A method of controlling a gas delivery apparatus including an apparatus controllable variable using an iterative algorithm to deliver a test gas (TG) for non-invasively determining a subject's pulmonary blood flow comprising iteratively generating and evaluating test values of a iterated variable based on an iterative algorithm in order output a test value of the iterated variable that meets a test criterion wherein iterative algorithm is characterized in that it defines a test mathematical relationship between the at least one apparatus controllable variable, the iterated variable and an end tidal concentration of test gas attained by setting the apparatus controllable variable, such that the iterative algorithm is determinative of whether iteration on the test value satisfies a test criterion or iteratively generates a progressively refined test value.

A respiratory ventilator device is described herein. The respiratory ventilator device includes an inhaled air assembly, an exhaled air assembly, and a control system operatively coupled to the inhaled air assembly and the exhaled air assembly. The inhaled air assembly is coupled to a patient respiratory circuit and configured to channel a volume of inhalation air to the patient's lungs to assist in patient inhalation. The exhaled air assembly is coupled to the patient respiratory circuit and configured to remove air from the patent's lungs to assist in a patient exhalation. The control system is configured to operate the respiratory ventilator system in an inhalation mode and an exhalation mode.

A wake-to-sleep transition for a subject is detected based on responsiveness to breathing cues provided to the subject. A pressurized flow of breathable gas to the airway of subject having one or more gas parameters that are adjusted to provide breathing cues to the subject. Based on a detected conformance of the respiration of the subject to the breathing cues, a determination is made as to whether the subject is awake or asleep.

Responsive determining that a client device is authorized for access to a ventilator, a user interface is provided, including a display of configuration information for the ventilator, the displayed configuration information including a current mode of operation of the ventilator and one or more ventilation settings affecting a current ventilation of a patient by the ventilator. A ventilation setting to modify the current ventilation of the patient is received and, before the current ventilation is modified by the received ventilation setting, a ventilation index for the received ventilation setting is determined based on comparing the current ventilation with the aggregated setting and outcome data for the plurality of patient ventilations, and a representation of the ventilation index is displayed responsive to receiving the ventilation setting. An instruction to modify the current ventilation of the patient based on the received setting and the determined ventilation index.

An arrangement for powering a pump in providing a controlled volume of water to a drip nozzle in a drip-feed humidifier. The pump arrangement including: a pump having a solenoid; a processing unit; and a power supply electrically connected to the solenoid via a switch which is controlled by the processing unit. The power supply is structured to supply power to the solenoid via the switch. The processing unit is programmed to modulate the power to the solenoid such that the pump is driven at or near a resonant frequency of the pump.

A humidifier assembly is configured to humidify a pressurized flow of breathable gas from a flow generator of a CPAP unit and includes a base configured to be attached to the flow generator, the base including a recess portion. A water receptacle is configured to be received within the recess portion of the base and includes a floor and a flange around an opening at the top of the water receptacle. A lid is hingedly attached to the base and is configured to pivot between an open position and a closed position. This lid includes a top wall, an outer depending wall, an inner depending wall in the form of a double wall, and an outlet pipe. A lid seal is attached to an underside of the top wall of the lid by way of a tongue and groove structure. A catch is located on the base and configured to lock the lid in the closed position.

The present invention relates to a member (14, 24, 26) of a patient interface (10) for providing a flow of breathable gas to a self-ventilating patient (12). The member (14, 24, 26) comprises a wear-out indicator (32) for indicating a wear-out of the member (14, 24, 26) to the patient (12). The wear-out indicator (32) comprises an elastic structure (34) that appears in a first colour in an unstressed condition and is configured to reversibly change its apparent colour when being stretched and returned to its unstressed condition again. The elastic structure (34) is configured to indicate a wear-out of the member (14, 24, 26) by appearing in a second colour in its unstressed condition when the structure (34) has lost at least a part of its elasticity, wherein the second colour is different from the first colour.

A system for stimulating body tissue may include a stimulation lead, sensors, and a control unit. The stimulation lead may include one or more energy sources. The control unit may include a processor and non-transitory computer readable medium, and an interface (e.g., touch screen interface) for receiving user inputs and communicating information to the user. The sensors may be configured to provide impedance measurements to the control unit. The control unit may calculate lung gas distributions and/or generate an image modeling lung gas distributions. Stimulation delivered by the stimulation may be adjusted based on the impedance measurements.

A portable, efficient, integrated humidification system for use, e.g., with a positive airway pressure devices. The portable, efficient, integrated humidification system described herein offers many advantages over current humidification systems! There are many advantages to a portable respiratory humidifier. Portability reduces the amount of space the humidifier occupies in the user's bedroom environment. Portability enhances travel for the user. With less to pack, carry, and manage, the user is more likely to remain adherent to therapy when not at home. Portability allows for better utilization in recreational vehicles, while camping, in foreign countries, in the sleeping cabins of trucks or airliners, and on marine craft.

Objective Pulmonary Function (PF) evaluation for respiratory fatigue is vital to the diagnosis and management of many pediatric respiratory diseases in the intensive care, emergency and outpatient settings. A non-invasive PF instrument utilizes sensors and software to access respiratory breathing patterns, vital parameters, asynchrony and measures the work of breathing. Software algorithms predict respiratory fatigue. The hardware includes a microcircuit board that individually links to rib cage (RC) and abdominal (ABD) inductance bands. The bands wirelessly transmit changes in RC and ABD circumference. Point-of-care, real-time indices of respiratory work, breathing patterns and respiratory fatigue indices are developed on a user-friendly graphical user interface. The diagnostic data can later be securely emailed as an attachment for entry into patients' electronic medical records or sent to a caretaker's computer, or used directly to control a respiratory therapy device. The system can also be used for telemedicine homecare.