CN110364267A - A kind of disease queue management system - Google Patents
A kind of disease queue management system Download PDFInfo
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- 201000010099 disease Diseases 0.000 title claims abstract description 35
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title claims abstract description 35
- 238000011160 research Methods 0.000 claims abstract description 53
- 238000012217 deletion Methods 0.000 claims abstract description 20
- 230000037430 deletion Effects 0.000 claims abstract description 20
- 238000012216 screening Methods 0.000 claims description 51
- 238000007726 management method Methods 0.000 claims description 49
- 230000006870 function Effects 0.000 claims description 27
- 238000000034 method Methods 0.000 claims description 20
- 238000013523 data management Methods 0.000 claims description 13
- 238000013461 design Methods 0.000 claims description 11
- 230000010354 integration Effects 0.000 claims description 7
- 238000012986 modification Methods 0.000 claims description 5
- 230000004048 modification Effects 0.000 claims description 5
- 238000012545 processing Methods 0.000 claims description 5
- 238000013479 data entry Methods 0.000 claims description 4
- 238000007405 data analysis Methods 0.000 claims description 2
- 238000004590 computer program Methods 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 2
- 238000000638 solvent extraction Methods 0.000 description 12
- 230000008569 process Effects 0.000 description 8
- 238000003745 diagnosis Methods 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 4
- 239000012472 biological sample Substances 0.000 description 3
- 230000008878 coupling Effects 0.000 description 3
- 238000010168 coupling process Methods 0.000 description 3
- 238000005859 coupling reaction Methods 0.000 description 3
- 238000013480 data collection Methods 0.000 description 3
- 238000013079 data visualisation Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000004891 communication Methods 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- 238000005192 partition Methods 0.000 description 2
- 238000007619 statistical method Methods 0.000 description 2
- 238000012550 audit Methods 0.000 description 1
- 238000013475 authorization Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
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- 230000004069 differentiation Effects 0.000 description 1
- 238000013507 mapping Methods 0.000 description 1
- 238000003032 molecular docking Methods 0.000 description 1
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- 238000004321 preservation Methods 0.000 description 1
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- 238000012800 visualization Methods 0.000 description 1
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Abstract
A kind of disease queue management system, the system comprises with lower module, administration of research activities module, specifically include function: application research, newly-increased, editor deletes disease queue, according to currently logged on user, shows the queue of the responsible queue of current login user and participation；Team Member's management, management study team and related participation member, carry out newly-increased editor and delete, and be associated with and correspond to group；Role Management is studied, system actor is managed, including newly-increased, editor, deletion, associated menu；File management is studied, the document information under current project, including project document and subject's document are managed, is added, file renames and delete operation.
Description
Technical Field
The invention belongs to the technical field of medical clinical research, and particularly relates to a disease queue management system.
Background
The diagnosis and treatment data of modern hospitals are rapidly accumulated, and the conventional recording mode for writing medical records cannot meet the scientific research requirement. Data in the systems of the hospital HIS, the LIS, the RIS and the like are independent from each other, so that the data cannot be directly exported for statistical analysis. Clinical data collection modes are different from Excel to SPSS, unified standards are lacked, data collection quality is uneven, and scientific research output is influenced.
For existing clinical research projects, different clinical study design types require different data acquisition modes, especially prospective studies involving the recording of follow-up data. The privacy of the diagnosis and treatment data of the hospital is strong, the hospital database needs to be accessed, and a data environment which is safe enough and relatively independent is needed. At present, hospitals have numerous scientific research projects, a unified management platform is lacked, and meanwhile, the roles in clinical scientific research projects are numerous, and the differentiation management is also needed.
Disclosure of Invention
The embodiment of the invention provides a disease queue management system, aiming at supporting the research process by taking clinical research as the center; a single disease category data warehouse is taken as a main part to serve the subject construction; establishing a clinical scientific research working platform; standardizing the management process of clinical research; the traceability of the research information is ensured.
In one embodiment of the present invention, a disease queue management system includes the following modules,
the research management module specifically comprises the functions of:
applying for research, newly adding, editing and deleting disease queues, and displaying queues in charge of and participating in the current login user according to the current login user;
managing team members, managing research team personnel and related participating members, performing new addition, editing and deletion, and associating corresponding groups;
researching role management, and managing system roles, including adding, editing, deleting and associating menus;
and researching file management, managing document information under the current project, including project documents and subject documents, and performing addition, file renaming and deletion operations.
The data entry module is used for checking the follow-up visit task information of the subject of the current project, displaying the visit progress of the subject in a list, completing the visit plan and filling the follow-up visit form of the current subject;
the case screening module is used for managing screened patient cases in the current disease queue, and comprises screening, grouping and deleting operations;
the form management module is used for managing CRF forms under the current project, including list display, addition, modification, form design, form copying, global parameter setting and deletion;
and the data management module is used for checking medical record information, managing all testees under the current project, and reporting errors, checking, deleting, uploading attachments and visiting the information of the testees.
The case screening module specifically comprises the following functions:
a screening list, which manages the screened patients in the current queue, and comprises screening, grouping and deleting operations;
screening rule configuration, namely managing the screening rules of the current queue, including adding, editing and deleting operations;
screening task setting, managing tasks of a current queue, including task configuration, starting/stopping, manual execution, editing and deleting operations;
and screening the logs and displaying the logs of task execution.
The embodiment of the invention is used for recording medical record information, follow-up visit information, biological sample information, basic research information and the like which enter patients in a special disease queue and can be used for scientific research, integrates full-dimensional data of scientific research of the patients, provides a more standard data management function, has a data visualization analysis function and is used for providing a preliminary scientific research clue. Thus, the beneficial effects obtained by the present invention include:
the system is used for establishing a prospective disease queue and follow-up visit, and recording structured data, wherein case data are all from a daily diagnosis and treatment process;
the system has a perfect data management function and a standard data management process, and the data collection quality is greatly improved;
the data security is greatly improved, traces are left in conventional operation, important operation is notified to a user, and all data are backed up in time;
the mobile terminal has a more standard follow-up design and supports data acquisition of the mobile terminal;
providing more efficient case screening rule design and supporting rapid grouping;
optimizing a data interface, and more efficiently capturing data generated in the diagnosis and treatment process;
can provide basic data visualization analysis;
provides clues for scientific research and can provide basis for individualized clinical decision.
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The above and other objects, features and advantages of exemplary embodiments of the present invention will become readily apparent from the following detailed description read in conjunction with the accompanying drawings. Several embodiments of the invention are illustrated by way of example, and not by way of limitation, in the figures of the accompanying drawings and in which:
FIG. 1 is a schematic diagram of a clinical study data management system according to one embodiment of the present invention
Detailed Description
In accordance with one or more embodiments, a disease cohort management system includes the following modules,
the research overview module specifically comprises:
the research progress shows the queue in which I participate in a list form according to the current login user; and displaying the number of cases in the scientific research queue and the statistics of the visiting progress in a chart form. The specific functional partitions are as follows:
1. queue that i participated in: the list shows the queues that the current loggers participate in.
2. The number of cases in a research queue: and displaying different queues and corresponding number of cases in a chart form.
3. Visit progress statistics: and displaying the case visiting progress corresponding to the project in a chart form, wherein the blue part is the number of visited persons, and the purple part is the number of non-visited persons.
Researching the calendar, the specific functional partition is as follows:
1. my calendar: and displaying all mode plans of the current login user in the current month in a calendar mode, and randomly performing task color by taking a project as a unit.
2. My event: and according to the date and the item selected by the user, displaying the backlog of the selected date and the item in a list.
The data entry module specifically includes again:
and the visit task is used for checking the follow-up task information of the subject of the current project. The list displays the visit progress of the subject and the completion condition of the visit plan. Follow-up form fill-out may be performed on the current subject. And specific function partitioning:
1. and filling out a follow-up form. The method comprises the following operation steps: 1. the subjects requiring the visit and the corresponding stage are selected. 2. Click on the link in the list, and 3 enter the form filling interface and fill in the corresponding data. 4. And saving the form.
2. Adding a private plan, and the operation steps are as follows: 1. and clicking the upper left corner of the form filling page to add a private plan. 2. And inputting a plan name and checking form information to be filled. And 3, clicking to save.
3. Different form data holds state descriptions. The form filling interface has several buttons of clear, save, submit, and data check, which are explained as follows:
and 4, rdr binding, namely, a form problem bound with rdr data appears after a problem title is completed with data filling, and the associated rdr data can be selected by clicking the icon.
The medical record screening module specifically comprises:
and screening lists, managing screened patients in the current queue, and comprising screening, grouping, deleting and the like. And specific function partitioning:
1. all the materials are put into a sieve, and the operation steps are as follows: 1. and clicking all the screening in the upper right corner of the query list, so that all the patient data in the list can be screened and added into the screening list.
2. And (2) batch screening, namely 1, checking data in the query list according to actual needs, 2, clicking batch screening, and adding the data into the screening list.
3. Batch deletion, operation steps: 1. and (4) checking data 2 in the query list according to actual needs, and clicking to delete in batches.
4. Screening, and operating: 1. according to actual requirements, selecting a needed patient, clicking a corresponding screening button and adding the patient into a screening list.
And 5, deleting, operating step: 1. according to actual requirements, a patient needing to be deleted is selected, and the corresponding deleting button is clicked.
6. All grouping, and the operation steps are as follows: 1. click on all entries in the top right of the filter list. 2. And filling the group time and the visit start time and grouping. 3. And (5) click determination.
And (4) screening rule configuration, namely managing the screening rules of the current queue. Including addition, editing and deletion. And specific function partitioning:
1. adding a rule newly, and the operation steps are as follows: 1. clicking the newly added rule on the upper right corner of the page. 2. And selecting the screening group required by the left side of the newly added interface, and clicking the newly added screening group. 3. And configuring corresponding screening conditions. 4. And selecting a corresponding storage mode according to actual requirements. Wherein,
(1) the screening group and the screening condition may be plural; the relationship between the screening group and the screening group is divided into ' and ' or ' two.
(2) Opening the template, and adding new rules based on the stored rule template.
(3) Saving the template: and saving the currently set rule as a template.
(4) Preservation: the current rule is saved.
(5) View result set: and taking the current rule as a screening condition, and directly importing the screened result sets into a screening queue, wherein the number of the screened result sets is at most 500 at one time.
2. Editing rules, and operating the steps: 1. and selecting a rule needing to be edited, and clicking to edit (stopping or deleting a task bound with the rule before editing the rule). 2. The current rule is modified. 3. And clicking to save.
3, deleting, and operating: and selecting a rule needing to be deleted, and clicking to delete. Before the rule is deleted, tasks bound with the rule need to be deleted.
And screening task setting and managing the tasks of the current queue. The method comprises task configuration, starting/stopping, manual execution, editing and deleting. And specific function partitioning:
1. configuring a new task, and the operation steps are as follows: 1. clicking the upper right corner to configure a new task. 2. Filling in corresponding task information 3, and clicking to determine.
2. Starting/stopping tasks, the operation steps are as follows: 1. and selecting the task needing starting/stopping, and clicking.
3. Manually executing, and the operation steps are as follows: 1. and selecting the task needing to be manually executed, and clicking the manual execution to immediately execute the current task once.
4. Editing tasks, and operating the steps: 1. and selecting a task needing to be edited, and clicking for editing (the task needs to be stopped before editing). 2. And modifying the task related information. 3 click determination.
5. Deleting, operating step: 1. and selecting the task to be deleted, clicking to delete, and determining.
And screening the logs, and displaying the logs of the task execution, wherein the logs exist as long as the tasks are executed regardless of the success of the task execution.
The research management module specifically includes:
new research, functional explanation: adding, editing and deleting queues; and displaying the queues which are in charge of me and the queues which are participated in me according to the current login user. And specific function partitioning:
1. newly adding disease seeds, and the operation steps are as follows: 1. click the new queue button. And 2, recording queue information. And 3, the click is completed.
2. Editing disease species, and operating steps: 1. and selecting a queue to be edited and clicking for editing. 2 modifying the queue information. 3 click determination.
3. Deleting the queue, and the operation steps are as follows: 1. and selecting the queue needing to be deleted and clicking to delete. 2. And clicking to confirm.
4. Queue i are responsible for: and displaying the queue of which the current login user is the responsible person in a list form.
5. Queue that i participated in: the list shows the queue with the currently enrolled patient as a participant.
And managing all researchers and related participating members in the management yard by the team members. The new edition deletion and the association of the corresponding group can be carried out. And specific function partitioning:
1. adding member information, and operating the steps: 1. and clicking the information of the new member. 2. And inputting related information. 3. And (5) click determination.
2. Editing member information, and operating the steps: 1. the member to be edited is selected. 2, modifying the relevant information and determining.
3. Association group, operation step: 1. a member requiring an association group is selected. 2. And associating corresponding group information, and determining.
4. Delete, 1. select the member that needs to be deleted. 2. Click delete and confirm twice.
And researching role management, and managing system roles, including adding, editing, deleting and associating menus. And specific function partitioning:
1. newly adding role information, and the operation steps are as follows: 1. and clicking the information of the newly added role. 2. And inputting related information. 3. And (5) click determination.
2. Editing role information, and operating the steps of: 1. and selecting the role to be edited and clicking for editing. 2. And modifying the role information. 3. And (5) click determination.
3. And the association menu is a current role and associates menu items. The method comprises the following operation steps: 1. selecting the character needing the associated menu clicks the associated menu. 2. And checking the corresponding menu. 3. And (5) click determination.
4. Deleting, operating step: 1. and selecting the roles to be deleted, and clicking to delete. 2. The deletion is confirmed.
And researching file management, managing document information under the current project, including project documents and subject documents, and adding, renaming and deleting files. And specific function partitioning:
1. adding a document, and the operation steps are as follows: 1. click to add the file. 2. A file and file type are selected. 3 click determination.
2. Renaming, operation steps: 1. and selecting the file to be renamed, and clicking renaming. 2. The file name is entered. 3 click determination.
3. Deleting, operating step: 1. and selecting the files needing to be deleted, clicking to delete, and determining.
File type maintenance, functional description: and maintaining all file types of the current project, including adding a file type, editing and deleting. The file type is used when the file is uploaded. The file type list is used for storing the application materials, the audit materials, the informed consent, and other four items which can not be edited and deleted. And specific function partitioning:
1. adding a file type newly, and the operation steps are as follows: 1. clicking the newly added file and inputting relevant information. 2. And (5) click determination.
2. Editing, and operating: 1. and 2, selecting the file type needing to be modified, and clicking to edit and modify the related information. 3. And (5) click determination.
3. Deleting, operating step: 1. the type of file to be deleted is selected. 2. Click delete and confirm twice. A form management module having a form management module further comprising:
and configuring a module, and managing a CRF form under the current project. The method comprises list display, addition, modification, form design, copying, global setting and deletion. And specific function partitioning:
1. list display and screening, and the operation steps are as follows: and inputting corresponding screening information in the screening box, clicking for screening, and screening out corresponding form information.
2. Adding a new form, and the operation steps are as follows: 1. click the newly added button in the upper right corner. And 2, inputting form information, wherein the form name is not repeatable. 3. And (5) click determination.
3. Modifying the form, and the operation steps are as follows: 1. and selecting the form to be modified, and clicking to edit. 2. And modifying the related information. 3. And (5) click determination.
4. Designing a form, and the operation steps are as follows: 1. and selecting the form to be set, and clicking the setting form. 2. And dragging the corresponding control from the right side to the left side area according to actual needs, and putting the control at a proper position. 3. Clicking the dragged control, and entering a control setting interface. 4. Setting control corresponding information (if the current control needs cdr binding, click determination after binding) and click determination. 5. Clicking the top right save button to save the current form.
5. And (4) rule configuration, wherein the rule configuration needs to enter a form design interface firstly and then enter a form rule configuration interface. The method comprises the following operation steps: 1. and selecting a form needing to be subjected to rule configuration, and clicking the form design. And 2, clicking the rule setting in the upper right corner of the form design interface. 3. Click on the creation rule. 4. And entering rule information. 5. Conditions and results are configured for the rules. 6. And clicking to save. Wherein,
(1) conditions and results are all questions of the current form, and the user chooses to do so.
(2) Conditions need to be added first, and the result is set according to the conditions. The calculation formula may have no added condition, and other rules need to be added.
(3).
6. Copying the form, and the operation steps are as follows: 1. and selecting a form to be copied and clicking to copy. 2. And inputting copy table information. 3. And (5) click determination.
7. Set global/cancel global: the global form is system visible and the non-global form is current project visible. The method comprises the following operation steps: 1. and selecting the form which needs to be set to be global, and clicking to set the global/cancel the global.
8. Deleting, operating step: 1. and selecting the form to be deleted, and clicking to delete. 2. And (5) click determination.
And the visit configuration is used for managing the stage (visit plan) of the current project, including adding a visit plan, editing and deleting. And specific function partitioning:
1. adding a visit plan, and operating the following steps: 1. and clicking a newly added visit plan. 2. And inputting related information. 3. And (5) click determination.
2. Editing, and operating: 1. and selecting a plan to be edited and clicking for editing. 2. And modifying the related information. 3. And (5) click determination.
3. Deleting, operating step: 1. and selecting an access plan needing to be deleted, and clicking to delete. 2. The deletion is confirmed. And the form mapping function description is a form corresponding to the project visit plan association plan. The method comprises the following operation steps:
1. a plan is selected that requires an associated form. 2. And clicking the associated form, checking the required form, and clicking for determination. The data management module specifically includes:
medical record information is checked, all subjects under the current project are managed, error checking, deleting, attachment uploading and visiting are performed, the subjects can be searched according to conditions and sorted according to time, and specific functions are divided into regions:
1. visiting and operating steps: 1. selecting a subject needing visiting, clicking the visiting, and entering a visiting interface.
2. The accessory comprises the following operation steps: 1. selecting the subject needing to upload the attachment, and clicking the attachment. 2 enter attachment viewing interface. And 3, clicking the added file at the upper left corner if the attachment needs to be uploaded. And 4, determining after relevant information is input.
3. Deleting, operating step: 1 selects the data to be deleted. 2 click delete and confirm.
4. 360-degree view of a patient, and the operation steps are as follows: 1. the subject is selected and the corresponding patient 360 button is clicked.
5. Editing, and operating: 1. selecting the subject needing editing. 2 modify the corresponding information. Click save and return 3.
6. Stopping visiting, and operating the steps of: 1, selecting the subject needing to stop visit. 2 click stop visit and secondary confirmation. And the patient stopping visiting can not start the visiting again and can not enter the visiting interface, and if the filled data needs to be checked, the data can be checked in the data visiting interface.
Data export, statistical analysis of all subjects and filled-in form data of the current project, and data download. And specific function partitioning:
1. data checking, operation steps: 1. click on the form selection. 2. Check the form 3 that wants to view, click the query button.
The system help module, including the help manual, helps the user to become familiar with the operation flow, and can be downloaded to local viewing by clicking a button.
A system maintenance module comprising
The user activity is used for displaying the login times of managers and other research color correction and can be inquired according to time.
System operation log, functional description: the method is used for displaying which modules are operated by a login user, and the user time query can be classified according to the queue.
The disease queue management system has the advantages that the disease queue management system provides a clinical scientific research management method, the management system also provides authorization management, form auxiliary filling, visualization tools, document checking and the like, and the clinical scientific research management level is greatly improved. The management system is based on the existing clinical data network structure, adopts various research and analysis methods for clinical data, and ensures the rigorous specification and high efficiency of the clinical research data.
In accordance with one or more embodiments, as shown in fig. 1, a clinical study data management system, the system collectively comprising,
the system comprises a plurality of clinical data sources, a plurality of data processing units and a plurality of data processing units, wherein each clinical data source comes from different medical departments of a hospital, and the formats of the clinical data are different;
a data integration platform for data integration after acquiring data from the clinical data source, including data analysis, data quality, data reporting, main data service and data integration service,
a data warehouse for extracting data from the data integration platform, including a scientific research data warehouse and a clinical data warehouse which are isolated from each other,
a disease cohort management system, the system comprising the following modules,
the research management module specifically comprises the functions of:
applying for research, newly adding, editing and deleting disease queues, and displaying queues in charge of and participating in the current login user according to the current login user;
managing team members, managing research team personnel and related participating members, performing new addition, editing and deletion, and associating corresponding groups;
researching role management, and managing system roles, including adding, editing, deleting and associating menus;
and researching file management, managing document information under the current project, including project documents and subject documents, and performing addition, file renaming and deletion operations.
The software developed according to the embodiment of the invention is used for recording medical record information, follow-up visit information, biological sample information, basic research information and the like which enter patients in a special disease queue and can be used for scientific research, integrating full-dimensional data of scientific research of the patients, providing a more standard data management function, having a data visualization analysis function and being used for providing a preliminary scientific research clue. The functions of the software include:
1. the system is used for establishing a prospective disease queue and follow-up visit, and recording structured data, wherein case data are all from a daily diagnosis and treatment process, and the system has a perfect data management function and a standard data management flow;
2. conventional operation is marked, important operation is informed to a user, and all data are backed up in time;
3. supporting data acquisition of a mobile terminal;
4. providing more efficient case screening rule design and supporting rapid grouping;
5. and a data interface is optimized, and data generated in the diagnosis and treatment process can be captured more efficiently.
The embodiment of the invention is used for docking the RDR database and the biological sample library of the hospital, avoids repeated entry of researchers to a certain extent, has a mobile follow-up function, can simplify the follow-up process, and improves compliance, thereby improving the research quality.
In the several embodiments provided in the present application, it should be understood that the disclosed system, 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 also be an electric, mechanical or other form of connection.
In addition, functional units in the embodiments of the present invention 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 invention essentially or partially contributes to the prior art, or all or part of the technical solution can be embodied in the form of a software product stored in a storage medium and including instructions for causing a computer device (which may be a personal computer, a server, or a network device) to execute all or part of the steps of the method according to the embodiments of the present invention. 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.
While the invention has been described with reference to specific embodiments, the invention is not limited thereto, and various equivalent modifications and substitutions can be easily made by those skilled in the art within the technical scope of the invention. Therefore, the protection scope of the present invention shall be subject to the protection scope of the claims.
Claims (8)
1. A disease queue management system, characterized in that the system comprises the following modules,
the research management module specifically comprises the functions of:
applying for research, newly adding, editing and deleting disease queues, and displaying queues in charge of and participating in the current login user according to the current login user;
managing team members, managing research team personnel and related participating members, performing new addition, editing and deletion, and associating corresponding groups;
researching role management, and managing system roles, including adding, editing, deleting and associating menus;
and researching file management, managing document information under the current project, including project documents and subject documents, and performing addition, file renaming and deletion operations.
2. The disease queue management system of claim 1, wherein the system further comprises:
the data entry module is used for checking the follow-up visit task information of the subject of the current project, displaying the visit progress of the subject in a list, completing the visit plan and filling the follow-up visit form of the current subject;
the case screening module is used for managing screened patient cases in the current disease queue, and comprises screening, grouping and deleting operations;
the form management module is used for managing CRF forms under the current project, including list display, addition, modification, form design, form copying, global parameter setting and deletion;
and the data management module is used for checking medical record information, managing all testees under the current project, and reporting errors, checking, deleting, uploading attachments and visiting the information of the testees.
3. The disease queue management system of claim 2, wherein the case screening module specifically comprises the functions of:
a screening list, which manages the screened patients in the current queue, and comprises screening, grouping and deleting operations;
screening rule configuration, namely managing the screening rules of the current queue, including adding, editing and deleting operations;
screening task setting, managing tasks of a current queue, including task configuration, starting/stopping, manual execution, editing and deleting operations;
and screening the logs and displaying the logs of task execution.
4. A disease cohort management platform, comprising a server having a memory; and
a processor coupled to the memory, the processor configured to execute instructions stored in the memory, the processor performing research management operations, in turn comprising:
applying for research, newly adding, editing and deleting disease queues, and displaying queues in charge of and participating in the current login user according to the current login user;
managing team members, managing research team personnel and related participating members, performing new addition, editing and deletion, and associating corresponding groups;
researching role management, and managing system roles, including adding, editing, deleting and associating menus;
and researching file management, managing document information under the current project, including project documents and subject documents, and performing addition, file renaming and deletion operations.
5. A disease queue management terminal, characterized in that the terminal issues a request to the disease queue management platform of claim 4, receiving a feedback of result data of said disease queue management platform.
6. A method for disease cohort management, comprising the steps of,
research management specifically comprises the following steps:
applying for research, newly adding, editing and deleting disease queues, and displaying queues in charge of and participating in the current login user according to the current login user;
managing team members, managing research team personnel and related participating members, performing new addition, editing and deletion, and associating corresponding groups;
researching role management, and managing system roles, including adding, editing, deleting and associating menus;
researching file management, managing document information under the current project, including project documents and subject documents, and performing addition, file renaming and deletion operations;
data entry, wherein the follow-up visit task information of the subject of the current project is checked, the visit progress of the subject is displayed in a list, the completion condition of the visit plan is displayed, and the follow-up visit form is filled in the current subject;
case screening, namely managing screened patient cases in the current disease queue, wherein screening, grouping and deleting operations are included;
form management, namely managing CRF forms under the current project, including list display, addition, modification, form design, copying, global parameter setting and deletion operation;
and the data management is used for checking medical record information, managing all testees under the current project, and reporting errors, checking, deleting, uploading attachments and visiting the information of the testees.
7. A storage medium on which a computer program is stored which, when executed by a processor, carries out the method of claim 6.
8. A clinical research data management system, comprising in combination,
the system comprises a plurality of clinical data sources, a plurality of data processing units and a plurality of data processing units, wherein each clinical data source comes from different medical departments of a hospital, and the formats of the clinical data are different;
the data integration platform is used for integrating data after acquiring the data from the clinical data source, and comprises data analysis, data quality, data report, main data service and data integration service;
the data warehouse is used for extracting data from the data integration platform and comprises a scientific research data warehouse and a clinical data warehouse, and the scientific research data warehouse and the clinical data warehouse are isolated from each other; and
the disease cohort management system of claim 1.
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