Patient transport apparatuses facilitate care of patients in a health care setting. Patient transport apparatuses comprise, for example, hospital beds, stretchers, cots, wheelchairs, and chairs. A conventional patient transport apparatus comprises a support structure having a base, a support frame, and a patient support surface upon which the patient is supported.
In some cases, a patient transport apparatus is needed to transport a patient to a hospital or other emergency medical facility in an emergency vehicle. During transport, it is desirable for the patient to be safely and securely restrained to the patient transport apparatus for their own safety and the safety of emergency medical personnel or other people within the emergency vehicle.
A harness system may be used to secure the patient to the patient transport apparatus. It is desirable for the harness system to be of suitable strength to withstand certain crash events. Conventional harness systems, however, comprise polyester webbing that may be difficult to clean when dirt, grease, body fluids, and/or other contaminants are trapped in the webbing. Typically, such harness systems are discarded once they reach an undesirable, soiled condition.
A harness system designed to address and/or overcome one or more of the aforementioned challenges is desired.
Referring to
The patient transport apparatus 30 shown in
The base 34, support frame 36, patient support deck 38, and patient support surface 42 each have a head end and a foot end corresponding to designated placement of the patient's head and feet on the patient transport apparatus 30. The construction of the support structure 32 may take on any known or conventional design, and is not limited to that specifically set forth above. In addition, a mattress (not shown) may be provided in certain embodiments, such that the patient rests directly on a patient support surface of the mattress while also being supported by the patient support surface 42.
Side rails 44 are coupled to the support frame 36 and thereby supported by the base 34. If the patient transport apparatus 30 is a hospital bed there may be more side rails. The side rails 44 may be fixed to the support frame 36 or may be movable between a raised position in which they block ingress and egress into and out of the patient transport apparatus 30, one or more intermediate positions, and a lowered position in which they are not an obstacle to such ingress and egress. In still other configurations, the patient transport apparatus 30 may not include any side rails.
Wheels 58 are coupled to the base 34 to facilitate transport over floor surfaces. The wheels 58 are arranged in each of four quadrants of the base 34 adjacent to corners of the base frame 35. In the embodiment shown, the wheels 58 are caster wheels able to rotate and swivel relative to the support structure 32 during transport. Each of the wheels 58 forms part of a caster assembly. Each caster assembly is mounted to the base 34. It should be understood that various configurations of the caster assemblies are contemplated. In addition, in some embodiments, the wheels 58 are not caster wheels and may be non-steerable, steerable, non-powered, powered, or combinations thereof. Additional wheels are also contemplated. For example, the patient transport apparatus 30 may comprise four non-powered, non-steerable wheels, along with one or more powered wheels.
A pair of loading wheels 64 (only one shown in
A lift device 70 is configured to raise and lower the patient support surface 42 between minimum and maximum heights relative to the floor surface and intermediate heights therebetween. The lift device 70 may be configured to operate in the same manner or a similar manner as the lift mechanisms shown in U.S. Pat. No. 7,389,552 or 7,398,571, both of which are hereby incorporated by reference in their entirety.
Referring to
Each of the harness assemblies 102-114 are configured to be attached to the support frame 36 and/or the patient support deck 38, but could be attached at any suitable location on the patient transport apparatus 30. In the embodiment shown, referring to
Referring to
The connecting harness assemblies 104, 106 are configured to be secured to the patient support deck 38 and/or the support frame 36. Each of the connecting harness assemblies 104, 106 comprises a connecting loop L and a pair of connectors C1 and/or C2 so that the connecting harness assemblies 104, 106 can be connected to the shoulder harness assemblies 102 and to each other. In the embodiment shown, the connectors C1, C2 on first connecting harness assembly 104 comprise an insertion latch and a buckle. The buckle is configured to releasably receive the insertion latch on one of the shoulder harness assemblies 102. The connectors C2 on second connecting harness assembly 106 comprise two buckles. One buckle is configured to releasably receive the insertion latch on the other shoulder harness assembly 102 and another buckle is configured to releasably receive the insertion latch on the first connecting harness assembly 104 to be secured across a waist of the patient.
The thigh harness assemblies 108, 110 are configured to be secured to the patient support deck 38 and/or the support frame 36 and connect to each other across thighs of the patient. Each of the thigh harness assemblies 108, 110 comprises a connecting loop L and a connector C1 or C2. In the embodiment shown, the connector C2 on first thigh harness assembly 108 comprises a buckle and the connector C1 on second thigh harness assembly 110 comprises an insertion latch configured to releasably engage the buckle.
The ankle harness assemblies 112, 114 are configured to be secured to the patient support deck 38 and/or the support frame 36 and connect to each other across ankles of the patient. Each of the ankle harness assemblies 112, 114 comprises a connecting loop L and a connector C1 or C2. In the embodiment shown, the connector C2 on first ankle harness assembly 112 comprises a buckle and the connector C1 on second ankle harness assembly 114 comprises an insertion latch configured to releasably engage the buckle.
Referring to
The first connecting harness assembly 104 comprises an elongate flexible restraint member 120 that attaches to the connectors C1, C2. The flexible restraint member 120 comprises first, second, and third joints J1, J2, J3. The first joint J1, a close-up of which is shown in
The fabric 124 may comprise webbing, such as that formed by woven fabric. The webbing may comprise polyester webbing or other suitable materials. It is also contemplated that the fabric 124 may be formed of nylon webbing, polypropylene webbing, cotton webbing, elastic webbing, and the like. The coated fabric 122 has a thickness suitable to accommodate the connectors C1, C2. In some cases, the coated fabric 122 has a combined thickness T1 (fabric 124 and outer layers of coating 126) of from 0.038 to 0.047 inches, from 0.040 to 0.045 inches, or of 0.047 inches or less. In the embodiment shown, the coated fabric 122 has a thickness T1 of about 0.042 inches. The fabric 124 may have a thickness T2 of less than 0.047 inches, less than 0.046 inches, or less than 0.045 inches. In some cases, the fabric 124 has a thickness T2 of from 0.025 to 0.045 inches, from 0.030 to 0.040 inches, or from 0.030 to 0.035 inches. In the embodiment shown, the fabric 124 has a thickness T2 of about 0.032 inches. Other thicknesses are also contemplated.
The coating 126 may be applied to the fabric 124 by spraying, lamination, extrusion and/or co-extrusion processes, dipping the fabric 124 into the coating 126, moving the fabric 124 through the coating 126, molding the coating 126 onto the fabric 124, or the like. The coating 126 may comprise polymeric material, such as polyurethane, or other suitable materials to ease cleaning of the flexible restraint member 120. The coating 126 may be non-porous and/or non-fibrous. The coating 126 eases cleaning of the flexible restraint member 120 by providing a smooth, continuous, outer surface for wiping and thereby cleaning (as compared to the fabric 124). The coating 126 may be waterproof, water-resistant, and/or impervious to contaminants, such as dirt, grease, and body fluids. By coating the fabric 124 with polyurethane or other similar material, users are able to more easily wipe contaminants off the flexible restraint member 120 as compared to uncoated fabric, which tends to trap such contaminants. The coating 126 may have a cross-sectional thickness (as shown in
Referring to
Referring to
Referring to
A covering is placed over the stitches 128 and the adhesive layers 130. In the embodiment shown, the covering comprises two separate covers 132 formed of rectangular patches sized to have the same width as the coated fabric 122 (other widths are also possible). In some cases, only a single cover 132 is used that wraps around to cover the stitches 128 on opposing surfaces. The covers 132 may be formed of urethane film or other suitable material. The covers 132 may comprise smooth, continuous, outer surfaces. The covers 132 may be non-porous and/or non-fibrous. The covers 132 may be waterproof, water-resistant, and/or impervious to contaminants to facilitate cleaning in the same manner as the coating 126.
As shown in
Referring briefly back to
The covers 132 may be sealed along their entire outer peripheries to the sections S1, S2 by any suitable sealing method, such as ultrasonic welding, radio frequency (RF) welding, adhesive, other heat sealing methods, or the like. In some cases, both the covers 132 are sealed to the coating 126 simultaneously, for instance, by placing the entire construction of covers 132, adhesive 130, and sections S1, S2 in an RF welding die. In this case, the bands B represent weld locations. In other cases, such as when using adhesive, the covers 132 may be attached separately with adhesive placed along the bands B between the covers 132 and the coating 126 on the sections S1, S2.
The covers 132 may be sized to have outer peripheries that extend beyond the outer periphery of the stitches 128 so that the covers 132 completely cover and provide a barrier between the stitches 128 and possible outside contaminants. In the embodiment shown, the covers 132 are sealed to the coating 126 outside the outer periphery of the stitches 128 such that the covers 132 and coating 126 have melded together (see, e.g.,
Referring specifically to
Referring back to
The third joint J3 is formed by sealing the other free end of the coated fabric 122 (opposite the free end 140) to an adjacent section, without any stitches or covers, but in a manner that also seals the other free end to eliminate any exposed fibers that may be present from the fabric 124. This is useful when the coated fabric 122 is manufactured in long lengths and cut into smaller lengths having two free ends with exposed fabric 124. In one embodiment, during assembly, the coating 126 at the other free end, and/or the coating 126 on the adjacent section to which the other free end is being attached, may be heated such that the coating 126 is flowable to seal off the fabric 124 at the other free end. When heating the coating 126 around the other free end, a smooth and tapered transition can be provided at the other free end of the coated fabric 122 with suitable dies, molds, etc. A similar third joint J3 is used to seal a free end of the coated fabric 122 in the harness assemblies 102, 110, and 114. In other embodiments, the free end of the coated fabric 122 can be sealed in other ways and/or using other suitable materials, such as adhesive, and the like. For instance, a separate cover (not shown) could be attached over the free end and adhered to the adjacent section to provide a barrier that protects any fabric 124 that would otherwise be exposed to contaminants.
As a result of the above-described construction of the flexible restraint member 120 and the joints J1, J2, J3 thereof, in the embodiment shown, there is no exposed fabric 124 or stitches 128 that would otherwise be susceptible to contamination and difficult to clean. In other words, the fabric 124 and stitches 128 are completely covered and sealed by the coating 126 and/or covers 132 such that the flexible restraint member 120 has generally smooth outer surfaces that can be easily cleaned after use. This will encourage continued reuse of the harness assemblies 102-114 and save costs associated with discarding soiled harness assemblies.
In some embodiments, the harness system 100 is configured to meet or exceed the requirements set forth in the SAE technical standards J3027 (which comprises SAE J2917 and SAE J2956). The harness system 100 may also be configured to meet or exceed the requirements set forth in the British Adopted European Standards BS EN 1789:2007 clause 4.5.9 and 5.4. One example of the harness system 100 that meets all the requirements of these standards is set forth below. In this example, each of the flexible restraint members 120 of the harness assemblies 102-114 comprises a single, continuous strap of coated fabric having a thickness of 0.042 inches and a width of 1.88 inches. The coated fabric 122 comprises polyester webbing with a polyurethane coating. The coating 126 has a thickness of 0.005 inches. The first and second joints J1, J2 are formed with the stitches 128 comprising nylon thread sized at 138/TEX 135/GOVT. FF. The stitches 128 are provided in a stitching pattern that comprises a box X stitch pattern (for the first joints J1) or circular pattern (for the second joints J2). The adhesive 130 applied onto the stitching pattern comprises double-sided self-adhesive tape, such as product no. 4965 manufactured by Tesa Tape, Inc. of Charlotte, N.C. The covers 132 comprise urethane film that is RF welded to the coated fabric 122. The covers 132 have a thickness of 0.015 inches.
It is to be appreciated that the terms “include,” “includes,” and “including” have the same meaning as the terms “comprise,” “comprises,” and “comprising.”
Several embodiments have been discussed in the foregoing description. However, the embodiments discussed herein are not intended to be exhaustive or limit the invention to any particular form. The terminology which has been used is intended to be in the nature of words of description rather than of limitation. Many modifications and variations are possible in light of the above teachings and the invention may be practiced otherwise than as specifically described.
This application is a continuation of U.S. patent application Ser. No. 15/497,693 which was filed on Apr. 26, 2017, the disclosure of which is hereby incorporated herein by reference.
Number | Name | Date | Kind |
---|---|---|---|
3970329 | Lewis | Jul 1976 | A |
4534075 | Schnitzler | Aug 1985 | A |
4569095 | Holling | Feb 1986 | A |
4977630 | Oswalt | Dec 1990 | A |
5400448 | Zwickey | Mar 1995 | A |
5577515 | Stout et al. | Nov 1996 | A |
5634222 | Zwickey | Jun 1997 | A |
5860176 | Norberg | Jan 1999 | A |
6007092 | Martz | Dec 1999 | A |
6740607 | Veiga | May 2004 | B2 |
6898811 | Zucker | May 2005 | B2 |
7389552 | Reed et al. | Jun 2008 | B1 |
7398571 | Souke et al. | Jul 2008 | B2 |
7861341 | Ayette | Jan 2011 | B2 |
7905233 | Hopper | Mar 2011 | B2 |
8001634 | Ayette | Aug 2011 | B2 |
8302231 | Moffitt | Nov 2012 | B2 |
8434827 | Young et al. | May 2013 | B2 |
8615829 | Kenalty | Dec 2013 | B2 |
9205007 | Chinn | Dec 2015 | B2 |
9757286 | Beaulieu | Sep 2017 | B2 |
10080693 | Scheenstra et al. | Sep 2018 | B1 |
10080694 | Scheenstra et al. | Sep 2018 | B1 |
10085902 | Chia | Oct 2018 | B2 |
20020105176 | Hammer et al. | Aug 2002 | A1 |
20040045089 | Zucker | Mar 2004 | A1 |
20080168603 | Ayelle et al. | Jul 2008 | A1 |
20100064432 | Duquette | Mar 2010 | A1 |
20100084526 | Moffitt | Apr 2010 | A1 |
20110056022 | Ayette | Mar 2011 | A1 |
20120084920 | Zucker | Apr 2012 | A1 |
20120151679 | Kenalty | Jun 2012 | A1 |
20130340170 | Chinn | Dec 2013 | A1 |
20140025939 | Smith | Jan 2014 | A1 |
20140217764 | Bradley et al. | Aug 2014 | A1 |
20140259391 | Karlsson | Sep 2014 | A1 |
20150143634 | Beaulieu | May 2015 | A1 |
20150313778 | Chia | Nov 2015 | A1 |
20160000625 | Duquette | Jan 2016 | A1 |
20190008707 | Scheenstra | Jan 2019 | A1 |
Entry |
---|
Article entitled “Medical Application for Biothane Coated Webbing” from the website biothane.us; https://www.biothane.us/applications/medical/. |
Biothane Product Data Brochure, 8 pages, bioplastics.us, published at least by Apr. 25, 2017. |
Chest Restraint Shoulder Harness, BioThane G1, Yellow, for Stryker 6500; https://www.boundtree.com/3175-67025-chest-restraint-product-38475-181.as- px?search=3175-67025. |
Dick Medical Supply 2016/2017 Product Catalog, 24 pages. |
Ferno Model 417-1 Series Harness Restraint Brochure dated Sep. 2013; 4 pages, Ferno-Washington, Inc. |
How to Sew Biothane 1 instructional video, posted Sep. 22, 2016 by BioThane Coated Webbing; URL: https://www.youtube.com/watch?v=9KQZFIQb-il. |
How to Sew Biothane 2 instructional video, posted Sep. 23, 2016 by BioThane Coated Webbing; URL: https://www.youtube.com/watch?v=exyrEj-7QGI. |
Masson Inc., “PathoShield(R) Coated Webbing” and “PathoShield(R) Welds”, extracted from web.archive.org, published at least as early as Apr. 26, 2017; 2 pages. |
Masson Inc., “PathoShield(R) Coated Webbing” and “PathoShield(R) Welds”, URL: http://www.massoninc.com/pathoshield.php. |
SAE J3027 Explained, The Stryker Solution, Stryker Brochure dated Nov. 6, 2014; 3 pages, McCoy Miller. |
Stryker Power-PRO XT Ref 6506 Operations/Maintenance Manual; 67 pages, Stryker Medical, published at least by Apr. 25, 2017. |
Stryker X-Restraint Cot Straps instructional Video, posted Feb. 29, 2016 by Ettore Dimiceli; URL: https://www.youtube.com/watch?v=9sZFDvWBLig. |
Number | Date | Country | |
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20190008707 A1 | Jan 2019 | US |
Number | Date | Country | |
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Parent | 15497693 | Apr 2017 | US |
Child | 16127543 | US |