The present technology relates generally to cough-assist devices with humidified cough assistance. In one example, a system includes a cough-assist device having a first phase configured to provide insufflating gas to a patient circuit and a second phase configured to draw exsufflating gas from the patient circuit. A humidifier is disposed between the cough-assist device and a distal end of the patient circuit, the humidifier including a chamber configured to contain heated water and fluidically coupled to the cough-assist device and the patient circuit. The system further includes a bypass configured to (a) direct insufflating gas from the cough-assist device through a first route to the patient circuit such that the insufflating gas is humidified in the chamber, and (b) route exsufflating gas from the patient circuit through a second route to the cough-assist device such that the exsufflating gas bypasses the chamber.

A method of predicting an unintentional leak in a respiratory system during a sleep session includes causing, during the sleep session, pressurized air to be delivered from a respiratory device to a user via a conduit coupled to a user interface. The method also includes receiving historical first data associated with pressurized air delivered from the respiratory device during one or more prior sleep sessions; receiving current first data associated with the pressurized air being delivered from the respiratory device during the sleep session; receiving historical second data associated with the user during one or more prior sleep sessions; and receiving, via one or more second sensors, current second data associated with the user during the current sleep session. The method determines, a likelihood that an unintentional leak in the respiratory system will occur within a predetermined amount of time.

The disclosed device serves for artificial respiration and has a blower connected to a control. The blower is held by a supporting part, which assumes the task of decoupling and other functions. The blower and the supporting part are arranged in a blower box. Both the control and the blower box are arranged in a housing. The control is connected to at least one indicating device and also to at least one operating element.

Provided are concepts for controlling a high flow nasal therapy (HFNT) device used by a subject. In particular, physiological and movement parameter values of the subject are leveraged in order to generate a control signal for the HFNT device. These parameters may indicate an activity level of the subject, as well as the condition of the subject, providing information useful for setting appropriate operating conditions of the HFNT device. Thus, a means for automatically controlling a HFNT device based on needs of the subject may be provided, improving subject comfort during therapy, and ease of use of the HFT device.

A system is provided for delivering gas to a patient during a medical procedure. The system comprises a heater arranged to heat at least one of the gas and a humidification liquid. The system comprises a controller arranged to control the system according to a first mode during delivery of a first flow rate of gas and a second mode during delivery of a second flow rate of gas. The controller monitors an electrical characteristic of the heater to select the mode of operation and/or to determine an operating state of the system.

The present technology relates generally to cough-assist devices with humidified cough assistance. In one example, a system includes a cough-assist device having a first phase configured to provide insufflating gas to a patient circuit and a second phase configured to draw exsufflating gas from the patient circuit. A humidifier is disposed between the cough-assist device and a distal end of the patient circuit, the humidifier including a chamber configured to contain heated water and fluidically coupled to the cough-assist device and the patient circuit. The system further includes a bypass configured to (a) direct insufflating gas from the cough-assist device through a first route to the patient circuit such that the insufflating gas is humidified in the chamber, and (b) route exsufflating gas from the patient circuit through a second route to the cough-assist device such that the exsufflating gas bypasses the chamber.

An apparatus for treating a respiratory disorder in a patient includes a power supply, a first power supply circuit coupled to the power supply, a pressure generator to generate a flow of air, a transducer to generate a flow signal representing a property of the flow of air, and motor power supply circuitry. The motor power supply circuitry includes: a motor controller to control operation of a motor in the pressure generator based on the flow signal; one or more storage elements to store energy generated by motor deceleration; an energy dissipation circuit to dissipate a portion the energy generated by the deceleration of the motor; and an energy transfer circuit to couple the one or more storage elements to the first power supply circuit and transfer the energy generated by motor deceleration and/or the energy stored by the one or more storage elements to the first power supply circuit.

A newborn respiration monitoring system includes a flow sensor that measures a gas flow and a CO.sub.2 sensor that measures a CO.sub.2 within the breathing circuit for an infant. The system further includes a resuscitation module executable on a processor of a computing system to receive the flow measurement and the CO.sub.2 measurement and determine respiratory information for the infant. A digital display is communicatively connected to the computing system and displays the respiratory information.

An example device comprises: a cradle to support a resuscitator bag; a paddle arm comprising: a paddle surface disposed opposite the cradle; and a pair of arms extending from the paddle surface; a housing comprising: top, bottom, front and rear sides, and an opening at the front side, towards the top side; the paddle surface extending through the opening; the pair of arms, of the paddle arm, rotatably attached to the housing at an end opposite the paddle surface towards the rear side; a nut assembly rotatably attached to the pair of arms therebetween; a screw threaded through the nut assembly; and a motor rotatably attached to the housing towards the bottom side of the housing; the motor configured to: drive the screw relative to the nut assembly to move the paddle arm towards and away from the cradle, to compress and release the resuscitator bag when located therebetween.

A cooling element for use within a cooling device of a closed-circuit respirator, includes an element housing, which has a liquid-tight cap and is filled with a coolant, which has a melting point below 50° C., especially below 45° C., preferably below 40° C. A sensor element is arranged in contact with the coolant within the element housing such that the sensor element can be moved in a direction of the gravity acting on the sensor element in the liquid state of the coolant during the use of the closed-circuit respirator by a user of the closed-circuit respirator.