Abstract: A method, including capturing, from an imaging system, a three-dimensional (3D) image of a body cavity, and using the captured 3D image to construct a simulated surface of the body cavity. A probe having a location sensor is inserted into the body cavity, and in response to multiple location measurements received from the location sensor, multiple positions are mapped within respective regions of the body cavity so as to generate respective mapped regions of the simulated surface. Based on the simulated surface and the respective mapped regions, one or more unmapped regions of the simulated surface are delineated, and the simulated surface of the body cavity is configured to indicate the delineated unmapped regions.

Abstract: An imaging system includes an imaging device (10) configured to acquire an image in a multi-beat acquisition mode. A quality scoring module (115) is stored in memory and is configured to evaluate changes in the image between portions of a multi-beat cycle to compute a quality score (136) indicating a suitability of the image. A display (118) is included for viewing the image and displaying the quality score as real-time feedback for the image.

Abstract: In one aspect, the present disclosure describes a method for detecting cerebrospinal fluid (CSF) flow of a subject in which magnetic resonance imaging signals of a selected region of interest of the subject's anatomy are acquired. Preferably, the selected region of interest comprises the cerebro-spinal anatomy. A central location of the selected region of interest of the subject's anatomy is determined and used to determine a mean intensity value associated with image pixels of the central location. The mean intensity value is then used to establish interior and exterior outlines of the the selected region of interest of the subject's anatomy so that the CSF flow within the interior and exterior anatomical outlines may be measured or detected.

Abstract: A system for detecting an abnormality in a subject's cerebrovascular response to a vasoactive stimulus in at least one region of interest (ROI) of the subject's brain The system comprises a system for generating the vasoactive stimulus (SVS), the SVS including a gas delivery device and a control system operable to deliver controlled amounts of carbon dioxide effective to attain at least one of a series of targeted increments or decrements in the subject's PetCO2, for a series of respective intervals; an imaging system comprising an MRI scanner for generating response signals corresponding to the subject's vasoactive response to the vasoactive stimulus; and a computer for analyzing the response signals, the computer including program code for computing at least one value representing a quantitative measure of the subject's cerebrovascular reactivity for the ROI, wherein the at least one value is obtained for a specific portion of the subject's vasoactive response in the ROI, the specific portion of the subject

Abstract: An ultrasound transducer assembly (10) is disclosed comprising a plurality of transducer elements (32) for transmitting and receiving ultrasound waves (24) each having a substrate (40) and a flexible membrane (46) disposed in a distance from a substrate. An AC voltage control unit (56) is provided for controlling an AC voltage provided to each of the transducer elements, and a DC voltage control unit (60) for controlling a DC bias voltage provided to the transducer elements in order to bring the flexible membranes in a collapse mode into contact with the substrate. The DC voltage control unit is adapted to disconnect the DC bias voltage from the transducer elements temporarily during the operation of the ultrasound transducer assembly to limit the collapse mode.

Abstract: A method for operating a medical robot, a medical robot, and a medical work station. The invention relates to a method for operating a medical robot (2). The robot (2) includes a robot arm (5) having a plurality of members (7), drives (15) provided for moving the members (7), and an attaching device (9). The robot (2) also has a control device (6) for activating the drives (15), and a sound generating device (3) attached to the attaching device (9), which is provided to apply sound to a living organism (10), in particular a high-intensity focused ultrasound.

Abstract: A palpation assisting apparatus includes a synchronization controller configured to synchronize a timing of acquiring pressure data output from a pressure sensor attached to a position in contact with a lesion part with a timing of acquiring positional information of a marker attached to a position corresponding to the pressure sensor, and an entering part configured to store, in a storage part, the pressure data and the positional information of the marker that are acquired at the synchronized timing in association with time information indicating a time at which the pressure data and the positional information are acquired.

Abstract: A method and an electronic device for measuring blood pressure are provided. The method includes illuminating, by a PPG sensor included in the electronic device, skin of a user and measuring a PPG signal based on an illumination absorption by the skin. Further, the method also includes extracting, by the electronic device, a plurality of parameters from the PPG signal, wherein the parameters may comprise PPG features, Heart Rate Variability (HRV) features, Acceleration Plethysmograph (APG) features, and non-linear features. The method also includes estimating, by the electronic device, the BP based on the extracted plurality of parameters.

Abstract: A therapy system includes a therapy source (2) emitting radiation or waves, an ultrasound probe (14), a patient rest as well as a multi-axis positioning system (X, Y, Z) with several drives, by way of which the patient rest and the therapy source (2) can be moved to one another in all three spatial directions. A control device (26) is coupled to the ultrasound probe (14) and configured such that in at least one operating mode, the control device (26) simultaneously activates the drives of the multi-axis positioning system (X, Y, Z) such that the patient rest is moved relative to the therapy source along a selectable movement path (B) which lies within the plane of an ultrasound picture (20) which is currently recorded by the ultrasound probe (14). A method for positioning a patient rest relative to a therapy source is also provided.

Abstract: The invention provides for a medical apparatus (400, 500, 600, 700, 800) comprising a magnetic resonance imaging system (402) for acquiring magnetic resonance thermometry data (442) from a subject (418). The magnetic resonance imaging system comprises a magnet (404) with an imaging zone (408). The medical apparatus further comprises a memory (432) for storing machine executable instructions (460, 462, 464, 466, 10, 660). The medical apparatus further comprises a processor (426) for controlling the medical apparatus, wherein execution of the machine executable instructions causes the processor to: acquire (100, 200, 300) the magnetic resonance thermometry data from multiple slices (421, 421?, 421?) within the imaging zone by controlling the magnetic resonance imaging system; and interpolate (102, 202, 204, 302, 304) a three dimensional thermal dose estimate (444) in accordance with the magnetic resonance thermometry data.

Abstract: A medical probe, consisting of a flexible insertion tube, having a distal end for insertion into a body cavity of a patient, and a distal tip, which is disposed at the distal end of the flexible insertion tube is configured to be brought into contact with tissue in the body cavity. The probe also includes a coupling member, which couples the distal tip to the distal end of the insertion tube and which consists of a tubular piece of an elastic material having a plurality of intertwined helical cuts therethrough along a portion of a length of the piece.

Abstract: Methods and compositions for treating a patient for a condition characterized by an excess blood concentration of dissolved gas in at least one targeted region of the patient are provided. The method comprises administering a composition comprising a perfluorocarbon droplet emulsion into the blood of the patient; insonifying the at least one target region sufficient to achieve formation of microbubbles by droplet vaporization of at least a portion of the perfluorocarbon droplets present in the blood; whereby a concentration gradient favoring movement of gas molecules from the blood into the microbubbles is established for a time frame.

Abstract: A surgical site is simultaneously illuminated by less than all the visible color components that make up visible white light, and a fluorescence excitation illumination component by an illuminator in a minimally invasive surgical system. An image capture system acquires an image for each of the visible color components illuminating the surgical site and a fluorescence image, which is excited by the fluorescence excitation component from the illuminator. The minimally invasive surgical system uses the acquired images to generate a background black and white image of the surgical site. The acquired fluorescence image is superimposed on the background black and white image, and is highlighted in a selected color, e.g., green. The background black and white image with the superimposed highlighted fluorescence image is displayed for a user of the system. The highlighted fluorescence image identifies tissue of clinical interest.

Abstract: For noise reduction in elasticity imaging, frequency compounding is used. Displacements caused by the acoustic radiation force impulse are measured using signals at different frequencies, either due to transmission of tracking pulses and reception at different frequencies or due to processing received signals at different sub-bands. The displacements are (a) combined to compound and the compounded displacements are used to determine elasticity or (b) are used to determine elasticity and the elasticities from information at the different frequencies are compounded.

Abstract: A system includes acquisition of a predetermined number of three-dimensional sub-frames from patient tissue using a T1-weighted radial sampling sequence and without contrast agent, determination of a matching one of a plurality of the three-dimensional images reconstructed from respective subsets of the predetermined number of three-dimensional sub-frames, based on a first three-dimensional image reconstructed from a first-acquired one of the predetermined number of three-dimensional sub-frames, and subtraction of the matching one of the plurality of the three-dimensional images from the first three-dimensional image to generate a second three-dimensional image.

Abstract: A urethral catheter and its method of use to identify a patient's urethral anatomic course for the precise placement of a treatment element into the patient's prostate are provided. An echo-opaque urethral catheter including an echogenic material and a radio-opaque material in at least an image portion thereof is introduced into a urethra until its echogenic and radio-opaque image portion is generally aligned with a treatment site of the prostate. An image probe positioned relative to the treatment site is activated to obtain a real time image of the prostate and urethra by ultrasound or X-ray imaging. The echo-opaque urethral catheter includes an elongated flexible catheter, at least the image portion of which, is coated with, incorporates within or is enclosed by the echogenic and radio-opaque materials that enhance ultrasound and radio visualization.

Abstract: An interactive visual guidance tool for an imaging acquisition and display system and configured for user navigation with respect to a blockage of a field of view (216) detects, and spatially defines, the blockage. It also integrates, with the image for joint visualization, an indicium (244) that visually represents the definition. The indicium is moved dynamically according to movement, relative to the blockage, of the field of view. The indicium can be shaped like a line segment, or two indicia (244, 248) can be joined in a “V” shape to frame a region of non-blockage. The defining maybe based on determining whether ultrasound beams in respective directions are blocked. Included, for deriving the image, in some embodiments are imaging channels for receiving image data for which a metric of coherence, i.e., similarity among channel data, is computed. The determination for a direction is based on the metric for locations in that direction.

Abstract: An information providing method which is implementable by using an ultrasound apparatus includes obtaining ultrasound image data which relates to an object; displaying, on a first area of a screen, a gain setup window for setting a gain of the obtained ultrasound image data; receiving a gain which is set by a user on the gain setup window; and displaying, on a second area of the screen, an ultrasound image of the object to which the set gain is applied.

Abstract: Systems and methods of M-mode ultrasound imaging allows for M-mode imaging along user-defined paths. In various embodiments, the user-defined path can be a non-linear path or a curved path. In some embodiments, a system for M-mode ultrasound imaging can comprise a multi-aperture probe with at least a first transmitting aperture and a second receiving aperture. The receiving aperture can be separate from the transmitting aperture. In some embodiments, the transmitting aperture can be configured to transmit an unfocused, spherical, ultrasound ping signal into a region of interest. The user-defined path can define a structure of interest within the region of interest.

Abstract: A 3D ultrasonic diagnostic imaging system produces 3D display images at a 3D frame rate of display which is equal to the acquisition rate of a 3D image dataset. The volumetric region being imaged is sparsely sub-sampled by separated scanning beams. Spatial locations between the beams are filled in with interpolated values or interleaved with acquired data values from other 3D scanning intervals depending upon the existence of motion in the image field. A plurality of different beam scanning patterns are used, different ones of which have different spatial locations where beams are located and beams are omitted. In a preferred embodiment the determination of motion and the consequent decision to use interpolated or interleaved data for display is determined on a pixel-by pixel basis.