A blood vessel visualization apparatus for visualizing a blood vessel inside a living body with light that has been transmitted through the living body includes: an irradiation unit configured to emit light from a contact portion with skin of the living body, the irradiation unit including: a fixing portion configured to be fixed to a target site of the living body, wherein the fixing portion includes a surface configured to contact the skin of the living body, and a plurality of light sources located in a light source arrangement area at the surface of the fixing portion that is configured to contact the skin of the living body. A brightness and/or a light distribution angle of respective ones of the light sources differ according to positions of the light sources in the light source arrangement area.

Embodiments of negative pressure wound therapy systems, apparatuses, and methods for operating the systems and apparatuses are disclosed. In some embodiments, the apparatus includes a negative pressure source, a connector port, at least one switch, and a controller. The negative pressure source is connected through the connector port to either (i) a wound dressing having a canister configured to store fluid aspirated from the wound or (ii) a wound dressing without a canister between the connector port and the wound dressing. The controller determines, based on a signal received from the at least one switch, whether the canister is positioned in the fluid flow path and adjusts one or more operational parameters of negative pressure wound therapy based on the determination. The switch is activated by the connection of either the canister or canisterless wound dressing to the apparatus.

The present disclosure relates to a dispenser. Specifically, the dispenser comprises a housing and a stop member fixedly positioned in the housing configured to receive at least a portion of a container and an actuator engagable by a user, whereby contents of the container are released.

A system for compounding medications. The system includes one or more compounding devices, and a central computer system. The central computer system receives requests, at least some of which require the compounding of one or more medications, and pushes assignments of respective compounding tasks to the one or more compounding devices. The assignments are made in accordance with a set of rules designed to promote efficient use of compounding resources.

An airway adaptor providing a measurement chamber for gas measurement by a mainstream gas analyzer includes a body having a first end and a second end and configured to connect in a ventilation circuit carrying ventilation gas to and from a patient. The body forms a primary path that includes the measurement chamber and is configured to allow ventilation gas to pass between the first end and the second end and at least one secondary path separated from the primary path and located on an outer perimeter of the primary path. The at least one secondary path is configured to contain liquid away from the measurement chamber.

A system and method for monitoring the health of dialysis patients with Raman spectroscopy measurements of one or more target analytes is described. The methods include irradiating one or more fluids of interest with light to produce one or more spectrum and detecting the spectrum with a detector. The fluids of interest are preferably those related to dialysis, including hemodialysis and peritoneal dialysis. In a preferred embodiment, the fluids are irradiated with monochromatic light, and one or more Raman spectra are detected as a result of the irradiation. The fluids may be irradiated within the dialysis tubing itself, or removed from the dialysis tubing and irradiated in a separate chamber. The Raman spectra of one or more target analytes of a dialysis patient may be followed over time or compared to one or more reference spectra, thereby providing information on the health of dialysis patients.

Medical devices and methods and apparatuses for identifying fluids in a conduit of a device are provided. An exemplary medical device includes a reservoir for holding a fluid and a conduit for dispensing the fluid from the reservoir. Further, the medical device includes a spectroscopy device for examining the fluid.

A blood filtering machine having a blood circuit, which has a plurality of ducts made of a transparent material, and a measuring system, which has a plurality of optical sensors coupled to respective ducts. Each optical sensor has a reading window placed in a point of the respective duct, a light emitter and a light receiver. The measuring system comprises one single spectrometer, an optical mixer comprising a plurality of inputs, each connected to the light receiver of a respective one of the optical sensors, and an output, which is connected to an input of the spectrometer, and a control unit is configured to activate the light emitter of one optical sensor at a time so as to measure a parameter of one organic fluid at a time.

System and methods are disclosed that promote a sleep stage of a user. The systems and methods determine a current sleep stage of a user during a sleep session, with the user using a respiratory therapy system during the sleep session. The systems and methods further predict an undesired sleep stage upcoming for the user during the sleep session based, at least in part, on (i) one or more user parameters, information from one or more previous sleep sessions, or a combination thereof, and (ii) the current sleep stage. The systems and methods adjust one or more control parameters of the respiratory therapy system, of one or more devices in an environment of the user, or of a combination thereof to promote a desired sleep stage of the user, thereby optimizing sleep of the user.

The present disclosure is related to a method and system for providing personalised haemodialysis for subject. The method includes obtaining concentration of electrolytes and of metabolic content in blood sample flowing into and out of dialyser through first blood bypass tube and second blood bypass tube, respectively. The first and the second blood bypass tube are arranged in first sensor and second sensor. Similarly, concentration of electrolytes and metabolic content in dialysate fluid flowing into and out of dialyser through first and second dialysate tube, respectively. The first dialysate tube and second dialysate tube are arranged to pass through third sensor and fourth sensor. Further, variations are identified in concentration obtained for electrolytes and metabolic content in blood sample with respect to concentration obtained for electrolytes and metabolic content in dialysate fluid, respectively. Thereafter, removal of electrolytes and metabolic content is performed from blood sample.