Abstract: A cover for protecting a tissue site may comprise a shell layer, an adhesive disposed on the shell layer, and a contact layer disposed adjacent to the adhesive. The contact layer may have a first pattern of apertures and bridges, and the shell layer may have a second pattern of apertures overlaying the bridges. In some examples, the adhesive may have a bond strength that is greater than the tensile modulus of the shell layer. The contact layer may have an open area of about 40 percent to about 50 percent of the total area of the contact layer. A release liner may be disposed adjacent to the contact layer. Perforations through the shell layer and the contact layer can define a sacrificial segment configured to be separated from the shell layer and the contact layer. A handling bar may be coupled to the sacrificial segment.

Abstract: A reduced-pressure system for treating a tissue site on a patient includes a distribution manifold that adheres to a tissue site to allow retention without external support. The distribution manifold includes a porous member and a tissue-fixation element. The tissue-fixation element maintains the porous member substantially adjacent to the tissue site while a sealing member is applied. In one instance, the tissue-fixation element is a soluble adhesive that partially covers either the tissue-facing side of the porous member or a tissue-facing side of a fluid-permeable substrate layer that is on the tissue-facing side of the porous member. Other systems, distributions manifolds, and methods are presented.

Abstract: In some examples, a dressing suitable for treating a tissue site may include a sealing member configured to form a sealed enclosure relative to the tissue site. A fluid buffer may be configured to be positioned at a sealing member aperture in fluid communication between the sealed enclosure and an ambient environment external to the sealed enclosure. Other dressings, apparatus, systems, and methods are disclosed.

Abstract: A method of manufacturing a load structure may include forming a panel having a first side and a second side, clearing a fill passage through the panel, providing a tool having a first portion, a second portion, and a cavity disposed between the first and second portions, disposing a film onto a surface of the first portion of the tool, disposing the panel within the cavity such that the second side of the panel engages the second portion of the tool, and the first side of the panel is spaced apart from the surface of the first portion of the tool defining a void, and injecting a coating through the fill passage such that the coating fills the void and the film adheres to the first side of the panel.

Abstract: Systems, methods, and devices related to removing fluids from a patient are provided. In one instance, fluid is removed from the patient and delivered to a canister using reduced pressure. Reduced pressure is supplied to the canister via a reduced-pressure delivery conduit that includes a moisture processing device and a hydrophobic filter. The moisture processing device condenses moisture from the air to prevent condensation from occluding the hydrophobic filter. The moisture processing devices includes an expanded volume and one or more liquid-impermeable, vapor-permeable membranes. The liquid-impermeable, vapor-permeable membrane allows vapor to egress the moisture processing device. Other systems, methods, and devices are presented.

Abstract: This disclosure describes devices, systems, and methods related to a compound film. An exemplary compound film includes a first layer including a first polymer composition including polyurethane and a second layer including a second polymer composition removably coupled to the first layer. The compound film further includes light switchable adhesive coupled to the second layer and configured to transition from a first state to a second state, the light switchable adhesive has a first peel strength in the first state that is greater than a second peel strength of the light switchable adhesive in the second state. A third peel strength between the first layer and the second layer is less than the second peel strength between the light switchable adhesive in the first state and a bond site.

Abstract: A dressing for treating a tissue site with negative pressure may include a first layer having a first side, a second side, and fenestrations having a raised edge extending from the first side. The raised edge is configured to expand in response to a pressure gradient across the first layer. The dressing also includes a second layer adjacent to the first side. The second layer includes a manifold. The dressing also includes a cover coupled to the second layer opposite the first layer. The cover includes a polymer drape.

Abstract: A dressing for treating a tissue site with negative pressure may comprise a first polymer film having a plurality of fluid restrictions, and a second polymer film comprising a plurality of standoffs disposed adjacent to the first polymer film. The first polymer film and the second polymer film may be substantially transparent to allow observation of the tissue site. In some embodiments, at least some of the standoffs may be offset from the fluid restrictions. The second polymer film may comprise fluid passages adjacent to the standoffs in some examples.

Abstract: Embodiments of the present invention are directed to action recipes for a crowdsourced digital assistant. Users can define an action recipe by recording a set of inputs across one or more applications, by providing multiple sub-commands in a single on-the-fly command, by providing one or more associated commands, or otherwise. An action recipe dataset is generated, and stored and indexed on a user device and/or on an action cloud server. As such, any user can invoke an action recipe by providing an associated command to a crowdsourced digital assistant application on a user device. The crowdsourced digital assistant searches for a matching command on the user device and/or the action cloud server, and if a match is located, the corresponding action recipe dataset is accessed, and the crowdsourced digital assistant emulates the actions in the action recipe on the user device.

Abstract: Systems, methods, and apparatuses are presented that facilitate the provision of reduced pressure to a tissue site by using a delivery-and-fluid-storage bridge, which separates liquids and gases and provides a flow path for reduced pressure. In one instance, a delivery-and-fluid-storage bridge includes a delivery manifold for delivering reduced pressure to a treatment manifold at the tissue site and an absorbent layer proximate the delivery manifold adapted to receive and absorb liquids. The delivery manifold and the absorbent layer are encapsulated in an encapsulating pouch. A first aperture is formed proximate a first longitudinal end of the delivery-and-fluid-storage bridge for fluidly communicating reduced pressure to the delivery manifold from a reduced-pressure source, and a second aperture is formed on a patient-facing side of the delivery-and-fluid-storage bridge. Reduced pressure is transferred to the tissue site via the second aperture. Other systems, apparatuses, and methods are disclosed.

Abstract: A method of manufacturing a load structure may include first forming a panel having a first side and a second side. The method may then include trimming the panel, including clearing a fill passage through the panel from the first side to the second side. The method may then include applying an over rim coating on the second side of the panel via an over rim tool by which a resin may be injected through the fill passage to the second side. The method may further include performing final trimming of the panel, and finally performing final assembly to form the load structure.

Abstract: A citric acid containing dressing for treating a tissue site with negative pressure may comprise a cover, a manifold, and a perforated polymer film and/or a sealing layer. The sealing layer can be a perforated silicone gel having a treatment aperture. The dressing can further contain an adhesive. The cover, the manifold, and the perforated polymer film and/or the sealing layer may be assembled in a stacked relationship with the cover and the sealing layer enclosing the manifold. Citric acid may be present on or incorporated in, for example, the perforated polymer film and/or the sealing layer.

Abstract: A system and method for performing tissue therapy may include applying a reduced pressure to a tissue site of a patient. A fluid parameter associated with applying a reduced pressure to the tissue site may be sensed. An audible fluid leak location sound may be generated in response to sensing the fluid parameter. The audible fluid leak location sound may be altered in response to sensing that the fluid parameter changes. By altering the audible fluid leak location sound in response to sensing a change of the fluid parameter, a clinician may detect location of a fluid leak at the drape by applying force to the drape. The force applied to the drape may be a clinician pressing a finger onto an edge of the drape.

Abstract: In one example embodiment, a system for treating a tissue site is disclosed that may comprise a manifold including a non-porous film having a plurality of closed cells defined by a sealed region perforated with apertures extending through the sealed region, wherein the manifold is adapted to contact the tissue site. The system may further comprise a cover adapted to provide a fluid seal between a therapeutic environment including the manifold proximate one side of the cover and a local external environment on the other side of the cover. In one embodiment, the plurality of closed cells is adapted to form distal channels with the cover and the apertures are adapted to provide fluid communication between the distal channels and the tissue site. The system may further comprise a negative-pressure source fluidly coupled to the therapeutic environment and adapted to provide negative pressure through the distal channels and the apertures to the tissue site.

Abstract: A dressing for treating a tissue site with negative pressure includes a manifold having a first surface and a second surface opposite the first surface. The dressing also includes a first layer adjacent to the first surface and a second layer adjacent to the second surface. The first layer and the second layer each include a polymer film. The dressing also includes a plurality of fluid restrictions in the polymer film adjacent to at least the first surface, and a plurality of bonds between the first layer and the second layer. The plurality of bonds defines separable sections of the manifold. Each of the separable sections of the manifold has at least one rounded edge.

Abstract: Disclosed herein are embodiments of a wound dressing layer. The wound dressing layer may include an open-cell foam. The foam may have a 50% compression force deflection of not more than about 4.8 kPa. The foam may also have a density of at least 24 kg/m3. The foam may exhibit a density increase of a factor of at least 12 at about ?75 mmHg.

Abstract: Foam wound inserts with high-density and low-density regions, methods for making wound inserts, wound-treatment methods, and wound-treatment systems.

Abstract: A dressing or wound filler comprising a laminate structure of materials. In one example embodiment, a dressing may include a first layer comprising a first film, a second layer adjacent to the first layer and comprising a foam, and a third layer comprising a second film. The first layer and the second layer may further include a plurality of perforations or fenestrations. The third layer may include a plurality of raised features. The perforations or fenestrations of the first and second layers may be positioned or aligned with the raised features of the third layer so as to facilitate tearing of the dressing for sizing and application purposes. In some embodiments, the first layer may comprise a polyurethane film, the second layer may comprise a polyurethane foam, and the third layer may comprise an additional polyurethane film.

Abstract: Body-fluid containers, methods, and systems are presented that include a container that has a container housing formed, at least in part, by a liquid-impermeable, vapor-permeable material. The liquid-impermeable, vapor-permeable material allows water to evaporate and be transmitted outside of the container. The evaporation allows more fluid to be processed by the container than the container could otherwise hold. Other systems, methods, and apparatuses are presented.

Abstract: A low-profile dressing interface or connector may comprise at least two side-by-side fluid pathways fluidly coupled to a recessed space of the connector, one for providing negative pressure to a tissue interface and the other for sensing negative pressure within the recessed space adjacent the tissue interface. The apparatus may comprise a top layer having a plurality of closed cells with tapered sidewalls. The apparatus may also comprise a base layer forming a sealed space between the top layer and the base layer. The base layer may further include a plurality of closed cells having tapered sidewalls. The apparatus may then further comprise a barrier coupled between the top layer and the base layer to form two fluid pathways within the sealed space.