Abstract: An apparatus for abdominal dressing that adds liquid coils in the form of a manifold is disclosed. The manifold includes heating coils to warm the bowel with heated water in a counter current method. This takes advantage of the large surface area of the bowel to exchange heat with the heater coils, but allows the abdominal dressing to maintain the initial function: remove pathologic fluid from the abdomen. Methods of treating patients with an open abdomen are also disclosed.

Abstract: Hydrostatic pressure of aqueous solutions—supplied from reservoir under rate control through tube to port of airtightly applied open pore dressing pad—is eliminated by levelling reservoir placed on rest with pad. Dressing pad may overlie a tissue culturing scaffold. A drip chamber with angulated channel permits drops to fall freely and be counted. Injection port elastic membrane prevents air inlet to pad while suction is applied at port, permitting fluid given under rate control through membrane to distribute evenly in pad. A drainage port flange, wholly covered by an open grid, is described. Acute wound bleeding is detected by computer-controlled serial weighing of a movement-stabilized drainage fluid canister with warning of abnormal flow rate increase.

Abstract: An apparatus for treating skin includes a chamber defined by a surface and a rim extending from the surface. A source of vacuum is capable of removing air from inside the chamber so that air outside the chamber flows into the chamber. Impedance of the air flowing between the rim of the chamber positioned adjacent the skin surface causes the pressure inside the chamber to decrease relative to ambient. A pressure sensor can determine when the pressure inside the chamber decreases to a threshold value. A controller can receive a signal from the pressure sensor when the threshold value is reached, which causes the rate of removal of the air from inside the chamber by the source of vacuum to be increased. The rim of the chamber forms a substantially fluid tight seal with the skin. The skin is drawn toward an inner surface of the chamber.

Abstract: A method for treating a wound with sutures is disclosed. One method includes placing the body and shaft of the device within a cavity of the wound; attaching a first end of at least one suture to a first side of the wound; passing a second end of the at least one suture through the body and coupling it to the shaft; attaching a second end of the at least one suture to the second side of the wound; and rotating the shaft with respect to the body to pull the first side of the wound and the second side of the wound toward one another.

Abstract: A suction head in fluid communication with a pump head provides a sub-ambient working pressure to a medical site, enabling drainage thereof to a waste container and/or enhancing healing at the site. A passive pressure regulator enables the working pressure to be maintained at a desired level independent of the fluid flow through the system.

Abstract: An apparatus (1) for cleansing wounds (5) in which irrigant fluid from a reservoir connected to a conformable wound dressing (2) and wound exudate from the dressing are moved by a device (18) (which may be a single pump or two pumps) for moving fluid through a flow path (6, 7, 9, 10) which passes through the dressing with a means for providing simultaneous aspiration and irrigation of the wound, and means for supplying thermal energy to the fluid in the wound. The former provides a desired balance of fluid at a controlled nominal flow rate that removes materials deleterious to wound healing, while distributing materials that are beneficial in promoting wound healing over the wound bed. The latter maintains a temperature at the wound bed under the wound dressing at a level that promotes wound healing.

Abstract: An apparatus includes a pressure housing configured to be coupled to a vacuum source and a diaphragm sealingly coupled to the pressure housing. The diaphragm is configured to move in response to the vacuum source. A magnet is coupled to the diaphragm. A magnetic switch is disposed opposite the magnet and is configured to be actuated by the magnet when the magnet is a predetermined distance from the magnetic switch. The magnetic switch is configured to selectively actuate the vacuum source.

Abstract: An apparatus (1) for cleansing wounds (5) in which irrigant fluid from a reservoir (12) connected to a conformable wound dressing (2) and wound exudate from the dressing are moved by a device (which may be a single pump or two pumps) for moving fluid through a flow path which passes through the dressing and a means for providing simultaneous aspiration and irrigation of the wound, and means for supplying physiologically active agents to the wound. The former provides a desired balance of fluid at a controlled nominal flow rate that removes materials deleterious to wound healing, while distributing materials that are beneficial in promoting wound healing over the wound bed. The latter maintains physiologically active agents at a level that promotes wound healing.

Abstract: A reduced-pressure treatment system for treating a tissue site on a patient includes a gasket releasably attached around a perimeter of the tissue site that may remain in place for an extended time and allows an over-drape to be attached to it. The system and method further may include a manifold sized and configured to be placed in contact with the tissue site; the over-drape positioned over the manifold and sealed to the gasket to create a sealed space between the over-drape and the tissue site; and a reduced-pressure source fluidly coupled to the sealed space to deliver reduced pressure to the tissue site. A method is also presented.

Abstract: A personal care apparatus (1) is provided with a suction nozzle configuration (4) which has two different suction nozzles (15, 22) with two different suction sections (27, 26), wherein the suction nozzles (15, 22) are held adjustably in relation to each other along a path of motion (16) which is preferably perpendicularly to their suction sections (27, 26), so that by means of an adjustment of this type in each case one of the suction nozzles (15, 22) may be adjusted with its suction section (27, 26) into an operating position permitting suctorial interaction with an area of the skin.

Abstract: [Problem] To provide a breast pump capable of securely holding a breast of a user and intensively stimulating a particular potion of the breast.

Abstract: Described generally herein are tissue therapy devices, which may comprise a sealant layer and a suction apparatus. The sealant layer functions so as to create a sealed enclosure between it and the surface of a patient by forming, preferably, an airtight seal around an area of tissue that requires negative pressure therapy. The tissue therapy device may comprise a suction apparatus. The suction apparatus is typically in fluid communication with the sealant layer and functions so as to reduce the amount of pressure present underneath the sealant layer. The reduced pressure is self-created by the suction apparatus. Together the sealant layer and the suction apparatus preferably create a closed reduced pressure therapy system. Preferably, the pressure under the sealant layer is reduced by expanding the volume of the enclosure space and thereby decreasing the density of the air molecules under the sealant layer.

Abstract: An apparatus for stimulating healing of a wound, includes a porous pad adapted to contact a surface of the wound on an affected part of a body. An envelope for receiving the porous pad and the affected part of the body is provided, and the envelope includes a re-sealable opening that permits the wound to be inspected. A connector is fluidly connected to an interior of the envelope and to a source of negative pressure.

Abstract: A reduced pressure treatment system is provided for delivering a reduced pressure to a tissue site comprising a distribution manifold including a backing substrate with a first side and a second side and a plurality of protrusions positioned on the first side of the backing substrate, each of the protrusions having a substantially circular cross-sectional shape and having a diameter of between about 0.1 and 2.0 millimeters, the backing substrate having a plurality of apertures formed therein to allow fluid communication between the first side and the second side opposite the first side. A reduced pressure source fluidly connects to the apertures of the backing substrate to deliver the reduced pressure through the apertures, between the protrusions, and to the tissue.

Abstract: A wound treatment system includes a sponge including a first surface adapted to confront a wound bed of a patient, a drape in contact with a second surface of the sponge, and a vacuum source for distributing a vacuum force through the sponge. The system also includes a wound separator having a sidewall defining an interior chamber, wherein at least a portion of an exterior of the sidewall confronts at least an interior portion of the sponge. An ostomy appliance is operatively connected to the wound separator to receive substances passing out of the wound separator.

Abstract: A system for applying suction to a wound uses a reference airflow for monitoring system operation. A reference airflow (or “controlled leak”) to the suction source is provided when the system is in operation, such that deviation from the reference airflow can be monitored as an indication of a change in operation, such as a leak in the seal of the wound cover, a blockage of airflow from crimping of the suction conduit or overfill of the waste collector, or an inadvertent turn off or disconnect from the suction source.

Abstract: A skin care device includes a suction nozzle to be brought into contact with skin to suction skin impurities therefrom, a suction pump for generating a suction force of the suction nozzle, a mist nozzle installed near the suction nozzle, for ejecting a mist of liquid, a tank for storing therein a liquid to be supplied to the mist nozzle, a liquid supply pump for supplying the liquid to the mist nozzle from the tank, a drive motor for driving the suction pump and the liquid supply pump at the same time, and a liquid amount control unit for controlling an amount of the liquid ejected from the mist nozzle. The liquid amount control unit is a flow rate regulation device disposed between the tank and the mist nozzle.

Abstract: The illustrative embodiments described herein are directed to an apparatus and method for managing reduced pressure at a tissue site. The apparatus includes a reduced pressure source that generates reduced pressure. The reduced pressure is delivered to the tissue site via a delivery tube. The apparatus includes a single pressure sensor. The single pressure sensor detects an actual reduced pressure at the tissue site. The apparatus also includes a controller. The controller determines a responsiveness of the actual reduced pressure measured by the single pressure sensor to an increase in reduced pressure generated by the reduced pressure source. The apparatus includes an indicator. The indicator emits a signal when the controller determines that the actual reduced pressure measured by the single pressure sensor is nonresponsive to the increase in reduced pressure generated by the reduced pressure source.

Abstract: An apparatus and method used for medical and/or cosmetic treatment of a tissue, such as skin tightening, skin laxity and/or wrinkle reduction and or other skin flaws, including an energy source, a vacuum chamber and rollers which may facilitate easy sliding of the apparatus from one treated area to another. The rollers may also prevent excessive friction of the skin during the treatment. The energy source can be configured to emit energy based on the position of the apparatus on the skin (i.e., the position of the rollers), as well as the pressure within the vacuum chamber. The vacuum level and energy emission can be changed or pulsed based on the treatment regime.

Abstract: A tissue treatment apparatus and method are provided for treating tissue by the application of the time-varying sub-atmospheric pressure. The apparatus includes a cover adapted to cover a wound and adapted to maintain sub-atmospheric pressure the site of the wound. The apparatus further includes a source of suction configured to generate a time-varying sub-atmospheric pressure having a periodic waveform comprising a gradual change in pressure. The suction source cooperates with the cover to supply the time-varying sub-atmospheric pressure under the cover to the wound. The time-varying sub-atmospheric pressure may vary between a first pressure value below the inherent tissue tension of the wound tissue and a second pressure value above the inherent tissue tension of the wound tissue.

Abstract: A disposable wound-healing device is disclosed that incorporates a housing having a fluid-impermeable material having a cavity and a perimeter that can be sealed in an air-tight manner over a wound region of a patient. The device is capable of producing a negative pressure over the wound region by either removing oxygen from within the cavity, or absorbing fluid into the cavity and then removing the fluid from the cavity. The oxygen may be removed via chemical absorption, by an electrochemical cell or by a chemical reaction that cannibalizes oxygen from the cavity. The fluid may be removed through the use of osmotic or electro-osmotic cells, or through a one-way valve. The negative partial pressure over the wound region promotes healing.

Abstract: A skin care device includes a suction nozzle for drawing and removing sebum or other impurities from a user's skin while contacting the skin, a suction pump for generating a suction force for the suction nozzle, a mist nozzle, provided at a position around the suction nozzle, for spraying liquid, a liquid storage tank for storing the liquid to be supplied to the mist nozzle, a liquid supply pump for supplying the liquid in the liquid storage tank to the mist nozzle, and a drive motor for operating the suction pump and the liquid supply pump at the same time. Further, the suction pump and the liquid supply pump are disposed opposite to each other.

Abstract: A skin care device includes a suction pump for generating a suction force, a suction nozzle detachably attached to a mounting portion of the suction pump and having a first end portion having a suction port with a smaller opening and a second end portion having a suction portion with a larger opening, and a sealing member disposed between an inner peripheral surface of the mounting portion and an outer peripheral surface of the suction nozzle, for sealing a gap between the mounting portion and the suction nozzle. Both of the first end portion and the second end portion are capable of being attached to the mounting portion.

Abstract: An apparatus for use in extracting milk from a human breast includes a pliant receiving member having an inner receiving portion sized to receive the human breast and an adjacent inner connecting portion defining an opening extending therethrough. The receiving member has an inner surface defining a recess located in the inner receiving portion and a passageway extending from the recess to the opening to provide fluid communication between the recess and the opening during use. The passageway provides fluid communication between the recess and the opening such that negative pressure can be generated between the recess and the breast.

Abstract: Disclosed is an apparatus for the treatment of a wound on a patient. The apparatus is capable of administering localized negative pressure therapy to the wound using a hospital wall vacuum source and a drain line for removing exudate from the wound. The apparatus may also be capable of administering localized hyperbaric oxygen therapy to the wound using a hospital wall oxygen source and a supply line for supplying oxygen to the wound. The apparatus includes at least one regulator to control the application of negative pressure therapy and hyperbaric oxygen therapy.

Abstract: A dressing for treating wounds, especially chronic wounds, includes a liquid-absorbing wound pad. A reservoir for receiving liquid is located on the side of the wound pad facing away from the body. The wound pad is connected to the reservoir via valves and/or a semi-permeable membrane so as to create a directed liquid flow from the wound pad into the reservoir.

Abstract: The invention relates to a drainage device (100) for the treatment of wounds using reduced pressure, comprising (a) a gas-type wound-covering element (3), which, in the state in contact with the body of the patient, is fastened cohesively at the skin surface around the region of the wound and forms a sealed wound space, remaining between the respective wound and the wound-covering element (3); (b) at least one drainage tube (4), which can be connected to means generating the reduced pressure and can be inserted into the wound space approximately parallel to the wound-covering element (3); and (c) at least one absorption body (2) in the form of at least one layer (7) of a textile section (33), which is interspersed with super-absorbing particles and enclosed in an envelope. Due to the size of the pores of the envelope, the absorbed wound secretions remain within the absorption body (2) and, with that, underneath the wound-covering element (3) until the absorption body is removed from the wound space.

Abstract: In one example, the present invention is directed to wound-healing patche that passively or actively draw fluids from a wound using an internal, integral vacuum source. The patches may also include electrodes and electronics for electrostimulation, and bioactive compounds that promote healing, such as anti-inflammatory agents.

Abstract: A bandage is provided for use with a wound having a wound surface. The bandage is connectable to a vacuum source and may include a flexible cover positioned over the wound and a collar coupled to the cover. The cover includes a port and is configured to seal to a patient's healthy skin surrounding the wound. The collar may be coupled to the cover and include a passageway in communication with the port of the cover. The passageway is configured to receive at least a portion of a tube in communication with the vacuum source. The bandage may also include a sealer coupled to the collar. The sealer may be configured to provide a substantially airtight seal between the tube and the passageway to create a sealed environment capable of maintaining a negative pressure between the cover and the wound surface.

Abstract: The present invention is a deformable liquid handling member, having an inner region circumscribed and hermetically sealed by a wall region, which comprises a membrane assembly to separate a first zone outside of the member from a second zone within the inner region of the member. Thereby, the second zone is connected to a suction source capable of receiving liquid, and the first zone is positioned in liquid communication with a liquid releasing source during its intended use. The membrane assembly is capable of maintaining a pressure differential between the second zone and the first zone without permitting air to penetrate from said first zone to said second zone. Further, the inner region comprises an inner material, which has a volume expansion factor of more than 3, preferably 5, more preferably 10, and can have a creep recovery of more than 60%, preferably more than 90%.

Abstract: The apparatus includes at least two skin-contacting elements, the elements having narrow end faces and a mounting assembly for holding the elements closely adjacent to each other. A driving assembly reciprocally moves one element relative to the adjacent element(s) at a frequency that produces an action on the pores of the skin to loosen sebaceous plugs present in the pores, by permitting their ready removal from the skin.

Abstract: A portable wound treatment apparatus, for stimulating the healing of superficial wounds, comprises a housing containing a suction pump and a canister for containing fluids drawn from the wound. The housing is supported on a harness or belt worn by the patient. The canister is connected to a porous wound dressing at the wound site via a plurality of tubes, a multi-lumen tube or a combination thereof. A rechargeable battery pack may be incorporated within the housing or externally thereto. The external battery pack may be shaped to balance the housing on the harness or belt. Pressure transducers are provided to monitor and report pressures at the wound site or internal to the canister. Monitored pressures may also be utilized to determine the filled state of the canister and, thereafter, either report this state to the operator or automatically discontinue suction from the wound, or both.

Abstract: A wound therapy device is disclosed. The wound therapy device may include a housing for covering at least a portion of a wound and for sealing to a body surface of a patient. The housing may also include a liquid collector for retaining liquid therein and a vacuum connection for coupling to a vacuum source. The vacuum connection may be in gaseous communication with the liquid collector. The vacuum connection may be separated from the liquid collector by a liquid barrier.

Abstract: An apparatus for measuring skin permeable gas, which can be used to obtain clinical information by noninvasive and bloodless operations and is useful for in-home medical care and health management. The apparatus includes a device for collecting skin permeable gas including a container for storing skin permeable gas; a partition, disposed at a lower section inside the container, having an opening at the center thereof; and an operating member for opening and closing the opening of the partition.

Abstract: A tool for cementing a liner to the glenoid cavity of a scapula. The tool comprises an elongated, hollow, rigid tube having distal and proximal ends with the distal end of the tube having either an angular portion or a curved portion which has a plurality of openings formed therein. The tube has a length such that the distal end thereof may be positioned in the glenoid vault and so that the proximal end of the tube may be placed in communication with a source of suction. An elongated sleeve member is slidably mounted on the tube and preferably has a sealing gasket at its distal end which may be moved into sealing engagement with the coracoid process around the opening formed therein. A flexible obturator is selectively extended through the tube to clear the tube of debris.

Abstract: A method and apparatus for providing concurrent applications of intermittent pneumatic compression therapy and vacuum assisted closure therapy generally comprises a wound dressing for introduction of a negative pressure into a wound on a patient's foot and a foot wrap for application of positive, compressive forces to substantially all of the patients foot. A suction pump, having an associated vacuum sensor and first feedback mechanism, supplies negative pressure to the wound dressing. A ventable source of pressurized gas, having an associated pressure transducer and second feedback mechanism, supplies positive force to the foot wrap. At least one control system is operably associated with the suction pump and ventable source of pressurized gas for controlling the negative and positive applications of pressure to the patient's foot. Controlled modes for operation include continuous or intermittent application of one or both therapies and simultaneous or cycled application of the therapies.

Abstract: An improved smoke evacuation system and method for removing gaseous byproducts of surgical procedures and noxious vapors from chemicals is provided. The smoke and vapor evacuation system includes a vacuum head positionable at a surgical site or incorporated into a workstation. The vacuum head includes a plenum, and a plenum support for preventing the plenum from collapsing when a vacuum or low pressure is established therein, and is adapted to facilitate the use of the system in a variety of surgical or commercial procedures at a variety of surgical sites or commercial workstations.

Abstract: A method, and apparatus (10) for the controlled acceleration, and/or retardation of the body's inflammatory response generally comprises a foam pad (11) for insertion substantially into a wound site, a heating, a cooling pad (13) for application over the wound site (12), a wound drape (14) or sealing enclosure of the foam pad (11), the heating, and cooling pad (13) at wound site (12). The foam pad (11) is placed in fluid communication with a vacuum source for promotion of the controlled acceleration or retardation of the body's inflammatory response. The heating, and cooling provision controls the local metabolic function as part of the inflammatory response.

Abstract: A wound treatment appliance is provided for treating a wound, which appliance comprises a semi-rigid or rigid wound covering device and a vacuum system to provide a supply of reduced pressure to the wound covering device. The wound covering device may be comprised of an impermeable overlay, a stopper, and a suction drain. Alternatively, the wound covering device may be comprised of an impermeable overlay and a suction drain. The wound covering device may also be comprised of an impermeable overlay that has at least one channel that is a part thereof, wherein the at least one channel is used to provide reduced pressure to the wound and may remove fluid aspirated from the wound. The vacuum system may be comprised of at least a vacuum pump or a suction bulb, or a combination of the same. Finally, methods for using the wound treatment appliance are provided.

Abstract: A biocompatible wound dressing comprised of a pad for insertion substantially into a wound site and a wound drape for sealing enclosure of the foam pad at the wound site. The pad, comprised of a foam or other like material having relatively few open cells in contact with the areas upon which cell growth is to be encouraged so as to avoid unwanted adhesions, but having sufficiently numerous open cells so that drainage and negative pressure therapy may continue unimpaired, is placed in fluid communication with a vacuum source for promotion of fluid drainage, as known in the art. The pad is further comprised of an ultra-low density fused-fibrous ceramic, or a bioabsorbable branched polymer, or cell growth enhancing matrix or scaffolding.

Abstract: A wound treatment apparatus has a vacuum bandage covering a wound of a patient, a vacuum source coupled to the vacuum bandage, and a controller that operates the vacuum source to apply negative pressure to the wound through the bandage in a controlled manner. The controller is programmed to limit the rate of change of the negative pressure applied to the wound. A caregiver has the ability to change one or more negative pressure setpoint values and the controller of the wound treatment apparatus controls the rate of change of the negative pressure to reduce patient discomfort.

Abstract: A portable closed wound drainage system that uses a pouch shaped dressing which is inserted into a wound. At least a portion of the outer surface of the pouch is porous to allow exudates to enter. Exudates are removed from the pouch by flexible tubing which is secured inside the pouch at one end, and secured at the other end to a portable drain/suction unit. The pouch contains porous material, and may optionally contain beads and fillers which are antibacterial in nature. The tubing can have a single or multi-lumen structure with perforations in the side walls of the end of the tube that is inserted in the pouch to allow body fluids to enter laterally. The portable drain/suction unit is preferably a portable battery powered device. The pouch and the tube are sealed by a flexible sealing material which is applied to the outer surface of the skin around the periphery of the pouch and the tubing as it exits the pouch.

Abstract: An improved smoke evacuation system (10), a method for removing gaseous byproducts of surgical procedures, and noxious vapors from chemicals, is provided. The smoke, and vapor evacuation system includes a vacuum head (18) positioned at a surgical site or incorporated into a workstation. The vacuum head includes a plenum (28), a plenum support for preventing the plenum from collapsing when a vacuum or low pressure is established therein, and is adapted to facilitate the use of the system in a variety of surgical or commercial procedures at a variety of surgical sites or commercial workstations.

Abstract: The present invention provides a liquid removal system for applications where there is a need for liquid removal including laboratories and workshops as well as medical applications as well as dental applications. The liquid removal system exhibits improved wearing comfort by comprising an interface device which is compressible in the longitudinal and/or transverse dimension.

Abstract: Disclosed is a method and apparatus for accomplishing a noninvasive screen for breast disease markers, including breast cancer markers and cytologically abnormal cells. Intraductal fluid is noninvasively aspirated using compression, heating and suction cycles. The removed sample is thereafter assayed for the presence of cytologically abnormal cells and/or one or more breast disease markers. In addition to the diagnostic applications of the disclosed method and apparatus, a therapeutic application is also contemplated wherein intraductal fluids are noninvasively aspirated using compression, heating and suction cycles to remove toxic buildups within the fluid.

Abstract: A wound dressing member is provided for use in a vacuum bandage connected to a vacuum source. The wound dressing member is also provided for use with a wound having a wound surface. The wound dressing member includes a wound facing surface adapted to be in contact with and generally conform to the wound surface and a plurality of discrete holes formed in the wound facing surface. The member further includes a port configured to communicate with the vacuum source and with each hole formed in the wound facing surface. The wound dressing member further includes a stand-off having interconnected portions coupled to the wound facing surface and configured to provide a space between the wound facing surface and the wound surface.

Abstract: The present invention provides a liquid removal system for applications where there is a need for liquid removal including laboratories and workshops as well as medical applications and dental applications. The urine acquisition zone of the liquid removal system of the present invention has a skin hydration value of less than 200 milligrams and hence reduces phenomena related to liquid rewet from the liquid removal system.

Abstract: A canister rack system for a microdermabrasion machine has a base with bores. The base has conduits for crystal passage through the canister rack. The canisters are mountable upon the canister rack and include supply and storage canisters. The supply canister has a feeding conduit for the exit of crystal from the supply canister and the storage canister has a return conduit and a filtered conduit. The canister rack bores are formed at the base so that the conduits from the storage canister and supply canister meet with their respective conduits to form an airtight seal. A Horizontal locking pin protrudes from each canister and locks into a pair of horizontal slots formed in the canister rack. A vertical locking pin protrudes from the base of the canister rack and locks into a slot formed in each canister. A latch attaches each canister to the canister rack.

Abstract: A wound vacuum therapy dressing kit is provided for use with a wound drainage system having a vacuum source. The kit may include a wound dressing member, a sealing film, and a wound measurement device. The wound dressing member may include a wound contacting surface configured to be in contact with and generally conform to a wound surface of a patient. The member may be adapted to be coupled to the vacuum source for communicating suction from the vacuum source to the wound surface. The sealing film of the kit may be provided for placement over the member and may be configured to adhere to a patient's healthy skin surrounding the wound. The wound measurement device may include a transparent top portion and a transparent bottom portion configured for placement adjacent the wound surface. The top portion may include a drawing surface and a grid associated with the drawing surface.

Abstract: An apparatus for measuring skin permeable gas is provide, wherein such an apparatus can be used to obtain clinical information by noninvasive and bloodless operations and are useful for in-home medical care and health management.