The present technology relates to the field of medical monitoring, and, in particular, to non-contact detecting and monitoring of patient breathing. Systems, methods, and computer readable media are described for calculating a change in depth of a region of interest (ROI) on a patient. In some embodiments, the systems, methods, and/or computer readable media can identify steep changes in depths. For example, the systems, methods, and/or computer readable media can identify large, inaccurate changes in depths that can occur at edge regions of a patient. In these and other embodiments, the systems, methods, and/or computer readable media can adjust the identified steep changes in depth before determining one or more patient respiratory parameters.

A patient interface is configured to deliver a pressurized flow of respiratory gas to a patient's airways. The patient interface includes a cradle base configured to cradle the patients nose in use. Two protrusions extend from the cradle base and are configured to be inserted into the patients nares in use. Each of the protrusions have formed therein an opening configured to allow a continuous flow of air therethrough. In addition, a plenum base forms a plenum chamber together with the cradle base. The cradle base is configured so that movement of the cradle base is decoupled from the plenum base.

One or more sensors are configured for detection of characteristics of moving objects and living subjects for human identification or authentication. One or more processors, such as in a system of sensors or that control a sensor, may be configured to process signals from the one or more sensors to identify a person. The processing may include evaluating features from the signals such as breathing rate, respiration depth, degree of movement and heart rate etc. The sensors may be radio frequency non-contact sensors with automated detection control to change detection control parameters based on the identification of living beings, such as to avoid sensor interference.

A device and method of generating an enriched gas within a nasal vestibule of a patient includes a housing, a chamber, a chamber inlet, a pump, a molecular sieve bed, a release outlet, and a breath duct. The chamber is configured to be received within the nasal vestibule. The pump is configured to direct an ambient air from an ambient environment into the chamber. The molecular sieve bed is positioned within the chamber and configured to collect a predetermined molecule from the ambient air thereby generating the enriched gas. The release outlet is configured to discharge the enriched gas from the chamber into the nasal vestibule. The breath duct longitudinally extends through the housing such that the breath duct is configured to fluidly communicate a fluid flow through the housing for nasal breathing by the patient while the chamber is positioned within the nasal vestibule.

In an example, a ventilator includes a first container and a second container in fluidic communication with each other via a liquid. The second container includes a second container space surrounded by the second container and a second liquid surface. A hydrostatic pressure in the second container space results from a pressure differential defined by a difference between the first liquid surface elevation in the first container and the second liquid surface elevation. The second container space increases in size with an increase in the breathing gas supplied from a gas supply line to the second container space. An inhalation line is configured to open to permit a flow of the breathing gas from an inhalation inlet in the second container space to an inhalation outlet outside of the liquid and outside of the second container and coupled to a patient, causing the second container space to decrease in size.

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 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.

The present disclosure pertains to a method and system configured for cough synchronization in a mechanical insufflation-exsufflation system. The system is configured to synchronize (712) the transition from an insufflation mode to an exsufflation mode to a patient initiated cough by detecting cough effort of the patient e.g. at the end of the insufflation phase. The detection of cough effort of the patient is based on one or more parameters associated with gas in the system. Upon detecting that the patient is initiating a cough, the system automatically switches the insufflation mode to the exsufflation mode to assist the patient to generate an effective cough.

Systems and methods for producing oxygen enriched air using vacuum pressure swing adsorption (VPSA) are disclosed. In one implementation, an oxygen concentrator includes a canister system having at least one canister, a pumping system having at least one motor-controlled pump, a set of valves pneumatically coupling the canister system and the pumping system, and a controller. The canister is configured to receive a gas separation adsorbent. The controller is configured to control operation of the pumping system and the set of valves to: selectively pneumatically couple the motor-controlled pump and the canister so as to pressurize the canister and selectively pneumatically couple the motor-controlled pump and the canister so as to evacuate the canister.

A portable oxygen concentrator includes a compressor and a controller. The compressor includes a motor, at least one chamber, and at least one piston operably coupled to the motor and movable within the at least one chamber. In some embodiments, the controller is configured to: determine actual motor speeds for commutations steps of the motor during a first rotational cycle; determine an average motor speed during the first rotational cycle; determine a voltage pattern based at least on a comparison of the average motor speed during the first rotational cycle and the actual motor speeds for the commutation steps of the motor during the first rotational cycle; and cause the voltage pattern to be applied to the motor during a second rotational cycle to reduce differences between applied motor torque and variable torque load imparted by the at least one piston.