The present disclosure provides techniques for a ventilator system with a removable airway. A ventilator system may include a removable airway and a base unit. The removable airway may include an air inlet port, a patient inhalation port, an air exhaust port, a patient exhalation port, a first portion of a pressure sensor, and a first portion of a flow sensor. The base unit may include two pinch valves, a second portion of the pressure sensor, and a second portion of the flow sensor. In some cases, the airway does not comprise any openings other than the air inlet port, the air exhaust port, the patient inhalation port, and the patient exhalation port. In some cases, air inside the removable airway does not contact any part of the base unit without first exiting the air exhaust port.

The present disclosure provides techniques for a ventilator system with a removable airway. A ventilator system may include a removable airway and a base unit. The removable airway may include an air inlet port, a patient inhalation port, an air exhaust port, a patient exhalation port, a first portion of a pressure sensor, and a first portion of a flow sensor. The base unit may include two pinch valves, a second portion of the pressure sensor, and a second portion of the flow sensor. In some cases, the airway does not comprise any openings other than the air inlet port, the air exhaust port, the patent inhalation port, and the patient exhalation port. In some cases, air inside the removable airway does not contact any part of the base unit without first exiting the air exhaust port.

Presented are manual ventilator systems, methods for making/using such ventilator systems, and clamshell, accordion-style ventilators operable by a lone operator. A ventilator device includes first and second panels pivotably attached together in a clamshell configuration. Each panel has an inlet port, an outlet port, and an internal channel that fluidly connects the inlet and outlet ports. A one-way valve is fluidly connected to the first panel’s outlet port and restricts airflow therethrough in one direction. Another one-way valve is fluidly connected to the second panel’s inlet port and restricts airflow therethrough in an opposite direction. A concertinaed bellows is fluidly connected to the first panel’s outlet port and the second panel’s inlet port. The bellows is sandwiched between and attached to the two panels such that pivoting the panels away from each other expands and fills the bellows whereas pivoting the panels towards each other compresses and evacuates the bellows.

A patient interface for delivering breathable gas to a patient includes a sealing portion including a nose tip engagement portion adapted to form a seal with the patient's nose tip, an upper lip engagement portion adapted to form a seal with the patient's upper lip and/or base of the patient's nares, and nostril engagement flaps adapted to form a seal with the patient's nares. The nose tip engagement portion, the upper lip engagement portion, and the nostril engagement flaps are all structured to extend or curve outwardly from a supporting wall defining an air path.

The technology relates to a variable flow vent assembly for a conduit mask configured to deliver a flow of breathable gas at a positive pressure to an airway entrance of a patient and allow a flow of exhaled gas from the airway of the patient to exit the vent assembly to ambient. The variable flow vent assembly is further configured to include a valve, wherein the valve is arranged to allow for the regulation of the flow of breathable gas to the patient and the regulation of the vent flow rate of exhaled gas leaving the vent assembly to ambient. By changing certain characteristics of the valve and by tuning the valve through variants in design, the resultant vent flow rate for a given air pressure can be altered in order to obtain the best treatment outcome for the patients individual requirements.

A CPAP device is configured to deliver a pressurized flow of respiratory gas to a patient's airways and includes a flow generator with a blower configured to pressurize the flow of respiratory gas. A flexible face seal is positioned at an outlet end of a blower discharge path. The flexible face seal includes an aperture and a lip curling inwardly from a perimeter of the flexible face seal. A tub configured to hold a body of water and humidify the pressurized flow of respiratory gas includes a heat conducting base plate and a side wall. A base supports both the flow generator and the tub and includes a floor with a heater plate and a spring biased catch configured to secure the tub to the base. The spring biased catch is configured so that applying a downward force on the tub so that the tub presses against the floor of the base secures the tub to the base and allows the tub to be released from the base.

The present disclosure pertains to a system and method for facilitating pressure support therapy, mechanical inexsufflation therapy, and suctioning therapy for a subject. The system and method described herein offer a novel combination of mechanical inexsufflation with suctioning from a vacuum system. The invasive nature of current closed suctioning systems poses many potential risks, such as tissue trauma, less optimum secretion clearance at the peripheral airway, and lung decruitment. The system and method described herein provide a non-invasive method of suctioning with a suctioning volume measurement and a monitoring alarm to ensure a baseline lung volume and a positive end expiratory pressure (PEEP) level are maintained. This non-invasive method of suctioning is provided together with mechanical inexsufflation and pressure support therapy.

A respiratory pressure therapy (RPT) device for pressurising breathable air to treat a respiratory disorder in a patient includes a pressure generator configured to pressurise breathable air, an RPT device inlet configured to receive breathable air from externally of the RPT device to be pressurised by the pressure generator, an RPT device outlet configured to be connected to an air circuit to direct breathable air pressurised by the pressure generator to the patient, a dock having a dock outlet and a dock inlet, and an external housing to enclose the pressure generator. The external housing forms an opening sized to alternatively receive an end cap or a water reservoir.

A CPAP device includes a flow generator with a blower configured to pressurize the flow of respiratory gas. A flexible face seal is positioned at an outlet end of a blower discharge path. The flexible face seal includes an aperture and a lip curling inwardly from a perimeter of the flexible face seal. A tub configured to hold a body of water and humidify the pressurized flow of respiratory gas includes a heat conducting base plate and a side wall. The side wall has a substantially flat portion that surrounds an air inlet opening. A base supports both the flow generator and the tub and includes a floor with a heater plate. A laterally positioned guide prevents the tub from being removed from the base in a vertical direction and includes a pair of C-shaped channel portions with open sides that face each other.

A water reservoir includes a reservoir base configured to hold a predetermined maximum volume of water to be used for humidification of pressurized breathable air, a reservoir lid pivotally connected to the reservoir base to allow the water reservoir to be movable between an open position and a closed position, the reservoir lid comprising an inlet and an outlet, and a seal configured to sealingly engage the reservoir lid and the reservoir base when the water reservoir is in the closed position, wherein the reservoir base includes an overfill protection element having an egress path for water at a predetermined location.