A dressing for treating a tissue site, particularly a peritoneal or abdominal site, is disclosed. The dressing may comprise: first and second layers, each being made from a liquid-impermeable material and being at least partially fenestrated, the layers being coupled together to define a chamber therebetween; and disposed within the chamber a third layer comprising a manifold having a central region, and a perimeter region containing perforations arranged in a pattern defining a plurality of sub-regions. The first and second layers can be coupled using a plurality of welds or bonds through the perimeter region perforations. Optionally, the manifold does not comprise, and the chamber does not contain, any manifolding elements extending outward from an outer edge of the perimeter region.

A negative pressure wound therapy system is configured for treating multiple wounds on a patient's body. The system preferably includes a source of negative air pressure, an air source, a first fluid collection volume, and a second fluid collection volume. The source of negative air pressure is in fluid communication with the first fluid collection volume, the first collection volume is in fluid communication with the second fluid collection volume, and the second fluid collection volume is in fluid communication with the air source, so that the source of negative air pressure, the first fluid collection volume, the second fluid collection volume, and the air source are fluidly connected in series.

A suction-based medical dressing assembly and method of dermal irrigation provides a flexible tube that is fluidly coupled to at least two bifurcated tube portions defined by a plurality of apertures. The tube has a proximal end opening for discharging ambient fluid. The length of the bifurcated tube portions is surrounded by an absorbent gauze material covered substantially with an occlusive sheet material, and having an adhesive strip thereon. A vacuum assembly creates a negative pressure in the tubes. The ambient fluid is absorbed by the absorbent material, and the negative pressure sucks the fluid through the apertures in the bifurcated tube portions for discharge through the opening in the tube. In operation, a patient applies the adhesive side of the occlusive device to the skin where liquid removal is desired and activates the vacuum-inducing source, thereby causing fluid runoff from the patient to be effectively removed for disposal.

Embodiments of negative pressure wound therapy devices and methods for controlling and operating such devices are disclosed. A negative pressure wound therapy apparatus can include a housing, a negative pressure source, controller, and output device supported by the housing. The negative pressure source can couple via a fluid flow path to a wound dressing and provides negative pressure to the wound dressing. The controller can operate the negative pressure source to provide negative pressure to the wound. The output device can provide identification data to an electronic device, and the identification data can be usable by the electronic device to access a label associated with the negative pressure wound therapy device.

A treatment system for applying negative pressure therapy and fluid instillation treatment to a tissue site, particularly an abdominal tissue site, is disclosed. In some embodiments, the treatment system may include a dressing member, a plurality of fluid removal pathways, a fluid instillation matrix, a drape, a negative-pressure source, and a fluid instillation source. Instillation fluid may be delivered from the fluid instillation source to the tissue site through the fluid instillation matrix, and negative pressure may be communicated and fluid withdrawn from the tissue site through the plurality of fluid removal pathways.

Embodiments described herein relate to apparatuses, systems, and methods for the treatment of wounds, for example using multiple wound dressings in combination with negative pressure wound therapy. A negative pressure would therapy apparatus can include a negative pressure source and a controller. The negative pressure source can include inlets configured to couple via fluid flow paths to wound dressings. The fluid flow paths can include pressure sensors configured to measure pressure in the fluid flow paths. The pressure sensors can include a first pressure sensor configured to measure pressure in the first fluid flow path and a second pressure sensor configured to measure pressure in the second fluid flow path. The controller can be configured to operate the negative pressure source and provide, based on measured pressure, indication of at least one operating condition associated with at least one of the fluid flow paths.

A device comprising: (a) a housing; (b) one or more pumps located within the housing, the one or more pumps configured to create a negative pressure and move fluid; (c) one or more connectors located at least partially within in the housing; (d) internal fluid paths connecting the one or more pumps to the one or more connectors; (e) one or more reservoirs connected to the one or more connectors, the one or more reservoirs being configured to collect the fluid moved by the one or more pumps; and (f) a processor configured to:(i) calculate a total volume of fluid collected in the one or more reservoirs; and (ii) indicate that the one or more reservoirs are full; wherein the fluid moved is a fluid from a wound or incision.

Disclosed herein are several embodiments of a negative 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, having an air leak channel separated from a suction channel.

A system, method, and apparatus are disclosed for dressing a wound. The apparatus comprises a liquid and gas permeable transmission layer, an absorbent layer for absorbing wound exudate, the absorbent layer overlying the transmission layer, a gas impermeable cover layer overlying the absorbent layer and comprising a first orifice, wherein the cover layer is moisture vapor permeable.

A system and apparatus for the collection of serous or serosanguinous fluid from a percutaneous site after surgery. A pump unit with one or more pumps or powered sources provide continuous negative pressure suction to draw fluid from the percutaneous site and pumps the fluid into disposable reservoirs with one-way valves that are easy to handle while maintaining sterility and a seal to prevent the loss of vacuum. Air is continuously removed from the reservoirs. Measurement and analysis of the output is performed automatically.