Abstract: An appendage massaging device that includes an appendage wrap having an inner band and an outer layer and one or more artificial muscles disposed between the inner band and the outer layer of the appendage wrap. Each of the one or more artificial muscles include a housing having an electrode region and an expandable fluid region, a dielectric fluid housed within the housing, and an electrode pair positioned in the electrode region of the housing. The electrode pair includes a first electrode fixed to a first surface of the housing and a second electrode fixed to a second surface of the housing. The electrode pair is actuatable between a non-actuated and an actuated state such that actuation from the non-actuated state to the actuated state directs the dielectric fluid into the expandable fluid region, expanding the expandable fluid region thereby applying pressure to the inner band of the appendage wrap.

Abstract: An adhesive sheet with flexibility for attaching a health appliance to a skin, including: a health appliance sticking portion which is a portion on which the health appliance is stuck; an adhesive portion for making the adhesive sheet adhere to the skin; first release paper stuck on the health appliance sticking portion in a peelable manner; and second release paper having an outer edge nearly identical to an outer edge of the adhesive portion in shape and size and stuck on the adhesive portion in a peelable manner so as to surround the first release paper, wherein the second release paper has stiffness that allows the second release paper to support the adhesive sheet and maintain a planar state in a state in which the first release paper is removed.

Abstract: The present disclosure describes systems, methods, devices for performing thought-controlled neuromuscular stimulation. Also described are methods for producing a neuromuscular stimulation cuff. The systems and methods generally relate to receiving and processing thought signals indicative of an intended action, and then delivering stimulation to effectuate the intended action through a neuromuscular stimulation cuff. The neuromuscular stimulation cuff includes a flexible printed circuit board having at least one finger and a plurality of electrogel discs disposed on the at least one finger. The neuromuscular stimulation cuff may be produced by providing a layer of polyimide, etching a conductive copper circuit including a plurality of electrodes into the layer of polyimide to form an etched circuit layer, adhering a cover layer onto the etched circuit layer to form a flexible printed circuit board (PCB), and cutting at least one finger from the flexible PCB.

Abstract: An apparatus for monitoring neural response and/or providing treatment includes an electrical stimulator configured to apply electrical stimulation, and one or more processors configured to analyze stimulation response. The one or more processors can be further configured to operate the electrical stimulator, adjust the electrical stimulation, and determine one or more wound characteristics based at least in part on at least one of the electrical stimulation or the stimulation response, e.g. a movement of a patient, a color absorption characteristic, or other physiological responses. An indication of the one or more wound characteristics can be provided.

Abstract: A dressing for applying pressure to a patient target site is provided. The dressing includes an elastic spacer longitudinally extending between first and second substrates. The elastic spacer is configured to be selectively moved between the first length and a second length. The second length is longer than the first length. A triggering element, when present, selectively maintains the elastic spacer at the second length and selectively prevents the elastic spacer from moving toward the first length. Portions of the triggering element are sequentially removable such that as each portion of the triggering element is removed, the elastic spacer sequentially moves from the second length toward the first length. The sequential movement of the elastic spacer from the second length toward the first length responsively urges the first and second substrates longitudinally toward one another to apply a predetermined amount of longitudinal force to the patient target site.

Abstract: Disclosed embodiments may relate to dressings configured to provide negative-pressure wound therapy to a tissue site, while simultaneously shielding a portion of the tissue site from the negative pressure. For example, dressing assembly embodiments may comprise an outer dressing configured for applying negative-pressure wound therapy to a tissue site, and an underlying isolation patch configured for use under the outer dressing. The isolation patch may be configured to seal the portion of the tissue site so that it does not experience the negative pressure. Additionally disclosed are other apparatus, dressings, systems, and methods.

Abstract: A therapeutic device includes a generally rigid but elastically deformable sheet body including a bridge portion, first and second support portions extending outwardly from the bridge portion in opposite directions along a longitudinal dimension, and adhesive or an adhesion member on a first surface along the bridge portion that is adapted for adhesion to skin of a user above a target site. The therapeutic device also includes first and second projections on the first surface proximate to lateral edges of the sheet body. The sheet body is configured to assume a neutral configuration in which the first and second projections space the bridge portion and the adhesive or the adhesion member apart from the target site by an air gap, a depressed position during affixation of the first surface to the target site, and an adhesion configuration after affixation of the first surface to the target site.

Abstract: Inflatable compression devices are disclosed. In some embodiments the devices provide compression to the torso of a patient, including at a pocket configured to receive a pacing device. In some embodiments at least one securing strap is displaceable with respect to a compression member. In some embodiments a compression member is displaceable relative to at least one securing strap.

Abstract: A wound dressing for use in the application of negative pressure to a wound, comprising a support member and a cover member positionable over the wound in use. The support member can have a first support element having a first portion aligned with a first axis and a body portion coupled with and extending away from the first portion, and a second support element having a first portion aligned with the first axis and a body portion coupled with and extending away from the first portion of the second support element. At least the body portion of each of the first support element and the second support element can be independently rotatable about the first axis. The support member can support at least a middle portion of the cover member above a surface of the wound so as to define a space between the wound cover and the wound.

Abstract: A reduced-pressure treatment system for debriding a treatment area of a tissue site and applying reduced pressure is disclosed. The reduced-pressure treatment system includes a hydrogel having a blocked acid debriding agent. The hydrogel is adapted to cover the treatment area and enhance autolytic debridement at the treatment area. The reduced-pressure treatment system includes a manifold that is adapted to cover the hydrogel and distribute reduced pressure to the tissue site. The reduce-pressure treatment system also includes a sealing drape for forming a fluid seal over the tissue site and manifold. Other systems, methods, and dressings are presented.

Abstract: Dressing for skin care, having a main compress covered by a membrane with an adhesive contour which extends beyond this compress and which is designed to be applied to the skin, this dressing having an inlet port for a treatment liquid on the main compress, and the membrane having, on at least part of the surface opposite this compress, a permeability that permits exchange of gases.

Abstract: A radial compression band employs a substantially rigid U-like cuff that fits over a patient's arm and then snaps onto a tightening band. A movable bubble member is positioned for movement along the band separate from the attachment to the patient and is inflatable to provide pressure to an incision or the like to accomplish hemostasis. A plural bubble member version provides multiple pressure application positions.

Abstract: A wearable medical bandage is provided having an energy harvesting generator that harvests mechanical energy from the user's natural body and muscle motions to produce electrical energy. The electrical energy induces an electric potential across the wound opening producing accelerated skin wound recovery under the voltage fluctuations produced by the power generator.

Abstract: A manifold for treating a tissue site may include a first side and a second side opposite the first side. The second side of the manifold may be configured to face the tissue site, and to contract a greater amount than the first side of the manifold when exposed to a compressive force. In some illustrative examples, the manifold may be configured to distribute reduced pressure to the tissue site, and to contract when exposed to the reduced pressure. The manifold may be suitable for use with dressing assemblies, treatment systems, and methods for treating a tissue site.

Abstract: In one example embodiment, a vibration apparatus can augment and enhance negative-pressure therapy systems. The apparatus can be attached to an external surface of a dressing, fluid conductor, or other components. The apparatus can generate low-amplitude vibrations, which can be transmitted through the components. Kinetic energy of the oscillations can agitate fluid in the components, which can lower the viscosity of the fluid and reduce the frequency of blockages in fluid conductors. Vibrations may also agitate a tissue site, which can encourage blood flow and granulation.

Abstract: 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.

Abstract: 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, for example using softer, kink-free conformable suction adapters.

Abstract: Scar formation is inhibited by simultaneously applying a vertical force and a lateral compression to the wound site during the healing process. Apparatus for applying such simultaneous forces can include a backing and a tissue displacement device. The backing holds the tissue displacement device over the wound. The tissue displacement device may be expanded to both apply the vertical force against the wound and to draw the backing radially or laterally inward to apply the desired compression forces to the wound.

Abstract: Connection pads for coupling fluid-instillation and negative pressure wound therapy (NPWT) apparatuses to wound dressing, and methods and wound dressings for breaching a drape after coupling a wound dressing to a fluid-instillation and/or NPWT apparatus.

Abstract: A reduced pressure dressing for applying reduced pressure treatment to a tissue site includes an interface layer adapted to be positioned at the tissue site. An absorbent layer is in fluid communication with the interface layer to absorb liquid from at least one of the interface layer and the tissue site. A pump is in fluid communication with the absorbent layer to deliver a reduced pressure to the tissue site. A cover is positioned over the pump, the absorbent layer, and the interface layer to maintain the reduced pressure at the tissue site, and a liquid-air separator is positioned between the absorbent layer and the pump to inhibit liquid from entering the pump.

Abstract: A hemostatic device has a band for being wrapped around a puncture site of a wrist, securing means for securing the band in a state where the band is wrapped around the wrist, and an inflation portion that interlocks with the band, and that is inflated by injecting gas. The inflation portion includes a first region which stretches when the gas is injected into the inflation portion, and a second region which is less likely to stretch compared to the first region and which is formed of a rigid material. The second region has a micropore which discharges the gas contained in the inflation portion with the lapse of time, in a state where the inflation portion is inflated.

Abstract: A method and apparatus are disclosed for dressing a wound. The apparatus comprises an absorbent layer for absorbing wound exudate, a liquid impermeable, gas permeable filter layer over the absorbent layer, a cover layer comprising at least one orifice and a first liquid and gas permeable transmission layer underlying the absorbent layer. The transmission layer is in fluid communication with the filter layer.

Abstract: Dressings, systems, and methods are disclosed that, in some embodiments, relate to treating a tissue site. In one embodiment, a dressing may include a manifold, a retention pouch, a sealing member, and a conduit interface. The manifold may be adapted to distribute reduced pressure to the tissue site, and the retention pouch may be adapted to retain and manage fluid extracted from the tissue site. The sealing member may cover the retention pouch and the manifold to provide a sealed space with the tissue site. The conduit interface may be in fluid communication with the sealed space and an exterior surface of the sealing member. The dressing may be utilized with a therapy device operable to control reduced pressure in the dressing and fluid flow over the sealing member.

Abstract: A hemostatic device includes a flexible band adapted to be wrapped around a patient's limb at a site on the limb where bleeding is to be stopped, a portion for securing the band in a wrapped state to the limb, a curved plate which is made of a material more rigid than the band and at least a portion of which is curved toward the inner peripheral side thereof, a main balloon which is provided on the inner peripheral side of the curved plate and which inflates when a fluid is introduced therein, and a pressing member which is provided between the curved plate and the main balloon so that at least a portion thereof overlaps with the balloon and which is adapted for pressing against the balloon. The device provides an excellent hemostatic effect and prevents numbness and poor circulation in areas peripheral to the site of attachment.

Abstract: A radial compression band employs a substantially rigid U-like cuff that fits over a patient's arm and then snaps onto a tightening band. A movable bubble member is positioned for movement along the band separate from the attachment to the patient and is inflatable to provide pressure to an incision or the like to accomplish hemostasis.

Abstract: A toroidal compression bandage includes: a soft fibrous material, defined by an absorbency of a predetermined amount; a compression bandage form comprised of soft fibrous absorbent material in a rolled, wrapped form and of a shape defined by a circle revolved in three-dimensional space about a circular axis coplanar with the circle, wherein the axis of revolution does not touch the rotated circle, to define a torus ring compression bandage; an aperture defined within a center area of the torus ring compression bandage as it is formed, the aperture having a predetermined diameter and configured for placement directly over a trauma wound to avoid contact with the trauma wound; and a compression surface defined on an underside of the torus ring compression bandage, the compression surface configured for circumferential placement around the trauma wound to avoid direct contact of the trauma wound, and for absorption placement around the trauma wound.

Abstract: A device (1) includes a first web of soft material (5), a projecting structure integral with the web and including multiple discrete projecting elements. The projecting elements include pieces of foam (3) spaced apart form one another and integral with the first web (5). The pieces of foam are compressed between the first web (5) and a second web (7) of soft material, the two webs mutually adhering between the projecting elements. The device is useful for treating various types of edemas and excessive tissue infiltration, as well as for repairing sports injury.

Abstract: A pressure-sensing compression bandage having a plurality of pressure sensors provided to indicate the pressures applied by and/or the pressure gradient created by, the applied bandage at various locations along its length when the bandage is applied to a limb or other extremity.

Abstract: A reduced-pressure treatment system for debriding a treatment area of a tissue site and applying reduced pressure is disclosed. The reduced-pressure treatment system includes a hydrogel having a blocked acid debriding agent. The hydrogel is adapted to cover the treatment area and enhance autolytic debridement at the treatment area. The reduced-pressure treatment system includes a manifold that is adapted to cover the hydrogel and distribute reduced pressure to the tissue site. The reduced-pressure treatment system also includes a sealing drape for forming a fluid seal over the tissue site and manifold. Other systems, methods, and dressings are presented.

Abstract: A bandage for use at an aggressive bleeding site of a patient is disclosed. The bandage includes a stretchable wrap, an auxiliary strap, a primary absorbent body, and at plural secondary absorbent bodies. The primary absorbent body is located on the inner surface of the wrap. The wrap is arranged to be wrapped about and tightly encircle a portion of the body of a patient at which the bleeding site is located to cause the primary absorbent body to apply pressure thereto. The auxiliary strap is secured to the wrap and is normally held in stowed position on the wrap, but arranged to be moved to an extended position whereupon the secondary absorbent bodies overlies said primary absorbent body and apply pressure thereto and to the underlying aggressive bleeding site.

Abstract: A reduced pressure dressing for applying reduced pressure treatment to a tissue site includes an interface layer adapted to be positioned at the tissue site. An absorbent layer is in fluid communication with the interface layer to absorb liquid from at least one of the interface layer and the tissue site. A pump is in fluid communication with the absorbent layer to deliver a reduced pressure to the tissue site. A cover is positioned over the pump, the absorbent layer, and the interface layer to maintain the reduced pressure at the tissue site, and a liquid-air separator is positioned between the absorbent layer and the pump to inhibit liquid from entering the pump.

Abstract: A reduced pressure dressing for applying reduced pressure treatment to a tissue site includes an interface layer adapted to be positioned at the tissue site. An absorbent layer is in fluid communication with the interface layer to absorb liquid from at least one of the interface layer and the tissue site. A pump is in fluid communication with the absorbent layer to deliver a reduced pressure to the tissue site. A cover is positioned over the pump, the absorbent layer, and the interface layer to maintain the reduced pressure at the tissue site, and a liquid-air separator is positioned between the absorbent layer and the pump to inhibit liquid from entering the pump.

Abstract: An electronic apparatus is provided. The electronic apparatus includes: a battery; at least one pressure sensor provided on a surface of the battery; and a controller electrically connected with the at least one pressure sensor. The at least one pressure sensor samples a pressure parameter on the surface of the battery. The controller acquires the pressure parameter, detects a magnitude relation between the pressure parameter and a predefined threshold value, and generates a control instruction for protecting the battery based on the detected magnitude relation.

Abstract: The devices, kits and methods described may be used for wound healing, including the treatment, amelioration, or prevention of scars and/or keloids by applying and/or maintaining a pre-determined strain in an elastic skin treatment device that is then affixed to the skin surface using skin adhesives to transfer a generally planar force from the bandage to the skin surface. Applicators are used to apply and/or maintain the strains, and some of the applicators are further configured to provide at least some mechanical advantage to the user when exerting loads onto the skin treatment device.

Abstract: The composite wound dressing apparatus promotes healing of a wound via the use of a vacuum pump. The vacuum pump applies a vacuum pressure to the wound to effectively draw wound fluid or exudate away from the wound bed. The vacuum pump is tethered to the wound dressing and is portable, preferably, carried by the patient in a support bag, which permits patient mobility. Moreover, the patient does not need to be constrained for any period of time while exudate is being removed from the wound.

Abstract: The present invention relates to apparatuses and methods for treating a wound by applying reduced or negative pressure to the wound. The apparatus can include a wound cover, a fluid collection container, a vacuum pump, an inflation pump, and one or more conduits. The wound cover can be configured to move between at least a relatively rigid, generally raised position and a relatively flexible, generally collapsed position according to a predetermined program or in response to input from a user or one or more sensors. In some embodiments, the wound cover can be configured to move between at least the relatively rigid, generally raised position and the relatively flexible, generally collapsed position by adjusting the air pressure in one or more channels in the wound cover or by adjusting the length of piezoelectric or other length changing material supported by the wound cover.

Abstract: Tissue compression devices having pressure indicators and methods of using the same. The tissue compression devices provide feedback to a user with respect to the pressure being applied to selected tissue at a selected location such as a radial artery to assist the user in applying the desired amount of pressure to the tissue (such as the pressure needed to achieve hemostasis at an access site). The pressure indication may be provided by a ring indicator that moves between two configurations (e.g., a concave configuration and a convex configuration), a bellow chamber in a housing, a bladder located below a bladder window, etc.

Abstract: Suture clip deployment devices for applying suture clips to sutures are described. Some embodiments can include a generally tubular main body and a vacuum port located at the distal end, a hollow inner body longitudinally slidable within the main body and extending from the main body at its distal end, and a suture recess located in the generally tubular main body. At least one suture clip configured to frictionally fit on an outer surface of the inner body is deployed during use. Clip deployment can occur after a vacuum source is applied to the device so as to draw the suture into the device. The suture lines can be retrieved through the suture recess, and the device can be actuated so as to deliver the suture clip off the delivery device and onto the suture, locking the suture in place.

Abstract: A dressing device has a device body, a bore extending into an inner surface of the device body, and a biasing element positioned within the bore for biasing the dressing element against the ulcer. The device body functions to offload pressure from an ulcer of a patient. The biasing element functions to support a dressing element against the ulcer to medicate the ulcer, and to prevent the formation of proud flesh.

Abstract: A therapeutic compression apparatus having a primary wrap, a foot wrap and a stirrup is provided. The primary wrap encircles a first portion of a leg and applies compression thereto. The foot wrap encircles at least a portion of the foot and applies compression thereto. The foot wrap may be integrated with the stirrup, detachably connected or provided separately. The compression apparatus may be configured such that one or more bladders are provided therein. The compression apparatus may include a pressure gauge and pump for controlling an amount of pressure applied to the treatment site. A bladder assembly with a number of fluid bladder configurations is also provided for use within a compression apparatus. The bladder may be configured to provide a gradient pressure profile to the treatment site when filled.

Abstract: The invention relates to knit fabric having zones having normal stress-elongation behavior and having predefined zones having increased stress-elongation behavior, for example, knitted fabrics of this type, in particular knit fabric of this type used as medical aids or sport aids, and methods for producing this knit fabric.

Abstract: A wound treatment device comprises a wound surface contacting plug and a cover for covering the wound surface and the plug, wherein said plug consists of a flat textile isolating material comprising at least one first surface layer, one second surface layer and one intermediate space arranged between said surface layers. At least the first surface layer is provided with a biocompatible surface and a structure which enables a liquid to pass and prevents a wound tissue from growing in said structure. The intermediate space is provided with isolating threads elastically holding the first surface layer and the second surface layer at a certain distance from each other.

Abstract: The present invention provides for an advanced postoperative compression binder comprising at least two overlapping stretchable bands. The bands are connected by stitches located within an overlapping portion of the bands. The stitches are spaced from first and seconds ends of the bands to allow individual compression-adjustments of the binder to allow compression to be adapted to the type of surgery or trauma performed and to a level of comfort desired by the patient. The invention provides for wound inspection and care without the need to open the total compression binder, which will maintain a degree of support during wound inspection and care, decrease pain and increase comfort for the patient.

Abstract: A topical cooling compressive hemostasis wound healing device and methods thereof for affecting a percutaneous access site wound or an acute surgical wound. The device delivers and transports cooling to affect and control vasculature and musculoskeletal motions surrounding the injury site during the blood coagulation, hemostasis, and wound healing phases. The device comprises a viscoelastic and thermally conductive surface to deliver and transport an adjustable compressive pressure to resist outward blood flow, thus improving patient safety and clinical outcomes. The device is anatomically conforming and treats not only the specific injury site, but also its surrounding anatomical structures together as means to prevent unpredictable delayed hemostasis breach. The device provides comfort to the patient by allowing mobility upon wound healing, thus reducing back pain and strain resulting from being in constrained position for a prolonged period of time which is known to cause additional medical events.

Abstract: Apparatuses and methods for treating a wound by applying reduced or negative pressure to the wound can include a wound cover, a fluid collection container, a vacuum pump, an inflation pump, and one or more conduits. The wound cover can be configured to move between at least a relatively rigid, generally raised position and a relatively flexible, generally collapsed position according to a predetermined program or in response to input from a user or one of more sensors. In some embodiments, the wound cover can be configured to move between at least the relatively rigid, generally raised position and the relatively flexible, generally collapsed position by adjusting the air pressure in one or more channels in the wound cover or by adjusting or by adjusting the length of piezoelectric or other length changing material supported by the wound cover.

Abstract: In one embodiment, a medical device for containing or applying a pressure or a combination thereof to an area of skin or wound of a user is provided. The medical device includes a bandage body, a pad component disposed thereon, body, an adhesive component, and an opening adjacent to the first end of the bandage body, wherein the opening is configured to receive at least a portion of the bandage body such that when the second end of the bandage body is received within the opening, the adhesive portion of bandage body can be attached to a portion of the bandage body such that the adhesive does not contact the user.

Abstract: An engineered designed article providing multi-directional support. Portions of three or more overlapping, circular-like bodies are integrated on a flexible planar membrane into products, such as bandages, headgear, tool handles, lumbar pillows, backpacks, cervical supports, and back supports, to offer a multi-directional, (360° quadrant) support or pressure-concentrating area, to enhance specific support at the medial, lateral, inferior and/or superior part of a body part. The article can be made of material that is waterproof, acts as a shock absorber, and provides multi-directional support. Medicaments can be infused into the pressure-concentrating area of the support or into the membrane itself. An aperture for accepting IV needles is also provided.

Abstract: The present invention relates generally to the field of hemostasis, including methods, compositions, and devices that can be employed to achieve hemostasis at an increased rate. More specifically the present invention relates to hemostatic compositions that achieve a hemostatic effect at a distance from the site of application of the composition, and a method for administering such a composition to effectively reduce localized vascular complications associated with treating a breach or puncture in a vein or artery and reduce the time to achieve hemostasis.

Abstract: A scar reducing device for stretching skin having a closed wound therein is provided. The device is for reducing scar formation. The device comprises first and second fasteners removably attachable to skin regions located proximate to the wound. The device also comprises an extension mechanism cooperating with said first and second fasteners. The extension mechanism is movable between contracted and extended configurations. When the fasteners are affixed to the skin, the mechanism forces the first and second fasteners away from one another with a predetermined tensile force, stretching the skin proximate to the wound. Use of the device is also provided, along with a method for reducing scarring of a closed wound.

Abstract: The multipurpose medical wrap serves as a dressing, covering, splint holder, and/or various other emergency medical uses. The wrap includes a central pad having two layers of material defining a plurality of internal pockets therebetween for the insertion of various treatment packs and/or splints therein. The pad includes a relatively soft sheet to protect the area to which it is applied, and a relatively thin, non-insulating sheet that allows the pad to be reversed for use in applying hot and cold packs and the like. An end flap extends from each end of the central pad for additional protection and/or treatment. A plurality of laterally overlapping straps extends from each side of the central pad. Corresponding opposite straps are interwoven to secure the wrap to the body, some straps being used to form a sling and/or torso securing swath when the wrap is used as an arm treatment.