CN111381053A - Instrument recommendation method, in-vitro diagnosis analyzer and computer storage medium - Google Patents
Instrument recommendation method, in-vitro diagnosis analyzer and computer storage medium Download PDFInfo
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- CN111381053A CN111381053A CN201811626358.XA CN201811626358A CN111381053A CN 111381053 A CN111381053 A CN 111381053A CN 201811626358 A CN201811626358 A CN 201811626358A CN 111381053 A CN111381053 A CN 111381053A
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- 238000000338 in vitro Methods 0.000 title claims abstract description 32
- 238000000034 method Methods 0.000 title claims abstract description 29
- 238000003745 diagnosis Methods 0.000 title abstract description 8
- 238000012360 testing method Methods 0.000 claims description 87
- 238000012545 processing Methods 0.000 claims description 15
- 230000015654 memory Effects 0.000 claims description 14
- 238000004590 computer program Methods 0.000 claims description 10
- 239000000126 substance Substances 0.000 claims description 4
- 239000000523 sample Substances 0.000 description 24
- 238000004458 analytical method Methods 0.000 description 13
- 239000003153 chemical reaction reagent Substances 0.000 description 8
- 230000004907 flux Effects 0.000 description 7
- 238000003018 immunoassay Methods 0.000 description 6
- 238000010586 diagram Methods 0.000 description 5
- 230000004044 response Effects 0.000 description 4
- 230000003287 optical effect Effects 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 2
- 238000004891 communication Methods 0.000 description 2
- 208000006454 hepatitis Diseases 0.000 description 2
- 231100000283 hepatitis Toxicity 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 206010028980 Neoplasm Diseases 0.000 description 1
- 238000012742 biochemical analysis Methods 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 206010012601 diabetes mellitus Diseases 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
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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
- G01N35/00722—Communications; Identification
- G01N35/00871—Communications between instruments or with remote terminals
Abstract
The embodiment of the invention discloses an instrument recommendation method, an in-vitro diagnosis analyzer and a computer storage medium, wherein the method comprises the following steps: acquiring instrument use data; obtaining a recommended value of an instrument parameter according to the instrument use data; and obtaining recommended information of the instrument according to the recommended value of the instrument parameter. Therefore, the instrument use data necessarily meet the use requirements, and therefore instrument recommendation information meeting the requirements can be generated according to the instrument use data, and a user can obtain the appropriate instrument recommendation information.
Description
Technical Field
The present invention relates to medical instruments, and more particularly, to an instrument recommendation method, an in vitro diagnostic analyzer, and a computer storage medium.
Background
When a user purchases an instrument (such as an immunoassay analyzer or a biochemical analyzer), how to select a proper instrument is an important and complicated problem; the better the configuration of the instrument, if it exceeds the daily needs of the user, but the corresponding price will also increase; conversely, if the configuration of the instrument is lower than the user's daily requirements, the user's work may be affected, for example, if the test throughput is insufficient, or the maximum on-machine test volume is insufficient, the user's operating time may be increased, or even the daily test requirements may not be met. The user usually selects and judges a proper instrument according to manual selection, but the manual judgment method is not objective and accurate and has low efficiency.
Disclosure of Invention
The embodiment of the invention is expected to provide an instrument recommendation method, an in-vitro diagnosis analyzer and a computer storage medium, which can generate instrument recommendation information meeting requirements according to instrument use data.
The embodiment of the invention provides an instrument recommendation method, which comprises the following steps:
acquiring instrument use data;
obtaining a recommended value of an instrument parameter according to the instrument usage data;
and obtaining recommended information of the instrument according to the recommended value of the instrument parameter.
Embodiments of the present invention also desirably provide an in vitro diagnostic analyzer comprising a processor and a memory, wherein,
the memory for storing instrument usage data, recommended values for instrument parameters, and a computer program executable on the processor;
the processor is used for acquiring instrument use data; obtaining a recommended value of an instrument parameter according to the instrument usage data; and obtaining recommended information of the instrument according to the recommended value of the instrument parameter.
The embodiment of the invention also provides an in-vitro diagnosis analyzer, which comprises an acquisition unit, a processing unit and an output unit; wherein the content of the first and second substances,
the acquisition unit is used for acquiring instrument use data;
the processing unit is used for obtaining a recommended value of an instrument parameter according to the instrument using data and obtaining instrument recommended information according to the recommended value of the instrument parameter;
and the output unit outputs the recommended value of the instrument parameter or the recommended information of the instrument.
Embodiments of the present invention also desirably provide a computer storage medium having a computer program stored thereon, where the computer program is executed by a processor to implement any one of the above-mentioned instrument recommendation methods.
In the embodiment of the invention, instrument use data is acquired; obtaining a recommended value of an instrument parameter according to the instrument use data; and obtaining recommended information of the instrument according to the recommended value of the instrument parameter. Therefore, the instrument use data necessarily meet the use requirements, and therefore instrument recommendation information meeting the requirements can be generated according to the instrument use data, and a user can obtain the appropriate instrument recommendation information.
Drawings
FIG. 1 is a flow chart of an instrument recommendation method of an embodiment of the present invention;
FIG. 2 is a schematic diagram of the structure of an in vitro diagnostic analyzer according to an embodiment of the present invention;
FIG. 3 is a schematic diagram of the hardware configuration of another in vitro diagnostic analyzer according to an embodiment of the present invention;
FIG. 4 is a schematic deployment diagram of an instrument recommendation in accordance with an embodiment of the present invention;
fig. 5 is a schematic view of an interaction flow for implementing instrument recommendation in an embodiment of the present invention.
Detailed Description
The technical solution in the embodiments of the present invention will be clearly and completely described below with reference to the accompanying drawings in the embodiments of the present invention.
In the related art, when instrument recommendation is performed, manual recommendation can be performed only by sales personnel or customer service personnel, and recommendation information may be inaccurate. For example, when performing an immunoassay or biochemical recommendation, the relevant recommendation is: through oral communication between salesmen and customers, the customers orally describe the demands of the customers, and the sales recommend proper instruments for the customers through knowledge and understanding of the customers; this recommendation has several problems: 1) the customer often has an understandably deep understanding of his needs; 2) when describing the needs of a client, the client often has difficulty in speaking index quantification; 3) misunderstanding and omission possibly exist in the process of communication between the sales staff and the customers; 5) the ability of the salesperson to select the appropriate instrument depends largely on the level of knowledge of the salesperson.
In view of the above problems, an embodiment of the present invention provides an instrument recommendation method, which can be applied to an instrument or a Laboratory (clinical Laboratory) Information System (LIS); the apparatus may be an immunoassay instrument or a biochemical instrument, for example.
Fig. 1 is a flowchart of an apparatus recommendation method according to an embodiment of the present invention, and as shown in fig. 1, the flowchart may include:
step 101: instrument usage data is acquired.
In the embodiment of the invention, the instrument use data comprises the test quantity distribution information of the instrument; illustratively, the test quantity distribution information of the instrument includes at least one of: distribution information of test items of the instrument, distribution information of test time of the instrument, sample test type distribution information of the instrument, and the like.
Here, the distribution information of the test items of the instrument includes distribution of various types of test items, and may be distribution of sample test types in each cycle within a preset statistical period, for example, the average number of test samples per day in the past month is 100, where 20 samples are tested for the first test item, 30 samples are tested for the second test item, and 50 samples are tested for the third test item. The usage data of the reagent or other consumable can be counted according to the corresponding reagent or other consumable needed by each test item. In the following, the test items are exemplified, and for an immunoassay analyzer or a biochemical analyzer, the supported test items include, but are not limited to, tumor test, diabetes test, hepatitis a test, hepatitis b test, and the like.
In the embodiment of the invention, if the instrument is a biochemical analyzer, consumables required by the biochemical analyzer comprise reagents, cleaning solutions and the like required by biochemical analysis; alternatively, if the apparatus is a biochemical analyzer, consumables to be used may include reagents required for immunoassay, cuvettes, separation solutions, enhanced cleaning solutions, and the like.
The distribution information of the test Time of the instrument may include at least one of an emergency sample response Time and a sample turn-around Time (TAT), for example, when the instrument is an immunoassay analyzer or a biochemical analyzer, the emergency sample response Time indicates a Time period from the entry of the emergency sample into the clinical laboratory to the output of the result report, and the TAT indicates a Time period from the entry of the sample into the clinical laboratory to the output of the result report.
Because different types of samples have different requirements on the testing time, for example, emergency samples require results within 1 hour, common outpatient samples require results within the same day, and physical examination samples require results within 48 hours, during data statistics, different types of samples can be respectively counted, the counted sample testing type distribution information can include distribution conditions of different types of samples, for example, 100 samples are tested on average each day, wherein the number of emergency samples, the number of outpatient samples, the number of physical examination samples, and the like, and the instrument parameters need to meet the testing requirements of various types of samples.
Step 102: and obtaining a recommended value of the instrument parameter according to the instrument use data.
In the embodiment of the invention, the corresponding recommended parameters can be calculated according to the statistical use data of the instrument. For example, it can be known how many samples the instrument needs to test on average per day through statistical historical data, the test items of the samples, the type of consumables required for testing the samples, the daily consumption of each consumable, the time required for testing the samples, etc. according to the statistical data, the recommended values of corresponding instrument parameters can be calculated, and the instrument parameters include analysis speed, analysis flux, the maximum on-machine quantity of consumables, the maximum on-machine quantity of samples, etc. Wherein the analysis flux represents the number of samples analyzed per unit time; the maximum on-machine amount of the consumable materials is used for representing the maximum consumable material amount which can be accommodated by the instrument; the maximum in-machine amount of a sample represents the maximum amount of sample that the instrument can accommodate at the same time. If the more the daily sample test quantity counted by the historical data is, the more the test items are, the higher the recommended values of the parameters such as the corresponding instrument analysis speed, the analysis flux, the maximum machine quantity of the consumables, the maximum machine quantity of the samples and the like are.
In addition, factors that affect the recommended values of these instrument parameters may include statistics of emergency samples, for example, because emergency samples may require a longer test time, if there are a greater number of emergency samples, or if the emergency samples are available for a longer time, the instrument parameters may also be adjusted, for example, to provide an instrument with a higher sample test speed. It will be appreciated that the instrument usage data reflects the instrument usage requirements of the user, and thus, the recommended values of the instrument parameters derived from the instrument usage data conform to the instrument usage requirements of the user.
Step 103: and obtaining recommended information of the instrument according to the recommended value of the instrument parameter.
For the implementation manner of this step, exemplarily, the recommended value of the instrument parameter may be compared with the parameter of at least one instrument to obtain the instrument recommended information; in practice, at least one of the instruments may be an instrument that is currently on the market or is about to be on the market, so that the corresponding instrument parameter is conveniently obtained.
It can be understood that, since the recommended value of the instrument parameter meets the instrument use requirement of the user, the instrument recommendation information obtained according to the recommended value of the instrument parameter also meets the instrument use requirement of the user.
Therefore, the instrument recommendation scheme provided by the embodiment of the invention can quantify the instrument use requirements of the user in an automatic mode, and the instrument recommendation information obtained according to the quantified information (instrument use data) has objectivity and accuracy.
As an implementation manner, the following several manners may be adopted to improve data security and protect client privacy:
1) the instrument usage data is stored locally, in particular, the instrument usage data may be stored in a local device that is not connected to the network, or the software that implements the storage of the instrument usage data is offline software.
2) Encrypting the instrument usage data; here, after encrypting the instrument use data, an unauthorized person (anyone or any device other than the instrument user) cannot acquire the corresponding instrument use data
3) Disabling access to the instrument usage data by an unauthorized person by adjusting access rights to the instrument usage data; for example, the data that the sales person may obtain is only a recommended value for an instrument parameter and does not include the user's instrument usage data.
In practical applications, the steps 101 to 103 may be implemented by a Processor in an external diagnostic analyzer or LIS, and the Processor may be at least one of an Application Specific Integrated Circuit (ASIC), a Digital Signal Processor (DSP), a Digital Signal Processing Device (DSPD), a Programmable Logic Device (PLD), a Field Programmable Gate Array (FPGA), a Central Processing Unit (CPU), a controller, a microcontroller, and a microprocessor.
As an implementation manner, after obtaining the instrument recommendation information, the device recommendation information can be output or prompt information can be generated, wherein the prompt information is used for prompting to check the instrument recommendation information; in practical applications, the processor in the in-vitro diagnostic analyzer or the LIS may output the instrument recommendation information to the display, or the processor in the in-vitro diagnostic analyzer or the LIS may output the generated reminding information to the display or the alarm. Therefore, after the instrument recommendation information is output or the reminding information is generated, a user can conveniently obtain the instrument recommendation information in time.
In the embodiment of the invention, the actual working condition of the in-vitro diagnostic analyzer can be obtained by collecting the use data of the in-vitro diagnostic analyzer, whether the current in-vitro diagnostic analyzer can better meet the requirement of daily work is judged according to the actual conditions of daily working load, distribution of sample test types, test speed and the like, the proper instrument parameters are obtained according to calculation, the proper instrument is recommended, and the recommended result is objective and accurate, so that various problems caused by the fact that a user selects the wrong instrument are avoided.
On the basis of the instrument recommendation method provided by the embodiment of the invention, the embodiment of the invention also provides an in-vitro diagnosis analyzer.
Fig. 2 is a schematic diagram of a structure of an in-vitro diagnostic analyzer according to an embodiment of the present invention, and as shown in fig. 2, the in-vitro diagnostic analyzer may include an obtaining unit 201, a processing unit 202, and an output unit 203; wherein the content of the first and second substances,
an acquisition unit 201 for acquiring instrument usage data;
the processing unit 202 is configured to obtain a recommended value of an instrument parameter according to the instrument usage data, and obtain instrument recommendation information according to the recommended value of the instrument parameter;
and the output unit 203 is used for outputting the recommended value of the instrument parameter or the instrument recommended information.
In the embodiment of the present invention, the instrument usage data acquired by the acquiring unit 201 includes the test quantity distribution information of the instrument; illustratively, the test quantity distribution information of the instrument includes at least one of: distribution information of test items of the instrument, distribution information of test time of the instrument, sample test type distribution information of the instrument, and the like.
Here, the distribution information of the test items of the instrument includes distribution conditions of various types of test items, and may be distribution conditions of sample test types per cycle within a preset statistical period. The usage data of the reagent or other consumable can be counted according to the corresponding reagent or other consumable needed by each test item.
The distribution information of the test time of the instrument may include at least one of emergency sample response time, TAT.
Because different types of samples have different requirements on testing time, the different types of samples can be respectively counted during data statistics, and the counted sample testing type distribution information can include distribution conditions of the different types of samples, for example, 100 samples are tested each day on average, wherein the number of emergency samples, the number of outpatient samples, the number of physical examination samples and the like, and the instrument parameters need to meet testing requirements of various types of samples.
In the embodiment of the present invention, the processing unit 202 may calculate the corresponding recommended parameter according to the statistical data of the usage of the apparatus. For example, it can be known how many samples the instrument needs to test on average per day through statistical historical data, the test items of the samples, the type of consumables required for testing the samples, the daily consumption of each consumable, the time required for testing the samples, etc. according to the statistical data, the recommended values of corresponding instrument parameters can be calculated, and the instrument parameters include analysis speed, analysis flux, the maximum on-machine quantity of consumables, the maximum on-machine quantity of samples, etc. If the more the daily sample test quantity counted by the historical data is, the more the test items are, the higher the recommended values of the parameters such as the corresponding instrument analysis speed, the analysis flux, the maximum machine quantity of the consumables, the maximum machine quantity of the samples and the like are.
In addition, the factors affecting the recommended values of these instrument parameters also include statistical data of emergency samples, and it is understood that the instrument usage data reflects the instrument usage requirements of the user, and thus the recommended values of the instrument parameters obtained from the instrument usage data conform to the instrument usage requirements of the user.
In an embodiment, the processing unit 202 is specifically configured to obtain the recommended device information by comparing the recommended value of the device parameter with at least one device parameter.
It can be understood that, since the recommended value of the instrument parameter meets the instrument use requirement of the user, the instrument recommendation information obtained according to the recommended value of the instrument parameter also meets the instrument use requirement of the user. Therefore, the in-vitro diagnosis analyzer provided by the embodiment of the invention can quantify the use requirements of the instrument of the user in an automatic mode, and further the recommended information of the instrument obtained according to the quantified information has objectivity and accuracy.
In an embodiment, to improve data security and protect client privacy, the processing unit 202 is further configured to:
storing the instrument usage data locally;
or, encrypting the instrument usage data;
alternatively, the instrument usage data is prevented from being accessed by an unauthorized person by adjusting access rights of the instrument usage data.
In an embodiment, the output unit 203 is further configured to generate a reminding message, where the reminding message is used to remind a user of viewing recommended information of an instrument; therefore, the user can conveniently obtain the recommended information of the instrument in time.
In practical applications, the acquiring Unit 201, the processing Unit 202, and the output Unit 203 can be implemented by a CPU, a microprocessor Unit (MPU), a DSP, or an FPGA located in the in vitro diagnostic analyzer.
In addition, each functional module in this embodiment may be integrated into one processing unit, or each unit may exist alone physically, or two or more units are integrated into one unit. The integrated unit can be realized in a form of hardware or a form of a software functional module.
Based on the understanding that the technical solution of the present embodiment essentially or a part contributing to the prior art, or all or part of the technical solution may be embodied in the form of a software product stored in a storage medium, and include several instructions for causing a computer device (which may be a personal computer, a server, or a network device, etc.) or a processor (processor) to execute all or part of the steps of the method of the present embodiment. And the aforementioned storage medium includes: various media capable of storing program codes, such as a usb disk, a removable hard disk, a Read Only Memory (ROM), a Random Access Memory (RAM), a magnetic disk, or an optical disk.
Specifically, the computer program instructions corresponding to an instrument recommendation method in the present embodiment may be stored on a storage medium such as an optical disc, a hard disc, or a usb disk, and when the computer program instructions corresponding to an instrument recommendation method in the storage medium are read or executed by an electronic device, the steps of any of the instrument recommendation methods in the foregoing embodiments are implemented.
Based on the same technical concept as the previous embodiment, referring to fig. 3, another in-vitro diagnostic analyzer 30 provided by the embodiment of the present invention is shown, which may include: a memory 31 and a processor 32; wherein the content of the first and second substances,
the memory 31 for storing instrument usage data, recommended values for instrument parameters and a computer program executable on the processor;
the processor 32 is used for acquiring instrument use data; obtaining a recommended value of an instrument parameter according to the instrument usage data; and obtaining recommended information of the instrument according to the recommended value of the instrument parameter.
In practical applications, the memory 31 may be a volatile memory (RAM); or a non-volatile memory (non-volatile memory) such as a ROM, a flash memory (flash memory), a Hard Disk (Hard Disk Drive, HDD) or a Solid-State Drive (SSD); or a combination of the above types of memories and provides instructions and data to the processor 32.
The processor 32 may be at least one of ASIC, DSP, DSPD, PLD, FPGA, CPU, controller, microcontroller, and microprocessor. It will be appreciated that the electronic devices used to implement the processor functions described above may be other devices, and embodiments of the present invention are not limited in particular.
In one embodiment, the instrument usage data includes test volume distribution information for an instrument-exemplary, the test volume distribution information for the instrument includes at least one of: distribution information of test items of the instrument, distribution information of test time of the instrument, and distribution information of test sample types of the instrument.
Here, the distribution information of the test items of the instrument includes distribution conditions of various types of test items, and may be distribution conditions of sample test types per cycle within a preset statistical period. The usage data of the reagent or other consumable can be counted according to the corresponding reagent or other consumable needed by each test item.
The distribution information of the test time of the instrument may include at least one of emergency sample response time, TAT.
Because different types of samples have different requirements on testing time, the different types of samples can be respectively counted during data statistics, and the counted sample testing type distribution information can include distribution conditions of the different types of samples, for example, 100 samples are tested each day on average, wherein the number of emergency samples, the number of outpatient samples, the number of physical examination samples and the like, and the instrument parameters need to meet testing requirements of various types of samples.
In the embodiment of the present invention, the processor 32 may calculate the corresponding recommended parameter according to the statistical data of the usage of the apparatus. For example, it can be known how many samples the instrument needs to test on average per day through statistical historical data, the test items of the samples, the type of consumables required for testing the samples, the daily consumption of each consumable, the time required for testing the samples, etc. according to the statistical data, the recommended values of corresponding instrument parameters can be calculated, and the instrument parameters include analysis speed, analysis flux, the maximum on-machine quantity of consumables, the maximum on-machine quantity of samples, etc. If the more the daily sample test quantity counted by the historical data is, the more the test items are, the higher the recommended values of the parameters such as the corresponding instrument analysis speed, the analysis flux, the maximum machine quantity of the consumables, the maximum machine quantity of the samples and the like are.
In addition, the factors affecting the recommended values of these instrument parameters also include statistical data of emergency samples, and it is understood that the instrument usage data reflects the instrument usage requirements of the user, and thus the recommended values of the instrument parameters obtained from the instrument usage data conform to the instrument usage requirements of the user.
In an embodiment, the processor 32 is specifically configured to obtain the recommended instrument information by comparing the recommended value of the instrument parameter with at least one instrument parameter.
It can be understood that, since the recommended value of the instrument parameter meets the instrument use requirement of the user, the instrument recommendation information obtained according to the recommended value of the instrument parameter also meets the instrument use requirement of the user. Therefore, the in-vitro diagnosis analyzer provided by the embodiment of the invention can quantify the use requirements of the instrument of the user in an automatic mode, and further the recommended information of the instrument obtained according to the quantified information has objectivity and accuracy.
In one embodiment, the processor 32 is further configured to store the instrument usage data locally for the purpose of improving data security and protecting customer privacy; or, encrypting the instrument usage data; alternatively, the instrument usage data is prevented from being accessed by an unauthorized person by adjusting access rights of the instrument usage data.
In an embodiment, the processor 32 is further configured to output the instrument recommendation information or generate a reminding message after obtaining the instrument recommendation information, where the reminding message is used to remind a user of viewing the instrument recommendation information; therefore, the user can conveniently obtain the recommended information of the instrument in time.
Fig. 4 is a schematic deployment diagram of an instrument recommendation scheme according to an embodiment of the present invention, and referring to fig. 4, according to the above-mentioned contents, the instrument recommendation method according to an embodiment of the present invention can be deployed in a software system of an in vitro diagnostic analyzer or LIS in the form of a computer program (see the instrument recommendation program in fig. 4) according to the permission of a user; after the instrument recommendation program is deployed in the software system, instrument usage data may be extracted by using the instrument recommendation program, that is, test quantity distribution information of the instrument of the user is collected.
As a variation of the embodiment of the present invention, a salesperson or a customer service staff may obtain a recommended value of an instrument parameter, and then the salesperson or the customer service staff compares the recommended value of the instrument parameter with at least one instrument parameter to obtain instrument recommendation information. Fig. 5 is a schematic view of an interaction flow for implementing instrument recommendation in an embodiment of the present invention, as shown in fig. 5, in the case that an instrument recommendation program is deployed based on fig. 4, and a user applies for a test (i.e., applies for obtaining instrument usage data), accumulated instrument usage data may be obtained after a period of time; after the salesperson or customer service staff obtains the recommended value of the instrument parameter, the most appropriate instrument is recommended for the customer by comparing the recommended value with the parameter of the instrument which is currently listed or is about to be listed.
The above-mentioned serial numbers of the embodiments of the present invention are merely for description and do not represent the merits of the embodiments.
Through the above description of the embodiments, those skilled in the art will clearly understand that the method of the above embodiments can be implemented by software plus a necessary general hardware platform, and certainly can also be implemented by hardware, but in many cases, the former is a better implementation manner. Based on such understanding, the technical solutions of the present invention may be embodied in the form of a software product, which is stored in a storage medium (such as ROM/RAM, magnetic disk, optical disk) and includes instructions for enabling a terminal (such as a mobile phone, a computer, a server, an air conditioner, or a network device) to execute the method according to the embodiments of the present invention.
While the present invention has been described with reference to the embodiments shown in the drawings, the present invention is not limited to the embodiments, which are illustrative and not restrictive, and it will be apparent to those skilled in the art that various changes and modifications can be made therein without departing from the spirit and scope of the invention as defined in the appended claims.
Claims (17)
1. An instrument recommendation method, the method comprising:
acquiring instrument use data;
obtaining a recommended value of an instrument parameter according to the instrument usage data;
and obtaining recommended information of the instrument according to the recommended value of the instrument parameter.
2. The method of claim 1, wherein the instrument usage data includes test volume distribution information for the instrument.
3. The method of claim 2, wherein the test quantity distribution information of the instrument comprises at least one of: distribution information of test items of the instrument, distribution information of test time of the instrument, and distribution information of test sample types of the instrument.
4. The method of claim 1, wherein deriving instrument recommendation information based on the recommended value of the instrument parameter comprises:
and comparing the recommended value of the instrument parameter with at least one instrument parameter to obtain instrument recommended information.
5. The method of claim 1, further comprising:
storing the instrument usage data locally;
or, encrypting the instrument usage data;
alternatively, the instrument usage data is prevented from being accessed by an unauthorized person by adjusting access rights of the instrument usage data.
6. The method according to any one of claims 1 to 5, further comprising:
and after obtaining the instrument recommendation information, outputting the instrument recommendation information or generating reminding information, wherein the reminding information is used for reminding to check the instrument recommendation information.
7. An in vitro diagnostic analyzer comprising a processor and a memory, wherein,
the memory for storing instrument usage data, recommended values for instrument parameters, and a computer program executable on the processor;
the processor is used for acquiring instrument use data; obtaining a recommended value of an instrument parameter according to the instrument usage data; and obtaining recommended information of the instrument according to the recommended value of the instrument parameter.
8. The in vitro diagnostic analyzer of claim 7, wherein the instrument usage data includes instrument test volume distribution information.
9. The in vitro diagnostic analyzer of claim 8, wherein the test quantity distribution information of the instrument comprises at least one of: distribution information of test items of the instrument, distribution information of test time of the instrument, and distribution information of test sample types of the instrument.
10. The in vitro diagnostic analyzer of claim 7, wherein the processor is specifically configured to derive instrument recommendation information by comparing the recommended value of the instrument parameter to at least one instrument parameter.
11. The in vitro diagnostic analyzer of claim 7, wherein the processor is further configured to store the instrument usage data locally; or, encrypting the instrument usage data; alternatively, the instrument usage data is prevented from being accessed by an unauthorized person by adjusting access rights of the instrument usage data.
12. The in vitro diagnostic analyzer of any one of claims 7 to 11, wherein the processor is further configured to output the instrument recommendation information or generate a reminder after obtaining the instrument recommendation information, wherein the reminder is used to remind the user to view the instrument recommendation information.
13. An in vitro diagnostic analyzer, characterized in that it comprises an acquisition unit, a processing unit and an output unit; wherein the content of the first and second substances,
the acquisition unit is used for acquiring instrument use data;
the processing unit is used for obtaining a recommended value of an instrument parameter according to the instrument using data and obtaining instrument recommended information according to the recommended value of the instrument parameter;
and the output unit outputs the recommended value of the instrument parameter or the recommended information of the instrument.
14. The in vitro diagnostic analyzer of claim 13, wherein the instrument usage data includes instrument test volume distribution information.
15. The in vitro diagnostic analyzer of claim 13, wherein the processing unit is specifically configured to derive instrument recommendation information by comparing the recommended value of the instrument parameter with at least one instrument parameter.
16. The in vitro diagnostic analyzer of claim 13, wherein the processing unit is further configured to store the instrument usage data locally; or, encrypting the instrument usage data; alternatively, the instrument usage data is prevented from being accessed by an unauthorized person by adjusting access rights of the instrument usage data.
17. A computer storage medium on which a computer program is stored, characterized in that the computer program realizes the method of any one of claims 1 to 6 when executed by a processor.
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