Abstract: A wound packing for use with suction is provided. The wound packing comprises a plurality of nonabsorbent synthetic polymeric fibers coupled together to form a nonabsorbent material suitable for placement in the wound of a mammal. A method for treating the wound in a mammal using the disclosed wound packing is also provided.

Abstract: A medical device is provided that encloses a wound and promotes wound drainage by suction. The device includes an enclosure to be placed over a wound, adhesively connected to the skin around the wound by a flange. Gauze type packing cylinders can be placed in the wound, and suction is provided either by a bulb type pump, or by a pair of regulators. When regulators are used, one alternates the suction that it provides, and the other is continuous, such that the level of suction is periodically varied. The suction facilitates the transfer of liquid from the wound to the packing cylinders and from the packing out of the enclosure. A leak detector is optionally provided.

Abstract: A wound packing for use with suction is provided. The wound packing comprises a plurality of nonabsorbent synthetic polymeric fibers coupled together to form a nonabsorbent material suitable for placement in the wound of a mammal. A method for treating the wound in a mammal using the disclosed wound packing is also provided.

Abstract: A suction regulator for controlling a level of negative pressure in a system in which compensatory clean airflow is used to isolate a control device for regulating suction delivered to a patient is disclosed. The regulator comprises an inlet; an outlet; a controller for controlling the suction delivered to the inlet; and a barrier for isolating the controller from the inlet.

Abstract: A suction regulator for controlling a level of negative pressure in a system in which compensatory clean airflow is used to isolate a control device for regulating suction delivered to a patient is disclosed. The regulator comprises an inlet; an outlet; a controller for controlling the suction delivered to the inlet; and a barrier for isolating the controller from the inlet.

Abstract: A wound therapy system is provided which includes at least one sensor placed in a wound for sensing information regarding status of a body of a living being, and a communication link for electronically passing the information regarding the at least one sensor to a controller. A method for providing wound therapy is also provided which includes the steps of providing at least one sensor, each sensor placed in a wound, sensing information regarding status of a body of a living being utilizing the at least one sensor, and passing the information from the at least one sensor to a controller, via a communication link, between the at least one sensor and the controller.

Abstract: A system for treating a wound with suction is provided. The system comprises a wound cover, a pump having an input port and an output port, the input port providing suction to the wound via the wound cover, and a reservoir coupled to the output port of the pump. The reservoir is adapted to receive effluent from the wound and the pump is capable of maintaining a controlled level of suction at the wound.

Abstract: A therapeutic device for promoting the healing of a wound in a mammal is disclosed. An exemplary device comprises a permeable structure having a plurality of depressions formed in a surface thereof. In use, the surface having the depressions is disposed adjacent a surface of the wound. A method of treating a wound comprises the steps of providing a permeable structure comprising a plurality of randomly disposed fibers and having i) a plurality of wound surface contact elements disposed between end portions of the structure, and ii) a plurality of voids defined by the contact elements; and applying the permeable structure to at least one surface of the wound.

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: The invention provides a vacuum tube attachment device for vacuum assisted wound dressings. The device is in the form of a patch that can be attached to the primary wound cover. The patch forms a substantially air-tight seal to the primary wound cover, and a vacuum tube is fixed to the patch such that the patch can be oriented on the wound cover to locate the tube near an opening in the cover to allow vacuum pressure to be communicated to the wound. The patch has an adhesive area around its perimeter for attaching the patch in a substantially air-tight seal to the wound cover at any convenient location on the cover. Several embodiments of the patch are described.

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: The invention provides a vacuum tube attachment device for vacuum assisted wound dressings. The device is in the form of a patch that can be attached to the primary wound cover. The patch forms a substantially air-tight seal to the primary wound cover, and a vacuum tube is fixed to the patch such that the patch can be oriented on the wound cover to locate the tube near an opening in the cover to allow vacuum pressure to be communicated to the wound. The patch has an adhesive area around its perimeter for attaching the patch in a substantially air-tight seal to the wound cover at any convenient location on the cover. Several embodiments of the patch are described.

Abstract: A system for treating a wound with suction is provided. The system comprises a wound cover, a pump having an input port and an output port, the input port providing suction to the wound via the wound cover, and a reservoir coupled to the output port of the pump. The reservoir is adapted to receive effluent from the wound and the pump is capable of maintaining a controlled level of suction at the wound.

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 medical device that seals a wound and facilitates wound drainage with suction is provided. In one exemplary embodiment, the device comprises a suction portion, having both an inlet valve and an outlet valve, for suctioning fluids from the wound, and a sealing portion for sealing the wound by engaging the skin adjacent the wound, the suction portion and sealing portion being integral with one another. A method for draining a wound comprises the steps of under-packing the wound with a packing material; sealing the wound; and applying suction to the wound to promote wound drainage and to promote intimate contact between the wound and the packing material.

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 wound contact device comprising a permeable material and a wound contact layer having voids extending through the contact layer to a depth in the permeable material. The wound contact layer can comprise a thin sheet or film forming a generally flat and smooth wound contact surface having essentially no discontinuities or gaps. The wound contact layer can comprise a thin sheet of highly calendered fabric forming a wound contact surface having a mean surface roughness in the range of about 0 microns to about 200 microns. In progressive wound healing, an embodiment of the wound contact device having the fabric contact surface is used in earlier healing stages and an embodiment of the wound contact device with film contact surface is used in later healing stages. The wound contact device is particularly useful in wound dressings for use in suction-assisted wound therapy.

Abstract: A tunnel dressing for use in treating a tunneling wound using negative pressure wound therapy. The tunnel dressing includes an elongate permeable member having a closed distal end for entering the wound and an open proximal end into which an applicator is removably disposed for guiding the dressing into the wound. The tunnel dressing has a support structure adapted to transport wound exudates away from the wound and to resist compression under suction. The tunnel dressing also has a wound contact surface adapted to minimize tissue entanglement to facilitate removal. The support structure and wound contact surface may be formed from the same material or from two adjacent layers of different material.

Abstract: A suction regulator for controlling a level of negative pressure in a system in which compensatory clean airflow is used to isolate a control device for regulating suction delivered to a patient is disclosed. The regulator comprises an inlet; an outlet; a controller for controlling the suction delivered to the inlet; and a barrier for isolating the controller from the inlet.

Abstract: Disclosed are methods of leasing or billing for the usage of a portable suction pump adapted for use in a suction-assisted would treatment system. The pump has means for recording time units corresponding to periods of time when the pump is operating and for providing reports of usage time. The pump further has means for detecting that the wound treatment system is operating normally so as to be compliant with standards for suction wound treatment, and for recording and reporting time of normal operation or compliant usage. The methods include leasing the pump at a payment schedule that is based upon the amount of actual usage time or the amount of compliant usage time. The lease payment may include an amount of pre-paid time units such that unused time units can be credited to a new or renewed lease for a replacement pump. The billing methods can also be based in whole or in part on a planned maintenance schedule for the pump.