摘要:
Anti-fouling treatments are applied to polymer substrates for preventing bacterial adhesion. The polymer substrate may comprise a medical device, such as a catheter. The treatment generally comprises a polymer layer graft polymerized to the surface of the polymer substrate. An anti-biofilm agent is contained in the polymer layer or applied to the surface. A polymer over-layer is then applied that encapsulates the anti-biofilm agent. The anti-biofilm agent prevents bacterial adhesion through the polymer over-layer.
摘要:
Anti-fouling treatments are applied to polymer substrates for preventing bacterial adhesion. The polymer substrate may comprise a medical device, such as a catheter. The treatment generally comprises a polymer layer graft polymerized to the surface of the polymer substrate. An anti-biofilm agent is contained in the polymer layer or applied to the surface. A polymer over-layer is then applied that encapsulates the anti-biofilm agent. The anti-biofilm agent prevents bacterial adhesion through the polymer over-layer.
摘要:
A medical device assembly for imparting a lubricious and/or antimicrobial liquid onto a medical device is provided. The medical device is surrounded by a pouch and includes a burst package or frangible cells for storage of the liquid prior to delivery onto the surface of the medical device. This helps prevent contamination of the medical device upon removal of the medical device from its pouch, insertion of the device into a body cavity, and implantation of the device into the body cavity.
摘要:
An oral care suction device that includes a suction control port cover. The oral care suction device includes a body having a fluid flow passage formed therethrough. The body has a suctioning feature is located on or joined at its distal end. The body also has an attachment feature located at its proximal end. The oral care suction device also includes a suction control port located intermediate the distal end and proximal end of the body and configured to be covered by a finger or a portion of the hand of a user to alter the level of suction through the suctioning feature while allowing one hand operation of the suctioning device. The suction control port defines a channel from an exterior of the body to the fluid flow passage. A breathable fabric is positioned to cover the suction control port so that contact of the finger or portion of the hand of a user with liquids and particles drawn into and through the fluid flow passage during suctioning is minimized.
摘要:
There is provided a device for performing a balloon dilation tracheostomy. The balloon has internal braces or “stays” extending from the center to the inside surface of the balloon, though other arrangements are possible. The braces control the ultimate expansion and final shape of the balloon when it is fully inflated, inhibiting the ability of parts of the balloon to herniate. The balloon should also expand more uniformly, allowing the practitioner to more confidently expand the tracheal stoma site and ensuring a successful dilation and tube placement.
摘要:
There is provided a novel tracheostomy tube flange. The flange is made of a flexible material and has a large open area for viewing of the underlying skin. The flange has holes for suturing the flange to the skin and slots for attachment of a strap to surround the neck and keep the flange and tube in place. The flange may swivel on the tube to allow for greater flexibility in attaching it to the skin. A stoma pad may be used with the flange to help keep the skin under the flange healthy.
摘要:
There is provided a tubular workpiece for blow-molding into an inflatable balloon component. The tubular workpiece is a raw tube having a lumen and composed of a thermoplastic polymer, the tube having an asymmetric wall thickness such that when the tube is preheated in a mold to a temperature sufficient to soften the material of the tube and inflated with a gas to generally uniformly stretch the material of the tube, the tube forms a balloon component. The balloon may be non-uniform in wall thickness depending on the type of mold used. The balloon may be attached according to conventional means to a hollow tube to produce a tracheostomy device.
摘要:
There is provided a moisture indicator for a heat and moisture exchange (HME) device that uses a pre-colorant and an activator applied to an inner surface of the HME device. The colorant undergoes a color change of Delta E (ΔE) of equal to or greater than 3 units upon exposure to moisture but not upon exposure to high humidity. The colorant is visually obvious to the unaided human eye under normal light conditions through the body of the device. The HME device with the visual indicator for moisture can indicate to the care-giver that it is time to change the HME device.