2288 results about "Ultrasound probe" patented technology

A surgical instrument for enhancing robotic surgery generally includes an elongate shaft with an ultrasound probe, an end effector at the distal end of the shaft, and a base at the proximal end of the shaft. The end effector includes an ultrasound probe tip and the surgical instrument is generally configured for convenient positioning of the probe tip within a surgical site by a robotic surgical system. Ultrasound energy delivered by the probe tip may be used to cut, cauterize, or achieve various other desired effects on tissue at a surgical site. In various embodiments, the end effector also includes a gripper, for gripping tissue in cooperation with the ultrasound probe tip. The base is generally configured to removably couple the surgical instrument to a robotic surgical system and to transmit forces from the surgical system to the end effector, through the elongate shaft. A method for enhancing robotic surgery generally includes coupling the surgical instrument to a robotic surgical system, positioning the probe tip in contact with tissue at a surgical site, and delivering ultrasound energy to the tissue.

A surgical instrument is provided including: an ultrasonic transducer for generating ultrasonic vibration; an ultrasonic probe for transmitting the ultrasonic vibration generated by the ultrasonic transducer to a distal end portion; a grasping member capable of grasping a living tissue as an object to be treated between the grasping member and a distal end portion of the ultrasonic probe by moving between positions close to and distant from the distal end portion of the ultrasonic probe; a conductive member configured of a conductive material for supplying high-frequency current to the living tissue, the conductive member being provided to the grasping member; and a non-conductive member configured of a non-conductive material and formed in a shape for blocking a contact between the conductive member and the ultrasonic probe and exposing a part of one surface of the conductive member on the ultrasonic probe side, the non-conductive member being provided to the grasping member so as to be located between the conductive member and the ultrasonic probe, thereby allowing high-frequency current to be effectively conducted to a living tissue.

An ultrasound probe for diagnostic medical ultrasound imaging, including an ultrasound transducer and a circuit having a plurality of states to limit the use of the ultrasound probe. Ultrasound probe use can be limited based on a unique identification number (e.g., selected by means of electrically programmable fuses) assigned to each ultrasound probe. Alternatively, the ultrasound system software monitors and updates the number of times that the ultrasound probe has been used. Another aspect of the invention is directed to an ultrasound system, including an ultrasound probe with multiple states, a circuit to program and to receive state data from the ultrasound probe and interpret the state data, and a cable to communicate state data between the ultrasound probe and the processor. Another aspect of the invention is directed to a method for using a limited use ultrasound probe, including the steps of determining the state of a circuit in the limited use ultrasound probe and determining if the ultrasound probe can be used.

Disclosed herein are methods and systems for producing hemostasis, tissue closure, or vessel closure by inserting a thermal delivery probe into a passageway and emitting thermal energy from the probe to produce the hemostasis or tissue closure. These methods and systems may be used following a percutaneous medical procedure that creates a passageway in tissue of patient, such as is caused by introduction of an access device into the patient. The thermal delivery probe may have one or more ultrasound transducers positioned in an elongated shaft.

The ultrasonic probe of the present invention includes an ultrasonic element unit for transmitting and receiving ultrasonic waves, an oscillation mechanism for causing oscillation to the ultrasonic element unit and a detector for detecting the oscillation of the ultrasonic element unit. The detector detects the oscillation angle and the oscillation origin of the ultrasonic element unit, and when the oscillation range of the ultrasonic element unit is divided at its oscillation origin into two regions of a positive region and a negative region, the detector detects in which area the ultrasonic element unit is located. In use of the ultrasonic probe, a control of origin return for returning the ultrasonic element unit to its oscillation origin is performed on the basis of the result of the detection by the detector.

Ultrasonic diagnostic equipment is equipped with an ultrasonic probe that transmits/receives ultrasound to/from an examined body, a probe position sensor that detects the position and the direction of the ultrasonic probe, an image generator that generates image data based upon the output of the ultrasonic probe, a probe position sensor that detects the position and the direction of a puncture probe inserted into the examined body, a display image generator that generates the data of a display image in which the end position of the puncture probe is fixed to a specific position in an image display area according to the position and the direction of the ultrasonic probe and the position and the direction of the puncture probe based upon the image data and a display for displaying the display image in the image display area.

An ultrasound diagnostic apparatus includes an ultrasound probe with transducers, memory storing probe identification information and binary state generation unit generating a binary electrical state corresponding to a probe identifier, probe identifier conversion unit converting the electrical state into the probe identifier, read unit reading the probe identification information from the memory, determination unit determining consistency between the probe identifier after conversion and the probe identification information read from the memory, and warning output unit outputting a predetermined warning if the probe identifier is inconsistent with the probe identification information.

A method to fabricate a catheter tip that encapsulates a mechanically actuated ultrasound transducer assembly is provided. In a representative procedure, the steps include providing an ultrasound transducer assembly (100) adapted for use with a catheter (300), the ultrasound transducer assembly (100) comprising a proximal end (102) and a distal end (104), a drive linkage (132) to an actuator (130), and a transducer array (110), the transducer array (110) electrically connected to an interconnect (120) adapted for passage to or through a body of the catheter (300), connecting the actuator (130), adapted for use with the ultrasound transducer assembly (100), to the drive linkage (132); and inserting the ultrasound transducer assembly (100) and the actuator (132) into a polymer or a plastic type or reinforced polymer sheath (140) comprising an acoustically transparent section, a closed end (142) at its distal end and an open end (144) at its proximal end, wherein the polymer sheath (140) provides a defined rigidity.

The invention is a transvaginal ultrasound probe having an attached echogenic needle that is useful in the treatment of uterine fibroids. The echogenic needle has an echogenic surface near its tip that allows the physician to visualize its location using ultrasound imaging. In one embodiment, the needle has an active electrode at its distal end. The active electrode supplies radio frequency energy to a fibroids causing necrosis of the targeted fibroid or by destroying the fibroid's vascular supply. The radio frequency needle preferably has a safety device that shuts-off energy if the needle punctures the uterine wall. In a second embodiment, the needle has a cryogen supply tube and cryogen supply. This embodiment destroys fibroid tissue by freezing it or its vascular supply when the tissue comes in contact with the needle's frozen distal end. The invention further includes the method of using the ultrasound probe with the attached needle.

An ultrasound imaging and therapy system is provided that includes an ultrasound probe and a diagnostic module to control the probe to obtain diagnostic ultrasound signals from a region of interest (ROI) of the patient. The ROI includes adipose tissue and the diagnostic module generates a diagnostic image of the ROI based on the ultrasound signals obtained. The system also includes a display to display the image of the ROI and a user interface to accept user inputs to designate a treatment space within the ROI that corresponds to the adipose tissue. The display displays the treatment space on the image. The system also includes a therapy module to control the probe to deliver, during a therapy session, a therapy to a treatment location based on a therapy parameter. The treatment location is within the treatment space defined by the user inputs.

An imaging probe for a biological sample includes an OCT probe and an ultrasound probe combined with the OCT probe in an integral probe package capable of providing by a single scanning operation images from the OCT probe and ultrasound probe to simultaneously provide integrated optical coherence tomography (OCT) and ultrasound imaging of the same biological sample. A method to provide high resolution imaging of biomedical tissue includes the steps of finding an area of interest using the guidance of ultrasound imaging, and obtaining an OCT image and once the area of interest is identified where the combination of the two imaging modalities yields high resolution OCT and deep penetration depth ultrasound imaging.

An ultrasonic probe assembly comprises a housing defining a longitudinal axis and having a linear motor assembly, a swivel base, and an extension arm disposed therewithin. An imaging transducer is mounted on a free end of the extension arm and is specifically adapted to be moved along an arcuate path as a result of mechanical interconnection of the swivel base to the linear motor assembly. The swivel base upon which the extension arm is mounted is configured to be pivotable about a pivot axis oriented transversely relative to the longitudinal axis such that reciprocative motion of the linear motor assembly is converted in swiveling motion of the swivel base and oscillating translation of the transducer along an arcuate path such that the transducer axis is oriented generally perpendicularly relative to an anatomical structure having a convexly shaped outer surface.

An ultrasound probe comprises a probe housing that has an inner surface and an outer surface. An array of transducer elements are within the probe housing. At least one sensor is formed between the inner and outer surfaces of the probe housing. The at least one sensor is configured to detect at least one parameter associated with an object in contact with the outer surface proximate the at least one sensor.

An ultrasound probe includes a transducer comprising an array of transducer elements removably disposed in a head portion. At least one or more stages of electronic circuit units is removably coupled to the transducer and configured to excite the transducer. A handle portion is detachably coupled to the head portion. The head portion and the handle portion are disposed enclosing the at least one or more stages of electronic circuit units. The ultrasound probe is used for one dimensional applications, two dimensional applications, and volumetric applications.

The present invention provides an apparatus and a method for an ultrasonic medical device operating in a torsional mode and a transverse mode. An ultrasonic probe of the ultrasonic medical device is placed in communication with a biological material. An ultrasonic energy source is activated to produce an electrical signal that drives a transducer to produce a torsional vibration of the ultrasonic probe. The torsional vibration produces a component of force in a transverse direction relative to a longitudinal axis of the ultrasonic probe, thereby exciting a transverse vibration along the longitudinal axis causing the ultrasonic probe to undergo both a torsional vibration and a transverse vibration. The torsional vibration and the transverse vibration cause cavitation in a medium surrounding the ultrasonic probe to ablate the biological material.

The present technique provides for the manufacture and/or use of an ultrasound probe configured to acquire non-imaging data in addition to imaging data. In particular, the ultrasound probe includes a micro-machined ultrasound transducer formed on the surface of a substrate using micro-electric mechanical systems techniques or other techniques associated with semiconductor processing. Non-imaging sensors are formed on the substrate, either on the surface or the interior, or on a substrate proximate to the substrate upon which the transducer is formed. The non-imaging sensors may be used to acquire non-imaging data in conjunction with the acquisition of imaging data by the transducer.

The present invention allows even soft tissue such as body tissue having a hierarchic structure of skin, fat, muscle and bone, etc., to be estimated and allows estimation only through a short-time pressing operation to thereby reduce damages to the soft tissue. The present invention is constructed of an ultrasonic probe for transmitting/receiving an ultrasonic signal, a target deformation amount calculation section for calculating an amount of deformation of a target shape from a time variation of data received from the ultrasonic probe, a movement mechanism for moving the ultrasonic probe, a probe control section for controlling the probe, a position sensor for measuring the position of the probe, a force sensor for measuring a force applied to the probe section, a viscoelasticity estimation section for estimating viscoelasticity of the target based on values obtained from the position sensor, force sensor, target deformation amount calculation section and a viscoelasticity display section for presenting the estimated viscoelasticity to the user.

A system and method for tracking completeness of co-registered medical image data is disclosed herein. The system and method tracks the position of an anatomical reference marker positionable on a patient and an ultrasound probe during an imaging session and co-registers medical images based on positional data received from the anatomical reference marker and the ultrasound probe. Using the co-registered image data, the system and method generates a surface contour of a region of interest (ROI) of the patient, such as a breast. The surface contour is defined to represent an interface between a chest wall structure and tissue of the ROI in a plurality of co-registered medical images. A completeness map of the image data within the defined surface contour during the imaging session is generated and overlaid on a graphic representation of the ROI.

A system and method for statistical design of an ultrasound probe and imager system, and an associated graphical user interface for selecting input parameters to be used in an ultrasound simulation. The process and computer code allow the performance of a probe and imager combination to be specified and jointly optimized in image quality terms. The designs produced optimize both the image quality and other CTQ (critical to quality) parameters, such as the distribution of regulatory power indices and mechanical index. These CTQs indirectly affect image quality through their effect on patient dose. The Transducer Design Advisor incorporates a graphical user interface for facilitating selection of a parameter set to be used in the simulation. The user selects a desired parameter set by navigating across and interacting with a succession of windows. The user specifies various geometric characteristics of the transducer and how the user wants to simulate the imager system. Finally, the user specifies weights for the various CTQs at different depths. Based on these inputs, the Transducer Design Advisor creates the files needed by the ultrasound simulator.

An object is to provide a pressing member, an ultrasonic probe and an ultrasonic diagnosing device that enhance the efficiency of uniformly pressing a subject and achieve a high-precision elastic image. Therefore, the contact surface of the pressing member with the subject is formed so that the vertical direction of the face of at least a part of the contact surface is different from the vertical direction of the face of the other part. The pressing member is detachably mounted on the probe or formed integrally with the probe.

An ultrasonic transducer probe having a highly integrated interface circuit array. Low-voltage transmit control signals from the system are transmitted on the system transmit channels via the ultrasound probe cable and into the interface circuit array. These transmit control signals are routed through the interface circuit array using a dense switching matrix. Once the low-voltage transmit control signals reach individual cells within the interface array, they are decoded and used to control local high-voltage pulser circuits to drive individual ultrasound transducer elements made up of selected subelements that are co-integrated with the interface electronics. The interface cell circuitry further comprises a high-voltage transmit/receive switch, which is closed when the high-voltage pulser is transmitting to protect the low-voltage components.

An ultrasound waveguide that is attachable to an ultrasound probe so as to identify a target area on a target object. The ultrasound waveguide has an ultrasound transducer coupling signal to be transmitted through a guide means. The ultrasound waveguide also has a positioning means for positioning the guide means in relation to the target area on the target object. The guide means is provided with a channel that provides a discontinuity within the guide means that causes a discontinuity in the ultrasound signal emitted by the probe. The presence of this discontinuity allow for proper alignment of the ultrasound waveguide with the target object.

A method of presenting a suggested path for an ultrasound probe along a patient's surface includes obtaining a three-dimensional, non-ultrasound image of the patient and an ultrasound image of the patient. A treatment area is defined within the within the three-dimensional, non-ultrasound image, and using the images, defining a scanning site contour of an anatomical structure of interest within the patient and an external contour of the patient's surface. A preferred path of the ultrasound scan is projected onto the external contour such that an operator can reproduce the ultrasound scan without knowledge of the anatomical structure of interest.

A backing material for suppressing the surface temperature rise of an ultrasonic probe. This backing material is provided on a back face of at least one vibrator for transmitting and/or receiving ultrasonic waves in an ultrasonic probe, and includes: a backing base material containing a polymeric material; and a heat conducting fiber provided in the backing base material, having a larger coefficient of thermal conductivity than that of the backing base material, and running through without disconnection from a first face of the backing material in contact with the at least one vibrator to a second face different from the first face.

An apparatus and method for indicating locus of an ultrasonic probe configured to transmit and receive ultrasonic waves toward a part of a subject wherein a position or movement of the ultrasonic probe is detected, and a locus of the ultrasonic probe on an image of the part of the subject is indicated according to the detected position or movement.

Method and formulations to extend the utility of ultrasound compliant adhesive hydrogel membranes from static to dynamic applications by modifying the surface of at least one face so as to transform the tactile nature of the surface from one that is adhesive and render it smooth and lubricious. Such modification thus provides one face that is smooth and lubricious and the other unmodified, hence providing one adhesive surface that can be attached to the skin of a patient, the face of an ultrasound probe or other surfaces that benefit from the adhesive/lubricious configuration of such modified adhesive hydrogels.

Various embodiments of an ultrasound probe for use with an ultrasound system are provided to enable local waveform generation with respect to the ultrasound probe. The ultrasound probe includes a plurality of transducer elements which are independently configured to transmit distinct waveforms. Certain embodiments include a variety of probes that house one or more waveform generators on application specific integrated circuits (ASICs).

A method and system for real-time ultrasound guided prostate needle biopsy based on a biomechanical model of the prostate from 3D planning image data, such as magnetic resonance imaging (MRI) data, is disclosed. The prostate is segmented in the 3D ultrasound image. A reference patient-specific biomechanical model of the prostate extracted from planning image data is fused to a boundary of the segmented prostate in the 3D ultrasound image, resulting in a fused 3D biomechanical prostate model. In response to movement of an ultrasound probe to a new location, a current 2D ultrasound image is received. The fused 3D biomechanical prostate model is deformed based on the current 2D ultrasound image to match a current deformation of the prostate due to the movement of the ultrasound probe to the new location.

An apparatus and method for using an ultrasonic medical device to treat chronic total occlusions comprises an ultrasonic probe, a transducer, a coupling engaging a proximal end of the ultrasonic probe to a distal end of the transducer and an ultrasonic energy source engaged to the transducer. The ultrasonic probe is inserted into a vasculature and placed in communication with the chronic total occlusion. The ultrasonic energy source produces an ultrasonic energy that is transmitted to the transducer, where the transducer creates a transverse ultrasonic vibration along the ultrasonic probe. The transverse ultrasonic vibration creates a plurality of transverse nodes and a plurality of transverse anti-nodes along the longitudinal axis of the ultrasonic probe, creating cavitation along a portion of the longitudinal axis of the ultrasonic probe to ablate the chronic total occlusion.

A cooling system for an ultrasonic imaging system is provided, the ultrasonic imaging system having a probe for transmitting and receiving acoustic signals through a tip of the probe to and from biological tissue contacting the tip at an outer surface of the tip. The cooling system includes a conduit for circulating cooling medium therein, and a heat exchanger in fluid communication with the circulating cooling medium and having means for removing heat from the circulating cooling medium, wherein at least a portion the conduit is in proximity to or contacts the outer surface of the probe tip. In a first embodiment the conduit includes an inlet fluid line extending from the heat exchanger to the tip of the probe for providing the circulating cooling medium from the heat exchanger to the probe tip, and an outlet cooling line extending from the tip of the probe to the heat exchanger for providing circulating cooling medium from the probe tip to the heat exchanger. In a second embodiment the heat exchanger is housed in the probe. In a third embodiment, the probe is housed within a housing, wherein a portion of the conduit extends from the tip of the probe along an external surface of the housing.