Patent classifications
A61F13/0216
Multi-lumen bridge for negative pressure wound therapy system
A bridge for facilitating delivery of reduced pressure to a wound site includes a reduced pressure lumen configured to be fluidly coupled to a reduced pressure source, a secondary pressure lumen configured to be fluidly coupled to a secondary pressure source, and one or more fluid adapters operable to be connected to a wound dressing disposed at the wound site. The one or more fluid adapters are positioned and configured with respect to the reduced pressure lumen to apply reduced pressure from the reduced pressure lumen to the wound site through the wound dressing and deliver exudate removed from the wound site through the reduced pressure lumen to the reduced pressure tubing. The secondary pressure lumen is fluidly coupled to the reduced pressure lumen to facilitate flow of the exudate removed from the wound site by the reduced pressure source using the secondary pressure source.
NEGATIVE PRESSURE WOUND THERAPY (NPWT) BANDAGE
A negative pressure wound therapy bandage for applying negative pressure to a wound, the bandage comprising: a membrane configured for disposition over a wound so as to form a wound chamber between the membrane and the wound, the membrane comprising a wound-side surface, an atmosphere-side surface, and an opening extending through the membrane from the wound-side surface to the atmosphere-side surface; and a pump assembly carried by the membrane, the pump assembly comprising: a pump body comprising a wall structure disposed about a pump chamber, wherein at least a portion of the wall structure is resilient, and further wherein the pump chamber communicates with the wound chamber through the opening formed in the membrane; and an atmosphere-side passageway extending through the wall structure so as to fluidically connect the pump chamber to the atmosphere.
Dressing using differential surface features for use in compartment spaces
A dressing for treating a tissue site, particularly an abdominal or peritoneal site, is disclosed. In some embodiments, the dressing may comprise a tissue interface formed from a first layer of a liquid-impermeable material and a plurality of manifolding bubbles formed as part of the first layer. In some embodiments, the tissue interface may further comprise a second layer of a permeable material, where the manifolding bubbles are formed as closed cells between the first layer and the second layer. The tissue interface may also include a third layer of liquid-impermeable material positioned adjacent to the second layer, where one or more fluid passageways may be formed between the second layer and third layer for delivering a therapeutic fluid to the tissue site.
DRESSING FOR BREAST CAVITIES
A dressing for an internal cavity may include a connector, a negative pressure pathway layer, an instillation pathway layer, a negative pressure manifold, and an instillation manifold. The negative pressure manifold can be disposed within the negative pressure pathway layer and the instillation manifold can be disposed within the instillation pathway layer. A proximate end of the negative pressure manifold can be fluidly coupled with a first channel of the connector. The proximate end of the instillation manifold can be fluidly coupled with a second channel of the connector. The negative pressure pathway layer and the instillation pathway layer can be configured to cooperatively form an inner volume therebetween. The inner volume may be configured to receive a space filler. The negative pressure pathway layer, the instillation pathway layer, and the space filler can be collectively configured to be positioned within the internal cavity.
VACUUM SEALED BANDAGE AND METHODS OF USE
The present disclosure relates to wound bandages. More specifically, the present disclosure describes a vacuum sealed bandage having a film layer that is manipulable into a wound by way of negative pressure imparted by a removable medical syringe. The vacuum sealed bandage of the present disclosure does not have a vacuum pump, does not constantly apply negative pressure to the wound through an electro-mechanical device or vacuum pump, and/or does not have chords or tubes positioned to opposite sides of the film layer or extending from one side of the film layer to another side of a film layer where the chord or tube is positioned between the film and the wound.
Apparatuses and methods for negative pressure wound therapy
Disclosed herein are several embodiments of a negative pressure appliance and methods of using the same in the treatment of wounds. Some embodiments are directed towards wound dressings comprising a liquid and gas permeable transmission layer, an absorbent layer for absorbing wound exudate, the absorbent layer overlying the transmission layer, a gas impermeable cover layer overlying the absorbent layer and comprising a first orifice, wherein the cover layer is moisture vapor permeable. Some embodiments are directed to improved fluidic connectors or suction adapters for connecting to a wound site, for example using softer, kink-free conformable suction adapters.
APPARATUSES AND METHODS FOR NEGATIVE PRESSURE WOUND THERAPY WITH SWITCHEABLE FLUID MANAGEMENT
Disclosed embodiments relate to wound therapy apparatuses and methods for use in negative pressure wound therapy (NPWT). Such wound therapy apparatuses and methods may reduce maceration during NPWT. The wound therapy apparatus may include a porous hydrophobic layer surrounded by a hydrophilic ring. The hydrophilic ring may serve to prevent passage of liquid while negative pressure is applied to the wound, but allow liquid passage to an absorbent ring when negative pressure is no longer applied. A transmission layer may also be included, underlying the absorbent layer.
SYSTEMS, APPARATUSES, AND METHODS FOR NEGATIVE-PRESSURE TREATMENT WITH REDUCED TISSUE IN-GROWTH AND EXTENDED WEAR TIME
Dressings, systems, and methods for treating a tissue site with negative pressure are described. The dressing includes a manifold having a first surface and a second surface opposite the first surface, a first layer adjacent to the first surface, and a second layer adjacent to the second surface. The first layer and the second layer each are formed from a polymer film. A plurality of fluid restrictions are formed in the polymer film adjacent to at least the first surface. A first plurality of bonds is formed between the first layer and the second layer. The first plurality of bonds define separable sections of the manifold. A second plurality of bonds is formed between the first layer and the second layer. The second plurality of bonds define a plurality of openings.
Contoured Dressing For Tissue Therapy
In some examples, a dressing assembly suitable for treating a tissue site may include a dressing bolster, a sealing skin, and a gasket member. The sealing skin may cover at least a portion of a first side of the dressing bolster while an opposing second side of the dressing bolster may be configured to be positioned in fluid communication with the tissue site. The gasket member may be configured to create a sealed space between the sealing skin and the tissue site. In some examples, the sealing skin may be liquid impermeable and integrally formed with the dressing bolster. Further, in some examples, the dressing bolster may have a contoured shape including a tissue housing. Other systems, dressings, apparatuses, and methods are disclosed.
Medical treatment systems and related methods thereof
A medical system including a compressible device, and a covering over the compressible device, wherein the covering includes a delivery configuration and a deployed configuration, wherein, in the delivery configuration, the covering at least partially covers the compressible device to maintain the compressible device in a compressed state, and wherein, in the deployed configuration, the covering is releasable from the device to transition the compressible device from the compressed state to an expanded state.