An example aerosol delivery device includes a mouthpiece having an airflow outlet, and an airflow passage extending between an airflow inlet and the airflow outlet. The example aerosol delivery device further includes a housing configured to receive a cartridge that includes an aerosolizable substance and a vapor element configured to heat the aerosolizable substance, and an internal power source configured to provide electrical power. The example aerosol delivery device further includes a controller coupled to the internal power source to receive a portion of the electrical power and configured to, when the cartridge is installed at the housing, cause the vapor element of the cartridge to heat the aerosolizable substance to release an aerosol into the airflow passage during an inhalation through the airflow outlet, and a connector configured to receive power from an external source to recharge the internal power source.

A process (10), with a computer program, a device (30) and a ventilation system (40) detect a leak in a patient gas module, which suctions and analyzes a continuous sample gas stream from a ventilated patient (20), in a ventilation system for ventilating a patient (20). The process includes a determination (12) of a first time curve of a carbon dioxide concentration in a breathing gas mixture of the patient (20) and the determination (14) of a second time curve of a concentration of another gas in the breathing gas mixture, which gas is different from carbon dioxide. The process (10) further includes a determination (16) of a statistical similarity indicator between the first time curve and the second time curve and the detection (18) of the leak based on the similarity indicator.

A medical device including an introducer; a first section configured to connect to a supply of therapeutic fluid; and a second section configured to connect to a supply of therapeutic elements. The therapeutic elements are drawn into the introducer by way of suction created by a flow of the therapeutic fluid through the introducer. The therapeutic elements are drawn into the introducer by way of suction created by a flow of the therapeutic fluid through the introducer.

An anesthesia vaporizer system includes a sump chamber, a variable volume reservoir within the sump chamber, and an anesthetic vaporizer. The variable volume reservoir is configured to contain anesthetic agent. A pressurized gas source is connected to the sump chamber and configured to maintain a constant pressure within the sump chamber to compress the variable volume reservoir to force the anesthetic agent through the anesthetic vaporizer, which vaporizes the liquid anesthetic agent for delivery to a patient.

An embodiment of a single use nitrous oxide solution delivery system can be used in a prehospital setting such as in ambulances. A container can be filled with a predetermined relative concentration of nitrous oxide and oxygen gases. The container is sized to be stored in a repository within an automated dispensing cabinet (ADC) for medications. The container is connected to a regulator which includes a main control dial configured to allow a health care provider to adjust the volumetric flow rate of the nitrous oxide and oxygen gas mixture used by a patient. A scavenger can be optionally connected to a patient's mask and configured to remove exhaled gas. Another embodiment of a single use nitrous oxide solution delivery system can be used within hospitals and other medical buildings.

Examples of a module for housing unrelated electronic and electromechanical equipment for use during surgery. The module can include a lower section and a tower-like upper section. The lower section can house unrelated electronic and electromechanical equipment. The tower-like upper section can be located on top of the lower section. A water-resistant cowling can enclose at least a portion of the lower section and the tower-like upper section. A cartridge containing one or more ultraviolet-C producing lights can be protectively housed within the tower-like upper section. The cartridge containing one or more ultraviolet-C producing lights can be configured to emerge upward from a top of the tower-like upper section to substantially seat itself on the top of the tower-like upper section when activated allowing the ultraviolet-C light to disinfect the patient and staff-contacting upper surfaces of the equipment in the operating room.

A system (1000) feeds substances to a patient (30) with a ventilation of the patient and with an oxygenation of the patient. The system (1000) has at least one ventilation system (1), a sedation by inhalation system (17) with a dispensing system (7), an oxygenation system (2), a breathing gas dispensing path (3), a purge gas dispensing path (4), a breathing gas connection system (5), a connection element (25) located adjacent to the patient, an oxygenation connection system (6) and a switching unit (8). The switching unit (8) is configured to distribute and to split a quantity of an inhalable substance dispensed into a gas mixture by means of the dispensing system (7) between the connection element (25) located adjacent to the patient and the oxygenation system (2). At least one control unit (9, 10, 11, 12) is configured to control the switching unit (8) and/or the system (1000).

A system (1000) feeds substances to a patient (30) with a ventilation of the patient and with an oxygenation of the patient. The system (1000) has at least one ventilation system (1), a sedation by inhalation system (17) with a dispensing system (7), an oxygenation system (2), a breathing gas dispensing path (3), a purge gas dispensing path (4), a breathing gas connection system (5), a connection element (25) located adjacent to the patient, an oxygenation connection system (6) and a switching unit (8). The switching unit (8) is configured to distribute and to split a quantity of an inhalable substance dispensed into a gas mixture by means of the dispensing system (7) between the connection element (25) located adjacent to the patient and the oxygenation system (2). At least one control unit (9, 10, 11, 12) is configured to control the switching unit (8) and/or the system (1000).

A respiration sensor fluid delivery device is provided. The device includes first and second nasal exhalation flow passages that extend through the device, wherein the first and second nasal exhalation flow passages can be aligned in parallel to one another with respect to a nasal respiratory flow direction. A housing of the respiration sensor fluid delivery device fluidly couples with one of a nasal cannula assembly and a respiratory mask assembly. The device provides for respiration monitoring of a subject via a sensor and fluid delivery, such as oxygen, to the subject. Methods of using a respiration sensor fluid delivery device and fluid delivery devices are also provided.

A respiration sensor fluid delivery device is provided. The device includes first and second nasal exhalation flow passages that extend through the device, wherein the first and second nasal exhalation flow passages can be aligned in parallel to one another with respect to a nasal respiratory flow direction. A housing of the respiration sensor fluid delivery device fluidly couples with one of a nasal cannula assembly and a respiratory mask assembly. The device provides for respiration monitoring of a subject via a sensor and fluid delivery, such as oxygen, to the subject. Methods of using a respiration sensor fluid delivery device and fluid delivery devices are also provided.