Disclosed herein are methods, systems, and devices for controlling a gas mixture within a mechanical ventilator. According to one embodiment, a computer implemented method includes receiving first peripheral arterial oxygen saturation (SpO.sub.2) data from a pulse oximeter via a pulse oximeter interface, wherein the pulse oximeter is configured to monitor a patient receiving invasive ventilation; determining a first mode of operation for a ventilator mechanism, wherein the ventilator mechanism is configured to provide at least a portion of the invasive ventilation; determining first partial pressure of oxygen (PaO.sub.2) data stored in a first lookup table using the first SpO.sub.2 data, wherein the first lookup table is derived from a sigmoid shaped oxyhemoglobin dissociation curve; determining first fraction of inspired oxygen in air (FiO.sub.2) data for setting a mixture in a gas blender in the ventilator mechanism based on the first PaO.sub.2 data and a variable offset; and providing the FiO.sub.2 data to the ventilator mechanism.

A method and system that is integrated in order to provide an automated control system for the user, which provides messaging to bedroom environmental control systems as a function of the status of the user's sleep state is disclosed herein. The system comprises a sleep monitoring sub-system and a bedroom environmental control sub-system. The sleep monitoring sub-system is configured to transmit the subject's sleep progression data to an interface for the bedroom environmental control system. The bedroom environmental control system is configured to modify a bedroom environment based on the subject's sleep progression data.

A fluid separation device includes a centrifuge in which a fluid is separated into at least two components, with an interface therebetween. At least a portion of one of the separated fluid components is removed from the centrifuge and flows through a vessel. Light is reflected off of the separated fluid component in the vessel and received and analyzed to determine its main wavelength. If the main wavelength is higher than a maximum value, a target location of the interface is changed. If the main wavelength is less than the maximum value, then the location of the interface is compared to the target location. When the interface is sufficiently close to the target location, the optical density of the separated fluid component in the vessel is compared to a minimum value. If the optical density is less than the minimum value, the target location of the interface is changed.

Described herein are an interactive apparatus and methods for sensing and measuring real-time characteristic patterns of a subject's use of a dry powder inhalation system. The inhaler device can be used in a wireless communication mode to communicate with a display to assess the subject's usage of the inhalation system concurrently as the inhalation is performed and thus the subject's inhalation can be evaluated as well as the performance of the inhalation system. The system can also detect the identity of the medicament, its dosage, lot, expiration, etc. and the characteristics profile of a dry powder formulation emitted from the inhalation system in use.

A nasal droplet delivery device and related methods for delivering precise and repeatable dosages to a subject via the nasal passageways and sinus cavities.

A method and system is provided that measures plasma protein levels of whole blood while a plasma donor is connected to an apheresis machine. A refractometer associated with the apheresis machine is capable of receiving a portion of a disposable tubing set including an integrated cuvette and prism. The integrated cuvette of the disposable tubing set can be inserted into a receiving space of the refractometer associated with the apheresis machine such that the light source and the sensor are oriented relative to the prism and a sensing surface of the integrated cuvette in a precise alignment. Calibration of the refractometer is made using anticoagulant pumped through the disposable tubing set including the integrated cuvette and prism. Based on a light intensity associated with this calibration, whole blood is then measured to determine plasma protein levels and donor eligibility.

An electronic device and method for providing information for stress relief are disclosed. The electronic device includes a user interface, at least one sensor, at least one processor operatively connected to the user interface and the at least one sensor, and a memory operatively connected to the at least one processor. The memory stores instructions to, when executed, cause the at least one processor to collect stress-related information through at least a part of the at least one sensor, identify contextual information of a user when stress calculated based on the collected stress-related information satisfies a designated condition, and guide at least one of a plurality of stress relief methods through the user interface at least based on the identified contextual information.

A system for monitoring percentage change in blood volume (ΔBV %) during dialysis treatment includes a sensor device configured to obtain hematocrit (Hct)-related measurements based on detecting light which has passed through extracorporeal blood of a patient undergoing the dialysis treatment; one or more controllers configured to: determine Hct values based on the Hct-related measurements obtained by the sensor device; determine ΔBV % values based on the determined Hct values; and generate a GUI having a ΔBV % plot based on the determined ΔBV % values; and a display device having a display configured to display the GUI having the ΔBV % plot. Zone indicators are provided on the display to distinguish between a first zone corresponding to a first ΔBV % profile, a second zone corresponding to a second ΔBV % profile, and a third zone corresponding to a third ΔBV % profile.

A method and system to manage a respiratory condition of a patient. An oxygen concentrator is configured to generate and deliver oxygen enriched air to the patient according to a selected dosage. The oxygen concentrator senses and collects physiological data of the patient and collects operational data during the generation and delivery of oxygen enriched air. The oxygen concentrator adjusts the dosage of oxygen enriched air based on the sensed physiological data. The oxygen concentrator transmits operational data and the physiological data to a health data analysis engine. The health data analysis engine collects the data transmitted by the oxygen concentrator. The health analysis engine detects a triggering event based on the collected data and determines an action to resolve the detected triggering event.

A method includes flowing spent dialysate through a spent dialysate line of a dialysis system into a fluid receptacle fluidly coupled to the spent dialysate line, reacting the spent dialysate with a chemical reagent contained within the fluid receptacle to generate a reacted sample, emitting electromagnetic radiation through the reacted sample using an emitter; detecting a level of one or more waste products present in the spent dialysate using a spectroscopy sensor positioned proximate the fluid receptacle.