The present invention offers various advantages as it allows switching of the position of the valve to allow release of selective inhalation-air from the air-reservoir. This principle is utilized in restoring the blood flow, accelerate tissue regeneration, improve physical performance, improve fluid intelligence, disease avoidance, disease recovery. The apparatus is useful for athletes to do altitude contrast training.

Embodiments of the present invention provide systems and methods for delivering respiratory treatment to a patient. For example, a treatment system may include a mechanism for delivering a positive pressure breath to a patient, and one or more limb flow control assemblies which modulate gas flow to and from the patient. Exemplary treatment techniques are embodied in anesthesia machines, mechanical ventilators, and manual ventilators.

A method of controlling a flow rate of gases supplied to a patient by a respiratory assistance device includes controlling the supply gases flow rate so as to deliver gases to the patient according to a predetermined gases pressure/flow rate profile for at least a portion of the breathing cycle. A profile may be achieved that provides the patient with a particular benefit or therapy.

The present invention relates to a device for positive pressure ventilation (PPV) and continuous positive airway pressure (CPAP) treatment comprising a fresh gas flow inlet, arranged to receive a fresh gas flow from a 5 fresh gas flow tube connectable thereto; a patient interface end, which is connectable with a patient interface; an outlet comprising an open end; a CPAP generator comprising first, second, and third connection portions, wherein the first connection portion is connected with the fresh gas flow inlet, the second connection portion is connected with the patient interface end, 10 and the third connection portion is connected with the outlet, wherein the CPAP generator is arranged to provide a primary fresh gas flow when receiving the fresh gas flow from the fresh gas flow inlet, and a generated CPAP level is adjustable by varying the fresh gas flow. The device further comprises a secondary flow channel comprising first and second ends, the 15 first end being connected with at least one of the second connection portion, the third connection portion, and the patient interface end, wherein the secondary flow channel is configured to provide a secondary fresh gas flow to be added, at least in the PPV mode, to the primary fresh gas flow; and a flow resistor arranged between the outlet and the first end of the secondary 20 flow channel to provide a resistance to a flow in a direction towards the outlet.

A nitrous oxide gas mixer includes at least one mixing chamber having at least one nitrous oxide gas connection and at least one oxygen gas connection for introduction of oxygen gas and nitrous oxide gas and at least one flow rate controller, by which a volume flow of the two gases can be respectively adjusted separately and/or together.

At least one O.sub.2 emergency button is mounted to the mixing chamber for emergency flooding the mixing chamber with oxygen gas and/or with ambient air.

An electronic flow monitor, a control method and an anesthesia machine. The electronic flow controller can comprise a control module, an oxygen gas branch for delivering oxygen gas, an equilibrium gas branch for delivering equilibrium gas, and a gas mixing branch for mixing the oxygen gas and the equilibrium gas. The control module can meter an oxygen gas flow and an equilibrium gas flow through flow sensors. A first flow controller can be disposed in the oxygen gas branch, and a second flow controller can be disposed in the equilibrium gas branch. The first flow controller may be used to regulate the gas flow in the oxygen gas branch between zero and a maximum value and the second flow controller may be used to regulate the gas flow in the equilibrium gas branch between zero and a maximum value.

Systems and methods provide a self-contained, intermittent positive airway pressure system for treating sleep apnea, snoring, and other respiratory disorders. The systems and methods provide an air flow director that can be worn in or over the nose of the individual in communication with an upper airway. The systems and methods provide an airflow regulation assembly that can also be worn in its entirety by the individual in communication with the air flow director. The airflow regulation assembly includes a source of positive pressure. The airflow regulation assembly intermittently operates the source of positive pressure to increase positive air pressure in the air flow director sufficient to resist tissue collapse in the upper airway during only a portion of the respiratory cycle less than the entire respiratory cycle.

Systems and methods for non-invasive ventilation are provided. The systems may include a gas source that provides breathing gases to a patient through one or more of a primary flow path (PFP) and a flushing flow path (FFP). The system may include a control assembly configured to open and restrict gas flow through the PFP. When the PFP is open, a significant portion of the gas flows through the PFP while the remaining gas flows through the FFP. When the PFP is restricted, a significant portion of the gas flows through the FFP. Increased flow through the FFP may have a high velocity (especially relative to the flow through the PFP). Gas delivered through the FFP may be used to flush dead space. One or both flow paths may contribute to inspiratory positive airway pressure (IPAP), expiratory positive airway pressure (EPAP), and/or positive end expiratory pressure (PEEP).

A method and system for controlling patient recovery from anesthesia with an inhalation anesthesia agent are provided, wherein the patient during the recovery is ventilated with a ventilator, and the method comprises decreasing inhalation anesthesia agent concentration in the patient breathing gas to a level enabling patient spontaneous breathing, monitoring the expiration of the patient to determine at least the expiratory O2 concentration, determining a target level for the expiratory O2 level for the patient during recovery, comparing the determined expiratory O2 concentration with the target level for the expiratory O2 level for the patient, and controlling the O2 concentration in the ventilation gas to allow the expiratory O2 level for the patient to match the target level for the expiratory O2 concentration.

A nitrous oxide gas mixer includes at least one mixing chamber having at least one nitrous oxide gas connection and at least one oxygen gas connection for introduction of oxygen gas and nitrous oxide gas and at least one flow rate controller, by which a volume flow of the two gases can be respectively adjusted separately and/or together. At least one O.sub.2 emergency button is mounted to the mixing chamber for emergency flooding the mixing chamber with oxygen gas and/or with ambient air.