Abstract: Disclosed is a liquid removal drypad and liquid removal system suitable for absorbing and removing liquid produced by an individual. The drypad can include one or more perforated conduits arranged with an absorbent material. A source of reduced pressure can be connected to the one or more perforated conduits to remove liquid from the drypad. The drypad can be positioned under a patient and liquid produced by the individual can be removed by applying reduced pressure to the drypad. The drypad can be made by combining one or more conduits with an absorbent material.

Abstract: A vented wound dressing barrier includes one or more membrane layers with a plurality of vents. The vents are cut along a perimeter of the vents through the one or more membrane layers. Each vent having a connection portion uncut relative to the one or more membrane layers thereby forming a hinge configured to allow the vents to open for drainage when exposed to fluid underlying the vented wound dressing barrier. The plurality of vents is each cut along the perimeter without removal of any of the membrane layer. The one or more membrane layers with the plurality of vents has a surface for covering a wound, the surface area in the absence of a fluid pressing on the vents having no openings or voids which reduce the surface area of a vented wound dressing barrier area covering a wound.

Abstract: Systems and methods encourage users to rotate injection sites and avoid lipodystrophy. Sleeves and/or lost-tooth gear dials and/or microswitches in or on injection pens or their caps, on vials, and on other portable devices manually adjust an indicator before or after an injection to show a current or next injection site in accordance with a site rotation plan. Injected medicine packaging and related printed indicia encourage site rotation. Optical devices employing optical mouse or projection technology help locate and/or distribute injection sites within a body area. A mobile phone app tracks injections and locations to select next injection site, and can use imaging to locate a target injection site and optionally diagnose lipodystrophic conditions and record them. Tactile and print media educational tools are presented to help users palpate and identify lipos in body areas having injection sites.

Abstract: A bandage system lances a skin tag from a person's body and thereafter projects the wound created. The system has a base layer that is adhesively attached to the person such that the skin tag passes through an opening of the base layer. A cutter is located atop the base layer and uses a pair of blades that are squeezed together to cut the skin tag protruding through the opening. After cutting, a protective layer is adhered to the base layer such that a medicine laden absorbent pad on the protective layer overlays the opening on the base layer absorbing any blood from the wound and applying the medicine to the wound. Thereafter, the system is worn as a typical bandage.

Abstract: An absorbent structure including a distribution layer and a storage layer is disclosed. The distribution layer has two or more stratums. The two or more stratums include a body facing stratum and a subsequent stratum below the body facing stratum. The density of the subsequent stratum is a fraction of the density of the body facing stratum and the porosity of the subsequent stratum is a multiple of the body facing stratum porosity.

Abstract: Provided are a support with an antibacterial layer, which exhibits excellent followability with respect to a curved surface and in which peeling does not easily occur between a support and an antibacterial layer even though the support with an antibacterial layer is bonded to a curved surface, and a laminate including the support with an antibacterial layer. The support with an antibacterial layer of the present invention includes a support and an antibacterial layer disposed in at least a portion on the support, in which the support contains a urethane resin, and the antibacterial layer contains a hydrophilic polymer and an antibacterial agent.

Abstract: A wound dressing for a burn or open wound is formed of a foam material body with an open center area. The thickness of the foam body creates a zone for air circulation and prevents contact with the wound. This may have a mesh, gauze or other air permeable cover over the open center area.

Abstract: A barrier for use in negative pressure wound therapy can include a base layer and surface structures. The barrier can be used to reduce or prevent tissue ingrowth. A method of using a negative pressure wound therapy system can include positioning a perforated barrier in a wound. After positioning the perforated barrier in the wound, positioning a pad in the wound on top of the perforated barrier, positioning a seal on top of the wound to at least partially seal the perforated barrier and the foam in the wound, and applying negative pressure wound therapy to the wound.

Abstract: An absorbent article can include a bodyside liner, an outer cover, and an absorbent body disposed between the bodyside liner and the outer cover. The bodyside liner can be treated with a surfactant. A component of the absorbent article can be treated with a hydrophobically modified polymer. The hydrophobically modified polymer can be configured to interact with the surfactant upon wetting of the absorbent article when the surfactant and the hydrophobically modified polymer are in an aqueous solution to increase surface tension of the aqueous solution.

Abstract: A support assembly for supporting a biological product (e.g., membrane) in an operative position. The support assembly has a base and a cover. A membrane receiving portion of the base defines a plurality of perforations that extend between top and bottom surfaces of the product receiving portion. The cover is releasably coupled to the base in a product-covering position in which the cover overlies the product receiving portion of the base. In the operative position, the biological product engages the top surface of the product receiving portion and the bottom surface of the cover.

Abstract: The invention relates to a system for treating an epistaxis, comprising: a compressible body designed to come into contact with walls of a nasal cavity of a patient, or surrounded by a veil of hemostatic properties; an envelope designed to envelop the compressible body; and a compression device for compressing the compressible body in the envelope, said compression device being designed so as to compress or release the compressible body.

Abstract: A system for treating a tissue site includes a pressure source to apply reduced pressure, and a manifold in fluid communication with the pressure source to provide reduced pressure to the tissue site. The system includes a drape for adhering to the tissue site to cover the tissue site and the manifold. The drape has a film layer having a thickness less than about 15 microns, and an adhesive coupled to the film layer. The adhesive seals the film layer to the tissue site to create a sealed space having the manifold therein. The adhesive is sufficiently thick to limit leaks between the film layer and the tissue site.

Abstract: Wound treatment materials can have at least two perforated biomatrix layers which are interconnected. Methods for preparing such wound treatment materials include the application of adhesives. Treatment of exuding wounds, and vacuum-assisted wound treatment therapy, can be carried out with the wound treatment materials.

Abstract: The present invention relates to a wound pad comprising fibers and being provided with at least a first and a second discrete group of incisions, wherein each one of said discrete groups of incisions comprises at least a first and a second incision, wherein said first and said second incision extend from a common starting point to a respective end point, wherein the end point of said first incision is spaced from the end point of said second incision, wherein the common starting point of said first group of incisions is provided on a first side of an imaginary line extending in the machine direction of said fibrous wound pad, and the common starting point of said second group of incisions is provided on a second side of said imaginary line, and wherein a first incision of said first group of incisions and a second incision of said second group of incisions each cross said imaginary line. The present invention also relates to a self-adhesive member for adhering to and cover a portion of a user's skin.

Abstract: Dressings, systems, and methods are disclosed for treating tissue with reduced pressure. A dressing for distributing reduced pressure to a tissue site includes a plurality of liquid-impermeable layers that are stacked and a plurality of spacers disposed at least partially between adjacent liquid-impermeable layers. The plurality of liquid-impermeable layers are fenestrated at least in part. The plurality of spacers and plurality of liquid-impermeable layers form a plurality of flow paths for allowing fluid flow under reduced pressure. Adjacent layers of the plurality of liquid-impermeable layers are stacked without foam between at least a majority of coextensive surfaces. Other dressings, systems, and methods are disclosed.

Abstract: Provided is a PSA sheet that has a high level of moisture resistance while maintaining good holding power with reduced gas emission. The PSA sheet provided by this invention comprises a moisture-impermeable layer and a PSA layer provided to one face of the moisture-impermeable layer. The PSA layer comprises a polymer A having a weight average molecular weight of 5×104 or higher as a base polymer and a polymer B having a number average molecular weight of 1000 or higher and a weight average molecular weight lower than 5×104.

Abstract: A system for treating a tissue site with negative-pressure is described. The system includes a manifold configured to be positioned adjacent to the tissue site and a drape configured to be positioned over the tissue site and the manifold to form a sealed space. The system also includes a negative-pressure source configured to provide negative-pressure to the sealed space. The drape includes a film layer, a layer of a bonding adhesive coupled to the film layer, and a mesh coupled to the layer of the bonding adhesive. The mesh includes a coating of a sealing adhesive and one or more bonding apertures. Methods of manufacturing the drape are also described.

Abstract: A system for treating a tissue site with negative-pressure is described. The system includes a manifold configured to be positioned adjacent to the tissue site and a drape configured to be positioned over the tissue site and the manifold to form a sealed space. The system also includes a negative-pressure source configured to provide negative-pressure to the sealed space. The drape includes a film layer, a layer of a bonding adhesive coupled to the film layer, and a mesh coupled to the layer of the bonding adhesive. The mesh includes a coating of a sealing adhesive and one or more bonding apertures. Methods of manufacturing the drape are also described.

Abstract: Wound dressings suitable for negative pressure wound therapy are disclosed. The wound dressings may include a body of porous material, the body of porous material may include a plurality of cuts which provide regions of flexibility within the body. Also disclosed are methods of manufacturing and methods of using such wound dressings. In addition, such wound dressings can include a retaining mechanism removably coupled to the material and configured to retain the material in the expanded conformation.

Abstract: Appurtenances to a wound dressing and systems for monitoring wound dressings are described. In some embodiments, a system for monitoring a wound dressing includes: an appurtenance to a wound dressing, wherein the appurtenance includes a sensor unit, an electronic identifier, and a transmitter unit operably attached to the sensor unit and to the electronic identifier; and a local unit including a receiver for the transmitter unit, a processor operably attached to the receiver, and a communication unit operably attached to the processor.

Abstract: The illustrative systems, methods, and dressings for applying reduced pressure to a tissue site are presented that involve quickly removing fluids from the tissue site to reduce or avoid maceration of the epidermis. One dressing includes a dressing material for transferring the reduced pressure to the tissue site and a drape covering at least a portion of the dressing material. The dressing material includes a hydrophobic tissue-interface layer adapted to contact the tissue site. The dressing material also includes a manifold adapted to distribute reduced pressure. The manifold may be a hydrophobic layer. The dressing material also includes one or more absorbent layers adapted to absorb liquid from the tissue site via the tissue-interface layer and the manifold. Other aspects are disclosed.

Abstract: Medical breathing tubes have a tubular body that defines a lumen extending between open terminal ends of the tubular body. An internal form is enclosed within the lumen and supportive of the tubular body. The internal form may be a coated encapsulated internal form where the coating secures the internal form to the tubular body. The internal form may provide for a series of alternative crests and troughs of the tubular body. A patient interface and/or a securement system may be attached to the tubular body.

Abstract: Techniques are described for using confinement structures and/or pattern gratings to reduce or prevent the wicking of sealant polymer (e.g., glue) into the optically active areas of a multi-layered optical assembly. A multi-layered optical structure may include multiple layers of substrate imprinted with waveguide grating patterns. The multiple layers may be secured using an edge adhesive, such as a resin, epoxy, glue, and so forth. A confinement structure such as an edge pattern may be imprinted along the edge of each layer to control and confine the capillary flow of the edge adhesive and prevent the edge adhesive from wicking into the functional waveguide grating patterns of the layers. Moreover, the edge adhesive may be carbon doped or otherwise blackened to reduce the reflection of light off the edge back into the interior of the layer, thus improving the optical function of the assembly.

Abstract: Appurtenances to cavity wound medical dressings are described. In some embodiments, an appurtenance to a cavity wound dressing includes: a substrate including at least one wound-facing surface, the wound-facing surface configured to be oriented facing a wound surface of a cavity wound; and a plurality of sensor units attached to the substrate, the plurality of sensor units oriented and positioned on the substrate relative to the wound surface of the cavity wound.

Abstract: Appurtenances to wound dressings are described, which include: a substrate configured to mechanically or chemically attach to a wound dressing; a transmission unit attached to a surface of the substrate, the transmission unit including circuitry and at least one antenna, the transmission unit configured to transmit a signal; and a projection operably attached to the transmission unit, the projection of a size and shape to extend into an interior region of the wound dressing and configured to sample a fluid associated with a wound.

Abstract: In some embodiments, an appurtenance to a wound dressing includes: a substrate with at least one surface of a size and shape to mate with a surface of a wound dressing; a plurality of projections attached to the substrate and positioned to secure the substrate to the wound dressing; one or more sensor units attached to the substrate, the one or more sensor units configured to sense a condition of the wound dressing; and a transmission unit attached to the substrate and operably coupled to the one or more sensor units, the transmission unit including circuitry configured to transmit information associated with the one or more sensor units.

Abstract: The present invention relates to method of preparing an absorbent wound care device comprising an active agent on a wound contacting surface, such as e.g. a protein or an enzyme, by the use of electrospraying, and a wound care device obtained by said method. The invention further relates to a wound care device comprising Thrombin and a polyurethane foam, and a method of treating bleeding.

Abstract: The invention relates to a wound dressing which is particularly suitable for therapeutically dressing wounds. Said wound dressing consists of a multi-layered structure comprising at least one layer containing at least one hydrocolloid, preferably collagen, (“hydrocolloid layer” or “collagen layer”) and at least one layer containing an activated carbon (“activated carbon layer”).

Abstract: An interface device for removing fluid from a surgical site by shaping the interface device in situ to place a set of openings, which are in fluid communication with a connection port adapted for connection to a vacuum source, in contact with at least a portion of the surgical site. This interface device having a connection port with a connection opening for connection to a vacuum source; a multiplicity of openings located on an exterior of the interface device and in fluid communication through the interface device to the connection port so that fluid may be drawn into the openings and removed by vacuum; and the interface device is adapted to allow a set of one or more hands to at least partially conform the interface device to at least a portion of the surgical site to place at least some of the multiplicity of openings in proximity to fluid.

Abstract: A method for closing a puncture wound on skin. The method including: adhering a first surface of a first member having an unrestrained shape to the skin and over the puncture; and subsequent to the adhering, removing a second member for restraining the first member in a restrained shape from the first member. Where at least a normal force is applied to the puncture wound due to the removal of the second member from the first member which causes the first member to change towards the unrestrained shape. The removing can further cause a force substantially perpendicular to the normal force which tends to close the puncture wound.

Abstract: An improved skin substitute is presented comprised of a silicone layer backed up with a woven nylon fabric layer, the silicone layer possessing a regular pattern of slits that permit the porosity of the skin substitute to be adjusted by clinicians by means of applying tension to the skin substitute that differentially opens the slits. A variety of therapeutic substances can be applied to the skin substitute to promote healing, including aloe and other medicinal preparations. A layer of water soluble or water insoluble anti-scar compound is also present, the preferred compound being salinomycin.

Abstract: There is provided a method for bonding together hydrogels by interposing a polyalkylene glycol between the gel surfaces to be bonded together of hydrogels. A method for bonding together hydrogels of the same type or different types, the method including: interposing a polyalkylene glycol between gel surfaces to be bonded together of the hydrogels and joining together the gel surfaces.

Abstract: The invention provides for a medical wrist band, specifically for infants and babies, which is economical to manufacture, durable, easy on the skin, does not cause allergic reactions and cannot be removed and reapplied without being damaged.

Abstract: A wound dressing provides a tenacious occlusive seal against the skin of a wearer, even in the presence of excessive blood or heavy perspiration. The preferred embodiment combines an adhesive backing layer with a hydrogel island providing superior hydrophilic gel adhesion. The product performs under extreme temperatures (i.e., 32-140° F.), and may be used to hold other dressings in place. The preferred embodiments are entirely translucent, and include a large pull-tab for easy removal. Two dressings may be packaged in a pliable re-sealable protective pouch, thereby forming a portable “kit.” Different “vented” embodiments are disclosed. A preferred structure includes a cover layer peripherally bonded to backing and hydrogel layers having a central aperture therethrough. The cover layer has one or more vent holes, and pressure is released through the central aperture and out the vent hole(s).

Abstract: The invention refers to a device for the negative pressure wound therapy comprising a cover material for the air-tight sealing of the wound and the wound surroundings; a means suitable for the generation of a negative pressure in the wound area, preferably a means for the functional connection of the wound area with a negative pressure source outside of the cover material in such a way that a negative pressure can be generated in the wound area and fluids can be drawn out of the wound area by suction; and a wound dressing, whereby the wound dressing contains an open-cell foam on the basis of a cross-linked polyorganosiloxane. The invention also refers to the use of open-cell foam on the basis of a cross-linked polyorganosiloxane for use in the negative pressure wound therapy, in particular in patients with a BMI of less than 18.

Abstract: This invention relates to a cosmetic sponge and a method of providing a cosmetic sponge incorporating a non-denatured collagen and other additives for skin care, cleaning, and cosmetic application.

Abstract: A device for the protection of skin lesions of various kinds, in particular lesions following biopsy interventions, comprising: a first sheet having a central opening; a spacing element on the first sheet, made of a non-rigid material soaked with substances having bacteriostatic, bactericidal, germicidal or fungicidal activity, and having a central opening of smaller size than the central opening in the first sheet, and the center of which is essentially coincident with the center of the opening in the first sheet, so that part of the spacing element comes into contact with the skin in an area surrounding the lesion; and a second sheet, made with a material having micro-porosity preferably lower than 0.5 ?m, placed over the spacing element so as to close the top of the central opening in said spacing element and to form, when the device is in contact with the skin, a closed chamber.

Abstract: A wound barrier pad is provided having a housing with a housing opening. The housing has a truncated conical shape. A base plate with an opening is disposed in the housing, and the housing is filled with a fluid or padding. The wound barrier pad may also be embodied to have a cylindrical shape, a rectangular shape or other shape. The wound barrier pad may be incorporated into a garment. In another embodiment the wound barrier pad includes a ring and an adhesive such that the wound barrier pad may be directly adhered to the patient, thus eliminating the need for the garment. In another embodiment there is a wound barrier device having a pad assembly and an anti-shear member. The anti-shear member reduces frictional forces on the skin of a patient.

Abstract: According to an embodiment of the present disclosure, a wound dressing system is presented. The wound dressing system includes a fluid permeable support layer, the support layer configured for positioning within a wound and adapted to generally conform to a topography of the wound, and to permit exudates from the wound to pass therethrough. The wound dressing system further includes a plurality of beads supported by the support layer, the beads defining an insulated inter-connected elongate member and an electrode embedded within and extending through at least a portion of the elongate member. Also, a current is generated by an external energy source that electrically flows through the electrode.

Abstract: A liner for incontinence includes a skin contact side sheet, a non-skin contact side sheet, and an absorbent body arranged between these sheets and including an absorbent material. The absorbent material includes 30 to 70 mass % of SAP. The liner includes a main body and wings in an intermediate region of the main body. An SAP basis weight in the intermediate region is larger than in front and rear regions of the main body. The main body includes a front compressed region which is positioned between the intermediate region and the front region immediately in front of a urinating position (UP) of a wearer when worn, side compressed regions which extend from the intermediate region to the front region and rear region, respectively, and a rear compressed region which extends in the rear region in substantially the width direction. At the compressed regions, the absorbent body is continuous.

Abstract: An improved skin substitute is presented comprised of a silicone layer backed up with a woven nylon fabric layer, the silicone layer possessing a regular pattern of slits that permit the porosity of the skin substitute to be adjusted by clinicians by means of applying tension to the skin substitute that differentially opens the slits. A variety of therapeutic substances can be applied to the skin substitute to promote healing, including aloe and other medicinal preparations.

Abstract: A wound treatment device comprises a wound surface contacting plug and a cover for covering the wound surface and the plug, wherein said plug consists of a flat textile isolating material comprising at least one first surface layer, one second surface layer and one intermediate space arranged between said surface layers. At least the first surface layer is provided with a biocompatible surface and a structure which enables a liquid to pass and prevents a wound tissue from growing in said structure. The intermediate space is provided with isolating threads elastically holding the first surface layer and the second surface layer at a certain distance from each other.

Abstract: The present invention relates to a bandage for use in negative-pressure wound therapy, more particularly for wounds in the abdominal region, comprising a flexible film as a wound contact layer and at least one conduit applied to the film, wherein the conduit communicates with the wound space through openings in the conduit and in the film.

Abstract: Methods, dressings, and systems for promoting epithelialization of a wound or other tissue are presented. The methods, dressings, and systems help form simulated rete pegs. In one instance, an epithelialization dressing is disclosed that may include a dressing body having a plurality of projections. A plurality of apertures is formed on a portion of the dressing body. The dressing helps manage fluids on the wound and the projections form cavities into which epithelial tissue migrates to from epithelial columns that function like rete pegs. Other dressings, methods, and systems are disclosed.

Abstract: Embodiments of the invention relate to a wound covering having a first strip-like element forming a first periphery and a second strip-like element that faces away from the first periphery, runs approximately parallel thereto, forming a second periphery, and is joined to the first strip-like element, there being formed between the first inner periphery of the strip-like element, facing away from the first periphery, and a second inner periphery of the second strip-like element, facing away from the second periphery, a drainage chamber, the depth of which in a depth direction extending at right angles to the periphery ensures a capillary action on bodily fluids received in the drainage chamber, in particular exudates.

Abstract: A hemostatic device for promoting the clotting of blood includes a gauze substrate, a clay material disposed on the gauze substrate, and also a polyol such as glycerol or the like disposed on the gauze substrate to bind the clay material. When the device is used to treat a bleeding wound, at least a portion of the clay material comes into contact with blood emanating from the wound to cause the clotting. A bandage that can be applied to a bleeding wound to promote the clotting of blood includes a flexible substrate and a gauze substrate mounted thereon. The gauze substrate includes a clay material and a polyol. A hemostatic sponge also includes a gauze substrate and a dispersion of hemostatic material and a polyol on a first surface of the substrate.

Abstract: A device for promoting the clotting of blood comprises a clay material in particle form and a receptacle for containing the clay material. At least a portion of the receptacle is defined by a mesh. Another device comprises a gauze substrate and a clay material disposed on the gauze substrate. Another device is a bandage comprising a substrate, a mesh mounted on the substrate, and particles of a clay material retained in the mesh. A hemostatic sponge comprises a substrate, a hemostatic material disposed on a first surface of the substrate, and a release agent disposed on a second surface of the substrate. The release agent is disposed on the wound-contacting surface of the substrate. When treating a bleeding wound, application of the hemostatic sponge causes at least a portion of the hemostatic material to come into contact with blood through the release agent and through the substrate.

Abstract: The present invention relates to wound treatment material comprising at least two perforated biomatrix layers interconnected by connecting means, as well as to methods for preparing such wound treatment materials and their use, in particular in the treatment of exuding wounds, and in the vacuum-assisted wound treatment therapy.

Abstract: A hyperbaric dressing has a fluid impermeable sheet and a fluid permeable layer with a sheet of porous material positioned between these two layers with passageways to permit fluid to flow out of the dressing.

Abstract: A wound dressing provides a tenacious occlusive seal against the skin of a wearer, even in the presence of excessive blood or heavy perspiration. The preferred embodiment combines an adhesive backing layer with a hydrogel island providing superior hydrophilic gel adhesion. The product performs under extreme temperatures (i.e., 32-140° F.), and may be used to hold other dressings in place. The preferred embodiments are entirely translucent, and include a large pull-tab for easy removal. Two dressings may be packaged in a pliable re-sealable protective pouch, thereby forming a portable “kit.” Different “vented” embodiments are disclosed. A preferred structure includes a cover layer peripherally bonded to backing and hydrogel layers having a central aperture therethrough. The cover layer has one or more vent holes, and pressure is released through the central aperture and out the vent hole(s).