Abstract: Apparatus and methods for clearing obstructions from a medical tube are disclosed. In an exemplary embodiment, a spool drive system is disclosed for actuating a guide wire within a medical tube. The spool drive system can be a hand held, disposable device having a spool housing with a spool therein for alternately advancing and withdrawing a guide wire through an inlet of the spool housing. A track can be spaced from and extend about a perimeter of the spool to direct the guide wire onto or off of the spool as the spool is rotated. Other embodiments and devices for actuating the guide wire, and methods therefor, also are disclosed.

Abstract: A wound therapy apparatus is disclosed that includes a wound interface securable to a skin surface around a wound bed to form an enclosed space over the wound bed that is fluid-tight. The wound therapy apparatus may include a dressing engaged with the wound interface to contact the wound bed. Gas within the enclosed space may have an O2 concentration greater than the O2 concentration in atmospheric air. The dressing may include a hydrophobic material, hydrophobic material, or a distal layer comprised of silicone having fenestrations therein, in various aspects. The pressure p0 within the enclosed space may vary over a pressure range pmin?p0?pmax. Related methods of use are also disclosed.

Abstract: The present disclosure provides systems and methods for transfer of tissue or other materials such as adipose tissue. The systems and methods can include a vessel and a syringe to facilitate transfer of tissue between one or more vessels and tissue implantation devices.

Abstract: Disclosed is a multiple bag system for fractionating blood, the system including a fluid collecting bag including at least one outlet port; at least first and second sampling bags, each including at least one inlet port and at least one outlet port; and a fluid transfer unit to transfer fluid from the collecting bag to the sampling bags. The fluid transfer unit includes an acoustic sorter. Also disclosed is a method for fractionating blood into blood products.

Abstract: A method for automated processing of a blood product, the method comprising providing a reusable separation apparatus controlled by a microprocessing unit, said apparatus configurable with settings and configured to associate with a disposable circuit comprising a separator and in communication with a source blood product having a first concentration and first volume. The apparatus and disposable circuit are configured to flow the source blood product into an inlet of the separator and separate supernatant of the source blood product from a first outlet of the separator into a filtrate container. The apparatus and disposable circuit are also configured to separate platelets and remaining supernatant from a second outlet of the separator into a retentate container, wherein the platelets and remaining supernatant in the retentate container have a second concentration greater than the first concentration and second volume less than the first volume.

Abstract: The present invention relates to a breast shield arrangement (1) for a breast pump (2) comprising: a breast shield (3) for receiving a user's breast therein, and a sensor (4) for transmitting an input signal into the breast and receiving a corresponding reception signal in response, said reception signal indicating changes in milk flow in the breast.

Abstract: A system for facilitating fluid connection between cannulae and a blood pump. The system includes a cannula having a distal end adapted to be in fluid communication with the circulatory system and a proximal end configured to couple to an inlet of the blood pump. Further included is a tunneling device configured to be inserted into a body of a patient to direct the proximal end of the cannula adjacent to the inlet and including a second connecting structure. Further included is a plug which has a first plug part and a second plug part. The first plug part includes a second connecting structure, the first and second connecting structures being selectively engageable. The second plug part is configured to be inserted in the proximal end of the cannula. The first and second plug parts are selectively disengageable to allow in situ disconnection between the cannula and tunneling device.

Abstract: A blood pump, such as an axial flow pump, having a pump housing, the pump housing defining a flow path and having a tapered portion adjacent to an outlet, tapering toward the outlet, an outflow cannula connected to the outlet of the pump housing, and an impeller and diffuser, disposed in the pump housing, the diffuser having a tapered body corresponding to the tapered portion of the pump housing, the diffuser body having at least one vane extending therefrom, the vein tapering in the same direction as the diffuser body. The present invention also includes a method of manufacturing the blood pump and a method of implanting the blood pump.

Abstract: The present invention provides an intravascular blood pump comprising a housing that is at least partially expandable and collapsible and having an impeller with one or more blades attached thereto. The housing having spanning sections that are aligned with the blade(s) and adapted to collapse into recesses or spaces defined or provided between or along the blade(s) and along the central rotor to which the blade(s)s are attached.

Abstract: A heart failure recovery device includes a fluid pump having an inlet and an outlet in fluid communication with a pump reservoir, and a pumping element disposed within the pump reservoir, the pumping element including a protrusion that in an active state is configured to rotate and move fluid away from the inlet and towards the outlet. A receiver coil can be electrically coupled to the fluid pump and is configured to subcutaneously absorb electromagnetic energy for powering the fluid pump. In certain embodiments, an implantable port provides fluid access to the pump reservoir for cleaning and maintaining the fluid pump. In other embodiments, a valve closes fluid access to at least one of the inlet and the outlet during periods when the device is not being used for treatment.

Abstract: A monitoring device operates on a pressure signal from a blood processing apparatus which has an extracorporeal blood circuit for pumping blood through a dialyzer, and a treatment fluid supply system for pumping a treatment fluid through the dialyzer. The monitoring device has a first input block for obtaining a first pressure signal, and a second input block for obtaining a second pressure signal. An emulation block generates, as a function of the second pressure signal, an emulated first pressure signal which emulates a concurrent signal response of the first pressure sensor, and a filtering block generates a filtered signal as a function of the first pressure signal and the emulated first pressure signal, so as to suppress, in the filtered signal compared to the first pressure signal, signal interferences originating from the treatment fluid supply system. A pulse detection block processes the filtered signal for detection of subject pulses.

Abstract: An apparatus for premixing fluids to form dialysate for an extracorporeal blood treatment includes at least a first feed portion for supplying at least a first fluid from at least a first fluid reservoir, at least a second feed portion for supplying at least a second fluid from at least a second fluid reservoir, a premixing portion being configured to premix fluids supplied via the feed portions in counter flow to form a fluid mixture and at least one drain portion for draining the fluid mixture premixed in the premixing portion as dialysate. A method carries out appropriate steps. In a conductivity measurement along the drain portion the conductivity of the premixed fluid mixture is measured by means of a digital filter adapted to be parameterized based on at least two state variables of the premixing process at least in two phases with a first predictive phase and a second corrective phase.

Abstract: A dialysis machine has a dialyzer (D), a water inlet system for supplying the dialyzer (D) with fresh dialysis fluid which is connected to the dialyzer and an external water supply and with a line for used dialysis fluid, which is in communication with the dialyzer (D). The water inlet system includes a container for water or other liquid, in particular for RO water. The dialysis machine includes a heat exchanger connected with the line for used dialysis fluid and with the water inlet system so that heat is transferred from the used dialysis fluid to the liquid present in the water inlet system. The container includes means for physical separation of the external water supply and the downstream portions of the water inlet system, preferably a free-fall path for incoming liquid from the water supply, and the heat exchanger is arranged downstream of the container.

Abstract: To provide a blood purification apparatus in which the hot-water-disinfection time can be optimized with consideration for environmental conditions. A blood purification apparatus provided with a dialyzer for giving dialysis treatment to a patient, and with a tube for introducing dialysate into or discharging drain liquid from the dialyzer. The apparatus includes a thermistor that is capable of detecting an environmental condition at a time of a hot-water-disinfection process in which the tube is disinfected with hot water or a parameter regarding the environmental condition, and an estimating device that estimates a hot-water-disinfection time required for the hot-water disinfection of the tube in accordance with the environmental condition or the parameter regarding the environmental condition detected by thermistor.

Abstract: A medical fluid management assembly includes: a pneumatic manifold including a plurality of pneumatic passageways and a plurality of pneumatic connectors; a pump and valve engine including a plurality of valve chambers and at least one pump chamber, the pump and valve engine including a plurality of pneumatic connectors mated sealingly and releaseably with the pneumatic connectors of the pneumatic manifold, the pump and valve engine further including a plurality of fluid connectors; and a fluid manifold including a plurality of fluid pathways and a plurality of fluid connectors mated sealingly and releaseably with the fluid connectors of the pump and valve engine.

Abstract: An assembly for an extracorporeal life support system with a suction line that features a venous cannula and a pressure line that features an arterial cannula furthermore includes a pump that is arranged between the suction line and the pressure line. This assembly has a discharge line with a discharge cannula, wherein the discharge cannula is longer than the arterial cannula, and wherein the discharge line is connected to the suction line or the pressure line.

Abstract: A femoral hip joint spacer including a prosthesis body having a ball head with a sliding surface, a neck, a collar and a stem. A fastening area is arranged on the stem. The femoral hip joint spacer further has a first connector for feeding a medical irrigation liquid into the body, a second connector for draining the irrigation liquid from the body, and an irrigation liquid inlet opening. The first connector is connected in a liquid-conveying manner to the irrigation liquid inlet opening and an irrigation liquid outlet opening. The second connector is connected in a liquid-conveying manner to the irrigation liquid outlet opening, an irrigation liquid discharge opening and an irrigation liquid intake opening. The irrigation liquid discharge opening is connected inside the body to the irrigation liquid inlet opening and the irrigation liquid intake opening is connected inside the body to the irrigation liquid outlet opening.

Abstract: A medical liquid vial is disclosed with a resilient inner bladder and a pre-stress member located with the bladder. Injector assemblies are also disclosed for injecting the vial contents into a patient by advancing the vial through a series of stages or positions. Methods of filling and use are also disclosed.

Abstract: Dual packaging for fill needles and safety needles are described herein. Such packaging can include hard packaging or blister packs. Also described herein are methods of opening the packaging and operating the needles disposed therein.

Abstract: An inserter for inserting a needle or cannula of an infusion set comprises a fixed inserter member and a movable inserter member movably connected to said fixed inserter member and adapted to receive the infusion set. The movable inserter member is movable from a first position to a second position to expose the needle or cannula. The movable inserter member is locked to the fixed inserter member in the first position to prevent accidentally exposing the needle or cannula.

Abstract: A method of securing an infusion set to a skin surface, comprising the steps of placing a needle or cannula of the infusion set in the skin surface, and controlling a minimum bend radius of the placed needle or cannula to resist deformation and fracture thereof.

Abstract: A needle assembly to prevent fluid/vapor escape so as to reduce or prevent fluid exposure to a clinician during use of the needle assembly. The needle assembly may include a handle portion with a needle extending therefrom, and a base portion releasably coupled to the handle portion. The base portion may include a safety assembly to shield a distal tip of the needle and prevent user contact therewith. The base portion may further include a self-sealing pad covering a bottom external surface thereof. The self-sealing pad may include an upper surface designed to mate with the base portion and a raised portion compressively positioned in the opening of the bottom external surface. The needle assembly may further include a fluid isolation component.

Abstract: A medical device for delivery of a fluid to a patient from a line terminating in a tubing needle. The medical device includes a cannula assembly for coupling the fluid into a cannula that is inserted into the patient. The cannula assembly has a first locking element disposed in a fixed position with respect to the cannula. Coupling the line to the cannula assembly is an infusion flap. The infusion flap includes a second locking element for engaging the first locking element of the cannula assembly and a lift tab for disconnecting the infusion flap from the cannula assembly. Coupling of the first and second locking elements requires initial mating of the infusion flap and cannula assembly followed by locking through rotation of the infusion flap with respect to the cannula assembly.

Abstract: A syringe pump configured to mechanically align a force sensor with an axis of a plunger of a syringe for a purpose of minimizing force measurement inaccuracies. The syringe pump includes a syringe pump housing that is configured to receive at least a portion of said syringe, wherein the syringe is selected from a plurality of syringes of different dimensions. A plunger retainer mechanism is pivotably coupled to the syringe pump housing and is configured to retain said plunger of said syringe. The plunger retainer mechanism pivots relative to the syringe pump housing based on a sensed dimension of the plunger to align a force sensor coupled to the plunger retainer mechanism with the axis of the plunger; and a syringe drive mechanism is operably coupled to the syringe pump housing and configured to shift the plunger relative to the portion of the syringe received by the syringe pump housing.

Abstract: An artificial pancreas system includes a continuous glucose monitoring device, a drug delivery device configured to exchange data with the continuous glucose monitoring device and containing a control algorithm, and possibly a remote controller configured to exchange data with the drug delivery device. The algorithm contains an insulin-glucose model, but is decoupled mathematically from the insulin injected by the user to offset the ingested carbohydrates. The control algorithm is designed to calculate two versions of insulin-on-board-patient-facing insulin-on-board (PFIOB) and system-facing insulin-on-board (SFIOB) to properly parse boluses and inform the system of only the insulin that is intended for high glucose correction, but not carbohydrate offsetting.

Abstract: A modular dental material dispenser can include multiple stackable, modular components, each having a syringe extending therethrough. The syringe of each component may include a detachable nozzle attachment to assist in efficiently dispensing the materials contained therein. Two or more modular components may be connected to provide a dispenser capable of dispensing multiple materials using different dispensing nozzles.

Abstract: With certain implementations, the configuration is such that a controller uses a first driver to move a pharmaceutical syringe attachment component closer to the distal end side than a needle removal position when a needle unit is attached to a pharmaceutical syringe unit or when the needle unit is removed from the pharmaceutical syringe unit, so when an injection needle is attached to the pharmaceutical syringe unit, or when the injection needle is removed from the pharmaceutical syringe unit, these operations can be executed without removing a distal end cap, which makes the device extremely convenient to use.

Abstract: In an embodiment, a medicament delivery system is provided. The medicament delivery system includes a container for storing a medicament prior to use, the container having a first end and a second end, an injection member in fluid communication with the container, an actuation mechanism associated with the container and configured to deliver the medicament from the container through the injection member when the actuation mechanism is activated. The medicament delivery system further includes at least one detection element associated with the system, wherein in a first mode of operation of the system, medicament is delivered through the injection member and in a second mode of operation of the system, medicament is not delivered through the injection member, and the mode of operation is dependent on an output from the at least one detection element.

Abstract: According to the invention, an auto-injector for administering a dose of a liquid medicament (M) comprises of a substantially cylindrical housing arranged to contain a pre-filled syringe filled with the medicament (M), a needle shroud slibably arranged with respect to the housing and adapted to rest on the skin of a patient receiving an injection, a releasable drive means arranged within the housing that is capable of, upon release, translating the needle shroud in a proximal direction (P) towards a safe position (PS) and a rotating collar rotatably arranged within the housing. The needle shroud in the safe position (PS) surrounds the injection needle after the injection has been carried out. The rotating collar engages the needle shroud in a manner that forces the rotating collar to rotate within the housing when the needle shroud is translated in the proximal direction (P).

Abstract: The housing for mounting an elongate-shaped container on an injection pen comprises an elongate-shaped body which extends along a longitudinal axis (X30) and which defines an interior volume (V32) for fully receiving the container. The body is provided, on the outside of a first axial end, with at least one first mechanical member for attaching a needle. The body is further provided, in the vicinity of a second axial end opposite the first axial end, with at least one second mechanical member for attaching the housing onto an injection pen. The housing further comprises, in the vicinity of the first axial end thereof, at least one third mechanical member for irreversibly locking a container in position, fully contained in the interior volume (V32) of the body of the housing. Said third locking member is formed by an elastically deformable tab intended to ensure locking of the container in position in the interior volume (V32) of the body of the housing, by axially retaining a flange of the container.

Abstract: A drive mechanism suitable for use in drug delivery devices is disclosed. The drive mechanism may be used with injector-type drug delivery devices, such as those permitting a user to set the delivery dose. The drive mechanism may include a housing, a dose dial sleeve, and a drive sleeve. A clutch is configured to permit rotation of the drive sleeve and the dose dial sleeve with respect to the housing when the dose dial sleeve and drive sleeve are coupled through the clutch. Conversely, when the dose dial sleeve and drive sleeve are in a de-coupled state, rotation of the dose dial sleeve with respect to the housing is permitted and rotation of the drive sleeve with respect to the housing is prevented. In the de-coupled state, axial movement of the drive sleeve transfers force in a longitudinal direction for actuation of a drug delivery device.

Abstract: An apparatus includes a needle, a cutter, a medication fluid path, and a filter assembly. The needle defines a tissue receiving feature. The cutter is movable relative to the needle to sever tissue protruding into the tissue receiving feature. The medication fluid path includes a first portion and a second portion. The first portion is configured to couple with a source of medication fluid. The tissue receiving feature is in fluid communication with the medication fluid path such that the first portion is upstream of the tissue receiving feature. The filter assembly is located in the second portion of the medication fluid path. The filter assembly is configured to permit air to pass through the filter assembly. The filter assembly is further configured to prevent medication fluid from passing through the filter assembly.

Abstract: A fluid injecting system (100) comprising an injector (A) having an injector body (10), a plunger shaft (30), a plunger assembly (20) having an inner plunger barrel (21) slidable within an outer plunger barrel (22), a fluid-cartridge (B) having a fluid (53) and a hypodermic needle (72) for injecting the fluid (53) at an injectable site. The fluid-cartridge (B) is configured to releasably engage with the injector (A). A vacuum (V) is created between the outer plunger barrel (22) and the inner plunger barrel (21) upon formation of a united plunger barrel (40). Also, forward movement of the united plunger barrel (40) transfers the fluid (53) from the fluid-cartridge (B) into the injectable site. The hypodermic needle (72) retracts within empty fluid-cartridge (B) due to release of the vacuum (V) and the injector (A) is disengaged from the fluid-cartridge (B) for reuse. Further, a fluid injecting method (300) is provided.

Abstract: A magazine (18) that stores a plurality of needles (56) configured to engage a medication pen (2) for medication delivery, the magazine (18) comprising a magazine housing (20) enclosing a removable array (26) having a plurality of hub chambers (22) each enclosing one of a plurality of needle hubs (50), a connector (28) in each of the plurality of hub chambers (22), each connector (28) engages one of the plurality of needle hubs (50), a plurality of peel tabs (30) each sealing one of the plurality of hub chambers (22), and an electronic indicator (62) to identify a status of the plurality of needle hubs (50), wherein the electronic indicator (62) identifies how many of the plurality of needle hubs (50) are unused.

Abstract: A breathing mask for use in administering inhalable medications to a patient in need of an inhaled drug is provided. The mask disclosed herein is particularly useful for use with very young children. The mask is made from a flexible molded plastic silicone or elastomeric material, and has an anthropometrically/anatomically/ergonomically contoured shape to provide a good seal, a comfortable fit, and minimal dead space within the mask. The airway is aligned with nose. There may be an orifice for use with a soother device to calm a child using the mask. Also provided is a visual flow indicator to provide an indication of the quality of the seal of the mask on the face.

Abstract: In one embodiment, a member for securely dispensing a substance to an intended user includes a first member configured to threadedly engage with a housing containing the substance; a second member coupled to the first member, the second member configured to fixedly secure the first member to the housing; a third member including a cavity sized and shaped to selectively receive the second member; and a valve coupled to the first member such that: when the second member is received within the cavity, the valve is in an open state that allows the substance to be dispensed from the housing to the intended user in response to a processor determining that a unique biometric attribute of the intended user is detected, and when the second member is not received within the cavity, the valve is in a closed state that prevents the substance from being dispensed from the housing.

Abstract: A metered dose inhaler (1) for dispensing aerosol doses comprises an actuation housing (2) adapted to receive a canister (4). The canister (4) is configured to move from a rest position to an activation position in which a valve (7) of the canister (4), positioned at a valve end (8) of the canister (4), is depressed against a bottom portion of the actuation housing such that an aerosol dose is released. The inhaler (1) further comprises a mechanical dose (10) counter comprising an indicator member which is constructed and arrangement to undergo a predetermined count-indicating motion when an aerosol dose is released. Moreover, the inhaler (1) comprises a triggering unit (11) for triggering at least one electrical switch (12) when the canister (4) is moved from the rest position to the activation position whereby an electrical signal is generated. Also part of the inhaler (1) is a processing unit for processing the signal generated by the switch (12) upon being triggered.

Abstract: A device (20) is disclosed for dispensing a fluid supplied from an external fluid source. The device comprises a transducer (32) adapted to receive a fluid from the fluid source, and a collapsible linkage and trip link (502) coupling the transducer and the fluid source. The linkage has a collapsible joint inhibiting discharge of the fluid source when in a locked orientation. The device (20) further comprises a moveable member coupled to the linkage such that inhalation forces on the device cause the linkage to collapse thereby discharging the fluid from the fluid source. The device may further include a dose counter coupled to the fluid source for registering the amount of doses administered from the fluid source.

Abstract: A respiratory device comprising a housing enclosing a chamber and an orientation indicator moveable with respect to the housing between a first position indicative of an orientation of the housing predetermined to be suitable for operation of the respiratory device, and a second position indicative of an orientation of the respiratory device predetermined to be less suitable for operation of the respiratory device. The orientation indicator is positioned in a location on the respiratory device visible to a user during the operation of the respiratory device.

Abstract: A method of providing pressure support to a patient that includes determining a measure associated with an inspiratory time of the patient during therapy, delivering a flow of breathing gas to the patient at an inspiratory positive airway pressure (IPAP) level during at least a portion of an inspiratory phase of the patient, delivering the flow of breathing gas to the patient at an expiratory positive airway pressure (EPAP) level that is less than the IPAP level during at least a portion of an expiratory phase of the patient, and automatically setting a rise time associated with a transition from the EPAP level to the IPAP level based on the measure associated with the inspiratory time of the patient. Also provided is a pressure support system adapted to perform the method.

Abstract: A device, for the pressure-supported or pressure-controlled ventilation of a patient with reduced spontaneous breathing, has a ventilator unit to supply a breathing air flow composed of cyclical ventilation strokes and a control unit generating a control signal to set a pressure and/or a volume flow of the breathing air flow. An EMG unit generates an EMG signal, which may be used as a basis for generating the control signal as a function of a breath of the patient. A unit for analyzing an EMG signal is provided, which analyzes at least one EMG signal recorded during an already concluded breath of the patient. The control unit is configured such that the ventilator unit control signal can be generated, at least at times, by taking into account the analysis of the EMG signal recorded during an already concluded breath of the patient.

Abstract: An airway has a ventilation tube with a mask attached to its distal end. The mask has a base and a sealing ring surrounding the base. The sealing ring has an exterior side surface extending around the base, an upper surface extending from the exterior side surface toward a center of the base, and an inner surface extending from the upper surface toward the center of the base. The exterior surface, upper surface, and inner surface define an inner volume within the sealing ring. The sealing ring and base define a cavity in the mask. An evacuation tube is attached to a proximal end of the mask and extends through the inner volume of the sealing ring to a distal end of the mask where it forms an opening on the mask distal end on the sealing ring exterior side surface.

Abstract: A respiratory mask assembly for delivering breathable gas to a patient includes a frame having a main body and a side frame member provided on each lateral side of the main body. Each side frame member includes an integrally formed first connector portion. A headgear assembly is removably attachable to the frame. The headgear assembly has a second connector portion adapted to be removably coupled with the first connector portion provided on the frame. The second connector portion is manually movable to a releasing position to detach the headgear assembly from the frame. The headgear assembly is rotationally adjustable with respect to the frame.

Abstract: A mask system and an air delivery conduit for use in the treatment of respiratory disorders. The air delivery conduit may comprise a textile having an airtight arrangement. A support structure may be provided to the conduit to provide form.

Abstract: A mask assembly for delivering pressurized gas to a patient comprising a mask having an inspiratory port and an expiratory port located on generally opposite sides, wherein said ports are sized, oriented, positioned, and/or spaced apart a sufficient distance to allow a cross-flow of pressurized gas to flow through the mask assembly; an outlet limb connected to the expiratory port and having an aperture in pneumatic communication with the breathing chamber; the aperture size being variable between a first, open configuration and at least one second configuration that is different from the first. A ventilation system for delivering pressurized gas to a patient comprising a seal formed with the patient's airways and in pneumatic communication with a plenum chamber; an exchanger positioned at least partially within the plenum chamber, and in pneumatic communication with inspiratory and expiratory flow paths, to recover heat and/or moisture from gas exhaled by the patient.

Abstract: A vapor delivery system having: a) a base unit configured to generate a supply of vapor; and b) a vapor control system configured to allow a user to selectively: a) cause vapor generated by the base unit to be discharged primarily to a surrounding space within which the base unit resides to thereby increase vapor density in the surrounding space; and b) cause vapor generated by the base unit to be discharged primarily to a vapor guide structure configured to: i) be placed operatively with respect to a user's face; and ii) guide discharging vapor generated by the base unit into at least one of the user's nose and mouth with the vapor guide structure placed operatively with respect to the user's face.

Abstract: A metering pump is joined to the stepping motor, includes an eccentric mechanism converting a revolving motion of the stepping motor into a reciprocating motion of a plunger, and makes a constant liquid delivery by sucking and discharging an anesthetic agent through variations in the cubic volume of a cylinder caused by the reciprocating motion of the plunger. The control section: calculates a suction and discharge cycle T of the metering pump on the basis of a set anesthetic-gas concentration and a fresh-gas flow rate; sets a discharge period T2 of the cycle T to be longer than a suction period T1 of the cycle T; and controls the revolution speed of the stepping motor so that the travelling speed of the plunger is kept constant during the discharge period T2.

Abstract: Device for use in the medical field as technical pulmonary re-expansion instrument sand comprising a T-body with one-way valve, a flow occlusion/release system, and pressure release valve, for use with patients with an artificial airway, be this an orotracheal tube or tracheostomy cannula.

Abstract: Disclosed herein are systems and methods for treating memory impairment, and more specifically to customized visual presentation for treating memory-related disorders and diseases. The disclosed systems and methods can predict clinical status of patients based on platform user behavior, such as those of patients. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

Abstract: The present disclosure describes a system configured to adjust the duration of individual sensory stimuli provided to a subject. The system is configured to determine a current amount of slow wave activity in the subject, responsive to the subject being presently in slow wave sleep, control one or more sensory stimulators to provide the individual sensory stimuli to the subject, determine habituation of the subject to the individual sensory stimuli and, responsive to the slow wave activity in the subject for a period of time following the providing of the individual sensory stimuli showing habituation, adjust the duration of the individual sensory stimuli.