Siemens Elema Ab

Siemens Aktiengesellschaft

Anders Larsson

Sven-Gunnar Olsson

Goeran Rydgren

Sven G Olsson

Stefan Brauer

Rolf Castor

Goran Rydgren

Tarmo Niininen

Patrik Jaerling

Goergan Rydgren

In a method an apparatus for vaporizing anesthetic liquids, in which a carrier gas is passed through a vaporizer so as to be saturated with vaporized anesthetic liquid, the vaporizer has a container, partially filled with anesthetic liquid, an inlet for a carrier gas, an outlet for carrier gas saturated with anesthetic and a pressure chamber. The carrier gas is supplied to the vaporizer at a pressure exceeding atmospheric pressure and is bubbled through the anesthetic liquid in the container in order to become saturated with anesthetic. The flow of gas at the outlet can be regulated as needed. Exact pressure and temperature conditions can be measured and/or regulated with a pressure meter, pressure regulator, thermometer and temperature regulator in order to regulate the partial pressure of anesthetic in the container.

Method for vaporizing an anesthetic liquid and vaporizer operating

In conjunction with the diagnosis of conditions in and treatment of the lungs, a small amount of NO is supplied to the lungs in some cases. A gas mixture for this purpose is disclosed in which an inert, non-toxic trace gas is present in an exact concentration in relation to NO, in order to simply and safely control the amount of NO then supplied to the lungs. The amount of NO supplied can be determined by determining the concentration of the trace gas. A method and device for administering breathing gas to a patient together with the aforementioned gas mixture are also disclosed.

Gas mixture and device for delivering the gas mixture to the lungs of a

In a method and a ventilator device for measuring the functional residual capacity, FRC, of lungs, a trace gas is mixed with a breathing gas in a gas mixer and the mixture os fed into the lungs via an inspiratory tube. When a predetermined concentration of trace gas is achieved in the lungs, the supply of trace gas is stopped, and a washout phase starts. During the washout phase, the concentration of trace gas in expired gas and the flow of expired gas are measured. The measurement values are sent to an analyzer which calculates the volume of trace gas in the lungs. Functional residual capacity can then be determined from the calculated volume of trace gas. The trace gas is preferably SF.sub.6.

Method for determining the functional residual capacity of lungs and a

A device which supplies breathing gas mixed with an additive gas to a patient for pulmonary diagnosis or pulmonary treatment includes a gas mixing unit through which a relatively large flow of breathing gas is achieved from a first gas source through a first pressure regulator and a second pressure regulator. The breathing gas passes through a connecting tube from which the patient can breathe spontaneously through an inspiration tube, thereby inhaling air from the connecting tube. Expired gas passes via an expiration tube to the connecting tube. Additive gas is supplied from a separate gas source via a second pressure regulator and a second flow regulator. The additive gas is supplied in a flow which is considerably smaller than the flow of breathing gas, permitting a very small but accurate concentration of the additive gas to be achieved in the breathing gas. The large flow prevents a reactive additive gas from reacting before being supplied to the patient.

Device for supplying breathing gas to the lungs of a respiratory subject

A method and apparatus for independent monitoring of a flow-through quantity and, potentially, of a concentration of a gas flow that is extremely small in comparison to a respiratory gas flow is provided. The valve for the control of this small gas flow can not be controlled via the overall gas flow. In order to be able to simply and reliably monitor the flow-through quantity and the concentration of this small gas flow without a gas analyzer and independently of gas flow regulators that are usually present, it is provided that the small gas flow be separately measured and compared to a value derived from the respiratory gas flow. Given the presence of prescribable criteria, an alarm is triggered and the flow-through quantity of the small gas flow is, for example, interrupted.

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Kaevlinge, Sweden

Anders Larsson