WO2020121721A1 - Diagnostic image system and diagnostic image management method - Google Patents

Diagnostic image system and diagnostic image management method 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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PCT/JP2019/044501
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French (fr)
Japanese (ja)
Inventor
駿介 加治木
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株式会社島津製作所
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Priority to JP2020559852A priority Critical patent/JP7111179B2/en
Publication of WO2020121721A1 publication Critical patent/WO2020121721A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B6/00Apparatus or devices for radiation diagnosis; Apparatus or devices for radiation diagnosis combined with radiation therapy equipment
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B6/00Apparatus or devices for radiation diagnosis; Apparatus or devices for radiation diagnosis combined with radiation therapy equipment
    • A61B6/12Arrangements 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

A diagnostic image system (1) equipped with an X-ray imaging device (2), a display unit (42) and a control unit (41) for executing a control for displaying an X-ray image (G) in a manner such that the test specimen collection position is distinguishable, and also executing a control for displaying specimen data (SD) which contains identification information (U), wherein the control unit is configured so as to display the recording status of the test specimen collection position on the X-ray image which is to be inputted by an operator on the basis of whether or not collection position information corresponding to the test specimen has been obtained.

Description

診断画像システムおよび診断画像管理方法Diagnostic image system and diagnostic image management method
 本発明は、診断画像システムおよび診断画像管理方法に関する。 The present invention relates to a diagnostic image system and a diagnostic image management method.
 従来、被検体(患者)の体内から血液や組織片などの検体試料を採取することにより、体内、臓器内における腫瘍などにより引き起こされる疾患の診断を行うことが知られている。ここで、従来、医師などが放射線画像診断装置によって被検体の透視画像を確認しながら、検体試料を採取するための採取デバイスを被検体内の採取位置まで送り込み、検体試料が採取されることが知られている。このような診断画像システムは、たとえば、牧田幸三、「原発性アルドステロン症における副腎静脈採血-副腎静脈サンプリング手技を成功させるためのコツ-」、日本インターベンショナルラジオロジー学会雑誌、2013年、Vol.28、No.2、p.204-210(以下、非特許文献1という)に開示されている。 Conventionally, it has been known to diagnose a disease caused by a tumor or the like in a body or an organ by collecting a specimen sample such as blood or a tissue piece from the body of a subject (patient). Here, conventionally, a doctor or the like sends a sampling device for collecting a specimen sample to a sampling position in the specimen while confirming a fluoroscopic image of the specimen by a radiographic image diagnostic apparatus, and the specimen sample may be collected. Are known. Such a diagnostic imaging system is described in, for example, 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).
 上記非特許文献1には、原発性アルドステロン症の診断のため、放射線画像診断装置による被検体のX線透視画像をリアルタイムで確認しながら、副腎の様々な部位の静脈から血液サンプリングを行うことが開示されている。副腎静脈サンプリングによって採取された各位置の血液(検体試料)を検体分析装置によって分析し、分析結果に基づいて確定診断が行われる。分析結果に基づいて確定診断がなされると、採取された試料の採取位置に基づいて病変部が特定され、病変部の部分切除などを行うか否かが決定される。なお、検体試料は、複数取得されるため、互いに識別可能な情報を付与することにより、個々の検体試料を識別可能にする。 In 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.
 上記非特許文献1に開示されている方法では、血液サンプルと採取位置との関連付けを行うために、カルテに副腎静脈のスケッチし、採取位置を記入しておく必要があるので、医師や作業者の負担が大きくなるという不都合がある。そこで、上記非特許文献1には記載されていないが、カルテにスケッチした副腎静脈に採取位置を記載することに代えて、医師などにより、放射線画像に対して検体試料の採取位置情報を登録することにより、放射線画像において検体試料の採取位置を確認することが考えられる。 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.
 ここで、放射線画像において検体試料の採取位置を確認する場合、医師などは、放射線画像に対して、各検体試料の採取位置情報が登録されているか否かを確認したい場合がある。しかしながら、放射線画像と試料データとを並べて表示するだけでは、試料データにおいて、放射線画像に対して検体試料の採取位置情報が登録されているか否かを一見して把握することが困難であるという問題点が生じる。 Here, when confirming 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. However, it is difficult to grasp at a glance whether or not the sampling position information of the specimen sample is registered with respect to the radiation image in the sample data simply by displaying the radiation image and the sample data side by side. Dots occur.
 この発明は、上記のような課題を解決するためになされたものであり、この発明の1つの目的は、放射線画像に対して検体試料の採取位置情報が登録されているか否かを、一見して容易に把握することが可能な診断画像システムおよび診断画像管理方法を提供することである。 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.
 上記目的を達成するために、この発明の第1の局面における診断画像システムは、臓器から採取される複数の検体試料の採取位置が判別可能な被検体の放射線画像を撮影する放射線撮影装置と、少なくとも、第1表示領域および第2表示領域を含む表示部と、放射線画像と、検体試料の採取位置情報とを取得し、取得した検体試料の採取位置情報に基づいて、検体試料の採取位置を判別可能なように放射線画像を第1表示領域に表示する制御を行うとともに、複数の検体試料のそれぞれを識別可能な情報を含む試料データを第2表示領域に表示する制御を行う制御部とを備え、制御部は、検体試料に対応する採取位置情報が取得されたか否かに基づいて、操作者によって行われる放射線画像への検体試料の採取位置情報の登録状況を表示するように構成されている。なお、本明細書において、「放射線画像への検体試料の採取位置情報の登録状況」とは、放射線画像に対して検体試料の位置情報が登録されているか否かを意味している。 In order to achieve the above-mentioned object, a diagnostic imaging system according to the first aspect of the present invention 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. There is. In the present specification, 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.
 この発明の第1の局面による診断画像システムでは、上記のように、検体試料に対応する採取位置情報が取得されたか否かに基づいて、操作者によって行われる放射線画像への検体試料の採取位置情報の登録状況を表示する制御を行う制御部を備える。これにより、第2表示領域において、放射線画像への検体試料の採取位置情報の登録状況を視覚的に把握することができる。その結果、医師などは、放射線画像に対して検体試料の採取位置情報が登録されているか否かを、一見して容易に把握することができる。なお、本明細書において、「表示領域」とは、画面上において、X線画像および試料データなどを表示する領域のことである。また、本明細書において「採取位置情報」とは、放射線画像上における検体試料を採取した位置の座標値、検体試料を採取した位置に付した標識および、採取位置を指し示す矢印など、放射線画像上において検体試料の採取位置を特定することが可能な情報を含む。 In the diagnostic image system according to the first aspect of the present invention, as described above, based on 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 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. In the present specification, the “display area” is an area on the screen for displaying an X-ray image, sample data, and the like. Further, in the present specification, "collection 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. In the above, the information that can specify the sampling position of the specimen sample is included.
 上記第1の局面による診断画像システムにおいて、好ましくは、制御部は、試料データをリスト形式によって表示するとともに、リスト形式によって表示した試料データの各行において、検体試料ごとに、採取位置情報の登録状況を表示するように構成されている。このように構成すれば、試料データの各行において、検体試料毎に採取位置情報の登録状況を確認することが可能となるので、医師などは、各検体試料の採取位置情報が放射線画像に登録されているか否かを容易に視覚的に把握することができる。 In the diagnostic image system according to the first aspect described above, preferably, 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. Is configured to display. With this configuration, it is possible to check the registration status of the collection position information for each specimen sample in each line of the sample data, so that the doctor or the like can register the collection position information of each specimen sample in the radiographic image. Whether or not it is possible to easily grasp visually.
 この場合、好ましくは、制御部は、リスト形式によって表示した試料データにおいて、採取位置情報の登録状況を示す標識を表示するとともに、標識および標識の表示領域の表示態様を、採取位置情報の登録状況に応じて異ならせて表示するように構成されている。このように構成すれば、放射線画像に対する採取位置情報の登録が完了している検体試料と、放射線画像に対する採取位置情報の登録が完了していない検体試料とを、識別可能に表示することができる。その結果、採取位置情報の状況に応じて標識および標識の表示領域の表示態様が異なるので、医師などは、採取位置情報の登録状況を表示する表示領域を確認することにより、検体試料ごとに、採取位置情報の登録状況を容易に視覚的に把握することができる。 In this case, preferably, in the sample data displayed in the list format, the control unit displays a sign indicating the registration status of the collection position information, and 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. .. As a result, since 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.
 上記第1の局面による診断画像システムにおいて、好ましくは、制御部は、操作者の入力によって放射線画像に対する採取位置情報の登録を行うとともに、放射線画像に採取位置情報が登録されていない検体試料がある場合に、未登録の検体試料が存在することを表示するように構成されている。このように構成すれば、医師などは、放射線画像に対する採取位置情報の登録漏れがあることを、登録操作を完了する前に視覚的に把握することができる。したがって、放射線画像に対する採取位置情報の登録漏れが生じることを抑制することができる。その結果、検体試料の採取位置が特定できなくなり、放射線画像に対して採取位置情報を登録できなくなることを抑制することができる。 In the diagnostic image system according to the first aspect, preferably, 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. With this configuration, 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.
 上記第1の局面による診断画像システムにおいて、好ましくは、検体試料を分析して分析結果を生成する検体分析装置をさらに備え、制御部は、複数の検体試料のそれぞれについて、分析の進捗状況を表示するように構成されている。このように構成すれば、医師などは、放射線画像に対する採取位置情報の登録状況に加えて、検体試料の分析の進捗状況を併せて視覚的に把握することができる。その結果、検体試料の状況を詳細に把握することができる。 The diagnostic image system according to the first aspect 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.
 この場合、好ましくは、制御部は、複数の検体試料のそれぞれについて、分析の進捗状況として、少なくとも分析が完了しているか否かを識別可能に表示するように構成されている。このように構成すれば、医師などは、検体試料毎に、分析が完了しているか否かを、一見して容易に把握することができる。その結果、医師などは、試料データを確認することにより、複数の検体試料のうち、分析が完了している検体試料を把握することができる。 In this case, preferably, the 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. With this configuration, a doctor or the like can easily see 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.
 上記検体分析装置を備える構成において、好ましくは、制御部は、複数の検体試料のそれぞれについて、分析の進捗状況として、検体試料の分析前、検体試料の分析中、検体試料の分析完了のいずれかを表示するように構成されている。このように構成すれば、医師などは、分析が完了していない検体試料について、分析前であるか分析中であるかを視覚的に把握することができる。 In the configuration including the sample analyzer, preferably, 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. Is configured to display. According to this structure, a doctor or the like can visually grasp whether the sample sample for which analysis has not been completed is being analyzed or being analyzed.
 上記検体分析装置を備える構成において、好ましくは、制御部は、複数の検体試料のそれぞれについて、検体分析装置による各分析工程のうち、進行中の分析工程を分析の進捗状況として表示するように構成されている。このように構成すれば、医師などは、検体試料の分析状況を、詳細に視覚的に把握することができる。 In the configuration including the sample analyzer, preferably, the 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.
 この発明の第2の局面における診断画像管理方法は、臓器から採取される複数の検体試料の採取位置が判別可能な被検体の放射線画像を取得するステップと、放射線画像と、検体試料の採取位置情報とを取得するステップと、取得した検体試料の採取位置情報に基づいて、検体試料の採取位置を判別可能なように放射線画像を第1表示領域に表示するとともに、複数の検体試料のそれぞれ識別可能な情報を含む試料データを第2表示領域に表示するステップと、検体試料に対応する採取位置情報が取得されたか否かに基づいて、操作者によって行われる放射線画像への検体試料の採取位置情報の登録状況を表示するステップとを含む。 The diagnostic image management method according to the second aspect of the present invention 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.
 この発明の第2の局面による診断画像管理方法では、上記のように、検体試料に対応する採取位置情報が取得されたか否かに基づいて、操作者によって行われる放射線画像への検体試料の採取位置情報の登録状況を表示するステップを含む。これにより、上記第1の局面における診断画像システムと同様に、放射線画像に対して検体試料の採取位置情報が登録されているか否かを、一見して容易に把握することが可能な診断画像管理方法を提供することができる。 In the diagnostic image management method according to the second aspect of the present invention, 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. As a result, similar to the diagnostic image system in the first aspect, it is possible to easily grasp at a glance whether or not the sampling position information of the specimen sample is registered in the radiographic image, and the diagnostic image management can be easily grasped. A method can be provided.
 本発明によれば、上記のように、放射線画像に対して検体試料の採取位置情報が登録されているか否かを、一見して容易に把握することが可能な診断画像システムおよび診断画像管理方法を提供することができる。 According to the present invention, as described above, it is possible to easily grasp at a glance whether or not the collection position information of the specimen sample is registered in the radiographic image, and the diagnostic image management method. Can be provided.
第1実施形態による診断画像システムの全体構成を示したブロック図である。It is a block diagram showing the whole diagnostic imaging system composition by a 1st embodiment. 第1実施形態による診断画像システムのX線撮影装置の構成例を示したブロック図である。It is a block diagram showing an example of composition of an X-ray imaging system of a diagnostic imaging system by a 1st embodiment. 第1実施形態による診断画像システムの検体分析装置の構成例を示したブロック図である。It is a block diagram showing an example of composition of a sample analyzer of a diagnostic imaging system by a 1st embodiment. 第1実施形態による診断画像システムにおける、X線画像と分析情報との関連付けを説明するための概念図である。It is a conceptual diagram for demonstrating the correlation with an X-ray image and analysis information in the diagnostic imaging system by 1st Embodiment. 第1実施形態による診断画像システムにおいて、表示部に表示される第1表示領域、第2表示領域および第3表示領域を示した模式図である。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. 第1実施形態による診断画像システムが、検体試料の採取位置情報の登録状況を表示する処理を説明するためのフローチャートである。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. 第1実施形態による診断画像システムにおいて、選択により特定される検体試料に対応する検体試料の採取位置情報および試料データを強調表示した模式図である。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. 第1実施形態による診断画像システムが、選択により特定される検体試料に対応する検体試料の採取位置情報および試料データを強調表示する処理を説明するためのフローチャートである。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. 第2実施形態による診断画像システムにおいて、選択により特定される検体試料に対応する検体試料の採取位置情報および試料データを強調表示した模式図である。In 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. 第3実施形態による診断画像システムにおいて、選択により特定される複数の検体試料に対応する複数の検体試料の採取位置情報および複数の試料データを強調表示した模式図である。In the diagnostic imaging system according to the third embodiment, it is a schematic diagram in which sampling position information and sample data of a plurality of sample samples corresponding to a plurality of sample samples specified by selection are highlighted. 第4実施形態による診断画像システムにおいて、採取位置情報が未登録の検体試料が存在することを示した模式図である。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. 第4実施形態による診断画像システムにおいて、採取位置情報が未登録の検体試料が存在することを生じする処理を説明するための示した模式図である。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. 第5実施形態による診断画像システムにおいて、検体試料の分析状況を表示した模式図である。It is a schematic diagram which displayed the analysis condition of the specimen sample in the diagnostic imaging system by 5th Embodiment. 第6実施形態による診断画像システムにおいて、検体試料の分析状況を表示した模式図である。FIG. 16 is a schematic diagram showing an analysis status of a specimen sample in the diagnostic imaging system according to the sixth embodiment. 第1実施形態の第1変形例による診断画像システムにおいて、選択により特定される検体試料に対応する検体試料の採取位置情報および試料データを強調表示した模式図である。In the diagnostic imaging system by the 1st modification of 1st Embodiment, it is the schematic diagram which highlighted the sampling position information and sample data of the sample sample corresponding to the sample sample specified by selection. 第1実施形態の第2変形例による診断画像システムの全体構成を示したブロック図である。It is a block diagram showing the whole diagnostic imaging system composition by the 2nd modification of a 1st embodiment. 第1実施形態の第3変形例による診断画像システムにおいて、表示部に表示される第1表示領域、第2表示領域および第3表示領域を示した模式図である。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.
 以下、本発明を具体化した実施形態を図面に基づいて説明する。 An embodiment of the present invention will be described below with reference to the drawings.
 [第1実施形態]
 図1~図5を参照して、第1実施形態による診断画像システム1の構成について説明する。
[First Embodiment]
The configuration of the diagnostic imaging system 1 according to the first embodiment will be described with reference to FIGS. 1 to 5.
 (診断画像システム)
 第1実施形態では、診断画像システム1が、原発性アルドステロン症の診断のための副腎静脈サンプリングに用いられる例を示す。
(Diagnostic imaging system)
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.
 図1に示すように、診断画像システム1は、被検体TのX線画像G(図2参照)を撮影するX線撮影装置2と、被検体Tから採取される検体試料の分析を行う検体分析装置3とを備えている。ここで、X線撮影装置2および検体分析装置3のそれぞれは、手術室R1および分析室R2に別々に設置されている。また、診断画像システム1は、ワークステーション4を備えている。ワークステーション4は、X線撮影装置2とともに、手術室R1に設置されている。ワークステーション4は、制御部41と、表示部42とを備えている。表示部42は、第1表示領域F1(図5参照)および第2表示領域F2(図5参照)を含んでいる。 As shown in FIG. 1, 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. Here, 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).
 制御部41は、X線画像Gと複数の検体試料の採取位置情報C(図5参照)とを、第1表示領域F1に表示する制御を行うとともに、複数の検体試料のそれぞれを識別可能な情報を含む試料データSD(図5参照)を第2表示領域F2に表示する制御を行うように構成されている。なお、X線撮影装置2は、請求の範囲の「放射線撮影装置」の一例である。また、X線画像Gは、請求の範囲の「放射線画像」の一例である。 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.
 診断画像システム1は、被検体T内の検体試料を採取するために、X線撮影装置2によって被検体Tの外部からX線画像Gを撮影する。検体試料を採取する際、検体採取デバイス10が被検体Tの内部に導入され、撮影されたX線画像Gを手がかりに、検体採取を担当する医師が検体採取デバイス10を検体試料の採取位置(図5参照)まで進入させ、検体試料を採取する。なお、副腎静脈サンプリングでは、検体採取デバイス10にカテーテルが用いられる。 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. When collecting a specimen sample, 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. In adrenal vein sampling, a catheter is used as the sample collection device 10.
 第1実施形態では、検体試料は、臓器から取得される。具体的には、臓器は、ホルモンを分泌する副腎AG(図5参照)である。検体試料は、副腎AGの副腎静脈から取得される、副腎静脈血である。なお、副腎AGは、請求の範囲の「臓器」の一例である。 In the first embodiment, the specimen sample is acquired from an organ. Specifically, 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.
 採取された検体試料は、検体採取デバイス10に取り込まれ、検体試料を収容するための検体容器Bに収容された後、検体容器Bが検体分析装置3に移送される。検査技師などの操作者が検体容器Bを検体分析装置3にセットすることにより、検体分析装置3が検体試料を受け付ける。検体容器Bは、たとえば採血管である。検体分析装置3は、取得した検体試料の分析を行う。 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.
 ここで、検体容器Bには、検体試料を特定するための試料特定情報が付されている。試料特定情報は、採取された検体試料を収容するための検体容器Bに付される識別情報Uである。識別情報Uは、たとえば検体容器Bにバーコードや2次元コードの形式で付される検体IDである。識別情報Uは、たとえばバーコードが印字されたラベルの形態で用意され、検体試料が採取される際に、操作者によって検体容器Bに貼付される。なお、識別情報Uは、請求の範囲の「複数の検体試料のそれぞれを識別可能な情報」の一例である。 Here, 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.
 (X線撮影装置)
 図2に示すように、X線撮影装置2は、被検体Tの外側から放射線を照射することによって、X線画像Gを撮影する装置である。なお、第1実施形態では、X線撮影装置2は、副腎AG(図5参照)から採取される検体試料の採取位置が判別可能な被検体TのX線画像Gを撮影するように構成されている。なお、「検体試料の採取位置が判別可能な被検体TのX線画像G」とは、検体試料を採取する位置に検体採取デバイス10を配置した状態で撮影された画像である。たとえば、検体採取デバイス10として、カテーテルを用いる場合、カテーテルの先端を検体試料の採取位置に配置した状態で撮影することにより、検体試料の採取位置が判別可能な被検体TのX線画像Gを取得する。
(X-ray equipment)
As shown in FIG. 2, the X-ray imaging apparatus 2 is an apparatus that captures an X-ray image G by irradiating the subject T with radiation. In addition, in the first embodiment, 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. ing. 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.
 X線撮影装置2は、被検体Tに放射線(X線)を照射する照射部21と、被検体Tを透過した放射線を検出する検出部22とを備えている。照射部21と検出部22とは、それぞれ、被検体Tが載置される天板23を挟んで対向するように配置されている。照射部21および検出部22は、移動機構24に移動可能に支持されている。天板23は、天板駆動部25により水平方向に移動可能である。被検体Tの関心領域を撮影できるように、移動機構24および天板駆動部25を介して照射部21、検出部22および天板23が移動される。関心領域は、被検体Tのうちで、検体試料の採取位置を含む領域である。X線撮影装置2は、移動機構24および天板駆動部25を制御する制御部26を備えている。 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.
 照射部21は、放射線源21aを含んでいる。放射線源21aは、たとえば、所定の高電圧が印加されることによりX線を発生させるX線管である。照射部21は、制御部26に接続されている。制御部26は、予め設定された撮影条件に従って照射部21を制御し、放射線源21aからX線を発生させる。 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.
 検出部22は、照射部21から照射され、被検体Tを透過したX線を検出し、検出したX線強度に応じた検出信号を出力する。検出部22は、たとえば、FPD(Flat Panel Detector)により構成されている。また、X線撮影装置2は、検出部22からX線検出信号を取得して、検出部22の検出信号に基づきX線画像Gを生成する画像処理部27を備えている。検出部22は、X線検出信号を画像処理部27に出力する。 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). Further, 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.
 画像処理部27は、たとえば、CPU(Central Processing Unit)などのプロセッサ(図示せず)と、ROM(Read Only Memory)およびRAM(Random Access Memory)などの記憶部(図示せず)とを含んで構成されるコンピュータであり、画像処理プログラムをプロセッサに実行させることにより画像処理部27として機能する。画像処理部27は、X線画像Gを生成するほか、X線画像Gの視認性を向上するための補正処理や、複数のX線画像Gを合成する合成処理などを行う機能を有している。また、画像処理部27は、生成したX線画像Gのサムネイル画像TH(図5参照)を生成する処理を行う。具体的には、画像処理部27は、生成したX線画像Gを縮小することにより、サムネイル画像THを生成する。 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.
 制御部26は、CPU(図示せず)、ROM(図示せず)およびRAM(図示せず)などを含んで構成されたコンピュータである。制御部26は、CPUが所定の制御プログラムを実行することにより、X線撮影装置2の各部を制御する制御部26として機能する。制御部26は、照射部21および画像処理部27の制御や、移動機構24および天板駆動部25の駆動制御を行う。 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.
 X線撮影装置2は、表示部26a、操作部26bおよび記憶部26cを備える。また、X線撮影装置2は、ネットワークN(図1参照)と接続するための通信部26dを備える。また、X線撮影装置2は、ワークステーション4と接続するための接続部26eを備える。表示部26aは、たとえば、液晶ディスプレイなどのモニタである。操作部26bは、たとえばキーボードおよびマウス、タッチパネルまたは他のコントローラーなどを含んで構成される。記憶部26cは、たとえばハードディスクドライブなどの記憶装置により構成される。制御部26は、画像処理部27により生成された画像を表示部26aに表示させる制御を行うように構成されている。 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.
 また、制御部26は、操作部26bを介した入力操作を受け付けるように構成されている。記憶部26cは、X線画像Gのデータ、識別情報Uのデータおよびサムネイル画像THのデータなどを記憶するように構成されている。接続部26eは、ワークステーション4と接続するように構成されている。接続部26eによってワークステーション4と接続されることにより、X線画像Gのデータ、識別情報Uのデータおよびサムネイル画像THのデータなどをワークステーション4に送信することができる。接続部26eは、たとえば、シリアル通信ポートを含む。 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.
 X線撮影装置2は、図1に示すように、採取された検体試料を収容するための検体容器Bに付される識別情報Uを読み取るための読取部28を備える。読取部28は、たとえば識別情報Uに応じたバーコードリーダー(または、2次元コードリーダー)であり、それぞれ検体容器Bに付される識別情報Uを読み取ることが可能である。制御部26は、検体試料が採取される際に、読取部28により読み出された識別情報UをX線画像Gに付与するように構成されている。たとえば、制御部26は、DICOM規格に準拠した形式の画像連結データ(DICOMファイル)にX線画像Gと識別情報Uとを記録することにより、X線画像Gに識別情報Uを付与する。 As shown in FIG. 1, 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.
 (検体分析装置)
 検体分析装置3は、被検体Tから採取された検体試料を取得して、診断に必要な成分の測定や細胞の検出などを行う装置である。第1実施形態では、図3において、検体分析装置3は、液体クロマトグラフ質量分析計である。検体分析装置3は、検体試料に含まれる目的成分の分離を行う液体クロマトグラフ部31(以下、LC部31という)と、分離された目的成分をイオン化し、目的イオンを質量数に応じて分離検出する質量分析部32(以下、MS部32という)とを備える。
(Sample analyzer)
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. In the first embodiment, in FIG. 3, 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).
 LC部31は、搬送液を収容する搬送液リザーバ(図示せず)と、搬送液を検体試料とともに送り出す送液ポンプ(図示せず)と、検体試料を導入する試料導入部(図示せず)と、搬送液中の検体試料を成分毎に分離する分離カラム(図示せず)とを主として含む。 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.
 MS部32は、LC部31の後段に設けられ、LC部31で分離された試料成分をイオン化するイオン化部(図示せず)と、生成されたイオンを質量分離して特定イオンを通過するための質量分離器(図示せず)と、質量分離器を通過したイオンを検出するイオン検出器(図示せず)とを主として含む。MS部32により、LC部31から順次溶出する試料成分について、質量毎の検出信号が出力される。 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.
 データ処理部33は、質量毎の検出信号からマススペクトルを作成し、検量線と対比することにより、検体試料中の所定成分の定量分析を行う。第1実施形態では、原発性アルドステロン症の診断のための副腎静脈サンプリングを行うため、検体分析装置3が分析する所定成分は、コルチゾールおよびアルドステロンである。 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. In the first embodiment, since adrenal vein sampling is performed for the diagnosis of primary aldosteronism, the predetermined components analyzed by the sample analyzer 3 are cortisol and aldosterone.
 検体分析装置3は、図3に示すように、表示部33a、操作部33b、記憶部33cおよび通信部33dを備える。検体分析装置3は、さらに読取部34(図1参照)を備える。データ処理部33は、検体試料が分析される際に、読取部34により読み出された識別情報Uを分析結果RAに付与するように構成されている。第1実施形態では、分析結果RAは、被検体Tの副腎AGから取得した検体試料に含まれる検査対象物質の存在量である。具体的には、副腎AGから分泌されるホルモンの存在量である。副腎AGから分泌されるホルモンには、副腎皮質ホルモンであるコルチゾールと、副腎皮質の球状体から分泌されるアルドステロンとが含まれる。第1実施形態では、分析結果RAは、コルチゾール濃度(図5のData1:xx)と、アルドステロン濃度(図5のData2:xx)とを含む。 As shown in FIG. 3, 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. In the first embodiment, 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. In the first embodiment, the analysis result RA includes the cortisol concentration (Data1:xx in FIG. 5) and the aldosterone concentration (Data2:xx in FIG. 5).
 図4に示すように、分析結果RAとX線画像Gとが、共通の識別情報Uを介して相互に対応付けられる。なお、相互に対応付けられるとは、分析結果RAとX線画像Gとが、共通の識別情報Uを介して一対一の関係に対応付けられることを意味する。なお、図4に示す例では、便宜上、1枚のX線画像Gに対して、1つの分析結果RAおよび分析の進捗状況PAを対応付ける例を示している。しかし、X線画像Gにおいて、複数の検体試料の採取位置が写っている場合、複数の検体試料の分析結果RAおよび分析の進捗状況PAが、X線画像Gに対して対応付けられる。 As shown in FIG. 4, 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. In the example shown in FIG. 4, for convenience, one X-ray image G is associated with one analysis result RA and analysis progress PA. However, in the X-ray image G, when the sampling positions of the plurality of sample specimens are shown, the analysis result RA of the plurality of specimen samples and the analysis progress PA are associated with the X-ray image G.
 (ワークステーション)
 図1に示すように、ワークステーション4は、制御部41、表示部42、操作部43、記憶部44および接続部45を備える。ワークステーション4は、たとえば、パーソナルコンピュータ(PC)を含む。
(Work station)
As shown in FIG. 1, 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).
 採取位置情報C(図5参照)は、ワークステーション4において、操作者により手動で登録される。具体的には、操作者は、第2表示領域F2(図5参照)において、編集開始ボタン(図示せず)を押下することにより、採取位置情報Cの登録を開始する。操作者は、編集開始ボタンの押下後、採取位置情報Cを登録したい検体試料を試料データSDから選択するとともに、X線画像G上の採取位置を選択することにより、検体試料の採取位置情報Cの登録を行う。また、操作者は、採取位置情報Cの登録が完了した場合には、編集終了ボタン(図示せず)を押下することにより、採取位置情報Cの登録を終了する。 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.
 第1実施形態では、制御部41は、X線画像Gと検体試料の採取位置情報Cとを取得するように構成されている。また、制御部41は、X線撮影装置2から複数のX線画像Gのそれぞれに対応する複数のサムネイル画像THを取得するように構成されている。また、制御部41は、検体試料の分析結果RAを取得するように構成されている。なお、採取位置情報Cとは、操作者によって登録されたX線画像G上における検体試料の採取位置の座標情報を含む情報である。 In the first embodiment, the 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.
 また、制御部41は、X線画像Gへの検体試料の採取位置情報Cの登録状況を表示するように構成されている。制御部41がX線画像Gへの検体試料の採取位置情報Cの登録状況を表示する構成の詳細については後述する。 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.
 また、制御部41は、操作者によって検体試料が選択された場合、選択により特定される検体試料に対応する検体試料の採取位置情報Cおよび試料データSDを強調表示するように構成されている。制御部41が選択により特定される検体試料に対応する検体試料の採取位置情報Cおよび試料データSDを強調表示する構成の詳細については後述する。 Further, 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.
 また、制御部41は、操作部43を介した入力操作を受け付けるように構成されている。制御部41は、たとえば、CPU、ROMおよびRAMなどを含んで構成されたコンピュータである。 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.
 表示部42は、第1表示領域F1と、第2表示領域F2と、第3表示領域F3とを含む。表示部42は、たとえば、液晶モニタを含む。 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.
 操作部43は、操作者の入力操作を受け付けるように構成されている。操作部43は、たとえば、マウスやキーボードなどを含む。 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.
 記憶部44は、X線画像Gのデータ、識別情報Uのデータ、検体試料の分析結果RAのデータ、X線画像Gへの採取位置情報Cの登録の状況、検体試料分析の進捗状況PAのデータなどを記憶するように構成されている。記憶部44は、たとえば、SSDまたはHDDなどを含む。 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.
 接続部45は、X線撮影装置2と接続されている。また、接続部45は、ネットワークNを介して検体分析装置3と接続されている。 The 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.
 また、ワークステーション4は、採取された検体試料を収容するための検体容器Bに付された識別情報Uを読み取るための読取部46を備える。制御部41は、読取部46により識別情報Uを読み取ったことに基づいて、識別情報Uに対応付けられたX線画像GをX線撮影装置2から取得するとともに、識別情報Uに対応付けられた分析結果RAおよび分析の進捗状況PAを検体分析装置3から取得するように構成されている。 Further, 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.
 (第1表示領域、第2表示領域および第3表示領域)
 図5を参照して、第1実施形態における制御部41が、X線画像G、試料データSD、サムネイル画像THなどを、表示部42に表示する構成について説明する。
(First display area, second display area, and third display area)
A configuration in which the control unit 41 according to the first embodiment displays the X-ray image G, the sample data SD, the thumbnail image TH, and the like on the display unit 42 will be described with reference to FIG. 5.
 図5に示すように、第1実施形態では、表示部42は、第1表示領域F1と、第2表示領域F2と、第3表示領域F3とを含む。制御部41は、副腎AGから採取される検体試料の採取位置情報Cが判別可能な被検体TのX線画像Gを第1表示領域F1に表示する。具体的には、制御部41は、取得したX線画像Gと、複数の検体試料の採取位置情報Cとを、第1表示領域F1に表示する制御を行うように構成されている。なお、図5に示す例では、検体試料を採取した位置に丸印C1を、採取位置情報Cとして図示している。 As shown in FIG. 5, in the first embodiment, 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. Specifically, 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. In the example shown in FIG. 5, a circle C1 is shown as the collection position information C at the position where the specimen sample is collected.
 また、制御部41は、識別情報Uを含む試料データSDを第2表示領域F2に表示するように構成されている。具体的には、制御部41は、第2表示領域F2において、試料データSDをリスト形式によって表示するように構成されている。また、制御部41は、第2表示領域F2において、検査情報Eを表示するように構成されている。なお、制御部41は、読取部46により識別情報Uを読み取ったことに基づいて、識別情報Uに対応付けられた試料データSDおよび検査情報Eを取得するよう様に構成されている。 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.
 検査情報Eは、検体試料が採取された被検体Tおよび被検体Tに対して実施された検査を識別可能な情報を有している。具体的には、検査情報Eは、検査ID、検査日時、患者名、患者ID、年齢および性別といった複数の項目を有している。検査IDは、行われている検査特有のIDが登録される項目である。検査日時は、検査が行われた日時が登録される項目である。患者名は、検査を受診した患者の名前が登録される項目である。患者IDは、患者名に対応するIDが登録される項目である。年齢および性別は、患者の年齢および性別のそれぞれが登録される項目である。ここで、検査ID、検査日時、患者名、患者ID、年齢および性別といった項目は、病院情報システム(Hospital Information Systems:HIS)に基づいたX線画像Gのタグ(たとえば、DICOMタグ)を読み込むことにより取得される。 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. Specifically, 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. Here, for items such as examination ID, examination date and time, patient name, patient ID, age, and gender, the tag (for example, DICOM tag) of the X-ray image G based on the hospital information system (HIS) should be read. Obtained by.
 試料データSDは、採取位置情報C、識別情報U、血管名(BV1、BV2・・・など)、分析結果RA(Data1:xx、Data2:xx)およびステータス(採取位置および分析)といった複数の項目を有している。試料データSDには、複数の検体試料のうちの任意の検体試料における、採取位置情報C、識別情報U、血管名、分析結果RAおよびステータスといった項目に関する情報が登録される。以下、複数の検体試料のうちの任意の検体試料を、たとえば、1番の数字が付された第1検体試料として、試料データSDの複数の項目を説明する。なお、第1検体試料は、X線画像Gにおいて1番の数字で示された場所から採取された検体試料である。 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. In the sample data SD, 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. Hereinafter, 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.
 採取位置項目は、第1検体試料の採取位置情報Cの番号(1番)が登録される項目である。第1実施形態では、採取位置項目には、後述する識別用目印IMが表示されている。識別情報項目は、第1検体試料が保存されている検体容器Bに付された識別情報Uが登録される項目である。血管名項目は、第1検体試料の採取位置情報Cの血管名が登録される項目である。分析結果項目は、第1検体試料を検体分析装置3において分析したことにより取得された分析結果RAが登録される項目である。ステータス項目は、第1表示領域F1中のX線画像Gに対する検体試料の採取位置情報Cの登録状況および検体試料の分析の進捗状況PAが登録される項目である。 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. In the first embodiment, 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.
 識別情報U、分析結果RA、採取位置情報Cの登録状況および分析の進捗状況PAといった項目は、ワークステーション4により、読取部46により識別情報Uを読み取ったことに基づいて取得される分析結果RAに基づいて、検体試料ごとに自動で登録される。採取位置情報Cの登録状況および分析の進捗状況PAの項目は、登録が行われたり分析が完了したりした場合など、状況が変化する度に自動的に更新される。 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.
 また、制御部41は、複数のX線画像Gのそれぞれに対応する複数のサムネイル画像THを、第3表示領域F3に表示するように構成されている。 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.
 第1実施形態では、制御部41は、試料データSDと、X線画像Gとに、複数の検体試料のそれぞれの採取位置が特定可能な共通の識別用目印IMを表示するように構成されている。第1実施形態では、制御部41は、円で囲まれた数字を、識別用目印IMとして表示する。また、制御部41は、サムネイル画像THにおいても、識別用目印IMを表示するように構成されている。具体的には、制御部41は、サムネイル画像THにおいて、X線画像Gとは表示態様を異ならせ、かつ、視認可能に、識別用目印IMを表示するように構成されている。 In the first embodiment, the 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. In the first embodiment, 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. Specifically, 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.
 ここで、複数の検体試料をリスト形式で表示する際に、図5の第2表示領域F2に含まれるステータス(採取位置)の項目を設けていない場合、検体試料の採取位置情報CがX線画像Gに登録されているか否かを一見して把握することが困難になっている。 Here, when the plurality of sample specimens are displayed in the list format and the item of the status (collection position) included in the second display area F2 of FIG. 5 is not provided, 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.
 (登録状況の表示)
 そこで、第1実施形態では、制御部41は、検体試料に対応する採取位置情報Cが取得されたか否かに基づいて、操作者によって行われるX線画像Gへの検体試料の採取位置情報Cの登録状況を表示するように構成されている。具体的には、図5の第2表示領域F2に示すように、制御部41は、試料データSDをリスト形式によって表示するとともに、リスト形式によって表示した試料データSDの各行において、検体試料ごとに、採取位置情報Cの登録状況を表示するように構成されている。
(Display of registration status)
Therefore, in the first embodiment, 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.
 また、制御部41は、リスト形式によって表示した試料データSDにおいて、採取位置情報Cの登録状況を示す標識MSを表示するとともに、標識MSおよび標識MSの表示領域DAMの表示態様を、採取位置情報Cの登録状況に応じて異ならせて表示するように構成されている。図5に示す例では、X線画像Gへの採取位置情報Cの登録が完了している検体試料は、標識MSの表示領域DAMにおいて、「○」を表示している。また、図5に示す例では、X線画像Gへの採取位置情報Cの登録が完了していない検体試料は、標識MSの表示領域DAMにおいて、「-」を表示している。制御部41は、X線画像Gに対して検体試料の採取位置情報Cが登録された際に、表示する標識MSを「-」から「○」へと変更する。また、図5に示す例では、X線画像Gへの採取位置情報Cの登録が完了していない検体試料の標識MSの表示領域DAMの背景色を、登録が完了している検体試料の標識MSの表示領域DAMの背景色と異ならせて表示している。なお、図5に示す例では、便宜上、標識MSの表示領域DAMの背景色の相違を、ハッチングの有無によって示している。 Further, the 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. In the example shown in FIG. 5, 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. Further, in the example shown in FIG. 5, 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. When the collection position information C of the specimen sample is registered in the X-ray image G, 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.
 また、第1実施形態では、制御部41は、複数の検体試料のそれぞれについて、分析の進捗状況PAを表示するように構成されている。具体的には、制御部41は、複数の検体試料のそれぞれについて、分析の進捗状況PAとして、少なくとも分析が完了しているか否かを識別可能に表示するように構成されている。図5に示す例では、分析が完了している検体試料は、分析の進捗状況PAの表示領域DASにおいて、「○」を表示している。また、図5に示す例では、分析が完了していない検体試料は、分析の進捗状況PAの表示領域DASにおいて、「―」を表示している。制御部41は、検体試料の分析が完了した際に、表示領域DASにおける分析の進捗状況PAの表示を「―」から「○」へと変更する。 Further, in the first embodiment, 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 “◯”.
 次に、図6を参照して、第1実施形態における検体試料の採取位置情報Cの登録状況を表示する処理について説明する。 Next, with reference to FIG. 6, a process of displaying the registration status of the sample sample collection position information C in the first embodiment will be described.
 ステップS1において、X線撮影装置2は、副腎AGから採取される複数の検体試料の採取位置が判別可能なX線画像Gを取得する。次に、ステップS2において、制御部41は、X線画像Gと複数の検体試料の採取位置情報Cとを取得する。その後、処理は、ステップS3へ進む。なお、選択された検体試料の強調表示を行うために、後述する図8のステップS5およびステップS6の処理がすでに行われている場合、制御部41は、ステップS1およびステップS2の処理を行わず、ステップS3から処理を開始する。 In 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. Next, in 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.
 ステップS3において、制御部41は、取得した検体試料の採取位置情報Cに基づいて、検体試料の採取位置を判別可能なようにX線画像Gを第1表示領域F1に表示するとともに、識別情報Uを含む試料データSDを第2表示領域F2に表示する。次に、ステップS4において、制御部41は、検体試料に対応する採取位置情報Cが取得されたか否かに基づいて、操作者によって行われるX線画像Gへの検体試料の採取位置情報Cの登録状況を表示し、処理を終了する。 In 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. Next, in 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.
 (強調表示)
 次に、図5および図7を参照して、制御部41が選択された検体試料を強調表示する構成について説明する。
(Highlighting)
Next, a configuration in which the control unit 41 highlights the selected specimen sample will be described with reference to FIGS. 5 and 7.
 医師などは、採取した検体試料の分析結果RAに基づいて、副腎AGにおける疾患の有無や、検体試料のサンプリングの成否を判定する。複数の検体試料を採取した場合、複数の検体試料の試料データSDをリスト形式で表示することが考えられる。しかしながら、試料データSDを単純にリスト形式で表示するだけでは、採取した検体試料の数が多い場合に、X線画像G上における医師などが確認したい検体試料に対応する検体試料の情報を、試料データSDから一見して把握することが難しい。 Doctors and the like judge the presence or absence of a disease in the adrenal AG and the success or failure of sampling of the specimen sample based on the analysis result RA of the collected specimen sample. When a plurality of specimen samples are collected, sample data SD of the plurality of specimen samples may be displayed in a list format. However, by simply displaying the sample data SD in a list format, when the number of collected sample specimens is large, 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.
 そこで、第1実施形態では、制御部41は、第1表示領域F1において検体試料の採取位置情報Cが選択された場合、第1表示領域F1および第2表示領域F2のそれぞれにおいて、選択により特定される検体試料に対応する検体試料の採取位置情報Cおよび試料データSDを強調表示するように構成されている。なお、検体試料の選択は、操作部43を介して医師などによって行われる。たとえば、検体試料の選択は、医師などがマウスを用いて検体試料の採取位置情報Cをクリックすることにより、検体試料が選択される。 Therefore, in the first embodiment, when the sample sample collection position information C is selected in the first display area F1, 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.
 図7に示すように、第1実施形態では、制御部41は、識別用目印IMの表示態様を変化させることにより、第1表示領域F1および第2表示領域F2のそれぞれにおいて、選択により特定される検体試料に対応する検体試料の採取位置情報Cおよび試料データSDを強調表示するように構成されている。なお、図7に示す例は、医師などにより、一番の採取位置情報Cにおける検体試料が選択された場合の模式図である。 As shown in FIG. 7, in the first embodiment, 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.
 図7に示す例では、制御部41は、識別用目印IMを太線で表示することにより、選択された検体試料の採取位置情報Cおよび試料データSDを強調表示している。図7に示す例では、試料データSDのうち、識別用目印IMのみを強調表示することにより、選択された検体試料に対応する試料データSDを強調して表示している。また、図7に示す例では、採取位置情報Cは、検体試料の採取位置を指し示す矢印C2を含み、制御部41は、検体試料の採取位置情報Cとして、採取位置を指し示す矢印C2についても、強調表示するように構成されている。 In the example shown in FIG. 7, 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. In the example shown in FIG. 7, among the sample data SD, only the identification mark IM is highlighted so that the sample data SD corresponding to the selected sample sample is highlighted. Further, in the example shown in FIG. 7, 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.
 また、制御部41は、検体試料が選択された場合に、第1表示領域F1および第2表示領域F2に加えて、第3表示領域F3においても選択された識別用目印IMを強調表示するように構成されている。すなわち、制御部41は、検体試料が選択された場合に、第1表示領域F1、第2表示領域F2、および、第3表示領域F3のそれぞれにおいて、選択された識別用目印IMを連動して強調表示するように構成されている。 Further, the 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.
 次に、図8を参照して、制御部41による選択された検体試料の強調表示処理について説明する。 Next, the highlighting process of the selected specimen sample by the control unit 41 will be described with reference to FIG.
 ステップS5において、X線撮影装置2は、副腎AGから取得される複数の検体試料の採取位置情報Cが判別可能なX線画像Gを取得する。次に、ステップS6において、制御部41は、X線画像Gと複数の検体試料の採取位置情報Cとを取得する。その後、処理は、ステップS7へ進む。なお、検体試料の採取位置情報Cの登録状況を表示するために、図6に示すステップS1およびステップS2の処理がすでに行われている場合、制御部41は、ステップS5およびステップS6の処理を行わず、ステップS7から処理を開始する。 In 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. Next, in 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.
 ステップS7において、制御部41は、検体試料の採取位置を識別可能なX線画像Gと複数の検体試料の採取位置情報Cを第1表示領域F1に表示するとともに、識別情報Uを含む試料データSDを第2表示領域F2に表示する。次に、ステップS8において、制御部41は、複数のX線画像Gのそれぞれに対応する複数のサムネイル画像THを取得するとともに、取得した複数のサムネイル画像THを第3表示領域F3に表示する。その後、処理は、ステップS9へ進む。 In 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. Next, in 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.
 ステップS9において、制御部41は、第1表示領域F1において検体試料の採取位置が選択された場合、第1表示領域F1および第2表示領域F2のそれぞれにおいて、選択により特定される検体試料に対応する検体試料の採取位置および検体試料の試料データSDを強調表示する。次に、ステップS10において、制御部41は、第1表示領域F1において検体試料の採取位置が選択された場合に、第3表示領域F3において、選択により特定される検体試料を強調表示する。なお、上記ステップS7とステップS8との処理は、同一のステップにおいて処理されてもよい。また、ステップS9とステップS10との処理は、同一のステップにおいて処理されてもよい。 In 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. Next, in 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.
 (第1実施形態の効果)
 第1実施形態では、以下のような効果を得ることができる。
(Effects of the first embodiment)
In the first embodiment, the following effects can be obtained.
 第1実施形態では、上記のように、診断画像システム1は、副腎AGから採取される検体試料の採取位置情報Cが判別可能な被検体TのX線画像Gを撮影するX線撮影装置2と、少なくとも、第1表示領域F1および第2表示領域F2を含む表示部42と、X線画像Gと、検体試料の採取位置情報Cとを取得し、取得した検体試料の採取位置情報Cに基づいて、検体試料の採取位置を判別可能なようにX線画像Gを第1表示領域F1に表示する制御を行うとともに、識別情報Uを含む試料データSDを第2表示領域F2に表示する制御を行う制御部41とを備え、制御部41は、検体試料に対応する採取位置情報Cが取得されたか否かに基づいて、操作者によって行われるX線画像Gへの検体試料の採取位置情報Cの登録状況を表示するように構成されている。これにより、第2表示領域F2において、X線画像Gへの検体試料の採取位置情報Cの登録状況を視覚的に把握することができる。その結果、医師などは、X線画像Gに対して検体試料の採取位置情報Cが登録されているか否かを、一見して容易に把握することができる。 In the first embodiment, as described above, 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.
 また、第1実施形態では、上記のように、制御部41は、試料データSDをリスト形式によって表示するとともに、リスト形式によって表示した試料データSDの各行において、検体試料ごとに、採取位置情報Cの登録状況を表示するように構成されている。これにより、試料データSDの各行において、検体試料毎に採取位置情報Cの登録状況を確認することが可能となるので、医師などは、各検体試料の採取位置情報CがX線画像Gに登録されているか否かを容易に視覚的に把握することができる。 Further, in the first embodiment, as described above, 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.
 また、第1実施形態では、上記のように、制御部41は、リスト形式によって表示した試料データSDにおいて、採取位置情報Cの登録状況を示す標識MSを表示するとともに、標識MSおよび標識MSの表示領域DAMの表示態様を、採取位置情報Cの登録状況に応じて異ならせて表示するように構成されている。これにより、X線画像Gに対する採取位置情報Cの登録が完了している検体試料と、X線画像Gに対する採取位置情報Cの登録が完了していない検体試料とを、識別可能に表示することができる。その結果、採取位置情報Cの状況に応じて標識MSおよび標識MSの表示領域DAMの表示態様が異なるので、医師などは、採取位置情報Cの登録状況を表示する表示領域DAMを確認することにより、検体試料ごとに、採取位置情報Cの登録状況を容易に視覚的に把握することができる。 Further, in the first embodiment, as described above, 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. Thereby, the specimen sample for which the collection position information C for the X-ray image G has been registered and the specimen sample for which the collection position information C for the X-ray image G has not been registered are displayed in a distinguishable manner. You can As a result, 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.
 また、第1実施形態では、上記のように、検体試料を分析して分析結果RAを生成する検体分析装置3をさらに備え、制御部41は、複数の検体試料のそれぞれについて、分析の進捗状況PAを表示するように構成されている。これにより、医師などは、X線画像Gに対する採取位置情報Cの登録状況に加えて、検体試料の分析の進捗状況PAを併せて視覚的に把握することができる。その結果、検体試料の状況を詳細に把握することができる。 Further, in the first embodiment, as described above, 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.
 また、第1実施形態では、上記のように、制御部41は、複数の検体試料のそれぞれについて、分析の進捗状況PAとして、少なくとも分析が完了しているか否かを識別可能に表示するように構成されている。これにより、医師などは、検体試料毎に、分析が完了しているか否かを、一見して容易に把握することができる。その結果、医師などは、試料データSDを確認することにより、複数の検体試料のうち、分析が完了している検体試料を把握することができる。 Further, in the first embodiment, as described above, 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.
 また、第1実施形態では、上記のように、診断画像管理方法は、副腎AGから採取される検体試料の採取位置情報Cが判別可能な被検体TのX線画像Gを撮影するステップS1と、X線画像Gと複数の検体試料の採取位置情報Cとを取得するステップS2と、取得した検体試料の採取位置情報Cに基づいて、検体試料の採取位置を判別可能なようにX線画像Gを第1表示領域F1に表示するとともに、識別情報Uを含む試料データSDを第2表示領域F2に表示するステップS3と、検体試料に対応する採取位置情報Cが取得されたか否かに基づいて、操作者によって行われるX線画像Gへの検体試料の採取位置情報Cの登録状況を表示するステップS4とを含む。これにより、診断画像システム1と同様に、X線画像Gに対して検体試料の採取位置情報Cが登録されているか否かを、一見して容易に把握することが可能な診断画像管理方法を提供することができる。 Further, in the first embodiment, as described above, 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. And the step S4 of displaying the registration status of the sampling position information C of the specimen sample on the X-ray image G performed by the operator. With this, similarly to the diagnostic image system 1, 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.
 [第2実施形態]
 次に、図1および図9を参照して、第2実施形態による診断画像システム100(図1参照)について説明する。制御部41が識別用目印IMの表示態様を異ならせることにより選択された検体試料を強調表示する上記第1実施形態とは異なり、第2実施形態では、診断画像システム100の制御部51は、識別用目印IMに加えて、試料データSDの行を、少なくとも、表示色の変更、字体の変更、文字の点滅、および拡大表示のいずれかによって、選択された検体試料を強調表示するように構成されている。なお、上記第1実施形態と同様の構成については同様の符号を付し、説明を省略する。
[Second Embodiment]
Next, a diagnostic imaging system 100 (see FIG. 1) according to the second embodiment will be described with reference to FIGS. 1 and 9. Unlike the first embodiment in which the control unit 41 highlights the selected specimen sample by changing the display mode of the identification mark IM, in the second embodiment, 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.
 図9に示すように、第2実施形態では、制御部51は、識別用目印IMに加えて、試料データSDの行を、少なくとも、表示色の変更、字体の変更、文字の点滅、および拡大表示のいずれかによって、選択された検体試料を強調表示するように構成されている。なお、図9に示す例は、試料データSDの行の表示色を変更することにより、選択された検体試料を強調表示している。また、図9に示す例は、便宜上、選択された検体試料の行にハッチングを付与することにより、表示色が変更されていることを図示している。 As shown in FIG. 9, in the second embodiment, in addition to the identification mark IM, 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. In the example shown in FIG. 9, the selected specimen sample is highlighted by changing the display color of the row of the sample data SD. Further, 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.
 なお、第2実施形態のその他の構成は、上記第1実施形態と同様である。 The other configurations of the second embodiment are the same as those of the first embodiment.
 (第2実施形態の効果)
 第2実施形態では、以下のような効果を得ることができる。
(Effects of Second Embodiment)
In the second embodiment, the following effects can be obtained.
 第2実施形態では、上記のように、制御部51は、識別用目印IMに加えて、試料データSDの行を、表示色の変更によって、選択された検体試料を強調表示するように構成されている。これにより、リスト表示された試料データSDにおいて、選択された検体試料が表示されている行をより一層強調して表示することができる。その結果、識別用目印IMのみを強調表示する場合と比較して、選択された検体試料が表示されている行の強調効果を向上させることが可能となるので、X線画像Gにおける検体試料の採取位置と、採取位置に対応する検体試料とを、より一層容易に把握することができる。 In the second embodiment, as described above, 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 display color to highlight the selected sample sample. ing. As a result, in the sample data SD displayed in the list, the line in which the selected specimen sample is displayed can be further emphasized and displayed. As a result, as compared with the case where only the identification mark IM is highlighted, it is possible to improve the highlighting effect of the row in which the selected sample specimen is displayed. The sampling position and the specimen sample corresponding to the sampling position can be more easily grasped.
 なお、第2実施形態のその他の効果は、上記第1実施形態と同様である。 The other effects of the second embodiment are the same as those of the first embodiment.
 [第3実施形態]
 次に、図1および図10を参照して、第3実施形態における診断画像システム110(図1参照)について説明する。制御部41が、選択により特定される1つの検体試料に対応する検体試料のX線画像Gにおける採取位置情報Cおよび検体試料の試料データSDを強調表示する上記第1実施形態とは異なり、第3実施形態における診断画像システム110の制御部61は、複数の検体試料が選択された場合に、選択により特定される複数の検体試料に対応する検体試料のX線画像Gにおける採取位置情報Cおよび検体試料の試料データSDを強調表示するように構成されている。なお、上記第1実施形態と同様の構成については同様の符号を付し、説明を省略する。
[Third Embodiment]
Next, a diagnostic image system 110 (see FIG. 1) according to the third embodiment will be described with reference to FIGS. 1 and 10. Unlike the first embodiment in which 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, When a plurality of specimen samples are selected, the control unit 61 of the diagnostic imaging system 110 according to the third embodiment 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.
 図10に示すように、第3実施形態では、制御部61は、複数の検体試料が選択された場合に、選択により特定される複数の検体試料に対応する検体試料のX線画像Gにおける採取位置情報Cおよび検体試料の試料データSDを、それぞれ強調表示するように構成されている。また、制御部61は、複数の検体試料が選択された場合に、選択により特定される複数の検体試料に対応する検体試料のX線画像Gにおける採取位置情報Cおよび検体試料の試料データSDを、それぞれ互いに識別可能に表示態様を異ならせて強調表示するように構成されている。 As shown in FIG. 10, in the third embodiment, when a plurality of specimen samples are selected, 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. In addition, when a plurality of specimen samples are selected, 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.
 図10に示す例では、選択された複数の検体試料に対応する識別用目印IMを太線で表示するとともに、それぞれの識別用目印IMの表示色を異ならせて表示している。なお、図10に示す例では、便宜上、識別用目印IMの表示色の相違を、識別用目印IMを太線で図示すること、および、識別用目印IMにハッチングを付すことにより表している。また、図10に示す例では、採取位置情報Cは、検体試料の採取位置を指し示す矢印C2および矢印C3を含み、制御部61は、検体試料の採取位置を指し示す矢印C2および矢印C3をそれぞれ識別可能に強調表示している。また、制御部61は、サムネイル画像THに表示した識別用目印IMについても、それぞれ識別可能に強調表示している。 In the example shown in FIG. 10, 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. Note that, in the example shown in FIG. 10, for convenience, 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. Further, in the example shown in FIG. 10, 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.
 なお、第3実施形態のその他の構成は、上記第1実施形態と同様である。 The other configurations of the third embodiment are the same as those of the first embodiment.
 (第3実施形態の効果)
 第3実施形態では、以下のような効果を得ることができる。
(Effect of the third embodiment)
In the third embodiment, the following effects can be obtained.
 第3実施形態では、上記のように、制御部61は、複数の検体試料が選択された場合に、選択により特定される複数の検体試料に対応する検体試料のX線画像Gにおける採取位置情報Cおよび検体試料の試料データSDを、それぞれ強調表示するように構成されている。これにより、医師などが複数の検体試料を選択した場合でも、各表示領域(第1表示領域F1、第2表示領域F2、および第3表示領域F3)において対応する検体試料を一見して把握することができる。その結果、1つの検体試料のみを強調表示する場合と比較して、一度に複数の検体試料を選択することが可能となるので、ユーザビリティ(ユーザの利便性)を向上させることができる。 In the third embodiment, as described above, when a plurality of specimen samples are selected, 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. With this, even when a doctor or the like selects a plurality of specimen samples, the corresponding specimen samples are grasped at a glance in each display area (first display area F1, second display area F2, and third display area F3). be able to. As a result, it is possible to select a plurality of sample samples at once as compared with the case where only one sample sample is highlighted, so that usability (user convenience) can be improved.
 また、第3実施形態では、上記のように、制御部61は、複数の検体試料が選択された場合に、選択により特定される複数の検体試料に対応する検体試料のX線画像Gにおける採取位置情報Cおよび検体試料の試料データSDを、それぞれ互いに識別可能に表示態様を異ならせて強調表示するように構成されている。これにより、医師などが複数の検体試料を選択した場合でも、各表示領域(第1表示領域F1、第2表示領域F2、および第3表示領域F3)における検体試料を1対1の関係で対応付けることができる。その結果、複数の検体試料が選択された場合でも、検体試料毎に、対応するX線画像G上の採取位置情報Cおよび試料データSDの行を容易に把握することができる。 Further, in the third embodiment, as described above, when a plurality of specimen samples are selected, 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. As a result, even when a doctor or the like selects a plurality of specimen samples, 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. As a result, even when a plurality of specimen samples are selected, it is possible to easily grasp the row of the sampling position information C and the sample data SD on the corresponding X-ray image G for each specimen sample.
 なお、第3実施形態のその他の効果は、上記第1実施形態と同様である。 The other effects of the third embodiment are similar to those of the first embodiment.
 [第4実施形態]
 次に、図1、図5および図11を参照して、第4実施形態における診断画像システム120(図1参照)について説明する。制御部41が、検体試料に対応する採取位置情報Cが取得されたか否かに基づいて、操作者によって行われるX線画像Gへの検体試料の採取位置情報Cの登録状況を表示する上記第1実施形態とは異なり、第4実施形態における診断画像システム120の制御部71は、操作者の入力によってX線画像Gに対する採取位置情報Cの登録を行うとともに、X線画像Gに採取位置情報Cが登録されていない検体試料がある場合に、未登録の検体試料が存在することを表示するように構成されている。なお、上記第1実施形態と同様の構成については同様の符号を付し、説明を省略する。
[Fourth Embodiment]
Next, 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. Unlike the first embodiment, the control unit 71 of the diagnostic imaging system 120 according to the fourth embodiment 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.
 第4実施形態では、制御部71は、操作者の入力によってX線画像Gに対する採取位置情報Cの登録を行うとともに、X線画像Gに採取位置情報Cが登録されていない検体試料がある場合に、未登録の検体試料が存在することを表示するように構成されている。 In the fourth embodiment, the 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.
 具体的には、制御部71は、操作者による入力操作を受け付けるように構成されている。制御部71は、操作者の選択操作による入力に基づいて、X線画像Gに対して、検体試料の採取位置情報Cの登録を行う。また、制御部71は、操作者によって編集終了ボタンが押下されたことにより、採取位置情報Cの登録を終了する。 Specifically, the 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.
 ここで、図5に示すように、X線画像Gに対して採取位置情報Cが登録されていない検体試料がある状態において、操作者が登録作業を完了(編集終了ボタンを押下)した場合、制御部71は、図11に示すようなメッセージを表示するように構成されている。なお、図11に示すメッセージは、単なる例示であり、採取位置情報Cが未登録の検体試料が存在することを操作者が把握することができれば、どのようなメッセージを表示してもよい。 Here, as shown in FIG. 5, when the operator completes the registration work (presses the edit end button) in the state where there is the specimen sample for which the collection position information C is not registered for the X-ray image G, 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.
 次に、図12を参照して、制御部71による採取位置情報Cが未登録の検体試料が存在すること表示する処理について説明する。 Next, with reference to FIG. 12, a process of displaying by the control unit 71 that there is an unregistered specimen sample in the collection position information C will be described.
 ステップS11において、制御部71は、操作者による登録完了の操作を受け付ける。次にステップS12において、制御部71は、X線画像Gに対して採取位置情報Cが登録されていない検体試料があるか否かを判定する。X線画像Gに対して採取位置情報Cが登録されていない検体試料がある場合、処理は、ステップS12へ進む。X線画像Gに対して採取位置情報Cが登録されていない検体試料がない場合、処理は終了する。 In step S11, the control unit 71 receives an operation of registration completion by the operator. Next, in 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.
 ステップS12において、制御部71は、採取位置情報Cが未登録の検体試料が存在することを表示し、処理を終了する。 In 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.
 なお、第4実施形態のその他の構成は、上記第1実施形態と同様である。 The other configurations of the fourth embodiment are the same as those of the first embodiment.
 (第4実施形態の効果)
 第4実施形態では、以下のような効果を得ることができる。
(Effects of Fourth Embodiment)
In the fourth embodiment, the following effects can be obtained.
 第4実施形態では、上記のように、制御部71は、操作者の入力によってX線画像Gに対する採取位置情報Cの登録を行うとともに、X線画像Gに採取位置情報Cが登録されていない検体試料がある場合に、未登録の検体試料が存在することを表示するように構成されている。これにより、医師などは、X線画像Gに対する採取位置情報Cの登録漏れがあることを、登録操作を完了する前に視覚的に把握することができる。したがって、X線画像Gに対する採取位置情報Cの登録漏れが生じることを抑制することができる。その結果、検体試料の採取位置が特定できなくなり、X線画像Gに対して採取位置情報Cを登録できなくなることを抑制することができる。 In the fourth embodiment, as described above, 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. When there is a specimen sample, it is configured to display that there is an unregistered specimen sample. As a result, a doctor or the like can visually recognize that there is omission of registration of the collection position information C for the X-ray image G before completing the registration operation. Therefore, the omission of registration of the sampling position information C for the X-ray image G can be suppressed. As a result, it is possible to prevent the collection position of the specimen sample from being unspecified and the collection position information C from being unable to be registered in the X-ray image G.
 なお、第4実施形態のその他の効果は、上記第1実施形態と同様である。 The other effects of the fourth embodiment are similar to those of the first embodiment.
 [第5実施形態]
 次に、図1および図13を参照して、第5実施形態における診断画像システム130(図1参照)について説明する。制御部41が、検体試料の分析の進捗状況PAとして、少なくとも分析が完了しているか否かを識別可能に表示する上記第1実施形態とは異なり、第5実施形態における診断画像システム130の制御部81は、複数の検体試料のそれぞれについて、分析の進捗状況PAとして、検体試料の分析前、検体試料の分析中、検体試料の分析完了のいずれかを表示するように構成されている。なお、上記第1実施形態と同様の構成については同様の符号を付し、説明を省略する。
[Fifth Embodiment]
Next, a diagnostic image system 130 (see FIG. 1) in the fifth embodiment will be described with reference to FIGS. 1 and 13. 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.
 図13に示すように、第5実施形態では、制御部81は、複数の検体試料のそれぞれについて、分析の進捗状況PAとして、検体試料の分析前、検体試料の分析中、検体試料の分析完了のいずれかを表示するように構成されている。分析状況の進捗状況PAは、検体試料の分析が進むにつれて変化する。制御部81は、検体分析装置3による検体試料の分析の状況を監視しており、分析状況の進捗状況PAが変化する度に、表示領域DASに表示する内容を変更する。すなわち、制御部81は、検体試料の分析が開始される前の状態では、表示領域DASに「分析前」と表示する。また、制御部81は、検体試料の分析が開始された際に、表示領域DASの表示を「分析前」から「分析中」に変更する。また、制御部81は、検体試料の分析が完了した際に、表示領域DASの表示を「分析中」から「分析完了」に変更する。 As shown in FIG. 13, in the fifth embodiment, 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”.
 なお、第5実施形態のその他の構成は、上記第1実施形態と同様である。 The other configurations of the fifth embodiment are the same as those of the first embodiment.
 (第5実施形態の効果)
 第5実施形態では、以下のような効果を得ることができる。
(Effects of the fifth embodiment)
In the fifth embodiment, the following effects can be obtained.
 第5実施形態では、上記のように、制御部81は複数の検体試料のそれぞれについて、分析の進捗状況PAとして、検体試料の分析前、検体試料の分析中、検体試料の分析完了のいずれかを表示するように構成されている。このように構成すれば、医師などは、分析が完了していない検体試料について、分析前であるか分析中であるかを視覚的に把握することができる。 In the fifth embodiment, as described above, the 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.
 なお、第5実施形態のその他の効果は、上記第1実施形態と同様である。 The other effects of the fifth embodiment are similar to those of the first embodiment.
 [第6実施形態]
 次に、図1および図14を参照して、第6実施形態における診断画像システム140(図1参照)について説明する。制御部41が、検体試料の分析の進捗状況PAとして、少なくとも分析が完了しているか否かを識別可能に表示する上記第1実施形態とは異なり、第6実施形態における診断画像システム140の制御部91は、複数の検体試料のそれぞれについて、検体分析装置3による各分析工程のうち、進行中の分析工程を分析の進捗状況PAとして表示するように構成されている。なお、上記第1実施形態と同様の構成については同様の符号を付し、説明を省略する。
[Sixth Embodiment]
Next, a diagnostic image system 140 (see FIG. 1) according to the sixth embodiment will be described with reference to FIGS. 1 and 14. Unlike the first embodiment in which 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. The unit 91 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.
 第6実施形態では、制御部91は、複数の検体試料のそれぞれについて、検体分析装置3による各分析工程のうち、進行中の分析工程を分析の進捗状況PAとして表示するように構成されている。 In the sixth embodiment, the 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. ..
 具体的には、図13に示すように、制御部91は、分析の進捗状況PAとして、登録前、前処理中、LC分析中、MS分析中、承認前、分析完了の分析工程のうち、対応する工程を、進行中の分析工程を分析の進捗状況PAとして表示するように構成されている。なお、「登録前」とは、検体分析装置3において、識別情報Uが読み込まれる前の状態である。また、「前処理中」とは、検体試料を分析するために必要な処理を行う工程が進行している状態である。また、「LC分析中」とは、検体試料を、LC部31において分離する工程が進行している状態である。また、「MS分析中」とは、MS部32における分析が進行している状態である。また、「承認前」とは、分析が終了し、得られた分析結果RAが承認される前の状態である。また、「分析完了」とは、分析が終了するとともに、得られた分析結果RAが承認された状態である。 Specifically, as shown in FIG. 13, 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. Further, “during pretreatment” is a state in which a step of performing a treatment necessary for analyzing a specimen sample is in progress. In addition, “during LC analysis” is a state in which the step of separating the specimen sample in the LC unit 31 is in progress. In addition, “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. Further, "analysis completed" is a state in which the analysis result RA obtained is approved when the analysis is completed.
 なお、検体分析装置3は、LC部31およびMS部32を備えていない場合もある。検体分析装置3がLC部31およびMS部32を備えていない場合、制御部81は、検体分析装置3によって実施される各工程を表示すればよい。 The sample analyzer 3 may not include the LC unit 31 and the MS unit 32. When the sample analyzer 3 does 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.
 なお、第6実施形態のその他の構成は、上記第1実施形態と同様である。 The other configurations of the sixth embodiment are similar to those of the first embodiment.
 (第6実施形態の効果)
 第6実施形態では、以下のような効果を得ることができる。
(Effects of the sixth embodiment)
In the sixth embodiment, the following effects can be obtained.
 第6実施形態では、上記のように、制御部81は、複数の検体試料のそれぞれについて、検体分析装置3による各分析工程のうち、進行中の分析工程を分析の進捗状況PAとして表示するように構成されている。これにより、医師などは、検体試料の分析状況を、詳細に視覚的に把握することができる。 In the sixth embodiment, as described above, the 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.
 なお、第6実施形態のその他の効果は、上記第1実施形態と同様である。 The other effects of the sixth embodiment are the same as those of the first embodiment.
 [変形例]
 なお、今回開示された実施形態は、すべての点で例示であって制限的なものではないと考えられるべきである。本発明の範囲は、上記した実施形態の説明ではなく請求の範囲によって示され、さらに請求の範囲と均等の意味および範囲内でのすべての変更(変形例)が含まれる。
[Modification]
It should be considered that the embodiments disclosed this time are exemplifications in all points and not restrictive. The scope of the present invention is shown not by the above description of the embodiments but by the scope of the claims, and further includes meanings equivalent to the scope of the claims and all modifications (modifications) within the scope.
 たとえば、上記第1~第6実施形態では、操作者によって、第1表示領域F1において、検体試料が選択された場合に、制御部41(51、61、71、81、91)が、第1表示領域F1、第2表示領域F2および第3表示領域F3において、選択により特定される検体試料の採取位置情報Cおよび試料データSD中の検体試料を強調表示する構成の例を示したが、本発明はこれに限られない。たとえば、制御部41(51、61、71、81、91)は、第2表示領域F2において、試料データSDが選択された場合に、第1表示領域F1、第2表示領域F2および第3表示領域F3において、選択により特定される検体試料の採取位置情報Cおよび試料データSD中の検体試料を強調表示しなくてもよい。 For example, in the first to sixth embodiments, 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 invention is not limited to this. For example, 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.
 また、操作者によって、第3表示領域F3において、検体試料が選択された場合に、制御部41(51、61、71、81、91)は、第1表示領域F1、第2表示領域F2および第3表示領域F3において、選択により特定される検体試料の採取位置情報Cおよび試料データSD中の検体試料を強調表示するように構成されていてもよい。すなわち、第1表示領域F1、第2表示領域F2および第3表示領域F3のいずれの表示領域において検体試料が選択された場合でも、制御部41(51、61、71、81、91)は、第1表示領域F1、第2表示領域F2および第3表示領域F3において、選択により特定される検体試料の採取位置情報Cおよび試料データSD中の検体試料を強調表示するように構成すればよい。 In addition, when the operator selects the specimen sample in the third display region F3, 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.
 また、上記第1~第6実施形態では、制御部41(51、61、71、81、91)が、第3表示領域F3において、サムネイル画像THを表示する構成の例を示したが、本発明はこれに限られない。たとえば、制御部41(51、61、71、81、91)は、第3表示領域F3において、サムネイル画像THを表示しなくてもよい。また、表示部42は、第3表示領域F3を含んでいなくてもよい。 In the first to sixth embodiments, the control unit 41 (51, 61, 71, 81, 91) displays the thumbnail image TH in the third display area F3. The invention is not limited to this. For example, the control unit 41 (51, 61, 71, 81, 91) does not have to display the thumbnail image TH in the third display area F3. In addition, the display unit 42 may not include the third display area F3.
 また、上記第1~第6実施形態では、制御部41(51、61、71、81、91)が、試料データSDをリスト形式で表示する構成の例を示したが、本発明はこれに限られない。制御部41(51、61、71、81、91)は、試料データSDをリスト形式で表示しなくてもよい。 Further, although the control unit 41 (51, 61, 71, 81, 91) 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 (51, 61, 71, 81, 91) does not have to display the sample data SD in the list format.
 また、上記第1~第6実施形態では、制御部41(51、61、71、81、91)が、分析結果RAを含む試料データSDを表示する構成の例を示したが、本発明はこれに限られない。制御部41(51、61、71、81、91)は、分析結果RAを含まない試料データSDを表示するように構成されていてもよい。試料データSDには、少なくとも、検体試料の識別情報Uと、採取位置情報Cの登録状況とが含まれていればよい。 In the first to sixth embodiments, the control unit 41 (51, 61, 71, 81, 91) 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 (51, 61, 71, 81, 91) 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.
 また、上記第1~第6実施形態では、制御部41(51、61、71、81、91)が、検体試料の分析の進捗状況PAを含む試料データSDを表示する構成の例を示したが、本発明はこれに限られない。制御部41(51、61、71、81、91)は、検体試料の分析の進捗状況PAを含まない試料データSDを表示するように構成されていてもよい。 In the first to sixth embodiments, the control unit 41 (51, 61, 71, 81, 91) displays the sample data SD including the progress PA of the sample sample analysis. However, the present invention is not limited to this. The control unit 41 (51, 61, 71, 81, 91) may be configured to display the sample data SD that does not include the progress status PA of the analysis of the sample sample.
 また、上記第1~第6実施形態では、1つの検体試料に対応する1つの識別用目印IMが、複数のサムネイル画像THのうちのいずれか1枚の画像に表示される構成の例を示したが、本発明はこれに限られない。たとえば、図15に示すように、1つの検体試料に対応する同一の数字が記された識別用目印IMが、複数のサムネイル画像THに表示されていてもよい。1つの検体試料に対応する同一の数字が記された識別用目印IMが、複数のサムネイル画像THに表示されている検体試料が選択された場合、制御部41(51、61、71、81、91)は、複数のサムネイル画像THにおいて、同一の数字が記された識別用目印IMを強調表示するように構成されればよい。 In the first to sixth embodiments, one identification mark IM corresponding to one specimen sample is displayed on any one of the thumbnail images TH. However, the present invention is not limited to this. For example, as shown in FIG. 15, 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. When the specimen sample displayed in the plurality of thumbnail images TH is selected as the identification mark IM with the same numeral corresponding to one specimen sample, the control unit 41 (51, 61, 71, 81, 91) may be configured to highlight the identification mark IM having the same number in the plurality of thumbnail images TH.
 また、上記第1~第6実施形態では、制御部41(51、61、71、81、91)が、手術室R1に設置されたワークステーション4に設けられる構成の例を示したが、本発明はこれに限られない。たとえば、図16に示すように、制御部41(51、61、71、81、91)は、ネットワークNを介してX線撮影装置2および検体分析装置3と接続された診断用情報処理装置5に設けられていてもよい。診断用情報処理装置5は、制御部52と、表示部53と、操作部54と、記憶部55と、通信部56とを備えている。診断用情報処理装置5は、読取部46を備えていない点を除いては、ワークステーション4と同様に構成されている。制御部52を、制御部41(51、61、71、81、91)と同様に構成することにより、選択により特定される検体試料に対応する検体試料の採取位置情報Cおよび試料データSDを強調表示するように構成してもよい。このように構成すれば、医師などの診断時において、検体試料の採取位置と試料データSDとを容易に把握可能な状態で診断を行うことができる。また、患者などに説明する場合でも、検体試料の採取位置と試料データSDとを容易に把握可能な状態で説明することができる。 In the first to sixth embodiments, 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 invention is not limited to this. For example, as shown in FIG. 16, the control unit 41 (51, 61, 71, 81, 91) 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. By configuring the control unit 52 in the same manner as the control unit 41 (51, 61, 71, 81, 91), 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.
 また、上記第1~第6実施形態では、制御部41(51、61、71、81、91)が、採取位置情報Cを丸印C1として、X線画像G上に表示する構成の例を示したが、本発明はこれに限られない。たとえば、第1表示領域F1において、X線画像Gとは別に、検体試料の採取位置の座標値を表示するように構成されていてもよい。採取位置情報Cとして、座標値を表示する構成の場合、制御部41(51、61、71、81、91)は、操作者によって座標値が選択されたことに基づいて、対応する採取位置情報Cおよび試料データSDを強調表示するように構成すればよい。また、制御部41(51、61、71、81、91)は、採取位置情報Cを第1表示領域F1に表示せず、採取位置情報Cの座標値の画素を操作者が選択することにより、採取位置情報Cおよび試料データSDを強調表示するように構成されていてもよい。 Further, in the first to sixth embodiments, an example of a configuration in which the control unit 41 (51, 61, 71, 81, 91) displays the sampling position information C as a circle C1 on the X-ray image G However, the present invention is not limited to this. For example, 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. When the coordinate value is displayed as the collection position information C, the control unit 41 (51, 61, 71, 81, 91) 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. In addition, the control unit 41 (51, 61, 71, 81, 91) 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.
 また、上記第1~第6実施形態では、制御部41(51、61、71、81、91)が、X線画像Gへの採取位置情報Cの登録状況として、登録されているか否かを表示する構成の例を示したが、本発明はこれに限られない。たとえば、制御部41(51、61、71、81、91)は、X線画像Gへの採取位置情報Cの登録が不要な検体試料の場合、標識MSの表示領域DAMにおいて、採取位置情報Cの登録が不要であることを識別可能に表示するように構成されていてもよい。このように構成すれば、X線画像Gへの採取位置情報Cの登録が必要な検体試料で、かつ、登録が漏れているのか、X線画像Gへの採取位置情報Cの登録が不要な検体試料なのかを容易に把握することができる。 In addition, in the first to sixth embodiments, 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. Although the example of the configuration to be displayed is shown, the present invention is not limited to this. For example, in the case of a specimen sample that does not require registration of the collection position information C in the X-ray image G, the control unit 41 (51, 61, 71, 81, 91) 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. With this configuration, it is not necessary to register the sampling position information C in the X-ray image G because it is a sample specimen that requires registration of the sampling position information C in the X-ray image G and whether registration is missing. It is possible to easily understand whether the sample is a sample.
 また、上記第1~第6実施形態では、接続部26eと、接続部45とを接続することにより、X線撮影装置2とワークステーション4とを直接接続する構成の例を示したが、本発明はこれに限られない。たとえば、X線撮影装置2とワークステーション4とは、ネットワークNを介して接続されていてもよい。 Further, in the above-described first to sixth embodiments, 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. For example, the X-ray imaging apparatus 2 and the workstation 4 may be connected via the network N.
 また、上記第2実施形態では、制御部51が、識別用目印IMに加えて、試料データSDの行を、表示色の変更によって、選択された検体試料を強調表示する構成の例を示したが、本発明はこれに限られない。たとえば、制御部51は、識別用目印IMに加えて、試料データSDの行を、字体の変更、文字の点滅、および拡大表示のいずれかによって、選択された検体試料を強調表示するように構成されていてもよい。 Further, in the second embodiment, an example of the configuration in which the 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 has been shown. However, the present invention is not limited to this. For example, 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.
 また、上記第1~第6実施形態では、分析の進捗状況PAとして、表示領域DASにおいて、「○」または「-」を表示する構成の例を示したが、本発明はこれに限られない。たとえば、図17に示すように、表示領域DASを設ける代わりに、分析結果RAの表示態様を異ならせることにより、分析の進捗状況PAを表示する構成であってもよい。具体的には、分析結果RAの表示色を異ならせることにより、「承認前」のステータスと、「分析完了」のステータスとを識別可能に表示するように構成すればよい。なお、図17では、便宜上、分析結果RAの表示色の違いを、白抜き文字か否かで表している。すなわち、通常の文字で表示された分析結果RA1は、ステータスが「承認前」であることを表している。また、白抜き文字で表示された分析結果RA2は、ステータスが「分析完了」であることを表している。また、図17の分析結果RAにおいて、「-」で表示された分析結果RA3は、ステータスが「分析前」であることを表している。 Further, in the above-described first to sixth embodiments, an example of the configuration in which “◯” or “−” is displayed in the display area DAS as the analysis progress status PA is shown, but the present invention is not limited to this. . For example, as shown in FIG. 17, instead of providing the display area DAS, the analysis progress status PA may be displayed by changing the display mode of the analysis result RA. Specifically, 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. Note that, in FIG. 17, for convenience, 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”.
 1、100、110、120、130、140 診断画像システム
 2 X線撮影装置(放射線撮影装置)
 3 検体分析装置
 41、51、61、71、81、91 制御部
 42 表示部
 AG 副腎(臓器)
 C 採取位置情報
 F1 第1表示領域
 F2 第2表示領域
 F3 第3表示領域
 G X線画像(放射線画像)
 RA 分析結果
 T 被検体
 U 識別情報(複数の検体試料のそれぞれを識別可能な情報)
1, 100, 110, 120, 130, 140 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)

Claims (9)

  1.  臓器から採取される複数の検体試料の採取位置が判別可能な被検体の放射線画像を撮影する放射線撮影装置と、
     少なくとも、第1表示領域および第2表示領域を含む表示部と、
     前記放射線画像と、前記検体試料の採取位置情報とを取得し、取得した前記検体試料の前記採取位置情報に基づいて、前記検体試料の前記採取位置を判別可能なように前記放射線画像を前記第1表示領域に表示する制御を行うとともに、複数の前記検体試料のそれぞれを識別可能な情報を含む試料データを前記第2表示領域に表示する制御を行う制御部とを備え、
     前記制御部は、前記検体試料に対応する前記採取位置情報が取得されたか否かに基づいて、操作者によって行われる前記放射線画像への前記検体試料の前記採取位置情報の登録状況を表示するように構成されている、診断画像システム。
    A radiation imaging apparatus for capturing a radiation image of a subject capable of discriminating the collection positions of a plurality of specimen samples collected from an organ,
    A display unit including at least a first display area and a second display area;
    The radiation image and the sampling position information of the specimen sample are acquired, and based on the acquired sampling position information of the specimen sample, the radiation image is stored in the radiation image so that the sampling position of the specimen sample can be determined. A control unit for performing control for displaying in one display area and for controlling for displaying sample data including information capable of identifying each of the plurality of specimen samples in the second display area,
    The control unit displays the registration status of the collection position information of the sample sample in the radiographic image performed by the operator based on whether the collection position information corresponding to the sample sample is acquired. A diagnostic imaging system configured to.
  2.  前記制御部は、前記試料データをリスト形式によって表示するとともに、リスト形式によって表示した前記試料データの各行において、前記検体試料ごとに、前記採取位置情報の登録状況を表示するように構成されている、請求項1に記載の診断画像システム。 The control unit is configured to display the sample data in a list format, and to display a registration status of the collection position information for each specimen sample in each line of the sample data displayed in the list format. The diagnostic imaging system according to claim 1.
  3.  前記制御部は、リスト形式によって表示した前記試料データにおいて、前記採取位置情報の登録状況を示す標識を表示するとともに、前記標識および前記標識の表示領域の表示態様を、前記採取位置情報の登録状況に応じて異ならせて表示するように構成されている、請求項2に記載の診断画像システム。 In the sample data displayed in a list format, the control unit displays a sign indicating the registration status of the collection position information, and the display mode of the sign and the display area of the sign is the registration status of the collection position information. The diagnostic imaging system according to claim 2, wherein the diagnostic imaging system is configured to be displayed differently according to.
  4.  前記制御部は、操作者の入力によって前記放射線画像に対する前記採取位置情報の登録を行うとともに、前記放射線画像に前記採取位置情報が登録されていない前記検体試料がある場合に、未登録の前記検体試料が存在することを表示するように構成されている、請求項1に記載の診断画像システム。 The control unit performs registration of the sampling position information for the radiation image by an operator's input, and when there is a sample sample in which the sampling position information is not registered in the radiation image, the unregistered sample The diagnostic imaging system of claim 1, wherein the diagnostic imaging system is configured to indicate the presence of a sample.
  5.  前記検体試料を分析して分析結果を生成する検体分析装置をさらに備え、
     前記制御部は、複数の前記検体試料のそれぞれについて、分析の進捗状況を表示するように構成されている、請求項1に記載の診断画像システム。
    Further comprising a sample analyzer that analyzes the sample sample to generate an analysis result,
    The diagnostic image system according to claim 1, wherein the control unit is configured to display a progress status of analysis for each of the plurality of specimen samples.
  6.  前記制御部は、複数の前記検体試料のそれぞれについて、分析の進捗状況として、少なくとも分析が完了しているか否かを識別可能に表示するように構成されている、請求項5に記載の診断画像システム。 The diagnostic image according to claim 5, wherein the control unit is configured to display, for each of the plurality of sample specimens, at least whether or not the analysis has been completed is identifiable as the progress status of the analysis. system.
  7.  前記制御部は、複数の前記検体試料のそれぞれについて、分析の進捗状況として、前記検体試料の分析前、前記検体試料の分析中、前記検体試料の分析完了のいずれかを表示するように構成されている、請求項5に記載の診断画像システム。 The control unit is configured to display, for each of the plurality of specimen samples, one of analysis progress of the specimen sample, analysis of the specimen sample, and completion of analysis of the specimen sample as the analysis progress status. The diagnostic imaging system according to claim 5, wherein:
  8.  前記制御部は、複数の前記検体試料のそれぞれについて、前記検体分析装置による各分析工程のうち、進行中の分析工程を分析の進捗状況として表示するように構成されている、請求項5に記載の診断画像システム。 The control unit is configured to display, for each of the plurality of sample samples, an ongoing analysis process among the analysis processes performed by the sample analyzer as a progress status of the analysis. Diagnostic imaging system.
  9.  臓器から採取される複数の検体試料の採取位置が判別可能な被検体の放射線画像を取得するステップと、
     前記放射線画像と、前記検体試料の採取位置情報とを取得するステップと、
     取得した前記検体試料の前記採取位置情報に基づいて、前記検体試料の採取位置を判別可能なように前記放射線画像を第1表示領域に表示するとともに、複数の前記検体試料のそれぞれ識別可能な情報を含む試料データを第2表示領域に表示するステップと、
     前記検体試料に対応する前記採取位置情報が取得されたか否かに基づいて、操作者によって行われる前記放射線画像への前記検体試料の前記採取位置情報の登録状況を表示するステップとを含む、診断画像管理方法。
    A step of acquiring a radiographic image of the subject capable of discriminating the sampling positions of a plurality of sample specimens collected from the organ;
    Acquiring the radiation image and the sampling position information of the specimen sample;
    Based on the acquired sampling position information of the specimen sample, the radiographic image is displayed in the first display area so that the sampling position of the specimen sample can be discriminated, and the plurality of specimen samples can be distinguished from each other. Displaying sample data including the following in the second display area,
    A step of displaying a registration status of the sampling position information of the sample sample in the radiographic image performed by an operator based on whether or not the sampling position information corresponding to the sample sample has been acquired. Image management method.
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