The invention relates to a wound dressing device for securing a dressing in position on a wound, wherein the wound dressing device comprises: a retaining device for encompassing a portion of the body; a dressing, and; a fastening element that can secure the dressing in position. The fastening element being configured at least substantially external to the retaining device, the dressing being configured at least substantially internal to the retaining device, such that the dressing can be secured to the fastening element through the retaining device. The invention also relates to a method of applying the device and to a combined dressing and fastening element.

A knitted compression article with tubular or pocketlike receiving members for receiving at least one finger or toe of a wearer of the compression article, with a spacer element being disposed at least between two adjacent receiving members. Putting on such garment parts can be made easier and the fabrication of such garment parts can be simplified and, in particular, can be carried out in a single continuous knitting process without the need for subsequent sewing steps by providing that each receiving member has a front ply and a back ply and that the front ply and the back ply are seamlessly knitted to each other so as to create a tubular or pocketlike receiving member, with the spacer element or each spacer element being formed by connecting the front ply and the back ply to each other by a machine knitting technique.

A tubular body is configured to be disposed around and to apply compression to an extremity. The tubular body includes a treatment area having a first filament and a second filament. Both the first filament and the second filament are disposed to engage the surface of the extremity. The first filament includes AgNP in a concentration effective to promote healing of a wound on the surface of the extremity. The second filament includes a metal having a composition that forms a galvanic couple with silver. The first filament and the second filament are arranged in the tubular body such that the AgNP and metal form galvanic couples across at least a portion of the treatment area when in the presence of a fluid in the wound of the extremity that produce an electric current in an amount effective to further promote healing of the wound.

A system is provided comprising a columnar sleeve of stretchable fabric, the sleeve produced in various skin tone colors and configured to slip upon an individual toe or finger and an absorbent padding configured for attachment to an inside surface of the sleeve, the padding configured to cover about one half of an interior circumference of the inside surface, the padding optionally infused with at least one of pain killers, antiseptics, and soothing gels. The system also comprises wax paper covering the padding prior to use of the sleeve, an applicator shaped to facilitate slipping the sleeve upon the individual toe or finger, and convex-shaped flex bands placed lengthwise into the sleeve. The flex bands exert downward pressure on one of a toe and a finger and are placed in a U-shape, thus promoting the downward pressure.

Systems, apparatuses, and methods for providing negative pressure to a tissue site are disclosed. Illustrative embodiments may include an apparatus or system comprising a dressing for treating a tissue site with negative pressure. For example, the dressing may comprise or consist essentially of a manifold and a contact layer. In some embodiments, the manifold may have a tubular shape with a central axis. The contact layer may comprise a polymer film completely or substantially enclosing the manifold in some examples. In further embodiments, the dressing may comprise a plurality of fluid restrictions in the contact layer, the fluid restrictions configured to open or expand in response to a pressure gradient across the polymer film.

Tubular bandage, in particular a finger or toe bandage which is formed as a tube comprising an outer layer which is connected to an inner layer, and wherein the outer layer has a diameter and an elasticity such that the bandage can be clamped adhesive-free around the body part to be treated, in the particular, said finger or said toe, and wherein the inner layer is made of an elastic wound-protective material, wherein said outer layer is made of an air-permeable and water-repellent material, and wherein, at the open endings, said outer layer extends in the longitudinal direction over the inner layer over a distance of more than 0.5 mm, such that the outer layer touches the body part to be treated, in particular a finger or toe, with its endings when applied.

An apparatus for protecting a post-amputation residuum comprises a shell defining a hollow interior cavity adapted for receiving and covering a distal portion of the residuum. The shell has an opening into the cavity at the distal end. A first and a second plurality of circumferentially spaced longitudinal slits extend from the proximal end and the distal end, respectively. A proximal portion of a compression sleeve is disposed over at least a portion of the residuum. A free distal portion of the sleeve extends through the opening in the shell and everts upon application of a longitudinal force to the distal portion of the sleeve in a proximal direction for folding over and covering the shell. The distal portion of the sleeve extends proximally of the shell to a position at least partially along the proximal portion of the sleeve for compressing the shell inwardly toward the residuum.

A wound dressing having a chromic material responsive to at least one stimuli. In one or more embodiments, a plurality of individual liquid expandable articles introduce the chromatic material to the wound. The individual liquid-expandable articles release stored mechanical energy and mechanically expand into expanded articles upon contact with a liquid associated with the wound. In response to the chromic material receiving the at least one stimuli the chromic material provides a color change evidencing how long the expanded articles have been in contact with the wound and where the expanded articles are within the wound. In one or more embodiments, determinations may be made about removing the expanded articles from the wound based on the color of the chromic material.

A method for dressing a wound. The method includes introducing a chromic material via at least one article to the wound and stimulating the chromic material with a stimuli. The method also includes providing a color change in response to stimulating the chromic material and indicating via the color change of the chromic material how long the article has been at least partially in contact with the wound. In one or more embodiments, the method may also include measuring the color change from information including a plurality of colors corresponding to a plurality of time periods and, in response to measuring the color change, determining a length of time the article has been in contact with the wound. The method may also include manually crumpling a distal end of a portion of the article such that the distal end of the portion is sized to be received within the wound and then manually separating the crumpled distal end from the rest of the article.

A wound dressing is made from a tubular inner layer and at least one outer layer disposed radially beyond the inner layer. The inner layer permits egress of fluid from weeping wounds, prevents desiccation of skin disposed beneath the inner layer, and prevents desiccation of ointment disposed between the inner layer and the skin. The at least one outer layer absorbs fluids that leak through the inner layer, protects the inner layer from outside contaminants, and prevents fluids from escaping. The at least one outer layer is affixed to the inner layer, and each of the layers is elastic in at least the radial direction. Optionally, a layer of ointment may be applied to an inner surface of the inner layer. Note that the tubular inner layer may be either pre-formed or formed at the time of application.