Abstract:
The present invention relates to a valve system for an inflatable portion of an indwelling medical device and more particularly to a valve system for fluid regulation of a catheter comprising a fluid inflatable portion that undergoes pressure changes within the body during use. The present invention also relates to methods of treatment using said valve system and indwelling medical devices comprising said valve systems.
Abstract:
An integrated system for assessing wound exudates from the wound of a patient is described. The system may contain functionality to detect, process and report various wound parameters. The system also may make treatment determinations based on these findings. The system may detect one or more physiological values of the wound exudates from the wound of the patient. The system may means for comparing the one or more detected physiological values to predetermined physiological values in order to obtain a comparison result in real time. The system may include a processor 15 which provides an electronic signal based on a comparison result in which the electronic signal may correspond to guidelines for treating the wound 13. The system may be integrated with other wound treatment devices, such as negative pressure wound therapy devices (NPWT) 9.
Abstract:
A stand-alone system for assessing wound exudates from the wound of a patient is described. The system contains functionality to detect, process and report various wound parameters. The system also may make treatment determinations based on these findings. The system may detect one or more physiological values of the wound exudates from the wound of the patient. The system may also compare detected physiological values to predetermined physiological values, in order to obtain a comparison result in real time. The system may include a processor (15) which provides an electronic signal based on the comparison result in which the electronic signal may corresponds to guidelines for treating the wound (3). The system described may be an accessory, which may be used on its own, or in conjunction with other wound treatment devices (9).
Abstract:
A drainable ostomy pouch includes a collection portion and a drain chute extending from the collection portion having a discharge opening for permitting emptying of contents from the pouch. The drain chute is foldable between an open condition in which the drain chute is extended from the collection portion, and a closed condition in which the drain chute is folded towards the collection portion; and a pocket for receiving at least a portion of the drain chute when the drain chute is in its closed condition.
Abstract:
An ostomy appliance including an ostomy pouch with a filter and a center pleated panel to protect the filter, facilitate deodorization and deter ballooning.
Abstract:
An ostomy appliance is disclosed with an inflatable seal for sealing against the stoma. The inflatable seal has a first inflatable chamber portion for fitting inside the stoma to seal against the internal tissue. The inflatable seal also has a second inflatable chamber portion for sealing externally against the stoma and peristomal skin. In one embodiment, a tube extends through the inflatable seal to provide a communication passage for discharge of body waste without removing the inflatable seal. The tube floats with respect to an adhesive mounting member to allow a waist between the first and second inflatable chamber portions to self-locate in the stoma.
Abstract:
A tube assembly for carrying malodoriforous matter from the human body comprises a silicone based tube having a central bore for the malodoriforous matter, and a tubular sleeve member comprising an odor barrier material, the silicone based tube and the tubular sleeve member being arranged one within the other such that the tubular sleeve member provides an odor barrier to obstruct leakage of odors from malodoriforous matter in the bore of the silicone based tube. The tube assembly is especially suitable for use in fecal or bowel management apparatus.
Abstract:
A medical compression product (“MCP”) for applying pressure to a limb of a patient may include one or more sensors integrally united therewith for measuring information indicative of the pressure applied by the MCP. The sensors may be permanently or removably attached to the MCP, and the sensors may be grouped into particular predetermined regions. The sensors may communicate (e.g., by use of wires or wirelessly) with a computer system that provides information to the user regarding the application of the MCP. The MCP may include bandages in the form of elongated fabric strips and tubular hosiery products. Wires connected to the sensors and communicating with the computer system may be aligned along or transverse to the longitudinal dimension of the bandage.
Abstract:
A controlled discharge ostomy appliance is described for use with an adhesive body fitment. The body fitment comprises an adhesive wafer having a stomal aperture that is manually shapeable by folding or rolling back a rim portion of the adhesive around the stomal aperture.
Abstract:
An ostomy coupling including a body-side coupling member, an appliance-side coupling member including plural fastener lugs, and a bracing member. The lugs flex independently of each other to provide plural independent latching fastenings. The bracing member is moved between a bracing position in which the bracing member locks the lugs by resisting flexing movement, and a non-bracing or dismounted position in which the lugs are free to flex. The ostomy coupling is used with an ostomy pouch or with a controlled evacuation device.