Abstract: An interface device comprises a cushion and a shell coupled thereto which together define an interior space with the face of a user. The shell includes an inlet port structured to have a conduit carrying a flow of treatment gas to the interior space selectively coupled thereto and a first aperture structured to allow the passage of ambient air into the interior space. A first sealing member is operatively coupled to the shell and is positioned such that the first sealing member is movable between a first state in which the first sealing member substantially seals the first aperture, and a second state wherein the sealing member does not substantially seal the first aperture. The first sealing member moves between the first state and the second state responsive to breathing of the patient.

Abstract: The mask for surface snorkeling comprises a rigid frame (2), a transparent visor (3), a soft face mask (4) applicable in an airtight way to the face of the user and having a membrane (7) which delimits an upper viewing chamber (8) being shaped to contain the eyes of the user and a lower breathing chamber (9) being shaped to contain the nose and mouth of the user, and a breathing circuit (5) connected to the lower chamber (9), a ventilation circuit of the upper chamber (8) independent and separated from the breathing circuit (5) also being provided.

Abstract: This disclosure describes systems and methods for managing a move of a patient being monitored or treated by a medical system, such as a medical ventilator. The disclosure describes a novel approach for preventing a patient from being moved from a first location to second different location that is connected to a monitoring and/or treatment system, before all of the necessary hoses have been disconnected from the patient. Further, the disclosure describes a novel approach of ensuring that all of the necessary hoses are reconnected to a patient being monitored or treated by a monitoring and/or treatment system after being moved from the first location to the second different location.

Abstract: A method of ventilating a patient controls an actuator, in accordance with a prescribed value for a respiratory parameter, to compress an inflatable bag to cause air to flow out of an output valve of the bag. The respiratory parameter may include tidal volume, pressure, volume limit, peak pressure, I:E ratio, inspiratory time, and/or breathing rate of the air flowing through the output valve. The method also senses the pressure flowing through the output valve, and sends a pressure signal to the controller. Additionally, the method senses the flow rate through the output valve, and sends a flow rate signal to the controller. The method also adjusts the compression of the actuator as a function of the flow rate signal and/or the pressure signal to adjust the output tidal volume, pressure, volume limit, peak pressure, I:E ratio, inspiratory time, and/or breathing rate to be in accordance with the prescribed value.

Abstract: A fluid sample dispenser includes a microdosing device for outputting, during an activation state, a fluid sample at a fluid sample outlet to the environment, wherein the microdosing device is placeable adjacent to a person's nose so that a distance between the outlet of the microdosing device and a nostril of the person's nose is within a predefined range, and a microdosing driver unit for adjusting a dosing rate of the scent sample output at the scent sample outlet by selectively activating the microdosing device.

Abstract: Described herein are passive nasal respiratory devices, in particular, passive nasal respiratory devices configured to achieve positive end-expiratory pressure (PEEP) in a subject wearing the device. PEEP devices may have a threshold pressure for opening during expiration. These devices may include a flap valve that opens on inhalation nested with a spring valve that opens when exhalation pressure exceeds a predetermined threshold. The device may be configured to be comfortably worn by a sleeping subject.

Abstract: A respiratory treatment device comprising at least one chamber, a chamber inlet configured to receive air into the at least one chamber, at least one chamber outlet configured to permit air to exit the at least one chamber, and a flow path defined between the chamber inlet and the at least one chamber outlet. A restrictor member positioned in the flow path is moveable between a closed position, where a flow of air along the flow path is restricted, and an open position, where the flow of air along the flow path is less restricted. A vane in fluid communication with the flow path is operatively connected to the restrictor member and is configured to reciprocate between a first position and a second position in response to the flow of air along the flow path.

Abstract: A CPAP compliance notification apparatus for use with a CPAP device having a flow generator, a CPAP hose, and a CPAP mask, the CPAP compliance notification apparatus, including a patient occupancy mat, an air pressure sensor, an air pressure tube, a compliance notification controller unit, a housing, a user interface, a programmable logic controller together with a patient to control parameters of the CPAP compliance notification apparatus in implementing a compliant CPAP treatment to the patient.

Abstract: The invention relates to a device for the regulation of PEEP and FiO2 of a ventilator for achieving an arterial oxygen partial pressure in the blood of a mechanically ventilated patient. At reading which is representative of the success of the oxygen supply, i.e. the oxygen saturation of the blood is measured with the device, and assigned to one of three regions, which are defined by two characteristic lines. A first control loop is designed to optimise PEEP and FiO2 on assigning a reading to a region which demands a change of the settings, or to retaining the settings with an assignment to the normal region between the characteristic lines. This first control loop carries out such an optimisation at predefined temporal intervals on account of the representative reading (SaO2REP) and a predefined necessary supply intensity. The ventilator is subsequently activated accordingly.

Abstract: A cuff pressure adjusting device includes: a gas feeding unit which feeds a gas into a cuff by a pressing manipulation performed by a user; a cuff pressure detection unit which detects a pressure in the cuff; and a display unit which displays the pressure detected by the cuff pressure detection unit. The gas feeding unit includes: an elastic hollow body which is deformed so as to reduce an inner volume with reception of a pressing manipulation; and a support member which is disposed adjacently to the elastic hollow body in a direction along which the pressing manipulation is performed.

Abstract: An electrically heated aerosol-generating device includes a main housing having a cavity, a closure body engageable with the main housing to enclose a cartridge in the cavity, and a heater assembly. The heater assembly includes an elongate piercing assembly configured to extend into the open-ended passage of the cartridge and one or more electric heaters. The piercing assembly has a first hollow shaft portion connected to the main housing and a second hollow shaft portion connected to the closure body. The first and second hollow shaft portions have first and second piercing surfaces configured to breakthrough first and second frangible seals when the cartridge is enclosed in the cavity.

Abstract: A connection assembly for a respiratory therapy system, comprising: an outlet assembly, said outlet assembly including an outlet housing and a swivelling disc located on said outlet housing, said outlet housing and said swivelling disc defining, at least in part, a recess; an outlet connector located at an end of a tube portion, said outlet connector including an electrical connector; and a cable having a first end to connect to the electrical connector and a second end to connect to at least one electrical component of the respiratory therapy system, said cable having a slack portion, wherein said outlet connector and said swivelling disc are rotatable in unison between a first position and a second position, and wherein the slack portion of the cable extends from the recess and wraps around the swivelling disc as the swivelling disc is rotated from the first position to the second position.

Abstract: This disclosure describes systems and methods for providing novel adaptive base flow scheduling during ventilation of a patient to optimize the accuracy of estimated exhaled tidal volume. Further, this disclosure describes systems and methods for providing novel adaptive inspiratory trigger threshold scheduling during the novel adaptive base flow scheduling.

Abstract: An aircraft inflatable harness assembly for an aircraft oxygen crew mask for providing regulated flow of oxygen on board an aircraft for an aircraft crew. The aircraft inflatable harness includes at least one inner inflatable tube having a normally deflated configuration and an inflated configuration. The inner inflatable tube has a first and second end, and is configured to inflate to cause expansion of the harness assembly to allow the harness assembly to be placed over a user's head. The inner inflatable tube includes a braided outer sleeve of elastic material. The outer sleeve is configured to have a first length when the inner inflatable tube is in a normally deflated configuration, and the outer sleeve is configured to longitudinally expand to a second length greater than the first length while remaining appreciably the same diameter in the radial direction when the inner inflatable tube is in an inflated configuration.

Abstract: The present invention provides a device (1) for assisting a cough comprising a hosing (3), a chamber (5) formed in the housing, a mouthpiece (7) communicating with the chamber and exposed out of the housing, and an electromagnetic valve (9) assembly for opening or closing the chamber at a pre-set frequency. The device for assisting a cough according to the present invention may produce a high cough pressure and thus form a strong cough airflow to loose and cough the lung mucus out of the airways, and may prevent the collapse of the patient's airway caused by the rapid release of the cough pressure.

Abstract: The present invention relates generally to methods for the delivery of beneficial respirable compounds such as moisture, anti-inflammation compounds, anti-irritants, fragrances, aromatherapy compounds, and low dose medications slowly and continuously over time using a mask containing a thickened aqueous gel media delivery system combined with, supported by, and coating solid bodies inside the filter. The present invention also relates generally to methods for the removal of harmful industrial gasses from inhaled air using a disposable filtration mask containing a fluid filter media composed of a thickened aqueous gel that can be readily modified by means of additives to enhance its filtration properties for specific gasses individually, or in combination. The fluid filter media is combined with, supported by, and coats solid bodies inside the filter which optimize contact between the fluid filtration gel and the incoming air containing harmful industrial gasses.

Abstract: A ventilator, or a breathing assistance apparatus, is disclosed to ventilate patients who may have breathing difficulties, said device comprising a inspiratory pressure control duct configured to be immersed in a first body of fluid; a positive end-expiratory pressure control duct configured to be immersed in a second body of fluid; at least one valve connected to the peak inspiratory pressure control duct and to the positive end-expiratory pressure control duct, and at least one controller communicably connected to the valve to control rate of cycling of the valve, thereby controlling number of breaths per minute, and to control the duration of peak inspiratory pressure also known as inspiratory time.

Abstract: The present disclosure pertains to a system and method for controlling insufflation pressure during inexsufflation of a subject. The system inexsufflates the subject such that tidal flow and/or tidal volume are monitored during insufflation, and insufflation pressure is adjusted to maintain the flow rate of the pressurized flow of breathable gas until a target tidal volume is reached for the insufflation. When the target tidal volume has substantially been reached, the system is causes gas to be evacuated from the airway of the subject. This may provide for more precise, customized therapy for the subject than is provided by conventional inexsufflation systems in which inspiratory flow may not be monitored and/or controlled. In one embodiment, the system comprises one or more of a pressure generator, a subject interface, one or more sensors, a processor, a user interface, electronic storage, and/or other components.

Abstract: An aircraft lavatory oxygen source includes an oxygen storage vessel having a manifold, and an actuator configured to break a pressure seal of the oxygen storage vessel to initiate a flow of oxygen. A flow path in the manifold includes one or more oxygen flow rate control orifices, and may include a variable orifice to control oxygen flow rate and pressure through an outlet of the manifold. The outlet includes a swivel connector fitting that rotates 360 degrees, and one or more oxygen distribution tubes connected with one or more removably attachable connectors, directly to the outlet, between portions of the tube, or to a breathing mask. The actuator can include a spring loaded mechanism, a pyrotechnic mechanism, an electrically powered solenoid or a pneumatic pressure initiated device.

Abstract: A system for improving an artificial respirator is disclosed. In particular, the system may be utilized to improve the quality of life of a user that utilizes an artificial respirator and to improve the quality of life of a caregiver of the user. In order to do so, the system may include an apparatus that suspends or activates one or more functions of the artificial respirator based on various conditions. As an example, if the system detects a threshold change in tension associated with a band supporting a respiration mask positioned on the user, the system may suspend a function of the artificial respirator. Similarly, if the system detects a temperature reading outside a temperature range, detects a unique sequence of inputs, detects a threshold distance between the user and the respiration mask, or detects other conditions, the system may suspend a function of the artificial respirator.