CN106529202A - Intelligent auditing system and method for medical specimen testing - Google Patents

Intelligent auditing system and method for medical specimen testing Download PDF

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Publication number
CN106529202A
CN106529202A CN201611184059.6A CN201611184059A CN106529202A CN 106529202 A CN106529202 A CN 106529202A CN 201611184059 A CN201611184059 A CN 201611184059A CN 106529202 A CN106529202 A CN 106529202A
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specimen
module
detection
data
information
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陶然
李娜
胡朝晖
王家健
莫南勋
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Shenzhen Jinyu Medical Laboratory Ltd
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Shenzhen Jinyu Medical Laboratory Ltd
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Priority to CN201611184059.6A priority Critical patent/CN106529202A/en
Publication of CN106529202A publication Critical patent/CN106529202A/en
Priority to CN201710375173.5A priority patent/CN107133482A/en
Priority to CN201710374886.XA priority patent/CN107229827A/en
Priority to CN201710374783.3A priority patent/CN107301315B/en
Priority to CN201710376471.6A priority patent/CN107358018B/en
Priority to CN201710375626.4A priority patent/CN107341337A/en
Withdrawn legal-status Critical Current

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    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16HHEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H50/00ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics
    • G16H50/30ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for calculating health indices; for individual health risk assessment
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16HHEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H10/00ICT specially adapted for the handling or processing of patient-related medical or healthcare data
    • G16H10/60ICT specially adapted for the handling or processing of patient-related medical or healthcare data for patient-specific data, e.g. for electronic patient records
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16HHEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H50/00ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics
    • G16H50/20ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for computer-aided diagnosis, e.g. based on medical expert systems

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  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Medical Informatics (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Biomedical Technology (AREA)
  • Primary Health Care (AREA)
  • General Health & Medical Sciences (AREA)
  • Databases & Information Systems (AREA)
  • Pathology (AREA)
  • Data Mining & Analysis (AREA)
  • Medical Treatment And Welfare Office Work (AREA)
  • Measuring And Recording Apparatus For Diagnosis (AREA)
  • Management, Administration, Business Operations System, And Electronic Commerce (AREA)
  • Analysing Materials By The Use Of Radiation (AREA)
  • Investigating Or Analysing Biological Materials (AREA)

Abstract

The invention discloses an intelligent auditing system for medical specimen testing, and relates to the technical field of medical testing. The intelligent auditing system comprises an abnormity prompt module, an information receiving module, a specimen receiving module, a data auditing module and a result auditing module; the specimen receiving module is used for recording to-be-tested specimen information of a specimen corresponding to a patient, extracting a standard specimen type corresponding to a testing item recorded in the information receiving module and comparing the standard specimen type with a to-be-tested specimen type; a haemolytic index threshold value, a lipemia index threshold value and an icterus index threshold value are stored in the data auditing module, and the data auditing module is used for receiving testing data of the specimen and comparing a haemolytic index, a lipemia index and an icterus index in the testing data with the threshold values; the result auditing module inputs the testing data to a data analysis model corresponding to the testing item and comparing a testing result of the specimen with a model analysis result. The invention further discloses an intelligent auditing method for medical specimen testing. The intelligent auditing system and method are beneficial for improving the efficiency of medical testing and increasing the intelligent degree of medical testing.

Description

A kind of intelligent checks System and method for for medical specimen detection
Technical field
The present invention relates to the technical field of medical treatment detection, and in particular to a kind of intelligent checks system for medical specimen detection System and method.
Background technology
China is the first big country of world population, although having received the factors such as conventional family planning policy affects the natural growth of the population Rate has been in downward trend year by year, but total number of people persistently rises, and the medical number of medical institutions accordingly increases;Cut-off year in 2014 Bottom, the aged of China's over-65s become the most country of the aged in the world more than 1.3 hundred million.In addition, life water It is flat lifted cause chronic disease increase, medical treatment consciousness increase caused by self health check-up frequency rise, be based on more than, between 2005-2014, The average compound growth rate of medical institutions of China quantity is 1.19%;Medical institutions' bedspace annual average compound growth rate is 7.77%, Clinical laboratory of medical institutions detection pressure is caused persistently to increase substantially.
The Central Committee of the Communist Party of China, State Council announce within 2009《With regard to deepening the suggestion of Health system reform》Open new one The tide of wheel medical reform, refer to public hospital's scale domination in method, encourage Private Capital to arrange medical institutions.Private mechanism will Substantial amounts of primary care is served, the sustainable growth of detection pressure is caused.
Nowadays, with the increase of inspection project, the increase of specimen amount, sample turnaround time will be prolonged according to original flow process It is long, but the clinical demand and laws and regulations requirement of the above requires that laboratory shortens the sample turnaround time as far as possible, how without any confusion Sample is classified, rationally effectively optimization experiment room testing process, the reasonable convenience of laboratory information system design into In order to shorten the key link of sample turnaround time.The classification of the project of independent laboratory development at present is mainly divided:Physics and chemistry mass spectrum is examined Test, genome inspection, pathological diagnosis, biochemical luminous inspection, immunological test, other comprehensive tests etc., because detection project it is many, plus Beginning a project, it is fast to weed out the old and bring forth the new, and the requirement to testing result auditor is also constantly lifted.
Exceptional sample, except sample is disturbed, such as lipidemia, haemolysis also need the project that artificial judgment screens, this portion including result The confirmation of point result needs to carry out artificial treatment, such as centrifugation survey again, push jack microscopy or contact it is clinical.This part sample expends a large amount of Time significantly can postpone other report send the time;Simultaneously under the pressure of sample turnaround time, lab assistant can Can neglect or the due handling process of simplification, cause the risk of result to be significantly increased.Nowadays, almost all of laboratory report List is accused by manually signing and issuing, it is about more than 1000 that one sign and issue report personnel to be signed and issued reporting quantities a working day, and And the most of limitation of these work is at night to morning (21:00-04:00) carry out, the time period prolonged computation is examined Nuclear Data, is easy to cause the dual fatigue of vision and body and mind, causes the generation of mistake;Meanwhile, if the result of report is related to learn Comparison and analysis between section, in addition it is also necessary to substantial amounts of manual historical record inquiry, the work of whole data analysiss will continue 6 hours with On.
The content of the invention
For the deficiencies in the prior art, the purpose of the present invention aims to provide a kind of intelligent checks for medical specimen detection System and method for, the detection to specimen are audited and are monitored, and point out abnormal conditions in time, are conducive to improving the effect of medical treatment detection Rate and intelligence degree.
For achieving the above object, the present invention is adopted the following technical scheme that:
A kind of intelligent checks system for medical specimen detection, includes:
Abnormal prompt module, for the abnormal conditions for pointing out to occur in detection process;
Contrasting data module, standard specimen types and the standard essential information being stored with corresponding to each detection project, deposits The reference information corresponding to each detection project is contained, the reference information is the conjunction corresponding to each index in each detection project Reason domain of walker or threshold values, be also stored with contrasting data module positive rate zone of reasonableness;
Information receiving module, for typing patient basis and detection project;
Specimen receiver module, corresponds to the specimen information to be measured of the specimen of patient, the specimen information bag to be measured for typing Specimen types to be measured are included, is additionally operable to receive the patient basis from information receiving module, the specimen receiver module is according to record The detection project for entering extracts corresponding standard essential information from contrasting data module, and by the specimen essential information and patient Essential information is compared item by item, when patient basis are not inconsistent with standard essential information, sends base to abnormal prompt module The prompting of this Information abnormity;The specimen receiver module extracts standard mark from contrasting data module according to the detection project of typing This type, standard specimen types are compared with specimen types to be measured, when specimen types to be measured are not inconsistent with standard specimen types, The abnormal prompting of specimen matching is sent to abnormal prompt module;
Data-auditing module, for receiving the detection data of specimen, the detection data is included corresponding to each of detection project Individual Indexs measure data, extract the reference information corresponding to detection project from contrasting data module, and by detection data with Reference information is compared, when the arbitrary Indexs measure data in detection data are not inconsistent with corresponding reasonable domain of walker or threshold values When, the prompting of Samples detection data exception is sent and by abnormal Indexs measure data is activation to exception to abnormal prompt module Reminding module;
As a result release module, for counting the positive rate of same day Samples detection, extracts the positive from contrasting data module Rate zone of reasonableness, the positive rate of same day Samples detection that statistics draws is compared with positive rate zone of reasonableness, when counting The positive rate of the same day Samples detection for going out not in positive rate zone of reasonableness when, send positive rate to abnormal prompt module abnormal Prompting.
Further, the standard essential information in contrasting data module includes sex and age, records in information receiving module The patient basis for entering include sex, age and allergies.
Further, the patient basis in information receiving module include the sampling time of sample to be tested, and specimen is received Specimen information to be measured in module includes the detection time of specimen to be measured, when specimen receiver module calculates the detection of specimen to be measured Between interval duration between the sampling time, when interval duration threshold value of the interval duration more than setting, specimen receiver module The abnormal prompting of detection time is sent to abnormal prompt module.
Further, also including audit log module, it is provided with according to date and time sequencing in the audit log module The audit log of arrangement, the audit log in units of patient, and correspondence is refreshed according to the newest detection date and time of patient The abnormal conditions occurred in detection process are uploaded to by sequence of the audit log in audit log module, the abnormal prompt module In the audit log of respective patient.
Further, in contrasting data module, reference information includes that hemolytic index threshold value, lipidemia index threshold and jaundice refer to Number threshold value.
A kind of intelligent checks method for medical specimen detection, includes following steps:
S1, in information receiving module typing patient basis and detection project;
S2, in specimen receiver module typing corresponding to patient specimen specimen information to be measured, the specimen information to be measured Including specimen types to be measured and specimen sampling time to be measured, the specimen receiver module receives the patient's base from information receiving module This information, and corresponding standard essential information is extracted from contrasting data module according to the detection project of typing, by the specimen Essential information is compared item by item with patient basis, when patient basis are not inconsistent with standard essential information, to exception Reminding module sends the abnormal prompting of essential information;The specimen receiver module is according to the detection project of typing from contrasting data module In extract standard specimen types, and the standard specimen types are compared with specimen types to be measured, treat mark when new typing When this type and the standard specimen types corresponding to the detection project of typing are not inconsistent, specimen matching is sent to abnormal prompt module different Normal prompting;
S3, data-auditing module receive specimen detection data, the detection data include corresponding to detection project each Indexs measure data, data-auditing module extract the reference information corresponding to detection project from contrasting data module, and will Detection data is compared with reference information, when the arbitrary Indexs measure data in detection data and corresponding reasonable domain of walker Or threshold values is not when being inconsistent, the prompting of Samples detection data exception is sent and by abnormal Indexs measure data to abnormal prompt module It is sent to abnormal prompt module;
S4, result release module count the positive rate of same day Samples detection, from contrasting data module extract positive rate Zone of reasonableness, the positive rate of the same day Samples detection that statistics is drawn are compared with positive rate zone of reasonableness, when statistics draws Same day Samples detection positive rate not in positive rate zone of reasonableness when, send to abnormal prompt module that positive rate is abnormal to be carried Show.
Further, in step S1, the patient basis of typing include sex, age and allergies;In step S2, should Standard essential information in contrasting data module includes sex and age.
Further, in step S1, the patient basis in information receiving module include the sampling time of sample to be tested; In step S2, the specimen information to be measured in specimen receiver module includes the detection time of specimen to be measured, and specimen receiver module is calculated The interval duration gone out between the detection time of specimen and specimen sampling time to be measured, when interval of the interval duration more than setting During long threshold value, specimen receiver module sends the abnormal prompting of detection time to abnormal prompt module.
Further, in step S3, reference information includes hemolytic index threshold value, lipidemia index threshold and icteric index threshold Value.
Further, also including step S5:
The abnormal conditions occurred in detection process are uploaded to the audit log of respective patient for S5, the abnormal prompt module In, it is provided with the audit log module according to date and time tactic audit log, the audit log with patient is Unit simultaneously refreshes correspondence sequence of the audit log in audit log module according to the newest detection date and time of patient.
The beneficial effects of the present invention is:Realize to Samples detection from receiving sample to drawing the whole detection stream of testing result The examination & verification and monitoring of journey, realizes the intellectuality examination & verification to Samples detection, substitutes traditional manual examination and verification, unified auditing standards, Avoid the auditing standards for varying with each individual or the mental status it is not good cause audit mistakes and omissions, improve review efficiency;Greatly reduce careful The cost of labor of core flow process;Automatically long specimen matching error, blood samples storage time, specimen data exception, detection number are investigated out According to abnormal conditions such as abnormal, detection perforated scrofula of neck, and abnormal prompt is carried out by abnormal prompt module, improve the pass to detecting abnormal conditions Note degree, is conducive to improving the quality of Samples detection.
Description of the drawings
Fig. 1 is a kind of structured flowchart of the intelligent checks system for medical specimen detection in the present invention.
Specific embodiment
Below, with reference to accompanying drawing and specific embodiment, the present invention is described further:
Embodiment 1
As shown in figure 1, a kind of intelligent checks system for medical specimen detection, includes:
Abnormal prompt module, the abnormal conditions to occurring in detection process are pointed out;
Contrasting data module, standard specimen types and the standard essential information being stored with corresponding to each detection project, mark Quasi- essential information includes the relevant informations such as sex, age, pregnant day;The reference information being stored with corresponding to each detection project, should Reference information is reasonable domain of walker or the threshold values corresponding to each index in each detection project, and the reference information includes haemolysis Index threshold, lipidemia index threshold and icteric index threshold value, be also stored with contrasting data module positive rate zone of reasonableness;
Information receiving module, for typing patient basis and detection project, patient basis include sex, age With the comparable data such as allergies, also including the sampling time of sample to be tested;
Specimen receiver module, for typing is corresponding to the specimen information to be measured of the specimen of patient and sends to data examination & verification Module, the specimen information to be measured include the detection time of specimen types to be measured and specimen to be measured, are additionally operable to reception and carry out self-information connect The patient basis for receiving module, it is right that the specimen receiver module is extracted from contrasting data module according to the detection project of typing The standard essential information answered, and the specimen essential information is compared with patient basis, when patient basis and mark When quasi- essential information is not inconsistent, the abnormal prompting of essential information is sent to abnormal prompt module;The specimen receiver module is according to typing Detection project extract standard specimen types from contrasting data module, by standard specimen types compared with specimen types to be measured Compared with when specimen types to be measured are not inconsistent with standard specimen types, to the prompting that the transmission specimen matching of abnormal prompt module is abnormal;Mark This receiver module also calculates the detection time of specimen to be measured and the interval duration between the sampling time, when the interval duration is more than During the interval duration threshold value of setting, specimen receiver module sends the abnormal prompting of detection time to abnormal prompt module;
Data-auditing module, for receiving the detection data of specimen, the detection data is included corresponding to each of detection project Individual Indexs measure data;Data-auditing module is linked with the data monitoring storehouse of detecting instrument equipment, receives the detection of specimen After data, data-auditing module searches for the quality detecting data of coherent detection instrument from the data monitoring storehouse of detecting instrument equipment, when Coherent detection instrument is searched in effective quality inspection time memory during renewal and the quality detecting data up to standard in quality detecting data, this intelligence Energy auditing system proceeds data examination & verification, when coherent detection instrument does not have the renewal of quality detecting data within effective quality inspection time Or quality detecting data it is not up to standard when, this intelligent checks system will terminate examination & verification to Samples detection data, effective quality inspection time setting It is one section of determination duration before the Samples detection time;By the detection project phase of detection data and typing in information receiving module Relatively, when the situation for finding to there is perforated scrofula of neck, the prompting of detection perforated scrofula of neck is sent to abnormal prompt module;Data-auditing module is from control The reference information corresponding to detection project is extracted in data module, and detection data is compared with reference information, work as inspection When the arbitrary Indexs measure data surveyed in data are not inconsistent with corresponding reasonable domain of walker or threshold values, send to abnormal prompt module The prompting of Samples detection data exception and by abnormal Indexs measure data is activation to abnormal prompt module;
As a result release module, provide automatically the detection project reported for arranging, when the detection for being set to automatic granting Mesh after corresponding all examination & verifications can onset detection and audit report automatically, as a result release module also count Announcement rate and theoretical automatic granting reporting rate, provide automatically reporting rate and reflect in the detection project that granting is reported automatically is set to Automatically the ratio of report is provided, theoretical reporting rate of providing automatically reflects the reason that can provide automatically report in all detection projects By maximum ratio;It is additionally operable to count the positive rate of same day Samples detection, extracts the reasonable model of positive rate from contrasting data module Enclose, the positive rate of the same day Samples detection that statistics is drawn is compared with positive rate zone of reasonableness, when the same day that statistics draws The positive rate of Samples detection not in positive rate zone of reasonableness when, send the abnormal prompting of positive rate to abnormal prompt module;When Same day specimen amount is counted to positive rate using Poisson distribution when reaching setting value, is made when same day specimen amount is less than setting value Positive rate is counted with binomial distribution;
Audit log module, is provided with the audit log module according to date and time tactic audit log, The audit log in units of patient, and correspondence audit log is refreshed in examination & verification day according to the newest detection date and time of patient The abnormal conditions occurred in detection process are uploaded to the examination & verification day of respective patient for sequence in will module, the abnormal prompt module In will.
This intelligent checks system is being carried out by data auditing system to be linked in the data monitoring storehouse of detecting instrument equipment Before the examination & verification of Samples detection data, judge whether the detecting instrument of correlation passes through quality inspection within effective quality inspection time;If related Detecting instrument within effective quality inspection time by quality inspection, then the detection data of specimen is measured on the instrument of normal operation, number According to effective, follow-up data examination & verification can be carried out;If the detecting instrument of correlation do not carry out within effective quality inspection time quality inspection or Not over quality inspection, then the detection data of specimen will be not trusted, data invalid, terminate data examination & verification.So as to substantially increase The reliability of testing result.
Embodiment 2
A kind of intelligent checks method for medical specimen detection, includes following steps:
S1, in information receiving module typing patient basis and detection project, patient basis include sex, year The comparable data such as age and allergic medicine history, also including the sampling time of specimen to be measured;
S2, in specimen receiver module typing corresponding to patient specimen specimen information to be measured, the specimen information to be measured Including the detection time of specimen types to be measured and specimen to be measured, specimen receiver module receives the patient's base from information receiving module This information, and corresponding standard essential information is extracted from contrasting data module according to the detection project of typing, by the specimen Essential information is compared with patient basis, and standard essential information includes the relevant informations such as sex, age, pregnant day, works as trouble When person's essential information is not inconsistent with standard essential information, the abnormal prompting of essential information is sent to abnormal prompt module;The specimen connects Receive module and standard specimen types are extracted from contrasting data module according to the detection project of typing, and by the standard specimen types Compared with specimen types to be measured, the standard specimen class of the specimen types to be measured when new typing and the detection project corresponding to typing When type is not inconsistent, the abnormal prompting of specimen matching is sent to abnormal prompt module;Specimen receiver module also calculates specimen to be measured Interval duration between detection time and sampling time, when interval duration threshold value of the interval duration more than setting, specimen connects Receive module the abnormal prompting of detection time is sent to abnormal prompt module;
S3, data-auditing module receive specimen detection data, the detection data include corresponding to detection project each Between Indexs measure data, detection data is compared with the detection project of typing in information receiving module, when discovery has perforated scrofula of neck Situation, to abnormal prompt module send detection perforated scrofula of neck prompting;It is right that data-auditing module is extracted from contrasting data module In the reference information of detection project, and detection data should be compared with reference information, when the arbitrary index in detection data When detection data is not inconsistent with corresponding reasonable domain of walker or threshold values, Samples detection data exception is sent to abnormal prompt module Prompting, and by abnormal Indexs measure data is activation to abnormal prompt module;
S4, result release module count the positive rate of same day Samples detection, from contrasting data module extract positive rate Zone of reasonableness, the positive rate of the same day Samples detection that statistics is drawn are compared with positive rate zone of reasonableness, when statistics draws Same day Samples detection positive rate not in positive rate zone of reasonableness when, send to abnormal prompt module that positive rate is abnormal to be carried Show.
The abnormal conditions occurred in detection process are uploaded to the audit log of respective patient for S5, the abnormal prompt module In, it is provided with the audit log module according to date and time tactic audit log, the audit log with patient is Unit simultaneously refreshes correspondence sequence of the audit log in audit log module according to the newest detection date and time of patient.
It will be apparent to those skilled in the art that technical scheme that can be as described above and design, make other various It is corresponding to change and deformation, and all these change and deformation should all belong to the protection domain of the claims in the present invention Within.

Claims (10)

1. it is a kind of for medical specimen detection intelligent checks system, it is characterised in that include:
Abnormal prompt module, for the abnormal conditions for pointing out to occur in detection process;
Contrasting data module, standard specimen types and the standard essential information being stored with corresponding to each detection project, is stored with Corresponding to the reference information of each detection project, the reference information be corresponding in each detection project each index it is reasonable Domain of walker or threshold values, be also stored with contrasting data module positive rate zone of reasonableness;
Information receiving module, for typing patient basis and detection project;
Specimen receiver module, corresponds to the specimen information to be measured of the specimen of patient for typing, and the specimen information to be measured includes Specimen types to be measured, are additionally operable to receive the patient basis from information receiving module, and the specimen receiver module is according to record The detection project for entering extracts corresponding standard essential information from contrasting data module, and by the specimen essential information and patient Essential information is compared, and when patient basis are not inconsistent with standard essential information, sends basic letter to abnormal prompt module The abnormal prompting of breath;The specimen receiver module extracts standard specimen from contrasting data module according to the detection project of typing Type, standard specimen types are compared with specimen types to be measured, when specimen types to be measured are not inconsistent with standard specimen types, to Abnormal prompt module sends the abnormal prompting of specimen matching;
Data-auditing module, for receiving the detection data of specimen, the detection data include corresponding to detection project each Indexs measure data, extract the reference information corresponding to detection project from contrasting data module, and by detection data and ginseng The information of examining is compared, when the arbitrary Indexs measure data in detection data are not inconsistent with corresponding reasonable domain of walker or threshold values When, the prompting of Samples detection data exception is sent and by abnormal Indexs measure data is activation to exception to abnormal prompt module Reminding module;
As a result release module, for counting the positive rate of same day Samples detection, extracts positive rate conjunction from contrasting data module Reason scope, the positive rate of same day Samples detection that statistics draws is compared with positive rate zone of reasonableness, when counting what is drawn The positive rate of same day Samples detection not in positive rate zone of reasonableness when, send to abnormal prompt module that positive rate is abnormal to be carried Show.
2. it is as claimed in claim 1 to be used for the intelligent checks system that medical specimen is detected, it is characterised in that the contrasting data Standard essential information in module includes sex and age, in information receiving module the patient basis of typing include sex, Age and allergies.
3. it is as claimed in claim 1 to be used for the intelligent checks system that medical specimen is detected, it is characterised in that described information is received Patient basis in module include the sampling time of sample to be tested, the specimen information bag to be measured in the specimen receiver module The detection time of specimen to be measured is included, the specimen receiver module calculates the detection time of specimen to be measured and between the sampling time Interval duration, when interval duration threshold value of the interval duration more than setting, specimen receiver module is sent to abnormal prompt module The abnormal prompting of detection time.
4. it is as claimed in claim 1 to be used for the intelligent checks system that medical specimen is detected, it is characterised in that also including examination & verification day Will module, is provided with the audit log module according to date and time tactic audit log, the audit log In units of patient, and correspondence audit log is refreshed in audit log module according to the newest detection date and time of patient Sequence, the abnormal prompt module are uploaded to the abnormal conditions occurred in detection process in the audit log of respective patient.
5. it is as claimed in claim 1 to be used for the intelligent checks system that medical specimen is detected, it is characterised in that the contrasting data In module, the reference information includes hemolytic index threshold value, lipidemia index threshold and icteric index threshold value.
6. it is a kind of for medical specimen detection intelligent checks method, it is characterised in that include following steps:
S1, in information receiving module typing patient basis and detection project;
S2, in specimen receiver module typing corresponding to patient specimen specimen information to be measured, the specimen information bag to be measured Specimen types to be measured and specimen sampling time to be measured is included, the specimen receiver module receives the patient's base from information receiving module This information, and corresponding standard essential information is extracted from contrasting data module according to the detection project of typing, by the specimen Essential information is compared item by item with patient basis, when patient basis are not inconsistent with standard essential information, to exception Reminding module sends the abnormal prompting of essential information;The specimen receiver module is according to the detection project of typing from contrasting data mould Standard specimen types are extracted in block, and the standard specimen types are compared with specimen types to be measured, when treating for new typing When survey specimen types and the standard specimen types corresponding to the detection project of typing are not inconsistent, specimen is sent to abnormal prompt module With abnormal prompting;
S3, data-auditing module receive the detection data of specimen, and the detection data includes referring to corresponding to each of detection project Mark detection data, data-auditing module extract the reference information corresponding to detection project from contrasting data module, and will inspection Survey data to compare with reference information, when the arbitrary Indexs measure data in detection data and corresponding reasonable domain of walker or When threshold values is not inconsistent, the prompting of Samples detection data exception the Indexs measure data by exception is sent to abnormal prompt module It is sent to abnormal prompt module;
S4, result release module count the positive rate of same day Samples detection, extract positive rate reasonable from contrasting data module Scope, the positive rate of the same day Samples detection that statistics is drawn are compared with positive rate zone of reasonableness, when working as that statistics draws The positive rate of day Samples detection not in positive rate zone of reasonableness when, send the abnormal prompting of positive rate to abnormal prompt module.
7. it is as claimed in claim 6 to be used for the intelligent checks method that medical specimen is detected, it is characterised in that step S1 In, the patient basis of typing include sex, age and allergies;In step S2, in the contrasting data module Standard essential information includes sex and age.
8. it is as claimed in claim 6 to be used for the intelligent checks method that medical specimen is detected, it is characterised in that step S1 In, the patient basis in information receiving module include the sampling time of sample to be tested;In step S2, the specimen receives mould Specimen information to be measured in block includes the detection time of specimen to be measured, and the specimen receiver module calculates the detection time of specimen With the interval duration between the specimen sampling time to be measured, when interval duration threshold value of the interval duration more than setting, specimen connects Receive module the abnormal prompting of detection time is sent to abnormal prompt module.
9. as described in claim 6 or 8 for medical specimen detection intelligent checks method, it is characterised in that the step In S3, the reference information includes hemolytic index threshold value, lipidemia index threshold and icteric index threshold value.
10. as described in claim 6 or 8 for medical specimen detection intelligent checks method, it is characterised in that also including step Rapid S5:
S5, the abnormal prompt module are uploaded to the abnormal conditions occurred in detection process in the audit log of respective patient, It is provided with the audit log module according to date and time tactic audit log, the audit log with patient is Unit simultaneously refreshes correspondence sequence of the audit log in audit log module according to the newest detection date and time of patient.
CN201611184059.6A 2016-12-20 2016-12-20 Intelligent auditing system and method for medical specimen testing Withdrawn CN106529202A (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
CN201611184059.6A CN106529202A (en) 2016-12-20 2016-12-20 Intelligent auditing system and method for medical specimen testing
CN201710375173.5A CN107133482A (en) 2016-12-20 2017-05-24 The data early warning method and device analyzed for inspection specimen
CN201710374886.XA CN107229827A (en) 2016-12-20 2017-05-24 Data checking early warning method and device for autoimmune disease detection and analysis
CN201710374783.3A CN107301315B (en) 2016-12-20 2017-05-24 Intelligent checks method and device for medical specimen detection
CN201710376471.6A CN107358018B (en) 2016-12-20 2017-05-24 Early warning method and device for prenatal and postnatal care examination project
CN201710375626.4A CN107341337A (en) 2016-12-20 2017-05-24 Project checking early warning method and device

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Application Number Priority Date Filing Date Title
CN201611184059.6A CN106529202A (en) 2016-12-20 2016-12-20 Intelligent auditing system and method for medical specimen testing

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CN106529202A true CN106529202A (en) 2017-03-22

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