WO2022080183A1 - 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
WO2022080183A1
WO2022080183A1 PCT/JP2021/036786 JP2021036786W WO2022080183A1 WO 2022080183 A1 WO2022080183 A1 WO 2022080183A1 JP 2021036786 W JP2021036786 W JP 2021036786W WO 2022080183 A1 WO2022080183 A1 WO 2022080183A1
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diagnostic
ultrasonic
image
findings
similarity
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PCT/JP2021/036786
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French (fr)
Japanese (ja)
Inventor
幸哉 宮地
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富士フイルム株式会社
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Priority to JP2022557385A priority Critical patent/JPWO2022080183A1/ja
Publication of WO2022080183A1 publication Critical patent/WO2022080183A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B8/00Diagnosis using ultrasonic, sonic or infrasonic waves

Definitions

  • the present invention relates to an ultrasonic diagnostic apparatus and a control method of an ultrasonic diagnostic apparatus that support a diagnosis using an ultrasonic image.
  • an ultrasonic image of each part of a subject is taken by using an ultrasonic diagnostic apparatus, and the obtained ultrasonic image is used to make a diagnosis of the part taken by the ultrasonic image.
  • an information processing apparatus as disclosed in Patent Document 1 has been developed so that a user can easily perform a diagnosis using an ultrasonic image.
  • the information processing apparatus of Patent Document 1 stores a plurality of frames of ultrasonic images taken in the past, and represents a case similar to the case of the site of the subject to be diagnosed from the multiple frames of the ultrasonic image. Search for an ultrasound image and display the ultrasound image.
  • a user who is unfamiliar with the diagnosis of a subject using an ultrasonic image may refer to an ultrasonic image representing a case similar to the site of the subject to be diagnosed by the information processing apparatus of Patent Document 1.
  • An object of the present invention is to provide an ultrasonic diagnostic apparatus capable of easily imparting diagnostic findings to an ultrasonic image by a user, and a control method for the ultrasonic diagnostic apparatus.
  • the ultrasonic diagnostic apparatus includes an ultrasonic probe and a diagnostic apparatus main body connected to the ultrasonic probe, and the diagnostic apparatus main body includes a plurality of diagnostic devices corresponding to a plurality of defined diagnostic findings as ultrasonic diagnostic images.
  • a monitor that displays the diagnostic findings icon, a similarity determination unit that determines the similarity between the ultrasonic diagnostic image and a plurality of image patterns corresponding to a plurality of diagnostic findings, and a similarity determination unit that determines the similarity. It is characterized by including an emphasis changing unit that changes the emphasis of a plurality of diagnostic findings icons on the monitor according to the degree.
  • the main body of the diagnostic device performs ultrasonic diagnosis of the input device for the user to perform an input operation and the diagnostic findings corresponding to the diagnostic findings icon selected via the input device from among the plurality of diagnostic findings icons displayed on the monitor. It is preferable to include a diagnostic finding linking portion linked to the image. It is preferable that the diagnostic findings associated with the ultrasonic diagnostic image by the diagnostic findings association unit are displayed on the monitor.
  • the emphasis changing unit changes the emphasis of the plurality of diagnostic findings icons so that the diagnostic findings icons corresponding to the diagnostic findings having a high degree of similarity are emphasized more strongly.
  • the emphasis changing unit can surround the diagnostic finding icon corresponding to the diagnostic finding having the highest degree of similarity among the plurality of diagnostic findings with a highlight line.
  • the emphasis degree changing unit can also display the diagnostic findings icon corresponding to the diagnostic findings having the highest degree of similarity among the plurality of diagnostic findings in a color different from that of other diagnostic findings icons.
  • the emphasis degree changing unit can display the diagnostic finding icon corresponding to the diagnostic finding having the highest degree of similarity among the plurality of diagnostic findings larger than the other diagnostic findings icons.
  • the ultrasound diagnostic image is an ultrasound image of the lungs of the subject, and at least one of the plurality of diagnostic findings includes one of B-line, hardening, normal, and no rung sliding. Is preferable.
  • the ultrasonic diagnostic image is a still image at the time of freezing, and the still image can be displayed on the monitor. Further, the ultrasonic diagnostic image may be a moving image. In this case, the ultrasonic diagnostic image is preferably a moving image at a predetermined time until the freeze.
  • the similarity determination unit determines the similarity of the ultrasonic images of the plurality of frames constituting the moving image with the plurality of image patterns corresponding to the plurality of diagnostic findings, and among the ultrasonic images of the plurality of frames, the similarity is determined.
  • the ultrasonic image with the highest degree is displayed on the monitor, and the emphasis changing unit can change the emphasis of the plurality of diagnostic findings icons based on the ultrasonic image with the highest degree of similarity.
  • the control method of the ultrasonic diagnostic apparatus displays an ultrasonic diagnostic image and a plurality of diagnostic findings icons corresponding to a plurality of defined diagnostic findings on a monitor, and displays the ultrasonic diagnostic image and a plurality of diagnostic findings on the monitor. It is characterized in that the similarity with a plurality of corresponding image patterns is determined, and the emphasis of the plurality of diagnostic findings icons on the monitor is changed according to the determined similarity.
  • an ultrasonic probe and a diagnostic device main body connected to the ultrasonic probe are provided, and the diagnostic device main body has a plurality of diagnostic findings icons corresponding to a plurality of diagnostic findings defined as an ultrasonic diagnostic image.
  • the monitor that displays the similarity determination unit that determines the similarity between the ultrasonic diagnostic image and the plurality of image patterns corresponding to the plurality of diagnostic findings, and the similarity determination unit that determines the similarity. Since it includes an emphasis changing unit that changes the emphasis of a plurality of diagnostic findings icons on the monitor, the user can easily give diagnostic findings to the ultrasonic image.
  • Embodiment 1 of this invention It is a block diagram which shows the structure of the ultrasonic diagnostic apparatus which concerns on Embodiment 1 of this invention. It is a block diagram which shows the structure of the transmission / reception circuit in Embodiment 1 of this invention. It is a block diagram which shows the structure of the ultrasonic image generation part in Embodiment 1 of this invention. It is a figure which shows the example of the plurality of diagnostic findings icons in Embodiment 1 of this invention. It is a figure which shows the example of the diagnostic findings icon whose emphasis degree was changed in Embodiment 1 of this invention. It is a flowchart which shows the operation of the ultrasonic diagnostic apparatus in Embodiment 1 of this invention.
  • FIG. 1 shows the configuration of the ultrasonic diagnostic apparatus 1 according to the first embodiment of the present invention.
  • the ultrasonic diagnostic apparatus 1 includes an ultrasonic probe 2 and a diagnostic apparatus main body 3.
  • the ultrasonic probe 2 includes an oscillator array 11, and a transmission / reception circuit 12 is connected to the oscillator array 11.
  • the diagnostic device main body 3 includes an image generation unit 13, and the image generation unit 13 is connected to the transmission / reception circuit 12 of the ultrasonic probe 2. Further, the display control unit 14 and the monitor 15 are sequentially connected to the image generation unit 13. Further, the image memory 16 is connected to the image generation unit 13. Further, the diagnostic apparatus main body 3 includes an image pattern memory 17. The similarity determination unit 18 is connected to the image memory 16 and the image pattern memory 17, and the emphasis change unit 19 is connected to the similarity determination unit 18. The emphasis changing unit 19 is connected to the display control unit 14. Further, the diagnostic finding linking portion 20 is connected to the image memory 16. The diagnostic finding linking unit 20 is connected to the display control unit 14.
  • the transmission / reception circuit 12 of the ultrasonic probe 2 the image generation unit 13, the display control unit 14, the image memory 16, the image pattern memory 17, the similarity determination unit 18, the emphasis change unit 19, and the diagnostic finding linking unit 20.
  • the main body control unit 21 is connected.
  • the input device 22 is connected to the main body control unit 21.
  • the processor 23 is composed of an image generation unit 13, a display control unit 14, a similarity determination unit 18, an emphasis degree changing unit 19, a diagnostic finding linking unit 20, and a main body control unit 21.
  • the oscillator array 11 of the ultrasonic probe 2 shown in FIG. 1 has a plurality of ultrasonic oscillators arranged one-dimensionally or two-dimensionally. Each of these ultrasonic transducers transmits ultrasonic waves according to a drive signal supplied from the transmission / reception circuit 12, receives ultrasonic echoes from a subject, and outputs a signal based on the ultrasonic echoes.
  • Each ultrasonic transducer is, for example, a piezoelectric ceramic represented by PZT (Lead Zirconate Titanate), a polymer piezoelectric element represented by PVDF (Poly Vinylidene Di Fluoride), and PMN-.
  • PT Lead Magnesium Niobate-Lead Titanate: lead magnesiumidene fluoride-lead titanate solid solution
  • the transmission / reception circuit 12 transmits ultrasonic waves from the oscillator array 11 and generates a sound line signal based on the received signal acquired by the oscillator array 11 under the control of the main body control unit 21.
  • the transmission / reception circuit 12 includes a pulser 31 connected to the oscillator array 11, an amplification unit 32 sequentially connected in series from the oscillator array 11, an AD (Analog Digital) conversion unit 33, and a beam. It has a former 34.
  • the pulsar 31 includes, for example, a plurality of pulse generators, and transmits from a plurality of ultrasonic oscillators of the oscillator array 11 based on a transmission delay pattern selected according to a control signal from the main body control unit 21.
  • Each drive signal is supplied to a plurality of ultrasonic transducers by adjusting the delay amount so that the ultrasonic waves to be generated form an ultrasonic beam.
  • a pulsed or continuous wave voltage is applied to the electrodes of the ultrasonic vibrator of the vibrator array 11, the piezoelectric body expands and contracts, and the pulsed or continuous wave ultrasonic waves are generated from the respective ultrasonic vibrators. Is generated, and an ultrasonic beam is formed from the combined wave of those sound waves.
  • the transmitted ultrasonic beam is reflected by, for example, a target such as a site of a subject, and propagates toward the oscillator array 11 of the ultrasonic probe 2.
  • the ultrasonic echo propagating toward the oscillator array 11 in this way is received by each ultrasonic oscillator constituting the oscillator array 11.
  • each ultrasonic oscillator constituting the oscillator array 11 expands and contracts by receiving the propagating ultrasonic echo, generates a received signal which is an electric signal, and amplifies these received signals. Output to 32.
  • the amplification unit 32 amplifies the signal input from each ultrasonic vibrator constituting the vibrator array 11, and transmits the amplified signal to the AD conversion unit 33.
  • the AD conversion unit 33 converts the signal transmitted from the amplification unit 32 into digital reception data.
  • the beam former 34 performs so-called reception focus processing by giving and adding delays to each received data received from the AD conversion unit 33. By this reception focus processing, each reception data converted by the AD conversion unit 33 is phase-adjusted and added, and a sound line signal in which the focus of the ultrasonic echo is narrowed down is acquired.
  • the image generation unit 13 has a configuration in which a signal processing unit 35, a DSC (Digital Scan Converter) 36, and an image processing unit 37 are sequentially connected in series.
  • a signal processing unit 35 a DSC (Digital Scan Converter) 36
  • an image processing unit 37 an image processing unit 37 is sequentially connected in series.
  • the signal processing unit 35 corrects the attenuation of the sound line signal received from the transmission / reception circuit 12 by the distance according to the depth of the ultrasonic reflection position using the sound velocity value set by the main body control unit 21. By performing the envelope detection process, a B-mode image signal, which is tomographic image information about the tissue in the subject, is generated.
  • the DSC 36 converts the B-mode image signal generated by the signal processing unit 35 into an image signal according to a normal television signal scanning method (raster conversion).
  • the image processing unit 37 performs various necessary image processing such as gradation processing on the B mode image signal input from the DSC 36, and then sends the B mode image signal to the display control unit 14 and the image memory 16.
  • the B-mode image signal processed by the image processing unit 37 is referred to as an ultrasonic image.
  • the image memory 16 is for storing the ultrasonic image generated by the image generation unit 13.
  • the ultrasonic image stored in the image memory 16 is read out under the control of the main body control unit 21, and is sent to the display control unit 14, the similarity determination unit 18, and the diagnostic finding linking unit 20.
  • Examples of the image memory 16 include a flash memory, an HDD (Hard Disc Drive), an SSD (Solid State Drive), an FD (Flexible Disc), and an MO disk (Magneto-Optical disc).
  • Magnetic disc Magnetic disc
  • MT Magnetic Tape
  • RAM Random Access Memory
  • CD Compact Disc: compact disc
  • DVD Digital Versatile Disc
  • SD card Secure Digital card
  • recording media such as USB memory (Universal Serial Bus memory) can be used.
  • the image pattern memory 17 stores a plurality of image patterns corresponding to a plurality of diagnostic findings defined for the site of the subject.
  • diagnostic findings on the lungs of a subject are known as so-called B-line, sclerosing, normal and without rung-sliding, and characteristic image patterns appearing in ultrasound images corresponding to these diagnostic findings. Is also known.
  • the image pattern corresponding to these diagnostic findings can be stored in the image pattern memory 17 in advance by the user, for example.
  • the image pattern memory 17 similarly to the image memory 16, for example, a flash memory, an HDD, an SSD, an FD, a MO disk, an MT, a RAM, a CD, a DVD, an SD card, a recording medium such as a USB memory, or the like can be used. Can be used.
  • the similarity determination unit 18 determines the similarity between the ultrasonic diagnostic image generated by the image generation unit 13 and stored in the image memory 16 and the plurality of image patterns stored in the image pattern memory 17. For example, when the image pattern memory 17 stores image patterns corresponding to four diagnostic findings of B line, curing, normality, and no rung sliding, the similarity determination unit 18 uses the four image patterns and ultrasonic waves. The similarity with the diagnostic image is determined, and four similarity values are obtained.
  • the ultrasonic diagnostic image includes a still image composed of a one-frame ultrasonic image generated by the image generation unit 13 and a moving image composed of a plurality of frames of ultrasonic images.
  • the similarity determination unit 18 may use, for example, a method using simple template matching, Csurka et al .: Visual Categorization with Bags of Keypoints, Proc. Of ECCV Workshop on Statistical Learning in Computer Vision, pp. Described in the machine learning method described in .59-74 (2004), or in Krizhevsk et al .: ImageNet Classification with Deep Convolutional Neural Networks, Advances in Neural Information Processing Systems 25, pp.1106-1114 (2012). It is possible to use a general image recognition method or the like using deep learning.
  • the emphasis changing unit 19 stores a plurality of diagnostic findings icons corresponding to a plurality of diagnostic findings on the site of the subject together with a predetermined display position on the monitor 15, and the plurality of diagnostic findings determined by the similarity determination unit 18.
  • the emphasis of multiple diagnostic findings icons is changed according to the similarity of each of the diagnostic findings.
  • the diagnostic findings icons J1 to J4 each have a design imitating the image pattern of the corresponding diagnostic findings so that the user can easily associate and recognize the diagnostic findings icons J1 to J4.
  • the emphasis changing unit 19 can change the emphasis of a plurality of diagnostic findings icons so that, for example, the diagnostic findings icons J1 to J4 corresponding to the diagnostic findings having a high degree of similarity are emphasized more strongly.
  • the emphasis changing unit 19 is normal (N), no rung sliding (S ( ⁇ )), B line (B), and hardening (C) with respect to the lung of the subject. ) (Consolidation), the four diagnostic findings icons J1 to J4 are stored together with the display positions arranged with the diagnostic findings icons J1, J2, J3, and J4 in order from the left.
  • the similarity is determined by the similarity determination unit 18 so that the values decrease in the order of, for example, B line, curing, normal, and no rung sliding
  • the emphasis changing unit 19 determines the similarity, as shown in FIG.
  • the emphasis of the diagnostic finding icon J3 can be changed by surrounding the diagnostic finding icon J3 corresponding to the diagnostic finding of the B line having the highest degree of similarity with the highlight line L1.
  • the plurality of diagnostic findings icons J1 to J4 whose emphasis is changed in this way are sent to the display control unit 14 and displayed on the monitor 15.
  • the normal diagnostic findings include the boundary of the thoracic membrane and the artifact (so-called A line) extending along the direction orthogonal to the depth direction due to the multiple reflection of the ultrasonic wave in the ultrasonic image. Moreover, it is a finding that the boundary of the thoracic membrane reflected in the ultrasonic image is displaced by a certain amount or more in a continuous multi-frame ultrasonic image (so-called rung sliding is recognized). Thus, the normal findings are those that include the A line and show rung sliding in the ultrasound image.
  • Findings without rung sliding include, in ultrasound images, pleural boundaries and artifacts (A-lines) extending along a direction orthogonal to the depth direction due to multiple reflections, and so-called pneumothorax, etc. Therefore, it is a finding that the boundary of the pleura reflected in the ultrasonic image is hardly displaced (no rung sliding is observed) in the continuous multi-frame ultrasonic image.
  • the findings without rung-sliding include the A-line in the ultrasound image, similar to the normal findings, but no rung-sliding is observed and generally indicate a suspicion of so-called pneumothorax. It has been known.
  • the diagnostic findings of the B line are findings in which a linear pattern along the depth direction is included in the ultrasonic image due to the accumulation of water in the pleura or the like. Further, the finding of hardening means a finding that a granular pattern is included in the ultrasonic image due to the accumulation of water in the lungs or the like.
  • the main body control unit 21 controls each part of the ultrasonic probe 2 and each part of the diagnostic apparatus main body 3 according to a program or the like recorded in advance.
  • the display control unit 14 controls the ultrasonic image generated by the image generation unit 13 and the plurality of diagnostic findings icons J1 to J4 whose emphasis is changed by the emphasis change unit 19 under the control of the main body control unit 21. After performing a predetermined process, the image is displayed on the monitor 15.
  • the monitor 15 performs various displays under the control of the display control unit 14.
  • the monitor 15 includes, for example, a display device such as an LCD (Liquid Crystal Display) and an organic EL display (Organic Electroluminescence Display).
  • the input device 22 is for the user to perform an input operation.
  • the input device 22 is composed of, for example, a keyboard, a mouse, a trackball, a touch pad, a touch panel, and other devices for the user to perform an input operation.
  • the diagnostic findings linking unit 20 links the diagnostic findings corresponding to the diagnostic findings icons selected by the user via the input device 22 among the diagnostic findings icons J1 to J4 displayed on the monitor 15 to the ultrasonic image. For example, as shown in FIG. 5, four diagnostic findings icons J1 to J4 are displayed on the monitor 15, and the diagnostic findings icons J3 corresponding to the diagnostic findings of the B line having the highest similarity are selected by the user via the input device 22. When this is done, the ultrasonic image used for determining the similarity by the similarity determination unit 18 is associated with the diagnostic findings of the B line corresponding to the diagnostic findings icon J3 selected by the user.
  • the processor 23 including the image generation unit 13, the display control unit 14, the similarity determination unit 18, the emphasis change unit 19, the diagnostic finding linking unit 20, and the main body control unit 21 is a CPU (Central Processing Unit). ), And a control program for causing the CPU to perform various processes, such as FPGA (Field Programmable Gate Array), DSP (Digital Signal Processor), and ASIC (Application Specific). Integrated Circuit: Application-specific integrated circuit), GPU (Graphics Processing Unit), and other ICs (Integrated Circuit: integrated circuit) may be used, or they may be combined. good.
  • the image generation unit 13, the display control unit 14, the similarity determination unit 18, the emphasis change unit 19, the diagnostic finding linking unit 20, and the main body control unit 21 are partially or wholly integrated into one CPU or the like. It can also be configured by letting it.
  • the ultrasonic diagnostic apparatus 1 includes a touch sensor arranged on the monitor 15 as an input device 22. Further, a plurality of image patterns corresponding to a plurality of diagnostic findings of the lung of the subject are stored in the image pattern memory 17. Further, the emphasis changing unit 19 stores a plurality of diagnostic findings icons J1 to J4 corresponding to a plurality of diagnostic findings in the lungs of the subject. Further, as shown in FIG. 7, for example, the monitor 15 has a first display area A1, a second display area A2, and a third display area A3.
  • the first display area A1 is an area for displaying the ultrasonic image U.
  • the second display area A2 includes a left / right switching button LR for setting one of the left and right lungs of the subject as an inspection site, and four inspection site selection icons P1 to P4 for selecting an inspection location of the subject.
  • the test site selection icons P1 to P4 correspond to the test site of the lung of the subject, respectively.
  • the inspection site selection icons P1 to P4 are "1R" to "4R” corresponding to the inspection location of the right lung and "1L" corresponding to the inspection location of the left lung by tapping the left / right switching button LR. -Switches to "4L".
  • the inspection site selection icons P1 to P4 correspond to the inspection sites of the right lung registered under the names “1R” to “4R”, respectively.
  • the body mark BM includes a schematic diagram M1 representing a body portion of a subject, a probe mark M2, and an inspection site mark M3.
  • the body mark BM including the schematic diagram M1 with the right lung facing the front side and the body mark BM including the schematic diagram M1 with the left lung facing the front side are switched.
  • a body mark BM including a schematic view M1 with the right lung facing the front side is shown.
  • the probe mark M2 and the inspection location mark M3 are arranged at positions on the schematic diagram M1 corresponding to each of the inspection location selection icons P1 to P4 to visually indicate the inspection location.
  • the body mark BM corresponding to the tapped inspection location selection icons P1 to P4 is displayed in the second display area A2 of the monitor 15.
  • the third display area A3 includes a user interface for inputting commands related to the operation of the ultrasonic diagnostic apparatus 1, such as a freeze button B1 for freezing the ultrasonic image U.
  • a freeze button B1 for freezing the ultrasonic image U.
  • to freeze the ultrasonic image U means to stop the generation of the ultrasonic image U continuously generated by the image generation unit 13 and sequentially displayed on the monitor 15, and the latest one frame of the ultrasonic image U is superposed on the monitor 15. It is to display the sound wave image U.
  • step S1 the user designates an inspection location for inspecting the lung of the subject via the input device 22, and the designated inspection location is accepted by the main body control unit 21.
  • the main body control unit 21 For example, when the user taps the left / right switching button LR to select the right lung as the inspection site and taps the inspection site selection icon P1 corresponding to the inspection location of "1R” to select the inspection location of "1R". Is accepted by the main body control unit 21.
  • the inspection location of "1R” is received in this way, for example, the character “1R” is displayed in the first display area A1 of the monitor 15, and the inspection of "1R" is displayed in the second display area A2.
  • the body mark BM corresponding to the location is displayed.
  • step S2 the user brings the ultrasonic probe 2 into contact with the body surface of the subject, and the ultrasonic image U is taken in this state.
  • the transmission / reception circuit 12 performs reception focus processing using preset sound velocity values under the control of the main body control unit 21 to generate a sound line signal.
  • the sound line signal generated by the transmission / reception circuit 12 in this way is transmitted to the image generation unit 13.
  • the image generation unit 13 generates an ultrasonic image U using the sound line signal transmitted from the transmission / reception circuit 12.
  • step S3 the ultrasonic image U generated in step S2 is sent to the display control unit 14 and displayed on the monitor 15, and the ultrasonic image U is stored in the image memory 16.
  • step S4 the main body control unit 21 determines whether or not an instruction to freeze the ultrasonic image U has been input by the user via the input device 22.
  • the main body control unit 21 determines that the freeze instruction has been given, for example, when the freeze button B1 displayed in the third display area A3 of the monitor 15 is tapped by the user. Further, the main body control unit 21 determines that the freeze instruction has not been given when the freeze button B1 is not tapped by the user.
  • step S2 If it is determined that the freeze instruction has not been given, the process returns to step S2, and the ultrasonic image U is newly captured.
  • the ultrasonic image U generated in step S2 is displayed on the monitor 15 and stored in the image memory 16 in the subsequent step S3.
  • step S3 the process proceeds to step S4, and it is determined whether or not the ultrasonic image U is frozen.
  • the ultrasonic image U is continuously generated and displayed on the monitor 15. Further, by repeating steps S2 to S4, the ultrasonic image U of a plurality of frames is stored in the image memory 16.
  • step S4 When it is determined in step S4 that the freeze instruction has been given, the generation of the ultrasonic image U is stopped and the ultrasonic image U of the latest frame is displayed on the monitor 15, so that the ultrasonic image U is displayed. It is frozen and proceeds to step S5.
  • the similarity determination unit 18 is a moving image of the plurality of frames of the ultrasonic image U stored in the image memory 16 by repeating steps S2 to S4, that is, a moving image at a predetermined time until freezing, that is, super The degree of similarity between each of the plurality of frames of the ultrasonic image U continuously generated within a predetermined time until the ultrasonic image U freezes and the plurality of image patterns stored in the image pattern memory 17. judge.
  • the defined time is set to a few seconds, for example, about 1 second to 3 seconds.
  • the diagnosis of B-line and curing is performed. Similarity can be determined for each finding using a one-frame ultrasound image U, but for diagnostic findings normal and without rung sliding, the movement of the pleural border within the ultrasound image U is discriminated. Therefore, it is preferable to determine the similarity using a continuous plurality of frames of ultrasonic images U.
  • the similarity determination unit 18 refers to the diagnostic findings of the B line, for example, the images corresponding to each of the plurality of frames of the ultrasonic image U generated at a predetermined time until the freeze and the diagnostic findings of the B line.
  • the similarity with the pattern can be calculated, and the similarity having the maximum value among the calculated values of the plurality of similarity can be determined as the similarity to the diagnostic findings of the B line.
  • the similarity determination unit 18 resembles each of the plurality of frames of the ultrasonic image U generated at a predetermined time until the freeze with respect to the diagnostic findings of curing and the image pattern corresponding to the diagnostic findings of curing.
  • the degree can be calculated, and the similarity having the maximum value among the calculated values of the plurality of similarity can be determined as the similarity to the diagnostic findings of hardening.
  • the similarity determination unit 18 can obtain the similarity determined for the ultrasonic image U in which the lungs of the subject are clearly captured as the final similarity.
  • the similarity determination unit 18 analyzes the ultrasonic image U of a plurality of frames generated at a predetermined time until the freeze, for example, with respect to the diagnostic findings of the B line, and the ultrasonic image of the plurality of frames.
  • the ultrasonic image U containing the largest number of linear patterns along the depth direction is selected, and the degree of similarity between the selected ultrasonic image U and the image pattern corresponding to the diagnostic findings of the B line is determined. You can also do it.
  • the similarity determination unit 18 best represents the characteristics of the diagnostic findings for determining the similarity from the ultrasonic images U of a plurality of frames generated at a predetermined time until the freeze.
  • the degree of similarity can also be determined using U. This makes it possible to improve the accuracy of determining the degree of similarity.
  • the image pattern memory 17 has an image corresponding to the normal diagnostic findings.
  • a pattern a series of multiple image patterns in which the pleural border is normally displaced are stored, and as an image pattern for diagnostic findings without rung sliding, a series of multiple images in which the pleural border is hardly displaced. It is preferable that the pattern is preserved.
  • the similarity determination unit 18 has a plurality of frames of ultrasonic image U generated at a predetermined time until the freeze and a plurality of image patterns corresponding to the normal diagnostic findings with respect to the normal diagnostic findings. Judge the degree of similarity with. Further, the similarity determination unit 18 has a plurality of frames of ultrasonic image U generated at a predetermined time until freeze and a plurality of image patterns corresponding to the diagnostic findings of curing for the diagnostic findings of curing. Determine the degree of similarity.
  • the emphasis changing unit 19 has diagnostic findings icons J1 to corresponding to the plurality of diagnostic findings whose similarity is determined in step S5 based on the similarity to the plurality of diagnostic findings determined in step S5. Change the emphasis of J4.
  • the emphasis changing unit 19 corresponds to the diagnostic findings icon J1 corresponding to the normal diagnostic findings, the diagnostic findings icon J2 corresponding to the diagnostic findings without rung sliding, and the diagnostic findings of the B line. It is assumed that the diagnostic findings icon J3 and the diagnostic findings icon J4 corresponding to the diagnostic findings of hardening are stored together with the display positions such that the diagnostic findings icons J1, J2, J3, and J4 are arranged from the left.
  • the emphasis changing unit 19 is, for example, as shown in FIG.
  • the emphasis of the diagnostic findings icon J3 can be changed.
  • step S7 under the control of the display control unit 14, the diagnostic findings icons J1 to J4 are displayed in the third display area A3 of the monitor 15 according to the emphasis degree changed in step S6, for example, as shown in FIG. To.
  • the diagnostic findings icons J1 to J4 correspond to the diagnostic findings icons J1 corresponding to the normal diagnostic findings, the diagnostic findings icons J2 corresponding to the diagnostic findings without rung sliding, and the diagnostic findings of the B line from the left.
  • the diagnostic findings icon J3 and the diagnostic findings icon J4 corresponding to the diagnostic findings of hardening are displayed on the monitor 15 in this order. Further, the diagnostic finding icon J3 corresponding to the diagnostic finding on the B line is surrounded by the highlighted line L1. Further, in the example of FIG. 8, the diagnostic findings icon J5 indicating that the diagnosis does not apply to any of the diagnostic findings is displayed below the diagnostic findings icons J1 to J4.
  • the diagnostic findings icons J1 to J4 are displayed on the monitor 15 according to the emphasis based on the similarity determined in step S5, so that the user is highlighted even if he / she is unfamiliar with the diagnosis of the subject.
  • an appropriate diagnostic finding can be easily given to the ultrasonic image U displayed on the monitor 15.
  • step S8 the main body control unit 21 receives the diagnostic findings icon selected by the user via the input device 22 among the diagnostic findings icons J1 to J4 displayed on the monitor 15.
  • the diagnostic finding linking unit 20 links the ultrasonic image U used for determining the similarity in step S5 and the diagnostic finding corresponding to the diagnostic finding icon selected by the user in step S8 to each other. ..
  • the diagnosis is made when the highest similarity among the similarity determined for the ultrasonic image U of a plurality of frames is determined as the final similarity for the diagnostic findings of the B line and the curing, respectively.
  • the finding linking unit 20 selects the ultrasonic image U having the highest degree of similarity to each of the B line and the diagnostic finding of hardening as the target of linking. Further, the diagnostic finding linking unit 20 targets the ultrasonic images U of a plurality of frames generated at a predetermined time until the freeze, respectively, with respect to the diagnostic findings of normal and without rung sliding.
  • step S10 under the control of the display control unit 14, the diagnostic findings corresponding to the diagnostic findings icon received in step S8 are displayed on the monitor 15.
  • the diagnostic finding icon J3 displayed at the left end is selected by the user, and the diagnostic finding "B" corresponding to the diagnostic finding icon J3 is the first display.
  • the region A1 it is displayed together with the ultrasonic image U associated with the diagnostic findings on the B line in step S9.
  • the similarity between the ultrasonic image U and the plurality of image patterns corresponding to the predetermined plurality of diagnostic findings is determined. Based on their similarity, the emphasis of the plurality of diagnostic findings icons J1 to J4 corresponding to the plurality of diagnostic findings is changed, and the diagnostic findings icons J1 to J4 are displayed on the monitor 15 according to the changed emphasis. , The user can easily give appropriate diagnostic findings to the ultrasonic image U displayed on the monitor 15 by confirming the diagnostic findings icons J1 to J4 whose emphasis is changed.
  • the emphasis is changed while the display order of the plurality of diagnostic findings icons J1 to J4 remains unchanged, for example, a diagnostic finding icon other than the diagnostic finding icon originally desired to be selected by the user is erroneously selected. It is possible to prevent it from being lost. Further, in the present invention, it is possible to set the display order of a plurality of diagnostic findings icons J1 to J4 for each facility such as a hospital where the ultrasonic diagnostic apparatus 1 is installed or for each user. Since the emphasis is changed while the display order of the plurality of diagnostic findings icons J1 to J4 remains unchanged, the user can use, for example, even if the plurality of diagnostic findings icons J1 to J4 are preset in any order. Which icon is most emphasized can be easily confirmed, and appropriate diagnostic findings can be easily given to the ultrasonic image U.
  • the transmission / reception circuit 12 is provided in the ultrasonic probe 2, but instead of being provided in the ultrasonic probe 2, it is provided in the diagnostic apparatus main body 3. You may. Further, although the image generation unit 13 is provided in the diagnostic device main body 3, it may be provided in the ultrasonic probe 2 instead of being provided in the diagnostic device main body 3. Further, as shown in FIG. 3, the image generation unit 13 includes a signal processing unit 35, a DSC 36, and an image processing unit 37, of which the signal processing unit 35 can be included in the ultrasonic probe 2.
  • connection method between the ultrasonic probe 2 and the diagnostic device main body 3 is not particularly limited, and may be a wired connection or a wireless connection.
  • the diagnostic device main body 3 may be a so-called handheld type that can be easily carried by the user, or may be a so-called stationary type.
  • the number of inspection location selection icons P1 to P4 is not limited to four.
  • the main body control unit 21 can store the number of inspection points and the set of corresponding inspection points. In this case, the number of inspection points stored by the user's input operation via the input device 22 is selected, and is selected by the user in the second display area A2 of the monitor 15 under the control of the display control unit 14.
  • the same number of inspection location selection icons as the number of inspection locations can be displayed. By switching the number of inspection points in this way, the present invention can be applied to a wider variety of inspections.
  • the similarity determination unit 18 is, for example, a one-frame ultrasonic image U displayed on the monitor 15 at the time of freezing and an image corresponding to a plurality of diagnostic findings. The degree of similarity of patterns can be determined. However, in order to accurately determine the similarity to the diagnostic findings of normal and no rung sliding, it is preferable to determine the similarity using a moving image.
  • the similarity determination unit 18 is, for example, When determining the similarity to diagnostic findings, normal and without rung-sliding, the movement of the image between the pleural boundary contained in the ultrasound image U and the pleural boundary to a certain depth position is taken into account. The degree of similarity can be determined. This can improve the accuracy of determining the similarity to the diagnostic findings of normal and without rung sliding. As a constant depth position, the depth position of the artifact extending along the direction orthogonal to the depth direction due to the multiple reflection of ultrasonic waves can be set.
  • the emphasis changing unit 19 changes the emphasis of the diagnostic finding icon J3 by surrounding the diagnostic finding icon J3 corresponding to the diagnostic finding having the highest similarity determined in step S5 with the highlight line L1.
  • the method of changing the emphasis is not limited to this.
  • the emphasis degree changing unit 19 can change the display mode of each of the plurality of diagnostic findings icons J1 to J4 according to the similarity degree determined by the similarity degree determination unit 18.
  • the emphasis changing unit 19 corresponds to the diagnostic findings of the B line as shown in FIG.
  • the diagnostic finding icon J3 can be surrounded by the double highlighted line L2
  • the diagnostic finding icon J4 corresponding to the diagnostic finding of hardening can be surrounded by the highlighted line L3.
  • the emphasis changing unit 19 can change the emphasis of the plurality of diagnostic findings icons J1 to J4 so that the diagnostic findings icons corresponding to the diagnostic findings having a high degree of similarity are emphasized more strongly.
  • the emphasis changing unit 19 also displays a display mode according to the degree of similarity with respect to the diagnostic finding icon J1 corresponding to the normal diagnostic finding and the diagnostic finding icon J2 corresponding to the diagnostic finding without rung sliding. It can be carried out.
  • the emphasis changing unit 19 displays the diagnostic findings icon corresponding to the diagnostic findings having the highest similarity among the plurality of diagnostic findings icons J1 to J4 on the monitor 15 in a color different from that of the other diagnostic findings icons. be able to. Further, the emphasis degree changing unit 19 can display the plurality of diagnostic findings icons J1 to J4 on the monitor 15 in different colors according to the degree of similarity to the plurality of diagnostic findings.
  • the emphasis changing unit 19 causes the diagnostic finding icon J3 corresponding to the diagnostic finding having the highest similarity to be displayed on the monitor 15 larger than the other diagnostic finding icons J1, J2 and J4. be able to. Further, the emphasis changing unit 19 can change the size of the plurality of diagnostic findings icons J1 to J4 according to the similarity to the plurality of diagnostic findings. For example, the emphasis changing unit 19 has the similarity. The size of the diagnostic findings icon corresponding to the higher diagnostic findings can be increased, and the size of the diagnostic findings icon corresponding to the diagnostic findings having a lower similarity can be reduced.
  • the diagnostic findings icons corresponding to the diagnostic findings having the lowest similarity can be deleted from the monitor 15.
  • the diagnostic apparatus main body 3 is a handheld type, since the monitor 15 is small, the diagnosis with a relatively high degree of similarity is made by deleting the diagnostic finding icon corresponding to the diagnostic finding with the lowest similarity from the monitor 15.
  • the diagnostic findings icon corresponding to the findings can be displayed in a large size, which makes it easier for the user to select the diagnostic findings icon.
  • the diagnostic finding linking unit 20 links the ultrasonic image U of a plurality of frames generated at a predetermined time until the freeze to the diagnostic findings of normal and without rung sliding, respectively.
  • the target is, a one-frame ultrasonic image U can also be the target of association.
  • the finding linking unit 20 targets the ultrasonic image U of the frame having the highest similarity with respect to the pleural boundary among the ultrasonic images U of a plurality of frames generated at a predetermined time until the freeze. be able to.
  • diagnostic finding icons J1 to J4 are exemplified, the number of diagnostic finding icons is not limited to four, and the degree of similarity is determined, for example, two, three, or five or more. It can be set according to the number of diagnostic findings to be performed. However, it is preferable that at least one of the plurality of diagnostic findings regarding the lungs of the subject includes any of the diagnostic findings of B-line, hardening, normal, and no rung sliding.
  • pleural effusion When the diagnostic findings due to the accumulation of so-called pleural effusion (PE: Pleural Effusion) are added to the lungs of the subject, the pleural effusion is accumulated in addition to the diagnostic findings of normal, no rung sliding, B line, and hardening. (N, PE), no rung sliding and pleural effusion (S (-), PE), B-line and pleural effusion (B, PE), hardening and pleural effusion (C, PE), total 8 Diagnostic findings are possible. In this case, for example, eight diagnostic findings icons J1 to J4 and J10 to J13 corresponding to the eight diagnostic findings as shown in FIG. 11 are displayed on the monitor 15.
  • the diagnostic findings icons J1 to J4 corresponding to the diagnostic findings of normal, no rung sliding, B line, and hardening, and the pleural effusion. It is also possible to display the pleural effusion icon E1 indicating that the pleural effusion is not recognized and the pleural effusion icon E2 indicating that the pleural effusion is recognized. In this case, the user selects any of the diagnostic findings icons J1 to J4 via the input device 22, and then selects any of the pleural effusion icons E1 and E2 to take into account the presence or absence of pleural effusion. Diagnostic findings can be imparted to the ultrasound image U.
  • FIGS. 4, 5 and 8 to 12 exemplify diagnostic findings icons J1 to J4 having a design corresponding to the ultrasonic image U taken by the so-called convex type ultrasonic probe 2.
  • the design of the diagnostic findings icons J1 to J4 may be set according to the type of the ultrasonic probe 2 used for the examination of the subject. For example, as shown in FIG. 13, diagnostic findings icons J6 to J9 having a design corresponding to an ultrasonic image U taken by a so-called linear ultrasonic probe 2 are exemplified.
  • the diagnostic finding icon J6 corresponds to the normal diagnostic finding
  • the diagnostic finding icon J7 corresponds to the diagnostic finding without rung sliding
  • the diagnostic finding icon J8 corresponds to the diagnostic finding of the B line
  • the diagnostic finding icon J9 corresponds to the diagnosis of hardening. Corresponds to the findings.
  • the diagnostic findings icons J14 to J17 in consideration of the accumulation of pleural effusion as shown in FIG. 14 can be displayed on the monitor 15.
  • diagnostic findings icons J14 to J17 having a design corresponding to the linear ultrasonic probe 2 are shown.
  • a pleural effusion icon having a design corresponding to the linear ultrasonic probe 2 can be displayed on the monitor 15 as in the embodiment shown in FIG.
  • a diagnostic finding icon having a design corresponding to the sector type ultrasonic probe 2 can be set.
  • the present invention is limited to the lung inspection. However, it can be applied to various test sites of the subject.
  • the present invention can be applied to a rectal examination of a subject.
  • diagnostic findings for example, three diagnostic findings of loose stool, standard and hard stool are set according to the hardness of the stool in the rectum, and as shown in FIG. 15, the diagnostic findings of loose stool correspond to the diagnostic findings.
  • the diagnostic findings icon J18, the diagnostic findings icon J19 corresponding to the standard diagnostic findings, and the diagnostic findings icon J20 corresponding to the diagnostic findings of hard stool are displayed on the monitor 15.
  • the three diagnostic findings icons J18 to J20 are displayed on the monitor 15 together with the ultrasonic image U1 in which the rectum of the subject is photographed.
  • the present invention can also be applied to an examination of the inferior vena cava of a subject.
  • diagnostic findings for example, there are respiratory fluctuations in the inferior large vein diameter and the inferior large vein diameter based on the size of the diameter of the inferior large vein and the presence or absence of respiratory fluctuations in the inferior large vein diameter. No respiratory fluctuations in large and inferior large vein diameters, normal inferior large vein diameter and respiratory fluctuations in inferior large vein diameter, normal inferior large vein diameter and no respiratory fluctuation in inferior large vein diameter, small inferior large vein diameter and Six diagnostic findings are set with inferior major venous diameter respiratory fluctuations and inferior major venous diameter small and inferior major venous diameter respiratory fluctuations.
  • the diameter of the inferior vena cava is 20 mm or more for "large inferior vena cava", the diameter of the inferior vena cava is larger than 10 mm and less than 20 mm for "normal inferior vena cava", and the diameter of the inferior vena cava is small. It means that the diameter of the vein is 10 mm or less.
  • “with inferior vena cava respiratory fluctuation” means that the change in the diameter of the inferior vena cava in exhaled breath is greater than 40% and 50% or less
  • "without inferior vena cava diameter breathable fluctuation” means that the change in inferior vena cava in exhaled breath is greater than 40%. It means that the change in diameter is 40% or less.
  • the present invention can also be applied to an examination of the liver of a subject.
  • diagnostic findings for example, diagnostic findings of normal, hepatic cyst, fatty liver, hepatic hemangiomas and intrahepatic lime can be set.
  • the present invention can also be applied to an examination of the gallbladder of a subject.
  • diagnostic findings for example, diagnostic findings of normal, gallbladder polyps, gallbladder wall stones, gallbladder stones, gallbladder adenomyomatosis and gallbladder wall thickening can be set.
  • the present invention can also be applied to an examination of a kidney of a subject.
  • diagnostic findings for example, diagnostic findings of normal, intrarenal calcification, renal stones, cystic kidney, renal angiomyolipoma, hydronephrosis, double renal pelvis and renal cyst can be set.
  • the present invention can also be applied to an examination of the heart of a subject.
  • diagnostic findings for example, based on the contractility of the left ventricle, the diagnostic findings of severe hypocontraction, hypocontraction, normal and hypercontraction can be set.
  • the width of the left ventricle in three orthogonal directions is measured from the ultrasonic image U corresponding to two cross sections of the left ventricle orthogonal to each other, and the value of the measured width is used. Can be calculated.
  • the present invention is applied to various test sites of the subject, and for example, the test site of the subject can be set by the input operation of the user via the input device 22. Thereby, the user can easily give appropriate diagnostic findings to the ultrasonic image U in the examination of various examination sites of the subject.
  • Embodiment 2 In the operation explanation of the ultrasonic diagnostic apparatus 1 using the flowchart of FIG. 6, the ultrasonic waves of a plurality of frames generated at a predetermined time until the freeze are triggered by the determination that the freeze instruction has been given in step S4. Although it is described that the image U is used to determine the similarity to a plurality of diagnostic findings in step S5, the ultrasound image U used to determine the similarity is manually selected by the user. You can also do it.
  • the operation of the ultrasonic diagnostic apparatus 1 in the second embodiment will be described with reference to the flowchart shown in FIG.
  • the flowchart of FIG. 16 is the flowchart of FIG. 6 in the first embodiment, in which steps S11 to S13 are provided instead of step S5.
  • step S4 Since steps S1 to S4 are the same as steps S1 to S4 in the flowchart shown in FIG. 6, detailed description thereof will be omitted. If it is determined in step S4 that the freeze instruction has been given, the process proceeds to step S11.
  • step S11 the frame range of the ultrasonic image U of a plurality of frames used for determining the similarity is designated by the user via the input device 22, and the designated frame range is accepted by the main body control unit 21.
  • the slide bar C1 and the freeze button B1 for designating the frame range are displayed in the third display area A3 of the monitor 15. .
  • the slide bar C1 slides between both ends of the slide bar C1 by being dragged by the user, and is one of a plurality of frames of ultrasonic images U generated from the start of the examination of the subject to the freeze. It includes a slide button C2 for selecting the ultrasonic image U of the frame.
  • the left end of the slide bar C1 corresponds to the ultrasonic image U generated first after the examination of the subject is started, and the right end of the slide bar C1 corresponds to the latest ultrasonic image U at the time of freezing.
  • the ultrasonic image U corresponding to the position of the slide button C2 is displayed in the first display area A1 of the monitor 15.
  • the ultrasonic image U of the first frame in the frame range used for determining the similarity is used.
  • the slide button C2 is further slid by the user, and the freeze button B1 is tapped again while being moved to the second position, so that the last frame of the frame range used for determining the similarity is used.
  • the ultrasonic image U is specified.
  • the frame range is designated in this way, and the designated frame range is accepted by the main body control unit 21.
  • step S12 the user inputs a command to start the determination of the similarity via the input device 22, and this command is accepted by the main body control unit 21.
  • step S13 the similarity determination unit 18 corresponds to the ultrasonic image U of a plurality of frames within the frame range specified by the user in step S11 and the plurality of diagnostic findings stored in the image pattern memory 17. Determine the degree of similarity with the image pattern.
  • step S6 the emphasis changing unit 19 changes the emphasis of the plurality of diagnostic findings icons J1 to J4 based on the similarity determined for each of the plurality of diagnostic findings in step S13.
  • step S7 a plurality of diagnostic findings icons J1 to J4 are displayed on the monitor 15 based on the emphasis changed in step S6.
  • step S8 the user selects one of the plurality of diagnostic findings icons J1 to J4 displayed on the monitor 15, and the main body control unit 21 accepts the selected diagnostic findings icons.
  • step S9 the diagnostic finding linking unit 20 associates the ultrasonic image U used for determining the similarity in step S13 with the diagnostic findings corresponding to the diagnostic findings icon whose selection was accepted in step S9. .. Finally, in step S10, the diagnostic findings associated with the ultrasonic image U in step S9 are displayed on the monitor 15.
  • the plurality of frames of the ultrasonic image U generated from the start of the examination of the subject to the freeze by the user via the input device 22 the plurality of frames of the ultrasonic image U used for determining the degree of similarity are super.
  • the frame range of the ultrasonic image U is specified, only one frame of the ultrasonic image U may be specified instead of the frame range being specified.
  • the slide button C2 is moved by the user, and the freeze button B1 is tapped while the ultrasonic image U of the desired frame is displayed on the monitor 15, so that the ultrasonic image of the frame displayed on the monitor 15 is displayed.
  • U is designated as the ultrasound image U used to determine the degree of similarity.
  • 1 ultrasonic diagnostic device 2 ultrasonic probe, 3 diagnostic device body, 11 oscillator array, 12 transmission / reception circuit, 13 image generation unit, 14 display control unit, 15 monitor, 16 image memory, 17 image pattern memory, 18 similarity Judgment unit, 19 emphasis change unit, 20 diagnostic finding linking unit, 21 main unit control unit, 22 input device, 23 processor, 31 pulser, 32 amplification unit, 33 AD conversion unit, 34 beam former, 35 signal processing unit, 36 DSC, 37 image processing unit, A1 1st display area, A2 2nd display area, A3 3rd display area, B1 freeze button, BM body mark, C1 slide bar, C2 slide button, E1, E2 chest water presence / absence icon, J1 ⁇ J20 diagnostic findings icon, L1 to L3 emphasis line, LR left / right switching button, M1 schematic diagram, M2 probe mark, M3 inspection location mark, P1 to P4 inspection location selection icon, U, U1 ultrasound image.

Abstract

An ultrasonic diagnostic device (1) comprises: an ultrasonic probe (2); and a diagnostic device body (3) connected to the ultrasonic probe (2), wherein the diagnostic device body (3) includes a monitor (15) which displays an ultrasonic diagnostic image and a plurality of diagnostic observation icons corresponding to a plurality of specific diagnostic observations, a similarity degree determination unit (18) which determines respective degrees of similarity between the ultrasonic diagnostic image and a plurality of image patterns corresponding to the plurality of diagnostic observations, and an emphasis degree changing unit (19) which changes the degrees of emphasis on the plurality of diagnostic observation icons on the monitor, according to the degrees of similarity determined by the similarity degree determination unit (18).

Description

超音波診断装置および超音波診断装置の制御方法Control method of ultrasonic diagnostic equipment and ultrasonic diagnostic equipment
 本発明は、超音波画像を用いた診断を支援する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 invention relates to an ultrasonic diagnostic apparatus and a control method of an ultrasonic diagnostic apparatus that support a diagnosis using an ultrasonic image.
 従来から、超音波診断装置を用いて被検体の各部の超音波画像が撮影され、得られた超音波画像を用いて、その超音波画像に撮影された部位に対する診断が行われている。超音波画像を用いた診断をユーザが容易に行うことができるように、例えば、特許文献1に開示されるような情報処理装置が開発されている。特許文献1の情報処理装置は、過去に撮影された複数フレームの超音波画像を保存し、この複数フレームの超音波画像から、診断対象となる被検体の部位の症例と類似する症例を表す超音波画像を検索し、その超音波画像を表示する。 Conventionally, an ultrasonic image of each part of a subject is taken by using an ultrasonic diagnostic apparatus, and the obtained ultrasonic image is used to make a diagnosis of the part taken by the ultrasonic image. For example, an information processing apparatus as disclosed in Patent Document 1 has been developed so that a user can easily perform a diagnosis using an ultrasonic image. The information processing apparatus of Patent Document 1 stores a plurality of frames of ultrasonic images taken in the past, and represents a case similar to the case of the site of the subject to be diagnosed from the multiple frames of the ultrasonic image. Search for an ultrasound image and display the ultrasound image.
特開2014-039852号公報Japanese Unexamined Patent Publication No. 2014-039852
 しかしながら、超音波画像を用いた被検体の診断に不慣れなユーザは、特許文献1の情報処理装置によって、診断対象となる被検体の部位と類似する症例を表す超音波画像を参照したとしても、診断対象の部位が撮影された超音波画像に対して、どのような診断所見を付与すべきかを判断することが困難な場合があった。 However, a user who is unfamiliar with the diagnosis of a subject using an ultrasonic image may refer to an ultrasonic image representing a case similar to the site of the subject to be diagnosed by the information processing apparatus of Patent Document 1. In some cases, it was difficult to determine what kind of diagnostic findings should be given to the ultrasonic image of the site to be diagnosed.
 本発明は、ユーザが超音波画像に対して診断所見を容易に付与することができる超音波診断装置およびその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。 An object of the present invention is to provide an ultrasonic diagnostic apparatus capable of easily imparting diagnostic findings to an ultrasonic image by a user, and a control method for the ultrasonic diagnostic apparatus.
 本発明に係る超音波診断装置は、超音波プローブと、超音波プローブに接続された診断装置本体とを備え、診断装置本体は、超音波診断画像と定められた複数の診断所見に対応する複数の診断所見アイコンとを表示するモニタと、超音波診断画像と複数の診断所見に対応する複数の画像パターンとの類似度をそれぞれ判定する類似度判定部と、類似度判定部により判定された類似度に応じてモニタにおける複数の診断所見アイコンの強調度を変更する強調度変更部とを含むことを特徴とする。 The ultrasonic diagnostic apparatus according to the present invention includes an ultrasonic probe and a diagnostic apparatus main body connected to the ultrasonic probe, and the diagnostic apparatus main body includes a plurality of diagnostic devices corresponding to a plurality of defined diagnostic findings as ultrasonic diagnostic images. A monitor that displays the diagnostic findings icon, a similarity determination unit that determines the similarity between the ultrasonic diagnostic image and a plurality of image patterns corresponding to a plurality of diagnostic findings, and a similarity determination unit that determines the similarity. It is characterized by including an emphasis changing unit that changes the emphasis of a plurality of diagnostic findings icons on the monitor according to the degree.
 診断装置本体は、ユーザが入力操作を行うための入力装置と、モニタに表示された複数の診断所見アイコンのうち、入力装置を介して選択された診断所見アイコンに対応する診断所見を超音波診断画像に紐付ける診断所見紐付け部とを含むことが好ましい。
 診断所見紐付け部により超音波診断画像に紐付けられた診断所見は、モニタに表示されることが好ましい。
The main body of the diagnostic device performs ultrasonic diagnosis of the input device for the user to perform an input operation and the diagnostic findings corresponding to the diagnostic findings icon selected via the input device from among the plurality of diagnostic findings icons displayed on the monitor. It is preferable to include a diagnostic finding linking portion linked to the image.
It is preferable that the diagnostic findings associated with the ultrasonic diagnostic image by the diagnostic findings association unit are displayed on the monitor.
 強調度変更部は、類似度が高い診断所見に対応する診断所見アイコンほど強く強調されるように、複数の診断所見アイコンの強調度を変更することが好ましい。
 この場合に、強調度変更部は、複数の診断所見のうち、類似度が最も高い診断所見に対応する診断所見アイコンを、強調線により囲むことができる。
 また、強調度変更部は、複数の診断所見のうち、類似度が最も高い診断所見に対応する診断所見アイコンを、他の診断所見アイコンとは異なる色により表示することもできる。
 また、強調度変更部は、複数の診断所見のうち、類似度が最も高い診断所見に対応する診断所見アイコンを、他の診断所見アイコンよりも大きく表示することができる。
It is preferable that the emphasis changing unit changes the emphasis of the plurality of diagnostic findings icons so that the diagnostic findings icons corresponding to the diagnostic findings having a high degree of similarity are emphasized more strongly.
In this case, the emphasis changing unit can surround the diagnostic finding icon corresponding to the diagnostic finding having the highest degree of similarity among the plurality of diagnostic findings with a highlight line.
Further, the emphasis degree changing unit can also display the diagnostic findings icon corresponding to the diagnostic findings having the highest degree of similarity among the plurality of diagnostic findings in a color different from that of other diagnostic findings icons.
Further, the emphasis degree changing unit can display the diagnostic finding icon corresponding to the diagnostic finding having the highest degree of similarity among the plurality of diagnostic findings larger than the other diagnostic findings icons.
 超音波診断画像は、被検体の肺を撮像した超音波画像であり、複数の診断所見のうち少なくとも1つは、Bライン、硬化、正常、ラングスライディング無し、のいずれかの診断所見を含むことが好ましい。 The ultrasound diagnostic image is an ultrasound image of the lungs of the subject, and at least one of the plurality of diagnostic findings includes one of B-line, hardening, normal, and no rung sliding. Is preferable.
 超音波診断画像は、フリーズ時の静止画像であり、静止画像がモニタに表示されることができる。
 また、超音波診断画像は、動画像であってもよい。
 この場合に、超音波診断画像は、フリーズまでの定められた時間における動画像であることが好ましい。
The ultrasonic diagnostic image is a still image at the time of freezing, and the still image can be displayed on the monitor.
Further, the ultrasonic diagnostic image may be a moving image.
In this case, the ultrasonic diagnostic image is preferably a moving image at a predetermined time until the freeze.
 また、類似度判定部は、動画像を構成する複数フレームの超音波画像について複数の診断所見に対応する複数の画像パターンとの類似度をそれぞれ判定し、複数フレームの超音波画像のうち、類似度が最も高い超音波画像がモニタに表示され、強調度変更部は、類似度が最も高い超音波画像に基づいて複数の診断所見アイコンの強調度を変更することができる。 Further, the similarity determination unit determines the similarity of the ultrasonic images of the plurality of frames constituting the moving image with the plurality of image patterns corresponding to the plurality of diagnostic findings, and among the ultrasonic images of the plurality of frames, the similarity is determined. The ultrasonic image with the highest degree is displayed on the monitor, and the emphasis changing unit can change the emphasis of the plurality of diagnostic findings icons based on the ultrasonic image with the highest degree of similarity.
 本発明に係る超音波診断装置の制御方法は、超音波診断画像と定められた複数の診断所見に対応する複数の診断所見アイコンとをモニタに表示し、超音波診断画像と複数の診断所見に対応する複数の画像パターンとの類似度をそれぞれ判定し、判定された類似度に応じてモニタにおける複数の診断所見アイコンの強調度を変更することを特徴とする。 The control method of the ultrasonic diagnostic apparatus according to the present invention displays an ultrasonic diagnostic image and a plurality of diagnostic findings icons corresponding to a plurality of defined diagnostic findings on a monitor, and displays the ultrasonic diagnostic image and a plurality of diagnostic findings on the monitor. It is characterized in that the similarity with a plurality of corresponding image patterns is determined, and the emphasis of the plurality of diagnostic findings icons on the monitor is changed according to the determined similarity.
 本発明によれば、超音波プローブと、超音波プローブに接続された診断装置本体とを備え、診断装置本体は、超音波診断画像と定められた複数の診断所見に対応する複数の診断所見アイコンとを表示するモニタと、超音波診断画像と複数の診断所見に対応する複数の画像パターンとの類似度をそれぞれ判定する類似度判定部と、類似度判定部により判定された類似度に応じてモニタにおける複数の診断所見アイコンの強調度を変更する強調度変更部とを含むため、ユーザが超音波画像に対して診断所見を容易に付与することができる。 According to the present invention, an ultrasonic probe and a diagnostic device main body connected to the ultrasonic probe are provided, and the diagnostic device main body has a plurality of diagnostic findings icons corresponding to a plurality of diagnostic findings defined as an ultrasonic diagnostic image. According to the monitor that displays, the similarity determination unit that determines the similarity between the ultrasonic diagnostic image and the plurality of image patterns corresponding to the plurality of diagnostic findings, and the similarity determination unit that determines the similarity. Since it includes an emphasis changing unit that changes the emphasis of a plurality of diagnostic findings icons on the monitor, the user can easily give diagnostic findings to the ultrasonic image.
本発明の実施の形態1に係る超音波診断装置の構成を示すブロック図である。It is a block diagram which shows the structure of the ultrasonic diagnostic apparatus which concerns on Embodiment 1 of this invention. 本発明の実施の形態1における送受信回路の構成を示すブロック図である。It is a block diagram which shows the structure of the transmission / reception circuit in Embodiment 1 of this invention. 本発明の実施の形態1における超音波画像生成部の構成を示すブロック図である。It is a block diagram which shows the structure of the ultrasonic image generation part in Embodiment 1 of this invention. 本発明の実施の形態1における複数の診断所見アイコンの例を示す図である。It is a figure which shows the example of the plurality of diagnostic findings icons in Embodiment 1 of this invention. 本発明の実施の形態1において強調度が変更された診断所見アイコンの例を示す図である。It is a figure which shows the example of the diagnostic findings icon whose emphasis degree was changed in Embodiment 1 of this invention. 本発明の実施の形態1における超音波診断装置の動作を示すフローチャートである。It is a flowchart which shows the operation of the ultrasonic diagnostic apparatus in Embodiment 1 of this invention. 本発明の実施の形態1においてモニタに表示された診断箇所選択ボタンと超音波画像の例を示す図である。It is a figure which shows the example of the diagnosis part selection button and the ultrasonic image displayed on the monitor in Embodiment 1 of this invention. 本発明の実施の形態1においてモニタに表示された複数の診断所見アイコンの例を示す図である。It is a figure which shows the example of the plurality of diagnostic findings icons displayed on the monitor in Embodiment 1 of this invention. 本発明の実施の形態1における診断所見アイコンの他の表示例である。It is another display example of the diagnostic findings icon in Embodiment 1 of this invention. 本発明の実施の形態1における診断所見アイコンのさらに他の表示例である。It is still another display example of the diagnostic findings icon in Embodiment 1 of this invention. 本発明の実施の形態1における診断所見アイコンの他の例である。It is another example of the diagnostic findings icon in Embodiment 1 of this invention. 本発明の実施の形態1における診断所見アイコンと一緒に表示される胸水有無アイコンの例である。It is an example of the pleural effusion presence / absence icon displayed together with the diagnostic finding icon in Embodiment 1 of this invention. 本発明の実施の形態1におけるリニア型の超音波プローブに対応する診断所見アイコンの例を示す図である。It is a figure which shows the example of the diagnostic findings icon corresponding to the linear type ultrasonic probe in Embodiment 1 of this invention. 本発明の実施の形態1におけるリニア型の超音波プローブに対応する診断所見アイコンの他の例を示す図である。It is a figure which shows the other example of the diagnostic findings icon corresponding to the linear type ultrasonic probe in Embodiment 1 of this invention. 本発明の実施の形態1においてモニタに表示された超音波画像と診断所見アイコンの他の例である。It is another example of the ultrasonic image and the diagnostic finding icon displayed on the monitor in Embodiment 1 of this invention. 本発明の実施の形態2における超音波診断装置の動作を示すフローチャートである。It is a flowchart which shows the operation of the ultrasonic diagnostic apparatus in Embodiment 2 of this invention. 本発明の実施の形態2においてモニタに表示されたスライドバーを示す図である。It is a figure which shows the slide bar displayed on the monitor in Embodiment 2 of this invention.
 以下、この発明の実施の形態を添付図面に基づいて説明する。
 以下に記載する構成要件の説明は、本発明の代表的な実施態様に基づいてなされるが、本発明はそのような実施態様に限定されるものではない。
 なお、本明細書において、「~」を用いて表される数値範囲は、「~」の前後に記載される数値を下限値および上限値として含む範囲を意味する。
 本明細書において、「同一」、「同じ」は、技術分野で一般的に許容される誤差範囲を含むものとする。
Hereinafter, embodiments of the present invention will be described with reference to the accompanying drawings.
The description of the constituent elements described below is based on the representative embodiments of the present invention, but the present invention is not limited to such embodiments.
In the present specification, the numerical range represented by using "-" means a range including the numerical values before and after "-" as the lower limit value and the upper limit value.
In the present specification, "same" and "same" include an error range generally accepted in the technical field.
実施の形態1
 図1に、本発明の実施の形態1に係る超音波診断装置1の構成を示す。超音波診断装置1は、超音波プローブ2と診断装置本体3を備えている。
 超音波プローブ2は、振動子アレイ11を備えており、振動子アレイ11に送受信回路12が接続されている。
Embodiment 1
FIG. 1 shows the configuration of the ultrasonic diagnostic apparatus 1 according to the first embodiment of the present invention. The ultrasonic diagnostic apparatus 1 includes an ultrasonic probe 2 and a diagnostic apparatus main body 3.
The ultrasonic probe 2 includes an oscillator array 11, and a transmission / reception circuit 12 is connected to the oscillator array 11.
 診断装置本体3は、画像生成部13を備えており、画像生成部13は、超音波プローブ2の送受信回路12に接続されている。また、画像生成部13に、表示制御部14およびモニタ15が順次接続されている。また、画像生成部13に画像メモリ16が接続されている。また、診断装置本体3は、画像パターンメモリ17を備えている。画像メモリ16および画像パターンメモリ17に、類似度判定部18が接続され、類似度判定部18に強調度変更部19が接続されている。強調度変更部19は、表示制御部14に接続されている。また、画像メモリ16に、診断所見紐付け部20が接続されている。診断所見紐付け部20は、表示制御部14に接続されている。 The diagnostic device main body 3 includes an image generation unit 13, and the image generation unit 13 is connected to the transmission / reception circuit 12 of the ultrasonic probe 2. Further, the display control unit 14 and the monitor 15 are sequentially connected to the image generation unit 13. Further, the image memory 16 is connected to the image generation unit 13. Further, the diagnostic apparatus main body 3 includes an image pattern memory 17. The similarity determination unit 18 is connected to the image memory 16 and the image pattern memory 17, and the emphasis change unit 19 is connected to the similarity determination unit 18. The emphasis changing unit 19 is connected to the display control unit 14. Further, the diagnostic finding linking portion 20 is connected to the image memory 16. The diagnostic finding linking unit 20 is connected to the display control unit 14.
 また、超音波プローブ2の送受信回路12、画像生成部13、表示制御部14、画像メモリ16、画像パターンメモリ17、類似度判定部18、強調度変更部19および診断所見紐付け部20に、本体制御部21が接続されている。また、本体制御部21に入力装置22が接続されている。
 また、画像生成部13、表示制御部14、類似度判定部18、強調度変更部19、診断所見紐付け部20および本体制御部21によりプロセッサ23が構成されている。
Further, the transmission / reception circuit 12 of the ultrasonic probe 2, the image generation unit 13, the display control unit 14, the image memory 16, the image pattern memory 17, the similarity determination unit 18, the emphasis change unit 19, and the diagnostic finding linking unit 20. The main body control unit 21 is connected. Further, the input device 22 is connected to the main body control unit 21.
Further, the processor 23 is composed of an image generation unit 13, a display control unit 14, a similarity determination unit 18, an emphasis degree changing unit 19, a diagnostic finding linking unit 20, and a main body control unit 21.
 図1に示す超音波プローブ2の振動子アレイ11は、1次元または2次元に配列された複数の超音波振動子を有している。これらの超音波振動子は、それぞれ送受信回路12から供給される駆動信号に従って超音波を送信すると共に、被検体からの超音波エコーを受信して、超音波エコーに基づく信号を出力する。各超音波振動子は、例えば、PZT(Lead Zirconate Titanate:チタン酸ジルコン酸鉛)に代表される圧電セラミック、PVDF(Poly Vinylidene Di Fluoride:ポリフッ化ビニリデン)に代表される高分子圧電素子およびPMN-PT(Lead Magnesium Niobate-Lead Titanate:マグネシウムニオブ酸鉛-チタン酸鉛固溶体)に代表される圧電単結晶等からなる圧電体の両端に電極を形成することにより構成される。 The oscillator array 11 of the ultrasonic probe 2 shown in FIG. 1 has a plurality of ultrasonic oscillators arranged one-dimensionally or two-dimensionally. Each of these ultrasonic transducers transmits ultrasonic waves according to a drive signal supplied from the transmission / reception circuit 12, receives ultrasonic echoes from a subject, and outputs a signal based on the ultrasonic echoes. Each ultrasonic transducer is, for example, a piezoelectric ceramic represented by PZT (Lead Zirconate Titanate), a polymer piezoelectric element represented by PVDF (Poly Vinylidene Di Fluoride), and PMN-. It is configured by forming electrodes at both ends of a piezoelectric body made of a piezoelectric single crystal or the like represented by PT (Lead Magnesium Niobate-Lead Titanate: lead magnesiumidene fluoride-lead titanate solid solution).
 送受信回路12は、本体制御部21による制御の下で、振動子アレイ11から超音波を送信し且つ振動子アレイ11により取得された受信信号に基づいて音線信号を生成する。送受信回路12は、図2に示すように、振動子アレイ11に接続されるパルサ31と、振動子アレイ11から順次直列に接続される増幅部32、AD(Analog Digital)変換部33、およびビームフォーマ34を有している。 The transmission / reception circuit 12 transmits ultrasonic waves from the oscillator array 11 and generates a sound line signal based on the received signal acquired by the oscillator array 11 under the control of the main body control unit 21. As shown in FIG. 2, the transmission / reception circuit 12 includes a pulser 31 connected to the oscillator array 11, an amplification unit 32 sequentially connected in series from the oscillator array 11, an AD (Analog Digital) conversion unit 33, and a beam. It has a former 34.
 パルサ31は、例えば、複数のパルス発生器を含んでおり、本体制御部21からの制御信号に応じて選択された送信遅延パターンに基づいて、振動子アレイ11の複数の超音波振動子から送信される超音波が超音波ビームを形成するようにそれぞれの駆動信号を、遅延量を調節して複数の超音波振動子に供給する。このように、振動子アレイ11の超音波振動子の電極にパルス状または連続波状の電圧が印加されると、圧電体が伸縮し、それぞれの超音波振動子からパルス状または連続波状の超音波が発生して、それらの超音波の合成波から、超音波ビームが形成される。 The pulsar 31 includes, for example, a plurality of pulse generators, and transmits from a plurality of ultrasonic oscillators of the oscillator array 11 based on a transmission delay pattern selected according to a control signal from the main body control unit 21. Each drive signal is supplied to a plurality of ultrasonic transducers by adjusting the delay amount so that the ultrasonic waves to be generated form an ultrasonic beam. As described above, when a pulsed or continuous wave voltage is applied to the electrodes of the ultrasonic vibrator of the vibrator array 11, the piezoelectric body expands and contracts, and the pulsed or continuous wave ultrasonic waves are generated from the respective ultrasonic vibrators. Is generated, and an ultrasonic beam is formed from the combined wave of those sound waves.
 送信された超音波ビームは、例えば、被検体の部位等の対象において反射され、超音波プローブ2の振動子アレイ11に向かって伝搬する。このように振動子アレイ11に向かって伝搬する超音波エコーは、振動子アレイ11を構成するそれぞれの超音波振動子により受信される。この際に、振動子アレイ11を構成するそれぞれの超音波振動子は、伝搬する超音波エコーを受信することにより伸縮して、電気信号である受信信号を発生させ、これらの受信信号を増幅部32に出力する。 The transmitted ultrasonic beam is reflected by, for example, a target such as a site of a subject, and propagates toward the oscillator array 11 of the ultrasonic probe 2. The ultrasonic echo propagating toward the oscillator array 11 in this way is received by each ultrasonic oscillator constituting the oscillator array 11. At this time, each ultrasonic oscillator constituting the oscillator array 11 expands and contracts by receiving the propagating ultrasonic echo, generates a received signal which is an electric signal, and amplifies these received signals. Output to 32.
 増幅部32は、振動子アレイ11を構成するそれぞれの超音波振動子から入力された信号を増幅し、増幅した信号をAD変換部33に送信する。AD変換部33は、増幅部32から送信された信号をデジタルの受信データに変換する。ビームフォーマ34は、AD変換部33から受け取った各受信データに対してそれぞれの遅延を与えて加算することにより、いわゆる受信フォーカス処理を行う。この受信フォーカス処理により、AD変換部33で変換された各受信データが整相加算され且つ超音波エコーの焦点が絞り込まれた音線信号が取得される。 The amplification unit 32 amplifies the signal input from each ultrasonic vibrator constituting the vibrator array 11, and transmits the amplified signal to the AD conversion unit 33. The AD conversion unit 33 converts the signal transmitted from the amplification unit 32 into digital reception data. The beam former 34 performs so-called reception focus processing by giving and adding delays to each received data received from the AD conversion unit 33. By this reception focus processing, each reception data converted by the AD conversion unit 33 is phase-adjusted and added, and a sound line signal in which the focus of the ultrasonic echo is narrowed down is acquired.
 画像生成部13は、図3に示すように、信号処理部35、DSC(Digital Scan Converter:デジタルスキャンコンバータ)36および画像処理部37が順次直列に接続された構成を有している。 As shown in FIG. 3, the image generation unit 13 has a configuration in which a signal processing unit 35, a DSC (Digital Scan Converter) 36, and an image processing unit 37 are sequentially connected in series.
 信号処理部35は、送受信回路12から受信した音線信号に対し、本体制御部21により設定される音速値を用いて超音波の反射位置の深度に応じて距離による減衰の補正を施した後、包絡線検波処理を施すことにより、被検体内の組織に関する断層画像情報であるBモード画像信号を生成する。 The signal processing unit 35 corrects the attenuation of the sound line signal received from the transmission / reception circuit 12 by the distance according to the depth of the ultrasonic reflection position using the sound velocity value set by the main body control unit 21. By performing the envelope detection process, a B-mode image signal, which is tomographic image information about the tissue in the subject, is generated.
 DSC36は、信号処理部35で生成されたBモード画像信号を通常のテレビジョン信号の走査方式に従う画像信号に変換(ラスター変換)する。
 画像処理部37は、DSC36から入力されるBモード画像信号に階調処理等の各種の必要な画像処理を施した後、Bモード画像信号を表示制御部14および画像メモリ16に送出する。以降は、画像処理部37により画像処理が施されたBモード画像信号を、超音波画像と呼ぶ。
The DSC 36 converts the B-mode image signal generated by the signal processing unit 35 into an image signal according to a normal television signal scanning method (raster conversion).
The image processing unit 37 performs various necessary image processing such as gradation processing on the B mode image signal input from the DSC 36, and then sends the B mode image signal to the display control unit 14 and the image memory 16. Hereinafter, the B-mode image signal processed by the image processing unit 37 is referred to as an ultrasonic image.
 画像メモリ16は、画像生成部13により生成された超音波画像を保存するためのものである。画像メモリ16に保存された超音波画像は、本体制御部21の制御の下で読み出され、表示制御部14、類似度判定部18および診断所見紐付け部20に送出される。 The image memory 16 is for storing the ultrasonic image generated by the image generation unit 13. The ultrasonic image stored in the image memory 16 is read out under the control of the main body control unit 21, and is sent to the display control unit 14, the similarity determination unit 18, and the diagnostic finding linking unit 20.
 画像メモリ16としては、例えば、フラッシュメモリ、HDD(Hard Disc Drive:ハードディスクドライブ)、SSD(Solid State Drive:ソリッドステートドライブ)、FD(Flexible Disc:フレキシブルディスク)、MOディスク(Magneto-Optical disc:光磁気ディスク)、MT(Magnetic Tape:磁気テープ)、RAM(Random Access Memory:ランダムアクセスメモリ)、CD(Compact Disc:コンパクトディスク)、DVD(Digital Versatile Disc:デジタルバーサタイルディスク)、SDカード(Secure Digital card:セキュアデジタルカード)、USBメモリ(Universal Serial Bus memory:ユニバーサルシリアルバスメモリ)等の記録メディア等を用いることができる。 Examples of the image memory 16 include a flash memory, an HDD (Hard Disc Drive), an SSD (Solid State Drive), an FD (Flexible Disc), and an MO disk (Magneto-Optical disc). Magnetic disc), MT (Magnetic Tape), RAM (Random Access Memory), CD (Compact Disc: compact disc), DVD (Digital Versatile Disc), SD card (Secure Digital card) : Secure digital card), recording media such as USB memory (Universal Serial Bus memory) can be used.
 画像パターンメモリ17は、被検体の部位に対して定められた複数の診断所見に対応する複数の画像パターンを保存するものである。例えば、被検体の肺に対する診断所見として、いわゆるBライン、硬化、正常およびラングスライディング無しの診断所見が知られており、これらの診断所見に対応して超音波画像中に現れる特徴的な画像パターンも知られている。これらの診断所見に対応する画像パターンは、例えばユーザにより予め画像パターンメモリ17に保存されることができる。 The image pattern memory 17 stores a plurality of image patterns corresponding to a plurality of diagnostic findings defined for the site of the subject. For example, diagnostic findings on the lungs of a subject are known as so-called B-line, sclerosing, normal and without rung-sliding, and characteristic image patterns appearing in ultrasound images corresponding to these diagnostic findings. Is also known. The image pattern corresponding to these diagnostic findings can be stored in the image pattern memory 17 in advance by the user, for example.
 また、画像パターンメモリ17として、画像メモリ16と同様に、例えば、フラッシュメモリ、HDD、SSD、FD、MOディスク、MT、RAM、CD、DVD、SDカード、または、USBメモリ等の記録メディア等を用いることができる。 Further, as the image pattern memory 17, similarly to the image memory 16, for example, a flash memory, an HDD, an SSD, an FD, a MO disk, an MT, a RAM, a CD, a DVD, an SD card, a recording medium such as a USB memory, or the like can be used. Can be used.
 類似度判定部18は、画像生成部13により生成され且つ画像メモリ16に保存された超音波診断画像と、画像パターンメモリ17に保存されている複数の画像パターンとの類似度をそれぞれ判定する。例えば、画像パターンメモリ17に、Bライン、硬化、正常およびラングスライディング無しの4つの診断所見に対応する画像パターンが保存されている場合に、類似度判定部18は、4つの画像パターンと超音波診断画像とのそれぞれの類似度を判定し、4つの類似度の値を得る。
 ここで、超音波診断画像は、画像生成部13により生成された1フレームの超音波画像からなる静止画像および複数フレームの超音波画像からなる動画像を含む。
The similarity determination unit 18 determines the similarity between the ultrasonic diagnostic image generated by the image generation unit 13 and stored in the image memory 16 and the plurality of image patterns stored in the image pattern memory 17. For example, when the image pattern memory 17 stores image patterns corresponding to four diagnostic findings of B line, curing, normality, and no rung sliding, the similarity determination unit 18 uses the four image patterns and ultrasonic waves. The similarity with the diagnostic image is determined, and four similarity values are obtained.
Here, the ultrasonic diagnostic image includes a still image composed of a one-frame ultrasonic image generated by the image generation unit 13 and a moving image composed of a plurality of frames of ultrasonic images.
 類似度を判定する方法として、類似度判定部18は、例えば、単純なテンプレートマッチングを用いる方法、Csurka et al.: Visual Categorization with Bags of Keypoints, Proc. of ECCV Workshop on Statistical Learning in Computer Vision, pp.59-74 (2004)に記載されている機械学習手法、あるいは、Krizhevsk et al.: ImageNet Classification with Deep Convolutional Neural Networks, Advances in Neural Information Processing Systems 25, pp.1106-1114 (2012)に記載されているディープラーニングを用いた一般画像認識手法等を用いることができる。 As a method for determining the similarity, the similarity determination unit 18 may use, for example, a method using simple template matching, Csurka et al .: Visual Categorization with Bags of Keypoints, Proc. Of ECCV Workshop on Statistical Learning in Computer Vision, pp. Described in the machine learning method described in .59-74 (2004), or in Krizhevsk et al .: ImageNet Classification with Deep Convolutional Neural Networks, Advances in Neural Information Processing Systems 25, pp.1106-1114 (2012). It is possible to use a general image recognition method or the like using deep learning.
 強調度変更部19は、被検体の部位に対する複数の診断所見に対応する複数の診断所見アイコンを、モニタ15における定められた表示位置と共に記憶しており、類似度判定部18により判定された複数の診断所見に対応するそれぞれの類似度に応じて、複数の診断所見アイコンの強調度を変更する。ここで、ユーザが診断所見アイコンJ1~J4と診断所見を容易に対応付けて認識できるように、診断所見アイコンJ1~J4は、それぞれ、対応する診断所見の画像パターンを模したデザインを有している。
 また、強調度変更部19は、例えば、類似度が高い診断所見に対応する診断所見アイコンJ1~J4ほど強く強調されるように、複数の診断所見アイコンの強調度を変更することができる。
The emphasis changing unit 19 stores a plurality of diagnostic findings icons corresponding to a plurality of diagnostic findings on the site of the subject together with a predetermined display position on the monitor 15, and the plurality of diagnostic findings determined by the similarity determination unit 18. The emphasis of multiple diagnostic findings icons is changed according to the similarity of each of the diagnostic findings. Here, the diagnostic findings icons J1 to J4 each have a design imitating the image pattern of the corresponding diagnostic findings so that the user can easily associate and recognize the diagnostic findings icons J1 to J4. There is.
Further, the emphasis changing unit 19 can change the emphasis of a plurality of diagnostic findings icons so that, for example, the diagnostic findings icons J1 to J4 corresponding to the diagnostic findings having a high degree of similarity are emphasized more strongly.
 例えば、強調度変更部19は、図4に示すように、被検体の肺に対して、正常(N)、ラングスライディング無し(S(-))、Bライン(B)、および、硬化(C)(コンソリデーション:Consolidation)の4つの診断所見アイコンJ1~J4を、左から順に、診断所見アイコンJ1、J2、J3、J4と配列した表示位置と共に記憶しているとする。類似度判定部18により、例えば、Bライン、硬化、正常、ラングスライディング無しの順に値が低くなるように類似度が判定された場合に、強調度変更部19は、図5に示すように、類似度が最も高いBラインの診断所見に対応する診断所見アイコンJ3を強調線L1により囲むことで、診断所見アイコンJ3の強調度を変更することができる。
 このようにして強調度が変更された複数の診断所見アイコンJ1~J4は、表示制御部14に送出され、モニタ15に表示される。
For example, as shown in FIG. 4, the emphasis changing unit 19 is normal (N), no rung sliding (S (−)), B line (B), and hardening (C) with respect to the lung of the subject. ) (Consolidation), the four diagnostic findings icons J1 to J4 are stored together with the display positions arranged with the diagnostic findings icons J1, J2, J3, and J4 in order from the left. When the similarity is determined by the similarity determination unit 18 so that the values decrease in the order of, for example, B line, curing, normal, and no rung sliding, the emphasis changing unit 19 determines the similarity, as shown in FIG. The emphasis of the diagnostic finding icon J3 can be changed by surrounding the diagnostic finding icon J3 corresponding to the diagnostic finding of the B line having the highest degree of similarity with the highlight line L1.
The plurality of diagnostic findings icons J1 to J4 whose emphasis is changed in this way are sent to the display control unit 14 and displayed on the monitor 15.
 ここで、正常の診断所見とは、超音波画像において、胸膜の境界と、超音波の多重反射に起因する、深さ方向に直交する方向に沿って延びるアーチファクト(いわゆるAライン)とが含まれ且つ超音波画像に写る胸膜の境界が、連続的な複数フレームの超音波画像において一定以上変位する(いわゆるラングスライディングが認められる)所見をいう。このように、正常の所見は、超音波画像においてAラインを含み且つラングスライディングが認められる所見である。ラングスライディング無しの所見とは、超音波画像において、胸膜の境界と、多重反射に起因する、深さ方向に直交する方向に沿って延びるアーチファクト(Aライン)とが含まれ、且つ、いわゆる気胸等により、超音波画像に写る胸膜の境界が、連続的な複数フレームの超音波画像においてほとんど変位しない(ラングスライディングが認められない)所見をいう。このように、ラングスライディング無しの所見は、正常の所見と同様に超音波画像においてAラインを含んでいるが、ラングスライディングが認められない所見であり、一般的に、いわゆる気胸の疑いを示すことが知られている。Bラインの診断所見とは、胸膜に水が溜まる等により深さ方向に沿った線状のパターンが超音波画像に含まれる所見をいう。また、硬化の所見とは、肺に水が溜まる等により粒状のパターンが超音波画像に含まれる所見をいう。 Here, the normal diagnostic findings include the boundary of the thoracic membrane and the artifact (so-called A line) extending along the direction orthogonal to the depth direction due to the multiple reflection of the ultrasonic wave in the ultrasonic image. Moreover, it is a finding that the boundary of the thoracic membrane reflected in the ultrasonic image is displaced by a certain amount or more in a continuous multi-frame ultrasonic image (so-called rung sliding is recognized). Thus, the normal findings are those that include the A line and show rung sliding in the ultrasound image. Findings without rung sliding include, in ultrasound images, pleural boundaries and artifacts (A-lines) extending along a direction orthogonal to the depth direction due to multiple reflections, and so-called pneumothorax, etc. Therefore, it is a finding that the boundary of the pleura reflected in the ultrasonic image is hardly displaced (no rung sliding is observed) in the continuous multi-frame ultrasonic image. Thus, the findings without rung-sliding include the A-line in the ultrasound image, similar to the normal findings, but no rung-sliding is observed and generally indicate a suspicion of so-called pneumothorax. It has been known. The diagnostic findings of the B line are findings in which a linear pattern along the depth direction is included in the ultrasonic image due to the accumulation of water in the pleura or the like. Further, the finding of hardening means a finding that a granular pattern is included in the ultrasonic image due to the accumulation of water in the lungs or the like.
 本体制御部21は、予め記録されたプログラム等に従って超音波プローブ2の各部および診断装置本体3の各部を制御する。
 表示制御部14は、本体制御部21の制御の下、画像生成部13により生成された超音波画像、強調度変更部19により強調度が変更された複数の診断所見アイコンJ1~J4等に対して所定の処理を施して、モニタ15に表示する。
The main body control unit 21 controls each part of the ultrasonic probe 2 and each part of the diagnostic apparatus main body 3 according to a program or the like recorded in advance.
The display control unit 14 controls the ultrasonic image generated by the image generation unit 13 and the plurality of diagnostic findings icons J1 to J4 whose emphasis is changed by the emphasis change unit 19 under the control of the main body control unit 21. After performing a predetermined process, the image is displayed on the monitor 15.
 モニタ15は、表示制御部14による制御の下、種々の表示を行う。モニタ15は、例えば、LCD(Liquid Crystal Display:液晶ディスプレイ)、有機ELディスプレイ(Organic Electroluminescence Display)等のディスプレイ装置を含む。 The monitor 15 performs various displays under the control of the display control unit 14. The monitor 15 includes, for example, a display device such as an LCD (Liquid Crystal Display) and an organic EL display (Organic Electroluminescence Display).
 入力装置22は、ユーザが入力操作を行うためのものである。入力装置22は、例えば、キーボード、マウス、トラックボール、タッチパッドおよびタッチパネル等のユーザが入力操作を行うための装置等により構成される。 The input device 22 is for the user to perform an input operation. The input device 22 is composed of, for example, a keyboard, a mouse, a trackball, a touch pad, a touch panel, and other devices for the user to perform an input operation.
 診断所見紐付け部20は、モニタ15に表示された診断所見アイコンJ1~J4のうち、入力装置22を介してユーザにより選択された診断所見アイコンに対応する診断所見を超音波画像に紐付ける。例えば、図5に示すように4つの診断所見アイコンJ1~J4がモニタ15に表示され、最も類似度が高いBラインの診断所見に対応する診断所見アイコンJ3が入力装置22を介してユーザにより選択された場合に、類似度判定部18により類似度の判定に使用された超音波画像と、ユーザに選択された診断所見アイコンJ3に対応するBラインの診断所見が紐付けられる。 The diagnostic findings linking unit 20 links the diagnostic findings corresponding to the diagnostic findings icons selected by the user via the input device 22 among the diagnostic findings icons J1 to J4 displayed on the monitor 15 to the ultrasonic image. For example, as shown in FIG. 5, four diagnostic findings icons J1 to J4 are displayed on the monitor 15, and the diagnostic findings icons J3 corresponding to the diagnostic findings of the B line having the highest similarity are selected by the user via the input device 22. When this is done, the ultrasonic image used for determining the similarity by the similarity determination unit 18 is associated with the diagnostic findings of the B line corresponding to the diagnostic findings icon J3 selected by the user.
 なお、画像生成部13、表示制御部14、類似度判定部18、強調度変更部19、診断所見紐付け部20および本体制御部21を含むプロセッサ23は、CPU(Central Processing Unit:中央処理装置)、および、CPUに各種の処理を行わせるための制御プログラムから構成されるが、FPGA(Field Programmable Gate Array:フィードプログラマブルゲートアレイ)、DSP(Digital Signal Processor:デジタルシグナルプロセッサ)、ASIC(Application Specific Integrated Circuit:アプリケーションスペシフィックインテグレイテッドサーキット)、GPU(Graphics Processing Unit:グラフィックスプロセッシングユニット)、その他のIC(Integrated Circuit:集積回路)を用いて構成されてもよく、もしくはそれらを組み合わせて構成されてもよい。 The processor 23 including the image generation unit 13, the display control unit 14, the similarity determination unit 18, the emphasis change unit 19, the diagnostic finding linking unit 20, and the main body control unit 21 is a CPU (Central Processing Unit). ), And a control program for causing the CPU to perform various processes, such as FPGA (Field Programmable Gate Array), DSP (Digital Signal Processor), and ASIC (Application Specific). Integrated Circuit: Application-specific integrated circuit), GPU (Graphics Processing Unit), and other ICs (Integrated Circuit: integrated circuit) may be used, or they may be combined. good.
 また、画像生成部13、表示制御部14、類似度判定部18、強調度変更部19、診断所見紐付け部20および本体制御部21は、部分的にあるいは全体的に1つのCPU等に統合させて構成されることもできる。 Further, the image generation unit 13, the display control unit 14, the similarity determination unit 18, the emphasis change unit 19, the diagnostic finding linking unit 20, and the main body control unit 21 are partially or wholly integrated into one CPU or the like. It can also be configured by letting it.
 次に、図6に示すフローチャートを用いて、本発明の実施の形態1に係る超音波診断装置1の動作を説明する。以下の動作説明では、被検体の肺を検査する例を説明するが、被検体の検査部位は肺に限定されない。 Next, the operation of the ultrasonic diagnostic apparatus 1 according to the first embodiment of the present invention will be described with reference to the flowchart shown in FIG. In the following operation explanation, an example of inspecting the lung of the subject will be described, but the inspection site of the subject is not limited to the lung.
 また、以下の動作説明において、超音波診断装置1は、入力装置22としてモニタ15に重ねて配置されたタッチセンサを備えている。
 また、画像パターンメモリ17に、被検体の肺の複数の診断所見に対応する複数の画像パターンが保存されている。また、強調度変更部19は、被検体の肺の複数の診断所見に対応する複数の診断所見アイコンJ1~J4を記憶している。
 また、モニタ15は、例えば図7に示すように、第1表示領域A1、第2表示領域A2および第3表示領域A3を有している。
Further, in the following operation description, the ultrasonic diagnostic apparatus 1 includes a touch sensor arranged on the monitor 15 as an input device 22.
Further, a plurality of image patterns corresponding to a plurality of diagnostic findings of the lung of the subject are stored in the image pattern memory 17. Further, the emphasis changing unit 19 stores a plurality of diagnostic findings icons J1 to J4 corresponding to a plurality of diagnostic findings in the lungs of the subject.
Further, as shown in FIG. 7, for example, the monitor 15 has a first display area A1, a second display area A2, and a third display area A3.
 第1表示領域A1は、超音波画像Uを表示するための領域である。
 第2表示領域A2は、被検体の左右の肺のいずれかを検査部位として設定するための左右切り替えボタンLRと、被検体の検査箇所を選択するための4つの検査箇所選択アイコンP1~P4と、ボディマークBMを含んでいる。検査箇所選択アイコンP1~P4は、それぞれ、被検体の肺の検査箇所に対応している。検査箇所選択アイコンP1~P4は、左右切り替えボタンLRがタップされることにより、右の肺の検査箇所に対応する「1R」~「4R」と、左の肺の検査箇所に対応する「1L」~「4L」に切り替わる。図7の例では、検査箇所選択アイコンP1~P4は、「1R」~「4R」という名称で登録されている右の肺の検査箇所にそれぞれ対応している。
The first display area A1 is an area for displaying the ultrasonic image U.
The second display area A2 includes a left / right switching button LR for setting one of the left and right lungs of the subject as an inspection site, and four inspection site selection icons P1 to P4 for selecting an inspection location of the subject. , Includes body mark BM. The test site selection icons P1 to P4 correspond to the test site of the lung of the subject, respectively. The inspection site selection icons P1 to P4 are "1R" to "4R" corresponding to the inspection location of the right lung and "1L" corresponding to the inspection location of the left lung by tapping the left / right switching button LR. -Switches to "4L". In the example of FIG. 7, the inspection site selection icons P1 to P4 correspond to the inspection sites of the right lung registered under the names “1R” to “4R”, respectively.
 また、ボディマークBMは、被検体の胴部分を表す模式図M1、プローブマークM2および検査箇所マークM3を含んでいる。左右切り替えボタンLRがタップされることにより、右の肺を前面側に向けた模式図M1を含むボディマークBMと左の肺を前面側に向けた模式図M1を含むボディマークBMに切り替わる。図7の例では、右の肺を前面側に向けた模式図M1を含むボディマークBMが示されている。 Further, the body mark BM includes a schematic diagram M1 representing a body portion of a subject, a probe mark M2, and an inspection site mark M3. By tapping the left / right switching button LR, the body mark BM including the schematic diagram M1 with the right lung facing the front side and the body mark BM including the schematic diagram M1 with the left lung facing the front side are switched. In the example of FIG. 7, a body mark BM including a schematic view M1 with the right lung facing the front side is shown.
 ボディマークBMにおいて、プローブマークM2および検査箇所マークM3は、検査箇所選択アイコンP1~P4のそれぞれに対応する模式図M1上の位置に配置されて、検査箇所を視覚的に示すものである。検査箇所選択アイコンP1~P4のいずれかがタップされると、タップされた検査箇所選択アイコンP1~P4に対応するボディマークBMがモニタ15の第2表示領域A2に表示される。 In the body mark BM, the probe mark M2 and the inspection location mark M3 are arranged at positions on the schematic diagram M1 corresponding to each of the inspection location selection icons P1 to P4 to visually indicate the inspection location. When any of the inspection location selection icons P1 to P4 is tapped, the body mark BM corresponding to the tapped inspection location selection icons P1 to P4 is displayed in the second display area A2 of the monitor 15.
 第3表示領域A3は、超音波画像UをフリーズさせるためのフリーズボタンB1等、超音波診断装置1の動作に関する指令を入力するためのユーザインターフェースを含んでいる。ここで、超音波画像Uをフリーズするとは、画像生成部13により連続的に生成され且つモニタ15に順次表示されている超音波画像Uの生成を停止し、モニタ15に最新の1フレームの超音波画像Uを表示することである。 The third display area A3 includes a user interface for inputting commands related to the operation of the ultrasonic diagnostic apparatus 1, such as a freeze button B1 for freezing the ultrasonic image U. Here, to freeze the ultrasonic image U means to stop the generation of the ultrasonic image U continuously generated by the image generation unit 13 and sequentially displayed on the monitor 15, and the latest one frame of the ultrasonic image U is superposed on the monitor 15. It is to display the sound wave image U.
 まず、ステップS1において、入力装置22を介してユーザにより、被検体の肺を検査するための検査箇所が指定され、指定された検査箇所が本体制御部21により受け付けられる。例えば、ユーザが、左右切り替えボタンLRをタップして右の肺を検査部位として選択し、「1R」の検査箇所に対応する検査箇所選択アイコンP1をタップして選択すると、「1R」の検査箇所が本体制御部21により受け付けられる。このようにして「1R」の検査箇所が受け付けられた場合に、例えば、モニタ15の第1表示領域A1に、「1R」の文字が表示され、第2表示領域A2に、「1R」の検査箇所に対応するボディマークBMが表示される。 First, in step S1, the user designates an inspection location for inspecting the lung of the subject via the input device 22, and the designated inspection location is accepted by the main body control unit 21. For example, when the user taps the left / right switching button LR to select the right lung as the inspection site and taps the inspection site selection icon P1 corresponding to the inspection location of "1R" to select the inspection location of "1R". Is accepted by the main body control unit 21. When the inspection location of "1R" is received in this way, for example, the character "1R" is displayed in the first display area A1 of the monitor 15, and the inspection of "1R" is displayed in the second display area A2. The body mark BM corresponding to the location is displayed.
 次に、ステップS2において、ユーザが超音波プローブ2を被検体の体表に接触させ、この状態で超音波画像Uの撮影が行われる。
 この際に、送受信回路12は、本体制御部21の制御の下で、予め設定された音速値を用いて受信フォーカス処理を行って、音線信号を生成する。このようにして送受信回路12により生成された音線信号は、画像生成部13に送出される。画像生成部13は、送受信回路12から送出された音線信号を用いて超音波画像Uを生成する。
Next, in step S2, the user brings the ultrasonic probe 2 into contact with the body surface of the subject, and the ultrasonic image U is taken in this state.
At this time, the transmission / reception circuit 12 performs reception focus processing using preset sound velocity values under the control of the main body control unit 21 to generate a sound line signal. The sound line signal generated by the transmission / reception circuit 12 in this way is transmitted to the image generation unit 13. The image generation unit 13 generates an ultrasonic image U using the sound line signal transmitted from the transmission / reception circuit 12.
 続くステップS3において、ステップS2で生成された超音波画像Uが表示制御部14に送出されてモニタ15に表示され、且つ、その超音波画像Uが画像メモリ16に保存される。 In the following step S3, the ultrasonic image U generated in step S2 is sent to the display control unit 14 and displayed on the monitor 15, and the ultrasonic image U is stored in the image memory 16.
 ステップS4において、本体制御部21は、入力装置22を介してユーザにより超音波画像Uをフリーズする指示が入力されたか否かを判定する。 In step S4, the main body control unit 21 determines whether or not an instruction to freeze the ultrasonic image U has been input by the user via the input device 22.
 本体制御部21は、例えば、モニタ15の第3表示領域A3に表示されているフリーズボタンB1がユーザによりタップされた場合に、フリーズの指示がなされたと判定する。また、本体制御部21は、ユーザによりフリーズボタンB1がタップされない場合に、フリーズの指示がなされていないと判定する。 The main body control unit 21 determines that the freeze instruction has been given, for example, when the freeze button B1 displayed in the third display area A3 of the monitor 15 is tapped by the user. Further, the main body control unit 21 determines that the freeze instruction has not been given when the freeze button B1 is not tapped by the user.
 フリーズの指示がなされていないと判定された場合に、ステップS2に戻り、超音波画像Uが新たに撮影される。このステップS2で生成された超音波画像Uは、続くステップS3においてモニタ15に表示されると共に、画像メモリ16に保存される。ステップS3が完了するとステップS4に進み、超音波画像Uがフリーズされたか否かが判定される。 If it is determined that the freeze instruction has not been given, the process returns to step S2, and the ultrasonic image U is newly captured. The ultrasonic image U generated in step S2 is displayed on the monitor 15 and stored in the image memory 16 in the subsequent step S3. When step S3 is completed, the process proceeds to step S4, and it is determined whether or not the ultrasonic image U is frozen.
 このようにしてステップS2~ステップS4が繰り返されることにより、超音波画像Uが連続的に生成され且つモニタ15に表示される。また、ステップS2~ステップS4の繰り返しにより、複数フレームの超音波画像Uが画像メモリ16に保存される。 By repeating steps S2 to S4 in this way, the ultrasonic image U is continuously generated and displayed on the monitor 15. Further, by repeating steps S2 to S4, the ultrasonic image U of a plurality of frames is stored in the image memory 16.
 フリーズの指示がなされたとステップS4で判定された場合には、超音波画像Uの生成が停止されると共に最新のフレームの超音波画像Uがモニタ15に表示されることにより、超音波画像Uがフリーズされて、ステップS5に進む。
 ステップS5において、類似度判定部18は、ステップS2~ステップS4の繰り返しにより画像メモリ16に保存された複数フレームの超音波画像Uのうち、フリーズまでの定められた時間における動画像、すなわち、超音波画像Uがフリーズされるまでの定められた時間内に連続的に生成された複数フレームの超音波画像Uのそれぞれと、画像パターンメモリ17に保存されている複数の画像パターンとの類似度を判定する。ここで、定められた時間は、例えば、1秒間~3秒間程度の数秒間に設定される。
When it is determined in step S4 that the freeze instruction has been given, the generation of the ultrasonic image U is stopped and the ultrasonic image U of the latest frame is displayed on the monitor 15, so that the ultrasonic image U is displayed. It is frozen and proceeds to step S5.
In step S5, the similarity determination unit 18 is a moving image of the plurality of frames of the ultrasonic image U stored in the image memory 16 by repeating steps S2 to S4, that is, a moving image at a predetermined time until freezing, that is, super The degree of similarity between each of the plurality of frames of the ultrasonic image U continuously generated within a predetermined time until the ultrasonic image U freezes and the plurality of image patterns stored in the image pattern memory 17. judge. Here, the defined time is set to a few seconds, for example, about 1 second to 3 seconds.
 ここで、例えば、Bライン、硬化、正常およびラングスライディング無しの4つの診断所見に対応するそれぞれの画像パターンと、超音波画像Uとの類似度が算出される場合に、Bラインおよび硬化の診断所見に対して、それぞれ、1フレームの超音波画像Uを用いて類似度が判定できるが、正常およびラングスライディング無しの診断所見に対しては、超音波画像U内の胸膜の境界の動きを判別する必要があるため、連続する複数フレームの超音波画像Uを用いて類似度を判定することが好ましい。 Here, for example, when the similarity between the respective image patterns corresponding to the four diagnostic findings of B-line, curing, normal and no rung sliding, and the ultrasonic image U is calculated, the diagnosis of B-line and curing is performed. Similarity can be determined for each finding using a one-frame ultrasound image U, but for diagnostic findings normal and without rung sliding, the movement of the pleural border within the ultrasound image U is discriminated. Therefore, it is preferable to determine the similarity using a continuous plurality of frames of ultrasonic images U.
 そのため、類似度判定部18は、Bラインの診断所見に対して、例えば、フリーズまでの定められた時間に生成された複数フレームの超音波画像UのそれぞれとBラインの診断所見に対応する画像パターンとの類似度を算出し、算出された複数の類似度の値のうち最大の値を有する類似度をBラインの診断所見に対する類似度として判定できる。また、類似度判定部18は、硬化の診断所見に対して、フリーズまでの定められた時間に生成された複数フレームの超音波画像Uのそれぞれと硬化の診断所見に対応する画像パターンとの類似度を算出し、算出された複数の類似度の値のうち最大の値を有する類似度を硬化の診断所見に対する類似度として判定できる。
 これにより、類似度判定部18は、被検体の肺が鮮明に写る超音波画像Uに対して判定された類似度を、最終的な類似度として得ることができる。
Therefore, the similarity determination unit 18 refers to the diagnostic findings of the B line, for example, the images corresponding to each of the plurality of frames of the ultrasonic image U generated at a predetermined time until the freeze and the diagnostic findings of the B line. The similarity with the pattern can be calculated, and the similarity having the maximum value among the calculated values of the plurality of similarity can be determined as the similarity to the diagnostic findings of the B line. Further, the similarity determination unit 18 resembles each of the plurality of frames of the ultrasonic image U generated at a predetermined time until the freeze with respect to the diagnostic findings of curing and the image pattern corresponding to the diagnostic findings of curing. The degree can be calculated, and the similarity having the maximum value among the calculated values of the plurality of similarity can be determined as the similarity to the diagnostic findings of hardening.
As a result, the similarity determination unit 18 can obtain the similarity determined for the ultrasonic image U in which the lungs of the subject are clearly captured as the final similarity.
 また、類似度判定部18は、Bラインの診断所見に対して、例えば、フリーズまでの定められた時間に生成された複数フレームの超音波画像Uを解析して、その複数フレームの超音波画像Uのうち、深さ方向に沿った線状のパターンを最も多く含む超音波画像Uを選出し、選出された超音波画像UとBラインの診断所見に対応する画像パターンとの類似度を判定することもできる。 Further, the similarity determination unit 18 analyzes the ultrasonic image U of a plurality of frames generated at a predetermined time until the freeze, for example, with respect to the diagnostic findings of the B line, and the ultrasonic image of the plurality of frames. Among U, the ultrasonic image U containing the largest number of linear patterns along the depth direction is selected, and the degree of similarity between the selected ultrasonic image U and the image pattern corresponding to the diagnostic findings of the B line is determined. You can also do it.
 このようにして、類似度判定部18は、フリーズまでの定められた時間に生成された複数フレームの超音波画像Uから、類似度を判定する診断所見の特徴を最もよく表している超音波画像Uを用いて類似度を判定することもできる。これにより、類似度の判定精度を向上できる。 In this way, the similarity determination unit 18 best represents the characteristics of the diagnostic findings for determining the similarity from the ultrasonic images U of a plurality of frames generated at a predetermined time until the freeze. The degree of similarity can also be determined using U. This makes it possible to improve the accuracy of determining the degree of similarity.
 また、正常およびラングスライディング無しの診断所見に対しては、胸膜の境界の変位を加味して類似度の判定が行われることが好ましいため、画像パターンメモリ17に、正常の診断所見に対応する画像パターンとして、胸膜の境界が正常に変位するような連続的な複数の画像パターンが保存され、ラングスライディング無しの診断所見に対する画像パターンとして、胸膜の境界がほとんど変位しないような連続的な複数の画像パターンが保存されることが好ましい。 Further, for the diagnostic findings of normal and no rung sliding, it is preferable that the similarity is determined by taking into account the displacement of the pleural boundary. Therefore, the image pattern memory 17 has an image corresponding to the normal diagnostic findings. As a pattern, a series of multiple image patterns in which the pleural border is normally displaced are stored, and as an image pattern for diagnostic findings without rung sliding, a series of multiple images in which the pleural border is hardly displaced. It is preferable that the pattern is preserved.
 この場合に、類似度判定部18は、正常の診断所見に対して、フリーズまでの定められた時間に生成された複数フレームの超音波画像Uと、正常の診断所見に対応する複数の画像パターンとの類似度を判定する。また、類似度判定部18は、硬化の診断所見に対して、フリーズまでの定められた時間に生成された複数フレームの超音波画像Uと、硬化の診断所見に対応する複数の画像パターンとの類似度を判定する。 In this case, the similarity determination unit 18 has a plurality of frames of ultrasonic image U generated at a predetermined time until the freeze and a plurality of image patterns corresponding to the normal diagnostic findings with respect to the normal diagnostic findings. Judge the degree of similarity with. Further, the similarity determination unit 18 has a plurality of frames of ultrasonic image U generated at a predetermined time until freeze and a plurality of image patterns corresponding to the diagnostic findings of curing for the diagnostic findings of curing. Determine the degree of similarity.
 続くステップS6において、強調度変更部19は、ステップS5で判定された複数の診断所見に対する類似度に基づいて、ステップS5で類似度が判定された複数の診断所見に対応する診断所見アイコンJ1~J4の強調度を変更する。 In the following step S6, the emphasis changing unit 19 has diagnostic findings icons J1 to corresponding to the plurality of diagnostic findings whose similarity is determined in step S5 based on the similarity to the plurality of diagnostic findings determined in step S5. Change the emphasis of J4.
 例えば、強調度変更部19は、図4に示すように、正常の診断所見に対応する診断所見アイコンJ1、ラングスライディング無しの診断所見に対応する診断所見アイコンJ2、Bラインの診断所見に対応する診断所見アイコンJ3および硬化の診断所見に対応する診断所見アイコンJ4を、左から診断所見アイコンJ1、J2、J3、J4と配列するような表示位置と共に記憶しているとする。Bライン、硬化、正常、ラングスライディング無しの順に値が低くなるようにステップS5でそれぞれの診断所見に対する類似度が判定された場合に、強調度変更部19は、例えば、図5に示すように、類似度が最も高いBラインの診断所見に対応する診断所見アイコンJ3を強調線L1により囲むことで、診断所見アイコンJ3の強調度を変更することができる。 For example, as shown in FIG. 4, the emphasis changing unit 19 corresponds to the diagnostic findings icon J1 corresponding to the normal diagnostic findings, the diagnostic findings icon J2 corresponding to the diagnostic findings without rung sliding, and the diagnostic findings of the B line. It is assumed that the diagnostic findings icon J3 and the diagnostic findings icon J4 corresponding to the diagnostic findings of hardening are stored together with the display positions such that the diagnostic findings icons J1, J2, J3, and J4 are arranged from the left. When the similarity to each diagnostic finding is determined in step S5 so that the values decrease in the order of B line, hardening, normal, and no rung sliding, the emphasis changing unit 19 is, for example, as shown in FIG. By surrounding the diagnostic findings icon J3 corresponding to the diagnostic findings of the B line having the highest degree of similarity with the highlight line L1, the emphasis of the diagnostic findings icon J3 can be changed.
 ステップS7において、表示制御部14の制御の下で、例えば図8に示すように、ステップS6で変更された強調度に従って、診断所見アイコンJ1~J4がモニタ15の第3表示領域A3に表示される。図8の例では、診断所見アイコンJ1~J4が、左から、正常の診断所見に対応する診断所見アイコンJ1、ラングスライディング無しの診断所見に対応する診断所見アイコンJ2、Bラインの診断所見に対応する診断所見アイコンJ3、硬化の診断所見に対応する診断所見アイコンJ4の順にモニタ15に表示されている。また、Bラインの診断所見に対応する診断所見アイコンJ3が強調線L1により囲まれている。また、図8の例では、いずれの診断所見にも当てはまらないことを表す診断所見アイコンJ5が、診断所見アイコンJ1~J4の下側に表示されている。 In step S7, under the control of the display control unit 14, the diagnostic findings icons J1 to J4 are displayed in the third display area A3 of the monitor 15 according to the emphasis degree changed in step S6, for example, as shown in FIG. To. In the example of FIG. 8, the diagnostic findings icons J1 to J4 correspond to the diagnostic findings icons J1 corresponding to the normal diagnostic findings, the diagnostic findings icons J2 corresponding to the diagnostic findings without rung sliding, and the diagnostic findings of the B line from the left. The diagnostic findings icon J3 and the diagnostic findings icon J4 corresponding to the diagnostic findings of hardening are displayed on the monitor 15 in this order. Further, the diagnostic finding icon J3 corresponding to the diagnostic finding on the B line is surrounded by the highlighted line L1. Further, in the example of FIG. 8, the diagnostic findings icon J5 indicating that the diagnosis does not apply to any of the diagnostic findings is displayed below the diagnostic findings icons J1 to J4.
 このように、診断所見アイコンJ1~J4が、ステップS5で判定された類似度に基づく強調度に従ってモニタ15に表示されるため、ユーザは、被検体に対する診断に不慣れな場合でも、強調表示された診断所見アイコンJ3を確認することにより、モニタ15に表示されている超音波画像Uに対して適切な診断所見を容易に付与することができる。 In this way, the diagnostic findings icons J1 to J4 are displayed on the monitor 15 according to the emphasis based on the similarity determined in step S5, so that the user is highlighted even if he / she is unfamiliar with the diagnosis of the subject. By confirming the diagnostic finding icon J3, an appropriate diagnostic finding can be easily given to the ultrasonic image U displayed on the monitor 15.
 ステップS8において、本体制御部21は、モニタ15に表示された診断所見アイコンJ1~J4のうち、入力装置22を介してユーザにより選択された診断所見アイコンを受け付ける。 In step S8, the main body control unit 21 receives the diagnostic findings icon selected by the user via the input device 22 among the diagnostic findings icons J1 to J4 displayed on the monitor 15.
 続くステップS9において、診断所見紐付け部20は、ステップS5で類似度の判定に使用された超音波画像Uと、ステップS8でユーザにより選択された診断所見アイコンに対応する診断所見を互いに紐付ける。 In the following step S9, the diagnostic finding linking unit 20 links the ultrasonic image U used for determining the similarity in step S5 and the diagnostic finding corresponding to the diagnostic finding icon selected by the user in step S8 to each other. ..
 例えば、Bラインおよび硬化の診断所見に対して、それぞれ、複数フレームの超音波画像Uに対して判定された類似度のうち最も高い類似度が最終的な類似度として判定された場合に、診断所見紐付け部20は、Bラインおよび硬化の診断所見のそれぞれに対して類似度が最も高い超音波画像Uを、紐付けの対象として選出する。
 また、診断所見紐付け部20は、正常およびラングスライディング無しの診断所見に対して、それぞれ、フリーズまでの定められた時間に生成された複数フレームの超音波画像Uを紐付けの対象とする。
For example, the diagnosis is made when the highest similarity among the similarity determined for the ultrasonic image U of a plurality of frames is determined as the final similarity for the diagnostic findings of the B line and the curing, respectively. The finding linking unit 20 selects the ultrasonic image U having the highest degree of similarity to each of the B line and the diagnostic finding of hardening as the target of linking.
Further, the diagnostic finding linking unit 20 targets the ultrasonic images U of a plurality of frames generated at a predetermined time until the freeze, respectively, with respect to the diagnostic findings of normal and without rung sliding.
 最後に、ステップS10において、表示制御部14の制御の下、ステップS8で受け付けられた診断所見アイコンに対応する診断所見がモニタ15に表示される。図8の例では、4つの診断所見アイコンJ1~J4のうち、左端に表示されている診断所見アイコンJ3がユーザにより選択され、診断所見アイコンJ3に対応する診断所見「B」が、第1表示領域A1において、ステップS9でBラインの診断所見に紐付けられた超音波画像Uと一緒に表示されている。 Finally, in step S10, under the control of the display control unit 14, the diagnostic findings corresponding to the diagnostic findings icon received in step S8 are displayed on the monitor 15. In the example of FIG. 8, among the four diagnostic findings icons J1 to J4, the diagnostic finding icon J3 displayed at the left end is selected by the user, and the diagnostic finding "B" corresponding to the diagnostic finding icon J3 is the first display. In the region A1, it is displayed together with the ultrasonic image U associated with the diagnostic findings on the B line in step S9.
 以上から、本発明の実施の形態1に係る超音波診断装置1によれば、超音波画像Uと、定められた複数の診断所見に対応する複数の画像パターンとの類似度がそれぞれ判定され、それらの類似度に基づいて、複数の診断所見に対応する複数の診断所見アイコンJ1~J4の強調度が変更され、変更された強調度に従って診断所見アイコンJ1~J4がモニタ15に表示されるため、ユーザは、強調度が変更された診断所見アイコンJ1~J4を確認することにより、モニタ15に表示されている超音波画像Uに対して適切な診断所見を容易に付与できる。 From the above, according to the ultrasonic diagnostic apparatus 1 according to the first embodiment of the present invention, the similarity between the ultrasonic image U and the plurality of image patterns corresponding to the predetermined plurality of diagnostic findings is determined. Based on their similarity, the emphasis of the plurality of diagnostic findings icons J1 to J4 corresponding to the plurality of diagnostic findings is changed, and the diagnostic findings icons J1 to J4 are displayed on the monitor 15 according to the changed emphasis. , The user can easily give appropriate diagnostic findings to the ultrasonic image U displayed on the monitor 15 by confirming the diagnostic findings icons J1 to J4 whose emphasis is changed.
 また、本発明においては、複数の診断所見アイコンJ1~J4の表示順が不変のまま強調度が変更されるため、例えば、ユーザが本来選択したい診断所見アイコン以外の診断所見アイコンを誤って選択してしまうことを抑制できる。
 また、本発明においては、超音波診断装置1が設置される病院等の施設毎またはユーザ毎に複数の診断所見アイコンJ1~J4の表示順を設定することもできる。複数の診断所見アイコンJ1~J4の表示順が不変のまま強調度が変更されるため、複数の診断所見アイコンJ1~J4がどのような順番で予め設定されている場合でも、ユーザは、例えば、どのアイコンが最も強調されているかを容易に確認することができ、適切な診断所見を超音波画像Uに容易に付与できる。
Further, in the present invention, since the emphasis is changed while the display order of the plurality of diagnostic findings icons J1 to J4 remains unchanged, for example, a diagnostic finding icon other than the diagnostic finding icon originally desired to be selected by the user is erroneously selected. It is possible to prevent it from being lost.
Further, in the present invention, it is possible to set the display order of a plurality of diagnostic findings icons J1 to J4 for each facility such as a hospital where the ultrasonic diagnostic apparatus 1 is installed or for each user. Since the emphasis is changed while the display order of the plurality of diagnostic findings icons J1 to J4 remains unchanged, the user can use, for example, even if the plurality of diagnostic findings icons J1 to J4 are preset in any order. Which icon is most emphasized can be easily confirmed, and appropriate diagnostic findings can be easily given to the ultrasonic image U.
 なお、図1に示すように、超音波診断装置1において、送受信回路12は、超音波プローブ2に備えられているが、超音波プローブ2に備えられる代わりに、診断装置本体3に備えられていてもよい。
 また、画像生成部13は、診断装置本体3に備えられているが、診断装置本体3に備えられる代わりに超音波プローブ2に備えられていてもよい。
 また、図3に示すように、画像生成部13は、信号処理部35、DSC36および画像処理部37を備えているが、そのうち、信号処理部35は超音波プローブ2に含まれることもできる。
As shown in FIG. 1, in the ultrasonic diagnostic apparatus 1, the transmission / reception circuit 12 is provided in the ultrasonic probe 2, but instead of being provided in the ultrasonic probe 2, it is provided in the diagnostic apparatus main body 3. You may.
Further, although the image generation unit 13 is provided in the diagnostic device main body 3, it may be provided in the ultrasonic probe 2 instead of being provided in the diagnostic device main body 3.
Further, as shown in FIG. 3, the image generation unit 13 includes a signal processing unit 35, a DSC 36, and an image processing unit 37, of which the signal processing unit 35 can be included in the ultrasonic probe 2.
 また、超音波プローブ2と診断装置本体3の接続方法は、特に限定されず、有線接続でもよく、無線接続でもよい。
 また、診断装置本体3は、ユーザが容易に携帯することが可能ないわゆるハンドヘルド型でもよく、いわゆる据え置き型でもよい。
Further, the connection method between the ultrasonic probe 2 and the diagnostic device main body 3 is not particularly limited, and may be a wired connection or a wireless connection.
Further, the diagnostic device main body 3 may be a so-called handheld type that can be easily carried by the user, or may be a so-called stationary type.
 また、図7では、4つの検査箇所選択アイコンP1~P4が例示されているが、検査箇所選択アイコンP1~P4の数は、4つに限定されない。例えば、本体制御部21は、検査箇所数と、対応する検査箇所のセットを記憶しておくことができる。この場合に、入力装置22を介したユーザの入力操作により記憶されている検査箇所数が選択され、表示制御部14の制御の下で、モニタ15の第2表示領域A2に、ユーザにより選択された検査箇所数と同一の数の検査箇所選択アイコンが表示されることができる。このようにして、検査箇所数を切り替えることにより、より多様な検査に本発明を適用することができる。 Further, in FIG. 7, four inspection location selection icons P1 to P4 are illustrated, but the number of inspection location selection icons P1 to P4 is not limited to four. For example, the main body control unit 21 can store the number of inspection points and the set of corresponding inspection points. In this case, the number of inspection points stored by the user's input operation via the input device 22 is selected, and is selected by the user in the second display area A2 of the monitor 15 under the control of the display control unit 14. The same number of inspection location selection icons as the number of inspection locations can be displayed. By switching the number of inspection points in this way, the present invention can be applied to a wider variety of inspections.
 また、ステップS5の類似度の判定において使用される超音波診断画像として、動画像が使用されることが説明されているが、1フレームの静止画像のみを使用することもできる。このように、1フレームの静止画像のみを使用する場合に、類似度判定部18は、例えば、フリーズ時にモニタ15に表示された1フレームの超音波画像Uと、複数の診断所見に対応する画像パターンの類似度を判定することができる。しかしながら、正常およびラングスライディング無しの診断所見に対する類似度を精度よく判定するためには、動画像を使用して類似度を判定することが好ましい。 Further, although it is explained that a moving image is used as the ultrasonic diagnostic image used in the determination of the similarity in step S5, only one frame of still image can be used. As described above, when only one frame of still image is used, the similarity determination unit 18 is, for example, a one-frame ultrasonic image U displayed on the monitor 15 at the time of freezing and an image corresponding to a plurality of diagnostic findings. The degree of similarity of patterns can be determined. However, in order to accurately determine the similarity to the diagnostic findings of normal and no rung sliding, it is preferable to determine the similarity using a moving image.
 また、正常の診断所見では、胸膜の境界から一定の深さ位置までの組織が、被検体の呼気または吸気に付随して変位することが知られているため、類似度判定部18は、例えば、正常およびラングスライディング無しの診断所見に対する類似度を判定する場合に、超音波画像Uに含まれる胸膜の境界と、胸膜の境界から一定の深さ位置までの間における画像の動きを加味して類似度を判定することができる。これにより、正常およびラングスライディング無しの診断所見に対する類似度を判定する精度を向上できる。
 なお、一定の深さ位置として、超音波の多重反射に起因する、深さ方向に対して直交する方向に沿って延びるアーチファクトの深さ位置が設定され得る。
In addition, since it is known from normal diagnostic findings that the tissue from the boundary of the pleura to a certain depth position is displaced with the exhalation or inspiration of the subject, the similarity determination unit 18 is, for example, When determining the similarity to diagnostic findings, normal and without rung-sliding, the movement of the image between the pleural boundary contained in the ultrasound image U and the pleural boundary to a certain depth position is taken into account. The degree of similarity can be determined. This can improve the accuracy of determining the similarity to the diagnostic findings of normal and without rung sliding.
As a constant depth position, the depth position of the artifact extending along the direction orthogonal to the depth direction due to the multiple reflection of ultrasonic waves can be set.
 また、ステップS6において、強調度変更部19は、ステップS5で判定された類似度が最も高い診断所見に対応する診断所見アイコンJ3を強調線L1により囲むことで診断所見アイコンJ3の強調度を変更しているが、強調度の変更方法は、これに限定されない。例えば、強調度変更部19は、類似度判定部18により判定された類似度に応じて複数の診断所見アイコンJ1~J4のそれぞれの表示態様を変更することもできる。 Further, in step S6, the emphasis changing unit 19 changes the emphasis of the diagnostic finding icon J3 by surrounding the diagnostic finding icon J3 corresponding to the diagnostic finding having the highest similarity determined in step S5 with the highlight line L1. However, the method of changing the emphasis is not limited to this. For example, the emphasis degree changing unit 19 can change the display mode of each of the plurality of diagnostic findings icons J1 to J4 according to the similarity degree determined by the similarity degree determination unit 18.
 例えば、Bラインの診断所見に対する類似度が最も高く、硬化の診断所見に対する類似度が次に高い場合に、強調度変更部19は、図9に示すように、Bラインの診断所見に対応する診断所見アイコンJ3を2重の強調線L2により囲み、硬化の診断所見に対応する診断所見アイコンJ4を強調線L3により囲むことができる。このように、強調度変更部19は、類似度が高い診断所見に対応する診断所見アイコンほど強く強調されるように、複数の診断所見アイコンJ1~J4の強調度を変更することができる。 For example, when the similarity to the diagnostic findings of the B line is the highest and the similarity to the diagnostic findings of hardening is the next highest, the emphasis changing unit 19 corresponds to the diagnostic findings of the B line as shown in FIG. The diagnostic finding icon J3 can be surrounded by the double highlighted line L2, and the diagnostic finding icon J4 corresponding to the diagnostic finding of hardening can be surrounded by the highlighted line L3. In this way, the emphasis changing unit 19 can change the emphasis of the plurality of diagnostic findings icons J1 to J4 so that the diagnostic findings icons corresponding to the diagnostic findings having a high degree of similarity are emphasized more strongly.
 また、図示しないが、強調度変更部19は、正常の診断所見に対応する診断所見アイコンJ1およびラングスライディング無しの診断所見に対応する診断所見アイコンJ2に対しても類似度に応じた表示態様を行うことができる。 Further, although not shown, the emphasis changing unit 19 also displays a display mode according to the degree of similarity with respect to the diagnostic finding icon J1 corresponding to the normal diagnostic finding and the diagnostic finding icon J2 corresponding to the diagnostic finding without rung sliding. It can be carried out.
 また、強調度変更部19は、複数の診断所見アイコンJ1~J4のうち、類似度が最も高い診断所見に対応する診断所見アイコンを、他の診断所見アイコンとは異なる色によりモニタ15に表示することができる。また、強調度変更部19は、複数の診断所見に対する類似度に応じて、複数の診断所見アイコンJ1~J4をそれぞれ異なる色によりモニタ15に表示することもできる。 Further, the emphasis changing unit 19 displays the diagnostic findings icon corresponding to the diagnostic findings having the highest similarity among the plurality of diagnostic findings icons J1 to J4 on the monitor 15 in a color different from that of the other diagnostic findings icons. be able to. Further, the emphasis degree changing unit 19 can display the plurality of diagnostic findings icons J1 to J4 on the monitor 15 in different colors according to the degree of similarity to the plurality of diagnostic findings.
 また、強調度変更部19は、図10に示すように、類似度が最も高い診断所見に対応する診断所見アイコンJ3を、他の診断所見アイコンJ1、J2およびJ4よりも大きくモニタ15に表示させることができる。
 また、強調度変更部19は、例えば、複数の診断所見に対する類似度に応じて複数の診断所見アイコンJ1~J4の大きさを変更することもできる、例えば、強調度変更部19は、類似度が高い診断所見に対応する診断所見アイコンほどサイズを大きくし、類似度が低い診断所見に対応する診断所見アイコンほどサイズを小さくすることができる。
Further, as shown in FIG. 10, the emphasis changing unit 19 causes the diagnostic finding icon J3 corresponding to the diagnostic finding having the highest similarity to be displayed on the monitor 15 larger than the other diagnostic finding icons J1, J2 and J4. be able to.
Further, the emphasis changing unit 19 can change the size of the plurality of diagnostic findings icons J1 to J4 according to the similarity to the plurality of diagnostic findings. For example, the emphasis changing unit 19 has the similarity. The size of the diagnostic findings icon corresponding to the higher diagnostic findings can be increased, and the size of the diagnostic findings icon corresponding to the diagnostic findings having a lower similarity can be reduced.
 また、診断所見アイコンJ1~J4の大きさを変更する際に、例えば、類似度が最も低い診断所見に対応する診断所見アイコンをモニタ15から消去することもできる。特に、診断装置本体3がハンドヘルド型である場合には、モニタ15が小さいため、類似度が最も低い診断所見に対応する診断所見アイコンをモニタ15から消去することにより、類似度が比較的高い診断所見に対応する診断所見アイコンを大きく表示することができ、ユーザが診断所見アイコンを選択しやすくなる。 Further, when changing the size of the diagnostic findings icons J1 to J4, for example, the diagnostic findings icons corresponding to the diagnostic findings having the lowest similarity can be deleted from the monitor 15. In particular, when the diagnostic apparatus main body 3 is a handheld type, since the monitor 15 is small, the diagnosis with a relatively high degree of similarity is made by deleting the diagnostic finding icon corresponding to the diagnostic finding with the lowest similarity from the monitor 15. The diagnostic findings icon corresponding to the findings can be displayed in a large size, which makes it easier for the user to select the diagnostic findings icon.
 また、ステップS9において、診断所見紐付け部20が、正常およびラングスライディング無しの診断所見に対して、それぞれ、フリーズまでの定められた時間に生成された複数フレームの超音波画像Uを紐付けの対象とすることが説明されているが、1フレームの超音波画像Uを紐付けの対象とすることもできる。例えば、画像パターンメモリ17に胸膜の境界に関する画像パターンが保存され、ステップS5において、類似度判定部18により、複数フレームの超音波画像Uにおける胸膜の境界に対する類似度が判定された場合に、診断所見紐付け部20は、フリーズまでの定められた時間に生成された複数フレームの超音波画像Uのうち、胸膜の境界に関する類似度が最も高いフレームの超音波画像Uを紐付けの対象とすることができる。 Further, in step S9, the diagnostic finding linking unit 20 links the ultrasonic image U of a plurality of frames generated at a predetermined time until the freeze to the diagnostic findings of normal and without rung sliding, respectively. Although it is explained that the target is, a one-frame ultrasonic image U can also be the target of association. For example, when an image pattern relating to the pleural boundary is stored in the image pattern memory 17, and the similarity determination unit 18 determines the similarity to the pleural boundary in the ultrasonic image U of a plurality of frames in step S5, the diagnosis is made. The finding linking unit 20 targets the ultrasonic image U of the frame having the highest similarity with respect to the pleural boundary among the ultrasonic images U of a plurality of frames generated at a predetermined time until the freeze. be able to.
 また、4つの診断所見アイコンJ1~J4が例示されているが、診断所見アイコンの数は4つに限定されるものではなく、例えば、2つ、3つまたは5つ以上等、類似度を判定する診断所見の数に応じて設定することができる。しかしながら、被検体の肺に関する複数の診断所見のうち少なくとも1つは、Bライン、硬化、正常、および、ラングスライディング無しのいずれかの診断所見を含むことが好ましい。 Further, although four diagnostic finding icons J1 to J4 are exemplified, the number of diagnostic finding icons is not limited to four, and the degree of similarity is determined, for example, two, three, or five or more. It can be set according to the number of diagnostic findings to be performed. However, it is preferable that at least one of the plurality of diagnostic findings regarding the lungs of the subject includes any of the diagnostic findings of B-line, hardening, normal, and no rung sliding.
 例えば、被検体の肺において、いわゆる胸水(PE:Pleural Effusion)の貯留に起因する診断所見を加味する場合には、正常、ラングスライディング無し、Bライン、硬化の診断所見に加えて、胸水の貯留(N,PE)、ラングスライディング無しおよび胸水の貯留(S(-),PE)、Bラインおよび胸水の貯留(B,PE)、硬化および胸水の貯留(C,PE)の、合計で8つの診断所見が考えられる。この場合に、例えば、図11に示すような8つの診断所見に対応する8つの診断所見アイコンJ1~J4、J10~J13がモニタ15に表示される。 For example, when the diagnostic findings due to the accumulation of so-called pleural effusion (PE: Pleural Effusion) are added to the lungs of the subject, the pleural effusion is accumulated in addition to the diagnostic findings of normal, no rung sliding, B line, and hardening. (N, PE), no rung sliding and pleural effusion (S (-), PE), B-line and pleural effusion (B, PE), hardening and pleural effusion (C, PE), total 8 Diagnostic findings are possible. In this case, for example, eight diagnostic findings icons J1 to J4 and J10 to J13 corresponding to the eight diagnostic findings as shown in FIG. 11 are displayed on the monitor 15.
 また、胸水の貯留の診断所見が加味される場合に、例えば、図12に示すように、正常、ラングスライディング無し、Bライン、硬化の診断所見に対応する診断所見アイコンJ1~J4と、胸水の貯留が認められないことを表す胸水有無アイコンE1と、胸水の貯留が認められることを表す胸水有無アイコンE2を表示することもできる。この場合に、ユーザは、入力装置22を介して診断所見アイコンJ1~J4のいずれかを選択した後に、胸水有無アイコンE1およびE2のいずれかを選択することにより、胸水の貯留の有無を加味した診断所見を超音波画像Uに付与することができる。 In addition, when the diagnostic findings of pleural effusion are taken into consideration, for example, as shown in FIG. 12, the diagnostic findings icons J1 to J4 corresponding to the diagnostic findings of normal, no rung sliding, B line, and hardening, and the pleural effusion. It is also possible to display the pleural effusion icon E1 indicating that the pleural effusion is not recognized and the pleural effusion icon E2 indicating that the pleural effusion is recognized. In this case, the user selects any of the diagnostic findings icons J1 to J4 via the input device 22, and then selects any of the pleural effusion icons E1 and E2 to take into account the presence or absence of pleural effusion. Diagnostic findings can be imparted to the ultrasound image U.
 なお、診断所見アイコンJ1~J4と胸水有無アイコンE1およびE2の6つのアイコンをモニタ15に同時に表示しなくてもよい。例えば、診断所見アイコンJ1~J4と胸水有無アイコンE1およびE2の6つのアイコンのうち、4つの診断所見アイコンJ1~J4のみをモニタ15に表示し、ユーザにより4つの診断所見アイコンJ1~J4のうちいずれか1つが選択された場合に、胸水有無アイコンE1およびE2をモニタ15に表示することもできる。このような表示を行うことにより、4つの診断所見アイコンJ1~J4のいずれかを選択した後に胸水有無アイコンE1またはE2を選択することをユーザに明確に示すことができ、ユーザが超音波画像Uへの診断所見の付与をより円滑に行うことができる。 It is not necessary to display the six icons of the diagnostic findings icons J1 to J4 and the pleural effusion icons E1 and E2 on the monitor 15 at the same time. For example, of the six icons J1 to J4 and the presence / absence of chest water icons E1 and E2, only the four diagnostic findings icons J1 to J4 are displayed on the monitor 15, and the user can display the four diagnostic findings icons J1 to J4. When any one is selected, the breast water presence / absence icons E1 and E2 can also be displayed on the monitor 15. By performing such a display, it is possible to clearly indicate to the user that the pleural effusion icon E1 or E2 is selected after selecting any of the four diagnostic findings icons J1 to J4, and the user can clearly indicate that the ultrasonic image U is selected. Diagnosis findings can be given to the patient more smoothly.
 また、図4、図5および図8~図12には、いわゆるコンベックス型の超音波プローブ2により撮影された超音波画像Uに対応するデザインを有する診断所見アイコンJ1~J4が例示されているが、被検体の検査に使用される超音波プローブ2の種類に応じて診断所見アイコンJ1~J4のデザインが設定されてもよい。例えば、図13に示すように、いわゆるリニア型の超音波プローブ2により撮影された超音波画像Uに対応するデザインを有する診断所見アイコンJ6~J9が例示されている。診断所見アイコンJ6は正常の診断所見に対応し、診断所見アイコンJ7はラングスライディング無しの診断所見に対応し、診断所見アイコンJ8はBラインの診断所見に対応し、診断所見アイコンJ9は硬化の診断所見に対応している。 Further, FIGS. 4, 5 and 8 to 12 exemplify diagnostic findings icons J1 to J4 having a design corresponding to the ultrasonic image U taken by the so-called convex type ultrasonic probe 2. , The design of the diagnostic findings icons J1 to J4 may be set according to the type of the ultrasonic probe 2 used for the examination of the subject. For example, as shown in FIG. 13, diagnostic findings icons J6 to J9 having a design corresponding to an ultrasonic image U taken by a so-called linear ultrasonic probe 2 are exemplified. The diagnostic finding icon J6 corresponds to the normal diagnostic finding, the diagnostic finding icon J7 corresponds to the diagnostic finding without rung sliding, the diagnostic finding icon J8 corresponds to the diagnostic finding of the B line, and the diagnostic finding icon J9 corresponds to the diagnosis of hardening. Corresponds to the findings.
 また、コンベックス型の超音波プローブ2を使用する場合と同様に、リニア型の超音波プローブ2を使用する場合にも、図14に示すような、胸水の貯留を加味した診断所見アイコンJ14~J17をモニタ15に表示することができる。図14の例では、リニア型の超音波プローブ2に対応するデザインを有する診断所見アイコンJ14~J17が示されている。
 また、図示しないが、図14に示される態様と同様に、リニア型の超音波プローブ2に対応するデザインを有する胸水有無アイコンをモニタ15に表示することもできる。
Further, as in the case of using the convex type ultrasonic probe 2, when using the linear type ultrasonic probe 2, the diagnostic findings icons J14 to J17 in consideration of the accumulation of pleural effusion as shown in FIG. 14 Can be displayed on the monitor 15. In the example of FIG. 14, diagnostic findings icons J14 to J17 having a design corresponding to the linear ultrasonic probe 2 are shown.
Further, although not shown, a pleural effusion icon having a design corresponding to the linear ultrasonic probe 2 can be displayed on the monitor 15 as in the embodiment shown in FIG.
 また、図示しないが、いわゆるセクタ型の超音波プローブ2が使用される場合に、セクタ型の超音波プローブ2に対応するデザインを有する診断所見アイコンが設定されることができる。 Further, although not shown, when a so-called sector type ultrasonic probe 2 is used, a diagnostic finding icon having a design corresponding to the sector type ultrasonic probe 2 can be set.
 また、図6のフローチャートを用いた実施の形態1の超音波診断装置1の動作において、被検体の肺を検査する例が説明されているが、本発明は、肺の検査に限定されるものではなく、被検体の種々の検査部位に適用されることができる。 Further, an example of inspecting the lung of a subject in the operation of the ultrasonic diagnostic apparatus 1 of the first embodiment using the flowchart of FIG. 6 is described, but the present invention is limited to the lung inspection. However, it can be applied to various test sites of the subject.
 例えば、本発明は、被検体の直腸の検査に適用することができる。この場合に、診断所見として、直腸内の便の硬さに応じて、例えば、軟便、標準および硬便の3つの診断所見を設定し、図15に示すように、軟便の診断所見に対応する診断所見アイコンJ18、標準の診断所見に対応する診断所見アイコンJ19、硬便の診断所見に対応する診断所見アイコンJ20がモニタ15に表示される。図15の例では、3つの診断所見アイコンJ18~J20は、被検体の直腸を撮影した超音波画像U1と一緒にモニタ15に表示されている。 For example, the present invention can be applied to a rectal examination of a subject. In this case, as diagnostic findings, for example, three diagnostic findings of loose stool, standard and hard stool are set according to the hardness of the stool in the rectum, and as shown in FIG. 15, the diagnostic findings of loose stool correspond to the diagnostic findings. The diagnostic findings icon J18, the diagnostic findings icon J19 corresponding to the standard diagnostic findings, and the diagnostic findings icon J20 corresponding to the diagnostic findings of hard stool are displayed on the monitor 15. In the example of FIG. 15, the three diagnostic findings icons J18 to J20 are displayed on the monitor 15 together with the ultrasonic image U1 in which the rectum of the subject is photographed.
 また、例えば、本発明は、被検体の下大静脈の検査に適用することもできる。この場合に、診断所見として、例えば、下大静脈の直径の大きさと下大静脈径の呼吸性変動の有無に基づいて、下大静脈径大および下大静脈径の呼吸性変動あり、下大静脈径大および下大静脈径の呼吸性変動無し、下大静脈径正常および下大静脈径呼吸性変動あり、下大静脈径正常および下大静脈径呼吸性変動無し、下大静脈径小および下大静脈径呼吸性変動あり、下大静脈径小および下大静脈径呼吸性変動無しの6つの診断所見が設定される。 Further, for example, the present invention can also be applied to an examination of the inferior vena cava of a subject. In this case, as diagnostic findings, for example, there are respiratory fluctuations in the inferior large vein diameter and the inferior large vein diameter based on the size of the diameter of the inferior large vein and the presence or absence of respiratory fluctuations in the inferior large vein diameter. No respiratory fluctuations in large and inferior large vein diameters, normal inferior large vein diameter and respiratory fluctuations in inferior large vein diameter, normal inferior large vein diameter and no respiratory fluctuation in inferior large vein diameter, small inferior large vein diameter and Six diagnostic findings are set with inferior major venous diameter respiratory fluctuations and inferior major venous diameter small and inferior major venous diameter respiratory fluctuations.
 ここで、「下大静脈径大」は下大静脈の直径が20mm以上、「下大静脈径正常」は下大静脈の直径が10mmより大きく20mm未満、「下大静脈径小」は下大静脈の直径が10mm以下であることを意味する。また、「下大静脈径呼吸性変動あり」は、呼気における下大静脈の直径の変化が40%より大きく50%以下、「下大静脈径呼吸性変動無し」は、呼気における下大静脈の直径の変化が40%以下であることを意味する。 Here, the diameter of the inferior vena cava is 20 mm or more for "large inferior vena cava", the diameter of the inferior vena cava is larger than 10 mm and less than 20 mm for "normal inferior vena cava", and the diameter of the inferior vena cava is small. It means that the diameter of the vein is 10 mm or less. In addition, "with inferior vena cava respiratory fluctuation" means that the change in the diameter of the inferior vena cava in exhaled breath is greater than 40% and 50% or less, and "without inferior vena cava diameter breathable fluctuation" means that the change in inferior vena cava in exhaled breath is greater than 40%. It means that the change in diameter is 40% or less.
 また、例えば、本発明は、被検体の肝臓の検査に適用することもできる。この場合に、診断所見として、例えば、正常、肝嚢胞、脂肪肝、肝血管腫および肝内石灰の診断所見を設定することができる。
 また、例えば、本発明は、被検体の胆嚢の検査に適用することもできる。この場合に、診断所見として、例えば、正常、胆嚢ポリープ、胆嚢壁在結石、胆嚢結石、胆嚢腺筋腫症および胆嚢壁肥厚の診断所見を設定することができる。
 また、例えば、本発明は、被検体の腎臓の検査に適用することもできる。この場合に、診断所見として、例えば、正常、腎内石灰化、腎結石、嚢胞腎、腎血管筋脂肪腫、水腎症、重複腎盂および腎嚢胞の診断所見を設定することができる。
Further, for example, the present invention can also be applied to an examination of the liver of a subject. In this case, as diagnostic findings, for example, diagnostic findings of normal, hepatic cyst, fatty liver, hepatic hemangiomas and intrahepatic lime can be set.
Further, for example, the present invention can also be applied to an examination of the gallbladder of a subject. In this case, as diagnostic findings, for example, diagnostic findings of normal, gallbladder polyps, gallbladder wall stones, gallbladder stones, gallbladder adenomyomatosis and gallbladder wall thickening can be set.
Further, for example, the present invention can also be applied to an examination of a kidney of a subject. In this case, as diagnostic findings, for example, diagnostic findings of normal, intrarenal calcification, renal stones, cystic kidney, renal angiomyolipoma, hydronephrosis, double renal pelvis and renal cyst can be set.
 また、例えば、本発明は、被検体の心臓の検査に適用することもできる。この場合に、診断所見として、例えば、左心室の収縮能に基づいて、重度収縮能低下、収縮能低下、正常および過収縮の診断所見を設定することができる。「重度収縮能低下」は、(左心室の1回の血液の拍出量)/(左心室の拡張末期の容積)×100=[(左心室の最大容積)-(左心室の最小容積)]/(左心室の最大容積)により算出される左室駆出能が30%以下の診断所見であり、「収縮能低下」は、左室駆出能が30%より大きく55%以下の診断所見であり、「正常」は、左室駆出能が55%より大きく70%未満の診断所見であり、「過収縮」は、左室駆出能が70%以上の診断所見である。 Further, for example, the present invention can also be applied to an examination of the heart of a subject. In this case, as diagnostic findings, for example, based on the contractility of the left ventricle, the diagnostic findings of severe hypocontraction, hypocontraction, normal and hypercontraction can be set. "Severe decrease in contractility" means (a single discharge of blood in the left ventricle) / (volume at the end of diastole of the left ventricle) x 100 = [(maximum volume of the left ventricle)-(minimum volume of the left ventricle)) ] / (Maximum volume of left ventricle) is a diagnostic finding that the left ventricular ejection ability is 30% or less, and "decreased contractility" is a diagnosis that the left ventricular ejection ability is larger than 30% and 55% or less. "Normal" is a diagnostic finding with a left ventricular ejection ability of more than 55% and less than 70%, and "hypercontraction" is a diagnostic finding with a left ventricular ejection ability of 70% or more.
 なお、左心室の容積は、例えば、左心室の互いに直交する2つの断面に対応する超音波画像Uから、それぞれ直交する3方向における左心室の幅を計測し、計測された幅の値を用いて算出することができる。 For the volume of the left ventricle, for example, the width of the left ventricle in three orthogonal directions is measured from the ultrasonic image U corresponding to two cross sections of the left ventricle orthogonal to each other, and the value of the measured width is used. Can be calculated.
 このようにして、本発明は、被検体の種々の検査部位に適用されるが、例えば、入力装置22を介したユーザの入力操作により、被検体の検査部位を設定することができる。これにより、ユーザは、被検体の種々の検査部位の検査において、超音波画像Uに対して適切な診断所見を容易に付与することができる。 In this way, the present invention is applied to various test sites of the subject, and for example, the test site of the subject can be set by the input operation of the user via the input device 22. Thereby, the user can easily give appropriate diagnostic findings to the ultrasonic image U in the examination of various examination sites of the subject.
実施の形態2
 図6のフローチャートを用いた超音波診断装置1の動作説明では、ステップS4でフリーズの指示がなされたと判定されたことをトリガとして、フリーズまでの定められた時間に生成された複数フレームの超音波画像Uを使用して、ステップS5で複数の診断所見に対する類似度が判定されることが説明されているが、類似度の判定に使用される超音波画像Uは、ユーザにより手動で選択されることもできる。
Embodiment 2
In the operation explanation of the ultrasonic diagnostic apparatus 1 using the flowchart of FIG. 6, the ultrasonic waves of a plurality of frames generated at a predetermined time until the freeze are triggered by the determination that the freeze instruction has been given in step S4. Although it is described that the image U is used to determine the similarity to a plurality of diagnostic findings in step S5, the ultrasound image U used to determine the similarity is manually selected by the user. You can also do it.
 図16に示すフローチャートを用いて、実施の形態2における超音波診断装置1の動作を説明する。図16のフローチャートは、実施の形態1における図6のフローチャートにおいて、ステップS5の代わりにステップS11~ステップS13が設けられたものである。 The operation of the ultrasonic diagnostic apparatus 1 in the second embodiment will be described with reference to the flowchart shown in FIG. The flowchart of FIG. 16 is the flowchart of FIG. 6 in the first embodiment, in which steps S11 to S13 are provided instead of step S5.
 ステップS1~ステップS4については、図6に示すフローチャートにおけるステップS1~ステップS4と同一であるため、詳細な説明は省略する。
 ステップS4において、フリーズの指示がなされたと判定された場合に、ステップS11に進む。
Since steps S1 to S4 are the same as steps S1 to S4 in the flowchart shown in FIG. 6, detailed description thereof will be omitted.
If it is determined in step S4 that the freeze instruction has been given, the process proceeds to step S11.
 ステップS11において、入力装置22を介してユーザにより、類似度の判定に使用する複数フレームの超音波画像Uのフレーム範囲が指定され、本体制御部21により、指定されたフレーム範囲が受け付けられる。 In step S11, the frame range of the ultrasonic image U of a plurality of frames used for determining the similarity is designated by the user via the input device 22, and the designated frame range is accepted by the main body control unit 21.
 この際に、例えば、表示制御部14の制御の下で、図16に示すように、フレーム範囲を指定するためのスライドバーC1とフリーズボタンB1がモニタ15の第3表示領域A3に表示される。スライドバーC1は、ユーザにドラッグされることによりスライドバーC1の両端の間をスライドして、被検体の検査が開始されてからフリーズまでに生成された複数フレームの超音波画像Uのうちの1フレームの超音波画像Uを選択するためのスライドボタンC2を含んでいる。スライドバーC1の左端は、被検体の検査が開始されてから最初に生成された超音波画像Uに対応し、スライドバーC1の右端は、フリーズ時の最新の超音波画像Uに対応しており、スライドボタンC2の位置に対応する超音波画像Uがモニタ15の第1表示領域A1に表示される。 At this time, for example, under the control of the display control unit 14, as shown in FIG. 16, the slide bar C1 and the freeze button B1 for designating the frame range are displayed in the third display area A3 of the monitor 15. .. The slide bar C1 slides between both ends of the slide bar C1 by being dragged by the user, and is one of a plurality of frames of ultrasonic images U generated from the start of the examination of the subject to the freeze. It includes a slide button C2 for selecting the ultrasonic image U of the frame. The left end of the slide bar C1 corresponds to the ultrasonic image U generated first after the examination of the subject is started, and the right end of the slide bar C1 corresponds to the latest ultrasonic image U at the time of freezing. , The ultrasonic image U corresponding to the position of the slide button C2 is displayed in the first display area A1 of the monitor 15.
 例えば、ユーザによりスライドボタンC2がスライドされ、第1の位置に移動された状態でフリーズボタンB1がタップされることにより、類似度の判定に使用されるフレーム範囲の最初のフレームの超音波画像Uが指定され、ユーザによりスライドボタンC2がさらにスライドされ、第2の位置に移動された状態でフリーズボタンB1が再度タップされることにより、類似度の判定に使用されるフレーム範囲の最後のフレームの超音波画像Uが指定される。例えばこのようにしてフレーム範囲が指定され、本体制御部21により、指定されたフレーム範囲が受け付けられる。 For example, when the slide button C2 is slid by the user and the freeze button B1 is tapped while the slide button C2 is moved to the first position, the ultrasonic image U of the first frame in the frame range used for determining the similarity is used. Is specified, the slide button C2 is further slid by the user, and the freeze button B1 is tapped again while being moved to the second position, so that the last frame of the frame range used for determining the similarity is used. The ultrasonic image U is specified. For example, the frame range is designated in this way, and the designated frame range is accepted by the main body control unit 21.
 続くステップS12において、入力装置22を介してユーザにより、類似度の判定を開始する指令が入力され、この指令が本体制御部21により受け付けられる。 In the following step S12, the user inputs a command to start the determination of the similarity via the input device 22, and this command is accepted by the main body control unit 21.
 ステップS13において、類似度判定部18は、ステップS11でユーザに指定されたフレーム範囲内の複数フレームの超音波画像Uと、画像パターンメモリ17に保存されている複数の診断所見に対応する複数の画像パターンとの類似度を判定する。 In step S13, the similarity determination unit 18 corresponds to the ultrasonic image U of a plurality of frames within the frame range specified by the user in step S11 and the plurality of diagnostic findings stored in the image pattern memory 17. Determine the degree of similarity with the image pattern.
 続くステップS6において、強調度変更部19は、ステップS13で複数の診断所見に対してそれぞれ判定された類似度に基づいて、複数の診断所見アイコンJ1~J4の強調度を変更する。
 ステップS7において、ステップS6で変更された強調度に基づいて、複数の診断所見アイコンJ1~J4がモニタ15に表示される。
In the following step S6, the emphasis changing unit 19 changes the emphasis of the plurality of diagnostic findings icons J1 to J4 based on the similarity determined for each of the plurality of diagnostic findings in step S13.
In step S7, a plurality of diagnostic findings icons J1 to J4 are displayed on the monitor 15 based on the emphasis changed in step S6.
 ステップS8において、モニタ15に表示された複数の診断所見アイコンJ1~J4のうち1つの診断所見アイコンがユーザにより選択され、本体制御部21により、選択された診断所見アイコンが受け付けられる。 In step S8, the user selects one of the plurality of diagnostic findings icons J1 to J4 displayed on the monitor 15, and the main body control unit 21 accepts the selected diagnostic findings icons.
 ステップS9において、診断所見紐付け部20は、ステップS13で類似度の判定に使用された超音波画像Uと、ステップS9で選択が受け付けられた診断所見アイコンに対応する診断所見とが紐付けられる。
 最後に、ステップS10において、ステップS9で超音波画像Uと紐付けられた診断所見がモニタ15に表示される。
In step S9, the diagnostic finding linking unit 20 associates the ultrasonic image U used for determining the similarity in step S13 with the diagnostic findings corresponding to the diagnostic findings icon whose selection was accepted in step S9. ..
Finally, in step S10, the diagnostic findings associated with the ultrasonic image U in step S9 are displayed on the monitor 15.
 以上から、類似度の判定に使用される複数フレームの超音波画像Uのフレーム範囲がユーザによって手動で指定される場合でも、実施の形態1と同様にして、ユーザは、強調度が変更された診断所見アイコンJ1~J4を確認することにより、モニタ15に表示されている超音波画像Uに対して適切な診断所見を容易に付与できる。 From the above, even when the frame range of the plurality of frames of the ultrasonic image U used for determining the similarity is manually specified by the user, the emphasis is changed by the user in the same manner as in the first embodiment. By confirming the diagnostic findings icons J1 to J4, appropriate diagnostic findings can be easily given to the ultrasonic image U displayed on the monitor 15.
 なお、入力装置22を介してユーザにより、被検体の検査が開始されてからフリーズまでの間に生成された複数フレームの超音波画像Uのうち、類似度の判定に使用される複数フレームの超音波画像Uのフレーム範囲が指定されることが説明されているが、フレーム範囲が指定される代わりに、1フレームの超音波画像Uのみが指定されてもよい。 Of the plurality of frames of the ultrasonic image U generated from the start of the examination of the subject to the freeze by the user via the input device 22, the plurality of frames of the ultrasonic image U used for determining the degree of similarity are super. Although it is explained that the frame range of the ultrasonic image U is specified, only one frame of the ultrasonic image U may be specified instead of the frame range being specified.
 例えば、ユーザによりスライドボタンC2が移動され、所望のフレームの超音波画像Uがモニタ15に表示された状態でフリーズボタンB1がタップされることにより、モニタ15に表示されているフレームの超音波画像Uが、類似度の判定に使用される超音波画像Uとして指定される。 For example, the slide button C2 is moved by the user, and the freeze button B1 is tapped while the ultrasonic image U of the desired frame is displayed on the monitor 15, so that the ultrasonic image of the frame displayed on the monitor 15 is displayed. U is designated as the ultrasound image U used to determine the degree of similarity.
1 超音波診断装置、2 超音波プローブ、3 診断装置本体、11 振動子アレイ、12 送受信回路、13 画像生成部、14 表示制御部、15 モニタ、16 画像メモリ、17 画像パターンメモリ、18 類似度判定部、19 強調度変更部、20 診断所見紐付け部、21 本体制御部、22 入力装置、23 プロセッサ、31 パルサ、32 増幅部、33 AD変換部、34 ビームフォーマ、35 信号処理部、36 DSC、37 画像処理部、A1 第1表示領域、A2 第2表示領域、A3 第3表示領域、B1 フリーズボタン、BM ボディマーク、C1 スライドバー、C2 スライドボタン、E1,E2 胸水有無アイコン、J1~J20 診断所見アイコン、L1~L3 強調線、LR 左右切り替えボタン、M1 模式図、M2 プローブマーク、M3 検査箇所マーク、P1~P4 検査箇所選択アイコン、U,U1 超音波画像。 1 ultrasonic diagnostic device, 2 ultrasonic probe, 3 diagnostic device body, 11 oscillator array, 12 transmission / reception circuit, 13 image generation unit, 14 display control unit, 15 monitor, 16 image memory, 17 image pattern memory, 18 similarity Judgment unit, 19 emphasis change unit, 20 diagnostic finding linking unit, 21 main unit control unit, 22 input device, 23 processor, 31 pulser, 32 amplification unit, 33 AD conversion unit, 34 beam former, 35 signal processing unit, 36 DSC, 37 image processing unit, A1 1st display area, A2 2nd display area, A3 3rd display area, B1 freeze button, BM body mark, C1 slide bar, C2 slide button, E1, E2 chest water presence / absence icon, J1 ~ J20 diagnostic findings icon, L1 to L3 emphasis line, LR left / right switching button, M1 schematic diagram, M2 probe mark, M3 inspection location mark, P1 to P4 inspection location selection icon, U, U1 ultrasound image.

Claims (13)

  1.  超音波プローブと、
     前記超音波プローブに接続された診断装置本体と
     を備え、
     前記診断装置本体は、
     超音波診断画像と定められた複数の診断所見に対応する複数の診断所見アイコンとを表示するモニタと、
     前記超音波診断画像と前記複数の診断所見に対応する複数の画像パターンとの類似度をそれぞれ判定する類似度判定部と、
     前記類似度判定部により判定された前記類似度に応じて前記モニタにおける前記複数の診断所見アイコンの強調度を変更する強調度変更部と
     を含む超音波診断装置。
    With an ultrasonic probe,
    It is equipped with a diagnostic device main body connected to the ultrasonic probe.
    The diagnostic device body is
    A monitor that displays ultrasonic diagnostic images and multiple diagnostic findings icons that correspond to multiple defined diagnostic findings.
    A similarity determination unit for determining the similarity between the ultrasonic diagnostic image and the plurality of image patterns corresponding to the plurality of diagnostic findings, respectively.
    An ultrasonic diagnostic apparatus including an emphasis degree changing unit that changes the emphasis degree of the plurality of diagnostic findings icons on the monitor according to the similarity degree determined by the similarity degree determination unit.
  2.  前記診断装置本体は、
     ユーザが入力操作を行うための入力装置と、
     前記モニタに表示された前記複数の診断所見アイコンのうち、前記入力装置を介して選択された前記診断所見アイコンに対応する前記診断所見を前記超音波診断画像に紐付ける診断所見紐付け部と
     を含む請求項1に記載の超音波診断装置。
    The diagnostic device body is
    An input device for the user to perform input operations, and
    Among the plurality of diagnostic findings icons displayed on the monitor, a diagnostic finding linking unit that links the diagnostic findings corresponding to the diagnostic findings icon selected via the input device to the ultrasonic diagnostic image. The ultrasonic diagnostic apparatus according to claim 1, which includes.
  3.  前記診断所見紐付け部により前記超音波診断画像に紐付けられた前記診断所見は、前記モニタに表示される請求項2に記載の超音波診断装置。 The ultrasonic diagnostic apparatus according to claim 2, wherein the diagnostic findings linked to the ultrasonic diagnostic image by the diagnostic findings linking unit are displayed on the monitor.
  4.  前記強調度変更部は、前記類似度が高い診断所見に対応する診断所見アイコンほど強く強調されるように、前記複数の診断所見アイコンの強調度を変更する請求項1~3のいずれか一項に記載の超音波診断装置。 One of claims 1 to 3 for changing the emphasis of the plurality of diagnostic findings icons so that the emphasis changing unit is emphasized more strongly as the diagnostic findings icon corresponding to the diagnostic findings having a higher similarity is emphasized. The ultrasonic diagnostic apparatus described in.
  5.  前記強調度変更部は、前記複数の診断所見のうち、前記類似度が最も高い診断所見に対応する診断所見アイコンを、強調線により囲む請求項4に記載の超音波診断装置。 The ultrasonic diagnostic apparatus according to claim 4, wherein the emphasis changing unit surrounds a diagnostic finding icon corresponding to the diagnostic finding having the highest similarity among the plurality of diagnostic findings with a highlight line.
  6.  前記強調度変更部は、前記複数の診断所見のうち、前記類似度が最も高い診断所見に対応する診断所見アイコンを、他の診断所見アイコンとは異なる色により表示する請求項4に記載の超音波診断装置。 The super-elevation according to claim 4, wherein the emphasis changing unit displays a diagnostic finding icon corresponding to the diagnostic finding having the highest similarity among the plurality of diagnostic findings in a color different from that of other diagnostic findings icons. Sound diagnostic equipment.
  7.  前記強調度変更部は、前記複数の診断所見のうち、前記類似度が最も高い診断所見に対応する診断所見アイコンを、他の診断所見アイコンよりも大きく表示する請求項4~6のいずれか一項に記載の超音波診断装置。 The emphasis changing unit is any one of claims 4 to 6 for displaying the diagnostic finding icon corresponding to the diagnostic finding having the highest similarity among the plurality of diagnostic findings larger than the other diagnostic findings icons. The ultrasonic diagnostic apparatus described in the section.
  8.  前記超音波診断画像は、被検体の肺を撮像した超音波画像であり、
     前記複数の診断所見のうち少なくとも1つは、Bライン、硬化、正常、ラングスライディング無し、のいずれかの診断所見を含む請求項1~7のいずれか一項に記載の超音波診断装置。
    The ultrasonic diagnostic image is an ultrasonic image of the lungs of a subject, and is an ultrasonic image.
    The ultrasonic diagnostic apparatus according to any one of claims 1 to 7, wherein at least one of the plurality of diagnostic findings includes any of the diagnostic findings of B line, hardening, normal, and no rung sliding.
  9.  前記超音波診断画像は、フリーズ時の静止画像であり、
     前記静止画像が前記モニタに表示される請求項1~8のいずれか一項に記載の超音波診断装置。
    The ultrasonic diagnostic image is a still image at the time of freezing, and is a still image.
    The ultrasonic diagnostic apparatus according to any one of claims 1 to 8, wherein the still image is displayed on the monitor.
  10.  前記超音波診断画像は、動画像である請求項1~8のいずれか一項に記載の超音波診断装置。 The ultrasonic diagnostic image according to any one of claims 1 to 8, wherein the ultrasonic diagnostic image is a moving image.
  11.  前記超音波診断画像は、フリーズまでの定められた時間における動画像である請求項10に記載の超音波診断装置。 The ultrasonic diagnostic image according to claim 10, wherein the ultrasonic diagnostic image is a moving image at a predetermined time until freeze.
  12.  前記類似度判定部は、前記動画像を構成する複数フレームの超音波画像について前記複数の診断所見に対応する前記複数の画像パターンとの類似度をそれぞれ判定し、
     前記複数フレームの超音波画像のうち、前記類似度が最も高い超音波画像が前記モニタに表示され、
     前記強調度変更部は、前記類似度が最も高い超音波画像に基づいて前記複数の診断所見アイコンの強調度を変更する請求項10または11に記載の超音波診断装置。
    The similarity determination unit determines the similarity of the ultrasonic images of the plurality of frames constituting the moving image with the plurality of image patterns corresponding to the plurality of diagnostic findings.
    Among the plurality of frames of ultrasonic images, the ultrasonic image having the highest similarity is displayed on the monitor.
    The ultrasonic diagnostic apparatus according to claim 10 or 11, wherein the emphasis changing unit changes the emphasis of the plurality of diagnostic findings icons based on the ultrasonic image having the highest similarity.
  13.  超音波診断画像と定められた複数の診断所見に対応する複数の診断所見アイコンとをモニタに表示し、
     前記超音波診断画像と前記複数の診断所見に対応する複数の画像パターンとの類似度をそれぞれ判定し、
     判定された前記類似度に応じて前記モニタにおける前記複数の診断所見アイコンの強調度を変更する
     超音波診断装置の制御方法。
    An ultrasonic diagnostic image and multiple diagnostic findings icons corresponding to multiple defined diagnostic findings are displayed on the monitor.
    The degree of similarity between the ultrasonic diagnostic image and the plurality of image patterns corresponding to the plurality of diagnostic findings is determined, respectively.
    A control method for an ultrasonic diagnostic apparatus that changes the emphasis of the plurality of diagnostic findings icons on the monitor according to the determined similarity.
PCT/JP2021/036786 2020-10-16 2021-10-05 Ultrasonic diagnostic device and method for controlling ultrasonic diagnostic device WO2022080183A1 (en)

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Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010237930A (en) * 2009-03-31 2010-10-21 Fujifilm Corp Case image retrieval device, method, and program
JP2010264175A (en) * 2009-05-18 2010-11-25 Aloka Co Ltd Ultrasonic diagnostic apparatus
JP2011118543A (en) * 2009-12-01 2011-06-16 Shizuoka Prefecture Case image retrieval device, method and program
JP2013511762A (en) * 2009-11-24 2013-04-04 コーニンクレッカ フィリップス エレクトロニクス エヌ ヴィ Protocol Guide Imaging Procedure

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010237930A (en) * 2009-03-31 2010-10-21 Fujifilm Corp Case image retrieval device, method, and program
JP2010264175A (en) * 2009-05-18 2010-11-25 Aloka Co Ltd Ultrasonic diagnostic apparatus
JP2013511762A (en) * 2009-11-24 2013-04-04 コーニンクレッカ フィリップス エレクトロニクス エヌ ヴィ Protocol Guide Imaging Procedure
JP2011118543A (en) * 2009-12-01 2011-06-16 Shizuoka Prefecture Case image retrieval device, method and program

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