Abstract: A system is described herein that can irrigate a tissue site using negative-pressure. The system may include a tissue interface configured to be placed adjacent to the tissue site, and a sealing member configured to be placed over the tissue interface to form a sealed space. The system may also include a negative-pressure source configured to be fluidly coupled to the sealed space and a fluid source. The system may further include an irrigation valve. The irrigation valve can have a fluid inlet configured to be fluidly coupled to the fluid source. The irrigation valve can also have a fluid outlet configured to be fluidly coupled to the sealed space. The irrigation valve may also include a clamp configured to be actuated by the negative-pressure source to regulate fluid flow from the fluid source through the fluid outlet.

Abstract: Systems, methods, and apparatuses for irrigating a tissue site are described. The system can include a tissue interface and a sealing member configured to be placed over the tissue site to form a sealed space, and a negative-pressure source fluidly coupled to the sealed space. The system includes an irrigation valve having a housing, a piston disposed in the housing, a fluid inlet to fluidly couple a fluid inlet chamber to a fluid source, and a fluid outlet to fluidly couple a fluid outlet chamber to the sealed space. A piston passage extends through the piston and fluidly couples the fluid inlet chamber and the fluid outlet chamber, and a biasing member is coupled to the piston to bias the irrigation valve to a closed position. The negative-pressure source is configured to move the piston between the closed position and an open position to draw fluid to the sealed space.

Abstract: Systems and methods for delivery of fluid to a wound therapy dressing. In exemplary embodiments, a pressure sensor measures the pressure at the wound therapy dressing and restricts fluid flow to the wound therapy dressing when a predetermined pressure is achieve.

Abstract: A system that may be adapted to distribute reduced pressure to a tissue site may include a dressing and a sealing member. The dressing may include a manifold layer, a storage layer, and a plurality of retainers. The manifold layer may be adapted to be positioned proximate the tissue site, and the storage layer may be positioned proximate the manifold layer. The plurality of retainers may be disposed in the storage layer. Each of the retainers may define a fluid communication channel through the storage layer. The retainers may be adapted to substantially preclude deformation of the storage layer into the fluid communication channels. The sealing member may be adapted to cover the dressing and to provide a fluid seal between the sealing member and the tissue site.

Abstract: Systems and methods for delivery of fluid to a wound therapy dressing. In exemplary embodiments, a pressure sensor measures the pressure at the wound therapy dressing and restricts fluid flow to the wound therapy dressing when a predetermined pressure is achieve.

Abstract: A conduit for treating a tissue site with reduced pressure may include a primary lumen and at least one secondary lumen. A wall of the conduit may include a first wall material and a second wall material. The first wall material may comprise a substantially non-absorbent material that is vapor impermeable and liquid impermeable. The second wall material may comprise an absorbent material that is vapor permeable and liquid impermeable. The second wall material may be positioned in fluid contact with the at least one secondary lumen. Other systems, apparatus, and methods are disclosed.

Abstract: A wound dressing includes a superabsorbent pad, a drape layer, a humidity chamber, a wick, and a humidity colorimeter sensor. The superabsorbent pad is configured to absorb wound fluid and has a first side and a second, wound- facing side. The drape layer is coupled to the first side of the superabsorbe nt pad and has a first side and a second, wound- facing side. The drape layer is substantially impermeable to liquid and substantially permeable to vapor. The humidity chamber is coupled to the first side of the drape layer opposite the superabsorbent pad. The wick extends through the drape layer and is configured to wick moisture between the superabsorbent pad and the humidity chamber. The humidity colorimeter sensor is located within the humidity chamber and configured to change color responsive to a humidity level within the humidity chamber.

Abstract: A dressing for treating a tissue site with negative pressure, a sealing tape, methods of use and methods of manufacturing the sealing tape are described. The dressing includes a tissue interface configured to be positioned adjacent to the tissue site and a sealing member configured to be positioned over the tissue interface and the tissue site to form a sealed environment. The dressing also includes a sealing tape having a carrier layer having a first side and a second side, a silicone adhesive layer bonded to the first side of the carrier layer, and an acrylic adhesive layer bonded to the second side of the carrier layer. A plurality of holes extend through the silicone adhesive layer, the acrylic adhesive layer, and the carrier layer. A first release liner is coupled to silicone adhesive layer, and a second release liner is coupled to the acrylic adhesive layer.

Abstract: A reduced pressure treatment system includes a porous pad positioned at a tissue site and a canister having a collection chamber, an inlet, and an outlet. The inlet is fluidly connected to the porous pad. A reduced pressure source is fluidly connected to the outlet of the canister to such that fluid from the tissue site may be drawn into the collection chamber. A hydrophobic filter is positioned adjacent the outlet to prevent liquid from exiting the collection chamber through the outlet. A baffle is positioned within the canister to create a tortuous path between the inlet and the outlet to prevent premature blocking of the hydrophobic filter.

Abstract: An apparatus for use in a multi-orientation liquid collection canister to collect liquid from a tissue site is provided. The apparatus includes a substantially planar, liquid-air separator disposed on at least one wall of the multi-orientation liquid collection canister to prevent the liquid from exiting the multi-orientation liquid collection canister. The apparatus further includes an elongated member connected to the liquid-air separator and extending away from the liquid-air separator into a first space of the multi-orientation liquid collection canister. The elongated member has a membrane defining a second space along at least a portion of a length of the elongated member. At least a portion of the membrane allows gaseous communication between the first space and the second space.

Abstract: In various embodiments, a support system includes a cover sheet with a number of layers. In certain embodiments, a top layer and a bottom layer are bonded to a middle spacer layer.

Abstract: An apparatus for use in a multi-orientation liquid collection canister to collect liquid from a tissue site is provided. The apparatus includes a substantially planar, liquid-air separator disposed on at least one wall of the multi-orientation liquid collection canister to prevent the liquid from exiting the multi-orientation liquid collection canister. The apparatus further includes an elongated member connected to the liquid-air separator and extending away from the liquid-air separator into a first space of the multi-orientation liquid collection canister. The elongated member has a membrane defining a second space along at least a portion of a length of the elongated member. At least a portion of the membrane allows gaseous communication between the first space and the second space.

Abstract: A reduced pressure treatment system includes a porous pad positioned at a tissue site and a canister having a collection chamber, an inlet, and an outlet. The inlet is fluidly connected to the porous pad. A reduced pressure source is fluidly connected to the outlet of the canister to such that fluid from the tissue site may be drawn into the collection chamber. A hydrophobic filter is positioned adjacent the outlet to prevent liquid from exiting the collection chamber through the outlet. A baffle is positioned within the canister to create a tortuous path between the inlet and the outlet to prevent premature blocking of the hydrophobic filter.

Abstract: Systems, methods, and apparatuses for providing installation therapy and negative-pressure therapy are described. The apparatus includes a housing and a moveable barrier disposed in the housing to form a dosing chamber and a pressure chamber. The apparatus also includes a therapy conduit configured to be fluidly coupled to a pressure source and to a canister. The apparatus further includes a fluid inlet fluidly coupled to the dosing chamber and configured to be fluidly coupled to a fluid source and a fluid outlet fluidly coupled to the dosing chamber and configured to be fluidly coupled to a dressing. A pressure inlet is fluidly coupled to the therapy conduit and the pressure chamber; and a check valve is disposed in the therapy conduit.

Abstract: Systems, apparatuses, and methods for instilling fluid to a tissue site in a negative-pressure therapy environment are described. Illustrative embodiments may include a pneumatically-actuated instillation pump that can draw a solution from a solution source during a negative-pressure interval, and instill the solution to a dressing during a venting interval. A pneumatic actuator may be mechanically coupled to a disposable distribution system that can provide a fluid path between the solution source and a distribution component. A bacterial filter may be disposed in the fluid path between the actuator and the distribution component to prevent contamination of the actuator during operation. The distribution system may be separated from the actuator and disposed of after operation, and the actuator may be re-used.

Abstract: Systems, methods, and apparatuses for providing instillation therapy with a negative-pressure source are described. The apparatus can include a housing having a dosing chamber and a negative-pressure chamber fluidly isolated from each other. The apparatus can also include a moveable barrier disposed in the housing between the dosing chamber and the negative-pressure chamber. The housing includes a fluid inlet in fluid communication with the dosing chamber and a fluid outlet in fluid communication with the dosing chamber. The housing can also include a negative-pressure inlet in fluid communication with the negative-pressure chamber and a biasing element coupled to the moveable barrier. The biasing element is operable to move the moveable barrier between a charge position and a discharge position.

Abstract: Systems, methods, and apparatuses for providing installation therapy and negative-pressure therapy are described. The apparatus includes a housing and a moveable barrier disposed in the housing to form a dosing chamber and a pressure chamber. The apparatus also includes a therapy conduit configured to be fluidly coupled to a pressure source and to a canister. The apparatus further includes a fluid inlet fluidly coupled to the dosing chamber and configured to be fluidly coupled to a fluid source and a fluid outlet fluidly coupled to the dosing chamber and configured to be fluidly coupled to a dressing. A pressure inlet is fluidly coupled to the therapy conduit and the pressure chamber; and a check valve is disposed in the therapy conduit.

Abstract: Methods, apparatuses, and systems for determining a pressure in a sealed therapeutic environment provided by a dressing are described. The system can include a tissue interface configured to be positioned adjacent a tissue site. At least a portion of the tissue interface is electrically conductive. The system also includes a sealing member configured to be disposed over the tissue interface to form the sealed therapeutic environment. The system includes a dressing interface configured to fluidly connect the sealed therapeutic environment with a therapy unit. The dressing interface is further configured to be electrically coupled to the tissue interface and the therapy unit.