Abstract: The invention comprises a diaper sensor device comprising at least two sensor units each comprising at least a temperature sensor and a humidity sensor; optionally a positional sensor; a microcontroller communicating with the sensors and comprising a transmitter for transmitting data from the sensors; a power unit supplying power to the sensors, the microcontroller and the transmitter; a flexible watertight casing; housing the sensors, the transmitter; and the power unit, and fastening means for fastening the diaper sensor device on the outside of the diaper. Furthermore the invention comprises a method and a system for determining the existence and class of human excreta in a diaper.

Abstract: Embodiments described herein relate to apparatuses, systems, and methods for the treatment of wounds, for example using multiple wound dressings in combination with negative pressure wound therapy. A negative pressure would therapy apparatus can include a negative pressure source and a controller. The negative pressure source can include inlets configured to couple via fluid flow paths to wound dressings. The fluid flow paths can include pressure sensors configured to measure pressure in the fluid flow paths. The pressure sensors can include a first pressure sensor configured to measure pressure in the first fluid flow path and a second pressure sensor configured to measure pressure in the second fluid flow path. The controller can be configured to operate the negative pressure source and provide, based on measured pressure, indication of at least one operating condition associated with at least one of the fluid flow paths.

Abstract: The invention relates to a connection device (2) for use in the negative pressure therapy of wounds, comprising a flexible conducting means (6) and a connecting body (4) made of an elastomeric flexible material which can be applied to a negative pressure dressing which covers the wound and seals the wound off from the atmosphere, wherein the connecting body (4) has a centrally arranged raised first area (8) which receives the conducting means (6), and a flatter flange-shaped second area (10) opposite the first area, which second area forms a contact plane (12) on the negative pressure dressing, wherein a conducting portion (46) which is closed on all sides and is formed by the central first area adjoins a free end of the delivery lumen (42) of the conducting means (6) which opens in the central first area, wherein said conducting portion first opens at a distal end into an interior (16) of the central first area (8) and from there is in fluid communication with the suction lumen (40) of the conducting means (

Abstract: A device and method for treating a wound of a patient with negative pressure is provided. The device comprises a heat-assisted pump system. The pump system can be powered in part by heat derived from the patient. The pump system may be configured to be highly planar, light weight, and portable. The pump system may comprise a Stirling engine or a thermal acoustic engine.

Abstract: The present invention provides a wound dressing tubing connector, comprising a first unit and a second unit which are releasably connectable and which when connected form a fluid path through the connector, wherein the first unit comprises an inlet and an outlet and wherein the second unit comprises an inlet and an outlet, in which the outlet of the first unit and the inlet of the second unit when connected together define the fluid path, and wherein the first unit and the second unit are connectable to form an air and fluid tight seal and wherein the first unit and/or the second unit comprises a pressure regulator valve in fluid communication with the fluid path. Also provided are systems, kits and methods of treatment.

Abstract: A collection bottle and a method for detecting a characteristic of a sample are provided. The collection bottle includes a body and a cover. The body of the collection bottle has an accommodating space. The cover of the collection bottle is removably assembled to the body of the collection bottle, and the cover includes a channel and a testing part. The channel of the collection bottle communicates the accommodating space and the outside environment. While the cover of the collection bottle is assembled to the body, the testing part extends toward the accommodating space.

Abstract: The present invention relates to a wound volume measuring method and device, wherein the method comprises the steps of: disposing a foam dressing on a wound site; hermetically sealing the wound site by attaching a film dressing on skin adjacent to the wound site; supplying a negative pressure to the hermetically sealed space formed between the film dressing and the wound site, and thereby discharging fluid into the hermetically sealed space; measuring the flow of the fluid discharged from the hermetically sealed space; and calculating the volume of the wound site on the basis of the measured fluid flow.

Abstract: The disclosure provides stable formulations of cationic biocides that are primarily used in the treatment and prevention of infections. The disclosure is also concerned with processes for forming stable emulsions of cationic biocides and petrolatum.

Abstract: Provided is a negative-pressure wound therapy apparatus capable of causing negative pressure in a closed space defined by a wound dressing and a wound region with a sufficient suction flow rate as needed even with a miniaturized pump device. In atypical use that needs a high suction flow rate, because a pump device (30) with a high suction flow rate is attached to a wound dressing (10) and sucks gas from a closed space (904) defined by a wound region (903) and the wound dressing (10), even when a pump device (20) for typical use is miniaturized and the suction flow rate of the pump device (20) is reduced, a therapy apparatus (100) can achieve a suction flow rate sufficient for atypical use. Thus, the pressure value in the closed space (904) can decrease to a desired value more quickly.

Abstract: Disclosed embodiments relate to apparatuses and methods for wound treatment. In certain embodiments, a negative pressure wound therapy apparatus includes one or more indicators configured to illuminate in a pattern to communicate at least one of a status of a pump assembly and/or of a dressing. The pattern is configured to enable an electronic device comprising at least one camera to capture the illumination pattern of the one or more indicators and to determine the status corresponding to the pattern of illumination. In some embodiments, a negative pressure wound therapy apparatus is powered by an energy generator that has a first side configured to be in contact with a skin surface of a patient and a second side configured to be exposed to atmosphere, and the energy generator is configured to utilize a temperature differential between the skin surface and the atmosphere to generate electrical energy to power the apparatus.

Abstract: A method for removing a stone from a patient comprising the steps of: providing a suction evacuation assembly which includes a sheath and one or more side arms; inserting and positioning a distal end of the sheath into a lumen or cavity of a patient's body containing a stones; connecting a tube to one of the side arms and to a collection bottle; connecting another tube to the collection bottle and a negative pressure system; visualizing the stone or foreign body using a scope inserted through the assembly; activating the negative pressure system in order to remove the stone from the cavity if the diameter of the stone is narrower than an inside diameter of the sheath and the side arm, or performing a lithotripsy on the stone to create fragments with a decreased diameter which allow the passage through the assembly; and collecting the stone in the collection bottle.

Abstract: The present disclosure illustrates a nasal aspiration and wash device which includes a shell member, a pump, a suction part and a spray part. The pump is disposed in the shell member. The suction part is disposed on the shell member and configured to flow external gas into the pump. The spray part is disposed in the shell member and configured to spray atomized liquid out. The suction part and the spray part are spaced apart from each other a distance. The nasal aspiration and wash device of the present disclosure is able to separately perform a nasal aspiration function and a nasal wash function without interfering with each other, and the user does not need to replace a functional assembly for using the two functions.

Abstract: A device and method are provided to facilitate the handling of a volume or fluid. The device includes an elongated tube having an open first end and a second end. The tube defines a reservoir for receiving the volume or fluid. A stanchion has a first end received within the reservoir of the tube and a second end projecting from the open end of the elongated tube. In operation, the elongated tube is deposited in a first capsule having fluid therein. The first capsule is centrifuged such that the volume of fluid is received in a reservoir in the tube through the open end. The tube is removed from the first capsule and positioned in a second capsule such that the open end of the tube is spaced from a closed end of the second capsule. The second capsule is centrifuged such that the volume of fluid is expelled from the reservoir of the tube.

Abstract: A cannula-catheter bonding method and apparatus can include a needle having a specifically configured connector end to reduce the risk of the connector end disengaging with an adapter (e.g., a catheter, a cannula, or a connector of a Huber needle assembly, etc.). The specifically configured needle connector end can be a formation, such as a barb, a bead, an annular structure, a rib, etc. The formation can be formed on the connector end, and may be elongated with a conical shaped nose leading to a base with a bottom. The formation can be used to prevent movement of the needle relative to the adapter. A method for producing the formation can include forming a mold for the formation in a plate, where the connector end can then be placed within the mold so that curable material can be disposed within the mold. Upon hardening of the curable material, the formation can take the shape of at least a portion of the mold.

Abstract: A system and apparatus for treating a tissue site with reduced pressure and collecting fluids from the tissue site is disclosed. The system may include a reduced-pressure source, a pouch in fluid communication with the reduced pressure source, and a dressing in fluid communication with the pouch. The pouch may include a first wall, a second wall having a periphery coupled to the first wall to form an interior, and a third wall extending through the interior to form a first chamber in fluid communication with the dressing and a second chamber in fluid communication with the reduced pressure source. A plurality of filters are positioned in the third wall. The filters permit fluid communication between the first chamber and the second chamber.

Abstract: The present disclosure provides an apparatus and methods of use for collecting particles. An example collection device includes (a) a vessel defining a chamber, wherein the vessel includes a distal end and a proximal end, (b) an inlet port extending from the proximal end of the vessel, wherein the inlet port is in fluid communication with the chamber, and (c) an outlet port extending from the proximal end of the vessel, wherein the inlet port is in fluid communication with the chamber, and wherein the outlet port includes a porous material positioned between the chamber and the outlet port.

Abstract: A reduced-pressure device for wound treatment includes a housing, an air pressure storage unit, a compression unit and a pressure indicating module. The air pressure storage unit is installed in the housing and comprises a pressure storage container, a piston assembly and a piston spring, and the compression unit is mounted on the piston assembly, and the pressure indicating module is engaged to the pressure storage container and the piston assembly. Therefore, the user can see the information shown on the pressure indicating module to be easily aware of how much capacity of negative pressure the reduced-pressure device can continuously be provided in order to determine when to operate the compression unit again for providing the desired negative pressure.

Abstract: Systems, methods, and devices are disclosed that involve a fistula-isolating device for use when reduced pressure is applied to a wound bed having a fistula. In one instance, the fistula-isolating device includes an adjustable passageway member and a perimeter member that contracts under reduced pressure and that automatically accommodates wound beds of different heights. In another instance, the fistula-isolating device involves a body shaped as a frustro-conical body that is readily sized for different depth wound beds. Other systems, methods, and devices are presented.

Abstract: A canister lid (101) for a canister (102) includes an annular perimeter (103) surrounding an interior portion (104). Rather than completely surrounding the interior portion, the annular perimeter is instead interrupted by a suction conduit (112) defined by a suction conduit (112) separating a first lobe (117) and a second lobe (118). The suction conduit (112) intersects the annular perimeter such that the first lobe is disposed interior of the annular perimeter while the second lobe is disposed exterior to the annular perimeter. The canister lid can further include one or more ports (110,111) extending from the interior portion. A canister (102) can include a valve (401) and can optionally be coupled to a hub mount vacuum source (1200) or a hub mount stand (1800).

Abstract: A therapeutic composition can include an amount of amniotic fluid having a therapeutically effective amount of at least one protein, hyaluronic acid, or both. The therapeutic composition can be substantially free of lanugo, vernix, and cells harvested with the amniotic fluid.

Abstract: A suction disc is configured for abutting against a dressing covering over a wound. The suction disc includes a base plate, a case, a negative pressure, a first sensing device and a second sensing device. The base plate has a first surface and a second surface opposite to each other. The first surface abuts against the dressing. The base plate has a first opening and a second opening respectively communicating with the first surface. The case has a first chamber and a second chamber. The case communicates with the second surface. The first chamber communicates with the first opening. The second chamber communicates with the second opening. The negative pressure device communicates with the second chamber. The negative pressure device provides a negative pressure to the second chamber. The first sensing device communicates with the first chamber. The second sensing device communicates with the second chamber.

Abstract: A wound dressing is provided. The dressing includes a moisture-transmissible backing layer having a first major surface, a second major surface, a backing layer perimeter, and a first opening; an absorbent adhesive gel adhered to the second major surface of the backing layer, the absorbent adhesive gel comprising an adhesive gel perimeter; and a porous layer having a first side, a second side, and a porous layer perimeter. The second major surface has a first adhesive disposed thereon. The first side of the porous layer is adhered to the absorbent adhesive gel. The porous layer is configured to facilitate passage of fluid to the first opening. One-hundred percent of the adhesive gel perimeter is overlapped by the backing layer. At least 50% of the porous layer perimeter is overlapped by the absorbent adhesive gel.

Abstract: Embodiments disclosed herein are directed to negative pressure treatment systems and wound dressing systems, apparatuses, and methods that may be used for the treatment of wounds. In particular, some embodiments are directed to improved wound dressings comprising a bridge portion connecting two or more portions of an absorbent layer that facilitates trimming of the wound dressing to suitable sizes. Some embodiments provide for trimming the dressing in a gap between two or more portions of an absorbent layer and sealing the exposed portion of dressing after trimming when the dressing is applied to skin surrounding a wound.

Abstract: A method and apparatus are described for moving a tray within a confined space while the tray is bounded by a chassis. The movement of the tray is effected by a driven gear moving along a rack. A driving gear for rotating the driven gear is mounted on a handle or integral with a rotatable handle. The handle is rotatable about a pivot mounted on the chassis to provide the driving force to move the driven gear along the rack.

Abstract: The present invention relates to an apparatus (1) for evacuating a system (3), comprising a pump (5), the pump (5) being suitable for being in connection with the system (3) with its inlet (7), a pressure tank (11) and a directional control valve (13), the pump (5) transporting a medium out of the system (3) and the pressure tank (11) into an ambience when the pressure tank (11) is connected to its inlet (7), wherein the directional control valve (13) is configured to switch the pressure tank (11) from the inlet (7) to the outlet (9) of the pump (5) when a predefined criterion is fulfilled. The present invention further relates to a breast pump (31) device comprising an apparatus (1) for evacuating a system (3) and a receiving funnel (27) for receiving a breast of a woman.

Abstract: The present disclosure relates to a wound management assembly. The wound management assembly comprises a housing and an exudate collector received in the housing. A gap is defined between the housing and the exudate collector to form a channel for fluid passage, wherein the fluid passes into and through the exudate collector and radially enters the channel.

Abstract: A sump port drain adapter apparatus is disclosed which provides a small, lightweight vessel to capture and collect gastric reflux or stomach contents exiting the smaller lumen, or sump line, of a double lumen nasogastric tube while providing airflow to the sump line to prevent the nasogastric tube from adhering to the stomach lining. The apparatus disclosed prevents clogging in the sump line, unnecessary patient gown and bedding changes, patient skin breakdown and decreases exposure to potentially infectious material for both the patient and healthcare workers.

Abstract: Some embodiments disclosed herein are directed to a pump assembly comprising a voice coil, a magnet and a diaphragm, wherein the voice coil is configured to move the diaphragm to pump a fluid through the pump assembly in response to a drive signal applied to the voice coil. Some embodiments disclosed herein are directed to an apparatus for applying negative pressure to a wound comprising a source of negative pressure configured to be coupled to a dressing, the source of negative comprising a voice coil actuator and a diaphragm, and a controller configured to produce a drive signal for the voice coil actuator.

Abstract: The purpose of the present invention is to provide a method for evaluating the possibility of suffering from pancreatic disease on the basis of the concentration of a pancreatic disease marker in a duodenal juice sample. The method for evaluating the possibility of suffering from pancreatic disease of the present invention has a step for (a) measuring the concentration of the pancreatic disease marker in a duodenal juice sample taken from a subject and a step for (b) evaluating the possibility of the subject suffering from pancreatic disease on the basis of the concentration of the pancreatic disease marker measured in step (a) and the age of the subject.

Abstract: An article having properties allowing same to absorb a body fluid. The article includes at least three paths for the propagation of fluid from a fluid capture zone to at least one storage and/or evaporation area, each fluid propagation path being delimited by a fluid barrier preventing the passage of liquid from one path to another.

Abstract: An integrated ocular fluid management system that, in one instance, includes a first chamber connected to a first input line and a first output line. A second chamber is connected to a second input line and a second output line. A first pump communicates with the first output line. A second pump communicates with the second input line. A first pressure regulator communicates with the first chamber. A second pressure regulator communicates with the second chamber. A first diaphragm is in the first chamber; and a second diaphragm is in the second chamber. A first controller controls at least one of the first pump and the first pressure regulator to maintain the first diaphragm in a predetermined position. A second controller controls operation of at least one of the second pump and the second pressure to maintain the second diaphragm in a predetermined position.

Abstract: The present invention is an intraocular surgery system using a Venturi pump and capable of preventing clogging due to nucleus fragments, despite a reduced aspiration flow rate.

Abstract: Systems, apparatuses, and methods for providing a negative-pressure therapy system are described. The system includes a first dressing, a second dressing, and a negative-pressure source. The negative-pressure source includes a first pump and a second pump. A first valve is fluidly coupled to the first dressing and the first pump to selectively permit fluid communication to the first dressing. A second valve is fluidly coupled to the second dressing and the second pump to selectively permit fluid communication to the second dressing. A cross-over valve is fluidly coupled to the first pump, the first valve, the second pump, and the second valve. The cross-over valve permits fluid communication between the first pump and the second valve and/or the second pump and the first valve. A controller is communicatively coupled to the first pump, the second pump, the first valve, the second valve, and the cross-over valve for operating the same.

Abstract: Some embodiments comprise a pump assembly for reduced pressure wound therapy, comprising a housing, a flow pathway through the pump, one or more valves in communication with the flow pathway, a pump supported within or by the housing, and a one-way flow valve in fluid communication with the pump. The pump assembly can have a pressure sensor in communication with the flow pathway through the pump, and at least one switch or button supported by the housing, the at least one switch or button being accessible to a user and being in communication with the controller. The one-way flow valve can be configured to substantially prevent a flow of gas through the one-way flow valve in a direction of flow away from the pump. The pump assembly can have a controller supported within or by the housing, the controller being configured to control an operation of the pump.

Abstract: Methods and devices for directing a waste fluid from a radiopharmaceutical synthesis system to a waste vessel are provided. In one example, the method includes serially connecting a primary waste vessel to a secondary waste vessel with a fluid conduit, including a waste valve connected to the fluid conduit extending between the primary waste vessel and secondary waste vessel; opening the waste valve so as to allow fluid communication between cavities of the primary and secondary waste vessels; drawing a low pressure in both waste vessels; closing the waste valve so as to fluidically isolate the secondary waste vessel from the primary waste vessel, discharging the waste fluid through a pump valve into the primary waste vessel, and opening the waste valve to evacuate the waste fluid from the primary waste vessel into the secondary waste vessel.

Abstract: A wound dressing, a method of manufacturing a wound dressing, and a method of treating a patient are disclosed. The wound dressing may include an absorbent layer for absorbing wound exudate; and an obscuring element for at least partially obscuring a view of wound exudate absorbed by the absorbent layer in use.

Abstract: A method and apparatus are disclosed for dressing a wound. The apparatus comprises a sealing layer comprising at least one orifice, an absorbent layer over the sealing layer, absorbing wound exude and a liquid impermeable, gas permeable filter layer over the absorbent layer.

Abstract: A drainage container device for collecting suctioned bodily fluids by means of a vacuum source includes a drainage container with a suction port to be connected with the vacuum source; an essentially one-piece container lid for closing and opening the drainage container, and with a drainage port to be connected with a patient drainage line; a suction bag for holding the suctioned bodily fluid, which is arranged on the container lid and accommodated by the drainage container; a channel that runs at least partially through the container lid, which joins an interior space of the suction bag with the suction port by way of an interior space of the drainage container, and is otherwise closed, and a protective element, in particular a filter, for avoiding overflow and/or contamination of the vacuum source by a suctioned bodily fluid.

Abstract: 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 to improved fluidic connectors or suction adapters for connecting to a wound site, for example using softer, kink-free conformable suction adapters.

Abstract: The transport carriage for flush solutions is characterized in that the flush solution is received in a flexible flush solution bag that is arranged in a rigid container, wherein a pressurized gas can be introduced into the flush solution bag or the rigid container.

Abstract: Provided are systems and methods for delivery of fluid to a wound therapy dressing. In exemplary embodiments, a pressure source provides negative pressure to a wound dressing and a biasing mechanism provides positive pressure to a fluid reservoir.

Abstract: A closing dressing bolster and assembly for use with a system for treating a linear wound on a patient includes a bolster body formed from a flexible closing bolster material having closing members that are operable to develop an inward closing force when the closing dressing bolster is placed under reduced pressure. In one aspect, when the closing dressing bolster is under reduced pressure, the system, dressing, or assembly develops an inward force realized at the linear wound and a compression force. A wicking-material holder and wicking material may be used as well. The member components may all be see-through to allow visual inspection of the wound without requiring removal of the dressing.

Abstract: A connection device for use in the negative pressure therapy of wounds, includes a flexible conduit having at least two lumens and being constructed for impingement with negative pressure and/or fluid media; a coupling body made of an elastomeric flexible material, and non-detachably molded onto a wound-side end section of the conduit and being constructed for arrangement on a negative pressure bandage which covers the wound and seals the wound against the atmosphere, wherein the conduit communicates with a wound space through at least one opening in the coupling body; and a fluid inlet section for insertion through an opening in the negative pressure bandage into the wound space. The fluid inlet section is formed on the coupling body and protrudes over a walling of the coupling body, which walling faces the negative pressure bandage. The fluid inlet section is fluidly connected interiorly of the coupling body with a further lumen for delivering a fluid medium.

Abstract: Systems and apparatuses for administering reduced pressure treatment to a tissue site include a reduced pressure source, a drape having a plurality of projections for contacting the tissue site, and an adhesive connected to at least a portion of the drape for sealing the drape to a portion of a patient's intact epidermis.

Abstract: Inline storage pouches and systems for receiving and retaining body fluids from an animal are presented. The inline storage pouch include a flexible pouch body has an interior portion with a fluid storage material disposed within the interior portion. In addition to receiving body fluids, the inline storage pouch may fluidly couple a pressure sensing conduit between a first port and a second port using a first bypass conduit. The first port may be a patient-port interface. The second port may be a device-port interface. Multiple sensors and bypass conduits may be included and associated with a microprocessor that is configured to locate blockages or determine when the inline storage pouch is full. Another inline storage pouch has two chambers and receives and discharges fluids from a pouch connector. Other pouches, systems, and methods are presented herein.

Abstract: A protective tissue cover having a sleeve configuration to slide onto the working portion of a surgical instrument, such as a retractor. At least the contact side of the protective tissue cover is constructed from smooth antimicrobial material that minimizes contact irritation with tissue. Alternative embodiments include various multiple-ply constructions that incorporate an antimicrobial layer, an absorbent layer, and other medical layers to assist in surgical procedures.

Abstract: A portable system for subatmospheric pressure therapy in connection with healing a surgical wound, including a wound dressing dimensioned for positioning relative to a wound bed of a subject and a subatmospheric pressure mechanism dimensioned to be carried or worn by the subject. The subatmospheric pressure mechanism includes a housing having a control unit adapted to draw a vacuum and a canister associated with the housing. The canister has a collection bag disposed therein, which is in fluid communication with the wound dressing to receive exudates from the wound bed. The collection bag is adapted to expand upon receipt of the fluids and has means to release gas from within the collection bag in connection with operation of the control unit. With this arrangement, the canister is attitude independent, i.e., the canister may be positioned on edge, on its side or on its end etc. while still maintaining operation of the control unit.

Abstract: Multi-conduit connector apparatuses for use in negative pressure wound therapy (NPWT) apparatuses to wound dressing, and methods for installing multi-conduit connector apparatuses in NPWT apparatuses.

Abstract: A wound treatment appliance is provided for treating all or a portion of a wound. In some embodiments, the appliance comprises an impermeable flexible overlay that covers all or a portion of the wound for purposes of applying a reduced pressure to the covered portion of the wound. In other embodiments, the impermeable flexible overlay comprises suction assistance means, such as channels, which assist in the application of reduced pressure to the area of the wound and removal of exudate from the wound. In other embodiments, the wound treatment appliance also includes a vacuum system to supply reduced pressure to the wound in the area under the flexible overlay. In yet other embodiments, the wound treatment appliance also includes wound packing means to prevent overgrowth of the wound or to encourage growth of the wound tissue into an absorbable matrix comprising the wound packing means. In still other embodiments, the appliance may include a suction drain.

Abstract: A wound drainage therapy system includes a wound seal unit, a fluid collector unit, a vacuum driving unit and an actuator. The fluid collector unit is detachably connected with the wound seal unit, and the fluid collector unit has a multiple-pipe integration module and a collection bag. The multiple-pipe integration module has a first row connection port group and a second row connection port group. The vacuum driving unit has a vacuum generator. The actuator has a motor, a negative pressure detector and a positive pressure detector, wherein the motor is used to drive the vacuum generator to operate and the motor is detachably connected with the vacuum generator. A connection port of the negative pressure detector and a connection port of the positive pressure detector are detachably connected with another two connection ports of the second row connection port group respectively.