A blood testing method and device

Abstract

This invention discloses a blood testing method applied to a blood testing device. The blood testing device includes multiple testing modules, each corresponding to different testing items. The method includes: receiving a blood testing instruction carrying testing indication information; determining a testing mode and corresponding testing items based on the testing indication information; and performing blood testing using the testing module corresponding to the testing item according to the testing mode. This blood testing method is convenient to operate, greatly saves resources, and offers diverse functions and high flexibility. Furthermore, a blood testing device is also provided.

Description

Technical Field

[0001] This invention relates to the field of medical testing technology, and in particular to a blood testing method and a blood testing device. Background Technology

[0002] In current technology, blood tests are generally performed separately. For example, routine blood tests and glycated blood glucose tests are performed separately. Each test requires the patient to have a blood sample drawn, which is not only painful for the patient but also cumbersome for the doctor.

[0003] Furthermore, if certain parameters in a blood test indicate a disease, patients will need to queue up again for blood tests and examinations, resulting in a waste of resources. Summary of the Invention

[0004] Therefore, it is necessary to propose a blood testing method and device that is resource-saving and easy to operate to address the above problems.

[0005] A blood testing method, the method being applied to a blood testing device, the blood testing device comprising: multiple testing modules, each testing module corresponding to different testing items;

[0006] Receive a blood test instruction, wherein the blood test instruction carries test indication information;

[0007] The detection mode and corresponding detection items are determined based on the detection indication information;

[0008] The blood is tested using a detection module corresponding to the detection item according to the detection mode.

[0009] A blood testing device includes: a controller and multiple testing modules, wherein the controller is connected to each testing module and different testing modules correspond to different testing items.

[0010] The controller is used to receive blood testing instructions, which carry testing indication information. Based on the testing indication information, the controller determines the testing mode and the corresponding testing items, and controls the testing module to test the blood according to the testing mode and the testing items.

[0011] The aforementioned blood testing method and apparatus include multiple testing modules, each corresponding to different testing items. Upon receiving a blood testing command, the testing mode and testing items are determined based on the testing indication information carried in the command. Then, the corresponding testing module is used to test the blood according to the testing mode. Because this blood testing device contains multiple testing modules, it can perform multiple tests. In other words, only one tube of blood is needed to complete multiple tests, making it convenient to operate and greatly saving resources. Furthermore, by setting different testing modes, it can handle various testing situations, offering diverse functions and high flexibility. Attached Figure Description

[0012] To more clearly illustrate the technical solutions in the embodiments of the present invention or the prior art, the drawings used in the description of the embodiments or the prior art will be briefly introduced below. Obviously, the drawings described below are only some embodiments of the present invention. For those skilled in the art, other drawings can be obtained based on these drawings without creative effort.

[0013] in:

[0014] Figure 1 Here is a flowchart of a blood testing method in one embodiment;

[0015] Figure 2 This is a schematic diagram of multiple detection modes in one embodiment;

[0016] Figure 3 This is an architectural diagram of a blood detection device in one embodiment;

[0017] Figure 4 This is an architectural diagram of a blood detection device in another embodiment;

[0018] Figure 5 This is an architectural diagram of the blood detection device in yet another embodiment;

[0019] Figure 6 This is a schematic diagram of the blood detection device in another embodiment;

[0020] Figure 7 This is an internal structural diagram of a blood testing device in one embodiment. Detailed Implementation

[0021] The technical solutions of the embodiments of the present invention will be clearly and completely described below with reference to the accompanying drawings. Obviously, the described embodiments are only some embodiments of the present invention, and not all embodiments. Based on the embodiments of the present invention, all other embodiments obtained by those skilled in the art without creative effort are within the scope of protection of the present invention.

[0022] like Figure 1 As shown, a blood testing method is proposed, which is applied to a blood testing device. The device includes multiple testing modules, each corresponding to different testing items. The blood testing method includes:

[0023] Step 102: Receive a blood test instruction, which carries test instruction information.

[0024] The detection indication information indicates the detection mode and detection items. The blood testing device receives blood testing instructions, which can be triggered manually or automatically by the machine; the triggering method is not limited here. Detection modules are modules used to perform testing operations on the blood. Detection modules can be customized, combined, added, or removed according to actual needs. Common detection modules include: complete blood count (CBC) module, glycated blood glucose (HbA1c) module, coagulation function module, blood typing module, C-reactive protein (CRP) module, virus detection module, etc.

[0025] Different testing modules correspond to different testing items. For example, the blood routine testing module is used to perform blood routine tests, while the glycated hemoglobin testing module is used to perform glycated hemoglobin tests.

[0026] Step 104: Determine the detection mode and corresponding detection items based on the detection instruction information.

[0027] The detection instruction information may include a detection mode identifier and a detection item identifier. The detection mode identifier indicates the detection mode to be used, and the detection item identifier indicates the item to be tested. In another embodiment, the detection instruction information includes a detection identifier, and the correspondence between the detection identifier, detection mode, and detection item is pre-stored. When the detection instruction information is obtained, the corresponding detection mode and detection item can be found based on the detection identifier. For example, pre-stored detection identifier 1 corresponds to the blood routine-glycated hemoglobin mode. The specific content of the blood routine-glycated hemoglobin mode is: first perform a blood routine test, and determine whether to perform a glycated hemoglobin test based on the test results. Stored detection identifier 2 corresponds to the pregnancy test mode. The specific content of the pregnancy test mode is: simultaneously perform a blood routine test and a glycated hemoglobin test (such as a thalassemia test).

[0028] Step 106: Use the detection module corresponding to the detection item to test the blood according to the detection mode.

[0029] The testing mode indicates the order in which tests are performed, including parallel testing, conditional testing, and standalone testing. Parallel testing means multiple tests are performed concurrently; for example, a complete blood count (CBC) and a thalassemia test can be performed simultaneously. Conditional testing means that the execution of a subsequent test depends on the results of the preceding test; that is, the execution of a later test is conditional. For example, if a CBC is performed first, and the MCV (mean corpuscular volume) and MCH (mean corpuscular hemoglobin) values ​​reach the warning range, it indicates that the patient in that sample is at risk of thalassemia, so the thalassemia test should be performed next. If the test results are normal, the thalassemia test is not required. Standalone testing means there is only one test; for example, if there is only a CBC test, then only the CBC module needs to be used to perform that test.

[0030] Different testing modules correspond to different testing items. Once the testing items are determined, the corresponding testing module is also determined. For example, the testing module corresponding to a complete blood count (CBC) test is a CBC testing module, the testing module corresponding to a glycated blood glucose (GG) test is a GG test module, and the testing module corresponding to a coagulation test is a coagulation test module, and so on.

[0031] The aforementioned blood testing method is applied to a blood testing device, which includes multiple testing modules, each corresponding to different testing items. Upon receiving a blood testing command, the device determines the testing mode and testing items based on the testing indication information carried in the command. Then, according to the testing mode, the corresponding testing module is used to test the blood. Because this blood testing device contains multiple testing modules, it can perform multiple tests. In other words, only one tube of blood is needed to complete multiple tests, making it convenient to operate and greatly saving resources. In addition, this blood testing method can handle various testing situations by setting different testing modes, offering versatility and high flexibility.

[0032] In one embodiment, the step of using a detection module corresponding to the detection item to test the blood according to the detection mode includes: when the detection mode is a composite parallel detection mode, there are multiple corresponding detection items; and parallel detection is performed using a detection module corresponding to each detection item.

[0033] The compound parallel testing mode refers to simultaneously testing multiple items, meaning multiple tests are performed in parallel, which saves time. For example, blood routine tests and glycated hemoglobin (HbA1c) tests can be performed in parallel using separate blood routine and HbA1c detection modules. It's important to understand that parallel testing doesn't necessarily mean strictly simultaneous testing or simultaneous output of results; rather, it tends to distribute samples among different detection modules after a single sample collection. Alternatively, it can be understood as the testing cycles of different modules at least partially overlapping in time after a single sample collection. HbA1c tests can be further subdivided into standard HbA1c testing (routine HbA1c testing), HbA1c variant testing (HbA1c testing when there are many variant proteins), and thalassemia testing. Generally, only one of these three HbA1c tests needs to be selected for testing. Therefore, the compound parallel mode can be: blood routine and standard HbA1c testing in parallel, or blood routine and HbA1c variant testing in parallel, or blood routine and thalassemia testing in parallel.

[0034] Of course, if it is necessary to test three items at the same time, then three testing modules can be used to test the three items simultaneously. For example, if it is necessary to test three items at the same time, such as blood routine test, glycated variation test and thalassemia test, then three testing modules can be used to test the three items at the same time.

[0035] In one embodiment, blood is tested using a detection module corresponding to the detection item according to the detection mode, including: when the detection mode is a composite condition detection mode, determining the execution order of multiple detection items; obtaining a first detection item in sequence, taking the first detection item as the current detection item, performing detection using a detection module corresponding to the current detection item, obtaining a detection result, and determining whether to execute the next detection item based on the detection result; if so, obtaining a second detection item, taking the second detection item as the current detection item, and proceeding to the step of performing detection using a detection module corresponding to the detection item, until all detection items are executed; if it is determined based on the detection result that the next detection item should not be executed, the detection ends.

[0036] The composite conditional testing mode refers to a testing method that may involve multiple tests, but the execution of a subsequent test depends on the result of the previous test. If the result of the previous test is normal, the next test is not required. If the result of the previous test is abnormal or indicates the need for further testing, then the next test must be performed. For example, in blood testing, a complete blood count (CBC) can be performed first. If the CBC result is normal, no further tests are needed. If the CBC result is abnormal, such as when MCV and MCH reach warning levels, then a glycation end product (GEP) test is required. The composite conditional testing mode avoids duplicate blood draws because if the previous test result is normal, the next test is not needed, thus eliminating potential risks and conserving testing resources.

[0037] In another embodiment, the glycation test is further subdivided into standard glycation testing (routine glycated hemoglobin testing), glycation variant testing (glycated hemoglobin testing when there are many variant proteins), and thalassemia testing (thalassemia testing). When performing blood tests, standard glycation testing can be performed first. If the test result is abnormal, the next test—whether to perform abnormal glycation testing or thalassemia testing—can be determined based on the anomaly. Specifically, if abnormal hemoglobin is detected, abnormal glycation testing is performed; if the test result indicates a risk of thalassemia, thalassemia testing is performed. In other words, the decision to proceed with the next test, and which test to perform, can be based on the test results.

[0038] In one embodiment, the step of using a detection module corresponding to the detection item to test the blood according to the detection mode includes: when the detection mode is a single-item detection mode, using a detection module corresponding to a single detection item to test the blood, obtaining the detection result, determining whether there is a risk based on the detection result, and if so, issuing a corresponding risk warning message.

[0039] In this context, "single-item testing mode" refers to testing only one item, such as only a complete blood count (CBC) or only a glycated blood glucose (GGR) test. This means the blood testing method can perform both combined and targeted single-item tests, offering versatility and allowing for flexible selection based on specific needs. During single-item testing, if the results indicate a risk, a corresponding risk warning will be issued. For example, after a CBC and preliminary analysis, if the MCV and MCH levels reach the warning range, a warning will be issued, indicating that the patient in this sample is at risk of thalassemia and suggesting a repeat test for thalassemia in the GGR mode. However, this warning can be displayed on the testing instrument or in the output report; whether further testing is initiated depends on further instructions, such as the patient's wishes or the doctor's needs.

[0040] In one embodiment, the step of using a detection module corresponding to the detection item to test the blood according to the detection mode includes: obtaining detection parameters corresponding to the detection item; and using the determined detection module to perform the detection according to the detection parameters.

[0041] Different tests require different parameters, meaning different indicators need to be detected in the blood. Therefore, after determining the specific tests, a testing module must be used based on the corresponding parameters. Different tests may correspond to the same testing module, so the parameters need to be obtained beforehand. For example, the glycation detection module has three types of tests: standard glycation detection, glycation variation detection, and thalassemia detection. Obviously, these three tests have different parameters.

[0042] In one embodiment, the blood testing device further includes: a sample injection module; the step of using a testing module corresponding to the testing item according to the testing mode to test the blood includes: determining the blood extraction volume according to the testing mode and the testing item, extracting blood from the sample injection module according to the blood extraction volume, and transmitting the extracted blood to the corresponding testing module for blood testing.

[0043] The blood testing device includes a sample injection module, from which blood is drawn for each of the different testing modules. The required blood volume may vary depending on the specific test, and different modes require different blood extraction methods. Therefore, the blood volume must be determined based on the testing mode and the specific test. For example, in a compound parallel mode, multiple blood samples (i.e., blood samples) for different tests need to be drawn at once—the composition and source of the blood samples can be freely chosen based on the actual situation. For instance, the blood sample composition can be serum, plasma, or whole blood. The source can be venous blood or capillary blood, etc. The blood sample can be determined according to actual needs and then sequentially transmitted to the corresponding testing modules. In a compound condition mode, blood samples need to be drawn separately for different tests; that is, the blood sample required for the first test is drawn first, and then, if necessary, the blood sample required for the second test is drawn. Of course, to reduce the number of operations of the sampling module, it is also possible to directly draw the blood sample required for multiple tests.

[0044] In one embodiment, determining the blood extraction volume based on the detection mode and the detection items, and extracting blood from the sample injection module based on the blood extraction volume, includes: when the detection mode is a composite parallel detection mode, obtaining the blood volume required for each detection item, and summing the blood volumes required for multiple detection items to obtain the total blood volume; extracting blood from the sample injection module based on the total blood volume; and transmitting the extracted blood to the corresponding detection module for blood testing, including: sequentially transmitting the total extracted blood volume to multiple detection modules and allocating the blood volume required for the corresponding detection items to each detection module.

[0045] When the testing mode is a composite parallel mode, in order to save time, a single blood extraction is adopted, that is, the total amount of blood required for each test item is extracted at once, and then the total amount of blood collected is transported from the sample injection module to each test module in sequence, and allocated to each test module according to the amount of blood required for the corresponding test item.

[0046] In one embodiment, the blood testing device further includes a waste liquid discharge module; the method further includes: transmitting the waste liquid generated after blood testing by each testing module to the waste liquid discharge module for processing. Of course, multiple testing modules can share a single waste liquid discharge module; alternatively, the waste liquid discharge module can include at least two waste liquid discharge sub-modules, which helps reduce the length of the waste liquid pipeline and facilitates the layout of different testing modules.

[0047] In one embodiment, the plurality of detection modules include: a routine blood count detection module and a glycated blood glucose detection module.

[0048] Specifically, based on the routine blood test module and the glycated blood glucose test module, multiple test modes can be preset, such as... Figure 2 The diagram shows multiple testing modes. These are categorized as: glycated blood glucose (GG) mode alone, complete blood count (CBC) mode alone, CBC-GG combined mode, CBC-GG combined mode under specific conditions, and pregnancy testing mode.

[0049] The three modes are: **Standard Glycation Mode:** This refers to performing glycation testing alone, which can be further divided into three different tests: standard glycation test, glycation variation test, and thalassemia test. **Standard Complete Blood Count (CBC) Test:** This refers to performing only a CBC. If the test results are abnormal, a risk warning will be issued. **CBC-Glycation Combined Mode:** This means performing a single sample and simultaneously conducting CBC and glycation tests (the glycation test can be either a standard glycation test or a glycation variation test). **CBC-Glycation Combined Conditional Mode:** This involves performing a CBC first and conducting a preliminary analysis of the results. When MCV and MCH reach the warning range, a warning message is issued; and based on the warning message, a blood sample is directly collected from that sample for thalassemia testing, avoiding the inconvenience of repeated registration and blood draws. **Pregnancy Test Mode:** This means performing a single sample and simultaneously conducting CBC and thalassemia testing.

[0050] like Figure 3 As shown, in one embodiment, a blood testing device is proposed, the blood testing device including: a controller 302 and a plurality of testing modules 304, the controller being connected to each testing module, and different testing modules corresponding to different testing items;

[0051] The controller 302 is used to receive blood testing instructions, which carry testing indication information. Based on the testing indication information, the controller determines the testing mode and the corresponding testing items, and controls the testing module 304 to test the blood according to the testing mode and the testing items.

[0052] In one embodiment, when the detection mode is a composite parallel detection mode, there are multiple corresponding detection items, and the controller is further configured to perform parallel detection using a detection module corresponding to each detection item.

[0053] In one embodiment, the controller is further configured to, when the detection mode is a composite condition detection mode, determine the execution order of multiple detection items; obtain a first detection item in sequence, take the first detection item as the current detection item, perform detection using the detection module corresponding to the current detection item, obtain a detection result, and determine whether to execute the next detection item based on the detection result; if so, obtain a second detection item, take the second detection item as the current detection item, and proceed to the step of performing detection using the detection module corresponding to the detection item, until all detection items are executed; if it is determined based on the detection result that the next detection item should not be executed, then the detection ends.

[0054] The execution order is preset, and different detection modes have different preset detection orders. Therefore, after obtaining the detection mode, the corresponding execution order can be obtained according to the detection mode.

[0055] In one embodiment, the controller is further configured to, when the detection mode is a single-item detection mode, use a detection module corresponding to a single detection item to detect the blood, obtain the detection result, determine whether there is a risk based on the detection result, and if so, issue a corresponding risk warning message.

[0056] In one embodiment, the controller is further configured to acquire detection parameters corresponding to the detection item, and perform detection using the determined detection module according to the detection parameters.

[0057] like Figure 4 As shown, in one embodiment, the blood testing device further includes: a sample injection module 306;

[0058] The controller is also used to determine the blood extraction volume according to the detection mode and the detection item, extract blood from the sample injection module according to the blood extraction volume, and transmit the extracted blood to the corresponding detection module for blood detection.

[0059] In one embodiment, the controller is further configured to, when the detection mode is a composite parallel detection mode, obtain the blood volume required for each detection item, accumulate the blood volumes required for multiple detection items to obtain the total blood volume; extract blood from the sample injection module according to the total blood volume; and sequentially transmit the extracted total blood volume to multiple detection modules, allocating the blood volume required for the corresponding detection item to each detection module.

[0060] like Figure 5 As shown, in one embodiment, the blood testing device further includes a waste liquid discharge module 308; the controller is also used to transmit the waste liquid generated after each testing module performs blood testing to the waste liquid discharge module for processing.

[0061] like Figure 6 As shown, in one embodiment, the plurality of detection modules include: a routine blood count detection module and a glycated blood glucose detection module.

[0062] Figure 7 An internal structural diagram of a blood testing device in one embodiment is shown. Figure 7 As shown, the blood testing device includes a processor (controller), multiple testing modules, and a memory connected via a system bus. The memory includes a non-volatile storage medium and internal memory. The non-volatile storage medium stores an operating system and may also store a computer program. When executed by the processor, this computer program enables the processor to implement the blood testing method. The internal memory may also store a computer program, which, when executed by the processor, enables the processor to perform the blood testing method. Those skilled in the art will understand that... Figure 7 The structure shown is merely a block diagram of a portion of the structure related to the present application and does not constitute a limitation on the blood testing device to which the present application is applied. A specific blood testing device may include more or fewer components than those shown in the figure, or combine certain components, or have different component arrangements.

[0063] A blood testing device includes a memory, a processor, and multiple testing modules. The memory stores a computer program, which, when executed by the processor, causes the processor to perform the following steps: receiving a blood testing instruction, the blood testing instruction carrying testing indication information; determining a testing mode and corresponding testing items based on the testing indication information; and using a testing module corresponding to the testing item to test the blood according to the testing mode.

[0064] In one embodiment, the step of using a detection module corresponding to the detection item to test the blood according to the detection mode includes: when the detection mode is a composite parallel detection mode, there are multiple corresponding detection items; and parallel detection is performed using a detection module corresponding to each detection item.

[0065] In one embodiment, blood is tested using a detection module corresponding to the detection item according to the detection mode, including: when the detection mode is a composite condition detection mode, determining the execution order of multiple detection items; obtaining a first detection item in sequence, taking the first detection item as the current detection item, performing detection using a detection module corresponding to the current detection item, obtaining a detection result, and determining whether to execute the next detection item based on the detection result; if so, obtaining a second detection item, taking the second detection item as the current detection item, and proceeding to the step of performing detection using a detection module corresponding to the detection item, until all detection items are executed; if it is determined based on the detection result that the next detection item should not be executed, the detection ends.

[0066] In one embodiment, the step of using a detection module corresponding to the detection item to test the blood according to the detection mode includes: when the detection mode is a single-item detection mode, using a detection module corresponding to a single detection item to test the blood, obtaining the detection result, determining whether there is a risk based on the detection result, and if so, issuing a corresponding risk warning message.

[0067] In one embodiment, the step of using a detection module corresponding to the detection item to test the blood according to the detection mode includes: obtaining detection parameters corresponding to the detection item; and using the determined detection module to perform the detection according to the detection parameters.

[0068] In one embodiment, the blood testing device further includes: a sample injection module; the step of using a testing module corresponding to the testing item according to the testing mode to test the blood includes: determining the blood extraction volume according to the testing mode and the testing item, extracting blood from the sample injection module according to the blood extraction volume, and transmitting the extracted blood to the corresponding testing module for blood testing.

[0069] In one embodiment, determining the blood extraction volume based on the detection mode and the detection items, and extracting blood from the sample injection module based on the blood extraction volume, includes: when the detection mode is a composite parallel detection mode, obtaining the blood volume required for each detection item, and summing the blood volumes required for multiple detection items to obtain the total blood volume; extracting blood from the sample injection module based on the total blood volume; and transmitting the extracted blood to the corresponding detection module for blood testing, including: sequentially transmitting the total extracted blood volume to multiple detection modules and allocating the blood volume required for the corresponding detection items to each detection module.

[0070] In one embodiment, the blood testing device further includes a waste liquid discharge module; when the computer program is executed by the processor, it is also used to perform the following steps: transmitting the waste liquid generated after each testing module performs blood testing to the waste liquid discharge module for processing.

[0071] In one embodiment, the plurality of detection modules include: a routine blood count detection module and a glycated blood glucose detection module.

[0072] A computer-readable storage medium storing a computer program, which, when executed by a processor, causes the processor to perform the following steps: receiving a blood testing instruction, the blood testing instruction carrying testing indication information; determining a testing mode and a corresponding testing item based on the testing indication information; and performing blood testing using a testing module corresponding to the testing item based on the testing mode.

[0073] In one embodiment, the step of using a detection module corresponding to the detection item to test the blood according to the detection mode includes: when the detection mode is a composite parallel detection mode, there are multiple corresponding detection items; and parallel detection is performed using a detection module corresponding to each detection item.

[0074] In one embodiment, blood is tested using a detection module corresponding to the detection item according to the detection mode, including: when the detection mode is a composite condition detection mode, determining the execution order of multiple detection items; obtaining a first detection item in sequence, taking the first detection item as the current detection item, performing detection using a detection module corresponding to the current detection item, obtaining a detection result, and determining whether to execute the next detection item based on the detection result; if so, obtaining a second detection item, taking the second detection item as the current detection item, and proceeding to the step of performing detection using a detection module corresponding to the detection item, until all detection items are executed; if it is determined based on the detection result that the next detection item should not be executed, the detection ends.

[0075] In one embodiment, the step of using a detection module corresponding to the detection item to test the blood according to the detection mode includes: when the detection mode is a single-item detection mode, using a detection module corresponding to a single detection item to test the blood, obtaining the detection result, determining whether there is a risk based on the detection result, and if so, issuing a corresponding risk warning message.

[0076] In one embodiment, the step of using a detection module corresponding to the detection item to test the blood according to the detection mode includes: obtaining detection parameters corresponding to the detection item; and using the determined detection module to perform the detection according to the detection parameters.

[0077] In one embodiment, the blood testing device further includes: a sample injection module; the step of using a testing module corresponding to the testing item according to the testing mode to test the blood includes: determining the blood extraction volume according to the testing mode and the testing item, extracting blood from the sample injection module according to the blood extraction volume, and transmitting the extracted blood to the corresponding testing module for blood testing.

[0078] In one embodiment, determining the blood extraction volume based on the detection mode and the detection items, and extracting blood from the sample injection module based on the blood extraction volume, includes: when the detection mode is a composite parallel detection mode, obtaining the blood volume required for each detection item, and summing the blood volumes required for multiple detection items to obtain the total blood volume; extracting blood from the sample injection module based on the total blood volume; and transmitting the extracted blood to the corresponding detection module for blood testing, including: sequentially transmitting the total extracted blood volume to multiple detection modules and allocating the blood volume required for the corresponding detection items to each detection module.

[0079] In one embodiment, the blood testing device further includes a waste liquid discharge module; when the computer program is executed by the processor, it is also used to perform the following steps: transmitting the waste liquid generated after each testing module performs blood testing to the waste liquid discharge module for processing.

[0080] In one embodiment, the plurality of detection modules include: a routine blood count detection module and a glycated blood glucose detection module.

[0081] Those skilled in the art will understand that all or part of the processes in the above embodiments can be implemented by a computer program instructing related hardware. The program can be stored in a non-volatile computer-readable storage medium, and when executed, it can include the processes of the embodiments described above. Any references to memory, storage, databases, or other media used in the embodiments provided in this application can include non-volatile and / or volatile memory. Non-volatile memory can include read-only memory (ROM), programmable ROM (PROM), electrically programmable ROM (EPROM), electrically erasable programmable ROM (EEPROM), or flash memory. Volatile memory can include random access memory (RAM) or external cache memory. By way of illustration and not limitation, RAM is available in various forms, such as static RAM (SRAM), dynamic RAM (DRAM), synchronous DRAM (SDRAM), dual data rate SDRAM (DDRSDRAM), enhanced SDRAM (ESDRAM), synchronous link DRAM (SLDRAM), RAMbus direct RAM (RDRAM), direct memory bus dynamic RAM (DRDRAM), and RAMbus dynamic RAM (RDRAM), etc.

[0082] The technical features of the above embodiments can be combined in any way. For the sake of brevity, not all possible combinations of the technical features in the above embodiments are described. However, as long as there is no contradiction in the combination of these technical features, they should be considered to be within the scope of this specification.

[0083] The embodiments described above are merely illustrative of several implementation methods of this application, and while the descriptions are specific and detailed, they should not be construed as limiting the scope of this patent application. It should be noted that those skilled in the art can make various modifications and improvements without departing from the concept of this application, and these all fall within the protection scope of this application. Therefore, the protection scope of this patent application should be determined by the appended claims.

Claims

1. A blood testing method, characterized in that, The method is applied to a blood testing device, which includes multiple testing modules, each corresponding to a different testing item. The method includes: Receive a blood test instruction, wherein the blood test instruction carries test indication information; The detection mode and corresponding detection items are determined based on the detection indication information. The detection mode is used to indicate the order in which the detection items are executed. The blood is tested using a detection module corresponding to the detection item according to the detection mode; According to the detection mode, the blood is tested using a detection module corresponding to the detection item, including: When the detection mode is a composite condition detection mode, the execution order of multiple detection items is determined; The first detection item is obtained in sequence, and the first detection item is taken as the current detection item. The detection module corresponding to the current detection item is used to perform the detection to obtain the detection result. Based on the detection result, it is determined whether to execute the next detection item. If so, then obtain the second detection item, take the second detection item as the current detection item, and proceed to the step of using the detection module corresponding to the detection item to perform the detection, until all detection items have been executed; If the test results determine that the next test item will not be performed, the test ends. The composite condition testing mode refers to a testing mode involving multiple testing items. During testing, whether a subsequent testing item is executed depends on the test result of the previous testing item. If the test result of the previous testing item is normal, there is no need to proceed with the next testing item. If the test result of the previous testing item is abnormal or indicates the need for further testing of the next testing item, then the next testing item needs to be executed.

2. The method according to claim 1, characterized in that, The step of using a detection module corresponding to the detection item to test the blood according to the detection mode includes: When the detection mode is a composite parallel detection mode, there are multiple corresponding detection items; Parallel testing is performed using the detection module corresponding to each detection item.

3. The method according to claim 1, characterized in that, The step of using a detection module corresponding to the detection item to test the blood according to the detection mode includes: When the detection mode is a single-item detection mode, the blood is tested using a detection module corresponding to a single detection item to obtain the test results. Based on the test results, it is determined whether there is a risk. If so, a corresponding risk warning message is issued.

4. The method according to claim 1, characterized in that, The step of using a detection module corresponding to the detection item to test the blood according to the detection mode includes: Obtain the detection parameters corresponding to the detection items; The detection is performed using the determined detection module based on the detection parameters.

5. The method according to claim 1, characterized in that, The blood testing device also includes: a sample injection module; The step of using a detection module corresponding to the detection item to test the blood according to the detection mode includes: The blood extraction volume is determined according to the detection mode and the detection items, and blood is extracted from the sample injection module according to the blood extraction volume. The extracted blood is transmitted to the corresponding detection module for blood testing.

6. The method according to claim 5, characterized in that, The step of determining the blood extraction volume based on the detection mode and the detection items, and extracting blood from the sample injection module according to the blood extraction volume, includes: When the detection mode is a composite parallel detection mode, the blood volume required for each detection item is obtained, and the blood volumes required for multiple detection items are added together to obtain the total blood volume. Blood is extracted from the injection module according to the total blood volume; The step of transmitting the extracted blood to the corresponding detection module for blood testing includes: The total amount of blood drawn is sequentially transmitted to multiple testing modules, and the amount of blood required for each testing module for the corresponding testing item is allocated.

7. The method according to claim 1, characterized in that, The blood testing device also includes: a waste liquid discharge module; The method further includes: The waste liquid generated after each blood test by the detection module is transferred to the waste liquid discharge module for processing.

8. The method according to claim 1, characterized in that, The multiple detection modules include: a routine blood test module and a glycated blood glucose test module.

9. A blood testing device, the blood testing device comprising: The system includes a controller and multiple detection modules, with the controller connected to each detection module. Different detection modules correspond to different detection items. The controller is used to receive blood testing instructions, which carry testing indication information. Based on the testing indication information, the controller determines the testing mode and corresponding testing items. The testing mode is used to indicate the order in which the testing items are executed. Based on the testing mode and the testing items, the controller controls the testing module to test the blood. According to the detection mode, the blood is tested using a detection module corresponding to the detection item, including: When the detection mode is a composite condition detection mode, the execution order of multiple detection items is determined; The first detection item is obtained in sequence, and the first detection item is taken as the current detection item. The detection module corresponding to the current detection item is used to perform the detection to obtain the detection result. Based on the detection result, it is determined whether to execute the next detection item. If so, then obtain the second detection item, take the second detection item as the current detection item, and proceed to the step of using the detection module corresponding to the detection item to perform the detection, until all detection items have been executed; If the test results determine that the next test item will not be performed, the test ends. The composite condition testing mode refers to a testing mode involving multiple testing items. During testing, whether a subsequent testing item is executed depends on the test result of the previous testing item. If the test result of the previous testing item is normal, there is no need to proceed with the next testing item. If the test result of the previous testing item is abnormal or indicates the need for further testing of the next testing item, then the next testing item needs to be executed.

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