A supply arrangement (100) and a process supply a medical device (50, 90) with a supply gas mixture. The supply gas mixture includes a carrier gas and an anesthetic and is generated by an anesthetic dispenser (3). A carrier gas mixing unit (9) generates the carrier gas from at least two carrier gas components. A carrier gas switch having a regular outlet and a discharge outlet selectively directs carrier gas components to the carrier gas mixing unit or to a discharge line (35). A gas mixture switch (6), having a regular outlet (41) and a discharge outlet (42) selectively directs the supply gas mixture to the medical device or to the discharge line (35). An anesthetic concentration sensor (5.1, 5.2) measures a concentration of anesthetic in the generated gas mixture. A control unit (2) controls the gas mixture switch based on measured concentration within or outside a predefined range.

Methods and systems are provided for anesthetic agent leakage diagnostics. In one embodiment, a method for diagnosing leaks in an anesthetic vaporizer includes calculating a leakage rate based on measurements of an anesthetic agent level in a sump of the anesthetic vaporizer, the measurements received from a fluid level sensor at a first time and a second time, and outputting a maintenance alert responsive to the leakage rate exceeding a threshold.

An absorption arrangement (100) includes a CO2 absorber (4) and a water trap (2). Such an absorption arrangement (100) is used with a process for filtering carbon dioxide from a gas mixture by absorption. The gas mixture flows from a source through the absorption arrangement (100) to a sink in the following way: through a supply fluid guide unit (3), through a lower deflecting fluid guide unit (9), through the CO2 absorber (4), through an upper deflecting fluid guide unit (6), through a connecting fluid guide unit (33), through the water trap (2) and through a discharge fluid guide unit (34). The gas mixture flows vertically or obliquely upward through the CO2 absorber (4) and vertically or obliquely downward through the connecting fluid guide unit (33) to the water trap (2).

An absorption arrangement (100) includes a CO2 absorber (4) and a water trap (2). Such an absorption arrangement (100) is used with a process for filtering carbon dioxide from a gas mixture by absorption. The gas mixture flows from a source through the absorption arrangement (100) to a sink in the following way: through a supply fluid guide unit (3), through a lower deflecting fluid guide unit (9), through the CO2 absorber (4), through an upper deflecting fluid guide unit (6), through a connecting fluid guide unit (33), through the water trap (2) and through a discharge fluid guide unit (34). The gas mixture flows vertically or obliquely upward through the CO2 absorber (4) and vertically or obliquely downward through the connecting fluid guide unit (33) to the water trap (2).

A ventilation system includes an electrochemical filter for depleting alkyl phenols, especially 2,6-diisopropyl phenol, in breathing gas. A method uses the filter for removing alkyl phenols, especially 2,6-diisopropyl phenol, from breathing gas.

A ventilation system includes an electrochemical filter for depleting alkyl phenols, especially 2,6-diisopropyl phenol, in breathing gas. A method uses the filter for removing alkyl phenols, especially 2,6-diisopropyl phenol, from breathing gas.

A method includes applying, via a respiratory therapy system, initial therapy settings for a user during a first sleep session in which the user uses the respiratory therapy system. First physiological data, which is received from one or more sensors, is generated during the first sleep session. Modified therapy settings are applied, via the respiratory therapy system, during a second sleep session of the user. Second physiological data is received from the one or more sensors. The second physiological data is generated by the one or more sensors during the second sleep session. A set of sleep-related parameters is determined based on changes between the first physiological data and the second physiological data. One or more of a recommended therapy or recommended therapy settings is determined based on the set of sleep-related parameters.

A method includes applying, via a respiratory therapy system, initial therapy settings for a user during a first sleep session in which the user uses the respiratory therapy system. First physiological data, which is received from one or more sensors, is generated during the first sleep session. Modified therapy settings are applied, via the respiratory therapy system, during a second sleep session of the user. Second physiological data is received from the one or more sensors. The second physiological data is generated by the one or more sensors during the second sleep session. A set of sleep-related parameters is determined based on changes between the first physiological data and the second physiological data. One or more of a recommended therapy or recommended therapy settings is determined based on the set of sleep-related parameters.

A delivery device for and a method of delivering gases to the nasal airway, in particular therapeutic gases and gases in combination with active substances, either as powders or liquids, for enhanced uptake of the active substances.

A delivery device for and a method of delivering gases to the nasal airway, in particular therapeutic gases and gases in combination with active substances, either as powders or liquids, for enhanced uptake of the active substances.