Abstract: Methods and devices for treating skin include a skin-contacting portion, an actuator and a processor, wherein activation of the actuator causes surface acoustic waves of Rayleigh, “pseudo” Rayleigh types to be produced on the skin around the actuator. In a location which is under the actuator, the actuator produces tension and repulsion of skin particles. These surface acoustic waves can be used to provide treatment to the skin, including wound healing, non-adhesion of bandages, reduced infection, reduced pain and cosmetic enhancements. The skin-contacting portion may be a patch or bandage, a glove, a hand-held device, or any other suitable configuration. The actuator is incorporated into the skin-contacting portion.

Abstract: Method and device for recording a vascular structure during intervention comprises steps or elements for detecting S1 an injection of a contrast agent 6 provided to the vicinity of a device landmark 5, monitoring S3 for a predetermined time the vicinity of the device landmark 5, generating S3a time-contrast curves based on the monitored vicinity of the device landmark 5, analyzing S4a the time-contrast curves, and determining S4b a best instant as a visibility optimum based on the time-contrast curves.

Abstract: Systems and methods are provided herein that generally involve measuring a prostate or other object. In some embodiments, a membrane can be sealed over a digit extension to form a closed volume. The closed volume can be inflated via an inflation tube, and a reference pattern can be disposed within the closed volume along with a measurement assembly. In use, a user can put on the glove, position the membrane in proximity to a rectal wall overlying a prostate, and inflate the membrane. As the user slides their finger across the rectal wall, optical fibers in the measurement assembly can move relative to a reference pattern, and a controller can sense light reflected through the fibers from the reference pattern. The controller can calculate or estimate various attributes of the prostate based on the reflected light, such as the palpable surface width or volume.

Abstract: A device (16) positions an ultrasound transducer (14) for ultrasound therapy to focus a treatment beam (12) emitted by the ultrasound transducer (14) at tissue of interest. The device (16) includes at least three anchors (20) which support the ultrasound transducer (14). The device (16) further includes at least three extendable structures (24), each with a coupling (22) that supports a corresponding one of the at least three anchors (20). A drive mechanism (100) of the device (16) independently drives each of the at least three extendable structures (24) towards or away from a subject to move the ultrasound transducer (14) within at least three degrees of freedom.

Abstract: An ultrasonic image generating device which generates a cross-sectional image of a specific cross-section of a subject from ultrasonic images obtained by scanning the subject from a plurality of directions using an ultrasonic probe, includes: a cross-section position identifying unit which obtains cross-section information indicating a position and an orientation of the specific cross-section; a positional information obtaining unit which obtains positional information including a position and an orientation of each of the ultrasonic images of the subject; a reference image selecting unit which selects at least one of the ultrasonic images as a reference image, the at least one of the ultrasonic images having a distance from the specific cross-section that is less than a first threshold and an orientation difference from the specific cross-section that is less than a second threshold; and a cross-sectional image generating unit which generates the cross-sectional image using the reference image.

Abstract: In an ultrasonic diagnostic device S according to the present invention, a reference signal generation unit 30 generates a reference signal to be used in correlation processing based on a direct reception signal obtained by receiving a first ultrasonic signal prior to being transmitted to a subject. Consequently, the ultrasonic diagnostic device S configured in this manner is able to generate a more suitable reference signal.

Abstract: An ultrasound machine is operated by executing a protocol. Executing the protocol configures the ultrasound machine, controls for operating the ultrasound machine and a display for the ultrasound machine. Protocols may be defined to provide a streamlined configuration of controls for operating the ultrasound machine, and to provide instructions that guide a user's operation of the ultrasound machine.

Abstract: There is provided an ultrasonic diagnosis apparatus capable of reducing an unnecessary signal component in a reception signal. A plurality of sign bits arranged in the channel direction are extracted from a plurality of element reception signals. A binarization circuit applies binarization processing to the plurality of sign bits to thereby generate a sign data array. An evaluation value computing unit computes an evaluation value (GSCF) based on a DC vicinity component contained in the sign data array on the frequency axis. This evaluation value is used to adjust the gain of the reception signal in a multiplier. With application of the binarization processing, excessive reduction of the reception signal can be prevented. Further, as the DC vicinity component is referenced, the side-lobe component can be appropriately reduced even if a certain degree of fluctuation exists in the main-lobe component.

Abstract: A fluoroscopy apparatus is adopted which includes a fluorescence-image generating section that generates a fluorescence image of a subject, a white-light-image generating section that generates a white-light image of the subject, a fluorescence-image correcting section that generates a corrected fluorescence image in which luminance values of pixels are normalized by dividing the luminance values of the pixels of the fluorescence image by the luminance values of the pixels of the white-light image, an error-image identifying section that standardizes white-light-image acquisition conditions and identifies an error region, which is a region in which the luminance values of the corrected fluorescence image exceed a preset allowable error range, on the basis of a gray level of the normalized white-light image, and a monitor that displays the error region.

Abstract: A cryocatheter for introduction into a body vessel or into an organ, with a catheter inner surrounded by a catheter sheath, and with a catheter tip arranged at its distal end, with a feed line for an expansion or cooling agent arranged in the catheter sheath or the catheter inner, and with a balloon, arranged close to the catheter tip, which can be expanded and contracted again by means of the expansion and cooling agent, is to be constructed in such a way that by simple manipulation it can be positioned at a precise target position in the body vessel and, in addition, it minimizes the burden on the patient from invasive interventions. For this purpose, in accordance with the invention an image capture device, with at least one imaging sensor for mapping the region of the vessel around the balloon, is positioned in the region of the catheter tip.

Abstract: The ultrasound diagnostic apparatus, ultrasound image generation apparatus and method transmit ultrasound waves to a subject into which a puncture tool is inserted, receive reflected waves reflected from the subject and the puncture tool, and generate echo signals of time-sequential frames based on the received reflected waves, and generate an ultrasound image of the subject based on the generated echo signals. These apparatus and method generate a differential echo signal between time-sequential frames from the echo signals, perform a tip detection process based on the differential echo signal to thereby detect at least one tip candidate including a tip end of the puncture tool, highlight a tip candidate of the puncture tool detected to thereby generate a tip image, and display the tip image of the highlighted puncture tool so as to be superimposed on the generated ultrasound image.

Abstract: The number of signal lines connecting an ultrasonic probe and an ultrasonic diagnostic apparatus main body is reduced or wireless communication is realized by reducing a volume of data of reception signals outputted from plural ultrasonic transducers. The ultrasonic probe includes: plural ultrasonic transducers for transmitting ultrasonic waves according to drive signals and receiving ultrasonic echoes to output reception signals; signal processing units for performing orthogonal detection processing or orthogonal sampling processing on the reception signals to generate two signals representing a complex baseband signal; sampling units for sampling the two signals to generate parallel sample data; a serializing unit for converting the parallel sample data into serial sample data; and a transmitting unit for transmitting the serial sample data.

Abstract: There is provided an ultrasonic diagnosis apparatus capable of reducing an unnecessary signal component in a reception signal. A sign data array formed of a plurality of sign data items arranged in an element arranging direction is extracted from a plurality of element reception signals having been subjected to delay processing but having not been subjected to summing processing. A factor computing unit computes a first factor indicating a level of sign coherence in the sign data array and a second factor indicating a sign transit density in the sign data array. The factor computing unit then computes a factor (evaluation value) for adjusting gain of the reception signal, based on the first factor and the second factor.

Abstract: Disclosed are systems and methods for power injectors incorporating a keep vein open functionality that is operable when an injection protocol (112) is suspended. The injector includes control logic (110) configured to include the injection protocol (112), and a separate drip mode injection protocol (114) executable only during a suspension of the injection protocol (112). In one embodiment, the drip mode injection protocol (114) is automatically or manually initiated immediately after and in response to the suspension of the injection protocol (112). In another embodiment, the drip mode injection protocol (114) is automatically initiated after a predetermined delay from start of the suspension of the injection protocol (112). The configuration parameters for the drip mode injection protocol (114) may be programmable prior to the initiation of an injection procedure, immediately prior to the execution of the drip mode injection protocol (114), or hard-coded into the injector.

Abstract: A medical examination device used for the detection of pre-cancerous and cancerous tissue has an illumination source, a visualization unit, a contacting optical probe, a detector and a process unit. One embodiment of the apparatus includes both a non-contacting macroscopic viewing device (the visualization unit) for visualizing an interior surface of the cervix, as well as a fiber optic wand (contacting optical probe) for spectrally analyzing a microscopic view of the tissue.

Abstract: An ultrasonic imaging system produces a sequence of images of the heart during a cardiac cycle. The images are analyzed to determine the motion, displacement, or change in size of segments of the myocardium. In a preferred embodiment the values determined are radial, longitudinal, or circumferential myocardial strain values. The displacement of the myocardial segments may be tracked during the cardiac cycle by speckle tracking or border detection. The motion, displacement, or change in size values for the segments are analyzed to produce a recruitment curve and anatomical display showing the relative times of recruitment of the different segments in the contractile and relaxation motion of the heart. Participation in and achievement of full recruitment may be determined by comparison against an initial recruitment threshold criterion and against a predetermine maximal recruitment milestone level.

Abstract: A medical instrument that comprises: a first-stage optic responsive to a tissue surface of a patient; a spectral separator optically responsive to the first stage optic and having a control input; an imaging sensor optically responsive to the spectral separator and having an image data output; and a diagnostic processor having an image acquisition interface with an input responsive to the imaging sensor and a filter control interface having a control output provided to the control input of the spectral separator.

Abstract: In order to simplify a manufacturing process and reduce cost and power consumption by providing an ultrasonic diagnostic apparatus including a carrier signal generating circuit excellent in IC implementation, a carrier signal generating circuit for generating an output voltage Vo applied to an ultrasonic probe 41 includes cascaded source follower type NMOSFETs 11 to 14, a variable current source 31, and a constant current source for biasing 32. The probe 41 can be made to generate the output voltage Vo with arbitrary amplitude by controlling a gate voltage V4 by controlling the output current value of the variable current source 31. In addition, a voltage applied to each NMOSFET can be divided by connecting the NMOSFETs 11 to 14 in a multi-stage manner. Accordingly, the withstand voltage of the NMOSFET may be low.

Abstract: A device for therapeutic treatment includes an acoustic transducer designed to emit power waves to treat a target, and an imaging probe designed to emit waves for providing an image representation of the target and its environment before, during and after the emission of the power waves issuing from the transducer. The probe and the transducer are integrally connected to one another other. The device also includes a display for displaying images taken by the probe, namely images at rest, taken before and/or after emission of the power waves, and interference images, taken during the emission of the power waves. The device additionally comprises a detector for detecting a change of structure of the interference images that is indicative of the efficacy of the power waves.

Abstract: A bioinformation acquisition apparatus to input a signal having uniform sensitivity and a high SN ratio at a high speed is provided. It includes a moving device moving an element group into the arrangement direction of the elements, and moves the element group situated at a first position at first time point to be situated at a second position at second time point. The element group receives an elastic wave emitted from a test object at the first time point at the first position, and the elastic wave from the test object at the second time point at the second position. The electric signal of a specified position of a test body from a first element of the elastic waves received at the first time point and the electric signal of the specified position from a second element received at the second time point are added to each other.