A breathing bag (20) has a tray section (21) and a bag section (22). The tray section (21) and the bag section enclose an inner volume (24) of variable size, the bag section dipping at least partially into the tray section to reduce the size of the inner volume. A system (10) includes the breathing bag, for a closed-circuit respirator (100), with a dispensing valve unit (40) having a dispensing valve (41) providing a quantity of gas in a breathing circuit. An actuating unit (42) is functionally connected mechanically to the dispensing valve for actuating the dispensing valve. A lever component (50) is functionally connected mechanically to the actuating unit for activating the actuating unit. A closed-circuit respirator has the system including the breathing bag and the dispensing valve unit. A process is provided for mounting the system, including breathing bag and dispensing valve unit, in the closed-circuit respirator.

Systems slow breathing with positive pressure therapy. In embodiments, a current interim breathing rate target is set, and periodically magnitude of a variable pressure waveform scaled to the current interim breathing rate target is increased if breathing rate is greater than the interim rate target to lengthen breath duration. The magnitude of the pressure increase may be a function of the difference between the interim rate target and the breathing rate. The interim rate target may be reduced in response to slowing breathing rate. The waveform cycles, inhalation to exhalation, when airflow decreases to a cycle threshold. Different interim rate targets have different cycle threshold functions that allow easier cycling as the interim rate targets decrease. Similarly, the waveform triggers, exhalation to inhalation, when airflow increases to a trigger threshold. Different interim rate targets have different trigger threshold functions that allow easier triggering as the interim rate targets decrease.

A system (10) configured to facilitate humidification of a pressurized flow of breathable gas delivered to a subject (12) comprises a pressure generator (14), a nebulizer (16), a heater (38), one or more hardware processors (22), and/or other components. The pressure generator is configured to generate a pressurized flow of breathable gas for delivery to an airway (24) within a trachea of the subject. The nebulizer is configured to provide fluid droplets (54) to the breathable gas. The heater is configured to heat a volume of the breathable gas before the droplets are supplied to the breathable gas. The breathable gas received by the subject exhibits a target temperature and humidity level at short distance d from the nebulizer due to one or more of a number of the droplets, an average size of the droplets, a gas flow rate, and/or an amount of heating power.

A ventilator system including an oxygen delivery cylinder, an air delivery unit, connecting tubes, and a digital display unit. The system further includes a Y connector configured to mix air and oxygen, to form a gas and pass said gas towards an outlet of the system. A water manometer that is configured to monitor a pressure of the gas in the system and blow off the excess pressure of the gas. A solenoid valve that is configured to adjust an end respiratory pressure obtained from a breathing device connected to the outlet of the system. The pressure of the gas being instantly delivered to the breathing device is measured by water manometer from a dead space near the outlet, thereby enabling a dual monitoring of the gas pressure being delivered to the breathing device.

A medical breathing gas delivery system design employs a manifold delivering gas in a controlled fashion to patients which includes two inhaled gas one-way valves, at least one pressure sensor for patient airway pressure monitoring, and one controlled exhalation pressure proportional control valve which may be overridden by patient exhaled pressure or if there is a power loss. The manifold is connected to a controlled source of breathing gas which may, for example, be a variable-speed fan, or a pressure-based gas flow controller with dynamic self-calibration employing a fast-acting valve and a pressure sensor, either of which yield predictable gas flow control with a minimum of components. The manifold exhalation pressure control valve and gas flow source may, for example, be controlled with a computer system which adjusts the valve power waveforms to attain the time-varying flow and pressure curves required by clinicians, then stores and displays the waveforms to enable long-term trend monitoring and alarm generation. Accurate gas mixing using the pressure-based gas flow control yields automatically calibrated mixes which are of use for patients in, for example, intensive care ventilation and in anesthesia machines for operating rooms.

A device (102) provides respiratory treatment for SDB (including mild OSA) and other respiratory conditions. A flow generator warms and humidifies gas at controlled flow levels. For example, the device (102) delivers breathable gas to the upper airway at flow rates of about 10-35 Liters/minute. Levels of flow rate, temperature and/or humidification of the device may be automatically adjusted in response to the detection of SDB events. The device may also automatically deliver adjustments of any of the levels in accordance with detected phases of respiratory cycles. In some embodiments, the device automatically delivers distinct levels to either of the nares based on independent control of flow to each nare. A warm-up procedure controls temperature and humidity at a desired target during a ramp-up of flow to the set therapy level. A cool-down procedure controls temperature above the dewpoint to avoid condensation internal to the device and patient interface.

High flow therapy is used to treat Cheyne-Stokes respiration and other types of periodic respiration disorders by periodic application of high flow therapy, adjustment of high flow therapy flow rates and/or periodic additions of CO2 or O2 into the air flow provided to the patient.

Therapy gas delivery systems that provide run-time-to-empty information to a user of the system and methods for administering therapeutic gas to a patient. The therapeutic gas delivery system may include a gas pressure sensor attachable to a therapeutic gas source that communicates therapeutic gas pressure data to a therapeutic gas delivery system controller, a gas temperature sensor positioned to measure gas temperature in the therapeutic gas source that communicates therapeutic gas temperature data to the therapeutic gas delivery system controller, at least one flow controller that communicates therapeutic gas flow rate data to the therapeutic gas delivery system controller, at least one flow sensor that communicates flow rate data to the therapeutic gas delivery system controller, and at least one display that communicates run-time-to-empty to a user of the therapeutic gas delivery system. The therapeutic gas delivery system controller of the system includes a processor that executes an algorithm to calculate the run-time-to-empty from the data received from the gas pressure sensor, temperature sensor, flow controller and flow sensor, and directs the result to the display.

Systems and methods for novel ventilation that allows the patient to trigger or initiate the delivery of a breath are provided. Further, systems and methods for triggering ventilation based on signal distortion of a monitored patient parameter are provided.

Disclosed is a device for supplying therapeutic gas, notably NO/N.sub.2 or O.sub.2/N.sub.2O mixtures, including an internal passage with a valve for conveying and controlling the flow of therapeutic gas in the internal passage, a control unit controlling the valve, a graphic display for displaying choices that can be selected by a user, and a selector, such as touch-sensitive keys displayed on the graphic display for making a selection from among the selectable choices displayed on the graphic display. The control unit is configured to count a total number of patients treated by administration of the therapeutic gas from the selection, by a user, via the selector, of a first given choice corresponding to the start of a treatment by administering the therapeutic gas to a patient concerned.