Abstract: Disclosed is a sensor patch (50) for attachment to a base plate for an ostomy appliance, and a method for manufacturing such sensor patch. The sensor patch having a proximal side and a distal side. The distal side being adapted for attachment to an adhesive surface of the base plate, wherein the adhesive surface of the base plate is adapted for attachment of the base plate to the skin surface of a user. The sensor patch comprises: a sensor assembly (204) comprising a plurality of electrodes (216), and a first adhesive sensor layer (52) forming the proximal side of the sensor patch and being adapted for attachment of the sensor patch to the skin surface of the user. The first adhesive sensor layer comprises a first centre portion (62) having a first centre thickness and a first outer rim portion (64) surrounding the first centre portion.

Abstract: A method for visually indicating that a door of a drug delivery device is open is described. A closing force to move the door is received. Then, it is detected that the door is not closed. A biasing element pushes the door to a perceptibly open position with an opening force when the door reaches the last 30 degrees of rotation of toward closure or when the door reaches the last 30% of range of movement during the rotation of the door. The perceptibly open position of the door is indicated relative to a drug delivery device housing.

Abstract: Improved urinary catheters are described. One example urinary catheter includes a catheter shaft with an internal lumen, extending between a distal discharge opening and a proximal drainage opening, arranged at a proximal tip of the catheter shaft. An overcoat layer encircles a portion of the catheter shaft, forming a closed deformable fluid filled cavity intermediate the overcoat layer and the outer surface of the shaft. The overcoat layer is elastically deformable to allow for movement of the fluid within the cavity during deployment. At least a portion at the proximal end is arranged to be compressed to a smaller diameter during insertion, and upon continued insertion of the catheter shaft through the urethra into at least the bladder neck, arranged to expand back toward a greater diameter, as the fluid is caused to flow toward the proximal end of the fluid filled cavity.

Abstract: An ostomy appliance comprising an inner wall and an outer wall that define a cavity for containing a stomal output, the ostomy appliance having an upper section, a lower section and a waisted section that is located between the upper section and the lower section. The upper section has a maximum width (A) that is greater than a maximum width (B) of the lower section and the waisted section has a minimum width (C) that is less than the maximum width (B) of the lower section. The waisted section has a left-hand edge that is smoothly rounded and a right-hand edge that is smoothly rounded, and both the left-hand edge and the right-hand edge smoothly blend, respectively, into left-hand edges and right-hand edges of the upper section and the lower section.

Abstract: A method of producing an arteriovenous (AV) fistula includes producing an anastomosis between a primary blood vessel (e.g., a vein) and a secondary blood vessel (e.g., an artery). A collateral (or competing) blood vessel in fluid communication with one of the primary blood vessel or the secondary blood vessel is identified. A reversible flow restrictor is then applied to the collateral blood vessel to reduce a blood flow rate through the collateral blood vessel. In some embodiments, the anastomosis can be produced percutaneously. In some embodiments, the reversible flow restriction (or a portion thereof) can be removed from the collateral blood vessel. In other embodiments, the reversible flow restriction (or a portion thereof) can be adjusted to allow increased blood flow therethrough while within the collateral blood vessel.

Abstract: Topical ocular delivery devices are provided. Aspects of the devices include a transducer configured to oscillate at an amplitude and frequency that provides for an emitted stream velocity which results in minimal discomfort during topical ocular delivery. Also provided are methods of using the devices, e.g., in topical ocular delivery applications.

Abstract: In an example, a fluid collection device includes a fluid impermeable barrier that at least partially defines a chamber. The fluid impermeable barrier also defines an opening extending therethrough. The opening is configured to be positioned adjacent to a female urethra or have a male urethra positioned therethrough. The fluid collection device also includes a conduit at least partially disposed in the chamber. The conduit defines at least one aperture that allows an interior of the conduit to be in fluid communication with the chamber. The fluid collection device further includes a valve. The valve includes a first aperture coupled to the conduit and a second aperture that is fluid couplable to at least one of an air source, a vacuum source, or a fluid storage container. The valve is configured to control fluid flow through the conduit responsive to direction from a user.

Abstract: Embodiments of the present invention are directed to devices, systems and methods adapted for implementing intermittent displacement of blood to mitigate peripheral nerve neuropathy such as that induced by chemotherapeutic agents (i.e., chemotherapy-induced neuropathy (CIN)) that are administered to a patient. Such devices, systems and methods advantageously provide for precise, uniform and controlled blood flow occluding (and optionally blood displacing) compression along irregular surfaces of an appendage of a patient. Such precise, uniform and controlled blood occluding compression is imparted upon the epidermal and dermis skin layers within the aforementioned areas of a patient's extremities to decrease the time that free nerve endings located in the epidermal and encapsulated nerve endings located in the dermis skin layers are exposed to nerve damaging chemotherapy chemicals, thereby substantially decreasing CIN caused by prolonged exposure to such chemicals.

Abstract: Embodiments of the present invention are directed to devices, systems and methods adapted for implementing intermittent displacement of blood to mitigate peripheral nerve neuropathy such as that induced by chemotherapeutic agents (i.e., chemotherapy-induced neuropathy (CIN)) that are administered to a patient. Such devices, systems and methods advantageously provide for precise, uniform and controlled blood flow occluding (and optionally blood displacing) compression along irregular surfaces of an appendage of a patient. Such precise, uniform and controlled blood occluding compression is imparted upon the epidermal and dermis skin layers within the aforementioned areas of a patient's extremities to decrease the time that free nerve endings located in the epidermal and encapsulated nerve endings located in the dermis skin layers are exposed to nerve damaging chemotherapy chemicals, thereby substantially decreasing CIN caused by prolonged exposure to such chemicals.

Abstract: An ostomy bag can include one or more sensors for measuring one or more metrics. An ostomy wafer can also include one or more sensors for measuring one or more metrics. The sensors can be temperature sensors and/or capacitive sensors, for example, and the metrics can include bag fill, leakage, skin irritation, and phase of stoma output, among others.

Abstract: A wound therapy system and method for clearing fluids from a conduit includes a wound dressing apparatus, a pneumatic pump, a valve, and a controller. The wound dressing apparatus is fluidly coupled to a wound, the pump, and the valve. The controller is configured to determine a volume of instillation fluid that has been delivered to the wound, to operate the pneumatic pump and the valve to apply a negative pressure to the wound dressing apparatus to purge a first portion of the instillation fluid, and to operate the pneumatic pump and the valve during a purge operation to deliver a volume of air through the wound dressing apparatus that is approximately equal to or greater than the volume of instillation fluid to purge a second portion of the instillation fluid from the wound dressing apparatus.

Abstract: A base plate for an ostomy system includes a monitor interface having a plurality of terminals for electrical coupling of a monitor device to the base plate and a coupling part to attach the base plate to the monitor device.

Abstract: A drainage catheter configured for draining bodily fluid from a patient is disclosed. The drainage catheter may comprise a catheter tube with a drainage lumen and a suture lumen. A suture of the drainage catheter may be disposed within the suture lumen. The suture may be coupled to a distal end of the catheter tube and extend proximally through a hub disposed at the proximal end of the catheter tube.

Abstract: Negative pressure wound therapy systems, apparatuses, and methods for operating the systems and apparatuses are disclosed. In some cases, the system can include a dressing having electronic circuitry that wirelessly communicates a dressing identifier and/or other dressing information to a controller of a pump assembly of the system. The controller can automatically modify one or more operational parameters of the pump assembly based on the dressing identifier and/or other dressing information wirelessly communicated. Duration of time over which the dressing has been in use can be monitored and provision of therapy by the pump assembly can be disabled responsive to a determination that the duration of time has reached operational lifetime of the dressing.

Abstract: An apparatus and associated methods relate to an external catheter configured with a urine collection bag having a semi-rigid and flexible internal tube adapted to permit fluid engagement with urine streaming from a patient, in a manner that does not require precisely locating a patient's buried, retracted or retractive penis supported by secure connection to the patient coincident to the outer circumference of the internal tube with an adhesive having a removable non-adhesive backing to prevent the dislodging or misplacement of the external catheter or obstruction of the flow of urine and the secure attachment of the tube to a transparent urine collection bag permitting visualization of the inner contents of the bag.

Abstract: A surgical suction device (10) comprising: a connector (12), a surgical cavity insertion tube (14), and a suction tip (16), wherein the surgical cavity insertion tube (14) is connected at a proximal end thereof to the connector (12) and at a distal end thereof to the suction tip (16), and the suction tip (16) comprises an inner hollow shaft (18) and an outer hollow shaft (20) coaxial to each other, the inner hollow shaft (18) having a first central opening (22) at a distal end thereof, and the outer hollow shaft (20) having an end wall (24) at a distal end thereof, wherein the end wall (24) has a second central opening (26) in axial alignment with the first central opening (22) of the inner hollow shaft (18), wherein the outer hollow shaft (20) has one or more openings (28) on a lateral wall (30) thereof.

Abstract: A nasal aspirator suction bin assembly comprises a suction bin base, which has a first connecting end connected with a host and a second connecting end connected with a suction bin cover; after the suction bin base is connected with the suction bin cover, a cavity is formed therein; the middle of the suction bin base is provided with an outlet tube, which runs through the suction bin base and extends into the cavity; the upper end of the suction bin cover is provided with a suction tube, which runs through the suction bin cover and extends into the cavity; a bracket is arranged in the cavity, and the bracket comprises a bracket tube which can be inserted on the outlet tube and a baffle arranged at the other free end of the bracket tube, and at least one air hole is arranged on the bracket tube to keep the suction tube and the outlet tube in communication all the time; the cavity is used to store the inhaled nasal fluid.

Abstract: This disclosure relates to blood flow reversal valves and related systems and methods. In certain aspects of the invention, a blood flow reversal valve includes a first member having a first passage and a second passage, and a second member having a first passage and a second passage. The first and second members are rotatably fixed relative to one another such that the first passage of the first member is aligned with the first passage of the second member and the second passage of the first member is aligned with the second passage of the second member. A flow directing element is disposed in the cavity and is moveable relative to the first and second members between a first position in which the first passage of the first member and the first passage of the second member are fluidly connected and a second position in which the first passage of the first member and the second passage of the second member are fluidly connected.

Abstract: The present disclosure generally relates to a removable enclosure for a mobile negative pressure wound therapy (NPWT) device, where the enclosure is arranged to reduce unwanted noise from a pump comprised with the negative pressure pump. The enclosure is specifically useful when operating the NPWT device during nighttime.

Abstract: According to certain aspects, a negative pressure wound therapy system can include a negative pressure therapy apparatus configured to apply negative pressure to a wound of a patient. The negative pressure therapy device can include a wound dressing configured to be placed over the wound, a negative pressure source supported by the wound dressing, and a controller. The controller can include a processor configured to determine operating data of the negative pressure therapy apparatus and transmit the operating data. The negative pressure wound therapy system can further include a wireless communication device having a controller with one or more processors. The controller of the wireless communication device can be configured to be communicatively coupled to the negative pressure therapy apparatus and further configured to receive the operating data transmitted by the controller of the negative pressure therapy apparatus. The controller can be further configured to output the operating data.