WO2014129203A1 - Ultrasonic diagnostic device and method for controlling ultrasonic diagnostic device - Google Patents

Ultrasonic diagnostic device and method for controlling ultrasonic diagnostic device Download PDF

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Publication number
WO2014129203A1
WO2014129203A1 PCT/JP2014/000954 JP2014000954W WO2014129203A1 WO 2014129203 A1 WO2014129203 A1 WO 2014129203A1 JP 2014000954 W JP2014000954 W JP 2014000954W WO 2014129203 A1 WO2014129203 A1 WO 2014129203A1
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Prior art keywords
unit
display
ultrasonic probe
ultrasonic
measurement
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PCT/JP2014/000954
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French (fr)
Japanese (ja)
Inventor
淳 三谷
俊輔 坂口
良信 渡辺
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コニカミノルタ株式会社
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Priority to JP2015501346A priority Critical patent/JPWO2014129203A1/en
Publication of WO2014129203A1 publication Critical patent/WO2014129203A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B8/00Diagnosis using ultrasonic, sonic or infrasonic waves
    • A61B8/08Detecting organic movements or changes, e.g. tumours, cysts, swellings
    • A61B8/0891Detecting organic movements or changes, e.g. tumours, cysts, swellings for diagnosis of blood vessels
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B8/00Diagnosis using ultrasonic, sonic or infrasonic waves
    • A61B8/13Tomography
    • A61B8/14Echo-tomography
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B8/00Diagnosis using ultrasonic, sonic or infrasonic waves
    • A61B8/42Details of probe positioning or probe attachment to the patient
    • A61B8/4245Details of probe positioning or probe attachment to the patient involving determining the position of the probe, e.g. with respect to an external reference frame or to the patient
    • A61B8/4254Details of probe positioning or probe attachment to the patient involving determining the position of the probe, e.g. with respect to an external reference frame or to the patient using sensors mounted on the probe
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B8/00Diagnosis using ultrasonic, sonic or infrasonic waves
    • A61B8/46Ultrasonic, sonic or infrasonic diagnostic devices with special arrangements for interfacing with the operator or the patient
    • A61B8/461Displaying means of special interest
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B8/00Diagnosis using ultrasonic, sonic or infrasonic waves
    • A61B8/54Control of the diagnostic device
    • A61B8/543Control of the diagnostic device involving acquisition triggered by a physiological signal
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01SRADIO DIRECTION-FINDING; RADIO NAVIGATION; DETERMINING DISTANCE OR VELOCITY BY USE OF RADIO WAVES; LOCATING OR PRESENCE-DETECTING BY USE OF THE REFLECTION OR RERADIATION OF RADIO WAVES; ANALOGOUS ARRANGEMENTS USING OTHER WAVES
    • G01S15/00Systems using the reflection or reradiation of acoustic waves, e.g. sonar systems
    • G01S15/88Sonar systems specially adapted for specific applications
    • G01S15/89Sonar systems specially adapted for specific applications for mapping or imaging
    • G01S15/8906Short-range imaging systems; Acoustic microscope systems using pulse-echo techniques
    • G01S15/8934Short-range imaging systems; Acoustic microscope systems using pulse-echo techniques using a dynamic transducer configuration
    • G01S15/8936Short-range imaging systems; Acoustic microscope systems using pulse-echo techniques using a dynamic transducer configuration using transducers mounted for mechanical movement in three dimensions
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01SRADIO DIRECTION-FINDING; RADIO NAVIGATION; DETERMINING DISTANCE OR VELOCITY BY USE OF RADIO WAVES; LOCATING OR PRESENCE-DETECTING BY USE OF THE REFLECTION OR RERADIATION OF RADIO WAVES; ANALOGOUS ARRANGEMENTS USING OTHER WAVES
    • G01S7/00Details of systems according to groups G01S13/00, G01S15/00, G01S17/00
    • G01S7/52Details of systems according to groups G01S13/00, G01S15/00, G01S17/00 of systems according to group G01S15/00
    • G01S7/52017Details of systems according to groups G01S13/00, G01S15/00, G01S17/00 of systems according to group G01S15/00 particularly adapted to short-range imaging
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B8/00Diagnosis using ultrasonic, sonic or infrasonic waves
    • A61B8/08Detecting organic movements or changes, e.g. tumours, cysts, swellings
    • A61B8/0858Detecting organic movements or changes, e.g. tumours, cysts, swellings involving measuring tissue layers, e.g. skin, interfaces

Definitions

  • the present disclosure relates to an ultrasonic diagnostic apparatus and a control method for the ultrasonic diagnostic apparatus.
  • IMT intima-media thickness
  • FIG. 9 is a schematic diagram showing a cross section (hereinafter, referred to as a long-axis cross section) in the major axis direction of the carotid artery blood vessel (the direction in which the blood vessel is elongated).
  • the blood vessel includes a blood vessel wall 200 and a blood vessel lumen 201.
  • the blood vessel wall 200 is composed of an inner membrane 204, a middle membrane 206, and an outer membrane 202 from the inside to the outside.
  • the inner media 203 is a complex of the inner membrane 204 and the media 206, and IMT indicates the thickness of the inner media 203.
  • the inner media 203 can be visually recognized between the blood vessel lumen 201 and the outer membrane 202.
  • the IMT measurement is usually based on a two-dimensional image which is an ultrasonic diagnostic image of a cross section (hereinafter referred to as “long-axis cross section”) along the long axis direction of the blood vessel (the direction in which the blood vessel has expanded). Is done. Specifically, the boundary between the blood vessel lumen 201 and the intima 204 in FIG. 14 (hereinafter referred to as “luminal intima boundary”) 205 and the boundary between the media 206 and the outer membrane 202 (hereinafter “medium”). IMT can be measured by detecting 207) (referred to as “outer membrane boundary”) and measuring the distance between the boundaries.
  • the IMT measurement must be performed regularly due to the nature of the disease, and it is desirable to perform the IMT measurement at the same position every time for accurate diagnosis. Conventionally, this has been done by manually setting the boundary using a distance measurement function mounted on a general-purpose ultrasonic diagnostic apparatus. In this case, the operator must perform the operation of extracting the IMT measurement target region and guiding the ultrasonic probe there. As a result, it was difficult for non-experts to measure, and it took inspection time to improve the accuracy of measurement. On the other hand, in recent years, an ultrasonic diagnostic apparatus that automatically performs part of an operation for IMT measurement has been proposed (for example, Patent Document 1).
  • An object of the present disclosure is to provide an ultrasonic diagnostic apparatus and an ultrasonic diagnostic apparatus control method that are more convenient for an operator.
  • An ultrasonic diagnostic apparatus configured to be connectable to a display device, and configured to be connected to an ultrasonic probe including an inclination angle measurement unit.
  • a tomographic image generated based on a received signal of a frame that satisfies the predetermined criterion when a received signal of the frame based on the reflected ultrasound acquired from the measurement object by the ultrasonic probe satisfies a predetermined criterion The table Is displayed on the vessel, characterized in that a freeze display processing unit to continue the display.
  • the above configuration suppresses unnecessary freeze display processing in the measurement of the characteristics of the subject including the IMT and the identification of the diagnostic site for the disease. Therefore, it is possible to specify a diagnostic site with a simple operation. Therefore, the usability of the ultrasonic diagnostic apparatus can be improved.
  • FIG. 1 is an example of a functional block diagram of an ultrasound diagnostic apparatus 1 according to Embodiment 1.
  • FIG. It is an example of the auxiliary figure for demonstrating the determination method of the heart rate synchronizing signal in the received signal determination part of the ultrasound diagnosing device 1 which concerns on Embodiment 1,
  • (a) is a schematic diagram of a blood vessel cross section,
  • (b) is. It is an example of the schematic diagram which shows the time change of the blood vessel diameter by a pulsation.
  • 3 is an example of a functional block diagram of a determination unit 11 of the ultrasound diagnostic apparatus 1 according to Embodiment 1.
  • FIG. 7 is an example of a schematic diagram for explaining the determination of the blood vessel center in the reception signal determination unit 111 of the ultrasonic diagnostic apparatus 1 according to Embodiment 1, and (a) is an ultrasonic probe arranged on the skin surface of a subject.
  • (b) shows a case where the ultrasonic wave does not pass through the vicinity of the blood vessel center 211.
  • 3 is an example of a schematic diagram for explaining a method for acquiring a heartbeat synchronization signal by a heartbeat synchronization signal acquisition unit of the ultrasound diagnostic apparatus 1 according to Embodiment 1.
  • FIG. 3 is an example of a flowchart showing an operation of the ultrasonic diagnostic apparatus 1 according to the first embodiment.
  • FIG. 3 is an example of an auxiliary diagram for explaining a function of an inclination angle determination unit in the ultrasonic diagnostic apparatus according to Embodiment 1.
  • FIG. 6 is an example of an auxiliary diagram for explaining a function of an inclination angle determination unit in the ultrasonic diagnostic apparatus according to Embodiment 2.
  • FIG. It is an example of the schematic diagram which showed the long-axis cross section of the blood vessel of a carotid artery.
  • an ultrasonic diagnostic apparatus generates a tomographic image for each frame by repeatedly transmitting and receiving ultrasonic waves to and from a subject including a carotid artery via an ultrasonic probe.
  • the generated tomographic image is sequentially updated and displayed on the display as a tomographic image, and the IMT value measured in a specific frame is displayed on the display.
  • the conventional ultrasonic diagnostic apparatus when the IMT value is displayed on the display, the tomographic image is sequentially updated and displayed for each frame, so that the tomographic image of the displayed frame and the IMT value measurement target are displayed.
  • the frame was not compatible.
  • a tomographic image of the frame is displayed on the display device as a still image and the display is continued (hereinafter referred to as “freeze display”). It is possible to do it.
  • a technique related to this for example, in Patent Document 2, when a predetermined standard satisfies a reception signal acquired via an ultrasonic probe or a signal that has been subjected to a predetermined process from the reception signal, A technique for freeze-displaying a tomographic image of a frame is disclosed. If this technique is used, it is considered that the tomographic image of the displayed frame can be made to correspond to the frame that is the measurement target of the IMT value.
  • the freeze display process is performed when the received signal satisfies a certain condition.
  • the ultrasonic probe is moved on the surface of the subject's skin and searching for a desired measurement target, if the received signal satisfies a certain condition, a freeze display process is performed. It will be.
  • the inventors have intensively studied a technique that can improve usability even when it is necessary to perform inspection at almost the same measurement position every time in periodic inspection, and according to the present embodiment.
  • the inventors have come up with an ultrasonic diagnostic apparatus and a method for controlling the ultrasonic diagnostic apparatus.
  • the ultrasonic diagnostic apparatus and the control method of the ultrasonic diagnostic apparatus according to the embodiment will be described in detail with reference to the drawings.
  • the present embodiment is not limited to this, and freeze display processing is performed in an examination using an ultrasonic diagnostic apparatus. It can be applied to all the necessary tests.
  • inclination angle of the ultrasound probe refers to the relative inclination of the ultrasound probe 2 with respect to a predetermined direction (for example, the direction of gravity, a specific direction in the subject). Means. At the same time, the angle of the ultrasonic probe is also determined for the positional relationship of the ultrasonic probe obtained based on the absolute position based on the position information of the ultrasonic probe with respect to a predetermined position (for example, the subject). means.
  • the ultrasonic diagnostic apparatus is an ultrasonic diagnostic apparatus configured to be connectable to a display device, configured to be connectable with an ultrasonic probe including an inclination angle measuring unit, and to be measured.
  • a state in which an inclination angle of the ultrasonic probe is included in a predetermined angle range, or a state in which an inclination angle variation is a predetermined reference value or less When the received signal of the frame based on the reflected ultrasound acquired from the measurement object by the ultrasonic probe satisfies a predetermined reference, a tomographic image generated based on the received signal of the frame that satisfies the predetermined reference is The indicator Characterized in that a freeze display processing unit to continue the display to display.
  • the tomographic image generation unit that generates a tomographic image for each frame based on the received signal
  • the display processing unit that displays the tomographic image on the display
  • the inclination angle measurement unit are sequentially acquired.
  • an inclination angle determination unit that determines whether or not an inclination angle of the ultrasonic probe is included in a predetermined angle range, and whether or not a reception signal of a frame acquired by the transmission / reception unit satisfies the predetermined criterion
  • a reception signal determination unit for determining whether or not the tilt angle determination unit receives the reflected ultrasonic wave based on the reception signal of one or more frames from the ultrasonic probe.
  • the freeze display processing unit is The one or more It may be configured to continue the display is displayed on the display device via the display processing unit tomographic image generated by the tomographic image generating unit based on the received signal of at least one frame included in the frame.
  • the tomographic image generation unit that generates a tomographic image for each frame based on the received signal
  • the display processing unit that displays the tomographic image on the display
  • the inclination angle measurement unit are sequentially acquired.
  • an inclination angle determination unit that determines whether or not an inclination angle variation of the ultrasonic probe is equal to or less than a predetermined reference value, and whether or not a reception signal of a frame acquired by the transmission / reception unit satisfies a predetermined reference.
  • Freeze display processing Is a configuration in which the tomographic image generated by the tomographic image generation unit based on the reception signal of at least one frame included in the one or more frames is displayed on the display device via the display processing unit and the display is continued. There may be.
  • the reception signal determination unit is configured to acquire a reflected ultrasonic wave based on the reception signal of the one or more frames from a predetermined region in the measurement target at a predetermined timing in a heartbeat cycle. It may be configured to determine that the predetermined criterion is satisfied when the vehicle is in the middle.
  • the apparatus further includes a measurement unit that measures the characteristics of the measurement target based on the received signal, and the freeze display processing unit is configured to transmit at least one frame included in the one or more frames by the measurement unit.
  • the measurement result of the characteristic measured based on the received signal may be displayed on the display unit and the display may be continued.
  • the characteristic may be IMT.
  • the tilt angle measurement unit is an angle sensor, and further includes a tilt angle calculation unit that calculates the tilt angle of the ultrasonic probe based on signals sequentially acquired from the angle sensor. There may be.
  • the control method of the ultrasonic diagnostic apparatus is a control method of the ultrasonic diagnostic apparatus configured such that an ultrasonic probe including an inclination angle measurement unit and a display can be connected to each other.
  • a transmission process for transmitting an ultrasonic wave to the subject including the measurement object via the ultrasonic probe, and a reception signal based on the reflected ultrasonic wave from the measurement object via the ultrasonic probe are framed.
  • the received signal of the frame based on the reflected ultrasound acquired from the measurement object by the ultrasound probe is generated based on the received signal of the frame that satisfies the predetermined criterion Refusal And having a freeze display processing step to continue the display to display an image on the display.
  • Embodiment 1 the ultrasonic diagnostic apparatus according to Embodiment 1 will be described with reference to the drawings.
  • FIG. 1 is a functional block diagram of an ultrasound diagnostic apparatus 1 according to Embodiment 1.
  • the ultrasonic diagnostic apparatus 1 includes a transmission / reception unit 6, an inclination angle calculation unit 7, a tomographic image generation unit 8, a heartbeat synchronization signal acquisition unit 9, a measurement unit 10, a determination unit 11, a freeze display processing unit 12, a display processing unit 13, and a control.
  • the controller 5 comprised from the part 14 is provided.
  • the ultrasonic diagnostic apparatus 1 is configured such that an ultrasonic probe 2, a display device 3, and an input device 4 can be connected.
  • FIG. 1 shows a state in which an ultrasound probe 2, a display device 3 and an input device 4 are connected to the ultrasound diagnostic apparatus 1.
  • each element connected to the ultrasonic diagnostic apparatus 1 will be described.
  • the ultrasonic probe 2 has a plurality of transducers (not shown) arranged in a one-dimensional direction (hereinafter referred to as “vibrator arrangement direction”), for example.
  • the ultrasonic probe 2 converts a pulsed or continuous wave electrical signal (hereinafter referred to as “transmission electrical signal”) supplied from a transmitting / receiving unit 6 described later into pulsed or continuous wave ultrasonic waves.
  • the ultrasonic probe 2 emits an ultrasonic beam composed of a plurality of ultrasonic waves emitted from a plurality of transducers in a state where the transducer-side outer surface of the ultrasonic probe 2 is in contact with the skin surface of the subject. Send to the measurement target (carotid artery).
  • the subject in order to acquire a tomographic image of the long-axis cross section of the carotid artery, the subject is placed on the subject so that the transducer arrangement direction of the ultrasonic probe 2 is along the long-axis direction of the carotid artery. Place on the skin surface.
  • the ultrasound probe 2 receives a plurality of reflected ultrasound waves from the subject, and converts the reflected ultrasound waves into electrical signals (hereinafter referred to as “received electrical signals”) by a plurality of transducers.
  • the received electrical signal is supplied to the transmission / reception unit 6.
  • the ultrasonic probe 2 having a plurality of transducers arranged in a one-dimensional direction is illustrated, but an ultrasonic probe that can be used in the present embodiment. 2 is not limited to this.
  • a two-dimensional array of transducers arranged in a two-dimensional direction, or a oscillating ultrasonic that mechanically oscillates a plurality of transducers arranged in a one-dimensional direction to acquire a three-dimensional tomographic image A probe may be used and can be appropriately used depending on the measurement.
  • the ultrasonic probe 2 may be provided with a part of functions of the transmission / reception unit 6 described later on the ultrasonic probe side.
  • a transmission electric signal is generated in the ultrasonic probe 2 based on a control signal (hereinafter referred to as “transmission control signal”) for generating a transmission electric signal output from the transmission / reception unit 6, and the transmission electric signal is generated.
  • a function of converting a signal into an ultrasonic wave may be provided on the ultrasonic probe side.
  • a function of generating a received signal described later based on the received electrical signal may be provided on the ultrasonic probe side.
  • the ultrasonic probe 2 has a built-in tilt angle measurement unit 21.
  • the tilt angle measurement unit 21 sequentially acquires information (hereinafter referred to as “sensor output information”) necessary for sequentially acquiring the tilt angle of the ultrasonic probe 2 being driven, and outputs the sensor output information. It outputs to the inclination angle calculation part 7 mentioned later of the ultrasonic diagnostic apparatus 1.
  • the tilt angle measuring unit 21 may be any sensor that can obtain sensor output information that allows the tilt angle calculating unit 7 to calculate the tilt angle of the ultrasound probe 2. Examples of the tilt angle measuring unit 21 include an acceleration sensor and a magnetic sensor. A sensor, an optical sensor, or a gyro sensor can be used. In the first embodiment, an example in which an acceleration sensor is used as the tilt angle measurement unit 21 has been described.
  • FIG. 1 shows a configuration in which the tilt angle measuring unit 21 is built in the ultrasonic probe 2, but depending on the type of the tilt angle measuring unit 21 to be used, the outside of the ultrasonic probe 2 is shown. It is good also as a structure which provides the inclination angle measurement part 21 in this.
  • the display 3 is a display device for so-called image display, and displays an image output from a display processing unit 13 described later on a display screen.
  • a liquid crystal display, a CRT, an organic EL display, or the like can be used as the display 3.
  • the input device 4 receives various operation inputs such as various settings / operations on the ultrasonic diagnostic apparatus 1 from the operator and outputs them to the control unit 14.
  • the input device 4 may be, for example, a touch panel configured integrally with the display device 3. In this case, various settings / operations of the ultrasonic diagnostic apparatus 1 can be performed by performing a touch operation or a drag operation on the operation keys displayed on the display device 3, and the ultrasonic diagnostic apparatus 1 can be operated by this touch panel. Configured to be possible.
  • the input device 4 may be, for example, a keyboard having various operation keys, or an operation panel having various operation buttons, levers, and the like. Further, it may be a trackball, a mouse, a flat pad or the like for moving the cursor display displayed on the display device 3. Alternatively, a plurality of these may be used, or a combination of these may be used.
  • the ultrasonic diagnostic apparatus 1 includes a controller 5 that controls the operation of the ultrasonic diagnostic apparatus 1 based on an operation input from the input unit 4.
  • the controller 5 includes the transmission / reception unit 6, the tilt angle calculation unit 7, the tomographic image generation unit 8, the heartbeat synchronization signal acquisition unit 9, the measurement unit 10, the determination unit 11, the freeze display processing unit 12, and the display processing unit 13. And a control unit 14.
  • Each block is controlled by the control unit 14.
  • the transmission / reception unit 6 is connected to the ultrasonic probe 2
  • the tilt angle calculation unit 7 is connected to the tilt angle measurement unit 21, and the display processing unit 13 is connected to the display 3.
  • the configuration of each block included in the controller 5 will be described.
  • the transmission / reception unit 6 is connected to the ultrasonic probe 2.
  • the transmission / reception unit 6 generates a transmission control signal related to transmission control of the ultrasonic beam of the ultrasonic probe 2, and transmits the pulsed or continuous wave transmission electric signal generated based on the transmission control signal to the ultrasonic probe. 2 is transmitted.
  • the transmission processing performed by the transmission / reception unit 6 means processing for generating a transmission control signal at least by the transmission / reception unit 6 and causing the ultrasonic probe 2 to transmit ultrasonic waves (beams) based on the transmission control signal.
  • the transmission / reception unit 6 performs reception processing for amplifying the received electrical signal from the ultrasound probe 2 and performing A / D conversion to generate a received signal. Then, this received signal is output to the tomographic image generation unit 8, the heartbeat synchronization signal acquisition unit 9, and the measurement unit 10.
  • the received signal includes, for example, a plurality of signals having a transducer arrangement direction and an ultrasonic transmission direction and a direction perpendicular to the transducer arrangement, and each signal is an electric signal converted from the amplitude of the reflected ultrasonic wave A. / D converted digital signal.
  • the transmission / reception unit 6 repeatedly performs transmission processing and reception processing continuously to construct a plurality of frames including a plurality of reception signals.
  • the reception process performed by the transmission / reception unit 6 means a process in which at least the transmission / reception unit 6 generates a reception signal based on the reflected ultrasound.
  • the “frame” is processed in order to construct a tomographic image based on one unit of received signals necessary for constructing one tomographic image, or on this one received signal.
  • the tilt angle calculation unit 7 acquires the angle of the ultrasonic probe 2 based on the sensor output information from the tilt angle measurement unit 21. That is, the tilt angle calculation unit 7 calculates the tilt of the ultrasonic probe 2 with reference to a predetermined direction (for example, the direction of gravity) based on the acceleration information output from the tilt angle measurement unit 21 that is an acceleration sensor. And obtained as the tilt angle. Then, the information related to the acquired inclination angle (hereinafter referred to as “inclination angle information”) is sequentially output to the determination unit 11.
  • inclination angle information information related to the acquired inclination angle
  • Tomographic image generation unit 8 converts each received signal in the frame into a luminance signal corresponding to the intensity, and generates the tomographic image data by performing coordinate conversion on the rectangular coordinate system. The tomographic image generation unit 8 sequentially performs this process for each frame and outputs the generated tomographic image to the determination unit 11.
  • the heartbeat synchronization signal acquisition unit 9 detects a heartbeat synchronization signal synchronized with the heartbeat of the subject from the received signal, and outputs the detected heartbeat synchronization signal to the determination unit 11.
  • the heartbeat synchronization signal acquisition unit 9 includes information for detecting a predetermined timing of the heartbeat synchronization signal, detects a predetermined timing for performing, for example, IMT measurement based on the detected heartbeat synchronization signal, and measures the timing. 10 is output. This timing may be the end timing of diastole during one heartbeat, for example, when the heart dilates after contraction and blood flow is minimized.
  • FIG. 2A and 2B are auxiliary diagrams for explaining a method of determining a heartbeat synchronization signal in a reception signal determination unit of the ultrasonic diagnostic apparatus 1, wherein FIG. 2A is a schematic diagram of a blood vessel cross section, and FIG. 2B is a blood vessel diameter due to pulsation. It is a schematic diagram which shows the time change of. 6 is an auxiliary diagram for explaining a method for determining a heartbeat synchronization signal in a reception signal determination unit of the ultrasound diagnostic apparatus 1 according to Embodiment 1.
  • the heartbeat synchronization signal acquisition unit 9 detects a pulse synchronization signal from the received signal using a known method described in, for example, Japanese Patent No. 4189405. Specifically, as shown in FIG.
  • measurement points A and B are set on the anterior wall of the blood vessel (the blood vessel wall located on the subject skin surface side in the long-axis cross section of the blood vessel) 209 and the rear wall 210.
  • the movement of the measurement points A and B is tracked by analyzing the signal intensity and phase of the received signal.
  • the artery repeatedly contracts and expands due to the heartbeat. Therefore, the distance between the measurement points A and B has a diameter change waveform indicating a periodic movement corresponding to the heart beat as shown in FIG. Obtainable. This diameter change waveform is acquired as a heartbeat synchronization signal.
  • a heartbeat synchronization signal can be acquired by a simple operation of merely bringing the ultrasound probe 2 into contact with the subject skin surface without requiring a special device such as an electrocardiograph or a heart sound meter.
  • a special device such as an electrocardiograph or a heart sound meter.
  • the acquisition of the heart rate synchronization signal described above is merely an example, and an electrocardiograph or a heart sound meter may be used.
  • the measurement unit 10 calculates a region of interest (hereinafter, abbreviated as “ROI”), which is an IMT measurement range, based on a received signal of a frame corresponding to a predetermined timing output from the heartbeat synchronization signal acquisition unit 9. Set. Then, a lumen inner membrane boundary and a media outer membrane boundary are detected from the received signal in the ROI, and a distance between them is measured. Of the measured distances within the ROI, for example, a value indicating the maximum value (that is, maximum thickness (maxIMT)) or an average value (that is, average thickness (meanIMT)) is calculated as the IMT value.
  • ROI region of interest
  • a known method disclosed in Japanese Patent Application Laid-Open No. 2010-119842, etc. can be used.
  • a known method disclosed in Japanese Patent No. 4829960 can be used for the detection of the lumen intima boundary and the medial epicardial boundary.
  • the measurement part 10 in Embodiment 1 has shown the structure which calculates IMT value from a received signal, it calculates IMT value from the signal (for example, tomographic image) in which the predetermined process was performed from the received signal. It is good also as a structure.
  • the determination unit 11 determines whether or not various standards when the measurement unit 10 performs IMT measurement satisfies a predetermined standard, and determines the measured IMT value when the various standards satisfy the predetermined standard. . That is, the determination unit 11 determines whether or not to perform freeze display processing, and determines that freeze display processing is performed if a predetermined criterion is satisfied, and reception of a frame determined to satisfy the predetermined criterion.
  • the IMT value measured based on the signal is determined as a measurement value.
  • (1) the tilt angle of the ultrasonic probe 2 when the reflected ultrasonic wave based on the received signal of the determination frame is acquired by the ultrasonic probe 2 appropriately measures the IMT.
  • a received signal received signal
  • first reference a reference tilt angle range that can be performed
  • second criterion a criterion that can appropriately measure IMT
  • “when the reflected ultrasound based on the received signal of the frame is acquired by the ultrasound probe 2” means to receive the reflected ultrasound based on the received signal of the frame. It means at least one of the time when the ultrasonic probe 2 transmits ultrasonic waves to the measurement object and the time when reflected ultrasonic waves are received from the measurement object.
  • FIG. 3 is a functional block diagram of the determination unit 11 of the ultrasonic diagnostic apparatus 1.
  • the determination unit 11 includes a reception signal determination unit 111, an inclination angle determination unit 112, a recording unit 113, and a measurement value determination unit 114. The configuration of each block included in the determination unit 11 will be described.
  • the reception signal determination unit 111 determines whether the reception signal and a signal that has been subjected to predetermined processing from the reception signal satisfy the second criterion. Specifically, the determination is made based on the second reference (1) and the second reference (2) that are the two references constituting the second reference, and the determination result relating to the determined frame is output to the recording unit 113.
  • the determination based on the second reference (1) is to determine whether the ultrasonic wave transmitted from the ultrasonic probe 2 arranged on the skin surface of the subject captures the vicinity of the blood vessel center in the carotid artery.
  • the reason for setting this standard is that the IMT measurement measures the distance between the lumen-intima boundary and the media-epicardium boundary, and a received signal that can clearly depict these boundaries as a tomographic image must be obtained. This is because the IMT measurement is not properly performed.
  • FIG. 4 is a schematic diagram for explaining the determination of the blood vessel center in the reception signal determination unit 111 of the ultrasonic diagnostic apparatus 1.
  • FIG. 4A is a diagram illustrating the ultrasonic probe 2 disposed on the skin surface of the subject.
  • (b) shows a case where the ultrasonic wave does not pass through the vicinity of the blood vessel center 211.
  • the positional relationship between the course of the ultrasonic wave transmitted / received from the ultrasonic probe 2 and the carotid artery blood vessel in the cross section cut in the direction perpendicular to the longitudinal direction with respect to the carotid artery blood vessel is shown.
  • Ultrasonic waves are reflected at boundaries where there is a difference in acoustic impedance, such as tissue boundaries, but are reflected more strongly at an angle close to 90 degrees with respect to the boundary surface, and clear reflected ultrasonic waves are obtained. Therefore, as shown in FIG. 4A, when the ultrasonic wave transmitted from the ultrasonic probe 2 arranged on the skin surface of the subject captures the vicinity of the blood vessel center 211 (the path of the ultrasonic wave is the blood vessel center 211). When in the vicinity), the ultrasound strikes approximately perpendicular to the luminal intima and medial epicardial boundaries of the blood vessel, and a strong and clear reflected ultrasound is obtained at these borders.
  • the received signal determination unit 111 evaluates whether the lumen-intima boundary and the media-endocardium boundary in the tomographic image data generated by the tomographic image generation unit 8 are clearly depicted. It can be determined whether or not the probe 2 is arranged at a position to be caught in the vicinity of the center of the blood vessel. Specifically, in the tomographic image data of the detected blood vessel boundary position and its peripheral part, it is detected whether there is a rise in luminance from the blood vessel lumen side to the inner media side of the detected lumen-intima boundary position.
  • the vicinity of the blood vessel center where the lumen inner membrane boundary and the media outer membrane boundary are clearly depicted as described above is the measured length of the ultrasonic wave transmitted from the ultrasonic probe 2 (in FIG. 4).
  • the distance from the center of the blood vessel cross section to the center of the blood vessel cross section corresponds to about 0.5 mm or less, but is not strictly limited.
  • the determination based on the second reference (2) is to determine whether or not the heartbeat synchronization signal for defining the timing in the IMT measurement has been properly acquired. This is a determination necessary when the heartbeat synchronization signal acquisition unit 9 acquires a heartbeat synchronization signal from the received signal. When the heartbeat synchronization signal acquisition unit 9 is an electrocardiograph or a heart sound meter, this condition is satisfied. Judgment is not required.
  • the blood vessel expands and contracts according to the amount of blood flow and the flow velocity flowing inside.
  • the blood flow velocity becomes maximum
  • the blood vessel diameter at that time becomes maximum
  • the thickness of the blood vessel wall becomes minimum.
  • the vessel diameter is minimized and the thickness of the vessel wall is maximized. That is, since the thickness of the blood vessel wall changes in synchronization with the heartbeat, the IMT value also changes depending on the timing of IMT measurement. Therefore, if the acquired heart rate synchronization signal cannot be acquired properly, appropriate IMT measurement cannot be performed, and thus the reception signal determination unit 111 determines whether or not the heart rate synchronization signal has been acquired appropriately.
  • reception signal determination unit 111 As a method of determining by the reception signal determination unit 111, for example, focusing on the degree of coincidence between (a) the determination method focusing on the characteristic amount of the blood vessel diameter change waveform and (b) the model waveform of the blood vessel diameter change waveform. The method of judging by this can be considered. Note that the reception signal determination unit 111 may include only one of (a) and (b), or may determine pulsation using both.
  • FIG. 5 is a schematic diagram for explaining a method for acquiring a heartbeat synchronization signal by the heartbeat synchronization signal acquisition unit of the ultrasonic diagnostic apparatus 1.
  • the method (a) it is determined whether or not the feature amount indicated by the amplitude or peak timing of the blood vessel diameter change waveform is within a range that can be taken by a person in a normal appropriate pulsation. For example, (A) maximum amplitude (Amax in FIG. 5), (B) minimum amplitude (Amin in FIG. 5), (C) timing at which the maximum amplitude is reached (Tmax in FIG. 5). ) And the timing at which the amplitude becomes minimum (Tmin in FIG. 5), (D) one heartbeat cycle (TR in FIG. 5) can be used.
  • the method (2) For example, by preparing a model waveform of a diameter change waveform in a predetermined period such as one heartbeat, comparing it with the blood vessel diameter change waveform output from the heartbeat synchronization signal acquisition unit 9, and calculating the degree of matching between them as a correlation coefficient Can be determined.
  • the model waveform and the blood vessel diameter change waveform output from the heartbeat synchronization signal acquisition unit 9 may differ in a predetermined period (for example, one heartbeat period). In this case, any waveform is used as a reference. By expanding or contracting the other waveform on the time axis, the two heartbeat periods become the same, and the correlation coefficient can be calculated.
  • the tilt angle determination unit 112 determines the tilt angle. Based on the tilt angle information output from the tilt angle calculation unit 7, the reflected ultrasonic wave that is the basis of the received signal of the frame to be determined is the supersonic wave. It is determined whether or not the inclination angle of the ultrasonic probe 2 when acquired by the acoustic probe satisfies the first reference. Specifically, when the ultrasonic probe 2 transmits an ultrasonic wave to the measurement object in order to receive the reflected ultrasonic wave based on the received signal of the frame to be determined, or receives the reflected ultrasonic wave from the measurement object. It is determined whether the inclination angle of the ultrasonic probe 2 at this time satisfies the first reference.
  • the ultrasonic probe 2 can appropriately measure the IMT when the reflected ultrasonic wave based on the received signal of the frame to be determined is received. It was in range. In that case, the determination result relating to the determined frame is output to the recording unit 113.
  • a reference tilt angle as a predetermined reference value is defined in advance.
  • the tilt angle determination unit 112 compares the reference tilt angle with the tilt angle corresponding to the frame output from the tilt angle calculation unit 7, and determines whether the tilt angle corresponding to this frame matches the reference tilt angle. To do.
  • this reference inclination angle is an angle at which measurement is to be performed.
  • the reference inclination angle may be an angle set in advance by an operator or the like, or may be an angle corresponding to a frame when IMT measurement has been performed on the same patient in the past.
  • the angle of the ultrasound probe 2 corresponding to the frame to be judged and the reference inclination angle do not necessarily coincide completely.
  • an angle range of ⁇ 5 ° from the reference inclination angle is set, and If the inclination angle of the ultrasound probe 2 corresponding to the frame is included in the frame, it may be determined that it matches the reference angle.
  • the recording unit 113 records the IMT measurement values for the tomographic image data, the determination results of the reception signal determination unit 111 and the tilt angle determination unit 112, and the IMT measurement values in the order of the timing of the ultrasonic transmission processing. . Thereby, the tomographic image data, the determination result, and the IMT measurement value in a certain frame are recorded in association with each other. The recording unit 113 records these information in association with each other, and then sequentially outputs the information to the measurement value determination unit 114 in the order of recording.
  • the measurement value determination unit 114 determines the IMT value as the measurement value based on the determination results of the reception signal determination unit 111 and the inclination angle determination unit 112 among the information output from the recording unit 113. That is, the IMT value measured based on the received signal of the frame in which the determination result of the reception signal determination unit 111 satisfies the first reference and the determination result of the tilt angle determination unit 112 satisfies the second reference is measured. Confirm as Then, for the frame for which the measurement value is confirmed, information indicating that the measurement value is confirmed is added to the information output from the recording unit 113 and output to the freeze display processing unit 12.
  • the information output from the recording unit 113 is output to the freeze display processing unit 12 for the frame for which the measurement value has not been determined.
  • the frame in which the measurement value is determined is a target on which the freeze display processing unit 12 performs the freeze display process.
  • the determination of the reception signal performed by the determination unit 11 is described in the first embodiment by taking IMT measurement as an example.
  • the present invention is not limited to IMT measurement, and the measurement type, measurement method, It can be determined appropriately according to the operator's setting.
  • the reference relating to the blood vessel center (second reference (1)) and the reference relating to the heartbeat synchronization signal have been described as the second reference (second reference (2)).
  • the criterion of the received signal in the IMT measurement in the present disclosure is not limited to this.
  • the determination standard of the received signal in the measurement of characteristics of subjects other than the IMT and the identification of the diagnostic site for the disease can be appropriately set according to the target disease and the site on the subject.
  • the determination standard of the received signal in the measurement of characteristics of subjects other than the IMT and the identification of the diagnostic site for the disease can be appropriately set according to the target disease and the site on the subject.
  • the freeze display processing unit 12 outputs frame information sequentially output from the recording unit 113 via the measurement value determining unit 114 to the display processing unit 13.
  • the frame information is information including at least one of tomographic image data, determination results of the reception signal determination unit 111 and the inclination angle determination unit 112, and an IMT measurement value for a frame in which IMT measurement is performed. It is. As described above, these pieces of information are recorded in the recording unit 113 in the order of timing of ultrasonic transmission processing.
  • the freeze display processing unit 12 monitors the input of information indicating that the measurement value from the measurement value determination unit 114 is confirmed.
  • the freeze display processing unit 12 inputs information indicating that the measurement value has been determined from the measurement value determination unit 114, the information on the frame in which the measurement value that is the target of the freeze display process is determined is the information that is the target of the freeze display process.
  • the freeze display processing unit 12 outputs the frame information output from the measurement value determination unit 114 to the display processing unit 13 after outputting the information to the display processing unit 13 as information on the frame subjected to the freeze display processing. Stop output.
  • the freeze display processing unit 12 can display the information of the frame in which the measurement value to be subjected to the freeze display process is determined via the display processing unit 13 described later, and can continue the display.
  • the freeze display process is to stop the update display of the tomographic image performed on the display by the display processing unit 13 described later and display the tomographic image of the frame subjected to the freeze display process as a still image. May be.
  • the tomographic image of the frame subjected to the freeze display process may be displayed as a still image.
  • the display processing unit 13 performs processing for displaying the tomographic image data supplied from the freeze display processing unit 12 and the measured value on the display screen of the display 3 when there is a confirmed IMT measurement result.
  • the display processing unit 13 Inputs the tomographic image data from the recording unit 113 via the measurement value determining unit 114 in the order in which the tomographic image data is sequentially generated (the order in which the received signals are acquired), and sequentially outputs them to the display unit 3 to display the display screen of the display unit 3 Is displayed updated.
  • the freeze display processing unit 12 receives information indicating that the measurement value is confirmed from the measurement value determining unit 114 (when the freeze display processing is performed in the freeze display processing unit 12), the display processing unit 13 Inputs the tomographic image of the frame corresponding to the measurement value determined via the measurement value determination unit 114 from the recording unit 113 and the determined IMT value, and outputs the tomographic image to the display 3.
  • the update of the tomographic image displayed on the display device 3 is stopped, the confirmed IMT value is displayed on the display device 3 together with the tomographic image of the frame corresponding to the confirmed measurement value, and the display of the IMT value is continued.
  • the display processing unit 13 receives information indicating that the measurement value has been confirmed from the measurement value determining unit 114 via the freeze display processing unit 12, and the display processing unit 13 mainly takes the display 3.
  • the tomographic image update display may be stopped and the tomographic image of the frame subjected to the freeze display process may be displayed on the display unit 3 as a still image.
  • Control unit 14 The control unit 14 controls each block included in the controller 5 based on an operator's instruction transmitted via the input device 4.
  • step 1 the ultrasonic probe 2 is placed on the surface of the subject skin, and the transmission / reception unit 6 performs transmission processing to transmit ultrasonic waves from the ultrasonic probe 2 toward the carotid artery.
  • the probe 2 receives reflected ultrasound from the subject including the carotid artery.
  • the transmission / reception unit 6 generates a reception signal by performing reception processing based on the reflected ultrasonic wave, and constructs one frame including a plurality of reception signals.
  • the transmission process and the reception process are repeated a plurality of times to construct a plurality of frames, and the reception signals for each frame are sequentially output to the tomographic image generation unit 8, the heartbeat synchronization signal acquisition unit 9, and the measurement unit 10 in the constructed order. .
  • step 2 (S002) the inclination angle measurement unit (acceleration sensor) 21 built in the ultrasonic probe 2 detects the sensor of the ultrasonic probe 2 at every timing of ultrasonic transmission processing (or reception processing). Acceleration information is acquired as output information, and is output to the tilt angle calculation unit 7 in the order of transmission processing timing. Then, the tilt angle calculation unit 7 acquires the tilt angle of the ultrasonic probe 2 with reference to a predetermined direction (for example, the direction of gravity) based on the acceleration information, and determines the tilt angle as tilt angle information. To the inclination angle determination unit 112 of the unit 11. The calculation of the angle of the ultrasound probe 2 by the tilt angle calculation unit 7 is performed in the order of sensor output information output from the tilt angle measurement unit 21.
  • a predetermined direction for example, the direction of gravity
  • step 1 (S001) is performed before step 2 (S002).
  • the transmission process in step 1 (S001) and the acquisition of sensor output information in step 2 (S002) are as follows. A configuration in which processing is performed in parallel may be used.
  • step 3 (S003) the tomographic image generation unit 8 converts the luminance signal corresponding to the intensity based on the received signal of the frame output from the transmission / reception unit 6, and coordinates the luminance signal to the orthogonal coordinate system. To generate a tomographic image.
  • This processing is sequentially performed in the order of the frames output from the transmission / reception unit 6 and is output to the determination unit 11 (the reception signal determination unit 111 and the recording unit 113). Note that the tomographic image data output to the recording unit 113 is recorded in the order of the output time series.
  • step 4 (S004) the heartbeat synchronization signal acquisition unit 9 detects a heartbeat synchronization signal synchronized with the heartbeat of the subject from the received signal, and outputs the detected heartbeat synchronization signal to the determination unit 11 and the measurement unit 10. Then, based on the received signal of the frame corresponding to the timing indicated by the output heartbeat synchronization signal, for example, the ROI is set using a known method disclosed in Japanese Patent Application Laid-Open No. 2010-119842, etc. For example, a known method disclosed in Japanese Patent No. 4829960 is used to detect a lumen-intima boundary and an intima-membrane boundary in the ROI, and measure the distance between the boundaries as an IMT.
  • step 3 is step 4 Although the configuration is performed before (S004), Step 3 (S003) and Step 4 (S004) may be performed simultaneously, and Step 4 (S004) is performed before Step 3 (S003). You may go to
  • the reception signal determination unit 111 determines the reception signal. Specifically, the received signal determination unit 111 makes a determination based on the second criterion (1) and the second criterion (2), and satisfies the second criterion (1) and the second criterion (2). For example, the fact that the frame satisfies the condition is recorded in the recording unit 113 together with the tomographic image data and the IMT measurement value related to the frame, and the process proceeds to step 6 (S006). On the other hand, if at least one of the second reference (1) and the second reference (2) does not satisfy the condition, the tomographic image data relating to the frame is recorded in the recording unit 113. Then, the tomographic image is output from the recording unit 113 to the measurement value determining unit 114. The tomographic image is output to the display processing unit 13 via the freeze display processing unit 12, and the process proceeds to step 9 (S009).
  • step 6 the tilt angle determination unit 112 determines the tilt angle. If the determination of the tilt angle satisfies the first criterion, the frame that satisfies the first criterion is recorded together with the frame that satisfies the second criterion for determination of the received signal. The data is recorded in the unit 113, and the process proceeds to step 7 (S007). On the other hand, for a frame that does not satisfy the first criterion, tomographic image data relating to that frame is recorded in the recording unit 113. Then, the tomographic image is output from the recording unit 113 to the measurement value determining unit 114. The tomographic image is output to the display processing unit 13 via the freeze display processing unit 12, and the process proceeds to step 9 (S009).
  • Step 5 (S005) is performed before Step 6 (S006). However, Step 5 (S005) and Step 6 (S006) may be performed simultaneously. (S005) may be performed prior to step 6 (S006).
  • Step 7 (S007) among the frames output from the recording unit 113 to the measurement value determining unit 114, the received signal determination satisfies the second reference and the tilt angle determination satisfies the first reference.
  • the IMT measurement result is determined as an appropriate IMT value, and the process proceeds to step 8 (S008). If there are a plurality of frames in which the determination of the received signal satisfies the second reference and the determination of the tilt angle satisfies the first reference, the IMT measurement result related to any of the frames is determined as an appropriate IMT value, and step 8 (S008).
  • the IMT measurement result related to the most recently acquired frame in time may be determined as an appropriate IMT value.
  • step 8 (S008) the freeze display processing unit 12 performs freeze display processing for the frame for which the IMT value is determined in step 7 (S007). Specifically, when the freeze display processing unit 12 inputs information indicating that the measurement value has been determined from the measurement value determination unit 114, the freeze display processing is performed on the information of the frame in which the measurement value to be subjected to the freeze display process is determined. Is output to the display processing unit 13 as information to be processed, and the process proceeds to step 9 (S009).
  • the frame information refers to, for example, tomographic image data, determination results of the reception signal determination unit 111 and the inclination angle determination unit 112, and an IMT measurement value for a frame in which IMT measurement is performed.
  • step 9 (S009) when there is at least the generated tomographic image data and the confirmed IMT measurement value, the display processing unit 13 displays at least one of the tomographic image data or the IMT value in the display screen in the display 3. Process to be displayed. That is, when the freeze display processing is performed by the freeze display processing unit 12, the display processing unit 13 displays the determined IMT value together with the tomographic image of the frame corresponding to the determined IMT measurement value on the display 3. Processing to continue the display is performed and the process is terminated.
  • the display processing unit 13 performs a process of sequentially updating and displaying the tomographic image data in the order in which the tomographic image data is sequentially generated (that is, the order in which the reception signals are acquired). finish.
  • FIG. 7 is an auxiliary diagram for explaining an inclination angle determination unit in the ultrasonic diagnostic apparatus 1.
  • FIG. 7 is a schematic diagram of the subject shown from the head side.
  • a broken-line arrow indicates an appropriate reference inclination angle ( ⁇ ) of the ultrasonic probe 2 arranged on the neck muscle surface when performing IMT measurement of the carotid artery.
  • a solid arrow indicates when the ultrasonic probe 2 acquires reflected ultrasonic waves in a state where the ultrasonic probe 2 is placed on the neck surface when acquiring the determination target frame determined by the inclination angle determination unit 112.
  • the inclination angle ( ⁇ 1 ) of the ultrasonic probe 2 is shown.
  • ⁇ and ⁇ 1 are defined as relative angles with respect to the gravitational direction of the ultrasonic wave emitting direction of the ultrasonic probe 2 (when there is a range, near the center of the range).
  • “when the ultrasonic probe 2 acquires reflected ultrasonic waves” means that the ultrasonic probe 2 receives ultrasonic waves in order to receive the reflected ultrasonic waves based on the reception signal of the frame. It refers to at least one of when transmitted or when a reflected ultrasonic wave is received from a measurement target.
  • the inclination in the inclination angle determination unit 112 In a configuration that does not perform angle determination, freeze display processing is performed.
  • a frame acquired at an inclination angle other than the reference inclination angle ( ⁇ ) at which proper measurement can be performed is a target for freeze display processing, and a tomographic image of that frame is displayed on the display 3 as a freeze display.
  • the freeze display process can be performed on a frame acquired in the vicinity of the reference inclination angle ( ⁇ ). Therefore, it is possible to suppress an unnecessary freeze display process in which a frame acquired at an inclination angle other than the reference inclination angle ( ⁇ ) capable of appropriate measurement is subjected to a freeze display process.
  • the inclination angle determination unit 112 has a predetermined inclination angle of the ultrasonic probe 2 when the reflected ultrasonic wave used as the basis of the received signal of the frame is acquired by the ultrasonic probe 2. It was set as the structure which determines with satisfy
  • the tilt angle determination unit 112 detects a change in the tilt angle of the ultrasonic probe 2 when the reflected ultrasound that is the basis of the received signal of the frame is acquired by the ultrasonic probe 2.
  • the second embodiment is different from the first embodiment in that it is determined that the first reference is satisfied when it is equal to or less than a predetermined reference value.
  • the reception signal determination unit 111 determines that the second reference is satisfied and is unnecessary. It is possible to prevent the freeze display process from being performed.
  • the configuration other than the inclination angle determination unit 112 is the same as each element shown in the first embodiment, and a description thereof is omitted.
  • the tilt angle determination unit 112 sequentially monitors and analyzes the tilt angle output from the tilt angle calculation unit 7. Specifically, the temporal variation of the inclination angle (hereinafter referred to as “inclination angle variation”) is calculated from the inclination angle sequentially output from the inclination angle calculation unit 7. For example, if the tilt angle of a certain frame (N) is 40 ° and the tilt angle of the immediately preceding frame (N ⁇ 1) is 30 °, the tilt angle variation of the frame (N) in this case is + 10 °. Can be calculated as Then, the calculation process of the inclination angle variation is sequentially repeated.
  • inclination angle variation the temporal variation of the inclination angle
  • the tilt angle determination unit 112 has a predetermined reference value in advance, and when a change in the tilt angle in a predetermined number of temporally continuous frames is equal to or less than the predetermined reference value, each of the predetermined number of frames is the first reference value. It is determined that the frame satisfies the above.
  • the tilt angle determination unit 112 does not satisfy the first reference. It is determined that the frame is a frame, and the tilt angle variation is determined based on the tilt angle of the next frame in which the tilt angle is subsequently varied.
  • FIG. 8 is an auxiliary diagram for explaining an inclination angle determination unit in the ultrasonic diagnostic apparatus according to the second embodiment.
  • FIG. 8 is a schematic diagram plotting the tilt angle fluctuations acquired by the tilt angle calculator 7 and showing the relationship with time.
  • the vertical axis represents the tilt angle fluctuations in each frame, and the horizontal axis represents the time axis.
  • the horizontal axis shows the new time as it goes to the right.
  • F1 to F20 indicate frames corresponding to the tilt angle fluctuation plots.
  • a predetermined number of temporally continuous frames are 5 frames
  • A a predetermined number of frames are F4 to F8
  • a predetermined number of frames are F12 to F16.
  • C Three examples in which the predetermined number of frames are set to F16 to F20 will be described.
  • the inclination angle determination unit 112 determines that the first reference is not satisfied. For example, it is assumed that the operator moves the ultrasonic probe 2 to a desired position. In such a case, the received signal determination unit 111 performs an unnecessary freeze display process when the received signal of any one of the frames F4 to F8 satisfies the second criterion. Therefore, in such a case, the tilt angle determination unit 112 determines that the tilt angle determination unit 112 does not satisfy the first reference and suppresses the freeze display process, and prevents the execution of an unnecessary freeze display process. .
  • the inclination angle determination unit 112 determines that the first reference is not satisfied. This is presumed that the operator arranges the ultrasonic probe 2 in the vicinity of a desired position, but performs fine adjustment of the position. Even in such a case, it is not desirable to perform the freeze display process, and the inclination angle determination unit 112 prevents the execution of the unnecessary freeze display process.
  • the inclination angle determination unit 112 determines that the first reference is satisfied. This is because the fluctuation angle of the ultrasonic probe 2 is within the reference value for a certain period of time, even if the ultrasonic probe 2 is arranged at an appropriate angle without blurring and freeze display is performed. It shows that good conditions are in place.
  • the frames of F16 to F20 are the target frames for determining the IMT measurement value in the measurement value determination unit 114. Of the frames F16 to F20, the frame that satisfies the second criterion in the received signal determination unit 111 is the IMT measurement value determination target frame, and this frame is the target of the freeze display process.
  • the freeze display process is performed for a frame acquired in a state where the inclination angle variation is equal to or less than the reference value. Can do. Therefore, it is possible to suppress an unnecessary freeze display process in which a frame acquired under an inclination angle variation that is equal to or greater than a reference value of an inclination angle variation that can be appropriately measured is subjected to a freeze display process.
  • the diagnostic part can be specified, and the usability of the ultrasonic diagnostic apparatus can be improved.
  • a condition for performing the freeze display process whether or not the determination result of the received signal is incorporated into the condition for performing the freeze display process using the determination result of the inclination angle of the ultrasonic probe depends on the purpose of the inspection / measurement. It is good also as a structure which can be set suitably according to it.
  • the ultrasonic probe 2 has the configuration of the ultrasonic probe 2 in which a plurality of piezoelectric elements are arranged in a one-dimensional direction.
  • the configuration of the ultrasonic probe 2 is not limited to this, and for example, an ultrasonic probe in which a plurality of piezoelectric transducer elements are two-dimensionally arranged can be used.
  • part or all of the processing units included in the ultrasonic diagnostic apparatus in each embodiment may be included in the ultrasonic probe 2.
  • each processing unit included in the ultrasonic diagnostic apparatus is typically realized as an LSI which is an integrated circuit. These may be individually made into one chip, or may be made into one chip so as to include a part or all of them.
  • circuits are not limited to LSI, and may be realized by a dedicated circuit or a general-purpose processor.
  • An FPGA Field Programmable Gate Array
  • reconfigurable processor that can reconfigure the connection and setting of circuit cells inside the LSI may be used.
  • ultrasonic diagnostic apparatus may be realized by a processor such as a CPU executing a program.
  • the present disclosure may be the above-described program, or a non-transitory computer-readable recording medium on which the above-described program is recorded.
  • the program can be distributed via a transmission medium such as the Internet.
  • division of functional blocks in the block diagram is an example, and a plurality of functional blocks can be realized as one functional block, a single functional block can be divided into a plurality of functions, or some functions can be transferred to other functional blocks. May be.
  • functions of a plurality of functional blocks having similar functions may be processed in parallel or time-division by a single hardware or software.
  • the freeze display process is performed based on the determination result of the received signal and the determination result of the inclination angle of the ultrasonic probe. It can be performed. Thereby, unnecessary freeze display processing can be suppressed in the measurement of the characteristics of the subject including the IMT and the specification of the diagnostic site for the disease, and the diagnostic site can be specified by a simple operation. Therefore, the usability of the ultrasonic diagnostic apparatus can be improved.
  • the ultrasonic diagnostic apparatus and the method for controlling the ultrasonic diagnostic apparatus according to the present disclosure it is possible to improve usability for the operator with the above configuration. Therefore, it can be widely used in an ultrasonic diagnostic apparatus capable of simple operation.

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Abstract

An ultrasonic diagnostic device which is configured to be connectable to a display comprises: a transmission reception unit which is configured to be connectable to an ultrasonic probe that includes a tilt angle measurement unit, and performs a transmission process which transmits an ultrasonic wave via the ultrasonic probe to a subject that includes a object to be measured and a reception process which obtains a received signal per frame based on a reflected ultrasonic wave from the object to be measured via the ultrasonic probe; and a freeze display processing unit which, in at least one of a state in which a tile angle of the ultrasonic probe is included in a predetermined angle range and a state in which a tilt angle variation is at a predetermined reference value or less, and when the received signal of the frame based on the reflected ultrasonic wave obtained from the object to be measured by the ultrasonic probe satisfies a predetermined criteria, displays on the display a tomographic image generated on the basis of the received signal of the frame that satisfies the predetermined criteria and continues the display.

Description

超音波診断装置および超音波診断装置の制御方法Ultrasonic diagnostic apparatus and control method of ultrasonic diagnostic apparatus
 本開示は、超音波診断装置および超音波診断装置の制御方法に関する。 The present disclosure relates to an ultrasonic diagnostic apparatus and a control method for the ultrasonic diagnostic apparatus.
 近年、脳梗塞や心筋梗塞などの虚血性疾患のような循環器系疾患に罹る患者が増加している。これらの疾患を予防するには、動脈硬化の兆候を早期に発見し治療を行うことが重要である。動脈硬化を判定する指標として、頚動脈における内膜中膜複合体の厚さ(Intima-Media Thickness:以下、IMTとする)の測定が注目されている。IMTは、頚動脈における初期の粥状硬化を知る重要な指標である。このIMTの測定には、非侵襲的かつ簡便に実施できるという理由で超音波検査が広く用いられている。 In recent years, an increasing number of patients have cardiovascular diseases such as ischemic diseases such as cerebral infarction and myocardial infarction. In order to prevent these diseases, it is important to detect signs of arteriosclerosis early and treat them. As an index for determining arteriosclerosis, measurement of intima-media thickness (hereinafter referred to as IMT) of the intima-media complex in the carotid artery has attracted attention. IMT is an important indicator of the initial atherosclerosis in the carotid artery. Ultrasonography is widely used for this IMT measurement because it can be performed non-invasively and simply.
 図9は、頚動脈の血管の長軸方向(血管が伸長した方向)における断面(以下、長軸断面とする)を示した模式図である。血管は、血管壁200と血管内腔201からなる。血管壁200は、内側から外側に向けて、内膜204、中膜206、外膜202から構成される。内中膜203は、内膜204と中膜206との複合体であり、IMTは内中膜203の厚さを指す。超音波診断装置を用いて、血管内腔201と外膜202との間に内中膜203を視認することができる。IMTの測定においては、通常、血管の長軸方向(血管が伸長した方向)に沿った断面(以後、「長軸断面」と称する)の超音波診断画像である2次元画像に基づきIMTの測定が行われる。具体的には、図14における血管内腔201と内膜204との境界(以後、「内腔内膜境界」とする)205、および中膜206と外膜202との境界(以後、「中膜外膜境界」とする)207を検出し、その境界間の距離を測定することでIMTを測定できる。 FIG. 9 is a schematic diagram showing a cross section (hereinafter, referred to as a long-axis cross section) in the major axis direction of the carotid artery blood vessel (the direction in which the blood vessel is elongated). The blood vessel includes a blood vessel wall 200 and a blood vessel lumen 201. The blood vessel wall 200 is composed of an inner membrane 204, a middle membrane 206, and an outer membrane 202 from the inside to the outside. The inner media 203 is a complex of the inner membrane 204 and the media 206, and IMT indicates the thickness of the inner media 203. Using the ultrasonic diagnostic apparatus, the inner media 203 can be visually recognized between the blood vessel lumen 201 and the outer membrane 202. In the IMT measurement, the IMT measurement is usually based on a two-dimensional image which is an ultrasonic diagnostic image of a cross section (hereinafter referred to as “long-axis cross section”) along the long axis direction of the blood vessel (the direction in which the blood vessel has expanded). Is done. Specifically, the boundary between the blood vessel lumen 201 and the intima 204 in FIG. 14 (hereinafter referred to as “luminal intima boundary”) 205 and the boundary between the media 206 and the outer membrane 202 (hereinafter “medium”). IMT can be measured by detecting 207) (referred to as “outer membrane boundary”) and measuring the distance between the boundaries.
 IMT測定は、その疾病の性質上、定期的に行う必要であり、正確な診断を行うためには毎回同一の位置でIMT測定を行うことが望ましい。従来、汎用の超音波診断装置に搭載されている距離測定機能を用いて手動で上記境界を設定することによりなされていた。この場合、IMTの測定対象領域を抽出しそこへ超音波探触子を案内する操作は、操作者が自ら行わなければならない。その結果、熟練者でなければ測定が難しく、また測定の精度を高めるためには検査時間を要した。これに対し、近年ではIMT測定のための操作の一部を自動的に行う超音波診断装置が提案されている(例えば、特許文献1)。 The IMT measurement must be performed regularly due to the nature of the disease, and it is desirable to perform the IMT measurement at the same position every time for accurate diagnosis. Conventionally, this has been done by manually setting the boundary using a distance measurement function mounted on a general-purpose ultrasonic diagnostic apparatus. In this case, the operator must perform the operation of extracting the IMT measurement target region and guiding the ultrasonic probe there. As a result, it was difficult for non-experts to measure, and it took inspection time to improve the accuracy of measurement. On the other hand, in recent years, an ultrasonic diagnostic apparatus that automatically performs part of an operation for IMT measurement has been proposed (for example, Patent Document 1).
特開2010-022565号公報JP 2010-022565 A WO2011/099103号公報WO2011 / 099103
 しかしながら、上記超音波診断装置においても、IMTを含む被検体の特性計測や疾患に対する診断部位の特定が、簡便な操作で行えるという点では不十分であり、超音波診断装置の使い勝手をさらに向上させることが必要である。本開示は、操作者にとりより使い勝手のよい超音波診断装置および超音波診断装置の制御方法を提供することを目的とする。 However, the above ultrasonic diagnostic apparatus is not sufficient in that the characteristic measurement of the subject including the IMT and the identification of the diagnostic site for the disease can be performed with a simple operation, and the usability of the ultrasonic diagnostic apparatus is further improved. It is necessary. An object of the present disclosure is to provide an ultrasonic diagnostic apparatus and an ultrasonic diagnostic apparatus control method that are more convenient for an operator.
 本開示の一態様に係る超音波診断装置は、表示器が接続可能に構成された超音波診断装置であって、傾斜角度測定部を備えた超音波探触子が接続可能に構成され、測定対象を含む被検体に対して前記超音波探触子を介して超音波を送信する送信処理と、前記超音波探触子を介して前記測定対象からの反射超音波に基づく受信信号をフレーム毎に取得する受信処理とを行う送受信部と、前記超音波探触子の傾斜角度が所定の角度範囲に含まれる状態、又は傾斜角度変動が所定の基準値以下である状態の少なくともいずれかにおいて、前記超音波探触子により前記測定対象から取得された反射超音波に基づくフレームの受信信号が所定の基準を満たすときに、前記所定の基準を満たしたフレームの受信信号に基づき生成された断層画像を前記表示器に表示させ当該表示を継続させるフリーズ表示処理部とを備えたことを特徴とする。 An ultrasonic diagnostic apparatus according to an aspect of the present disclosure is an ultrasonic diagnostic apparatus configured to be connectable to a display device, and configured to be connected to an ultrasonic probe including an inclination angle measurement unit. A transmission process for transmitting an ultrasonic wave to the subject including the object via the ultrasonic probe, and a reception signal based on the reflected ultrasonic wave from the measurement object via the ultrasonic probe for each frame. In at least one of a transmission / reception unit that performs a receiving process acquired in a state where the inclination angle of the ultrasonic probe is included in a predetermined angle range, or a state in which the inclination angle variation is equal to or less than a predetermined reference value, A tomographic image generated based on a received signal of a frame that satisfies the predetermined criterion when a received signal of the frame based on the reflected ultrasound acquired from the measurement object by the ultrasonic probe satisfies a predetermined criterion The table Is displayed on the vessel, characterized in that a freeze display processing unit to continue the display.
 本開示の一態様に係る超音波診断装置および超音波診断装置の制御方法によれば、上記構成により、IMTを含む被検体の特性計測や疾患に対する診断部位の特定において不要なフリーズ表示処理を抑制することができ、簡便な操作で診断部位の特定が可能となる。そのため、超音波診断装置の使い勝手を向上させることができる。 According to the ultrasonic diagnostic apparatus and the method for controlling the ultrasonic diagnostic apparatus according to one aspect of the present disclosure, the above configuration suppresses unnecessary freeze display processing in the measurement of the characteristics of the subject including the IMT and the identification of the diagnostic site for the disease. Therefore, it is possible to specify a diagnostic site with a simple operation. Therefore, the usability of the ultrasonic diagnostic apparatus can be improved.
実施の形態1に係る超音波診断装置1の機能ブロック図の一例である。1 is an example of a functional block diagram of an ultrasound diagnostic apparatus 1 according to Embodiment 1. FIG. 実施の形態1に係る超音波診断装置1の受信信号判定部における心拍同期信号の判定方法を説明するための補助図の一例であり、(a)は、血管断面の模式図、(b)は、拍動による血管径の時間的変化を示す模式図の一例である。It is an example of the auxiliary figure for demonstrating the determination method of the heart rate synchronizing signal in the received signal determination part of the ultrasound diagnosing device 1 which concerns on Embodiment 1, (a) is a schematic diagram of a blood vessel cross section, (b) is. It is an example of the schematic diagram which shows the time change of the blood vessel diameter by a pulsation. 実施の形態1に係る超音波診断装置1の判定部11の機能ブロック図の一例である。3 is an example of a functional block diagram of a determination unit 11 of the ultrasound diagnostic apparatus 1 according to Embodiment 1. FIG. 実施の形態1に係る超音波診断装置1の受信信号判定部111における血管中心の判定を説明するための模式図の一例であり、(a)は、被検体の皮膚表面に配置した超音波探触子2から送信された超音波が血管中心211近傍を捉えている場合、(b)は、超音波が血管中心211近傍を通らない場合を示す。FIG. 7 is an example of a schematic diagram for explaining the determination of the blood vessel center in the reception signal determination unit 111 of the ultrasonic diagnostic apparatus 1 according to Embodiment 1, and (a) is an ultrasonic probe arranged on the skin surface of a subject. When the ultrasonic wave transmitted from the touch element 2 captures the vicinity of the blood vessel center 211, (b) shows a case where the ultrasonic wave does not pass through the vicinity of the blood vessel center 211. 実施の形態1に係る超音波診断装置1の心拍同期信号取得部による心拍同期信号の取得方法を説明するための模式図の一例である。3 is an example of a schematic diagram for explaining a method for acquiring a heartbeat synchronization signal by a heartbeat synchronization signal acquisition unit of the ultrasound diagnostic apparatus 1 according to Embodiment 1. FIG. 実施の形態1に係る超音波診断装置1の動作を示すフローチャートの一例である。3 is an example of a flowchart showing an operation of the ultrasonic diagnostic apparatus 1 according to the first embodiment. 実施の形態1に係る超音波診断装置における傾斜角度判定部の機能を説明するための補助図の一例である。3 is an example of an auxiliary diagram for explaining a function of an inclination angle determination unit in the ultrasonic diagnostic apparatus according to Embodiment 1. FIG. 実施の形態2に係る超音波診断装置における傾斜角度判定部の機能を説明するための補助図の一例である。6 is an example of an auxiliary diagram for explaining a function of an inclination angle determination unit in the ultrasonic diagnostic apparatus according to Embodiment 2. FIG. 頚動脈の血管の長軸断面を示した模式図の一例である。It is an example of the schematic diagram which showed the long-axis cross section of the blood vessel of a carotid artery.
 ≪発明を実施するための形態に至った経緯について≫
 発明者らは、超音波診断装置を用いてIMTを測定する際の動作について検討した。一般的に、超音波診断装置は、超音波探触子を介して頚動脈を含む被検体に対し繰り返し超音波を送受信することでフレーム毎に断層画像を生成する。そして、生成した断層画像を断層画像として逐次表示器に更新表示を行うとともに、特定のフレームにおいて測定されたIMTの値を表示器に表示する。しかしながら、従来の超音波診断装置では、表示器にIMT値が表示される場合に、断層画像はフレーム毎に逐次更新表示されるため、表示されているフレームの断層画像とIMT値の測定対象となったフレームとが対応しないものとなっていた。
≪Background to the form for carrying out the invention≫
The inventors examined the operation when measuring IMT using an ultrasonic diagnostic apparatus. Generally, an ultrasonic diagnostic apparatus generates a tomographic image for each frame by repeatedly transmitting and receiving ultrasonic waves to and from a subject including a carotid artery via an ultrasonic probe. The generated tomographic image is sequentially updated and displayed on the display as a tomographic image, and the IMT value measured in a specific frame is displayed on the display. However, in the conventional ultrasonic diagnostic apparatus, when the IMT value is displayed on the display, the tomographic image is sequentially updated and displayed for each frame, so that the tomographic image of the displayed frame and the IMT value measurement target are displayed. The frame was not compatible.
 これに対し、IMT測定を行うことが可能な基準を満たしたフレームに対し、フレームの断層画像を静止画像として表示器に表示させ当該表示を継続する(以下、「フリーズ表示」とする)処理を行うことが考えられる。これに関連する技術として、例えば、特許文献2には、超音波探触子を介して取得した受信信号や受信信号から所定の処理が施された信号が所定の基準が満たしたときに、当該フレームの断層画像をフリーズ表示する技術が開示されている。この技術を用いれば、表示されているフレームの断層画像とIMT値の測定対象となったフレームとが対応させることができると考えられる。

 しかしながら、上述のような受信信号に基づいてフリーズ表示処理を行う構成では、受信信号が一定の条件を満たしている場合にはフリーズ表示処理が行われる。その結果、超音波探触子を被検体皮膚表面で動かして所望の測定対象を探索している際中に、受信信号が一定の条件を満たしている場合にはフリーズ表示処理が行われてしまうことになる。
On the other hand, for a frame that satisfies the criteria capable of performing IMT measurement, a tomographic image of the frame is displayed on the display device as a still image and the display is continued (hereinafter referred to as “freeze display”). It is possible to do it. As a technique related to this, for example, in Patent Document 2, when a predetermined standard satisfies a reception signal acquired via an ultrasonic probe or a signal that has been subjected to a predetermined process from the reception signal, A technique for freeze-displaying a tomographic image of a frame is disclosed. If this technique is used, it is considered that the tomographic image of the displayed frame can be made to correspond to the frame that is the measurement target of the IMT value.

However, in the configuration in which the freeze display process is performed based on the received signal as described above, the freeze display process is performed when the received signal satisfies a certain condition. As a result, while the ultrasonic probe is moved on the surface of the subject's skin and searching for a desired measurement target, if the received signal satisfies a certain condition, a freeze display process is performed. It will be.
 また、例えば、IMT測定のように定期的な検査を必要とし、その検査を毎回、ほぼ同一の測定位置で行う必要がある検査では、以下のような問題もある。すなわち、超音波探触子が必要な測定位置に当てられていないにもかかわらず、受信信号が一定の条件を満たしている場合にはフリーズ表示処理が行われてしまい、使い勝手の十分な向上が図れない。 Further, for example, in the inspection that requires a periodic inspection like IMT measurement and needs to perform the inspection at almost the same measurement position every time, there are the following problems. In other words, if the received signal satisfies a certain condition even though the ultrasonic probe is not placed at the required measurement position, the freeze display process is performed, and the usability is sufficiently improved. I can't figure it out.
 そこで、発明者らは、定期的な検査において毎回、ほぼ同一の測定位置で検査を行う必要がある場合においても、使い勝手を向上させることができる技術について鋭意検討を行い、本実施の形態に係る超音波診断装置および超音波診断装置の制御方法を想到するに至ったものである。 Therefore, the inventors have intensively studied a technique that can improve usability even when it is necessary to perform inspection at almost the same measurement position every time in periodic inspection, and according to the present embodiment. The inventors have come up with an ultrasonic diagnostic apparatus and a method for controlling the ultrasonic diagnostic apparatus.
 以下に、実施の形態に係る超音波診断装置および超音波診断装置の制御方法について図面を用いて詳細に説明する。なお、以下の説明では、被検体の特性として頚動脈のIMTを測定を例について説明するが、本実施の形態はこれに限定されず、超音波診断装置を用いた検査において、フリーズ表示処理を行う必要がある検査全般に適用することができる。 Hereinafter, the ultrasonic diagnostic apparatus and the control method of the ultrasonic diagnostic apparatus according to the embodiment will be described in detail with reference to the drawings. In the following description, an example of measuring the IMT of the carotid artery as the characteristics of the subject will be described. However, the present embodiment is not limited to this, and freeze display processing is performed in an examination using an ultrasonic diagnostic apparatus. It can be applied to all the necessary tests.
 なお、本明細書における「超音波探触子の傾斜角度」とは、所定の方向(例えば、重力方向、被検体における特定の方向)を基準とした超音波探触子2の相対的な傾きを意味する。併せて、所定の位置(例えば、被検体)を基準とした超音波探触子の位置情報に基づく絶対位置に基づき得られる超音波探触子の位置関係についても超音波探触子の角度を意味する。 In this specification, “inclination angle of the ultrasound probe” refers to the relative inclination of the ultrasound probe 2 with respect to a predetermined direction (for example, the direction of gravity, a specific direction in the subject). Means. At the same time, the angle of the ultrasonic probe is also determined for the positional relationship of the ultrasonic probe obtained based on the absolute position based on the position information of the ultrasonic probe with respect to a predetermined position (for example, the subject). means.
 以下、実施の形態に係る超音波診断装置および超音波診断装置の制御方法について、図面を参照しながら説明する。 Hereinafter, an ultrasonic diagnostic apparatus and a control method of the ultrasonic diagnostic apparatus according to the embodiment will be described with reference to the drawings.
 ≪本発明を実施するための形態の概要≫
 本実施の形態に係る超音波診断装置は、表示器が接続可能に構成された超音波診断装置であって、傾斜角度測定部を備えた超音波探触子が接続可能に構成され、測定対象を含む被検体に対して前記超音波探触子を介して超音波を送信する送信処理と、前記超音波探触子を介して前記測定対象からの反射超音波に基づく受信信号をフレーム毎に取得する受信処理とを行う送受信部と、前記超音波探触子の傾斜角度が所定の角度範囲に含まれる状態、又は傾斜角度変動が所定の基準値以下である状態の少なくともいずれかにおいて、前記超音波探触子により前記測定対象から取得された反射超音波に基づくフレームの受信信号が所定の基準を満たすときに、前記所定の基準を満たしたフレームの受信信号に基づき生成された断層画像を前記表示器に表示させ当該表示を継続させるフリーズ表示処理部とを備えたことを特徴とする。
<< Outline of Embodiment for Implementing the Present Invention >>
The ultrasonic diagnostic apparatus according to the present embodiment is an ultrasonic diagnostic apparatus configured to be connectable to a display device, configured to be connectable with an ultrasonic probe including an inclination angle measuring unit, and to be measured. A transmission process for transmitting an ultrasonic wave to the subject including the ultrasonic probe via the ultrasonic probe, and a reception signal based on the reflected ultrasonic wave from the measurement object via the ultrasonic probe for each frame. In at least one of a transmission / reception unit that performs a reception process to be acquired, a state in which an inclination angle of the ultrasonic probe is included in a predetermined angle range, or a state in which an inclination angle variation is a predetermined reference value or less, When the received signal of the frame based on the reflected ultrasound acquired from the measurement object by the ultrasonic probe satisfies a predetermined reference, a tomographic image generated based on the received signal of the frame that satisfies the predetermined reference is The indicator Characterized in that a freeze display processing unit to continue the display to display.
 また、別の態様では、前記受信信号に基づきフレーム毎に断層画像を生成する断層画像生成部と、前記断層画像を前記表示器に表示させる表示処理部と、前記傾斜角度測定部から逐次取得された前記超音波探触子の傾斜角度が所定の角度範囲に含まれるか否かを判定する傾斜角度判定部と、前記送受信部が取得したフレームの受信信号が前記所定の基準を満たすか否かを判定する受信信号判定部とを備え、前記傾斜角度判定部が、1以上のフレームの受信信号の基礎とされた反射超音波が前記超音波探触子に取得されたときの前記超音波探触子の傾斜角度が所定の角度範囲に含まれると判定し、前記受信信号判定部が、前記1以上のフレームの受信信号が前記所定の基準を満たすと判定したとき、前記フリーズ表示処理部は、前記1以上のフレームに含まれる少なくとも1のフレームの受信信号に基づき前記断層画像生成部により生成された断層画像を前記表示処理部を介して前記表示器に表示させ当該表示を継続させる構成であってもよい。 In another aspect, the tomographic image generation unit that generates a tomographic image for each frame based on the received signal, the display processing unit that displays the tomographic image on the display, and the inclination angle measurement unit are sequentially acquired. In addition, an inclination angle determination unit that determines whether or not an inclination angle of the ultrasonic probe is included in a predetermined angle range, and whether or not a reception signal of a frame acquired by the transmission / reception unit satisfies the predetermined criterion A reception signal determination unit for determining whether or not the tilt angle determination unit receives the reflected ultrasonic wave based on the reception signal of one or more frames from the ultrasonic probe. When it is determined that the tilt angle of the touch element is included in a predetermined angle range, and the reception signal determination unit determines that the reception signals of the one or more frames satisfy the predetermined criterion, the freeze display processing unit is The one or more It may be configured to continue the display is displayed on the display device via the display processing unit tomographic image generated by the tomographic image generating unit based on the received signal of at least one frame included in the frame.
 また、別の態様では、前記受信信号に基づきフレーム毎に断層画像を生成する断層画像生成部と、前記断層画像を前記表示器に表示させる表示処理部と、前記傾斜角度測定部から逐次取得された前記超音波探触子の傾斜角度変動が所定の基準値以下であるか否かを判定する傾斜角度判定部と、前記送受信部が取得したフレームの受信信号が所定基準を満たすか否かを判定する受信信号判定部とをさらに備え、前記傾斜角度判定部が、1以上のフレームの受信信号の基礎とされた反射超音波が前記超音波探触子に取得されたときの前記超音波探触子の傾斜角度変動が傾斜角度変動が所定の基準値以下であると判定し、前記受信信号判定部が、前記1以上のフレームの受信信号が前記所定の基準を満たすと判定したとき、前記フリーズ表示処理部は、前記1以上のフレームに含まれる少なくとも1のフレームの受信信号に基づき前記断層画像生成部が生成した断層画像を前記表示処理部を介して前記表示器に表示させ当該表示を継続させる構成であってもよい。 In another aspect, the tomographic image generation unit that generates a tomographic image for each frame based on the received signal, the display processing unit that displays the tomographic image on the display, and the inclination angle measurement unit are sequentially acquired. In addition, an inclination angle determination unit that determines whether or not an inclination angle variation of the ultrasonic probe is equal to or less than a predetermined reference value, and whether or not a reception signal of a frame acquired by the transmission / reception unit satisfies a predetermined reference. A reception signal determination unit for determining, wherein the tilt angle determination unit is configured to detect the ultrasonic probe when a reflected ultrasonic wave based on the reception signal of one or more frames is acquired by the ultrasonic probe. When the tilt angle variation of the touchor determines that the tilt angle variation is equal to or less than a predetermined reference value, and the reception signal determination unit determines that the reception signal of the one or more frames satisfies the predetermined criterion, Freeze display processing Is a configuration in which the tomographic image generated by the tomographic image generation unit based on the reception signal of at least one frame included in the one or more frames is displayed on the display device via the display processing unit and the display is continued. There may be.
 また、別の態様では、前記受信信号判定部は、前記1以上のフレームの受信信号の基礎とされた反射超音波が前記測定対象における所定の領域から心拍周期における所定のタイミングにて取得されているときに前記所定の基準を満たすと判定する構成であってもよい。 In another aspect, the reception signal determination unit is configured to acquire a reflected ultrasonic wave based on the reception signal of the one or more frames from a predetermined region in the measurement target at a predetermined timing in a heartbeat cycle. It may be configured to determine that the predetermined criterion is satisfied when the vehicle is in the middle.
 また、別の態様では、前記受信信号に基づき前記測定対象の特性を測定する測定部をさらに備え、前記フリーズ表示処理部は、前記測定部により前記1以上のフレームに含まれる少なくとも1のフレームの受信信号に基づき測定された前記特性の測定結果を前記表示器に表示させ当該表示を継続させる構成であってもよい。 In another aspect, the apparatus further includes a measurement unit that measures the characteristics of the measurement target based on the received signal, and the freeze display processing unit is configured to transmit at least one frame included in the one or more frames by the measurement unit. The measurement result of the characteristic measured based on the received signal may be displayed on the display unit and the display may be continued.
 また、別の態様では、前記特性はIMTである構成であってもよい。 In another aspect, the characteristic may be IMT.
 また、別の態様では、前記傾斜角度測定部は角度センサであり、前記角度センサから逐次取得した信号に基づき前記超音波探触子の傾斜角度を算出する傾斜角度算出部をさらに備えた構成であってもよい。 In another aspect, the tilt angle measurement unit is an angle sensor, and further includes a tilt angle calculation unit that calculates the tilt angle of the ultrasonic probe based on signals sequentially acquired from the angle sensor. There may be.
 本実施の形態に係る超音波診断装置の制御方法は、傾斜角度測定部を備えた超音波探触子と表示器とが各々接続可能に構成された超音波診断装置の制御方法であって、測定対象を含む被検体に対して前記超音波探触子を介して超音波を送信する送信処理と、前記超音波探触子を介して前記測定対象からの反射超音波に基づく受信信号をフレーム毎に取得する受信処理とを行う送受信ステップと、前記超音波探触子の傾斜角度が所定の角度範囲に含まれる状態、又は傾斜角度変動が所定の基準値以下である状態の少なくともいずれか一方において、前記超音波探触子により前記測定対象から取得された反射超音波に基づくフレームの受信信号が所定の基準を満たすときに、前記所定の基準を満たしたフレームの受信信号に基づき生成された断層画像を前記表示器に表示させ当該表示を継続させるフリーズ表示処理ステップとを有することを特徴とする。 The control method of the ultrasonic diagnostic apparatus according to the present embodiment is a control method of the ultrasonic diagnostic apparatus configured such that an ultrasonic probe including an inclination angle measurement unit and a display can be connected to each other. A transmission process for transmitting an ultrasonic wave to the subject including the measurement object via the ultrasonic probe, and a reception signal based on the reflected ultrasonic wave from the measurement object via the ultrasonic probe are framed. At least one of a transmission / reception step for performing reception processing acquired every time, a state in which the tilt angle of the ultrasonic probe is included in a predetermined angle range, and a state in which the tilt angle variation is equal to or less than a predetermined reference value The received signal of the frame based on the reflected ultrasound acquired from the measurement object by the ultrasound probe is generated based on the received signal of the frame that satisfies the predetermined criterion Refusal And having a freeze display processing step to continue the display to display an image on the display.
 ≪実施の形態1≫
 以下、実施の形態1に係る超音波診断装置について、図面を参照しながら説明する。
<< Embodiment 1 >>
Hereinafter, the ultrasonic diagnostic apparatus according to Embodiment 1 will be described with reference to the drawings.
 <全体構成>
 実施の形態1に係る超音波診断装置1の機能ブロック図である。超音波診断装置1は、送受信部6、傾斜角度算出部7、断層画像生成部8、心拍同期信号取得部9、測定部10、判定部11、フリーズ表示処理部12、表示処理部13および制御部14から構成される制御器5を備える。超音波診断装置1は、超音波探触子2、表示器3及び入力器4が接続可能に構成されている。図1は超音波診断装置1に、超音波探触子2、表示器3及び入力器4が接続された状態を示している。以降、超音波診断装置1に接続される各要素について説明する。
<Overall configuration>
1 is a functional block diagram of an ultrasound diagnostic apparatus 1 according to Embodiment 1. FIG. The ultrasonic diagnostic apparatus 1 includes a transmission / reception unit 6, an inclination angle calculation unit 7, a tomographic image generation unit 8, a heartbeat synchronization signal acquisition unit 9, a measurement unit 10, a determination unit 11, a freeze display processing unit 12, a display processing unit 13, and a control. The controller 5 comprised from the part 14 is provided. The ultrasonic diagnostic apparatus 1 is configured such that an ultrasonic probe 2, a display device 3, and an input device 4 can be connected. FIG. 1 shows a state in which an ultrasound probe 2, a display device 3 and an input device 4 are connected to the ultrasound diagnostic apparatus 1. Hereinafter, each element connected to the ultrasonic diagnostic apparatus 1 will be described.
 (超音波探触子2)
 超音波探触子2は、例えば一次元方向(以下、「振動子配列方向」とする)に配列された複数の振動子(不図示)を有する。超音波探触子2は、後述の送受信部6から供給されたパルス状または連続波の電気信号(以下、「送信電気信号」とする。)をパルス状または連続波の超音波に変換する。超音波探触子2は、超音波探触子2の振動子側外表面を被検体の皮膚表面に接触させた状態で、複数の振動子から発せられる複数の超音波からなる超音波ビームを測定対象(頚動脈)に向けて送信する。この際、例えば、頚動脈の長軸断面の断層画像を取得するためには、超音波探触子2の振動子配列方向が頚動脈の長軸方向に沿うように超音波探触子2を被検体皮膚表面に配置する。そして、超音波探触子2は、被検体からの複数の反射超音波を受信し、複数の振動子によりこれら反射超音波をそれぞれ電気信号(以下、「受信電気信号」とする)に変換し、受信電気信号を送受信部6に供給する。
(Ultrasonic probe 2)
The ultrasonic probe 2 has a plurality of transducers (not shown) arranged in a one-dimensional direction (hereinafter referred to as “vibrator arrangement direction”), for example. The ultrasonic probe 2 converts a pulsed or continuous wave electrical signal (hereinafter referred to as “transmission electrical signal”) supplied from a transmitting / receiving unit 6 described later into pulsed or continuous wave ultrasonic waves. The ultrasonic probe 2 emits an ultrasonic beam composed of a plurality of ultrasonic waves emitted from a plurality of transducers in a state where the transducer-side outer surface of the ultrasonic probe 2 is in contact with the skin surface of the subject. Send to the measurement target (carotid artery). At this time, for example, in order to acquire a tomographic image of the long-axis cross section of the carotid artery, the subject is placed on the subject so that the transducer arrangement direction of the ultrasonic probe 2 is along the long-axis direction of the carotid artery. Place on the skin surface. The ultrasound probe 2 receives a plurality of reflected ultrasound waves from the subject, and converts the reflected ultrasound waves into electrical signals (hereinafter referred to as “received electrical signals”) by a plurality of transducers. The received electrical signal is supplied to the transmission / reception unit 6.
 なお、実施の形態1においては、一次元方向に配列された複数の振動子を有する超音波探触子2を、例示しているが、本実施の形態に用いることができる超音波探触子2はこれに限定されない。例えば、振動子を二次元方向に配列した二次元配列振動子や、一次元方向に配列された複数の振動子を機械的に揺動させて三次元の断層画像を取得する揺動型超音波探触子を用いてもよく、測定に応じて適宜使い分けることができる。 In the first embodiment, the ultrasonic probe 2 having a plurality of transducers arranged in a one-dimensional direction is illustrated, but an ultrasonic probe that can be used in the present embodiment. 2 is not limited to this. For example, a two-dimensional array of transducers arranged in a two-dimensional direction, or a oscillating ultrasonic that mechanically oscillates a plurality of transducers arranged in a one-dimensional direction to acquire a three-dimensional tomographic image A probe may be used and can be appropriately used depending on the measurement.
 また、超音波探触子2は、後述する送受信部6の一部の機能を超音波探触子側に設けてもよい。例えば、送受信部6から出力された送信電気信号を生成するための制御信号(以下、「送信制御信号」とする)に基づき超音波探触子2内で送信電気信号を生成し、この送信電気信号を超音波に変換する機能を超音波探触子側に設けてもよい。また、受信した反射超音波を受信電気信号に変換した後、この受信電気信号に基づき後述の受信信号を生成する機能を超音波探触子側に設けてもよい。 Further, the ultrasonic probe 2 may be provided with a part of functions of the transmission / reception unit 6 described later on the ultrasonic probe side. For example, a transmission electric signal is generated in the ultrasonic probe 2 based on a control signal (hereinafter referred to as “transmission control signal”) for generating a transmission electric signal output from the transmission / reception unit 6, and the transmission electric signal is generated. A function of converting a signal into an ultrasonic wave may be provided on the ultrasonic probe side. Moreover, after converting the received reflected ultrasonic wave into a received electrical signal, a function of generating a received signal described later based on the received electrical signal may be provided on the ultrasonic probe side.
 超音波探触子2には、傾斜角度測定部21が内蔵されている。この傾斜角度測定部21は、駆動中の超音波探触子2の傾斜角度を逐次取得するために必要な情報(以下、「センサ出力情報」とする)を逐次取得し、そのセンサ出力情報を超音波診断装置1の後述する傾斜角度算出部7に出力する。傾斜角度測定部21は、傾斜角度算出部7で超音波探触子2の傾斜角度を算出可能なセンサ出力情報が得られるものであればよく、当該部21には、例えば、加速度センサ、磁気センサ、光学センサ、ジャイロセンサを用いることができる。なお、実施の形態1においては、傾斜角度測定部21として加速度センサを用いる例を示した。この場合、センサ出力情報は加速度情報である。また、図1においては、傾斜角度測定部21を超音波探触子2内に内蔵した構成を示しているが、使用する傾斜角度測定部21の種類に応じて超音波探触子2の外部に傾斜角度測定部21を設ける構成としてもよい。 The ultrasonic probe 2 has a built-in tilt angle measurement unit 21. The tilt angle measurement unit 21 sequentially acquires information (hereinafter referred to as “sensor output information”) necessary for sequentially acquiring the tilt angle of the ultrasonic probe 2 being driven, and outputs the sensor output information. It outputs to the inclination angle calculation part 7 mentioned later of the ultrasonic diagnostic apparatus 1. The tilt angle measuring unit 21 may be any sensor that can obtain sensor output information that allows the tilt angle calculating unit 7 to calculate the tilt angle of the ultrasound probe 2. Examples of the tilt angle measuring unit 21 include an acceleration sensor and a magnetic sensor. A sensor, an optical sensor, or a gyro sensor can be used. In the first embodiment, an example in which an acceleration sensor is used as the tilt angle measurement unit 21 has been described. In this case, the sensor output information is acceleration information. Further, FIG. 1 shows a configuration in which the tilt angle measuring unit 21 is built in the ultrasonic probe 2, but depending on the type of the tilt angle measuring unit 21 to be used, the outside of the ultrasonic probe 2 is shown. It is good also as a structure which provides the inclination angle measurement part 21 in this.
 (表示器3)
 表示器3は、いわゆる画像表示用の表示装置であって、後述する表示処理部13からの画像出力を表示画面に表示する。表示器3には、液晶ディスプレイ、CRT、有機ELディスプレイ等を用いることができる。
(Display 3)
The display 3 is a display device for so-called image display, and displays an image output from a display processing unit 13 described later on a display screen. As the display 3, a liquid crystal display, a CRT, an organic EL display, or the like can be used.
 (入力器4)
 入力器4は、操作者からの超音波診断装置1に対する各種設定・操作等の各種操作入力を受け付け、制御部14に出力する。
(Input device 4)
The input device 4 receives various operation inputs such as various settings / operations on the ultrasonic diagnostic apparatus 1 from the operator and outputs them to the control unit 14.
 入力器4は、例えば、表示器3と一体として構成されたタッチパネルであってもよい。この場合、表示器3に表示された操作キーに対してタッチ操作やドラッグ操作を行うことで超音波診断装置1の各種設定・操作を行うことができ、超音波診断装置1がこのタッチパネルにより操作可能に構成される。また、入力器4は、例えば、各種操作用のキーを有するキーボードや、各種操作用のボタン、レバー等を有する操作パネルであってもよい。また、表示器3に表示されるカーソル表示を動かすためのトラックボール、マウスまたはフラットパッド等であってもよい。または、これらを複数用いてもよく、これらを複数組合せた構成のものであってもよい。 The input device 4 may be, for example, a touch panel configured integrally with the display device 3. In this case, various settings / operations of the ultrasonic diagnostic apparatus 1 can be performed by performing a touch operation or a drag operation on the operation keys displayed on the display device 3, and the ultrasonic diagnostic apparatus 1 can be operated by this touch panel. Configured to be possible. The input device 4 may be, for example, a keyboard having various operation keys, or an operation panel having various operation buttons, levers, and the like. Further, it may be a trackball, a mouse, a flat pad or the like for moving the cursor display displayed on the display device 3. Alternatively, a plurality of these may be used, or a combination of these may be used.
 <各部構成>
 (制御器5)
 超音波診断装置1は、入力器4からの操作入力に基づき超音波診断装置1の動作を制御する制御器5を有する。制御器5は、上述のとおり、送受信部6、傾斜角度算出部7、断層画像生成部8、心拍同期信号取得部9、測定部10、判定部11、フリーズ表示処理部12、表示処理部13および制御部14を備える。それぞれのブロックは制御部14によって制御されている。送受信部6は超音波探触子2と、傾斜角度算出部7は傾斜角度測定部21と、表示処理部13は表示器3と、各々接続された構成となっている。以降、制御器5に含まれる各ブロックの構成について説明する。
<Configuration of each part>
(Controller 5)
The ultrasonic diagnostic apparatus 1 includes a controller 5 that controls the operation of the ultrasonic diagnostic apparatus 1 based on an operation input from the input unit 4. As described above, the controller 5 includes the transmission / reception unit 6, the tilt angle calculation unit 7, the tomographic image generation unit 8, the heartbeat synchronization signal acquisition unit 9, the measurement unit 10, the determination unit 11, the freeze display processing unit 12, and the display processing unit 13. And a control unit 14. Each block is controlled by the control unit 14. The transmission / reception unit 6 is connected to the ultrasonic probe 2, the tilt angle calculation unit 7 is connected to the tilt angle measurement unit 21, and the display processing unit 13 is connected to the display 3. Hereinafter, the configuration of each block included in the controller 5 will be described.
 (送受信部6)
 送受信部6は、超音波探触子2と接続される。送受信部6は、超音波探触子2の超音波ビームの送信制御に係る送信制御信号を生成し、この送信制御信号に基づき生成したパルス状または連続波の送信電気信号を超音波探触子2に供給する送信処理を行う。なお、送受信部6が行う送信処理とは、少なくとも送受信部6で送信制御信号を生成し、送信制御信号に基づいて超音波探触子2に超音波(ビーム)を送信させる処理を意味する。
(Transceiver 6)
The transmission / reception unit 6 is connected to the ultrasonic probe 2. The transmission / reception unit 6 generates a transmission control signal related to transmission control of the ultrasonic beam of the ultrasonic probe 2, and transmits the pulsed or continuous wave transmission electric signal generated based on the transmission control signal to the ultrasonic probe. 2 is transmitted. Note that the transmission processing performed by the transmission / reception unit 6 means processing for generating a transmission control signal at least by the transmission / reception unit 6 and causing the ultrasonic probe 2 to transmit ultrasonic waves (beams) based on the transmission control signal.
 また、送受信部6は、超音波探触子2からの受信電気信号を増幅してA/D変換を行い、受信信号を生成する受信処理を行う。そして、この受信信号を断層画像生成部8、心拍同期信号取得部9および測定部10に出力する。受信信号は、例えば、振動子配列方向と超音波の送信方向であって振動子配列と垂直な方向からなる複数の信号からなり、各信号は反射超音波の振幅から変換された電気信号をA/D変換したデジタル信号である。送受信部6は、送信処理および受信処理を繰り返し連続して行い、複数の受信信号からなるフレームを複数構築する。なお、送受信部6が行う受信処理とは、少なくとも送受信部6が反射超音波に基づく受信信号を生成する処理を意味する。 Also, the transmission / reception unit 6 performs reception processing for amplifying the received electrical signal from the ultrasound probe 2 and performing A / D conversion to generate a received signal. Then, this received signal is output to the tomographic image generation unit 8, the heartbeat synchronization signal acquisition unit 9, and the measurement unit 10. The received signal includes, for example, a plurality of signals having a transducer arrangement direction and an ultrasonic transmission direction and a direction perpendicular to the transducer arrangement, and each signal is an electric signal converted from the amplitude of the reflected ultrasonic wave A. / D converted digital signal. The transmission / reception unit 6 repeatedly performs transmission processing and reception processing continuously to construct a plurality of frames including a plurality of reception signals. The reception process performed by the transmission / reception unit 6 means a process in which at least the transmission / reception unit 6 generates a reception signal based on the reflected ultrasound.
 ここで、「フレーム」とは、1枚の断層画像を構築する上で必要な1つのまとまった受信信号の単位、またはこの1つのまとまった受信信号に基づき断層画像を構築するために処理された信号の単位、あるいは、この一つのまとまった受信信号に基づき構築された1枚の断層画像の単位ことをさす。 Here, the “frame” is processed in order to construct a tomographic image based on one unit of received signals necessary for constructing one tomographic image, or on this one received signal. A unit of signal or a unit of one tomographic image constructed on the basis of a single received signal.
 (傾斜角度算出部)
 傾斜角度算出部7は、傾斜角度測定部21からのセンサ出力情報に基づき、超音波探触子2の角度を取得する。すなわち、傾斜角度算出部7は、加速度センサである傾斜角度測定部21から出力される加速度情報に基づき、所定の方向(例えば、重力方向)を基準とした超音波探触子2の傾きを算出し傾斜角度として取得する。そして、取得した傾斜角度に係る情報(以下、「傾斜角度情報」とする。)を逐次、判定部11に出力する。
(Inclination angle calculation unit)
The tilt angle calculation unit 7 acquires the angle of the ultrasonic probe 2 based on the sensor output information from the tilt angle measurement unit 21. That is, the tilt angle calculation unit 7 calculates the tilt of the ultrasonic probe 2 with reference to a predetermined direction (for example, the direction of gravity) based on the acceleration information output from the tilt angle measurement unit 21 that is an acceleration sensor. And obtained as the tilt angle. Then, the information related to the acquired inclination angle (hereinafter referred to as “inclination angle information”) is sequentially output to the determination unit 11.
 (断層画像生成部8)
 断層画像生成部8は、フレーム内のそれぞれの受信信号を、その強度に対応した輝度信号へと変換し、その輝度信号を直交座標系に座標変換を施すことで断層画像データを生成する。断層画像生成部8はこの処理をフレーム毎に逐次行い、生成した断層画像を判定部11に出力する。
(Tomographic image generation unit 8)
The tomographic image generation unit 8 converts each received signal in the frame into a luminance signal corresponding to the intensity, and generates the tomographic image data by performing coordinate conversion on the rectangular coordinate system. The tomographic image generation unit 8 sequentially performs this process for each frame and outputs the generated tomographic image to the determination unit 11.
 (心拍同期信号取得部9)
 心拍同期信号取得部9は、受信信号から被検体の心拍に同期した心拍同期信号を検出し、検出した心拍同期信号を判定部11に出力する。また、心拍同期信号取得部9は、心拍同期信号の所定のタイミングを検出する情報を備え、検出した心拍同期信号に基づき例えばIMT測定を行うための所定のタイミングを検出し、そのタイミングを測定部10に出力する。このタイミングとは、一心拍中の、例えば、心臓が収縮後拡張して血流が最小となる心拡張末期のタイミングとしてもよい。
(Heartbeat synchronization signal acquisition unit 9)
The heartbeat synchronization signal acquisition unit 9 detects a heartbeat synchronization signal synchronized with the heartbeat of the subject from the received signal, and outputs the detected heartbeat synchronization signal to the determination unit 11. The heartbeat synchronization signal acquisition unit 9 includes information for detecting a predetermined timing of the heartbeat synchronization signal, detects a predetermined timing for performing, for example, IMT measurement based on the detected heartbeat synchronization signal, and measures the timing. 10 is output. This timing may be the end timing of diastole during one heartbeat, for example, when the heart dilates after contraction and blood flow is minimized.
 図2は、超音波診断装置1の受信信号判定部における心拍同期信号の判定方法を説明するための補助図であり、(a)は血管断面の模式図、(b)は拍動による血管径の時間的変化を示す模式図である。実施の形態1に係る超音波診断装置1の受信信号判定部における心拍同期信号の判定方法を説明するための補助図である。心拍同期信号取得部9は、例えば、特許第4189405号公報等に記載されている公知の方法を用いて受信信号から拍同期信号を検出する。具体的には、図2(a)に示すように血管の前壁(血管の長軸断面における被検体皮膚表面側に位置する血管壁)209と後壁210に測定点A、Bを設定し、受信信号の信号強度や位相を解析することで測定点A、Bの動きを追跡する。動脈は、心拍によって収縮拡張を繰り返しており、このため測定点A-B間の距離は、図2(b)に示すように心臓の拍動に対応した周期的な動きを示す径変化波形を得ることができる。この径変化波形を心拍同期信号として取得する。これにより、心電計や心音計のような特別な装置を必要とせず、超音波探触子2を被検体皮膚表面に当接させるだけの簡単な操作で心拍同期信号を取得することができる。ただし、上記で示した心拍同期信号の取得は、あくまで一例であって、心電計や心音計を用いてもよい。 2A and 2B are auxiliary diagrams for explaining a method of determining a heartbeat synchronization signal in a reception signal determination unit of the ultrasonic diagnostic apparatus 1, wherein FIG. 2A is a schematic diagram of a blood vessel cross section, and FIG. 2B is a blood vessel diameter due to pulsation. It is a schematic diagram which shows the time change of. 6 is an auxiliary diagram for explaining a method for determining a heartbeat synchronization signal in a reception signal determination unit of the ultrasound diagnostic apparatus 1 according to Embodiment 1. FIG. The heartbeat synchronization signal acquisition unit 9 detects a pulse synchronization signal from the received signal using a known method described in, for example, Japanese Patent No. 4189405. Specifically, as shown in FIG. 2A, measurement points A and B are set on the anterior wall of the blood vessel (the blood vessel wall located on the subject skin surface side in the long-axis cross section of the blood vessel) 209 and the rear wall 210. The movement of the measurement points A and B is tracked by analyzing the signal intensity and phase of the received signal. The artery repeatedly contracts and expands due to the heartbeat. Therefore, the distance between the measurement points A and B has a diameter change waveform indicating a periodic movement corresponding to the heart beat as shown in FIG. Obtainable. This diameter change waveform is acquired as a heartbeat synchronization signal. As a result, a heartbeat synchronization signal can be acquired by a simple operation of merely bringing the ultrasound probe 2 into contact with the subject skin surface without requiring a special device such as an electrocardiograph or a heart sound meter. . However, the acquisition of the heart rate synchronization signal described above is merely an example, and an electrocardiograph or a heart sound meter may be used.
 (測定部10)
 測定部10は、心拍同期信号取得部9から出力された所定のタイミングに対応するフレームの受信信号に基づき、IMT測定範囲である関心領域(Region of Interest:以下、「ROI」と略する)を設定する。そして、ROI内の受信信号から内腔内膜境界および中膜外膜境界を検出し、その間の距離を測定する。そして、計測されたROI内の距離のうち、例えば、最大値を示す値(すなわち、最大厚(maxIMT))や平均値(すなわち、平均厚(meanIMT))をIMT値として算出する。
(Measurement unit 10)
The measurement unit 10 calculates a region of interest (hereinafter, abbreviated as “ROI”), which is an IMT measurement range, based on a received signal of a frame corresponding to a predetermined timing output from the heartbeat synchronization signal acquisition unit 9. Set. Then, a lumen inner membrane boundary and a media outer membrane boundary are detected from the received signal in the ROI, and a distance between them is measured. Of the measured distances within the ROI, for example, a value indicating the maximum value (that is, maximum thickness (maxIMT)) or an average value (that is, average thickness (meanIMT)) is calculated as the IMT value.
 なお、ROIの設定は、例えば、特開2010-119842号公報等に開示されている公知の方法を用いることができる。また、内腔内膜境界および中膜外膜境界の検出については、特許4829960号等に開示されている公知の方法を用いることができる。 For setting the ROI, for example, a known method disclosed in Japanese Patent Application Laid-Open No. 2010-119842, etc. can be used. In addition, a known method disclosed in Japanese Patent No. 4829960 can be used for the detection of the lumen intima boundary and the medial epicardial boundary.
 なお、実施の形態1における測定部10は、受信信号からIMT値を算出する構成を示しているが、受信信号から所定の処理が施された信号(例えば、断層画像)からIMT値を算出する構成としてもよい。 In addition, although the measurement part 10 in Embodiment 1 has shown the structure which calculates IMT value from a received signal, it calculates IMT value from the signal (for example, tomographic image) in which the predetermined process was performed from the received signal. It is good also as a structure.
 (判定部11)
 判定部11は、測定部10でIMT測定を行った際の各種基準が所定の基準を満たすか否かの判定を行い、各種基準が所定の基準を満たす場合には測定したIMT値を確定する。すなわち、判定部11は、フリーズ表示処理を行うか否かを判定するものであって、所定の基準を満たせばフリーズ表示処理を行うと判定し、所定の基準を満たすと判定されたフレームの受信信号に基づき測定されたIMT値を測定値として確定する。判定部11では、(1)判定するフレームの受信信号が基礎とされた反射超音波が超音波探触子2に取得されたときの超音波探触子2の傾斜角度がIMTを適切に測定することが可能な基準傾斜角度範囲(以後、「第1基準」とする)に含まれるか否かの判定(以後、「傾斜角度の判定」とする)と、(2)受信信号(受信信号から所定の処理が施された信号を含む)が、IMTを適切に測定することが可能な基準(以下、「第2基準」とする)を満たしているかの判定(以下、「受信信号の判定」とする)とを行う。
(Determination unit 11)
The determination unit 11 determines whether or not various standards when the measurement unit 10 performs IMT measurement satisfies a predetermined standard, and determines the measured IMT value when the various standards satisfy the predetermined standard. . That is, the determination unit 11 determines whether or not to perform freeze display processing, and determines that freeze display processing is performed if a predetermined criterion is satisfied, and reception of a frame determined to satisfy the predetermined criterion. The IMT value measured based on the signal is determined as a measurement value. In the determination unit 11, (1) the tilt angle of the ultrasonic probe 2 when the reflected ultrasonic wave based on the received signal of the determination frame is acquired by the ultrasonic probe 2 appropriately measures the IMT. (2) a received signal (received signal); a determination as to whether it is included in a reference tilt angle range that can be performed (hereinafter referred to as “first reference”); (Including signals that have been subjected to a predetermined processing from the above) satisfy a criterion (hereinafter referred to as “second criterion”) that can appropriately measure IMT (hereinafter, “determination of received signal”). ”).
 ここで、「フレームの受信信号の基礎とされた反射超音波が超音波探触子2に取得されたとき」とは、当該フレームの受信信号の基礎とされた反射超音波を受信するために超音波探触子2が測定対象に超音波を送信した時間、又は測定対象から反射超音波を受信した時間の少なくとも一方をさす。 Here, “when the reflected ultrasound based on the received signal of the frame is acquired by the ultrasound probe 2” means to receive the reflected ultrasound based on the received signal of the frame. It means at least one of the time when the ultrasonic probe 2 transmits ultrasonic waves to the measurement object and the time when reflected ultrasonic waves are received from the measurement object.
 図3は、超音波診断装置1の判定部11の機能ブロック図である。判定部11は、図3に示すように、受信信号判定部111、傾斜角度判定部112、記録部113および測定値決定部114を有する。判定部11に含まれる各ブロックの構成について説明する。 FIG. 3 is a functional block diagram of the determination unit 11 of the ultrasonic diagnostic apparatus 1. As shown in FIG. 3, the determination unit 11 includes a reception signal determination unit 111, an inclination angle determination unit 112, a recording unit 113, and a measurement value determination unit 114. The configuration of each block included in the determination unit 11 will be described.
 [受信信号判定部111]
 受信信号判定部111は、受信信号及び受信信号から所定の処理が施された信号が、上述の第2基準を満たしているかを判定する。具体的には、第2基準を構成する2つの基準である第2基準(1)および第2基準(2)に基づき判定を行い、判定したフレームに係る判定結果を記録部113に出力する。
[Received signal determination unit 111]
The reception signal determination unit 111 determines whether the reception signal and a signal that has been subjected to predetermined processing from the reception signal satisfy the second criterion. Specifically, the determination is made based on the second reference (1) and the second reference (2) that are the two references constituting the second reference, and the determination result relating to the determined frame is output to the recording unit 113.
 第2基準(1)に基づく判定は、被検体の皮膚表面に配置した超音波探触子2から送信された超音波が、頚動脈における血管中心近傍を捉えているかを判定するものである。この基準を設けている理由は、IMT測定が内腔内膜境界と中膜外膜境界との距離を測定するものであるため、これら境界が明瞭に断層画像として描出できる受信信号が得られなければ、適切にIMT測定が行われないためである。 The determination based on the second reference (1) is to determine whether the ultrasonic wave transmitted from the ultrasonic probe 2 arranged on the skin surface of the subject captures the vicinity of the blood vessel center in the carotid artery. The reason for setting this standard is that the IMT measurement measures the distance between the lumen-intima boundary and the media-epicardium boundary, and a received signal that can clearly depict these boundaries as a tomographic image must be obtained. This is because the IMT measurement is not properly performed.
 この点を、図面を用いてより詳細に説明する。図4は、超音波診断装置1の受信信号判定部111における血管中心の判定を説明するための模式図であり、(a)は、被検体の皮膚表面に配置した超音波探触子2から送信された超音波が血管中心211近傍を捉えている場合、(b)は、超音波が血管中心211近傍を通らない場合を示す。頚動脈血管に対して長軸方向に垂直な方向に切断した断面における、超音波探触子2から送受信される超音波の進路と頚動脈血管との位置関係を示したものである。 This point will be described in more detail with reference to the drawings. FIG. 4 is a schematic diagram for explaining the determination of the blood vessel center in the reception signal determination unit 111 of the ultrasonic diagnostic apparatus 1. FIG. 4A is a diagram illustrating the ultrasonic probe 2 disposed on the skin surface of the subject. When the transmitted ultrasonic wave captures the vicinity of the blood vessel center 211, (b) shows a case where the ultrasonic wave does not pass through the vicinity of the blood vessel center 211. The positional relationship between the course of the ultrasonic wave transmitted / received from the ultrasonic probe 2 and the carotid artery blood vessel in the cross section cut in the direction perpendicular to the longitudinal direction with respect to the carotid artery blood vessel is shown.
 超音波は、組織境界等、音響インピーダンスに差異がある境界で反射するが、境界面に対して90度に近い角度であたるほど強く反射し、明瞭な反射超音波が得られる。したがって、図4(a)に示すように被検体の皮膚表面に配置した超音波探触子2から送信された超音波が血管中心211近傍を捉えている場合(超音波の進路が血管中心211近傍上にあるとき)、超音波は血管の内腔内膜境界および中膜外膜境界に略垂直にあたり、これら境界で強く明瞭な反射超音波が得られる。 Ultrasonic waves are reflected at boundaries where there is a difference in acoustic impedance, such as tissue boundaries, but are reflected more strongly at an angle close to 90 degrees with respect to the boundary surface, and clear reflected ultrasonic waves are obtained. Therefore, as shown in FIG. 4A, when the ultrasonic wave transmitted from the ultrasonic probe 2 arranged on the skin surface of the subject captures the vicinity of the blood vessel center 211 (the path of the ultrasonic wave is the blood vessel center 211). When in the vicinity), the ultrasound strikes approximately perpendicular to the luminal intima and medial epicardial boundaries of the blood vessel, and a strong and clear reflected ultrasound is obtained at these borders.
 一方、図4(b)に示すように被検体の皮膚表面に配置した超音波探触子2から送信された超音波が血管中心211近傍を通らない場合、超音波が血管の内腔内膜境界および中膜外膜境界に略垂直にあたらないため、弱く不明瞭な反射超音波しか得られないことになる。そのため、断層画像上では、内腔内膜境界及び中膜外膜境界がぼやけて分離されずに描出されたり、内腔内膜境界が描出されなかったりする受信信号しか得られないため、適切なIMT測定が行われないこととなる。 On the other hand, when the ultrasonic wave transmitted from the ultrasonic probe 2 disposed on the skin surface of the subject does not pass near the blood vessel center 211 as shown in FIG. Since it is not substantially perpendicular to the boundary and the epicardial boundary, only weak and unclear reflected ultrasonic waves can be obtained. Therefore, on the tomographic image, only the received signal that the lumen intima boundary and the medial epicardial boundary are depicted in a blurred manner without being separated or the lumen intima boundary is not depicted is obtained. IMT measurement will not be performed.
 したがって、受信信号判定部111が、断層画像生成部8で生成した断層画像データ中の内腔内膜境界及び中膜外膜境界が明瞭に描出されているか否かを評価することで、超音波探触子2が血管の中心近傍に捉える位置で配置されているか否かを判定することができる。具体的には、検出された血管境界位置およびその周辺部位の断層画像データにおいて、検出された内腔内膜境界位置の血管内腔側から内中膜側にかけて輝度の立ち上がりが存在するか、検出された中膜外膜境界位置の内中膜側から外膜側にかけて輝度の立ち上がりが存在するか、および検出された内腔内膜境界位置と中膜外膜境界位置の間に輝度の落ち込みがあるか等を評価することによって、血管境界の位置で断層画像に内腔内膜境界および中膜外膜境界が明瞭に描出されているか否かを判定することができる。 Therefore, the received signal determination unit 111 evaluates whether the lumen-intima boundary and the media-endocardium boundary in the tomographic image data generated by the tomographic image generation unit 8 are clearly depicted. It can be determined whether or not the probe 2 is arranged at a position to be caught in the vicinity of the center of the blood vessel. Specifically, in the tomographic image data of the detected blood vessel boundary position and its peripheral part, it is detected whether there is a rise in luminance from the blood vessel lumen side to the inner media side of the detected lumen-intima boundary position. There is a rise in luminance from the intima side to the adventitia side of the detected intima-media boundary position, and there is a drop in luminance between the detected intima-media boundary position and the intima-media boundary position. By evaluating whether or not there is, it is possible to determine whether or not the lumen intima boundary and the medial epicardial boundary are clearly depicted in the tomographic image at the position of the blood vessel boundary.
 なお、上述の内腔内膜境界及び中膜外膜境界が明瞭に描出される血管中心近傍とは、実測長としては、超音波探触子2から送信される超音波の進路(図4において破線で示す)から血管断面の中心までの間隔が0.5mm以内程度に相当するが、厳密に限定されるものではない。 Note that the vicinity of the blood vessel center where the lumen inner membrane boundary and the media outer membrane boundary are clearly depicted as described above is the measured length of the ultrasonic wave transmitted from the ultrasonic probe 2 (in FIG. 4). The distance from the center of the blood vessel cross section to the center of the blood vessel cross section corresponds to about 0.5 mm or less, but is not strictly limited.
 次に、第2基準(2)に基づく判定について説明する。第2基準(2)に基づく判定は、IMT測定においてタイミングを規定するための心拍同期信号が適切に取得できたか否かを判定するものである。これは、心拍同期信号取得部9が、受信信号から心拍同期信号を取得した場合に必要な判定であって、心拍同期信号取得部9が心電計や心音計である場合は、この条件の判定は不要である。 Next, the determination based on the second standard (2) will be described. The determination based on the second reference (2) is to determine whether or not the heartbeat synchronization signal for defining the timing in the IMT measurement has been properly acquired. This is a determination necessary when the heartbeat synchronization signal acquisition unit 9 acquires a heartbeat synchronization signal from the received signal. When the heartbeat synchronization signal acquisition unit 9 is an electrocardiograph or a heart sound meter, this condition is satisfied. Judgment is not required.
 血管はその内部に流れる血流の量や流速に応じて伸縮・拡張する。心臓の収縮期には血流速度が最大となり、そのときの血管径が最大となるとともに、血管壁の厚みが最小となる。一方、心臓の拡張期では血流が最小となるので、血管径が最小となるとともに、血管壁の厚みが最大となる。すなわち、心拍に同期して血管壁の厚みが変化するため、IMT測定のタイミングによりIMT値も変化することとなる。したがって、取得した心拍同期信号が適切に取得できていなければ、適切なIMT測定が行うことができないため、受信信号判定部111は、この心拍同期信号が適切取得できたか否かを判定する。 The blood vessel expands and contracts according to the amount of blood flow and the flow velocity flowing inside. During the systole of the heart, the blood flow velocity becomes maximum, the blood vessel diameter at that time becomes maximum, and the thickness of the blood vessel wall becomes minimum. On the other hand, since the blood flow is minimized during the diastole of the heart, the vessel diameter is minimized and the thickness of the vessel wall is maximized. That is, since the thickness of the blood vessel wall changes in synchronization with the heartbeat, the IMT value also changes depending on the timing of IMT measurement. Therefore, if the acquired heart rate synchronization signal cannot be acquired properly, appropriate IMT measurement cannot be performed, and thus the reception signal determination unit 111 determines whether or not the heart rate synchronization signal has been acquired appropriately.
 受信信号判定部111で判定する方法としては、例えば、(a)血管径変化波形の特徴量に着目して判定する方法と、(b)血管径変化波形のモデル波形との一致度に着目して判定する方法等が考えられる。なお、受信信号判定部111は、(a)、(b)のいずれか一方のみでもよいし、両方を用いて拍動の判定を行ってもよい。 As a method of determining by the reception signal determination unit 111, for example, focusing on the degree of coincidence between (a) the determination method focusing on the characteristic amount of the blood vessel diameter change waveform and (b) the model waveform of the blood vessel diameter change waveform. The method of judging by this can be considered. Note that the reception signal determination unit 111 may include only one of (a) and (b), or may determine pulsation using both.
 まず、(a)の方法について図面を用いて説明する。図5は、超音波診断装置1の心拍同期信号取得部による心拍同期信号の取得方法を説明するための模式図である。(a)の方法では、血管径変化波形の振幅やピークのタイミング等で示される特徴量が通常の適切な拍動において人間が取り得る範囲に入っているか否かを判定する。その特徴量のパラメータとしては、例えば、(A)最大振幅(図5中のAmax)、(B)最小振幅(図5中のAmin)、(C)最大振幅になるタイミング(図5中のTmax)と最小振幅になるタイミング(図5中のTmin)、(D)一心拍周期(図5中のTR)を用いることができる。 First, the method (a) will be described with reference to the drawings. FIG. 5 is a schematic diagram for explaining a method for acquiring a heartbeat synchronization signal by the heartbeat synchronization signal acquisition unit of the ultrasonic diagnostic apparatus 1. In the method (a), it is determined whether or not the feature amount indicated by the amplitude or peak timing of the blood vessel diameter change waveform is within a range that can be taken by a person in a normal appropriate pulsation. For example, (A) maximum amplitude (Amax in FIG. 5), (B) minimum amplitude (Amin in FIG. 5), (C) timing at which the maximum amplitude is reached (Tmax in FIG. 5). ) And the timing at which the amplitude becomes minimum (Tmin in FIG. 5), (D) one heartbeat cycle (TR in FIG. 5) can be used.
 なお、発明者らは、例えば、(A)のAmaxが1mm弱、(B)のAminがマイナス値、(C)のTmin<Tmax、(D)のTRが1秒程度であれば、適切に拍動を取得できていると判定することができることを実験的に確認している。 In addition, the inventors appropriately, for example, if Amax of (A) is less than 1 mm, Amin of (B) is a negative value, Tmin <Tmax of (C), and TR of (D) is about 1 second. It has been experimentally confirmed that it can be determined that pulsation has been acquired.
 次に、(2)の方法について説明する。例えば、1心拍といった所定の期間における径変化波形のモデル波形を準備し、心拍同期信号取得部9から出力された血管径変化波形と比較し、両者の整合度合いを相関係数として算出することにより判定することができる。なお、モデル波形と心拍同期信号取得部9から出力された血管径変化波形とでは、所定の期間(例えば、1心拍の期間)が異なる場合があるが、この場合、いずれかの波形を基準にもう一方の波形を時間軸上で拡張あるいは伸縮することで両者の1心拍期間が同一となり相関係数を算出することができる。 Next, the method (2) will be described. For example, by preparing a model waveform of a diameter change waveform in a predetermined period such as one heartbeat, comparing it with the blood vessel diameter change waveform output from the heartbeat synchronization signal acquisition unit 9, and calculating the degree of matching between them as a correlation coefficient Can be determined. The model waveform and the blood vessel diameter change waveform output from the heartbeat synchronization signal acquisition unit 9 may differ in a predetermined period (for example, one heartbeat period). In this case, any waveform is used as a reference. By expanding or contracting the other waveform on the time axis, the two heartbeat periods become the same, and the correlation coefficient can be calculated.
 [傾斜角度判定部112]
 傾斜角度判定部112は、傾斜角度の判定を行うものであって、傾斜角度算出部7から出力される傾斜角度情報に基づき、判定するフレームの受信信号の基礎とされた反射超音波が前記超音波探触子に取得されたときの超音波探触子2の傾斜角度が第1基準を満たしているか否かを判定する。具体的には、判定するフレームの受信信号の基礎とされた反射超音波を受信するために超音波探触子2が測定対象に超音波を送信したとき、又は測定対象から反射超音波を受信したときの超音波探触子2の傾斜角度が第1基準を満たしているかの判定する。第1基準を満たしている場合には、判定するフレームの受信信号が基礎とする反射超音波を受信したときに超音波探触子2は、IMTを適切に測定することが可能な基準傾斜角度範囲に存在していたこととなる。その場合、判定したフレームに係る判定結果を記録部113に出力する。
[Inclination angle determination unit 112]
The tilt angle determination unit 112 determines the tilt angle. Based on the tilt angle information output from the tilt angle calculation unit 7, the reflected ultrasonic wave that is the basis of the received signal of the frame to be determined is the supersonic wave. It is determined whether or not the inclination angle of the ultrasonic probe 2 when acquired by the acoustic probe satisfies the first reference. Specifically, when the ultrasonic probe 2 transmits an ultrasonic wave to the measurement object in order to receive the reflected ultrasonic wave based on the received signal of the frame to be determined, or receives the reflected ultrasonic wave from the measurement object. It is determined whether the inclination angle of the ultrasonic probe 2 at this time satisfies the first reference. When the first reference is satisfied, the ultrasonic probe 2 can appropriately measure the IMT when the reflected ultrasonic wave based on the received signal of the frame to be determined is received. It was in range. In that case, the determination result relating to the determined frame is output to the recording unit 113.
 傾斜角度判定部112における、超音波探触子2の傾斜角度が第1基準を満たしているか否かの判定方法について説明する。傾斜角度判定部112には、あらかじめ所定の基準値としての基準傾斜角度が規定されている。傾斜角度判定部112は、基準傾斜角度と傾斜角度算出部7から出力されたフレームに対応する傾斜角度とを比較し、このフレームに対応する傾斜角度が基準傾斜角度と一致するか否かを判定する。IMT測定の場合、診断の都度、毎回ほぼ同一の傾斜角度で測定を行うことが望ましい。そのため、この基準傾斜角度は測定を行うべき角度である。基準傾斜角度は、操作者等があらかじめ設定した角度としてもよく、同一患者に対して過去にIMT測定を行ったときのフレームに対応する角度としてもよい。 A method for determining whether or not the tilt angle of the ultrasound probe 2 satisfies the first reference in the tilt angle determination unit 112 will be described. In the tilt angle determination unit 112, a reference tilt angle as a predetermined reference value is defined in advance. The tilt angle determination unit 112 compares the reference tilt angle with the tilt angle corresponding to the frame output from the tilt angle calculation unit 7, and determines whether the tilt angle corresponding to this frame matches the reference tilt angle. To do. In the case of IMT measurement, it is desirable to perform measurement at substantially the same inclination angle every time diagnosis is performed. Therefore, this reference inclination angle is an angle at which measurement is to be performed. The reference inclination angle may be an angle set in advance by an operator or the like, or may be an angle corresponding to a frame when IMT measurement has been performed on the same patient in the past.
 また、判定するフレームに対応する超音波探触子2の角度と基準傾斜角度とが必ずしも完全に一致する必要はなく、例えば、基準傾斜角度から±5°の角度範囲を設定し、その範囲内にフレームに対応する超音波探触子2の傾斜角度が入れば基準角度に一致すると判定する構成であってもよい。 In addition, the angle of the ultrasound probe 2 corresponding to the frame to be judged and the reference inclination angle do not necessarily coincide completely. For example, an angle range of ± 5 ° from the reference inclination angle is set, and If the inclination angle of the ultrasound probe 2 corresponding to the frame is included in the frame, it may be determined that it matches the reference angle.
 [記録部113]
 記録部113は、断層画像データ、受信信号判定部111および傾斜角度判定部112の判定結果、IMT測定が行われたフレームに対してはIMT測定値を、超音波の送信処理のタイミング順に記録する。これにより、あるフレームにおける断層画像データ、判定結果、IMT測定値が関連付けされた状態で記録される。そして、記録部113は、これら情報を関連付けて記録した後、記録された順に逐次、測定値決定部114に出力する。
[Recording unit 113]
The recording unit 113 records the IMT measurement values for the tomographic image data, the determination results of the reception signal determination unit 111 and the tilt angle determination unit 112, and the IMT measurement values in the order of the timing of the ultrasonic transmission processing. . Thereby, the tomographic image data, the determination result, and the IMT measurement value in a certain frame are recorded in association with each other. The recording unit 113 records these information in association with each other, and then sequentially outputs the information to the measurement value determination unit 114 in the order of recording.
 [測定値決定部114]
 測定値決定部114は、記録部113から出力された情報のうち、受信信号判定部111および傾斜角度判定部112の判定結果に基づき、測定値としてIMT値を確定する。すなわち、受信信号判定部111の判定結果が第1基準を満たし、かつ傾斜角度判定部112の判定結果が第2基準を満たしと判定されたフレームの受信信号に基づき測定されたIMT値を測定値として確定する。そして、測定値が確定したフレームについては、記録部113から出力された情報に測定値が確定したことを示す情報を追加してフリーズ表示処理部12に出力する。
[Measurement value determination unit 114]
The measurement value determination unit 114 determines the IMT value as the measurement value based on the determination results of the reception signal determination unit 111 and the inclination angle determination unit 112 among the information output from the recording unit 113. That is, the IMT value measured based on the received signal of the frame in which the determination result of the reception signal determination unit 111 satisfies the first reference and the determination result of the tilt angle determination unit 112 satisfies the second reference is measured. Confirm as Then, for the frame for which the measurement value is confirmed, information indicating that the measurement value is confirmed is added to the information output from the recording unit 113 and output to the freeze display processing unit 12.
 一方、測定値が確定しなかったフレームについては、記録部113から出力された情報をフリーズ表示処理部12に出力する。なお、ここで測定値が確定したフレームは、フリーズ表示処理部12においてフリーズ表示処理が行われる対象となる。 On the other hand, the information output from the recording unit 113 is output to the freeze display processing unit 12 for the frame for which the measurement value has not been determined. Note that the frame in which the measurement value is determined is a target on which the freeze display processing unit 12 performs the freeze display process.
 以上、判定部11の構成について説明した。 The configuration of the determination unit 11 has been described above.
 なお、上記において、判定部11が行う受信信号の判定について、実施の形態1ではIMT測定を例に説明しているが、IMT測定に限定されるものではなく、測定の種類、測定のやり方、操作者の設定に応じて適宜定めることができる。 In the above description, the determination of the reception signal performed by the determination unit 11 is described in the first embodiment by taking IMT measurement as an example. However, the present invention is not limited to IMT measurement, and the measurement type, measurement method, It can be determined appropriately according to the operator's setting.
 また、IMT測定における受信信号の判定として、血管中心に係る基準(第2基準(1))と心拍同期信号に係る基準を第2基準(第2基準(2))として説明した。しかしながら、これは一例であって、本開示における、IMT測定における受信信号の判定基準は、これに限定されるものではない。また、IMT以外の他の被検体の特性計測や疾患に対する診断部位の特定における受信信号の判定基準についても、対象となる疾患や被検体上の部位に応じて適宜設定することができることはいうまでもない。 In addition, as the determination of the received signal in the IMT measurement, the reference relating to the blood vessel center (second reference (1)) and the reference relating to the heartbeat synchronization signal have been described as the second reference (second reference (2)). However, this is merely an example, and the criterion of the received signal in the IMT measurement in the present disclosure is not limited to this. In addition, it is needless to say that the determination standard of the received signal in the measurement of characteristics of subjects other than the IMT and the identification of the diagnostic site for the disease can be appropriately set according to the target disease and the site on the subject. Nor.
 (フリーズ表示処理部12)
 フリーズ表示処理部12は、記録部113から測定値決定部114を介して逐次出力されるフレームの情報を表示処理部13に出力する。ここで、フレームの情報とは、断層画像データ、受信信号判定部111および傾斜角度判定部112の判定結果、IMT測定が行われたフレームに対してはIMT測定値、の少なくとも1つからなる情報である。これらの情報は、上述のとおり、記録部113に超音波の送信処理のタイミング順に記録されている。
(Freeze display processor 12)
The freeze display processing unit 12 outputs frame information sequentially output from the recording unit 113 via the measurement value determining unit 114 to the display processing unit 13. Here, the frame information is information including at least one of tomographic image data, determination results of the reception signal determination unit 111 and the inclination angle determination unit 112, and an IMT measurement value for a frame in which IMT measurement is performed. It is. As described above, these pieces of information are recorded in the recording unit 113 in the order of timing of ultrasonic transmission processing.
 さらに、フリーズ表示処理部12は、測定値決定部114からの測定値が確定したことを示す情報の入力を監視する。フリーズ表示処理部12は、測定値決定部114から測定値が確定したことを示す情報を入力すると、フリーズ表示処理の対象となる測定値が確定したフレームの情報をフリーズ表示処理の対象となる情報として表示処理部13に出力する。すなわち、フリーズ表示処理部12は、フリーズ表示処理の対象となったフレームの情報として表示処理部13に出力した後は、測定値決定部114から出力されるフレームの情報の表示処理部13への出力を停止する。これにより、フリーズ表示処理部12は、後述する表示処理部13を介して、フリーズ表示処理の対象となる測定値が確定したフレームの情報を表示器に表示させ当該表示を継続することができる。

 なお、フリーズ表示処理は、後述する表示処理部13が表示器に対して行う断層画像の更新表示を停止し、フリーズ表示処理の対象となったフレームの断層画像を静止画として表示するものであってもよい。また、表示処理部13が表示器3に対して更新表示する断層画像とは別に、フリーズ表示処理の対象となったフレームの断層画像を静止画として表示する構成であってもよい。
Furthermore, the freeze display processing unit 12 monitors the input of information indicating that the measurement value from the measurement value determination unit 114 is confirmed. When the freeze display processing unit 12 inputs information indicating that the measurement value has been determined from the measurement value determination unit 114, the information on the frame in which the measurement value that is the target of the freeze display process is determined is the information that is the target of the freeze display process. To the display processing unit 13. That is, the freeze display processing unit 12 outputs the frame information output from the measurement value determination unit 114 to the display processing unit 13 after outputting the information to the display processing unit 13 as information on the frame subjected to the freeze display processing. Stop output. Thereby, the freeze display processing unit 12 can display the information of the frame in which the measurement value to be subjected to the freeze display process is determined via the display processing unit 13 described later, and can continue the display.

The freeze display process is to stop the update display of the tomographic image performed on the display by the display processing unit 13 described later and display the tomographic image of the frame subjected to the freeze display process as a still image. May be. In addition to the tomographic image that the display processing unit 13 updates and displays on the display device 3, the tomographic image of the frame subjected to the freeze display process may be displayed as a still image.
 (表示処理部13)
 表示処理部13は、フリーズ表示処理部12から供給される断層画像データ、確定したIMT測定結果がある場合はその測定値を表示器3の表示画面に表示する処理を行う。
(Display processing unit 13)
The display processing unit 13 performs processing for displaying the tomographic image data supplied from the freeze display processing unit 12 and the measured value on the display screen of the display 3 when there is a confirmed IMT measurement result.
 フリーズ表示処理部12が測定値決定部114から測定値が確定したことを示す情報を受け取らない場合(フリーズ表示処理部12にてフリーズ表示処理が行われていない場合)には、表示処理部13は、記録部113から測定値決定部114を介して断層画像データを逐次生成された順(受信信号を取得した順)に入力し、逐次、表示器3に出力して表示器3の表示画面に更新表示される。 When the freeze display processing unit 12 does not receive information indicating that the measurement value is confirmed from the measurement value determining unit 114 (when the freeze display processing unit 12 does not perform freeze display processing), the display processing unit 13 Inputs the tomographic image data from the recording unit 113 via the measurement value determining unit 114 in the order in which the tomographic image data is sequentially generated (the order in which the received signals are acquired), and sequentially outputs them to the display unit 3 to display the display screen of the display unit 3 Is displayed updated.
 他方、フリーズ表示処理部12が測定値決定部114から測定値が確定したことを示す情報を受け取った(フリーズ表示処理部12にてフリーズ表示処理が行われた場合)には、表示処理部13は、記録部113から測定値決定部114を介して確定した測定値に対応するフレームの断層画像と確定したIMT値を入力し、表示器3に当該断層画像を出力する。この場合、表示器3に表示させる断層画像の更新は停止され、確定した測定値に対応するフレームの断層画像とともに確定したIMT値が表示器3に表示され当該IMT値の表示が継続される。 On the other hand, when the freeze display processing unit 12 receives information indicating that the measurement value is confirmed from the measurement value determining unit 114 (when the freeze display processing is performed in the freeze display processing unit 12), the display processing unit 13 Inputs the tomographic image of the frame corresponding to the measurement value determined via the measurement value determination unit 114 from the recording unit 113 and the determined IMT value, and outputs the tomographic image to the display 3. In this case, the update of the tomographic image displayed on the display device 3 is stopped, the confirmed IMT value is displayed on the display device 3 together with the tomographic image of the frame corresponding to the confirmed measurement value, and the display of the IMT value is continued.
 なお、フリーズ表示処理は、表示処理部13が測定値決定部114からフリーズ表示処理部12を介して測定値が確定したことを示す情報を受け取り、表示処理部13が主体的に表示器3に対して行う断層画像の更新表示を停止し、フリーズ表示処理の対象となったフレームの断層画像を静止画として表示器3に表示されるものであってもよい。 In the freeze display process, the display processing unit 13 receives information indicating that the measurement value has been confirmed from the measurement value determining unit 114 via the freeze display processing unit 12, and the display processing unit 13 mainly takes the display 3. Alternatively, the tomographic image update display may be stopped and the tomographic image of the frame subjected to the freeze display process may be displayed on the display unit 3 as a still image.
 (制御部14)
 制御部14は、入力器4を介して伝達される操作者の指示に基づき、制御器5に含まれる各ブロックを制御する。
(Control unit 14)
The control unit 14 controls each block included in the controller 5 based on an operator's instruction transmitted via the input device 4.
 ≪動作について≫
 以上の構成からなる超音波診断装置1の制御方法について、操作者の動作も踏まえて図6のフロー図を用いて説明する。
≪About operation≫
A control method of the ultrasonic diagnostic apparatus 1 having the above configuration will be described with reference to the flowchart of FIG.
 <ステップ1(S001>
 ステップ1(S001)では、超音波探触子2を被検体皮膚表面に配置し、送受信部6が送信処理行うことで超音波探触子2から超音波を頚動脈に向けて送信し、超音波探触子2で頚動脈を含む被検体からの反射超音波を受信する。送受信部6では反射超音波に基づき受信処理を行うことで受信信号を生成し、複数の受信信号からなる1つのフレームを構築する。そして、この送信処理および受信処理を複数回繰り返し行い複数のフレームを構築し、構築した順にフレーム毎の受信信号を逐次、断層画像生成部8、心拍同期信号取得部9および測定部10に出力する。
<Step 1 (S001)
In step 1 (S001), the ultrasonic probe 2 is placed on the surface of the subject skin, and the transmission / reception unit 6 performs transmission processing to transmit ultrasonic waves from the ultrasonic probe 2 toward the carotid artery. The probe 2 receives reflected ultrasound from the subject including the carotid artery. The transmission / reception unit 6 generates a reception signal by performing reception processing based on the reflected ultrasonic wave, and constructs one frame including a plurality of reception signals. Then, the transmission process and the reception process are repeated a plurality of times to construct a plurality of frames, and the reception signals for each frame are sequentially output to the tomographic image generation unit 8, the heartbeat synchronization signal acquisition unit 9, and the measurement unit 10 in the constructed order. .
 <ステップ2(S002)>
 ステップ2(S002)では、超音波探触子2に内蔵された傾斜角度測定部(加速度センサ)21が、超音波の送信処理(又は受信処理)のタイミング毎に超音波探触子2のセンサ出力情報として加速度情報を取得し、送信処理のタイミング順に傾斜角度算出部7に出力する。そして、傾斜角度算出部7では、加速度情報に基づき、所定の方向(例えば、重力方向)を基準とした超音波探触子2の傾斜角度を取得し、この傾斜角度を傾斜角度情報として、判定部11の傾斜角度判定部112に出力する。この傾斜角度算出部7による超音波探触子2の角度の算出は、傾斜角度測定部21から出力されるセンサ出力情報の順に行われる。
<Step 2 (S002)>
In step 2 (S002), the inclination angle measurement unit (acceleration sensor) 21 built in the ultrasonic probe 2 detects the sensor of the ultrasonic probe 2 at every timing of ultrasonic transmission processing (or reception processing). Acceleration information is acquired as output information, and is output to the tilt angle calculation unit 7 in the order of transmission processing timing. Then, the tilt angle calculation unit 7 acquires the tilt angle of the ultrasonic probe 2 with reference to a predetermined direction (for example, the direction of gravity) based on the acceleration information, and determines the tilt angle as tilt angle information. To the inclination angle determination unit 112 of the unit 11. The calculation of the angle of the ultrasound probe 2 by the tilt angle calculation unit 7 is performed in the order of sensor output information output from the tilt angle measurement unit 21.
 なお、図6では、ステップ1(S001)がステップ2(S002)より先に行われる構成となっているが、ステップ1(S001)の送信処理とステップ2(S002)のセンサ出力情報の取得は、並列に処理が行われる構成であってもよい。 In FIG. 6, step 1 (S001) is performed before step 2 (S002). However, the transmission process in step 1 (S001) and the acquisition of sensor output information in step 2 (S002) are as follows. A configuration in which processing is performed in parallel may be used.
 <ステップ3(S003)>
 ステップ3(S003)では、断層画像生成部8が、送受信部6から出力されるフレームの受信信号に基づき、その強度に対応した輝度信号へと変換し、その輝度信号を直交座標系に座標変換を施すことで断層画像を生成する。この処理は、送受信部6から出力されるフレームの順に逐次行われ、判定部11(受信信号判定部111および記録部113)へと出力される。なお、記録部113に出力された断層画像データは、出力された時系列順に記録される。
<Step 3 (S003)>
In step 3 (S003), the tomographic image generation unit 8 converts the luminance signal corresponding to the intensity based on the received signal of the frame output from the transmission / reception unit 6, and coordinates the luminance signal to the orthogonal coordinate system. To generate a tomographic image. This processing is sequentially performed in the order of the frames output from the transmission / reception unit 6 and is output to the determination unit 11 (the reception signal determination unit 111 and the recording unit 113). Note that the tomographic image data output to the recording unit 113 is recorded in the order of the output time series.
 <ステップ4(S004)>
 ステップ4(S004)では、心拍同期信号取得部9が、受信信号から被検体の心拍に同期した心拍同期信号を検出し、検出した心拍同期信号を判定部11と測定部10に出力する。そして、出力された心拍同期信号が示すタイミングに対応するフレームの受信信号に基づき、例えば、特開2010-119842号公報等に開示されている公知の手法を用いてROIの設定を行い、さらに、例えば、特許4829960号等に開示されている公知の方法を用いてROI内の内腔内膜境界および中膜外膜境界を検出を行い、その境界間の距離をIMTとして測定し、判定部11に出力する。IMT測定は、例えば、maxIMTやmeanIMTをIMT値として算出する。心拍同期信号が示すタイミングは、一心拍中の、例えば、心臓が収縮後拡張して血流が最小となる心拡張末期のタイミングとしてもよい
 なお、図6では、ステップ3(S003)がステップ4(S004)より先に行われる構成となっているが、ステップ3(S003)とステップ4(S004)とを同時に行ってもよく、また、ステップ4(S004)をステップ3(S003)よりも先に行ってもよい。
<Step 4 (S004)>
In step 4 (S004), the heartbeat synchronization signal acquisition unit 9 detects a heartbeat synchronization signal synchronized with the heartbeat of the subject from the received signal, and outputs the detected heartbeat synchronization signal to the determination unit 11 and the measurement unit 10. Then, based on the received signal of the frame corresponding to the timing indicated by the output heartbeat synchronization signal, for example, the ROI is set using a known method disclosed in Japanese Patent Application Laid-Open No. 2010-119842, etc. For example, a known method disclosed in Japanese Patent No. 4829960 is used to detect a lumen-intima boundary and an intima-membrane boundary in the ROI, and measure the distance between the boundaries as an IMT. Output to. In the IMT measurement, for example, maxIMT and meanIMT are calculated as IMT values. The timing indicated by the heartbeat synchronization signal may be the end timing of diastole during one heartbeat, for example, when the heart expands after contraction and blood flow is minimized. In FIG. 6, step 3 (S003) is step 4 Although the configuration is performed before (S004), Step 3 (S003) and Step 4 (S004) may be performed simultaneously, and Step 4 (S004) is performed before Step 3 (S003). You may go to
 <ステップ5(S005)>
 ステップ5(S005)では、受信信号判定部111が受信信号の判定を行う。具体的には、受信信号判定部111が、上述の第2基準(1)および第2基準(2)に基づき判定を行い、第2基準(1)および第2基準(2)を満たしていれば、条件を満たしたフレームであることをそのフレームに係る断層画像データおよびIMT測定値とともに記録部113に記録し、ステップ6(S006)に移行する。一方、第2基準(1)および第2基準(2)の少なくともいずれか一方がその条件を満たしていなければ、そのフレームに係る断層画像データを記録部113に記録する。そして、記録部113からその断層画像を測定値決定部114へ出力する。その断層画像はフリーズ表示処理部12を介して表示処理部13に出力され、ステップ9(S009)に移行する。
<Step 5 (S005)>
In step 5 (S005), the reception signal determination unit 111 determines the reception signal. Specifically, the received signal determination unit 111 makes a determination based on the second criterion (1) and the second criterion (2), and satisfies the second criterion (1) and the second criterion (2). For example, the fact that the frame satisfies the condition is recorded in the recording unit 113 together with the tomographic image data and the IMT measurement value related to the frame, and the process proceeds to step 6 (S006). On the other hand, if at least one of the second reference (1) and the second reference (2) does not satisfy the condition, the tomographic image data relating to the frame is recorded in the recording unit 113. Then, the tomographic image is output from the recording unit 113 to the measurement value determining unit 114. The tomographic image is output to the display processing unit 13 via the freeze display processing unit 12, and the process proceeds to step 9 (S009).
 <ステップ6(S006)>
 ステップ6(S006)では、傾斜角度判定部112で傾斜角度の判定を行う。そして、傾斜角度の判定が、上述の第1基準を満たしていれば、第1基準を満たしたフレームであることを、受信信号の判定の第2基準を満たしたフレームであることに併せて記録部113に記録し、ステップ7(S007)に移行する。一方、第1基準を満たしていないフレームについては、そのフレームに係る断層画像データを記録部113に記録する。そして、記録部113からその断層画像を測定値決定部114へ出力する。その断層画像はフリーズ表示処理部12を介して表示処理部13に出力され、ステップ9(S009)に移行する。
<Step 6 (S006)>
In step 6 (S006), the tilt angle determination unit 112 determines the tilt angle. If the determination of the tilt angle satisfies the first criterion, the frame that satisfies the first criterion is recorded together with the frame that satisfies the second criterion for determination of the received signal. The data is recorded in the unit 113, and the process proceeds to step 7 (S007). On the other hand, for a frame that does not satisfy the first criterion, tomographic image data relating to that frame is recorded in the recording unit 113. Then, the tomographic image is output from the recording unit 113 to the measurement value determining unit 114. The tomographic image is output to the display processing unit 13 via the freeze display processing unit 12, and the process proceeds to step 9 (S009).
 なお、図6では、ステップ5(S005)がステップ6(S006)より先に行われる構成となっているが、ステップ5(S005)とステップ6(S006)とを同時に行ってもよく、ステップ5(S005)をステップ6(S006)よりも先に行ってもよい。 In FIG. 6, Step 5 (S005) is performed before Step 6 (S006). However, Step 5 (S005) and Step 6 (S006) may be performed simultaneously. (S005) may be performed prior to step 6 (S006).
 <ステップ7(S007)>
 ステップ7(S007)では、記録部113から測定値決定部114に出力されたフレームのうち、受信信号の判定が第2基準を満たし、かつ傾斜角度の判定が第1基準を満たしたフレームに係るIMT測定結果を適切なIMT値として確定し、ステップ8(S008)に移行する。受信信号の判定が第2基準を満たし、かつ傾斜角度の判定が第1基準を満たしたフレームが複数ある場合には、いずれかのフレームに係るIMT測定結果を適切なIMT値として確定し、ステップ8(S008)に移行する。例えば、時間的に最も新しく取得したフレームに係るIMT測定結果を適切なIMT値として確定してもよい。
<Step 7 (S007)>
In step 7 (S007), among the frames output from the recording unit 113 to the measurement value determining unit 114, the received signal determination satisfies the second reference and the tilt angle determination satisfies the first reference. The IMT measurement result is determined as an appropriate IMT value, and the process proceeds to step 8 (S008). If there are a plurality of frames in which the determination of the received signal satisfies the second reference and the determination of the tilt angle satisfies the first reference, the IMT measurement result related to any of the frames is determined as an appropriate IMT value, and step 8 (S008). For example, the IMT measurement result related to the most recently acquired frame in time may be determined as an appropriate IMT value.
 <ステップ8(S008)>
 ステップ8(S008)では、フリーズ表示処理部12が、ステップ7(S007)でIMT値が確定したフレームについて、フリーズ表示処理を行う。具体的には、フリーズ表示処理部12は、測定値決定部114から測定値が確定したことを示す情報を入力すると、フリーズ表示処理の対象となる測定値が確定したフレームの情報をフリーズ表示処理の対象となる情報として表示処理部13に出力し、ステップ9(S009)に移行する。ここで、フレームの情報とは、例えば、断層画像データ、受信信号判定部111および傾斜角度判定部112の判定結果、IMT測定が行われたフレームに対してはIMT測定値である。
<Step 8 (S008)>
In step 8 (S008), the freeze display processing unit 12 performs freeze display processing for the frame for which the IMT value is determined in step 7 (S007). Specifically, when the freeze display processing unit 12 inputs information indicating that the measurement value has been determined from the measurement value determination unit 114, the freeze display processing is performed on the information of the frame in which the measurement value to be subjected to the freeze display process is determined. Is output to the display processing unit 13 as information to be processed, and the process proceeds to step 9 (S009). Here, the frame information refers to, for example, tomographic image data, determination results of the reception signal determination unit 111 and the inclination angle determination unit 112, and an IMT measurement value for a frame in which IMT measurement is performed.
 <ステップ9(S009)>
 ステップ9(S009)では、表示処理部13は、少なくとも生成された断層画像データと確定したIMT測定値がある場合には、その断層画像データ又はIMT値の少なくとも一方を表示器3中の表示画面に表示する処理を行う。すなわち、表示処理部13は、フリーズ表示処理部12にてフリーズ表示処理が行われた場合に、確定したIMT測定値に対応するフレームの断層画像とともに確定したIMT値を表示器3に表示し当該表示を継続させる処理を行い、プロセスを終了する。
<Step 9 (S009)>
In step 9 (S009), when there is at least the generated tomographic image data and the confirmed IMT measurement value, the display processing unit 13 displays at least one of the tomographic image data or the IMT value in the display screen in the display 3. Process to be displayed. That is, when the freeze display processing is performed by the freeze display processing unit 12, the display processing unit 13 displays the determined IMT value together with the tomographic image of the frame corresponding to the determined IMT measurement value on the display 3. Processing to continue the display is performed and the process is terminated.
 他方、表示処理部13は、フリーズ表示処理が行われていない場合は、断層画像データを逐次生成した順(すなわち、受信信号を取得した順)に逐次、更新して表示する処理を行いプロセスを終了する。 On the other hand, when the freeze display process is not performed, the display processing unit 13 performs a process of sequentially updating and displaying the tomographic image data in the order in which the tomographic image data is sequentially generated (that is, the order in which the reception signals are acquired). finish.
 <傾斜角度の判定の効果について>
 次に、実施の形態1に係る超音波診断装置1における傾斜角度の判定の効果について、図面を用いて説明する。図7は、超音波診断装置1における傾斜角度判定部を説明するための補助図である。図7は頭部側から示した被検体の模式図である。破線矢印は頚動脈のIMT測定を行うときに首筋表面に配置する超音波探触子2の適切な基準傾斜角度(θ)を示したものである。実線矢印は傾斜角度判定部112で判定される判定対象フレームを取得する際に、超音波探触子2を首筋表面に配置した状態で、超音波探触子2が反射超音波を取得したときの超音波探触子2の傾斜角度(θ1)を示している。ここで、θおよびθ1は、一例として、超音波探触子2の超音波出射方向(範囲がある場合はその範囲の中央付近)の重力方向に対する相対角度をして規定している。
<Effect of determination of tilt angle>
Next, the effect of the determination of the tilt angle in the ultrasonic diagnostic apparatus 1 according to Embodiment 1 will be described using the drawings. FIG. 7 is an auxiliary diagram for explaining an inclination angle determination unit in the ultrasonic diagnostic apparatus 1. FIG. 7 is a schematic diagram of the subject shown from the head side. A broken-line arrow indicates an appropriate reference inclination angle (θ) of the ultrasonic probe 2 arranged on the neck muscle surface when performing IMT measurement of the carotid artery. A solid arrow indicates when the ultrasonic probe 2 acquires reflected ultrasonic waves in a state where the ultrasonic probe 2 is placed on the neck surface when acquiring the determination target frame determined by the inclination angle determination unit 112. The inclination angle (θ 1 ) of the ultrasonic probe 2 is shown. Here, as an example, θ and θ 1 are defined as relative angles with respect to the gravitational direction of the ultrasonic wave emitting direction of the ultrasonic probe 2 (when there is a range, near the center of the range).
 ここでも、「超音波探触子2が反射超音波を取得したとき」とは、当該フレームの受信信号の基礎とされた反射超音波を受信するために超音波探触子2が超音波を送信したとき、又は測定対象から反射超音波を受信したときの少なくとも一方をさす。 Here, “when the ultrasonic probe 2 acquires reflected ultrasonic waves” means that the ultrasonic probe 2 receives ultrasonic waves in order to receive the reflected ultrasonic waves based on the reception signal of the frame. It refers to at least one of when transmitted or when a reflected ultrasonic wave is received from a measurement target.
 例えば、超音波探触子2を首筋表面に配置した角度(θ1)で、受信信号判定部111の判定結果が上述の第2基準を満たすと判定された場合、傾斜角度判定部112における傾斜角度判定を行わない構成では、フリーズ表示処理が行われてしまう。この場合、適正な測定ができる基準傾斜角度(θ)以外の傾斜角度で取得されたフレームがフリーズ表示処理の対象となり、そのフレームの断層画像が表示器3にフリーズ表示される。 For example, when it is determined that the determination result of the reception signal determination unit 111 satisfies the above-described second reference at the angle (θ 1 ) at which the ultrasound probe 2 is disposed on the neck surface, the inclination in the inclination angle determination unit 112 In a configuration that does not perform angle determination, freeze display processing is performed. In this case, a frame acquired at an inclination angle other than the reference inclination angle (θ) at which proper measurement can be performed is a target for freeze display processing, and a tomographic image of that frame is displayed on the display 3 as a freeze display.
 これに対し、傾斜角度判定部112の判定結果をフリーズ表示処理をするための基準とすることで、基準傾斜角度(θ)近傍で取得されたフレームを対象としてフリーズ表示処理を行うことができる。そのため、適正な測定ができる基準傾斜角度(θ)以外の傾斜角度で取得されたフレームがフリーズ表示処理されるという不要なフリーズ表示処理を抑制することができる。 On the other hand, by using the determination result of the inclination angle determination unit 112 as a reference for performing the freeze display process, the freeze display process can be performed on a frame acquired in the vicinity of the reference inclination angle (θ). Therefore, it is possible to suppress an unnecessary freeze display process in which a frame acquired at an inclination angle other than the reference inclination angle (θ) capable of appropriate measurement is subjected to a freeze display process.
 すなわち、IMTを含む被検体の特性計測や疾患に対する診断部位の特定において、不要なフリーズ表示処理を抑制することができる。これにより、簡便な操作で診断部位の特定ができ、超音波診断装置の使い勝手を向上させることができる。 That is, unnecessary freeze display processing can be suppressed in the measurement of the characteristics of the subject including the IMT and the identification of the diagnostic site for the disease. Thereby, a diagnostic site | part can be pinpointed by simple operation and the usability of an ultrasonic diagnosing device can be improved.
 ≪実施の形態2≫
 実施の形態1では、傾斜角度判定部112は、フレームの受信信号の基礎とされた反射超音波が超音波探触子2に取得されたときの前記超音波探触子2の傾斜角度が所定の角度範囲に含まれるときに第1基準を満たすと判定する構成とした。 実施の形態2では、傾斜角度判定部112は、フレームの受信信号の基礎とされた反射超音波が超音波探触子2に取得されたときの前記超音波探触子2の傾斜角度変動が所定の基準値以下であるときに第1基準を満たすと判定する構成とした点で、実施の形態1と相違する。係る構成により、操作者が超音波探触子2を被検体皮膚表面上で動かし測定対象を探索している際中に、受信信号判定部111が第2基準を満たしていると判定し不要なフリーズ表示処理が行われることを防止することができる。傾斜角度判定部112以外の構成については、実施の形態1に示した各要素と同じであり説明を省略する。
<< Embodiment 2 >>
In the first embodiment, the inclination angle determination unit 112 has a predetermined inclination angle of the ultrasonic probe 2 when the reflected ultrasonic wave used as the basis of the received signal of the frame is acquired by the ultrasonic probe 2. It was set as the structure which determines with satisfy | filling the 1st reference | standard when it is included in the angle range. In the second embodiment, the tilt angle determination unit 112 detects a change in the tilt angle of the ultrasonic probe 2 when the reflected ultrasound that is the basis of the received signal of the frame is acquired by the ultrasonic probe 2. The second embodiment is different from the first embodiment in that it is determined that the first reference is satisfied when it is equal to or less than a predetermined reference value. With such a configuration, when the operator moves the ultrasonic probe 2 on the subject skin surface and searches for the measurement target, the reception signal determination unit 111 determines that the second reference is satisfied and is unnecessary. It is possible to prevent the freeze display process from being performed. The configuration other than the inclination angle determination unit 112 is the same as each element shown in the first embodiment, and a description thereof is omitted.
 具体的には、実施の形態2に係る構成では、傾斜角度判定部112は、傾斜角度算出部7から出力される傾斜角度を逐次監視し解析する。具体的には、傾斜角度算出部7から逐次出力される傾斜角度から傾斜角度の時間的な変動(以後、「傾斜角度変動」とする)を算出する。例えば、あるフレーム(N)の傾斜角度が40°であり、このフレームの直前のフレーム(N-1)の傾斜角度が30°とすると、この場合のフレーム(N)の傾斜角度変動は+10°として算出することができる。そして、この傾斜角度変動の算出処理を、逐次繰り返し行う。 Specifically, in the configuration according to the second embodiment, the tilt angle determination unit 112 sequentially monitors and analyzes the tilt angle output from the tilt angle calculation unit 7. Specifically, the temporal variation of the inclination angle (hereinafter referred to as “inclination angle variation”) is calculated from the inclination angle sequentially output from the inclination angle calculation unit 7. For example, if the tilt angle of a certain frame (N) is 40 ° and the tilt angle of the immediately preceding frame (N−1) is 30 °, the tilt angle variation of the frame (N) in this case is + 10 °. Can be calculated as Then, the calculation process of the inclination angle variation is sequentially repeated.
 そして、傾斜角度判定部112は、あらかじめ所定の基準値を備え、時間的に連続する所定数のフレームにおける傾斜角度変動が所定の基準値以下であるときに、所定数のフレームそれぞれが第1基準を満たしたフレームであると判定する。 The tilt angle determination unit 112 has a predetermined reference value in advance, and when a change in the tilt angle in a predetermined number of temporally continuous frames is equal to or less than the predetermined reference value, each of the predetermined number of frames is the first reference value. It is determined that the frame satisfies the above.
 一方、時間的に連続する複数のフレームにおける傾斜角度変動のうち、例えば、1つのフレームが所定の基準値を超えた場合は、傾斜角度判定部112は所定数のフレームが第1基準を満たさないフレームであると判定し、続いて出力される傾斜角度の変動した次フレームの傾斜角度に基づき、傾斜角度変動の判定を行う。 On the other hand, among the tilt angle fluctuations in a plurality of temporally continuous frames, for example, when one frame exceeds a predetermined reference value, the tilt angle determination unit 112 does not satisfy the first reference. It is determined that the frame is a frame, and the tilt angle variation is determined based on the tilt angle of the next frame in which the tilt angle is subsequently varied.
 上記のように傾斜角度判定部112が判定する理由について、図面を用いて説明する。 The reason why the inclination angle determination unit 112 determines as described above will be described with reference to the drawings.
 図8は、実施の形態2に係る超音波診断装置における傾斜角度判定部を説明するための補助図である。図8は、傾斜角度算出部7で取得した傾斜角度変動をプロットし、時間との関係を示した概略図であり、縦軸が各フレームにおける傾斜角度変動、横軸が時間軸を示す。横軸は右側ほど新しい時刻を示す。F1~F20は、傾斜角度変動のプロットに対応したフレームを示している。ここでは、例えば、時間的に連続する所定数のフレームを5フレームとした場合、(A)所定数のフレームをF4~F8とした場合、(B)所定数のフレームをF12~F16とした場合、(C)所定数のフレームをF16~F20とした場合の3つの例を傾斜角度判定部112で判定した例を説明する。 FIG. 8 is an auxiliary diagram for explaining an inclination angle determination unit in the ultrasonic diagnostic apparatus according to the second embodiment. FIG. 8 is a schematic diagram plotting the tilt angle fluctuations acquired by the tilt angle calculator 7 and showing the relationship with time. The vertical axis represents the tilt angle fluctuations in each frame, and the horizontal axis represents the time axis. The horizontal axis shows the new time as it goes to the right. F1 to F20 indicate frames corresponding to the tilt angle fluctuation plots. Here, for example, when a predetermined number of temporally continuous frames are 5 frames, (A) a predetermined number of frames are F4 to F8, and (B) a predetermined number of frames are F12 to F16. (C) Three examples in which the predetermined number of frames are set to F16 to F20 will be described.
 (A)の場合、F4のフレームを除く他のフレームの傾斜角度変動は基準値を超えており、傾斜角度判定部112は第1基準を満たさないと判定する。これは、例えば、操作者が超音波探触子2を動かして所望の位置に移動させている場合が想定される。係る場合には、受信信号判定部111でF4~F8のいずれかのフレームの受信信号が上述の第2基準を満たしているとき不要なフリーズ表示処理を行うことになる。したがって、傾斜角度判定部112は、このような場合、傾斜角度判定部112は第1基準を満たさないと判定してフリーズ表示処理を行うことを抑制し、不要なフリーズ表示処理の実行を防止する。 In the case of (A), the inclination angle variation of the other frames excluding the frame of F4 exceeds the reference value, and the inclination angle determination unit 112 determines that the first reference is not satisfied. For example, it is assumed that the operator moves the ultrasonic probe 2 to a desired position. In such a case, the received signal determination unit 111 performs an unnecessary freeze display process when the received signal of any one of the frames F4 to F8 satisfies the second criterion. Therefore, in such a case, the tilt angle determination unit 112 determines that the tilt angle determination unit 112 does not satisfy the first reference and suppresses the freeze display process, and prevents the execution of an unnecessary freeze display process. .
 (B)の場合、F13のフレームの傾斜角度変動のみが基準値を超えており、その他のフレームの傾斜角度変動は基準値内に収まっている。この場合も(A)と同様に、傾斜角度判定部112は第1基準を満たさないと判定する。これは、操作者が超音波探触子2を所望の位置近傍に配置しているものの、その位置の微調整等を行っていることが想定される。このような場合もフリーズ表示処理を行うことは望ましくなく、傾斜角度判定部112はし、不要なフリーズ表示処理の実行を防止する。 In the case of (B), only the inclination angle fluctuation of the frame of F13 exceeds the reference value, and the inclination angle fluctuations of the other frames are within the reference value. Also in this case, similarly to (A), the inclination angle determination unit 112 determines that the first reference is not satisfied. This is presumed that the operator arranges the ultrasonic probe 2 in the vicinity of a desired position, but performs fine adjustment of the position. Even in such a case, it is not desirable to perform the freeze display process, and the inclination angle determination unit 112 prevents the execution of the unnecessary freeze display process.
 (C)の場合、F16~F20全てのフレームの傾斜角度変動が、基準値内に収まっているため、傾斜角度判定部112は第1基準を満たしていると判定する。これは、一定期間、超音波探触子2の変動角度が基準値内に収まっているということは、ブレがなく適切な角度に超音波探触子2が配置され、フリーズ表示を行ってもよい条件が整っていることを示している。係る場合、F16~F20のフレームが、測定値決定部114においてIMT測定値を決定するための対象フレームとなる。そして、F16~F20のフレームのうち、受信信号判定部111において第2基準を満たすフレームがIMT測定値の確定対象フレームとなり、このフレームがフリーズ表示処理の対象となる。 In the case of (C), since the inclination angle fluctuations of all the frames F16 to F20 are within the reference value, the inclination angle determination unit 112 determines that the first reference is satisfied. This is because the fluctuation angle of the ultrasonic probe 2 is within the reference value for a certain period of time, even if the ultrasonic probe 2 is arranged at an appropriate angle without blurring and freeze display is performed. It shows that good conditions are in place. In such a case, the frames of F16 to F20 are the target frames for determining the IMT measurement value in the measurement value determination unit 114. Of the frames F16 to F20, the frame that satisfies the second criterion in the received signal determination unit 111 is the IMT measurement value determination target frame, and this frame is the target of the freeze display process.
 上記した構成におる傾斜角度判定部112の判定結果をフリーズ表示処理をするための基準とすることで、傾斜角度変動が基準値以下の状態で取得されたフレームを対象としてフリーズ表示処理を行うことができる。そのため、適正な測定ができる傾斜角度変動の基準値以上の傾斜角度変動下で取得したフレームがフリーズ表示処理されるというような不要なフリーズ表示処理を抑制することができる。 By using the determination result of the inclination angle determination unit 112 having the above-described configuration as a reference for performing the freeze display process, the freeze display process is performed for a frame acquired in a state where the inclination angle variation is equal to or less than the reference value. Can do. Therefore, it is possible to suppress an unnecessary freeze display process in which a frame acquired under an inclination angle variation that is equal to or greater than a reference value of an inclination angle variation that can be appropriately measured is subjected to a freeze display process.
 これにより、操作者が超音波探触子2を被検体皮膚表面上で動かし測定対象を探索している際中に不要なフリーズ表示処理が行われることを抑制することができ、簡便な操作で診断部位の特定ができ、超音波診断装置の使い勝手を向上させることができる。 Thereby, it is possible to suppress unnecessary freeze display processing from being performed while the operator moves the ultrasonic probe 2 on the surface of the subject skin and searches for the measurement target. The diagnostic part can be specified, and the usability of the ultrasonic diagnostic apparatus can be improved.
 <変形例>
 以上、各実施の形態に係る超音波診断装置について説明した。なお、本開示は、各実施の形態に限定されるものではない。
<Modification>
The ultrasonic diagnostic apparatus according to each embodiment has been described above. Note that the present disclosure is not limited to each embodiment.
 実施の形態1においては、フリーズ表示処理を行う条件として、受信信号の判定結果と超音波探触子の傾斜角度の判定結果を用いる説明をした。しかしながら、フリーズ表示処理を行う条件として、超音波探触子の傾斜角度の判定結果を用いて、受信信号の判定結果をフリーズ表示処理を行う条件に組み込むか否かは、検査・測定の目的に応じて適宜設定することができる構成としてもよい。 In the first embodiment, description has been made using the determination result of the received signal and the determination result of the inclination angle of the ultrasonic probe as the conditions for performing the freeze display process. However, as a condition for performing the freeze display process, whether or not the determination result of the received signal is incorporated into the condition for performing the freeze display process using the determination result of the inclination angle of the ultrasonic probe depends on the purpose of the inspection / measurement. It is good also as a structure which can be set suitably according to it.
 また、実施の形態においては、超音波探触子2は、複数の圧電素子が一次元方向に配列された超音波探触子2構成を示した。しかしながら、超音波探触子2の構成は、これに限定されるものではなく、例えば、複数の圧電変換素子が2次元に配列された超音波探触子を用いることも可能である。 In the embodiment, the ultrasonic probe 2 has the configuration of the ultrasonic probe 2 in which a plurality of piezoelectric elements are arranged in a one-dimensional direction. However, the configuration of the ultrasonic probe 2 is not limited to this, and for example, an ultrasonic probe in which a plurality of piezoelectric transducer elements are two-dimensionally arranged can be used.
 また、各実施の形態における超音波診断装置に含まれる処理部の一部又は全部が、超音波探触子2に含まれてもよい。 Further, part or all of the processing units included in the ultrasonic diagnostic apparatus in each embodiment may be included in the ultrasonic probe 2.
 また、各実施の形態に係る超音波診断装置に含まれる各処理部は典型的には集積回路であるLSIとして実現される。これらは個別に1チップ化されてもよいし、一部又は全てを含むように1チップ化されてもよい。 Further, each processing unit included in the ultrasonic diagnostic apparatus according to each embodiment is typically realized as an LSI which is an integrated circuit. These may be individually made into one chip, or may be made into one chip so as to include a part or all of them.
 また、集積回路化はLSIに限るものではなく、専用回路又は汎用プロセッサで実現してもよい。LSI製造後にプログラムすることが可能なFPGA(Field Programmable Gate Array)、又はLSI内部の回路セルの接続や設定を再構成可能なリコンフィギュラブル・プロセッサを利用してもよい。 Further, the integration of circuits is not limited to LSI, and may be realized by a dedicated circuit or a general-purpose processor. An FPGA (Field Programmable Gate Array) that can be programmed after manufacturing the LSI or a reconfigurable processor that can reconfigure the connection and setting of circuit cells inside the LSI may be used.
 また、各実施の形態に係る、超音波診断装置の機能の一部又は全てを、CPU等のプロセッサがプログラムを実行することにより実現してもよい。 Further, some or all of the functions of the ultrasonic diagnostic apparatus according to each embodiment may be realized by a processor such as a CPU executing a program.
 さらに、本開示は上記プログラムであってもよいし、上記プログラムが記録された非一時的なコンピュータ読み取り可能な記録媒体であってもよい。また、上記プログラムは、インターネット等の伝送媒体を介して流通させることができるのは言うまでもない。 Further, the present disclosure may be the above-described program, or a non-transitory computer-readable recording medium on which the above-described program is recorded. Needless to say, the program can be distributed via a transmission medium such as the Internet.
 また、ブロック図における機能ブロックの分割は一例であり、複数の機能ブロックを一つの機能ブロックとして実現したり、一つの機能ブロックを複数に分割したり、一部の機能を他の機能ブロックに移してもよい。また、類似する機能を有する複数の機能ブロックの機能を単一のハードウェア又はソフトウェアが並列又は時分割に処理してもよい。 In addition, division of functional blocks in the block diagram is an example, and a plurality of functional blocks can be realized as one functional block, a single functional block can be divided into a plurality of functions, or some functions can be transferred to other functional blocks. May be. In addition, functions of a plurality of functional blocks having similar functions may be processed in parallel or time-division by a single hardware or software.
 また、上記のステップが実行される順序は、本開示を具体的に説明するために例示するためのものであり、上記以外の順序であってもよい。また、上記ステップの一部が、他のステップと同時(並列)に実行されてもよい。 Further, the order in which the above steps are executed is for illustration in order to specifically describe the present disclosure, and may be in an order other than the above. Also, some of the above steps may be executed simultaneously (in parallel) with other steps.
 また、各実施の形態に係る超音波診断装置、及びその変形例の機能のうち少なくとも一部を組み合わせてもよい。 Also, at least a part of the functions of the ultrasonic diagnostic apparatus according to each embodiment and its modification may be combined.
 さらに、本実施の形態に対して当業者が思いつく範囲内の変更を施した各種変形例も本開示に含まれる。 Furthermore, the present disclosure also includes various modifications in which the present embodiment has been modified within the scope conceived by those skilled in the art.
 ≪まとめ≫
 以上、説明したとおり、実施の形態1に係る超音波診断装置および超音波診断装置の制御方法によれば、受信信号の判定結果および超音波探触子の傾斜角度の判定結果に基づきフリーズ表示処理を行うことができる。これにより、IMTを含む被検体の特性計測や疾患に対する診断部位の特定において不要なフリーズ表示処理を抑制することができ、簡便な操作で診断部位の特定が可能となる。そのため、超音波診断装置の使い勝手を向上させることができる。
≪Summary≫
As described above, according to the ultrasonic diagnostic apparatus and the control method of the ultrasonic diagnostic apparatus according to the first embodiment, the freeze display process is performed based on the determination result of the received signal and the determination result of the inclination angle of the ultrasonic probe. It can be performed. Thereby, unnecessary freeze display processing can be suppressed in the measurement of the characteristics of the subject including the IMT and the specification of the diagnostic site for the disease, and the diagnostic site can be specified by a simple operation. Therefore, the usability of the ultrasonic diagnostic apparatus can be improved.
 ≪補足≫
 以上で説明した実施の形態は、いずれも本開示の好ましい一具体例を示すものである。実施の形態で示される数値、形状、材料、構成要素、構成要素の配置位置及び接続形態、工程、工程の順序などは一例であり、本開示を限定する主旨ではない。また、実施の形態における構成要素のうち、本開示の最上位概念を示す独立請求項に記載されていない工程については、より好ましい形態を構成する任意の構成要素として説明される。
<Supplement>
Each of the embodiments described above shows a preferred specific example of the present disclosure. Numerical values, shapes, materials, constituent elements, arrangement positions and connection forms of constituent elements, processes, order of processes, and the like shown in the embodiments are merely examples, and are not intended to limit the present disclosure. In addition, among the constituent elements in the embodiment, steps that are not described in the independent claims indicating the highest concept of the present disclosure are described as arbitrary constituent elements constituting a more preferable form.
 また、本開示の理解の容易のため、上記各実施の形態で挙げた各図の構成要素の縮尺は実際のものと異なる場合がある。また本開示は上記各実施の形態の記載によって限定されるものではなく、本開示の要旨を逸脱しない範囲において適宜変更可能である。 Also, in order to facilitate understanding of the present disclosure, the scales of the constituent elements in the drawings described in the above embodiments may differ from actual ones. The present disclosure is not limited by the description of each of the above embodiments, and can be appropriately changed without departing from the gist of the present disclosure.
 さらに、超音波診断装置においては基板上に回路部品、リード線等の部材も存在するが、電気的配線、電気回路について当該技術分野における通常の知識に基づいて様々な態様を実施可能であり、本開示の説明として直接的には無関係のため、説明を省略している。尚、上記示した各図は模式図であり、必ずしも厳密に図示したものではない。 Furthermore, in the ultrasonic diagnostic apparatus, there are members such as circuit components and lead wires on the substrate, but various modes can be implemented based on ordinary knowledge in the technical field regarding electrical wiring and electrical circuits. The description is omitted because it is not directly relevant to the description of the present disclosure. Each figure shown above is a schematic diagram, and is not necessarily illustrated strictly.
 本開示に係る超音波診断装置および超音波診断装置の制御方法によれば、上記構成とすることで、操作者にとって使い勝手を向上させることが可能となる。したがって、簡便な操作が可能な超音波診断装置において広く活用することができる。 According to the ultrasonic diagnostic apparatus and the method for controlling the ultrasonic diagnostic apparatus according to the present disclosure, it is possible to improve usability for the operator with the above configuration. Therefore, it can be widely used in an ultrasonic diagnostic apparatus capable of simple operation.
 1 超音波診断装置
 2 超音波探触子
 3 表示器
 4 入力器
 5 制御器
 6 送受信部
 7 傾斜角度算出部
 8 断層画像生成部
 9 心拍同期信号取得部
 10 測定部
 11 判定部
 12 フリーズ表示処理部
 13 表示処理部
 14 制御部
 21 傾斜角度測定部
 111 受信信号判定部
 112 傾斜角度判定部
 113 記録部
 114 測定値決定部
 200 頚動脈
 201 血管内腔
 202 外膜
 203 内中膜
 204 内膜
 205 内腔内膜境界
 206 中膜
 207 中膜外膜境界
 208 IMT測定範囲
 209 前壁
 210 後壁
 211 血管中心
DESCRIPTION OF SYMBOLS 1 Ultrasonic diagnostic apparatus 2 Ultrasonic probe 3 Display 4 Input device 5 Controller 6 Transmission / reception part 7 Inclination angle calculation part 8 Tomographic image generation part 9 Heart rate synchronization signal acquisition part 10 Measurement part 11 Judgment part 12 Freeze display process part DESCRIPTION OF SYMBOLS 13 Display processing part 14 Control part 21 Inclination angle measurement part 111 Reception signal determination part 112 Inclination angle determination part 113 Recording part 114 Measurement value determination part 200 Carotid artery 201 Blood vessel lumen 202 Outer membrane 203 Intima 204 Intima 205 Intraluminal Membrane boundary 206 Middle membrane 207 Middle membrane outer membrane boundary 208 IMT measurement range 209 Front wall 210 Rear wall 211 Blood vessel center

Claims (8)

  1.  表示器が接続可能に構成された超音波診断装置であって、
     傾斜角度測定部を備えた超音波探触子が接続可能に構成され、
     測定対象を含む被検体に対して前記超音波探触子を介して超音波を送信する送信処理と、前記超音波探触子を介して前記測定対象からの反射超音波に基づく受信信号をフレーム毎に取得する受信処理とを行う送受信部と、
     前記超音波探触子の傾斜角度が所定の角度範囲に含まれる状態、又は傾斜角度変動が所定の基準値以下である状態の少なくともいずれかにおいて、前記超音波探触子により前記測定対象から取得された反射超音波に基づくフレームの受信信号が所定の基準を満たすときに、前記所定の基準を満たしたフレームの受信信号に基づき生成された断層画像を前記表示器に表示させ当該表示を継続させるフリーズ表示処理部と
     を備えた超音波診断装置。
    An ultrasonic diagnostic apparatus configured to be connectable to a display,
    An ultrasonic probe equipped with an inclination angle measurement unit is configured to be connectable,
    A transmission process for transmitting an ultrasonic wave to the subject including the measurement object via the ultrasonic probe, and a reception signal based on the reflected ultrasonic wave from the measurement object via the ultrasonic probe are framed. A transmission / reception unit that performs reception processing to be acquired every time;
    Acquired from the measurement object by the ultrasonic probe in at least one of the state in which the inclination angle of the ultrasonic probe is included in a predetermined angle range or the state in which the fluctuation of the inclination angle is a predetermined reference value or less. When the received signal of the frame based on the reflected ultrasonic wave satisfies a predetermined criterion, the tomographic image generated based on the received signal of the frame satisfying the predetermined criterion is displayed on the display device and the display is continued. An ultrasonic diagnostic apparatus comprising a freeze display processing unit.
  2.  前記受信信号に基づきフレーム毎に断層画像を生成する断層画像生成部と、
     前記断層画像を前記表示器に表示させる表示処理部と、
     前記傾斜角度測定部から逐次取得された前記超音波探触子の傾斜角度が所定の角度範囲に含まれるか否かを判定する傾斜角度判定部と、
     前記送受信部が取得したフレームの受信信号が前記所定の基準を満たすか否かを判定する受信信号判定部とを備え、
     前記傾斜角度判定部が、1以上のフレームの受信信号の基礎とされた反射超音波が前記超音波探触子に取得されたときの前記超音波探触子の傾斜角度が所定の角度範囲に含まれると判定し、
     前記受信信号判定部が、前記1以上のフレームの受信信号が前記所定の基準を満たすと判定したとき、
     前記フリーズ表示処理部は、前記1以上のフレームに含まれる少なくとも1のフレームの受信信号に基づき前記断層画像生成部により生成された断層画像を前記表示処理部を介して前記表示器に表示させ当該表示を継続させる
     請求項1に記載の超音波診断装置。
    A tomographic image generator for generating a tomographic image for each frame based on the received signal;
    A display processing unit for displaying the tomographic image on the display;
    A tilt angle determination unit that determines whether or not the tilt angle of the ultrasonic probe sequentially acquired from the tilt angle measurement unit is included in a predetermined angle range;
    A reception signal determination unit that determines whether a reception signal of a frame acquired by the transmission / reception unit satisfies the predetermined criterion;
    The tilt angle of the ultrasonic probe when the reflected ultrasonic wave based on the reception signal of one or more frames is acquired by the ultrasonic probe is within a predetermined angle range. Determined to be included,
    When the received signal determining unit determines that the received signal of the one or more frames satisfies the predetermined criterion,
    The freeze display processing unit causes the display unit to display a tomographic image generated by the tomographic image generation unit based on a reception signal of at least one frame included in the one or more frames via the display processing unit. The ultrasonic diagnostic apparatus according to claim 1, wherein the display is continued.
  3.  前記受信信号に基づきフレーム毎に断層画像を生成する断層画像生成部と、
     前記断層画像を前記表示器に表示させる表示処理部と、
     前記傾斜角度測定部から逐次取得された前記超音波探触子の傾斜角度変動が所定の基準値以下であるか否かを判定する傾斜角度判定部と、
     前記送受信部が取得したフレームの受信信号が所定基準を満たすか否かを判定する受信信号判定部とをさらに備え、
     前記傾斜角度判定部が、1以上のフレームの受信信号の基礎とされた反射超音波が前記超音波探触子に取得されたときの前記超音波探触子の傾斜角度変動が傾斜角度変動が所定の基準値以下であると判定し、
     前記受信信号判定部が、前記1以上のフレームの受信信号が前記所定の基準を満たすと判定したとき、
     前記フリーズ表示処理部は、前記1以上のフレームに含まれる少なくとも1のフレームの受信信号に基づき前記断層画像生成部が生成した断層画像を前記表示処理部を介して前記表示器に表示させ当該表示を継続させる
     請求項1に記載の超音波診断装置。
    A tomographic image generator for generating a tomographic image for each frame based on the received signal;
    A display processing unit for displaying the tomographic image on the display;
    A tilt angle determination unit that determines whether or not the tilt angle variation of the ultrasonic probe sequentially acquired from the tilt angle measurement unit is equal to or less than a predetermined reference value;
    A reception signal determination unit that determines whether a reception signal of the frame acquired by the transmission / reception unit satisfies a predetermined criterion;
    The tilt angle variation of the ultrasonic probe when the reflected angle based on the reception signal of one or more frames is acquired by the ultrasonic probe is the tilt angle variation. It is determined that it is below a predetermined reference value,
    When the received signal determining unit determines that the received signal of the one or more frames satisfies the predetermined criterion,
    The freeze display processing unit causes the display to display a tomographic image generated by the tomographic image generation unit based on a reception signal of at least one frame included in the one or more frames via the display processing unit. The ultrasonic diagnostic apparatus according to claim 1.
  4.  前記受信信号判定部は、前記1以上のフレームの受信信号の基礎とされた反射超音波が前記測定対象における所定の領域から心拍周期における所定のタイミングにて取得されているときに前記所定の基準を満たすと判定する
     請求項2又は3の何れか1項に記載の超音波診断装置。
    The received signal determination unit is configured to obtain the predetermined reference when a reflected ultrasonic wave based on the received signal of the one or more frames is acquired from a predetermined region of the measurement target at a predetermined timing in a heartbeat cycle. The ultrasonic diagnostic apparatus according to claim 2, wherein it is determined that the condition is satisfied.
  5.  前記受信信号に基づき前記測定対象の特性を測定する測定部をさらに備え、
     前記フリーズ表示処理部は、前記測定部により前記1以上のフレームに含まれる少なくとも1のフレームの受信信号に基づき測定された前記特性の測定結果を前記表示器に表示させ当該表示を継続させる
     請求項2又は3の何れか1項に記載の超音波診断装置。
    A measuring unit that measures the characteristics of the measurement object based on the received signal;
    The freeze display processing unit causes the display unit to display a measurement result of the characteristic measured based on a reception signal of at least one frame included in the one or more frames by the measurement unit, and continues the display. The ultrasonic diagnostic apparatus according to any one of 2 and 3.
  6.  前記特性はIMTである
     請求項5に記載の超音波診断装置。
    The ultrasonic diagnostic apparatus according to claim 5, wherein the characteristic is IMT.
  7.  前記傾斜角度測定部は角度センサであり、
     前記角度センサから逐次取得した信号に基づき前記超音波探触子の傾斜角度を算出する傾斜角度算出部をさらに備えた
     請求項1に記載の超音波診断装置。
    The tilt angle measurement unit is an angle sensor,
    The ultrasonic diagnostic apparatus according to claim 1, further comprising an inclination angle calculation unit that calculates an inclination angle of the ultrasonic probe based on a signal sequentially acquired from the angle sensor.
  8.  傾斜角度測定部を備えた超音波探触子と表示器とが各々接続可能に構成された超音波診断装置の制御方法であって、
     測定対象を含む被検体に対して前記超音波探触子を介して超音波を送信する送信処理と、前記超音波探触子を介して前記測定対象からの反射超音波に基づく受信信号をフレーム毎に取得する受信処理とを行う送受信ステップと、
     前記超音波探触子の傾斜角度が所定の角度範囲に含まれる状態、又は傾斜角度変動が所定の基準値以下である状態の少なくともいずれか一方において、前記超音波探触子により前記測定対象から取得された反射超音波に基づくフレームの受信信号が所定の基準を満たすときに、前記所定の基準を満たしたフレームの受信信号に基づき生成された断層画像を前記表示器に表示させ当該表示を継続させるフリーズ表示処理ステップと
     を有する超音波診断装置の制御方法。
    A method for controlling an ultrasonic diagnostic apparatus configured such that an ultrasonic probe having an inclination angle measurement unit and a display can be connected to each other,
    A transmission process for transmitting an ultrasonic wave to the subject including the measurement object via the ultrasonic probe, and a reception signal based on the reflected ultrasonic wave from the measurement object via the ultrasonic probe are framed. A transmission / reception step for performing reception processing acquired every time;
    In at least one of the state in which the inclination angle of the ultrasonic probe is included in a predetermined angle range or the state in which the inclination angle variation is equal to or less than a predetermined reference value, the ultrasonic probe removes the object from the measurement target. When the received signal of the frame based on the acquired reflected ultrasound satisfies a predetermined standard, the tomographic image generated based on the received signal of the frame satisfying the predetermined standard is displayed on the display unit and the display is continued. A control method for an ultrasonic diagnostic apparatus, comprising: a freeze display processing step.
PCT/JP2014/000954 2013-02-25 2014-02-24 Ultrasonic diagnostic device and method for controlling ultrasonic diagnostic device WO2014129203A1 (en)

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CN112237443B (en) * 2020-11-11 2024-05-17 深圳开立生物医疗科技股份有限公司 Ultrasonic imaging data acquisition method and related device

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