The present invention is a device for transcutaneous application of CO.sub.2, which comprises: a therapeutic chamber comprising at least a portion to receive a part of a patient's body to which the carbon dioxide is to be applied, an inlet/outlet pipe connecting the chamber with a CO.sub.2 distribution system, the said pipe connecting the chamber with a CO.sub.2 distribution system, wherein a gate valve for sealing the chamber is installed in the chamber where the inlet/outlet pipe is installed; the CO.sub.2 distribution system comprising a housing where at least the following components are installed: a first pipe with a first valve for suction of air out of the chamber, a second pipe with a second valve for supplying CO.sub.2 from a tank; wherein the first and second pipe are combined into the inlet/outlet pipe upstream of the valves; at least one ventilator for ensuring air flow through the said valves and inlet/outlet pipe, an outlet pipe for leading the used air from the chamber through the wall to the external environment of the building where the device is installed; and at least one tank for storing CO.sub.2 suitably connected to the second pipe.

Systems, devices, and methods for delivery of a topical substance, including medicaments and/or cosmetic formulas, with carbon dioxide to the surface of the skin. The systems regulate the pH, temperature and viscosity of the topical substance, which provides benefits to the treatment of the skin. For beauty treatments, the systems lessen wrinkles of the skin and hydrate at the same time. For medicaments with active ingredients, the systems enhance delivery and ionic state using pH adjustment. The systems include devices that contain a reservoir of carbon dioxide, which flows through a heat control path where the temperature of the carbon dioxide is adjusted to a desired setting. The temperature-controlled carbon dioxide then mixes with the topical substance in a chamber, which is pressed against or applied to the skin to achieve the benefits.

A decubitus ulcer healing airflow device includes a motorized airflow intake fan disposed within a housing body devised to be attached to a bed rail A tubular airflow outlet is attached to a rear side of the housing body. An air filter slideably engages an access slot and is disposed between a protective grill and an airflow intake fan. At least one strap has a central elastomeric central section engageable onto the bed rail and a pair of u-shaped outer ends. Each strap engages a respective one of a pair of strap support holders disposed on each or one of a top and bottom side of the housing body. A slotted compartment, within the airflow outlet, contains a fragrance or a vaporized medicine to assist in healing the ulcers.

The apparatus according to the invention is adapted for transcutaneous treatment by gas. The apparatus (10) comprises a rigid-wall cabinet (20) and having an upper opening and at least one openable panel, wherein a seat (25) is arranged inside the cabinet (20), and the cabinet (20) comprises at least one gas concentration measurement unit (29a), and the cabinet (20) further comprises a gas inlet (30) for feeding the treatment gas and a gas outlet (31) for discharging the treatment gas; a gas supply unit (40) coupled to the gas inlet (30) of the cabinet (20) via a pipe (41) and through an interposed controllable valve (42); and a gas tank (50) connected to the gas supply unit (40). The apparatus further comprises a ventilation unit (60) connected to the gas outlet (31) of the cabinet (20) through an interposed controllable valve (63), said ventilation unit (60) being coupled via a further pipe (62) to a space (70) hermetically separated from the room containing the cabinet (20), and wherein said ventilation unit (60) is designed so that it can discharge the entire volume of the treatment gas from the inner space of the cabinet (20) within at most 5 seconds. The apparatus further comprises a control unit (80) for receiving the signals of the gas concentration measurement unit (29a) and for controlling operation of the valves (42, 63) and said ventilation unit (60) based on at least the signals of the gas concentration measurement unit (29a).

An apparatus for use in applying a therapy to a human limb includes a bag for surrounding all or part of the limb. The apparatus also includes a connection arrangement, mounted to a wall of the bag in a distal portion of the bag, that enables therethrough a flow of a gas between a pressure-regulating device and an interior space of the bag. The apparatus also includes a gas-permeable strip affixed to an interior surface of the bag and having a length equal to at least 70% of the bag's length. The distal end of the strip is in communication with the connection arrangement in the distal portion of the bag, and a proximal end of the strip is disposed in a proximal portion of the bag. The strip contains a partially compressible, gas-permeable material forming a lengthwise gas-flow pathway.

A configurable oxygen concentrator for providing various flow rates and volumes of concentrated oxygen to a patient includes an electro-mechanical assembly having a housing with a first face, a second face and an outer surface. The oxygen concentrator also includes a first battery, a second battery, a first adsorbent container and a second adsorbent container. The first and second batteries are removably mountable to the first face and the first and second adsorbent containers are removably mountable to the second face to permit modification of the concentrated oxygen capacity and operating life of the concentrator as the patient progresses through different stages of a breathing disease. The first battery has a first battery capacity that is less than a second battery capacity of the second battery. The first adsorbent container has a first adsorbent capacity that is less than a second adsorbent capacity of the second adsorbent container.

An apparatus for cleansing wounds, in which wound exudate is removed from a wound bed and selectively cleansed and returned to the wound. The cleansing means removes materials deleterious to wound healing, and the cleansed fluid, still containing materials that are beneficial in promoting wound healing, is returned to the wound bed. The associated wound dressing and cleansing means are conformable to the wound, and may have irrigant fluid circulated from a reservoir by a device for moving fluid through a flow path which passes through the dressing and a means for fluid cleansing and back to the dressing.

A combination therapy pad that includes a first layer and a second layer operatively coupled to the first layer. A fiber-optic array is disposed between the first layer and the second layer. A third layer is operatively coupled to the first layer. The third layer includes a vacuum tube in fluid communication with a vacuum source and a therapeutic fluid tube in fluid communication with a therapeutic fluid source. The third layer provides at least one of vacuum therapy and therapeutic fluid treatment to a wound area.

Systems, apparatuses, and methods for providing negative-pressure therapy with oxygen therapy are claimed. An apparatus for providing negative pressure therapy with normobaric or hypobaric oxygen therapy may include dressing having a tissue interface and a cover. Additionally, in some embodiments, the apparatus may include a negative-pressure source and an oxygen-concentrating or oxygen-generating source, each of which may be coupled to or configured to be coupled to the tissue interface. The tissue interface can enable fluid transport during negative-pressure therapy cycles, and disbursement of normobaric or hyperbaric oxygen during oxygen therapy cycles. For example, some embodiments of the tissue interface may comprise structures or foams constructed from polyurethane, silicone, or polyvinyl chloride. The cover should be versatile enough to conform to a tissue site, yet be sufficiently inelastic or become sufficiently inelastic to contain and sustain the pressure from the application of topical normobaric oxygen therapy or hypobaric oxygen therapy.

This disclosure includes negative pressure wound therapy dressings with local oxygen generation for topical wound therapy. The dressings (18) for facilitating delivery of oxygen and application of negative pressure to target tissue include a manifold (46) that defines a plurality of gas passageways (50) and is configured to allow communication of oxygen to the target tissue; an oxygen-generating material (146) that is configured to release oxygen when exposed to water; a gas-occlusive layer (74) configured to be disposed over the manifold and the oxygen-generating material and coupled to tissue surrounding the target tissue such that an interior volume containing the manifold and the oxygen-generating material is defined between the gas-occlusive layer and the target tissue; and a port (94) coupled to the gas-occlusive layer and configured to be coupled to a negative pressure source.