Patent classifications
A61F13/00055
Compression strain and negative pressure delivery indicator for a wound dressing
An indicator configured to be attached to a wound dressing includes first and second parts. The wound dressing is configured to collapse in response to an applied negative pressure. The first and second indicator parts are configured to move relative to one another as the wound dressing is collapsed. The movement of the first and second indicator parts is configured to allow a user to easily visualize the compression of the wound dressing and monitor the application of the negative pressure to the wound dressing. A marker is provided along a top surface of the first part and a window is formed on the second part. The changes in the portion of the marker that is visible in the window as the first part is slid into or under the second part are configured to provide for easier detection of the collapse of the wound dressing by the user.
Wearable sensor
A system includes a disposable patch having a first side and an opposite second side, the disposable patch having a body formed from a flexible material, a plurality of sensors positioned on the disposable patch, an electrically conductive pattern on the disposable patch wherein segments of the electrically conductive pattern are electrically connected to the plurality of sensors, and a reusable patch for positioning on the disposable patch, the reusable patch having a plurality of conductive connection points. The conductive pattern of the disposable patch and the conductive connection points of the reusable patch configured such that in an operative position the conductive connection points of the reusable patch are electrically connected to the conductive pattern such that one or more electrical components of the reusable patch are electrically connected to the plurality of sensors of the disposable patch through the conductive pattern.
Self contained wound dressing with micropump
A composite wound dressing apparatus promotes healing of a wound via the use of a micropump system housed within or above a wound dressing member. The micropump system includes a miniature pump that applies a subatmospheric pressure to the wound to effectively draw wound fluid or exudate away from the wound bed without the need for a cumbersome external vacuum source. Hence, the wound dressing and micropump system is portable which allows the patient mobility that is unavailable when an external vacuum source is used. The patient does not need to be constrained for any period of time while exudate is being removed from the wound.
DRESSING APPARATUS AND METHODS FOR FACILITATING HEALING
A dressing apparatus and methods for facilitating healing, the apparatus and methods involving a dressing member, an electromagnetically conductive element mechanically coupled with the dressing member, and a primary RFID device configured to transmit at least one output signal to the electromagnetically conductive element, to receive at least one return signal from the electromagnetically conductive element, and to provide an alert if the at least one return signal has a strength corresponding to at least approximately a threshold amount of fluid present in the dressing member, whereby healing is facilitated.
Medical wetness sensing devices and related systems and methods
A medical wetness sensing device includes a cover, a first and second electrically conductive portions housed in the cover, an electrically insulative portion housed in the cover, and a compressible portion. The cover defines an outer surface. The first and second electrically conductive portions are exposed along an inner surface of the device. The first and second electrically conductive portions are configured to transmit a test signal indicating an absence or presence of a liquid on the inner surface. The electrically insulative portion electrically isolates the first electrically conductive portion from the second electrically conductive portion. The compressible portion is flexible, compressible, and configured such that the inner surface of the device is conformable to skin of a wearer of the device. The compressible portion is formed by at least one of the cover, the first and second electrically conductive portions, and the electrically insulative portion.
OPTICAL SENSING SYSTEMS AND METHODS FOR SENSOR ENABLED WOUND DRESSINGS AND SYSTEMS
In some cases, a method of coating a wound dressing includes coating a wound facing side of a substantially flexible substrate of the wound dressing with a coating, the wound facing side of the substrate supporting at least one optical sensor and reducing and/or controlling surface texture of the coating to improve detection by the at least one optical sensor. In some cases, a wound dressing includes a substantially flexible substrate supporting at least one optical sensor, the at least one optical sensor including a light source and a detector configured to sense reflected light, a void in the substrate, the void positioned between the light source and the detector, and coating applied to the substrate and covering the at least one optical sensor. The void can prevent transmission of light emitted by the light source to the detector through the coating.
Negative pressure wound therapy system
A negative pressure wound therapy system includes a dressing, a tube, a flow restriction pad, and an in-line filter. The dressing is configured for placement in a wound bed. The tube includes a first end and a second end. The first end is configured to be operably coupled to the dressing. The second end is configured to engage a negative pressure source. The flow restriction pad is configured to be coupled to the dressing proximate the first end of the tube. The flow restriction pad includes a tortuous fluid flow path that is configured to restrict or reduce an amount of a fluid drawn from the dressing into the tube and induce a backpressure between the dressing and the tube. The in-line filter is positioned within the tube between the first end and the second end. The in-line filter configured to substantially prevent the fluid entering the tube.
VACUUM DRESSING WITH CONTROL FEEDBACK
A wound management system (WMS) is provided that includes dressings, bandages, or implantable medical devices that are equipped with filters, environmental controls, and sensors that promote the formation of a natural biologic seal between the skin and the dressing to form a barrier to microbial invasion into the body that accelerates healing and mitigates wound or exit site infection. Percutaneous access devices (PAD) used with the WMS or other devices including peritoneal dialysis (PD) catheters, Steinman pin, Kirschner wires, and chronic indwelling venous access catheters that require skin penetration. The WMS minimizes risk of exit site infection by reducing the bioburden in the exit tunnel environment in the acute and subacute phases of the PD catheter post-implant. Visualization of the wound without taking off the dressing is provided via a window in the wound area or exit-site to visually monitor for signs of infection and the presence of exudate.
APPARATUSES AND METHODS FOR WOUND THERAPY
Some arrangements disclosed herein relate to devices and methods for treating a wound, comprising applying negative pressure to the wound through a cover applied over a wound, monitoring the internal pressure in the wound, and controlling the closure of the wound by controlling the amount that a wound packing material positioned under the cover collapses within the wound based on the monitored internal pressure. The wound packing material collapse can be controlled to ensure that the monitored internal pressure does not exceed a threshold value. Additionally, some embodiments or arrangements disclosed herein relate to a visualization element to visualize a location of a wound surface. The visualization element can comprise a radiopaque member that is configured to be positioned on or adjacent to a surface of an open wound.
APPARATUS, SYSTEM, AND METHOD FOR DETECTING A TARGET SUBSTANCE
Described herein are apparatus, methods, and systems for detecting the presence of a targeted substance. The apparatus comprises a detection layer comprising an indicator that is configured to display a signal upon the detection of an interaction with the targeted substance. In some examples, the apparatus can include a top layer coupled to a top surface of the detection layer and a bottom layer coupled to a bottom surface of the detection layer.