A nightstand designed to support and contain various CPAP machines and associated CPAP equipment including air tubing, cleaning devices and distilled water storage. Separate drawers and compartments are provided to house the CPAP machine, CPAP cleaning device, and water supply containers. Various openings are designed to increase utility and convenience in the operation and storage of CPAP devices and associated equipment. A pump may be provided to transfer water from water supply containers to the CPAP machine reservoir. The CPAP nightstand is designed to be located at bedside and provides easy access to the CPAP machine and its ancillary devices while keeping all equipment in dedicated drawers. Each dedicated drawer provides openings to allow passage of air tubing, water hoses and power cords. The CPAP nightstand also has generic drawers for additional storage.

Apparatus for performing a procedure at a target site of a patient's body, the apparatus comprising: a continuous positive airway pressure (CPAP) apparatus that provides CPAP to the patient's lungs; a medical device for performing the procedure at the target site; and a controller that controls the CPAP apparatus to provide CPAP to the patient's lungs during performance of the procedure.

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.

An inhalation monitoring system includes an inhaler having a medicament delivery apparatus configured to deliver medicament to a user during an inhalation of the user; inhalation monitoring apparatus, configured to, during the inhalation, gather data for determining a measure of the user's lung function and/or lung health; and a processor configured to receive the data from the inhalation monitoring apparatus and, using the data, determine a measure of the user's lung function and/or lung health.

Techniques described herein can identify usage information for sensors. In one example, an anesthesia device can include a processor to obtain usage information from a first flow sensor coupled to the anesthesia device. The processor can also determine the usage information exceeds a predetermined limit and generate an alert indicating the first flow sensor is to be replaced.

A ventilation monitoring system for assisting in proper placement of an endotracheal tube in a subject includes: a capnography sensor configured to be placed in fluid communication with the endotracheal tube and to provide information representative of the subject's breath; and a processor in communication with the capnography sensor. The processor is configured to provide an indication of proper endotracheal tube placement when (1) a first indication of the subject's breath and a positive result of a first auscultation are identified within a first predetermined time period, and (2) a second indication of the subject's breath and a positive result of a second auscultation are identified within a second predetermined time period. The first auscultation includes auscultation of a subject's left lung, right lung, left axillary region, right axillary region, or abdomen. The second auscultation includes auscultation of another region of the subject different from the first auscultation.

A method includes data associated with a sleep session of a user, including respiration data associated with the user during at least a portion of the sleep session and audio data reproducible as one or more sounds during at least a portion of the sleep session. The method also includes determining a respiration signal associated with the user during the sleep session based, at least in part, on at least a portion of the data. The method also includes identifying an event experienced by the user during the sleep session based, at least in part on, at least a portion of the data. The method also includes causing to be communicated to the user via a user device a graphical representation of a portion of the respiration signal and an event indication that aids in identifying the identified event within the graphical representation of the portion of the respiration signal.

A ventilation management system communicatively couples a remote device such as a mobile device to one or more ventilators for monitoring of ventilator data, including ventilator configuration data, patient physiological statistics, and notifications. When a command to modify a configuration parameter of the ventilator is received while the ventilator is unavailable for communication, the command is cached and provided when the ventilator becomes available. When ventilator becomes available, the system receives an indication that the configuration parameter was modified at the ventilator, an operating condition of the ventilator, and a physiological statistic of a patient associated with the ventilator, the operating condition and physiological statistic having been cached by the ventilator while the ventilator is unavailable. The operating condition of the ventilator, the physiological statistic of the patient, and the indication that the configuration parameter was modified is provided to the remote computing device for display.

A first medical device can receive a physiological parameter value from a second medical device. The second physiological parameter value may be formatted according to a protocol not used by the first medical device such that the first medical device is not able to process the second physiological parameter value to produce a displayable output value. The first medical device can pass the physiological parameter data from the first medical device to a separate translation module and receive translated parameter data from the translation module at the first medical device. The translated parameter data can be processed for display by the first medical device. The first medical device can output a value from the translated parameter data for display on the first medical device or an auxiliary device.

For the production of an assembly for a patient ventilation system, at least one conducting connection is first prepared between contact pins of a component receptacle of a connector for the insertion of at least one electronic component and sheath wires which are guided along a tube sheath of a breathing air tube portion of the assembly. This prepared conducting connection is overmolded to form an inner conduction carrier housing sleeve of the connector. The conducting connection is connected to the sheath wires and the inner conduction carrier housing sleeve is overmolded to form an outer connector housing of the connector in which the component receptacle is implemented. This results in an assembly manufacturing process that is suitable for mass production.