CN108269618A - Genetic test status tracking management system and method based on wechat small routine - Google Patents
Genetic test status tracking management system and method based on wechat small routine Download PDFInfo
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- CN108269618A CN108269618A CN201810074354.9A CN201810074354A CN108269618A CN 108269618 A CN108269618 A CN 108269618A CN 201810074354 A CN201810074354 A CN 201810074354A CN 108269618 A CN108269618 A CN 108269618A
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Abstract
The invention discloses the genetic test status trackings based on wechat small routine to manage system, and backstage includes database module；Operable interface includes the document management module being connect with database module and the detection being connect with document management module request submits module, detection request to check module and individual center module.The present invention internet+thinking be introduced into traditional genetic test service center, user can momentarily be used using mobile phone by wechat, with more efficient reasonable manner unicom patient, doctor and genetic test mechanism, it allows patient and doctor can understand the latest developments of detection in time, and examining report is checked anywhere or anytime, solves existing patient, the problem of inefficient and easy error in cooperation of doctor and third party's genetic test mechanism, greatly facilitate patient and doctor, simultaneously also communication burden is alleviated to third party's genetic test mechanism, improve efficiency, the each side for the whole flow process that lets on all has enjoyed the facility that the system is brought.
Description
Technical field
The invention belongs to technical field of gene detection, and in particular to it is a kind of based on the genetic test state of wechat small routine with
Track manages system and method.
Background technology
Genetic disease refers to because of the inhereditary material exception in fertilized eggs or the hereditary information exception institute entrained by reproduction cell
The character of caused filial generation is abnormal, i.e., carries ospc gene in sperm and ovum, be then passed to children and cause disease, and this
Disease can be also transmitted to the next generation by a little female after getting married.Genetic test can diagnose the illness, and can be used for the pre- of disease risks
It surveys, medical diagnosis on disease is to cause the mutator of genetic disease with genetic test, and current most widely used genetic test is newborn
The auxiliary diagnosis of the inspection of youngster's genetic disease, the diagnosis of genetic disease and certain common diseases.
During existing medical diagnosis on disease, hospital generally requires the part idagnostic logout and cdna sample of patient to provide
Analyzing and diagnosing is carried out based on detection company to third-party, third party detects company and finally returns to a papery report to hospital,
Generally require to wait for several weeks the time of even one or two months from third company's cdna collection sample to delivery Final Report, at this
In the section time, patient and doctor can not know the progress of third party's genetic test company, and unique channel can only find doctor,
The doctor contact third party's genetic test company that finds time goes and finds out what's going on and returns result to patient.
Further, since third party's genetic test company needs to refer to the clinical symptoms letter of some patientss during diagnosis
Breath, these information can only allow doctor to issue permit papery or directly and third party's genetic test company given by way of piece, which imitates
Rate is low and easy error.
Furthermore since a genetic test needs the longer time period, doctors is waited to take gene so usually will appear
After examining report, at this moment situation that patient has left hospital generally requires doctor and actively contacts patient or patient irregularly to hospital
It seeks advice from its report on progress, inefficiency and is difficult to operate.In addition, patient may change the place of examination, even if it has taken genetic test
Papery is reported, needs to carry, it is impossible to be lost and be damaged.
For third party's genetic test company, it is also desirable to continuously distribute manpower and come from doctor to cope with
Raw various consultings detection progress phone, waste of manpower and easily malfunctions.As it can be seen that existing patient, doctor and third party's base
Because this collaboration mode of detection company is inefficient, easy error and is unfavorable for the diagnosis of genetic disease.
Invention content
For above-mentioned deficiency of the prior art, the genetic test status tracking provided by the invention based on wechat small routine
Management system and method, which solves doctor and patient in existing acquisition genetic test outcome procedure, can not obtain detection progress, doctor
The problem of submitting patient data's trouble, patient that can not obtain examining report waste and genetic test company manpower and materials in time.
In order to reach foregoing invention purpose, the technical solution adopted by the present invention is：Genetic test based on wechat small routine
Status tracking manages system, including operable interface and backstage；
The backstage is the database module of deployment beyond the clouds；
The operable interface include the document management module that is connect with database module and with the file management mould
The detection request of block connection submits module, detection request to check module and individual center module；
The individual center module includes user register unit, information modification unit, other people is authorized to check reporting unit, be
System message checks unit, suggestion feedback unit and patient's adding device.
Beneficial effects of the present invention are：The present invention based on wechat small routine genetic test status tracking management system and
Method, internet+thinking be introduced into traditional genetic test service center, the system background dispose beyond the clouds, user
It can momentarily be used by wechat using smart mobile phone, with more efficient reasonable manner unicom patient, doctor and third party's base
It because of testing agency, allows patient and doctor that can understand the latest developments of detection in time, and check examining report anywhere or anytime, solves
Determined inefficient and easy error in cooperation of existing patient, doctor and third party's genetic test mechanism the problem of, greatly
Patient and doctor are facilitated, while also alleviates communication burden to third party's genetic test mechanism, substantially improves existing procedure,
Efficiency is improved, each side for the whole flow process that lets on all has enjoyed the facility that the system is brought.
Further, the operable interface of wechat small routine further includes the science popularization classroom mould being connect with document management module
Block.
Above-mentioned further scheme has the beneficial effect that：Science popularization classroom module understands study genetic test and correlation convenient for user
The knowledge of genetic disease improves the safe and healthy consciousness of users.
Further, the database module is used to store all data informations in the system, and the data include using
Family register when fill in relevant information, detection request submit when fill in essential information, detection request check in progress msg,
Data information in the data information and science popularization classroom that are preserved in document management module；
The document management module passes through the module and checks for preserving for submitting the data submitted during detection request
The data submitted with modification；
The detection request submits module genetic test to be submitted to ask for user, by the module writes essential information simultaneously
Submit genetic test request；
The detection request checks that module checks the processing progress information of detection request for user, and passes through the module label
Send out examining report；
Science popularization classroom module is used to provide genetic disease popular science knowledge related to genetic test.
Above-mentioned further scheme has the beneficial effect that：Modules cooperate, provide to the user efficiently, easily gene
Detection service.
Further, the user register unit for new user's registration and fills in relevant information；
Described information modification unit for user according to the variations of actual conditions, related letter during time update user's registration
Breath；
It is described that other people is authorized to check that reporting unit authorizes the right for checking genetic test report to other people for patient；
The system message checks unit for genetic test progress message to be automatically transmitted to user；
The suggestion feedback unit is used to the query of user submitting to third party's genetic test company, and pass through system and disappear
Breath checks that unit checks corresponding reply situation；
Patient's adding device fills in the relevant information for needing the patient for carrying out genetic test for doctor.
Above-mentioned further scheme has the beneficial effect that：Individual center module is used to record the essential information of user, convenient for use
Information solicitation and modification of the family to genetic test object, it is ensured that user checked is the genetic test report oneself submitted.
Genetic test status tracking management method based on wechat small routine, includes the following steps：
S1, new user's registration is carried out in individual center module, fills in relevant information, obtain login account and login system；
S2, submission genetic test is asked, and fill in essential information in detection asks to submit module；
S3, check that module checks that progress msg is asked and its detected in submitted genetic test by detecting request；
S4, the query to examining report is proposed, and check in system by individual center mould information feedback unit in the block
Corresponding return information is checked in unit.
Further, new user registration course is specially in the step S1：The relevant information of user is filled in, including user
Identity selects and its contact method；
It can select to fill in individual center mould patient's adding device in the block in the new user registration course or authorize him
People checks information in reporting unit；
The user identity includes doctor and patient；
When the user is doctor, the related letter for the patient for needing to carry out genetic test is filled in patient's adding device
Breath；
When the user is patient, in mandate, other people check in reporting unit the relevant information for filling in licensee.
Further, the essential information in the step S2 include name, gender, the date of birth, illness history, family history,
Photo and documentation.
Above-mentioned further scheme has the beneficial effect that：User submits perfect personal essential information, more accurate convenient for obtaining
True examining report.
Further, progress msg is detected in the step S3 and includes sampling, gene sequencing, data analysis, generation detection
Report and doctor's audit are signed and issued.
Above-mentioned further scheme has the beneficial effect that：Understand genetic test progress in time convenient for user, carry out corresponding standard
Standby work.
Further, in the step S3, when user is doctor, to the inspection report of third party's genetic test company generation
Announcement check and audits and sign and issue；
When user be patient when, check doctor sign and issue after audit report.
Above-mentioned further scheme has the beneficial effect that：Doctor first checks examining report, is made according to report content and finally examined
Break after signing and issuing, checked for patient, examining report result is checked convenient for user.
Further, can heredity be checked by science popularization classroom module in any one step in the step S1~S4
Disease and genetic test knowledge.
Above-mentioned further scheme has the beneficial effect that：By science popularization classroom module patient can understand at any time genetic test and
The relevant knowledge of genetic disease improves its safe and healthy knowledge.
Description of the drawings
Fig. 1 is that the genetic test status tracking based on wechat small routine in the present embodiment manages system structure diagram.
Fig. 2 is the genetic test status tracking management method flow chart based on wechat small routine in the present embodiment.
Specific embodiment
The specific embodiment of the present invention is described below, in order to facilitate understanding by those skilled in the art this hair
It is bright, it should be apparent that the present invention is not limited to the range of specific embodiment, for those skilled in the art,
As long as various change in the spirit and scope of the present invention that appended claim limits and determines, these variations are aobvious and easy
See, all are using the innovation and creation of present inventive concept in the row of protection.
As shown in Figure 1, the genetic test status tracking management system based on wechat small routine, including operable interface with after
Platform；Database module of the backstage for deployment beyond the clouds；Operable interface includes the document management module being connect with database module,
And the detection request being connect with document management module submits module, detection request to check module, individual center module and science popularization
Classroom module.
Wherein, individual center module include user register unit, information modification unit, authorize other people check reporting unit,
System message checks unit, suggestion feedback unit and patient's adding device.
Database module is used to store all data informations in the system, and data include the correlation filled in during user's registration
Information, detection ask the essential information filled in when submitting, detection to ask the progress msg in checking, preserved in document management module
Data information and science popularization classroom in data information.
Document management module is used to preserve the data submitted when user submits detection to ask；User can pass through file at any time
Submission data is checked and changed to management module.
Detection request submits module by the module writes information and to submit base for the genetic test of user to be submitted to ask
Because detection is asked.
Module is checked in detection request：After user has submitted genetic test request, check that module is checked by detecting request
Detect the processing progress information of request；After examining report generates and is signed and issued by doctor, patient can check inspection in the module
Observe and predict announcement；Doctor can check the detection request oneself submitted or the inspection request that oneself patient submits in the module, understand inspection
Survey the progress of request processing.
Science popularization classroom module understands and is learned convenient for user for providing genetic disease popular science knowledge related to genetic test
It practises.
In individual center module：User register unit is for new user's registration and fills in relevant information, it is ensured that user can only
It checks and oneself submits genetic test request；The contact method filled in during registration, convenient in time by genetic test report generation information
Short massage notice user.
Information modification unit for user according to the variations of actual conditions, relevant information during time update user's registration,
User is notified in time after being generated convenient for examining report.
Other people is authorized to check that reporting unit function only opens registered user for patient, sometimes child or baby during patient
Youngster, registered user are its mother, if its mother knows about the snowball of detection progress, father can will check detection by the unit
Progress and the right of report authorize mother；Meanwhile need to fill in the relevant information of mother.
System message checks that unit for genetic test progress message to be automatically transmitted to user, understands in time convenient for user
Situation；Genetic test process link includes：Sampling, extraction DNA, gene sequencing, data analysis, making examining report and doctor examine
Core is signed and issued, and in detection process, often proceeds to a new link, and system can send out a piece of news to user automatically, within the message
Can remind user which link current genetic test is in, also it is surplus how long, user understands progress by the module and believes in time
Breath.
Suggestion feedback unit：After patient takes genetic test report after doctor, the query of generation or have what is be intended by
Opinion feeds back to third party's genetic test company by suggestion feedback unit, and passes through system message and check that unit checks phase
The reply situation answered.
Patient's adding device function only develops user for doctor, and doctor will need to carry out genetic test in oneself patient
Patient information is filled in, and genetic test is submitted to ask and check genetic test progress and examining report for user convenient for doctor.
In one embodiment of the invention, as shown in Fig. 2, the genetic test status tracking management based on wechat small routine
Method includes the following steps：
S1, new user's registration is carried out in individual center module, fills in relevant information, obtain login account and login system.
The relevant information of user is filled in, including user identity selection and its contact method；It can be in new user registration course
Selection fills in individual center mould patient's adding device in the block or other people is authorized to check information in reporting unit；User identity includes
Doctor and patient；When user is doctor, the relevant information for needing the patient for carrying out genetic test is filled in patient's adding device；
When user is patient, in mandate, other people check in reporting unit the relevant information for filling in licensee.
S2, submission genetic test is asked, and fill in essential information in detection asks to submit module.
Essential information includes name, gender, date of birth and illness history etc.；If there is family history, family can also be provided
History information, while photo some hereditary diseases can also be provided have apparent face or physical characteristic, these features and can pass through
It takes pictures upload and some other documentations etc.；Doctor can in the patient for being added to patient information selected as its carry
Genetic test request is handed over, and fills in essential information.
S3, check that module checks that progress msg is asked and its detected in submitted genetic test by detecting request；
Detection progress msg includes sampling, gene sequencing, data analysis, generation examining report and doctor's audit and signs and issues.When
When user is doctor, the audit report of third party's genetic test company generation check and audits and signs and issues；When user is suffers from
During person, check doctor sign and issue after audit report.
S4, the query to examining report is proposed, and check in system by individual center mould information feedback unit in the block
Corresponding return information is checked in unit.
Can be checked in any one step in above-mentioned steps S1~S4 by science popularization classroom module genetic disease and
Genetic test knowledge.
In one embodiment of the invention, third party's genetic test by system background management and can check doctor and trouble
The genetic test request and problem suggestion feedback that person user submits, and according to the job schedule of oneself, change doctor and patient institute
The genetic test progress status that can be checked.
Beneficial effects of the present invention are：The present invention based on wechat small routine genetic test status tracking management system and
Method, internet+thinking be introduced into traditional genetic test service center, the system background dispose beyond the clouds, user
It can momentarily be used by wechat using smart mobile phone, with more efficient reasonable manner unicom patient, doctor and third party's base
It because of testing agency, allows patient and doctor that can understand the latest developments of detection in time, and check examining report anywhere or anytime, solves
Determined inefficient and easy error in cooperation of existing patient, doctor and third party's genetic test mechanism the problem of, greatly
Patient and doctor are facilitated, while also alleviates communication burden to third party's genetic test mechanism, substantially improves existing procedure,
Efficiency is improved, each side for the whole flow process that lets on all has enjoyed the facility that the system is brought.
Claims (10)
1. the genetic test status tracking management system based on wechat small routine, which is characterized in that including operable interface with after
Platform；
The backstage is the database module of deployment beyond the clouds；
The operable interface includes the document management module being connect with database module and connects with the document management module
The detection request connect submits module, detection request to check module and individual center module；
The individual center module includes user register unit, information modification unit, other people is authorized to check that reporting unit, system disappear
Breath checks unit, suggestion feedback unit and patient's adding device.
2. the genetic test status tracking management system according to claim 1 based on wechat small routine, which is characterized in that
The operable interface of wechat small routine further includes the science popularization classroom module being connect with document management module.
3. the genetic test status tracking management system according to claim 2 based on wechat small routine, which is characterized in that
The database module is used to store all data informations in the system, and the data include what is filled in during user's registration
Relevant information, detection ask the essential information filled in when submitting, detection to ask the progress msg in checking, in document management module
Data information in the data information and science popularization classroom of preservation；
The document management module passes through the module and checks and repair for preserving for submitting the data submitted during detection request
Change the data of submission；
The detection request submits module genetic test to be submitted to ask for user, by the module writes essential information and submits
Genetic test is asked；
The detection request checks that module checks the processing progress information of detection request for user, and passes through the module and sign and issue inspection
Observe and predict announcement；
Science popularization classroom module is used to provide genetic disease popular science knowledge related to genetic test.
4. the genetic test status tracking management system according to claim 2 based on wechat small routine, which is characterized in that
The user register unit is for new user's registration and fills in relevant information；
Described information modification unit for user according to the variations of actual conditions, relevant information during time update user's registration；
It is described that other people is authorized to check that reporting unit authorizes the right for checking genetic test report to other people for patient；
The system message checks unit for genetic test progress message to be automatically transmitted to user；
The suggestion feedback unit is used to the query of user submitting to third party's genetic test company, and pass through system message and look into
See that unit checks corresponding reply situation；
Patient's adding device fills in the relevant information for needing the patient for carrying out genetic test for doctor.
5. the genetic test status tracking management method based on wechat small routine, which is characterized in that include the following steps：
S1, new user's registration is carried out in individual center module, fills in relevant information, obtain login account and login system；
S2, submission genetic test is asked, and fill in essential information in detection asks to submit module；
S3, check that module checks that progress msg is asked and its detected in submitted genetic test by detecting request；
S4, the query to examining report is proposed, and check unit in system by individual center mould information feedback unit in the block
In check corresponding return information.
6. the genetic test status tracking management method according to claim 5 based on wechat small routine, which is characterized in that
New user registration course is specially in the step S1：The relevant information of user is filled in, identity selection and its connection including user
It is mode；
Selection fills in individual center mould patient's adding device in the block or other people is authorized to check report in the new user registration course
Accuse the information in unit；
The user identity includes doctor and patient；
When the user is doctor, the relevant information for needing the patient for carrying out genetic test is filled in patient's adding device；
When the user is patient, in mandate, other people check in reporting unit the relevant information for filling in licensee.
7. the genetic test status tracking management method according to claim 5 based on wechat small routine, which is characterized in that
Essential information in the step S2 includes name, gender, date of birth, illness history, family history, photo and documentation.
8. the genetic test status tracking management method according to claim 6 based on wechat small routine, which is characterized in that
Progress msg is detected in the step S3 and includes sampling, gene sequencing, data analysis, generation examining report and doctor's audit label
Hair.
9. the genetic test status tracking management method according to claim 9 based on wechat small routine, which is characterized in that
In the step S3, when user is doctor, the audit report of third party's genetic test company generation check careful
Core is simultaneously signed and issued；
When user be patient when, check doctor sign and issue after audit report.
10. the genetic test status tracking management method according to claim 5 based on wechat small routine, feature exist
In can checking genetic disease and genetic test by science popularization classroom module in any one step in the step S1~S4
Knowledge.
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Application publication date: 20180710 |