Configuration method of automatic auditing rule, automatic auditing method and sample analysis system

Abstract

The embodiment of the invention discloses a configuration method of an automatic auditing rule, an automatic auditing method and a sample analysis system, which are used for displaying an auditing rule configuration interface of the automatic auditing rule and comprise a biological sample detection item selection area and a rule configuration area. A user can visually view each biological sample detection item through the biological sample detection item selection area, and view rule configuration items corresponding to different biological sample detection items in the rule configuration area. A user can intuitively and conveniently configure or modify automatic auditing rules of different biological sample detection items, and can autonomously complete rule configuration. Besides, the user can independently set the auditing rules for different biological sample detection items, so that the corresponding auditing rules can be matched for different biological sample detection items in the auditing process, manual modification on site according to the change of the biological sample detection items is not needed, and the auditing efficiency is improved. And the auditing efficiency of the sample inspection result is improved.

Description

Technical Field

[0001] The present application relates to the technical field of medical equipment, and in particular to a configuration method of automatic review rules, an automatic review method, and a sample analysis system. Background Art

[0002] In vitro diagnostic tests are commonly used in the healthcare industry to help diagnose a patient's medical condition. In vitro diagnostic tests refer to testing procedures that analyze a sample / specimen. After analyzing the patient sample, the laboratory produces a test result. The doctor or other medical practitioner then uses the test result to help diagnose one or more medical conditions.

[0003] In vitro diagnostic tests are usually implemented by in vitro diagnostic analyzers, and the test results of the in vitro diagnostic tests are the sample test results of the samples obtained by the in vitro diagnostic analyzer. After obtaining the sample test results, the sample test results need to be reviewed to determine the validity of the sample test results, classify the sample test results, and confirm whether they need further testing. Suspicious or abnormal sample test results may have a significant impact on the workflow of technicians. Sample test results with questionable or abnormal results may need to be re-tested by technicians to confirm the validity of the sample test results or determine the properties of the sample test results. In addition, certain sample test results may cause subsequent tests to be indicated or cancelled. For example, abnormally low or high sample test results will require re-performing previously performed tests to confirm whether the previous sample test results are correct. This process of conducting tests, evaluating sample test results, re-testing, recalculating sample test results, and reporting sample test results to medical personnel makes the task of managing laboratories and their workflows a complex task.

[0004] The existing technology can automatically review the sample inspection results, but the review rules in the current automatic review method require the service engineer to confirm the requirements with the user during installation and then configure the review rules. If the review rules need to be modified later, the service engineer needs to be instructed to modify them. The current automatic review method is not convenient for users to set or modify the rules. Summary of the invention

[0005] The following is a summary of the subject matter described in detail in this application. This summary is not intended to limit the scope of the claims.

[0006] The embodiments of the present application provide a configuration method of automatic review rules, an automatic review method, and a sample analysis system, which can facilitate users to configure automatic review rules.

[0007] In a first aspect, an embodiment of the present application provides a method for configuring an automatic review rule, where the automatic review rule is used to automatically review the sample test results generated by an in vitro diagnostic analyzer, and the configuration method includes:

[0008] Displaying an audit rule configuration interface of the automatic audit rule, the audit rule configuration interface includes a biological sample detection item selection area and a rule configuration area, wherein the biological sample detection item selection area includes at least one biological sample detection item, and the rule configuration area includes at least one rule configuration item corresponding to the biological sample detection item, and the rule configuration item is used to configure the automatic audit rule, and the automatic audit rule is used to automatically compare each rule configuration item with the sample test result to determine whether the sample test result passes the audit;

[0009] A first instruction is received to select at least one biological sample detection item, and a review rule of a rule configuration item corresponding to the biological sample detection item is configured.

[0010] In a second aspect, an embodiment of the present application provides a method for automatically reviewing sample test results, which is used to automatically review sample test results generated by an in vitro diagnostic analyzer. The method for automatically reviewing sample test results includes the following steps:

[0011] The automatic review rules are configured by applying the method for configuring the automatic review rules of the first aspect of the embodiment of the present application;

[0012] Obtain sample test results;

[0013] The sample inspection results are audited according to the automatic audit rules to obtain the audit results.

[0014] In a third aspect, an embodiment of the present application provides a sample analysis system, including:

[0015] At least one in vitro diagnostic analyzer for testing the sample to obtain a sample test result;

[0016] a control device, communicatively connected to at least one in vitro diagnostic analyzer, for obtaining sample test results from the in vitro diagnostic analyzer, the control device comprising a processor and a display;

[0017] The processor is used to control the display to display an audit rule configuration interface of the automatic audit rule, the audit rule configuration interface includes a biological sample detection item selection area and a rule configuration area, wherein the biological sample detection item selection area includes at least one biochemical analysis detection item, the rule configuration area includes at least one rule configuration item corresponding to the biochemical analysis detection item, the rule configuration item is used to configure the automatic audit rule, and the automatic audit rule is used to automatically compare each rule configuration item with the sample test result to determine whether the sample test result passes the audit;

[0018] The processor is also used to receive a first instruction to select at least one biochemical analysis detection item, and configure the review rules of the rule configuration items corresponding to the biochemical analysis detection item.

[0019] In a fourth aspect, an embodiment of the present application provides an electronic device, comprising a memory and a processor, wherein the memory stores a computer program, and when the processor executes the computer program, it implements the method for configuring the automatic review rules of the first aspect of the embodiment of the present application, or implements the method for automatically reviewing the sample inspection results of the second aspect of the embodiment of the present application.

[0020] In a fifth aspect, an embodiment of the present application provides a computer-readable storage medium, which stores a computer program. When the computer program is executed by a processor, it implements the method for configuring the automatic review rules of the first aspect of the embodiment of the present application, or implements the method for automatically reviewing the sample inspection results of the second aspect of the embodiment of the present application.

[0021] In a sixth aspect, an embodiment of the present application provides a computer program product, including a computer program, which, when executed by a processor, implements the method for configuring the automatic review rules of the first aspect of the embodiment of the present application, or implements the method for automatically reviewing the sample inspection results of the second aspect of the embodiment of the present application.

[0022] The embodiments of the present application include at least the following beneficial effects:

[0023] The configuration method of automatic audit rules and the automatic audit method and sample analysis system provided in the embodiment of the present application display the audit rule configuration interface of the automatic audit rules, and the audit rule configuration interface includes a biological sample detection project selection area and a rule configuration area. Among them, the biological sample detection project selection area includes at least one biological sample detection project, and the rule configuration area includes at least one rule configuration item corresponding to the biological sample detection project, so that the user can intuitively view each biological sample detection project through the biological sample detection project selection area, and view the rule configuration items corresponding to different biological sample detection projects in the rule configuration area. By receiving the first instruction of the user to operate according to the content displayed on the audit rule configuration interface, at least one biological sample detection project is selected according to the first instruction, and the audit rules of the rule configuration items corresponding to the biological sample detection project are configured. In the embodiment of the present application, the user can configure or modify the automatic audit rules of different biological sample detection projects very intuitively and conveniently, and can complete the rule configuration independently without making an appointment or instructing the service engineer to set or modify. In addition, in the embodiment of the present application, the user can independently set the review rules for different biological sample detection items, so that the corresponding review rules can be matched for different biological sample detection items during the review process. There is no need to manually modify on-site according to changes in the biological sample detection items, which greatly improves the review efficiency of the sample test results. BRIEF DESCRIPTION OF THE DRAWINGS

[0024] The accompanying drawings are used to provide further understanding of the technical solution of the present application and constitute a part of the specification. Together with the embodiments of the present application, they are used to explain the technical solution of the present application and do not constitute a limitation on the technical solution of the present application.

[0025] Figure 1 A system principle block diagram of a sample analysis system provided by an embodiment of the present invention;

[0026] Figure 2 A block diagram of the structural principle of an electronic device provided by an embodiment of the present invention;

[0027] Figure 3 A method flow chart of a method for configuring automatic audit rules provided by an embodiment of the present invention;

[0028] Figure 4 A schematic diagram of an audit rule configuration interface provided by an embodiment of the present invention;

[0029] Figure 5 A schematic diagram of an interface of a configuration window for a rule configuration item provided by an embodiment of the present invention;

[0030] Figure 6 is a method flow chart of an embodiment of step 320;

[0031] Figure 7 is a method flow chart of another embodiment of step 320;

[0032] Figure 8 A method flow chart of a method for configuring automatic audit rules provided by an embodiment of the present invention;

[0033] Fig. 9 A method flow chart of a method for configuring automatic audit rules provided by an embodiment of the present invention;

[0034] Fig.10 A schematic diagram of an interface of an automatic review flow chart provided by an embodiment of the present invention;

[0035] Fig.11 A method flow chart of a method for configuring automatic audit rules provided by an embodiment of the present invention;

[0036] Fig.12 A method flow chart of a method for configuring automatic audit rules provided by an embodiment of the present invention;

[0037] Fig.13 A method flow chart of a method for configuring automatic audit rules provided by an embodiment of the present invention;

[0038] Fig.14 A schematic diagram of an interface of test statistical results provided by an embodiment of the present invention;

[0039] Fig.15 A method flow chart of an automatic review method for sample inspection results provided by an embodiment of the present invention. DETAILED DESCRIPTION

[0040] The present application is further described below in conjunction with the accompanying drawings and specific embodiments. The described embodiments should not be regarded as limiting the present application, and all other embodiments obtained by ordinary technicians in this field without creative work are within the scope of protection of the present application.

[0041] In the following description, reference is made to “some embodiments”, which describe a subset of all possible embodiments, but it can be understood that “some embodiments” may be the same subset or different subsets of all possible embodiments and may be combined with each other without conflict.

[0042] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as those commonly understood by those skilled in the art to which this application belongs. The terms used herein are only for the purpose of describing the embodiments of this application and are not intended to limit this application.

[0043] In vitro diagnostic tests are commonly used in the healthcare industry to help diagnose a patient's medical condition. In vitro diagnostic tests refer to testing procedures that analyze a sample / specimen. After analyzing the patient sample, the laboratory produces a test result. The doctor or other medical practitioner then uses the test result to help diagnose one or more medical conditions.

[0044] In vitro diagnostic tests are usually implemented by in vitro diagnostic analyzers, and the test results of the in vitro diagnostic tests are the sample test results of the samples obtained by the in vitro diagnostic analyzer. After obtaining the sample test results, the sample test results need to be reviewed to determine the validity of the sample test results, classify the sample test results, and confirm whether they need further testing. Suspicious or abnormal sample test results may have a significant impact on the workflow of technicians. Sample test results with questionable or abnormal results may need to be re-tested by technicians to confirm the validity of the sample test results or determine the properties of the sample test results. In addition, certain sample test results may cause subsequent tests to be indicated or cancelled. For example, abnormally low or high sample test results will require re-performing previously performed tests to confirm whether the previous sample test results are correct. This process of conducting tests, evaluating sample test results, re-testing, recalculating sample test results, and reporting sample test results to medical personnel makes the task of managing laboratories and their workflows a complex task.

[0045] The existing technology can automatically review the sample inspection results, but the review rules in the current automatic review method require the service engineer to confirm the requirements with the user during installation and then configure the review rules. If the review rules need to be modified later, the service engineer needs to be instructed to modify them (the existing technology uses programming code to complete the rule modification). The current automatic review method is not convenient for users to set or modify the rules.

[0046] Based on this, an embodiment of the present invention provides a configuration method for automatic review rules and an automatic review method, a sample analysis system, an electronic device, a computer-readable storage medium and a computer program product, which can facilitate users to configure automatic review rules, improve the operability of the configuration of review rules and improve the efficiency of automatic review of the inspection results.

[0047] See also Figure 1As shown, an embodiment of the present invention provides a sample analysis system, which includes an electronic device 101 and at least one in vitro diagnostic analyzer 102, wherein the in vitro diagnostic analyzer 102 is used to detect the sample and obtain the test result of the sample. In one embodiment, the sample is a biochemical sample, for example, it can be a biological tissue, and the test result of the sample can include test data of multiple parameters, and the parameter reflects a certain property of the sample. For example, the test result of the sample can include WBC (White Blood Cell count), RBC (Red Blood Cell count), PLT (Platelet count), vitamin content (Vitamin) and other items in the blood routine test results.

[0048] In one embodiment, the electronic device may be a computer device, for example, a terminal device (such as a mobile phone), a computer device, a server, a cloud host or a network device, etc. The electronic device can communicate with an in vitro diagnostic analyzer and obtain the test results of the in vitro diagnostic analyzer for samples of different biological sample detection items. The electronic device can communicate with the in vitro diagnostic analyzer via wired or wireless means. In addition, the in vitro diagnostic analyzer can be accessed via the Internet of Things or the Internet to obtain the test results of the samples.

[0049] In another embodiment, the electronic device may not communicate with the in vitro diagnostic analyzer. For example, it may be an independent computer device that reads the test results of the samples stored in an external storage device for review. For example, the user can connect a USB flash drive or a mobile hard disk that stores the sample test results to the electronic device, and the electronic device reads the sample test results in the USB flash drive or the mobile hard disk. This also belongs to obtaining the sample test results of the in vitro diagnostic analyzer.

[0050] In one embodiment, the sample analysis system is an in vitro diagnostic analysis assembly line, that is, various in vitro diagnostic analyzers are arranged in the form of an assembly line, and can automatically complete various tests on samples in sequence, wherein the electronic device serves as a control device to centrally control the various in vitro diagnostic analyzers and uniformly review the test results of the samples.

[0051] In one embodiment, the electronic device performs an automatic audit method on the obtained sample test results, determines whether the sample test results meet the requirements of the audit rules, and obtains the audit results, wherein the audit results can be whether the sample test results pass the audit or fail the audit, or whether certain result items in the sample test results pass the audit or fail the audit. The audit results can be stored in the built-in memory of the electronic device, or stored in an external storage device, or sent to other computer devices or network devices for subsequent processing (can be sent wirelessly, wired, via the Internet or a local area network).

[0052] See also Figure 2 As shown, in one embodiment, the electronic device includes a control device, a memory and a display, wherein the display is used to display the audit rule configuration interface of the automatic audit rule, the memory is used to store the automatic audit rule, and the control device is used to configure the automatic audit rule and automatically audit the inspection result of the sample according to the automatic audit rule. The control device obtains the first instruction input by the user, and configures (creates) the automatic audit rule according to the first instruction or modifies the automatic audit rule already stored in the memory. In one embodiment, the controller can receive the first instruction input by the user through the communication port, for example, the user inputs the first instruction through another control device, and sends the first instruction to the electronic device, or sends the first instruction to the electronic device through the Internet / local area network. This operation mode can be called the user's remote operation. In another embodiment, the electronic device also includes an input device, the user can operate the input device, and the input device then obtains the first instruction operated by the user and sends the first instruction to the control device. This operation mode can also be called the user's local operation. In one embodiment, the input device can be a keyboard, a mouse, a trackball, a touchpad or a touch screen, etc., for example, it can be a touch screen integrated with the display.

[0053] The present application embodiment provides a method for configuring an automatic audit rule. Figure 2 The electronic device shown is executed for explanation. It can be understood that the configuration method can also be executed by other devices, and this application is not limited to this. Figure 3 As shown, the configuration method of automatic audit rules includes the following steps 310 to 320:

[0054] Step 310: display the audit rule configuration interface of the automatic audit rule.

[0055] See also Figure 4As shown, in this step, the control device of the electronic device controls the display to display the audit rule configuration interface 400, and the audit rule configuration interface 400 includes a biological sample detection item selection area 410 and a rule configuration area 420, wherein the biological sample detection item selection area 410 includes at least one biological sample detection item 411, and the rule configuration area 420 includes at least one rule configuration item corresponding to the biological sample detection item 411, and the rule configuration item is used to configure the automatic audit rule. The automatic audit rule is used to automatically compare each rule configuration item with the sample test result to determine whether the sample test result has passed the audit. The user can intuitively view each biological sample detection item 411 through the biological sample detection item selection area 410, and view the rule configuration items corresponding to different biological sample detection items 411 in the rule configuration area 420.

[0056] In one embodiment, participating Figure 4 As shown, the rule configuration area 420 includes a first rule display area 421 and a second rule display area 422, and the rule configuration items include at least one rule classification entry 430 and at least one group of rule configuration entries 440 corresponding to the rule classification entry 430. At least one rule classification entry 430 is displayed in the first rule display area 421, and at least one group of rule configuration entries 440 corresponding to the rule classification entry 430 is displayed in the second rule display area 422. In this embodiment, the rule classification entry 430 is used to classify each group of rule configuration entries 440 so that the user can quickly locate and find the rule configuration entry 440 that needs to be configured.

[0057] For example, see Figure 4 As shown, in one embodiment, a plurality of biological sample detection items 411 are displayed in the item selection area 410, including a vitamin D (Vitamin D) detection item, an alanine aminotransferase (ALT) detection item, an albumin (ALB) detection item and a human chorionic gonadotropin (HCG) detection item, wherein the ALB detection item is selected.

[0058] The first rule display area 421 displays multiple rule classification entries 430 corresponding to the selected ALB detection item. The rule classification entries 430 in the first rule display area 421 include "rules related to instrument information", "rules related to patient information and sample information", "rules related to data analysis", "report integrity rules", "result rationality rules", "special rules and classification rules", "all single-item main rules except multi-item rules", "result rationality rules and report integrity rules", among which "result rationality rules and report integrity rules" are in the selected state.

[0059] The second rule display area 422 displays a plurality of rule configuration entries 440 corresponding to the selected “result rationality rule and report integrity rule” classification entry 430. The plurality of rule configuration entries 440 are classified into a group, wherein Figure 4 The multiple rule configuration entries 440 shown in the figure are classified into a group named "result rationality rules and report integrity rules", which includes multiple rule configuration entries 440, including "rules related to patient information and sample information", "rules related to gender and structure", etc. The user can perform further rule configuration operations according to the displayed rule configuration entries 440 (see the detailed description of the following step 320).

[0060] In another embodiment, the rule configuration area 420 may also not set the first rule display area 421, that is, the first rule display area 421 and the second rule display area 422 are not performed, but the rule configuration entries 440 corresponding to each biological sample detection item 411 are directly displayed in the rule configuration area 420 according to each biological sample detection item 411 in the item selection area 410, that is, the rule configuration entries 440 are not grouped and classified.

[0061] Step 320 , receiving a first instruction to select at least one biological sample detection project, and configuring the review rules of the rule configuration items corresponding to the biological sample detection project.

[0062] In this step, the control device in the electronic device obtains the first instruction input by the user. Wherein, the user can input the first instruction through the input device of the electronic device (such as a keyboard, a mouse, a touch screen, etc.). In another embodiment, the user can also send the first instruction to the electronic device through other control devices outside the electronic device (such as a mobile terminal, another computer device, etc.), for example, the first instruction is sent to the electronic device remotely by another computer. It can be understood that the first instruction is input by the user according to the content displayed on the display in the above step 310, that is, the user can confirm which rule configuration items 440 correspond to different biological sample detection items 411 in the biological sample detection item selection area 410 through the above step 310, and confirm the rule configuration items 440 that need to be configured, or after finding the rule configuration items 440 to be configured through the above step 310, the first instruction is input to the electronic device, and the first instruction is input by the user according to the instructions of the above step 310, including the configuration information of the rule configuration items 440 displayed in the configuration step 310. The control device determines at least one biological sample detection item selected by the user according to the configuration information in the first instruction, and configures the review rule of the rule configuration item corresponding to the rule classification item according to the configuration information in the first instruction.

[0063] The configuration method of the automatic audit rule provided in the embodiment of the present application is to display the audit rule configuration interface of the automatic audit rule through the display, and the audit rule configuration interface includes a biological sample detection project selection area and a rule configuration area. Wherein, the biological sample detection project selection area includes at least one biological sample detection project, and the rule configuration area includes at least one rule configuration item corresponding to the biological sample detection project, so that the user can intuitively view each biological sample detection project through the biological sample detection project selection area, and view the rule configuration items corresponding to different biological sample detection projects in the rule configuration area. By receiving the first instruction of the user to operate according to the display content of the audit rule configuration interface, at least one biological sample detection project is selected according to the first instruction, and the audit rules of the rule configuration items corresponding to the biological sample detection project are configured. In the embodiment of the present application, by converting the software engineering language with high technical threshold into a visual setting item form, the user can configure the desired rules according to the needs and habits, so that the automatic audit rules of different biological sample detection projects can be configured or modified very intuitively and conveniently, and the user can independently complete the rule configuration for each rule configuration item without making an appointment or instructing the service engineer to set or modify it. In addition, in the embodiment of the present application, the user can independently set the review rules for different biological sample detection items, so that the corresponding review rules can be matched for different biological sample detection items during the review process. There is no need to manually modify on-site according to changes in the biological sample detection items, which greatly improves the review efficiency of the sample test results.

[0064] In another embodiment, the control device determines at least one biological sample detection item selected by the user and a rule classification item corresponding to the biological sample detection item according to the configuration information in the first instruction, and configures the review rule according to the configuration information in the first instruction.

[0065] In one embodiment, the first instruction may include multiple instruction messages, that is, the first instruction is a collection of multiple instruction messages, wherein the multiple instruction messages in the first instruction may be sent to the control device simultaneously or at different times. For example, the first instruction includes a selection message for selecting a biological sample detection item 411 and a configuration message for configuring a rule configuration item 440 corresponding to the biological sample detection item 411. The control device first receives the selection message, locates and selects the biological sample detection item 411 specified by the user (for example, the selection message is to select the "ALB detection item"), and displays the corresponding rule configuration item 440 according to the specified biological sample detection item 411. Then, the control device receives the configuration message corresponding to the rule configuration item 440, and configures the review rule of the rule configuration item 440 according to the configuration message.

[0066] The above-mentioned selection messages and configuration messages can be classified as the first instruction. In another embodiment, the first instruction may also include multiple selection messages or multiple configuration messages, for example, including a first selection message for selecting the biological sample detection project 411, a second selection message for selecting the rule classification entry 430, a third selection message for selecting and configuring the rule configuration entry 440, and a configuration message for configuring the rule configuration entry 440, and for example, including a first selection message for selecting the biological sample detection project 411, a second selection message for selecting the rule classification entry 430, and a first configuration message for configuring one of the rule configuration entries 440 and a second configuration message for configuring another rule configuration entry 440. In this embodiment, the number and content of the instruction messages contained in the first instruction are not limited. The first instruction may also have only one instruction message, for example, only the configuration message of the rule configuration entry 440 corresponding to the biological sample detection project 411 selected by the user, and the control device directly configures the specified rule configuration entry 440 after receiving this message.

[0067] In one embodiment, the control device controls the display to display the configuration window of the rule configuration item 440 selected by the user according to the first instruction, for example, see Figure 5 As shown, the controller receives a selection message for the "gender and result related rules" rule configuration entry 440 in the first instruction, and controls the display to display the configuration window of the "gender and result related rules" rule configuration entry 440. The user sets the male patient detection value range rule to "≤27" or "≥135" according to the configuration window. At this time, the controller receives a configuration message corresponding to the configuration, and configures the review rules according to the configuration message.

[0068] In one embodiment, the rule configuration entries 440 corresponding to each rule classification entry 430 are all displayed in the second rule display area 422, see Figure 4 As shown, the second rule display area 422 is a scrollable display area, and the rule configuration entries 440 corresponding to each rule classification entry 430 are all listed in the second rule display area 422, wherein the user can adjust the content of the display range in the second rule display area 422 to view different rule configuration entries 440. By listing the rule configuration entries 440 in the second rule display area 422, it is convenient for the user to view and check all the rule configuration entries 440, thereby improving the ease of configuration of the rule configuration entries 440 and reducing the difficulty of user operation.

[0069] Based on the display mode of the second rule display area 422, see Figure 6 As shown, in one embodiment, the above step 320 specifically includes the following steps 610 to 620.

[0070] Step 610, receiving a first instruction, selecting at least one of the biological sample detection items and the rule classification item corresponding to the biological sample detection item according to the selection message in the first instruction, and adjusting the display interface of the second rule display area according to the selected rule classification item so that it jumps to the position of the rule configuration item corresponding to the rule classification item.

[0071] In this step, the controller determines the rule classification entry 430 selected by the user according to the selection message of the first instruction, and controls the display to adjust the display interface of the second rule display area 422 (it can also be considered to adjust the display content in the second rule display area 422), so that the display interface jumps to the position of the rule configuration entry 440 corresponding to the selected rule classification entry 430. In this way, the user can quickly jump to the configuration entry 440 that needs to be configured by selecting the rule classification entry 430 in the first rule display area 421, for example, see Figure 4 As shown, in one embodiment, the control device receives a selection message in the first instruction, which indicates that the rule classification entry 430 of "result rationality rule and report integrity rule" in the first rule display area 421 is selected. Then, the control device adjusts the display interface of the second rule display area 422 so that the rule configuration entry 440 corresponding to "result rationality rule and report integrity rule" is displayed in the second rule display area 422, for example Figure 4 The rule configuration entry 440 of "Rules related to patient information and sample information" is shown. In this step, the user can easily jump to the required rule configuration entry 440 through the rule classification entry 430 in the first rule display area 421, which greatly improves the ease of use of user configuration rules.

[0072] Step 620: Configure the review rule of the rule configuration item corresponding to the rule classification item according to the configuration message in the first instruction.

[0073] In one embodiment, the controller configures the review rules of the rule configuration items corresponding to the rule classification items according to the configuration message in the first instruction, wherein the user can use the following configuration information: Figure 5 The rule configuration interface shown is used to send the configuration message.

[0074] In another embodiment, the second rule display area 422 only displays the rule configuration entry 440 corresponding to the rule classification entry 430 selected by the user, see Figure 7 As shown, the above step 320 specifically includes the following steps 710 to 720:

[0075] Step 710, receiving a first instruction, selecting at least one biological sample detection item and a rule classification item corresponding to the biological sample detection item according to a selection message in the first instruction, and displaying a rule configuration item corresponding to the selected rule classification item in a second rule display area.

[0076] In one embodiment of this step, the controller determines the rule classification entry 430 selected by the user based on the selection message of the first instruction, and controls the display to adjust the display interface of the second rule display area 422 so that the display interface of the second rule display area 422 only displays the rule configuration entry 440 corresponding to the selected rule classification entry 430.

[0077] Step 720: Configure the review rules of the rule configuration items corresponding to the rule classification items according to the configuration message in the first instruction.

[0078] In one embodiment of this step, the controller configures the audit rules of the rule configuration items corresponding to the rule classification items according to the configuration message in the first instruction, wherein the user can use the following Figure 5 The rule configuration interface shown is used to send the configuration message.

[0079] See also Figure 4 As shown, in one embodiment of the present application, the first rule display area 421 includes a target control 450 for displaying the enabled state of each rule classification entry. The target control 450 is used to control whether all rule configuration entries 440 corresponding to the rule classification entry 430 are enabled. If the user enables the selected rule classification entry 430 through the target control 450, the rule configuration entry 440 configured for the selected rule classification entry 430 is applicable to the current automatic audit rule. If the user cancels the enablement of the selected rule classification entry 430 through the target control 450, the rule configuration entry 440 configured for the selected rule classification entry 430 is no longer applicable to the current automatic audit rule. In one embodiment, enabling and disabling the selected rule classification entry 430 is equivalent to adding and reducing audit items in the automatic audit rule. In one embodiment, see Figure 4 As shown, one target control 450 corresponds to one rule classification entry 430. In another embodiment, one target control 450 may be set to control the enabling state of multiple rule classification entries 430. The target control 450 may be represented in a variety of different forms. For example, in one embodiment, see Figure 4 As shown, a target control 450 is set in the row where each rule classification entry 430 in the rule configuration area 420 is located. The target control 450 is the state of the switch button. When the target control 450 is enabled, the switch button is on the right side, and when the target control 450 is disabled, the switch button is on the left side. Figure 4As shown, the target control 450 corresponding to the "report integrity rule" in the first rule display area 421 is in an enabled state, while the target control 450 corresponding to the "all single-project main rules except multi-project rules" in the first rule display area 421 is in a disabled state. In addition, the target control 450 may also have other presentation styles. In one embodiment, the target control 450 may be a check box set next to the rule classification entry 430. When the check box is selected, it indicates that the corresponding rule classification entry 430 is in an enabled state. When the check box is unchecked, it indicates that the corresponding rule classification entry 430 is in a disabled state. In another embodiment, the target control 450 may also be a control for operating the display state of the rule classification entry 430. For example, after clicking the rule classification entry 430, the color or font, glyph, background color, etc. of the text displayed on the rule classification entry 430 may change to indicate its enabled state.

[0080] See also Figure 8 As shown, the configuration method of the automatic audit rules of the embodiment of the present application also includes the following steps 810 to 820:

[0081] Step 810: Receive a second instruction for operating the target control, and set the enabled state of the rule configuration corresponding to each rule classification entry according to the second instruction.

[0082] In this step, the control device receives a second instruction from the user to operate the target control 450. In one embodiment, the user can operate the target control 450 through the input device to generate the second instruction. The control device sets the state of each rule classification entry 430 corresponding to the target control 450 according to the second instruction. For example, the control device can control the display to change the display state of the target control 450 to indicate the enabled state of the rule classification entry 430. In one embodiment, see Figure 4 As shown, a target control 450 is set in the row where each rule classification entry 430 in the rule configuration area 420 is located. After receiving the second instruction, the control device changes the display state of the target control 450 and records the enabled state of the rule classification entry 430 corresponding to each target control 450. In one embodiment, the control device can receive multiple second instructions respectively to set the state of the target control 450 corresponding to each second instruction. In another embodiment, the control device can receive one second instruction to set the state of multiple target controls 450 at the same time.

[0083] By using the target control 450 corresponding to the rule classification entry 430 to configure the automatic audit rules, a visual setting of the logical layering is achieved, and the operation method is very intuitive and convenient. The user can directly use the target control 450 to uniformly set the enabled status of a certain type (or a certain group) of rule configuration entries, which greatly simplifies the user's configuration operations and effectively reduces the difficulty of the user's configuration rules.

[0084] Step 820, configuring the automatic review rules according to the enabled state of the target control corresponding to each rule classification entry.

[0085] In this step, the controller configures the automatic audit rules according to the enabled state of the rule classification entries 430 corresponding to each target control 450 in the above step 810. In one embodiment, if the current state of the target control 450 is switched from off to enabled, the control device determines each rule configuration entry 440 of the rule classification entry 430 corresponding to the target control 450, configures the automatic audit rules, and adds the audit rules corresponding to these rule configuration entries 440 to the automatic audit rules. If the current state of the target control 450 is switched from enabled to off, the control device determines each rule configuration entry 440 of the rule classification entry 430 corresponding to the target control 450, configures the automatic audit rules, and cancels the audit rules corresponding to these rule configuration entries 440 in the automatic audit rules.

[0086] See also Fig. 9 As shown, the configuration method of the automatic audit rule of the embodiment of the present application also includes the following steps 910:

[0087] Step 910, display the automatic review flow chart corresponding to the rule configuration item.

[0088] See also Fig.10 As shown, in this step, the control device controls the display to display the automatic audit flowchart 1000 corresponding to the rule configuration item. The automatic audit flowchart 1000 includes an audit execution node 1010 and an audit path 1020 connected between each of the audit execution nodes 1010. Through the audit execution nodes 1010 and the audit path 1020 in the automatic audit flowchart 1000, the user can intuitively understand the audit process of the automatic audit rules and the order of rule audits, and can confirm whether the configured automatic audit rules are correct according to the automatic audit flowchart 1000. In one embodiment, the audit execution nodes 1010 of the automatic audit flowchart 1000 correspond to each rule configuration item or each rule configuration entry 440. In another embodiment, see Fig.10 As shown, the audit execution nodes 1010 of the automatic audit flowchart 1000 correspond to the various rule classification entries 430 in the first rule display area 421 respectively.

[0089] See also Fig.11 As shown, the configuration method of the automatic audit rule of another embodiment of the present application further includes the following steps 1110:

[0090] Step 1110, displaying the automatic review flow chart of the rule configuration items corresponding to the biochemical analysis detection items.

[0091] In this step, multiple automatic review flow charts 1000 are included, wherein different automatic review flow charts 1000 correspond to different biological sample detection items 411. In another embodiment, when the automatic review flow chart 1000 needs to be displayed, the currently selected biological sample detection item 411 is confirmed, for example, Fig.10 As shown, in addition to the automatic review flowchart 1000 , a biological sample detection item selection area 410 is also displayed, that is, the currently displayed automatic review flowchart 1000 is generated according to a biological sample detection item 411 selected by the user in the biological sample detection item selection area 410 .

[0092] In one embodiment, after the control device obtains the flowchart display instruction of the user, it controls the display to switch the displayed screen according to the flowchart display instruction of the user, so that the display displays the automatic review flowchart 1000. In another embodiment, the automatic review flowchart 1000 can be displayed on the same screen as the review rule configuration interface 400, or displayed on the same screen as some elements in the review rule configuration interface 400, for example, Fig.10 As shown, the display interface of the display screen simultaneously displays the automatic review flowchart 1000, the biological sample detection item selection area 410, and the rule configuration area 420. Among them, the currently displayed automatic review flowchart 1000 corresponds to the biological sample detection item 411 selected in the biological sample detection item selection area 410, and the review execution node 1010 of the currently displayed automatic review flowchart 1000 corresponds to the rule classification item 430 in the first rule display area 421. In this way, the user can select and view the automatic review flowchart 1000 corresponding to different biological sample detection items 411, and confirm whether the setting of the corresponding rule classification item 430 is correct through the status of the review execution node 1010 of the automatic review flowchart 1000.

[0093] See also Fig.12 As shown, the configuration method of the automatic audit rule of the embodiment of the present application also includes the following steps 1210:

[0094] Step 1210, displays the automatic audit flowchart corresponding to the rule configuration item, the automatic audit flowchart includes audit execution nodes corresponding to each rule classification item, and audit paths connected between each audit execution node, wherein the enabled status of the audit execution nodes corresponding to the enabled rule classification items is displayed.

[0095] In this step, the automatic audit flowchart 1000 lists multiple audit execution nodes 1010 corresponding to each rule classification entry 430. As described in the above embodiment, the enable status of different rule classification entries 430 in the first rule display area 421 can be set to conveniently set whether the corresponding rule configuration entry 440 is enabled. For example, the enable status of the rule classification entry 430 can be set by setting the target control 450 in the rule classification entry 430. Since there is a corresponding relationship between the audit execution node 1010 and the rule classification entry 430 in the automatic audit flowchart 1000, the enable status display of the corresponding audit execution node 1010 can be synchronously set according to the enable status of the classification entry 430. For example, the enabled audit execution node 1010 can be represented by high brightness, and the disabled audit execution node 1010 can be represented by low brightness.

[0096] In one embodiment, the above step 1210 may be modified as follows, that is, an automatic audit flowchart corresponding to the rule configuration item is displayed, and the automatic audit flowchart includes audit execution nodes corresponding to each enabled rule classification item, and an audit path connected between each audit execution node. The difference between this embodiment and the above step 1210 is that the enabled status display is not set for the audit execution node 1010, but only the audit execution node 1010 corresponding to the enabled rule classification item 430 is displayed, and the audit execution node 1010 of the unenabled rule classification item 430 is deleted or hidden in the automatic audit flowchart 1000.

[0097] In one embodiment, see Fig.10 As shown, the audit rule configuration interface 400 and the automatic audit flowchart 1000 are displayed on the same screen, and the rule classification entries 430 corresponding to each audit execution node 1010 in the automatic audit flowchart 1000 are displayed in the rule configuration area 420 of the audit rule configuration interface 400. When the audit rule configuration interface 400 and the automatic audit flowchart 1000 are displayed on the same screen, the configuration method of the automatic audit rules of the embodiment of the present application further includes the following steps:

[0098] A third instruction is received to select at least one rule classification entry in the rule configuration area, and to set the rule classification entry to an enabled state or a disabled state.

[0099] In this step, the user may input a third instruction to the electronic device, the third instruction being used to select at least one rule classification entry 430 in the rule configuration area 420 and set the enabled state of the rule classification entry 430. In one embodiment, the third instruction may be a control instruction for the target control 450 of the selected rule classification entry 430.

[0100] In one embodiment, see Fig.10 As shown, in the process of displaying the automatic review flowchart 1000, the association status of each biological sample detection item 411 in the biological sample detection item selection area 410 is also displayed to determine whether it is adapted to the rule configuration item corresponding to the currently displayed automatic review flowchart 1000. In this embodiment, different biological sample detection items 411 can be set with the same automatic review rule configuration. Therefore, the association status of the biological sample detection items 411 associated with the currently displayed automatic review flowchart 1000 can be displayed in the biological sample detection item selection area 410. In one embodiment, see Fig.10 As shown, an enable status control 412 can be set next to each biological sample detection item 411 in the biological sample detection item selection area 410, and the association status of different biological sample detection items 411 and the currently displayed automatic review flowchart 1000 can be displayed through the enable status control 412. In one embodiment, the enable status control 412 can be in the shape of a switch. When the switch is turned to the right, it indicates that the corresponding biological sample detection item 411 is applied to the current automatic review flowchart 1000 and / or the setting of the first rule display area 421.

[0101] In one embodiment, the configuration method of the automatic review rules of the embodiment of the present application further includes the following steps:

[0102] Receive the fourth instruction to select at least one biological sample detection project 411 in the biological sample detection project selection area 410, and configure the audit rules of the selected biological sample detection project 411 according to the rule configuration items corresponding to the automatic audit flowchart 1000. In this step, in addition to displaying the association status of each biological sample detection project 411 with the current automatic audit flowchart 1000 in the biological sample detection project selection area 410, the association status of each biological sample detection project 411 can also be set according to the fourth instruction input by the user, so that it can adapt to the audit configuration of the current automatic audit flowchart 1000. This can facilitate users to uniformly configure the rules of different biological sample detection projects 41 in batches, thereby improving the ease of use and operability of the audit rule configuration. In one embodiment, the fourth instruction is an action instruction to enable the enablement status control 412 corresponding to the biological sample detection project 411.

[0103] In another embodiment, the method for configuring the automatic audit rules further includes the following steps:

[0104] A fifth instruction is received to select at least one biochemical analysis test item in the biological sample test item selection area, and to cancel the association between the review rule corresponding to the biochemical analysis test item and the automatic review flow chart.

[0105] In this step, the association status of each biological sample detection item 411 can be set according to the fifth instruction input by the user, so that it is unassociated with the audit configuration of the current automatic audit flowchart 1000. In one embodiment, the fifth instruction is an action instruction to set the enable status control 412 corresponding to the biological sample detection item 411 to be disabled.

[0106] See also Fig.13 As shown, the configuration method of the automatic audit rule of the embodiment of the present application also includes the following steps 1310 to 1340:

[0107] Step 1310, obtaining sample test results corresponding to the biochemical analysis test items.

[0108] In this step, the electronic device can obtain the sample test results of the in vitro diagnostic analyzer through wired, wireless, local area network or Internet according to the description of the above embodiment. In addition, the electronic device can also connect to an external storage device to obtain the prepared sample test results. In one embodiment, the sample test results can also be pre-prepared sample test results for testing.

[0109] Step 1320, auditing the sample test results according to the rule configuration items corresponding to the biochemical analysis test items to obtain the audit results.

[0110] In this step, the control device in the electronic device determines the configured rule configuration items according to the current biochemical analysis test project to perform an audit operation on the sample test results to obtain an audit result. The audit result can be whether the sample test results pass the audit or fail the audit, or whether certain result items in the sample test results pass the audit or fail the audit. The audit result can be stored in the built-in memory of the electronic device, or can be stored in an external storage device, or sent to other computer devices or network devices for subsequent processing.

[0111] Step 1330, performing statistical calculation on the audit results to obtain test statistical results;

[0112] Step 1340, display the test statistical results.

[0113] In this step, see Fig.14As shown, the control device further performs statistical calculations on the audit results to obtain test statistical results. The control device controls the display to display the test statistical results, wherein the test statistical results can be displayed independently, or displayed on the same screen with the audit rule configuration interface 400, or some elements of the audit rule configuration interface 400 (e.g., at least one of the biological sample detection item selection area 410, the first rule display area 421, or the second rule display area 422).

[0114] In one embodiment, the test statistical results may be displayed in at least one of the following ways:

[0115] A schematic diagram showing the pass rate and / or pass rate percentage of the test samples;

[0116] Alternatively, the pass rates of different biochemical analysis test items may be displayed;

[0117] Or, display the pass rate of different rule configuration items;

[0118] Alternatively, the pass rates of different rule configuration items under different biochemical analysis test items are displayed;

[0119] Alternatively, the pass rates of different biochemical analysis test items under different rule configuration items are displayed.

[0120] The test statistics can be used to determine the problems that occur during the verification process of the automatic audit rules. For example, the automatic audit pass rate of a certain rule and a certain project can be accurately located to find out the accuracy of the rule configuration. Fig.14 As shown, the test statistical results include a chart statistics area 1410 that displays the data statistical results in a chart format. In one embodiment, it also includes a project statistics area 1420 for statistically analyzing the audit pass rate of different biological sample detection projects, and an audit rule statistics area 1430 for statistically analyzing the audit pass rate of different audit rules, wherein the pass rate, failure rate, and rule missing rate of the overall automatic audit rules can be seen through the sample automatic audit ratio. The pass rate of each project can be understood through the project pass rate. If it is found that the automatic audit pass rate of a project is very low, the reasons can be checked through two tables: 1. Check the sample audit pass status of each rule in each project; 2. Check the sample audit pass status of each project in each rule. Based on this, it can be found out which rule of which project has a problem and modify the rule.

[0121] See also Fig.15 As shown, the embodiment of the present application provides a method for automatically reviewing sample test results, which is used to automatically review sample test results generated by an in vitro diagnostic analyzer, wherein the method for automatically reviewing sample test results includes the following steps:

[0122] Step 1510: Apply the method for configuring automatic audit rules of any of the above embodiments to configure the automatic audit rules.

[0123] Step 1520, obtain sample inspection results.

[0124] Step 1530, audit the sample inspection results according to the automatic audit rules to obtain the audit results.

[0125] The automatic audit method of the sample test result provided in the embodiment of the present application, displays the audit rule configuration interface of the automatic audit rule through the display, and the audit rule configuration interface includes a biological sample detection project selection area and a rule configuration area. Wherein, the biological sample detection project selection area includes at least one biological sample detection project, and the rule configuration area includes at least one rule configuration item corresponding to the biological sample detection project, so that the user can intuitively view each biological sample detection project through the biological sample detection project selection area, and view the rule configuration items corresponding to different biological sample detection projects in the rule configuration area. By receiving the first instruction of the user to operate according to the content displayed on the audit rule configuration interface, at least one biological sample detection project is selected according to the first instruction, and the audit rules of the rule configuration items corresponding to the biological sample detection project are configured. In the embodiment of the present application, by converting the software engineering language with high technical threshold into a visual setting item form, the user can configure the desired rules according to the needs and habits, so that the automatic audit rules of different biological sample detection projects can be configured or modified very intuitively and conveniently, and the user can independently complete the rule configuration for each rule configuration item without making an appointment or instructing the service engineer to set or modify. In addition, in the embodiment of the present application, the user can independently set the review rules for different biological sample detection items, so that the corresponding review rules can be matched for different biological sample detection items during the review process. There is no need to manually modify on-site according to changes in the biological sample detection items, which greatly improves the review efficiency of the sample test results.

[0126] See also Figure 1 As shown, an embodiment of the present application provides a sample analysis system, including:

[0127] At least one in vitro diagnostic analyzer for testing the sample to obtain a sample test result;

[0128] a control device, communicatively connected to at least one in vitro diagnostic analyzer, for obtaining sample test results from the in vitro diagnostic analyzer, the control device comprising a processor and a display;

[0129] The processor is used to control the display to display an audit rule configuration interface of the automatic audit rule, the audit rule configuration interface includes a biological sample detection item selection area and a rule configuration area, wherein the biological sample detection item selection area includes at least one biochemical analysis detection item, the rule configuration area includes at least one rule configuration item corresponding to the biochemical analysis detection item, the rule configuration item is used to configure the automatic audit rule, and the automatic audit rule is used to automatically compare each rule configuration item with the sample test result to determine whether the sample test result passes the audit;

[0130] The processor is also used to receive a first instruction to select at least one biochemical analysis detection item, and configure the review rules of the rule configuration items corresponding to the biochemical analysis detection item.

[0131] The method for controlling the automatic audit rules by the control device and controlling the content displayed by the display device are specifically described in the description of the configuration method of the automatic audit rules in any of the above embodiments, which will not be repeated here.

[0132] The sample analysis system provided in the embodiment of the present application displays the audit rule configuration interface of the automatic audit rule through the display, and the audit rule configuration interface includes a biological sample detection project selection area and a rule configuration area. Among them, the biological sample detection project selection area includes at least one biological sample detection project, and the rule configuration area includes at least one rule configuration item corresponding to the biological sample detection project, so that the user can intuitively view each biological sample detection project through the biological sample detection project selection area, and view the rule configuration items corresponding to different biological sample detection projects in the rule configuration area. By receiving the first instruction of the user to operate according to the content displayed on the audit rule configuration interface, at least one biological sample detection project is selected according to the first instruction, and the audit rules of the rule configuration items corresponding to the biological sample detection project are configured. In the embodiment of the present application, by converting the software engineering language with high technical threshold into a visual setting item form, the user can configure the desired rules according to the needs and habits, so that the automatic audit rules of different biological sample detection projects can be configured or modified very intuitively and conveniently, and the user can independently complete the rule configuration for each rule configuration item without making an appointment or instructing the service engineer to set or modify it. In addition, in the embodiment of the present application, the user can independently set the review rules for different biological sample detection items, so that the corresponding review rules can be matched for different biological sample detection items during the review process. There is no need to manually modify on-site according to changes in the biological sample detection items, which greatly improves the review efficiency of the sample test results.

[0133] An embodiment of the present application provides an electronic device, including a memory and a processor, wherein the memory stores a computer program, and when the processor executes the computer program, it implements the configuration method of the automatic review rules as in the above embodiment, or is also used to execute the automatic review method of the sample inspection results as in the above embodiment.

[0134] An embodiment of the present application provides a computer storage medium having a computer program stored thereon, which is applied to an ultrasonic imaging device. When the computer program is executed by a processor, it implements the configuration method of the automatic review rules as in the above embodiment, or is also used to execute the automatic review method of the sample inspection results of the above embodiment.

[0135] The embodiment of the present application provides a computer program product or a computer program, which includes a computer instruction stored in a computer-readable storage medium. The processor of the computer device reads the computer instruction from the computer-readable storage medium, and the processor executes the computer instruction, so that the computer device executes the configuration method of the automatic review rule of the above embodiment, or is also used to execute the automatic review method of the sample inspection result of the above embodiment.

[0136] The embodiment of the present application also provides a computer program product, which includes a computer program, and the computer program is stored in a computer-readable storage medium. The processor of the computer device reads the computer program from the computer-readable storage medium, and the processor executes the computer program, so that the computer device executes the configuration method of the automatic review rule of the above embodiment, or is also used to execute the automatic review method of the sample inspection result of the above embodiment.

[0137] The terms "first", "second", "third", "fourth", etc. (if any) in the specification of the present application and the above-mentioned drawings are applicable to distinguish similar objects, and are not necessarily used to describe a specific order or sequence. It should be understood that the data used in this way can be interchangeable where appropriate, so that the embodiments of the present application described herein can be implemented in an order other than those illustrated or described herein, for example. In addition, the terms "including" and "having" and any of their variations 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 necessarily limited to those steps or units that are clearly listed, but may include other steps or units that are not clearly listed or inherent to these processes, methods, products or devices.

[0138] It should be understood that in the present application, "at least one (item)" means one or more, and "plurality" means two or more. "And / or" is used to describe the association relationship of associated objects, indicating that three relationships may exist. For example, "A and / or B" can mean: only A exists, only B exists, and A and B exist at the same time, where A and B can be singular or plural. The character " / " generally indicates that the objects associated before and after are in an "or" relationship. "At least one of the following" or similar expressions refers to any combination of these items, including any combination of single or plural items. For example, at least one of a, b or c can mean: a, b, c, "a and b", "a and c", "b and c", or "a and b and c", where a, b, c can be single or multiple.

[0139] It should be understood that in the description of the embodiments of the present application, the meaning of multiple (or multiple items) is more than two, greater than, less than, exceed, etc. are understood to not include the number, and above, below, within, etc. are understood to include the number.

[0140] In the several embodiments provided in the present application, it should be understood that the disclosed systems, devices and methods can be implemented in other ways. For example, the device embodiments described above are only schematic. For example, the division of units is only a logical function division. There may be other division methods in actual implementation. For example, 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 an indirect coupling or communication connection through some interfaces, devices or units, which can be electrical, mechanical or other forms.

[0141] The units described as separate components may or may not be physically separated, and the components shown as units may or may not be physical units, and 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 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 storage medium. Based on this understanding, the technical solution of the present application is essentially 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, and the computer software product is stored in a storage medium, including a number of instructions to enable 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 various embodiments of the present application. The aforementioned storage medium includes: U disk, mobile hard disk, read-only memory (Read-Only Memory, referred to as ROM), random access memory (Random Access Memory, referred to as RAM), disk or optical disk and other media that can store program codes.

[0144] It should also be understood that the various implementation methods provided in the embodiments of the present application can be combined arbitrarily to achieve different technical effects.

[0145] The above is a specific description of the preferred implementation of the present application, but the present application is not limited to the above implementation mode. Technical personnel familiar with the field can also make various equivalent modifications or substitutions under the shared conditions without violating the spirit of the present application. These equivalent modifications or substitutions are all included in the scope defined by the claims of the present application.

Claims

1. A method for configuring an automatic review rule, wherein the automatic review rule is used to automatically review the sample test results generated by an in vitro diagnostic analyzer, characterized in that: The configuration method comprises: Displaying an audit rule configuration interface of the automatic audit rule, the audit rule configuration interface comprising a biological sample detection item selection area and a rule configuration area, wherein the biological sample detection item selection area comprises at least one biological sample detection item, the rule configuration area comprises at least one rule configuration item corresponding to the biological sample detection item, the rule configuration item is used to configure the automatic audit rule, and the automatic audit rule is used to automatically compare each of the rule configuration items with the sample inspection result to determine whether the sample inspection result has passed the audit; A first instruction is received to select at least one of the biological sample detection items, and an audit rule of the rule configuration item corresponding to the biological sample detection item is configured.

2. The configuration method according to claim 1, characterized in that: The rule configuration area includes a first rule display area and a second rule display area, the rule configuration item includes at least one rule classification entry and at least one group of rule configuration entries corresponding to the rule classification entry, at least one rule classification entry is displayed in the first rule display area, and at least one group of rule configuration entries corresponding to the rule classification entry is displayed in the second rule display area.

3. The configuration method according to claim 2, characterized in that: The receiving of the first instruction to select at least one of the biological sample detection items, and configuring the review rules of the rule configuration items corresponding to the biological sample detection items, includes: A first instruction is received to select at least one of the biological sample detection items and the rule classification item corresponding to the biological sample detection item, and to configure the review rule of the rule configuration item corresponding to the rule classification item.

4. The configuration method according to claim 2, characterized in that: The rule configuration corresponding to each of the rule classification items is displayed in the second rule display area; the receiving of the first instruction to select at least one of the biological sample detection items and the rule classification item corresponding to the biological sample detection item, and configuring the review rule of the rule configuration item corresponding to the rule classification item, includes: receiving a first instruction, selecting at least one of the biological sample detection items and the rule classification item corresponding to the biological sample detection item according to a selection message in the first instruction, and adjusting a display interface of the second rule display area according to the selected rule classification item so as to jump to a position of the rule configuration item corresponding to the rule classification item; The audit rule of the rule configuration item corresponding to the rule classification item is configured according to the configuration message in the first instruction.

5. The configuration method according to claim 2, characterized in that: The receiving of the first instruction to select at least one of the biological sample detection items and the rule classification item corresponding to the biological sample detection item, and configuring the review rule of the rule configuration item corresponding to the rule classification item, includes: receiving a first instruction, selecting at least one of the biological sample detection items and the rule classification item corresponding to the biological sample detection item according to a selection message in the first instruction, and displaying the rule configuration item corresponding to the selected rule classification item in the second rule display area; The audit rules of the rule configuration items corresponding to the rule classification items are configured according to the configuration message in the first instruction.

6. The configuration method according to any one of claims 2 to 5, characterized in that: The first rule display area includes a target control for displaying the activation status of each rule classification entry, and the method further includes: receiving a second instruction for operating the target control, and setting an enabled state of the rule configuration corresponding to each of the rule classification entries according to the second instruction; The automatic audit rules are configured according to the enabled state of the target control corresponding to each of the rule classification entries.

7. The configuration method according to any one of claims 1 to 6, characterized in that: Also include one of the following: Display the automatic review flow chart corresponding to the rule configuration item; Alternatively, an automatic review flow chart of the rule configuration items corresponding to the biochemical analysis detection items is displayed.

8. The configuration method according to claim 7, characterized in that: The automatic review flow chart and the biological sample detection item selection area are displayed on the same screen.

9. The configuration method according to claim 2, characterized in that: The configuration method further includes one of the following: Displaying an automatic audit flowchart corresponding to the rule configuration item, the automatic audit flowchart comprising audit execution nodes corresponding to each of the rule classification items, and audit paths connected between the audit execution nodes, wherein the audit execution nodes corresponding to the enabled rule classification items are displayed in an enabled state; Alternatively, an automatic audit flowchart corresponding to the rule configuration item is displayed, wherein the automatic audit flowchart includes audit execution nodes corresponding to each enabled rule classification item, and an audit path connected between each audit execution node.

10. The configuration method according to claim 9, characterized in that: The automatic review flow chart corresponding to the display rule configuration item includes: The audit rule configuration interface and the automatic audit flowchart are displayed on the same screen, and the rule classification entries corresponding to each audit execution node in the automatic audit flowchart are displayed in the rule configuration area of ​​the audit rule configuration interface.

11. The configuration method according to claim 10, characterized in that: The configuration method further includes: A third instruction is received to select at least one of the rule classification entries in the rule configuration area, and to set the rule classification entry to an enabled state or a disabled state.

12. The configuration method according to claim 10, characterized in that: In the process of displaying the automatic review flow chart, at least one of the biochemical analysis test items is also displayed in the biological sample test item selection area of ​​the review rule configuration interface.

13. The configuration method according to claim 12, characterized in that: In the process of displaying the automatic review flowchart, the association status of whether each of the biochemical analysis test items in the biological sample test item selection area is adapted to the rule configuration item corresponding to the automatic review flowchart is also displayed.

14. The configuration method according to claim 12 or 13, characterized in that: The configuration method further includes at least one of the following: receiving a fourth instruction to select at least one of the biochemical analysis detection items in the biological sample detection item selection area, and configuring the review rule of the selected biochemical analysis detection item according to the rule configuration item corresponding to the automatic review flow chart; Alternatively, a fifth instruction is received to select at least one of the biochemical analysis detection items in the biological sample detection item selection area, and to cancel the association between the review rule corresponding to the biochemical analysis detection item and the automatic review flowchart.

15. The configuration method according to claim 1, characterized in that: The configuration method further includes: Obtaining the sample test results corresponding to the biochemical analysis test items; Performing an audit operation on the sample test result according to the rule configuration item corresponding to the biochemical analysis test item to obtain an audit result; Performing statistical calculations on the audit results to obtain test statistical results; Display the test statistics.

16. The configuration method according to claim 15, characterized in that: The displaying of the test statistical results comprises at least one of the following: A schematic diagram showing the pass rate and / or pass rate percentage of the test samples; Alternatively, the passing rates of different biochemical analysis test items are displayed; Alternatively, the pass rates of different rule configuration items are displayed; Alternatively, the passing rates of different rule configuration items under different biochemical analysis detection items are displayed; Alternatively, the pass rates of different biochemical analysis test items under different rule configuration items are displayed.

17. A method for automatically reviewing sample test results, for automatically reviewing sample test results generated by an in vitro diagnostic analyzer, characterized in that: The automatic review method for sample inspection results comprises the following steps: Applying the method for configuring automatic audit rules according to any one of claims 1 to 16 to configure the automatic audit rules; Obtaining the sample test result; An audit operation is performed on the sample inspection result according to the automatic audit rule to obtain an audit result.

18. A sample analysis system, characterized in that: include: At least one in vitro diagnostic analyzer for testing the sample to obtain a sample test result; a control device, communicatively connected to the at least one in vitro diagnostic analyzer, for obtaining the sample test result from the in vitro diagnostic analyzer, the control device comprising a processor and a display; The processor is used to control the display to display an audit rule configuration interface of the automatic audit rule, wherein the audit rule configuration interface includes a biological sample detection item selection area and a rule configuration area, wherein the biological sample detection item selection area includes at least one biochemical analysis detection item, and the rule configuration area includes at least one rule configuration item corresponding to the biochemical analysis detection item, and the rule configuration item is used to configure the automatic audit rule, and the automatic audit rule is used to automatically compare each of the rule configuration items with the sample test result to determine whether the sample test result has passed the audit; The processor is further configured to receive a first instruction to select at least one of the biochemical analysis detection items, and configure the review rules of the rule configuration items corresponding to the biochemical analysis detection items.

19. The sample analysis system according to claim 18, characterized in that: The rule configuration area includes a first rule display area and a second rule display area, the rule configuration item includes at least one rule classification entry and at least one group of rule configuration entries corresponding to the rule classification entry, at least one rule classification entry is displayed in the first rule display area, and at least one group of rule configuration entries corresponding to the rule classification entry is displayed in the second rule display area.

20. The sample analysis system according to claim 19, characterized in that: In the process of receiving a first instruction to select at least one of the biological sample detection items and configuring the review rules of the rule configuration items corresponding to the biological sample detection items, the processor also receives a first instruction to select at least one of the biological sample detection items and the rule classification items corresponding to the biological sample detection items, and configures the review rules of the rule configuration items corresponding to the rule classification items.

21. The sample analysis system according to any one of claims 18 to 20, characterized in that: The controller is also used to control the display to display the automatic review flow chart corresponding to the rule configuration item, or to display the automatic review flow chart of the rule configuration item corresponding to the biochemical analysis detection item.

22. The sample analysis system according to claim 19, characterized in that: The controller is also used to control the display to display an automatic audit flowchart corresponding to the rule configuration item, wherein the automatic audit flowchart includes audit execution nodes corresponding to each of the rule classification items, and audit paths connected between each of the audit execution nodes, wherein the audit execution nodes corresponding to the enabled rule classification items are displayed in an enabled state; Alternatively, the controller is also used to control the display to display an automatic audit flowchart corresponding to the rule configuration item, wherein the automatic audit flowchart includes audit execution nodes corresponding to each enabled rule classification entry, and an audit path connected between each audit execution node.

23. An electronic device comprising a memory and a processor, wherein the memory stores a computer program, wherein: When the processor executes the computer program, the processor implements the method for configuring the automatic review rules described in any one of claims 1 to 16 or the method for automatically reviewing the sample inspection results described in claim 17.

24. A computer-readable storage medium storing a computer program, characterized in that: When the computer program is executed by a processor, it implements the method for configuring the automatic review rules described in any one of claims 1 to 16 or the method for automatically reviewing the sample inspection results described in claim 17.

25. A computer program product, comprising a computer program, characterized in that When the computer program is executed by a processor, it implements the method for configuring the automatic review rules described in any one of claims 1 to 16 or the method for automatically reviewing the sample inspection results described in claim 17.

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