Method and system for determining real time analyte concentration including an analyte sensor having a portion in fluid contact with an interstitial fluid under a skin layer, an on-body electronics including a housing coupled to the analyte sensor and configured for positioning on the skin layer, the on-body electronics housing including a plurality of electrical contacts, on the housing; and a data analysis unit having a data analysis unit housing and a plurality of probes, on the housing. Each of the probes configured to electrically couple to a respective electrical contact when the data analysis unit is positioned in physical contact with the on-body electronics. The one or more signals on the probes correspond to one or more of a substantially real time monitored analyte concentration level (MACL), MACL over a predetermined time period, or a rate of change of the MACL, or combinations thereof, are provided.

Systems and methods for providing infant monitoring and support avoid image degradation, for x-ray imaging, related to sensors used for infant monitoring by separating an infant-supporting body from a sensor-carrying body. The sensor-carrying body, and with it any number of related sensors, is moved out of the way during x-ray imaging.

A monitoring system and method tracks a patient's position over time and ensures that proper turning or other manipulation is done within the time prescribed. Preferably, the techniques herein continuously monitor patient position and alert medical or other personnel of the need for turning or other patient manipulation. The system may be implemented within a medical or other care facility, or within a patient's home.

The device comprises: a first support layer (C1) having detection means including several electrodes (11) arranged, in use, in contact with the skin of a user on at least one muscle, or part thereof, and configured for acquiring a plurality of electromyographic signals, said first support layer (C1) being mechanically and electrically attached in a detachable manner to a second support layer (C2); and said second support layer (C2) which includes electronic means (BE) configured for performing the conditioning of said acquired electromyographic signals, conversion thereof to a digital format and transmission through a communication channel (26) to a master electronic unit (27), wherein said master electronic unit (27) is configured for controlling said electronic means (BE) and to further transmit the received conditioned and digitized electromyographic signals to a control unit (30) for monitoring thereof.

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.

In one aspect, a sensory, motor and/or cognitive analysis device includes a casing unit structured to include a contact side conformable to a forehead region of a user; a data acquisition unit structured to include one or more sensors to detect electrophysiological signals of the user when the user makes contact with the device; a data processing unit encased within the casing unit and in communication with the data acquisition unit to amplify and digitize the detected electrophysiological signals as data, to process the data, to store the data, and to transmit the data to a remote computer system; and a power supply unit encased within the casing unit to provide electrical power, in which the device is operable to acquire physiological and/or behavioral signal data from the user used to determine a quantitative and/or qualitative information set associated with a cognitive or sensory assessment.

A sensing guidewire device used to measure physiological parameters within a living body. In one embodiment, the device is used to measure the fractional flow reserve (FFR) across a stenotic lesion in a patient's vasculature. The device includes a sensor that is adapted to be affixed near the distal end of a guidewire. The guidewire contains a corewire, processed to enclose electrical conductors in a sealed, off-centered interstice or channel, with an outer diameter approximate to the outer diameter of the device, running substantially the full length of the device, and has a homogenous outer surface. The enclosed eccentric channel provides space for electrical conductors to move freely. The corewire can have a tapered segment to create desirable flexibility. A solid connector comprised of alternating conductive and insulating elements for connecting the conductors to an external device is disclosed. The guidewire can be advanced through a patient's blood vessels, returning pressure measurements across vessel blockages that allow for accurate assessment of blockage severity and lead to better clinical outcomes.

A modular hand-held point of care testing system, which includes a plurality of different assay adapters configured to receive a plurality of different assay devices that perform assays on one or more samples; a shared door that that interchangeably receives the plurality of different assay adapters; wherein at least two of the plurality of assay adapters or at least two of the assay devices comprise different identifiers that distinguish the assays from each other; an apparatus comprising a portable frame configured to interchangeably receive the shared door and a means for decoding the different identifiers when received by the frame; and a means for reading assay results.

Physiological monitoring can be provided through a wearable monitor that includes a flexible extended wear electrode patch and a removable reusable monitor recorder. A pair of flexile wires is interlaced or sewn into a flexible backing, serving as electrode signal pickup and electrode circuit traces. The wearable monitor sits centrally on the patient's chest along the sternum, which significantly improves the ability to sense cutaneously cardiac electric signals, particularly those generated by the atrium. The electrode patch is shaped to fit comfortably and conformal to the contours of the chest approximately centered on the sternal midline. To counter the dislodgment due to compressional and torsional forces, non-irritating adhesive is provided on the underside, or contact, surface of the electrode patch, but only on the distal and proximal ends. Interlacing the flexile wires into the flexile backing also provides structural support and malleability against compressional, tensile and torsional forces.

Systems and methods for integrating a continuous glucose sensor, including a receiver, a medicament delivery device, and optionally a single point glucose monitor are provided. Manual integrations provide for a physical association between the devices wherein a user (for example, patient or doctor) manually selects the amount, type, and/or time of delivery. Semi-automated integration of the devices includes integrations wherein an operable connection between the integrated components aids the user (for example, patient or doctor) in selecting, inputting, calculating, or validating the amount, type, or time of medicament delivery of glucose values, for example, by transmitting data to another component and thereby reducing the amount of user input required. Automated integration between the devices includes integrations wherein an operable connection between the integrated components provides for full control of the system without required user interaction.