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WO2020121721A1 - Système d'imagerie diagnostique et procédé de gestion d'imagerie diagnostique - Google Patents

Système d'imagerie diagnostique et procédé de gestion d'imagerie diagnostique Download PDF

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Publication number
WO2020121721A1
WO2020121721A1 PCT/JP2019/044501 JP2019044501W WO2020121721A1 WO 2020121721 A1 WO2020121721 A1 WO 2020121721A1 JP 2019044501 W JP2019044501 W JP 2019044501W WO 2020121721 A1 WO2020121721 A1 WO 2020121721A1
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Prior art keywords
sample
specimen
position information
control unit
analysis
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English (en)
Japanese (ja)
Inventor
駿介 加治木
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Shimadzu Corp
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Shimadzu Corp
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Priority to JP2020559852A priority Critical patent/JP7111179B2/ja
Publication of WO2020121721A1 publication Critical patent/WO2020121721A1/fr
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B6/00—Apparatus or devices for radiation diagnosis; Apparatus or devices for radiation diagnosis combined with radiation therapy equipment
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B6/00—Apparatus or devices for radiation diagnosis; Apparatus or devices for radiation diagnosis combined with radiation therapy equipment
    • A61B6/12—Arrangements for detecting or locating foreign bodies

Definitions

  • the present invention relates to a diagnostic image system and a diagnostic image management method.
  • Non-Patent Document 1 Kozo Makita, “Adrenal Vein Blood Collection in Primary Aldosteronism-Tips for Successful Adrenal Vein Sampling Procedure”, Journal of the Japanese Society of Interventional Radiology, 2013, Vol. 28, No. 2, p. No. 204-210 (hereinafter referred to as Non-Patent Document 1).
  • Non-Patent Document 1 for diagnosis of primary aldosteronism, blood sampling is performed from veins of various parts of the adrenal gland while confirming an X-ray fluoroscopic image of a subject in real time by a radiographic image diagnostic apparatus. It is disclosed. Blood (sample sample) at each position collected by adrenal vein sampling is analyzed by a sample analyzer, and a definitive diagnosis is made based on the analysis result. When the definitive diagnosis is made based on the analysis result, the lesioned part is specified based on the sampling position of the sampled sample, and whether or not partial excision of the lesioned part is performed is determined. Since a plurality of sample specimens are acquired, the individual specimen samples can be identified by adding information that allows them to be identified.
  • Non-Patent Document 1 In the method disclosed in Non-Patent Document 1 described above, it is necessary to sketch the adrenal vein in the chart and enter the collection position in order to associate the blood sample with the collection position. However, there is an inconvenience that the burden on the user increases. Therefore, although not described in Non-Patent Document 1, instead of describing the collection position in the adrenal vein sketched on the chart, a doctor or the like registers the collection position information of the specimen sample in the radiation image. Therefore, it is possible to confirm the sampling position of the specimen sample in the radiation image.
  • a doctor or the like may want to confirm whether or not the sampling position information of each specimen sample is registered in the radiation image.
  • the present invention has been made to solve the above problems, and one object of the present invention is to see at a glance whether or not the sampling position information of a specimen sample is registered in a radiographic image. To provide a diagnostic image system and a diagnostic image management method that can be easily grasped.
  • a diagnostic imaging system is a radiographic apparatus that captures a radiographic image of a subject whose collection positions of a plurality of specimen samples collected from an organ can be determined, At least a display unit including the first display area and the second display area, a radiation image, and sampling position information of the sample specimen is acquired, and the sampling position of the specimen sample is determined based on the acquired sampling position information of the specimen sample.
  • a control unit that controls to display a radiographic image in the first display area so as to be distinguishable, and controls to display sample data including information that can identify each of a plurality of specimen samples in the second display area.
  • the control unit is configured to display the registration status of the sampling position information of the specimen sample in the radiographic image performed by the operator based on whether the sampling position information corresponding to the specimen sample is acquired.
  • the “registration status of the sampling position information of the specimen sample in the radiation image” means whether or not the position information of the specimen sample is registered in the radiation image.
  • the sampling position of the sample in the radiographic image performed by the operator is performed.
  • a control unit for performing control to display the registration status of information is provided. Accordingly, in the second display area, it is possible to visually grasp the registration status of the sampling position information of the specimen sample in the radiation image. As a result, a doctor or the like can easily grasp at a glance whether or not the sampling position information of the specimen sample is registered in the radiographic image.
  • the “display area” is an area on the screen for displaying an X-ray image, sample data, and the like.
  • selection position information means the coordinate value of the position where the specimen sample is collected on the radiographic image, the marker attached to the position where the specimen sample is collected, and the arrow indicating the collection position on the radiographic image.
  • the information that can specify the sampling position of the specimen sample is included.
  • the control unit displays the sample data in a list format, and in each line of the sample data displayed in the list format, the registration status of the sampling position information for each sample specimen.
  • the control unit displays the sample data in a list format, and in each line of the sample data displayed in the list format, the registration status of the sampling position information for each sample specimen.
  • the control unit displays a sign indicating the registration status of the collection position information
  • the display mode of the sign and the display area of the sign is the registration status of the collection position information. It is configured to be displayed differently according to. According to this structure, it is possible to distinguishably display the specimen sample for which the registration of the sampling position information for the radiation image is completed and the specimen sample for which the registration of the sampling position information for the radiation image is not completed. ..
  • the display mode of the indicator and the display area of the indicator differs depending on the situation of the collection position information, a doctor or the like confirms the display area for displaying the registration situation of the collection position information, and for each sample specimen, The registration status of the collection position information can be easily visually grasped.
  • the control unit registers the sampling position information with respect to the radiation image by an operator's input, and there is a specimen sample in which the sampling position information is not registered with the radiation image. In this case, the presence of an unregistered specimen sample is displayed.
  • a doctor or the like can visually recognize that there is omission of registration of the collection position information for the radiation image before the registration operation is completed. Therefore, it is possible to suppress the omission of registration of the sampling position information for the radiographic image. As a result, it is possible to prevent the collection position of the specimen sample from being unspecified, and the collection position information from being unable to be registered in the radiation image.
  • the diagnostic image system preferably further includes a sample analyzer that analyzes the sample sample and generates an analysis result, and the control unit displays the progress status of the analysis for each of the plurality of sample samples. Is configured to. According to this structure, a doctor or the like can visually grasp the progress status of the analysis of the specimen sample in addition to the registration status of the sampling position information for the radiographic image. As a result, the situation of the sample specimen can be grasped in detail.
  • control unit is configured to display, as the progress status of the analysis, at least whether or not the analysis is completed for each of the plurality of sample specimens in a distinguishable manner.
  • a doctor or the like can easily see at a glance whether or not the analysis is completed for each sample specimen.
  • a doctor or the like can grasp the sample sample of which analysis has been completed among the plurality of sample samples by confirming the sample data.
  • the control unit for each of the plurality of sample samples, as the progress status of the analysis, one of before analysis of the sample sample, during analysis of the sample sample, and completion of analysis of the sample sample.
  • the control unit for each of the plurality of sample samples, as the progress status of the analysis, one of before analysis of the sample sample, during analysis of the sample sample, and completion of analysis of the sample sample.
  • the control unit for each of the plurality of sample samples, as the progress status of the analysis, one of before analysis of the sample sample, during analysis of the sample sample, and completion of analysis of the sample sample.
  • control unit is configured to display an ongoing analysis step among the analysis steps by the sample analyzer for each of the plurality of sample samples as the progress status of the analysis. Has been done. With this configuration, a doctor or the like can visually grasp the analysis status of the sample specimen in detail.
  • the diagnostic image management method includes a step of acquiring a radiation image of a subject whose collection positions of a plurality of sample specimens collected from an organ can be determined, a radiation image, and a specimen sample collection position. And a radiographic image is displayed in the first display area so that the sampling position of the sample sample can be determined based on the acquired information and the sampled sample position information. Based on the step of displaying the sample data including the possible information in the second display area and whether or not the sampling position information corresponding to the sample is acquired, the sampling position of the sample in the radiographic image performed by the operator Displaying the registration status of the information.
  • the diagnostic image management method As described above, based on whether or not the collection position information corresponding to the specimen sample is acquired, the specimen sample is collected from the radiation image by the operator. The step of displaying the registration status of the position information is included.
  • a method can be provided.
  • FIG. 6 is a schematic diagram showing a first display area, a second display area, and a third display area displayed on a display unit in the diagnostic image system according to the first embodiment.
  • FIG. 6 is a flowchart for explaining a process in which the diagnostic image system according to the first embodiment displays a registration status of sampling position information of a specimen sample.
  • FIG. 6 is a schematic diagram in which sampled sample position information and sample data corresponding to a sample sample specified by selection are highlighted in the diagnostic imaging system according to the first embodiment.
  • 6 is a flowchart for explaining a process in which the diagnostic imaging system according to the first embodiment highlights sample sample collection position information and sample data corresponding to a sample sample specified by selection.
  • the diagnostic imaging system according to the second embodiment it is a schematic diagram in which sampling position information and sample data of a specimen sample corresponding to a specimen sample specified by selection are highlighted.
  • FIG. 14 is a schematic diagram showing that there is a sample specimen whose collection position information is not registered in the diagnostic image system according to the fourth embodiment.
  • FIG. 12 is a schematic diagram for explaining a process that causes the presence of a sample specimen whose collection position information is unregistered in the diagnostic image system according to the fourth embodiment. It is a schematic diagram which displayed the analysis condition of the specimen sample in the diagnostic imaging system by 5th Embodiment.
  • FIG. 16 is a schematic diagram showing an analysis status of a specimen sample in the diagnostic imaging system according to the sixth embodiment.
  • FIG. 14 is a schematic diagram showing a first display area, a second display area, and a third display area displayed on the display unit in the diagnostic image system according to the third modified example of the first embodiment.
  • the first embodiment shows an example in which the diagnostic imaging system 1 is used for adrenal vein sampling for the diagnosis of primary aldosteronism.
  • the diagnostic imaging system 1 includes an X-ray imaging apparatus 2 that captures an X-ray image G (see FIG. 2) of a subject T, and a sample that analyzes a sample sample collected from the subject T. And an analyzer 3.
  • each of the X-ray imaging apparatus 2 and the sample analyzer 3 is separately installed in the operating room R1 and the analysis room R2.
  • the diagnostic image system 1 also includes a workstation 4.
  • the workstation 4 is installed in the operating room R1 together with the X-ray imaging apparatus 2.
  • the workstation 4 includes a control unit 41 and a display unit 42.
  • the display unit 42 includes a first display area F1 (see FIG. 5) and a second display area F2 (see FIG. 5).
  • the control unit 41 controls the X-ray image G and the collection position information C (see FIG. 5) of the plurality of specimen samples to be displayed in the first display area F1, and can identify each of the plurality of specimen samples.
  • the sample data SD including information (see FIG. 5) is configured to be displayed in the second display area F2.
  • the X-ray imaging apparatus 2 is an example of the “radiation imaging apparatus” in the claims.
  • the X-ray image G is an example of the “radiation image” in the claims.
  • the diagnostic imaging system 1 captures an X-ray image G from the outside of the subject T by the X-ray imaging device 2 in order to collect a specimen sample in the subject T.
  • the specimen collecting device 10 is introduced into the inside of the subject T, and the doctor in charge of the specimen collection uses the specimen collecting device 10 at the specimen sample collecting position ( (See Fig. 5) and collect the specimen sample.
  • a catheter is used as the sample collection device 10.
  • the specimen sample is acquired from an organ.
  • the organ is adrenal AG (see FIG. 5) that secretes hormones.
  • the specimen sample is adrenal venous blood obtained from the adrenal vein of adrenal AG.
  • the adrenal gland AG is an example of the “organ” in the claims.
  • the collected specimen sample is taken into the specimen collecting device 10, is accommodated in the specimen container B for accommodating the specimen sample, and then the specimen container B is transferred to the specimen analyzer 3.
  • An operator such as a laboratory technician sets the sample container B on the sample analyzer 3, and the sample analyzer 3 receives the sample sample.
  • the sample container B is, for example, a blood collection tube.
  • the sample analyzer 3 analyzes the acquired sample sample.
  • the sample container B is provided with sample specifying information for specifying a sample sample.
  • the sample specifying information is the identification information U attached to the sample container B for containing the collected sample sample.
  • the identification information U is, for example, a sample ID attached to the sample container B in the form of a barcode or a two-dimensional code.
  • the identification information U is prepared, for example, in the form of a label on which a barcode is printed, and is attached to the sample container B by the operator when the sample sample is collected.
  • the identification information U is an example of “information capable of identifying each of a plurality of sample specimens” in the claims.
  • the X-ray imaging apparatus 2 is an apparatus that captures an X-ray image G by irradiating the subject T with radiation.
  • the X-ray imaging apparatus 2 is configured to take an X-ray image G of the subject T in which the collection position of the specimen sample collected from the adrenal gland AG (see FIG. 5) can be determined.
  • the “X-ray image G of the subject T in which the sampling position of the sample is discriminable” is an image captured with the sample collecting device 10 arranged at the position for collecting the sample. For example, when a catheter is used as the sample collection device 10, an X-ray image G of the subject T in which the sample sample collection position can be determined is obtained by photographing the tip of the catheter at the sample sample collection position. get.
  • the X-ray imaging apparatus 2 includes an irradiation unit 21 that irradiates the subject T with radiation (X-rays) and a detector 22 that detects the radiation that has passed through the subject T.
  • the irradiation unit 21 and the detection unit 22 are arranged so as to face each other with the top plate 23 on which the subject T is placed interposed.
  • the irradiation unit 21 and the detection unit 22 are movably supported by the moving mechanism 24.
  • the top 23 can be moved in the horizontal direction by the top driver 25.
  • the irradiation unit 21, the detection unit 22, and the top 23 are moved via the moving mechanism 24 and the top driving unit 25 so that the region of interest of the subject T can be imaged.
  • the region of interest is a region of the subject T including the sampling position of the specimen sample.
  • the X-ray imaging apparatus 2 includes a control unit 26 that controls the moving mechanism 24 and the top plate driving unit 25.
  • the irradiation unit 21 includes a radiation source 21a.
  • the radiation source 21a is, for example, an X-ray tube that generates X-rays by applying a predetermined high voltage.
  • the irradiation unit 21 is connected to the control unit 26.
  • the control unit 26 controls the irradiation unit 21 according to preset imaging conditions, and causes the radiation source 21a to generate X-rays.
  • the detection unit 22 detects the X-rays emitted from the irradiation unit 21 and transmitted through the subject T, and outputs a detection signal according to the detected X-ray intensity.
  • the detection unit 22 is composed of, for example, an FPD (Flat Panel Detector).
  • the X-ray imaging apparatus 2 includes an image processing unit 27 that acquires an X-ray detection signal from the detection unit 22 and generates an X-ray image G based on the detection signal of the detection unit 22.
  • the detection unit 22 outputs the X-ray detection signal to the image processing unit 27.
  • the image processing unit 27 includes, for example, a processor (not shown) such as a CPU (Central Processing Unit) and a storage unit (not shown) such as a ROM (Read Only Memory) and a RAM (Random Access Memory).
  • the computer is configured and functions as the image processing unit 27 by causing the processor to execute the image processing program.
  • the image processing unit 27 has a function of generating an X-ray image G, a correction process for improving the visibility of the X-ray image G, a combining process of combining a plurality of X-ray images G, and the like. There is. Further, the image processing unit 27 performs a process of generating the thumbnail image TH (see FIG. 5) of the generated X-ray image G. Specifically, the image processing unit 27 reduces the generated X-ray image G to generate the thumbnail image TH.
  • the control unit 26 is a computer including a CPU (not shown), a ROM (not shown), a RAM (not shown), and the like.
  • the control unit 26 functions as the control unit 26 that controls each unit of the X-ray imaging apparatus 2 by the CPU executing a predetermined control program.
  • the control unit 26 controls the irradiation unit 21 and the image processing unit 27, and drives the moving mechanism 24 and the top plate driving unit 25.
  • the X-ray imaging apparatus 2 includes a display unit 26a, an operation unit 26b, and a storage unit 26c.
  • the X-ray imaging apparatus 2 also includes a communication unit 26d for connecting to the network N (see FIG. 1). Further, the X-ray imaging apparatus 2 includes a connecting portion 26e for connecting to the workstation 4.
  • the display unit 26a is, for example, a monitor such as a liquid crystal display.
  • the operation unit 26b includes, for example, a keyboard and a mouse, a touch panel or another controller.
  • the storage unit 26c is configured by a storage device such as a hard disk drive.
  • the control unit 26 is configured to perform control to display the image generated by the image processing unit 27 on the display unit 26a.
  • the control unit 26 is also configured to receive an input operation via the operation unit 26b.
  • the storage unit 26c is configured to store the data of the X-ray image G, the data of the identification information U, the data of the thumbnail image TH, and the like.
  • the connecting portion 26e is configured to connect to the workstation 4. By being connected to the workstation 4 by the connecting unit 26e, the data of the X-ray image G, the data of the identification information U, the data of the thumbnail image TH, etc. can be transmitted to the workstation 4.
  • the connection unit 26e includes, for example, a serial communication port.
  • the X-ray imaging apparatus 2 includes a reading unit 28 for reading the identification information U attached to the sample container B for containing the collected sample specimen.
  • the reading unit 28 is, for example, a bar code reader (or a two-dimensional code reader) corresponding to the identification information U, and can read the identification information U attached to each sample container B.
  • the control unit 26 is configured to add the identification information U read by the reading unit 28 to the X-ray image G when the specimen sample is collected. For example, the control unit 26 adds the identification information U to the X-ray image G by recording the X-ray image G and the identification information U in image concatenated data (DICOM file) in a format conforming to the DICOM standard.
  • DICOM file image concatenated data
  • the sample analyzer 3 is a device that acquires a sample sample collected from the subject T and measures components necessary for diagnosis and detects cells.
  • the sample analyzer 3 is a liquid chromatograph mass spectrometer.
  • the sample analyzer 3 ionizes the liquid chromatograph unit 31 (hereinafter, referred to as LC unit 31) that separates the target component contained in the sample, and separates the target component according to the mass number.
  • a mass spectrometric unit 32 for detecting hereinafter referred to as MS unit 32).
  • the LC unit 31 includes a carrier liquid reservoir (not shown) that stores the carrier liquid, a liquid feed pump (not shown) that sends the carrier liquid together with the sample specimen, and a sample introduction unit (not shown) that introduces the sample specimen. And a separation column (not shown) that separates the specimen sample in the carrier liquid for each component.
  • the MS unit 32 is provided after the LC unit 31, and is used for mass-separating the generated ions and an ionization unit (not shown) that ionizes the sample components separated by the LC unit 31 and passes the specific ions. Mass separator (not shown) and an ion detector (not shown) for detecting ions that have passed through the mass separator. The MS unit 32 outputs a detection signal for each mass of the sample components that are sequentially eluted from the LC unit 31.
  • the data processing unit 33 creates a mass spectrum from the detection signal for each mass and compares it with the calibration curve to perform quantitative analysis of a predetermined component in the specimen sample.
  • the predetermined components analyzed by the sample analyzer 3 are cortisol and aldosterone.
  • the sample analyzer 3 includes a display unit 33a, an operation unit 33b, a storage unit 33c, and a communication unit 33d.
  • the sample analyzer 3 further includes a reading unit 34 (see FIG. 1).
  • the data processing unit 33 is configured to add the identification information U read by the reading unit 34 to the analysis result RA when the sample sample is analyzed.
  • the analysis result RA is the abundance of the test substance contained in the sample sample acquired from the adrenal gland AG of the sample T. Specifically, it is the amount of hormones secreted from adrenal AG. Hormones secreted from the adrenal gland include cortisol, which is a corticosteroid, and aldosterone, which is secreted from spheroids of the adrenal cortex.
  • the analysis result RA includes the cortisol concentration (Data1:xx in FIG. 5) and the aldosterone concentration (Data2:xx in FIG. 5).
  • the analysis result RA and the X-ray image G are associated with each other via common identification information U. Note that being associated with each other means that the analysis result RA and the X-ray image G are associated with one-to-one relationship via the common identification information U.
  • one X-ray image G is associated with one analysis result RA and analysis progress PA.
  • the analysis result RA of the plurality of specimen samples and the analysis progress PA are associated with the X-ray image G.
  • the workstation 4 includes a control unit 41, a display unit 42, an operation unit 43, a storage unit 44, and a connection unit 45.
  • the workstation 4 includes, for example, a personal computer (PC).
  • the collection position information C (see FIG. 5) is manually registered by the operator at the workstation 4. Specifically, the operator starts registration of the collection position information C by pressing an edit start button (not shown) in the second display area F2 (see FIG. 5). After pressing the edit start button, the operator selects the sample sample SD for which the sample position information C is to be registered from the sample data SD, and also selects the sample position on the X-ray image G, thereby collecting the sample sample position information C. To register. When the registration of the collection position information C is completed, the operator presses an edit end button (not shown) to end the registration of the collection position information C.
  • control unit 41 is configured to acquire the X-ray image G and the sampling position information C of the specimen sample.
  • the control unit 41 is also configured to acquire a plurality of thumbnail images TH corresponding to each of the plurality of X-ray images G from the X-ray imaging apparatus 2.
  • the control unit 41 is also configured to acquire the analysis result RA of the sample specimen.
  • the sampling position information C is information including coordinate information of the sampling position of the specimen sample on the X-ray image G registered by the operator.
  • the control unit 41 is also configured to display the registration status of the sampling position information C of the specimen sample on the X-ray image G. Details of the configuration in which the control unit 41 displays the registration status of the sampling position information C of the specimen sample on the X-ray image G will be described later.
  • control unit 41 when the operator selects the sample sample, the control unit 41 is configured to highlight the sampling position information C and the sample data SD of the sample sample corresponding to the sample sample specified by the selection.
  • the details of the configuration in which the control unit 41 highlights the sampling position information C and the sample data SD of the sample corresponding to the sample specified by selection will be described later.
  • the control unit 41 is also configured to receive an input operation via the operation unit 43.
  • the control unit 41 is, for example, a computer including a CPU, a ROM, a RAM, and the like.
  • the display unit 42 includes a first display area F1, a second display area F2, and a third display area F3.
  • the display unit 42 includes, for example, a liquid crystal monitor.
  • the operation unit 43 is configured to receive the input operation of the operator.
  • the operation unit 43 includes, for example, a mouse and a keyboard.
  • the storage unit 44 stores the data of the X-ray image G, the data of the identification information U, the data of the analysis result RA of the specimen sample, the registration status of the sampling position information C in the X-ray image G, and the progress status PA of the specimen sample analysis. It is configured to store data and the like.
  • the storage unit 44 includes, for example, SSD or HDD.
  • connection unit 45 is connected to the X-ray imaging apparatus 2.
  • the connection unit 45 is connected to the sample analyzer 3 via the network N.
  • the workstation 4 includes a reading unit 46 for reading the identification information U attached to the sample container B for storing the collected sample specimen.
  • the control unit 41 acquires the X-ray image G associated with the identification information U from the X-ray imaging apparatus 2 based on the reading of the identification information U by the reading unit 46, and associates the X-ray image G with the identification information U.
  • the analysis result RA and the analysis progress PA are obtained from the sample analyzer 3.
  • the display unit 42 includes a first display area F1, a second display area F2, and a third display area F3.
  • the control unit 41 displays the X-ray image G of the subject T in which the collection position information C of the specimen sample collected from the adrenal gland can be discriminated in the first display area F1.
  • the control unit 41 is configured to perform control to display the acquired X-ray image G and the collection position information C of the plurality of specimen samples in the first display area F1.
  • a circle C1 is shown as the collection position information C at the position where the specimen sample is collected.
  • the control unit 41 is also configured to display the sample data SD including the identification information U in the second display area F2. Specifically, the control unit 41 is configured to display the sample data SD in a list format in the second display area F2. Further, the control unit 41 is configured to display the inspection information E in the second display area F2. The control unit 41 is configured to acquire the sample data SD and the inspection information E associated with the identification information U based on the reading of the identification information U by the reading unit 46.
  • the test information E has information that can identify the subject T from which the sample specimen was collected and the test performed on the subject T.
  • the examination information E has a plurality of items such as examination ID, examination date and time, patient name, patient ID, age, and sex.
  • the examination ID is an item in which an ID unique to the examination being performed is registered.
  • the inspection date and time is an item in which the date and time when the inspection was performed is registered.
  • the patient name is an item in which the name of the patient who has undergone the examination is registered.
  • the patient ID is an item in which an ID corresponding to the patient name is registered.
  • the age and sex are items in which the age and sex of the patient are registered.
  • the tag for example, DICOM tag
  • the sample data SD includes a plurality of items such as collection position information C, identification information U, blood vessel name (BV1, BV2%), analysis result RA (Data1:xx, Data2:xx) and status (collection position and analysis). have.
  • information on items such as collection position information C, identification information U, blood vessel name, analysis result RA, and status in any sample sample among a plurality of sample samples is registered.
  • a plurality of items of the sample data SD will be described by using an arbitrary sample among the plurality of sample samples as a first sample sample with a number 1 attached thereto, for example.
  • the first specimen sample is the specimen sample collected from the place indicated by the number 1 in the X-ray image G.
  • the collection position item is an item in which the number (1) of the collection position information C of the first specimen sample is registered.
  • an identification mark IM described later is displayed in the collection position item.
  • the identification information item is an item in which the identification information U attached to the sample container B in which the first sample specimen is stored is registered.
  • the blood vessel name item is an item in which the blood vessel name of the collection position information C of the first sample specimen is registered.
  • the analysis result item is an item in which the analysis result RA acquired by analyzing the first sample sample in the sample analyzer 3 is registered.
  • the status item is an item in which the registration status of the sampling position information C of the specimen sample for the X-ray image G in the first display area F1 and the progress status PA of the analysis of the specimen sample are registered.
  • Items such as the identification information U, the analysis result RA, the registration status of the sampling position information C, and the analysis progress PA are acquired by the workstation 4 based on the reading of the identification information U by the reading unit 46. Based on the above, it is automatically registered for each specimen sample.
  • the items of the registration status of the sampling position information C and the progress status PA of the analysis are automatically updated every time the status changes, such as when the registration is performed or the analysis is completed.
  • the control unit 41 is also configured to display a plurality of thumbnail images TH corresponding to the plurality of X-ray images G in the third display area F3.
  • control unit 41 is configured to display, on the sample data SD and the X-ray image G, a common identification mark IM that can specify the sampling positions of the plurality of sample specimens. There is.
  • the control unit 41 displays a number surrounded by a circle as the identification mark IM.
  • the control unit 41 is also configured to display the identification mark IM even in the thumbnail image TH.
  • the control unit 41 is configured to display the identification mark IM in the thumbnail image TH in a display mode different from that of the X-ray image G and in a visually recognizable manner.
  • the specimen sample collection position information C is X-ray. It is difficult to grasp at a glance whether or not the image G is registered.
  • the control unit 41 based on whether or not the sampling position information C corresponding to the sample sample is acquired, the sampling position information C of the sample sample on the X-ray image G performed by the operator. It is configured to display the registration status of. Specifically, as shown in the second display area F2 of FIG. 5, the control unit 41 displays the sample data SD in a list format, and in each line of the sample data SD displayed in the list format, for each sample specimen. The registration status of the collection position information C is displayed.
  • control unit 41 displays the marker MS indicating the registration status of the sampling position information C in the sample data SD displayed in the list format, and displays the display mode of the marker MS and the display area DAM of the marker MS as the sampling position information.
  • the display is made different according to the registration status of C.
  • the sample sample for which the collection position information C has been registered in the X-ray image G is indicated by “ ⁇ ” in the display area DAM of the label MS.
  • the specimen sample for which the collection position information C has not been registered in the X-ray image G is displayed as “-” in the display area DAM of the label MS.
  • the control unit 41 changes the marker MS to be displayed from “ ⁇ ” to “ ⁇ ”. Further, in the example shown in FIG. 5, the background color of the display area DAM of the label MS of the specimen sample for which the collection position information C has not been registered in the X-ray image G is changed to the label of the specimen sample for which registration has been completed.
  • the background color of the display area DAM of the MS is displayed differently. In the example shown in FIG. 5, for the sake of convenience, the difference in background color of the display area DAM of the marker MS is indicated by the presence or absence of hatching.
  • the control unit 41 is configured to display the analysis progress PA of each of the plurality of sample specimens. Specifically, the control unit 41 is configured to display, for each of the plurality of sample specimens, at least whether or not the analysis is completed, as the analysis progress status PA so as to be identifiable. In the example shown in FIG. 5, the sample sample for which analysis has been completed displays “ ⁇ ” in the display area DAS of the analysis progress PA. Further, in the example shown in FIG. 5, the sample sample for which analysis has not been completed displays “-” in the display area DAS of the analysis progress PA. When the analysis of the sample specimen is completed, the control unit 41 changes the display of the analysis progress status PA in the display area DAS from “ ⁇ ” to “ ⁇ ”.
  • step S1 the X-ray imaging apparatus 2 acquires an X-ray image G capable of discriminating the sampling positions of a plurality of specimen samples collected from the adrenal gland AG.
  • step S2 the control unit 41 acquires the X-ray image G and the sampling position information C of the plurality of sample specimens. Thereafter, the process proceeds to step S3. Note that if the processing of steps S5 and S6 of FIG. 8 to be described later has already been performed in order to highlight the selected specimen sample, the control unit 41 does not perform the processing of steps S1 and S2. , The process starts from step S3.
  • step S3 the control unit 41 displays the X-ray image G in the first display area F1 so that the sampling position of the sample specimen can be determined based on the acquired sampling position information C of the specimen sample, and the identification information.
  • the sample data SD including U is displayed in the second display area F2.
  • step S4 the control unit 41 determines the sampling position information C of the sample sample on the X-ray image G performed by the operator based on whether the sampling position information C corresponding to the sample sample is acquired. The registration status is displayed and the process ends.
  • sample data SD of the plurality of specimen samples may be displayed in a list format.
  • the information on the specimen sample corresponding to the specimen sample to be confirmed by the doctor or the like on the X-ray image G is displayed as the sample data. It is difficult to understand at a glance from the data SD.
  • the control unit 41 specifies the selection in each of the first display area F1 and the second display area F2.
  • the sampling position information C and the sample data SD of the sample sample corresponding to the sample sample to be displayed are configured to be highlighted.
  • the selection of the specimen sample is performed by a doctor or the like via the operation unit 43. For example, when selecting a specimen sample, a doctor or the like clicks the sampling position information C of the specimen sample with a mouse to select the specimen sample.
  • the control unit 41 is specified by selection in each of the first display area F1 and the second display area F2 by changing the display mode of the identification mark IM.
  • the sample position information C and the sample data SD of the sample sample corresponding to the sample sample are highlighted. Note that the example shown in FIG. 7 is a schematic diagram in the case where the doctor or the like selects the sample specimen in the first collection position information C.
  • the control unit 41 highlights the sampling position information C and the sample data SD of the selected specimen sample by displaying the identification mark IM with a thick line.
  • the collection position information C includes an arrow C2 indicating the collection position of the sample specimen, and the control unit 41 also collects the arrow C2 indicating the collection position as the collection position information C of the specimen sample. It is configured to highlight.
  • control unit 41 highlights the selected identification mark IM in the third display area F3 in addition to the first display area F1 and the second display area F2 when the sample specimen is selected. Is configured. That is, the control unit 41 links the selected identification mark IM in each of the first display region F1, the second display region F2, and the third display region F3 when the specimen sample is selected. It is configured to highlight.
  • step S5 the X-ray imaging apparatus 2 acquires an X-ray image G with which the collection position information C of a plurality of specimen samples acquired from the adrenal gland can be determined.
  • step S6 the control unit 41 acquires the X-ray image G and the sampling position information C of the plurality of sample specimens. Thereafter, the processing proceeds to step S7. If the processing of steps S1 and S2 shown in FIG. 6 has already been performed in order to display the registration status of the collection position information C of the specimen sample, the control unit 41 performs the processing of steps S5 and S6. Without performing, the process starts from step S7.
  • step S7 the control unit 41 displays the X-ray image G capable of identifying the sampling position of the specimen sample and the sampling position information C of the plurality of specimen samples in the first display area F1, and the sample data including the identification information U. SD is displayed in the second display area F2.
  • step S8 the control unit 41 acquires a plurality of thumbnail images TH corresponding to each of the plurality of X-ray images G, and displays the acquired thumbnail images TH in the third display area F3. Then, a process progresses to step S9.
  • step S9 when the sampling position of the specimen sample is selected in the first display area F1, the control unit 41 corresponds to the specimen sample specified by the selection in each of the first display area F1 and the second display area F2. The sampling position of the sample to be sampled and the sample data SD of the sample to be sampled are highlighted.
  • step S10 when the sampling position of the specimen sample is selected in the first display area F1, the control unit 41 highlights the specimen sample specified by the selection in the third display area F3.
  • the processes of steps S7 and S8 may be performed in the same step. Further, the processes of step S9 and step S10 may be processed in the same step.
  • the diagnostic imaging system 1 uses the X-ray imaging apparatus 2 that captures the X-ray image G of the subject T in which the collection position information C of the specimen sample collected from the adrenal AG can be determined. And at least the display unit 42 including the first display area F1 and the second display area F2, the X-ray image G, and the sampling position information C of the specimen sample, and the acquired sampling position information C of the specimen sample Based on this, control is performed to display the X-ray image G in the first display area F1 so that the sampling position of the specimen sample can be determined, and control to display the sample data SD including the identification information U in the second display area F2. And a control unit 41 for performing the above.
  • the control unit 41 based on whether or not the sampling position information C corresponding to the sample is acquired, performs the sampling position information of the sample on the X-ray image G performed by the operator. It is configured to display the registration status of C. Accordingly, in the second display area F2, the registration status of the sampling position information C of the specimen sample in the X-ray image G can be visually grasped. As a result, a doctor or the like can easily grasp at a glance whether or not the sampling position information C of the specimen sample is registered in the X-ray image G.
  • the control unit 41 displays the sample data SD in the list format, and in each line of the sample data SD displayed in the list format, the sampling position information C for each specimen sample. Is configured to display the registration status of. This makes it possible to check the registration status of the collection position information C for each sample in each line of the sample data SD, so that the doctor or the like registers the collection position information C of each sample in the X-ray image G. It is possible to easily visually grasp whether or not the operation is performed.
  • the control unit 41 displays the marker MS indicating the registration status of the collection position information C in the sample data SD displayed in the list format, and displays the marker MS and the marker MS.
  • the display mode of the display area DAM is configured to be displayed differently according to the registration status of the collection position information C.
  • the display mode of the marker MS and the display area DAM of the marker MS differs depending on the status of the collection position information C, so that a doctor or the like confirms the display area DAM for displaying the registration status of the collection position information C.
  • the registration status of the collection position information C can be easily visually grasped for each specimen sample.
  • the sample analyzer further includes the sample analyzer 3 that analyzes the sample sample and generates the analysis result RA, and the control unit 41 has the progress of the analysis for each of the plurality of sample samples. It is configured to display the PA. Thereby, the doctor or the like can visually grasp the progress status PA of the analysis of the specimen sample in addition to the registration status of the sampling position information C for the X-ray image G. As a result, the situation of the sample specimen can be grasped in detail.
  • the control unit 41 displays the analysis progress status PA for each of the plurality of sample specimens in a distinguishable manner as to whether or not the analysis is completed. It is configured. Thereby, a doctor or the like can easily grasp at a glance whether or not the analysis is completed for each sample specimen. As a result, a doctor or the like can grasp the sample sample of which analysis has been completed among the plurality of sample samples by confirming the sample data SD.
  • the diagnostic image management method includes the step S1 of capturing the X-ray image G of the subject T in which the sampling position information C of the sample sample collected from the adrenal AG can be determined. , Step S2 of acquiring the X-ray image G and the collection position information C of the plurality of specimen samples, and the X-ray image so that the collection position of the specimen sample can be discriminated based on the acquired collection position information C of the specimen sample. Based on step S3 of displaying G in the first display area F1 and sample data SD including the identification information U in the second display area F2, and whether or not the sampling position information C corresponding to the specimen sample is acquired.
  • a diagnostic image management method capable of easily grasping at a glance whether or not the sampling position information C of the specimen sample is registered in the X-ray image G is provided. Can be provided.
  • a diagnostic imaging system 100 (see FIG. 1) according to the second embodiment will be described with reference to FIGS. 1 and 9.
  • the control unit 51 of the diagnostic image system 100 In addition to the identification mark IM, the line of the sample data SD is configured to highlight the selected specimen sample by at least one of the display color change, the font change, the character blinking, and the enlarged display. Has been done.
  • the same components as those in the first embodiment are designated by the same reference numerals and the description thereof will be omitted.
  • the control unit 51 controls at least the line of the sample data SD to change the display color, change the font, blink the character, and enlarge the character.
  • Any of the displays is configured to highlight the selected specimen sample.
  • the selected specimen sample is highlighted by changing the display color of the row of the sample data SD.
  • the example illustrated in FIG. 9 illustrates that the display color is changed by adding hatching to the row of the selected sample specimen for convenience.
  • control unit 51 is configured to highlight the line of the sample data SD in addition to the identification mark IM by changing the display color to highlight the selected sample sample. ing.
  • the line in which the selected specimen sample is displayed can be further emphasized and displayed.
  • a diagnostic image system 110 (see FIG. 1) according to the third embodiment will be described with reference to FIGS. 1 and 10.
  • the control unit 41 highlights the sampling position information C in the X-ray image G of the specimen sample corresponding to one specimen sample specified by selection and the sample data SD of the specimen sample
  • the control unit 61 of the diagnostic imaging system 110 collects the sampling position information C in the X-ray image G of the specimen samples corresponding to the plurality of specimen samples specified by the selection and
  • the sample data SD of the sample specimen is configured to be highlighted.
  • the same components as those in the first embodiment are designated by the same reference numerals and the description thereof will be omitted.
  • the control unit 61 collects the specimen samples corresponding to the plurality of specimen samples specified in the selection in the X-ray image G.
  • the position information C and the sample data SD of the sample sample are respectively highlighted.
  • the control unit 61 obtains the sampling position information C and the specimen data SD of the specimen sample in the X-ray image G of the specimen sample corresponding to the plurality of specimen samples specified by the selection.
  • the display modes are configured to be different from each other so as to be distinguishable from each other and to be highlighted.
  • the identification marks IM corresponding to a plurality of selected sample specimens are displayed in bold lines, and the display colors of the identification marks IM are displayed differently.
  • the difference in display color of the identification mark IM is represented by showing the identification mark IM with a thick line and by hatching the identification mark IM.
  • the collection position information C includes an arrow C2 and an arrow C3 indicating the collection position of the sample specimen, and the control unit 61 identifies the arrow C2 and the arrow C3 indicating the collection position of the specimen sample, respectively. It is highlighted as possible.
  • the control unit 61 also highlights the identification marks IM displayed on the thumbnail image TH so that they can be identified.
  • the control unit 61 collects position information in the X-ray image G of the specimen samples corresponding to the plurality of specimen samples specified by the selection.
  • the sample data SD of C and the sample of the sample are respectively highlighted.
  • the control unit 61 collects the specimen samples corresponding to the plurality of specimen samples specified in the selection in the X-ray image G.
  • the position information C and the sample data SD of the sample sample are configured to be highlighted in different display modes so as to be distinguishable from each other.
  • the specimen samples in the respective display areas first display area F1, second display area F2, and third display area F3 are associated in a one-to-one relationship. be able to.
  • a diagnostic image system 120 (see FIG. 1) in the fourth embodiment will be described with reference to FIGS. 1, 5 and 11.
  • the control unit 41 displays the registration status of the sampling position information C of the sample on the X-ray image G performed by the operator based on whether the sampling position information C corresponding to the sample is acquired.
  • the control unit 71 of the diagnostic imaging system 120 registers the sampling position information C for the X-ray image G according to the operator's input, and collects the sampling position information in the X-ray image G. When there is a sample sample in which C is not registered, it is configured to display that there is an unregistered sample sample.
  • the same components as those in the first embodiment are designated by the same reference numerals and the description thereof will be omitted.
  • control unit 71 registers the sampling position information C with respect to the X-ray image G by an operator's input, and there is a specimen sample in which the sampling position information C is not registered in the X-ray image G. Is configured to display that there is an unregistered sample specimen.
  • control unit 71 is configured to receive an input operation by the operator.
  • the control unit 71 registers the sampling position information C of the specimen sample in the X-ray image G based on the input by the operator's selection operation.
  • the control unit 71 also ends the registration of the collection position information C when the operator presses the edit end button.
  • the control unit 71 is configured to display a message as shown in FIG. Note that the message shown in FIG. 11 is merely an example, and any message may be displayed as long as the operator can understand that there is a sample sample whose collection position information C is not registered.
  • step S11 the control unit 71 receives an operation of registration completion by the operator.
  • step S12 the control unit 71 determines whether or not there is a specimen sample for which the collection position information C is not registered for the X-ray image G. If there is a specimen sample for which the collection position information C is not registered for the X-ray image G, the process proceeds to step S12. If there is no specimen sample for which the collection position information C is not registered for the X-ray image G, the process ends.
  • step S12 the control unit 71 displays that there is a specimen sample for which the collection position information C is not registered, and ends the processing.
  • the control unit 71 registers the sampling position information C for the X-ray image G by the input of the operator, and the sampling position information C is not registered in the X-ray image G.
  • the control unit 71 registers the sampling position information C for the X-ray image G by the input of the operator, and the sampling position information C is not registered in the X-ray image G.
  • the control unit 71 registers the sampling position information C for the X-ray image G by the input of the operator, and the sampling position information C is not registered in the X-ray image G.
  • the control unit 71 registers the sampling position information C for the X-ray image G by the input of the operator, and the sampling position information C is not registered in the X-ray image G.
  • the control unit 41 controls the diagnostic imaging system 130 in the fifth embodiment unlike the first embodiment in which at least whether or not the analysis is completed is displayed as the progress status PA of the analysis of the sample in a distinguishable manner.
  • the unit 81 is configured to display, as the analysis progress status PA, each of a plurality of sample samples, that is, “before sample sample analysis”, “during sample sample analysis”, or “sample sample analysis completed”.
  • the same components as those in the first embodiment are designated by the same reference numerals and the description thereof will be omitted.
  • the control unit 81 sets the analysis progress status PA of each of the plurality of sample samples as analysis progress status PA before sample sample analysis, during sample sample analysis, and sample sample analysis completion. Is configured to display either.
  • the progress PA of the analysis status changes as the analysis of the specimen sample progresses.
  • the control unit 81 monitors the status of the analysis of the sample sample by the sample analyzer 3, and changes the content displayed in the display area DAS every time the progress status PA of the analysis status changes. That is, the control unit 81 displays “before analysis” in the display area DAS before the analysis of the sample specimen is started. In addition, the control unit 81 changes the display of the display area DAS from “before analysis” to “during analysis” when the analysis of the sample specimen is started. Further, when the analysis of the sample specimen is completed, the control unit 81 changes the display of the display area DAS from “under analysis” to “analysis completed”.
  • control unit 81 sets, as the analysis progress status PA for each of the plurality of sample samples, one of the sample sample before analysis, the sample sample during analysis, and the sample sample analysis completed. Is configured to display. According to this structure, a doctor or the like can visually recognize whether the sample sample for which analysis has not been completed is before analysis or during analysis.
  • a diagnostic image system 140 (see FIG. 1) according to the sixth embodiment will be described with reference to FIGS. 1 and 14.
  • the control unit 41 identifiably indicates at least whether or not the analysis is completed as the progress PA of the analysis of the sample specimen
  • the control of the diagnostic image system 140 in the sixth embodiment is configured to display the ongoing analysis process among the analysis processes by the sample analyzer 3 for each of the plurality of sample samples as the analysis progress PA.
  • the same components as those in the first embodiment are designated by the same reference numerals and the description thereof will be omitted.
  • control unit 91 is configured to display the ongoing analysis process among the analysis processes performed by the sample analyzer 3 as the analysis progress PA for each of the plurality of sample samples. ..
  • the control unit 91 sets, as the analysis progress status PA, among the analysis steps of pre-registration, pre-processing, LC analysis, MS analysis, pre-approval, and analysis completion.
  • the corresponding process is configured to display the ongoing analysis process as the analysis progress PA.
  • the “before registration” is a state before the identification information U is read in the sample analyzer 3.
  • “during pretreatment” is a state in which a step of performing a treatment necessary for analyzing a specimen sample is in progress.
  • “during LC analysis” is a state in which the step of separating the specimen sample in the LC unit 31 is in progress.
  • MS analysis in progress is a state in which analysis in the MS unit 32 is in progress.
  • the “before approval” is a state before the analysis is completed and the obtained analysis result RA is approved.
  • “analysis completed” is a state in which the analysis result RA obtained is approved when the analysis is completed.
  • the sample analyzer 3 may not include the LC unit 31 and the MS unit 32.
  • the control unit 81 may display each process performed by the sample analyzer 3.
  • control unit 81 displays, for each of the plurality of sample samples, the analysis process in progress among the analysis processes by the sample analyzer 3 as the analysis progress PA. Is configured. As a result, a doctor or the like can visually grasp the analysis status of the sample specimen in detail.
  • the controller 41 when the operator selects the specimen sample in the first display area F1, the controller 41 (51, 61, 71, 81, 91) causes the first In the display area F1, the second display area F2, and the third display area F3, an example of a configuration is shown in which the sampling position information C of the specimen sample specified by selection and the specimen sample in the sample data SD are highlighted.
  • the control unit 41 when the sample data SD is selected in the second display area F2, the control unit 41 (51, 61, 71, 81, 91) causes the first display area F1, the second display area F2, and the third display area F2. In the area F3, it is not necessary to highlight the sampling position information C of the specimen sample specified by selection and the specimen sample in the sample data SD.
  • the control unit 41 (51, 61, 71, 81, 91) causes the first display region F1, the second display region F2, and In the third display area F3, the sampling position information C of the specimen sample specified by selection and the specimen sample in the specimen data SD may be configured to be highlighted. That is, the control unit 41 (51, 61, 71, 81, 91), even when the sample specimen is selected in any of the first display area F1, the second display area F2, and the third display area F3, In the first display area F1, the second display area F2, and the third display area F3, the sampling position information C of the specimen sample specified by selection and the specimen sample in the specimen data SD may be highlighted.
  • the control unit 41 displays the thumbnail image TH in the third display area F3.
  • the invention is not limited to this.
  • the control unit 41 (51, 61, 71, 81, 91) does not have to display the thumbnail image TH in the third display area F3.
  • the display unit 42 may not include the third display area F3.
  • control unit 41 displays the sample data SD in the list format in the first to sixth embodiments
  • the present invention is not limited to this. Not limited.
  • the control unit 41 does not have to display the sample data SD in the list format.
  • the control unit 41 displays the sample data SD including the analysis result RA, but the present invention is not limited to this. It is not limited to this.
  • the control unit 41 may be configured to display the sample data SD that does not include the analysis result RA. It is sufficient that the sample data SD includes at least the identification information U of the sample and the registration status of the collection position information C.
  • control unit 41 displays the sample data SD including the progress PA of the sample sample analysis.
  • the control unit 41 may be configured to display the sample data SD that does not include the progress status PA of the analysis of the sample sample.
  • one identification mark IM corresponding to one specimen sample is displayed on any one of the thumbnail images TH.
  • the present invention is not limited to this.
  • the identification mark IM in which the same number is written corresponding to one specimen sample may be displayed in a plurality of thumbnail images TH.
  • the control unit 41 51, 61, 71, 81, 91
  • the control unit 41 may be configured to highlight the identification mark IM having the same number in the plurality of thumbnail images TH.
  • the control unit 41 (51, 61, 71, 81, 91) is provided in the workstation 4 installed in the operating room R1 by way of example.
  • the control unit 41 includes a diagnostic information processing apparatus 5 connected to the X-ray imaging apparatus 2 and the sample analyzer 3 via the network N. May be provided.
  • the diagnostic information processing device 5 includes a control unit 52, a display unit 53, an operation unit 54, a storage unit 55, and a communication unit 56.
  • the diagnostic information processing device 5 has the same configuration as the workstation 4 except that the reading unit 46 is not provided.
  • the sampling position information C and the sample data SD of the sample sample corresponding to the sample sample specified by selection are emphasized. It may be configured to display. According to this structure, at the time of diagnosis by a doctor or the like, the diagnosis can be performed in a state where the sampling position of the sample and the sample data SD can be easily grasped. Further, even when explaining to a patient or the like, it is possible to explain in a state where the sampling position of the specimen sample and the sample data SD can be easily grasped.
  • the control unit 41 displays the sampling position information C as a circle C1 on the X-ray image G
  • the present invention is not limited to this.
  • the first display area F1 may be configured to display the coordinate value of the sampling position of the specimen sample separately from the X-ray image G.
  • the control unit 41 determines that the corresponding collection position information is based on the coordinate value being selected by the operator. It may be configured so that C and the sample data SD are highlighted.
  • control unit 41 does not display the sampling position information C in the first display area F1 and the operator selects the pixel of the coordinate value of the sampling position information C. , The sampling position information C and the sample data SD may be highlighted.
  • whether the control unit 41 (51, 61, 71, 81, 91) is registered as the registration status of the sampling position information C in the X-ray image G is determined.
  • the control unit 41 displays the collection position information C in the display area DAM of the marker MS. May be configured to be displayed in such a manner that the registration is unnecessary.
  • connection unit 26e an example of a configuration in which the X-ray imaging apparatus 2 and the workstation 4 are directly connected by connecting the connection unit 26e and the connection unit 45 has been shown.
  • the invention is not limited to this.
  • the X-ray imaging apparatus 2 and the workstation 4 may be connected via the network N.
  • control unit 51 highlights the selected specimen sample by changing the display color of the line of the sample data SD in addition to the identification mark IM.
  • the present invention is not limited to this.
  • the control unit 51 is configured to highlight the line of the sample data SD, in addition to the identification mark IM, by changing the font, blinking the characters, or enlarging the selected sample sample. It may have been done.
  • the analysis progress status PA may be displayed by changing the display mode of the analysis result RA.
  • the status of “before approval” and the status of “analysis completed” may be configured to be distinguishably displayed by changing the display color of the analysis result RA.
  • the difference in display color of the analysis result RA is represented by whether or not it is a white character. That is, the analysis result RA1 displayed in normal characters indicates that the status is “before approval”. Further, the analysis result RA2 displayed in white characters indicates that the status is "analysis completed”. Further, in the analysis result RA of FIG. 17, the analysis result RA3 indicated by “ ⁇ ” indicates that the status is “before analysis”.
  • Diagnostic image system 2 X-ray imaging apparatus (radiography apparatus) 3 sample analyzer 41, 51, 61, 71, 81, 91 control unit 42 display unit AG adrenal gland (organ) C Collection position information F1 1st display area F2 2nd display area F3 3rd display area G X-ray image (radiation image) RA analysis result T analyte U identification information (information that can identify each of multiple specimens)

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Abstract

L'invention concerne un système (1) d'imagerie diagnostique comportant: un dispositif (2) de radiographie à rayons X; une unité (42) d'affichage; une unité de commande (41) destinée à la fois à la commande de l'affichage d'images (G) à rayons X permettant la différenciation d'emplacements de collecte d'échantillons spécimens, et la commande de l'affichage de données (SD) d'échantillon contenant des informations (U) d'identification. L'unité de commande est conçue de façon à afficher, en fonction de l'acquisition ou non de données d'emplacements de collecte correspondant à un échantillon spécimen, le statut de l'enregistrement effectué par un opérateur, des données d'emplacements de collecte de l'échantillon spécimen par rapport à des images à rayons X.
PCT/JP2019/044501 2018-12-13 2019-11-13 Système d'imagerie diagnostique et procédé de gestion d'imagerie diagnostique Ceased WO2020121721A1 (fr)

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