WO2021135365A1 - 测试结果确定方法及装置 - Google Patents

测试结果确定方法及装置 Download PDF

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Publication number
WO2021135365A1
WO2021135365A1 PCT/CN2020/114206 CN2020114206W WO2021135365A1 WO 2021135365 A1 WO2021135365 A1 WO 2021135365A1 CN 2020114206 W CN2020114206 W CN 2020114206W WO 2021135365 A1 WO2021135365 A1 WO 2021135365A1
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Prior art keywords
test
target
calibration curve
signal value
normal
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PCT/CN2020/114206
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English (en)
French (fr)
Inventor
吴振焦
张晶鑫
吴栋杨
李临
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科美诊断技术股份有限公司
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Publication of WO2021135365A1 publication Critical patent/WO2021135365A1/zh

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    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B40/00—ICT specially adapted for biostatistics; ICT specially adapted for bioinformatics-related machine learning or data mining, e.g. knowledge discovery or pattern finding
    • G16B40/10—Signal processing, e.g. from mass spectrometry [MS] or from PCR
    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B45/00—ICT specially adapted for bioinformatics-related data visualisation, e.g. displaying of maps or networks
    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H10/00—ICT specially adapted for the handling or processing of patient-related medical or healthcare data
    • G16H10/40—ICT specially adapted for the handling or processing of patient-related medical or healthcare data for data related to laboratory analysis, e.g. patient specimen analysis

Definitions

  • This application relates to the field of medical technology, in particular to a method and device for determining test results.
  • the various processes of the diagnostic equipment are controlled by manual management, and the analysis of the test results of some special test items (such as the test items that are usually less measured, etc.) needs to be analyzed by professionals, which will undoubtedly increase human resources.
  • the input of the company has increased the labor cost, and people without professional skills cannot analyze and get the results.
  • This application provides a method and device for determining test results to solve the problem of analyzing the test results of special test items in the prior art, which needs to rely on professionals for analysis, which will undoubtedly increase the investment in human resources and increase the labor cost, and there is no Professionals are unable to analyze the problem of getting results.
  • this application discloses a method for determining test results, which is applied to a diagnostic device or a terminal connected to the diagnostic device, including:
  • the test result corresponding to the target test signal value is determined.
  • the obtaining multiple normal test samples corresponding to the target test item includes:
  • the multiple test samples are determined.
  • the obtaining a target calibration curve corresponding to the target test item based on the multiple normal test samples includes:
  • the target calibration curve is drawn in a pre-generated preset page.
  • the determining the test result corresponding to the target test signal value based on the target calibration curve includes:
  • the test result corresponding to the target test signal value is obtained by analyzing.
  • the analyzing and obtaining the test result corresponding to the target test signal value according to the display result in the preset page includes:
  • the terminal establishes a connection with the diagnostic device through a controller area network bus.
  • test result determination device which is applied to a diagnostic equipment or a terminal connected to the diagnostic equipment, and includes:
  • the target calibration curve determination module is configured to determine whether there is a target calibration curve corresponding to the target test item after obtaining the target test signal value corresponding to the target test item;
  • the normal test sample acquisition module is configured to acquire multiple normal test samples corresponding to the target test item when the target calibration curve does not exist;
  • a target calibration curve acquisition module configured to acquire a target calibration curve corresponding to the target test item based on the multiple normal test samples
  • the test result determination module is configured to determine the test result corresponding to the target test signal value based on the target calibration curve.
  • the normal test sample acquisition module includes:
  • the normal test liquid obtaining unit is used to obtain the normal sample test liquid of different doses corresponding to the target test item;
  • the test sample determining unit is configured to determine the multiple test samples according to the normal sample test liquids of different doses.
  • the target calibration curve acquisition module includes:
  • the normal data value acquisition unit is used to test different doses of normal sample test liquid to obtain multiple normal test signal values
  • the target calibration curve drawing unit is configured to draw the target calibration curve in a pre-generated preset page based on the multiple normal test signal values.
  • test result determining module includes:
  • a target calibration curve display unit configured to display the target calibration curve in a pre-generated preset page
  • the target data value display unit is configured to display the target test signal value in the preset page according to the dose of the test sample solution corresponding to the target test item;
  • the test result analysis unit is configured to analyze and obtain the test result corresponding to the target test signal value according to the display result in the preset page.
  • test result analysis unit includes:
  • the positioning data value determination subunit is used to determine the positioning test data value according to the dose of the test sample liquid and the target calibration curve;
  • the target data value determining subunit is used to determine whether the target test signal value is within the threshold interval of the positioning test data value
  • the normal test result determining subunit is configured to determine that the test result corresponding to the target test signal value is a normal test result when the target test signal value is within the threshold interval;
  • the abnormal test result determining subunit is configured to determine that the test result corresponding to the target test signal value is an abnormal test result when the target test signal value is outside the threshold interval.
  • the terminal establishes a connection with the diagnostic device through a controller area network bus.
  • this application includes the following advantages:
  • the embodiment of the present application provides a test result determination solution. After obtaining the target test signal value corresponding to the target test item, it is determined whether there is a target calibration curve corresponding to the target test item. In the case that there is no target calibration curve, Obtain multiple normal test samples corresponding to the target test item, obtain the target calibration curve corresponding to the target test item based on the multiple normal test samples, and determine the test result corresponding to the target test signal value based on the target calibration curve. The embodiment of the application determines the test result corresponding to the target test item by drawing the calibration curve of the target test item, without arranging professional and technical personnel for analysis, saving labor costs, and personnel without relevant professional skills can also directly obtain the test results. The result analysis is relatively simple.
  • FIG. 1 shows a schematic structural diagram of an automatic laser chemiluminescence detector provided by an embodiment of the present application
  • FIG. 2 shows a schematic structural view of the front side of a fully automatic laser chemiluminescence detector provided by an embodiment of the present application after the housing is removed;
  • FIG. 3 shows a schematic structural view of the reverse side of a fully automatic laser chemiluminescence detector provided by an embodiment of the present application after the housing is removed;
  • Figure 4 shows a schematic structural diagram of a slat clamping device provided by an embodiment of the present application
  • FIG. 5 shows a flow chart of the steps of a method for determining a test result provided by an embodiment of the present application
  • FIG. 6 shows a schematic structural diagram of a test result determination device provided by an embodiment of the present application.
  • Fig. 7 schematically shows a block diagram of a computing processing device for executing the method according to the present invention.
  • Fig. 8 schematically shows a storage unit for holding or carrying program codes for implementing the method according to the present invention.
  • the diagnostic equipment in the embodiments of the present application can be described as follows using a fully automatic photo-induced chemiluminescence detector as an example.
  • a fully automatic photo-induced chemiluminescence detector as an example.
  • Figure 1, Figure 2, Figure 3 and Figure 4 the structure of the fully automatic laser chemiluminescence detector The following description is made.
  • the fully automated photo-induced chemiluminescence detector can include: a plate rack module 83, a pushing device 84, a sample addition arm module 4, a sample addition module 85, a sample rack module 86, and temperature
  • Samples and reagents are added to the reaction cup on the slats, and the slats on the sample adding module 85 are pushed into the incubation module 87 through the pushing device 84, and enter the detection module 88 for detection after the incubation is completed.
  • the plate rack module 83 is installed at the front of the rack 2, the housing 1 is provided outside the rack 2, the turntable is installed behind the plate rack module 83, the incubation module 87 is installed on one side of the turntable, the sample rack module 86 and The reagent modules 5 are respectively located on both sides of the plate rack module 83.
  • the pushing device 84 includes an X-direction pushing mechanism 6 and a Y-direction pushing mechanism 7. The slats on the plate-taking rack module 83 are pushed onto the turntable 19 through the Y-direction pushing mechanism 7 , The slats 3 on the turntable 19 are pushed into the incubation module 87 through the X to the pushing mechanism 6 and enter the detection module 88 for detection after the incubation is completed.
  • the incubation module 87 includes an incubation board 8 and a first sliding mechanism.
  • the incubation board 8 is slidably connected to the frame 2 through the first sliding mechanism.
  • the incubation board 8 is provided with a slat clamping device 90.
  • the incubation module 87 includes two incubation plates 8 arranged parallel to each other, which are respectively slidably connected to the frame 2 through a set of first sliding mechanisms.
  • the first sliding mechanism includes a first motor 9 and a first sliding rail 10.
  • the incubation plates 8 is arranged on the first slide rail 10, the first motor 9 is connected to the incubation plate 8 through the first timing belt 11, and the first motor 9 rotates to drive the incubation plate 8 to slide along the first slide rail 10.
  • the incubation is divided into two incubation plates 87, which can achieve different incubation times, and the speed of the rotation of the first motor 9 can determine the speed of the incubation plate 8 to move back and forth, thereby achieving different degrees of shaking and mixing, and the operation is more flexible.
  • the method for determining a test result may be applied to a diagnostic device or a terminal connected to the diagnostic device, and specifically may include the following steps:
  • Step 101 After obtaining the target test signal value corresponding to the target test item, determine whether there is a target calibration curve corresponding to the target test item.
  • the terminal can be a mobile electronic device such as a mobile phone, a PAD (Portable Android Device, tablet computer), or a PC (Personal Computer) terminal such as a desktop computer and a notebook computer.
  • a mobile electronic device such as a mobile phone, a PAD (Portable Android Device, tablet computer), or a PC (Personal Computer) terminal such as a desktop computer and a notebook computer.
  • PAD Portable Android Device, tablet computer
  • PC Personal Computer
  • the diagnostic equipment may be equipment used in medical diagnosis or inspection, which includes but is not limited to: a biochemical analyzer, a chemiluminescence immunoassay analyzer, a fluorescence immunoassay analyzer, an immune turbidity analyzer, a biochemical immune integrated machine, and a gene sequencer.
  • a biochemical analyzer e.g., a biochemical analyzer, a chemiluminescence immunoassay analyzer, a fluorescence immunoassay analyzer, an immune turbidity analyzer, a biochemical immune integrated machine, and a gene sequencer.
  • a fully automatic photo-induced chemiluminescence detector is used to describe this embodiment in detail.
  • CAN Controller Area Network
  • the principle of CAN bus is to connect the CAN bus, sensors, controllers and actuators by serial data lines. It is more than just connecting cables in a tree structure. Its communication protocol is equivalent to the data link layer in the ISO/OSI reference model. The network can detect and correct data errors caused by electromagnetic interference during data transmission according to the protocol.
  • target test items refer to items that need to be tested with less tests.
  • the target test signal value refers to the test result signal value obtained by testing the target test item.
  • the diagnostic equipment takes a fully automatic photoinduced chemiluminescence detector as an example, as shown in Figures 2 and 3, when the detection module 88 is used After testing the target test item, a test result signal value can be obtained.
  • the target calibration curve refers to the calibration curve formed by drawing the normal test signal value corresponding to the target test item. Through the target calibration curve, the target test signal value can be determined and analyzed to determine the test result of the target test item, that is, the test result data value is obtained.
  • the target calibration curve is used to analyze the target test signal value of the target test item to determine whether the test result corresponding to the target test item is a normal result.
  • step 102 is executed.
  • Step 102 If the target calibration curve does not exist, obtain multiple normal test samples corresponding to the target test item.
  • the normal test sample refers to the test sample used to generate the target calibration curve. Multiple normal test samples are normal test samples of different doses. By testing the normal test samples, the normal test results of the target test items can be obtained.
  • the foregoing step 102 may include:
  • Sub-step A1 Obtain different doses of normal sample test liquid corresponding to the target test item.
  • the normal sample test solution refers to a sample test solution that can obtain a normal test result after testing the sample test solution corresponding to the target test item.
  • Different doses refer to different test doses, such as 1 drop of test liquid, 3 drops of test liquid, etc.
  • Sub-step A2 Determine the multiple test samples according to the different doses of the normal sample test liquid.
  • step 103 After obtaining multiple normal test samples corresponding to the target test item, step 103 is executed.
  • Step 103 Obtain a target calibration curve corresponding to the target test item based on the multiple normal test samples.
  • the multiple normal test samples can be tested separately.
  • the diagnostic equipment takes a fully automatic photo-induced chemiluminescence detector as an example, and the detection module 88 can be used to test multiple normal test samples. Test samples for testing, etc.
  • test signal value corresponding to each normal test sample can be obtained, and the target calibration curve corresponding to the target test item can be generated in combination with the test signal value.
  • target calibration curve corresponding to the target test item can be generated in combination with the test signal value.
  • the foregoing step 103 may include:
  • Sub-step B1 Test different doses of normal sample test liquid to obtain multiple normal test signal values.
  • the normal sample test solution of different doses can be tested, so that the normal sample test solution corresponding to each normal sample test solution of different doses can be obtained. Test signal value.
  • sub-step B2 After testing different doses of normal sample test solutions to obtain multiple normal test signal values, sub-step B2 is performed.
  • Sub-step B2 based on the multiple normal test signal values, draw the target calibration curve in a pre-generated preset page.
  • a preset page refers to a page that is generated in advance.
  • the preset page may be a web page or an html page, and may be specifically determined according to business requirements, which is not limited in the embodiment of the present application.
  • the target calibration curve can be drawn on the preset page in combination with the multiple normal test signal values. Specifically, first, multiple normal test signal values can be marked in the preset page, and then , Draw a smooth curve between two normal test signal values. After drawing a smooth curve between two of the multiple normal test signal values, a calibration curve can be obtained, namely the target calibration curve corresponding to the target test item.
  • step 104 After obtaining the target calibration curve corresponding to the target test item based on the multiple normal test samples, step 104 is executed.
  • Step 104 Determine a test result corresponding to the target test signal value based on the target calibration curve.
  • the test result corresponding to the target test signal value can be determined according to the target calibration curve, that is, to determine whether the result of the target test item is a normal result or an abnormal result. Specifically, it can be combined with the following specific implementations The method is described in detail.
  • the foregoing step 104 may include:
  • Sub-step C1 Display the target calibration curve in a pre-generated preset page.
  • the target calibration curve after obtaining the target calibration curve and the target test signal value corresponding to the target test item, the target calibration curve may be displayed in a preset page.
  • Sub-step C2 Display the target test signal value in the preset page according to the dose of the test sample solution corresponding to the target test item.
  • the test sample liquid refers to the test liquid corresponding to the target test item.
  • the target calibration curve displayed in the preset page is the normal test signal value displayed when the target test item is at different doses.
  • the target calibration curve is displayed in the preset page, when the target test signal value can be measured according to the target test item, the dose of the sample solution is tested, and the target test signal value is displayed in the preset page.
  • the sub-step C3 is executed.
  • Sub-step C3 According to the display result in the preset page, analyze and obtain the test result corresponding to the target test signal value.
  • the test result corresponding to the target test signal value can be obtained by analyzing the display result in the preset page.
  • the aforementioned sub-step C3 may include:
  • Sub-step D1 Determine the positioning test data value according to the dose of the test sample solution and the target calibration curve.
  • the calibration test data value refers to the test data value on the target calibration curve used for matching and positioning with the target test signal value.
  • the corresponding positioning test data value on the target calibration curve can be determined according to the dose value.
  • sub-step D2 is executed.
  • Sub-step D2 Determine whether the target test signal value is within the threshold interval of the positioning test data value.
  • the threshold interval refers to an interval preset by business personnel to determine whether the target test signal value is a normal value.
  • the specific range of the threshold interval may be determined according to business requirements, which is not limited in the embodiment of the present application.
  • the positioning test data value After the positioning test data value is determined, it can be determined whether the target test signal value is within the threshold interval of the positioning test data value.
  • sub-step D3 is executed.
  • sub-step D4 is executed.
  • Sub-step D3 when the target test signal value is within the threshold interval, determining that the test result corresponding to the target test signal value is a normal test result.
  • Sub-step D4 when the target test signal value is outside the threshold interval, it is determined that the test result corresponding to the target test signal value is an abnormal test result.
  • the test result corresponding to the target test signal value is a normal test result.
  • the test result corresponding to the target test signal value is an abnormal test result.
  • the test result corresponding to the target test item is determined by drawing the calibration curve of the target test item, without arranging professional technicians for analysis.
  • the method for determining the test result determines whether there is a target calibration curve corresponding to the target test item after obtaining the target test signal value corresponding to the target test item, and the target calibration curve is obtained when there is no target calibration curve.
  • the multiple normal test samples corresponding to the test item are based on the multiple normal test samples to obtain the target calibration curve corresponding to the target test item, and the test result corresponding to the target test signal value is determined based on the target calibration curve.
  • the embodiment of the application determines the test result corresponding to the target test item by drawing the calibration curve of the target test item, without arranging professional and technical personnel for analysis, saving labor costs, and personnel without relevant professional skills can also directly obtain the test results.
  • the result analysis is relatively simple.
  • test result determining apparatus can be applied to a diagnostic device or a terminal connected to the diagnostic device, and specifically may include the following modules:
  • the target calibration curve determination module 210 is configured to determine whether there is a target calibration curve corresponding to the target test item after obtaining the target test signal value corresponding to the target test item;
  • the normal test sample obtaining module 220 is configured to obtain multiple normal test samples corresponding to the target test item when the target calibration curve does not exist;
  • the target calibration curve acquisition module 230 is configured to acquire the target calibration curve corresponding to the target test item based on the multiple normal test samples;
  • the test result determining module 240 is configured to determine the test result corresponding to the target test signal value based on the target calibration curve.
  • the normal test sample obtaining module 220 includes:
  • the normal test liquid obtaining unit is used to obtain the normal sample test liquid of different doses corresponding to the target test item;
  • the test sample determining unit is configured to determine the multiple test samples according to the normal sample test liquids of different doses.
  • the target calibration curve acquisition module 230 includes:
  • the normal data value acquisition unit is used to test different doses of normal sample test liquid to obtain multiple normal test signal values
  • the target calibration curve drawing unit is configured to draw the target calibration curve in a pre-generated preset page based on the multiple normal test signal values.
  • test result determining module 240 includes:
  • a target calibration curve display unit configured to display the target calibration curve in a pre-generated preset page
  • the target data value display unit is configured to display the target test signal value in the preset page according to the dose of the test sample solution corresponding to the target test item;
  • the test result analysis unit is configured to analyze and obtain the test result corresponding to the target test signal value according to the display result in the preset page.
  • test result analysis unit includes:
  • the positioning data value determination subunit is used to determine the positioning test data value according to the dose of the test sample liquid and the target calibration curve;
  • the target data value determining subunit is used to determine whether the target test signal value is within the threshold interval of the positioning test data value
  • the normal test result determining subunit is configured to determine that the test result corresponding to the target test signal value is a normal test result when the target test signal value is within the threshold interval;
  • the abnormal test result determining subunit is configured to determine that the test result corresponding to the target test signal value is an abnormal test result when the target test signal value is outside the threshold interval.
  • the terminal establishes a connection with the diagnostic device through a controller area network bus.
  • the test result determining device determines whether there is a target calibration curve corresponding to the target test item after obtaining the target test signal value corresponding to the target test item, and obtains the target if there is no target calibration curve.
  • the multiple normal test samples corresponding to the test item are based on the multiple normal test samples to obtain the target calibration curve corresponding to the target test item, and the test result corresponding to the target test signal value is determined based on the target calibration curve.
  • the embodiment of the application determines the test result corresponding to the target test item by drawing the calibration curve of the target test item, without arranging professional and technical personnel for analysis, saving labor costs, and personnel without relevant professional skills can also directly obtain the test results.
  • the result analysis is relatively simple.
  • an embodiment of the present application also provides an electronic device, including: a processor, a memory, and a computer program stored on the memory and capable of running on the processor.
  • a processor executes the program, Realize the above-mentioned test result determination method.
  • the embodiment of the present application also provides a computer-readable storage medium on which a computer program is stored, and when the program is executed by a processor, the above method for determining the test result is realized.
  • the device embodiments described above are merely illustrative, where the units described as separate components may or may not be physically separated, and the components displayed as units may or may not be physical units, that is, they may be located in One place, or it can be distributed to multiple network units. Some or all of the modules can be selected according to actual needs to achieve the objectives of the solutions of the embodiments. Those of ordinary skill in the art can understand and implement it without creative work.
  • the various component embodiments of the present invention may be implemented by hardware, or by software modules running on one or more processors, or by a combination of them.
  • a microprocessor or a digital signal processor (DSP) may be used in practice to implement some or all of the functions of some or all of the components in the computing processing device according to the embodiments of the present invention.
  • DSP digital signal processor
  • the present invention can also be implemented as a device or device program (for example, a computer program and a computer program product) for executing part or all of the methods described herein.
  • Such a program for realizing the present invention may be stored on a computer-readable medium, or may have the form of one or more signals.
  • Such a signal can be downloaded from an Internet website, or provided on a carrier signal, or provided in any other form.
  • FIG. 7 shows a computing processing device that can implement the method according to the present invention.
  • the computing processing device traditionally includes a processor 1010 and a computer program product in the form of a memory 1020 or a computer readable medium.
  • the memory 1020 may be an electronic memory such as flash memory, EEPROM (Electrically Erasable Programmable Read Only Memory), EPROM, hard disk, or ROM.
  • the memory 1020 has a storage space 1030 for executing program codes 1031 of any method steps in the above methods.
  • the storage space 1030 for program codes may include various program codes 1031 respectively used to implement various steps in the above method. These program codes can be read from or written into one or more computer program products.
  • These computer program products include program code carriers such as hard disks, compact disks (CDs), memory cards, or floppy disks. Such computer program products are usually portable or fixed storage units as described with reference to FIG. 8.
  • the storage unit may have storage segments, storage spaces, etc. arranged similarly to the memory 1020 in the computing processing device of FIG. 7.
  • the program code can be compressed in an appropriate form, for example.
  • the storage unit includes computer-readable codes 1031', that is, codes that can be read by, for example, a processor such as 1010. These codes, when run by a computing processing device, cause the computing processing device to execute the method described above. The various steps.
  • any reference signs placed between parentheses should not be constructed as a limitation to the claims.
  • the word “comprising” does not exclude the presence of elements or steps not listed in the claims.
  • the word “a” or “an” preceding an element does not exclude the presence of multiple such elements.
  • the invention can be implemented by means of hardware comprising several different elements and by means of a suitably programmed computer. In the unit claims listing several devices, several of these devices may be embodied in the same hardware item.
  • the use of the words first, second, and third, etc. do not indicate any order. These words can be interpreted as names.

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Abstract

一种测试结果确定方法及装置。所述方法包括：在获取到目标测试项对应的目标测试信号值之后，确定是否存在所述目标测试项对应的目标校准曲线（101）；在不存在所述目标校准曲线的情况下，获取所述目标测试项对应的多个正常测试样本（102）；基于所述多个正常测试样本，获取所述目标测试项对应的目标校准曲线（103）；基于所述目标校准曲线，确定所述目标测试信号值对应的测试结果（104）。所述方法通过绘制目标测试项的校准曲线确定目标测试项对应的测试结果，无需安排专业技术人员进行分析，节省了人力成本，并且，没有相关专业技术的人员也可以直接获取到测试结果，结果分析较为简单。

Description

测试结果确定方法及装置
本申请要求在2019年12月31日提交中国专利局、申请号为201911423245.4、发明名称为“测试结果确定方法及装置”的中国专利申请的优先权，其全部内容通过引用结合在本申请中。
技术领域
本申请涉及医疗技术领域，特别是涉及一种测试结果确定方法及装置。
背景技术
随着诊断设备的不断应用，能够实现样本测试结果的准确性和检测高效性。
目前，诊断设备的各个流程均是由人工管理控制的，而对于某些特殊测试项(如平时测量较少的测试项等)的测试结果分析，需要依靠专业人员进行分析，无疑会增加人力资源的投入，增加了人力成本，且没有专业技术的人是无法分析得到结果的。
发明内容
本申请提供一种测试结果确定方法及装置，以解决现有技术中的对于特殊测试项的测试结果分析，需要依靠专业人员进行分析，无疑会增加人力资源的投入，增加了人力成本，且没有专业技术的人是无法分析得到结果的问题。
为了解决上述问题，本申请公开了一种测试结果确定方法，应用于诊断设备或与诊断设备连接的终端，包括：
在获取到目标测试项对应的目标测试信号值之后，确定是否存在所述目标测试项对应的目标校准曲线；
在不存在所述目标校准曲线的情况下，获取所述目标测试项对应的多个正常测试样本；
基于所述多个正常测试样本，获取所述目标测试项对应的目标校准曲线；
基于所述目标校准曲线，确定所述目标测试信号值对应的测试结果。
可选地，所述获取所述目标测试项对应的多个正常测试样本，包括：
获取所述目标测试项对应的不同剂量的正常样本测试液；
根据所述不同剂量的正常样本测试液，确定所述多个测试样本。
可选地，所述基于所述多个正常测试样本，获取所述目标测试项对应的目标校准曲线，包括：
对不同剂量的正常样本测试液进行测试，得到多个正常测试信号值；
基于所述多个正常测试信号值，在预先生成的预置页面内绘制得到所述目标校准曲线。
可选地，所述基于所述目标校准曲线，确定所述目标测试信号值对应的测试结果，包括：
在预先生成的预置页面内显示所述目标校准曲线；
根据所述目标测试项对应的测试样本液的剂量，将所述目标测试信号值显示于所述预置页面内；
根据所述预置页面内的显示结果，分析得到所述目标测试信号值对应的测试结果。
可选地，所述根据所述预置页面内的显示结果，分析得到所述目标测试信号值对应的测试结果，包括：
根据所述测试样本液的剂量和所述目标校准曲线，确定定位测试数据值；
确定所述目标测试信号值是否位于所述定位测试数据值的阈值区间内；
在所述目标测试信号值位于所述阈值区间内时，确定所述目标测试信号值对应的测试结果为正常测试结果；
在所述目标测试信号值位于所述阈值区间之外时，确定所述目标测试信号值对应的测试结果为异常测试结果。
可选地，所述终端通过控制器局域网络总线与所述诊断设备建立连接。
为了解决上述问题，本申请公开了一种测试结果确定装置，应用于诊断设备或与诊断设备连接的终端，包括：
目标校准曲线确定模块，用于在获取到目标测试项对应的目标测试信号值之后，确定是否存在所述目标测试项对应的目标校准曲线；
正常测试样本获取模块，用于在不存在所述目标校准曲线的情况下，获取所述目标测试项对应的多个正常测试样本；
目标校准曲线获取模块，用于基于所述多个正常测试样本，获取所述目标测试项对应的目标校准曲线；
测试结果确定模块，用于基于所述目标校准曲线，确定所述目标测试信号值对应的测试结果。
可选地，所述正常测试样本获取模块包括：
正常测试液获取单元，用于获取所述目标测试项对应的不同剂量的正常样本测试液；
测试样本确定单元，用于根据所述不同剂量的正常样本测试液，确定所述多个测试样本。
可选地，所述目标校准曲线获取模块包括：
正常数据值获取单元，用于对不同剂量的正常样本测试液进行测试，得到多个正常测试信号值；
目标校准曲线绘制单元，用于基于所述多个正常测试信号值，在预先生成的预置页面内绘制得到所述目标校准曲线。
可选地，所述测试结果确定模块包括：
目标校准曲线显示单元，用于在预先生成的预置页面内显示所述目标校准曲线；
目标数据值显示单元，用于根据所述目标测试项对应的测试样本液的剂量，将所述目标测试信号值显示于所述预置页面内；
测试结果分析单元，用于根据所述预置页面内的显示结果，分析得到所述目标测试信号值对应的测试结果。
可选地，所述测试结果分析单元包括：
定位数据值确定子单元，用于根据所述测试样本液的剂量和所述目标校准曲线，确定定位测试数据值；
目标数据值确定子单元，用于确定所述目标测试信号值是否位于所述定位测试数据值的阈值区间内；
正常测试结果确定子单元，用于在所述目标测试信号值位于所述阈值区间内时，确定所述目标测试信号值对应的测试结果为正常测试结果；
异常测试结果确定子单元，用于在所述目标测试信号值位于所述阈值区间之外时，确定所述目标测试信号值对应的测试结果为异常测试结果。
可选地，所述终端通过控制器局域网络总线与所述诊断设备建立连接。
与现有技术相比，本申请包括以下优点：
本申请实施例提供了一种测试结果确定方案，通过在获取到目标测试项对应的目标测试信号值之后，确定是否存在目标测试项对应的目标校准曲线，在不存在目标校准曲线的情况下，获取目标测试项对应的多个正常测试样本，基于多个正常测试样本，获取目标测试项对应的目标校准曲线，基于目标校准曲线确定目标测试信号值对应的测试结果。本申请实施例通过绘制目标测试项的校准曲线确定目标测试项对应的测试结果，无需安排专业技术人员进行分析，节省了人力成本，并且，没有相关专业技术的人员也可以直接获取到测试结果，结果分析较为简单。
上述说明仅是本发明技术方案的概述，为了能够更清楚了解本发明的技术手段，而可依照说明书的内容予以实施，并且为了让本发明的上述和其它目的、特征和优点能够更明显易懂，以下特举本发明的具体实施方式。
附图说明
为了更清楚地说明本发明实施例或现有技术中的技术方案，下面将对实施例或现有技术描述中所需要使用的附图作一简单地介绍，显而易见地，下面描述中的附图是本发明的一些实施例，对于本领域普通技术人员来讲，在不付出创造性劳动的前提下，还可以根据这些附图获得其他的附图。
图1示出了本申请实施例提供的一种全自动激光化学发光检测仪的结构示意图；
图2示出了本申请实施例提供的一种全自动激光化学发光检测仪去除外壳后正面的结构示意图；
图3示出了本申请实施例提供的一种全自动激光化学发光检测仪去除外壳后反面的结构示意图；
图4示出了本申请实施例提供的一种板条夹紧装置的结构示意图；
图5示出了本申请实施例提供的一种测试结果确定方法的步骤流程图；
图6示出了本申请实施例提供的一种测试结果确定装置的结构示意图；
图7示意性地示出了用于执行根据本发明的方法的计算处理设备的框图；以及
图8示意性地示出了用于保持或者携带实现根据本发明的方法的程序代码的存储单元。
具体实施例
为使本申请的上述目的、特征和优点能够更加明显易懂，下面结合附图和具体实施方式对本申请作进一步详细的说明。
本申请实施例中的诊断设备可以以全自动光激化学发光检测仪为例进行如下描述，接下来，结合图1、图2、图3和图4，对全自动激光化学发光检测仪的结构进行如下描述。
如图1、2、3和4所示，全自动光激化学发光检测仪可以包括：取板架模块83、推送装置84、加样臂模块4、加样模块85、样本架模块86、温育模块87、试剂模块5和检测模块88，其中，取板架模块83上的板条3通过推送装置84推送到加样模块85上，通过加样臂模块4向位于加样模块85上的板条上的反应杯内加入样本和试剂，加样模块85上的板条通过推送装置84推送进入温育模块87，在温育结束之后进入检测模块88检测。
取板架模块83设于机架2的前部，在机架2外部设有外壳1，转盘设于取板架模块83的后方，温育模块87设于转盘一侧，样本架模块86和试剂模块5分别位于取板架模块83的两侧，推送装置84包括X向推送机构6和Y向推送机构7，取板架模块83上的板条通过Y向推送机构7推送到转盘19上，转盘19上的板条3通过X向推送机构6推送进入温育模块87，在温育结束之后进入检测模块88检测。
温育模块87包括温育板8和第一滑行机构，温育板8通过第一滑行机构与机架2滑动连接，温育板8上设有板条夹紧装置90。
温育模块87包括两个相互平行设置的温育板8，分别通过一套第一滑行机构与机架2滑动连接，第一滑行机构包括第一电机9和第一滑轨10，温育板8设于第一滑轨10上，第一电机9通过第一同步带11与温育板8相连接，第一电机9转动进而带动温育板8沿着第一滑轨10滑动。
温育分两个温育板87分别进行，可以实现分别温育不同时间，并且第一电机9转动的快慢可以决定温育板8来回移动的速度，进而实现不同程度的震荡混匀，操作更加灵活多变。
接下来，结合具体实施例，针对本申请提供的测试结果确定方法进行详细描述。
参照图5，示出了本申请实施例提供的一种测试结果确定方法的步骤流程图，该测试结果确定方法可以应用于诊断设备或与诊断设备连接的终端，具体可以包括如下步骤：
步骤101：在获取到目标测试项对应的目标测试信号值之后，确定是否存在所述目标测试项对应的目标校准曲线。
在本申请实施例中，终端可以为手机、PAD(Portable Android Device，平板电脑)等移动电子设备，也可以为台式电脑、笔记本电脑等PC(Personal Computer，个人计算机)端，具体地，可以根据业务需求而定，本申请实施例对此不加以限制。
诊断设备可以为医疗诊断或检验时使用的设备，其包括但不限于：生化分析仪、化学发光免疫分析仪、荧光免疫分析仪、免疫比浊分析仪、生化免疫一体机和基因测序仪。本申请中采用全自动光激化学发光检测仪对本实施例进行详细说明。
在终端与全自动光激化学发光检测仪之间预先建立有通信连接，具体地，终端可以通过控制器局域网络总线(Controller Area Network，CAN)或网线与全自动光激化学发光检测仪连接通信连接，CAN总线原理是通过CAN总线、传感器、控制器和执行器由串行数据线连接起来。它不仅仅是将电缆按树形结构连接起来，其通信协议相当于ISO/OSI参考模型中的数据链路层，网络可根据协议探测和纠正数据传输过程中因电磁干扰而产生的数据错误。
在终端与全自动光激化学发光检测仪通过CAN总线建立通信连接之后，可以实现终端与全自动光激化学发光检测仪之间的数据交互。
在本申请中，目标测试项是指需要进行测试的平时测试较少的项目。
目标测试信号值是指对目标测试项进行测试所得到的测试结果信号值，例如，诊断设备以全自动光激化学发光检测仪为例，如图2和图3所示，在采用检测模块88对目标测试项进行测试之后，可以得到一个测试结 果信号值。
可以理解地，上述示例仅是为了更好地理解本申请实施例的技术方案而列举的示例，不作为对本申请实施例的唯一限制。
目标校准曲线是指目标测试项所对应的正常测试信号值绘制形成的校准曲线，通过目标校准曲线可以确定目标测试信号值进行分析，以确定目标测试项的测试结果，即得到测试结果数据值。
对于目标校准曲线的生成过程将在下述实施例主动进行详细描述，本申请在此不再加以赘述。
在确定存在目标测试项对应的目标校准曲线时，则采用目标校准曲线对目标测试项的目标测试信号值进行分析，以确定目标测试项对应的测试结果是否为正常结果。
而在确定终端内未保存目标测试项对应的目标校准曲线时，则执行步骤102。
步骤102：在不存在所述目标校准曲线的情况下，获取所述目标测试项对应的多个正常测试样本。
正常测试样本是指用于生成目标校准曲线的测试样本，多个正常测试样本即为不同剂量的正常测试样本，通过对正常测试样本进行测试，可以获取到目标测试项的正常测试结果。
在确定终端内不存在目标校准曲线时，则可以获取目标测试项对应的多个正常测试样本，具体地，可以结合下述具体实现方式进行详细描述。
在本申请的一种具体实现方式中，上述步骤102可以包括：
子步骤A1：获取所述目标测试项对应的不同剂量的正常样本测试液。
在本申请实施例中，正常样本测试液是指经过对目标测试项所对应的样本测试液进行测试，能够得到正常测试结果的样本测试液。
不同剂量是指不同的测试剂量，如1滴测试液、3滴测试液等。
在获取目标测试项的多个正常样本测试液时，可以获取目标测试项对应的不同剂量的正常样本测试液，进而，执行子步骤A2。
子步骤A2：根据所述不同剂量的正常样本测试液，确定所述多个测试样本。
在获取不同剂量的正常样本测试液之后，可以将不同剂量的正常样本测试液添加至反应杯内，并在不同剂量的正常样本测试液对应的反应杯内添加相应剂量的测试试剂，从而能够得到多个测试样本。
在获取目标测试项对应的多个正常测试样本之后，执行步骤103。
步骤103：基于所述多个正常测试样本，获取所述目标测试项对应的目标校准曲线。
在获取目标测试项对应的多个正常测试样本之后，可以分别对多个正常测试样本进行测试，例如，诊断设备以全自动光激化学发光检测仪为例，可以采用检测模块88对多个正常测试样本进行测试等。
在对多个正常测试样本进行测试之后，可以获取每个正常测试样本所对应的测试信号值，结合测试信号值可以生成目标测试项对应的目标校准曲线，具体地，可以结合下述具体实现方式进行详细描述。
在本申请的一种具体实现方式中，上述步骤103可以包括：
子步骤B1：对不同剂量的正常样本测试液进行测试，得到多个正常测试信号值。
在本申请实施例中，在获取目标测试项对应的不同剂量的正常样本测试项之后，可以对不同剂量的正常样本测试液进行测试，从而可以得到每个不同剂量的正常样本测试液对应的正常测试信号值。
在对不同剂量的正常样本测试液进行测试得到多个正常测试信号值之后，执行子步骤B2。
子步骤B2：基于所述多个正常测试信号值，在预先生成的预置页面内绘制得到所述目标校准曲线。
预置页面是指预先生成的页面，预置页面可以为一个web页面，也可以为一个html页面，具体地可以根据业务需求而定，本申请实施例对此不加以限制。
在获取多个正常测试信号值之后，可以结合多个正常测试信号值在预置页面内绘制得到目标校准曲线，具体地，首先，可以将多个正常测试信号值标注在预置页面内，然后，在两个正常测试信号值之间绘制一个平滑曲线，在多个正常测试信号值中两两之间绘制平滑曲线之后，可得到一个 校准曲线，即目标测试项对应的目标校准曲线。
在基于多个正常测试样本获取目标测试项对应的目标校准曲线之后，执行步骤104。
步骤104：基于所述目标校准曲线，确定所述目标测试信号值对应的测试结果。
在得到目标测试相对应的目标校准曲线之后，可以根据目标校准曲线确定目标测试信号值对应的测试结果，即判定目标测试项的结果是正常结果还是异常结果，具体地，可以结合下述具体实现方式进行详细描述。
在本申请的一种具体实现方式中，上述步骤104可以包括：
子步骤C1：在预先生成的预置页面内显示所述目标校准曲线。
在本申请实施例中，在获取到目标测试项对应的目标校准曲线和目标测试信号值之后，可以将目标校准曲线显示于预置页面内。
在预置页面内显示目标校准曲线之后，执行子步骤C2。
子步骤C2：根据所述目标测试项对应的测试样本液的剂量，将所述目标测试信号值显示于所述预置页面内。
测试样本液是指目标测试项对应的测试液。
在预置页面内显示的目标校准曲线是在目标测试项在处于不同剂量时显示的正常测试信号值。
在将目标校准曲线显示于预置页面内之后，可以根据目标测试项测得目标测试信号值时，测试样本液的剂量，将目标测试信号值显示于预置页面内。
在根据目标测试项对应的测试样本液的剂量将目标测试信号值显示于预置页面内之后，执行子步骤C3。
子步骤C3：根据所述预置页面内的显示结果，分析得到所述目标测试信号值对应的测试结果。
在将目标测试信号值和目标校准曲线显示于预置页面内之后，可以根据预置页面内的显示结果分析得到目标测试信号值对应的测试结果。
具体地，可以结合下述具体实现方式进行详细描述。
在本申请的一种具体实现方式中，上述子步骤C3可以包括：
子步骤D1：根据所述测试样本液的剂量和所述目标校准曲线，确定定位测试数据值。
在本申请实施例中，定标测试数据值是指目标校准曲线上的用于与目标测试信号值进行匹配定位的测试数据值。
在获取目标测试项的测试样本液的剂量之后，可以根据该剂量值确定出目标校准曲线上对应的定位测试数据值。
在确定出定位测试数据值之后，执行子步骤D2。
子步骤D2：确定所述目标测试信号值是否位于所述定位测试数据值的阈值区间内。
阈值区间是指由业务人员预先设置的用于判定目标测试信号值是否为正常值的区间。
对于阈值区间的具体范围可以根据业务需求而定，本申请实施例对此不加以限制。
在确定定位测试数据值之后，可以判断目标测试信号值是否位于定位测试数据值的阈值区间内。
在确定目标测试信号值位于定位测试数据值的阈值区间内时，执行子步骤D3。
在确定目标测试信号值位于定位测试数据值的阈值区间之外时，执行子步骤D4。
子步骤D3：在所述目标测试信号值位于所述阈值区间内时，确定所述目标测试信号值对应的测试结果为正常测试结果。
子步骤D4：在所述目标测试信号值位于所述阈值区间之外时，确定所述目标测试信号值对应的测试结果为异常测试结果。
在确定目标测试信号值位于定位测试数据值的阈值区间内时，则可以确定目标测试信号值对应的测试结果为正常测试结果。
而在确定目标测试信号值位于定位测试数据值的阈值区间之外时，则可以确定目标测试信号值对应的测试结果为异常测试结果。
本申请实施例通过绘制目标测试项的校准曲线确定目标测试项对应的测试结果，无需安排专业技术人员进行分析。
本申请实施例提供的测试结果确定方法，通过在获取到目标测试项对应的目标测试信号值之后，确定是否存在目标测试项对应的目标校准曲线，在不存在目标校准曲线的情况下，获取目标测试项对应的多个正常测试样本，基于多个正常测试样本，获取目标测试项对应的目标校准曲线，基于目标校准曲线确定目标测试信号值对应的测试结果。本申请实施例通过绘制目标测试项的校准曲线确定目标测试项对应的测试结果，无需安排专业技术人员进行分析，节省了人力成本，并且，没有相关专业技术的人员也可以直接获取到测试结果，结果分析较为简单。
对于前述的各方法实施例，为了简单描述，故将其都表述为一系列的动作组合，但是本领域技术人员应该知悉，本申请并不受所描述的动作顺序的限制，因为依据本申请，某些步骤可以采用其他顺序或者同时进行。其次，本领域技术人员也应该知悉，说明书中所描述的实施例均属于优选实施例，所涉及的动作和模块并不一定是本申请所必须的。
参照图6，示出了本申请实施例提供的一种测试结果确定装置的结构示意图，该测试结果确定装置可以应用于诊断设备或与诊断设备连接的终端，具体可以包括如下模块：
目标校准曲线确定模块210，用于在获取到目标测试项对应的目标测试信号值之后，确定是否存在所述目标测试项对应的目标校准曲线；
正常测试样本获取模块220，用于在不存在所述目标校准曲线的情况下，获取所述目标测试项对应的多个正常测试样本；
目标校准曲线获取模块230，用于基于所述多个正常测试样本，获取所述目标测试项对应的目标校准曲线；
测试结果确定模块240，用于基于所述目标校准曲线，确定所述目标测试信号值对应的测试结果。
可选地，所述正常测试样本获取模块220包括：
正常测试液获取单元，用于获取所述目标测试项对应的不同剂量的正常样本测试液；
测试样本确定单元，用于根据所述不同剂量的正常样本测试液，确定所述多个测试样本。
可选地，所述目标校准曲线获取模块230包括：
正常数据值获取单元，用于对不同剂量的正常样本测试液进行测试，得到多个正常测试信号值；
目标校准曲线绘制单元，用于基于所述多个正常测试信号值，在预先生成的预置页面内绘制得到所述目标校准曲线。
可选地，所述测试结果确定模块240包括：
目标校准曲线显示单元，用于在预先生成的预置页面内显示所述目标校准曲线；
目标数据值显示单元，用于根据所述目标测试项对应的测试样本液的剂量，将所述目标测试信号值显示于所述预置页面内；
测试结果分析单元，用于根据所述预置页面内的显示结果，分析得到所述目标测试信号值对应的测试结果。
可选地，所述测试结果分析单元包括：
定位数据值确定子单元，用于根据所述测试样本液的剂量和所述目标校准曲线，确定定位测试数据值；
目标数据值确定子单元，用于确定所述目标测试信号值是否位于所述定位测试数据值的阈值区间内；
正常测试结果确定子单元，用于在所述目标测试信号值位于所述阈值区间内时，确定所述目标测试信号值对应的测试结果为正常测试结果；
异常测试结果确定子单元，用于在所述目标测试信号值位于所述阈值区间之外时，确定所述目标测试信号值对应的测试结果为异常测试结果。
可选地，所述终端通过控制器局域网络总线与所述诊断设备建立连接。
本申请实施例提供的测试结果确定装置，通过在获取到目标测试项对应的目标测试信号值之后，确定是否存在目标测试项对应的目标校准曲线，在不存在目标校准曲线的情况下，获取目标测试项对应的多个正常测试样本，基于多个正常测试样本，获取目标测试项对应的目标校准曲线， 基于目标校准曲线确定目标测试信号值对应的测试结果。本申请实施例通过绘制目标测试项的校准曲线确定目标测试项对应的测试结果，无需安排专业技术人员进行分析，节省了人力成本，并且，没有相关专业技术的人员也可以直接获取到测试结果，结果分析较为简单。
另外地，本申请实施例还提供了一种电子设备，包括：处理器、存储器以及存储在所述存储器上并可在所述处理器上运行的计算机程序，所述处理器执行所述程序时实现上述测试结果确定方法。
本申请实施例还提供了一种计算机可读存储介质，其上存储有计算机程序，该程序被处理器执行时实现上述测试结果确定方法。
本说明书中的各个实施例均采用递进的方式描述，每个实施例重点说明的都是与其他实施例的不同之处，各个实施例之间相同相似的部分互相参见即可。
最后，还需要说明的是，在本文中，诸如第一和第二等之类的关系术语仅仅用来将一个实体或者操作与另一个实体或操作区分开来，而不一定要求或者暗示这些实体或操作之间存在任何这种实际的关系或者顺序。而且，术语“包括”、“包含”或者其任何其他变体意在涵盖非排他性的包含，从而使得包括一系列要素的过程、方法、商品或者设备不仅包括那些要素，而且还包括没有明确列出的其他要素，或者是还包括为这种过程、方法、商品或者设备所固有的要素。在没有更多限制的情况下，由语句“包括一个……”限定的要素，并不排除在包括所述要素的过程、方法、商品或者设备中还存在另外的相同要素。
以上对本申请所提供的一种测试结果确定方法和一种测试结果确定装置，进行了详细介绍，本文中应用了具体个例对本申请的原理及实施方式进行了阐述，以上实施例的说明只是用于帮助理解本申请的方法及其核心思想；同时，对于本领域的一般技术人员，依据本申请的思想，在具体实施方式及应用范围上均会有改变之处，综上所述，本说明书内容不应理解为对本申请的限制。
以上所描述的装置实施例仅仅是示意性的，其中所述作为分离部件说明的单元可以是或者也可以不是物理上分开的，作为单元显示的部件可以是或者也可以不是物理单元，即可以位于一个地方，或者也可以分布到多个网络单元上。可以根据实际的需要选择其中的部分或者全部模块来实现本实施例方案的目的。本领域普通技术人员在不付出创造性的劳动的情况下，即可以理解并实施。
本发明的各个部件实施例可以以硬件实现，或者以在一个或者多个处理器上运行的软件模块实现，或者以它们的组合实现。本领域的技术人员应当理解，可以在实践中使用微处理器或者数字信号处理器(DSP)来实现根据本发明实施例的计算处理设备中的一些或者全部部件的一些或者全部功能。本发明还可以实现为用于执行这里所描述的方法的一部分或者全部的设备或者装置程序(例如，计算机程序和计算机程序产品)。这样的实现本发明的程序可以存储在计算机可读介质上，或者可以具有一个或者多个信号的形式。这样的信号可以从因特网网站上下载得到，或者在载体信号上提供，或者以任何其他形式提供。
例如，图7示出了可以实现根据本发明的方法的计算处理设备。该计算处理设备传统上包括处理器1010和以存储器1020形式的计算机程序产品或者计算机可读介质。存储器1020可以是诸如闪存、EEPROM(电可擦除可编程只读存储器)、EPROM、硬盘或者ROM之类的电子存储器。存储器1020具有用于执行上述方法中的任何方法步骤的程序代码1031的存储空间1030。例如，用于程序代码的存储空间1030可以包括分别用于实现上面的方法中的各种步骤的各个程序代码1031。这些程序代码可以从一个或者多个计算机程序产品中读出或者写入到这一个或者多个计算机程序产品中。这些计算机程序产品包括诸如硬盘，紧致盘(CD)、存储卡或者软盘之类的程序代码载体。这样的计算机程序产品通常为如参考图8所述的便携式或者固定存储单元。该存储单元可以具有与图7的计算处理设备中的存储器1020类似布置的存储段、存储空间等。程序代码可以例如以适当形式进行压缩。通常，存储单元包括计算机可读代码1031’，即可以由例如诸如1010之类的处理器读取的代码，这些代码当由计算处理设备运行时，导致该计算处理设 备执行上面所描述的方法中的各个步骤。
本文中所称的“一个实施例”、“实施例”或者“一个或者多个实施例”意味着，结合实施例描述的特定特征、结构或者特性包括在本发明的至少一个实施例中。此外，请注意，这里“在一个实施例中”的词语例子不一定全指同一个实施例。
在此处所提供的说明书中，说明了大量具体细节。然而，能够理解，本发明的实施例可以在没有这些具体细节的情况下被实践。在一些实例中，并未详细示出公知的方法、结构和技术，以便不模糊对本说明书的理解。
在权利要求中，不应将位于括号之间的任何参考符号构造成对权利要求的限制。单词“包含”不排除存在未列在权利要求中的元件或步骤。位于元件之前的单词“一”或“一个”不排除存在多个这样的元件。本发明可以借助于包括有若干不同元件的硬件以及借助于适当编程的计算机来实现。在列举了若干装置的单元权利要求中，这些装置中的若干个可以是通过同一个硬件项来具体体现。单词第一、第二、以及第三等的使用不表示任何顺序。可将这些单词解释为名称。
最后应说明的是：以上实施例仅用以说明本发明的技术方案，而非对其限制；尽管参照前述实施例对本发明进行了详细的说明，本领域的普通技术人员应当理解：其依然可以对前述各实施例所记载的技术方案进行修改，或者对其中部分技术特征进行等同替换；而这些修改或者替换，并不使相应技术方案的本质脱离本发明各实施例技术方案的精神和范围。

Claims (12)

  1. 一种测试结果确定方法，应用于诊断设备或与所述诊断设备连接的终端，其特征在于，包括：
    在获取到目标测试项对应的目标测试信号值之后，确定是否存在所述目标测试项对应的目标校准曲线；
    在不存在所述目标校准曲线的情况下，获取所述目标测试项对应的多个正常测试样本；
    基于所述多个正常测试样本，获取所述目标测试项对应的目标校准曲线；
    基于所述目标校准曲线，确定所述目标测试信号值对应的测试结果。
  2. 根据权利要求1所述的方法，其特征在于，所述获取所述目标测试项对应的多个正常测试样本，包括：
    获取所述目标测试项对应的不同剂量的正常样本测试液；
    根据所述不同剂量的正常样本测试液，确定所述多个正常测试样本。
  3. 根据权利要求2所述的方法，其特征在于，所述基于所述多个正常测试样本，获取所述目标测试项对应的目标校准曲线，包括：
    对所述不同剂量的正常样本测试液进行测试，得到多个正常测试信号值；
    基于所述多个正常测试信号值，在预先生成的预置页面内绘制得到所述目标校准曲线。
  4. 根据权利要求1所述的方法，其特征在于，所述基于所述目标校准曲线，确定所述目标测试信号值对应的测试结果，包括：
    在预先生成的预置页面内显示所述目标校准曲线；
    根据所述目标测试项对应的测试样本液的剂量，将所述目标测试信号值显示于所述预置页面内；
    根据所述预置页面内的显示结果，分析得到所述目标测试信号值对应的测试结果。
  5. 根据权利要求4所述的方法，其特征在于，所述根据所述预置页面内的显示结果，分析得到所述目标测试信号值对应的测试结果， 包括：
    根据所述测试样本液的剂量和所述目标校准曲线，确定定位测试数据值；
    确定所述目标测试信号值是否位于所述定位测试数据值的阈值区间内；
    在所述目标测试信号值位于所述阈值区间内时，确定所述目标测试信号值对应的测试结果为正常测试结果；
    在所述目标测试信号值位于所述阈值区间之外时，确定所述目标测试信号值对应的测试结果为异常测试结果。
  6. 根据权利要求1所述的方法，其特征在于，所述终端通过控制器局域网络总线与所述诊断设备建立连接。
  7. 一种测试结果确定装置，应用于诊断设备或与所述诊断设备连接的终端，其特征在于，包括：
    目标校准曲线确定模块，用于在获取到目标测试项对应的目标测试信号值之后，确定是否存在所述目标测试项对应的目标校准曲线；
    正常测试样本获取模块，用于在不存在所述目标校准曲线的情况下，获取所述目标测试项对应的多个正常测试样本；
    目标校准曲线获取模块，用于基于所述多个正常测试样本，获取所述目标测试项对应的目标校准曲线；
    测试结果确定模块，用于基于所述目标校准曲线，确定所述目标测试信号值对应的测试结果。
  8. 根据权利要求7所述的装置，其特征在于，所述正常测试样本获取模块包括：
    正常测试液获取单元，用于获取所述目标测试项对应的不同剂量的正常样本测试液；
    测试样本确定单元，用于根据所述不同剂量的正常样本测试液，确定所述多个正常测试样本。
  9. 根据权利要求8所述的装置，其特征在于，所述目标校准曲线获取模块包括：
    正常数据值获取单元，用于对所述不同剂量的正常样本测试液进行测试，得到多个正常测试信号值；
    目标校准曲线绘制单元，用于基于所述多个正常测试信号值，在 预先生成的预置页面内绘制得到所述目标校准曲线。
  10. 根据权利要求7所述的装置，其特征在于，所述测试结果确定模块包括：
    目标校准曲线显示单元，用于在预先生成的预置页面内显示所述目标校准曲线；
    目标数据值显示单元，用于根据所述目标测试项对应的测试样本液的剂量，将所述目标测试信号值显示于所述预置页面内；
    测试结果分析单元，用于根据所述预置页面内的显示结果，分析得到所述目标测试信号值对应的测试结果。
  11. 一种计算机程序，包括计算机可读代码，当所述计算机可读代码在计算处理设备上运行时，导致所述计算处理设备执行根据权利要求1-6中的任一个所述的测试结果确定方法。
  12. 一种计算机可读介质，其中存储了如权利要求11所述的计算机程序。
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