Abstract: An apparatus for negative-pressure treatment of a tissue site may comprise a fluid reservoir having a variable volume; a first fluid passage fluidly coupled to the fluid reservoir; a first check valve configured to prevent egress through the first fluid passage; a second fluid passage fluidly coupled to the fluid reservoir; and a second check valve configured to prevent ingress through the second fluid passage. In some embodiments, the first check valve and the second check valve may be configured to open if downstream negative pressure is greater than upstream negative pressure. The first fluid passage may be configured to be coupled to a dressing or tissue interface, and the second fluid passage may be configured to be coupled to a negative-pressure source. The apparatus may provide a mobile, re-usable, self-emptying, self-charging source of negative pressure that can manage fluid and temporary or transitional negative-pressure treatment.

Abstract: Apparatuses, systems, and methods for optimizing fluid storage in a negative pressure therapy system are described. A fluid storage canister includes a first section, a second section, a fluid flow pathway, and a forced air module. The first section is fluidly coupled to a dressing and stores fluid, and the second section is fluidly coupled to a therapy unit and stores fluid. The fluid flow pathway is disposed between the first section and the second section. The forced air module generates a fluid flow through the fluid flow pathway.

Abstract: A customizable wound treatment system for treating multiple zones of a wound includes a dressing configured for use with a first zone and a second zone of a wound that includes a first foam layer placed over the first zone, a second foam layer placed over the second zone, a first drape layer disposed over the first foam layer and beneath the second foam layer, and a second drape layer disposed over the second foam layer. The customizable wound treatment system includes a negative pressure source pneumatically coupled to the first foam layer and the second foam layer and operable to create a negative pressure at the first zone and the second zone and a fluid instillation pump fluidly coupled to the first foam layer and configured to instill a treatment fluid to the first zone.

Abstract: The present disclosure relates to a network system. The system is formed by at least two negative pressure wound therapy (NPWT) devices. The first NPWT device includes a wireless radio, user interface, controller, and processing circuit. The wireless radio wirelessly communicates with the second NPWT device. The user interface displays operational status of therapy operation, receives a command of operational change from a user, and displays wireless radio connection strength between the first NPWT device and the NPWT device. The controller controls therapy operation of the first NPWT device based on input from the user interface. The processing circuit causes the wireless radio to communicate with the second NPWT device, determines wireless radio connection strength between the first NPWT device and the second NPWT device based on communication between the first NPWT device and the second NPWT device, and causes the user interface to display determined wireless radio connection strength.

Abstract: A negative pressure wound therapy (NPWT) system includes a therapy unit (102), a first pump (112), a piezo-electric pump (116), and a controller (202). The first pump (112) is configured to draw a negative pressure at a wound site (105) through a first tubular member (122). The piezo-electric pump (116) is fluidly coupled with the first tubular member (122) through a bypass tubular member (124) and is configured to detect a fluid indication. The controller (202) includes processing circuitry configured to obtain feedback signals from the piezo-electric pump (116) and determine if fluid is present at the piezo-electric pump (116) based on the feedback signals.

Abstract: The present disclosure relates to a network system. The system is formed by at least two negative pressure wound therapy (NPWT) devices. The first NPWT device includes a wireless radio, user interface, controller, and processing circuit. The wireless radio wirelessly communicates with the second NPWT device. The user interface displays operational status of therapy operation, receives a command of operational change from a user, and displays wireless radio connection strength between the first NPWT device and the NPWT device. The controller controls therapy operation of the first NPWT device based on input from the user interface. The processing circuit causes the wireless radio to communicate with the second NPWT device, determines wireless radio connection strength between the first NPWT device and the second NPWT device based on communication between the first NPWT device and the second NPWT device, and causes the user interface to display determined wireless radio connection strength.

Abstract: A wound therapy system includes a dressing an instillation pump fluidly communicable with the dressing and configured to provide instillation fluid to the dressing, a negative pressure pump fluidly communicable with the dressing and configured to remove air from the dressing, and a control circuit communicably coupled to the instillation pump and the negative pressure pump. The control circuit is configured to control the instillation pump to provide an amount of the instillation fluid to the dressing, provide a soak period, and control the negative pressure pump to provide a cyclic variation of negative pressure at the dressing.

Abstract: A cutting template for use with a negative pressure wound therapy system includes a substantially rigid body. The body includes a top surface, a bottom surface, a height, and a recess. The top surface is configured to engage a drape layer. The bottom surface is configured to engage a dressing layer. The height is defined between the top surface and the bottom surface. The height is configured to create a gap between the drape layer and the dressing layer. The recess is disposed substantially about a perimeter of the body. The recess is configured to receive an edge of a cutting tool so that an opening is formed in the drape layer when the edge is traversed about the perimeter.

Abstract: A wound therapy system includes a dressing an instillation pump fluidly communicable with the dressing and configured to provide instillation fluid to the dressing, a negative pressure pump fluidly communicable with the dressing and configured to remove air from the dressing, and a control circuit communicably coupled to the instillation pump and the negative pressure pump. The control circuit is configured to control the instillation pump to provide an amount of the instillation fluid to the dressing, provide a soak period, and control the negative pressure pump to provide a cyclic variation of negative pressure at the dressing.

Abstract: In one example embodiment, a system for treating a tissue site is disclosed comprising a dressing adapted to contact the tissue site and provide a fluid seal between a therapeutic environment and a local external environment, and a solution source fluidly coupled to the dressing and adapted to deliver an antimicrobial solution comprising a peroxy ?-keto carboxylic acid, such as peroxy pyruvic acid, to the tissue interface. The system may further comprise a negative-pressure source fluidly coupled to the dressing and adapted to provide negative pressure to the therapeutic environment after delivery of the antimicrobial fluid to the therapeutic environment.

Abstract: A dressing that includes a contact layer having walls defining a plurality of holes and a retainer layer comprising portions protruding into holes of a contact layer is provided herein. Systems, methods and kits using the dressing for debriding a tissue site are also provided herein.

Abstract: A dressing that includes a contact layer having walls defining a plurality of holes and a retainer layer comprising portions protruding into holes of a contact layer is provided herein. Systems, methods and kits using the dressing for debriding a tissue site are also provided herein.

Abstract: In one example embodiment, a system for treating a tissue site is disclosed comprising a dressing adapted to contact the tissue site and provide a fluid seal between a therapeutic environment and a local external environment, and a solution source fluidly coupled to the dressing and adapted to deliver an antimicrobial solution comprising a peroxy ?-keto carboxylic acid, such as peroxy pyruvic acid, to the tissue interface. The system may further comprise a negative-pressure source fluidly coupled to the dressing and adapted to provide negative pressure to the therapeutic environment after delivery of the antimicrobial fluid to the therapeutic environment.

Abstract: Disclosed embodiments relate to dressings for treating a tissue site with negative pressure. Some dressing embodiments may be configured to allow the depth of the dressing to be expandable. For example, dressing embodiments may comprise a segmented manifold having one or more vertical expansion joints between segments of the manifold. Some embodiments may comprise a first layer adjacent to a first surface of the manifold and a second layer adjacent to a second surface of the manifold. In some embodiments, the first layer may comprise one or more folds configured to extend between adjacent segments, and the second layer may also comprise one or more folds configured to extend between adjacent segments; and the folds in the first layer may match the folds in the second layer to jointly form the vertical expansion joints. Additionally disclosed are other apparatus, dressings, systems, and methods.

Abstract: A wound therapy system includes a dressing sealable over a wound, a conduit comprising a first inner diameter, coupled to the dressing, and fluidly communicable with the wound space, and a canister fluidly communicable with the conduit. A therapy unit is coupled to the canister and includes a pump, a sensor configured to measure a pressure, a valve controllable between an open position and a closed position, and a control circuit. The control circuit is configured to control the pneumatic pump to remove air to establish a negative pressure, control the valve to repeatedly alternate between the open closed positions to allow a controlled rate of airflow through the valve, receive measurements of the pressure from the sensor, and determine a volume of the wound space based on the pressure measurements. A portion of the conduit comprises a second inner diameter that is less than the first inner diameter.

Abstract: Dressings, systems, and methods for treating a tissue site are described. The dressing can include a first layer having a first side and a second side and a plurality of through-holes extending through the first layer from the first side to the second side. The dressing can also include a second layer configured to be positioned adjacent the second side of the first layer. The second layer can have a plurality of fluid restrictions and a plurality of perforations disposed in the second layer. The plurality of perforations can be configured to be aligned with the plurality of through-holes in the first layer.

Abstract: In one example embodiment, a system for treating a tissue site is disclosed comprising a dressing adapted to contact the tissue site and provide a fluid seal between a therapeutic environment and a local external environment, and a solution source fluidly coupled to the dressing and adapted to deliver an antimicrobial solution comprising a peroxy ?-keto carboxylic acid, such as peroxy pyruvic acid, to the tissue interface. The system may further comprise a negative-pressure source fluidly coupled to the dressing and adapted to provide negative pressure to the therapeutic environment after delivery of the antimicrobial fluid to the therapeutic environment.

Abstract: A wound therapy system includes a therapy unit, a wound dressing and an optional controller. The therapy unit is configured to deliver instillation fluid to a wound site. The wound dressing is formed from a plurality of discrete, individual blocks that are selectively separable from one another along a plurality of separation-lines, allowing the wound dressing to be customized to the shape and size of the wound site. By calculating the remaining blocks that define the wound dressing following customization, the volume of the wound dressing may be determined. The controller may be configured to deliver fluid to the wound site based on this calculated volume. The controller may also optionally be used to gauge the healing of the wound site over time by monitoring the changes in volume of customized wound dressings as wound dressings are replaced during the course of treatment of the wound site.

Abstract: This disclosure describes a wound sealing film containing a first layer having a first surface and a second surface, said first layer contains a first polymer composition, a second layer having a first surface and a second surface, said second layer contains an adhesive, and a third layer having a first surface and a second surface, said third layer contains a polymeric gel, wherein the second layer is positioned between the first layer and the third layer, method of making and using the wound sealing film. In some aspects, a wound sealing film can contain a first layer containing a first polymer composition, and a combined layer containing a polymeric gel and an adhesive.

Abstract: 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.