Abstract:
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.
Abstract:
An apparatus for protecting a wound. The apparatus includes a waterproof shield element to cover a wound area of a user's body, where the elevated top surface of the shield element is elevated away from the user's body. A retention mechanism selectively retains the shield element against the user's body, utilizing the elevated top surface to create a normal force between the shield element and the user's body to thereby form an effective seal between the shield element and the user's body.
Abstract:
A reduced-pressure, deep-tissue closure device for applying a closing force on a deep tissue includes a contractible matrix that is formed with a first plurality of apertures and which has a first side and a second, inward-facing side. The contractible matrix is for disposing proximate to the deep tissue. A reduced-pressure source is fluidly coupled to the contractible matrix and operable to deliver reduced pressure to the contractible matrix. When under reduced pressure, the contractible matrix grips the deep tissue adjacent the contractible matrix and provides a closing force on the deep tissue. A system and method are also presented.
Abstract:
Systems and apparatuses for administering reduced pressure treatment to a tissue site include a reduced pressure source, a drape having a plurality of projections for contacting the tissue site, and an adhesive connected to at least a portion of the drape for sealing the drape to a portion of a patient's intact epidermis.
Abstract:
A see-through dressing assembly is presented for use with a reduced-pressure system for treating a wound on a patient using reduced pressure that allows visual observation of the wound during treatment. The dressing assembly includes a bolster for providing a directed force when under reduced pressure, a sealing member for covering the bolster and providing a seal over the bolster and a patient's epidermis, and wherein the bolster and sealing member are formed from see-through materials sufficient to allow perception of color from a point external to the system. Other systems, dressings, and methods are presented.
Abstract:
An open-cavity, reduced-pressure treatment device and system for treating a cavity in a patient's body, such as an abdominal cavity, is presented. In one instance, an open-cavity, reduced-pressure treatment device includes a plurality of encapsulated leg members, each having an interior portion with a leg manifold member and formed with fenestrations operable to allow fluid flow into the interior portion, and a central connection member fluidly coupled to the plurality of encapsulated leg members. The central connection member has a connection manifold member. The open-cavity, reduced-pressure treatment devices, systems, and methods allow for, among other things, removal of fluids.
Abstract:
Adjustable covers, systems, and methods are presented that include an adjustable cover that may be adjusted to an appropriate size by hand without requiring cutting tools and without substantial leaks. In one instance, the adjustable covering includes a drape member with a plurality of non-leaking tear paths. Each non-leaking tear path includes a weakened path of the drape member that may be torn. The adjustable covering may further include a first plurality of tear starters formed on a first initiation edge of the drape member. Each tear starter of the first plurality of tear starters is aligned with one of the plurality of tear paths. Each of the first plurality of tear starters is adapted to facilitate the initiation of a tear along a tear path. The grains of the drape member, a backing layer, and support layer may also be in the same direction. Other adjustable covers, systems, and methods are presented.
Abstract:
The invention relates to a wound dressing for absorbing exudate from a wound on which the wound dressing is placed. The wound dressing includes a porous, highly absorptive fiber dressing and a negative surface charge on a surface of the dressing.
Abstract:
Disclosed are solid dressings for treated wounded tissue in mammalian patients, such as a human, comprising a haemostatic layer consisting essentially of fibrinogen and a fibrinogen activator, wherein the fibrinogen is present in an amount between 3.0 mg/cm2 of the wound facing surface of the dressing and 13.0 mg/cm2 of the wound facing surface of the dressing. Also disclosed are methods for treating wounded tissue.
Abstract:
The invention refers to a disposable absorbent article such as a diaper, a pant or a sanitary napkin. The disposable absorbent article further comprises a structure which is able to elongate and simultaneously convert from an initial flat configuration into an erected configuration.