Sample analysis system and sample loading information display method

By directly displaying the status logo of the sample holder or kit in the management interface of the coagulation analyzer, the problem of users needing to frequently switch pages is solved, and the multiplexing of sample loading and the improvement of information processing speed is achieved.

CN119510796APending Publication Date: 2025-02-25MEDCAPTAIN MEDICAL TECH
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Patent Information

Application Number
CN202411671836.4
Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Filing Date
2024-11-20
Publication Date
2025-02-25

AI Technical Summary

Technical Problem

In the use of the coagulation analyzer, the status information of the sample holder and the kit are located on different display pages, which leads to users need to switch the display page through the tab button, which is cumbersome and reduces the speed of user information processing.

Method used

A sample analysis system is designed, including a loading device, a display device and a control device. By displaying the status mark of the sample holder or kit in the management interface through the loading display bit, the multiplexing of the sample loading bits is realized, and the loading information of the sample loading bits is directly displayed.

Benefits of technology

It improves the convenience of user operations, reduces the number of times users switch pages, speeds up user information processing, and enhances user interface dependence.

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Abstract

The invention provides a sample analysis system and a sample loading information display method. The system comprises an analysis device, a sample loading device, a display device and a control device. The sample analysis system firstly displays a management interface, the management interface comprises a sample loading display area, then the loading object information of the sample loading position can be obtained according to the sample loading device, and a sample frame state identifier or a kit state identifier is displayed at the sample loading display position. Therefore, the sample loading position can be used for loading the sample frame and the kit, the reuse of the sample loading position is realized, the actual loading object of the sample loading position can be displayed, a user can conveniently and intuitively know the loading object information of the sample loading position, the convenience degree of user operation is improved, and the user information processing speed is accelerated.
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Description

Technical Field

[0001] The present application relates to the field of medical equipment, and specifically to a sample analysis system and a sample loading information display method. Background Art

[0002] A coagulation analyzer is an instrument for laboratory examination of thrombosis and hemostasis. The working principle of a coagulation analyzer is mainly to mix the sample with the reagent by a specific method, detect the change in the physical properties of the mixture, and then discharge the mixture. The page display of the coagulation analyzer can provide users with relevant information, which is helpful for the diagnosis and treatment of bleeding and thrombotic diseases.

[0003] Currently, in the use of coagulation analyzers, sample racks and reagent kits are loaded at different locations, and the sample rack status information and reagent kit status information are displayed on the management interface of the display, but the sample rack status information and the reagent kit status information are located on different display pages, respectively. Users need to switch display pages through tab buttons to understand the sample rack status information or the reagent kit status information, which makes user operations cumbersome and reduces the user's information processing speed. Summary of the invention

[0004] The present application proposes a sample analysis system and a sample loading information display method, which realizes the reuse of sample loading positions and can display the actual load of the sample loading positions, thereby improving the convenience of user operation and accelerating the user information processing speed.

[0005] In a first aspect, an embodiment of the present application provides a sample analysis system, comprising:

[0006] A sample loading device, comprising a sample loading platform and a dispatching mechanism, wherein the sample loading platform comprises a sample loading position, and the dispatching mechanism is used to transport the load at the sample loading position;

[0007] Display device;

[0008] A control device is used to control the display device to display a management interface, wherein the management interface includes a first display area, the first display area includes a sample loading display position, and the sample loading display position displays a reagent kit status mark when the load corresponding to the sample loading position is a reagent kit, and displays a sample rack status mark when the load corresponding to the sample loading position is a sample rack.

[0009] In a second aspect, an embodiment of the present application provides a method for displaying sample loading information, which is applied to a control device of the sample analysis system as described above, and the method includes:

[0010] Display management interface, the management interface includes a sample display position;

[0011] According to the acquired loading information of the sample loading position, a sample rack status mark or a reagent kit status mark is displayed at the sample loading display position.

[0012] It can be seen that in the present application, the sample analysis system first displays the management interface, which includes a sample loading display area, and then can obtain the loading information of the sample loading position according to the sample loading device, and display the sample rack status mark or the reagent kit status mark in the sample loading display position. In this way, the sample loading position can load both the sample rack and the reagent kit, realizing the reuse of the sample loading position, and can display the actual loading of the sample loading position, so that the user can intuitively understand the loading information of the sample loading position, improve the convenience of user operation, and speed up the user information processing speed. BRIEF DESCRIPTION OF THE DRAWINGS

[0013] In order to more clearly illustrate the embodiments of the present application or the technical solutions in the prior art, the drawings required for use in the embodiments or the description of the prior art will be briefly introduced below. Obviously, the drawings described below are only some embodiments of the present application. For ordinary technicians in this field, other drawings can be obtained based on these drawings without paying creative work.

[0014] Figure 1 It is a schematic diagram of the composition of a sample analysis system provided in an embodiment of the present application;

[0015] Figure 2 is a schematic diagram of a management interface provided in an embodiment of the present application;

[0016] Figure 3 It is a schematic diagram of the composition of a coagulation analyzer provided in an embodiment of the present application;

[0017] Figure 4a - Figure 4c is a schematic diagram of an emergency sample setting provided in an embodiment of the present application;

[0018] Figure 4a , Figure 4b ,as well as Figure 4d is a schematic diagram of another emergency sample setting provided in an embodiment of the present application;

[0019] Figure 5 is a schematic diagram of the display method of each logo provided in the embodiment of the present application;

[0020] Figure 6 is a schematic diagram of another management interface provided in an embodiment of the present application;

[0021] Figure 7 is a schematic diagram of a second display area provided in an embodiment of the present application;

[0022] Figure 8 This is a schematic diagram of viewing reagent information provided by an embodiment of the present application;

[0023] Fig. 9 This is a schematic diagram of a one-key uninstallation provided in an embodiment of the present application;

[0024] Fig.10 This is another schematic diagram for viewing reagent information provided in an embodiment of the present application;

[0025] Fig.11 is a schematic diagram of an uninstallation reminder provided in an embodiment of the present application;

[0026] Fig.12 is a schematic diagram of a reagent container view provided in an embodiment of the present application;

[0027] Fig.13 is a schematic diagram of another reagent container view provided in an embodiment of the present application;

[0028] Fig.14 This is a schematic diagram of viewing sample information provided by an embodiment of the present application;

[0029] Fig.15 It is a flow chart of a method for displaying sample loading information provided in an embodiment of the present application. DETAILED DESCRIPTION

[0030] In order to enable those skilled in the art to better understand the solution of the present application, the technical solution in the embodiments of the present application will be clearly and completely described below in conjunction with the drawings in the embodiments of the present application. Obviously, the described embodiments are only part of the embodiments of the present application, not all of the embodiments. Based on the embodiments in the present application, all other embodiments obtained by ordinary technicians in this field without creative work are within the scope of protection of this application.

[0031] The terms "first", "second", etc. in the specification and claims of this application and the above-mentioned drawings are used to distinguish different objects, rather than to describe a specific order. In addition, the terms "including" and "having" and any variations thereof are intended to cover non-exclusive inclusions. For example, a process, method, system, product or device that includes a series of steps or units is not limited to the listed steps or units, but optionally includes steps or units that are not listed, or optionally includes other steps or units inherent to these processes, methods, products or devices.

[0032] Reference to "embodiments" herein means that a particular feature, structure, or characteristic described in conjunction with the embodiments may be included in at least one embodiment of the present application. The appearance of the phrase in various locations in the specification does not necessarily refer to the same embodiment, nor is it an independent or alternative embodiment that is mutually exclusive with other embodiments. It is explicitly and implicitly understood by those skilled in the art that the embodiments described herein may be combined with other embodiments.

[0033] In the embodiments of the present application, "and / or" describes the association relationship of the associated objects, indicating that three relationships may exist. For example, A and / or B can represent the following three situations: A exists alone; A and B exist at the same time; B exists alone. Among them, A and B can be singular or plural.

[0034] In the embodiment of the present application, the symbol " / " can indicate that the objects associated with each other are in an "or" relationship. In addition, the symbol " / " can also indicate a division sign, that is, performing a division operation. For example, A / B can indicate A divided by B.

[0035] In the embodiments of the present application, "equal to" can be used in conjunction with greater than, and is applicable to the technical solution adopted when greater than, and can also be used in conjunction with less than, and is applicable to the technical solution adopted when less than. When equal to is used in conjunction with greater than, it is not used in conjunction with less than; when equal to is used in conjunction with less than, it is not used in conjunction with greater than.

[0036] At present, in the use of coagulation analyzers, the loading platform can only place samples. The coagulation analyzer displays the sample rack status information and the reagent kit status information on different display pages of its display. Users need to switch the display page through the tab button to understand the relevant information. The visualization effect is poor and the user's interface dependence is low, so the user's operation convenience is low and the user's information processing speed is reduced.

[0037] In response to the above problems, an embodiment of the present application provides a sample analysis system and a sample loading information display method. The embodiment of the present application is described in detail below in conjunction with the accompanying drawings.

[0038] See also Figure 1 , Figure 1 Schematic diagram of the composition of a sample analysis system provided in an embodiment of the present application. Figure 1 As shown, the sample analysis system 10 may include an analysis device 101, a sample loading device 102, a display device 103, and a control device 104. The control device 104 may be connected to the analysis device 101 to instruct the analysis device 101 to perform various operations, such as adding samples, incubating, adding reagents, mixing, and testing; the sample loading device 102 includes a sample loading platform 1021 and a scheduling mechanism 1022, the sample loading platform 1021 has a sample loading position for placing a load, and the control device 104 may be connected to the sample loading device 102 to control the scheduling mechanism 1022 to transfer the load placed at the sample loading position to the target position of the analysis device 101; the control device 104 may be connected to the display device 103 to control the display device 103 to display different contents according to the acquired information.

[0039] The analysis device 101 is used to detect the sample to be tested to obtain the test result. The analysis device may include components such as a sample adding unit, a reagent storage unit and a test unit. The reagent storage unit may be used to place the reagent kit. The sample adding unit may absorb the sample to be tested or the reagent, and transfer the absorbed sample to be tested or the reagent to the reaction cup to form a reaction liquid. The reaction liquid in the reaction cup is then tested by the test unit, thereby achieving the purpose of detecting the sample to be tested to obtain the test result. The sample analysis system may be a coagulation analyzer or a part of a coagulation analyzer.

[0040] The loading device 102 includes a loading platform 1021 and a scheduling mechanism 1022. The loading platform 1021 includes a plurality of loading positions, such as loading position 1, loading position 2, loading position 3, etc. The scheduling mechanism 1022 is configured to transfer the load of the loading position to the analysis device. The load of the loading position can be a sample rack or a reagent kit. For example, Figure 3 The coagulation analyzer shown has a total of 17 sample loading positions, each of which can be used to load a sample rack or a reagent kit. When the sample loading position is loaded with a sample rack, the scheduling mechanism can transfer the sample rack to the next step area, such as the sample suction area, and then transfer the sample rack back to the sample loading platform after the sample suction is completed, waiting for the user to collect and unload the machine; when the sample loading position is loaded with a reagent kit, the scheduling mechanism can transfer the reagent kit to the reagent storage unit. When unloading the reagent kit, the scheduling mechanism can also place the reagent kit in the reagent storage unit back to the sample loading platform, waiting for the user to take it and unload it. Each sample loading position of the sample loading platform 1021 can load both sample racks and reagent kits, realizing the reuse of the sample loading positions.

[0041] Among them, the control device 104 is used to control the display device 103 to display the management interface 20, and the management interface 20 includes a first display area 110, and the first display area 110 is used to display the status information of each loading position of the loading platform 1021. The first display area includes multiple loading display positions, and the multiple loading display positions correspond to the multiple loading positions of the loading platform 1021 one by one. Each loading display position displays a reagent kit status mark when the load of the corresponding loading position is a reagent kit, and displays a sample rack status mark when the load of the corresponding loading position is a sample rack. The sample rack status mark and the reagent kit status mark have different visual elements, which can facilitate users to intuitively understand the load information of the loading position.

[0042] See also Figure 2 , Figure 2 Schematic diagram of a management interface provided by an embodiment of the present application. Figure 2As shown, the management interface 20 may include a first display area 110, and the first display area 110 may include multiple sample loading display positions. The sample loading display position may be displayed as a reagent kit status mark 122 to indicate that the load corresponding to the sample loading position is a reagent kit. The sample loading display position may also be displayed as a sample rack status mark 121 to indicate that the load corresponding to the sample loading position is a sample rack. That is, the sample loading position of the sample analysis system of the present application is a multiplexed sample loading position, which can be loaded with both a sample rack and a reagent kit. The display device intuitively displays the actual load of each sample loading position through different visual marks, which not only improves the visualization effect, but also facilitates the user to intuitively understand the load information of the sample loading position, and displays the sample rack status information and the reagent kit status information in the same area, which improves the convenience of user operation and speeds up the user information processing speed.

[0043] Furthermore, the first display area includes a plurality of sample loading display positions, and the sample loading display positions display number information, and the number information matches the number of the corresponding sample loading position.

[0044] Among them, see Figure 3 , Figure 3 Schematic diagram of the composition of a coagulation analyzer provided in an embodiment of the present application. Figure 3 As shown, the coagulation analyzer may include a loading platform 1021 and a display device 103. At the loading platform 1021, there are 17 loading positions, and each loading position is numbered from 1 to 17 in order from left to right. This relationship can be displayed in the management interface 20 of the display device, such as Figure 2 As shown, in the management interface 20, there is a number mark below each sample display position in the first display area 110, and the number of each number mark corresponds to the number sequence of the sample positions. For example, the sample display position numbered 4 can reflect Figure 3 The placement of the fourth loading position from left to right in the figure.

[0045] In addition, since the loading capacity of sample racks is large, in order to meet the detection requirements, a part of the loading positions of the loading platform 1021 can be used only for placing sample racks, and another part of the loading positions of the loading platform 1021 can be used to place both sample racks and reagent kits. Figure 3 As shown, the sample loading positions numbered 1-12 can only support the placement of sample racks, and the sample loading positions numbered 13-17 can be used to place both sample racks and reagent kits. Figure 2The multiple loading display positions can be divided into a sample position display area 111 and a reuse position display area 112. Each loading display position in the sample position display area 111 can display a sample rack status mark or an idle mark, that is, the loading display positions numbered 1-12 can display a sample rack status mark (such as a loading display position with a number of 4) or an idle mark (such as a loading display position with a number of 6) according to actual conditions; the loading display positions in the reuse position display area 112 can display a sample rack status mark, a reagent kit status mark or an idle mark according to actual conditions, that is, the loading display positions numbered 13-17 can be displayed as a sample rack status mark (such as a loading display position with a number of 16), or as a reagent kit status mark (such as a loading display position with a number of 15), or as an idle mark (such as a loading display position with a number of 17). The loading positions corresponding to the reuse position display area 112 in the loading platform 1021 can be loaded with both sample racks and reagent kits, thereby realizing multiplexing of the loading positions.

[0046] Furthermore, in order to facilitate the user to intuitively distinguish the sample position display area 111 from the multiplexed position display area 112, a separation mark is provided between the sample position display area 111 and the multiplexed position display area 112. Figure 6 As shown, the sample bit display area 111 and the multiplexed bit display area 112 can be distinguished by a dividing line, or as shown in FIG. Figure 7 As shown, in the first display area 110, the distance between the sample position display area 111 and the multiplexed position display area 112 is greater than the distance between any other two adjacent sample display positions, such as the distance between the sample display position numbered 12 and the sample display position numbered 13 is greater than the distance between any other two adjacent sample display positions. In particular, specific number identifiers can also be designed to distinguish between sample positions and multiplexed positions. For example, the number identifiers of the sample display positions in the sample position display area 111 can be displayed in numbers, and the number identifiers of the sample display positions in the multiplexed position display area 112 can be represented by letters. It should be noted that in the sample analysis system, the sample loading platform 1021 can be divided into a sample position area and a multiplexed position area, and the positional relationship between the sample position area and the multiplexed position area can correspond to the positional relationship between the sample position display area 111 and the multiplexed position display area 112 of the management interface 20. For example, Figure 3 In the coagulation analyzer, the first 12 sample loading positions from left to right are the sample position area, and the last 5 sample loading positions are the multiplexing position area. The sample loading positions in the sample position area and the multiplexing position area have different appearances, so that the user can intuitively understand whether the sample loading position is a sample position or a multiplexing position based on the appearance of the sample loading position, thereby improving the user's operation convenience and accelerating the user's information processing speed.

[0047] It should be noted that the sample analysis system may also include an analysis device and a control device, and the analysis device and the control device may be located inside the sample analysis system. Figure 3 Cannot be displayed directly.

[0048] It should be noted that the specific number of loading positions provided in this application is only for illustration purposes only and is not intended to be limiting.

[0049] It can be seen that the sample analysis system displays the coding information of the sample display position and the number of the sample position respectively, so that the user can intuitively understand the correspondence between the sample display position and the sample position, improves the visualization of the sample position, enhances the user's interface dependence, and speeds up the user's information processing speed.

[0050] In a possible embodiment, the control device displays an emergency sign on the sample display position in response to emergency operation information input by the user.

[0051] Among them, the emergency mark displayed on the loading display position indicates that the sample rack loaded on the loading position corresponding to the loading display position has an emergency sample, and the sample analysis system needs to give priority to the samples in the sample rack of the loading position. The emergency mark can be displayed in a variety of ways. For example, the emergency mark can be displayed in a red border of the loading display position to remind the user that the sample rack placed on the loading position has an emergency sample.

[0052] Among them, the emergency operation information can be that the user pre-designates a certain loading position as an emergency sample position, and the corresponding loading display position displays an emergency mark. For example, the user can set a certain loading position as an emergency sample position in advance, and display the emergency mark in the loading display position corresponding to the emergency sample position. When a sample rack is placed in the emergency sample position, the sample rack in the emergency sample position will be defaulted as an emergency sample rack. In this way, the user can place the sample rack that needs to be processed first in the pre-set emergency sample position, and the sample analysis system will give priority to the samples in the emergency sample position, which improves the convenience of user operation and speeds up the user information processing speed.

[0053] Among them, the emergency operation information can also be that the user selects a certain loading position as an emergency sample position according to his own needs after the sample rack is loaded, and the corresponding loading display position displays the emergency mark. For example, if it is temporarily necessary to give priority to the samples of the sample rack at a certain loading position, the user can switch the loading position to the emergency sample position (that is, switch the sample rack of the loading position to the emergency sample rack), so that the sample analysis system gives priority to the samples placed in the loading position. In this way, the user can change the emergency status of the sample rack according to actual needs after the sample rack is loaded, switch the non-emergency sample rack to the emergency sample rack, or switch the emergency sample rack to the non-emergency sample rack, which improves the flexibility of user operation and speeds up the user information processing speed.

[0054] It can be seen that in this example, the user can pre-set the sample loading position as the emergency sample position before the sample rack is loaded on the machine, or switch the sample loading position to the emergency sample position according to his or her own needs after the sample rack is loaded on the machine, so that the sample analysis system can give priority to processing the samples in the sample rack at this loading position, thereby improving the convenience of user operation and speeding up the user information processing speed.

[0055] In a possible embodiment, the sample rack status identifier includes multiple sample identifiers, and the sample identifier indicates sample information of the corresponding sample container on the sample rack; the control device switches the ordinary sample identifier to the emergency sample identifier or switches the emergency sample identifier to the ordinary sample identifier in response to the emergency switching information input by the user.

[0056] The sample identifiers include emergency sample identifiers and common sample identifiers. The user can switch the common sample to the emergency sample or the emergency sample to the common sample by quickly switching the sample identifiers in the first display area according to their needs.

[0057] For example, see Figure 4a - Figure 4c , Figure 4a - Figure 4c is a schematic diagram of an emergency sample setting provided in an embodiment of the present application. Specifically, Figure 4a As shown, when the screen of the display device is small, the user can click the sample rack status mark 121, such as Figure 4b As shown, the enlarged sample rack status mark 124 can be called out, and the user can directly double-click the common sample mark 131 in the enlarged sample rack status mark 124 to switch the sample corresponding to the common sample mark 131 to the emergency sample, such as Figure 4c As shown, the position of the common sample identifier 131 is displayed as the emergency sample identifier 132, indicating that the corresponding sample has been successfully switched to the emergency sample, and the display device can also display a message "has been set as an emergency sample" to inform the user that the setting is successful. Similarly, the user can directly double-click the emergency sample identifier in the enlarged sample rack status identifier to switch the sample corresponding to the emergency sample identifier to a common sample, and display its position as a common sample identifier, indicating that the corresponding sample has been successfully switched to a common sample, and the display device can also display a message "has been set as a common sample" to inform the user that the setting is successful.

[0058] Also, see Figure 4a , Figure 4b ,as well as Figure 4d , Figure 4a , Figure 4b ,as well as Figure 4d Schematic diagram of another emergency sample setting provided in the embodiment of the present application. Figure 4a As shown, the user can click on the sample rack status indicator 121, such as Figure 4b As shown, the enlarged sample rack status mark 124 can be called out, and after the user clicks the common sample mark 133 in the enlarged sample rack status mark 124, as shown in FIG. Figure 4d As shown, the management page will pop up an emergency secondary confirmation pop-up window 134, which can display "Are you sure to set it as emergency?" to the user to remind the user to make a secondary confirmation. If the user is sure to switch the ordinary sample to an emergency sample, the "Set as emergency" operation control in the emergency secondary confirmation pop-up window 134 can be clicked, and the ordinary sample identifier 133 will be switched to the emergency sample identifier. Similarly, the process of switching the emergency sample to the ordinary sample can be similar to the above process, which will not be repeated here.

[0059] It can be seen that the user can adjust the emergency status of the samples in each sample container on the sample rack through the display device, which improves the visualization of sample switching, improves the convenience of user operation, and speeds up user information processing.

[0060] In a possible embodiment, the control device switches the display mode of the sample rack status indicator of the sample loading display position based on the acquired sample rack status information.

[0061] The sample rack status information indicates that the sample rack is in an untested state, a testing state, a test completed state or a fault state. When the sample rack status information changes, the display mode of the corresponding sample rack status identifier is also adjusted accordingly.

[0062] See also Figure 5 , Figure 5 Schematic diagram of the display mode of each logo provided in the embodiment of the present application. Figure 5 As shown, when the user puts the sample rack in the sample loading position, the sample rack has been loaded but has not been transferred, that is, the sample rack is in an untested state. At this time, the display mode of the sample rack status mark can be a green stroke (such as Figure 5 501 in the figure) and green display (503 in the figure) to indicate that the sample loading position has been placed in the sample rack but is in an untested state. Specifically, it can be Figure 6 When the sample rack is transported and enters the test process (such as scanning, sampling or testing), the sample rack status indicator can be displayed in a green outline (such as Figure 5 501) and green flashing (such as Figure 5 504) to indicate that the sample rack is currently in the testing state, which may be Figure 6When the sample rack completes the test, it will be transferred to the sample loading position again, that is, the sample rack is in the test completed state, and the display mode of the sample rack status mark can be gray stroke (such as Figure 5 508) and gray (such as Figure 5 506) to indicate that the sample rack has completed the test, which can be Figure 6 When the sample rack fails in any process (e.g., code scanning failure, test failure, unloading failure, etc.), the sample rack is in a fault state, and the sample rack status indicator can be displayed in a yellow outline (e.g., Figure 5 502) and flashing yellow (such as Figure 5 505), or a yellow outline and yellow display may be displayed to indicate that the sample rack has a fault. Figure 6 The status identifier of the sample rack numbered 7.

[0063] It can be seen that in this example, different display modes of the sample rack status identification can be switched according to the status information of the sample rack, and the sample rack status identification graphic is vivid, which can efficiently convey important information to the user, so that the user can intuitively understand the specific status of the sample rack according to the sample rack status identification, thereby improving the visualization of the sample rack, improving the user's operation convenience, and accelerating the user's information processing speed.

[0064] In a possible embodiment, the sample loading display position displays an empty mark when there is no load at the sample loading position.

[0065] The loading position is displayed as an empty mark, indicating that the loading position has no load. The user can place a sample rack or a reagent kit in the loading position according to his own needs, or do not perform any processing on the loading position.

[0066] Among them, Figure 5 As shown, when there is no object loaded at the loading position, the loading display position may display an idle mark 510, indicating that there is no sample rack or reagent kit at the loading position. It can be seen that in this example, when there is no object loaded at the loading position, the loading display position may display an idle mark, and the user can know that there is no object loaded at the loading position through the idle mark.

[0067] In a possible embodiment, the sample loading display position displays an occupancy mark when the load corresponding to the sample loading position is in a testing or transporting state.

[0068] Among them, when the sample loading display position shows an occupied mark, it prompts that the load at the corresponding sample loading position is in the testing or transportation state. At this time, although there is no load at the sample loading position, another load cannot be placed at the sample loading position. After the test or transportation is completed, the load transferred from the sample loading position will be placed back at the sample loading position. Therefore, when the sample loading display position shows an occupied mark, if it is detected that there is another load at the corresponding sample loading position, that is, the user places another load in the sample loading position, the sample analysis system can issue an alarm prompt. For example, if Figure 6 As shown, the occupancy mark can be specifically the sample display area numbered 4, which is specifically green stroked and green flashing, which can indicate that the sample rack corresponding to the sample loading position is in a testing state, and the user cannot place another sample rack at the sample loading position. If the user places another sample rack at the sample loading position, the management interface can pop up a warning pop-up window, and the warning pop-up window displays "Sample loading error occurred at sample loading position No. 4!", or an alarm sounds to remind the user to remove another sample rack.

[0069] It can be seen that in this example, when the load in the sample loading position is in the testing or operating state, the sample loading display position displays an occupied mark to remind the user that another load cannot be placed in the sample loading position, avoiding confusion in the sample analysis system and speeding up the user's information processing speed.

[0070] In a possible embodiment, the sample rack status identifier includes a plurality of sample identifiers, and the sample identifiers indicate sample information of corresponding sample containers on the sample rack; and the control device switches the display mode of the sample identifiers based on the acquired sample information.

[0071] The sample information indicates that the sample is in a state of not applying for a test, applying for a test, being tested, completed, abnormal, failed, or waiting for retest. Different states of the sample can be represented by different display modes. When the sample information changes, the display mode of the corresponding sample identification is also adjusted accordingly.

[0072] For example, the display method of the sample identification corresponding to the sample container can be Figure 5 507, at this time, the sample in the sample container may be in the state of not applying for test, applying for test, testing or completed; when the sample in the sample container is detected to be abnormal, the display mode of the sample identification can be Figure 5 511 in the sample container indicates that the sample in the corresponding sample container is abnormal. Specifically, it can be Figure 6 The sample loading display position numbered 6 indicates that the sample in the sample container at position 6 of the sample rack corresponding to the sample loading display position is in an abnormal state. It should be noted that the display method of the sample identification in this application is only exemplary, and the specific display method is not limited in this application.

[0073] It can be seen that in this example, the control device can determine the sample information corresponding to the sample according to the test or transportation status of each sample, and switch the display mode of the sample identification according to the sample information, so that the user can intuitively understand the sample information according to different sample identifications in the management interface, which improves the visualization of the sample information, improves the convenience of user operation, and speeds up the user information processing speed.

[0074] In a possible embodiment, the control device switches the display mode of the reagent kit status indicator of the sample loading display position based on the acquired reagent kit status information.

[0075] The reagent kit status information indicates that the reagent kit is in a non-transported state, in a transported state, or in a faulty state. Different status information of the reagent kit can be represented by different display modes. When the status information of the reagent kit changes, the display mode of the corresponding reagent kit status indicator is also adjusted accordingly. For example, when the user puts the reagent kit in the loading position, the reagent kit has been loaded but has not been transported. At this time, the display mode of the reagent kit status indicator can be a green border and a green solid display to indicate that the reagent kit is in a non-transported state. Specifically, it can be Figure 6 When the reagent kit is transported (for example, transported to the code scanning area, etc.), the reagent kit status indicator may be displayed with a green border and a constant green color to indicate that the reagent kit is in the transport state. Specifically, Figure 6 The loading display position numbered D in the figure; when the reagent kit fails in any process (for example, code scanning fails, etc.), the display mode of the reagent kit status logo can be a yellow border and a constant yellow display, or a yellow border and a flashing yellow display, to indicate that the reagent kit transport fails. Specifically, it can be Figure 6 The sample loading position numbered B in the figure is shown.

[0076] It can be seen that in this example, the reagent kit status identification has multiple display modes, and the current status of the reagent kit can be displayed by switching the display mode of the reagent kit status identification, and the reagent kit status identification graphic is vivid, which can efficiently convey important information to the user, so that the user can intuitively understand the status of the reagent kit according to the reagent kit status identification, thereby improving the visualization of the reagent kit status information, improving the user's operation convenience, and accelerating the user's information processing speed.

[0077] In a possible embodiment, the sample analysis system further includes a plurality of indicator lights, and a display mode of the indicator lights matches a display mode of a corresponding sample loading display position.

[0078] Among them, Figure 3As shown, there is a corresponding indicator light under each loading position. There are a total of 17 loading positions, corresponding to which there are 17 indicator lights, and the display mode of the indicator lights is the same as that of the loading display position. For example, when the display mode of the loading display position is green, the corresponding indicator light is green; when the display mode of the loading display position is green flashing, the corresponding indicator light is green flashing; when the display mode of the loading display position is yellow, the corresponding indicator light is yellow; when the display mode of the loading display position is gray, the corresponding indicator light is off.

[0079] It can be seen that in this example, the display mode of the display indicator light can be matched with the display mode of the sample loading display position, so that the user can understand the status of the sample rack or reagent kit in the corresponding sample loading position through the indicator light, which improves the visualization of the sample loading position status, improves the user's operation convenience, and speeds up the user's information processing speed.

[0080] In a possible embodiment, the management interface includes a second display area, and the second display area includes a reagent project status identifier and / or a reagent container identifier.

[0081] The reagent item status identifier indicates reagent information of the corresponding reagent item, and the reagent container identifier indicates reagent information of the corresponding reagent container.

[0082] like Figure 2 As shown, the management interface 20 may include a second display area 210, the second display area is used to display the reagent information of each reagent item, the second display area 210 may include multiple reagent item status identifiers, each reagent item status identifier may represent the reagent information of the corresponding reagent item, and the reagent information may include the name, total amount or remaining amount of the reagent item. For example, Figure 2 The reagent item status indicator 221 includes reagent remaining quantity information presented in the form of a bar graph, and reagent name information "PT", reagent specification information "400T" and reagent available remaining quantity information "300T" presented in text form.

[0083] The second display area can also be used to display reagent information of the reagent containers in each reagent kit. Figure 7 , Figure 7 is a schematic diagram of a second display area provided in an embodiment of the present application. Figure 7 As shown, the second display area 210 includes multiple reagent container identifiers 241, each reagent container identifier 241 can represent the reagent information of the corresponding reagent container, and the reagent information of the reagent container is at least one of the remaining information, calibration information, number information and validity information of the reagent stored in the reagent container.

[0084] Among them, the remaining amount information can be the reagent remaining amount in the reagent container; the calibration information can indicate the calibration status of the reagent in the reagent container, which can be normal, uncalibrated, or calibration expired; the number of times information can indicate the number of times the reagent in the reagent container can be used, which can be the number of times it can be used and the number of times remaining; the validity period information can be the actual number of remaining valid days in the reagent container. Different colors, logos, or animations can be used as visual identifiers to indicate the reagent information of the reagent container, for example, Figure 7 In 242, "uncalibrated" is displayed in the reagent container label to indicate that the calibration information of the reagent is uncalibrated; Figure 7 243, displaying "expired" in the reagent container label can indicate that the calibration information of the reagent is out of calibration; Figure 7 In 244, a red line is displayed in the reagent container mark to indicate that the reagent remaining amount is small, that is, the reagent is about to run out. In this way, the user can intuitively understand the reagent information of the reagent container through the reagent container mark, which improves the visualization of the reagent container, improves the user's operation convenience, and speeds up the user's information processing speed.

[0085] The reagent container can also be used to place calibration products or quality control products. When the reagent container stores calibration products, the corresponding reagent container identifier 241 can be used to indicate the calibration product information of the reagent container, such as the calibration product name, the number of times it can be used, etc. When the reagent container stores quality control products, the corresponding reagent container identifier 241 can be used to indicate the quality control product information of the reagent container, such as the quality control product name, the number of times it can be used, etc.

[0086] In addition, if Figure 7 As shown, the drug information of each reagent container can be displayed in the second display area in the form of a card, that is, one card displays the drug information in one reagent container. It should be noted that the drug in the reagent container can be a reagent, a calibrator or a quality control product, and the drug information here can indicate the corresponding reagent information, calibrator information or quality control product information according to the actual loading situation of the reagent container. Figure 7 In the second display area shown, there are at least 24 display positions (or cards) of reagent containers. When the number of reagent containers on the machine exceeds 24, the user can display more display positions (or cards) by turning pages, sliding or enlarging the adaptive area of ​​the second display area. In particular, in the second display area, the order of the cards is consistent with the order in which the corresponding reagent containers are put on the machine, that is, the reagent container status identifiers are sorted from early to late according to the time of being put on the machine, so that the user can find and identify the reagent according to the time of being put on the machine.

[0087] It should be noted that when the second display area only contains the reagent item status indicator, it can be called the reagent item view (for example Figure 6 or Figure 2), the second display area may be referred to as a reagent container view when it only contains the reagent container identifier (e.g. Figure 7 ), the user can switch the second display area to the reagent item view or the reagent container view according to their own needs. For example, Figure 2 In the example, when the second display area is a reagent item view, the user can click the reagent container view mark 231 to enter the reagent item view. Figure 7 Reagent container view shown; Figure 7 In the example, when the second display area is a reagent container view, the user can click the reagent item view mark 232 to enter the reagent container view. Figure 2 In particular, when the sample analysis system undertakes a small number of projects, the reagent project status mark and the reagent container mark can be set to be displayed on the same page, that is, the second display area can contain both the reagent project status mark and the reagent container mark.

[0088] It can be seen that in this example, the second display area can display the reagent project view so that the user can timely understand the detailed information of the reagent project, and can also display the reagent container view so that the user can timely understand the detailed information of the reagent container, thereby improving the visualization of the reagent information, improving the user's operation convenience, and speeding up the user's information processing speed.

[0089] In a possible embodiment, the control device adjusts the display mode of the reagent project status identifier based on the acquired reagent information of the reagent project; or adjusts the display mode of the reagent container identifier based on the acquired reagent information of the reagent container.

[0090] Specifically, the reagent information of the reagent project includes remaining quantity information; the control device determines the project stage of the reagent project based on the remaining quantity information, and adjusts the display mode of the reagent project status indicator when the project stage changes.

[0091] The project stage indicates whether the reagent remaining amount of the reagent project is in a sufficient stage, a low stage, an exhausted stage or an unready stage, and each stage corresponds to a specific remaining amount range. The remaining amount information can be the reagent remaining amount of the reagent project, and the reagent remaining amount of each reagent project is obtained by adding the remaining amount of all reagent containers loaded with the reagent. The control device can determine the project stage of the reagent project according to the remaining amount range of the reagent remaining amount of the reagent project, thereby adjusting the display mode of the reagent project status mark. For example, Figure 6 As shown in the figure, when the balance of the reagent project is between 200T and 400T, the project stage of the reagent project is in the sufficient stage, and the display mode of the reagent project status indicator can be a purple data column, such as Figure 6223; When the reagent remaining amount of the reagent project is between 50 and 199T, the project stage of the reagent project is in the low quantity stage, and the display mode of the reagent project status identification can be a yellow data column with a height less than the height of the purple data column, such as Figure 6 225; when the reagent remaining amount of the reagent project is between 1 and 49T, the project stage of the reagent project is in the exhaustion stage, and the display mode of the reagent project status mark can be an orange data column with a height less than the height of the yellow data column; when the reagent remaining amount of the reagent project is 0T, the project stage of the reagent project is in the unready stage, and the display mode of the reagent project status mark can be a red data column with a height less than the height of the orange data column, such as Figure 6 224. The display mode of the reagent project status mark is adjusted through the reagent project remaining information, so that the user can intuitively understand the reagent remaining stage of the reagent project through the reagent project status mark, thereby improving the visualization of the reagent project, improving the user's operation convenience, and accelerating the user's information processing speed.

[0092] See also Figure 8 , Figure 8 Schematic diagram of viewing detailed information of a reagent provided in the embodiment of the present application. Figure 8 As shown, the user can click on the reagent container identification 241 to enter the reagent detailed information pop-up window 251, and the reagent detailed information pop-up window 251 displays the reagent detailed information corresponding to the selected reagent container identification 241, such as the reagent name, remaining amount, specification, batch number, location, status or effective days and other related data. The reagent detailed information pop-up window 251 can also display the function buttons of priority use, editing, and uninstallation. The user can click "priority use" so that when there are multiple reagent containers with the same reagent, the reagent in the reagent container is used first; the user can click "edit" to modify the content in the reagent detailed information pop-up window 251; the user can click "uninstall" to uninstall the reagent container.

[0093] Please note that the user can also unload all reagent containers. Fig. 9 , Fig. 9 Schematic diagram of a one-click uninstallation provided by an embodiment of the present application. Fig. 9 As shown, the user can click the more button 223 in the second display area, and the second display area displays a one-key uninstall function button. After the user clicks the function button, the control device can uninstall all reagent containers. In addition, if there are other uncommon function entrances, they can be included in the list of more buttons, leaving the important display area for the reagent container logo or the reagent project status logo, with visual emphasis and clear functions.

[0094] It can be seen that in this example, the control device can adjust the display mode of the reagent project status identification according to the reagent information of the reagent project, or adjust the display mode of the reagent container identification according to the reagent information of the reagent container, so that the control device can detect the change of the reagent information in time, and control the display device to display the reagent related information in time, so that the user can view the reagent information conveniently and intuitively in the second display area, the visualization of the reagent information is improved, and the user can perform related operations, which improves the user's operation convenience and speeds up the user information processing speed.

[0095] In a possible embodiment, the second display area includes at least two reagent container identifiers and an associated identifier.

[0096] The association identifier is used to associate the at least two reagent container identifiers to indicate that the reagent containers corresponding to the at least two reagent container identifiers are stored on the same reagent kit.

[0097] The association mark can be displayed in a variety of ways. The association mark can be presented in a graphic form. For example, when the reagent kit is loaded with reagent container A and reagent container B, the reagent container mark corresponding to reagent container A and the reagent container mark corresponding to reagent container B have the same icon (for example, a dot, a small box, a triangle, etc.), and the icon is the association mark to indicate that reagent container A and reagent container B are located in the same reagent kit. Fig. 9 As shown, both reagent container labels have a first association mark 261, which can indicate that the reagent container with the reagent name "PT" and the reagent container with the reagent name "yyy calibrator" are located in the same reagent kit. The association mark can also be presented in text. For example, when the reagent kit is loaded with reagent container C and reagent container D, the association mark can be the same text information (for example, the adapter number or the sample loading position number, etc.) on the reagent container label corresponding to reagent container C and the reagent container label corresponding to reagent container D, to indicate that reagent container C and reagent container D are located in the same reagent kit. Fig. 9 As shown, both reagent container identifiers have a second association identifier 262, which can indicate that the reagent container with the reagent name "reagent name" and the reagent container with the reagent name "PT" are located in "reagent kit 1". The association identifier can be presented in the form of graphics or text, enriching the display method of the association identifier, so that the user can intuitively view the relationship between the reagent containers.

[0098] In a possible embodiment, the association mark can connect the mutually related reagent container marks to form a combined reagent container mark, and each reagent container mark constituting the combined reagent container mark is displayed independently. The combined reagent container mark indicates that a plurality of different reagent containers are located in the same reagent kit. When the reagent container marks and the combined reagent container marks in the second display area are sorted, each reagent container mark in the combined reagent container mark moves synchronously, and the relative position relationship remains unchanged. In this way, even after sorting, the user can still intuitively understand the association relationship between the reagent containers through the combined reagent container mark, thereby improving the accuracy of user operation and the quality of user information processing.

[0099] In one possible embodiment, the reagent container identification can be presented in the form of a card, and the combined reagent container identification can be presented in the form of a combined card. Figure 7 The reagent container identification 241 is represented by a reagent card. When the reagent container E and the reagent container F are in the same reagent kit, the reagent card corresponding to the reagent container E and the reagent card corresponding to the reagent container F can be combined and connected. Specifically, the background color of the reagent card of the reagent container F and the background color of the reagent card of the reagent container E can be connected, and a dividing line is drawn in the middle to indicate that the same reagent kit is shared but the reagents are independent. Fig. 9 As shown, the combined reagent container identification 263 may indicate that the reagent container storing "xxx quality control product" and the reagent container storing "yyy quality control product" are located in the same reagent kit, but the reagents in the two reagent containers are independent.

[0100] like Fig.10 As shown, the combined reagent container identification 263 includes two reagent container identifications that are independently displayed. If the user wants to view the reagent detailed information of any reagent container identification in the combined reagent container identification 263, any reagent container identification (such as the target reagent container identification 245) in the combined reagent container identification 263 can be clicked to input the viewing operation instruction, and then the control device responds to the viewing operation instruction, and displays the target reagent information pop-up window 252 in the management interface, and the target reagent information pop-up window 252 displays the detailed information corresponding to the target reagent container identification 245, such as the reagent name, the available number of times, the reagent type or the reagent state. In addition, the target reagent information pop-up window 252 also includes an operation control, and the operation control includes a priority use control, an edit control and an uninstall control. Specifically, the user can click the priority use control to set the target reagent to use first, the user can edit the information in the target pop-up window by editing the control, and the user can uninstall the target reagent by uninstalling the control. In this way, the user can view or operate the reagent in the single bottle reagent container in the test kit through the sample analysis system, improve the visualization of the reagent container, improve the user's convenience of operation, and speed up the user's information processing speed.

[0101] It should be noted that, since the reagent containers in the same reagent kit are loaded and unloaded synchronously, when the user performs an unloading operation on the reagent container, the management interface displays a prompt message when it is determined that the reagent container corresponding to the target reagent container identifier selected by the user has an associated container. The associated container refers to a reagent container on the same reagent kit as the reagent container corresponding to the target reagent container identifier selected by the user. Specifically, when the user performs an unloading operation on a single reagent container, the user needs to be reminded. For example, Fig.10 As shown, the user can click the uninstall control in the reagent information pop-up window 252 to input the uninstall operation instruction, and then the control device responds to the uninstall operation instruction, such as Fig.11 As shown, Fig.11 It is a schematic diagram of an uninstallation reminder provided in an embodiment of the present application. The control display device displays a prompt message 253 in the management interface. The prompt message 253 displays the content "If the yyy quality control product is uninstalled, the xxx quality control product will also be uninstalled. Are you sure to uninstall the quality control product?" to remind the user that if the yyy quality control product is uninstalled, the xxx quality control product will be uninstalled at the same time. The user can make a second confirmation, that is, the user can click "Confirm" to execute the uninstallation of the target reagent or "Cancel" to cancel the uninstallation of the target reagent.

[0102] Furthermore, when the second display area displays multiple reagent container identifiers, the control device can switch the arrangement of the multiple reagent container identifiers based on the arrangement operation instruction input by the user. Specifically, the user can click Fig. 9 The management interface displays a function button for classification sorting, and when the user clicks the function button to start classification sorting, the display device can arrange the reagent container identifiers in the second display area in a specific order (for example, based on associated identifiers); when the user clicks the function button again to cancel the classification sorting, the display device can arrange them in a default order (for example, the position of the sample loading station or the time of loading).

[0103] Among them, the arrangement mode includes a classified sorting mode and an unclassified sorting mode. In the classified sorting mode, the second display area includes a single reagent display area and a combination reagent display area. The reagent container corresponding to the reagent container identifier in the combination reagent display area has an associated container. In the unclassified sorting mode, multiple reagent container identifiers are arranged in the order of the machine-on time on the corresponding reagent container. For example, in the classified sorting mode, please refer to Fig.12 , Fig.12 Schematic diagram of a reagent container provided in an embodiment of the present application. Fig.12As shown, the second display area 210 can be divided into a single reagent display area 211 and a combination reagent display area 212. The single reagent display area 211 includes a plurality of reagent container identifiers 241, and these reagent container identifiers can be arranged in the order of the corresponding reagent containers being put on the machine; the combination reagent display area 212 includes a plurality of combination reagent container identifiers 263, and these combination reagent container identifiers can be arranged in the order of the time when the corresponding reagent containers (or reagent kits) are put on the machine; the reagent container identifiers in the single reagent display area 211 can be arranged in front of the combination reagent container identifiers in the combination reagent display area 212, that is, the single reagent display area 211 can be located above the combination reagent display area 212. In addition, no additional partition can be added between the single reagent display area 211 and the combination reagent display area 212. In the non-classified sorting mode, please refer to Fig.13 , Fig.13 Schematic diagram of another reagent container view provided in the embodiment of the present application. Fig.13 As shown, the reagent container identification 241 and the combined reagent container identification 263 in the second display area 210 are mixed together and displayed in the order of the reagent container loading time. It should be noted that the number of reagent container identifications in the second display area is subject to requirements, and the horizontal position can be an even number, such as Fig.13 As shown, each row can have up to 8 reagent container identifiers. If a row contains both reagent container identifiers and combined reagent container identifiers, such as Fig.13 In the second row of the second display area shown, after the arrangement of 5 reagent container identifiers and 1 combined reagent container identifier, there is only a position that can display one reagent container identifier. If the second combined reagent container identifier cannot be fully displayed in the second row, the position can be left vacant without any filling, and the second combined reagent container identifier can be fully displayed in the third row to prevent misunderstanding or confusion. It should be noted that if the second display area cannot completely contain all reagent container identifiers and combined reagent container identifiers, the user can scroll the second display area up and down to view all reagent container identifiers and combined container reagent identifiers.

[0104] It can be seen that in this example, the situation in which a single reagent kit carries multiple reagent containers can be represented by an associated logo and displayed in the second display area, so that the user can intuitively view this relationship, the visualization of the reagent kit is improved, the user's dependence on the interface is enhanced, and the user can perform related operations, which improves the convenience of user operation and speeds up user information processing.

[0105] In a possible embodiment, the management interface includes a third display area, and the third display area includes a consumables status indicator; the control device adjusts the display mode of the consumables status indicator based on the acquired consumables status information.

[0106] Among them, the consumables-related materials include reaction cups, enhanced cleaning fluid, and ordinary cleaning fluid. Different consumables have different corresponding consumable status identifiers. The consumable status information can indicate the remaining information of the corresponding consumables. For example, the reaction cup status information can indicate the quantity stage of the reaction cup, including sufficient, insufficient, and exhausted states; the enhanced cleaning fluid status information can indicate the available quantity stage of the enhanced cleaning fluid, including sufficient, insufficient, and exhausted states; the ordinary cleaning fluid status information can indicate the available quantity stage of the ordinary cleaning fluid, including sufficient, insufficient, and exhausted states. Fig. 9 As shown, in the third display area 310, when the reaction cup status information indicates that the number of reaction cups is in an insufficient state, the display mode of the reaction cup status mark may be 321, indicating that the number of reaction cups is small, and "small amount" is highlighted in yellow to remind the user to replenish the reaction cups as soon as possible; when the enhanced cleaning liquid status information indicates that the available amount of the enhanced cleaning liquid is in a sufficient state, the display mode of the enhanced cleaning liquid status mark may be 322, indicating that the remaining amount of the enhanced cleaning liquid is sufficient; when the ordinary cleaning liquid status information indicates that the available amount of the ordinary cleaning liquid is in a sufficient state, the ordinary cleaning liquid status mark may be 323, indicating that the remaining amount of the ordinary cleaning liquid is sufficient.

[0107] In addition, since the sample analysis system needs to detect the sample to be tested in the analysis device, waste and waste liquid will be generated. The waste and waste liquid will be collected by the waste bin and the waste liquid barrel, respectively, and then transferred by the user. The third display area may also include a waste container status indicator. The control device adjusts the display mode of the waste container status indicator based on the acquired waste container status information. Different waste containers correspond to different waste container status indicators. The waste container status information can indicate the loading information of the corresponding waste container. For example, the waste bin status information can be the content stage of the waste in the waste bin, specifically including empty, almost full, and overflowing states; the waste liquid barrel status information can be the content stage of the waste liquid in the waste liquid barrel, specifically including empty, almost full, and overflowing states. Fig. 9 As shown, in the third display area 310, when the waste bin status information indicates that the waste content stage is about to be full, the waste bin status mark can be displayed in 324, indicating that the waste bin is about to be filled with waste, and "almost full" is highlighted in yellow to remind the user to transfer the waste in the waste bin as soon as possible; when the waste liquid barrel status information indicates that the waste liquid content stage is about to be full, the waste liquid barrel status mark can be displayed in 325, indicating that the waste liquid barrel is about to be filled with waste liquid, and "almost full" is highlighted in yellow to remind the user to transfer the waste liquid in the waste liquid barrel as soon as possible. In this way, the user can intuitively and timely understand the status of the waste container through the waste container status mark, which improves the visualization of the waste container and speeds up the user's information processing speed.

[0108] It can be seen that in this example, the control device can monitor the status information related to consumables and waste containers, and control the display device to display the third display area in the management interface, so that the user can understand the status of each consumable and the status of each waste container through the consumable status mark and the waste container mark, so that the consumable can be added or the waste container can be processed in time according to the status of the consumable and the status of the waste container. The visualization of consumables and waste containers is improved, the user's interface dependence is enhanced, and the user can perform related operations, which speeds up the user information processing speed.

[0109] In a possible embodiment, the control device displays a sample rack information pop-up window on the management interface in response to a sample rack viewing operation instruction input by the user for a target sample rack identifier, wherein the sample rack information pop-up window displays sample detailed information or operation controls corresponding to each sample identifier in the target sample rack identifier, and the operation controls include additional items or emergency settings.

[0110] The target sample rack identifier can be any sample rack identifier in the first display area. The sample detailed information can include the reagent items that the sample needs to participate in the test, the sample number in the sample analysis system, and the sample test status. The number can be used as the identity information of the sample. The sample test status can indicate that the sample is in the unapplied test state, the applied test state, the testing state, the completed test state, the abnormal state, or the failed state. The operation controls can include an emergency setting control and an additional item control. The emergency setting control is used to switch the state of the sample corresponding to the sample identifier to an emergency sample or a normal sample. The additional item control is used to add the reagent items that the sample needs to participate in the test. Please refer to Fig.14 , Fig.14 Schematic diagram of viewing sample information provided by an embodiment of the present application. Fig.14As shown, the user can click on the sample rack status mark 123 to input the sample rack viewing operation instruction. In response to the viewing operation instruction, the control device displays a sample rack information pop-up window 135 on the management interface. The sample rack information pop-up window 135 contains sample detailed information and operation controls corresponding to the six sample identifiers in the sample rack status mark. Specifically, for position 1, there is no sample, so there is no sample detailed information and operation control; for position 2, there is a sample, PT, APTT, and DD are the reagent items that the sample needs to participate in the test, and the number 407 is the identity information of the sample in the sample analysis system. The abnormal status is used to indicate that the sample is in an abnormal state, and the emergency The diagnosis setting button is in the selected state, as shown in 1351 in the figure, indicating that the sample is an emergency sample. The user can click the emergency cancel control 1351 to switch the sample to a normal sample, and can also click the add item button 1352 to add reagent items that need to participate in the sample test; for the sample at position 4, the four coagulation items are the reagent items that need to participate in the test of the sample, and the status of not applied is used to indicate that the sample is in an unapplied test state. The user can click the emergency setting control 1353 to switch the sample to an emergency sample; the sample detailed information and operation controls of the sample information of positions 3, 5, and 6 can be seen intuitively in the figure and will not be repeated here.

[0111] It can be seen that in this example, the control device can display the sample rack information pop-up window on the management interface based on the sample rack viewing operation instructions, which can efficiently convey important information to the user, so that the user can timely understand the detailed information of each sample in the sample rack through the sample rack information pop-up window, and can also set separate emergencies and set additional items through the sample rack information pop-up window, thereby improving the visualization of the sample rack, improving the convenience of user operation, and accelerating the speed of user information processing.

[0112] See also Fig.15 , Fig.15 is a flow chart of a method for displaying sample loading information provided in an embodiment of the present application. The method for displaying sample loading information can be applied to the control device of the sample analysis system described in the present application, such as Fig.15 As shown, the method for displaying loading information may include the following steps.

[0113] S1501, displaying a management interface, wherein the management interface includes a sample display position.

[0114] S1502, displaying a sample rack status mark or a reagent kit status mark at the sample loading display position according to the acquired loading information of the sample loading position.

[0115] The loading information may indicate that the loading object of the loading position is a sample rack or a reagent kit. When the loading information indicates that the loading object of the loading position is a sample rack, the corresponding loading display position is a sample rack status mark (such as Figure 5 508 in the example), when the loading information indicates that the loading object at the loading position is a reagent kit, the corresponding loading display position is a reagent kit status indicator (such as Figure 5 509 in the figure). The user can determine that the object loaded at the corresponding loading position is a sample rack according to the sample rack status mark, or determine that the object loaded at the corresponding loading position is a reagent kit according to the reagent kit status mark.

[0116] It can be seen that in this example, the sample loading position is a multiplexed sample loading position, which can be loaded with both sample racks and reagent kits. The display device intuitively displays the actual load of each sample loading position through different visual labels, which not only improves the visualization effect, but also makes it convenient for users to intuitively understand the load information of the sample loading position, and displays the sample rack status information and the reagent kit status information in the same area, which improves the convenience of user operation and speeds up the user information processing speed.

[0117] It should be noted that if Fig. 9 As shown, the management interface may also include a fourth display area 410, which may be used to record the test data of the day, so that the user can quickly obtain the process and revenue concept. For example, the fourth display area 410 may specifically include the number of all samples, the number of emergency samples, the number of applied samples, the number of samples being tested, the number of completed samples, and the number of abnormal samples, such as Fig. 9 As shown, the number of all samples is 22 to indicate that there are 22 samples in the applied test state, the number of emergency samples is 10 to indicate that there are 10 emergency samples, the number of samples being tested is 12 to indicate that there are 12 samples in the testing state, and the number of abnormal samples is 4 to indicate that there are 4 samples in the abnormal state. In addition, the fourth display area 410 may also include the number of completed samples, such as Figure 5 As shown in 410, the number of completed samples is 4, indicating that there are 4 samples in the completed test state, and the number can be displayed in green to increase the user's attention to the number of completed samples. It can also be known that the number of abnormal samples is 4, and the number can be displayed in red to increase the user's attention to the number of abnormal samples. In addition, the statistics area can also be configured with the remaining completion time to help the user grasp the test progress.

[0118] It should be noted that the management interface can be divided into the whole machine status area at the top, the status display area in the middle, and the function module switching operation area at the bottom. The top and bottom areas are shared with other pages, making the management interface highly unified and concise, with a single function and no redundant content that affects user observation. The status display area in the middle is divided into the consumables display area (i.e. the third display area), the reagent remaining / reagent container status display area (i.e. the second display area), the machine status display area (i.e. the first display area), and the data statistics area (i.e. the fourth display area) according to the functional focus. It has obvious boundaries, clear fonts, vivid graphics, and effectively concentrates on visual functions, which can efficiently convey key information to users.

[0119] It should be noted that the management interface can not only display the first display area, the second display area, the third display area, and the fourth display area, but the management interface can also be expanded or customized to display different content modules according to the user's own needs. For example, the management interface can add the display of the calibration curve, display only the reagent remaining amount or only the reagent container status, hide the consumables area, or add the display of a brief result list, etc.

[0120] The above embodiments can be implemented in whole or in part by software, hardware, firmware or any other combination. When implemented using software, the above embodiments can be implemented in whole or in part in the form of a computer program product. The computer program product includes one or more computer instructions or computer programs. When the computer instructions or computer programs are loaded or executed on a computer, the process or function described in the embodiment of the present application is generated in whole or in part. The computer can be a general-purpose computer, a special-purpose computer, a computer network, or other programmable device. The computer instructions can be stored in a computer-readable storage medium, or transmitted from one computer-readable storage medium to another computer-readable storage medium. For example, the computer instructions can be transmitted from one website site, computer, server or data center to another website site, computer, server or data center by wired or wireless means. The computer-readable storage medium can be any available medium that a computer can access or a data storage device such as a server or data center that contains one or more available media sets. The available medium can be a magnetic medium (e.g., a floppy disk, a hard disk, a tape), an optical medium (e.g., a DVD), or a semiconductor medium. The semiconductor medium can be a solid-state hard disk.

[0121] An embodiment of the present application also provides a computer storage medium, wherein the computer storage medium stores a computer program for electronic data exchange, wherein the computer program enables a computer to execute part or all of the steps of any method recorded in the above method embodiments, and the above computer includes an electronic device.

[0122] It should be noted that, for the aforementioned method embodiments, for the sake of simplicity, they are all expressed as a series of action combinations, but those skilled in the art should be aware that the present application is not limited by the described order of actions, because according to the present application, certain steps can be performed in other orders or simultaneously. Secondly, those skilled in the art should also be aware that the embodiments described in the specification are all preferred embodiments, and the actions and modules involved are not necessarily required by the present application.

[0123] In the above embodiments, the description of each embodiment has its own emphasis. For parts that are not described in detail in a certain embodiment, reference can be made to the relevant descriptions of other embodiments.

[0124] In addition, the light theme colors and dark theme colors provided in this application are only for example, and the specific images in the display interface provided in this application are only for example to facilitate the explanation of this application. Therefore, this application does not impose any restrictions on the color and / or theme color of the display interface and the specific graphics of the display interface.

[0125] In the several embodiments provided in the present application, it should be understood that the disclosed device can be implemented in other ways. For example, the device embodiments described above are only schematic, such as the division of the above-mentioned units, which is only a logical function division. There may be other division methods in actual implementation, such as multiple units or components can be combined or integrated into another system, or some features can be ignored or not executed. Another point is that the mutual coupling or direct coupling or communication connection shown or discussed can be through some interfaces, and the indirect coupling or communication connection of devices or units can be electrical or other forms.

[0126] The units described above as separate components may or may not be physically separated, and the components shown as units may or may not be physical units, that is, they may be located in one place or distributed on multiple network units. Some or all of the units may be selected according to actual needs to achieve the purpose of the solution of this embodiment.

[0127] In addition, each functional unit in each embodiment of the present application may be integrated into one processing unit, or each unit may exist physically separately, or two or more units may be integrated into one unit. The above-mentioned integrated unit may be implemented in the form of hardware or in the form of software functional units.

[0128] If the above-mentioned integrated unit is implemented in the form of a software functional unit and sold or used as an independent product, it can be stored in a computer-readable memory. Based on this understanding, the technical solution of the present application, or the part that contributes to the prior art, or all or part of the technical solution can be embodied in the form of a software product, which is stored in a memory and includes several instructions for a computer device (which can be a personal computer, a server or a network device, etc.) to perform all or part of the steps of the above-mentioned methods of each embodiment of the present application. The aforementioned memory includes: U disk, read-only memory (ROM), random access memory (RAM), mobile hard disk, disk or optical disk, etc., and other media that can store program codes.

[0129] A person skilled in the art can understand that all or part of the steps in the various methods of the above embodiments can be completed by instructing related hardware through a program, and the program can be stored in a computer-readable memory, and the memory can include: a flash drive, a read-only memory (English: Read-Only Memory, abbreviated as: ROM), a random access memory (English: Random Access Memory, abbreviated as: RAM), a magnetic disk or an optical disk, etc.

[0130] The embodiments of the present application are introduced in detail above. Specific examples are used in this article to illustrate the principles and implementation methods of the present application. The description of the above embodiments is only used to help understand the method and core idea of ​​the present application. At the same time, for general technical personnel in this field, according to the idea of ​​the present application, there will be changes in the specific implementation method and application scope. In summary, the content of this specification should not be understood as a limitation on the present application.

Claims

1. A sample analysis system, characterized in that: include: A sample loading device, comprising a sample loading platform and a dispatching mechanism, wherein the sample loading platform comprises a sample loading position, and the dispatching mechanism is used to transport the load at the sample loading position; Display device; A control device is used to control the display device to display a management interface, wherein the management interface includes a first display area, the first display area includes a sample loading display position, and the sample loading display position displays a reagent kit status mark when the load at the sample loading position is a reagent kit, and displays a sample rack status mark when the load at the sample loading position is a sample rack.

2. The sample analysis system according to claim 1, characterized in that: The loading display position displays an idle mark when there is no object loaded in the loading position; Alternatively, the sample loading display position displays an occupancy mark when the load at the sample loading position is in a testing or transporting state.

3. The sample analysis system according to claim 1, characterized in that: The first display area includes a sample bit display area and a multiplexed bit display area; The loading display position of the sample position display area is only used to display the sample rack status mark; the loading display position of the multiplex position display area is used to display the sample rack status mark or the reagent kit status mark.

4. The sample analysis system according to claim 1, characterized in that: The control device displays an emergency mark on the sample display position in response to the emergency operation information input by the user.

5. The sample analysis system according to claim 1, characterized in that: The sample rack status identifier includes a plurality of sample identifiers, and the sample identifiers indicate sample information of corresponding sample containers on the sample rack; wherein the sample identifiers include emergency sample identifiers and common sample identifiers; The control device switches the common sample identifier to the emergency sample identifier or switches the emergency sample identifier to the common sample identifier in response to the emergency switching information input by the user.

6. The sample analysis system according to claim 1, characterized in that: The control device switches the display mode of the sample rack status indicator of the sample loading display position based on the acquired sample rack status information; The sample rack status information indicates that the sample rack is in an untested state, a testing state, a test completed state or a fault state.

7. The sample analysis system according to claim 1, characterized in that: The sample rack status identifier includes a plurality of sample identifiers, and the sample identifiers indicate sample information of corresponding sample containers on the sample rack; The control device switches the display mode of the sample identification based on the acquired sample information; wherein the sample information indicates that the sample is in a state of not applying for test, a state of applying for test, a state of being tested, a state of completed test, an abnormal state, a failed state, or a state of waiting for retest.

8. The sample analysis system according to claim 1, characterized in that: The control device switches the display mode of the reagent kit status indicator of the sample loading display position based on the acquired reagent kit status information; The reagent kit status information indicates that the reagent kit is in a non-transportation state, a transporting state, or a fault state.

9. The sample analysis system according to claim 1, characterized in that: The first display area includes a plurality of sample loading display positions, and the sample loading display positions display number information, and the number information matches the number of the corresponding sample loading position.

10. The sample analysis system according to claim 1, characterized in that: The sample analysis system further includes a plurality of indicator lights, and the display mode of the indicator lights matches the display mode of the corresponding sample loading display positions.

11. The sample analysis system according to claim 1, characterized in that: The management interface includes a second display area or a third display area; The second display area includes a reagent item status mark or a reagent container mark; The third display area includes a consumables status indicator.

12. A method for displaying loading information, characterized in that: A control device for a sample analysis system according to any one of claims 1 to 11, wherein the method comprises: Display management interface, the management interface includes a sample display position; According to the acquired loading information of the sample loading position, a sample rack status mark or a reagent kit status mark is displayed at the sample loading display position.