Abstract: Dressings, systems, and methods for treating a tissue site with negative pressure are described. The dressing includes a manifold having a first surface and a second surface opposite the first surface, 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 are formed from a polymer film. A plurality of fluid restrictions are formed in the polymer film adjacent to at least the first surface. A first plurality of bonds is formed between the first layer and the second layer. The first plurality of bonds define separable sections of the manifold. A second plurality of bonds is formed between the first layer and the second layer. The second plurality of bonds define a plurality of openings.

Abstract: A chiller includes an evaporator, a compressor including a prime mover, a first pressure sensor that detects a first pressure in the evaporator, a second pressure sensor that detects a second pressure in a condenser, and a controller. The controller determines a predicted energy level of the compressor based on the first pressure and the second pressure, the predicted energy level associated with liquid droplet flow into the compressor, compares the predicted energy level to an operating energy level, and modifies the at least one of the input power and the input current to the prime mover based on the comparison satisfying a modification condition.

Abstract: Embodiments generally relate to a screening element, screen assembly, and associated fixing systems, components and methods. Such embodiments can be used for exterior protection of windows and/or building facades, particularly in commercial buildings and the like. Some embodiments relate to a lightweight screening element, awning or louvre blade that can be readily fixed and applied to the exterior of buildings or built structures so as to provide a screen. Some embodiments relate to a screening element, comprising: an elongate panel defining a first portion and a second portion angled relative to the first portion; and at least one solar panel connected to the first portion of the elongate panel.

Abstract: A conduit includes a first end configured to be fluidly coupled to a wound site, and a second end configured to be fluidly coupled to a canister. The conduit additionally includes a central lumen extending between the first end and the second end. The conduit further includes a male interlocking member on a first side of the conduit and a female interlocking member on a second side of the conduit. Both the first side and the second side extend along a length of the conduit between the first end and the second end. The female interlocking member is configured to receive the male interlocking member.

Abstract: Devices for delivering a flowable tissue dressing material for treating a tissue site are described. The devices include a first zone including a first reactant, such as a polyol, and a second zone including a second reactant, such as a multi-isocyanate, which can be mixed together to form a flowable tissue dressing material. The device can also include a flowable tissue dressing material including a reacted polymer present in a carrier. Kits and methods including and/or using the devices are also described.

Abstract: An apparatus for filling a wound can include an array of at least four truncated ellipsoids interconnected to define at least one fluid path through, for example perpendicular to, the array. The longest principal axis of each ellipsoid may be perpendicular to the array. Each truncated ellipsoid may be a spheroid and/or may include an approximately elliptical contact surface at each contact surface between two interconnected ellipsoids. Each fluid pathway may have four continuously-curved concave sides and may have a parallelogram-shaped cross-section with continuously-curved concave edges. A dressing may include the apparatus, a dressing layer coupled to the apparatus, a backing layer disposed over a surface of the dressing layer opposite the apparatus, and an attachment device disposed on at least a margin of the backing layer. Methods of treating various tissue sites using the apparatus or dressing with negative-pressure therapy are also disclosed.

Abstract: A load structure may include a first honeycomb layer, a second honeycomb layer, and/or an attachment feature. The second honeycomb layer may be connected to the first honeycomb layer. The attachment feature may be connected to at least one of the first honeycomb layer or the second honeycomb layer. A method of manufacturing a load structure may include providing a first honeycomb layer, a second honeycomb layer, and an attachment feature, disposing an adhesive layer onto at least one of the first honeycomb layer or the second honeycomb layer, connecting an attachment feature to the first honeycomb layer or the second honeycomb layer, and/or disposing the first honeycomb layer onto the second honeycomb layer.

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.

Abstract: Dressings for treating a tissue site with negative pressure are disclosed, which may include a dressing having at least three layers assembled in a stacked relationship. In one example embodiment, a first film may comprise a non-porous material and a plurality of fluid restrictions. A first manifold layer may be adjacent to the first film and may comprise a second film of a transparent material having blisters and a manifold area. The first manifold layer may further comprise apertures configured to allow fluid transfer through the second film. A second manifold layer may be adjacent to the first manifold layer and may comprise foam having a contact area that is less than the manifold area of the first manifold layer.

Abstract: A dressing includes a manifold layer and a drape coupled to the manifold layer and configured to seal the manifold layer over a wound. The drape has an opening extending therethrough. A connection pad is positioned at the opening and configured to couple the dressing to a tube. The connection pad includes an outer ring coupled to the drape and a center dimple extending away from the drape and defining a volume between the center dimple and a plane defined by the outer ring. The dressing also includes an absorbent manifolding structure positioned between the center dimple and the manifold layer and formed to substantially match a shape of the volume.

Abstract: A load structure may include a panel having a core, and a coating of polyurethane around the core. The load structure may also have a layer of carpet or felt on at least a portion of a first side of the panel. The load structure may further include an over mold coating on a second side of the panel.

Abstract: A dressing for a wound can include a body layer formed from an absorbent material. The dressing can also include multiple wicking cores disposed within the body layer. Each of the multiple wicking cores can be configured to provide a visual indication at a different state of liquid absorption in the body layer.

Abstract: Dressings for closing an opening through a surface of a tissue site are described. The dressing includes a cover adapted to form a sealed space over the opening and a bolster. The bolster is adapted to be positioned adjacent the opening and includes a first plurality of holes. The holes have an average width to length ratio causing the plurality of holes to collapse in a direction substantially perpendicular to the opening. Systems, apparatuses, kits and methods including and/or using the dressing for closing the opening are also described.

Abstract: 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.

Abstract: In an example is a system for providing treatment to a tissue site. The system may include a tissue interface for transporting fluid to the tissue site. The system may further include a cover for providing a sealed space including the tissue interface. The system may further include a negative-pressure source fluidly coupled to the tissue interface and providing negative pressure. The system may further include a hyperoxic fluid source fluidly coupled to the tissue interface and providing a hyperoxic fluid. The system may further include a controller for controlling the negative pressure and the hyperoxic fluid so as to maintain the sealed space at a negative pressure while the hyperoxic fluid is provided to the sealed space.

Abstract: A dressing includes a first felted foam layer, a superabsorbent material printed on the first felted foam layer, and a second felted foam layer coupled to the first felted foam layer. The superabsorbent material is confined between the first felted foam layer and the second felted foam layer.

Abstract: A wound dressing includes a hydrophilic foam layer, a plurality of wicking strips, and a drape layer. The hydrophilic foam layer is configured to engage a wound bed and has a first side and a second side, the second side configured to face the wound bed. The plurality of wicking strips also have a first side and a second side, the second side configured to face the first side of the hydrophilic foam layer. The drape layer also has a first side and a second side, the second side configured to face the first side of the plurality of wicking strips. One or more of the plurality of wicking strips also have a removable tab, wherein the tab extends beyond a periphery of the wound dressing.

Abstract: Dressings for treating a tissue site with negative pressure are disclosed, which may include a dressing having at least three layers assembled in a stacked relationship. In one example embodiment, a first film may comprise a non-porous material and a plurality of fluid restrictions. A first manifold layer may be adjacent to the first film and may comprise a second film of a transparent material having blisters and a manifold area. The first manifold layer may further comprise apertures configured to allow fluid transfer through the second film. A second manifold layer may be adjacent to the first manifold layer and may comprise foam having a contact area that is less than the manifold area of the first manifold layer.

Abstract: Systems and methods are provided for providing a consistent experience for users of cloud-based block storage volumes. While cloud storage aims to remove hardware considerations for an end user's experience, block storage performance can nevertheless vary according to hardware configuration, such as the specific model of underlying hardware used to support a volume or the specific network location of that hardware. Embodiments of the present disclosure address that inconsistent performance by associating a volume with a performance profile, which can represent a desired distribution of performance for the volume. Each read or write can be compared to the profile, and may be selectively delayed to match the desired performance. This enables the cloud provider to vary physical hardware or network configurations without effect on block storage performance from the point of view of an end user.

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.