CN111351947A - Sample analysis device and sample detection result processing method - Google Patents
Sample analysis device and sample detection result processing method Download PDFInfo
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- CN111351947A CN111351947A CN201811572048.4A CN201811572048A CN111351947A CN 111351947 A CN111351947 A CN 111351947A CN 201811572048 A CN201811572048 A CN 201811572048A CN 111351947 A CN111351947 A CN 111351947A
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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
Abstract
The application discloses a sample analysis device and a sample detection result processing method. The method comprises the following steps: selecting at least one result marker; detecting a sample to be detected to obtain sample detection data; judging whether the selected result mark needs to be sent to the LIS according to the sample detection data; if necessary, sending the sample detection data and the selected result mark to the LIS; if not, the sample detection data is sent to the LIS. Therefore, before the sample test, because the result mark which needs to be concerned when the sample test result is audited is customized in advance, after the test is finished, the customized result mark is only sent to the LIS end, and thus the audit of the sample test result by a testing doctor is not interfered.
Description
Technical Field
The present application relates to the technical field of Laboratory information management, and in particular, to a sample analysis device connected to an LIS (Laboratory information management system) and a sample detection result processing method.
Background
The LIS system is one of the important components of hospital information management, is connected with each analyzer in a laboratory (clinical laboratory) through a computer network, and is mainly used for acquiring sample detection data of the analyzer and performing operations such as storage, browsing, auditing, printing and the like on the sample detection data. In the prior art, as shown in fig. 1, a biochemical analyzer or an immunoassay analyzer is responsible for testing a sample on a test tube rack or a sample tray, and then sending a test result to the LIS end, and a checking physician reviews data related to the test result on the LIS end and sends a review report. The audited test results require each analyzer to provide information, including concentration values for sample testing and result indicia. The result marking refers to the problem which is generated in the running process of the instrument and has influence on the test result, and the influence reason needs to be marked on the influenced test result so as to further judge whether the result is reliable or not according to the marks. Of course, the data alarm does not necessarily have to be a fault, but may affect the test result, and therefore special attention is required.
When the test results are reviewed, the examining physician usually only pays attention to the "> (i.e., exceeds the upper limit of the linear range), < (i.e., is smaller than the lower limit of the linear range), PRO (i.e., potential examination abnormality), BOE (i.e., substrate exhaustion)" and other markers affecting the correctness of the results, but may not pay attention to the "RGTE (i.e., reagent expired), EXT (calibration parameter delay)" and other markers. However, the analyzer sends all the result markers to the LIS side, and these redundant markers may severely interfere with the review of the results by the examining physician if the LIS side does not perform a filtered display.
In addition, since the types of result marks sent to the LIS end are various, each mark has different meanings, and in order to know the meaning of a certain result mark, a user usually needs to browse a product help manual of an analysis instrument, which causes inconvenience to the result auditing work.
Disclosure of Invention
According to a first aspect of the present application, there is provided a method of processing results of a sample test, comprising selecting at least one result marker; detecting a sample to be detected to obtain sample detection data; judging whether the selected result mark needs to be sent to the LIS according to the sample detection data; if necessary, sending the sample detection data and the selected result mark to the LIS; if not, the sample detection data is sent to the LIS.
According to a second aspect of the present application, there is provided a sample analysis device comprising: the detection instrument is used for detecting a sample to be detected to obtain sample detection data; the human-computer interaction module is used for displaying the result marks which can be selected by the user and receiving at least one selected result mark; a communication port for communicating with the LIS; and the processor is used for judging whether the selected result mark needs to be sent to the LIS according to the sample detection data, controlling the communication interface to send the sample detection data and the selected result mark to the LIS if the sample detection data needs to be sent to the LIS, and controlling the communication interface to send the sample detection data to the LIS through the communication interface if the sample detection data does not need to be sent to the LIS.
The beneficial effect of this application is: the result mark selected by the user is provided through the man-machine interaction module, so that the user can customize the result mark, and only the customized result mark is sent to the LIS end after the sample test is finished, so that the result examination by a testing physician is not interfered. In one embodiment, the corresponding meanings of the result marks are provided, so that a user can conveniently check the corresponding meanings of the marks, and convenience is brought to the result auditing work.
Drawings
FIG. 1 is a schematic diagram of a prior art sample detection system;
FIG. 2 is a schematic view of a sample detection system according to an embodiment of the present application;
FIG. 3 is a schematic diagram of the composition of a sample analysis device according to an embodiment of the present application;
FIG. 4 is a schematic view of a results presentation interface of an example of the present application;
FIG. 5 is a schematic view of a system setup interface according to an example of the present application;
FIGS. 6 and 9 are schematic diagrams of a markup customization interface component of an example of the present application;
FIGS. 7 and 8 are schematic diagrams of an exemplary transmission settings interface assembly of the present application;
fig. 10 is a schematic flow chart of a sample detection result processing method according to an embodiment of the present application.
Detailed Description
The present invention will be described in further detail with reference to the following detailed description and accompanying drawings. Wherein like elements in different embodiments are numbered with like associated elements. In the following description, numerous details are set forth in order to provide a better understanding of the present application. However, those skilled in the art will readily recognize that some of the features may be omitted or replaced with other elements, materials, methods in different instances. In some instances, certain operations related to the present application have not been shown or described in detail in order to avoid obscuring the core of the present application from excessive description, and it is not necessary for those skilled in the art to describe these operations in detail, so that they may be fully understood from the description in the specification and the general knowledge in the art.
Furthermore, the features, operations, or characteristics described in the specification may be combined in any suitable manner to form various embodiments. Also, the various steps or actions in the method descriptions may be transposed or transposed in order, as will be apparent to one of ordinary skill in the art. Thus, the various sequences in the specification and drawings are for the purpose of describing certain embodiments only and are not intended to imply a required sequence unless otherwise indicated where such sequence must be followed.
The numbering of the components as such, e.g., "first", "second", etc., is used herein only to distinguish the objects as described, and does not have any sequential or technical meaning. The term "connected" and "coupled" when used in this application, unless otherwise indicated, includes both direct and indirect connections (couplings).
One of the design ideas of the embodiment of the present application is as follows: in order to conveniently audit the detection result of the sample, the mark which needs to be paid attention when the audit result is customized in advance before the sample is detected, so that the result mark which is not needed after the detection is finished can not be sent to the LIS terminal, and the audit of the detection result of the sample is facilitated. The second design idea of the embodiment of the application is as follows: when a result mark with unclear meaning is encountered (for example, when the detection result is audited or the mark is customized in advance), the meaning of the result mark can be quickly located, and the operation of auditing the result or customizing the mark is convenient.
Based on this, one embodiment of the present application provides a sample testing system 10, as shown in fig. 2, comprising a sample analysis device 100 and an LIS200, wherein the LIS200 communicates with the sample analysis device 100 and receives test results and corresponding result-labeling information (if any) from the sample analysis device 100. As shown in fig. 3, the sample analysis device 100 comprises a detection instrument 101, a processor 103, a human-computer interaction module 105 and a communication interface 107.
The detecting instrument 101 is used for detecting a sample to be detected to obtain sample detection data. The detection instrument may be, for example, a biochemical analyzer, an immunoassay tester, or the like.
The human-machine interaction module 105 may include an input portion for presenting result indicia available for selection by a user and an output portion for receiving at least one selected result indicia. The input section may accept input from an input device such as a keyboard, mouse, light pen, handwriting input panel, voice input device, or the like. The output section may be, for example, a display, which may be a touch screen display. The display may include one display or may include a plurality of displays, without limiting the number of displays.
The human-computer interaction module 105 is further configured to present a result display interface for displaying the sample test data and the result flag sent to the LIS. As shown in fig. 4, an exemplary results presentation interface, wherein the right side of the results presentation interface schematically presents the results of the testing of the sample and the corresponding results indicia (if any). In one implementation, when the cursor or the like moves to a result marker, the processor 103 controls the result presentation interface to present the meaning of the result marker accordingly, e.g., when the cursor moves to the result marker "BOE", the meaning "substrate exhaustion" of "BOE" may be presented in a floating window manner at the result marker "BOE" on the result presentation interface.
The human-computer interaction module 105 can also display a sample detection related system setup interface. As shown in fig. 5, an exemplary system setup interface through which a user (e.g., a testing physician) can set sample testing, such as automatic retest settings, margin limit settings, calculation item settings, print settings, combination item settings, LIS settings, reference range settings, user settings, display settings, and the like. The system setting interface is provided with a configuration interface, and the configuration interface comprises a mark customizing interface component arranged on the system setting interface and is used for at least presenting a plurality of result marks selected by a user and corresponding meanings of each result mark.
FIG. 6 illustrates an example markup customization interface component. As shown in FIG. 6, a plurality of interface elements and/or controls corresponding to a plurality of tabs are presented in a list on the tab customization interface component. FIG. 6 schematically lists a number of labels including ABS, RBK, BOE, NLN, EXP, LIN, PRO, >, <, # @! ↓! And so on, each result mark is represented by a symbol + key, the user selects the mark of interest by clicking and selecting the corresponding key (i.e. the customization of the result mark is realized), and all marks are presented in a list mode. Of course, all the result marks may be presented in other forms, such as in a drop-down box manner, or in an icon manner; in addition, each mark can be represented in other manners, such as a check box, an icon, and the like.
Still referring to fig. 6, in the markup customization interface component presented in a list dialog of fig. 6, a first column is displayed as a symbol of a result markup presented by a key, and a second column is displayed as a description of the meaning of each result markup, so that it is convenient for a user to quickly refer to the meaning of each markup while selecting the markup of interest. In the example of fig. 6, a plurality of text boxes are presented in a list manner, but it is also possible to set each mark and its meaning in another manner not limited to a list, for example, a user clicks a certain icon on a system setting interface to automatically pop up a page on which a plurality of marks and their corresponding meanings are listed in a text manner; as another example, each result token and its meaning are presented using a drop-down box.
In yet another example, the configuration interface includes a transport settings control disposed on the system settings interface for user selection to trigger (e.g., a control on the system settings interface shown in FIG. 5 that presents a "LIS settings" icon). The transmission setting interface component is used for presenting the transmission setting interface component when being triggered. As shown in fig. 7, an example of a transfer setup interface component is shown for presenting at least transfer options for the resulting tagged information to be transferred to the LIS host 200 for setting up by the user. Fig. 7 schematically shows some transmission options such as transport, server IP, serial port, data bit, item list, communication, protocol type, etc. Additionally, a markup setup control (i.e., a control illustrating a "LIS markup customization" icon presented) is provided on the transport setup interface component shown in fig. 7 for user selection to trigger, and when triggered, is used to present a markup customization interface component such as that shown in fig. 6.
For the input portion of the human-machine-interaction module 105, it may be used to receive at least one result token entered or selected by the user. For example, after the user opens the system setting interface shown in fig. 5, the user clicks a key corresponding to the "LIS setting" icon, the transmission setting interface component shown in fig. 7 or fig. 8 may be presented, the user clicks a key corresponding to the "LIS mark customization" icon on the transmission setting interface component, the mark customization interface component shown in fig. 6 or fig. 9 may be presented, and the user clicks a key corresponding to the mark of interest on the mark customization interface component interface, for example, clicks a key corresponding to ">, <, PRO, and BOE" one by one, and then selects "save", and then completes receiving the mark customization information input by the user from the input part of the human-machine interaction module 105.
The processor 103 may determine from the sample test data whether the selected result flag needs to be sent to the LIS200, and if so, control the communication interface 107 to send the sample test data and the selected result flag to the LIS200, and if not, control the communication interface 107 to send the sample test data to the LIS200 through the communication interface 107. For example, selected result markers include PRO, BOE, >, < etc., which are anomaly identifications, and if the test result is normal, there is no need to send these markers; if the test result shows that abnormal conditions such as substrate exhaustion (BOE), prozone inspection abnormity (PRO), certain test data larger than ">" or smaller than "<" reference critical value and the like exist, result marks corresponding to the abnormal conditions are sent while the test result is sent, and when a doctor examines the sample detection result, the result marks can be checked to decide whether the examination is passed or retesting is needed. For other non-selected markers, even if there is a corresponding abnormality, such as "RGTE (reagent expired), EXT (calibration expired)", they are not sent to the LIS because they do not affect much or the validity of the sample test results, and therefore, the physician does not need to pay attention when reviewing the sample test results.
As can be seen from the above description, in the sample analysis system 10 according to an embodiment of the present application, the result flag sent by the sample analysis apparatus to the LIS terminal 200 can be customized in advance, that is, the sample analysis apparatus 100 provides a customizable function of the result flag sent to the LIS terminal 200.
Based on the sample analysis system 10 and the corresponding sample analysis device 100, an embodiment of the present application provides a sample detection result processing method, which is applied to a sample analysis device, as shown in fig. 10, and includes:
step S101: selecting at least one result marker;
step S103: detecting a sample to be detected to obtain sample detection data;
step S105: judging whether the selected result mark needs to be sent to the LIS according to the sample detection data, if so, executing the step S107, and if not, executing the step S109;
step S107: sending the sample detection data and the selected result mark to the LIS;
step S109: the sample detection data is sent to the LIS.
In the embodiment of the present invention, determining whether the selected result flag needs to be sent to the LIS according to the sample detection data includes: judging whether the detection data is consistent with the selected result mark, if so, sending the result mark to the LIS; if not, not sending the result mark of the non-conformity to the LIS; for example, if a user-selected result flag comprises "<", ">", and if a certain item in the sample detection data is greater than the corresponding reference threshold, then ">" this result flag needs to be sent to the LIS; if a certain item in the sample detection data is smaller than the corresponding reference threshold, then the "<" result flag needs to be sent to the LIS.
In addition, determining whether the selected result marker needs to be sent to the LIS based on the sample detection data may further include: judging whether an abnormal condition corresponding to the selected at least one result mark exists or not, if so, indicating that the result mark corresponding to the abnormal condition needs to be sent; if not, the selected at least one result indicia need not be transmitted. For example, if the selected result markers include BOE (substrate depletion), PRO (pre-strip examination abnormalities), and the sample test data (including the sample test result data and test procedure log information) indicates that there are substrate depletion or pre-strip examination abnormalities, then these result markers need to be sent to the LIS for reference when the physician reviews the sample test results.
In one example, the method further includes providing a configuration interface, specifically including: and creating a mark customizing interface component, wherein at least a plurality of result marks selected by a user and corresponding meanings of each result mark are presented on the mark customizing interface component. In one specific implementation, the markup customization interface component can be in a list form or a drop-down box form to present a plurality of interface elements and/or controls corresponding to a plurality of markup items.
In another example, the configuration interface is disposed on a system setup interface of an instrument on which the sample is tested. In one particular implementation of this embodiment, the creating of the branding customization interface component includes: providing a transmission setting control for being selected and triggered by a user on a system setting interface; when the processor captures that the transmission setting control is triggered, a transmission setting interface component is created, at least a transmission option for transmitting result marking information to the LIS is presented on the transmission setting interface component for setting by a user, and a marking setting control for the user to select and trigger is also provided on the transmission setting interface component; and when the processor captures that the mark setting control is triggered, creating the mark customizing interface component.
In yet another example, the method further comprises: and providing a result display interface, wherein the result display interface is used for displaying the sample test data and the result mark sent to the LIS. In one implementation, upon capturing a signal that the cursor moves to a result mark, the meaning of the result mark may be correspondingly presented on the result presentation interface.
Reference is made herein to various exemplary embodiments. However, those skilled in the art will recognize that changes and modifications may be made to the exemplary embodiments without departing from the scope hereof. For example, the various operational steps, as well as the components used to perform the operational steps, may be implemented in differing ways depending upon the particular application or consideration of any number of cost functions associated with operation of the system (e.g., one or more steps may be deleted, modified or incorporated into other steps).
Additionally, as will be appreciated by one skilled in the art, the principles herein may be reflected in a computer program product on a computer readable storage medium, which is pre-loaded with computer readable program code. Any tangible, non-transitory computer-readable storage medium may be used, including magnetic storage devices (hard disks, floppy disks, etc.), optical storage devices (CD-ROMs, DVDs, Blu Ray disks, etc.), flash memory, and/or the like. These computer program instructions may be loaded onto a general purpose computer, special purpose computer, or other programmable data processing apparatus to produce a machine, such that the instructions which execute on the computer or other programmable data processing apparatus create means for implementing the functions specified. These computer program instructions may also be stored in a computer-readable memory that can direct a computer or other programmable data processing apparatus to function in a particular manner, such that the instructions stored in the computer-readable memory produce an article of manufacture including means for implementing the function specified. The computer program instructions may also be loaded onto a computer or other programmable data processing apparatus to cause a series of operational steps to be performed on the computer or other programmable apparatus to produce a computer implemented process such that the instructions which execute on the computer or other programmable apparatus provide steps for implementing the functions specified.
While the principles herein have been illustrated in various embodiments, many modifications of structure, arrangement, proportions, elements, materials, and components particularly adapted to specific environments and operative requirements may be employed without departing from the principles and scope of the present disclosure. The above modifications and other changes or modifications are intended to be included within the scope of this document.
The foregoing detailed description has been described with reference to various embodiments. However, one skilled in the art will recognize that various modifications and changes may be made without departing from the scope of the present disclosure. Accordingly, the disclosure is to be considered in an illustrative and not a restrictive sense, and all such modifications are intended to be included within the scope thereof. Also, advantages, other advantages, and solutions to problems have been described above with regard to various embodiments. However, the benefits, advantages, solutions to problems, and any element(s) that may cause any element(s) to occur or become more pronounced are not to be construed as a critical, required, or essential feature or element of any or all the claims. As used herein, 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, system, article, or apparatus. Furthermore, the term "coupled," and any other variation thereof, as used herein, refers to a physical connection, an electrical connection, a magnetic connection, an optical connection, a communicative connection, a functional connection, and/or any other connection.
Those skilled in the art will recognize that many changes may be made to the details of the above-described embodiments without departing from the underlying principles of the invention. Accordingly, the scope of the invention should be determined from the following claims.
Claims (14)
1. A sample detection result processing method is applied to sample analysis equipment and comprises the following steps:
selecting at least one result marker;
detecting a sample to be detected to obtain sample detection data;
judging whether the selected result mark needs to be sent to the LIS according to the sample detection data;
if necessary, sending the sample detection data and the selected result mark to the LIS;
if not, the sample detection data is sent to the LIS.
2. The method of claim 1, further comprising providing a configuration interface, the providing a configuration interface comprising:
and creating a mark customizing interface component, wherein at least a plurality of result marks selected by a user and corresponding meanings of each result mark are presented on the mark customizing interface component.
3. The method of claim 2, wherein the configuration interface is disposed on a system setup interface of the sample analysis device.
4. The method of claim 3, wherein the creation of the branding customization interface component comprises:
providing a transmission setting control for being selected and triggered by a user on the system setting interface;
when the transmission setting control is triggered, creating a transmission setting interface component, wherein at least a transmission option for transmitting result marking information to the LIS is presented on the transmission setting interface component for setting by a user, and a marking setting control for the user to select and trigger is also provided on the transmission setting interface component;
and when the mark setting control is triggered, creating the mark customized interface component.
5. The method of claim 1, further comprising: and providing a result display interface, wherein the result display interface is used for displaying the sample test data and the result mark sent to the LIS.
6. The method of claim 5, wherein the method further comprises: when a signal that the cursor moves to a result mark is captured, the result presentation interface presents the meaning of the result mark accordingly.
7. The method of claim 1, wherein said determining whether the selected outcome indicia needs to be sent to the LIS based on the sample detection data comprises: judging whether the detection data is consistent with the selected result mark, if so, sending the result mark to the LIS; if not, not sending the result mark of non-conformity to the LIS.
8. The method of claim 1, wherein said determining whether the selected outcome indicia needs to be sent to the LIS based on the sample detection data comprises: judging whether an abnormal condition corresponding to the selected at least one result mark exists or not, if so, indicating that the result mark corresponding to the abnormal condition needs to be sent; if not, the selected at least one result indicia need not be transmitted.
9. The method of claim 2, wherein the markup customization interface component presents interface elements and/or controls corresponding to a plurality of result markup in a list form or a drop-down box form thereon.
10. A sample analysis apparatus, comprising:
the detection instrument is used for detecting a sample to be detected to obtain sample detection data;
the human-computer interaction module is used for displaying the result marks which can be selected by the user and receiving at least one selected result mark;
a communication interface for communicating with the LIS;
and the processor is used for judging whether the selected result mark needs to be sent to the LIS according to the sample detection data, controlling the communication interface to send the sample detection data and the selected result mark to the LIS if the sample detection data needs to be sent to the LIS, and controlling the communication interface to send the sample detection data to the LIS through the communication interface if the sample detection data does not need to be sent to the LIS.
11. The sample analysis device as claimed in claim 10, wherein the human-computer interaction module is configured to display a system setup interface, the system setup interface having a configuration interface, the configuration interface including a mark customization interface component disposed on the system setup interface for presenting at least a plurality of result marks for selection by the user and a corresponding meaning of each result mark.
12. The sample analysis device of claim 11, wherein the configuration interface comprises a transmission setting control disposed on the system setting interface for selection by a user to trigger, the transmission setting control is configured to present a transmission setting interface component when triggered, the transmission setting interface component is configured to present at least a transmission option for transmitting the resulting marking information to the LIS for setting by the user, a marking setting control is further provided on the transmission setting interface component for selection by the user to trigger, and the marking setting control is configured to present the marking customization interface component when triggered.
13. The sample analysis device of claim 10, wherein the human-computer interaction module is further configured to present a result presentation interface for presenting the sample test data and the result indicia sent to the LIS; the processor is further used for controlling the result showing interface to correspondingly show the meaning of a result mark when capturing a signal that the cursor moves to the result mark.
14. The sample analysis device of claim 11, wherein the markup customization interface component presents interface elements and/or controls of the multiple result markup in a list form or a drop-down box form thereon.
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