CN111105868B - Data management method, in-vitro diagnosis device and storage medium - Google Patents
Data management method, in-vitro diagnosis device and storage medium Download PDFInfo
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- CN111105868B CN111105868B CN201811270352.3A CN201811270352A CN111105868B CN 111105868 B CN111105868 B CN 111105868B CN 201811270352 A CN201811270352 A CN 201811270352A CN 111105868 B CN111105868 B CN 111105868B
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- 238000000338 in vitro Methods 0.000 title claims abstract description 90
- 238000013523 data management Methods 0.000 title claims abstract description 73
- 238000000034 method Methods 0.000 title claims abstract description 59
- 238000003745 diagnosis Methods 0.000 title claims abstract description 30
- 238000012217 deletion Methods 0.000 claims abstract description 42
- 230000037430 deletion Effects 0.000 claims abstract description 42
- 239000003153 chemical reaction reagent Substances 0.000 claims abstract description 7
- 238000003908 quality control method Methods 0.000 claims abstract description 7
- 238000004064 recycling Methods 0.000 claims description 33
- 238000011084 recovery Methods 0.000 claims description 16
- 238000012163 sequencing technique Methods 0.000 claims description 5
- 230000001960 triggered effect Effects 0.000 claims description 4
- 239000008280 blood Substances 0.000 description 9
- 210000004369 blood Anatomy 0.000 description 9
- 238000010586 diagram Methods 0.000 description 7
- 238000001514 detection method Methods 0.000 description 6
- 238000007726 management method Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 4
- 238000009666 routine test Methods 0.000 description 4
- 230000003068 static effect Effects 0.000 description 4
- 238000012545 processing Methods 0.000 description 3
- 230000009286 beneficial effect Effects 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 230000001360 synchronised effect Effects 0.000 description 2
- 238000012742 biochemical analysis Methods 0.000 description 1
- 230000023555 blood coagulation Effects 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 238000013515 script Methods 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
Classifications
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- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H40/00—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices
- G16H40/60—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices
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- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06F—ELECTRIC DIGITAL DATA PROCESSING
- G06F11/00—Error detection; Error correction; Monitoring
- G06F11/07—Responding to the occurrence of a fault, e.g. fault tolerance
- G06F11/14—Error detection or correction of the data by redundancy in operation
- G06F11/1402—Saving, restoring, recovering or retrying
- G06F11/1471—Saving, restoring, recovering or retrying involving logging of persistent data for recovery
Abstract
The invention provides a data management method, in-vitro diagnosis equipment and storage medium, wherein the method comprises the following steps: presenting at least one set of data on a data management interface; the at least one set of data includes target data, the target data stored in the first storage space including at least one of: sample data, reagent data, calibration data, or quality control data; receiving a first deletion instruction for target data, wherein the first deletion instruction indicates that the target data is deleted from the first storage space; moving the target data to a temporary data area; and if a restoring instruction for target data is received through the data management interface, restoring the target data from the temporary data area to the first storage space.
Description
Technical Field
The present invention relates to the field of medical technology, and in particular, to a data management method, an in vitro diagnostic device, and a storage medium.
Background
In the related art, in the process of operating data by using in-vitro diagnostic equipment, if the data is deleted due to misoperation or improper operation, the storage space occupied by the deleted data is recovered, so that the deleted data cannot be recovered.
Disclosure of Invention
In view of the foregoing, it is desirable to provide a data management method, an in-vitro diagnostic device, and a storage medium, which can realize effective management of data.
In a first aspect, an embodiment of the present invention provides a data management method, applied to an in vitro diagnostic device, the method including:
presenting at least one set of data on a data management interface; the at least one set of data includes target data, the target data stored in the first storage space including at least one of: sample data, reagent data, calibration data, or quality control data;
receiving a first deletion instruction for target data, wherein the first deletion instruction indicates that the target data is deleted from the first storage space;
moving the target data to a temporary data area;
and if a restoring instruction for target data is received through the data management interface, restoring the target data from the temporary data area to the first storage space.
In the above scheme, the data in the temporary data area is classified and stored, and all data in the same type can be restored by one key.
In the above scheme, the method further comprises:
acquiring the storage time length of each group of data in the temporary data area;
and recycling the storage space occupied by the data with the storage time exceeding the preset time.
In the above scheme, the method further comprises:
acquiring the residual storage space capacity of the in-vitro diagnosis device;
when the residual storage space capacity is smaller than a preset threshold value, sequencing each group of data in the temporary data area;
and based on the sorting result, sequentially recycling the storage space occupied by each group of data until the size of the residual storage space is not smaller than the preset threshold value.
In the above scheme, the sorting the data of each group in the temporary data area includes:
acquiring creation time of each group of data in the temporary data area;
and ordering the data of each group in the temporary data area based on the front and back of the creation time.
In the above scheme, the sorting the data of each group in the temporary data area includes:
acquiring the operated times of each group of data in the temporary data area;
and sorting the data of each group in the temporary data area based on the number of times of the operated.
In the above scheme, the method further comprises:
receiving a second deleting instruction for the data in the temporary data area;
and recycling the storage space occupied by the deleted data indicated by the second deleting instruction.
In the above scheme, the method further comprises:
presenting data stored in the temporary data area and deletion information corresponding to each group of data in a list form in an interface of the temporary data area;
the deletion information includes at least one of: the time of moving to the temporary data area, the storage time length and the data creation time.
In a second aspect, embodiments of the present invention also provide an in vitro diagnostic device, comprising:
a presentation unit for presenting at least one set of data on the data management interface; the at least one set of data includes target data, the target data stored in the first storage space including at least one of: sample data, reagent data, calibration data, or quality control data;
a receiving unit configured to receive a first deletion instruction for target data, the first deletion instruction indicating deletion of the target data from the first storage space;
a moving unit for moving the target data to a temporary data area;
and the data management interface is used for restoring the target data from the temporary data area to the first storage space when receiving a restoring instruction for the target data.
In the above aspect, the in vitro diagnostic device further comprises:
a first obtaining unit, configured to obtain a storage duration of each group of data in the temporary data area;
the first recovery unit is used for recovering the storage space occupied by the data with the storage time exceeding the preset time.
In the above aspect, the in vitro diagnostic device further comprises:
a second acquisition unit configured to acquire a remaining storage space capacity of the in-vitro diagnostic device;
the sorting unit is used for sorting the data of each group in the temporary data area when the residual storage space capacity is smaller than a preset threshold value;
and the second recycling unit is used for recycling the storage space occupied by the data in sequence based on the sorting result until the size of the residual storage space is not smaller than the preset threshold value.
In the above scheme, the sorting unit is further configured to obtain creation time of each set of data in the temporary data area;
and ordering the data of each group in the temporary data area based on the front and back of the creation time.
In the above scheme, the sorting unit is further configured to obtain the number of times that each group of data in the temporary data area is operated;
and sorting the data of each group in the temporary data area based on the number of times of the operated.
In the above aspect, the in-vitro diagnostic device further comprises a third recovery unit;
the receiving unit is further configured to receive a second deletion instruction for data in the temporary data area, and trigger the third recycling unit;
and the third recycling unit is used for recycling the storage space occupied by the deleted data indicated by the second deleting instruction.
In the above scheme, the data in the temporary data area is classified and stored, and all data in the same type can be restored by one key.
In the above aspect, the presenting unit is further configured to present, in an interface of the temporary data area, data stored in the temporary data area and deletion information corresponding to each group of data in a list form;
the deletion information includes at least one of: the time of moving to the temporary data area, the storage time length and the data creation time.
In a third aspect, embodiments of the present invention also provide an in vitro diagnostic device comprising:
a memory for storing executable instructions;
and the processor is used for realizing the data management method provided by the embodiment of the invention when executing the executable instructions stored in the memory.
In a fourth aspect, an embodiment of the present invention further provides a storage medium storing executable instructions, where the executable instructions implement the data management method provided by the embodiment of the present invention when the executable instructions are executed.
The data management method, the in-vitro diagnosis equipment and the storage medium provided by the embodiment of the invention have the following beneficial technical effects:
when a user indicates to delete target data from the data management interface, the in-vitro diagnosis device does not recover the storage space occupied by the target data, but moves the target data to a temporary data area, the storage space occupied by the data stored in the temporary data area is in a state of being ready for recovery, and when the user triggers a recovery instruction through the data management interface, the target data is recovered to the original first storage space; in this way, in the process that the user checks or operates the data through the data management interface, if the user performs data deletion under the condition of non-subjective intention, or finds that the previously deleted data still has use value, because the storage space occupied by the data in the temporary data area is not recovered, that is, the data is not erased from the disk, the user can still restore the deleted data.
Drawings
Fig. 1 is a schematic flow chart of a data management method according to an embodiment of the present invention;
FIG. 2 is a schematic diagram of a data management interface according to an embodiment of the present invention;
FIG. 3 is a second flowchart of a data management method according to an embodiment of the present invention;
fig. 4 is a flowchart illustrating a data management method according to an embodiment of the present invention;
fig. 5 is a flow chart diagram of a data management method according to an embodiment of the present invention;
fig. 6 is a schematic diagram of the composition and structure of an in vitro diagnostic device 100 according to an embodiment of the present invention;
fig. 7 is a schematic diagram of a hardware composition structure of an in vitro diagnostic device according to an embodiment of the present invention.
Detailed Description
In order to make the objects, technical solutions and advantages of the present invention more apparent, the present invention will be described in further detail below with reference to the accompanying drawings, wherein the described embodiments are some, but not all embodiments of the present invention. All other embodiments, which can be made by one of ordinary skill in the art without undue burden from the invention, are within the scope of the invention in accordance with embodiments of the present invention.
It should be noted that, in the embodiments of the present invention, the terms "comprises," "comprising," or any other variation thereof, are intended to cover a non-exclusive inclusion, such that a method or apparatus that comprises a list of elements does not include only those elements but may include other elements not expressly listed or inherent to such method or apparatus. Without further limitation, the element defined by the phrase "comprising one … …" does not exclude the presence of other related elements (e.g., a step in a method or a unit in an apparatus, where the unit may be a part of a circuit, a part of a processor, a part of a program or software, etc.) in a method or apparatus comprising the element.
For example, the data management method provided in the embodiment of the present invention includes a series of steps, but the data management method provided in the embodiment of the present invention is not limited to the provided steps, and similarly, the in vitro diagnostic device provided in the embodiment of the present invention includes a series of units, but the in vitro diagnostic device provided in the embodiment of the present invention is not limited to include explicitly provided units, and may also include units that are required to be set for acquiring related information or performing processing based on the information.
The data management method provided by the embodiment of the invention is explained next. The data management method provided by the embodiment of the invention is applied to the in-vitro diagnosis equipment, the in-vitro diagnosis equipment is used for medical detection in the medical technical field, and the detection result is displayed in a data management interface, and in practical application, the in-vitro diagnosis equipment can be a blood analyzer, a biochemical analysis detection equipment, a blood coagulation detection equipment, a urine detection equipment and the like; correspondingly, the software of the in-vitro diagnosis equipment is used for controlling the operation of the in-vitro diagnosis equipment and managing the detection result of the in-vitro diagnosis equipment; when the in vitro diagnostic device is a blood analyzer, the corresponding data may be blood routine test data.
Fig. 1 is a schematic flow chart of a data management method according to an embodiment of the present invention, which is applied to an in vitro diagnostic device, referring to fig. 1, and the data management method according to the embodiment of the present invention includes:
step 101: at least one set of data is presented on the data management interface, the at least one set of data including target data.
Here, in practical application, for the in vitro diagnostic device provided by the embodiment of the present invention, the target data may be at least one of the following: sample data, reagent data, calibration data, or quality control data; the user can view and operate the data/target data through the data management interface, and the at least one group of data presented by the data management interface is stored in a first storage space, such as a specific storage partition or a hard disk of the device; fig. 2 is a schematic diagram of a data management interface provided in an embodiment of the present invention, referring to fig. 2, the current data management interface presents 5 sets of data, and when a mouse selects a set of data, operations such as deletion, sorting, etc. can be performed on the data.
Step 102: a first delete instruction for target data is received, the first delete instruction indicating deletion of the target data from the data management interface.
Still taking fig. 2 as an example, in the process of data management, there may be a situation that only a part of data is needed currently and temporarily unwanted data needs to be deleted, after the data needing to be deleted is selected through the data management interface, a first deletion instruction is triggered to instruct to delete the selected data from the current data management interface, the data or information presented by the data management interface is stored in a storage address, such as a certain folder of a D disc of the device, after the selected target data is deleted according to the first deletion instruction, the target data is deleted from the storage address, and the data management interface does not display the relevant information of the target data before the target data is not restored.
Step 103: and moving the target data to a temporary data area.
Here, the storage space occupied by the data stored in the temporary data area is in a state of being ready for reclamation.
After receiving a first deleting instruction triggered by a user, the in-vitro diagnosis equipment moves target data indicating deletion to a temporary data area and marks the storage space occupied by the target data as a state of being ready for recycling, namely, the in-vitro diagnosis equipment does not erase the data in the storage space occupied by the target data although receiving the first deleting instruction, but only marks the storage space occupied by the target data as a state of being ready for recycling, so that if the data is deleted by the user under the condition of non-subjective intention, or the user finds that the data still has use value, the user can restore the deleted data because the storage space occupied by the data of the temporary data area is not recycled, namely, the data is not erased from a disk.
Step 104: and if a restoring instruction for target data is received through the data management interface, restoring the target data from the temporary data area to the first storage space.
In one embodiment, the data of the temporary data area is classified and stored, and all data of the same type can be restored by one key.
In practical implementation, in order to realize effective management of the storage space of the device, the in-vitro diagnostic device periodically reclaims the storage space occupied by the data meeting the specific reclaiming condition in the temporary data area.
In an embodiment, the device manages the data with the storage time length exceeding a certain time length in the temporary data area, and optionally, the in-vitro diagnosis device obtains the storage time length of each group of data in the temporary data area; and recycling the storage space occupied by the data with the storage time exceeding the preset time. In practical application, the preset time length can be set based on practical requirements, and the data with the storage time length exceeding the preset time length can be regarded as the data which is no longer needed by a user and can be permanently deleted; for example, the in-vitro diagnosis device deletes the data stored for more than 30 days in the temporary data area, namely, recovers the storage space occupied by the data stored for more than 30 days; therefore, the effective management of the equipment storage space is realized, and the unnecessary occupation of the equipment storage space is reduced.
In an embodiment, the in-vitro diagnosis device may periodically detect the remaining capacity of the storage space of the own magnetic disk, and manage the data in the temporary data area when the remaining capacity of the storage space is smaller than a preset threshold, and optionally, the in-vitro diagnosis device obtains the remaining capacity of the own magnetic disk; when the capacity of the residual storage space is smaller than a preset threshold value, sequencing each group of data in the temporary data area, and based on the sequencing result, sequentially recovering the storage space occupied by the data until the size of the residual storage space is not smaller than the preset threshold value; therefore, the residual storage space capacity of the in-vitro diagnosis equipment is not smaller than the preset capacity, the data with the preset capacity can be stored sufficiently, and the situation that the storage space of the equipment is insufficient when a user needs to store important data is avoided. In practical applications, the threshold value of the remaining storage space capacity may be set according to practical needs.
Here, the order of the respective sets of data in the temporary data area will be described.
In practical applications, the earlier the user indicates deleted data, the less likely the user restores the data, so in an embodiment, each set of data in the temporary data area may be ordered based on the creation time of the data, and specifically, the in vitro diagnostic device obtains the creation time of each set of data in the temporary data area; the data sets in the temporary data area are ordered based on the front and rear of the creation time (e.g., the data sets in the temporary data area are ordered in the order of front to rear of the creation time). Thus, when the device performs the storage space reclamation of the data, the storage space occupied by the data with the previous creation time, that is, the storage space occupied by the data which the user instructed to delete earlier, can be reclaimed preferentially.
In practical application, the more data the user views/operates, the higher the use value is for the user, and the greater the possibility of the user restoring the data is, so in an embodiment, the data of each group in the temporary data area may be ordered based on the number of times the data is operated, specifically, the in vitro diagnostic device obtains the number of times each group of data in the temporary data area is operated; the data sets in the temporary data area are ordered based on the number of times the operation is performed (e.g., the data sets in the temporary data area are ordered in order of the number of times the operation is performed from less to more). Thus, when the device performs the recovery of the storage space of the data, the storage space occupied by the data having the smaller number of operations can be recovered preferentially.
In practical application, there is a situation that a user actively performs storage space recycling, and the user triggers a second deleting instruction for deleting data in the temporary data area, in an embodiment, the in-vitro diagnostic device receives the second deleting instruction for the data in the temporary data area, and recycling the storage space occupied by the deleted data indicated by the second deleting instruction.
In practical application, there is a case that a user restores data in the temporary data area, the user triggers a restoration instruction for restoring the data in the temporary data area, and in an embodiment, the in-vitro diagnostic device receives the restoration instruction for the data in the temporary data area; and removing the data corresponding to the restore instruction from the temporary data area, so that the removed data can be presented on the data management interface. Therefore, even if the user performs false deletion on the data in the process of data viewing/operation, the data can still be restored, and the user experience is improved.
In practical application, the user may also view/manage the data stored in the temporary data area at the interface of the temporary data area, so as to facilitate the user's viewing/management, in an embodiment, in the interface of the temporary data area, the in vitro diagnostic device presents the data stored in the temporary data area in the form of a list, and the deletion information corresponding to each group of data; wherein the deletion information includes at least one of: the time of moving to the temporary data area, the storage time length and the data creation time. Therefore, the user can manage the data stored in the temporary data area based on the presented information, and the user does not need to independently check the deleting information of each group of data, so that the user experience is improved.
Fig. 3 is a flow chart of a data management method according to an embodiment of the present invention, which is applied to an in vitro diagnostic device, referring to fig. 3, the data management method according to an embodiment of the present invention includes:
step 201: the in vitro diagnostic device presents multiple sets of data on a data management interface.
In practical implementation, when the in-vitro diagnostic device is a blood analyzer, the corresponding data may be blood routine test data.
Step 202: a delete instruction for the target data is received.
Here, the deletion instruction instructs to delete the target data from the data management interface.
Step 203: and moving the target data to the temporary data area, and marking the storage space occupied by the target data as a state of preparation for recovery.
In actual implementation, the storage space occupied by the data stored in the temporary data area is in a state of being ready for recycling, that is, the storage space occupied by the data stored in the temporary data area is in a state of being ready for recycling.
Step 204: a restore instruction for the target data is received.
Step 205: the target data is removed from the temporary data area such that the removed data can be presented on the data management interface.
By applying the embodiment of the invention, the storage space occupied by the data in the temporary data area is not recovered, namely the data is not erased from the disk, so that a user can restore the deleted data when needed, and the user experience is improved.
Fig. 4 is a flow chart of a data management method according to an embodiment of the present invention, which is applied to an in vitro diagnostic device, referring to fig. 4, and the data management method according to the embodiment of the present invention includes:
step 301: the in vitro diagnostic device presents multiple sets of data on a data management interface.
In practical implementation, when the in-vitro diagnostic device is a blood analyzer, the corresponding data may be blood routine test data.
Step 302: a delete instruction for the target data is received.
Here, the deletion instruction instructs to delete the target data from the data management interface.
Step 303: and moving the target data to the temporary data area, and marking the storage space occupied by the target data as a state of preparation for recovery.
In actual implementation, the storage space occupied by the data stored in the temporary data area is in a state of being ready for recycling, that is, the storage space occupied by the data stored in the temporary data area is in a state of being ready for recycling.
Step 304: and acquiring the storage time length of each group of data in the temporary data area.
Step 305: and recycling the storage space occupied by the data with the storage time exceeding the preset time.
By applying the embodiment of the invention, the in-vitro diagnosis equipment can automatically realize the recovery of the storage space occupied by the data with the storage time exceeding a certain time in the temporary data area, realize the effective management of the storage space of the equipment and reduce the unnecessary occupation of the storage space of the equipment.
Fig. 5 is a flow chart of a data management method according to an embodiment of the present invention, which is applied to an in vitro diagnostic device, referring to fig. 5, and the data management method according to the embodiment of the present invention includes:
step 401: the in vitro diagnostic device presents multiple sets of data on a data management interface.
In practical implementation, when the in-vitro diagnostic device is a blood analyzer, the corresponding data may be blood routine test data.
Step 402: a delete instruction for the target data is received.
Here, the deletion instruction instructs to delete the target data from the data management interface.
Step 403: and moving the target data to the temporary data area, and marking the storage space occupied by the target data as a state of preparation for recovery.
In actual implementation, the storage space occupied by the data stored in the temporary data area is in a state of being ready for recycling, that is, the storage space occupied by the data stored in the temporary data area is in a state of being ready for recycling.
Step 404: and acquiring the residual storage space capacity of the in-vitro diagnosis equipment, and sequencing each group of data in the temporary data area when the residual storage space capacity is smaller than a preset threshold value.
Here, the threshold value of the remaining storage space capacity may be set according to actual needs.
In one embodiment, the in vitro diagnostic device may implement the ordering of the sets of data in the temporary data area by:
acquiring creation time of each group of data in the temporary data area; and ordering the data of each group in the temporary data area based on the front and back of the creation time. Illustratively, the in-vitro diagnostic device orders the sets of data in the temporary data area in a front-to-back order of creation time.
In one embodiment, the in vitro diagnostic device may further implement ordering of the sets of data in the temporary data area by:
acquiring the operated times of each group of data in the temporary data area; and sorting the data of each group in the temporary data area based on the number of times of the operated. Illustratively, the in-vitro diagnostic device orders the sets of data in the temporary data area in an order in which the number of times the data is operated is from small to large.
Step 405: and based on the sorting result, sequentially recycling the storage space occupied by the data until the size of the residual storage space is not smaller than a preset threshold value.
Next, an in vitro diagnostic device implementing the data management method according to the above embodiment of the present invention will be described. Fig. 6 is a schematic diagram of the composition structure of an in-vitro diagnostic device 100 according to an embodiment of the present invention, referring to fig. 6, the in-vitro diagnostic device 100 includes:
a presentation unit 11 for presenting at least one set of data on a data management interface; the at least one set of data includes target data; the target data is stored in the first storage space, and comprises at least one of the following: sample data, reagent data, calibration data, or quality control data;
a receiving unit 12, configured to receive a first deletion instruction for target data, where the first deletion instruction indicates that the target data is deleted from the data management interface;
a moving unit 13 for moving the target data to a temporary data area; the storage space occupied by the data stored in the temporary data area is in a state of being reserved for recovery;
and the data management interface is used for restoring the target data from the temporary data area to the first storage space when receiving a restoring instruction for the target data.
In an embodiment, the in vitro diagnostic device further comprises:
a first obtaining unit, configured to obtain a storage duration of each group of data in the temporary data area;
the first recovery unit is used for recovering the storage space occupied by the data with the storage time exceeding the preset time.
In an embodiment, the in vitro diagnostic device further comprises:
a second acquisition unit configured to acquire a remaining storage space capacity of the in-vitro diagnostic device;
the sorting unit is used for sorting the data of each group in the temporary data area when the residual storage space capacity is smaller than a preset threshold value;
and the second recycling unit is used for recycling the storage space occupied by the data in sequence based on the sorting result until the size of the residual storage space is not smaller than the preset threshold value.
In an embodiment, the sorting unit is further configured to obtain creation time of each set of data in the temporary data area;
and ordering the data of each group in the temporary data area based on the front and back of the creation time.
In an embodiment, the sorting unit is further configured to obtain the number of times each set of data in the temporary data area is operated;
and sorting the data of each group in the temporary data area based on the number of times of the operated.
In an embodiment, the in vitro diagnostic device further comprises a third recovery unit;
the receiving unit is further configured to receive a second deletion instruction for data in the temporary data area, and trigger the third recycling unit;
and the third recycling unit is used for recycling the storage space occupied by the deleted data indicated by the second deleting instruction.
In an embodiment, the presenting unit is further configured to present, in an interface of the temporary data area, data stored in the temporary data area and deletion information corresponding to each group of data in a list form;
the deletion information includes at least one of: the time of moving to the temporary data area, the storage time length and the data creation time.
It should be noted here that: the description of the in-vitro diagnosis equipment is similar to the description of the control method of the software interface layout, and the description of the beneficial effects of the same method is omitted. For technical details not disclosed in the embodiments of the in vitro diagnostic device according to the present invention, please refer to the description of the embodiments of the method according to the present invention.
Next, the hardware structure of the in vitro diagnostic device according to the embodiment of the present invention will be described in detail, and fig. 7 is a schematic diagram of the hardware composition structure of the in vitro diagnostic device according to the embodiment of the present invention, it will be understood that fig. 7 only shows an exemplary structure of the in vitro diagnostic device, but not all the structures, and part of or all the structures shown in fig. 7 may be implemented as required. The in-vitro diagnosis device provided by the embodiment of the invention comprises: at least one processor 21, a memory 22, at least one network interface 24, and a user interface 23. The various components in the in vitro diagnostic device are coupled together by a bus system 25. It will be appreciated that the bus system 25 is used to enable connected communications between these components. The bus system 25 includes a power bus, a control bus, and a status signal bus in addition to the data bus. But for clarity of illustration the various buses are labeled as bus system 25 in fig. 7.
The user interface 23 may include a display, keyboard, mouse, trackball, click wheel, keys, buttons, touch pad, touch screen, or the like.
The memory 22 may be volatile memory or nonvolatile memory, and may include both volatile and nonvolatile memory. The nonvolatile Memory may be a Read Only Memory (ROM), a programmable Read Only Memory (PROM, programmable Read-Only Memory), an erasable programmable Read Only Memory (EPROM, erasable Programmable Read-Only Memory), a Flash Memory (Flash Memory), or the like. The volatile memory may be random access memory (RAM, random Access Memory), which acts as external cache memory. By way of example and not limitation, many forms of RAM are available, such as static random access memory (SRAM, static Random Access Memory), synchronous static random access memory (SSRAM, synchronous Static Random Access Memory). The memory 22 described in embodiments of the present invention is intended to comprise these and any other suitable types of memory.
The processor 21 may be an integrated circuit chip with signal processing capabilities such as a general purpose processor, which may be a microprocessor or any conventional processor, or the like, a digital signal processor (DSP, digital Signal Processor), or other programmable logic device, discrete gate or transistor logic, discrete hardware components, or the like.
The memory 22 is capable of storing executable instructions 221 to support the operation of the in vitro diagnostic device, examples of which include: various forms of software modules, such as programs, plug-ins, and scripts, for operating on the in vitro diagnostic device may include, for example, an operating system including various system programs, such as a framework layer, a core library layer, a driver layer, etc., for implementing various basic services and processing hardware-based tasks, and application programs.
Correspondingly, the embodiment of the invention also provides an in-vitro diagnosis device, which comprises:
a memory for storing executable instructions;
and the processor is used for realizing the data management method provided by the embodiment of the invention when executing the executable instructions stored in the memory.
The embodiment of the invention also provides a storage medium which stores executable instructions, and the executable instructions are used for realizing the data management method provided by the embodiment of the invention when being executed.
Those of ordinary skill in the art will appreciate that: all or part of the steps for implementing the above method embodiments may be implemented by hardware associated with program instructions, where the foregoing program may be stored in a computer readable storage medium, and when executed, the program performs steps including the above method embodiments; and the aforementioned storage medium includes: a removable storage device, a read-only memory, a random access memory, a magnetic or optical disk, or other various media capable of storing program code.
Alternatively, the above-described integrated units of the present invention may be stored in a computer-readable storage medium if implemented in the form of software functional modules and sold or used as separate products. Based on such understanding, the technical solutions of the embodiments of the present invention may be embodied in essence or a part contributing to the prior art in the form of a software product stored in a storage medium, including several instructions for causing a computer device (which may be a personal computer, a server, or a network device, etc.) to execute all or part of the methods described in the embodiments of the present invention. And the aforementioned storage medium includes: a removable storage device, ROM, RAM, magnetic or optical disk, or other medium capable of storing program code.
The foregoing is merely exemplary embodiments of the present invention and is not intended to limit the scope of the present invention. Any modification, equivalent replacement, improvement, etc. made within the spirit and scope of the present invention are included in the protection scope of the present invention.
Claims (12)
1. A data management method applied to an in vitro diagnostic device, the method comprising:
presenting at least one set of data on a data management interface; the at least one set of data includes target data, the target data stored in the first storage space including at least one of: sample data, reagent data, calibration data, or quality control data;
receiving a first deletion instruction for target data, wherein the first deletion instruction indicates that the target data is deleted from the data management interface, and the first deletion instruction indicates that the target data is deleted from the first storage space; the first deleting instruction is triggered after the data to be deleted is selected through the data management interface;
moving the target data to a temporary data area, and marking the storage space occupied by the target data as a state of preparation for recovery;
if a restoring instruction for the target data is received through the data management interface, restoring the target data from the temporary data area to the first storage space;
the method comprises the steps that an in-vitro diagnosis device obtains the residual storage space capacity of the in-vitro diagnosis device; the residual storage space capacity is the storage space residual capacity of a self-disk of the in-vitro diagnosis equipment;
when the residual storage space capacity is smaller than a preset threshold value, the in-vitro diagnosis device sorts the data of each group in the temporary data area based on the number of times the data are operated; the number of times the data is manipulated is obtained based on the number of times the user views/manipulates the data, the number of times the data is manipulated characterizing the value of use of the data;
and the in-vitro diagnosis equipment sequentially recovers the storage space occupied by each group of data based on the sequencing result until the size of the residual storage space is not smaller than the preset threshold value.
2. The method of claim 1, wherein the data of the temporary data area is stored in a classified manner, and all data of the same type can be restored by one-key.
3. The method of claim 1 or 2, wherein the method further comprises:
acquiring the storage time length of each group of data in the temporary data area;
and recycling the storage space occupied by the data with the storage time exceeding the preset time.
4. The method of claim 1, wherein the method further comprises:
receiving a second deleting instruction for the data in the temporary data area;
and recycling the storage space occupied by the deleted data indicated by the second deleting instruction.
5. The method of any one of claims 1 to 4, further comprising:
presenting data stored in the temporary data area and deletion information corresponding to each group of data in a list form in an interface of the temporary data area;
the deletion information includes at least one of: the time of moving to the temporary data area, the storage time length and the data creation time.
6. An in vitro diagnostic device, characterized in that it comprises:
a presentation unit for presenting at least one set of data on the data management interface; the at least one set of data includes target data, the target data stored in the first storage space including at least one of: sample data, reagent data, calibration data, or quality control data;
a receiving unit configured to receive a first deletion instruction for target data, the first deletion instruction indicating deletion of the target data from the data management interface, and the first deletion instruction indicating deletion of the target data from the first storage space; the first deleting instruction is triggered after the data to be deleted is selected through the data management interface;
the mobile unit is used for moving the target data to the temporary data area and marking the storage space occupied by the target data as a state of preparation for recovery; and the data management interface is used for restoring the target data from the temporary data area to the first storage space when receiving a restoring instruction for the target data;
a second acquisition unit configured to acquire a remaining storage space capacity of the in-vitro diagnostic device; the residual storage space capacity is the storage space residual capacity of a self-disk of the in-vitro diagnosis equipment;
a sorting unit, configured to sort each group of data in the temporary data area based on the number of times the data is operated when the remaining storage space capacity is smaller than a preset threshold; the number of times the data is operated is acquired based on the number of times the user views or operates the data, and the number of times the data is operated characterizes the use value of the data;
and the second recycling unit is used for recycling the storage space occupied by the data in sequence based on the sorting result until the size of the residual storage space is not smaller than the preset threshold value.
7. The in vitro diagnostic device of claim 6 wherein said in vitro diagnostic device further comprises:
a first obtaining unit, configured to obtain a storage duration of each group of data in the temporary data area;
the first recovery unit is used for recovering the storage space occupied by the data with the storage time exceeding the preset time.
8. The in-vitro diagnostic device according to claim 6, wherein the in-vitro diagnostic device further comprises a third recovery unit;
the receiving unit is further configured to receive a second deletion instruction for data in the temporary data area, and trigger the third recycling unit;
and the third recycling unit is used for recycling the storage space occupied by the deleted data indicated by the second deleting instruction.
9. The in vitro diagnostic device according to claim 6, wherein,
and the data of the temporary data area is stored in a classified mode, and all data of the same type can be restored by one key.
10. The in vitro diagnostic device according to any one of the claims 6 to 9, wherein,
the presentation unit is further configured to present, in an interface of the temporary data area, data stored in the temporary data area and deletion information corresponding to each group of data in a list form;
the deletion information includes at least one of: the time of moving to the temporary data area, the storage time length and the data creation time.
11. An in vitro diagnostic device, characterized in that it comprises:
a memory for storing executable instructions;
a processor for implementing the data management method according to any one of claims 1 to 5 when executing executable instructions stored in said memory.
12. A storage medium storing executable instructions which, when executed, implement the data management method of any one of claims 1 to 5.
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