CROSS REFERENCE TO RELATED APPLICATIONSThe current application is a continuation of U.S. Non-Provisional patent application Ser. No. 15/898,107, filed on Feb. 15, 2018, entitled “BANDAGING DEVICE”, which claims priority to U.S. Provisional patent application Ser. No. 62/459,474, filed on Feb. 15, 2017, entitled “BANDAGING DEVICE”, each of which are incorporated by reference herein in their entirety.
BACKGROUNDThe present invention relates generally to wound care, and in particular to a device for bandaging a wound without adhering to the wearer's skin, or causing discomfortor an adverse reaction by the wearer.
A wound to a person can include a puncture, cut, scrape or blunt force trauma, particularly originating at the person's skin. Wounds are typically treated by application of a wound care device to the wound, and often directly.
Wound care devices include a range of different dressings and pads that can be applied to limit or control blood flow from a wound, facilitate or promote clotting at the wound site, and/or protect a wound site from contamination. Most preferred wound care devices include an elastic or adhesive bandage. Elastics bandages are highly adaptable to treat a range of wounds and conform to virtually any body part, and provide many benefits at the wound site, including applying varying degrees of compression and support to the wound, as well as providing a sterile barrier around the wound. Adhesive bandages irritate the patient's skin, pull on hair near the wound, or might interfere with the wound itself
However, existing wound care devices, in particular those with elastic or adhesive bandages, have a limited ability to limit or control blood flow, are difficult to attach effectively to wounds in certain locations or on certain parts of the body, can irritate the patient's skin, and may interfere with the clinician's ability to see the wound or other relevant parts of the patient's body. Further, some conventional wound care devices can be difficult to apply to the wound or attach to the patient.
SUMMARYThe present invention overcomes these limitations of the prior art, providing a simple, inexpensive wound care device that can be effectively attached to a wide range of wound locations without the use of any adhesives, can apply controlled, consistent pressure to the wound, and can be configured to allow the clinician to see relevant areas of the patient's body.
In some aspects, a wound care device for compressively covering a wound on a body part of a patient is disclosed. The wound care device includes a contact pad having a thickness, and an elongated securing strap connected with the contact pad. The elongated securing strap has a top side, a bottom side, a proximal end and a distal end, and the contact pad is connected on the bottom side toward the proximal end of the elongated securing strap. The elongated securing strap further has an inelastic strap segment formed of a substantially inelastic material, an elastic strap segment formed of a substantially elastic material, and an attachment strap segment at the distal end of the elongated securing strap proximate the elastic strap segment and being configured to securely attach to the top side of the elongated securing strap when the contact pad covers the wound of the patient and the elongated securing strap is wound around the body part of the patient. The elastic strap segment cooperates with the attachment strap segment when the attachment strap segment is attached to the top side of the elongated securing strap to apply a compression force by the elongated securing strap to the thickness of the contact pad to compress the contact pad on the wound. The thickness of the contact pad allows the elongated securing strap to be offset from the skin of the patient to provide further compression force.
In some other aspects, a wound care device includes an elongated securing strap having a top side, a bottom side, a proximal end and a distal end. The elongated securing strap has an inelastic strap segment formed of a substantially inelastic material, an elastic strap segment formed of a substantially elastic material, and an attachment strap segment at the distal end of the elongated securing strap proximate the elastic strap segment and being configured to securely attach to the top side of the elongated securing strap when the elongated securing strap is wound around the body part of the patient. The device further includes a contact pad connected on the bottom side toward the proximal end of the elongated securing strap. The elastic strap segment cooperates with the attachment strap segment when the attachment strap segment is attached to the top side of the elongated securing strap to apply a compression force by the elongated securing strap to the contact pad to compress the contact pad on the wound.
In yet other aspects, a method of compressively covering a wound on a body part of a patient is presented. In some implementations, the method includes applying, to the wound, a contact pad connected to a bottom side of an elongated securing strap, the elongated securing strap having a top side, a bottom side, a proximal end and a distal end. The elongated securing strap has an inelastic strap segment formed of a substantially inelastic material, an elastic strap segment formed of a substantially elastic material, and an attachment strap segment at the distal end of the elongated securing strap proximate the elastic strap segment. The method further includes wrapping the elongated securing strap around the body part of the patient while maintaining the application of the contact pad to the wound. The method further includes attaching the attachment strap segment to the top side of the elongated securing strap while at least partially elongating the elastic strap segment of the elongated securing strap, to apply a compression force by the elongated securing strap to the contact pad to compress the contact pad on the wound.
The details of one or more embodiments are set forth in the accompanying drawings and the description below. Other features and advantages will be apparent from the description and drawings, and from the claims.
BRIEF DESCRIPTION OF THE DRAWINGSThese and other aspects will now be described in detail with reference to the following drawings.
FIG. 1 is a diagram showing the top view of an exemplary embodiment of the wound care device described herein.
FIG. 2 is a diagram showing the side view of an exemplary embodiment of the wound care device described herein.
FIG. 3 is a diagram showing the top view of an exemplary embodiment of the wound care device described herein.
FIG. 4 is a diagram showing the side view of an exemplary embodiment of the wound care device described herein.
FIG. 5 is a photograph showing an exemplary embodiment of the wound care device on a patient's arm.
FIG. 6 is a diagram showing a perspective view of an exemplary embodiment of the wound care device described herein rolled for storage.
Like reference symbols in the various drawings indicate like elements.
DETAILED DESCRIPTIONThis document describes a simple, inexpensive wound care device that can be effectively attached to a wide range of wound locations without the use of any adhesives, can apply controlled, consistent pressure to the wound, and can be configured to allow the clinician to see relevant areas of the patient's body.
The following description is presented to enable any person skilled in the art to make and use the implementations described herein. For purposes of explanation, specific nomenclature is set forth to provide a thorough understanding of the present inventions. Descriptions of specific embodiments or applications are provided only as examples. Various modifications to the embodiments or implementations will be readily apparent to those skilled in the art, and general principles defined herein may be applied to other embodiments and applications without departing from the spirit and scope of the invention. Thus, the present disclosure is not intended to be limited to the embodiments shown, but is to be accorded the widest possible scope consistent with the principles and features disclosed herein. Moreover, in the present disclosure various devices are described and set forth with regard to several embodiments. It is contemplated that features of the disclosed embodiments may be combined in any manner as may be desired for various applications and implementations.
Referring toFIGS. 1-6, in various exemplary embodiments, awound care device100 may include a securingstrap102, awound contact pad104, anelastic strap segment106 and anattachment strap segment108. In some implementations, thesecuring strap102 is elongated and has a top side, a bottom side, a proximal end and a distal end. In these implementations, the elongated securing strap includes aninelastic strap segment110 formed of a substantially inelastic material, and theelastic strap segment106 is formed of a substantially elastic material. Theattachment strap segment108 is positioned or connected at the distal end of theelongated securing strap102 proximate theelastic strap segment106, and is configured to securely attach to the top side of the elongatedsecuring strap102 when the elongatedsecuring strap102 is wound or wrapped around the body part of the patient.
In some implementations, theinelastic strap segment110 of the elongatedsecuring strap102 has a length configured so as to be the only contact with the patient's body part apart from thecontact pad104 covering the wound of the patient. Accordingly, in some implementations, theelastic strap segment106 has a length that is less than one-third of a length of theinelastic strap segment110, and more particularly less than one-sixth of the length of theinelastic strap segment110.
As shown inFIG. 5, thesecuring strap102 may be wrapped around the part of the body where the wound is located such that the attachment strap segment comes into contact with the back side of the securing strap and attaches thereto. In various exemplary embodiments, the attachment strap segment has an attaching surface that can attach to the back of the securing strap at any point or at a range of locations to allow the user to adjust the length and apply the bandage to a range of different sized body parts, and to allow the user to adjust the amount of pressure or compression exerted on the wound. The attaching surface can include, without limitation, hooks, loops, snaps, pins, adhesive material(s), or the like. In some preferred implementations, at least the inelastic strap segment of the securingstrap102 is formed of a fabric or woven fabric, and the attaching surface of theattachment strap segment108 includes a number of small hooks that can attach to the fabric or woven fabric of the top surface of the inelastic strap segment of thesecuring strap102.
As shown inFIGS. 1-4, thewound contact pad104 may be positioned on the front surface of securingstrap102 at a location distal from theattachment strap segment108. In various exemplary embodiments, however, the location of thecontact pad104 on the securingstrap102 can be varied to effectively position thecontact pad104 for wounds in various locations on various parts of the body.
In various exemplary embodiments, thecontact pad104 may be affixed to thesecuring strap102, or it may be provided separate from the securing strap and provided with an adhesive surface on the side opposite to the side that will be in contact with the wound such that thecontact pad104 can be attached to thesecuring strap102 at any location along thesecuring strap102. The ability to affix thecontact pad104 at any location the securing strap allows the clinician to customize the position of thecontact pad104 to bandage the wound effectively regardless of location. Aseparate contact pad104 may also be trimmed or cut to customize thecontact pad104 based on the nature or characteristics of the wound or the wound site.
In various exemplary embodiments, thecontact pad104 may be made of any suitable material, including non-stick pads, gauze, or any other appropriate wound care materials. Thecontact pad104 may also be constructed of a multi-layered material, and it may be any suitable thickness. For example, for applications where targeted compression is desirable, thecontact pad104 may include more rigid materials and/or may be either elevated or made of a thicker material such that additional compression is targeted directly on the wound site. Thecontact pad104 may also be made from a highly absorbent and/or fluid retaining material such as super absorbent polymers (SAPs), sometimes referred to as slush powders, cellulose or fiber-based absorbent materials, or any other suitable absorbent material.
In some implementations, thecontact pad104 has a first thickness, in an uncompressed state, of between 0.1 and 2 centimeters or more, and a second thickness in a compressed state of 0.01 and 1 centimeters or more. The second thickness, which displaces the securing strap from the patient's skin at the wound site proximate thecontact pad104, can be adjusted according to an amount of compression applied to thecontact pad104 by theelastic strap segment106 cooperating with theattachment strap segment108.
Thecontact pad104 is preferably thicker than typical bandages or absorbent surfaces in order to provide additional downward compression because of an angle of the securingstrap102, and in particular the inelastic strap segment, down from thecontact pad104, to stop blood flow. Thecontact pad104 thickness also offsets the securingstrap102 from the patient's skin proximate the wound and/orcontact pad104, to further reduce pain, skin irritation, blistering and/or skin breakdown experienced with conventional bandage devices.
Anelastic strap segment106 may be attached to the securingstrap102 using any appropriate means, including without limitation adhesives, stitching, welding (such as radio frequency or ultrasonic welding), etc. While shown inFIGS. 1 and 2 as overlapping with the securingstrap102, theelastic strap segment106 can be attached in any suitable way including overlapping on the side of the securingstrap102 opposite to the side with thecontact pad104, overlapping on the same side of the securingstrap102 as thecontact pad104, or abutting the end of the securingstrap102. Theelastic strap segment106 is shown located at one end, i.e. distal end, of the securingstrap102, but in various exemplary embodiments it may be positioned at either end of the securingstrap102, or it can be located at an intermediate point within the securingstrap102.
Theelastic strap segment106 cooperates with theattachment strap segment108, when theattachment strap segment108 is attached to the top side of the elongated securingstrap102, to apply a compression force by the elongated securingstrap102 to the thickness of the contact pad to compress the contact pad on the wound. Preferably, when the securingstrap102 is wrapped or wound around a body part of a patient, only the inelastic strap segment of the securingstrap102 contacts the patient's skin, other than the contact made by thecontact pad104 to the wound and the patient's skin proximate the wound.
In various exemplary embodiments, the elastic strap segment can be eliminated or integrated into the securing strap, and the attachment strap segment can be attached directly to the securing strap, or can be formed on the securing strap itself by affixing a removable attachment material to the securing strap directly. Theattachment strap segment108 can include a hook-and-loop type fastener, such as only micro-hooks for attaching to the top side of the securingstrap102.
The securingstrap102 itself can be made from an appropriate elastic or inelastic material, or from various materials having different amounts of elasticity to manage the location and degree of compression. For instance, the securingstrap102 can be made of cloth or synthetic materials, or multiple layers of fabric such as cotton, hemp, bamboo, microfiber, or even plastic fibers such as a thermoplastic, such as polylactic acid (PLA), dual polylactic acid (DPLA), or the like.
Theattachment strap segment108 may be attached to theelastic strap segment106 or it may be attached to an end of the securingstrap102. Theattachment strap segment106 may be attached in any suitable configuration including overlapping or abutting and using any suitable attachment means including without limitation adhesives, stitching, welding, etc.
In some implementations, such as shown inFIGS. 1 and 2, thecontact pad104 being placed proximate a proximal end of the securingstrap102, and theelastic strap segment106 andattachment strap segment108, respectively, being placed at a distal end of the securingstrap102, allows a clinician to: a) place or contact thecontact pad104 to a wound site on a body part of a patient; b) while holding thecontact pad104 in place, wrap the securingstrap102 around the body part of the patient until the distal end of the securing strap overlaps the proximal end of the securing strap, and preferably overlaps the top side of the securingstrap102 opposite a position of thecontact pad104; c) position theattachment strap segment108 on the top side of the securingstrap102 to elongate theelastic strap segment106, to apply a desired compression force to the securingstrap102 and onto thecontact pad104, in which, preferably, only the inelastic strap segment of the securingstrap102 contacts the patient's skin other than thecontact pad104; and d) secure theattachment strap segment108 on the top side of the securingstrap102 to maintain thecontact pad104 on the wound site of the body part.
In various exemplary embodiments, theattachment strap segment108 may be provided with a means for removably attaching theattachment strap segment108 to the securingstrap102 and/or theelastic strap segment106. In an exemplary embodiment, the front surface of theattachment strap segment108 may include hook and loop type of fasteners that can removable attach to the back surface of the securingstrap102 and/or the back surface of theelastic strap segment106. Any other suitable attachment means may be used, including adhesives, hooks, etc. In various exemplary embodiments, the attachment means is configured such that it can be removably attached to the back surface of the securingstrap102 or theelastic strap segment106 at any location.
To use thewound care device100, thecontact pad104 may be positioned on the wound, and the securingstrap102 may be wrapped around the body part where the wound is located such that the attachment strap segment can be put in contact with and removably attached to the back side of the securing strap103 and/or theelastic strap segment106. Theelastic strap segment106 can be stretched or contracted to adjust the location of such attachment, and thereby control the tightness of thewound care device100 and the amount of pressure the contact pad exerts on the wound.
Referring toFIG. 6, thewound care device100 can be rolled up for storage and shipping, such that the attachment strap segment can be removably attached to the securingstrap102 or theelastic strap segment106 to maintain the wound care device in a rolled up configuration.
The resulting wound care device avoids any contact between adhesives or similar substances and the patient's skin, while providing secure wound care applied with appropriate pressure. It will be readily understood that the various exemplary components described above can by rearranged into various different configurations.
Although a few embodiments have been described in detail above, other modifications are possible. Other embodiments may be within the scope of the following claims.