Disclosed embodiments relate to apparatuses and methods for wound treatment. In certain embodiments, a wound treatment apparatus includes a wound dressing configured to be positioned over a wound to provide a substantially fluid impermeable seal over the wound. The wound dressing further includes a wound contact layer configured to be positioned in contact with the wound, a transmission layer positioned above the wound contact layer and configured to transmit wound fluid away from the wound, an absorbent layer positioned above the transmission layer and configured to absorb wound fluid, and a backing layer positioned above the absorbent layer and including an orifice. The apparatus also includes an oxygen source configured to supply oxygen to the wound through the orifice.

A wound dressing comprising a component wherein said component comprises a planar backing sheet and a yarn wherein the yarn extends through the planar backing sheet from the first side of the sheet to form a plurality of tufts on the second side of the planar backing sheet. Also disclosed is a component comprising an elastomeric planar backing sheet and an absorbent yarn and a component comprising a planar backing sheet and a monofilament yarn wherein in each case the yarn extends through the planar backing sheet from the first side of the sheet to form a plurality of tufts on the second side of the planar backing sheet. Also disclosed is a method of manufacturing the components, a wound dressing or a negative pressure apparatus comprising the components and a method of treating a wound using said wound dressing or negative pressure apparatus comprising the components.

Tissue dressing materials and associated methods of forming such dressing materials are disclosed. In one example embodiment, a dressing material may include a foam and a film formed on a first side of the foam. The film may be integrally-formed on the side of the foam. The film may include a plurality of apertures. A method of making the dressing material may include placing a pre-polymer mixture and water into a mold to create the dressing material comprising a foam and an integral film on at least one surface of the foam. The method may further include forming a plurality of openings in at least the integral film, with the openings being formed within the mold or subsequent to removal of the dressing material from the mold.

A negative pressure device includes a drape covering a dressing site on a patient, a sealing element connected with the drape, a flexible gas chamber housing disposed outwardly from the drape with respect to the enclosed chamber, and a reactor. The drape is made from a thin sheet film and is capable of maintaining a negative pressure underneath the drape. The sealing element and the drape are configured so that the sealing element cooperates with the drape to define an enclosed volume covered by the drape and surrounded by the sealing element when applied to skin. The flexible gas chamber housing defines a flexible gas chamber. The reactor is positioned with respect to the enclosed volume and the flexible gas chamber to consume a gas found in air within the enclosed volume and the flexible gas chamber.

A wound treatment system includes a wound dressing, a negative-pressure source, a light-emitting device, an image recognition module, and a control module. The wound dressing includes a housing with an opening, and a barrier layer with a conduit pathway separating the inside of the housing from the opening to form a receiving space. The negative-pressure source is fluidly connected to the wound dressing to remove tissue exudate of the wound. The light-emitting device is disposed in the receiving space, optically coupled to the barrier layer and can emit light of different wavelength bands as the detection light required by the image recognition module disposed on a side of the opening of the housing of the wound dressing and provide specific wavelengths of phototherapy required by different stages of the wound.

A negative pressure wound therapy system includes a dressing, a tube, a flow restriction pad, and an in-line filter. The dressing is configured for placement in a wound bed. The tube includes a first end and a second end. The first end is configured to be operably coupled to the dressing. The second end is configured to engage a negative pressure source. The flow restriction pad is configured to be coupled to the dressing proximate the first end of the tube. The flow restriction pad includes a tortuous fluid flow path that is configured to restrict or reduce an amount of a fluid drawn from the dressing into the tube and induce a backpressure between the dressing and the tube. The in-line filter is positioned within the tube between the first end and the second end. The in-line filter configured to substantially prevent the fluid entering the tube.

Various arrangements of fluidics systems are disclosed. In one arrangement, an aspiration circuit for a fluidics system is disclosed that selectively controls aspiration. The aspiration circuit comprises an aspiration line operatively connected to a surgical instrument, an aspiration exhaust line operatively connected to a waste receptacle; an aspiration vent line connected at a first end to the aspiration line; and a selectively variable vent valve operatively connected to the aspiration vent line. The variable vent valve may be selectively moved to vary aspiration pressure within the aspiration line. Other fluidics systems are disclosed that include a selectively positionable irrigation valve that may also be incorporated into a fluidics system that includes a variable vent valve.

A combination hanger arm extension and pump cover device can be used with an instillation unit. The device includes a body portion that has a first end and a second end. A hook extends from the first end, and a tab extends from the body proximate the hook. A panel is disposed proximate the second end. A substantially rectangular sleeve extends at least partially through the body. The sleeve is disposed between the first and second end.

Wound therapy compression garments and layered dressing kits are described. In an aspect, a kit includes a compression garment and one or more fenestrated dressing layers. The compression garment includes a plurality of hydrophobic longitudinal wales arranged to form a fabric with a plurality of hydrophilic transverse elastomeric threads under variable tension connecting adjacent ones of the hydrophobic longitudinal wales in such way as to deliver elastic compression at a wound site. The hydrophobic longitudinal wales and the hydrophilic transverse elastomeric threads cooperate to generate hydrostatic pressure for transporting fluid away from the wound site. The fenestrated dressing layer(s) is configured to form a textured interface with the compression garment and increase movement of fluid away from the wound site.

A specimen collection cassette for a medical fluid collection system. A housing defines a first void space and a second void space, and an outlet opening in fluid communication with the first and second void spaces. An aperture may be within a wall separating the first and second void spaces with the aperture providing fluid communication between the first and second void spaces. First and second fittings receive a suction line for drawing fluid into the first and second void spaces, respectively. A fluid communication path is established from the first fitting to the outlet opening through the first void space, aperture, and the second void space, and a bypass fluid communication path is established from the second bore to the outlet opening through the second void space. The cassette is operable in one or both of a tissue sample collection mode and a bypass mode.