CN113125777A - Sample test item arrangement method and device - Google Patents
Sample test item arrangement method and device Download PDFInfo
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- CN113125777A CN113125777A CN201911416785.XA CN201911416785A CN113125777A CN 113125777 A CN113125777 A CN 113125777A CN 201911416785 A CN201911416785 A CN 201911416785A CN 113125777 A CN113125777 A CN 113125777A
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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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- 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
- G01N35/0099—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
- 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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- 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
- G01N35/10—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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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 sample test items corresponding to a plurality of samples to be tested; obtaining at least one first sample test item needing dilution processing and at least one second sample test item needing no dilution processing in the plurality of sample test items; arranging each first sample test item and each second sample test item in reaction cups of two batches respectively; and marking a first position of the reaction cup where each first sample test item is positioned and a second position of the reaction cup where each second sample test item is positioned in the preset page. According to the method and the device, the time of the user can be saved, and the experience of the user 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.
In this arrangement, diluted items and undiluted items may be arranged on the same strip, and the undiluted items may be tested only after the diluted items are waiting for the undiluted items, which will increase the waiting time of the undiluted items, resulting in a long waiting time for the user of the undiluted items, and reduce the user experience.
Disclosure of Invention
The application provides a sample test item arrangement method and device, which are used for solving the problems that in the prior art, a non-diluted test item can be tested after waiting for the diluted test item to be diluted, the waiting time of the non-diluted test item can be increased undoubtedly, the waiting time of a user of the non-diluted test item is longer, and the user experience is reduced.
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 sample test items corresponding to a plurality of samples to be tested;
obtaining at least one first sample test item needing dilution processing and at least one second sample test item needing no dilution processing in the plurality of sample test items;
arranging each first sample test item and each second sample test item in reaction cups of two batches respectively;
and marking a first position of the reaction cup where each first sample test item is positioned and a second position of the reaction cup where each second 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,
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;
and setting a first strip corresponding to the sample test item needing dilution processing in the plurality of strips and a second strip corresponding to the sample test item not needing dilution processing.
Optionally, the arranging each of the first sample test items and each of the second sample test items in two batches of reaction cups respectively includes:
arranging the first sample test items in each reaction cup on the first strip in sequence;
and sequentially arranging the second sample test items in the reaction cups on the second strip.
Optionally, after marking a first position of the cuvette where each of the first sample test items is located and a second position of the cuvette where each of the second sample test items is located in the preset page, the method further includes:
generating a first adding instruction corresponding to the first sample test item and a second adding instruction corresponding to the second sample test item;
sending the first adding instruction and the second adding instruction to the diagnostic equipment, so that the diagnostic equipment controls the sample adding arm module to add the test sample corresponding to the first sample test item into the reaction cup corresponding to the first sample test item according to the first adding instruction and the mark position corresponding to each first sample test item; and controlling the sample adding arm module to add the test sample corresponding to the second sample test item into the reaction cup corresponding to the second sample test item by the diagnostic equipment according to the second adding instruction and the mark position corresponding to each second 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 sample test items corresponding to a plurality of samples to be tested;
the dilution test item acquisition module is used for acquiring at least one first sample test item needing dilution processing and at least one second sample test item needing no dilution processing from the plurality of sample test items;
the sample test item arrangement module is used for respectively arranging each first sample test item and each second sample test item in reaction cups of two batches;
and the reaction cup position marking module is used for marking a first position of the reaction cup where each first sample test item is positioned and a second position of the reaction cup where each second 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:
drawing and generating a plurality of the slats and a plurality of reaction cups on each slat in the preset page;
and setting a first strip corresponding to the sample test item needing dilution processing in the plurality of strips and a second strip corresponding to the sample test item not needing dilution processing.
Optionally, the sample test item arrangement module includes:
the first test item arrangement unit is used for sequentially arranging each first sample test item in each reaction cup on the first strip;
and the second test item arrangement unit is used for sequentially arranging the second sample test items in the reaction cups on the second strip.
Optionally, the apparatus further comprises:
the adding instruction generating module is used for generating a first adding instruction corresponding to the first sample test item and a second adding instruction corresponding to the second sample test item;
an adding instruction sending module, configured to send the first adding instruction and the second adding instruction to the diagnostic device, so that the diagnostic device controls the sample adding arm module to add the test sample corresponding to the first sample test item into the reaction cup corresponding to the first sample test item according to the first adding instruction and the mark position corresponding to each of the first sample test items; and controlling the sample adding arm module to add the test sample corresponding to the second sample test item into the reaction cup corresponding to the second sample test item by the diagnostic equipment according to the second adding instruction and the mark position corresponding to each second 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 the steps of determining a plurality of samples to be tested according to state information of a diagnosis device by generating a preset page, obtaining sample test items corresponding to the plurality of samples to be tested, obtaining at least one first sample test item needing dilution processing in the plurality of sample test items and at least one second sample test item needing no dilution processing, respectively arranging the first sample test items and the second sample test items in reaction cups of two batches, and marking a first position of the reaction cup where each first sample test item is located and a second position of the reaction cup where each second sample test item is located in the preset page. The embodiment of the application arranges the non-diluted test items and the diluted test items in batches, so that the problem that the non-diluted test items can be tested after waiting for the diluted test items to be diluted is solved, the waiting time of the non-diluted test items can be increased undoubtedly, the waiting time of users of the non-diluted test items is long, the user experience is reduced, the user time can be saved, and the user experience 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 fully automatic light-activated chemiluminescence detector includes a plurality of slats, each of the slats is provided with a plurality of reaction cups, 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: and setting a first strip corresponding to the sample test item needing dilution processing in the plurality of strips and a second strip corresponding to the sample test item not needing dilution processing.
The first strip means a strip corresponding to a sample test item to be subjected to dilution processing.
The second strip refers to a strip corresponding to a sample test item that does not require a dilution process.
In the application, the first lath corresponding to the sample test item needing coefficient processing in the plurality of laths and the second lath corresponding to the sample test item not needing dilution processing can be set according to the number of items needing dilution processing and the number of items not needing dilution processing in the sample test item corresponding to the sample to be tested on the full-automatic light-activated chemical luminescence detector.
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 sample test items corresponding to a plurality of samples to be tested.
After a plurality of samples to be tested are determined, a sample test item corresponding to each sample to be tested may be obtained, and it may be understood that one sample to be tested may correspond to one sample test item, and one sample to be tested may also correspond to a plurality of sample test items, and specifically, may be determined according to business requirements, which is not limited in this embodiment of the present application.
After sample test items corresponding to a plurality of samples to be tested are obtained, step 104 is executed.
Step 104: at least one first sample test item requiring dilution processing and at least one second sample test item not requiring dilution processing among the plurality of sample test items are obtained.
The first sample test item refers to a sample test item that needs to be subjected to dilution processing among the plurality of sample test items.
The second sample test item refers to a sample test item that does not require dilution processing among the plurality of sample test items.
After obtaining the sample test items corresponding to the plurality of samples to be tested, at least one first sample test item requiring dilution processing and at least one second sample test item not requiring dilution processing can be obtained from the plurality of sample test items.
After acquiring at least one first sample test item requiring dilution processing and at least one second sample test item not requiring dilution processing among the plurality of sample test items, step 105 is performed.
Step 105: arranging each of the first sample test items and each of the second sample test items in two batches of cuvettes, respectively.
After obtaining at least one first sample test item requiring dilution processing among the plurality of sample test items, and at least one second sample test item not requiring dilution processing, the first sample test items and the second sample test items may be arranged in two batches of cuvettes, respectively, and, in particular, the arrangement of the first strip corresponding to the sample test item requiring the dilution process and the second strip corresponding to the sample test item not requiring the dilution process has been set in the previous step, and then, after obtaining at least one first sample test item requiring dilution processing among the plurality of sample test items, and at least one second sample test item not requiring dilution processing, the first sample test items may be arranged in sequence in the reaction cups on the first strip and the second sample test items may be arranged in sequence in the reaction cups on the second strip.
After the first sample test items and the second sample test items are arranged in the reaction cups of the two batches, respectively, step 106 is performed.
Step 106: and marking a first position of the reaction cup where each first sample test item is positioned and a second position of the reaction cup where each second sample test item is positioned in the preset page.
The first position is the position of the cuvette where the first sample test item marked within the preset page is located.
The second position is the position of the cuvette where the second sample test item marked within the preset page is located.
After arranging the first sample test items and the second sample test items in the cuvettes of the two batches, respectively, a first position of the cuvette where the first sample test item is located may be marked in the preset page, and a second position of the cuvette where the second sample test item is located may be marked in the preset page. Therefore, the state observation of each first sample test item and each second sample test item can be realized, and the visual display of the sample test items is realized.
After the positions of the reaction cups where the first sample test items and the second sample test items are located are marked in the preset page, the full-automatic light-activated chemiluminescence detector can control the sample adding arm module to add corresponding test samples into the reaction cups corresponding to the sample test items according to the marked positions of the first sample test items and the second sample test items, and specifically, the full-automatic light-activated chemiluminescence detector can be described in detail by combining the following specific implementation modes.
In a specific implementation manner of the present application, the step 106 may include:
step B1: and generating a first adding instruction corresponding to the first sample test item and a second adding instruction corresponding to the second sample test item.
In the embodiment of the present application, the first adding instruction refers to an adding instruction corresponding to the first sample test item, that is, an instruction for adding the test sample into the corresponding reaction cup according to the first sample test item.
The second adding instruction is an adding instruction corresponding to the second sample test item, that is, an instruction for adding the test sample into the corresponding reaction cup according to the second sample test item.
After marking the first position of the reaction cup where each first sample test item is located and the second position of the reaction cup where each second sample test item is located in the preset page, a first adding instruction corresponding to the first sample test item and a second adding instruction corresponding to the second sample test item can be generated.
After the first add instruction and the second add instruction are generated, step B2 is performed.
Step B2: sending the first adding instruction and the second adding instruction to the diagnostic equipment, so that the diagnostic equipment controls the sample adding arm module to add the test sample corresponding to the first sample test item into the reaction cup corresponding to the first sample test item according to the first adding instruction and the mark position corresponding to each first sample test item; and controlling the sample adding arm module to add the test sample corresponding to the second sample test item into the reaction cup corresponding to the second sample test item by the diagnostic equipment according to the second adding instruction and the mark position corresponding to each second sample test item.
After the first adding instruction and the second adding instruction are generated, the first adding instruction and the second adding instruction can be sent to the full-automatic light-activated chemical light-emitting detector, so that the full-automatic light-activated chemical light-emitting detector controls the sample adding arm module to add the test sample corresponding to the first sample test item into the reaction cup corresponding to the first sample test item according to the first adding instruction and the marking position corresponding to each first sample test item.
And controlling the sample adding arm module to add the test sample corresponding to the second sample test item into the reaction cup corresponding to the second sample test item by the full-automatic light-activated chemical light-emitting detector according to the second adding instruction and the mark position corresponding to each second sample test item.
The embodiment of the application arranges the non-diluted test items and the diluted test items in batches, so that the problem that the non-diluted test items can be tested after waiting for the diluted test items to be diluted is solved, the waiting time of the non-diluted test items can be increased undoubtedly, the waiting time of users of the non-diluted test items is longer, and the user experience is reduced.
The arrangement method of the sample test items provided in the embodiment of the application includes the steps of generating a preset page, determining a plurality of samples to be tested according to state information of a diagnosis device, obtaining sample test items corresponding to the plurality of samples to be tested, obtaining at least one first sample test item needing dilution processing in the plurality of sample test items, and at least one second sample test item needing no dilution processing, arranging the first sample test items and the second sample test items in reaction cups of two batches respectively, and marking a first position of the reaction cup where each first sample test item is located and a second position of the reaction cup where each second sample test item is located in the preset page. The embodiment of the application arranges the non-diluted test items and the diluted test items in batches, so that the problem that the non-diluted test items can be tested after waiting for the diluted test items to be diluted is solved, the waiting time of the non-diluted test items can be increased undoubtedly, the waiting time of users of the non-diluted test items is long, the user experience is reduced, the user time can be saved, and the user experience 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 sample test items corresponding to a plurality of samples to be tested;
a dilution test item obtaining module 240, configured to obtain at least one first sample test item that needs to be subjected to dilution processing and at least one second sample test item that does not need to be subjected to dilution processing from among the plurality of sample test items;
the sample test item arrangement module 250 is configured to arrange each of the first sample test items and each of the second sample test items in two batches of cuvettes respectively;
the cuvette position marking module 260 is configured to mark a first position of a cuvette where each of the first sample test items is located and a second position of a cuvette where each of the second sample test items 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:
drawing and generating a plurality of the slats and a plurality of reaction cups on each slat in the preset page;
and setting a first strip corresponding to the sample test item needing dilution processing in the plurality of strips and a second strip corresponding to the sample test item not needing dilution processing.
In a specific implementation manner of the present application, the sample test item arrangement module 250 includes:
the first test item arrangement unit is used for sequentially arranging each first sample test item in each reaction cup on the first strip;
and the second test item arrangement unit is used for sequentially arranging the second sample test items in the reaction cups on the second strip.
In a specific implementation manner of the present application, the apparatus further includes:
the adding instruction generating module is used for generating a first adding instruction corresponding to the first sample test item and a second adding instruction corresponding to the second sample test item;
an adding instruction sending module, configured to send the first adding instruction and the second adding instruction to the diagnostic device, so that the diagnostic device controls the sample adding arm module to add the test sample corresponding to the first sample test item into the reaction cup corresponding to the first sample test item according to the first adding instruction and the mark position corresponding to each of the first sample test items; and controlling the sample adding arm module to add the test sample corresponding to the second sample test item into the reaction cup corresponding to the second sample test item by the diagnostic equipment according to the second adding instruction and the mark position corresponding to each second 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 sample test item arrangement device provided in the embodiment of the application determines a plurality of samples to be tested according to state information of a diagnostic device by generating a preset page, obtains sample test items corresponding to the plurality of samples to be tested, obtains at least one first sample test item needing dilution processing in the plurality of sample test items, and at least one second sample test item needing no dilution processing, arranges each first sample test item and each second sample test item in reaction cups of two batches respectively, and marks a first position of the reaction cup where each first sample test item is located and a second position of the reaction cup where each second sample test item is located in the preset page. The embodiment of the application arranges the non-diluted test items and the diluted test items in batches, so that the problem that the non-diluted test items can be tested after waiting for the diluted test items to be diluted is solved, the waiting time of the non-diluted test items can be increased undoubtedly, the waiting time of users of the non-diluted test items is long, the user experience is reduced, the user time can be saved, and the user experience 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 sample test items corresponding to a plurality of samples to be tested;
obtaining at least one first sample test item needing dilution processing and at least one second sample test item needing no dilution processing in the plurality of sample test items;
arranging each first sample test item and each second sample test item in reaction cups of two batches respectively;
and marking a first position of the reaction cup where each first sample test item is positioned and a second position of the reaction cup where each second sample test item is positioned 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;
and setting a first strip corresponding to the sample test item needing dilution processing in the plurality of strips and a second strip corresponding to the sample test item not needing dilution processing.
3. The method of claim 2, wherein said arranging each of said first sample test items and each of said second sample test items in two batches of cuvettes comprises:
arranging the first sample test items in each reaction cup on the first strip in sequence;
and sequentially arranging the second sample test items in the reaction cups on the second strip.
4. The method of claim 1, further comprising, after marking a first location of a cuvette in which each of the first sample test items is located and a second location of a cuvette in which each of the second sample test items is located within the preset page:
generating a first adding instruction corresponding to the first sample test item and a second adding instruction corresponding to the second sample test item;
sending the first adding instruction and the second adding instruction to the diagnostic equipment, so that the diagnostic equipment controls the sample adding arm module to add the test sample corresponding to the first sample test item into the reaction cup corresponding to the first sample test item according to the first adding instruction and the mark position corresponding to each first sample test item; and controlling the sample adding arm module to add the test sample corresponding to the second sample test item into the reaction cup corresponding to the second sample test item by the diagnostic equipment according to the second adding instruction and the mark position corresponding to each second sample test item.
5. The method of claim 1, wherein the terminal establishes a connection with the diagnostic device through a controller area network bus.
6. 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 sample test items corresponding to a plurality of samples to be tested;
the dilution test item acquisition module is used for acquiring at least one first sample test item needing dilution processing and at least one second sample test item needing no dilution processing from the plurality of sample test items;
the sample test item arrangement module is used for respectively arranging each first sample test item and each second sample test item in reaction cups of two batches;
and the reaction cup position marking module is used for marking a first position of the reaction cup where each first sample test item is positioned and a second position of the reaction cup where each second sample test item is positioned in the preset page.
7. The apparatus of claim 6, wherein the diagnostic device comprises a plurality of strips, each strip having a plurality of reaction cups disposed thereon,
the device further comprises:
drawing and generating a plurality of the slats and a plurality of reaction cups on each slat in the preset page;
and setting a first strip corresponding to the sample test item needing dilution processing in the plurality of strips and a second strip corresponding to the sample test item not needing dilution processing.
8. The apparatus of claim 7, wherein the sample test item arrangement module comprises:
the first test item arrangement unit is used for sequentially arranging each first sample test item in each reaction cup on the first strip;
and the second test item arrangement unit is used for sequentially arranging the second sample test items in the reaction cups on the second strip.
9. The apparatus of claim 6, further comprising:
the adding instruction generating module is used for generating a first adding instruction corresponding to the first sample test item and a second adding instruction corresponding to the second sample test item;
an adding instruction sending module, configured to send the first adding instruction and the second adding instruction to the diagnostic device, so that the diagnostic device controls the sample adding arm module to add the test sample corresponding to the first sample test item into the reaction cup corresponding to the first sample test item according to the first adding instruction and the mark position corresponding to each of the first sample test items; and controlling the sample adding arm module to add the test sample corresponding to the second sample test item into the reaction cup corresponding to the second sample test item by the diagnostic equipment according to the second adding instruction and the mark position corresponding to each second sample test item.
10. The apparatus of claim 6, wherein the terminal establishes a connection with the diagnostic device via a controller area network bus.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201911416785.XA CN113125777A (en) | 2019-12-31 | 2019-12-31 | Sample test item arrangement method and device |
| PCT/CN2020/114208 WO2021135367A1 (en) | 2019-12-31 | 2020-09-09 | Sample test item arrangement method and apparatus |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201911416785.XA CN113125777A (en) | 2019-12-31 | 2019-12-31 | Sample test item arrangement method and device |
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| CN113125777A true CN113125777A (en) | 2021-07-16 |
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| CN201911416785.XA Pending CN113125777A (en) | 2019-12-31 | 2019-12-31 | Sample test item arrangement method and device |
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| WO (1) | WO2021135367A1 (en) |
Cited By (1)
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|---|---|---|---|---|
| CN114609400A (en) * | 2022-05-11 | 2022-06-10 | 深圳市帝迈生物技术有限公司 | Sample distribution method, sample analyzer and storage medium |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN115617699A (en) * | 2022-12-16 | 2023-01-17 | 歌尔股份有限公司 | Product mixed line testing method, device, equipment and storage medium |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0100663B1 (en) * | 1982-07-30 | 1987-11-19 | Corning Glass Works | Dilution cups for spectrophotometer analyzer |
| CN103769022B (en) * | 2014-01-16 | 2015-10-14 | 东软安德医疗科技有限公司 | A kind of automatic biochemical analytical equipment and reaction cup group thereof |
| CN203881777U (en) * | 2014-04-01 | 2014-10-15 | 重庆科斯迈生物科技有限公司 | Reaction cup strip mounting base of chemical luminescence immunity analyzer |
| CN106706938B (en) * | 2017-02-14 | 2018-03-09 | 迈克医疗电子有限公司 | A kind of test sample method, test sample control device and sample testing system |
| CN106980024A (en) * | 2017-03-28 | 2017-07-25 | 杭州凯坤科技有限公司 | A kind of full-automatic light-induced chemiluminescent detector |
| CN207047210U (en) * | 2017-07-03 | 2018-02-27 | 北京大学人民医院 | A kind of townhouse pipe puts base |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114609400A (en) * | 2022-05-11 | 2022-06-10 | 深圳市帝迈生物技术有限公司 | Sample distribution method, sample analyzer and storage medium |
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