Abstract: A reduced-pressure, wound closure system is presented that generates a closing force on a surface wound and optionally provides reduced pressure to a body cavity or tissue site. The sealed contracting member, when placed under reduced pressure, generates the closing force. One illustrative system includes a first attachment member and a second attachment member, a sealed contracting member coupled to the first attachment member and the second attachment member, and wherein the closing force is generated between the first attachment member and the second attachment member when reduced pressure is supplied to the sealed contracting member. Other systems and methods are presented.

Abstract: The illustrative embodiments described herein are directed to a system and method for administering reduced pressure at a tissue site. The apparatus includes a reduced pressure source. The reduced pressure source generates a reduced pressure. The apparatus includes a tube having a plurality of lumens. The plurality of lumens includes at least one collection lumen. The reduced pressure source applies the reduced pressure to the tissue site through the plurality of lumens such that the at least one collection lumen receives fluid from the tissue site. The at least one collection lumen stores the fluid received from the tissue site.

Abstract: A modular, reduced-pressure, wound-closure system for generating a closing force on a surface wound on a patient includes a sealed contracting member, a plurality of attachment base members, and a plurality of connecting members. The combination of the plurality of attachment base members and plurality of connecting members forms a circumferential wall around the surface wound. The sealed contracting member is operable to be disposed within an interior space defined by the circumferential wall and coupled to at least of portion of the circumferential wall. When reduced pressure is provided to the sealed contracting member, the sealed contracting member contracts and the circumferential wall delivers a closing force. Other systems and methods are presented.

Abstract: An apparatus for connecting multi-lumen conduits may include a conduit adapter and a conduit collar. The conduit adapter may include a housing, a bayonet connector, and a support member connecting the housing and the bayonet connector. The support member has an aperture that permits fluid communication through the support member. One end of the conduit collar is sized for insertion into the housing, and a second end is adapted to receive a first multi-lumen conduit. The housing also is adapted to receive a second multi-lumen conduit. The bayonet connector engages a primary lumen of the first multi-lumen conduit and the second multi-lumen conduit such that the primary lumen of the second multi-lumen conduit fluidly communicates with the primary lumen of the first multi-lumen conduit. The conduit adapter and the conduit collar are capable of 360 degree rotation relative to each other about a common axis.

Abstract: A manually-activated reduced pressure treatment system includes a substantially rigid housing, and an end cap slidingly received by the housing. An inner chamber is disposed between the end cap and housing, and a volume of the inner chamber is variable in amount depending on the position of the end cap within the housing. The end cap is slidingly movable between an uncompressed position at which the volume of the inner chamber is at a maximum value and a compressed position at which the volume of the inner chamber is at a minimum value. A position indicating member is associated with the end cap and housing to indicate the position of the end cap relative to the housing at predetermined positions between the uncompressed position and the compressed position.

Abstract: The illustrative embodiments described herein are directed to a system and method for administering reduced pressure at a tissue site. The apparatus includes a reduced pressure source. The reduced pressure source generates a reduced pressure. The apparatus includes a tube having a plurality of lumens. The plurality of lumens includes at least one collection lumen. The reduced pressure source applies the reduced pressure to the tissue site through the plurality of lumens such that the at least one collection lumen receives fluid from the tissue site. The at least one collection lumen stores the fluid received from the tissue site.

Abstract: A patient cooling system comprises an inflatable patient mattress and a patient enclosure or tent supported by a framework of inflatable tubes drawing air off of the same air supply used to supply the mattress and to cool the tent. The framework of inflatable tubes is divided into left and right sections, which are further subdivided into lower body and upper body sections. An inflatable connector with a stem and protuberance is provided to secure the framework in a closed position. The patient-supporting mattress comprises a plurality of inflatable compartments extending transversely across the width of the mattress that can be alternately pressurized for pressure relief therapy. Radially collapsible, sleeved openings in the tent panel enable connection of conduits or patient care lines to the patient.

Abstract: Systems, methods, and apparatuses for debriding a tissue site, such as a wound, involve using solid CO2 particles and reduced pressure to cut and remove undesired tissue in a controlled manner. The system may urge the undesired tissue into a treatment cavity and then cut the undesired tissue with impinging CO2 particles. The CO2 particles sublime into a gas and present little or no mess. Other systems, methods, and apparatuses are presented.

Abstract: A manually-activated reduced pressure treatment system includes a substantially rigid housing, and an end cap slidingly received by the housing. An inner chamber is disposed between the end cap and housing, and a volume of the inner chamber is variable in amount depending on the position of the end cap within the housing. The end cap is slidingly movable between an uncompressed position at which the volume of the inner chamber is at a maximum value and a compressed position at which the volume of the inner chamber is at a minimum value. A position indicating member is associated with the end cap and housing to indicate the position of the end cap relative to the housing at predetermined positions between the uncompressed position and the compressed position.

Abstract: An apparatus for connecting multi-lumen conduits may include a conduit adapter and a conduit collar. The conduit adapter may include a housing, a bayonet connector, and a support member connecting the housing and the bayonet connector. The support member has an aperture that permits fluid communication through the support member. One end of the conduit collar is sized for insertion into the housing, and a second end is adapted to receive a first multi-lumen conduit. The housing also is adapted to receive a second multi-lumen conduit. The bayonet connector engages a primary lumen of the first multi-lumen conduit and the second multi-lumen conduit such that the primary lumen of the second multi-lumen conduit fluidly communicates with the primary lumen of the first multi-lumen conduit. The conduit adapter and the conduit collar are capable of 360 degree rotation relative to each other about a common axis.

Abstract: Apparatuses, systems, and methods involve using reduced pressure to position a portion of tissue in a cutting head and cutting the tissue to debride a tissue site. A cutting head includes a debridement conduit having a distal end and a proximal end. A portion of the debridement conduit adjacent to the distal end comprises a tissue treatment area. The cutting head also includes an opening to the tissue treatment area formed at the distal end of the debridement conduit. The tissue treatment area is adapted to receive the portion of tissue through the opening under reduced pressure. The cutting head also includes a selectively moveable cutting member associated with the debridement conduit at the tissue treatment area. The cutting member is for cutting the portion of tissue from the tissue site while the portion of tissue resides in the debridement conduit. Other methods, systems, and apparatuses are disclosed.

Abstract: A wound therapy combination comprising a suction head and a surgical drape. The suction head comprises a planar flange portion and a tubular connector piece on a first face that communicates with an aperture extending to a second face. The second face is formed with projections that define flow channels for facilitating flow of liquids to the aperture.

Abstract: A system for stimulating the healing of tissue comprises a porous pad positioned within a wound cavity, and an airtight dressing secured over the pad, so as to provide an airtight seal to the wound cavity. A proximal end of a conduit is connectable to the dressing. A distal end of the conduit is connectable to a negative pressure source, which may be an electric pump housed within a portable housing, or wall suction. A canister is positioned along the conduit to retain exudates suctioned from the wound site during the application of negative pressure. A first hydrophobic filter is positioned at an opening of the canister to detect a canister full condition. A second hydrophobic filter is positioned between the first filter and the negative pressure source to prevent contamination of the non-disposable portion of the system by exudates being drawn from the wound. An odor filter is positioned between the first and second hydrophobic filters to aid in the reduction of malodorous vapors.

Abstract: An apparatus to provide thermal control to a patient comprises a neck member having a surface defining at least one opening, the surface configured to be spaced apart from a neck area of the patient. The neck member includes an air inlet to receive cooled air from an air source. The at least one opening is in fluid communication with the air inlet to direct cooled air from the air source and toward the neck area of the patient to provide the thermal control to the patient.

Abstract: A system for stimulating the healing of tissue comprises a porous pad positioned within a wound cavity, and an airtight dressing secured over the pad, so as to provide an airtight seal to the wound cavity. A proximal end of a conduit is connectable to the dressing. A distal end of the conduit is connectable to a negative pressure source, which may be an electric pump housed within a portable housing, or wall suction. A canister is positioned along the conduit to retain exudates suctioned from the wound site during the application of negative pressure. A first hydrophobic filter is positioned at an opening of the canister to detect a canister full condition. A second hydrophobic filter is positioned between the first filter and the negative pressure source to prevent contamination of the non-disposable portion of the system by exudates being drawn from the wound. An odor filter is positioned between the between the first and second hydrophobic filters to aid in the reduction of malodorous vapors.

Abstract: A method for stimulating new tissue growth is provided in which a limb is introduced into an interior portion of an outer cover. A porous component is applied to at least a portion of the limb within the outer cover. An opening through which the limb was introduced is sealed, and a negative pressure is applied to the interior portion to stimulate new tissue growth.

Abstract: A therapeutic apparatus for stimulating the healing of a wound site includes a polyurethane foam positioned at the wound site and a connector having a disc-like cup and an elbow-shaped spout. The connector is positioned in contact with the polyurethane foam, and the elbow-shaped spout is configured for connection to a tube that is capable of delivering negative pressure through the elbow-shaped spout and to the polyurethane foam. The therapeutic apparatus further includes a drape having a hole, the drape being positioned over the connector such that the elbow-shaped spout extends through the hole in the drape.

Abstract: A disposable portable therapeutic cooling system that utilizes convective cooling and re-circulated air to efficiently, safely, and effectively cool the head and body of the patient, clothed or not, after a life-threatening health event, such as a cardiac arrest or stroke.

Abstract: A reduced-pressure, deep-tissue closure device for applying a closing force on a deep tissue includes a contractible matrix that is formed with a first plurality of apertures and which has a first side and a second, inward-facing side. The contractible matrix is for disposing proximate to the deep tissue. A reduced-pressure source is fluidly coupled to the contractible matrix and operable to deliver reduced pressure to the contractible matrix. When under reduced pressure, the contractible matrix grips the deep tissue adjacent the contractible matrix and provides a closing force on the deep tissue. A system and method are also presented.

Abstract: A system for applying reduced pressure to tissue includes a multi-lumen reduced pressure delivery tube having a proximate end, a distal end, a primary lumen extending through the conduit from the proximate end to the distal end, and an ancillary lumen extending through the conduit from the proximate end to the distal end. A vacuum pump is coupled to the proximate end of the primary lumen, and a reduced pressure adapter is coupled to the distal end of the reduced pressure delivery tube. The adapter includes channels to direct liquid away from the ancillary lumens and into the primary lumen.