A ventilation system includes a processor in communication with a mechanical ventilator and a user interface comprising a quick start mode for allowing an individual to operate the system with little or no respiratory care expertise until a respiratory care practitioner can take over operation is disclosed. The ventilation system further includes a function that permits seamless transition between modes of operation.

A medical ventilation monitoring system is provided. The system includes: a patient ventilation unit defining an airflow path, and arranged so that when the unit is applied to a patient, the airflow path is in fluid communication with the patient's airway. The patient ventilation unit includes: an airflow sensor positioned to sense the presence of ventilation airflow to or from the patient and a communication link. The system also includes at least one processor arranged to communicate with the ventilation unit by the communication link. The at least one processor is configured to: provide an initial treatment protocol for providing care to the patient, receive data regarding a current condition of the patient from the ventilation unit, and determine an updated treatment protocol. The updated treatment protocol includes applying ventilation at an updated ventilation volume or at an updated ventilation rate based on information from the airflow sensor.

An apparatus for humidifying a flow of pressurised, breathable air includes varying a first pressure of the flow of breathable gas to vary a level of thermal engagement between the conductive portion of the reservoir and the heater plate, varying a height of the variable portion varies a level of thermal engagement between the conductive portion of the reservoir and the heater plate, use of a humidifier reservoir base component with a maximum water capacity substantially equal to the predetermined maximum volume of water of the humidifier reservoir or the use of intersecting inlet and outlet axes.

A compliance monitoring module for an inhaler comprising: a miniature pressure sensor, a sensor port of said sensor being configured to be pneumatically coupled to a flow channel of said inhaler through which a user can inhale; a processor configured to: receive data from a sensing element of the pressure sensor; receive data from a mode sensor configured to detect when the inhaler changes from an inactive mode to an active mode; and based on said data from said pressure sensor sensing element and said data from said mode sensor, compile a compliance report; and a transmitter configured to issue said compliance report.

A device for use in pulmonary surgery is presented. The device comprises a dispensing apparatus 300, 400, 900, a delivery apparatus 100, 1000, 1100, in fluid communication with said dispensing apparatus, and a pressurized gas input 338. The dispensing apparatus is configured to provide a pressurized gas, a fibrinogen stream, and a thrombin stream to the delivery apparatus. The delivery apparatus is configured to mix the fibrogen stream and the thrombin stream in the pressurized gas stream to form a fibrin reaction mixture comprising a cellular foam 700.

A breathing assistance apparatus user interface is described which presents animated information related to the management of the apparatus. The user interface is provided on a display screen of the apparatus. The animated illustrations can correspond to operational modes, warnings, user instructions, fault conditions, status, menu options, and the like. The animations can include a sequence of images shown in rapid succession which depict moving icons or objects, scrolling text, flashing colors, or any combination of these or the like. The user interface can combine static information along with animations.

A capnography module for a patient monitoring system includes a hardware switching mechanism and a software mechanism for switching the capnography module automatically between a mainstream monitoring mode and a sidestream monitoring mode. The hardware switching mechanism along with software detection is capable of detecting the connection of a mainstream capnography sensor and a sidestream sampling line and generates flags to notify the software switching mechanism which sensor or line is connected. The software switching mechanism notifies a controller board in the module which monitoring system is available and the controller board operates the module in the respective mode. The capnography module also includes a connector latching mechanism for securing the mainstream capnography sensor to the module and preventing accidental disconnection.

An electronic apparatus including an adjustment determination unit structured to receive patient interface device information for a patient interface device including one or more adjustable features and a 3-D model of a patient's face, and to calculate adjustment information for the patient interface device corresponding to the patient's face using the patient interface device information and the 3-D model of the patient's face and an output unit structured to output the adjustment information.

Methods, systems, and apparatuses are described that indicate an amount at which various gas flow rates should be manually adjusted in order to achieve targeted total flow rates and concentration levels.

A device to monitor movement of a tracheostomy tube is described. The device includes a faceplate that is releasably attached to a tracheostomy collar such that the faceplate may be used without the tracheostomy collar. The tracheostomy collar includes a sensor component and an actuator component each located proximate the faceplate. The actuator component actuates when the sensor component moves from a first position to a second position. The second position is further from the actuator component than the first position. The sensor component transmits a signal to an alarm assembly in response to the actuator component actuating. The alarm assembly produces an alert in response to receiving the signal from the sensor component.