A multifunctional wound treatment dressing for administering different therapeutic treatments to an open, chronic wound of a human or animal body. The multifunctional wound treatment dressing includes an occlusive wrapping adapted for placing over a wound. The multifunctional wound treatment dressing further includes at least two of the group of electrical, optical or mechanical stimulation means adapted for transmitting electrical, optical or mechanical energy towards the wound to stimulate healing of the wound and/or means for applying a negative (i.e. sub-atmospheric) pressure to the wound. Thus, a variety of different healing stimulation treatments may be performed together or in sequence by wearing the same occlusive wrapping without the need of changing/removing temporarily the wrapping for each change of treatment method.

A treatment system including one or more of a wound dressing having one or more of a substrate element, a dressing member disposed on the substrate element, an adhesive element disposed on the substrate element, and a tether connecting the wound dressing to a treatment device.

Systems and methods for pain management are disclosed herein. In some embodiments, a vibrating pain management device includes a vibration generator attachable to a wearable patch having first and second arms for attaching the patch to a wearer. The patch is at least partially stretchable.

Embodiments herein provide hemostatic compositions comprising a plurality of liquid-expandable articles arranged on a backing material. In general, embodiments include methods for treating hemorrhagic injuries. More specifically, there is provided a method to effect rapid hemostatic response and control hemorrhage by introducing a hemostatic composition into a bleeding wound cavity. An embodiment also provides a method of preparing or manufacturing such a hemostatic composition.

A pressure system and method for managing post-operative swelling. The pressure system has a balloon with a quadrilateral basal skirt that surrounds a surgical site on a patient. A plurality of strap-receiving slots is located in the skirt. Adhesive pads are affixed to the patient outside the skirt. One or more tensioning straps are deployed between the strap-receiving slots and the adhesive pads so that tension can be applied to the straps and to the skirt in order to press the balloon upon the surgical site. Optionally, means for generating visual feedback cues are provided to enable the operator to determine appropriate compression and assess skin recoil feedback. Such means may signify swelling reduction and skin turgor.

A viscoelastic wound closure dressing. The dressing can include a viscoelastic backing having a first major surface configured to face skin when in use, a first end, a second end, and a middle section located between the first end and the second end. The wound closure dressing can further include a skin-contact adhesive on the first major surface of the viscoelastic backing adjacent the first end and the second end. A majority of the first major surface of the middle section can be free of the skin-contact adhesive. The viscoelastic backing can recover, at room temperature: (i) no more than 40% of its deformation after 10 seconds, after being strained to 50% elongation for 30 minutes, and (ii) at least 70% of its deformation after 48 hours, after being strained to 50% elongation for 30 minutes.

An adhesive therapeutic cover comprises at least one lift device and a single sheet of at least a two-ply material that includes a cover material with an adhesive on a bottom surface and a backing layer. The cover material defines at least one opening therethrough or at least one opening area which is removable after application of the cover material to a patient to form an opening through the cover material. The at least one lift device comprises a connector adhered or adherable to the cover material in alignment with the opening or opening area. The connector can be connected to a pressurized source of a flowable lifting agent, to urge the flowable lifting agent through the connector and the opening to separate the cover material from patient skin. Sensors can be provided to monitor and/or control the flow of lifting agent through the lifting device during removal of the cover from the patient.

The present disclosure relates to apparatus for covering a burn or other wound in ways that prevent or limit touching the wound. The present disclosure describes Burn Bandages that may include domes or structures that bridge over a wide range of a burn or wound size. In certain instances these structures may expand in one or more directions as they are adjusted to fit to a particular burn or wound size. Such bridging structures may include airways, openings, or voids that promote air/oxygen flow to the wound as the Burn Bandage sits upon surfaces or pads that contact healthy surrounding tissue while they cover a wound site. The apparatus may be any shape including, yet not limited to, a circle, a rectangle, a square, a hexagon, an octagon, an oval, a cone, a cylinder, have a semi-cylindrical shape, or that have any another geometric shape.

Kits and systems are disclosed that include one or more segments of elastically deformable membrane in combination with one or more external fixation members and optionally in combination with one or more tension protector pads. Also disclosed are methods of use of the kits and systems in methods that involve stretching the elastically deformable membrane and applying the stretched membrane to the skin of a patient, and releasing the tension on the membrane, thus causing compression of the skin to which the membrane is applied. The method may further include the optional steps of inserting one or more external fixation members through the membrane/skin combination and into a bone segment, applying a distraction force to the one or more external fixation members, and separating at least a portion of the membrane so as to release a portion of the tension in the skin at a rate that is similar to a rate at which the distraction force is applied.

A system for treating a tissue site includes a pressure source to apply reduced pressure, and a manifold in fluid communication with the pressure source to provide reduced pressure to the tissue site. The system includes a drape for adhering to the tissue site to cover the tissue site and the manifold. The drape has a film layer having a thickness less than about 15 microns, and an adhesive coupled to the film layer. The adhesive seals the film layer to the tissue site to create a sealed space having the manifold therein. The adhesive is sufficiently thick to limit leaks between the film layer and the tissue site.