Patent Application
20100106120
This disclosure relates to wound dressings, and more particularly to a wound dressing and a support delivery system designed to conform to highly contoured areas of the body.
Wound dressings using an absorbent central area surrounded by a larger adhesive film are known. For example, U.S. Pat. No. 5,738,642 (the '642 patent) shows a wound dressing and delivery system comprising a thick absorbent pad placed in the center of a thin backing. A carrier frame surrounds the perimeter of the wound dressing, providing support (e.g. rigidity) to the backing to facilitate handling of the dressing during application to a wound. Such dressings are often applied to relatively flat areas of the body, such as the chest or abdomen.
The present disclosure provides a wound dressing having a backing material surrounding an absorbent pad, and delivery system that facilitates the handling and application of the wound dressing. The wound dressing is readily handled and applied with one hand, which frees up the other hand to help position the patient or parts of the patient to ensure better application of the wound dressing. The wound dressing is constructed so as to have improved adhesion to highly contoured areas of the body, such as a toe, finger or heel, and to permit easy application to these surfaces.
In certain embodiments, the wound dressing and delivery system comprise an adhesive layer on a first side of a backing layer, with absorbent pad or other material applied or attached to the adhesive layer. A dressing support layer is positioned on a second side of the backing layer, and is configured to deliver the wound dressing to a wound. The dressing support layer further comprises a tab, wherein the tab overlaps at least a portion of the absorbent pad on the opposite side of the backing layer of the wound dressing.
These and various other advantages and features characterizing the invention are pointed out with particularity in the claims annexed hereto and forming a part hereof. However, for a better understanding of the invention, its advantages, and objects obtained by its use, reference should be made to the accompanying drawings and descriptive matter, in which embodiments of the invention are illustrated and described.
The invention will be further described with reference to the drawings, wherein corresponding reference characters indicate corresponding parts throughout the several views, and wherein:
a-c depict the wound dressing of
While the invention is amenable to various modifications and alternative forms, specifics thereof have been shown by way of example in the drawings and will be described in detail. It should be understood, however, that the intention is not to limit the invention to the particular embodiments described. On the contrary, the intention is to cover all modifications, equivalents, and alternatives falling within the spirit and scope of the invention.
The present disclosure is directed to a wound dressing and delivery system, as well as to methods of positioning and applying the wound dressing to a patient, especially with one hand. The wound dressing and delivery system are particularly suited for application over a highly contoured surface of a patient, such as a finger, toe or heel. The wound dressing permits an absorbent material to be placed against the wound, while the delivery system aids in positioning the wound dressing on the body over the wound site, and forming a seal around the wound.
In some embodiments, the wound dressing comprises an absorbent pad, a backing layer, and an adhesive layer on the backing layer facing the absorbent pad. The adhesive layer and backing layer form a perimeter around the absorbent pad and hold the absorbent pad in place on a wound. The perimeter formed by the adhesive layer and backing layer keeps the absorbent pad properly positioned, and may also help maintain a sterile environment around the wound.
The delivery system described herein provides an easy and effective way to position and apply the wound dressing to a patient with one hand and is particularly well suited for application of a wound dressing to a highly contoured area of the body such as to the fingers, toes, or a heel. The wound dressings described herein are generally comprised of a backing layer having an adhesive layer on one side of the backing layer, and an absorbent pad on the adhesive layer. A support layer is releasably adhered to the backing layer on the side opposite the adhesive layer. The support layer includes a tab that overlaps a portion of the absorbent pad located on the opposite side of the backing. In some embodiments, the tab is covered with a bond block material, or is free of adhesive in order to permit easy handling of the tab. The wound dressing may further comprise a release liner to protect the adhesive until the dressing is ready for use.
Turning now to the figures,
At least one dressing support layer 16 is positioned over the wound dressing 10. In the embodiment shown in
In an embodiment, the tab portion is not secured to the backing 14 by use of a bond block material or liner to facilitate handling the wound dressing 10 by the tab 20. Examples of suitable bond block materials are described in US 2007156075 (Heinecke), the entire disclosure of which is incorporated by reference herein.
The wound dressing 10 typically includes a carrier film 24 to protect the adhesive layer 17, until the wound dressing is ready for use. To facilitate removal, the carrier film 24 may have a tab 26 which overhangs the end portion 18 of the support layer 16. The carrier film 24 covers the surface of the wound dressing applied to the patient, generally making contact with the absorbent pad 12 and the periphery of the adhesive layer 17. The carrier film 24 remains attached to wound dressing 10 until a user is ready to apply the dressing. The carrier film 24 may be a single piece or multiple piece release liner, and may be part of or laminated to the package (not shown) containing the dressing, or merely enclosed along with the dressing within the package. The carrier film 24 keeps the adhesive clean during storage and shipping of the wound dressing 10.
The wound dressing 10 is typically applied to a patient by first cleaning the wound and making sure the area around the wound is ready to receive a dressing. The carrier film 24 is then removed from the dressing, for example, by grasping tab 26 and peeling away the carrier film 24, exposing the bottom of the absorbent pad 12 and the perimeter of the adhesive layer 17 on the backing layer 14. As the wound dressing 10 is held by tab 20, the center of the absorbent pad 12 is brought in contact with the wound, and then the edges 15 of the dressing 10 are gently pressed against the patient, thereby bringing the exposed adhesive perimeter of the backing layer 14 in contact with the patient to form a seal around the wound.
After the dressing 10 is properly in position and adhered to a patient's skin, the support layer 16 can be removed. Generally removal of support layer 16 is accomplished by grasping the tab 20 and then using a peeling motion toward the edge 15 of the dressing 10 to remove the support layer 16. Alternatively, tab 18 could be used to remove the support layer 16.
The wound dressing 10 of
Turning now to
In an embodiment, the wound dressing has a length (including the tabs) of approximately 8.5 cm. In a further embodiment, such as the circular wound dressing shown in
In order to improve the conformability of the backing material on a highly contoured surface of a patient, the support layer should cover only a limited portion of the outer perimeter of the wound dressing. In one embodiment, the support layer 16, 56, 66 covers less than 40% of the perimeter of the backing, and in a further embodiment, the support layer covers less than 20% of the perimeter of the backing. In still a further embodiment, the support layer covers 0% of the perimeter of the backing, for example in the embodiments shown in
The wound dressings described herein are well suited for placement with one hand to highly contoured areas of the body such the toes or fingers. The placement of the tab opposite the absorbent pad, enables the user to easily position the dressing on a wound.
a-c show the wound dressing of
When the support layer is removed from the backing layer 14, the force applied to the edge of the backing layer is generally perpendicular to the perimeter of the dressing 10. This force contrasts with peel forces of conventional support layers, which are parallel to the perimeter of the wound dressing, and which often lift the perimeter off the surface of the patient, potentially loosening the dressing or creating a path for leakage of fluids from the wound.
The absorbent pad 12 of dressing is sometimes referred to as an “island pad” because the backing layer extends substantially beyond the absorbent pad 12, typically beyond the entire periphery of the absorbent pad 12. For example, the diameter of the absorbent pad can be 2.5 cm, while a backing for this pad can be 7.2 cm by 7.2 cm.
The absorbent pad 12 can comprise a foam, a hydrocolloid or a hydrogel pad having a thickness of at least 1 mm (e.g., most preferably 3-9 mm), and the backing layer 14 can comprise a transparent elastic polymeric film (e.g., urethane) having a thickness no greater than 1 mm (e.g., most preferably 0.021-0.10 mm). It will be appreciated that in this embodiment the absorbent pad 12 is thicker, than the backing layer 14. The backing layer construction in this embodiment should be sufficiently stiff such that it will not fold over onto itself where it is not adequately supported by the support layer 16 or the absorbent pad 12. Typically, sufficient stiffness of the backing is obtained when at least a portion of the backing layer construction is comprised of a thickness greater than 0.070 mm. Other portions of the backing layer can be as thin as 0.021 mm (21 microns).
The support layer 16 is attached to the second major surface of the backing layer 14 (over the low adhesion backing). The bond between the support layer 16 and the backing layer 14 is stronger than the bond between the pressure sensitive adhesive 17 and the carrier layer 24 so that the backing layer 14 remains attached to the support layer 16 when the carrier layer 24 is removed from the dressing 10. A portion of the support layer is typically attached to the backing layer by heat seal bonding although other methods may be employed.
As one skilled in the art would appreciate, other implementations are appropriate in order to add or take away from the aspects the various embodiments of the wound dressings as described herein. For example, the backing layer 14 can be multiple films or coatings without diverging from the invention or deviating from the meaning of the term “film” as used herein. Similarly, the absorbent pad 12 can include multiple sub-layers, including films, webs, sheets, etc. Also, additional layers and films of other materials can be added between the materials described herein without deviating from the invention.
Additional aspects of various components of the invention will now be described in greater detail.
Absorbent pad 12 can be manufactured of any of a variety of materials including, but not limited to, woven or nonwoven cotton or rayon. Absorbent pad 12 is useful for containing a number of substances, optionally including antimicrobial agents, drugs for transdermal drug delivery, chemical indicators to monitor hormones or other substances in a patient, etc.
The absorbent may include a hydrocolloid composition, including the hydrocolloid compositions described in U.S. Pat. Nos. 5,622,711 and 5,633,010, the disclosures of which are hereby incorporated by reference. The hydrocolloid absorbent may comprise, for example, a natural hydrocolloid, such as pectin, gelatin, or carboxymethylcellulose (CMC) (Aqualon Corp., Wilmington, Del.), a semi-synthetic hydrocolloid, such as cross-linked carboxymethylcellulose (X4ink CMC) (e.g. Ac-Di-Sol; FMC Corp., Philadelphia, Pa.), a synthetic hydrocolloid, such as cross-linked polyacrylic acid (PAA) (e.g., CARBOPOL™ No. 974P; B.F. Goodrich, Brecksville, Ohio), or a combination thereof. Generally, the hydrocolloid absorbent component comprises from about 5 percent to about 60 percent by weight of the absorbent composition. When preparing an absorbent composition for use in a wound dressing the hydrocolloid absorbent preferably comprises from about 20 percent to about 40 percent by weight of the composition. Absorbent materials may also chosen from other synthetic and natural materials including polymer gels and foams.
Suitable backing materials for backing layer include, for example, nonwoven fibrous webs, woven fibrous webs, knits, films, porous films, and other familiar backing materials. The backing materials are typically translucent or transparent polymeric elastic films. The backing can be a high moisture vapor permeable film backing U.S. Pat. No. 3,645,835, the disclosure of which is hereby incorporated by reference, describes methods of making such films and methods for testing their permeability. A combination of the aforementioned backings could also be used.
In an embodiment, the backing material is a polyurethane film. In a further embodiment, a polyurethane film backing laminated to a non-woven material is used. Such non-woven materials are described in U.S. Pat. No. 5,088,483 (Heinecke) and U.S. Pat. No. 6,881,875 (Swenson), the entire disclosures of which is incorporated by reference herein. The thickness of the backing may range from about 21 to 1000 microns. In an embodiment, the thickness ranges from about 70 to about 500 microns. The backing layer construction in this embodiment should be sufficiently stiff such that it will not fold over onto itself where it is not adequately supported by the support layer 16 or the absorbent pad 12. Typically, sufficient stiffness of the backing is obtained when at least a portion of the backing layer construction is comprised of a thickness greater than 0.070 mm (70 microns).
The backing advantageously should transmit moisture vapor at a rate equal to or greater than human skin. In some embodiments, the adhesive coated backing layer transmits moisture vapor at a rate of at least 300 g/m2/24 hrs/37° C./100-10% RH, frequently at least 700 g/m2/24 hrs/37° C./100-10% RH, and most typically at least 2000 g/m2/24 hrs/37° C./100-10% RH using the inverted cup method.
The backing layer 14 is generally conformable to anatomical surfaces. As such, when the backing layer 14 is applied to an anatomical surface, it conforms to the surface even when the surface is moved. The backing layer 14 is also conformable to animal anatomical joints. When the joint is flexed and then returned to its unflexed position, the backing layer 14 can be made such that it stretches to accommodate the flexion of the joint, but is resilient enough to continue to conform to the joint when the joint is returned to its unflexed condition.
A description of this characteristic of backing layers 14 for use with the present invention can be found in issued U.S. Pat. Nos. 5,088,483 and 5,160,315, the disclosures of which are hereby incorporated by reference in their entirety. Specific suitable backing materials are elastomeric polyurethane, co-polyester, or polyether block amide films. These films combine the desirable properties of resiliency, high moisture vapor permeability, and transparency found in backings.
The material used to form the support layer 16 is generally more rigid than the backing layer 14 to provide adequate support to the backing layer and dressing 10 during application to a patient. The support layer 16 can be heat-sealable to the backing layer 14 with or without a low adhesion coating described above. In general, the support layer materials can include, but are not limited to, polyethylene/vinyl acetate copolymer-coated papers and polyester films. One example of a suitable support layer material is a polyethylene/vinyl acetate copolymer coated super calendared Kraft paper (1-80BKG-157 PE; Loparex of Willowbrook, Ill.). The support layer 16 can include a slit or perforations to form an area of weakness along a portion of the length of the support layer in order to facilitate folding of the dressing.
Various pressure sensitive adhesives can be used to form adhesive layer 17 on the backing layer 14 to make it adhesive. The pressure sensitive adhesive is usually reasonably skin compatible and “hypoallergenic”, such as the acrylate copolymers described in U.S. Pat. No. RE 24,906, the disclosure of which is hereby incorporated by reference. Particularly useful is a 97:3 iso-octyl acrylate:acrylamide copolymer, as is 70:15:15 isooctyl acrylate:ethyleneoxide acrylate:acrylic acid terpolymer described in U.S. Pat. No. 4,737,410, the disclosure of which is hereby incorporated by reference is suitable. Additional useful adhesives are described in U.S. Pat. Nos. 3,389,827, 4,112,213, 4,310,509, 4,323,557, WO 99/27975, and WO 99/28539, the disclosures of which are hereby incorporated by reference. Inclusion of medicaments or antimicrobial agents in the adhesive is also contemplated, as described in U.S. Pat. Nos. 4,310,509 and 4,323,557, both of which are also hereby incorporated by reference.
The pressure sensitive adhesive layer is generally provided on one major surface of the backing layer in order to make it adhesive, and a low adhesion coating (low adhesion backsize or LAB) is provided on the other major surface of the backing layer 14 on the side that comes in contact with the support layer. The low adhesion coating reduces the need to change the dressing due to unwanted dressing removal when other tapes or devices are placed on the dressing and removed, and reduces the surface friction of the dressing on linen or other fabrics, thereby offering additional protection against the accidental removal of dressing. A description of a low adhesion backing material suitable for use with the present invention can be found in U.S. Pat. Nos. 5,531,855 and 6,264,976, which are compatible with a heat seal bond described below, and are incorporated herein in their entirety.
Carrier films 24 suitable for use with the invention can be made of kraft papers, polyethylene, polypropylene, polyester or composites of any of these materials. The films are preferably coated with release agents such as fluorochemicals or silicones. For example, U.S. Pat. No. 4,472,480, the disclosure of which is hereby incorporated by reference, describes low surface energy perfluorochemical liners. The liners are papers, polyolefin films, or polyester films coated with silicone release materials. Examples of commercially available silicone coated release papers are POLYSLIK™, silicone release papers available from Rexam Release (Bedford Park, Ill.) and silicone release papers supplied by Loparex Inc. (Willowbrook, Ill.).
As various changes could be made in the above constructions, compositions and methods without departing from the scope of the invention as defined in the claims, it is intended that all matter contained in the above description or shown in the accompanying drawings be interpreted as illustrative and not in a limiting sense.
| Number | Date | Country | |
|---|---|---|---|
| 61108397 | Oct 2008 | US |
