The present disclosure pertains to a system (10) configured to prevent damage from liquid spills in a humidified pressure support therapy device (50). The system is configured to decouple a humidification chamber (42) in a humidifier from a pressure generator (14) of the pressure support therapy device when a cover (48) of the humidifier is opened. This eliminates and/or reduces the possibility of liquid in an overfilled humidification chamber unintentionally and/or otherwise entering the pressure generator and damaging sensitive mechanical and/or electrical components. In some embodiments, the system includes one or more of the pressure generator, the humidifier, a subject interface (16), a sensor (18), a decoupler (100), a processor (20), electronic storage (22), a user interface (24), and/or other components.

Apparatus (20) for fitting to the machine end of a tracheostomy tube (10) includes both an HME and a speaking valve (30). The HME includes two exchange elements (28, 29) at opposite ends of a housing (23) extending laterally of a coupling (25) for fitting on the tube. The speaking valve has a cylindrical sleeve (31) extending across the housing midway along its length and in line with the tube. The sleeve is rotatable about its axis and has two openings (36) on opposite sides that can be aligned with the exchange elements of the HME to allow gas to flow from the tube through the exchange elements, bypassing the speaking valve. When the patient wishes to speak, he twists and rotates the speaking valve to block flow to the exchange elements and instead to allow air to be inhaled via the valve.

The self-inflating bag control system is characterized in that it comprises a bag controlling valve which is connected to at least two gas pumps and at least one gas parameter sensor via the gas distribution tubes. It comprises at least one gas pressing device connected to the valve via a gas parameter sensor via gas flow tubes. A control unit with a control panel is connected to the system through a gas sensor, which includes a sub-unit for setting the parameters of the gas flowing into the self-expanding bag, a measuring and analyzing the parameters of the gas flowing in the system by measuring the pressure and volume of the gas from the as parameters sensor, and a warn-alarm sub-unit, which generates a warning and/or alarm signal on the basis of the gas parameters read from the measurement and analysis subunit.

Systems and methods for collecting breathing gas properties via a medical ventilatory filter and wirelessly transmitting the data to another device. For example, the filter includes a first housing enclosing filtration media for filtering breathing gases flowing through the filter, the first housing defining a first port and a second port exposed to the breathing gases; and a sensor assembly. The sensor assembly includes a first sensor coupled to the first port, the first sensor configured to capture measurement data for a first gas property of breathing gases flowing through the filter; a second sensor coupled to the second port, the second sensor configured to capture measurement data for a first gas property of the breathing gases flowing through the filter; and a second housing. The second housing includes a processor and communication circuitry operative to wirelessly communicate the sensor data to a computing device located remotely from the filter.

A vent adaptor for a for a respiratory pressure therapy (RPT) system, the vent adaptor comprising: a vent assembly comprising: a vent housing defining a central orifice for the flow of pressurized gas to pass through the vent assembly from the delivery conduit to the patient interface, the vent housing having an annular surface around the central orifice, and the annular surface having a plurality of holes to discharge pressurized gas to atmosphere; and a membrane positioned adjacent to the annular surface; a heat and moisture exchanger (HME); and a diffusing member.

A patient interface includes a sealing arrangement adapted to provide an effective seal with the patient's nose, an inlet conduit arrangement adapted to deliver breathable gas to the sealing arrangement, and a cover that substantially encloses the sealing arrangement and/or the inlet conduit arrangement.

A conduit for a breathing circuit includes a heater associated, at least in part, with a hydrophilic layer. The purpose of the heater is to evaporate any condensed liquid collecting in the conduit, which is first sucked up by the hydrophilic layer. The heated wick reduces the risk of collected water being passed to the patient and causing choking fits or discomfit. It is preferred that the heated wick lies freely in the conduit to settle at low points in the conduit where condensation may collect.

An air delivery system for providing a supply of air from a source of air at positive pressure to an interfacing structure located at the entrance to the airways of a patient includes a manifold adapted to connect with the supply of positive air pressure and at least one tube connected to the manifold and adapted to deliver the supply of air to the interfacing structure. Each tube is structured to allow movement between an open phase in which the tube allows the passage of air and a collapsed phase in which the tube is collapsed. Each tube is structured such that weight of a typical patient's head against bedding apparel is sufficient to collapse the tube from the open phase to the collapsed phase.

An ultrasound scanning apparatus comprises an ultrasound scanning unit, an ultrasound controller for controlling the operation of the ultrasound scanning unit, detecting the operation state of the ultrasound scanning unit, generating a first enable signal when detecting that the operation state of the ultrasound scanning unit is transferred from an operating state to a non-operating state and generating a second enable signal when detecting that the operation state of the ultrasound scanning unit is transferred from the non-operating state to the operating state, and an enable output end for transmitting the first enable signal or the second enable signal to the breathing machine to control the running of the breathing machine.

In one embodiment, a method for accurate leak estimation in a flow generation system includes measuring a total flow through the flow generation system, measuring a pressure in in the primary flow circuit of the flow generation system, determining when the measured pressure is within a predetermined threshold of EPAP, and calculating an intentional leak flowrate and an unintentional leak flowrate based on the relationship Q.sub.FS(t)=Q.sub.IL(t)+Q.sub.UL(t) when the measured pressure is within the predetermined threshold. In another embodiment, a flow generation system includes in one embodiment an airflow generator connected in-line to a flow sensor, a pressure sensor and a patient interface connection by a first gas flow circuit, and a controller electrically coupled to the airflow generator, the flow sensor and the pressure sensor. The controller sends a control signal to the airflow generator based on a first flow value measured from the flow sensor and an unintentional leak flow value that is derived from a proportional relationship with an intentional leak flow value.