This disclosure describes devices, systems, and methods related to a connector for a dressing, such as a dressing of a hyperbaric oxygen therapy system. An example of a connector includes a connector body configured to define at least a portion of a first channel. The connector also includes a viewing member coupled to the connector body. The connector further includes a deformable member positioned within the first channel. The deformable member is configured to deform based on a pressure associated with the deformable member and to provide a visual indication, via the viewing member, of the pressure.

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.

Disclosed herein are several embodiments of a reduced pressure appliance and methods of using the same in the treatment of wounds. Some embodiments are directed to improved fluidic connectors or suction adapters for connecting to a wound site, for example using softer, kink-free conformable suction adapters. Certain embodiments are directed to connectors used to connect fluid passage tube used in transmitting negative pressure to a fabric channel used in a suction adapter.

Disclosed herein are embodiments of a wound treatment apparatus employing hydrophobic and hydrophilic dressing materials and/or coating of the layers of a wound dressing. In some embodiments, the hydrophobic and hydrophilic dressing materials and/or coating controls the migration of fluid within the wound dressing.

Embodiments of negative pressure wound therapy systems, apparatuses, and methods for operating the systems and apparatuses are disclosed. In some embodiments, the apparatus includes a negative pressure source, a connector port, at least one switch, and a controller. The negative pressure source is connected through the connector port to either (i) a wound dressing having a canister configured to store fluid aspirated from the wound or (ii) a wound dressing without a canister between the connector port and the wound dressing. The controller determines, based on a signal received from the at least one switch, whether the canister is positioned in the fluid flow path and adjusts one or more operational parameters of negative pressure wound therapy based on the determination. The switch is activated by the connection of either the canister or canisterless wound dressing to the apparatus.

A system for wirelessly controlling a dressing interface that performs negative pressure wound therapy and fluid instillation therapy at a wound site. The system comprises a core module comprising: i) a plurality of sensors configured to determine a plurality of physical parameter data associated with the wound site; ii) a processor coupled to the plurality of sensors and configured to read the physical parameter data from the plurality of sensors; iii) a wireless transceiver coupled to the processor and configured to communicate with an external therapy controller; and iv) at least a first internal peripheral device coupled to the processor. The system further comprises at least a first external peripheral interface coupled to the core module and configured to communicate with the processor, wherein the core module and the at least a first external peripheral interface are disposed within a housing of the dressing interface.

A dressing for treating tissue with negative pressure is provided herein comprising a composite of dressing layers, including a release film, a perforated coated polymer film, a manifold, and an adhesive cover. Additionally, a method of manufacturing the dressing may comprise applying a cross-linkable polymer to a polymer film, curing the cross-linkable polymer to a gel layer to form a coated polymer film, and perforating the coated polymer film to form fluid restrictions, such as slits and/or slots, though the coated polymer film.

A medical device for use with an associated tube inserted into an incision formed in skin or tissue of a patient includes a dressing including an opening sized to receive and allow movement of the associated tube. A valve is operatively connected with the opening of the dressing and includes a main body; and an opening formed in a portion of the main body. The opening is sized and dimensioned to accommodate the surgical tube.

A wound therapy device includes a wound dressing and a humidifier configured to deliver humid air to a wound site to which the wound dressing is applied. The humidifier may be a remote structure that is fluidly connected to the wound dressing applied about a patient's skin at a wound site. Alternatively, the humidified may be integrated with the wound dressing to define an integral, portable therapy device that may be worn by the patient. The wound therapy device may be a standalone wound treatment device, or may be used in conjunction with other wound treatment devices, such as, e.g., negative pressure wound therapy devices.

An assembly for coupling a dressing to a tube connected to a pump includes a hydrophobic film layer comprising a perforation extending therethrough, an indicator coupled to a first side of the hydrophobic film layer and positioned proximate the perforation, a felted foam layer coupled to a second side of the hydrophobic film layer and fluidly communicable with the indicator via the perforation, and a connection pad coupled to the first side of the hydrophobic film layer and coupleable to the tube.