CN113392948A - Medical laboratory sample detection bar code registration method and device - Google Patents
Medical laboratory sample detection bar code registration method and device Download PDFInfo
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- CN113392948A CN113392948A CN202110779896.8A CN202110779896A CN113392948A CN 113392948 A CN113392948 A CN 113392948A CN 202110779896 A CN202110779896 A CN 202110779896A CN 113392948 A CN113392948 A CN 113392948A
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- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06K—GRAPHICAL DATA READING; PRESENTATION OF DATA; RECORD CARRIERS; HANDLING RECORD CARRIERS
- G06K19/00—Record carriers for use with machines and with at least a part designed to carry digital markings
- G06K19/06—Record carriers for use with machines and with at least a part designed to carry digital markings characterised by the kind of the digital marking, e.g. shape, nature, code
- G06K19/06009—Record carriers for use with machines and with at least a part designed to carry digital markings characterised by the kind of the digital marking, e.g. shape, nature, code with optically detectable marking
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- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06F—ELECTRIC DIGITAL DATA PROCESSING
- G06F16/00—Information retrieval; Database structures therefor; File system structures therefor
- G06F16/30—Information retrieval; Database structures therefor; File system structures therefor of unstructured textual data
- G06F16/33—Querying
- G06F16/3331—Query processing
- G06F16/334—Query execution
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- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06F—ELECTRIC DIGITAL DATA PROCESSING
- G06F16/00—Information retrieval; Database structures therefor; File system structures therefor
- G06F16/30—Information retrieval; Database structures therefor; File system structures therefor of unstructured textual data
- G06F16/36—Creation of semantic tools, e.g. ontology or thesauri
- G06F16/374—Thesaurus
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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
- G16H10/00—ICT specially adapted for the handling or processing of patient-related medical or healthcare data
- G16H10/40—ICT specially adapted for the handling or processing of patient-related medical or healthcare data for data related to laboratory analysis, e.g. patient specimen analysis
Abstract
The application discloses a medical laboratory sample detection bar code registration method and a device, wherein the method comprises the following steps: converting a preset detection combination obtained after splitting a target test specimen into pre-registered specimen information according to a pre-registered dictionary, and constructing a project list according to the pre-registered specimen information, wherein the project list comprises specimen bar codes, specimen professional groups and registration early warning time; distributing pre-registered sample information in the project list to a pre-registered list of a first target professional group according to a sample bar code, a sample professional group and a pre-registration rule, wherein the pre-registration rule comprises a preset time priority rule and a preset sample priority rule; the pre-registered specimen information received in the pre-registration list is registered on the target instrument by the professional group within the registration warning time range. The method solves the technical problems that the existing sample detection bar code registration method cannot track the sample in real time, forms closed-loop management, is greatly dependent on manpower, causes low working efficiency and is easy to cause doctor-patient disputes.
Description
Technical Field
The application relates to the technical field of laboratory information management, in particular to a medical laboratory sample detection bar code registration method and device.
Background
With the rapid development of clinical test medicine and the gradual improvement of test management, more and more accurate test items are introduced by the clinical laboratory of each hospital, so that the accuracy and the timeliness of disease diagnosis are greatly improved, and great help is provided for doctors and patients. However, because of the precise and specialized design of the examination items, the examination items on an order sheet often relate to a plurality of professional groups, and the difficulty of timely, accurately and completely issuing examination reports by the clinical laboratory is higher and higher due to the imperfect information circulation between different professional groups.
In order to reduce the internal turnover time (TAT) of a laboratory and improve the on-time issuing proportion of a test report, a clinical laboratory strictly manages the TAT, and inspectors can pay attention to samples close to the requirement of test return time in different modes.
For example, scheme one: the LIS system is provided with a countdown function and related equipment, such as a large screen of a laboratory, and when a sample is close to the requirement of testing and reporting time, reminding information is displayed on a department workstation, large screen information is updated, and the sample information close to the requirement of testing and reporting time is prompted. After receiving the prompt message, the worker will first try to locate the specimen in the professional group, such as searching the on-machine information on the production line or searching in the unarchived specimen processing area; if the specimen cannot be found in the current professional group, the professional group in which the specimen possibly exists is presumed according to experience, and the other professional groups continue to search.
Scheme II: and (3) manually inquiring information of each item in the professional group at a fixed frequency (set according to different professional groups and different test items, such as once every two hours), counting the number and the state of the samples within the test return time requirement range, and if the samples with the requirements close to the test return time are found, performing urgent processing on the samples after the samples are positioned by the method described above.
The third scheme is as follows: and associating the IP address of the computer used for signing the specimen with the specific professional group, and pre-registering the specimen signed by the specific computer to a fixed professional group to-be-detected list associated with the specimen. Through this kind of mode, the very first time obtains the sample information after the sample can be signed for at laboratory foreground to specific specialty group, makes things convenient for the staff in time to follow up, accomplishes the sample and detects.
The three solutions either require a large amount of labor cost investment or the management mode is relatively fixed, so that the real operation condition of a changeable laboratory is difficult to deal with. A plurality of laboratories are forced to modify the bar code generating logic of the specimen, and after doctors prescribe medical orders, the bar codes are generated according to the preset information of the specimen container type, the specimen type, the professional group to which the specimens belong and the like, so that the number of the common tubes among different professional groups is reduced as much as possible. The unavailable management measures increase the blood sampling amount and the number of blood sampling tubes of the patient, and cause huge physical, psychological and economic burdens on the patient. Or, the performance assessment management mode prompts the staff to strengthen the management of the specimen and the report, however, the strict management mode of the behavior of the staff not only increases the working pressure of the staff, but also can not fundamentally solve the problems faced by the laboratory at present.
Generally speaking, the prior art cannot guarantee that all combinations to be detected in the sample barcode reach a closed loop. Moreover, existing solutions rely on significant labor costs. Finally, in the management of the medical laboratory, the circulation of the specimen has the corresponding requirement on the inspection return time, and all closed loops of the combination to be inspected cannot be well guaranteed, so that the TAT management requirement of the medical laboratory on the specimen cannot be met, the requirements of patients cannot be met, and medical disputes can be caused.
Disclosure of Invention
The application provides a medical laboratory sample detection bar code registration method and device, which are used for solving the technical problems that the existing sample detection bar code registration method cannot avoid sample omission, is high in dependence on manpower, causes low working efficiency and is easy to cause doctor-patient disputes.
In view of the above, a first aspect of the present application provides a medical laboratory specimen detection barcode registration method, including:
converting a preset detection combination obtained after splitting a target test specimen into pre-registered specimen information according to a pre-registered dictionary, and constructing a project list according to the pre-registered specimen information, wherein the project list comprises specimen bar codes, specimen professional groups and registration early warning time;
distributing the pre-registered sample information in the project list to a pre-registered list of a first target professional group according to the sample bar code, the sample professional group and a pre-registered rule, wherein the pre-registered rule comprises a preset time priority rule and a preset sample priority rule;
registering the pre-registered specimen information received in the pre-registration list on a target instrument by a professional group within the registration pre-warning time range.
Preferably, the registering the pre-registered specimen information received in the pre-registration list on the target instrument by a professional group within the registration pre-warning time range further includes:
and judging whether the pre-registered specimen information does not complete the registration operation in the project list, if so, performing professional group-to-group operation according to a second target professional group determined by the project list based on a preset handover principle.
Preferably, the registering the pre-registered specimen information received in the pre-registration list on a target instrument by a professional group within the registration warning time range further includes:
adding the pre-registered specimen information which cannot be registered to a delayed pre-registration list through the professional group, and recording a delay reason and a delay registration early warning time.
Preferably, the registering the pre-registered specimen information received in the pre-registration list on a target instrument by a professional group within the registration warning time range further includes:
and if the pre-registered specimen information is not registered on the target instrument within the registration early warning time, triggering an early warning mechanism.
Preferably, the registering the pre-registered specimen information received in the pre-registration list on the target instrument by a professional group within the registration pre-warning time range further includes:
deleting the pre-registered specimen information of which the registration operation is completed in the pre-registered list.
Preferably, the registering the pre-registered specimen information received in the pre-registration list on the target instrument by a professional group within the registration pre-warning time range further includes:
and adopting a preset double-person auditing flow standard to audit all the inspection results which are inspected on the target instrument.
Preferably, the registering the pre-registered specimen information received in the pre-registration list on the target instrument by a professional group within the registration pre-warning time range further includes:
and comparing and detecting the detection result according to preset medical advice information and the item list, wherein the comparison and detection are used for judging whether the medical advice detection items are finished and whether the examination of the detection result is finished.
The present application provides in a second aspect a medical laboratory specimen detection barcode registration apparatus, comprising:
the specimen conversion module is used for converting a preset detection combination obtained after the target inspection specimen is split into pre-registered specimen information according to a pre-registered dictionary, and constructing a project list according to the pre-registered specimen information, wherein the project list comprises specimen bar codes, specimen professional groups and registration early warning time;
the specimen distribution module is used for distributing the pre-registered specimen information in the project list to a pre-registered list of a first target professional group according to the specimen bar code, the specimen professional group and a pre-registered rule, wherein the pre-registered rule comprises a preset time priority rule and a preset sample priority rule;
and the specimen registration module is used for registering the pre-registered specimen information received in the pre-registration list on a target instrument through a professional group within the registration early warning time range.
Preferably, the method further comprises the following steps:
and the sample grouping conversion module is used for judging whether the pre-registered sample information does not complete the registration operation in the project list, and if so, performing professional grouping conversion operation according to a second target professional group determined by the project list based on a preset handover principle.
Preferably, the method further comprises the following steps:
and the delayed registration module is used for adding the pre-registered specimen information which cannot be subjected to registration operation to a delayed pre-registration list through the professional group, and recording a delay reason and a delayed registration early warning time.
According to the technical scheme, the embodiment of the application has the following advantages:
in the present application, a medical laboratory specimen detection barcode registration method is provided, including: converting a preset detection combination obtained after splitting a target test specimen into pre-registered specimen information according to a pre-registered dictionary, and constructing a project list according to the pre-registered specimen information, wherein the project list comprises specimen bar codes, specimen professional groups and registration early warning time; distributing pre-registered sample information in the project list to a pre-registered list of a first target professional group according to a sample bar code, a sample professional group and a pre-registration rule, wherein the pre-registration rule comprises a preset time priority rule and a preset sample priority rule; the pre-registered specimen information received in the pre-registration list is registered on the target instrument by the professional group within the registration warning time range.
According to the medical laboratory sample detection bar code registration method, each target test sample is split, a corresponding project list is constructed, then pre-registered sample information in the project list is subjected to sample distribution according to a sample professional group, sample sorting guidance can be effectively provided, and the problem caused by instrument registration directly according to sample bar codes is solved; finally, the internally received information of the pre-registered specimen is registered on a target instrument for inspection through a professional group, the registration early warning time can provide intelligent TAT (timing sequence entry) control, and an integral registration mechanism can ensure that a preset detection combination achieves closed-loop management. Automatic and intelligent sample sorting and registration are carried out according to the relation characteristics between different target test samples and professional groups, and the dependence on manual management is reduced; and the whole circulation process is recorded through a list, so that the traceability is strong. Therefore, the method and the device can solve the technical problems that the existing sample detection bar code registration method cannot avoid sample omission, is greatly dependent on manpower, causes low working efficiency and is easy to cause doctor-patient disputes.
Drawings
Fig. 1 is a schematic flow chart of a medical laboratory specimen detection barcode registration method according to an embodiment of the present application;
fig. 2 is a schematic structural diagram of a medical laboratory specimen detection barcode registration apparatus according to an embodiment of the present application.
Detailed Description
In order to make the technical solutions of the present application better understood, the technical solutions in the embodiments of the present application will be clearly and completely described below with reference to the drawings in the embodiments of the present application, and it is obvious that the described embodiments are only a part of the embodiments of the present application, and not all of the embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present application.
Interpretation of terms:
LIS: a Laboratory Information management System (LIS) is a set of Information management System specially designed for a medical Laboratory, and can form a network by using experimental instruments and computers, so that the intelligent, automatic and standardized management of complex operation processes such as patient sample entry, experimental data access, analysis, report auditing and release, experimental data statistical analysis and the like is realized. The method is beneficial to improving the management level of a laboratory, reducing the occurrence of leaks and improving the experiment quality.
TAT: the turn around Time (Turnaround Time) inside the laboratory is the Time (in minutes) from the reception of the specimen to the transmission of the report from the laboratory.
Professional groups: different working groups are separated from the laboratory according to different experimental details, such as a biochemical group, an immunological group, an emergency treatment group, a molecular diagnosis group and the like.
The applicant finds that the commonly described "closed loop of barcode flow" in a laboratory refers to the closed loop of the flow of the sample barcode, but actually, due to the blank of some control flows, it cannot be really guaranteed that all combinations to be detected in the barcode reach closed loop management. Several existing solutions all have certain limitations and inconvenience and rapidness, and cannot provide powerful support for the overall operation of a laboratory.
For example, in the first scheme, the countdown function only performs analysis of the test report issuance timeout early warning and the report issuance timeout reason through TAT management, and cannot notify relevant professional groups that there is a sample to be processed immediately after the sample arrives at a laboratory, or cannot provide sample turnaround records and other auxiliary information of the sample in a department after issuing the timeout early warning. Although the department personnel can position the specimen, complete the inspection and issue the report within the requirement range of the inspection return time in most cases after receiving the overtime early warning, once the condition that the specimen cannot be quickly positioned occurs, the clinical experience of the department personnel is needed to deduce the range of the possible specimen, such as an unarchived specimen processing area, other related professional groups and the like, and great manpower and time are spent to complete the operation, and meanwhile, when the specimen is searched for in the specific requirement range of the inspection return time, the processing of other specimens can be delayed, so that the TAT of more specimens is prolonged.
In contrast to the first solution, by manually querying each item in the professional group with a fixed frequency, the professional group can acquire the information of the specimen that has arrived at the laboratory earlier, but this solution requires more human input. Meanwhile, the same as the first scheme, the scheme cannot provide sample turnover records and other auxiliary information of the samples in the department, once the samples cannot be located quickly, the range of the possible samples needs to be deduced by depending on clinical experience of personnel in the department, huge manpower and time are spent for completing the operation, and meanwhile, when the samples are required to be searched for specific near inspection return time, the processing of other samples can be delayed, so that the TAT of more samples is prolonged.
And thirdly, correlating the IP address of the computer used for signing the specimen with the specific professional group, and pre-registering the specimen signed by the specific computer to a fixed professional group to-be-detected list associated with the specimen. Through this kind of mode, the very first time obtains the sample information after the sample can be signed for at laboratory foreground to specific specialty group, makes things convenient for the staff in time to follow up, accomplishes the sample and detects. However, this solution is relatively rigid, cannot guide specimen classification, and cannot assist information communication among different professional groups. If the staff who signs the specimen is unfamiliar with the specimen classification rules or the specimen signing process and uses a wrong computer to sign the specimen, the specimen detected by a certain professional group (A) is pre-registered to another professional group (B), so that the detection professional group A cannot obtain the specimen information, and the professional group B has the specimen pre-registered information but does not actually receive the specimen, so that the specimen cannot be positioned and the unnecessary specimen searching and positioning are caused.
Based on the problems existing in the above schemes, the application provides a registration scheme for detecting a barcode, which is used for solving the technical problems existing in the above technical schemes.
In view of the above, the following is an embodiment of a method for registering a barcode for detecting a specimen in a medical laboratory.
For ease of understanding, referring to fig. 1, an embodiment of a method for barcode registration for medical laboratory specimen detection provided herein includes:
It should be noted that each target detection sample corresponds to a sample barcode, a plurality of different preset detection combinations can be split from the same sample barcode, the preset detection combinations are sample combinations, and a sample combination is detected on one or more corresponding instruments to obtain a detection result, but the sample combinations and the instruments are in a many-to-many relationship, so that the effect of directly performing instrument registration according to the sample barcode is poor.
The pre-registered dictionary records specimen professional groups to which different specimen combinations belong and registration early warning time, after all target inspection specimens are split and combined, the target inspection specimens can be inquired according to the pre-registered dictionary, the specimen professional groups and the registration early warning time of the pre-registered inspection combinations are judged, pre-registered specimen information is obtained, the pre-registered specimen information is combined to construct an item list, namely, a plurality of pieces of pre-registered specimen information possibly exist in the item list, and one piece of pre-registered specimen information corresponds to one specimen combination to be detected.
For example, the detection items of the target test specimen are a + B + C, the split preset detection combination is a combination a, a combination B and a combination C, and the combined specimen professional group and the registration early warning time information can be queried in the pre-registration dictionary, so that 3 pieces of pre-registration specimen information are obtained, and an item list is formed.
The registration early warning time means that pre-registration specimen information needs to be successfully registered on a corresponding instrument before the time point, and the time can be specific to minutes and seconds.
And 102, distributing pre-registered sample information in the item list to a pre-registered list of a first target professional group according to the sample bar code, the sample professional group and a pre-registered rule, wherein the pre-registered rule comprises a preset time priority rule and a preset sample priority rule.
The distribution process is essentially a sorting process, that is, pre-registered sample information is sorted into corresponding first target professional groups, each first target professional group is provided with a pre-registered list, and the list is a sample task required to be checked in the professional group, that is, the pre-registered sample information in the distribution process.
The specimen specialty group serves as a guide for intelligent assignment, determining a first target specialty group. The pre-registration rule is set according to the registration sequence of a plurality of pre-registration sample information, and is generally distributed according to a preset time priority rule, and the pre-registration rule is distributed to a professional group for registration in an urgent or relatively short registration early warning time; the preset sample priority rule means that some samples are easy to be polluted or have related regulation requirements, and if the samples need to be registered preferentially, the samples are distributed preferentially according to the rule. The specific value may be determined according to a preset time priority rule or a preset sample priority rule, and the specific value may be in accordance with actual requirements, and is not limited herein.
And 103, registering the pre-registered sample information received in the pre-registered list on the target instrument through a professional group within the registration early warning time range.
According to the registration early warning time, the pre-registered sample information allocated to the pre-registered list is registered on the target instrument one by one, and then the sample inspection is performed. In the process, even if the operator has an operation error and does not send the specimen to the corresponding professional group, the professional group can inquire the item list corresponding to the information of the pre-registered specimen according to the information recorded in the pre-registered list, and find the movement track of the specimen from the record of the item list, so that the source tracing of the specimen is realized, and the specimen can be registered in time without missing.
Further, step 103, thereafter, further includes:
and judging whether the pre-registered sample information does not complete the registration operation or not exists in the project list, if so, performing professional group transfer operation according to a second target professional group determined by the project list based on a preset handover principle.
Only one combination to be detected may be in a project list, and the inspection can be performed after the registration is completed, so that the inspection task is completed. However, in many cases, a plurality of combinations to be detected, that is, a plurality of pieces of pre-registered specimen information exist in a project list, and the pre-registered specimen information may or may not be inspected in the same professional group, and if the pre-registered specimen information is inspected in a professional group, the pre-registered specimen information is assigned to a professional group for registration; if the sample is in a different professional group, the sample needs to be transferred to the next professional group to continue to complete the inspection task after the professional group where the instrument which is registered preferentially completes the inspection.
The specific professional grouping and grouping operation can be divided into two types: 1. grouping to the current professional group; 2. and transferring the group to other professional groups. Specifically, the group transfer operation is completed according to the preset handover principle which is actually formulated, and details are not repeated herein.
The preset handover principle generally includes that operators of two handover professional groups check the specimen for two persons, and simultaneously record information such as handover persons and handover time of the two persons. The first target professional group and the second target professional group are professional groups to which the pre-registered specimen information belongs, and can be determined according to an initial pre-registered dictionary; for example, the professional group to which the first piece of pre-registered specimen information belongs in the current project list is a biochemical group, and the professional group to which the second piece of pre-registered specimen information belongs is an immunological group.
When the pre-registered sample information is registered on the target instrument, the information required to be registered simultaneously comprises a professional group, a current instrument number, a current sample number, a current serial number, a check date and a registrant, so that the inquiry and the indication are facilitated.
Further, step 103 further includes:
and adding pre-registered specimen information which cannot be subjected to registration operation to a delayed pre-registration list through a professional group, and recording a delay reason and a delayed registration early warning time.
When a laboratory has signed a specimen, that is, a professional group has received the information of the allocated pre-registered specimen, and added the specimen to the pre-registered list, but the instrument matching registration cannot be performed according to the original plan due to instrument failure and the like, such a combination of specimens needs to be added to the deferred pre-registered list. Besides the record of the bar code and the combination related information of the specimen, the list also needs to record the name of the patient corresponding to the specimen to be detected, the department to which the patient belongs, the specimen sign-in time, the original registration early warning time, the reason delay and the registration delay early warning time, and finally needs to update the actual registration time and calculate the specific delay time. The deferred pre-registration list needs to be checked manually, which is not described in detail.
Further, step 103 further includes:
and if the pre-registered sample information is not registered on the target instrument within the registration early warning time, triggering an early warning mechanism.
And timing by adopting a server, and if the timing exceeds the registration early warning time of certain pre-registered sample information and the registration operation is not finished, judging that the sample combination registration operation is overtime. If the time is overtime, an early warning mechanism needs to be triggered, specifically, an overtime list needs to be established, the information of the overtime pre-registered sample is recorded, besides, the information of a sample bar code, the name of a patient, the name of the affiliated department, the sign-in time of the sample and the like needs to be recorded, finally, the actual registration time needs to be updated, the specific overtime duration is calculated, and relevant prompts are given. The timeout list needs to be checked manually, which is not described in detail.
Further, step 103, thereafter, further includes:
the pre-registered specimen information in which the registration operation is completed in the pre-registration list is deleted. The deleted information is information in a pre-registered list of professional groups; the registration can be deleted after the completion, so that the occupation of a memory is avoided, and the repeated registration can be avoided.
Further, step 103, thereafter, further includes:
and adopting a preset double-person auditing flow standard to audit all the inspection results which are inspected on the target instrument. The review process of the inspection result continues to be a double review process in a general medical laboratory, and can be specifically realized according to the prior art, which is not described herein again.
Further, step 103, thereafter, further includes:
and comparing and detecting the detection result according to the preset medical advice information and the item list, wherein the comparison detection is used for judging whether the medical advice detection item is finished and whether the examination of the detection result is finished.
And each sample combination can find the medical advice when the sample is signed according to the corresponding sample bar code, namely preset medical advice information which contains various items to be detected, if the detection result of the to-be-detected combination shows that the preset medical advice information contains all the items to be detected, and the examination operation is executed aiming at the examination result, the detection task and the examination task of the sample are completed.
According to the medical laboratory sample detection bar code registration method provided by the embodiment of the application, each target test sample is split, the corresponding item list is constructed, then the pre-registered sample information in the item list is subjected to sample distribution according to the sample professional group, sample sorting guidance can be effectively provided, and the problem caused by instrument registration directly according to the sample bar code is solved; finally, the internally received information of the pre-registered specimen is registered on a target instrument for inspection through a professional group, the registration early warning time can provide intelligent TAT (timing sequence entry) control, and an integral registration mechanism can ensure that a preset detection combination achieves closed-loop management. Automatic and intelligent sample sorting and registration are carried out according to the relation characteristics between different target test samples and professional groups, and the dependence on manual management is reduced; and the whole circulation process is recorded through a list, so that the traceability is strong. Therefore, the embodiment of the application can solve the technical problems that the existing sample detection bar code registration method cannot avoid sample omission, is highly dependent on manpower, causes low working efficiency and is easy to cause doctor-patient disputes.
The above is an embodiment of a medical laboratory sample detection barcode registration method provided by the present application, and the following is an embodiment of a medical laboratory sample detection barcode registration apparatus provided by the present application.
To facilitate understanding, referring to fig. 2, the present application provides an embodiment of a medical laboratory specimen detection barcode registration apparatus, comprising:
the specimen conversion module 201 is used for converting a preset detection combination obtained after the target inspection specimen is split into pre-registered specimen information according to the pre-registered dictionary, and constructing a project list according to the pre-registered specimen information, wherein the project list comprises specimen bar codes, specimen professional groups and registration early warning time;
the specimen distribution module 202 is used for distributing the pre-registered specimen information in the project list to a pre-registered list of a first target professional group according to a specimen bar code, a specimen professional group and a pre-registration rule, wherein the pre-registration rule comprises a preset time priority rule and a preset sample priority rule;
and the specimen registration module 203 is used for registering the pre-registered specimen information received in the pre-registration list on the target instrument through the professional group within the registration early warning time range.
Further, still include:
and the sample grouping conversion module 204 is configured to determine whether pre-registered sample information does not complete the registration operation in the project list, and if so, perform a professional grouping conversion operation according to a second target professional group determined by the project list based on a preset handover principle.
Further, still include:
and a deferred registration module 205, configured to add pre-registration specimen information that cannot be registered to the deferred pre-registration list through a professional group, and record a reason for deferral and a deferred registration early warning time.
In the several embodiments provided in the present application, it should be understood that the disclosed apparatus and method may be implemented in other ways. For example, the above-described apparatus embodiments are merely illustrative, and for example, the division of the units is only one logical division, and other divisions may be realized in practice, for example, a plurality of units or components may be combined or integrated into another system, or some features may be omitted, or not executed. In addition, the shown or discussed mutual coupling or direct coupling or communication connection may be an indirect coupling or communication connection through some interfaces, devices or units, and may be in an electrical, mechanical or other form.
The units described as separate parts may or may not be physically separate, and parts displayed as units may or may not be physical units, may be located in one place, or may be distributed on a plurality of network units. Some or all of the units can be selected according to actual needs to achieve the purpose of the solution of the embodiment.
In addition, functional units in the embodiments of the present application may be integrated into one processing unit, or each unit may exist alone physically, or two or more units are integrated into one unit. The integrated unit can be realized in a form of hardware, and can also be realized in a form of a software functional unit.
The integrated unit, if implemented in the form of a software functional unit and sold or used as a stand-alone product, may be stored in a computer readable storage medium. Based on such understanding, the technical solution of the present application may be substantially implemented or contributed to by the prior art, or all or part of the technical solution may be embodied in a software product, which is stored in a storage medium and includes instructions for executing all or part of the steps of the method described in the embodiments of the present application through a computer device (which may be a personal computer, a server, or a network device). And the aforementioned storage medium includes: a U disk, a removable hard disk, a Read-Only Memory (ROM), a Random Access Memory (RAM), a magnetic disk or an optical disk, and other various media capable of storing program codes.
The above embodiments are only used for illustrating the technical solutions of the present application, and not for limiting the same; although the present application has been described in detail with reference to the foregoing embodiments, it should be understood by those of ordinary skill in the art that: the technical solutions described in the foregoing embodiments may still be modified, or some technical features may be equivalently replaced; and such modifications or substitutions do not depart from the spirit and scope of the corresponding technical solutions in the embodiments of the present application.
Claims (10)
1. A medical laboratory specimen detection bar code registration method is characterized by comprising the following steps:
converting a preset detection combination obtained after splitting a target test specimen into pre-registered specimen information according to a pre-registered dictionary, and constructing a project list according to the pre-registered specimen information, wherein the project list comprises specimen bar codes, specimen professional groups and registration early warning time;
distributing the pre-registered sample information in the project list to a pre-registered list of a first target professional group according to the sample bar code, the sample professional group and a pre-registered rule, wherein the pre-registered rule comprises a preset time priority rule and a preset sample priority rule;
registering the pre-registered specimen information received in the pre-registration list on a target instrument by a professional group within the registration pre-warning time range.
2. The medical laboratory specimen detection barcode registration method according to claim 1, wherein the registering the pre-registered specimen information received in the pre-registration list on a target instrument by a professional group within the registration pre-warning time range further comprises:
and judging whether the pre-registered specimen information does not complete the registration operation in the project list, if so, performing professional group-to-group operation according to a second target professional group determined by the project list based on a preset handover principle.
3. The medical laboratory specimen detection barcode registration method according to claim 1, wherein the registering the pre-registered specimen information received in the pre-registration list on a target instrument by a professional group within the registration warning time range further comprises:
adding the pre-registered specimen information which cannot be registered to a delayed pre-registration list through the professional group, and recording a delay reason and a delay registration early warning time.
4. The medical laboratory specimen detection barcode registration method according to claim 1, wherein the registering the pre-registered specimen information received in the pre-registration list on a target instrument by a professional group within the registration warning time range further comprises:
and if the pre-registered specimen information is not registered on the target instrument within the registration early warning time, triggering an early warning mechanism.
5. The medical laboratory specimen detection barcode registration method according to claim 1, wherein the registering the pre-registered specimen information received in the pre-registration list on a target instrument by a professional group within the registration pre-warning time range further comprises:
deleting the pre-registered specimen information of which the registration operation is completed in the pre-registered list.
6. The medical laboratory specimen detection barcode registration method according to claim 1, wherein the registering the pre-registered specimen information received in the pre-registration list on a target instrument by a professional group within the registration pre-warning time range further comprises:
and adopting a preset double-person auditing flow standard to audit all the inspection results which are inspected on the target instrument.
7. The medical laboratory specimen detection barcode registration method according to claim 6, wherein the registering the pre-registered specimen information received in the pre-registration list on a target instrument by a professional group within the registration pre-warning time range further comprises:
and comparing and detecting the detection result according to preset medical advice information and the item list, wherein the comparison and detection are used for judging whether the medical advice detection items are finished and whether the examination of the detection result is finished.
8. A medical laboratory specimen detection barcode registration device, characterized by comprising:
the specimen conversion module is used for converting a preset detection combination obtained after the target inspection specimen is split into pre-registered specimen information according to a pre-registered dictionary, and constructing a project list according to the pre-registered specimen information, wherein the project list comprises specimen bar codes, specimen professional groups and registration early warning time;
the specimen distribution module is used for distributing the pre-registered specimen information in the project list to a pre-registered list of a first target professional group according to the specimen bar code, the specimen professional group and a pre-registered rule, wherein the pre-registered rule comprises a preset time priority rule and a preset sample priority rule;
and the specimen registration module is used for registering the pre-registered specimen information received in the pre-registration list on a target instrument through a professional group within the registration early warning time range.
9. The medical laboratory specimen detection barcode registration device according to claim 8, further comprising:
and the sample grouping conversion module is used for judging whether the pre-registered sample information does not complete the registration operation in the project list, and if so, performing professional grouping conversion operation according to a second target professional group determined by the project list based on a preset handover principle.
10. The medical laboratory specimen detection barcode registration device according to claim 8, further comprising:
and the delayed registration module is used for adding the pre-registered specimen information which cannot be subjected to registration operation to a delayed pre-registration list through the professional group, and recording a delay reason and a delayed registration early warning time.
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