CN117741170A - Quality control product experiment item registration method and detection control method - Google Patents
Quality control product experiment item registration method and detection control method Download PDFInfo
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Abstract
The invention relates to the technical field of medical instruments, in particular to a quality control product experimental project registering method and a detection control method. The quality control product detection control method determines the type of the reagent according to the position information of the current quality control product and determines the first feasibility of the current project according to the first experimental project, so that the reagent can be automatically selected and adjusted to be compatible with multiple human reagents and single human reagents.
Description
Technical Field
The invention relates to the technical field of medical equipment, in particular to a quality control product experimental project registration method and a detection control method.
Background
The sample analyzer is an instrument for detecting and analyzing samples, in the related art, most of reagents used by the sample analyzer are bottled reagents (multi-person reagents), the bottled reagents are used by a plurality of samples, but in some application scenes, the quantity of detection items is small, so that the bottled reagents cannot be used in the effective period after being unsealed, and reagent waste is caused. Therefore, POCT-type (point of care testing) sample analyzers that use single-person reagent card strips have been developed. However, the single reagent card strip is opposite to bottled reagent, cannot adapt to the application scene with a large sample size, has the problem of low efficiency, and is complex to operate because the reagent card strip needs to be repeatedly loaded for a commonly developed detection project; i.e. only one of the reagent bottles or only one of the reagent strips cannot fully accommodate all scenarios of sample analysis. At present, how to accommodate multiple human reagents and single human reagents on a sample analyzer is a problem to be solved.
Disclosure of Invention
The present invention aims to solve at least one of the technical problems existing in the prior art. Therefore, the invention provides a quality control product experimental project registration method which can register the experimental project of the quality control product so as to be compatible with multiple human reagents and single human reagents; the invention also provides a quality control product detection control method which can be compatible with multiple reagents and single reagents, can flexibly select and use multiple reagent bottles and single reagent card strips according to the number of quality control product samples, and can be suitable for application scenes of different quality control product sample numbers.
In a first aspect, an embodiment of the present invention provides a quality control product experimental project registration method, including
Displaying a first interactive interface, wherein the first interactive interface displays at least one first graph and at least one second graph, the first graph corresponds to the reagent card strip, and the second graph corresponds to the sample tube;
responding to a first operation instruction, determining the selected second graph as a first target object, and displaying a second interactive interface, wherein the second interactive interface is displayed with a first operation control and a second operation control;
responding to a second operation instruction of the first operation control, determining a quality control file corresponding to the first target object, and determining quality control experiment item information according to the quality control file of the first target object;
Determining position information of a target reagent card strip and first experimental item information in response to a third operation instruction of the second operation control, wherein the first experimental item information is obtained by scanning a code of the target reagent card strip or manually inputting the code;
and responding to a fourth operation instruction, and associating the first target object, the quality control product experimental project information, the position information of the target reagent card strip and the first experimental project information.
The embodiment of the invention has at least the following beneficial effects:
according to the embodiment of the invention, through the related operation of the first operation control and the second operation control, the quality control experiment item of the sample analyzer can be registered and correlated with the related information of the reagent card strip, so that the quality control detection can be carried out on the sample analyzer by using a single reagent, and the quality control item and the reagent can be matched in the process of being compatible with multiple reagents and a single reagent.
In a second aspect, an embodiment of the present invention provides a quality control product experimental project registration method, including:
displaying a first interactive interface, wherein the first interactive interface displays at least one first graph and at least one second graph, the first graph corresponds to the reagent card strip, and the second graph corresponds to the sample tube;
Responding to an eighteenth operation instruction, determining the selected first graph as a fifth target object, and determining first experimental item information and position information of a target reagent card strip, wherein the first experimental item information is obtained by scanning a code of the target reagent card strip or manually inputting the code;
responding to a first operation instruction, determining the selected second graph as a first target object, and displaying a second interactive interface, wherein the second interactive interface is displayed with a first operation control;
responding to a second operation instruction of the first operation control, determining a quality control file corresponding to the first target object, and determining quality control experiment item information according to the quality control file of the first target object;
and responding to a fourth operation instruction, and associating the first target object, the quality control product experimental project information, the position information of the target reagent card strip and the first experimental project information.
The embodiment of the invention has at least the following beneficial effects:
according to the embodiment of the invention, through the related operation of the first graph and the first operation control, the quality control experiment item of the sample analyzer can be registered and correlated with the related information of the reagent card strip, so that the quality control detection can be carried out on the sample analyzer by using a single reagent, and the quality control item and the reagent can be matched in the process of being compatible with multiple reagents and a single reagent.
In a third aspect, an embodiment of the present invention provides a quality control product detection control method, including:
acquiring associated information of a current quality control product, wherein the associated information comprises position information of the current quality control product, quality control product experimental project information, position information of a target reagent card strip and first experimental project information, the quality control product experimental project information is used for representing the experimental project information of the current quality control product, and the first experimental project information is used for representing the reagent information of a single person;
determining the reagent type of the current quality control product according to the position information of the current quality control product, wherein the reagent type is a single-person reagent or a multi-person reagent;
under the condition that the reagent type is a single reagent, determining a current experiment item according to the quality control product experiment item information;
determining a first feasibility of the current experiment item according to the first experiment item information;
determining the position information of a target reagent according to the current experiment item, the first experiment item information and the position information of the target reagent card strip under the condition that the first feasibility of the current experiment item is characterized in the affirmative;
or determining the reagent type corresponding to the current experiment item as a multi-person reagent in the case that the first feasibility of the current experiment item is characterized as negative.
The embodiment of the invention has at least the following beneficial effects:
according to the embodiment of the invention, the reagent type is determined according to the position information of the current quality control product, and the first feasibility of the current project is determined according to the first experimental project, so that the automatic selection and adjustment of the reagent can be realized, and the automatic selection of the single reagent and the multiple reagent in the process of being compatible with the multiple reagents and the single reagent is realized.
In a fourth aspect, an embodiment of the present invention provides a quality control product detection control method, including:
acquiring associated information of a current quality control product, wherein the associated information comprises quality control product experimental project information, position information of a target reagent card strip and first experimental project information, the quality control product experimental project information is used for representing the experimental project information of the current quality control product, and the first experimental project information is used for representing the reagent information of a single person;
determining the reagent type of the current quality control product according to the quality control product experimental project information, wherein the reagent type is a single-person reagent or a multi-person reagent;
under the condition that the reagent type is a single reagent, determining a current experiment item according to the quality control product experiment item information;
determining a first feasibility of the current experiment item according to the first experiment item information;
Determining the position information of a target reagent according to the current experiment item, the first experiment item information and the position information of the target reagent card strip under the condition that the first feasibility of the current experiment item is characterized in the affirmative;
or determining the reagent type corresponding to the current experiment item as a multi-person reagent in the case that the first feasibility of the current experiment item is characterized as negative.
The embodiment of the invention has at least the following beneficial effects:
according to the embodiment of the invention, the reagent type is determined according to the quality control product experimental project information, and the first feasibility of the current project is determined according to the first experimental project, so that the automatic selection and adjustment of the reagent can be realized, and the automatic selection of the single reagent and the multiple reagent in the process of being compatible with the multiple reagents and the single reagent is realized.
In a fifth aspect, an embodiment of the present invention provides a sample analyzer, including:
the first display module is used for displaying a first interactive interface, at least one first graph and at least one second graph are displayed on the first interactive interface, the first graph corresponds to the reagent card strip, and the second graph corresponds to the sample tube;
The first response module is used for responding to a first operation instruction, determining the selected second graph as a first target object, and displaying a second interactive interface, wherein the second interactive interface is displayed with a first operation control and a second operation control;
the second response module is used for responding to a second operation instruction of the first operation control, determining a quality control file corresponding to the first target object, and determining quality control experiment item information according to the quality control file of the first target object;
the third response module is used for responding to a third operation instruction of the second operation control to determine the position information of the target reagent card strip and the first experimental item information, wherein the first experimental item information is obtained by scanning a code of the target reagent card strip or manually inputting the code;
and the fourth response module is used for responding to a fourth operation instruction and correlating the first target object, the quality control product experimental project information, the position information of the target reagent card strip and the first experimental project information.
The embodiment of the invention has at least the following beneficial effects:
according to the embodiment of the invention, through the related operation of the first operation control and the second operation control, the quality control experiment item of the sample analyzer can be registered and correlated with the related information of the reagent card strip, so that the quality control detection can be carried out on the sample analyzer by using a single reagent, and the quality control item and the reagent can be matched in the process of being compatible with multiple reagents and a single reagent.
In a sixth aspect, an embodiment of the present invention provides a sample analyzer, including:
the second display module is used for displaying a first interactive interface, at least one first graph and at least one second graph are displayed on the first interactive interface, the first graph corresponds to the reagent card strip, and the second graph corresponds to the sample tube;
the fifth response module is used for responding to an eighteenth operation instruction, determining the selected first graph as a fifth target object, and determining first experimental project information and position information of a target reagent card strip, wherein the first experimental project information is obtained by scanning a code of the target reagent card strip or is obtained by manually inputting the code;
the sixth response module is used for responding to the first operation instruction, determining the selected second graph as a first target object, and displaying a second interactive interface, wherein the second interactive interface displays a first operation control;
a seventh response module, configured to determine a quality control file corresponding to the first target object in response to a second operation instruction for the first operation control, and determine quality control experiment item information according to the quality control file of the first target object;
And the eighth response module is used for responding to a fourth operation instruction and correlating the first target object, the quality control product experiment item information, the position information of the target reagent card strip and the first experiment item information.
The embodiment of the invention has at least the following beneficial effects:
according to the embodiment of the invention, through the related operation of the first graph and the first operation control, the quality control product experimental project of the sample analyzer can be registered and correlated with the related information of the reagent card strip, so that the quality control detection can be carried out on the sample analyzer by using a single reagent, and the automatic selection of the single reagent and the multiple reagents in the process of being compatible with the multiple reagents and the single reagent is realized.
In a seventh aspect, an embodiment of the present invention provides a sample analyzer, including:
the first acquisition module is used for acquiring the associated information of the current quality control product, wherein the associated information comprises the position information of the current quality control product, the experimental project information of the quality control product, the position information of the target reagent card strip and the first experimental project information, the experimental project information of the quality control product is used for representing the experimental project information of the current quality control product, and the first experimental project information is used for representing the reagent information of a single person;
The first determining module is used for determining the reagent type of the current quality control product according to the position information of the current quality control product, wherein the reagent type is a single person reagent or a plurality of person reagents;
the second determining module is used for determining a current experiment item according to the quality control product experiment item information under the condition that the reagent type is a single reagent;
the third determining module is used for determining the first feasibility of the current experiment item according to the first experiment item information;
a fourth determining module, configured to determine, when the first feasibility of the current experiment item is characterized in affirmative, location information of a target reagent according to the current experiment item, the first experiment item information, and the location information of the target reagent card strip;
or determining the reagent type corresponding to the current experiment item as a multi-person reagent in the case that the first feasibility of the current experiment item is characterized as negative.
The embodiment of the invention has at least the following beneficial effects:
according to the embodiment of the invention, the reagent type is determined according to the position information of the current quality control product, and the first feasibility of the current project is determined according to the first experimental project, so that the automatic selection and adjustment of the reagent can be realized, and the automatic selection of the single reagent and the multiple reagent in the process of being compatible with the multiple reagents and the single reagent is realized.
In an eighth aspect, an embodiment of the present invention provides a sample analyzer, including:
the second acquisition module is used for acquiring the associated information of the current quality control product, wherein the associated information comprises quality control product experimental project information, position information of a target reagent card strip and first experimental project information, the quality control product experimental project information is used for representing the experimental project information of the current quality control product, and the first experimental project information is used for representing the reagent information of a single person;
the fifth determining module is used for determining the reagent type of the current quality control product according to the quality control product experimental project information, wherein the reagent type is a single-person reagent or a multi-person reagent;
a sixth determining module, configured to determine a current experiment item according to the quality control item information when the reagent type is a single reagent;
a seventh determining module, configured to determine, according to the first experiment item information, a first feasibility of the current experiment item;
an eighth determining module, configured to determine, when the first feasibility of the current experiment item is characterized in affirmative, location information of a target reagent according to the current experiment item, the first experiment item information, and the location information of the target reagent card strip;
Or determining the reagent type corresponding to the current experiment item as a multi-person reagent in the case that the first feasibility of the current experiment item is characterized as negative.
The embodiment of the invention has at least the following beneficial effects:
according to the embodiment of the invention, the reagent type is determined according to the quality control product experimental project information, and the first feasibility of the current project is determined according to the first experimental project, so that the automatic selection and adjustment of the reagent can be realized, and the automatic selection of the single reagent and the multiple reagent in the process of being compatible with the multiple reagents and the single reagent is realized.
Additional aspects and advantages of the invention will be set forth in part in the description which follows, and in part will be obvious from the description, or may be learned by practice of the invention.
Drawings
The foregoing and/or additional aspects and advantages of the invention will become apparent and may be better understood from the following description of embodiments taken in conjunction with the accompanying drawings in which:
FIG. 1 is a schematic view of a sample cartridge according to an embodiment of the present invention;
FIG. 2 is a schematic view of a reagent card strip loading rack according to an embodiment of the present invention;
FIG. 3 is a flowchart showing steps of a quality control experiment item registration method according to an embodiment of the present invention;
FIG. 4 is a schematic diagram of a first interactive interface according to an embodiment of the present invention;
FIG. 5 is a schematic diagram of a third interface according to an embodiment of the present invention;
FIG. 6 is a schematic diagram of a fourth interface according to an embodiment of the present invention;
FIG. 7 is a schematic diagram of a fifth interface according to an embodiment of the present invention;
FIG. 8 is a schematic diagram of a sixth interactive interface according to an embodiment of the present invention;
FIG. 9 is a second schematic diagram of a first interactive interface according to an embodiment of the present invention;
FIG. 10 is a third schematic diagram of a first interactive interface according to an embodiment of the present invention;
FIG. 11 is a second flowchart illustrating a quality control experiment item registration method according to an embodiment of the present invention;
FIG. 12 is a flowchart illustrating steps of a quality control product detection control method according to an embodiment of the present invention;
FIG. 13 is a second flowchart illustrating a quality control detecting and controlling method according to an embodiment of the present invention;
FIG. 14 is one of the functional block diagrams of a sample analyzer according to an embodiment of the present invention;
FIG. 15 is a second schematic block diagram of a sample analyzer according to an embodiment of the present invention;
FIG. 16 is a third schematic block diagram of a sample analyzer according to an embodiment of the present invention;
FIG. 17 is a fourth block diagram of a sample analyzer according to an embodiment of the present invention.
Reference numerals:
sample cartridge 100, loading channel 110, sample tube loading bay 120, sample tube 121, reagent card stripe loading bay 130, reagent card stripe 131, first channel bitmap 210, first graphic 211, second graphic 212, first operational control 220, loading card stripe 231, manual entry card stripe 232, third operational control 240, quality control file list 250, quality control file item 251, fourth operational control 252, quality control file edit control 253, reagent type configuration control 260, sixth operational control 270, second channel bitmap 280, third channel bitmap 290, experiment item option 291, first display module 311, first response module 312, second response module 313, third response module 314, fourth response module 315, second display module 321, fifth response module 322, sixth response module 323, seventh response module 324, eighth response module 325, first acquisition module 331, first determination module 332, second determination module 333, third determination module 334, fourth determination module 341, fifth determination module 342, seventh determination module 343, eighth determination module 345.
Detailed Description
Embodiments of the present invention are described in detail below, examples of which are illustrated in the accompanying drawings, wherein like or similar reference numerals refer to like or similar elements or elements having like or similar functions throughout. The embodiments described below by referring to the drawings are illustrative only and are not to be construed as limiting the invention.
In the description of the present invention, the meaning of "a number" means one or more, the meaning of "a plurality" means two or more, and greater than, less than, exceeding, etc. are understood to not include the present number, and "above", "below", "within", etc. are understood to include the present number. If any, the terms "first," "second," etc. are used for distinguishing between technical features only, and should not be construed as indicating or implying a relative importance or implicitly indicating the number of technical features indicated or implicitly indicating the precedence of the technical features indicated.
In the description of the present invention, unless explicitly defined otherwise, terms such as "disposed," "mounted," "connected," and the like are to be construed broadly and the specific meaning of the terms in the present invention can be reasonably determined by those skilled in the art in combination with the specific contents of the technical solutions.
PT: prothrombin time, prothrombin time;
APTT: activated Partial Thromboplastin Time time to partial thromboplastin activation
TT: thrombinTime, thrombin time
FIB: fibrinogen, fibrinogen
FDP: fibrin/Fibrinogen Degradation Products, fibrin (ogen) degradation products
DD: D-Dimer, D-Dimer
AT-III: antithrombin III
The sample analyzer is applied to the field of medical treatment or biochemical analysis, and has the function of detecting a sample to be detected, wherein the sample to be detected can be blood, urine, body fluid or the like. In the related art, a sample analyzer includes a sample storage module and a reagent storage module, wherein the sample storage module is used for storing a plurality of test tubes (also referred to as sample tubes), the reagent storage module is used for storing a plurality of reagent bottles, and each reagent bottle can store different or same types of reagents. In general, the reagent bottle has a large reagent storage amount, can be used by a plurality of persons, for example, can be used by tens of detection samples, and is suitable for a scene with a large sample amount, for example, a large hospital or a large detection mechanism. However, in the case of an application scenario in which the sample size is small, the reagent stored in the reagent bottle has a limit of the life, and particularly, after the reagent bottle is opened, the reagent cannot be used continuously once the period of the life is exceeded. In order to solve the above-mentioned problems, the related art provides a reagent card strip 131 for storing a reagent for single-person detection without using a large reagent bottle, wherein single-person is a relatively multi-person, a certain amount of reagent is packaged and the amount of reagent should meet the use requirement for performing one-sample detection (single-person use). It should be noted that, in the related art, the POCT sample analyzer can only use a single reagent card, and the sample analyzer of the present embodiment can be compatible with a single reagent and multiple reagents.
Referring to fig. 1 and 2, the sample analyzer of the present embodiment includes a case, a sample compartment 100, a reagent storage module, a distribution module, an incubation detection module, and a detection cup, wherein the sample compartment 100 is installed in the case, at least one loading channel 110 is provided on the sample compartment 100, and the loading channel 110 is used for installing a loading rack, wherein the loading rack may be a sample tube loading rack 120 for placing a sample tube 121, a reagent card strip loading rack 130 for placing a reagent card strip 131 and a sample tube 121, or a reagent card strip loading rack for placing only a reagent card strip 131 (i.e. a placing position of the sample tube 121 is not provided on the reagent card strip loading rack 130). The sample tube 121 is used for storing a sample to be tested, the reagent storage module is used for storing a reagent bottle, and the reagent card strip 131 or the reagent bottle is stored with a reagent, wherein the reagent comprises AT least one of PT reagent, APTT reagent, TT reagent, FIB reagent, FDP reagent, DD reagent and AT-III reagent. In this embodiment, according to the flexible choice of the user, the reagent card strip 131 and the sample tube 121 can share the physical space of the sample chamber 100 for loading, and no additional space is required to be opened up in the sample analyzer to additionally place the reagent card strip, which is beneficial to miniaturization of the sample analyzer. And because reagent card strip 131 and sample tube 121 all satisfy single person's detection and use, as the consumptive material that needs the repeated loading change, the convenient user operation of sharing sample storehouse. The distribution module is used for injecting the sample collected from the sample tube 121 into the detection cup and injecting the reagent collected from the reagent bottle or the reagent card strip 131 into the detection cup, and the incubation detection module is used for incubating the sample in the detection cup and detecting the sample in the detection cup to obtain a detection result. In addition, the medical test analysis needs quality control, and the reliability and consistency of the result are ensured by performing quality control tests daily to monitor the stability and reliability of the instrument. Because the sample analyzer can be loaded with a plurality of human reagents and can also be loaded with a single human reagent, for example, for coagulation analysis, the number of times of making part of items in seven coagulation items is high, the reagent in a reagent bottle is required to be used for detection, the number of times of making part of items is low, and the reagent of a reagent card strip is required to be used for detection; for example, even in a large hospital or a large detection facility, there are strong seasons and off-seasons, the reagent usage in the reagent bottle should be used in a large amount, and the reagent usage in the reagent card should be used in a small amount in the off-seasons, and therefore, how to accommodate a plurality of human reagents and a single human reagent on the sample analyzer is a problem to be solved urgently.
Referring to fig. 3, the embodiment discloses a quality control product experimental project registration method, which includes S110-S150, for implementing registration of quality control product experimental projects in the process of compatible multi-person reagent and single-person reagent, so as to determine whether to suck multi-person reagent or single-person reagent when quality control product analysis is performed. It should be noted that, the steps in this embodiment are labeled only for facilitating examination and understanding, and not limiting the execution sequence of the steps, and in practical application, the steps may be adaptively adjusted according to the logic relationship between the steps. The contents of the individual steps are described in detail below with reference to fig. 1, 2 and 4:
s110, displaying a first interactive interface, wherein the first interactive interface is displayed with at least one first graph 211 and at least one second graph 212, the first graph 211 corresponds to the reagent card strip 131, and the second graph 212 corresponds to the sample tube 121;
illustratively, the number of loading channels 110 on the sample analyzer may be one or more, and the present embodiment uses 4 loading channels 110 as an example, and correspondingly, 4 first channel bitmaps 210 are displayed on the first interaction interface. Since each loading lane 110 may be used for mounting the reagent card strip loading rack 130 or for mounting the sample tube loading rack 120, the target lane may be divided into a first lane type for characterizing the case where the loading lane 110 mounts the reagent card strip loading rack 130 and a second lane type for characterizing the case where the loading lane 110 mounts the sample tube loading rack 120, depending on the type of the loading rack. In order to facilitate the user to distinguish the channel types of the loading channel 110, the first channel bitmap 210 is displayed in different channel patterns according to the channel types, for example, in the case that the channel type of the target channel is the first channel type, the first channel bitmap 210 is displayed in the first channel pattern; in the case where the channel type of the target channel is the second channel type, the first channel bitmap 210 is displayed as a second channel pattern, wherein the first channel pattern is configured with the first graphic 211 and the second channel pattern is configured with the second graphic 212, and in some application scenarios, the first channel pattern may be configured with the first graphic 211 and the second graphic 212. In the case of a single-lot reagent application, the reagent card strip 131 needs to be placed by the reagent card strip loading rack 130 to store the single-lot reagent, and thus, at least one of the target channels is of the first channel type, i.e., at least one first channel bitmap 210 is displayed as a first channel pattern.
S120, responding to the first operation instruction, determining the selected second graph 212 as a first target object, and displaying a second interactive interface, wherein the second interactive interface is displayed with a first operation control 220 and a second operation control;
for example, the number of loading channels 110 may be one or more, and the reagent card strip loading rack 130 may be used to place one or more sample tubes 121, and similarly, the sample tube loading rack 120 may be used to place a plurality of sample tubes 121, so that when performing quality control detection, the placement position of the quality control product needs to be determined first. Because the positions of the second graphics 212 on the first channel bitmap 210 correspond to the mounting positions of the sample tubes 121 on the loading frame one by one, in response to the first operation instruction, the selected second graphics 212 are determined to be the first target object, the placement position of the quality control product can be determined, and the attribute interface of the second graphics 212, that is, the second interaction interface, is displayed, where the first operation instruction may be a click, double click or long press operation instruction. The second interactive interface may be displayed in a local area of the current interface, or the second interactive interface may be another interface different from the current interface.
S130, responding to a second operation instruction of the first operation control 220, determining a quality control file corresponding to the first target object, and determining quality control experiment item information according to the quality control file of the first target object;
The first operation control 220 may be an operation control such as a single-box control or a drop-down list, and the second operation instruction may be a click operation on the single-box, or a selection operation for an option of the drop-down list. In order to simplify the interface design, the embodiment takes a drop-down list as an example, and a plurality of options related to the quality control files are configured in the drop-down list, for example, each quality control file is indexed and distinguished by a sample number, where the quality control files can be preset or configured by user definition. When the quality control file corresponding to the first target object is determined, quality control item information can be determined according to the quality control file of the first target object.
S140, determining the position information of the target reagent card strip and the first experimental item information in response to a third operation instruction of the second operation control, wherein the first experimental item information is obtained by scanning a code of the target reagent card strip or manually inputting;
for example, in order to achieve compatibility of the multiple-part reagent and the single-part reagent, the position information of the target reagent card strip and the first experimental item information are determined in response to the third operation instruction of the second operation control so as to facilitate subsequent information association, wherein the first experimental item information determined based on the third operation instruction is configured to use the single-part reagent, namely, the corresponding reagent is sucked according to the position of the target reagent card strip when detection is performed. The first experiment item information may be one or more items of PT, APTT, TT, FIB, FDP, DD or AT-III, and of course, according to different data storage formats, the first experiment item information may only include identifiers of a plurality of experiment items, such as PT, APTT, etc., or may also include identifiers of a plurality of experiment items and corresponding reagent position information, where the reagent position information is obtained by scanning a code of a target reagent card or manually inputting the code, and may be selected according to different user habits or requirements of application scenarios, so that flexibility is high. Therefore, the first experimental project information is obtained by scanning the code of the target reagent card strip or manually inputting, so that the information inputting diversity is improved, and the requirements of different application scenes can be met.
And S150, responding to a fourth operation instruction, and associating the first target object, the quality control product experimental project information, the position information of the target reagent card strip and the first experimental project information.
The fourth operation instruction may be an operation instruction for a certain operation control, for example, an operation instruction for a "save" control, or an operation instruction for a current interface, for example, an operation instruction of clicking, double clicking, long pressing, or sliding in a designated area. When the quality control product is required to be detected, the sample analyzer needs to determine information such as the position of the quality control product to be detected, the item to be detected, the type of the used reagent, the position of the reagent and the like, through the steps, the position of the quality control product to be detected can be known by determining a first target object, the item to be detected can be known by determining the experimental item information of the quality control product through a quality control file, the position of the reagent and the type of the used reagent can be determined to be a single person reagent or a plurality of persons reagent through determining the position information and the first experimental item information of the target object, the quality control product, the position information of the target reagent card and the first experimental item information, and the sample analyzer can automatically select the corresponding reagent according to the related information when the quality control product is detected so as to execute the related detection item.
Thus, through the related operations of the first operation control 220 and the second operation control, the quality control product experimental project of the sample analyzer can be registered and correlated with the related information of the reagent card strip 131, so that the quality control detection can be performed on the sample analyzer by using a single reagent, and the quality control product and the reagent can be matched in the process of being compatible with multiple reagents and a single reagent.
With continued reference to fig. 4, in some application examples, the second interactive interface further displays a third operation control 240, and step S130, in response to a second operation instruction for the first operation control 220, determines a quality control file corresponding to the first target object, includes:
s131, determining the quality control type of the target reagent card strip in response to a fifth operation instruction to the third operation control 240;
and S132, updating the quality control file options associated with the first operation control 220 according to the quality control type of the target reagent card strip.
The quality control files are classified according to different quality control methods, wherein the quality control methods are used for monitoring and evaluating the accuracy and reliability of the experimental results, and whether the experimental results are within an acceptable range or not is judged by setting a series of quality control rules and limiting conditions, and whether the experimental results are abnormal or not is judged, for example, the quality control methods comprise Westgard multi-rule quality control and L-J quality control, and it should be understood that the Westgard multi-rule quality control and the L-J quality control are common quality control methods in the technical field, and the definitions and contents of the Westgard multi-rule quality control and the L-J quality control are not repeated herein. The third operation control 240 may be an operation control such as a single selection box, a check box or a drop-down list, in order to simplify the interface design, the drop-down list is taken as an example of the third operation control 240, the drop-down options of the third operation control 240 include Westgard multi-rule quality control and L-J quality control, and the quality control type of the target reagent card strip can be determined through the fifth operation instruction of the third operation control 240, and when the quality control types of the target reagent card strip are different, the quality control files associated with the first operation control 220 are also different, so that the display of the quality control files can be simplified by updating the quality control file options associated with the first operation control 220, and the management and the use of the quality control files are facilitated.
The quality control file may be customized according to the requirement of the user, referring to fig. 5 and fig. 6, and step S130, in response to a second operation instruction for the first operation control 220, determines a quality control file corresponding to the first target object, and further includes:
s133, responding to a sixth operation instruction, displaying a third interactive interface, wherein the third interactive interface is displayed with a quality control file list 250 and a fourth operation control 252;
the sixth operation instruction may be an operation instruction for a certain operation control in the current interactive interface, for example, an operation instruction for a "quality control" operation control of the current interactive interface, or an operation instruction for the current interactive interface, for example, an operation instruction for clicking, double-clicking, sliding or the like in a designated area, for example, an operation instruction for executing sliding in the current interactive interface, so as to implement switching of the current interactive interface. The fourth interactive interface may be displayed in a local area of the current interactive interface or may be an interface other than the current interactive interface. The quality control file list 250 is used for displaying a quality control file list, so that a user can browse and select a corresponding quality control file. In the default state, one or more quality control file options may be preconfigured in the quality control file list 250, or the quality control file list 250 may be emptied, so that the user may configure the quality control file in a self-defined manner.
S134, responding to a seventh operation instruction of the fourth operation control 252, displaying a fourth interactive interface, wherein the fourth interactive interface is displayed with a quality control file editing control 253 and a fifth operation control;
illustratively, fourth operational control 252 is a "new" operational control whose primary function is to add a quality control file option to quality control file list 250. The fourth interactive interface may be displayed in a local area of the current interactive interface or may be an interface other than the current interactive interface.
S135, responding to an eighth operation instruction of the quality control file editing control 253, and acquiring quality control file information;
illustratively, the quality control file editing control 253 has a function of enabling a user to input related information to obtain quality control file information, thereby generating corresponding quality control file options. The quality control file information may be information such as a quality control file name, quality control product information, quality control items, and the like, wherein the quality control items may be PT, APTT, TT, FIB, and the like.
And S136, closing the fourth interaction interface in response to a ninth operation instruction of the fifth operation control, and adding a quality control file item 251 corresponding to the quality control file in the quality control file list 250 according to the quality control file information.
For example, the fifth operation control may be a "save" control, and by clicking the fifth operation control, closing the fourth interactive interface, a corresponding quality control file item 251 is generated according to the quality control file information, and the quality control file item 251 is added to the quality control file list 250.
Through the arrangement, the user can carry out self-defined configuration on the quality control file according to different scene requirements, and the flexibility of use is improved.
With continued reference to fig. 6, in some application examples, the fourth interactive interface further displays a reagent type configuration control 260, and step S135, in response to an eighth operation instruction for the quality control file editing control 253, acquires quality control file information, includes:
s1351, in response to the eighth operation instruction of the reagent type configuration control 260 and the quality control file editing control 253, determining the reagent type and acquiring the quality control file information, wherein the reagent type is a single person reagent or a plurality of person reagents.
For example, the reagent type configuration control 260 may be an operation control such as a single selection box or a drop-down list, for example, two options including a single reagent and a plurality of reagents are configured in the drop-down list, the user determines the reagent type corresponding to the current quality control file through the selection operation of the reagent type configuration control 260, and the quality control file can be edited by the quality control file editing control 253, so that the reagent type and project information of the quality control product can be determined on the sample analyzer, and the plurality of reagents and the single reagent can be compatible.
In addition, referring to fig. 5, in step S136, in response to the ninth operation instruction of the fifth operation control, the fourth interactive interface is closed, and a quality control file item 251 corresponding to the quality control file is added to the quality control file list 250 according to the quality control file information, and then the method further includes:
s1371, rendering the quality control file item 251 into a marked state;
and S1372, updating the quality control file options associated with the first operation control 220 according to the quality control file item 251.
For example, one or more quality control file items 251 are displayed in the quality control file list 250, and the user may select one or more quality control file items 251 according to actual needs. The fifth operation control may be an operation instruction for a certain operation control, for example, an operation instruction for a "save" control, or an operation instruction for a current interface, for example, an operation instruction such as clicking, double clicking, long pressing, or sliding in a designated area. By operating the fifth operation control, a quality control file item 251 corresponding to the quality control file is added in the quality control file list 250, and then the newly added quality control file item 251 is rendered into a marked state to indicate that the quality control file item 251 is in an available state, so that the quality control file option associated with the first operation control 220 can be updated according to the quality control file item 251, so that a user can select the corresponding quality control file option, namely, select the corresponding quality control file through the operation of the first operation control 220.
Referring to fig. 5, in some application examples, step S136, in response to a ninth operation instruction of the fifth operation control, closes the fourth interaction interface, and adds a quality control file item 251 corresponding to the quality control file in the quality control file list 250 according to the quality control file information, and then further includes:
s1381, responding to a tenth operation instruction, and determining a second target object in the quality control file list 250;
s1382, rendering the second target object into a marked state or an unmarked state;
s1383, updating the quality control file options associated with the first operation control 220 according to the rendering state of the second target object.
For example, one or more quality control file items 251 are displayed in the quality control file list 250, and the user may select one or more quality control file items 251 according to actual needs. The tenth operation instruction may be an operation instruction for clicking, double clicking, long pressing, or the like on one of the quality control file items 251 in the quality control file list 250, or may be a frame selection operation instruction for a plurality of quality control file items 251 in the quality control file list 250, so as to determine the selected quality control file item 251 as the second target object. Rendering the second target object into a marked state or an unmarked state is convenient for the user to intuitively understand whether the second target object is in an available state, for example, an "enable" attribute is configured in the quality control file list 250, and when the "enable" attribute of the quality control file item 251 is displayed as a tick, it indicates that the quality control file item 251 is rendered into the marked state, and vice versa. In this way, according to the rendering state of the second target object, the quality control file option associated with the first operation control 220 is updated, so that the user can configure the quality control file item 251 to be in an available state or configure the quality control file item 251 to be in a disabled or standby state according to the actual application scene requirement, so as to meet the analysis requirements of different application scenes, and be beneficial to improving the diversity of the application scenes.
With continued reference to fig. 5, in some application examples, the third interactive interface further displays a sixth operation control 270, and in step S133, in response to the sixth operation instruction, the third interactive interface is displayed, and then further includes:
s1331, responding to an eleventh operation instruction of the sixth operation control 270, and determining the quality control type of the current quality control file.
For example, as described above, the quality control method includes Westgard multi-rule quality control and L-J quality control, in order to facilitate management and display of different quality control files, the third interactive interface is displayed with a sixth operation control 270, where the sixth operation control 270 may be an operation control such as a single box or a drop-down list, for example, the drop-down list is taken as an example of the sixth operation control 270, and the drop-down options of the sixth operation control 270 include Westgard multi-rule quality control and L-J quality control, and by using an eleventh operation instruction on the sixth operation control 270, the quality control type of the current quality control file may be determined.
Step S1331, in response to the eleventh operation instruction of the sixth operation control 270, determines the quality control type of the current quality control file, and then further includes:
s1332, updating the quality control file list 250 according to the quality control type of the current quality control file.
For example, when the quality control types are different, the quality control file items 251 of the quality control file list 250 are also different, and the quality control file list 250 is updated according to the quality control type of the current quality control file, so that the user can conveniently screen and manage different quality control files according to the quality control type, and the display of the quality control file items 251 is also facilitated to be simplified.
Referring to fig. 4 and fig. 7, in some application examples, the second operation control is a loading card bar 231 control, and step S140, in response to a third operation instruction for the second operation control, determines location information of the target reagent card bar and information of the first experiment item, includes:
s141, responding to a third operation instruction for loading the card bar 231 control, displaying a fifth interaction interface, wherein the fifth interaction interface is displayed with at least one second channel bitmap 280 corresponding to the target channel, and the second channel bitmap 280 is configured with at least one first graph 211;
s142, responding to a twelfth operation instruction, and determining the selected at least one first graph 211 in the at least one second channel bitmap 280 as a third target object;
s143, determining the position information of the target reagent card strip according to the position information of the third target object;
s144, responding to code scanning operation of the target reagent card strip, and acquiring first experimental project information.
The fifth interactive interface may be displayed in a local area of the current interactive interface, or may be an interface different from the current interactive interface. The second channel bitmap 280 corresponds to the target channels, for example, the number of the second channel bitmaps 280 is the same as the number of the target channels, and the position numbers correspond to each other. The twelfth operation instruction may be an operation instruction such as clicking, double clicking or long pressing for the second channel bitmap 280, by determining the third target object, the position information of the target channel that needs to be loaded by the reagent card strip 131 may be obtained, and by performing code scanning operation on the target reagent card strip, the relevant information of the reagent card strip 131 is automatically entered, so as to obtain the first experimental project information. When the user needs to load a plurality of reagent card strips, the above operation may be repeated to perform the recording, or the installation sequence of the plurality of reagent card strips may be determined according to the determination sequence of the first graph 211 in step S142, for example, the user clicks the first graph 211 with the sequence number 1 first and then clicks the first graph 211 with the sequence number 2 first, so as to indicate that two reagent card strips are sequentially installed on the installation positions with the sequence numbers 1 and 2, thereby facilitating the recording and the installation of the plurality of reagent card strips.
Referring to fig. 4 and 8, in other application examples, the second operation control is a manual entry card bar 232 control, and step S140, in response to a third operation instruction for the second operation control, determines location information of the target reagent card bar and information of the first experiment item, includes:
s145, responding to a third operation instruction of manually entering the card bar 232 control, displaying a sixth interactive interface, wherein the sixth interactive interface is displayed with at least one experiment item option 291 and at least one third channel bitmap 290 corresponding to a target channel, and the third channel bitmap 290 is configured with at least one first graph 211;
s146, in response to the thirteenth operation instruction, determining the selected at least one first graph 211 in the at least one third channel bitmap 290 as a fourth target object;
s147, determining the position information of the target reagent card strip according to the position information of the fourth target object;
s148, in response to a fourteenth operation instruction to the at least one experiment item option 291, the first experiment item information is determined.
Illustratively, in addition to the manner in which the scan code automatically enters the reagent card strip 131, the user may also manually enter relevant information for the reagent card strip 131. The sixth interactive interface may be displayed in a local area of the current interactive interface, or may be another interface different from the current interactive interface. The third channel bitmap 290 corresponds to the target channel, e.g., the number of second channel bitmaps 280 is the same as the number of target channels, and the position numbers correspond one-to-one. By determining the fourth target object, it is possible to know the positional information of the target channel on which the reagent card strip 131 needs to be loaded, and manually enter the first experimental item information by operating the experimental item option 291. The experiment item option 291 may be a preset option control or a manually input operation control, for example, lot number information of the reagent is input in the sixth interactive interface through an input box, so that the lot number information is added to the first experiment item information, and the lot number of the "PT" reagent is "2022032201" and the lot number of the "APTT" reagent is "2022032202" as shown in fig. 8.
Step S120, in response to the first operation instruction, determines the selected second graphic 212 as the first target object, and displays the second interactive interface, which further includes:
s121, responding to a fifteenth operation instruction, displaying a seventh interaction interface, wherein a seventh operation control is displayed on the seventh interaction interface;
s122, responding to a sixteenth operation instruction of the seventh operation control, and displaying an eighth interactive interface;
s123, responding to card swiping operation, and acquiring and displaying information of the target reagent card strip in the eighth interactive interface.
For example, the seventh interactive interface and the eighth interactive interface may each be displayed in a partial area of the current interactive interface or may be other interfaces different from the current interface. The seventh operation control may be a "swiping card" operation control, for example, before the reagent card strip 131 is loaded, the "swiping card" operation control needs to be clicked on a "reagent interface", that is, a seventh interaction interface, so as to enter the "swiping card interface", that is, an eighth interaction interface, and swiping a card by aligning the reagent card with a card swiping area of the sample analyzer, and after the swiping card is successful, reagent information related to the reagent card strip 131 in the card may be imported into the sample analyzer, where the reagent card may be a card capable of recording information such as a radio frequency induction card or a magnetic card, and reagent information in the reagent card includes ID, curve information, positional information of each reagent on the reagent card strip 131, validity period of the reagent, and specification information. And when the reagent information is successfully imported, displaying the information of the target reagent card strip in the eighth interactive interface so as to facilitate the visual understanding of the related information by a user.
Referring to fig. 9 and fig. 10, in some application examples, the second interactive interface further displays a reagent type configuration control 260, and step S130, in response to a second operation instruction for the first operation control 220, determines a quality control file corresponding to the first target object, and determines quality control experiment item information according to the quality control file of the first target object, including:
s1301, responding to a second operation instruction of the first operation control 220, and determining a quality control file corresponding to the first target object;
s1302, responding to a seventeenth operation instruction of the reagent type configuration control 260, and determining a reagent type corresponding to the first target object, wherein the reagent type is a single person reagent or a plurality of person reagents;
and S1303, determining quality control product experimental project information according to the quality control file and the reagent type corresponding to the first target object.
For example, unlike step S1351, step S1351 is directed to the reagent type configuration control 260 displayed in the fourth interactive interface, and steps S1301-S1303 are directed to the reagent type configuration control 260 displayed in the second interactive interface, where, of course, the reagent type configuration control 260 may be configured in the fourth interactive interface or the second interactive interface according to the requirements of the actual application scenario, for example, please refer to fig. 9, in the second interactive interface, the number of reagent type configuration controls 260 is only one and corresponds to the quality control file, and please refer to fig. 10, the number of reagent type configuration controls 260 is plural, and each reagent type configuration control 260 may independently configure the reagent of each experiment item; the reagent type configuration control 260 may also be configured in the fourth and second interactive interfaces, but the option contents of the reagent type configuration control 260 in the fourth and second interactive interfaces need to be synchronized. For example, referring to fig. 6 and 9, in the case that the reagent type of one of the quality control files is configured as a single reagent by the reagent type configuration control 260 in the fourth interactive interface, the reagent type of the quality control file should also be displayed as a single reagent in the second interactive interface.
Referring to fig. 4, 9 or 10, in some application examples, step S110 of displaying a first interactive interface includes:
s112, displaying a first interactive interface, where the first interactive interface displays a plurality of first channel bitmaps 210 corresponding to the target channel, and at least one first channel bitmap 210 is displayed as a first channel pattern, and the first channel pattern is configured with at least one first graphic 211 and at least one second graphic 212.
Illustratively, when the loading channel 110 mounts the reagent card strip loading rack 130, the first channel bitmap 210 corresponding to the loading channel 110 is displayed as a first channel pattern, as shown by the two first channel bitmaps 210 on the left side, and of course, in the case that all the loading channels 110 mount the reagent card strip loading rack 130, the illustrated 4 first channel bitmaps 210 may all be displayed as the first channel patterns. The first channel pattern is configured with first patterns 211 and second patterns 212, and the number of the first patterns 211 and the second patterns 212 may be one or more, and each first channel bitmap 210 is shown with two first patterns 211 and one second pattern 212. The first operation instruction in step S120 may be directed to any one of the plurality of second patterns 212, and of course, if there is and only one of the second patterns 212, the target object of the first operation instruction may be unambiguously determined.
Referring to fig. 4, 9 or 10, in another application example, step S110, displaying a first interactive interface includes:
s112, displaying a first interactive interface, where the first interactive interface displays a plurality of first channel bitmaps 210 corresponding to the target channel, at least one first channel bitmap 210 is displayed as a first channel pattern and at least one first channel bitmap 210 is displayed as a second channel pattern, the first channel pattern is configured with at least one first graphic 211, and the second channel pattern is configured with at least one second graphic 212.
Illustratively, the number of loading channels 110 may be a plurality, e.g., 4, and 4 loading channels 110 may mount a sample tube loading rack 120 or a reagent card strip loading rack 130, and when one of the loading channels 110 mounts a reagent card strip loading rack 130, the corresponding first channel bitmap 210 of the loading channel 110 is displayed as a first channel pattern, as shown by the first channel bitmap 210 on the left side, but the first channel bitmap 210 on the left side may not be configured with the second pattern 212; when one of the loading channels 110 mounts the sample tube loading rack 120, the corresponding first channel bitmap 210 of that loading channel 110 is displayed as a second channel pattern, as shown by the first channel bitmap 210 on the right side. The number of second patterns 212 in the second channel pattern is the same as the number of sample tubes 121 that can be placed on the sample tube carrier 120. At this time, the second pattern 212 in step S120 may be the second pattern 212 in the first channel pattern, or may be the second pattern 212 in the second channel pattern, that is, the same operation may be performed on the second pattern 212 corresponding to any sample tube 121.
Referring to fig. 14, based on the above quality control product experimental item registration method, the present embodiment further provides a sample analyzer, which includes a first display module 311, a first response module 312, a second response module 313, a third response module 314, and a fourth response module 315, where the inventive concept of the sample analyzer is the same as that of the above quality control product experimental item registration method, and the details not related in the embodiments may refer to the above quality control product experimental item registration method example, which will not be described in detail below:
the first display module 311 is configured to display a first interactive interface, where the first interactive interface displays at least one first graphic 211 and at least one second graphic 212, the first graphic 211 corresponds to the reagent card strip 131, and the second graphic 212 corresponds to the sample tube 121;
the first response module 312 is configured to determine the selected second graphic 212 as a first target object in response to the first operation instruction, and display a second interactive interface, where the second interactive interface displays the first operation control 220 and the second operation control;
the second response module 313 is configured to determine a quality control file corresponding to the first target object in response to the second operation instruction for the first operation control 220, and determine quality control experiment item information according to the quality control file of the first target object;
The third response module 314 is configured to determine, in response to a third operation instruction for the second operation control, location information of the target reagent card strip and first experimental item information, where the first experimental item information is obtained by scanning a code of the target reagent card strip or is obtained by manually inputting the code;
and the fourth response module 315 is configured to correlate the first target object, the quality control experiment item information, the position information of the target reagent card strip, and the first experiment item information in response to the fourth operation instruction.
According to the embodiment, through the related operation of the first operation control and the second operation control, the quality control product experimental project of the sample analyzer can be registered and correlated with the related information of the reagent card strip, so that the quality control detection can be carried out on the sample analyzer by using a single reagent, and the quality control product and the reagent can be matched in the process of being compatible with multiple reagents and a single reagent.
Referring to fig. 11, the present embodiment further provides a quality control product experimental project registration method, which includes steps S210 to S250, for implementing registration of quality control product experimental projects in a process of being compatible with multiple human reagents and single human reagents, so as to determine whether to suck multiple human reagents or suck single human reagents when performing quality control product analysis. It should be noted that, the steps in this embodiment are labeled only for facilitating examination and understanding, and not limiting the execution sequence of the steps, and in practical application, the steps may be adaptively adjusted according to the logic relationship between the steps. The contents of the individual steps are described in detail below with reference to fig. 1, 2 and 4:
S210, displaying a first interactive interface, wherein the first interactive interface is displayed with at least one first graph 211 and at least one second graph 212, the first graph 211 corresponds to the reagent card strip 131, and the second graph 212 corresponds to the sample tube 121;
s220, responding to an eighteenth operation instruction, determining the selected first graph 211 as a fifth target object, and determining first experimental item information and position information of a target reagent card strip, wherein the first experimental item information is obtained by scanning a code of the target reagent card strip or manually inputting;
s230, responding to the first operation instruction, determining the selected second graph 212 as a first target object, and displaying a second interactive interface, wherein the second interactive interface is displayed with a first operation control 220;
s240, responding to a second operation instruction of the first operation control 220, determining a quality control file corresponding to the first target object, and determining quality control experiment item information according to the quality control file of the first target object;
and S250, responding to a fourth operation instruction, and associating the first target object, the quality control product experimental project information, the position information of the target reagent card strip and the first experimental project information.
The steps S110 to S130 are different from the steps S110 to S150 in that after determining the first target object, the first experimental item information and the position information of the target reagent card strip are determined by the related operation of the second operation control, and the steps S210 to S250 are that before determining the first target object, the selected first graph 211 is determined as the fifth target object, the first experimental item information and the position information of the target reagent card strip are determined, and then the selected second graph 212 is determined as the first target object, so as to determine the quality control item experimental item information. Thus, the embodiment provides two different operation modes, which can meet the operation habits of different users and is beneficial to enhancing the user experience. Specifically, the number of the first patterns 211 in the first channel bitmap 210 is the same as the mountable number of the reagent card stripes 131, and the positions are in one-to-one correspondence. The selected first graph 211 can be determined as a fifth target object through operation instructions such as clicking, double clicking or long pressing, so that the installation position of the target reagent card strip is determined, and then after the user manually inputs related information of the reagent card strip 131 through code scanning, the reagent card strip 131 is installed at a corresponding position, so that the corresponding position of the reagent can be positioned during subsequent quality control analysis.
It is to be understood that, in order to avoid redundancy, the content not related to the embodiment of the quality control experiment item registration method may refer to the embodiment of the quality control experiment item registration method described above. For example, regarding the inventive concept of the reagent type configuration control 260, reference may be made to step S1351 or steps S1301 to S1303; the inventive concept related to the card swiping operation can refer to steps S121 to S123; the inventive concept regarding the first channel pattern and the second channel pattern may refer to step S111; the inventive concept of the quality control file information can refer to steps S1371-S1372, S1381-S1383 or steps S1331-S1332.
Referring to fig. 15, based on the above quality control product experimental item registration method, the present embodiment further provides a sample analyzer, including a second display module 321, a fifth response module 322, a sixth response module 323, a seventh response module 324, and an eighth response module 325, where the inventive concept of the sample analyzer is the same as that of the above quality control product experimental item registration method, and details not related to the embodiment of the above quality control product experimental item registration method may be referred to below without further description:
the second display module 321 is configured to display a first interactive interface, where the first interactive interface displays at least one first graphic 211 and at least one second graphic 212, the first graphic 211 corresponds to the reagent card strip 131, and the second graphic 212 corresponds to the sample tube 121;
A fifth response module 322, configured to determine, in response to the eighteenth operation instruction, the selected first graphic 211 as a fifth target object, and determine first experimental item information and position information of the target reagent card strip, where the first experimental item information is obtained by scanning a code of the target reagent card strip or is obtained by manually inputting the code;
a sixth response module 323, configured to determine, in response to the first operation instruction, the selected second graphic 212 as a first target object, and display a second interaction interface, where the second interaction interface displays the first operation control 220;
the seventh response module 324 is configured to determine a quality control file corresponding to the first target object in response to the second operation instruction for the first operation control 220, and determine quality control experiment item information according to the quality control file of the first target object;
and an eighth response module 325, configured to correlate the first target object, the quality control experiment item information, the position information of the target reagent card strip, and the first experiment item information in response to the fourth operation instruction.
According to the embodiment, through the related operation of the first graph and the first operation control, the quality control product experimental project of the sample analyzer can be registered and correlated with the related information of the reagent card strip, so that the quality control detection can be carried out on the sample analyzer by using a single reagent, and the quality control product and the reagent can be matched in the process of being compatible with multiple reagents and a single reagent.
According to the method, the quality control test items can be registered in the sample analyzer, and after the quality control test items are registered, the sample analyzer can perform quality control detection according to the related information, so referring to fig. 12, the embodiment further provides a quality control test control method, which comprises steps S310 to S360, for judging whether to suck a plurality of reagents or a single reagent in a process of being compatible with the plurality of reagents and the single reagent. It should be noted that, the steps in this embodiment are labeled only for facilitating examination and understanding, and not limiting the execution sequence of the steps, and in practical application, the steps may be adaptively adjusted according to the logic relationship between the steps. The following details are made with reference to the content of the individual steps:
s310, acquiring associated information of a current quality control product, wherein the associated information comprises position information of the current quality control product, quality control product experiment item information, position information of a target reagent card strip and first experiment item information, the quality control product experiment item information is used for representing experiment item information of the current quality control product, and the first experiment item information is used for representing reagent information of a single person;
s320, determining the reagent type of the current quality control product according to the position information of the current quality control product, wherein the reagent type is a single-person reagent or a multi-person reagent;
S330, under the condition that the reagent type is a single reagent, determining a current experiment item according to the quality control product experiment item information;
s340, determining the first feasibility of the current experiment item according to the first experiment item information;
s350, under the condition that the first feasibility of the current experiment item is characterized in the affirmative, determining the position information of the target reagent according to the current experiment item, the first experiment item information and the position information of the target reagent card strip;
or, if the first feasibility of the current experiment item is characterized as negative, determining the reagent type corresponding to the current experiment item as a multi-person reagent in S360.
For example, according to the quality control product experimental project registration method in steps S110 to S150 or steps S210 to S250, the correlation of quality control product experimental project information, position information of the target reagent card strip and first experimental project information can be implemented on the target sample tube, and when quality control product detection is performed, quality control products in the plurality of sample tubes 121 can be sequentially detected to determine the position information of the current quality control product. According to the embodiment, the reagent type of the current quality control product is determined according to the position information of the current quality control product, so that automatic configuration of the reagent type can be realized, user operation is reduced, and the user experience is enhanced, for example, the placement position of the current quality control product is on the reagent card strip loading frame 130, the reagent type of the current quality control product is determined to be a single reagent, namely, the corresponding reagent is sucked from the reagent card strip 131 for quality control product detection, and if the placement position of the current quality control product is not on the reagent card strip loading frame 130, the reagent type of the current quality control product is determined to be a plurality of human reagents, namely, the corresponding reagent is sucked from the reagent bottle for quality control product detection. In practical applications, the type of the reagent on the reagent card 131 may not meet the requirement of quality control product detection, for example, FIB reagent is needed for quality control product detection, but the quality control product detection cannot be performed due to lack of FIB reagent caused by unconfiguration or consumption depletion of the reagent card 131, so that the first feasibility of the current experiment item is determined by performing feasibility analysis on the current experiment item, and if the first feasibility is characterized as affirmative, the position information of the target reagent is determined, so that the sample analyzer can absorb the corresponding reagent according to the position information of the target reagent; under the condition that the first feasibility is characterized as negative, the multi-person reagent is used instead, namely, the type of the reagent corresponding to the current experiment item is determined to be the multi-person reagent, for example, the current experiment item comprises an APTT item, but the reagent card strip 131 lacks APTT reagent, namely lacks single-person APTT reagent, and the reagent storage amount of the reagent bottle is more than that of the reagent card strip 131, so that the APTT reagent can be sucked from the reagent bottle of the APTT, namely, the multi-person reagent is adopted for quality control detection. Therefore, the mixed use of the single reagent and the multiple reagents can be realized, so that the single reagent and the multiple reagents are compatible on the sample analyzer, and the flexibility of quality control product detection is improved.
Step S360, determining the reagent type corresponding to the current experiment item as a multi-person reagent under the condition that the feasibility of the current experiment item is represented as negative, and then further comprising:
s371, acquiring reagent information of a plurality of human reagents;
s372, determining the second feasibility of the current experiment item according to the reagent information of the multiple human reagents;
s373, determining the position information of a target reagent according to the reagent information of the multiple human reagents under the condition that the second feasibility of the current experimental project is characterized in the affirmative;
or, if the second feasibility of the current experimental project is characterized as negative, performing alarm processing S374.
The reagent information of the multiple human reagents may be configured in a pre-stored manner and may be obtained in a manner such as table look-up or index, for example, the current experiment item includes an APTT item, but lacks an APTT reagent of a single human, and according to the reagent information of the multiple human reagents, it may be determined whether the multiple human reagents have an APTT reagent and whether the stock of the APTT reagent meets the quality control detection requirement, that is, the second feasibility of the current experiment item is determined. In the event that the second feasibility is characterized as affirmative, determining the location information of the target reagent based on the reagent information of the multi-human reagent, thereby enabling the sample analyzer to aspirate the corresponding multi-human reagent from the corresponding location. And in the event that the second feasibility is characterized as negative, an alarm is provided, such as a prompt "lack of reagent, no test is initiated.
Therefore, the reagent type can be determined according to the position information of the current quality control product, and the first feasibility of the current project can be determined according to the first experimental project, so that the reagent can be automatically selected and adjusted to be compatible with multiple human reagents and single human reagents.
Referring to fig. 16, based on the above quality control product detection control method, the present embodiment further provides a sample analyzer, which includes a first obtaining module 331, a first determining module 332, a second determining module 333, a third determining module 334, and a fourth determining module 335, where the inventive concept of the sample analyzer is the same as that of the above quality control product detection control method, and the content not related in the embodiment may refer to the above quality control product detection control method example, and will not be described in detail below:
the first obtaining module 331 is configured to obtain association information of a current quality control product, where the association information includes location information of the current quality control product, quality control product experiment item information, location information of a target reagent card strip, and first experiment item information, the quality control product experiment item information is used to represent experiment item information of the current quality control product, and the first experiment item information is used to represent reagent information of a single person;
The first determining module 332 is configured to determine, according to the position information of the current quality control, a reagent type of the current quality control, where the reagent type is a single person reagent or multiple person reagents;
the second determining module 333 is configured to determine, according to the quality control product experimental project information, a current experimental project in case that the reagent type is a single reagent;
a third determining module 334, configured to determine a first feasibility of the current experiment item according to the first experiment item information;
a fourth determining module 335, configured to determine, if the first feasibility of the current experiment item is characterized in the affirmative, location information of the target reagent according to the current experiment item, the first experiment item information and the location information of the target reagent card strip;
or, in the case that the first feasibility of the current experiment item is characterized as negative, determining the reagent type corresponding to the current experiment item as a multi-human reagent.
According to the embodiment, the reagent type is determined according to the position information of the current quality control product, and the first feasibility of the current project is determined according to the first experimental project, so that automatic selection and adjustment of the reagent can be realized, and automatic selection of the single reagent and the multiple reagents in the process of being compatible with the multiple reagents and the single reagent is realized.
In addition, in the above, in the steps S1351 or S1301 to S1303, the reagent type is determined by the reagent type configuration control 260 when the quality control experiment item is registered, and accordingly, a single person reagent or multiple person reagents can be selected according to the reagent type when the quality control is detected. Therefore, referring to fig. 13, the present embodiment also provides a quality control product detection control method, including steps S410 to S460, and it should be noted that the steps in the present embodiment are labeled only for facilitating examination and understanding, and not limiting the execution sequence of the steps, and in practical application, the steps may be adaptively adjusted according to the logic relationship between the steps. The following details are made with reference to the content of the individual steps:
s410, acquiring associated information of a current quality control product, wherein the associated information comprises quality control product experimental project information, position information of a target reagent card strip and first experimental project information, the quality control product experimental project information is used for representing experimental project information of the current quality control product, and the first experimental project information is used for representing reagent information of a single person;
s420, determining the reagent type of the current quality control product according to the quality control product experimental project information, wherein the reagent type is a single-person reagent or a multi-person reagent;
S430, under the condition that the reagent type is a single reagent, determining a current experiment item according to the quality control product experiment item information;
s440, determining the first feasibility of the current experiment item according to the first experiment item information;
s450, determining the position information of a target reagent according to the current experiment item, the first experiment item information and the position information of the target reagent card strip under the condition that the first feasibility of the current experiment item is characterized in the affirmative;
or, if the first feasibility of the current experiment item is characterized as negative, determining the reagent type corresponding to the current experiment item as a multi-person reagent, wherein S460 is the same as the reagent type corresponding to the current experiment item.
For example, through the related operations in steps S1351 or S1301 to S1303, the information of the quality control product experiment item may carry the reagent type, so that the reagent type of the current quality control product may be determined according to the information of the quality control product experiment item, for example, the quality control product experiment item includes four items, i.e., PT, APTT, TT and FIB, where the reagent type of the APTT is a multiple-person reagent, i.e., the reagent needs to be sucked from the reagent bottle, and the reagent types of the remaining three items are a single-person reagent, i.e., the reagent needs to be sucked from the reagent card 131. When the single reagent can not meet the detection requirement, the multi-person reagent is selected for detection, so that the mixed use of the single reagent and the multi-person reagent can be realized, the single reagent and the multi-person reagent are compatible on the sample analyzer, and the quality control product detection flexibility is improved.
Step S460, determining the reagent type corresponding to the current experiment item as a multi-person reagent under the condition that the feasibility of the current experiment item is represented as negative, and then further comprising:
s471, acquiring reagent information of a plurality of human reagents;
s472, determining the second feasibility of the current experiment item according to the reagent information of the multiple human reagents;
s473, determining the position information of the target reagent according to the reagent information of the multiple human reagents under the condition that the second feasibility of the current experimental project is characterized in the affirmative;
or, if the second feasibility of the current experimental project is characterized as negative, performing alarm processing S474.
Similar to steps S371-S374, if a plurality of human reagents can meet the detection requirement, the corresponding reagents are sucked from the reagent bottles, and if a plurality of human reagents cannot meet the detection requirement, an alarm is performed, for example, a prompt "lack of reagent, and failure to start the test" is given.
Therefore, the reagent type can be determined according to the quality control product experimental project information, and the first feasibility of the current project can be determined according to the first experimental project, so that the reagent can be automatically selected and adjusted to be compatible with multiple reagents and single reagents.
Referring to fig. 17, based on the above quality control product detection control method, the present embodiment further provides a sample analyzer, which includes a second obtaining module 341, a fifth determining module 342, a sixth determining module 343, a seventh determining module 344, and an eighth determining module 345, where the inventive concept of the sample analyzer is the same as that of the above quality control product detection control method, and the content not related in the embodiment may refer to the above quality control product detection control method embodiment, and will not be described in detail below:
the second obtaining module 341 is configured to obtain association information of a current quality control product, where the association information includes quality control product experiment item information, position information of a target reagent card strip, and first experiment item information, the quality control product experiment item information is used to represent experiment item information of the current quality control product, and the first experiment item information is used to represent reagent information of a single person;
a fifth determining module 342, configured to determine, according to the quality control item information, a reagent type of the current quality control item, where the reagent type is a single reagent or multiple reagents;
a sixth determining module 343, configured to determine, according to the quality control experiment item information, a current experiment item in case that the reagent type is a single reagent;
A seventh determining module 344, configured to determine a first feasibility of the current experiment item according to the first experiment item information;
an eighth determining module 345, configured to determine, if the first feasibility of the current experiment item is characterized in affirmative, location information of the target reagent according to the current experiment item, the first experiment item information and the location information of the target reagent card strip;
or, in the case that the first feasibility of the current experiment item is characterized as negative, determining the reagent type corresponding to the current experiment item as a multi-human reagent.
According to the embodiment, the reagent type is determined according to the quality control product experimental project information, and the first feasibility of the current project is determined according to the first experimental project, so that automatic selection and adjustment of the reagent can be realized, and automatic selection of the single reagent and the multiple reagents in the process of being compatible with the multiple reagents and the single reagent is realized.
The embodiments of the present invention have been described in detail with reference to the accompanying drawings, but the present invention is not limited to the above embodiments, and various changes can be made within the knowledge of one of ordinary skill in the art without departing from the spirit of the present invention.
Claims (16)
1. The quality control product experimental project registration method is characterized by comprising the following steps of:
Displaying a first interactive interface, wherein the first interactive interface displays at least one first graph and at least one second graph, the first graph corresponds to the reagent card strip, and the second graph corresponds to the sample tube;
responding to a first operation instruction, determining the selected second graph as a first target object, and displaying a second interactive interface, wherein the second interactive interface is displayed with a first operation control and a second operation control;
responding to a second operation instruction of the first operation control, determining a quality control file corresponding to the first target object, and determining quality control experiment item information according to the quality control file of the first target object;
determining position information of a target reagent card strip and first experimental item information in response to a third operation instruction of the second operation control, wherein the first experimental item information is obtained by scanning a code of the target reagent card strip or manually inputting the code;
and responding to a fourth operation instruction, and associating the first target object, the quality control product experimental project information, the position information of the target reagent card strip and the first experimental project information.
2. The quality control product experiment item registration method according to claim 1, wherein the second interactive interface further displays a third operation control, and the determining, in response to the second operation instruction for the first operation control, the quality control file corresponding to the first target object further includes:
Responding to a fifth operation instruction of the third operation control, and determining the quality control type of the target reagent card strip;
and updating the quality control file options associated with the first operation control according to the quality control type of the target reagent card strip.
3. The quality control experiment item registration method according to claim 1, wherein the determining, in response to the second operation instruction for the first operation control, the quality control file corresponding to the first target object further includes:
responding to a sixth operation instruction, displaying a third interactive interface, wherein the third interactive interface is displayed with a quality control file list and a fourth operation control;
responding to a seventh operation instruction of the fourth operation control, displaying a fourth interactive interface, wherein the fourth interactive interface is displayed with a quality control file editing control and a fifth operation control;
responding to an eighth operation instruction of the quality control file editing control to acquire quality control file information;
and closing the fourth interaction interface in response to a ninth operation instruction of the fifth operation control, and adding a quality control file item corresponding to the quality control file in the quality control file list according to the quality control file information.
4. The quality control product experiment item registration method according to claim 3, wherein the fourth interactive interface further displays a reagent type configuration control, and the responding to the eighth operation instruction of the quality control file editing control to obtain quality control file information includes:
and responding to an eighth operation instruction of the reagent type configuration control and the quality control file editing control, determining a reagent type and acquiring quality control file information, wherein the reagent type is a single person reagent or a plurality of persons reagent.
5. The quality control product experiment item registration method according to claim 3, wherein the responding to the ninth operation instruction of the fifth operation control closes the fourth interaction interface, and adds a quality control file item corresponding to the quality control file in the quality control file list according to the quality control file information, and further comprises:
rendering the quality control file items into a marked state;
and updating the quality control file options associated with the first operation control according to the quality control file items.
6. The quality control product experiment item registration method according to claim 5, wherein the responding to the ninth operation instruction of the fifth operation control closes the fourth interaction interface, and adds a quality control file item corresponding to the quality control file in the quality control file list according to the quality control file information, and further comprises:
Responding to a tenth operation instruction, and determining a second target object in the quality control file list;
rendering the second target object into a marked state or an unmarked state;
and updating the quality control file options associated with the first operation control according to the rendering state of the second target object.
7. The quality control experiment item registration method of claim 3, wherein the third interactive interface further displays a sixth operation control, and the displaying the third interactive interface in response to the sixth operation instruction further includes:
and responding to an eleventh operation instruction of the sixth operation control, and determining the quality control type of the current quality control file.
8. The quality control experiment item registration method according to claim 7, wherein the determining the quality control type of the current quality control file in response to an eleventh operation instruction to the sixth operation control further comprises:
and updating the quality control file list according to the quality control type of the current quality control file.
9. The quality control product experimental item registration method according to claim 1, wherein the second operation control is a loading card bar control, and the determining the position information of the target reagent card bar and the first experimental item information in response to the third operation instruction of the second operation control includes:
Responding to a third operation instruction for loading the card bar control, displaying a fifth interaction interface, wherein the fifth interaction interface is displayed with at least one second channel bitmap corresponding to a target channel, and the second channel bitmap is configured with at least one first graph;
in response to a twelfth operation instruction, determining the selected at least one first graphic in the at least one second channel bitmap as a third target object;
determining the position information of the target reagent card strip according to the position information of the third target object;
and responding to the code scanning operation of the target reagent card strip, and acquiring the first experimental project information.
10. The quality control product experimental item registration method according to claim 1, wherein the second operation control is a manual entry card bar control, and the determining the position information of the target reagent card bar and the first experimental item information in response to the third operation instruction of the second operation control includes:
responding to a third operation instruction of the manual entry card bar control, displaying a sixth interactive interface, wherein the sixth interactive interface displays at least one experimental item option and at least one third channel bitmap corresponding to a target channel, and the third channel bitmap is configured with at least one first graph;
In response to a thirteenth operation instruction, determining the selected at least one first graphic in the at least one third channel bitmap as a fourth target object;
determining the position information of the target reagent card strip according to the position information of the fourth target object;
the first experimental item information is determined in response to a fourteenth operational instruction for the at least one experimental item option.
11. The quality control experiment item registration method according to claim 1, wherein the determining the selected second graphic as the first target object in response to the first operation instruction, and displaying the second interactive interface, further comprises:
responding to a fifteenth operation instruction, displaying a seventh interactive interface, wherein a seventh operation control is displayed on the seventh interactive interface;
responding to a sixteenth operation instruction of the seventh operation control, and displaying an eighth interactive interface;
and responding to the card swiping operation, and acquiring and displaying the information of the target reagent card strip in the eighth interactive interface.
12. The quality control product experimental project registration method according to claim 1, wherein the second interactive interface further displays a reagent type configuration control, the determining a quality control file corresponding to the first target object in response to a second operation instruction for the first operation control, and determining quality control product experimental project information according to the quality control file of the first target object includes:
Responding to a second operation instruction of the first operation control, and determining a quality control file corresponding to the first target object;
determining a reagent type corresponding to the first target object in response to a seventeenth operation instruction of the reagent type configuration control, wherein the reagent type is a single-person reagent or a multi-person reagent;
and determining quality control product experimental project information according to the quality control file and the reagent type corresponding to the first target object.
13. The quality control experiment item registration method according to any one of claims 1 to 12, wherein displaying the first interactive interface includes:
displaying a first interactive interface, the first interactive interface displaying at least one first channel bitmap corresponding to a target channel, at least one of the first channel bitmaps being displayed as a first channel pattern configured with at least one first graphic and at least one second graphic,
or displaying a first interactive interface, wherein the first interactive interface displays a plurality of first channel bitmaps corresponding to a target channel, at least one first channel bitmap is displayed as the first channel pattern, and at least one first channel bitmap is displayed as a second channel pattern, the first channel pattern is configured with at least one first graph, and the second channel pattern is configured with at least one second graph.
14. The quality control product experimental project registration method is characterized by comprising the following steps of:
displaying a first interactive interface, wherein the first interactive interface displays at least one first graph and at least one second graph, the first graph corresponds to the reagent card strip, and the second graph corresponds to the sample tube;
responding to an eighteenth operation instruction, determining the selected first graph as a fifth target object, and determining first experimental item information and position information of a target reagent card strip, wherein the first experimental item information is obtained by scanning a code of the target reagent card strip or manually inputting the code;
responding to a first operation instruction, determining the selected second graph as a first target object, and displaying a second interactive interface, wherein the second interactive interface is displayed with a first operation control;
responding to a second operation instruction of the first operation control, determining a quality control file corresponding to the first target object, and determining quality control experiment item information according to the quality control file of the first target object;
and responding to a fourth operation instruction, and associating the first target object, the quality control product experimental project information, the position information of the target reagent card strip and the first experimental project information.
15. The quality control product detection control method is characterized by comprising the following steps:
acquiring associated information of a current quality control product, wherein the associated information comprises position information of the current quality control product, quality control product experiment item information, position information of a target reagent card strip and first experiment item information, or the associated information comprises quality control product experiment item information, position information of the target reagent card strip and first experiment item information, the quality control product experiment item information is used for representing the experiment item information of the current quality control product, and the first experiment item information is used for representing the reagent information of a single person;
determining the reagent type of the current quality control product according to the position information of the current quality control product or the quality control product experimental project information, wherein the reagent type is a single-person reagent or a multi-person reagent;
under the condition that the reagent type is a single reagent, determining a current experiment item according to the quality control product experiment item information;
determining a first feasibility of the current experiment item according to the first experiment item information;
determining the position information of a target reagent according to the current experiment item, the first experiment item information and the position information of the target reagent card strip under the condition that the first feasibility of the current experiment item is characterized in the affirmative;
Or determining the reagent type corresponding to the current experiment item as a multi-person reagent in the case that the first feasibility of the current experiment item is characterized as negative.
16. The quality control article detection control method according to claim 15, wherein in the case where the feasibility of the current experiment item is characterized as negative, determining the reagent type corresponding to the current experiment item as a multi-human reagent, further comprises:
acquiring reagent information of a plurality of human reagents;
determining a second feasibility of the current experiment item according to the reagent information of the multiple human reagents;
determining the position information of a target reagent according to the reagent information of the multiple human reagents under the condition that the second feasibility of the current experimental project is characterized in the affirmative;
or, in case the second feasibility of the current experimental project is characterized as negative, performing alarm processing.
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Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN113866431A (en) * | 2020-06-30 | 2021-12-31 | 深圳迈瑞生物医疗电子股份有限公司 | Sample analysis system and quality control method and test method thereof |
| CN114093444A (en) * | 2022-01-10 | 2022-02-25 | 深圳市帝迈生物技术有限公司 | Reagent loading control method, reagent loading control device, computer equipment and storage medium |
| CN114200151A (en) * | 2022-02-17 | 2022-03-18 | 宁波海壹生物科技有限公司 | Full-automatic chemiluminescence immunoassay analyzer management system |
| CN114239627A (en) * | 2021-12-20 | 2022-03-25 | 中元汇吉生物技术股份有限公司 | Quality control product importing method, device, equipment and computer readable storage medium |
| CN115298550A (en) * | 2020-03-23 | 2022-11-04 | 株式会社日立高新技术 | Automatic analysis system |
| CN115343487A (en) * | 2021-05-12 | 2022-11-15 | 深圳迈瑞生物医疗电子股份有限公司 | Sample analysis system and reagent specifying method |
| CN115798659A (en) * | 2022-12-02 | 2023-03-14 | 中元汇吉生物技术股份有限公司 | Quality control method, quality control system, analyzer and computer storage medium |
| CN116936066A (en) * | 2022-03-31 | 2023-10-24 | 深圳迈瑞生物医疗电子股份有限公司 | Sample analysis system and information editing method |
| WO2023216638A1 (en) * | 2022-05-12 | 2023-11-16 | 深圳市帝迈生物技术有限公司 | Testing apparatus for testing coagulation item and reagent card |
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Patent Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115298550A (en) * | 2020-03-23 | 2022-11-04 | 株式会社日立高新技术 | Automatic analysis system |
| CN113866431A (en) * | 2020-06-30 | 2021-12-31 | 深圳迈瑞生物医疗电子股份有限公司 | Sample analysis system and quality control method and test method thereof |
| CN115343487A (en) * | 2021-05-12 | 2022-11-15 | 深圳迈瑞生物医疗电子股份有限公司 | Sample analysis system and reagent specifying method |
| CN114239627A (en) * | 2021-12-20 | 2022-03-25 | 中元汇吉生物技术股份有限公司 | Quality control product importing method, device, equipment and computer readable storage medium |
| CN114093444A (en) * | 2022-01-10 | 2022-02-25 | 深圳市帝迈生物技术有限公司 | Reagent loading control method, reagent loading control device, computer equipment and storage medium |
| CN114200151A (en) * | 2022-02-17 | 2022-03-18 | 宁波海壹生物科技有限公司 | Full-automatic chemiluminescence immunoassay analyzer management system |
| CN116936066A (en) * | 2022-03-31 | 2023-10-24 | 深圳迈瑞生物医疗电子股份有限公司 | Sample analysis system and information editing method |
| WO2023216638A1 (en) * | 2022-05-12 | 2023-11-16 | 深圳市帝迈生物技术有限公司 | Testing apparatus for testing coagulation item and reagent card |
| CN117092325A (en) * | 2022-05-12 | 2023-11-21 | 深圳市帝迈生物技术有限公司 | Detection device and reagent card for detecting coagulation project |
| CN115798659A (en) * | 2022-12-02 | 2023-03-14 | 中元汇吉生物技术股份有限公司 | Quality control method, quality control system, analyzer and computer storage medium |
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