Abstract: The present invention is a nasal respiratory assembly and methods of using the same wherein the assembly comprises a mask, a ventilator hose and a strap. The mask has a top surface, a base, an exhaust port having a one-way valve and two rotatable intake ports. The hose has a first end and a second end adapted to be received by the first and second intake ports, and at least a third end to connect to the ventilator. The hose and/or the mask further contain a rotatable medication delivery port to allow treatment delivery in close proximity to the patient. ; The rotatable intake ports are located on either side of the mask so that the pressurized air is not delivered directly into the patient's nasal cavities.

Abstract: Embodiments of an inhaler device include a housing, a withdrawing assembly disposed within the housing for facilitating withdrawal of medicament from a target blister of a blister strip, the withdrawing assembly including an opening element adapted for opening the target blister of the blister strip while the target blister is positioned in the withdrawing assembly, and a dispensing element adapted for directing the withdrawn medicament toward the exterior of the inhaler device. A blister track is disposed within the housing for guiding each blister of the blister strip to the withdrawing assembly in succession, an advancing mechanism for advancing the blister strip by a predetermined distance each time the advancing mechanism is engaged, and an engaging element for engaging the advancing mechanism to advance the blister strip. The blister track includes a primary coil structure, a secondary coil structure, and a tertiary coil structure.

Abstract: A patient interface has a single loop headstrap and a mask for covering at least the nostrils of the user. The single loop headstrap extends from the mask at either end. A short length of supple conduit is coupled to the mask by a swivel or ball joint to allow rotation of the conduit relative to the mask through different angles and orientations.

Abstract: A system and method for automated inspiratory muscle strength exercise includes software for setting a mechanical ventilator for a pressure regulated breath with an initial pressure target that is at the highest pressure setting a patient can tolerate and increasing the pressure target as tolerated.

Abstract: A breathing mask arrangement includes an arch body, a sealing lip means for bearing against the surface of the face of a mask user, a respiratory gas conduit means for feeding respiratory gas to a mask internal space which is defined by the arch body and which is in communication with the nose and/or mouth opening of the user of the mask, and an application structure for application of the sealing lip means jointly with the arch body, wherein the application structure has a carrier portion on which a respiratory gas conduit member is releasably coupled.

Abstract: A pressure support device implements compensation for variations in air density of its operating environment. A pressurized flow of breathable gas is generated for delivery to the airway of a subject. One or more parameters associated with the ambient environment of the pressure support device are determined. These parameters can include one or more of an ambient barometric air pressure, an ambient air temperature, or ambient air humidity. In some embodiments, one or more assumed parameters associated with the ambient environment of the pressure support device are determined based on typical sleeping conditions of the subject. An ambient air density of the ambient environment of the pressure support device is estimated based on one or more of the parameters and/or assumed parameters. A flow rate of the pressurized flow of breathable gas is adjusted based on the estimated ambient air density of the ambient environment of the pressure support device.

Abstract: Systems and methods for compensating long term sensitivity drift of catalytic type electrochemical gas sensors used in systems for delivering therapeutic nitric oxide (NO) gas to a patient by compensating for drift that may be specific to the sensors. In at least some instances, the long term sensitivity drift of catalytic type electrochemical gas sensors can be addressed using calibration schedules, which can factor in the absolute change in set dose of NO being delivered to the patient that can drive one or more baseline calibrations. The calibration schedules can reduce the amount of times the sensor goes offline. Systems and methods may factor in actions occurring at the delivery system and/or aspects of the surrounding environment, prior to performing a baseline calibration, and may postpone the calibration and/or rejected using the sensor's output for the calibration.

Abstract: Systems and methods for providing respiratory therapy with varying flow rates are disclosed. A system comprises a source of breathing gas, a patient interface, and a flow control device. The flow control device is configured to automatically change a rate of the flow of breathing gas. The flow control device may vary the rate of the flow of breathing gas at a frequency slower than a frequency of breathing of the patient. A method comprises coupling a patient interface to the patient, providing the flow of breathing gas to an inlet port of the patient interface, and automatically changing a rate of the flow of breathing gas with a flow control device in communication with the flow of breathing gas. The method may also comprise varying the rate of the flow of breathing gas at a frequency slower than a frequency of breathing of the patient.

Abstract: It is discloses a patient interface 3000 comprising a seal forming portion 11, a pad 10, and a cushion 20. The seal forming portion 11 may comprise a base surface 111 and a plurality of fibers 112 fixed to and extending away from said base surface 111 for contacting a patient's skin. The cushion 20 may comprise at least along a portion of the circumference a first structure 22 having an elongate section 24 joined with at least one end section 26 oriented substantially perpendicular or at an angle to the elongate section 24. A first end A of the elongate section 24 may be connected or connectable to a frame member 30. The end section 26 may be provided at an opposing second end B of the elongate section 24. The pad 10 may comprise a resilient foam material layer with the seal forming portion 11. The pad 10 may be adapted to be connected to the cushion 20.

Abstract: A system and a method for generating a respirable dry powder aerosol (15) from a liquid solution or liquid suspension at a respirable dry powder aerosol volume flow (91). A liquid aerosol generating nozzle (3) generates from the liquid solution or liquid suspension a liquid aerosol (13) that is diluted by dilution gas (4) and dried in a cylindrical evaporation chamber (6) to generate a dry powder aerosol (14) that is subsequently concentrated by a cylindrical single linear slit aerosol concentrator (9). The system and method may include heliox as a gas, specifically dilution gas (4), for enhancing both the drying process in the cylindrical evaporation chamber (6) and for enhancing the concentration efficiency, but also as a nozzle gas (2) for enhancing generating the liquid aerosol (13) from the liquid solution or liquid suspension.

Abstract: Systems and methods for compensating long term sensitivity drift of catalytic type electrochemical gas sensors used in systems for delivering therapeutic nitric oxide (NO) gas to a patient by compensating for drift that may be specific to the sensors. In at least some instances, the long term sensitivity drift of catalytic type electrochemical gas sensors can be addressed using calibration schedules, which can factor in the absolute change in set dose of NO being delivered to the patient that can drive one or more baseline calibrations. The calibration schedules can reduce the amount of times the sensor goes offline. Systems and methods may factor in actions occurring at the delivery system and/or aspects of the surrounding environment, prior to performing a baseline calibration, and may postpone the calibration and/or rejected using the sensor's output for the calibration.

Abstract: The invention relates to a respiratory circuit appliance with a respiratory line, a CO2 absorber (6) in the respiratory line, and a cooling device for cooling the respiratory gas after it exits the CO2 absorber. Provision is made that the cooling device cools a heating pump with a compressor (33) for compressing/condensing a cooling medium, a condenser (30), which receives the condensed cooling medium, and in so doing releases heat to the surroundings, and with a heat exchanger body (8) which receives the cooled cooling medium and is in heat-conducting contact with a section of the respiratory line.

Abstract: A respiratory mask (10) for delivering inspiratory gas to a wearer, the mask comprising a mask body (12) shaped to define a cavity adapted to fit about the mouth and nose of the patient, wherein the mask body comprises a nose cavity portion (18) and a mouth cavity portion (16), the nose cavity portion comprising an inspiratory gas inlet port (26) and wherein the mouth portion comprises an expiratory gas monitoring port (34) at a location spaced from the inlet port. The gas monitoring port and may comprise an integral connector for a monitoring line and may be used to monitor carbon dioxide levels.

Abstract: A closed circuit breathing apparatus (2) and a method of operating the same, the method comprising: determining whether a sufficient amount of replenishing gas is being supplied to a breathing circuit (4); sensing pressure within the breathing circuit (4) using a pressure sensor (6); generating a pressure signal representative of the sensed pressure; determining whether the pressure signal is representative of breathing; and generating an alert if it is determined that both an insufficient amount of replenishing gas, such as oxygen, is being supplied to the breathing circuit (4) and that the pressure signal is representative of breathing.

Abstract: Described are systems and methods for compensating long term sensitivity drift of catalytic type electrochemical gas sensors used in systems for delivering therapeutic nitric oxide (NO) gas to a patient by compensating for drift that may be specific to the sensors atypical use in systems for delivering therapeutic nitric oxide gas to a patient. The long term sensitivity drift of catalytic type electrochemical gas sensors may be addressed using calibration schedules, which can factor in the absolute change in set dose of NO being delivered to the patient that can drive one or more baseline calibrations. The calibration schedules can be used to reduce the amount of times the sensor goes offline.

Abstract: A tool for inserting an endotracheal tube, comprising a tubular sheath defining therein a longitudinally extending lumen, is provided. The tool comprises a longitudinal insertion member, and a guide member configured to facilitate relative longitudinal motion between the insertion member and the endotracheal tube when the insertion member is received within its lumen.

Abstract: The present disclosure pertains to an exhalation valve system (10) configured to control gas flow during exhalation of a subject (12). In some embodiments, the system comprises one or more of a pressure generator (14), a subject interface (16), one or more sensors (18), one or more processors (20), electronic storage (22), user interface (23), and/or other components. The system is configured to adjust a rebreathing level of the subject based on detected occurrences of disordered breathing events. By rebreathing exhaled air (and/or other breathable gas) a subject may minimize and/or prevent central sleep apneas. The system monitors the breathing of the subject to detect occurrences of respiratory events related to central sleep apnea. The system monitors accumulated retrograde breathing and adjusts the volume of exhaled rebreathing and/or other system settings affecting the subject's breathing. Through these adjustments, the system may prevent and/or reduce respiratory events related to central sleep apnea.

Abstract: A nebulization structure includes a carrier unit, a vibration unit, a nebulization unit and a position-limiting unit. The carrier unit has a first carrier portion and a first surrounding portion extended from an outer perimeter of the first carrier portion, and the first carrier portion has a through hole. The vibration unit includes an annular vibrating sheet disposed on the carrier unit. The nebulization unit is disposed on the first carrier portion, and the nebulization unit has a plurality of micro holes communicated with the through hole. The position-limiting unit has a first position-limiting portion disposed on the nebulization unit and a second position-limiting portion extended from an outer perimeter of the first position-limiting portion and along the first surrounding portion. The nebulization unit is positioned between the first carrier portion and the position-limiting unit, and the first position-limiting portion has an opening for exposing the micro holes.

Abstract: Devices and methods for delivering air to a patient are provided. A device includes a first portion having a first airflow inlet and a first impeller configured to move in response to airflow from the first airflow inlet contacting the first impeller, the first portion defining a first airflow path; a second portion having a second airflow inlet, a second impeller, and an outlet for communicating airflow to a patient, the second portion defining a second airflow path; and means for coupling the first portion and the second portion, such that movement of the first impeller causes corresponding movement of the second impeller, wherein the second impeller is configured to impel air through the second airflow inlet and out of the outlet to the patient, upon movement of the second impeller and wherein the first and second airflow paths are not in fluid communication.

Abstract: The present invention provides an improved filter connection system for a gas mask, comprising: a filter, a mounting means that attaches the filter to the gas mask, and a retainer means to hold the filter within the mounting means. The mounting means includes a protruding means; a valving assembly in communication with the protruding means, wherein the valving assembly enables air to flow from the fitter to the mask when the retainer means retains the protruding means, and disables air flow from the filter to the mask when the protruding means disengages from the retainer means; and a sealing means located within or adjacent to the valving assembly to prevent air from outside of the filter from entering the mounting means.