Patent classifications
A61F13/00021
DEVICES AND METHODS FOR TREATING AND CLOSING WOUNDS WITH NEGATIVE PRESSURE
The present invention relates to a negative pressure wound closure system and methods for using such a system. Preferred embodiments of the invention facilitate closure of the wound by preferentially contracting to provide for movement of the tissue.
LOW-GROWTH TISSUE INTERFACE
A tissue interface for treating a tissue site and systems and methods of manufacturing the same are described. The tissue interface can include a plurality of shapes and a plurality of ribs. Each rib of the plurality of ribs can have a first end coupled to a respective shape of the plurality of shapes and a second end coupled to at least one other rib of the plurality of ribs. The tissue interface can also include a sheet of felted open-cell foam and a plurality of holes formed in the sheet. Each hole can extend through the sheet. Each hole can have a first end and a second end joined by a gauge section. The first end and the second end can form shoulders that are wider than the gauge section.
Mucoadhesive Patch and Uses Thereof
The present invention provides a mucoadhesive patch for attachment to a mucosal surface in a patient, the patch comprising a fibrous polymeric mat substrate and a plurality of polymeric flock particles that are attached to the substrate.
MICRO BALLOON-ON-TUBE WOUND FILLER
A dressing, system, and method for use with negative-pressure treatment is described. The dressing includes a tube formed from a non-porous material. The tube can have a first end, a second end, a lumen extending from the first end to the second end, and a wall surrounding the lumen. At least one blister is formed in the wall of the tube, the at least one blister proximate to the second end of the tube. At least one aperture is formed in the wall of the second end of the tube. The at least one aperture is configured to provide fluid communication across the wall from the lumen to an exterior of the tube.
Device for use in endoluminal vacuum therapy
The device (10, 36, 38, 42, 68) applies a negative pressure to an endoluminal surface in the body of a patient to facilitate healing of a wound in the endoluminal surface. The device comprises a flexible porous element (14) with a peripheral outer face (32) for contact with the wound, the outer face being defined between opposite proximal and distal ends of the porous element. A suction tube (30) for being connected to a suction source externally of the patient's body is provided in fluid communication with the porous element to apply a negative pressure to the wound via the outer face (32) of the porous element (14) upon operation of the suction source. The porous element (14) has at least one through passageway (16) extending from its proximal end to its distal end for passage of bodily substances of the patient through the porous element. The device can also include a drainage tube (22) for collection and drainage of the bodily substances from the patient, wherein the drainage tube is received in the through passageway of the porous element. The device is particularly suitable for assisted healing of anastomotic wounds but its use is not limited thereto.
Wound pads
Described are wound pads for use, e.g., as cavity wound fillers, having shapes with rounded corners, the projection on an X-Y plane of at least one corner having a curvature distinct from that of the projection of the other corners. Negative pressure systems and kits that includes such wound pads, and methods of using such wound pads are also described.
Multiple-wound negative pressure wound therapy using multiple fluid collection volumes
A negative pressure wound therapy system treats multiple wounds on a patient's body. The system includes a source of negative air pressure, an air source, first and second fluid collection volumes, first and second wound-covering domes disposed over first and second wounds, a valve assembly disposed between the source of negative air pressure and the first and second fluid collection volumes, and between the air source and the first and second domes. The valve assembly has first and second operational modes. In the first, the valve assembly puts the source of negative air pressure in fluid communication with the first fluid collection volume, and the air source in fluid communication with the first dome. In the second, the valve assembly puts the source of negative air pressure in fluid communication with the second fluid collection volume, and the air source in fluid communication with the second dome.
WOUND DRESSING CONTAINING A VACUUM PUMP
The present invention relates to a wound healing PVA sponge dressing using negative capillary pressure of the dressing material together with auxiliary negative pressure for wound treatment. The PVA sponge dressing is pretreated with gram positive and gram negative biocidal 5 dyes for insertion into or over a wound. A negative pressure pump is mounted to the PVA sponge dressing to produce additional capillary pressure for withdrawing fluid or water vapor from the sponge dressing and a cover is mounted over the sponge material and negative pressure pump forming a unitary sealed package for placement over a wound.
FLUID CONTAINMENT LAYER AND PAD CONTAINING FLUID CONTAINMENT LAYER
A fluid containment layer adapted to be used in a pad for absorption, containment, and/or controlled release of liquid or gel, where the fluid containment layer absorbs and/or holds a liquid or gel, such as a disinfecting liquid or gel. The fluid containment layer is resilient and returns to its original shape upon pressure applied thereto. The fluid containment layer includes generally vertically oriented fibers. The fluid containment layer may be used in a self-disinfecting pad.
STERILIZATION OF MEDICAL DRESSINGS WITH ENHANCED ANTIMICROBIAL PROPERTIES
The present invention relates to a sponge dressing for treating wounds comprised of a polymer sponge containing a plurality of antimicrobial dyes with at least one dye being gram positive and at least one other dye being gram negative and a silicon adhesive secured to a sponge surface. The sponge dressing can be exposed initially to gamma radiation and later sterilized by ethylene oxide or alternatively it can be sterilized by ethylene oxide and later irradiated by gamma radiation. The sponge dressing has a morphology characterized by an average pore throat diameter of 0.5-500 μm and a porosity ranging from about 60% to about 99.5%. The sponge dressing can also contain at least one biofilm reducing agent, at least one chelating agent and an ionic and non-ionic surfactant.