The present invention relates to line management device, and more particularly to a line management device that can hold tubing, namely tubing used during medical treatment and/or patient monitoring.
Current line management devices are formed from generally inelastic material, such as plastics or resins, which can break overtime and, in some cases, can create a pinch point for a caregiver when inserting a tube into the device. The devices also inherently pose a cleaning challenge due to its multiple and tight surfaces.
Accordingly, a line management device is provided that includes a body with one or more slots for receiving tubing and which is configured to deflect when subject to a side load or deform when mounted to a curved surface but without affecting the shape of the slots.
In one form, a line management device includes a body with one or more slots extending into the body. The body includes a base, which is adapted to releasably mount the device to a support surface. The base is configured to adapt to a non-planar surface without affecting the shape of the slot.
In another form, a line management device includes a body with one or more slots extending into the body. The body extends from a base, which is adapted to releasably mount the device to a support surface. The body and base are configured to allow the body to deflect relative to the base but without affecting the shape of the slot.
In any of the above, the body includes a plurality of slots. Further, the size of the slots may vary in length and/or width. In yet a further aspect, one or more of the slots may be color coded for a specific use.
In any of the above, the body and the base may be monolithic. For example, the body and the base made be formed from a foam, such as cross-linked polyethylene foam or a urethane foam and further can be molded, such as cast molding or injection molding. Alternately, the body and the base may be formed together as a hollow member from a thin polymer material, such as plastic. The density of the foam may vary, for example, in a range of about 1-6 lbs./ft3, of about 2-5 lbs./ft3, or about 3-4 lbs./ft3.
In any of the above, the body and the base may have an antimicrobial component, such as by a coating, such as MICROBAN or by incorporating antimicrobial components, such as antimicrobial powder, antimicrobial bodies, antimicrobial elements, such as wires, etc. into the body and/or base during the forming process. Suitable antimicrobial component may be formed from silver, copper, or their alloys or the like.
In any of the above, the body may have a generally cylindrical shape with a curved outer surface and a central axis extending generally parallel to the curved outer surface, with the slots extending into the curved outer surface.
In any of the above, the body may have a thickness in a range of about ¾″ to 2″, or any dimension in between, including about 1″ or about 1½″.
In any of the above, the device may have a height in a range of about 1½″ to 3½″, or any dimension in between including in a range of about 2″ to 3″ inches, or about 2½″.
In any of the above, the body may have a generally cylindrical shape with a curved outer surface and a central axis extending generally parallel to the curved outer surface, with the slots extending into the curved outer surface.
In any of the above, the base may comprise a generally planar member. For example, the base may have a thickness in a range of ⅛″ to ½″, or any dimension in between including in a range of about 3/16″ to ⅜″ or about ¼″.
In any of the above, the base may have a length in a range of 1″ to 3″, or any dimension in between including in a range of about 1½″ to 2½″ or about 2″.
In any of the above, the base may have a width in a range of about ¾″ to 2″, or any dimension in between, including about 1″ or about 1½″.
In any of the above, the base may have an adhesive layer to mount the device to a support surface. For example, the adhesive surface may be provided by a double-sided adhesive tape or the adhesive may be applied to the base with a release paper over the adhesive.
Before the embodiments of the invention are explained in more detail below, it is to be understood that the invention is not limited to the details of operation or to the details of construction and the arrangement of the components set forth in the following description or illustrated in the drawings. The invention may be implemented in various other embodiments and is capable of being practiced or being carried out in alternative ways not expressly disclosed herein. Also, it is to be understood that the phraseology and terminology used herein are for the purpose of description and should not be regarded as limiting. The use of “including” and “comprising” and variations thereof is meant to encompass the items listed thereafter and equivalents thereof as well as additional items and equivalents thereof. Further, enumeration may be used in the description of various embodiments. Unless otherwise expressly stated, the use of enumeration should not be construed as limiting the invention to any specific order or number of components. Nor should the use of enumeration be construed as excluding from the scope of the invention any additional steps or components that might be combined with or into the enumerated steps or components.
Referring to
As best seen in
Referring to
In the illustrated embodiment, body 12 includes multiple slots, including one slot 16 with a rounded end and with a width that is suitable for inserting and holding larger tubing, such as breathing liens or arterial lines. The other slots 14 are configured with a tear drop shape with a width and height to accommodate multiple, stacked smaller tubes, such as IV tubing. As would be understood, with multiple slots, the material between the slots can then form fingers that can easily flex and tilt about their base at the end of the slots in the direction of the unoccupied slot.
Device 10 also includes a base 18, which in the illustrated embodiment is integrally formed with body 12 so that the body and the base are monolithic. Device 10 optionally includes a tapered transition between the body and the base so base 18 is wedge shaped, and body 12 may deflect relative to base 18, for example when device is impacted by a load, such as when a caregiver bumps into the device. One result is that the body can deflect relative to the base but without affecting the shape of the slots.
For example, the body and the base may be molded as a unitary member and be formed from an elastic material, such as foam or structural gel. A suitable structure gel may include a SEB, SEBS, SEP, SEPS, SEEP, SEEPS polymer combined with a mineral oil, for example, as is commonly known in the gel art. A suitable foam includes a cross-linked polyethylene foam or a urethane foam. The density of the foam may vary, for example, in a range of about 1-6 lbs./ft3, of about 2-5 lbs./ft3, or about 3-4 lbs./ft3. In either case, the device can be molded, such as cast molding or injection molding. When formed from urethane foam, device may be formed with a conventional in-mold coating, which could include antimicrobial properties. Suitable antimicrobial coatings may include MICROBAN. During the forming process, the material surrounding the slots may be formed using a different color, as noted above, to provide color coding. Alternately, the color coding can be applied post forming.
Alternately, the body and the base may be formed, such as by molding, as a hollow member from a thin polymeric material, such as plastic. For example, the wall thickness may range from several thousands of an inch to tens of thousands of an inch, for example in a range of 10/1000th of an inch to 50/1000th of an inch so that the body and base can compress and deflect in a similar manner as described above.
Base 18 is adapted to releasably mount the device to a support surface, for example a hospital bed barrier, such a side rail, footboard, and/or headboard. For example, the base may have an adhesive layer, including a 2 sided adhesive tape, that releasably mounts the device to a support surface, such as a double-side adhesive tape or an adhesive applied to the base with a release paper over the adhesive. Alternately, the device may incorporate a COMMAND STRIP, available from 3M.
Further, the base may be configured to adapt to a non-planar surface, for example, to an IV pole or IV pole mount. For further details of another embodiment of the line management device that is formed as a pole mount version reference is made to
As noted above, when forming device 10, device 10 may be covered with a coating that has antimicrobial properties. Alternately or in addition, the body and the base may have an antimicrobial component, such as by incorporating antimicrobial components, such as antimicrobial powder, antimicrobial bodies, antimicrobial elements, such as wires, etc. into the body and/or base during the forming process. Suitable antimicrobial component may be formed from silver, copper, or their alloys or the like.
Referring again to
To provide sufficient mass and structure to device 10, body 12 may have a thickness (as measured along axis 12c) in a range of about ¾″ to 2″, or any dimension in between, including about 1″ or about 1½″. Further, the device may have a height in a range of about 1½″ to 3½″, or any dimension in between including about in a range of about 2″ to 3″ inches, or about 2½″.
Referring to
As best seen
For further details, for example, of the slots 114, 116, the material and method of forming device 110, reference is made above to device 10.
Referring to
In the illustrated embodiment, slots 214 each include a generally cylindrical portion 214a and a narrowed neck 214b, which is formed between the respective adjacent surfaces of the adjacent segments. Optionally, the adjacent segments may be configured so that they have no gap or a very small gap (e.g. 0.02-0.06 inches) between them so that they touch or nearly touch, and, hence, the narrowed necks 214b could go down to zero width or close to zero width. Further, each slot 214 may have a longitudinal extent that extends into the body, with the longitudinal extents of each slot being substantially the same so that the depth or height of each slot in device 210 is about the same. Similarly each slot includes a lateral extent, which at its widest point is generally the same as the lateral extent of each adjacent slot so that the slots may have similar dimensions, though as described above and below the dimensions of the slots may vary. For example, the depth of the slots may be optionally in a range of about 0.5 to 1.5 inches or about 0.75 inches, with the diameter of the cylindrical portion of the slots optionally in a range of about 0.2 to 0.8 inches or about 0.5 inches.
The dimensions of the body of the device may also vary. For example, in the three slot version, device 210 may have a length in a range of about 3.0 to 4.0 inches or be in a range of about 3.5 to 3.75 inches. Device 210 may have a width in a range of about 1.0 to 2.0 inches or be in a range of about 1.25 to 1.75 inches. The height may range from about 0.75 to 1.50 inches or be in a range of about 1.0 to 1.25 inches. For a four slot version, noted below, the length may be increased.
Referring to
Referring to
Slots 414 are similar to slots 214 and 314 in that they each have cylindrical portion 414a and a narrowed neck 414b. Optionally, as shown in
Optionally, device 410 may include a second plurality of slots 416 that extend partially into each segment 412a 412b, 412c, 412d, and 412e to form smaller slots for holding smaller tubes or tubing. Slots 416 may have a rounded distal end but may be defined by generally parallel facing surfaces of the respective segment, which may allow stacking of the tubes in the slots.
Referring again to
The above description is that of several embodiments of the invention. Various alterations and changes can be made from these embodiments without departing from the spirit and broader aspects of the invention as defined in the appended claims, which are to be interpreted in accordance with the principles of patent law including the doctrine of equivalents. This disclosure is presented for illustrative purposes and should not be interpreted as an exhaustive description of all embodiments of the invention or to limit the scope of the claims to the specific elements illustrated or described in connection with these embodiments. For example, and without limitation, any individual element(s) of the described invention may be replaced by alternative elements that provide substantially similar functionality or otherwise provide adequate operation. This includes, for example, presently known alternative elements, such as those that might be currently known to one skilled in the art, and alternative elements that may be developed in the future, such as those that one skilled in the art might, upon development, recognize as an alternative. Further, the disclosed embodiments include a plurality of features that are described in concert and that might cooperatively provide a collection of benefits. The present invention is not limited to only those embodiments that include all of these features or that provide all of the stated benefits, except to the extent otherwise expressly set forth in the issued claims. Any reference to claim elements in the singular, for example, using the articles “a,” “an,” “the” or “said,” is not to be construed as limiting the element to the singular.
This application claims the benefit of provisional application entitled LINE MANAGEMENT DEVICE, filed Jul. 31, 2013, U.S. Ser. No. 61/860,859.
Number | Date | Country | |
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61860859 | Jul 2013 | US |