CN113125775A - Sample test item arrangement method and device - Google Patents
Sample test item arrangement method and device Download PDFInfo
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- CN113125775A CN113125775A CN201911416744.0A CN201911416744A CN113125775A CN 113125775 A CN113125775 A CN 113125775A CN 201911416744 A CN201911416744 A CN 201911416744A CN 113125775 A CN113125775 A CN 113125775A
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- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
- G01N35/0099—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor comprising robots or similar manipulators
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
- G01N35/00584—Control arrangements for automatic analysers
- G01N35/0092—Scheduling
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- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
- G01N35/10—Devices for transferring samples or any liquids to, in, or from, the analysis apparatus, e.g. suction devices, injection devices
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- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
- G01N35/10—Devices for transferring samples or any liquids to, in, or from, the analysis apparatus, e.g. suction devices, injection devices
- G01N35/1009—Characterised by arrangements for controlling the aspiration or dispense of liquids
- G01N35/1011—Control of the position or alignment of the transfer device
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
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Abstract
The application provides a method and a device for arranging sample test items. The method comprises the following steps: generating a preset page; determining a plurality of samples to be tested according to the state information of the diagnostic equipment; obtaining a plurality of sample test items which are required to be subjected to incubation treatment and correspond to the plurality of samples to be tested; arranging each sample test item in the reaction cups of the corresponding batch according to the incubation time corresponding to each sample test item; and marking the position of each sample test item in the reaction cup in the preset page. The test in the same incubation time period is placed on the same plate, so that the incubation time can be ensured, and the accuracy of the test result is improved.
Description
Technical Field
The present application relates to the field of medical technology, and in particular, to a method and an apparatus for arranging sample test items.
Background
With the continuous application of the diagnostic equipment, the accuracy and the detection efficiency of the sample test result can be realized.
At present, in a diagnostic apparatus, test samples are generally arranged in sequence according to whether reaction cups placed on a strip are empty or not.
However, with this arrangement, when test items with different incubation times are arranged in the reaction cups on the same strip batch, the same strip stays in the same incubation time, so that tests with different incubation times cannot be placed on the same strip, otherwise the incubation time of part of the tests is too long or not enough, and the test result is inaccurate.
Disclosure of Invention
The application provides a sample test item arrangement method and a sample test item arrangement device, which aim to solve the problem that in the prior art, the retention time of the same strip in incubation is the same, so tests with different incubation times cannot be placed on the same strip, otherwise, the incubation time of partial tests is too long or not enough, and the test result is inaccurate.
In order to solve the above problems, the present application discloses an arrangement method of sample test items, which is applied to a diagnostic device or a terminal connected to the diagnostic device, and includes:
generating a preset page;
determining a plurality of samples to be tested according to the state information of the diagnostic equipment;
obtaining a plurality of sample test items which are required to be subjected to incubation treatment and correspond to the plurality of samples to be tested;
arranging each sample test item in the reaction cups of the corresponding batch according to the incubation time corresponding to each sample test item;
and marking the position of each sample test item in the reaction cup in the preset page.
Optionally, the diagnostic apparatus comprises a plurality of strips, each strip having a plurality of reaction cups disposed thereon,
after the generating a preset page, the method further comprises:
drawing and generating a plurality of the slats and a plurality of reaction cups on each slat in the preset page;
acquiring at least two incubation periods according to the test requirements;
each of the incubation periods is set to correspond to at least one of the strips.
Optionally, the arranging each sample test item in the reaction cups of the corresponding batch according to the incubation time corresponding to each sample test item includes:
determining an incubation period for each of the sample test items based on the incubation time for that sample test item;
arranging each of the sample test items in a cuvette on at least one of the strips corresponding to the incubation period according to the incubation period corresponding to each of the sample test items.
Optionally, the arranging each of the sample test items in a reaction cup on at least one plate corresponding to the incubation period comprises:
and arranging the sample test items belonging to the at least one strip in sequence according to the state information of the reaction cups on the at least one strip.
Optionally, the diagnostic device comprises a sample application arm module,
after marking the position of each sample test item in the reaction cup in the preset page, the method further comprises the following steps:
generating a sample adding instruction corresponding to the at least one sample test item;
and sending the sample adding instruction to the diagnostic equipment, and controlling the sample adding arm module to add the test sample corresponding to the at least one sample test item into the reaction cup corresponding to the at least one sample test item by the diagnostic equipment according to the sample adding instruction and the marking position corresponding to the at least one sample test item.
Optionally, the terminal establishes a connection with the diagnostic device through a controller area network bus.
In order to solve the above problems, the present application discloses an arrangement apparatus for sample test items, which is applied to a diagnostic device or a terminal connected to the diagnostic device, and comprises:
the preset page generating module is used for generating a preset page;
the to-be-tested sample determining module is used for determining a plurality of to-be-tested samples according to the state information of the diagnostic equipment;
the sample test item acquisition module is used for acquiring a plurality of sample test items which are required to be subjected to incubation treatment and correspond to the plurality of samples to be tested;
the sample test item arrangement module is used for arranging each sample test item in the reaction cups of the corresponding batch according to the incubation time corresponding to each sample test item;
and the reaction cup position marking module is used for marking the position of the reaction cup where each sample test item is positioned in the preset page.
Optionally, the diagnostic apparatus comprises a plurality of strips, each strip having a plurality of reaction cups disposed thereon,
the device further comprises:
the lath reaction cup drawing module is used for drawing and generating a plurality of laths and a plurality of reaction cups on each lath in the preset page;
the incubation period acquisition module is used for acquiring at least two incubation periods according to the test requirement;
an incubation period setting module for setting each of said incubation periods to correspond to at least one slat.
Optionally, the sample test item arrangement module includes:
a temperature period determination unit for determining an incubation period in which the sample test item is located according to the incubation time of each sample test item;
the sample test item arrangement unit is used for arranging each sample test item in the reaction cup on at least one strip corresponding to the incubation period according to the incubation period corresponding to each sample test item.
Optionally, the sample test item arranging unit includes:
and the sample test item arrangement subunit is used for sequentially arranging the sample test items belonging to the at least one strip according to the state information of the reaction cups on the at least one strip.
Optionally, the diagnostic device comprises a sample application arm module,
the device further comprises:
the sample adding instruction generating module is used for generating a sample adding instruction corresponding to the at least one sample test item;
and the sample adding instruction sending module is used for sending the sample adding instruction to the diagnostic equipment, and the diagnostic equipment controls the sample adding arm module to add the test sample corresponding to the at least one sample test item into the reaction cup corresponding to the at least one sample test item according to the sample adding instruction and the mark position corresponding to the at least one sample test item.
Optionally, the terminal establishes a connection with the diagnostic device through a controller area network bus.
Compared with the prior art, the method has the following advantages:
the embodiment of the application provides an arrangement scheme of sample test items, which includes that a preset page is generated, a plurality of samples to be tested are determined according to state information of a diagnosis device, a plurality of sample test items which are corresponding to the plurality of samples to be tested and need to be subjected to incubation processing are obtained, the sample test items are arranged in reaction cups of corresponding batches according to incubation time corresponding to the sample test items, and the positions of the reaction cups where the sample test items are located are marked in the preset page. According to the embodiment of the application, the test in the same incubation time period is placed on the same plate strip, so that the incubation time can be ensured, and the accuracy of the test result is improved.
Drawings
Fig. 1 is a schematic structural diagram illustrating a fully automatic laser chemiluminescence detector according to an embodiment of the present disclosure;
FIG. 2 is a schematic structural diagram of a front side of a fully automatic laser chemiluminescence detector provided by an embodiment of the present application after a housing is removed;
FIG. 3 is a schematic view illustrating a structure of a fully automatic laser chemiluminescence detector according to an embodiment of the present disclosure, after a housing is removed;
fig. 4 is a schematic structural diagram illustrating a slat clamping device according to an embodiment of the present disclosure;
FIG. 5 is a flowchart illustrating steps of a method for arranging sample test items according to an embodiment of the present disclosure;
FIG. 6 is a schematic diagram of a reaction cup well provided in an embodiment of the present application;
fig. 7 is a schematic structural diagram illustrating an arrangement apparatus for sample test items according to an embodiment of the present disclosure.
Detailed Description
In order to make the aforementioned objects, features and advantages of the present application more comprehensible, the present application is described in further detail with reference to the accompanying drawings and the detailed description.
The diagnosis device in the embodiment of the present application may be described as follows by taking a fully automatic laser-activated chemiluminescence detector as an example, and then, the structure of the fully automatic laser-activated chemiluminescence detector is described as follows with reference to fig. 1, fig. 2, fig. 3, and fig. 4.
As shown in fig. 1, 2, 3 and 4, the fully automatic light-activated chemiluminescence detector may include: the device comprises a plate taking frame module 83, a pushing device 84, a sample adding arm module 4, a sample adding module 85, a sample frame module 86, an incubation module 87, a reagent module 5 and a detection module 88, wherein the plate strip 3 on the plate taking frame module 83 is pushed to the sample adding module 85 through the pushing device 84, a sample and a reagent are added into a reaction cup on the plate strip on the sample adding module 85 through the sample adding arm module 4, the plate strip on the sample adding module 85 is pushed into the incubation module 87 through the pushing device 84, and the plate strip enters the detection module 88 for detection after the incubation is finished.
Get the frame module 83 and locate the front portion of frame 2, be equipped with shell 1 in frame 2 outside, the carousel is located the rear of getting frame module 83, temperature culture module 87 is located carousel one side, sample frame module 86 and reagent module 5 are located the both sides of getting frame module 83 respectively, pusher 84 includes X to push mechanism 6 and Y to push mechanism 7, it pushes to carousel 19 through Y to push mechanism 7 to get the lath on the frame module 83, lath 3 on the carousel 19 passes through X to push mechanism 6 and gets into temperature culture module 87, get into detection module 88 after the temperature culture finishes and detect.
The incubation module 87 comprises an incubation plate 8 and a first slide mechanism by which the incubation plate 8 is slidably connected to the frame 2, the incubation plate 8 being provided with a slat clamping device 90.
The incubation module 87 comprises two incubation plates 8 arranged in parallel, and the two incubation plates are respectively connected with the frame 2 in a sliding manner through a set of first sliding mechanism, the first sliding mechanism comprises a first motor 9 and a first sliding rail 10, the incubation plates 8 are arranged on the first sliding rail 10, the first motor 9 is connected with the incubation plates 8 through a first synchronous belt 11, and the first motor 9 rotates to drive the incubation plates 8 to slide along the first sliding rail 10.
The incubation is divided into two incubation plates 87 to be respectively carried out, different times of incubation can be respectively realized, and the speed of the incubation plate 8 moving back and forth can be determined by the rotation speed of the first motor 9, so that the oscillation mixing in different degrees can be realized, and the operation is more flexible and changeable.
Next, the method for arranging the sample test items provided in the present application will be described in detail with reference to specific embodiments.
Referring to fig. 5, a flowchart illustrating steps of a method for arranging sample test items according to an embodiment of the present application is shown, where the method for arranging sample test items can be applied to a diagnostic device or a terminal connected to the diagnostic device, and specifically includes the following steps:
step 101: and generating a preset page.
In this embodiment of the application, the terminal may be a mobile electronic Device such as a mobile phone and a PAD (Portable Android Device), and may also be a Personal Computer (PC) terminal such as a desktop Computer and a notebook Computer, and specifically, may be determined according to a service requirement, which is not limited in this embodiment of the application.
The diagnostic device may be a device used in medical diagnosis or testing, including but not limited to: biochemical analyzer, chemiluminescence immunity analyzer, fluorescence immunity analyzer, immune turbidimetry analyzer, biochemical immunity integrated machine and gene sequencer. This embodiment is described in detail with a fully automatic light-activated chemiluminescent detector.
The communication connection is pre-established between the terminal and the full-automatic light-activated chemiluminescence detector, specifically, the terminal CAN be connected with the full-automatic light-activated chemiluminescence detector through a Controller Area Network (CAN) or a Network cable, and the CAN bus is connected through a serial data line through a CAN bus, a sensor, a Controller and an actuator. The network can detect and correct data errors caused by electromagnetic interference in the data transmission process according to the protocol, and the communication protocol of the network is equivalent to a data link layer in an ISO/OSI reference model.
After the terminal and the full-automatic light-activated chemical light-emitting detector are in communication connection through the CAN bus, data interaction between the terminal and the full-automatic light-activated chemical light-emitting detector CAN be realized.
The target test item refers to a test item for performing a test, and the target test item may be a hepatitis b five item, an alpha fetoprotein test item, and the like, specifically, the target test item may be determined according to business requirements, and the embodiment of the present application is not limited thereto.
The test index is an index of the target test item obtained after the target test item is tested, that is, test data obtained by testing the target test item.
After the target test item is obtained, the target test item can be tested, and after the test is completed, a test index corresponding to the target test item is obtained.
In the present application, the strip and the plurality of reaction cups on the strip can also be drawn in a preset page, and in particular, the following specific implementation manner can be combined for detailed description.
In a specific implementation manner of the present application, the diagnostic apparatus may include a plurality of strips, each strip having a plurality of reaction cups disposed thereon, and after step 102, the method may further include:
step A1: and drawing and generating a plurality of the slats and a plurality of reaction cups on each slat in the preset page.
In this application embodiment, full-automatic light-activated chemiluminescence detector can include a plurality of laths, is provided with a plurality of reaction cup holes on every lath, and a reaction cup can all be placed in every reaction cup hole, can be used for holding user's test sample in the reaction cup to accomplish the test of a user's test item.
After the preset page is generated, a plurality of strips and a plurality of reaction cups on each strip can be drawn in the preset page, as shown in fig. 6, each column of circular holes corresponds to one strip, 8 reaction cup holes are arranged on each strip, and one reaction cup can be placed in each reaction cup hole.
Step A2: at least two incubation periods were taken according to test requirements.
Step A3: each of the incubation periods is set to correspond to at least one of the strips.
In the present application, at least two incubation periods may be obtained according to the test requirement corresponding to each sample to be tested, and then, each incubation period is set to correspond to at least one slat, that is, a mapping relationship between different incubation periods and different slats is set.
After a preset page is generated, step 102 is performed.
Step 102: and determining a plurality of samples to be tested according to the state information of the diagnostic equipment.
The state information refers to information of the running state of the full-automatic light-activated chemiluminescence detector, and in the application, the state information refers to information when a test sample of a target user needs to be called to a reaction cup.
The sample to be tested refers to the sample to be tested which is placed in the sample test tube hole.
In this application, can be according to the state information of full-automatic light-activated chemiluminescence detector, determine a plurality of examination to be tested samples that need carry out the test, specifically, can determine a plurality of examination to be tested samples according to the test sample that holds in the sample test tube that places on the sample frame module.
After determining a plurality of samples to be tested according to the status information of the fully-automatic light-activated chemiluminescence detector, step 103 is executed.
Step 103: and obtaining a plurality of sample test items needing incubation processing corresponding to the plurality of samples to be tested.
In obtaining a plurality of samples to be tested, a plurality of sample test items to be subjected to an incubation process in the plurality of samples to be tested may be obtained. For example, the samples to be tested include a sample 1, a sample 2, a sample 7 and a sample 10, wherein the samples to be tested to be subjected to the incubation treatment are the sample 1, the sample 3, the sample 5, the sample 7 and the sample 9, and the sample 1, the sample 3, the sample 5, the sample 7 and the sample 9 are regarded as sample test items to be subjected to the incubation treatment.
After obtaining a plurality of sample test items to be incubated, corresponding to the plurality of samples to be tested, step 104 is performed.
Step 104: arranging each sample test item in the reaction cups of the corresponding batch according to the incubation time corresponding to each sample test item.
After obtaining a plurality of sample test items to be incubated, the sample test items may be arranged in the reaction cups of the corresponding batch according to the incubation time corresponding to each sample test item, and specifically, the following detailed description may be made in conjunction with the following specific implementation manner.
In a specific implementation manner of the present application, the step 104 may include:
substep B1: determining an incubation period for each of the sample test items based on the incubation time for that sample test item.
In an embodiment of the present application, after obtaining the incubation time for each sample test item, the incubation period in which the sample test item is located may be determined, and in turn, sub-step B2 is performed.
Substep B2: arranging each of the sample test items in a cuvette on at least one of the strips corresponding to the incubation period according to the incubation period corresponding to each of the sample test items.
After determining the incubation period of each sample test item, each sample test item may be arranged in the cuvette of at least one strip corresponding to the incubation period according to the incubation period corresponding to each sample test item and the mapping relationship between the incubation period and the at least one strip established in the above process. Specifically, the sample test items belonging to at least one strip may be sequentially arranged according to the status information of the cuvettes on at least one strip, for example, whether there is a free cuvette on the strip corresponding to the incubation period where the sample test item is located, so as to complete the arrangement of the sample test items.
Step 105: and marking the position of each sample test item in the reaction cup in the preset page.
After the sample test items are arranged in the reaction cups of the corresponding batch, the positions of the reaction cups where the sample test items are positioned can be marked in the preset page, so that the state observation of the sample test items can be realized, and the visual display of the sample test items can be realized.
The fully-automatic light-activated chemiluminescence detector can comprise a sample adding arm module, and after the position of a reaction cup where each sample test item is located is marked in a preset page, the sample adding arm module can be controlled to add a test sample into the reaction cup corresponding to each sample test item according to the marked position of each sample test item, and the detailed description can be specifically combined with the following specific implementation mode.
In a specific implementation manner of the present application, after the step 105, the method may further include:
step C1: and generating a sample adding instruction corresponding to the at least one sample test item.
In the embodiment of the present application, the sample adding instruction is an instruction to add a test sample corresponding to at least one sample test item into the cuvette.
After the position of the reaction cup where each sample test item is located is marked in the preset page, a sample adding instruction corresponding to at least one sample test item can be generated.
After the sample adding instruction corresponding to the at least one sample test item is generated, step C2 is executed.
Step C2: and sending the sample adding instruction to the diagnostic equipment, and controlling the sample adding arm module to add the test sample corresponding to the at least one sample test item into the reaction cup corresponding to the at least one sample test item by the diagnostic equipment according to the sample adding instruction and the marking position corresponding to the at least one sample test item.
After a sample adding instruction corresponding to at least one sample test item is generated, the sample adding instruction can be sent to the full-automatic light-activated chemiluminescence detector, and the full-automatic light-activated chemiluminescence detector controls the sample adding arm module to add a corresponding test sample into the reaction cup corresponding to the at least one sample test item according to the sample adding instruction and the marking position corresponding to the at least one sample test item.
According to the arrangement method of the sample test items, a preset page is generated, a plurality of samples to be tested are determined according to the state information of the diagnosis equipment, a plurality of sample test items which are corresponding to the plurality of samples to be tested and need to be subjected to incubation processing are obtained, the sample test items are arranged in reaction cups of corresponding batches according to the incubation time corresponding to the sample test items, and the positions of the reaction cups where the sample test items are located are marked in the preset page. According to the embodiment of the application, the test in the same incubation time period is placed on the same plate strip, so that the incubation time can be ensured, and the accuracy of the test result is improved.
While, for purposes of simplicity of explanation, the foregoing method embodiments have been described as a series of acts or combination of acts, it will be appreciated by those skilled in the art that the present application is not limited by the order of acts or acts described, as some steps may occur in other orders or concurrently with other steps in accordance with the application. Further, those skilled in the art should also appreciate that the embodiments described in the specification are preferred embodiments and that the acts and modules referred to are not necessarily required in this application.
Referring to fig. 7, a schematic structural diagram of an arrangement apparatus of sample test items provided in an embodiment of the present application is shown, where the arrangement apparatus of sample test items may be applied to a diagnostic device or a terminal connected to the diagnostic device, and specifically includes the following modules:
the preset page generating module 210 is configured to generate a preset page;
a to-be-tested sample determining module 220, configured to determine a plurality of to-be-tested samples according to the state information of the diagnostic apparatus;
a sample test item obtaining module 230, configured to obtain a plurality of sample test items that need to be subjected to incubation processing and correspond to the plurality of samples to be tested;
the sample test item arrangement module 240 is configured to arrange each sample test item in a corresponding batch of cuvettes according to the incubation time corresponding to each sample test item;
and the reaction cup position marking module 250 is used for marking the position of the reaction cup where each sample test item is located in the preset page.
In one particular implementation of the present application, the diagnostic device comprises a plurality of strips, each strip having a plurality of reaction cups disposed thereon,
the device further comprises:
the lath reaction cup drawing module is used for drawing and generating a plurality of laths and a plurality of reaction cups on each lath in the preset page;
the incubation period acquisition module is used for acquiring at least two incubation periods according to the test requirement;
an incubation period setting module for setting each of said incubation periods to correspond to at least one slat.
In a specific implementation manner of the present application, the sample test item arrangement module 240 includes:
a temperature period determination unit for determining an incubation period in which the sample test item is located according to the incubation time of each sample test item;
the sample test item arrangement unit is used for arranging each sample test item in the reaction cup on at least one strip corresponding to the incubation period according to the incubation period corresponding to each sample test item.
In a specific implementation manner of the present application, the sample test item arranging unit includes:
and the sample test item arrangement subunit is used for sequentially arranging the sample test items belonging to the at least one strip according to the state information of the reaction cups on the at least one strip.
In one particular implementation of the present application, the diagnostic device includes a sample application arm module,
the device further comprises:
the sample adding instruction generating module is used for generating a sample adding instruction corresponding to the at least one sample test item;
and the sample adding instruction sending module is used for sending the sample adding instruction to the diagnostic equipment, and the diagnostic equipment controls the sample adding arm module to add the test sample corresponding to the at least one sample test item into the reaction cup corresponding to the at least one sample test item according to the sample adding instruction and the mark position corresponding to the at least one sample test item.
In a specific implementation manner of the present application, the terminal establishes a connection with the diagnostic device through a controller area network bus.
The arrangement device for the sample test items, provided by the embodiment of the application, determines a plurality of samples to be tested according to the state information of the diagnostic equipment by generating a preset page, obtains a plurality of sample test items to be incubated, corresponding to the plurality of samples to be tested, arranges the sample test items in the reaction cups of the corresponding batches according to the incubation time corresponding to the sample test items, and marks the positions of the reaction cups where the sample test items are located in the preset page. According to the embodiment of the application, the test in the same incubation time period is placed on the same plate strip, so that the incubation time can be ensured, and the accuracy of the test result is improved.
Additionally, an embodiment of the present application further provides an electronic device, including: the device comprises a processor, a memory and a computer program which is stored on the memory and can run on the processor, wherein the processor realizes the arrangement method of the sample test items when executing the program.
The embodiment of the 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 program realizes the arrangement method of the sample test items.
The embodiments in the present specification are described in a progressive manner, each embodiment focuses on differences from other embodiments, and the same and similar parts among the embodiments are referred to each other.
Finally, it should also be noted that, herein, relational terms such as first and second, and the like may be used solely to distinguish one entity or action from another entity or action without necessarily requiring or implying any actual such relationship or order between such entities or actions. Also, the terms "comprises," "comprising," or any other variation thereof, are intended to cover a non-exclusive inclusion, such that a process, method, article, or apparatus that comprises a list of elements does not include only those elements but may include other elements not expressly listed or inherent to such process, method, article, or apparatus. Without further limitation, an element defined by the phrase "comprising an … …" does not exclude the presence of other like elements in a process, method, article, or apparatus that comprises the element.
The method and the device for arranging the sample test items provided by the present application are introduced in detail, and the principle and the implementation manner of the present application are explained by applying specific examples, and the description of the above examples is only used to help understanding the method and the core concept of the present application; meanwhile, for a person skilled in the art, according to the idea of the present application, there may be variations in the specific embodiments and the application scope, and in summary, the content of the present specification should not be construed as a limitation to the present application.
Claims (10)
1. A sample test item arrangement method is applied to a diagnostic device or a terminal connected with the diagnostic device, and is characterized by comprising the following steps:
generating a preset page;
determining a plurality of samples to be tested according to the state information of the diagnostic equipment;
obtaining a plurality of sample test items which are required to be subjected to incubation treatment and correspond to the plurality of samples to be tested;
arranging each sample test item in the reaction cups of the corresponding batch according to the incubation time corresponding to each sample test item;
and marking the position of each sample test item in the reaction cup in the preset page.
2. The method of claim 1, wherein the diagnostic device comprises a plurality of strips, each strip having a plurality of reaction cups disposed thereon,
after the generating a preset page, the method further comprises:
drawing and generating a plurality of the slats and a plurality of reaction cups on each slat in the preset page;
acquiring at least two incubation periods according to the test requirements;
each of the incubation periods is set to correspond to at least one of the strips.
3. The method of claim 2, wherein arranging each of the sample test items in a corresponding batch of cuvettes according to the incubation time corresponding to each of the sample test items comprises:
determining an incubation period for each of the sample test items based on the incubation time for that sample test item;
arranging each of the sample test items in a cuvette on at least one of the strips corresponding to the incubation period according to the incubation period corresponding to each of the sample test items.
4. The method of claim 3, wherein said arranging each of said sample test items in a reaction cup on at least one plate corresponding to said incubation period comprises:
and arranging the sample test items belonging to the at least one strip in sequence according to the state information of the reaction cups on the at least one strip.
5. The method of claim 1, wherein the diagnostic device comprises a sample application arm module,
after marking the position of each sample test item in the reaction cup in the preset page, the method further comprises the following steps:
generating a sample adding instruction corresponding to the at least one sample test item;
and sending the sample adding instruction to the diagnostic equipment, and controlling the sample adding arm module to add the test sample corresponding to the at least one sample test item into the reaction cup corresponding to the at least one sample test item by the diagnostic equipment according to the sample adding instruction and the marking position corresponding to the at least one sample test item.
6. The method of claim 1, wherein the terminal establishes a connection with the diagnostic device through a controller area network bus.
7. A sample test item arrangement device applied to a diagnostic device or a terminal connected with the diagnostic device is characterized by comprising:
the preset page generating module is used for generating a preset page;
the to-be-tested sample determining module is used for determining a plurality of to-be-tested samples according to the state information of the diagnostic equipment;
the sample test item acquisition module is used for acquiring a plurality of sample test items which are required to be subjected to incubation treatment and correspond to the plurality of samples to be tested;
the sample test item arrangement module is used for arranging each sample test item in the reaction cups of the corresponding batch according to the incubation time corresponding to each sample test item;
and the reaction cup position marking module is used for marking the position of the reaction cup where each sample test item is positioned in the preset page.
8. The apparatus of claim 7, wherein the diagnostic device comprises a plurality of strips, each strip having a plurality of reaction cups disposed thereon,
the device further comprises:
the lath reaction cup drawing module is used for drawing and generating a plurality of laths and a plurality of reaction cups on each lath in the preset page;
the incubation period acquisition module is used for acquiring at least two incubation periods according to the test requirement;
an incubation period setting module for setting each of said incubation periods to correspond to at least one slat.
9. The apparatus of claim 8, wherein the sample test item arrangement module comprises:
a temperature period determination unit for determining an incubation period in which the sample test item is located according to the incubation time of each sample test item;
the sample test item arrangement unit is used for arranging each sample test item in the reaction cup on at least one strip corresponding to the incubation period according to the incubation period corresponding to each sample test item.
10. The apparatus of claim 9, wherein the sample test item arranging unit comprises:
and the sample test item arrangement subunit is used for sequentially arranging the sample test items belonging to the at least one strip according to the state information of the reaction cups on the at least one strip.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201911416744.0A CN113125775A (en) | 2019-12-31 | 2019-12-31 | Sample test item arrangement method and device |
| PCT/CN2020/114207 WO2021135366A1 (en) | 2019-12-31 | 2020-09-09 | Arrangement method for sample testing items, and apparatus |
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| Application Number | Priority Date | Filing Date | Title |
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| CN201911416744.0A CN113125775A (en) | 2019-12-31 | 2019-12-31 | Sample test item arrangement method and device |
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| CN113125775A true CN113125775A (en) | 2021-07-16 |
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| CN201911416744.0A Pending CN113125775A (en) | 2019-12-31 | 2019-12-31 | Sample test item arrangement method and device |
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| CN113743912A (en) * | 2021-09-30 | 2021-12-03 | 浙江艾凯普计算机系统服务有限公司 | Electronic component reliability experiment scheduling method and device based on time |
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| CN113930331A (en) * | 2021-10-09 | 2022-01-14 | 苏州国科均豪生物科技有限公司 | Temperature control method, medium and PCR detection system for incubation of fluorescence immunoassay analyzer |
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| DE4210963A1 (en) * | 1992-04-02 | 1993-10-07 | Baxter Deutschland | Automatic device for the photometric analysis of liquid samples |
| JP2000121511A (en) * | 1998-10-13 | 2000-04-28 | Hitachi Koki Co Ltd | Automatic separation and extraction device and its control method |
| FR2893138B1 (en) * | 2005-11-10 | 2008-01-25 | Maxmat Sa Sa | AUTOMATIC BIOLOGICAL ANALYSIS APPARATUS. |
| JP2008058129A (en) * | 2006-08-31 | 2008-03-13 | Hitachi High-Technologies Corp | Autoanalyzer |
| CN101566624A (en) * | 2008-11-14 | 2009-10-28 | 北京量质科技有限公司 | Full-automatic medical inspection and detection system |
| CN102565439B (en) * | 2011-12-29 | 2013-07-24 | 长春迪瑞医疗科技股份有限公司 | Incubation part device for full-automatic chemiluminescence immunity analyzer and control method for incubation part device |
| CN107389962A (en) * | 2017-09-21 | 2017-11-24 | 苏州新波生物技术有限公司 | A kind of Full-automatic chemiluminescence immunoassay analysis meter for possessing multiple independent reaction passages |
| CN110118876A (en) * | 2018-02-06 | 2019-08-13 | 北京科美生物技术有限公司 | A kind of multiple batches of operation method |
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| CN113743912A (en) * | 2021-09-30 | 2021-12-03 | 浙江艾凯普计算机系统服务有限公司 | Electronic component reliability experiment scheduling method and device based on time |
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