CN111584057A

CN111584057A - Method and device for updating state of instrument

Info

Publication number: CN111584057A
Application number: CN201910120057.8A
Authority: CN
Inventors: 于怀博; 高雪红; 姚言义; 郑文洋; 何明; 张震
Original assignee: Shenzhen Increcare Biotech Co Ltd
Current assignee: Shenzhen Increcare Biotech Co Ltd
Priority date: 2019-02-18
Filing date: 2019-02-18
Publication date: 2020-08-25
Anticipated expiration: 2039-02-18
Also published as: CN111584057B

Abstract

The application relates to a method and a device for updating instrument states. The method comprises the steps of determining a state identification group to be updated in an instrument state bar; the instrument status bar is displayed in an operation interface of the in-vitro diagnosis equipment; monitoring the instrument state corresponding to each state identifier in the state identifier group in real time; when the instrument state corresponding to at least one state identifier is monitored to change, the changed instrument state is obtained; and updating the changed state of the instrument to the state identifier in the corresponding state identifier group. By adopting the scheme, the checking efficiency of the state of the instrument can be improved.

Description

Method and device for updating state of instrument

Technical Field

The present application relates to the field of in vitro diagnosis technologies, and in particular, to a method and an apparatus for updating an instrument state.

Background

With the development of computer technology, computers connected to in vitro diagnostic devices have appeared, and items and other identifiers in a display interface of the computer can be selected through a mouse, so that the in vitro diagnostic devices perform detection corresponding to the selected items. However, since the in-vitro diagnostic apparatus and the computer are independent, the volume is too large and the operation is complicated.

Therefore, an integrated in-vitro diagnostic device with a display screen appears, the display screen of the device is a touch display screen, and corresponding operation can be performed on a display interface more conveniently and intuitively when the device is used. However, in the display interface of the touch display screen of the conventional integrated in-vitro diagnostic apparatus, if the instrument state of the apparatus needs to be known, the user must go to the page corresponding to the instrument state that the user wants to know to view. For example, if the consumable status of the device is to be known, the user must go to the consumable status page to check, which results in the failure to check the consumable status of the extracorporeal diagnostic device on the non-consumable status page, and the checking efficiency of the instrument status is low.

Disclosure of Invention

In view of the foregoing, it is desirable to provide an apparatus status updating method and apparatus that can improve efficiency of viewing an apparatus status.

A method for updating the state of an instrument, which is applied to an in-vitro diagnostic device, comprises the following steps:

determining a state identification group to be updated in an instrument state bar; the instrument status bar is displayed in an operation interface of the in-vitro diagnosis equipment;

monitoring the instrument state corresponding to each state identifier in the state identifier group in real time;

when the instrument state corresponding to at least one state identifier is monitored to change, the changed instrument state is obtained;

and updating the changed state of the instrument to the corresponding state identifier in the state identifier group.

In one embodiment, the determining the group of status identifiers to be updated in the instrument status bar includes:

detecting touch operation triggered in an instrument status bar;

switching and displaying a selectable state identification group in the instrument state bar according to the touch operation;

and determining the currently displayed state identification group in the instrument state bar as a state identification group to be updated.

In one embodiment, the updating the changed instrument state to the corresponding state identifier in the state identifier group includes:

determining a state identifier corresponding to the changed state of the instrument in the state identifier group;

acquiring a display mode corresponding to the determined state identifier according to the changed state of the instrument;

and updating the changed state of the instrument to the determined state identifier according to the display mode.

In one embodiment, the instrument status bar is displayed in a floating manner in an operation interface of the in-vitro diagnosis device; the method further comprises the following steps:

acquiring a hidden instruction;

hiding at least one part of the instrument status bar according to the hiding instruction.

In one embodiment, the method further comprises:

when any state identifier in the instrument state bar is triggered, determining a state identifier group to which the triggered state identifier belongs as a target state identifier group;

popping up a first instrument state list associated with the target state identification group;

and displaying the first instrument state associated information corresponding to each state identifier in the target state identifier group to the first instrument state list.

In one embodiment, the method further comprises:

displaying a plurality of status list entries in the first instrument status list;

determining a selected state list entry from the plurality of state list entries;

switching to a second instrument state list associated with the selected state list entry;

and displaying the second instrument state related information corresponding to the selected state list entry into the second instrument state list.

In one embodiment, the first device state associated information includes a first device state page entry, the second device state associated information includes a second device state page entry, and the method further includes:

when a first instrument state page entry of any first instrument state associated information in the first instrument state list is triggered, jumping to a first instrument state page corresponding to the first instrument state list;

and when a second instrument state page entry of any second instrument state associated information in the second instrument state list is triggered, jumping to a second instrument state page corresponding to the second instrument state list.

In one embodiment, the first instrument state list is one of a consumable state list, a sample state list, a quality control state list, a calibration state list and an alarm state list;

the plurality of state list entries comprise at least two of a consumable state list entry, a sample state list entry, a quality control state list entry, a calibration state list entry and an alarm state list entry;

the second instrument state list comprises at least two of a consumable state list, a sample state list, a quality control state list, a calibration state list and an alarm state list.

In one embodiment, the status identifier group comprises at least one of an inspection progress identifier group, a consumable status identifier group, an inspection result identifier group and an alarm status identifier group;

the state mark in the detection progress mark group comprises at least one of a detected progress mark and an undetected progress mark;

the state marks in the consumable state mark group comprise at least one of a reagent allowance mark, a substrate allowance mark, a cleaning liquid allowance mark, a waste box capacity mark, a separation liquid allowance mark, a reaction cup allowance mark and a waste liquid barrel capacity mark;

the state identifier in the detection result identifier group comprises at least one of an emergency call result identifier, a conventional result identifier, a quality control result identifier and a calibration result identifier;

the status flags in the alarm status flag group include at least one of an emergency alert status flag and a no emergency alert status flag.

An apparatus for updating a state of an instrument, the apparatus comprising:

the state identification group determining module is used for determining a state identification group to be updated in the instrument state bar; the instrument status bar is displayed in an operation interface of the in-vitro diagnosis equipment;

the instrument state monitoring module is used for monitoring the instrument state corresponding to each state identifier in the state identifier group in real time;

the instrument state acquisition module is used for acquiring the changed instrument state when the instrument state corresponding to at least one state identifier is monitored to be changed;

and the instrument state updating module is used for updating the changed instrument state to the corresponding state identifier in the state identifier group.

According to the method and the device for updating the instrument state, the instrument state corresponding to the state identifier in the state identifier group to be updated is monitored in real time, and the monitored changed instrument state is updated and displayed by using the instrument state bar capable of being displayed in the operation interface of the in-vitro diagnostic equipment, so that the real-time instrument state of the in-vitro diagnostic equipment can be displayed on any operation interface of the in-vitro diagnostic equipment, and the viewing efficiency of the instrument state is improved.

Drawings

FIG. 1 is a diagram showing an internal structure of an in-vitro diagnostic apparatus according to an embodiment;

FIG. 2 is a diagram of an embodiment of a system for updating an instrument state;

FIG. 3 is a flow diagram illustrating a method for updating a status of an instrument according to one embodiment;

FIG. 4 is a diagram illustrating an instrument status bar displaying an identification group of test results according to an embodiment;

FIG. 5 is a diagram illustrating an instrument status bar showing consumable status identifier groups according to an embodiment;

FIG. 6 is a schematic diagram of an instrument status bar showing an identification group of test results in accordance with another embodiment;

FIG. 7 is a diagram showing an instrument status bar displaying a test result identifier set according to still another embodiment;

FIG. 8 is a diagram illustrating an instrument status bar displaying a set of alarm status identifiers according to one embodiment;

FIG. 9 is a diagram illustrating an instrument status bar popping up an alarm status list in accordance with an embodiment;

FIG. 10 is a diagram of an alarm state page in one embodiment;

FIG. 11 is a diagram illustrating an embodiment of an instrument status bar popping up a consumable status list;

FIG. 12 is a diagram of a consumable status page in accordance with another embodiment;

FIG. 13 is a diagram illustrating a pop-up sample status list from an instrument status bar in accordance with one embodiment;

FIG. 14 is a diagram of an instrument status bar popping up a sample status list in accordance with another embodiment;

FIG. 15 is a diagram of a sample results page in one embodiment;

FIG. 16 is a diagram illustrating an example of a pop-up quality control status list from the status bar of the instrument;

FIG. 17 is a diagram illustrating a pop-up quality control status list from the status bar of an instrument according to another embodiment;

FIG. 18 is a diagram of a quality control results page in accordance with an embodiment;

FIG. 19 is a diagram illustrating an instrument status bar popping up a list of calibration states in one embodiment;

FIG. 20 is a diagram illustrating a pop-up calibration status list from the status bar of the instrument in accordance with an alternative embodiment;

FIG. 21 is a diagram of a calibration results page in one embodiment;

FIG. 22 is a diagram showing an instrument status bar displaying a test result identifier set according to still another embodiment;

FIG. 23 is a block diagram showing an apparatus for updating the state of an instrument according to an embodiment.

Detailed Description

In order to make the objects, technical solutions and advantages of the present application more apparent, the present application is described in further detail below with reference to the accompanying drawings and embodiments. It should be understood that the specific embodiments described herein are merely illustrative of the present application and are not intended to limit the present application.

It will be understood that, as used herein, the terms "first," "second," and the like may be used herein to describe various objects, but the objects are not limited by these terms. These terms are only used to distinguish a first object from another object.

The method for updating the instrument status provided by the present application can be applied to an in vitro diagnostic apparatus shown in fig. 1, where the in vitro diagnostic apparatus includes a memory, a processor, a display screen, and an instrument status sensor, the instrument status sensor is used to detect the instrument status of the in vitro diagnostic apparatus, the memory stores a computer program, and the computer program implements a method for updating the instrument status when executed by the processor. It is understood that the in-vitro diagnostic device may also comprise physical components for performing in-vitro diagnostic functions based on the instrument status.

The in-vitro diagnosis device can be an integrated in-vitro diagnosis device with a display screen integrated with the in-vitro diagnosis device, and the display screen of the in-vitro diagnosis device can be a touch display screen. The display screen of the in-vitro diagnostic apparatus may display an operation interface 200 as shown in fig. 2, an instrument status bar 201 is displayed in the operation interface 200, and the instrument status bar 201 includes a status identifier group to be updated. The in-vitro diagnostic apparatus may switch to display different operation interfaces 200 through the detected touch operation.

Specifically, the in-vitro diagnostic device determines a state identifier group to be updated in the instrument state bar 201, and monitors the instrument state corresponding to each state identifier in the state identifier group to be updated in real time; when the instrument state corresponding to at least one state identifier is monitored to change, the changed instrument state is obtained; and updating the changed state of the instrument to the state identifier in the corresponding state identifier group.

In one embodiment, as shown in fig. 3, a method for updating the status of an apparatus is provided, which is described by taking the method as an example for being applied to the extracorporeal diagnostic apparatus in fig. 1, and comprises the following steps:

step S302, determining a state identification group to be updated in an instrument state bar; the instrument status bar is displayed in the operation interface of the in vitro diagnostic device.

The instrument state refers to a state of the in-vitro diagnostic apparatus, such as a consumable state, a detection progress, a detection result, an alarm state, and the like of the in-vitro diagnostic apparatus. The consumable state refers to the use condition of the consumable material, such as whether a reagent is sufficient or not and whether a cleaning solution is sufficient or not, the detection progress refers to the real-time progress of the in-vitro diagnosis equipment during in-vitro diagnosis, the detection result refers to the result obtained by the in-vitro diagnosis equipment after completing in-vitro diagnosis, and the alarm state refers to whether an emergency alarm exists in the in-vitro diagnosis equipment or not, such as the emergency alarm generated due to insufficient reagent, instrument faults and the like.

The instrument status bar is a status bar for showing the status of the instrument. The status identifier group is a group including a plurality of status identifiers of the same type, for example, the status identifier group is a consumable status group, and then a plurality of status identifiers included in the consumable status group are status identifiers related to consumables. The operation interface of the in-vitro diagnostic device refers to any interface displayed on the display screen of the in-vitro diagnostic device.

Specifically, an instrument status bar may be displayed on any operation interface of the in-vitro diagnostic apparatus. The instrument status bar may be fixedly disposed in any region of the operation interface of the in-vitro diagnostic apparatus, and the position of the instrument status bar is unchanged along with the change of the operation interface. Of course, the instrument status bar may be a movable instrument status bar, and the in-vitro diagnostic device moves the position of the instrument status bar in the operation interface according to the detected touch operation. And the in-vitro diagnosis equipment determines the state identification group displayed by the instrument state bar in the currently displayed operation interface as the state identification group to be updated.

In one embodiment, the instrument status bar may be composed of one graphic or a plurality of graphics, and when the instrument status bar is composed of a plurality of graphics, the in vitro diagnostic apparatus may treat each of the graphics composing the instrument status bar as an identification group region, and one identification group region may accommodate one status identification group.

In one embodiment, the instrument status bar may be formed of two shapes, for example, the shape of the instrument status bar may be as shown in FIG. 2, and the first identifier group area 202 and the second identifier group area 203 may each accommodate one status identifier group.

And step S304, monitoring the instrument state corresponding to each state identifier in the state identifier group in real time.

The state identifier refers to an identifier for displaying a state of the instrument, for example, the state identifier may be specifically an icon, and different states of the instrument are displayed by colors of the icon. For example, the a-state identifier is a state identifier belonging to the consumable state identifier group, and the a-state identifier may be icons of various consumable materials for in vitro diagnosis, and the different consumable states of each consumable material are shown by the colors of the icons.

Specifically, different state identifier groups correspond to different types of instrument states, and the instrument states of the different state identifier groups are determined according to different data. For example, the detection progress identification group corresponds to an instrument state related to the detection progress, the instrument state of each identification in the detection progress identification group is determined according to the current detection progress of the in vitro diagnostic equipment, the consumable state identification group corresponds to an instrument state related to the consumable, and the instrument state of each identification in the consumable state identification group is determined according to the current state of each consumable material of the in vitro diagnostic equipment. The in-vitro diagnostic equipment monitors the instrument state corresponding to each state identifier in the state identifier group to be updated in real time so as to determine whether the instrument state corresponding to at least one state identifier in the state identifier group to be updated changes.

Step S306, when the instrument state corresponding to at least one state identifier is monitored to change, the changed instrument state is obtained.

Specifically, the in-vitro diagnostic device compares the instrument state corresponding to each state identifier monitored each time to obtain a comparison result. Of course, the in-vitro diagnostic device may also subtract the preset time interval from the current time point to obtain a historical time point according to the preset time interval, and compare the instrument state corresponding to each state identifier monitored at the current time point with the instrument state corresponding to each state identifier monitored at the historical time point to obtain a comparison result. And if the obtained comparison result shows that the change exists, determining that the state of the instrument corresponding to the state mark of which the comparison result shows that the change exists is changed. And acquiring the changed state corresponding to the state identifier of which the corresponding state of the instrument is changed.

And step S308, updating the changed state of the instrument to the state identifier in the corresponding state identifier group.

Specifically, the in-vitro diagnostic device determines a state identifier group corresponding to the changed instrument state, determines a state identifier corresponding to the changed instrument state in the corresponding state identifier group, and updates the changed instrument state to the corresponding state identifier in the corresponding state identifier group.

In the method for updating the instrument state, the instrument state corresponding to the state identifier in the state identifier group to be updated is monitored in real time, and the monitored changed instrument state is updated and displayed by using the instrument state bar which can be displayed in the operation interface of the in-vitro diagnostic equipment, so that the real-time instrument state of the in-vitro diagnostic equipment can be displayed on any operation interface of the in-vitro diagnostic equipment, and the viewing efficiency of the instrument state is improved.

In one embodiment, determining the set of state identifiers to be updated in the instrument status bar comprises: touch operations triggered in the instrument status bar are detected. And switching and displaying the selectable state identification group in the instrument state bar according to the touch operation. And determining the currently displayed state identification group in the instrument state bar as a state identification group to be updated.

Specifically, the status identifier group in the instrument status bar of the in-vitro diagnostic apparatus may be customized in advance according to different requirements. And the in-vitro diagnosis equipment detects touch operation triggered in the instrument status bar and switches and displays the selectable status identifier group in the instrument status bar according to the touch operation. And the in-vitro diagnosis equipment determines the currently displayed state identification group in the instrument state bar as the state identification group to be updated.

Further, as shown in fig. 2, a second identifier group area 203 in the instrument status bar may be provided with a switching control 204 for triggering a touch operation, and when the in-vitro diagnostic apparatus detects that the switching control 204 is triggered, a next selectable status identifier group is switched and displayed in the second identifier group area 203. If the currently displayed status identifier group in the instrument status bar is the status identifier group displayed in the first identifier group region 202 and the second identifier group region 203, the in-vitro diagnostic apparatus determines the status identifier group displayed in the first identifier group region 202 and the second identifier group region 203 as the status identifier group to be updated.

In this embodiment, the selectable state identifier group can be switched and displayed according to the touch operation triggered in the instrument state bar, and the currently displayed state identifier group is determined as the state identifier group to be updated, so that a user can select to view the state identifier group from the selectable state identifier group according to a requirement to display, and update each state identifier in the currently displayed state identifier group in real time, thereby further improving the viewing efficiency of the instrument state.

In one embodiment, updating the changed instrument state to the state identifier in the corresponding state identifier group includes: in the state identifier group, state identifiers corresponding to the changed instrument states are determined. And acquiring a display mode corresponding to the determined state identifier according to the changed state of the instrument. And updating the changed state of the instrument to the determined state identifier according to a display mode.

Specifically, each state identifier in each state identifier group has a corresponding display mode group, and the display mode group includes display modes corresponding to different instrument states. And the in-vitro diagnostic equipment determines the state identifier corresponding to the changed state of the instrument in the state identifier group corresponding to the changed state of the instrument. And the in-vitro diagnosis equipment acquires a display mode group corresponding to the state identifier corresponding to the changed state of the instrument, and determines a display mode matched with the changed state of the instrument in the acquired display mode group. And updating the changed state of the instrument to the state identifier corresponding to the changed state of the instrument according to the determined display mode.

For example, as shown in fig. 4, the detection result identifier group displays an emergency result identifier 401, a normal result identifier 402, a quality control result identifier 403, and a calibration result identifier 404, and when there is no detection item, the emergency result identifier 401, the normal result identifier 402, the quality control result identifier 403, and the calibration result identifier 404 are all blue. When the in vitro diagnostic device detects the presence of a calibrant delay, calibration result indicator 404 is displayed in yellow. The emergency result flag 401 is displayed as cyan when the in-vitro diagnostic apparatus detects that an emergency is in detection, the regular result flag 402 is displayed as cyan when the in-vitro diagnostic apparatus detects that a regular is in detection, the quality control result flag 403 is displayed as cyan when the in-vitro diagnostic apparatus detects that a quality control detection is in progress, and the calibration result flag 404 is displayed as cyan when the in-vitro diagnostic apparatus detects that a calibration is in progress.

The upper right corner of the emergency results identifier 401, the general results identifier 402, the quality control results identifier 403, and the calibration results identifier 404 may be displayed with a countdown. For example, as shown in fig. 22, the upper right corner of the emergency treatment result mark is blue, and is displayed with "3 m", which indicates that the emergency treatment test is completed for 3 minutes.

In the consumable status identifier group shown in fig. 5, when each consumable identifier corresponds to a different instrument status, different display colors may be provided, the display color of the consumable identifier indicates a normal status when it is blue, indicates an early warning status when it is yellow, indicates an alarm status when it is red, indicates an invalid status when it is gray, and indicates an unloaded status when it is black and white. For example, the reagent remaining amount indicator 501 indicates that the reagent remaining amount is sufficient when it is blue, indicates that the reagent remaining amount is insufficient when it is yellow, indicates that the reagent is used up when it is red, indicates that an ineffective reagent is present when it is gray, and indicates that an overdue reagent is present when it is black and white. The substrate residue indicator 502 indicates that the substrate residue is in a normal state when it is blue, that the substrate residue is insufficient when it is yellow, that the substrate is used up when it is red, and that the substrate is not loaded when it is white with black. The remaining cleaning liquid level indicator 503 is blue to indicate that the remaining cleaning liquid level is normal, yellow to indicate that the remaining cleaning liquid level is insufficient, red to indicate that the cleaning liquid is used up, and black and white to indicate that the cleaning liquid is not loaded. Wherein, the cleaning solution can be an intensified cleaning solution.

The waste bin capacity indicator 504 is blue to indicate that the waste bin is full, yellow to indicate that the waste bin is low, and red to indicate that the waste bin is full. The remaining separation liquid indicator 505 is blue to indicate that the remaining separation liquid is normal, yellow to indicate that the remaining separation liquid is insufficient, and red to indicate that the separation liquid is used up. The cuvette remaining mark 506 indicates that the number of cuvettes is normal when it is blue, indicates that the number of cuvettes is insufficient when it is yellow, and indicates that the cuvettes are used up when it is red. The waste liquid tank capacity mark 507 indicates that the waste liquid tank is normal in capacity when blue, indicates that the waste liquid tank is insufficient in capacity when yellow, and indicates that the waste liquid tank is full when red.

As shown in fig. 6, when the detection corresponding to the emergency result identifier, the conventional result identifier, the quality control result identifier and the calibration result identifier is completed and the detection results are normal, the upper right corner areas of the emergency result identifier, the conventional result identifier, the quality control result identifier and the calibration result identifier are green and all have a square root.

As shown in fig. 7, when an abnormality occurs in the detection result of the in-vitro diagnostic apparatus, there may be cases where: and if the emergency detection result is unqualified, the emergency result mark is red as a whole. And when the upper right corner area of the emergency treatment result mark is red and H is displayed, the emergency treatment result is higher. And when the upper right corner area of the regular result mark is red and is displayed with 'L', the regular detection result is low. The upper right corner area of the quality control result mark is red and is displayed with! When "is used," the quality control result is out of control. When the calibration result marks that the upper right corner area is red and shows "X", the calibration result fails. When the detection results with lower results and higher results exist in emergency treatment or routine detection, the H and the L are displayed in a switching mode. When all the detections are completed, the state flag corresponding to the invalid detection result changes to gray. For example, if the emergency detection result is invalid, the indication of the emergency result is changed to gray.

When the instrument status bar is in a display state or a hidden state, the instrument status bar is immediately popped up and displayed in the middle position of the operation interface as long as the in vitro diagnosis equipment monitors that the emergency alarm information exists. And automatically pops up an alarm state identifier group in the second identifier group area of the instrument status bar, as shown in fig. 8, the alarm state identifier group displays an emergency alert state identifier 800.

As shown in fig. 8, when the in-vitro diagnostic apparatus detects that the emergency alert state flag 800 is triggered, an alert state list is popped up, and as shown in fig. 9, detailed information of the instrument state related information corresponding to the emergency alert state is displayed in the alert state list. The detail information corresponding to the emergency alert state may be used as an entry of an alert state page, and when the in-vitro diagnosis device detects that the detail information corresponding to any emergency alert state is triggered, the in-vitro diagnosis device enters the alert state page as shown in fig. 10. When the in vitro diagnosis equipment does not detect that the emergency alarm information exists and an alarm state identification group is displayed in the second identification group area of the instrument status bar, the 'no emergency alarm' with black fonts is displayed in the alarm state identification group.

In this embodiment, the display mode corresponding to the determined state identifier may be obtained according to the changed state of the instrument, and then different states of the instrument are displayed according to different display modes, so that a user may more intuitively and clearly understand the state of the instrument represented by each state identifier.

In one embodiment, the instrument status bar is displayed in a floating manner in an operation interface of the in-vitro diagnosis device; the method for updating the state of the instrument further comprises the following steps: acquiring a hidden instruction; and hiding at least one part of the instrument status bar according to the hiding instruction.

In particular, the instrument status bar may be displayed in suspension in the operation interface of the in vitro diagnostic apparatus. The in-vitro diagnostic device may move the instrument status bar displayed in suspension in the currently displayed operation interface according to the detected drag operation. When the in-vitro diagnosis equipment detects that any boundary of the instrument status bar is overlapped with any boundary of the operation interface, a hiding instruction is obtained, and at least one part of the instrument status bar is hidden according to the hiding instruction. So that the area of the operation interface occupied by the instrument status bar is reduced.

In one embodiment, hiding at least a portion of the instrument status bar may hide a ninth portion of the instrument status bar and display a tenth portion of the instrument status bar. And when the in-vitro diagnosis equipment detects touch operation on one tenth of the displayed instrument status bar, acquiring a display instruction, and completely displaying the instrument status bar in the currently displayed operation interface according to the display instruction. Further, the in-vitro diagnostic apparatus may acquire the display instruction according to the long press operation detected in the tenth part of the display performed in the instrument status bar. And judging whether the long-press operation condition is the condition that whether the detected duration of the continuous click operation reaches the preset target duration or not, and if so, determining the detected continuous click operation as the long-press operation.

In this embodiment, the displayed instrument status bar can be hidden through the detected touch operation, and the hidden instrument status bar is displayed, so that a user can freely switch between the displayed instrument status bar and the hidden instrument status bar according to needs.

In one embodiment, the method for updating the state of the instrument further comprises: when any state identifier in the instrument state bar is triggered, determining a state identifier group to which the triggered state identifier belongs as a target state identifier group. A first instrument state list associated with the target state identification group is popped up. And displaying the first instrument state associated information corresponding to each state identifier in the target state identifier group to a first instrument state list.

The first instrument state list is used for displaying first instrument state associated information corresponding to each state identifier of the target state identifier group. The first instrument state related information refers to instrument state related information corresponding to each state identifier in the target state identifier group. The instrument state related information refers to detailed information of the instrument state.

Specifically, different status identifier groups have different instrument status lists, such as a consumable status identifier group has a consumable status list, a detection result identifier group has a detection result list, and an alarm status identifier group has an alarm status list. When the in-vitro diagnosis equipment detects that any state identifier in the instrument state identifier column is triggered, determining a state identifier group to which the triggered state identifier belongs as a target state identifier group. And popping up a first instrument state list associated with the target state identification group, and displaying first instrument state associated information corresponding to each state identification in the target state identification group to the first instrument state list.

In one embodiment, the instrument state list corresponding to the state identification group may be multiple. For a state identifier group in which a plurality of corresponding instrument state lists exist, the in-vitro diagnostic apparatus may be provided with an instrument state list corresponding to each state identifier in the state identifier group. When the in-vitro diagnosis equipment detects that any state identifier in the instrument state bar is triggered, determining a state identifier group to which the triggered state identifier belongs as a target state identifier group. And when the target state identification group is determined to be associated with a plurality of instrument state lists, acquiring the instrument state list corresponding to the triggered state identification, and popping up the instrument state list corresponding to the triggered state identification.

For example, taking the state identifier group as the detection result identifier group as an example, as shown in fig. 4, the detection result identifier group displays an emergency result identifier 401, a normal result identifier 402, a quality control result identifier 403, and a calibration result identifier 404. The emergency result identifier 401 and the conventional result identifier 402 correspond to a common sample state list. The quality control result identifier 403 corresponds to a quality control state list, and the calibration result identifier 404 corresponds to a calibration state list. The set of test result identifiers corresponds to a total of 3 different instrument status lists. When the in-vitro diagnosis equipment detects that the emergency result identifier 401 or the conventional result identifier 402 is triggered, popping up a sample state list; when the in-vitro diagnostic equipment detects that the quality control result identifier 403 is triggered, popping up a quality control state list; when the in-vitro diagnostic device detects that the calibration result identifier 404 is triggered, a calibration status list is popped up.

In this embodiment, one status identifier group may correspond to a plurality of instrument status lists, and the user may preset a default instrument status list according to the requirement.

In one embodiment, the method for updating the state of the instrument further comprises: a plurality of status list entries are displayed in a first instrument status list. A selected state list entry from the plurality of state list entries is determined. Switching to a second instrument status list associated with the selected status list entry. And displaying the second instrument state related information corresponding to the selected state list entry into a second instrument state list.

Wherein, the entry of the state list refers to an entry for switching to the corresponding instrument state list. The second instrument state list is a list for displaying second instrument state associated information, and the second instrument state associated information is instrument state associated information corresponding to each state identifier in a state identifier group corresponding to a state list entry selected from the plurality of state list entries.

Specifically, when the in-vitro diagnostic apparatus detects that the first instrument status list pops up, a plurality of status list entries are displayed in the first instrument status list, and the displayed plurality of status list entries may include all status list entries of the instrument status list corresponding to all selectable status identification groups in the instrument status bar. The in-vitro diagnosis equipment determines a state list entry selected from a plurality of displayed state lists, switches to a second instrument state list associated with the selected state list entry when a second instrument state list associated with the selected state list entry is not the same as a first instrument state list popped up currently, determines second instrument state associated information of each state identifier in a state identifier group corresponding to the selected state list entry, and displays the determined second instrument state associated information to the second instrument state list.

It is understood that when the second instrument state list associated with the selected state list entry is the same as the currently popped first instrument state list, the extracorporeal diagnosis apparatus continues to display the first instrument state list.

In this embodiment, the currently popped first instrument state list can be switched to the second instrument state list through the selected state list entry, so that a user can freely switch among different instrument state lists conveniently according to requirements.

In one embodiment, a plurality of status list entries may also be displayed in the second instrument status list, and the displayed plurality of status list entries may include all status list entries of all instrument status lists corresponding to all selectable status identifier groups in the instrument status bar. The user may return to the first instrument status list by selecting a status list entry of the plurality of status list entries corresponding to the first instrument status list. Of course, the user may also switch the currently displayed second instrument status list to another instrument status list by selecting a status list entry corresponding to another instrument status list from the plurality of status list entries.

In one embodiment, the first device state associated information includes a first device state page entry, the second device state associated information includes a second device state page entry, and the method for updating the device state further includes: and when a first instrument state page entry of any first instrument state associated information in the first instrument state list is triggered, jumping to a first instrument state page corresponding to the first instrument state list. And when a second instrument state page entry of any second instrument state associated information in the second instrument state list is triggered, jumping to a second instrument state page corresponding to the second instrument state list.

Wherein the first instrument state page entry refers to an entry for entering the first instrument state page. A second instrument state page entry refers to an entry for entering a second instrument state page.

Specifically, the first apparatus state related information may include detailed summary information and corresponding detailed information, the detailed summary information may be information displayed by default, and the detailed information may be information that can be hidden. The detail information may be entered as a first instrument status page. When the first instrument state related information is displayed in the first instrument state list, the in-vitro diagnostic device may display the detailed summary information in the first instrument state related information by default. When any detail summary information displayed in the first instrument state list is triggered, detail information corresponding to the triggered detail summary information is displayed. And when the in-vitro diagnosis device detects that any detail information in the first instrument state list is triggered, jumping to a first instrument state page corresponding to the first instrument state list.

The second apparatus state related information may also include detailed summary information and corresponding detailed information, where the detailed summary information may be information displayed by default, and the detailed information may be information that can be hidden. The detail information may be entered as a second instrument status page. When the second instrument state related information is displayed in the second instrument state list, the in-vitro diagnostic device may display the detailed summary information in the second instrument state related information by default. When any detail summary information displayed in the second instrument state list is triggered, detail information corresponding to the triggered detail summary information is displayed. And when the in-vitro diagnosis device detects that any detail information in the second instrument state list is triggered, jumping to a second instrument state page corresponding to the second instrument state list.

In one embodiment, the first instrument state list is one of a consumable state list, a sample state list, a quality control state list, a calibration state list and an alarm state list; the plurality of state list entries comprise at least two of a consumable state list entry, a sample state list entry, a quality control state list entry, a calibration state list entry and an alarm state list entry; the second instrument state list comprises at least two of a consumable state list, a sample state list, a quality control state list, a calibration state list and an alarm state list.

Specifically, the first instrument state list is taken as a consumable state list, the plurality of state list entries include a consumable state list entry, a sample state list entry, a quality control state list entry, a calibration state list entry and an alarm state list entry, and the second instrument state list includes a consumable state list, a sample state list, a quality control state list, a calibration state list and an alarm state list.

As shown in fig. 5, a consumable status group is displayed in the second identifier group area of the status identifier bar, and the consumable status group includes a reagent remaining amount identifier 501, a substrate remaining amount identifier 502, a cleaning solution remaining amount identifier 503, a waste tank capacity identifier 504, a separation solution remaining amount identifier 505, a cuvette remaining amount identifier 506, and a waste tank capacity identifier 507. When the in-vitro diagnostic equipment detects that any one state identifier of a reagent allowance identifier 501, a substrate allowance identifier 502, a cleaning solution allowance identifier 503, a waste box capacity identifier 504, a separation solution allowance identifier 505, a reaction cup allowance identifier 506 and a waste liquid barrel capacity identifier 507 is triggered, a consumable state list is popped up. As shown in fig. 11.

As shown in fig. 11, a consumable part status list entry 1101, a sample status list entry 1102, a quality control status list entry 1103, a calibration status list entry 1104, and an alarm status list entry 1105 are displayed in the consumable part status list 1100. When the sample status list entry 1102 is triggered, the consumable status list 1100 is switched to the second instrument status list: a list of sample states. When the quality control status list entry 1103 is triggered, the consumable part status list 1100 is switched to the second instrument status list: and (5) quality control state list. When the calibration status list entry 1104 is triggered, the consumable status list 1100 is switched to a second instrument status list: a list of alignment states. When the alarm status list entry 1105 is triggered, the consumable part status list 1100 is switched to the second instrument status list: and (4) an alarm state list.

Further, when the in vitro diagnostic device detects that any one status identifier of the reagent residual amount identifier 501, the substrate residual amount identifier 502, the cleaning solution residual amount identifier 503, the waste box capacity identifier 504, the separation solution residual amount identifier 505, the reaction cup residual amount identifier 506 and the waste liquid barrel capacity identifier 507 is triggered again, the consumable state list is retrieved.

In one embodiment, the currently displayed set of status identifiers may be the set of status identifiers associated with the currently displayed list of instrument statuses. For example, when the consumable state list 1100 in fig. 11 is switched to the sample state list, the quality control state list, or the calibration state list, the in-vitro diagnostic apparatus switches the consumable state identifier group to the detection result identifier group. When the consumable state list 1100 is switched to the alarm state list, the consumable state identifier group is switched to the alarm state identifier group.

In one embodiment, the status identifier group includes at least one of a test progress identifier group, a consumable status identifier group, a test result identifier group, and an alarm status identifier group. The state identification in the detection progress identification group comprises at least one of a detected progress identification and an undetected progress identification. The state marks in the consumable state mark group comprise at least one of a reagent allowance mark, a substrate allowance mark, a cleaning liquid allowance mark, a waste box capacity mark, a separation liquid allowance mark, a reaction cup allowance mark and a waste liquid barrel capacity mark. The state identifier in the detection result identifier group comprises at least one of an emergency call result identifier, a conventional result identifier, a quality control result identifier and a calibration result identifier. The status flags in the alarm state flag group include at least one of an emergency alert state flag and a no emergency alert state flag.

Specifically, the status identifier group to be updated may only include the detection progress identifier group, and the detection progress identifier group is displayed in the first identifier group area. The selectable status identifier groups may include a consumable status identifier group, a detection result identifier group, and an alarm status identifier group. The status identifier group to be updated may include one of the selectable status identifier groups in addition to the detection progress identifier group, and one of the selectable status identifier groups is displayed in the second identifier group area. Of course, the optional state identification group may be user-defined.

For example, as shown in fig. 5, a detection progress flag group is displayed in the first flag group area, and status flags in the detection progress flag group may include a detected progress flag 508 and an undetected progress flag 509. The detected progress indicator 508 is used to indicate the percentage of detected progress, and the undetected progress indicator 509 is used to indicate the countdown of the remaining detection time, for example, if the detected progress indicator 508 is 50%, the percentage of the detected completed item is 50%, and if the undetected progress indicator 509 is 56m, the remaining detection time is 56 minutes.

When the in-vitro diagnostic apparatus starts to perform in-vitro diagnostic tests, the first marker set region is displayed in cyan overall, and cyan represents an undetected portion. The detected progress flag 508 displays a detection progress of 0%. And along with the completion of the detection of each item in the in-vitro diagnosis, the first identification group area gradually appears green, and the green represents the detected part. Furthermore, the detected progress indicator 508 is gradually increased from 0%, 1%, 2%. the green portion appearing in the first indicator group region also gradually increases from bottom to top, and the cyan portion gradually decreases from bottom to top. Until the detected progress indicator 508 is 100%, the first indicator group area is filled with the green portion, and the cyan portion disappears. The first identifier group area may directly display "free" when the in vitro diagnostic device has no detection progress.

In one embodiment, the detailed summary information of the instrument status related information of each consumable corresponding to the consumable status is displayed in the consumable status list 1100 shown in fig. 11, and the detailed summary information of the consumable may be used as an entry of a consumable status page, and when the in-vitro diagnostic apparatus detects that the detailed summary information corresponding to any consumable is triggered, the consumable status page shown in fig. 12 is entered.

In an embodiment, after the sample state column pops up the sample state list, as shown in fig. 13, the sample state list displays details summary information of the instrument state related information of each sample corresponding to the sample state, the details summary information of each sample includes a test sequence number, a sample number, a test type, a sample type, and a detection state of the sample, the test type of the sample has an emergency and a routine score, the sample type has several types, such as serum, plasma, whole blood, and urine, the detection state has several states, such as application, in-test, completion, and exception, if the detection result of the item corresponding to the sample has a deviation, the "completion" font is set to red, and the "exception" result is also set to red. If no sample detection item exists currently, the interface displays detailed summary information of the historical sample.

The test sequence number in the sample state list corresponds to the sample detection priority, that is, the test sequence number 1 is the first detection completion, the test sequence number 2 is the second detection completion, and the test sequence number 3 is the third detection completion. When the detail summary information of any sample is triggered, the corresponding detail information is displayed. For example, as shown in fig. 14, when the detail summary information of the sample with the test sequence number of 1 is triggered, the detail information corresponding to the sample with the test sequence number of 1 is displayed. The detail information corresponding to the sample comprises information such as name, result, unit, identification and the like of the item corresponding to the sample; if the result is high, the result is marked with a red font and an up arrow, and so is the result low, which is marked with a red font and a down arrow.

The detail information of the sample can be used as an entry of a sample result page, and when the in-vitro diagnosis device detects that the detail information of any sample is triggered, the sample result page shown in fig. 15 is entered. The user can perform operations such as querying, trending, exporting, printing and the like in the sample result page.

In one embodiment, after the quality control state column pops up the quality control state list, as shown in fig. 16, the quality control state list displays detail summary information of the instrument state related information of each quality control item corresponding to the quality control state, the detail summary information of each quality control item includes a test sequence number, a quality control batch number, a quality control name, a state, and completion time of the quality control item, the state of the quality control item has several states of application, in-detection, completion, and abnormality, and if the detection result of the item corresponding to the quality control has a deviation, the "completion" font is set to red, and the "abnormality" result is also set to red; and if no quality control item exists currently, the quality control state list shows detailed summary information of the historical quality control item. The test sequence number of the quality control item is equivalent to the quality control priority, that is, the test sequence number 1 is the first quality control completion, the test sequence number 2 is the second quality control completion, and the test sequence number 3 is the third quality control completion.

And when the detail summary information of any quality control item is triggered, displaying the corresponding detail information. For example, as shown in fig. 17, when the detail summary information of the quality control item with the test sequence number of 3 is triggered, the detail information corresponding to the quality control item with the test sequence number of 3 is displayed. The detail information corresponding to the quality control item comprises information such as the name, result, identification, target value and the like of the quality control item; if the actual detection result of the quality control item is not within the standard range of the target value, the mark is out of control, and if the actual detection result of the quality control item is within the standard range of the target value, the mark is normal.

The detailed information of the quality control item may be used as an entry of a quality control result page, and when the in-vitro diagnosis device detects that the detailed information of any quality control item is triggered, the in-vitro diagnosis device enters the quality control result page as shown in fig. 18. The user can perform operations such as query, trend, export, printing and the like in the quality control result page.

In an embodiment, after the calibration state column pops up the calibration state list, as shown in fig. 19, the calibration state list displays detail summary information of the instrument state association information of each calibration item corresponding to the calibration state, where the detail summary information of each calibration item includes a calibrated test sequence number, a calibration lot number, an item, a calibration state, and calibration time, and the calibration state includes states of application, calibrated, deferred, and the like; if there is no calibration item currently, the calibration status list shows detailed summary information of the historical calibration items. The calibrated test sequence number is equivalent to the calibration priority, that is, the test sequence number 1 is the first calibration completion, the test sequence number 2 is the second calibration completion, the test sequence number 3 is the third calibration completion, and so on, and the in vitro diagnostic apparatus may change the calibration priority according to the detected long press operation.

When the detailed summary information of any calibration item is triggered, the corresponding detailed information is displayed. For example, as shown in fig. 20, when the detail summary information of the calibration item "AFP" with the test sequence number of 1 is triggered, the detail information corresponding to the calibration item "AFP" is displayed. The detail information of the calibration items comprises level marks, concentrations and luminous values corresponding to the calibration items.

The detail information of the calibration items may be used as an entry of a calibration result page, and when the in-vitro diagnostic device detects that the detail information of any calibration item is triggered, the calibration result page shown in fig. 21 is entered. The user can perform operations such as inquiry, trend, export, printing and the like in the calibration result page.

It should be understood that, although the steps in the flowchart of fig. 3 are shown in order as indicated by the arrows, the steps are not necessarily performed in order as indicated by the arrows. The steps are not performed in the exact order shown and described, and may be performed in other orders, unless explicitly stated otherwise. Moreover, at least a portion of the steps in fig. 3 may include multiple sub-steps or multiple stages that are not necessarily performed at the same time, but may be performed at different times, and the order of performance of the sub-steps or stages is not necessarily sequential, but may be performed in turn or alternately with other steps or at least a portion of the sub-steps or stages of other steps.

In one embodiment, as shown in fig. 23, there is provided an apparatus 2300 for updating an instrument status, comprising: a status identifier group determination module 2301, an instrument status monitoring module 2302, an instrument status acquisition module 2303 and an instrument status update module 2304, wherein:

a status identifier group determining module 2301, configured to determine a status identifier group to be updated in the instrument status bar; the instrument status bar is displayed in an operation interface of the in-vitro diagnosis equipment;

the instrument state monitoring module 2302 is used for monitoring the instrument state corresponding to each state identifier in the state identifier group in real time;

an instrument state obtaining module 2303, configured to obtain a changed instrument state when it is monitored that an instrument state corresponding to at least one state identifier changes;

the instrument state updating module 2304 is configured to update the changed instrument state to the state identifier in the corresponding state identifier group.

In one embodiment, the status identification group determination module 2301 is further configured to detect a touch operation triggered in the instrument status bar; switching and displaying the selectable state identification group in the instrument state bar according to touch operation; and determining the currently displayed state identification group in the instrument state bar as a state identification group to be updated.

In one embodiment, the instrument state update module 2304 is further configured to determine a state identification corresponding to the changed instrument state in the set of state identifications; acquiring a display mode corresponding to the determined state identifier according to the changed state of the instrument; and updating the changed state of the instrument to the determined state identifier according to a display mode.

In one embodiment, the status bar of the instrument is displayed in a floating manner in an operation interface of the in-vitro diagnostic equipment, and the updating device of the status bar of the instrument further comprises a status bar hiding module for acquiring a hiding instruction; and hiding at least one part of the instrument status bar according to the hiding instruction.

In one embodiment, the apparatus for updating the state of the instrument further includes a state list pop-up module, configured to determine, when any state identifier in the instrument state bar is triggered, a state identifier group to which the triggered state identifier belongs as a target state identifier group; popping up a first instrument state list associated with the target state identification group; and displaying the first instrument state associated information corresponding to each state identifier in the target state identifier group to a first instrument state list.

In one embodiment, the status list popup module is further configured to display a plurality of status list entries in the first instrument status list; determining a selected state list entry from the plurality of state list entries; switching to a second instrument state list associated with the selected state list entry; and displaying the second instrument state related information corresponding to the selected state list entry into a second instrument state list.

In one embodiment, the first device state associated information includes a first device state page entry, the second device state associated information includes a second device state page entry, and the device for updating the device state further includes a page jump module, configured to jump to a first device state page corresponding to the first device state list when the first device state page entry of any one of the first device state associated information in the first device state list is triggered; and when a second instrument state page entry of any second instrument state associated information in the second instrument state list is triggered, jumping to a second instrument state page corresponding to the second instrument state list.

In one embodiment, the status identifier group comprises at least one of a detection progress identifier group, a consumable status identifier group, a detection result identifier group and an alarm status identifier group; the state identification in the detection progress identification group comprises at least one of a detected progress identification and an undetected progress identification; the state marks in the consumable state mark group comprise at least one of a reagent allowance mark, a substrate allowance mark, a cleaning liquid allowance mark, a waste box capacity mark, a separation liquid allowance mark, a reaction cup allowance mark and a waste liquid barrel capacity mark; the state identifier in the detection result identifier group comprises at least one of an emergency call result identifier, a conventional result identifier, a quality control result identifier and a calibration result identifier; the status flags in the alarm state flag group include at least one of an emergency alert state flag and a no emergency alert state flag.

For the specific definition of the device for updating the state of the instrument, reference may be made to the above definition of the method for updating the state of the instrument, which is not described herein again. The modules in the device for updating the state of the instrument can be wholly or partially realized by software, hardware and a combination thereof. The modules can be embedded in a hardware form or independent from a processor in the computer device, and can also be stored in a memory in the computer device in a software form, so that the processor can call and execute operations corresponding to the modules.

In one embodiment, an in-vitro diagnostic apparatus is provided, the internal structure of which can be as shown in fig. 1. The in-vitro diagnosis device comprises a memory, a processor, a display screen and an instrument state sensor, wherein the instrument state sensor is used for detecting the instrument state of the in-vitro diagnosis device, the memory stores a computer program, and the computer program realizes an updating method of the instrument state when being executed by the processor.

It will be understood by those skilled in the art that the structure shown in fig. 1 is a block diagram of only a part of the structure related to the present application, and does not constitute a limitation to the extracorporeal diagnostic apparatus to which the present application is applied, and a specific extracorporeal diagnostic apparatus may include more or less components than those shown in the drawings, or combine some components, or have a different arrangement of components.

In one embodiment, an in vitro diagnostic apparatus is provided, comprising a memory and a processor, the memory storing a computer program which when executed by the processor performs the steps of: determining a state identification group to be updated in an instrument state bar; the instrument status bar is displayed in an operation interface of the in-vitro diagnosis equipment; monitoring the instrument state corresponding to each state identifier in the state identifier group in real time; when the instrument state corresponding to at least one state identifier is monitored to change, the changed instrument state is obtained; and updating the changed state of the instrument to the state identifier in the corresponding state identifier group.

In one embodiment, a computer-readable storage medium is provided, having a computer program stored thereon, which when executed by a processor, performs the steps of: determining a state identification group to be updated in an instrument state bar; the instrument status bar is displayed in an operation interface of the in-vitro diagnosis equipment; monitoring the instrument state corresponding to each state identifier in the state identifier group in real time; when the instrument state corresponding to at least one state identifier is monitored to change, the changed instrument state is obtained; and updating the changed state of the instrument to the state identifier in the corresponding state identifier group.

It will be understood by those skilled in the art that all or part of the processes of the methods of the embodiments described above can be implemented by hardware instructions of a computer program, which can be stored in a non-volatile computer-readable storage medium, and when executed, can include the processes of the embodiments of the methods described above. Any reference to memory, storage, database, or other medium used in the embodiments provided herein may include non-volatile and/or volatile memory, among others. Non-volatile memory can include read-only memory (ROM), Programmable ROM (PROM), Electrically Programmable ROM (EPROM), Electrically Erasable Programmable ROM (EEPROM), or flash memory. Volatile memory can include Random Access Memory (RAM) or external cache memory. By way of illustration and not limitation, RAM is available in a variety of forms such as Static RAM (SRAM), Dynamic RAM (DRAM), Synchronous DRAM (SDRAM), Double Data Rate SDRAM (DDRSDRAM), Enhanced SDRAM (ESDRAM), Synchronous Link DRAM (SLDRAM), Rambus Direct RAM (RDRAM), direct bus dynamic RAM (DRDRAM), and memory bus dynamic RAM (RDRAM).

The technical features of the above embodiments can be arbitrarily combined, and for the sake of brevity, all possible combinations of the technical features in the above embodiments are not described, but should be considered as the scope of the present specification as long as there is no contradiction between the combinations of the technical features.

The above-mentioned embodiments only express several embodiments of the present application, and the description thereof is more specific and detailed, but not construed as limiting the scope of the invention. It should be noted that, for a person skilled in the art, several variations and modifications can be made without departing from the concept of the present application, which falls within the scope of protection of the present application. Therefore, the protection scope of the present patent shall be subject to the appended claims.

Claims

1. A method for updating the state of an instrument, which is applied to an in-vitro diagnostic device, comprises the following steps:

2. The method of claim 1, wherein determining the set of state identifiers to be updated in the instrument status bar comprises:

detecting touch operation triggered in an instrument status bar;

3. The method of claim 1, wherein updating the changed instrument state to the state identifier in the corresponding state identifier group comprises:

4. The method of claim 1, wherein the instrument status bar is displayed in suspension in an operator interface of an in vitro diagnostic device; the method further comprises the following steps:

acquiring a hidden instruction;

5. The method of claim 1, further comprising:

6. The method of claim 5, further comprising:

7. The method of claim 6, wherein the first instrument state association information comprises a first instrument state page entry, wherein the second instrument state association information comprises a second instrument state page entry, and wherein the method further comprises:

8. The method of claim 6, wherein the first instrument state list is one of a consumable state list, a sample state list, a quality control state list, a calibration state list, and an alarm state list;

9. The method according to any one of claims 1 to 8, wherein the status identifier group comprises at least one of a test progress identifier group, a consumable status identifier group, a test result identifier group, and an alarm status identifier group;

10. An apparatus for updating a status of an instrument, the apparatus comprising: