A pressure support device (4) for providing pressure support therapy to a patient includes a pressure generating system (6, 18) structured to generate pressure to provide pressure compensation to the patient via a patient circuit (12, 14), one or more sensors (22, 27, 28) structured to gather data indicative of disordered breathing events of the patient, and a processing unit (24) structured to control the pressure generating system to provide a pressure compensation regimen to the patient; to analyze outputs of the one or more sensors while pressure support therapy is provided to the patient to determine if the pressure compensation regimen provided to the patient is effective to relieve one or more disordered breathing events, and to output an alert if it is determined that the pressure compensation regimen provided to the patient is not effective in relieving the one or more disordered breathing events.

A portable medical ventilator using pulse flow from an oxygen concentrator to gain higher oxygen concentration includes a positive pressure source to deliver pressurized air to the patient and a negative pressure source to trigger the oxygen concentrator. A patient circuit attached to a patient interface mask connects the ventilator to the patient. The ventilator includes a controller module that is configured to generate a signal to the negative pressure device to trigger the concentrator to initiate one or more pulses of oxygen from the oxygen concentrator. The oxygen pulses are delivered to the patient interface directly through multi-tube or a multi lumen patient circuit. The oxygen does not mix with air in the ventilator or in the patient circuit and bypasses the leaks in the patient circuit and/or patient interface.

The present disclosure describes a bi-valve for use with a flowmeter or other source of oxygen or other medical gas, that allows a medical practitioner to easily and quickly switch from delivering oxygen or other gas from the flowmeter or other gas source to a given mask or other device, to another mask or other device. This is accomplished far faster and easier than is done under current practice. Current practice results in the patient being off oxygen or other gas for a short, but very significant period of time, which poses a serious risk of desaturation in the patient. The bi-valve may include a casing, an inlet, and two outlets, with a knob for selecting which output the oxygen or other gas is to be delivered to. The device may be a very simple ball valve device, with the only moving parts being the knob and the ball.

A flow generator is configured to pressurize a flow of breathable gas to within a range of about 2-30 cm H.sub.2O for delivery to a patient's airways. The flow generator includes a blower with at least one impeller and a motor configured to drive the at least one impeller. The flow generator also includes a substantially planar blower mount configured to support the blower. The blower mount includes a flexible blower receptacle portion configured to receive and support the blower. The blower receptacle portion includes an outlet opening that is axially aligned with an air outlet of the blower. The flow generator also includes housing that encloses the blower and the blower mount. The housing has an inner surface that engages a perimeter of the blower mount.

The invention relates to a respiratory device (10) for the artificial respiration of a patient (12), comprising: —a respiration gas source assembly (15, 62), —a flow-changing device (16), —a humidifier device (38) which is designed to increase the value of the absolute humidity of the inspiratory respiration gas flow (AF), said humidifier device (38) having a liquid store (40) and an evaporation device (76) with a variable output for this purpose, —a respiration gas line assembly (30), —a proximal temperature sensor (48) which detects the temperature of the respiration gas flow (AF) in the proximal longitudinal end region (30a) of the respiration gas line assembly (30), —a humidity sensor assembly (66) which directly or indirectly detects the absolute humidity of the inspiratory respiration gas flow (AF), —a flow sensor (44), and —a controller (18) which is designed to control the operational output of the evaporation device (76)

A relay administration device 50 for use in connection to a nitric oxide administration device 20 which supplies NO generated from air, includes an NO densitometer 506, a flowmeter 507 or pressure gauge 504, a control unit 600 which calculates a dosage of NO to be administered to a patient based on an NO concentration measured by the NO densitometer 506 and a value of the flowmeter 507 or the pressure gauge 504, and a two-way valve 505 which is configured to increase a flow rate when the calculated dosage is less than a predetermined value and to decrease the flow rate when the calculated dosage is greater than a predetermined value.

A ventilation therapy apparatus and a control method, includes: an apparatus body, a respiratory pipe and a patient interface. The apparatus body further includes: a signal acquisition module, a target pressure acquisition module and a first control module. The signal acquisition module is configured for acquiring an output pressure value and an output flow value of a signal collection point of the apparatus body; the target pressure acquisition module is configured for acquiring a target pressure value at the patient interface; the first calculation module is configured for, calculating an actual pressure value at the patient interface according to the output pressure value and the output flow value of the signal collection point; the first control module is configured for adjusting an output flow of the apparatus body according to the actual pressure value and the target pressure value. In the present disclosure, it is capable to determine the actual pressure value at the patient interface by the output parameters feedback of the signal collection point of the apparatus body, and determine the patient's respiratory state according to the comparison between the actual pressure value and the target pressure value, and output the gas with a corresponding threshold, therefore the gas pressure of the airflow received by the patient may reach a preset target pressure range, and achieve the therapeutic effect.

A connection device, for mechanical ventilation and monitoring of spontaneous breathing of a patient (P), includes a fluid-guiding unit (9, 11, 15) and establishes a fluid connection between a medical arrangement (100) and a patient-side coupling unit (19). A volume flow sensor (90) measures an indicator of volume flow of fluid through the fluid-guiding unit. A volume flow sensor component (2) engages with an interior of the fluid-guiding unit. A homogenization unit (10) is nonrotatably inserted into the interior between the patient-side coupling unit and the component and includes two sieves and a connection element, which connects the sieves together. The homogenization unit homogenizes the flow of fluid through the fluid-guiding unit. An inner profile of the fluid-guiding unit and an outer profile of the homogenization unit together form a mechanical coding, which determines a defined rotation position of the homogenization unit in relation to the fluid-guiding unit.

The present technology is directed to ventilator systems that can provide both ventilation therapy and oxygen therapy. The systems described herein may include a ventilation assembly that can provide inspiratory gas to a patient circuit and an oxygen assembly that can provide pulses of oxygen to an oxygen delivery circuit. In some embodiments, the oxygen delivery circuit is distinct from the patient circuit. For example, the patient circuit can include a corrugated conduit coupled a ventilation mask, and the oxygen delivery circuit can include a nasal cannula. The ventilation mask can be positioned over the nasal cannula so that the patient can receive both the inspiratory gases and the pulses of oxygen.

The present invention relates to an electrically operable resuscitation device comprising a piston/cylinder assembly including a rigid cylinder including at least one gas inlet and at least one gas outlet, a piston to travel in said cylinder, and at least one valve, the or each valve configured to allow gas to be displaced into said cylinder through said at least one gas inlet during at least one of a first stroke direction and second stroke direction of said piston in said cylinder, and for allowing gas to displaced through said at least one gas outlet during an opposite of said at least one of the first stroke direction and second stroke direction of said piston in said cylinder; a motor, selected from one of a stepper motor and feedback motor and stepper motor with feedback and linear motor, operatively connected to said piston to move said piston in said cylinder; a patient interface in ducted fluid connection with said piston/cylinder assembly to receive gas via said at least one gas outlet and to deliver said gas to said patient.