According to one embodiment, there is provided an X-ray diagnostic apparatus which comprises an X-ray generation unit configured to irradiate an object with X-rays; an X-ray detection unit configured to detect X-rays applied by the X-ray generation unit and transmitted through the object; an image generation unit configured to generate an X-ray image based on X-rays detected by the X-ray detection unit; a recording unit configured to record pressure data acquired by using a pressure sensor provided on a guide wire; a measurement position setting unit configured to set a measurement position for a pressure by the pressure sensor using the X-ray image; and a display unit configured to display the X-ray image almost in real time and superimpose and display the measurement position set by the measurement position setting unit.

A method of calibrating a monitoring device to generate calibrated vital sign data using a calibration device includes positioning the monitoring device in a first position on a patient, generating vital sign data with a sensing assembly of the positioned monitoring device, and processing the vital sign data with the calibration device to determine if the vital sign data is calibrated vital sign data or uncalibrated vital sign data. The method also includes generating a calibrated data signal if the vital sign data is calibrated vital sign data, generating a reposition signal if the vital sign data is uncalibrated vital sign data, and repositioning the monitoring device on the patient until the calibrated data signal is generated.

Devices, systems, and methods for the localization of body lumen junctions and other intraluminal structure are disclosed. Various embodiments permit clinicians to identify and locate lesions and/or anatomical structures within a lumen and accurately place leads and/or devices within a lumen, through determining the intralumen conductance and/or cross-sectional area at a plurality of locations within the body lumen.

Examples are disclosed that relate to sensor devices configured to sense bending in multiple joints. One example provides a sensor device configured to span a first articulable joint and a second articulable joint. The sensor device comprises a plurality of electrodes arranged in a stack and connected to a base. The plurality of electrodes comprise a first electrode arranged at a first joint region of the sensor device that is configured to be positioned at the first articulable joint, a second electrode arranged at a second joint region of the sensor device that is configured to be positioned at the second articulable joint, and a reference electrode.

A method for re-configuring a biomedical laser device. The biomedical laser device is pre-configured to be operable in one or more operational modes, and is provided with set of operational parameters that are employed for at least one of: given medical procedure, given medical treatment, activation of given drug, illumination of given dye. The method includes collecting information indicative of light output properties of biomedical laser device measured during given operational mode; detecting deviation in measured light output properties with respect to predefined light output properties for given operational mode; determining new set of operational parameters that are to be employed for at least one of: new medical procedure, new medical treatment, activation of new drug, illumination of new dye; and sending new set of operational parameters to biomedical laser device for re-configuring biomedical laser device to be operable in a new operational mode.

A physiological monitor is provided for determining a physiological parameter of a medical patient with a multi-stage sensor assembly. The monitor includes a signal processor configured to receive a signal indicative of a physiological parameter of a medical patient from a multi-stage sensor assembly. The multi-stage sensor assembly is configured to be attached to the physiological monitor and the medical patient. The monitor of certain embodiments also includes an information element query module configured to obtain calibration information from an information element provided in a plurality of stages of the multi-stage sensor assembly. In some embodiments, the signal processor is configured to determine the physiological parameter of the medical patient based upon said signal and said calibration information.

Electrode array for monitoring of physiological parameters and devices including or utilizing same, the electrode array including an active electrode configured to provide an electrical signal and at least two inactive electrodes configured to collect the electrical signal transferred from the active electrode, wherein each of the at least two inactive electrodes are positioned at a different predetermined distance from the active electrode.

The subject matter disclosed herein relates to systems, methods and/or devices for calibrating sensor data to be used in estimating a blood glucose concentration. A relationship between sensor measurements and reference readings may be used to estimate a relationship between sensor measurements and blood glucose concentration. Such sensor measurements may be weighted according to a decreasing function of uncertainty associated with sensor values.

A device is for estimating a blood pressure of a user by a combination of an acoustic mode employing acoustic emitters and acoustic detectors and an optical mode using light sources and photodetectors forming source—detector pairs. The device includes an acoustic selection unit to determine the pertinent acoustic emitter—acoustic detector pair as well as an optical selection unit to determine the pertinent light source—photodetector pairs.

A method includes, receiving multiple measurements, which are acquired using a registration tool including an ultrasound (US) transducer and a position sensor of a position-tracking system. The measurements are acquired by positioning the registration tool, while maintaining a gap from skin tissue, at multiple respective locations on a patient head and acquiring respective position measurements of the position sensor and respective US measurements of the skin tissue at the locations. First positions, of the skin tissue at the multiple locations, are calculated based on the position measurement and the US measurements obtained using the registration tool. Second positions, of the skin tissue at the multiple locations, are identified in an anatomical image of the patient head. The anatomical image is registered with a coordinate system of the position tracking system, by correlating the first positions and the second positions, so as to enable tracking a medical instrument, which is inserted into the patient head and includes another position sensor of the position-tracking system, using the anatomical image registered with the position-tracking system.