the illustrated embodiment. In other embodiments, one or more of them can be formed in one piece. In one illustrated embodiment, the system further includes an adapter assembly, referred to below as a spreader bar adapter assembly, which is operative to connect between an existing spreader bar of a lifter apparatus and the support assembly so as to lift the support assembly in a desired manner. Intended to be used for bed bound patients having the propensity to develop pressure ulcers, this newly designed device modifies localized pressure in the areas normally prone to restricted blood flow when a patient is not capable of repositioning under their own power; thus aiding the prevention and/or healing of pressure sores/ulcers. Further beneficial effects include increased airflow in the patient's midsection, lowered skin temperatures, as well as potentially increased pressure to the legs and feet.
A patient repositioning system 10 as illustrated in the accompanying drawing figures will now be described. As shown in
The frame base 14 is operative to be anchored or affixed to a foot end of a bed or bed frame B, such as using well-known tie-down straps as shown in
As best seen in the detailed perspective and side-elevation schematic views of the support frame 12 in
The sling 16 is shown in detail in
In the illustrated embodiment, lateral connecting regions 32 of the sling 16 are placed over the foot and head segments 28, 30 along corresponding portions of their respective lengths and retained by hook-and-loop (such as Velcro® or similar) type fasteners. Likewise, the head end connecting region 35 of the sling 16 is similarly placed over and connected to the frame head board 22 by a hook-and-loop fastener connection. Complementary patches of the hook-and-loop type fasteners are affixed respectively to the sling connecting regions 32, 35 (such as by stitching) and to the corresponding members of the frame 12 (such as by adhesive). In other embodiments of a support assembly, a sling can be attached to a frame using any other suitable method, including but not limited to grommets over hooks imbedded in the poles, a rope or ropes threaded and/or tied between the sling and frame, or other such devices.
The lateral stabilizer cushions 45, which may, for example, be formed as fabric tubes filled with a soft material (e.g., cotton or other batting material), attached to a top side of the flexible sheet 24 by suitable means such as hook-and-loop fasteners or stitching, provide raised soft obstructions to restrain sliding movement of a person supported on the sling 16 when the sling is tilted to one side in accordance with a system and method of the disclosure.
The hanging straps 47 can be, for example, straps of nylon or polyester webbing stitched at one end to a lateral side of the sling 16, each folded over and stitched to itself at an opposite end to form a loop or eyelet. Straps 47 attached to the sling 16 at a plurality of points along each lateral side, such as four points as shown in
The lateral connecting regions 32 extend longitudinally over substantially an entire length of each lateral side of the sling 16, with gaps provided to accommodate a respective pair of attachment points of a lifting harness 39 of each frame pole 20, each of which connects to a suitable lifter for lifting a patient on the support assembly 11 according to systems and methods described in more detail below. When attached to the frame poles 20 in this manner, the sling 16 is operative to bear all or substantially all of a patient's weight, and to transmit the patient's weight to the frame poles, without the sling 16 breaking or its connecting portions separating from the frame poles 20.
When the support assembly 11 is passively in place under a patient on the bed B (that is, when the lifter is disconnected and/or not applying any lifting force) so that the frame 12 is not bearing any of the patient's weight, it can be desirable to move one or both frame poles 20 out of the way to provide a caregiver unobstructed access to a patient's side(s). To facilitate this access, one or both lateral connecting regions 32 of the sling 16 can be removable from a central section 41 of the sling 16 that includes the flexible sheet 24. In the illustrated embodiment, the sling 16 comprises a pair of quick-disconnect lateral sections 49, each lateral section 49 comprising the connecting regions 32 of the respective lateral side of the sling 16 and being removably connected to the central section 41 along its respective lateral side by a zipper 37. Similarly, the head end connecting region 35 can also be conveniently removable from the central region of the sling 16, by a zipper or other suitable removable connection (removable connection not shown). Either frame pole 20 can thus be freed from the flexible sheet 24 without detaching the connecting regions 32 from the frame pole 20, by simply unzipping the corresponding zipper 37 and sliding the frame head board 22 off of the frame pole 20 (if necessary, first freeing the frame head board 22 from the flexible sheet 24 before sliding it off of the frame pole 20, by detaching the head end connecting region 35 of the sling from the frame head board 22, or in other embodiments not shown, from the central section 41 of the sling 16). This allows the selected frame pole 20 to be pivoted forwardly away from the flexible sheet 24, independently of the other frame pole 20 and the frame board 22, or to be removed entirely by further disconnecting the frame pole 20 from the base 14, thus providing a caregiver unobstructed access to the corresponding side of a patient on the flexible sheet 24. Alternatively, both lateral sections 49 of the sling 16 can be disconnected from the central section 41, and either the head end connecting region 35 of the sling detached from the frame head board 22, or in embodiments not shown, a head end section of the sling comprising the head end connecting region 35 similarly disconnected from the central section 41, thus freeing the entire patient support frame 12 to be pivoted forwardly away from the flexible sheet 24 as a unit, for access to a patient thereon from three sides, without the need to slide the frame head board 22 off of either frame pole 20. In other embodiments of a support assembly according to this disclosure, a sling can connect to the frame poles and head board using other suitable connectors and/or other suitable techniques as known in the art.
In embodiments, the support assembly is constructed in appropriate dimensions and of suitable materials to be able to lift individuals of different weight (such as a three-hundred-pound person or a four-hundred-pound person) supported on the sling to a position in which the sling initially loses contact with a top side of a mattress, so as to shift all of the person's weight off of the mattress and provide a small air gap, such as a one-inch air gap, between the sling and the mattress. Without limitation, suitable materials for base, frame poles, and headboard include metal, wood, PVC, and similar materials. For example, the foot and head segments 28, 30 can be 1.5-inch by 0.75-inch extruded aluminum bars, connected by a suitable hinge (such as a marine hinge) fastened to their adjacent top sides. The segments 28, 30 can have lengths of, for example, about forty-six inches and thirty-three inches, respectively, so that the frame poles 20 have a total length of about seventy-nine inches. The sling 16 can be constructed of canvas and/or felt, with the interior region 26 comprising a suitable mesh fabric or other breathable and liquid permeable material, and the elastic lumbar strap 43 comprising any suitable stretch material.
When the sling 16 is attached to the frame poles 20 and frame head board 22 as described, the flexible sheet 24 is operative to extend over a sufficient area of a back side of a patient's body to comfortably lift the patient's weight entirely off the bed B, preferably so that the bottom side of the sling is just out of contact with the top side of the mattress at the lowest point where the top side of the sling touches the patient's body. More particularly, the flexible sheet 24 covers a large enough area to extend from below the patient's buttocks to above the patient's head when the patient is supported on the mattress, with the joints of the frame poles 20 approximately aligned with the patient's hip joints, when the patient is supported on the mattress as well as when the patient is suspended above the mattress and supported on the sling 16. Still more particularly, the flexible sheet 24 extends from below the patient's knees (such as from a mid-calf region or lower) to above the patient's head when the patient is so positioned.
As seen in the detailed view of the frame 12 of
In addition, the foot support 18 further comprises a hook-and-loop fastener patch 44 formed on its foot engaging surface 38. According to an embodiment illustrated in
According to aspects of the present disclosure, a support assembly can be used: (A) For patient transfer, in conjunction with various suitable external lifting devices; (B) For patient repositioning from a mattress to a sling in conjunction with various suitable external lifting devices; and (C) For patient repositioning from a mattress to a sling and tilting the sling to a desired side, in conjunction with an external lifting device according to this disclosure. A lifting device suitable for use according to aspect (A) or (B) can be any one of a variety of interchangeable automated external lifters, including existing lifters, such as any of several patient lifts available under the names Hoyer, Liko, Invacare, and others. A suitable lifter typically includes a lifter base, at least one motor/motive device, and at least one spreader bar that is driven up and down by the motive device. The spreader bar is operative to connect to the support assembly and to transmit a lifting force from the motive device to the support assembly to raise the support assembly with a patient supported thereon. The motor or motive device can be electromagnetic, hydraulic, pneumatic, or of any other suitable type.
In an embodiment of a patient repositioning system and method according to this disclosure, as illustrated in
More particularly, as mentioned previously, each frame pole 20 includes an integrated lifting harness 39 (illustrated as a cable harness assembly, while other types of lifting connectors are possible, while a flexible and/or collapsible tension linkage is preferred, such as a strap, cord, band, rope, chain, or a combination thereof, so that the lifting connector does not inhibit the patient support frame from being passively lifted and/or folded up to a sitting position from below, such as when a mattress under the patient support frame is itself raised and/or folded up to a sitting position by a powered bed frame) with lower ends, the lower ends being connected to at least one attachment point on each of the foot segment 28 and head segment 30 (illustrated as one attachment point per segment, but more attachment points are possible in other embodiments), respectively, of the corresponding frame pole 20. The spacing between the connectors 54 corresponds to a width of the support frame 12, allowing each connector 54 to connect to a respective one of the connectors 39 of the assembled support frame 12 and to pull straight up on each frame pole 20 via the connectors 39 while the adapter spreader bar 52 is raised by an external lifter, from which it is suspended by attaching the connectors 56 to a pair of more narrowly spaced apart connecting features 57 of an external lifter spreader bar 58.
According to another aspect of the invention, a new lifter is provided for use with a support assembly according to the previously described aspect. In an embodiment shown in
Each linear actuator 68 has a corresponding fixed member, illustrated as a cylinder 72, and a corresponding extension member movably connected to the fixed member for movement in opposed linear extension and retraction directions to extended and retracted positions, the extension member in the extended position having a non-overlapping length segment extending distally past a distal end of the fixed member, the extension member in the retracted position having an overlapping length segment extending proximally past the distal end of the fixed member. The extension member is illustrated as a piston 74, the cylinder 72 being connected to and supported on the corresponding lifter base 66, the piston 74 being operative to extend upwardly from and retract downwardly into the cylinder 72 (“upward,” “upwardly,” “downward,” and “downwardly” will be understood to be inclusive of approximately vertical directions, such as within ten degrees, preferably within five degrees, or still more preferably within two degrees of the vertical, positive z direction). The upper ends of the pistons 74 are connected to the suspension bar 70 at laterally spaced apart positions, in the opposite lateral end regions 76 of the suspension bar 70.
A suspension bar according to this disclosure is adapted to be connected to lateral support members of a patient support frame, such as those of the patient support frame 12 of the previously described embodiment. More particularly, a suspension bar can include connectors to connect directly to a harness or the like of each lateral support member, or the suspension bar and the lateral support member can be adapted to connect to a pair of hangers that are in turn connected to the lateral support members so as to transmit tensile loads from the lateral support members to the suspension bar. Such hangers can be constructed as assemblies; thus, a pair of hanger assemblies 78 are shown in
The linear actuators 68 are operative to extend and retract the pistons 74 out of and into their respective cylinders 72, each independently of the other, so as to independently raise and lower the opposite lateral end regions 76 of the suspension bar 70, either by different amounts or by the same amount of vertical displacement as desired, so as to raise and lower the connectors 39 and their corresponding frame poles 20 by the same amount or different amounts of vertical displacement, and thus to different elevations. As follows, the lifter 64 can thus produce bidirectional rotational adjustments of the frame 12, and the sling 16 supported thereon; that is, pivoting of the frame 12 about a transverse (x) axis and rotation of the distal/head end of the frame 12 about a longitudinal (y) axis.
The first bidirectional rotational adjustment is pivoting of the frame 12 about a transverse (x) axis where the frame pole forward ends 25 are connected to the frame base 14, which effects raising and lowering the angle of inclination of the sling 16 relative to the bed B. Thus, when it is desired simply to shift the weight of a patient off of a mattress and onto the sling 16, the linear actuators 68 can be operated so as to extend and retract the pistons 74 at the same time, by the same amounts, thus raising and lowering the frame poles 20 suspended from the lifting harnesses 39 upwardly and downwardly by equal distances, so as to produce the same change in angle of inclination of each frame pole 20 about the transverse (x) axis. In this manner, the weight of a supine or upright seated patient can be lifted slightly off of the mattress, while remaining approximately centered on the patient's body (e.g., aligned with the patient's spine) and downwardly directed between the frame poles 20.
The second bidirectional rotational adjustment is rotation of the frame 12 about a longitudinal (y) axis, to the right or left side. This effects turning a patient toward that side, and/or laterally shifting the patient's weight so as to laterally shift the distribution of pressure over areas of the patient's body closer to that side. Thus, when it is desired to shift a patient's weight laterally and/or turn a patient, the linear actuators 68 can be operated to extend or retract the pistons 74 by different amounts so as to raise or lower the connectors 39 and their corresponding frame poles 20 by different amounts, which in turn tilts the flexible sheet 24 of the sling 16 toward the lower frame pole 20, as best seen in
The preceding description of the disclosure has been presented for purposes of illustration and description and is not intended to be exhaustive or to limit the disclosure to the precise form disclosed. The description was selected to best explain the principles of the present teachings and practical application of these principles to enable others skilled in the art to best utilize the disclosure in various embodiments and various modifications as are suited to the particular use contemplated. It should be recognized that the words “a” or “an” are intended to include both the singular and the plural. Conversely, any reference to plural elements shall, where appropriate, include the singular.
It is intended that the scope of the disclosure not be limited by the specification, but be defined by the claims set forth below. In addition, although narrow claims may be presented below, it should be recognized that the scope of this disclosure is much broader than presented by the claim(s). It is intended that broader claims will be submitted in one or more applications that claim the benefit of priority from this application. Insofar as the description above and the accompanying drawings disclose additional subject matter that is not within the scope of the claim or claims below, the additional disclosures are not dedicated to the public and the right to file one or more applications to claim such additional disclosures is reserved.
This application claims the priority benefit of U.S. provisional patent application No. 63/435,249, filed Dec. 24, 2022 and entitled PATIENT REPOSITIONING SYSTEM AND METHOD, the entire contents of which are hereby incorporated by reference herein for all purposes.
Number | Date | Country | |
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63435249 | Dec 2022 | US |