Abstract: An intravascular imaging device is provided. In one embodiment, the intravascular imaging device includes a flexible elongate member sized and shaped for insertion into a vessel of a patient, the flexible elongate member having a proximal portion and a distal portion; a conductor extending between the proximal and distal portions of the flexible elongate member; an imaging assembly disposed at the distal portion of the flexible elongate member, the imaging assembly including: a flex circuit including a body and a tab extending therefrom, the tab having a conductive portion coupled to the conductor; and a support member around which the flex circuit is disposed, the support member including a shelf on which tab is positioned.

Abstract: Disclosed are wearable ultrasound probes for use in trauma triage and assessment. The probes define a finger-receiving aperture and include an ultrasound array disposed adjacent the distal end wherein the ultrasound array is angled toward the bottom side of the probe about 10-50 degrees from the longitudinal axis and a second ultrasound array adjacent the distal end and proximal to the first ultrasound array, wherein the second ultrasound array is angled about 105-155 degrees from the first ultrasound array.

Abstract: A system, according to various embodiments, includes eyewear (or any other suitable wearable device) that includes at least one environmental pollution monitoring sensor (e.g., at least one light pollution, air pollution, radioactive pollution, thermal pollution, and/or noise pollution sensor) that may be used to monitor the presence of environmental pollution adjacent a wearer of the eyewear. The system may further include one or more health monitoring sensors to determine the health effects of the environmental pollution on the wearer. In certain circumstances, the system may alert the user to potentially harmful environmental conditions, or convey preventative healthcare advice to the wearer.

Abstract: This disclosure generally relates to systems and methods for facilitating determination of morphology (e.g., shape) and structure (e.g., size, rigidity) and/or penetrating channels (e.g., microchannels) of occlusions (e.g., clots, fluid obstructions, tumors, chronic total occlusions) involving magnetic particles (e.g., nanoparticles, microparticles) controlled by an external magnetic control system.

Abstract: Various methods and systems are provided for a guided at-home ultrasound imaging session. In one example, a system for ultrasonically scanning a tissue sample includes a hand-held ultrasound probe including a transducer array of transducer elements, a probe position tracking device including one or more position sensors coupled to the ultrasound probe, and a controller. The controller is configured to, during an imaging session, determine a position of the ultrasound probe relative to a target position based on position data collected by the probe position tracking device, and responsive to an indication that the ultrasound probe is at the target position, acquire image data with the transducer array.

Abstract: A wireless handheld ultrasound system an ultrasound front end to transmit ultrasonic waves into a subject and convert received ultrasonic echoes into digital data; an image processor coupled to the ultrasound front end to convert the digital data into an image; and a power section coupled to the ultrasound front end and the image processor. The power section may include a battery; a charging circuit to charge the battery; and a wireless power transducer coupled to the charging circuit to convert wireless power received from an external source into electrical energy for the charging circuit.

Abstract: An ultrasound imaging system includes an array of ultrasound transducer elements chat send ultrasound energy into an object when energized for respective transmission time periods and provide responses to ultrasound energy emitted from the object for respective reception time periods, a reception modulation circuit modulating the responses with irregular sequences of modulation coefficients, a combiner circuit combining the modulated responses, and an image reconstruction processor configured to computer-process the combined modulated responses into one or more images of the object.

Abstract: Handheld ultrasound devices and replaceable tips for such devices are provided. For example, a handheld ultrasound device comprises a handle and a tip that includes a sensor for transmitting and receiving ultrasound waves. The handle and the tip may be a single, integral, unit or the tip may be separable from the handle. In either embodiment, the handle and tip together are a fully self-contained unit. Also provided are handheld ultrasound sterile assemblies, comprising a handheld ultrasound device and a sheath that fully covers the device to provide a sterile barrier for the device. Further, tips for handheld ultrasound devices are provided. The tips may be a replaceable component of the handheld ultrasound devices. For example, the tips may be configured for one-time use, and the tip rather than the entire handheld ultrasound device may be replaced between procedures such that a new tip is used in a subsequent procedure.

Abstract: The present disclosure provides a system and method for using widely available ultrasound imaging to overcome the limitations of imaging guidewires and other small objects that may be subwavelength in size relative to an ultrasound wavelength. The system and method can reduce the use of X-rays and exposure to the dangerous effects of radiation and avoids the expense of MRI technology. The subwavelength object, such as a guidewire, can be detected using several methods and associated systems described herein, including the object changing positions at a frequency that creates a brighter ultrasound image of the object as the object progresses across a scanned region of the ultrasound detector. In some embodiments, the movement of the small object causes a different speckle signature than the object itself would otherwise generate. Analysis of changes in speckle patterns due to progressive movement of an object can yield a detectable object.

Abstract: An elastography device includes a probe with a single ultrasound transducer; or a plurality of ultrasound transducers, and a low frequency vibrator arranged to induce a displacement of said single ultrasound transducer or plurality of ultrasound transducers towards a tissue. The device is configured to emit a sequence of ultrasound pulses and to acquire echo signals received in response to track how elastic waves, induced by the displacement, travel in the tissue. The device is configured to generate, for one or more of the ultrasound pulses emitted a temporal offset upon emission, and/or a temporal offset upon reception, so that a difference thereof varies as a function of 2·d/vus, where d is the displacement of the single transducer or plurality of ultrasound transducers, and where vus is the speed of ultrasound in said tissue.

Abstract: The present invention relates to an apparatus, method and system for detecting and locating dental cavitations in jawbones using Through-Transmission Alveolar Ultrasonography (TAU). The apparatus comprises a measuring unit comprising an ultrasonic transducer and a round ultrasonic receiver. The apparatus is a handhold and is configured to define the geometric position of the ultrasonic transducer and the ultrasonic receiver with respect to each other so as to achieve a high-resolution ultrasound image of the jawbone with minimal errors and in order to improve diagnosis of dental cavitations.

Abstract: The disclosure relates to a magnetic resonance imaging device configured to exert a high-frequency electromagnetic field on an object under test in a static magnetic field and to reconstruct an image based on magnetic resonance signals. The magnetic resonance imaging device comprises a receiving coil comprising a plurality of receiving coil elements and configured to receive magnetic resonance signals and feed the magnetic resonance signals to a receiver, and a coupler configured to be coupled with at least a first receiving coil element of the receiving coil, the coupler being directionally coupled with at least the receiver, the first receiving coil element being configured to receive a high-frequency electromagnetic wave signal through the coupler. The directional coupling between the coupler and the receiver is so regulated that the first receiving coil element transmits the high-frequency electromagnetic wave signal to the object under test to sense a physiological movement signal.

Abstract: Systems and methods for detecting features in ultrasound images and delineating boundaries that representative of the detected features. A method can include determining a boundary of a feature in a displayed ultrasound image, determining a closed polygon that represents the feature based on the boundary, and determining information of the feature using the dimensions of the closed polygon. The ultrasound image and graphical representations of the feature (e.g., the boundary, the closed polygon) can be displayed in a user interface on a touch screen display. The method can include receiving user input indicative of a location of the feature, and adjusting the feature boundary and closed polygon based on user input. The method can also include determining an area and/or a perimeter of the feature based on the closed polygon.

Abstract: The ultrasonic diagnostic apparatus according to a present embodiment includes processing circuitry. The processing circuitry is configured to: acquire at least one of optical image data and sound data as data related to a confirmation item corresponding to a disorder name of a subject or an examination type for an ultrasonic scan; associate the ultrasonic image data acquired by the ultrasonic scan with the data related to the confirmation item; and store the association in a memory.

Abstract: The present discussion relates to structures and devices to facilitate application of an ultrasound therapy beam to a target anatomic region in a replicable manner. In certain aspects, adjustable positioning structures are described that allow a general probe positioning structure to be configured for a specific patient in a manner that allows the device to be used repeatedly to target the anatomic region, even when in non-clinical settings. In other aspects, a probe positioning structure is fabricated that is specific to a respective patient anatomy, such that use of the probe positioning structure provides repeatable targeting of the target anatomic region, even when in non-clinical settings.

Abstract: A method for imaging may include directing a PET scanner to perform scans of a subject injected with a tracer during a first time period. The method may also include generating PET images by reconstructing the PET data that are generated by the PET scanner based on the scans of the subject. The method may also include determining a first portion of a blood input function of the tracer in the subject based on the PET images. The method may also include determining an integral of a second portion of the blood input function based on a kinetic model, the PET data, and the first portion of the blood input function. The method may also include determining kinetic parameters of the kinetic model based on the PET data, the first portion of the blood input function, and the integral of the second portion of the blood input function.

Abstract: An optical shape sensing system includes an attachment mechanism (130) being configured to secure an optical shape sensing fiber to an instrument, the optical shape sensing fiber being connected to the instrument and configured to identify a position and orientation of the instrument. An optical shape sensing module (115) is configured to receive feedback from the optical shape sensing fiber and register the position of the instrument relative to an operating environment. A position response module (144) is configured to provide feedback to an operator based on position or orientation of the instrument to guide usage of the instrument.

Abstract: Systems and methods for monitoring and controlling delivery of a therapeutic compound to a brain of a subject using FUS-BBBD are disclosed. The method includes treating the brain of the subject with focused ultrasound in combination with microbubbles for blood-brain barrier disruption (FUS-BBBD), administering the therapeutic agent to the subject; and obtaining a map of a concentration of the therapeutic agent delivered to the brain of the subject using passive cavitation imaging (PCI). The delivery of focused sound may be modulated to match the map of the concentration of the therapeutic agent delivered to the brain of the subject to a desired spatial distribution of the therapeutic agent.

Abstract: The present disclosure relates to an apparatus for mounting on a guide member for insertion into an anatomical cavity, the apparatus comprising a body defining a cavity for receiving a guide member therethrough, a drive arrangement for moving the body along a guide member disposed through the body, a probe secured to the body for, in use, obtaining a measurement from, taking a sample of, applying a substance to, or applying a therapy to, an environment of the body, and a measurement arrangement for measuring a position relative to the guide member disposed through the body.

Abstract: An implantable ultrasound generating treating device (12) to induce spinal cord or spinal nerves treatment, suitable for implantation in the spinal canal and comprises an elongate support member (22, 32) and an array of several treatment transducers (20) distributed along the elongate support member. The several treatment transducers (20) comprise radial transducers emitting an ultrasound treatment beam oriented radially, wherein the treatment transducers (20) have a resonant frequency comprised between 0.5 and 4 MHz. The device has articulating portions so that the implantable device can adapt its shape to a curved elongation path. Also disclosed is an apparatus including the implantable ultrasound generating treating device and methods comprising inserting the implantable ultrasound generating treating device (12) inside the spinal canal of the spine of the patient.