Sample analysis system and reagent state information display method

Abstract

The invention provides a sample analysis system and a reagent state information display method. The system includes a reagent storage device, a display device, and a control device. The sample analysis system firstly displays a management interface which comprises a reagent state display area, and then displays at least two reagent container identifiers and associated identifiers in the reagent state display area according to the obtained reagent information of the reagent containers. The management interface can display the physical relationship that the same kit is loaded with a plurality of reagent containers so as to represent the association relationship that the reagent containers share the same kit but the reagents are mutually independent, so that the reagent containers are prevented from being unloaded by mistake, the accuracy of user operation is improved, and the user information processing quality is improved.

Description

Technical Field

[0001] The present application relates to the field of medical applications, and in particular to a sample analysis system and a reagent status information display method. Background Art

[0002] At present, in the use of coagulation analyzers, the display page of the display can only display the status information of each reagent container, and the physical relationship of each reagent container cannot be displayed through the display page. Since multiple reagent containers may be loaded in the same reagent kit, when the reagent in a reagent container is used up, the reagent container is directly unloaded, and other reagent containers on the reagent kit will also be unloaded together. If the reagents in other reagent containers have not been used up, this unloading method will cause other reagent containers to be unloaded by mistake, resulting in reagent waste. Summary of the invention

[0003] The present application proposes a sample analysis system and a reagent status information display method. The display interface of the display device can display the physical relationship between multiple reagent containers loaded in the same reagent kit to prompt that multiple reagent containers share the same reagent kit but are independent of each other, thereby avoiding reagent containers from being accidentally unloaded, improving the accuracy of user operations, and improving the quality of user information processing.

[0004] In a first aspect, an embodiment of the present application provides a sample analysis system, comprising:

[0005] A reagent storage device, used for storing a reagent kit, wherein the reagent kit is loaded with a reagent container;

[0006] Display device;

[0007] A control device is used to control the display device to display a management interface, wherein the management interface includes a reagent status display area, wherein the reagent status display area displays at least two reagent container identifiers and an associated identifier; wherein the reagent container identifier is used to indicate reagent information of the corresponding reagent container, and the associated 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 located on the same reagent kit.

[0008] In a second aspect, an embodiment of the present application proposes a method for displaying reagent status information, which is applied to a control device in the sample analysis system as described above, and the method includes:

[0009] Display a management interface, the management interface including a reagent status display area;

[0010] According to the reagent information of the reagent container obtained, at least two reagent container identifiers and an associated identifier are displayed in the reagent status display area; the reagent container identifier is used to indicate the reagent information of the corresponding reagent container, and the associated 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 located on the same reagent kit.

[0011] It can be seen that in the present application, the sample analysis system can first display the management interface, which includes a reagent status display area, and then display at least two reagent container identifiers and an associated identifier in the reagent status display area according to the reagent information of the reagent container obtained. In this way, the management interface can display the physical relationship of multiple reagent containers loaded in the same reagent kit through the associated identifier to indicate that these reagent containers share the same reagent kit, but the associated relationship between the reagent containers is independent of each other, thereby avoiding the reagent container from being unloaded by mistake, improving the accuracy of user operations, and improving the quality of user information processing. BRIEF DESCRIPTION OF THE DRAWINGS

[0012] 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.

[0013] Figure 1 It is a schematic diagram of the composition of a sample analysis system provided in an embodiment of the present application;

[0014] Figure 2 is a schematic diagram of a reagent status display area provided in an embodiment of the present application;

[0015] Figure 3 is a schematic diagram of another reagent status display area provided in an embodiment of the present application;

[0016] Figure 4 is a schematic diagram of viewing detailed information of a reagent provided in an embodiment of the present application;

[0017] Figure 5 is another schematic diagram for viewing detailed information of a reagent provided in an embodiment of the present application;

[0018] Figure 6 is a schematic diagram of an uninstallation reminder provided in an embodiment of the present application;

[0019] Figure 7 is a schematic diagram of a reagent container view provided in an embodiment of the present application;

[0020] Figure 8is a schematic diagram of another reagent container view provided in an embodiment of the present application;

[0021] Fig. 9 It is a schematic diagram of a reagent project view provided in an embodiment of the present application;

[0022] Fig.10 It is a schematic diagram of another reagent project view provided in an embodiment of the present application;

[0023] Fig.11 It is a schematic diagram of the composition of a coagulation analyzer provided in an embodiment of the present application;

[0024] Figure 12a-Figure 12c is a schematic diagram of an emergency sample setting provided in an embodiment of the present application;

[0025] Fig.12a , Figure 12b ,as well as Fig.12d is a schematic diagram of another emergency sample setting provided in an embodiment of the present application;

[0026] Fig.13 is a schematic diagram of the display method of each logo provided in the embodiment of the present application;

[0027] Fig.14 This is a schematic diagram of viewing sample information provided by an embodiment of the present application;

[0028] Fig.15 It is a flow chart of a reagent status information display method provided in an embodiment of the present application. DETAILED DESCRIPTION

[0029] 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.

[0030] 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.

[0031] 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.

[0032] 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.

[0033] 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.

[0034] 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.

[0035] 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 changes in the physical properties of the mixture, and then discharge the mixture.

[0036] Currently, in coagulation analyzers, the display page of the display can only display the status information of each reagent container, and the physical relationship between the reagent containers cannot be shown through the display page. Since multiple reagent containers may be loaded in the same reagent kit, when one reagent container is unloaded, the other reagent containers on the reagent kit will be unloaded together, causing other reagent containers to be accidentally unloaded.

[0037] In view of the above problems, an embodiment of the present application provides a sample analysis system and a reagent status information display method, which will be 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 1As shown, the sample analysis system 10 may include a reagent storage device 101, a display device 102, and a control device 103. The control device 103 may be connected to the reagent storage device 101 to automatically load the reagent kit into the reagent storage device; the control device 103 may be connected to the display device 102 to control the display device to display different contents according to the acquired information.

[0039] The reagent storage device 101 is used to store a reagent kit, and the reagent kit is loaded with a reagent container.

[0040] The control device 103 is used to control the display device 102 to display the management interface 20, see Figure 2 , Figure 2 Schematic diagram of a reagent status display area provided in an embodiment of the present application. Figure 2 As shown, the management interface 20 includes a reagent status display area 210, which is used to display the status information of each reagent container in the reagent storage device. The reagent status display area 210 includes at least two reagent container identifiers 241, each reagent container identifier is used to indicate the reagent information of the corresponding reagent container. The reagent status display area 210 also includes an association identifier, which is used to associate the at least two reagent container identifiers to indicate that the reagent containers corresponding to the two reagent container identifiers are located on the same reagent kit.

[0041] It can be seen that in this example, the sample analysis system can display the physical relationship between multiple reagent containers loaded in the same reagent kit through associated identification to prompt that these reagent containers share the same reagent kit, but each reagent container is independent of each other, thereby avoiding the reagent containers from being accidentally unloaded, improving the accuracy of user operations, and improving the quality of user information processing.

[0042] In a possible embodiment, the association identifier may be presented in the form of graphics or text.

[0043] The association mark can be presented in the form of a graphic. For example, when the reagent kit contains 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 (e.g., a dot, a small box, a triangle, etc.). This icon is the association mark, indicating that reagent container A and reagent container B are in the same reagent kit. Figure 3 , Figure 3 Schematic diagram of another reagent status display area provided in an embodiment of the present application. Figure 3 As shown, both reagent container identifiers have the first associated identifier 261, which may indicate that the reagent container corresponding to the reagent name "PT" and the reagent container corresponding to the reagent name "yyy calibrator" are located in the same reagent kit.

[0044] The associated identifier may also be presented in the form of text. For example, when the reagent kit is loaded with reagent container C and reagent container D, the associated identifier may be the same text information (e.g., the number of the adapter or the number of the loading position, etc.) on the reagent container identifier corresponding to reagent container C and the reagent container identifier corresponding to reagent container D, to indicate that reagent container C and reagent container D are located in the same reagent kit. Figure 3 As shown, both reagent container identifiers have the second association identifier 262, which may indicate that the reagent container corresponding to the reagent name "reagent name" and the reagent container corresponding to the reagent name "PT" are both located in the same "reagent kit 1".

[0045] Among them, each reagent container identification 241 in the reagent status display area 210 can also be arranged according to the physical position of each reagent container in the reagent storage device. For example, the reagent status display area 210 includes a plurality of reagent kit identifications, and the arrangement of the plurality of reagent kit identifications is the same as the arrangement of the plurality of reagent kits in the reagent storage device, and a reagent container identification is displayed on the reagent kit identification to indicate that the reagent container corresponding to the reagent container identification is loaded on the reagent kit corresponding to the reagent kit identification. If only one reagent container is loaded on the reagent kit, only one reagent container identification is displayed on the reagent kit identification corresponding to the reagent kit; if two or more reagent containers are loaded on the reagent kit, two or more reagent container identifications will be displayed on the reagent kit identification corresponding to the reagent kit to indicate that the two or more reagent containers are loaded in the same reagent kit. At this time, the reagent kit identification directly displays the physical relationship of the reagent containers corresponding to each reagent container identification through the reagent kit identification relative to the association identification of the present application.

[0046] It can be seen that in this example, the association mark can be presented in the form of graphics or text, which enriches the display method of the association mark, allowing the user to intuitively view the synchronous unloading relationship between reagent containers, thereby improving the accuracy of user operations and improving the quality of user information processing.

[0047] In a possible embodiment, the association mark connects mutually associated reagent container marks to form a combined reagent container mark, and each reagent container mark constituting the combined reagent container mark is displayed independently.

[0048] Among them, the combined reagent container identification indicates that multiple different reagent containers are located in the same reagent kit. When the reagent container identification and the combined reagent container identification in the reagent status display area are sorted, each reagent container identification in the combined reagent container identification 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 identification, which improves the accuracy of user operation and improves the quality of user information processing.

[0049] In a possible embodiment, the reagent container identification is presented in the form of a card, and the combined reagent container identification is presented in the form of a combined card.

[0050] The reagent container identifier 241 may be as follows: Figure 2 In the figure, the reagent card is used to indicate that 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 reagent container E and the reagent container F share the same reagent kit, but the reagent container E and the reagent container F are independent of each other. Figure 3 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.

[0051] In addition, if Figure 2 As shown, in the reagent status display area, the drug information of each reagent container can be displayed 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. 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 2 In the reagent status 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 reagent status display area. In particular, in the reagent status 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.

[0052] It can be seen that in this example, presenting reagent container identifiers in the form of cards and presenting combined reagent container identifiers in the form of combined cards allows users to intuitively understand the association between reagent containers, improves the accuracy of user operations, and improves the quality of user information processing.

[0053] In a possible embodiment, the control device causes the management interface to display a reagent information pop-up window in response to a viewing operation input by the user for the target reagent container identifier; the reagent information pop-up window displays reagent detail information or operation controls matching the target reagent container identifier, and the operation controls include at least one of a priority use control, an edit control, and an uninstall control.

[0054] The target reagent container identifier may be any reagent container identifier selected by the user in the reagent status display area 210. For example, see Figure 4 , Figure 4 Schematic diagram of viewing detailed information of a reagent provided in the embodiment of the present application. Figure 4 As shown, the user can enter the reagent detailed information pop-up window 251 by clicking on the reagent container identification 241. 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 function buttons such as priority use, edit, and uninstall. The user can click "priority use" so that when there are multiple reagent containers storing 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.

[0055] The target reagent container identifier may also be any reagent container identifier selected by the user in the combination of reagent container identifiers. Figure 5 , Figure 5 Schematic diagram of another method for viewing detailed information of a reagent provided in the embodiment of the present application. Figure 5 As shown, the combined reagent container identification 263 includes two independently displayed reagent container identifications. If the user wants to view the reagent detailed information of any reagent container identification in the combined reagent container identification 263, the user can click on any reagent container identification in the combined reagent container identification 263 (such as Figure 5 The target reagent container identification 245 is 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 detailed information corresponding to the target reagent container identification 245, such as the reagent name, the number of times available, the reagent type or the reagent status, etc. 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 set the priority use of the target reagent by clicking the priority use control, the user can edit the information in the target pop-up window by using the edit control, and the user can uninstall the target reagent by using the uninstall control.

[0056] It can be seen that in this example, the user can view the detailed reagent information of any reagent container and can also operate any reagent container, which not only improves the convenience of user operation, but also improves the accuracy of user operation and the quality of user information processing.

[0057] In a possible embodiment, in response to the unloading operation instruction input by the user, the control device causes the management interface to display 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.

[0058] Among them, 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. Since all reagent containers in the same reagent kit are loaded and unloaded synchronously with the reagent kit, when the user unloads the reagent container, when it is determined that the reagent container corresponding to the target reagent container identifier selected by the user has an associated container, the management interface will display a prompt message to avoid the associated container from being unloaded by mistake. Specifically, when the user unloads a single reagent container, the user needs to be reminded. For example, Figure 5 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 Figure 6 As shown, Figure 6 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.

[0059] It should be noted that the user can also unload all reagent containers. Figure 3 As shown, the user can click the more button 223 in the reagent status display area, and the reagent status 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 item status logo, with visual emphasis and clear functions.

[0060] It can be seen that in this example, when there is an associated container in the reagent container unloaded by the user, the control device can control the display device to display a prompt message on the management interface to remind the user, thereby avoiding the reagent container from being unloaded by mistake, improving the accuracy of user operations, and improving the quality of user information processing.

[0061] In a possible embodiment, the reagent status display area displays a plurality of reagent container identifiers; and the control device switches the arrangement of the plurality of reagent container identifiers based on an arrangement operation instruction input by a user.

[0062] Users can click Figure 3 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 reagent status 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).

[0063] Furthermore, the arrangement method includes a classified arrangement method and an unclassified arrangement method; in the classified arrangement method, the reagent status display area includes a single reagent display area and a combination reagent display area, and the reagent containers corresponding to the reagent container identifications in the combination reagent display area all have associated containers; in the unclassified arrangement method, the multiple reagent container identifications are arranged in order based on the time when the corresponding reagent containers were put on the machine.

[0064] Among them, in the classification sorting method, please refer to Figure 7 , Figure 7 Schematic diagram of a reagent container provided in an embodiment of the present application. Figure 7 As shown, the reagent status 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 a centralized manner according to the order in which the corresponding reagent containers are loaded onto 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 a centralized manner according to the order in which the corresponding reagent containers (or reagent kits) are loaded onto 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.

[0065] In the case of non-classified sorting, please refer to Figure 8 , Figure 8 Schematic diagram of another reagent container view provided in the embodiment of the present application. Figure 8 As shown, the reagent container identification 241 and the combined reagent container identification 263 in the reagent status 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 reagent status display area is subject to requirements, and the horizontal position can be an even number, such as Figure 8 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 Figure 8In the second row of the reagent status 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. In addition, if the reagent status display area cannot completely contain all reagent container identifiers and combined reagent container identifiers, the user can scroll the reagent status display area up and down to view all reagent container identifiers and combined container reagent identifiers.

[0066] It can be seen that in this example, the reagent container identifications can be sorted and displayed, so that the user can intuitively determine the reagent container according to the reagent container identification, which improves the visualization of the reagent container, and the classification and sorting can make the management interface more orderly. The user can intuitively distinguish between single reagent containers and combined reagent containers, which improves the accuracy of user operations and improves the quality of user information processing.

[0067] In a possible embodiment, the control device adjusts the display mode of the reagent container identification based on the acquired reagent information of the reagent container.

[0068] The reagent status display area can be used to display the reagent information of the reagent container in each reagent kit, such as Figure 2 As shown, the reagent status display area 210 includes a plurality of 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 includes at least one of remaining amount information, calibration information, number of times information and validity period information. The remaining amount information can be the reagent remaining amount in the reagent container; the calibration information can represent the calibration status of the reagent in the reagent container, specifically normal, uncalibrated, calibration expired; the number of times information can represent the number of times status of the reagent in the reagent container, specifically the number of times it can be used and the number of times remaining; the validity period information can be the actual remaining valid days in the reagent container. Different colors, identifiers, or animations can be used as visual identifiers to represent the reagent information of the reagent container, for example, Figure 2 In 242, "uncalibrated" is displayed in the reagent container label to indicate that the calibration information of the reagent is uncalibrated; Figure 2 243, displaying "expired" in the reagent container label can indicate that the calibration information of the reagent is out of calibration; Figure 2 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.

[0069] 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.

[0070] It can be seen that in this example, the control device can 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 conveniently and intuitively view the reagent information of the reagent container in the reagent status display area, which improves the visualization of the reagent information, and the user can perform related operations, which improves the user's operation convenience and speeds up the user information processing speed.

[0071] In a possible embodiment, the management interface includes a reagent item switching control; and the control device displays a reagent item status identifier in the reagent status display area based on a triggering operation of the reagent item switching control.

[0072] The reagent item status indicator indicates the reagent information of the corresponding reagent item. Fig. 9 , Fig. 9 Schematic diagram of a reagent project view provided in the embodiment of the present application. Fig. 9 As shown, the reagent status display area is used to display the reagent information of each reagent item. The reagent status display area 210 may include multiple reagent item status identifiers, each of which may indicate the reagent information of the corresponding reagent item. The reagent information may include the name, total amount or remaining amount of the reagent item. For example, Fig. 9 The reagent item status indicator 221 includes the reagent remaining information presented in the form of a bar graph, and the reagent name information "PT", the reagent specification information "400T" and the reagent available remaining information "300T" presented in text form. When the reagent status display area only includes the reagent item status indicator, it can be called a reagent item view (for example, Fig. 9 ), the reagent status display area only includes the reagent container identifier and can be called a reagent container view (e.g. Figure 2 ), the user can switch the reagent status display area to the reagent item view or reagent container view according to their needs. For example, Fig. 9 In the reagent status display area, when the reagent item view is displayed, the user can click the reagent container switching control 231 to enter the reagent item view. Figure 2 Reagent container view shown; Figure 2In the example, when the reagent status display area is a reagent container view, the user can click the reagent item switching control 232 to enter the following Fig. 9 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.

[0073] In this way, the reagent status 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.

[0074] In a possible embodiment, the control device adjusts the display mode of the reagent item status identifier based on the acquired reagent information of the reagent item.

[0075] 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.

[0076] The project stage indicates whether the reagent remaining amount of the reagent project is in the sufficient stage, the low stage, the exhausted stage or the 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, please refer to Fig.10 , Fig.10 Schematic diagram of another reagent project view provided in the embodiment of the present application. Fig.10 As shown, when the remaining amount 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 Fig.10 223; When the reagent remaining amount of the reagent project is between 50-199T, the project stage of the reagent project is in the low quantity stage, and the display mode of the reagent project status indicator can be a yellow data column with a height less than the height of the purple data column, such as Fig.10225; when the reagent remaining amount of the reagent project is between 1-49T, 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 Fig.10 224. 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.

[0077] In this way, the control device can adjust the display mode of the reagent container identification according to the reagent information of the reagent item, 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 conveniently and intuitively view the reagent information of the reagent item in the reagent status display area, thereby improving the visualization of the reagent information, and the user can perform related operations, thereby improving the user's operation convenience and accelerating the user information processing speed.

[0078] In a possible embodiment, the management interface further includes a loading position status display area.

[0079] Among them, the sample analysis system can also include a loading device and an analysis device. The control device can be connected to the analysis device to command the analysis device to perform various operations, such as adding samples, incubation, adding reagents, mixing and testing. The loading device includes a loading platform and a scheduling mechanism. The loading platform has a loading position for placing the load. The control device can be connected to the loading device to control the scheduling mechanism to transfer the load placed on the loading position to the target position of the analysis device. Specifically, the analysis device is used to detect the sample to be tested to obtain the test result. The analysis device can include components such as a loading unit, a reagent storage unit and a test unit. The reagent storage unit can be used to place a reagent kit. The loading unit can 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, and then the reaction liquid in the reaction cup is detected by the test unit, thereby achieving the purpose of detecting the sample to be tested to obtain the test result.

[0080] The sample analysis system can be a coagulation analyzer or a part of a coagulation analyzer. The reagent storage device can be the above-mentioned reagent storage unit; the loading device includes a loading platform and a scheduling mechanism, the loading platform includes a plurality of loading positions, such as loading position 1, loading position 2, loading position 3, etc., the scheduling mechanism is configured to transfer the load of the loading position to the analysis device, and the load of the loading position can be a sample rack or a reagent kit. For example, Fig.11 The coagulation analyzer shown has a total of 17 loading positions, each of which can be used to load a sample rack or a reagent kit. When the loading object of the loading position is 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 loading platform after the sample suction is completed, waiting for the user to collect and unload the machine; when the loading object of the loading position is 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 loading platform, waiting for the user to take it and unload it. Each loading position of the loading platform 1021 can load both sample racks and reagent kits, realizing the reuse of the loading positions. The reagent storage device can be the above-mentioned loading platform.

[0081] Correspondingly, the control device is used to control the display device to display the management interface 20, such as Fig. 9 As shown, the management interface 20 includes a sample loading position status display area 110, and the sample loading position status display area 110 is used to display the status information of each sample loading position of the sample loading platform 1021. The sample loading position status display area includes multiple sample loading display positions, and the multiple sample loading display positions correspond to the multiple sample loading positions of the sample loading platform 1021 one by one. Each sample loading display position displays a reagent kit status mark when the load at the corresponding sample loading position is a reagent kit, and displays a sample rack status mark when the load at the corresponding sample loading position is a sample rack. The sample rack status mark and the reagent kit status mark have different visual elements, which can help users intuitively understand the load information of the sample loading position. Please refer to the following figure. Fig. 9 As shown, the management interface 20 may include a sample loading position status display area 110, and the sample loading position status 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, and 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.

[0082] Furthermore, the sample loading position status 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.

[0083] Among them, see Fig.11 , Fig.11 Schematic diagram of the composition of a coagulation analyzer provided in an embodiment of the present application. Fig.11 As shown, the coagulation analyzer may include a loading platform 1021 and a display device 102. There are 17 loading positions on the loading platform 1021, and each loading position is numbered from 1 to 17 from left to right. This relationship can be displayed in the management interface 20 of the display device, such as Fig. 9 As shown, in the management interface 20, there is a number mark below each sample display position in the sample position status 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.

[0084] 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. Fig.11 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 placed in both sample racks and reagent kits. Fig. 9 The 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.

[0085] 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. Fig.10 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 2 As shown, in the sample loading position status 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 the other two adjacent sample loading display positions, such as the distance between the sample loading display position numbered 12 and the sample loading display position numbered 13 is greater than the distance between the other two adjacent sample loading display positions. In particular, it is also possible to distinguish between sample positions and multiplexed positions by designing specific number identifications, for example, the number identifications of the sample loading display positions in the sample position display area 111 can be displayed in numbers, and the number identifications of the sample loading 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, Fig.11 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.

[0086] 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. Fig.11 Cannot be displayed directly.

[0087] 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.

[0088] 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.

[0089] 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.

[0090] 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.

[0091] 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.

[0092] 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.

[0093] 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.

[0094] 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.

[0095] The sample identifiers include emergency sample identifiers and common sample identifiers. Users can switch common samples to emergency samples or emergency samples to common samples according to their needs by quickly switching the sample identifiers in the sample loading status display area.

[0096] For example, see Figure 12a-Figure 12c , Figure 12a-Figure 12c is a schematic diagram of an emergency sample setting provided in an embodiment of the present application. Specifically, Fig.12a As shown, when the screen of the display device is small, the user can click the sample rack status mark 121, such as Figure 12b 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 Fig.12c 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.

[0097] Also, see Fig.12a , Figure 12b ,as well as Fig.12d , Fig.12a , Figure 12b ,as well as Fig.12d FIG. 1 is a schematic diagram of another emergency sample setting provided in an embodiment of the present application. Fig.12a As shown, the user can click on the sample rack status indicator 121, such as Figure 12b 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. Fig.12d 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.

[0098] 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.

[0099] 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.

[0100] 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.

[0101] See also Fig.13 , Fig.13 Schematic diagram of the display mode of each logo provided in the embodiment of the present application. Fig.13 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 Fig.13 501) and green display (such as Fig.13 503) to indicate that the sample loading position has been placed in the sample rack but is in an untested state. Specifically, it can be Fig.10 When the sample rack is transported and enters the test process (such as scanning, sampling or testing), the sample rack status logo can be displayed in a green outline (such as Fig.13 501) and green flashing (such as Fig.13 504) to indicate that the sample rack is currently in the testing state, which may be Fig.10 When 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 Fig.13 508) and gray (such as Fig.13 506) to indicate that the sample rack has completed the test, which can be Fig.10 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., Fig.13 502) and flashing yellow (such as Fig.13 505), or a yellow outline and yellow display may be displayed to indicate that the sample rack has a fault. Fig.10 The status identifier of the sample rack numbered 7.

[0102] 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.

[0103] In a possible embodiment, the sample loading display position displays an empty mark when there is no load at the sample loading position.

[0104] 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.

[0105] Among them, Fig.13 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.

[0106] 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.

[0107] 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 Fig.10 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.

[0108] 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.

[0109] 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.

[0110] The sample information indicates that the sample is in a state of not applying for a test, applying for a test, being tested, having completed a test, abnormal, or failed. Different states of the sample can be indicated by different display modes. When the sample information changes, the display mode of the corresponding sample identification is also adjusted accordingly.

[0111] For example, the display method of the sample identification corresponding to the sample container can be Fig.13 507, 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 Fig.13 511 in the sample container indicates that the sample in the corresponding sample container is abnormal. Specifically, it can be Fig.10 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.

[0112] 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.

[0113] 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.

[0114] 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 Fig.10When the reagent kit is transported (for example, transported to the code scanning area, etc.), the reagent kit status indicator may be displayed in a green frame and green color to indicate that the reagent kit is in the transport state. Specifically, Fig.10 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 Fig.10 The sample loading position numbered B in the figure is shown.

[0115] 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.

[0116] 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.

[0117] Among them, Fig.11 As 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.

[0118] 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.

[0119] In a possible embodiment, the management interface includes a consumables status display area, and the consumables status display area includes a consumables status mark; the control device adjusts the display mode of the consumables status mark based on the acquired consumables status information.

[0120] 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. Figure 3 As shown, in the consumables status 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 can 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 can 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 can be 323, indicating that the remaining amount of the ordinary cleaning liquid is sufficient.

[0121] 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 consumable status 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. Figure 3 As shown, in the consumables status 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.

[0122] 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 consumable status 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.

[0123] 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.

[0124] The target sample rack identifier can be any sample rack identifier in the sample loading status 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 the emergency setting control and the 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.14 As 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 in the management interface. The sample rack information pop-up window 135 contains sample detailed information and operation controls corresponding to the 6 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 setting button is in a selected state, that is, Fig.14As shown in 1351, it means 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 unapplied 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.

[0125] 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.

[0126] See also Fig.15 , Fig.15 is a flow chart of a method for displaying reagent status information provided in an embodiment of the present application. The method for displaying reagent status information can be applied to a control device of a sample analysis system described in the present application, such as Fig.15 As shown, the reagent status information display method may include the following steps.

[0127] S1501, displaying a management interface, wherein the management interface includes a reagent status display area.

[0128] S1502: Display at least two reagent container identifiers and associated identifiers in the reagent status display area according to the acquired reagent information of the reagent container.

[0129] Among them, the reagent status display area can be used to display the reagent information of the reagent container in each reagent kit, and the reagent container identification is used to indicate the reagent information of the corresponding reagent container, and the reagent information of the reagent container may include at least one of the remaining amount information, calibration information, number of times information and validity period information. The remaining amount information may be the reagent remaining amount in the reagent container; the calibration information may indicate the calibration status of the reagent in the reagent container, which may be normal, uncalibrated, or calibration expired; the number of times information may indicate the number of times status of the reagent in the reagent container, which may be the number of times that can be used and the number of times remaining; the validity period information may be the actual remaining valid days in the reagent container. The user can understand the reagent information of the reagent container through the reagent container identification.

[0130] The association mark is used to associate the at least two reagent container marks to indicate that the reagent containers corresponding to the at least two reagent container marks are located on the same reagent kit. The association mark can be displayed in a variety of ways (e.g., graphics or text). The user can understand the association relationship between the reagent containers based on the association mark.

[0131] It can be seen that in this example, the management interface can display the physical relationship of multiple reagent containers loaded with the same reagent kit to indicate that the reagent containers share the same reagent kit but the reagents are independent of each other. Users can understand the relevant information of the reagent containers through the reagent container identifiers and understand the association relationship between the reagent containers through the association identifiers, thereby avoiding the reagent containers from being accidentally unloaded, reducing the error rate of user operations, and improving the quality of user information processing.

[0132] It should be noted that if Figure 3 As shown, the management interface may also include a sample statistics display area 410, which can be used to record the test data of the day, so that users can quickly obtain the process and revenue concept. For example, the sample statistics 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 Figure 3 As shown, the number of all samples is 22, indicating that there are 22 samples in the applied test state, the number of emergency samples is 10, indicating that there are 10 emergency samples, the number of samples being tested is 12, indicating that there are 12 samples in the testing state, and the number of abnormal samples is 4, indicating that there are 4 samples in the abnormal state. In addition, the sample statistics display area 410 can also include the number of completed samples, such as Fig.13 As shown in the sample statistics display area 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 sample statistics display area can also be configured with the remaining completion time to help the user grasp the test progress.

[0133] 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 consumables status display area), the reagent remaining / reagent container status display area (i.e., the reagent status display area), the machine status display area (i.e., the sample position status display area), and the data statistics area (i.e., the sample statistics 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.

[0134] It should be noted that the management interface can not only display the loading position status display area, reagent status display area, consumables status display area, and sample statistics 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 calibration curves, display only the reagent remaining amount or only the reagent container status, hide the consumables area, or add a brief result list.

[0135] 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.

[0136] 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 described in the above method embodiments, and the above computer includes an electronic device.

[0137] 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.

[0138] 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.

[0139] 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.

[0140] 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.

[0141] 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.

[0142] 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.

[0143] 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.

[0144] 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.

[0145] 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 reagent storage device, used for storing a reagent kit, wherein the reagent kit is loaded with a reagent container; Display device; A control device is used to control the display device to display a management interface, wherein the management interface includes a reagent status display area, wherein the reagent status display area displays at least two reagent container identifiers and an associated identifier; wherein the reagent container identifier is used to indicate reagent information of the corresponding reagent container, and the associated 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 located on the same reagent kit.

2. The sample analysis system according to claim 1, characterized in that: The association mark connects the mutually associated reagent container marks to form a combined reagent container mark, and each reagent container mark constituting the combined reagent container mark is displayed independently.

3. The sample analysis system according to claim 1, characterized in that: The control device responds to the unloading operation instruction input by the user, and when it is determined that the reagent container corresponding to the target reagent container identifier selected by the user has an associated container, causes the management interface to display a prompt message.

4. The sample analysis system according to claim 1, characterized in that: The control device causes the management interface to display a reagent information pop-up window in response to a viewing operation input by a user for a target reagent container identifier; The reagent information pop-up window displays reagent detail information or an operation control that matches the target reagent container identifier, and the operation control includes at least one of a priority use control, an edit control, and an uninstall control.

5. The sample analysis system according to claim 1, characterized in that: The reagent status display area displays multiple reagent container identifiers; The control device switches the arrangement of the plurality of reagent container identifiers based on an arrangement operation instruction input by a user.

6. The sample analysis system according to claim 5, characterized in that: The arrangement method includes a classified arrangement method and a non-classified arrangement method; In the classified arrangement mode, the reagent status display area includes a single reagent display area and a combination reagent display area, and the reagent container corresponding to the reagent container identifier in the combination reagent display area has an associated container; In the non-classified arrangement mode, the multiple reagent container identifiers are arranged in order based on the time when the corresponding reagent containers were loaded onto the machine.

7. The sample analysis system according to claim 1, characterized in that: The control device adjusts the display mode of the reagent container identification based on the acquired reagent information of the reagent container; The reagent information includes at least one of remaining quantity information, calibration information, number of times information and validity period information.

8. The sample analysis system according to claim 1, characterized in that: The management interface includes a reagent item switching control; The control device displays a reagent item status mark in the reagent status display area based on a triggering operation of the reagent item switching control, and adjusts a display mode of the reagent item status mark based on the acquired reagent information of the reagent item.

9. The sample analysis system according to claim 1, characterized in that: The management interface also includes a loading position status display area or a consumables status display area.

10. A method for displaying reagent status information, characterized in that: A control device applied to a sample analysis system according to any one of claims 1 to 9, wherein the method comprises: Display a management interface, the management interface including a reagent status display area; According to the reagent information of the reagent container obtained, at least two reagent container identifiers and an associated identifier are displayed in the reagent status display area; the reagent container identifier is used to indicate the reagent information of the corresponding reagent container, and the associated 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 located on the same reagent kit.

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