A system and apparatus for treating a tissue site with reduced pressure and collecting fluids from the tissue site is disclosed. The system may include a reduced-pressure source, a pouch in fluid communication with the reduced pressure source, and a dressing in fluid communication with the pouch. The pouch may include a first wall, a second wall having a periphery coupled to the first wall to form an interior, and a third wall extending through the interior to form a first chamber in fluid communication with the dressing and a second chamber in fluid communication with the reduced pressure source. A plurality of filters are positioned in the third wall. The filters permit fluid communication between the first chamber and the second chamber.

In various aspects, the wound therapy apparatus disclosed herein includes a wound interface that defines an enclosed space over a wound bed that is fluid tight when secured to a skin surface around the wound bed. The wound therapy apparatus includes a control group that cooperates with the wound interface to regulate input of input fluid comprising a gas having an O.sub.2 concentration greater than atmospheric air into the enclosed space and to regulate the withdrawal of output fluid from the enclosed space in order to vary an actual pressure p.sub.a within the enclosed space generally between a minimum pressure p.sub.min and a maximum pressure p.sub.max. Related methods of use of the wound therapy apparatus are disclosed herein.

In some embodiments, a wound monitoring and/or therapy apparatus can include a wound dressing configured to be positioned over a wound. The wound dressing can support one or more sensors. The one or more sensors can include an optical sensor array cluster, which can include an optical sensor and single light source. In some embodiments, the wound dressing can include a substantially stretchable wound contact layer that includes a wound facing side and a non-wound facing side opposite the wound facing side, the wound facing side configured to be positioned in contact with a wound. The non-wound facing side of the wound contact layer can support a plurality of electronic components and a plurality of electronic connections that connect at least some of the plurality of the electronic components. The electronic components can include one or more sensors configured to obtain measurements of the wound or the periwound, or both.

A housing of a pump unit is fixed to a drape of a wound dressing by a joint portion. A suction chamber that is brought into a negative pressure by driving of a piezoelectric pump directly communicates with a closed space through an opening and an inlet. Hence, a therapy device does not need to include a pipe that allows the closed space and the pump unit to communicate with each other. Therefore, since the therapy device does not need to include the pipe that allows the pump unit to communicate with the closed space, detachment of the pump unit from the wound dressing owing to coming-off of the pipe is avoided. Since the housing is fixed to the drape by the joint portion, the pump unit can be prevented from detaching from the wound dressing.

A wound therapy system includes a dressing sealable over a wound and defining a wound space between the dressing and the wound, tubing fluidly communicable with the wound space, and a canister fluidly communicable with the tubing. The canister, the tubing, and the dressing define a sealed space that includes the wound space. The wound therapy system also includes a therapy unit coupled to the canister. The therapy unit includes a sensor configured to measure a pressure in the sealed space, a valve positioned between the sealed space and a surrounding environment and controllable between an open position and a closed position, and a control circuit. The control circuit is configured to control the valve to alternate between the open position and the closed position to allow airflow through the valve, receive measurements from the sensor, and determine a volume of the wound space based on the measurements.

A wound therapy apparatus is disclosed that includes a wound interface securable to a skin surface around a wound bed to form an enclosed space over the wound bed that is fluid-tight. The wound therapy apparatus may include a dressing engaged with the wound interface to contact the wound bed. Gas within the enclosed space may have an O.sub.2 concentration greater than the O.sub.2 concentration in atmospheric air. The dressing may include a hydrophobic material, hydrophobic material, or a distal layer comprised of silicone having fenestrations therein, in various aspects. The pressure p.sub.0 within the enclosed space may vary over a pressure range p.sub.minp.sub.0p.sub.max. Related methods of use are also disclosed.

Disclosed herein are devices, systems and methods for delivering reduced pressure to a load-bearing wound site. The device can include a distal port configured to connect to a wound dressing positioned over the wound site; a proximal port located a distance from the distal port and configured to connect to a reduced pressure source, and a conduit body having an inner channel extending between the distal port and the proximal port. When the distal port is applied to the wound dressing positioned over the wound site the proximal port is positioned at a non-load bearing location remote from the wound dressing. The inner channel has a non-circular profile having a width larger than a height of the conduit body.

Dressings, systems, and methods are disclosed, in some embodiments, that involve treating a tissue site with reduced pressure. In one embodiment, a reduced-pressure dressing may include a dressing bolster, a retention pouch, and a sealing member. The dressing bolster may be adapted to apply a compressive force to the tissue site capable of closing a wound or incision therein. The retention pouch may be adapted to retain and manage fluid extracted from the tissue site to keep the tissue site substantially free of fluid and to prevent clogging of the reduced-pressure dressing. The sealing member may provide a seal over the retention pouch, the dressing bolster, and a portion of the epidermis of the patient. Other dressings, systems, and methods are disclosed.

Dressings, systems, and methods are disclosed that, in some embodiments, relate to treating a tissue site. In one embodiment, a dressing may include a manifold, a retention pouch, a sealing member, and a conduit interface. The manifold may be adapted to distribute reduced pressure to the tissue site, and the retention pouch may be adapted to retain and manage fluid extracted from the tissue site. The sealing member may cover the retention pouch and the manifold to provide a sealed space with the tissue site. The conduit interface may be in fluid communication with the sealed space and an exterior surface of the sealing member. The dressing may be utilized with a therapy device operable to control reduced pressure in the dressing and fluid flow over the sealing member.

Some embodiments provide in-line negative pressure wound therapy (NPWT) sampling assessment systems, comprising: a housing; a wound fluid input port configured to fluidly couple with a first wound fluid lumen extending from a wound treatment site; a wound fluid output port configured to fluidly couple with a NPWT control unit; an in-line sampling chamber positioned within the housing and comprising a theranostic sampling element, wherein the first in-line sampling chamber is configured to: removably and fluidly couple between the input port and the output port in-line with a wound fluid path between the wound treatment site and the NPWT control unit with the first theranostic sampling element positioned so that at least some of the wound fluid contacts at least a portion of the first theranostic sampling element; and decouple out of the wound fluid path without interrupting a negative pressure treatment process applied at the wound treatment site.