Abstract: An olfactory cognitive ability test system includes an olfactory stimulator configured to accommodate an olfactory stimulating material, and an olfactory stimulation terminal configured to recognize the olfactory stimulator and to perform an olfactory cognitive ability test based on an olfactory stimulation protocol. The olfactory stimulation terminal is provided based on a mobile device, and an amount of the olfactory stimulating material or an amount of an olfactory stimulation may be adjusted to a fixed amount in the olfactory stimulator by a user's operation.

Abstract: A berg balance testing apparatus includes: a floor frame that is a stage on which the examinee takes movements; a plurality of first sensors that is disposed in sections divided to have a predetermined area on the floor frame and senses positions of the feet of the examinee; a second sensor that is disposed at a predetermined distance from the first sensors and senses movements of the examinee; a controller that performs a berg balance test on movements of the examinee on the basis of information sensed and transmitted by the first sensors and the second sensor; and a display that receives berg balance test guide and test result information from the controller and outputs the information through images.

Abstract: A biological function measurement and analysis system, a biological function measurement and analysis method, and a recording medium storing program code causing a computer to execute the biological function measurement and analysis method. The biological function measurement and analysis system includes an input acceptance unit configured to accept selection of a biological function to be measured, and a measurement and analysis procedure determining unit configured to access a memory in which measurement and analysis procedure data, indicating a combination of measurement and analysis of reaction of a live subject caused by stimulation on a biological-function-by-biological-function basis, is stored to specify measurement and analysis procedure data corresponding to the selected biological function.

Abstract: Disclosed embodiments include a complete system and platform, and a method which allows for monitoring and supporting treatment for elderly care in clinic, home, and other normal daily environments. The system includes: (1) a pressure sensitive device for receiving force response from the elderly and convert the force response into digitalized pressure data, (2) a computing device for running a movement disorder assessment module to receive digitalized pressure data, display visual instructions and feedback, and process the digitalized pressure data for calculation of movement disorder scores, and (3) a cloud based digital diary to store, access and analyze the movement disorder scores, and generate reports on demand. The method will calculate the movement disorder scores based on the digitalized pressure data. A pressure sensitive device is also disclosed.

Abstract: The invention generally relates to motion analysis systems and methods of use thereof. In certain aspects, the system includes an image capture device, at least one accelerometer, and a central processing unit (CPU) with storage coupled thereto for storing instructions that when executed by the CPU cause the CPU to receive a first set of motion data from the image capture device related to at least one joint of a subject while the subject is performing a task and receive a second set of motion data from the accelerometer related to the at least one joint of the subject while the subject is performing the task. The CPU also calculates kinematic and/or kinetic information about the at least one joint of a subject from a combination of the first and second sets of motion data, and outputs the kinematic and/or kinetic information for purposes of assessing a movement disorder.

Abstract: A method for assessing a cognition and movement disease or disorder in a subject suspected to suffer therefrom. A cognition and/or fine motoric activity parameter is determined from a dataset of activity measurements obtained from the subject using a mobile device. The determined activity parameter is compared to a reference, and the cognition and movement disease or disorder is assessed. Also disclosed is a method for identifying whether a subject will benefit from a therapy for a cognition and movement disease or disorder. The steps just described are performed along with the step of identifying the subject as one who benefits from the therapy if the cognition and movement disease or disorder is assessed. Also disclosed is a mobile device comprising a processor, at least one sensor, a database and software which is tangibly embedded in said device and, when running on said device, carries out the disclosed methods.

Abstract: Embodiments disclosed herein are directed to devices, systems, and methods for monitoring pregnancy of a female pregnant subject. For example, a pregnancy monitoring system can detect movement or motion of a pregnant subject and/or of the fetus in the pregnant subject. Additionally or alternatively, the pregnancy monitoring system can detect internal and/or external source loads applied to the pregnant subject. In an embodiment, the pregnancy monitoring system can compare and/or correlate two or more loads, one to another (e.g., to produce an output that is at least partially based on such comparison and that is related to the wellbeing of the pregnant subject and/or of the fetus). For example, the pregnancy monitoring system can include a controller that is configured to determine and compare two or more loads based on signals received from one or more sensors that can be positioned on the pregnant subject.

Abstract: A skin inspection device for identifying abnormalities. The device comprises a transparent panel having an inspection area. An array of temperature sensors are provided on the transparent panel to record the temperature of an area of skin of a target. One or more image capture devices are provided for capturing an image of the area of skin of a target located in the inspection area. The captured image and recorded temperature being analysed to identify abnormalities in the area of skin of the target. A processor is operably coupled to the one or more image capture devices and the array of temperature sensors for controlling operations thereof. The processor is operable to generate indicia indicative of the emergence of ulcers and/or other skin abnormalities.

Abstract: A tongue-image-based diagnostic system and a tongue-image-based diagnostic method are disclosed. The diagnostic system includes a parameter collector configured to acquire environmental parameter information; a model establishment circuitry configured to perform a training process using image training data and the environmental parameter information and establish an estimation model; and an analysis circuitry configured to analyze acquired image information using the estimation model, and generate an analysis result corresponding to the acquired image information.

Abstract: A posture analysis device (10) is a device for analyzing the posture of a subject, and includes a data acquisition unit (11) configured to acquire image data to which the depth of each pixel is added, from a depth sensor that is disposed to capture an image of the subject, a skeleton information creation unit (12) configured to create skeleton information for specifying positions of a plurality of sites of the subject based on the image data, a state specifying unit (13) configured to specify states of the back, the upper limbs, and the lower limbs of the subject based on the skeleton information, and a posture analysis unit (14) configured to analyze the posture of the subject based on the specified states of the back, the upper limbs, and the lower limbs of the subject.

Abstract: A biofeedback virtual reality (VR) system and methods are provided for improving, optimizing, or minimizing the physiological or psychological effects of a medical condition, such as a physiological or psychological condition of a patient. The biofeedback VR System monitors one or more physiological parameters while presenting an immersive VR environment. The system and method comprise a closed-loop biofeedback system where a user (i.e., patient) observes a VR Experience provided by the VR System. The VR System monitors one or more physiological parameters while guiding the user to an improved (or optimized) physiological state through improvement of one or more of the physiological parameters. In some embodiments, a social experience is included in the VR, where the user engages with one or more other users in the VR Experience.

Abstract: A method of performing closed-loop dialysis treatment during hemodialysis is provided. The method involves determining an initial ultrafiltration rate and setting an ultrafiltration pump of a dialysis system to the determined ultrafiltration rate. A series of measurements and calculations are made to ensure that a rate of change of blood volume during treatment follows a specified profile. A threshold may be used to keep the rate of change of blood volume tracking the profile. Patient fluid dynamics may be measured in real-time and used to determine the ultrafiltration pump rate.

Abstract: The present disclosure relates to blood pressure calibration period determining methods and devices. One example method includes obtaining, by a blood pressure measurement device, first physiological status information and second physiological status information of a tested person, where the first physiological status information is related information that causes a change in blood pressure of the tested person within a first time period after the blood pressure is calibrated, and where the second physiological status information is related information that causes a change in the blood pressure of the tested person within a second time period before the blood pressure is calibrated, and determining, by the blood pressure measurement device, a blood pressure calibration period based on a degree of change of the first physiological status information relative to the second physiological status information.

Abstract: A sensing element comprises a transistor having a gate electrode, a source electrode, a gate electrode and a semiconductor nanostructure connecting between the source and the gate electrodes. The semiconductor nanostructure is modified by a functional moiety covalently attached thereto. A voltage source is connected to the gate electrode. A controller controls a gate voltage applied by the voltage source to the gate electrode such as to reverse a redox reaction occurring when the moiety contacts a redox reactive agent.

Abstract: A capacitive sensor may include a stretchable substrate, a first conductor assembly disposed on the substrate, a second conductor assembly disposed on the substrate and above the first conductor, and a redundancy member coupled to the one of the conductor assemblies. A capacitive sensor may include a first serpentine conductor assembly disposed on the substrate and having first and second terminal ends coupled to the substrate, a second serpentine conductor assembly disposed above and overlapping the first conductor assembly and having first and second terminal ends coupled to the substrate, wherein each of the terminal ends of the first conductor assembly is offset from the corresponding terminal ends of the second conductor assemblies. A sensor system may include a stretchable sensor, an electronics module coupled to the stretchable sensor, and a strain relief member extending from the stretchable sensor and coupling to the electronics module.

Abstract: A wearable device to wear on a head of a user includes a flexible band generally shaped to correspond to the user's head, the band having at least a front portion to contact at least part of a frontal region of the user's head, a rear portion to contact at least part of an occipital region of the user's head, and at least one side portion extending between the front portion and the rear portion to contact at least part of an auricular region of the user's head. A deformable earpiece is connected to the at least one side portion, the deformable earpiece including conductive material to provide at least one bio-signal sensor to contact at least part of the auricular region of the user's head. At least one additional bio-signal sensor is disposed on the band to receive bio-signals from the user.

Abstract: A wearable defibrillator includes garment configured to be worn by a patient, treatment electrodes configured to apply electric current to the patient, and an alarm module configured to provide audio, visual, and haptic notifications. The notifications are configured to indicate that an electric current will be administered imminently, and prompt the patient to provide a response input. The wearable defibrillator includes a motion sensor configured to detect motion and a lack of motion of the patient, and a controller in electrical communication with the alarm module and the motion sensor. The controller is configured to monitor for the response input, cause administration of the electric current to be delayed or cancelled if the response input is received and motion of the patient is detected, and cause administration of the electric current to be delivered if no response input from the patient is received and a lack of motion is detected.

Abstract: A silver coated needle, a medical device comprising the needle and a method for electrochemically detecting penetration through a semi-permeable membrane such as the round window membrane of a subject are described. Penetration through the membrane by the needle can be detected by observing the voltage change as the needle penetrates through the membrane.

Abstract: A wireless circuit includes a housing having at least one opening, and sensor connected to the housing at the opening. The sensor includes a first layer having a first dimension and a second layer having a second dimension shorter than the first dimension. The second layer may be positioned entirely within the housing and a surface of said first layer may be exposed to an exterior of the housing.

Abstract: A body movement detection sensor includes a sensor section having a piezoelectric film, a right belt member, a left belt member, and an engagement member configured to engage the right and left belt members. In the body movement detection sensor, the piezoelectric film exhibits piezoelectric effect in a length direction, the right belt member and the left belt member have substantially no elasticity, the body movement detection sensor further includes an elastic sheet directly or indirectly connected to the right belt member and the left belt member, the piezoelectric film and the elastic sheet are arranged substantially without irregularities when viewed from a side, and the elastic sheet has a maximum amount of expansion larger than an amount of change of a thorax during breathing and has a length equal to or smaller than one-sixth of a total length of the right belt member and the left belt member.

Abstract: A system for performing a diagnostic or therapeutic procedure within a subject includes a device having a distal portion configured for insertion within a lumen or duct of the subject, the device including an elongate body having a longitudinal axis, the elongate body comprising a polymeric material and having a proximal end and a distal end, one or more electrically-conductive tracings carried on a first surface of the elongate body and configured to carry a signal, and one or more conductors embedded within the polymeric material and configured to carry a signal.

Abstract: A jacket that includes a first portion, a second portion, and an interface. The interface is movably coupled to the first portion and the second portion. The first portion comprises multiple medical modules. The multiple medical modules include at least one medical sensor and a physiological signal conduit for transferring a physiological signal from an inner side of the first portion to an exterior side of the first portion. The first and second portions are configured to be detachably coupled to a mobile phone. When the jacket is at a closed position then the first portion, the second portion and the interface define an inner space that is configured to receive the mobile phone and the first and second portions contact opposite sides of the mobile phone. When the jacket is at an open position, then only one of the first and second portions contacts the mobile phone.

Abstract: A bio-information measuring apparatus bio-information measuring method are provided. The bio-information measuring apparatus includes: a pulse wave obtainer configured to obtain a pulse wave signal, and a processor configured to correct a feature of the obtained pulse wave signal based on a variation in an amplitude of the obtained pulse wave signal, and to measure bio-information based on the corrected feature.

Abstract: A method and system used to detect characteristic information of internal body tissues applies multiple AC currents of different frequencies simultaneously to a human or animal body. After the modulated voltage signals are received, they are demodulated. Information from both the cardiovascular system and the surrounding tissues is extracted from the carrier waves of specified frequencies. System identification or channel estimation procedures are performed to separate the information from the cardiovascular circulation system and the surrounding tissues. The resistance and capacitance of the cardiovascular system and surrounding tissues are calculated separately. The calculated resistance and capacitance values are used to represent the states of body fluid and cardiovascular circulation. As a result, relevant state information is obtained accurately and reliably to enable accurate measurements of targeted tissues for acquiring health states.

Abstract: Time-efficient identification of a brain network input-output (IO) dynamics model for brain stimulation includes generating an input stochastic-switched noise-modulated waveform characterized by at least one parameter modulated according to a stochastic-switched noise sequence, inputting the input stochastic-switched noise-modulated waveform to a clinical brain-response system, recording one or more time-correlated outputs of the clinical brain-response system responsive to the input stochastic-switched noise-modulated waveform, and identifying a brain network IO dynamics model that optimally correlates the input stochastic-switched noise-modulated waveform to the one or more time-delimited outputs of the clinical brain-response system. A desired brain response to an input electrical signal may be obtained using the model, such as by modulating the input electrical signal using a closed-loop control algorithm based on the brain network IO dynamics model.

Abstract: Systems and methods for detecting an anomaly in a cardiovascular signal using hierarchical extremas and repetitions. The traditional systems and methods provide for some anomaly detection in the cardiovascular signal but do not consider the discrete nature and strict rising and falling patterns of the cardiovascular signal and frequency in terms of hierarchical maxima points and minima points. Embodiments of the present disclosure provide for detecting the anomaly in the cardiovascular signal using hierarchical extremas and repetitions by smoothening the cardiovascular signal, deriving sets of hierarchical extremas using window detection, identifying signal patterns based upon the sets of hierarchical extremas, identifying repetitions in the signal patterns based upon occurrences and randomness of occurrences of the signal patterns and classifying the cardiovascular signal as anomalous and non-anomalous for detecting the anomaly in the cardiovascular signal.

Abstract: A system includes a wearable sensor device including an accelerometer configured to be worn by a person and to record sensor data during an activity performed by the person; an analysis element configured to receive the sensor data from the wearable sensor, determine sensor orientation data of the wearable sensor during the activity based on the sensor data, translate the sensor orientation data of the wearable sensor to person orientation data of the person during the activity, determine, for the person during the activity, (a) a lift rate, (b) a maximum sagittal flexion, (c) an average twist velocity, (d) a maximum moment, and (e) a maximum lateral velocity, and determine a score representative of an injury risk to the person during the activity based on such data; and a tangible feedback element configured to provide at least one tangible feedback based on the score so as to reduce the injury risk.

Abstract: The present invention relates to a device (10, 10a, 10b), system (1, 2, 3) and method for detection of an asthma attack or asthma of a subject. For this purpose, the device comprises a light sensor input (11), e.g. a 2D camera, for obtaining light sensor data of the scene and a thermal sensor input (12), e.g. a thermal camera, for obtaining thermal sensor data of a scene including a subject while breathing. An analysis unit (13) obtains these data and derives respiratory effort information indicating respiratory efforts of the subject from the obtained light sensor data and/or the obtained thermal sensor data and derives airflow information indicating airflow during respiration of the subject from the obtained thermal sensor data. Further, the analysis unit (13) predicts or detects an asthma attack or asthma based on analysis of the respiratory effort information and the airflow information, said analysis evaluating deviations from predetermined or healthy correlations between respiratory efforts and airflow.

Abstract: A method of calculating body fluid and blood flow in a human or animal body using multi-frequencies alternating electrical currents, determining the tissues' multi-frequency impedance and reactance changes, calculating the body fluid, blood flow and physiological parameter. With the simultaneous measurements of body's or tissues' impedance and reactance from multi-frequencies, it is possible either to compensate for the frequency-dependencies or to find the dependencies' cross relationship, and thus measure body fluid and blood flow more accurately.

Abstract: An approach is provided for synchronizing an impedance cardiography (“ICG”) measurement period with an electrocardiography (“ECG”) signal to reduce patient (105) auxiliary current. The approach involves measuring an ECG signal of a patient via an ECG device (103). The approach also involves processing the ECG signal to cause, at least in part, a detection of one or more ECG features of the signal. The approach further involves synchronizing a start, a stop, or a combination thereof of a measurement of an ICG signal of the patient via an ICG device (101) based, at least in part, on the detection of the one or more ECG features. The measurement of the ICG signal includes injecting an electrical current into the patient (105) for a duration of the measurement.

Abstract: A method for determining and responding in real-time to an increased risk of death relating to a patient with epilepsy is provided. The method includes receiving cardiac data and determining a cardiac index based upon the cardiac data. The method includes determining an increased risk of death associated with epilepsy if the indices are extreme, issuing a warning of the increased risk of death and logging information related to the increased risk of death. Also presented is a second method for determining and responding in real-time to an increased risk of death relating to a patient with epilepsy comprising receiving at least one of arousal data, responsiveness data or awareness data and determining an arousal index, a responsiveness index or an awareness index, where the indices are based on arousal data, responsiveness data or awareness data respectively.

Abstract: A patient monitoring system can have a display screen or portion thereof with graphic user interface for displaying indications of a patient's oxygen state. The indications can include the patient's SpO2, dissolved oxygen index, and/or an increasing or decreasing trend of dissolved oxygen index. The displays of oxygen state indications can be compact, and/or able to provide direct visual information to a user of various aspects of the patient's oxygen state. The display elements can be used to represent any other physiological parameters.

Abstract: A system for multi-mode breast x-ray imaging which comprises a compression arm assembly for compressing and immobilizing a breast for x-ray imaging, an x-ray tube assembly, and an x-ray image receptor is provided. The system is configured for a plurality of imaging protocols and modes.

Abstract: Various embodiments of medical detector systems as well as their methods of operation are disclosed. In one embodiment, one or more detectors are coupled to wearable structures for detecting at least a first tracer within a body portion. In another embodiment, one or more detectors are coupled to a wearable structure, where the detector corresponds to a CMOS chip that directly detects a first radioactive tracer.

Abstract: A system includes a multi-sectional articulating arm including a first section pivotally secured to a second section, the second section pivotally secured to a third section, a wall mount secured to the first section opposite the second section, and a mounting bracket secured to an end of the third section opposite the second section.

Abstract: A medical image diagnosis apparatus according to an embodiment obtains a first position of a predetermined part of an image taking target included in a medical robot system, a first direction of a rotation axis of the image taking target, and a first rotation angle of the image taking target, within a coordinate system of the medical image diagnosis apparatus. The medical image diagnosis apparatus derives information that brings the coordinate system of the medical image diagnosis apparatus and the coordinate system of the medical robot system into correspondence with each other, on the basis of the first position, the first direction, and the first rotation angle, as well as a second position of the predetermined part, a second direction of the rotation axis, and a second rotation angle of the image taking target, within a coordinate system of the medical robot system.

Abstract: A computer-implemented system and method for generating a medical image is provided. In some embodiments, the medical image is generated by determining a location and an alignment for a first tracking detector with respect to a particle beam system. The direction of a beam generated from the particle beam system is determined. A first position of a first particle from a detected particle hit on the first tracking detector is also determined. A determination is made as to a first residual range of the first particle from a detected particle hit on a residual range detector. The system reconstructs a path for the first particle based on the location, the alignment, the first position, and the first residual range of the first particle. The resulting medical image that is generated by the system is based on the reconstructed path for the first particle.

Abstract: A method of setting operating conditions of a detector in an imaging system includes searching for a detector that is not registered in the imaging system; acquiring detector profile information from the searched detector; registering the detector based on the detector profile information; allocating a predetermined marker to the registered detector to represent activation or non-activation thereof; transmitting control information including the allocated predetermined marker to the detector; receiving detector correction information from the detector; and setting operating conditions of the detector based on the received detector correction information.

Abstract: The present disclosure is related to systems and methods for monitoring a medical device. The medical device may include a tube configured to generate radiation rays and a detector configured to receive radiation rays emitted from the tube. The tube may include an anode target and a filament. The detector may include a plurality of detecting units. The method may include obtaining imaging data acquired by the detector via detecting radiation rays emitted from the tube. The method may also include determining a first feature parameter associated with the radiation rays based on the imaging data. The method may further include monitoring the medical device based on the first feature parameter associated with the radiation rays.

Abstract: This document describes a system for determining positioning of an intubation tube in a patient. The system can include a first acoustic sensor configured to be disposed to listen to one of a lung and a stomach of the patient and to provide a first signal. The system includes a signal processing unit, coupled to the first acoustic sensor, configured to analyze spectral components of the first signal and determine whether a frequency of the spectral components of the first signal are characteristic of sounds induced by ventilation via the intubation tube of airflow to the lung or the stomach of the patient.

Abstract: A system, device (140) and method for the non-invasive ultrasound or any other imaging based measurement system of the intravascular blood pressure is presented, wherein the blood pressure measurements are performed by means of the image time series processing estimating the volumes of the oscillating traceable regions. The new generalized M-mode being the set of M-modes corresponding to all ultrasound channels is introduced. The invention is applicable to any medium transparent for imaging waves capable to be converted into the image series calibrated to the pressure changes of the liquid.

Abstract: Disclosed herein are systems and methods for providing real-time monitoring of a probe within a target zone. An apparatus for tracking the probe comprises a transducer assembly comprising a two-dimensional array of transducer elements. The two-dimensional array comprises a plurality of transverse arrays and a plurality of longitudinal arrays. The monitoring system further comprises a processor configured to activate and receive data from at least one transverse array extending along a transverse axis that is transverse to the target zone and to a direction of travel of the probe, and two or more longitudinal arrays extending along longitudinal axes that are transverse to the transverse axis. The two or more longitudinal arrays may be activated sequentially in a programmed sequence. Based on the data, the processor can determine the position of the probe within the target zone, and display the probe on a transverse cross-section view of the target zone via a software-generated special effect.

Abstract: A catheter extension can include an extension body with a sheath defining a lumen, a cable extending within the lumen, a proximal connector attached to the sheath and configured to couple to a catheter drive mechanism, and a distal connector attached to the sheath and configured to couple to a catheter. An axial biasing member can be coupled to the cable and integrated into either the proximal or distal connector and configured to exert a force on the cable in a first axial direction and permit movement of the cable in a second axial direction. An axial key can be coupled to the cable and integrated into the connector opposite the axial biasing member. The axial key can include a tab attached to the cable and a slot with an inner profile that complements a tab outer profile that can permit the tab to move in within the slot.

Abstract: Embodiments of the present invention include a laser catheter that includes a catheter body, a light guide, and a distal tip that extends beyond the exit aperture of the light guide. In some embodiments, an imaging device is disposed on the distal tip such that the imaging device is distal relative to the exit aperture of the light guide. In some embodiments, the imaging device can be gated to record images during and or slightly beyond periods when the laser catheter is not activated.

Abstract: The present disclosure relates to a probe structure that includes a probe configured to transmit or receive acoustic energy and having a first end and a second end opposite the first end, a probe hub defining a cavity for receiving at least a portion of the probe, and a joint coupled to the second end of the probe and configured to allow the probe to pivot within the probe hub.

Abstract: An ultrasound diagnosis apparatus and method enabling general users to easily acquire ultrasound images even when the users are unskilled at using ultrasound diagnosis apparatuses, including a probe comprising an analog front-end controller, an analog-to-digital converter, a field-programmable gate array, and a communication module, the probe being configured to acquire ultrasound data of an object.

Abstract: High frequency ultrasound transducers configured for use with high frequency ultrasound diagnostic imaging systems are disclosed herein. In one embodiment, an ultrasound transducer includes a concave lens having an average thickness in a center portion that that is substantially equal to an odd multiple a ¼-wavelength of the center frequency of the ultrasound transducer.

Abstract: Devices, systems, and methods are disclosed for use in tomographic ultrasound imaging, large aperture ultrasound imaging and therapeutic ultrasound that provide for coupling acoustic signal transducers to body structures for transmitting and receiving acoustic signals. The acoustic signal transmission couplants can conform to the receiving medium (e.g., skin) of the subject such that there is an acoustic impedance matching between the receiving medium and the transducer. In one aspect, an acoustic coupling medium includes a hydrogel including polymerizable material that form a network structured to entrap an aqueous fluid inside the hydrogel.

Abstract: A cradle apparatus configured to detachably support an ultrasound diagnostic apparatus, the cradle apparatus including: a base portion configured to support a bottom portion of the ultrasound diagnostic apparatus; a back supporting portion extending from the base portion along an attaching/detaching direction of the ultrasound diagnostic apparatus, the back supporting portion being configured to support a back portion of the ultrasound diagnostic apparatus on a side opposite to a front portion of the ultrasound diagnostic apparatus, the front portion being provided with a display device; and a guide disposed in the back supporting portion and configured to be fitted with a rail provided in the back portion of the ultrasound diagnostic apparatus so as to allow the ultrasound diagnostic apparatus to slide along the attaching/detaching direction.

Abstract: A high frequency ultrasound array having a number of transducer elements that are formed in sheet of piezoelectric material. A frame having a coefficient of thermal expansion that is similar to that of the piezoelectric material surrounds the piezoelectric material and is separated from the piezoelectric material by a filling material. Kerf cuts that define the individual elements in the sheet of piezoelectric material extend across a full width of the sheet. In some embodiments, sub-dice kerf cuts that divide a single transducer element into two or more sub-elements also extend all the way across the width of the sheet. A lens positioned in front of the transducer elements can have a radius machined therein to focus ultrasound signals.